U.S. patent application number 15/485203 was filed with the patent office on 2017-08-03 for oxazole compound and pharmaceutical composition.
This patent application is currently assigned to Otsuka Pharmaceutical Co., Ltd.. The applicant listed for this patent is Otsuka Pharmaceutical Co., Ltd.. Invention is credited to Junpei HARUTA, Hidetaka HIYAMA, Masaya KATO, Hideki KITAGAKI, Minoru OKADA, Norifumi SATO, Tomonori SHIBATA, Tetsuyuki UNO.
Application Number | 20170216260 15/485203 |
Document ID | / |
Family ID | 37879936 |
Filed Date | 2017-08-03 |
United States Patent
Application |
20170216260 |
Kind Code |
A1 |
OKADA; Minoru ; et
al. |
August 3, 2017 |
OXAZOLE COMPOUND AND PHARMACEUTICAL COMPOSITION
Abstract
The present invention provides a oxazole compound represented by
Formula (1), or a salt thereof: ##STR00001## wherein R.sup.1 is an
aryl group which may have one or more substituents; R.sup.2 is an
aryl group or a nitrogen atom-containing heterocyclic group each of
which may have one or more substituents; and W is a divalent group
represented by --Y.sup.1-A.sup.1- or --Y.sup.2--C(.dbd.O)-- wherein
Y.sup.1 is a group such as --C(.dbd.O)--, A.sup.1 is a group such
as a lower alkylene group, and Y.sup.2 is a group such as a
piperazinediyl group. The oxazole compound has a specific
inhibitory action against phosphodiesterase 4.
Inventors: |
OKADA; Minoru; (Hyogo,
JP) ; KATO; Masaya; (Hyogo, JP) ; SATO;
Norifumi; (Hyogo, JP) ; UNO; Tetsuyuki;
(Hyogo, JP) ; KITAGAKI; Hideki; (Hyogo, JP)
; HARUTA; Junpei; (Hyogo, JP) ; HIYAMA;
Hidetaka; (Hyogo, JP) ; SHIBATA; Tomonori;
(Hyogo, JP) |
|
Applicant: |
Name |
City |
State |
Country |
Type |
Otsuka Pharmaceutical Co., Ltd. |
Tokyo |
|
JP |
|
|
Assignee: |
Otsuka Pharmaceutical Co.,
Ltd.
Tokyo
JP
|
Family ID: |
37879936 |
Appl. No.: |
15/485203 |
Filed: |
April 11, 2017 |
Related U.S. Patent Documents
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Application
Number |
Filing Date |
Patent Number |
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14104871 |
Dec 12, 2013 |
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15485203 |
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12090951 |
Mar 26, 2009 |
8637559 |
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PCT/JP2006/323066 |
Nov 14, 2006 |
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14104871 |
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Current U.S.
Class: |
1/1 |
Current CPC
Class: |
A61P 25/16 20180101;
A61P 37/08 20180101; A61P 19/02 20180101; A61P 37/00 20180101; A61K
31/4439 20130101; A61P 25/24 20180101; A61P 11/00 20180101; A61P
27/02 20180101; A61P 27/16 20180101; A61P 17/00 20180101; A61K
31/421 20130101; A61P 17/14 20180101; A61K 31/4709 20130101; A61P
25/22 20180101; C12N 9/16 20130101; C07D 263/34 20130101; C07D
263/32 20130101; C07D 413/06 20130101; C07D 413/12 20130101; A61K
31/497 20130101; A61P 25/28 20180101; A61P 43/00 20180101; A61P
25/18 20180101; A61P 17/06 20180101; A61P 11/06 20180101; A61P 1/04
20180101; C12Y 301/04012 20130101; A61P 29/00 20180101; A61K
31/5377 20130101; A61K 31/496 20130101 |
International
Class: |
A61K 31/421 20060101
A61K031/421; A61K 31/497 20060101 A61K031/497; C12N 9/16 20060101
C12N009/16; A61K 31/496 20060101 A61K031/496; A61K 31/5377 20060101
A61K031/5377; A61K 31/4439 20060101 A61K031/4439; A61K 31/4709
20060101 A61K031/4709 |
Foreign Application Data
Date |
Code |
Application Number |
Nov 15, 2005 |
JP |
2005-330590 |
Claims
1-14. (canceled)
15. A method for obtaining cells expressing phosphodiesterase (PDE)
4, comprising: preparing a vector containing cDNA encoding human
PDE4, introducing the vector into mammalian cells, cultivating the
cells in a medium, and collecting the cells
16. The method of claim 15, wherein the cells are COS-7 cells.
17. The method of claim 15, wherein the vector is a plasmid
vector.
18-24. (canceled)
Description
TECHNICAL FIELD
[0001] The present invention relates to new oxazole compounds and
pharmaceutical compositions.
BACKGROUND ART
[0002] Various oxazole compounds have been developed and are
disclosed in documents such as WO 03/072102, WO 98/15274, etc.
However, the oxazole compounds of the present invention are not
disclosed in any literature.
[0003] Some compounds having a specific inhibitory action against
phosphodiesterase 4 (PDE4) have been reported. However, known PDE4
inhibitors have problems of side effects such as vomit induction,
nausea, etc. and/or a defect of insufficient PDE4 inhibitory
action. Therefore, known PDE4 inhibitors are not clinically used as
therapeutic agents.
DISCLOSURE OF THE INVENTION
[0004] An object of the present invention is to provide a compound
that has a PDE4 inhibitory action and is free from the
above-mentioned problems of the prior art.
[0005] The present inventors conducted extensive research to solve
the above problems, and succeeded in synthesizing an oxazole
compound with a novel structure, the compound having high
specificity and a strong PDE4 inhibitory action. Further, the
present inventors found that the oxazole compound is capable of
exhibiting preventive and/or therapeutic effects on PDE-mediated
diseases, and in particular atopic dermatitis, based on its PDE4
inhibitory action. Furthermore, the inventors found that the
compound has low penetration into blood when administered
transdermally, and thus has low systemic side effects.
[0006] The present inventors further found that the oxazole
compound is capable of exhibiting a tumor necrosis factor-.alpha.
(TNF-.alpha.) production inhibitory action.
[0007] In chronic inflammatory diseases such as autoimmune diseases
and allergic diseases, cytokines produced by immunocompetent cells
are known to be important inflammatory mediators, and among such
cytokines, TNF-.alpha. is presumed to play a particularly important
role. Therefore, the oxazole compound of the present invention is
extremely effective for the treatment of TNF-.alpha.-mediated
diseases.
[0008] The present invention has been accomplished by further
research based on the above findings.
[0009] The present invention provides a oxazole compound, a
pharmaceutical composition comprising said compound, a use of said
compound, a method for treating or preventing a disorder, and a
process for producing said compound, as described in Item 1 to 14
below.
[0010] Item 1. An oxazole compound represented by Formula (1)
##STR00002##
wherein R.sup.1 is an aryl group which may have one or more
substituents selected from the following (1-1) to (1-11): (1-1)
hydroxy groups, (1-2) unsubstituted or halogen-substituted lower
alkoxy groups, (1-3) lower alkenyloxy groups, (1-4) lower
alkynyloxy groups, (1-5) cyclo C.sub.3-8 alkyl lower alkoxy groups,
(1-6) cyclo C.sub.3-8 alkyloxy groups, (1-7) cyclo C.sub.3-8
alkenyloxy groups, (1-8) dihydroindenyloxy groups, (1-9) hydroxy
lower alkoxy groups, (1-10) oxiranyl lower alkoxy groups, and
(1-11) protected hydroxy groups;
[0011] R.sup.2 is an aryl group or a nitrogen atom-containing
heterocyclic group each of which may have one or more substituents
selected from the following (2-1) to (2-10):
(1-1) hydroxy groups, (2-2) unsubstituted or halogen-substituted
lower alkoxy groups, (2-3) unsubstituted or halogen-substituted
lower alkyl groups, (2-4) lower alkenyloxy groups, (2-5) halogen
atoms, (2-6) lower alkanoyl groups, (2-7) lower alkylthio groups,
(2-8) lower alkylsulfonyl groups, (2-9) oxo groups, and (2-10)
lower alkoxy lower alkoxy groups; and W is a divalent group
represented by Formula (i) or (ii):
--Y.sup.1-A.sup.1- Formula (i)
--Y.sup.2--C(.dbd.O)-- Formula (ii)
wherein A.sup.1 is a lower alkenylene group, or a lower alkylene
group which may have one or more substituents selected from the
group consisting of hydroxy groups and lower alkoxycarbonyl groups,
Y.sup.1 is a direct bond, --C(.dbd.O)--, --C(.dbd.O)--N(R.sup.3)--,
--N(R.sup.4)--C(.dbd.O)--, --S(O).sub.m--NH--, or --S(O).sub.n--
wherein R.sup.3 and R.sup.4 are each independently a hydrogen atom
or a lower alkyl group, and m and n are each independently an
integer from 0 to 2, and Y.sup.2 is a piperazinediyl group, or a
divalent group represented by Formula (iii) or (iv):
--C(.dbd.O)-A.sup.2-N(R.sup.5)-- Formula (iii)
-A.sup.3-N(R.sup.6)-- Formula (iv)
wherein A.sup.2 and A.sup.3 are each independently a lower alkylene
group, and R.sup.5 and R.sup.6 are each independently a hydrogen
atom or a lower alkyl group; or a salt thereof.
[0012] Item 2. The compound according to item 1,
wherein R.sup.1 is a phenyl group which has 1 to 3 substituents
selected from the following (1-2), (1-3), (1-4) and (1-5): (1-2)
unsubstituted or halogen-substituted lower alkoxy groups, (1-3)
lower alkenyloxy groups, (1-4) lower alkynyloxy groups, and (1-5)
cyclo C.sub.3-8 alkyl lower alkoxy groups; R.sup.2 is a phenyl
group or a pyridyl group each of which may have 1 to 3 substituents
selected from the group consisting of the following (2-2), (2-3),
(2-4) and (2-5): (2-2) unsubstituted or halogen-substituted lower
alkoxy groups, (2-3) unsubstituted or halogen-substituted lower
alkyl groups, (2-4) lower alkenyloxy groups, and (2-5) halogen
atoms; W is a divalent group represented by Formula (i):
--Y.sup.1-A.sup.1- Formula(i)
wherein A.sup.1 is a lower alkylene group, and Y.sup.1 is
--C(.dbd.O)-- or --C(.dbd.O)--N(R.sup.3)-- wherein R.sup.3 is a
hydrogen atom.
[0013] Item 3. The compound according to item 2,
wherein R.sup.1 is a phenyl group having two substituents selected
from the following (1-2), (1-3), (1-4) and (1-5): (1-2)
unsubstituted or halogen-substituted lower alkoxy groups, (1-3)
lower alkenyloxy groups, (1-4) lower alkynyloxy groups, and (1-5)
cyclo C.sub.3-8 alkyl lower alkoxy groups; R.sup.2 is a phenyl
group or a pyridyl group each of which may have 1 to 2 substituents
selected from the following (2-2), (2-3), (2-4) and (2-5): (2-2)
unsubstituted or halogen-substituted lower alkoxy groups, (2-3)
unsubstituted or halogen-substituted lower alkyl groups, (2-4)
lower alkenyloxy groups, and (2-5) halogen atoms; and W is a
divalent group represented by Formula (i):
--Y.sup.1-A.sup.1- Formula (i)
wherein A.sup.1 is a lower alkylene group, and Y.sup.1 is
--C(.dbd.O)-- or --C(.dbd.O)--N(R.sup.3)-- wherein R.sup.3 is a
hydrogen atom.
[0014] Item 4. The compound according to item 3,
wherein R.sup.1 is a phenyl group substituted on the phenyl ring
with two lower alkoxy groups, a phenyl group substituted on the
phenyl ring with one lower alkoxy group and one cyclo C.sub.3-8
alkyl lower alkoxy group, a phenyl group substituted on the phenyl
ring with one lower alkoxy group and one halogen-substituted lower
alkoxy group, a phenyl group substituted on the phenyl group with
one lower alkoxy group and one lower alkenyloxy group, a phenyl
group substituted on the phenyl ring with one halogen-substituted
lower alkoxy group and one cyclo C.sub.3-8 alkyl lower alkoxy
group, a phenyl group substituted on the phenyl ring with one
halogen-substituted lower alkoxy group and one lower alkenyloxy
group, or a phenyl group substituted on the phenyl ring with two
halogen-substituted lower alkoxy groups; R.sup.2 is a lower
alkoxyphenyl group, a lower alkenyloxyphenyl group, a
halogen-substituted lower alkoxyphenyl group, a lower alkylpyridyl
group, or a phenyl group substituted on the phenyl ring with one
lower alkoxy group and one halogen atom; and W is a divalent group
represented by Formula (i):
--Y.sup.1-A.sup.1- Formula (i)
wherein A.sup.1 is a C.sub.1-4 alkylene group, and Y.sup.1 is
--C(.dbd.O)-- or --C(.dbd.O)--N(R.sup.3)-- wherein R.sup.3 is a
hydrogen atom.
[0015] Item 5. The compound according to item 4,
wherein R.sup.1 is a phenyl group substituted on the phenyl ring
with two lower alkoxy groups, a phenyl group substituted on the
phenyl ring with one lower alkoxy group and one cyclo C.sub.3-8
alkyl lower alkoxy group, a phenyl group substituted on the phenyl
ring with one lower alkoxy group and one halogen-substituted lower
alkoxy group, a phenyl group substituted on the phenyl group with
one lower alkoxy group and one lower alkenyloxy group, a phenyl
group substituted on the phenyl ring with one halogen-substituted
lower alkoxy group and one cyclo C.sub.3-8 alkyl lower alkoxy
group, a phenyl group substituted on the phenyl ring with one
halogen-substituted lower alkoxy group and one lower alkenyloxy
group, or a phenyl group substituted on the phenyl ring with two
halogen-substituted lower alkoxy groups; R.sup.2 is a lower
alkoxyphenyl group, a lower alkenyloxy phenyl group, a
halogen-substituted lower alkoxyphenyl group, a lower alkylpyridyl
group, or a phenyl group substituted on the phenyl ring with one
lower alkoxy group and one halogen atom; and W is a divalent group
represented by Formula (i):
--Y.sup.1-A.sup.1- Formula (i)
wherein A.sup.1 is a C.sub.1-4 alkylene group, and
Y.sup.1 is --C(.dbd.O)--.
[0016] Item 6. The compound according to item 4,
wherein R.sup.1 is a phenyl group substituted on the phenyl ring
with one lower alkoxy group and one halogen-substituted lower
alkoxy group, a phenyl group substituted on the phenyl ring with
one halogen-substituted lower alkoxy group and one cyclo C.sub.3-8
alkyl lower alkoxy group, or a phenyl group substituted on the
phenyl ring with one halogen-substituted lower alkoxy group and one
lower alkenyloxy group; R.sup.2 is a lower alkoxyphenyl group or a
lower alkylpyridyl group; and W is a divalent group represented by
Formula (i):
--Y.sup.1-A.sup.1- Formula (i)
wherein A.sup.1 is a C.sub.1-4 alkylene group, and Y.sup.1 is
--C(.dbd.O)--N(R.sup.3)-- wherein R.sup.3 is a hydrogen atom.
[0017] Item 7. A pharmaceutical composition comprising the compound
or salt according to any one of items 1 to 6 as an active
ingredient and a pharmaceutically acceptable carrier.
[0018] Item 8. A pharmaceutical composition for treating or
preventing phosphodiesterase 4-mediated and/or tumor necrosis
factor-.alpha.-mediated diseases, the composition comprising the
compound or salt according to any one of items 1 to 6.
[0019] Item 9. A pharmaceutical composition for treating or
preventing atopic dermatitis, the composition comprising the
compound or salt according to any one of items 1 to 6.
[0020] Item 10. A process for producing a pharmaceutical
composition, the process comprising mixing the compound or salt
according to any one of items 1 to 6 with a pharmaceutically
acceptable carrier.
[0021] Item 11. Use of the compound or salt according to any one of
items 1 to 6 as a drug.
[0022] Item 12. Use of the compound or salt according to any one of
items 1 to 6 as a phosphodiesterase 4 inhibitor and/or tumor
necrosis factor-.alpha. production inhibitor.
[0023] Item 13. A method for treating or preventing
phosphodiesterase 4-mediated and/or tumor necrosis
factor-.alpha.-mediated diseases, the method comprising
administering the compound or salt according to any one of items 1
to 6 to human or animal.
[0024] Item 14. A process for producing an oxazole compound
represented by Formula (1):
##STR00003##
wherein R.sup.1, R.sup.2 and W are the same as defined in item 1,
or a salt thereof, the process comprising a reaction of a compound
represented by Formula (2):
##STR00004##
wherein R.sup.2 and W are the same as defined above, and X is a
halogen atom, or a salt thereof, with a compound represented by
Formula (3):
##STR00005##
wherein R.sup.1 is the same as defined above, or a salt
thereof.
[0025] In Formula (1), R.sup.1 is preferably a phenyl group. The
phenyl group represented by R.sup.1 preferably has 1 to 3, and more
preferably 2, substituents selected from the group consisting of
(1-2) unsubstituted or halogen-substituted lower alkoxy groups,
(1-3) lower alkenyloxy groups, (1-4) lower alkynyloxy groups, and
(1-5) cyclo C.sub.3-8 alkyl lower alkoxy groups.
[0026] In Formula (1), R.sup.2 is preferably a phenyl group or a
pyridyl group. The phenyl group or pyridyl group represented by
R.sup.2 preferably has 1 to 3, and more preferably 1, substituents
selected from the group consisting of (2-2) unsubstituted or
halogen-substituted lower alkoxy groups, (2-3) unsubstituted or
halogen-substituted lower alkyl groups, (2-4) lower alkenyloxy
groups, and (2-5) halogen atoms.
[0027] In Formula (1), W is preferably a divalent group represented
by Formula (i) --Y.sup.1-A.sup.1-. A.sup.1 is preferably a lower
alkylene group; Y.sup.1 is preferably --C(.dbd.O)-- or
--C(.dbd.O)--N(R.sup.3)--; and R.sup.3 is preferably a hydrogen
atom.
[0028] Among the oxazole compounds of the present invention, those
represented by Formula (1A) and salts thereof are preferable, and
those represented by Formula (1B) and salts thereof are more
preferable.
##STR00006##
wherein R.sup.1 is a phenyl group having two substituents selected
from the following (1-2), (1-3), (1-4) and (1-5): (1-2)
unsubstituted or halogen-substituted lower alkoxy groups, (1-3)
lower alkenyloxy groups, (1-4) lower alkynyloxy groups, and (1-5)
cyclo C.sub.3-8 alkyl lower alkoxy groups; R.sup.2 is a phenyl
group or a pyridyl group each of which may have one or more
substituents selected from the following (2-2), (2-3), (2-4) and
(2-5): (2-2) unsubstituted or halogen-substituted lower alkoxy
groups, (2-3) unsubstituted or halogen-substituted lower alkyl
groups, (2-4) lower alkenyloxy groups, and (2-5) halogen atoms; and
W is a divalent group represented by Formula (i):
--Y.sup.1-A.sup.1- Formula (i)
wherein A.sup.1 is a lower alkylene group, and Y.sup.1 is
--C(.dbd.O)-- or --C(.dbd.O)--N(R.sup.3)-- wherein R.sup.3 is a
hydrogen atom.
##STR00007##
wherein R.sup.1 is a phenyl group substituted on the phenyl ring
with two lower alkoxy groups, a phenyl group substituted on the
phenyl ring with one lower alkoxy group and one cyclo C.sub.3-8
alkyl lower alkoxy group, a phenyl group substituted on the phenyl
ring with one lower alkoxy group and one halogen-substituted lower
alkoxy group, a phenyl group substituted on the phenyl group with
one lower alkoxy group and one lower alkenyloxy group, a phenyl
group substituted on the phenyl ring with one halogen-substituted
lower alkoxy group and one cyclo C.sub.3-8 alkyl lower alkoxy
group, a phenyl group substituted on the phenyl ring with one
halogen-substituted lower alkoxy group and one lower alkenyloxy
group, or a phenyl group substituted on the phenyl ring with two
halogen-substituted lower alkoxy groups; R.sup.2 is a lower
alkoxyphenyl group, a lower alkenyloxyphenyl group, a
halogen-substituted lower alkoxyphenyl group, a lower alkylpyridyl
group, or a phenyl group substituted on the phenyl ring with one
lower alkoxy group and one halogen atom; and W is a divalent group
represented by Formula (i):
--Y.sup.1-A.sup.1- Formula (i)
wherein A.sup.1 is a C.sub.1-4 alkylene group, and Y.sup.1 is
--C(.dbd.O)-- or --C(.dbd.O)--N(R.sup.3)-- wherein R.sup.3 is a
hydrogen atom.
[0029] The present invention is described below in further
detail.
Compound Represented by Formula (1)
[0030] In Formula (1), R.sup.1 is an aryl group. The aryl group may
have 1 to 3, and preferably 2, substituents selected from the group
consisting of (1-1) hydroxy groups, (1-2) unsubstituted or
halogen-substituted lower alkoxy groups, (1-3) lower alkenyloxy
groups, (1-4) lower alkynyloxy groups, (1-5) cyclo C.sub.3-8 alkyl
lower alkoxy groups, (1-6) cyclo C.sub.3-8 alkyloxy groups, (1-7)
cyclo C.sub.3-8 alkenyloxy groups, (1-8) dihydroindenyloxy groups,
(1-9) hydroxy lower alkoxy groups, (1-10) oxiranyl lower alkoxy
groups, and (1-11) protected hydroxy groups.
[0031] In Formula (1), R.sup.2 is an aryl group or a nitrogen
atom-containing heterocyclic group. The aryl group and heterocyclic
group may have 1 to 3, and preferably 1, substituent selected from
the group consisting of (2-1) hydroxy groups, (2-2) unsubstituted
or halogen-substituted lower alkoxy groups, (2-3) unsubstituted or
halogen-substituted lower alkyl groups, (2-4) lower alkenyloxy
groups, (2-5) halogen atoms, (2-6) lower alkanoyl groups, (2-7)
lower alkylthio groups, (2-8) lower alkylsulfonyl groups, (2-9) oxo
groups, and (2-10) lower alkoxy lower alkoxy groups.
[0032] In Formula (1), W is a divalent group represented by Formula
(i) or (ii):
--Y.sup.1-A.sup.1- Formula (i)
--Y.sup.2--C(.dbd.O)-- Formula (ii)
wherein A.sup.1 is a lower alkenylene group, or a lower alkylene
group which may have 1 to 3, and preferably 1, substituent selected
from the group consisting of hydroxy groups and lower
alkoxycarbonyl groups; Y.sup.1 is a direct bond, --C(.dbd.O)--,
--C(.dbd.O)--N(R.sup.3)--, --N(R.sup.4)--C(.dbd.O)--,
--S(O).sub.m--NH--, or --S(O).sub.n-- wherein R.sup.3 and R.sup.4
are each independently a hydrogen atom or a lower alkyl group, and
m and n are each independently an integer from 0 to 2; and Y.sup.2
is a piperazinediyl group, or a divalent group represented by
Formula (iii) or (iv):
--C(.dbd.O)-A.sup.2-N(R.sup.5)-- Formula (iii)
-A.sup.3-N(R.sup.6)-- Formula (iv)
wherein A.sup.2 and A.sup.3 are each independently a lower alkylene
group, and R.sup.5 and R.sup.6 are each independently a hydrogen
atom or a lower alkyl group.
[0033] Examples of aryl groups include phenyl, naphthyl, etc.
[0034] Examples of halogen atoms include fluorine, chlorine,
bromine, iodine, etc.
[0035] Lower alkyl groups are straight- or branched-chain alkyl
groups having 1 to 6 carbon atoms, and examples thereof include
methyl, ethyl, n-propyl, isopropyl, n-butyl, isobutyl, tert-butyl,
sec-butyl, 1-ethylpropyl, n-pentyl, neopentyl, n-hexyl, isohexyl,
3-methylpentyl, etc.
[0036] Unsubstituted or halogen-substituted lower alkyl groups are
straight- or branched-chain alkyl groups having 1 to 6 carbon atoms
as defined above, or such alkyl groups substituted with 1 to 7
halogen atoms. Examples thereof include methyl, ethyl, n-propyl,
isopropyl, n-butyl, isobutyl, tert-butyl, sec-butyl, 1-ethylpropyl,
n-pentyl, neopentyl, n-hexyl, isohexyl, 3-methyl pentyl,
fluoromethyl, difluoromethyl, trifluoromethyl, chloromethyl,
dichloromethyl, trichloromethyl, bromomethyl, dibromomethyl,
dichlorofluoromethyl, 2-fluoroethyl, 2,2-difluoroethyl,
2,2,2-trifluoroethyl, pentafluoroethyl, 2-chloroethyl,
3,3,3-trifluoropropyl, heptafluoropropyl, heptafluoroisopropyl,
3-chloropropyl, 2-chloropropyl, 3-bromopropyl,
4,4,4-trifluorobutyl, 4,4,4,3,3-pentafluorobutyl, 4-chlorobutyl,
4-bromobutyl, 2-chlorobutyl, 5,5,5-trifluoropentyl, 5-chloropentyl,
6,6,6-trifluorohexyl, 6-chlorohexyl, etc.
[0037] Lower alkenyloxy groups are groups composed of an oxygen
atom and a C.sub.2-6 straight- or branched-chain alkenyl group
having 1 to 3 double bonds. Lower alkenyloxy groups have cis and
trans forms. More specific examples thereof include vinyloxy,
1-propenyloxy, 2-propenyloxy, 1-methyl-1-propenyloxy,
2-methyl-1-propenyloxy, 2-methyl-2-propenyloxy, 2-propenyloxy,
2-butenyloxy, 1-butenyloxy, 3-butenyloxy, 2-pentenyloxy,
1-pentenyloxy, 3-pentenyloxy, 4-pentenyloxy, 1,3-butadienyloxy,
1,3-pentadienyloxy, 2-penten-4-yloxy, 3-methyl-2-butenyloxy,
2-hexenyloxy, 1-hexenyloxy, 5-hexenyloxy, 3-hexenyloxy,
4-hexenyloxy, 3,3-dimethyl-1-propenyloxy, 2-ethyl-1-propenyloxy,
1,3,5-hexatrienyloxy, 1,3-hexadienyloxy, 1,4-hexadienyloxy,
etc.
[0038] Examples of lower alkynyloxy groups include groups composed
of an oxygen atom and a C.sub.2-6 straight- or branched-chain
alkynyl group having 1 to 3 triple bonds. More specific examples
thereof include ethynyloxy, 2-propynyloxy, 2-butynyloxy,
3-butynyloxy, 1-methyl-2-propynyloxy, 2-pentynyloxy, 2-hexynyloxy,
etc.
[0039] Examples of cyclo C.sub.3-6 alkyl groups include
cyclopropyl, cyclobutyl, cyclopentyl, cyclohexyl, cycloheptyl,
cyclooctyl, etc.
[0040] Preferable examples of lower alkoxy groups include C.sub.1-6
straight- or branched-chain alkoxy groups. Specifically, such
groups include methoxy, ethoxy, n-propoxy, isopropoxy, n-butoxy,
isobutoxy, tert-butoxy, sec-butoxy, 1-ethylpropoxy, n-pentoxy,
neopentoxy, n-hexyloxy, isohexyloxy, 3-methylpentoxy, etc.
[0041] Examples of cyclo C.sub.2-6 alkyl lower alkoxy groups
include the above-mentioned lower alkoxy groups which have 1 to 3,
and preferably 1, cyclo C.sub.3-6 alkyl group as listed above. More
specific examples thereof include cyclopropylmethoxy,
cyclobutylmethoxy, cyclohexylmethoxy, 2-cyclopropylethoxy,
1-cyclobutylethoxy, cyclopentylmethoxy, 3-cyclopentylpropoxy,
4-cyclohexylbutoxy, 5-cycloheptylpentoxy, 6-cyclooctylhexyloxy,
1,1-dimethyl-2-cyclohexylethoxy, 2-methyl-3-cyclopropylpropoxy,
etc.
[0042] Examples of cyclo C.sub.3-6 alkyloxy groups include
cyclopropyloxy, cyclobutyloxy, cyclopentyloxy, cyclohexyloxy,
cycloheptyloxy, cyclooctyloxy, etc.
[0043] Examples of cyclo C.sub.3-6 alkenyloxy groups include
cyclopropenyloxy, cyclobutenyloxy, cyclopentenyloxy,
cyclohexenyloxy, cycloheptenyloxy, cyclooctenyloxy, etc.
[0044] Examples of dihydroindenyloxy groups include
2,3-dihydroinden-1-yloxy, 2,3-dihydroinden-2-yloxy, etc.
[0045] Examples of hydroxy lower alkoxy groups include lower alkoxy
groups (preferably C.sub.1-6 straight- or branched-chain alkoxy
groups) having 1 to 5, and preferably 1 to 3, hydroxy groups. More
specific examples thereof include hydroxymethyloxy,
2-hydroxyethyloxy, 1-hydroxyethyloxy, 3-hydroxypropyloxy,
2,3-dihydroxypropyloxy, 4-hydroxybutyloxy, 3,4-dihydroxybutyloxy,
1,1-dimethyl-2-hydroxyethyloxy, 5-hydroxypentyloxy,
6-hydroxyhexyloxy, 3,3-dimethyl-3-hydroxypropyloxy,
2-methyl-3-hydroxypropyloxy, 2,3,4-trihydroxybutyloxy,
perhydroxyhexyloxy, etc.
[0046] Examples of oxiranyl lower alkoxy groups include C.sub.1-6
straight- or branched-chain alkoxy groups having 1 or 2 oxyranyl
groups such as, for example, oxiranylmethoxy, 2-oxiranylethoxy,
1-oxiranylethoxy, 3-oxiranylpropoxy, 4-oxiranylbutoxy,
5-oxiranylpentyloxy, 6-oxiranylhexyloxy,
1,1-dimethyl-2-oxiranylethoxy, 2-methyl-3-oxiranylpropoxy, etc.
[0047] Examples of protecting groups of protected hydroxy groups
include lower alkanoyl and other acyl groups; phenyl(lower)alkyl
groups which may have one or more suitable substituents (e.g.,
benzyl, phenethyl, 3-phenylpropyl, 4-methoxybenzyl, trityl, etc.);
trisubstituted silyl groups [e.g., tri(lower)alkylsilyl groups
(e.g., trimethylsilyl, t-butyldimethylsilyl, etc.) and the like];
tetrahydropyranyl; etc.
[0048] Examples of nitrogen atom-containing heterocyclic groups
include pyrrolidinyl, imidazolidinyl, piperidyl,
hexahydropyrimidinyl, piperazinyl, octahydroisoindolyl, azepanyl,
azocanyl, pyrrolyl, dihydropyrrolyl, imidazolyl, dihydroimidazolyl,
triazolyl, dihydrotriazolyl, pyrazolyl, pyridyl and N-oxides
thereof, dihydropyridyl, pyrimidinyl, dihydropyrimidinyl,
pyrazinyl, dihydropyrazinyl, pyridazinyl, tetrazolyl, indolyl,
isoindolyl, indolinyl, isoindolinyl, hexahydroisoindolinyl,
benzoimidazolyl, quinolyl, isoquinolyl, indazolyl, quinazolinyl,
dihydroquinazolinyl, benzotriazolyl, carbazolyl, oxazolyl,
isooxazolyl, oxadiazolyl, oxazolidinyl, isooxazolidinyl,
morpholinylbenzoxazolyl, dihydrobenzoxazolyl, benzoxazinyl,
dihydrobenzoxazinyl, benzoxazolyl, benzooxadiazolyl, triazolyl,
dihydrothiazolyl, isothiazolyl, thiadiazolyl, dihydrothiazinyl,
thiazolyzinyl, benzothiazolyl, benzothiadiazolyl, etc.
[0049] Unsubstituted or halogen-substituted lower alkoxy groups are
straight- or branched-chain alkoxy groups having 1 to 6 carbon
atoms, or such alkoxy groups substituted with 1 to 7 halogen atoms.
Examples thereof include methoxy, ethoxy, n-propoxy, isopropoxy,
n-butoxy, isobutoxy, tert-butoxy, sec-butoxy, 1-ethylpropoxy,
n-pentoxy, neopentoxy, n-hexyloxy, isohexyloxy, 3-methylpentoxy,
fluoromethoxy, difluoromethoxy, trifluoromethoxy, chloromethoxy,
dichloromethoxy, trichloromethoxy, bromomethoxy, dibromomethoxy,
dichlorofluoromethoxy, 2-fluoroethoxy, 2,2-difluoroethoxy,
2,2,2-trifluoroethoxy, pentafluoroethoxy, 2-chloroethoxy,
3,3,3-trifluoropropoxy, heptafluoropropoxy, heptafluoroisopropoxy,
3-chloropropoxy, 2-chloropropoxy, 3-bromopropoxy,
4,4,4-trifluorobutoxy, 4,4,4,3,3-pentafluorobutoxy, 4-chlorobutoxy,
4-bromobutoxy, 2-chlorobutoxy, 5,5,5-trifluoropentoxy,
5-chloropentoxy, 6,6,6-trifluorohexyloxy, 6-chlorohexyloxy,
etc.
[0050] Examples of lower alkanoyl groups include formyl, acetyl,
propionyl, butyryl, isobutyryl, pentanoyl, tert-butylcarbonyl,
hexanoyl, and other C.sub.1-6 straight- or branched-chain alkanoyl
groups.
[0051] Examples of lower alkylthio groups include methylthio,
ethylthio, n-propylthio, isopropylthio, n-butylthio,
tert-butylthio, n-pentylthio, n-hexylthio, and other C.sub.1-6
straight- or branched-chain alkylthio groups.
[0052] Preferable examples of lower alkylsulfonyl groups include
C.sub.1-6 straight- or branched-chain alkylsulfonyl groups. More
specific examples thereof include methylsulfonyl, ethylsulfonyl,
n-propylsulfonyl, isopropylsulfonyl, n-butylsulfonyl,
isobutylsulfonyl, tert-butylsulfonyl, sec-butylsulfonyl,
n-pentylsulfonyl, isopentylsulfonyl, neopentylsulfonyl,
n-hexylsulfonyl, isohexylsulfonyl, 3-methylpentylsulfonyl, etc.
[0053] Lower alkenylene groups include, for example, vinylidene,
propylene, butenylene, and other C.sub.2-6 straight- or
branched-chain alkenylene groups having 1 to 3 double bonds.
[0054] Preferable examples of lower alkoxycarbonyl groups include
groups composed of a C.sub.1-6 straight- or branched-chain alkoxy
group and a carbonyl group. Specific examples thereof include
methoxycarbonyl, ethoxycarbonyl, n-propoxycarbonyl,
isopropoxycarbonyl, n-butoxycarbonyl, isobutoxycarbonyl,
tert-butoxycarbonyl, sec-butoxycarbonyl, n-pentoxycarbonyl,
neopentoxycarbonyl, n-hexyloxycarbonyl, isohexyloxycarbonyl,
3-methylpentoxycarbonyl, etc.
[0055] Lower alkylene groups include, for example, ethylene,
trimethylene, 2-methyltrimethylene, 2,2-dimethyltrimethylene,
1-methyltrimethylene, methylmethylene, ethylmethylene,
tetramethylene, pentamethylene, hexamethylene, and other C.sub.1-6
straight- or branched-chain alkylene groups.
[0056] Examples of lower alkoxy lower alkoxy groups include
alkoxyalkoxy groups in which the two alkoxy moieties are each
independently a C.sub.1-6 straight- or branched-chain alkoxy group.
Specific examples thereof include methoxymethoxy, 2-methoxyethoxy,
3-methoxypropoxy, 4-methoxybutoxy, 5-methoxypentoxy,
6-methoxyhexyloxy, ethoxymethoxy, 2-ethoxyethoxy, n-propoxymethoxy,
isopropoxymethoxy, n-butoxymethoxy, etc.
[0057] Examples of C.sub.1-4 alkylene groups include ethylene,
trimethylene, 2-methyltrimethylene, 2,2-dimethyltrimethylene,
1-methyltrimethylene, methylmethylene, ethylmethylene,
tetramethylene, and other C.sub.1-4 straight- or branched-chain
alkylene groups.
Production Process for Compound Represented by Formula (1)
[0058] The oxazole compound represented by Formula (1) can be
produced by various processes, one example of which is shown in
Reaction Scheme 1.
##STR00008##
wherein R.sup.1, R.sup.2 and W are as defined in Formula (1), and X
is a halogen atom.
[0059] Compound (1) is produced by reacting Compound (2) with
Compound (3).
[0060] The reaction of Compound (2) with Compound (3) is usually
performed in a suitable solvent. A wide variety of known solvents
can be used as long as they do not inhibit the reaction. Examples
of such solvents include dimethylformamide, dimethylsulfoxide,
acetonitrile, and other aprotic polar solvents; acetone, methyl
ethyl ketone, and other ketone solvents; benzene, toluene, xylene,
tetralin, liquid paraffin, and other hydrocarbon solvents;
methanol, ethanol, isopropanol, n-butanol, tert-butanol, and other
alcohol solvents; tetrahydrofuran, dioxane, dipropyl ether, diethyl
ether, dimethoxyethane, diglyme, and other ether solvents; ethyl
acetate, methyl acetate, and other ester solvents; mixtures
thereof; etc. Such solvents may contain water.
[0061] The proportion of Compound (3) to Compound (2) is usually
0.5 to 5 mol, and preferably 0.5 to 3 mol, per mol of Compound
(2).
[0062] The reaction of Compound (2) with Compound (3) is usually
performed by continuing stirring at -20 to 200.degree. C., and
preferably at 0 to 150.degree. C., for 30 minutes to 60 hours, and
preferably 1 to 30 hours.
[0063] Compound (3) used as a starting material is an easily
available known compound. Compound (2) encompasses novel compounds,
and a production process for such a compound is described
hereinafter (Reaction Scheme 9).
[0064] Among the oxazole compounds represented by Formula (1),
those in which W is a divalent group represented by
--Y.sup.1-A.sup.1- wherein Y.sup.1 is --C(.dbd.O)--N(R.sup.3)--
(hereinafter referred to as "Compound (1a)") can be produced by,
for example, the process shown in Reaction Scheme 2.
##STR00009##
wherein R.sup.1, R.sup.2, R.sup.3 and A.sup.1 are as defined in
Formula (1).
[0065] Compound (1a) is produced by reacting Compound (4) or a
reactive derivative thereof at the carboxy group, with Compound (5)
or a reactive derivative thereof at the amino or imino group.
[0066] Preferable examples of reactive derivatives of Compound (4)
include acid halides, acid anhydrides, activated amides, activated
esters, etc. Preferable examples of reactive derivatives include
acid chlorides; acid azides; dialkylphosphoric acids,
phenylphosphoric acid, diphenylphosphoric acid, dibenzylphosphoric
acid, phosphoric acid halides, and other substituted phosphoric
acids, dialkylphosphorous acid, sulfurous acid, thiosulfuric acid,
sulfuric acid, methanesulfonic acid, and other sulfonic acids,
acetic acid, propionic acid, butyric acid, isobutyric acid, pivalic
acid, pentanoic acid, isopentanoic acid, 2-ethylbutyric acid,
trichloroacetic acid, and other aliphatic carboxylic acids, and
mixed acid anhydrides with acids such as benzoic acid or other
aromatic acids; symmetrical acid anhydrides; activated amides with
imidazole, 4-substituted imidazole, dimethylpyrazole, triazole or
tetrazole; cyanomethyl ester, methoxymethyl ester,
dimethyliminomethyl ester, vinyl ester, propargyl ester,
p-nitrophenyl ester, 2,4-dinitrophenyl ester, trichlorophenyl
ester, pentachlorophenyl ester, mesylphenyl ester, and other
activated esters, esters with N,N-dimethylhydroxylamine,
1-hydroxy-2-(1H)-pyridone, N-hydroxysuccinimide,
N-hydroxyphthalimide, 1-hydroxy-1H-benzotriazol, and other
N-hydroxy compounds; etc. Such reactive derivatives can be selected
as desired, according to the type of Compound (4) used.
[0067] When using Compound (4) in the form of a free acid or a salt
thereof in the above reaction, it is preferable to perform the
reaction in the presence of condensing agent(s). A wide variety of
condensing agents known in this field can be used, including, for
example, N,N'-dicyclohexylcarbodiimide;
N-cyclohexyl-N'-morpholinoethylcarbodiimide;
N-cyclohexyl-N'-(4-diethylaminocyclohexyl)carbodiimide;
N,N'-diethylcarbodiimide; N,N'-diisopropylcarbodiimide;
N-ethyl-N'-(3-dimethylaminopropyl)carbodiimide and hydrochlorides
thereof; N,N'-carbonylbis(2-methylimidazole);
pentamethyleneketene-N-cyclohexylimine;
diphenylketene-N-cyclohexylimine; ethoxyacetylene,
1-alkoxy-1-chloroethylene; trialkyl phosphite; ethyl polyphosphate;
isopropyl polyphosphate; phosphorus oxychloride (phosphoryl
chloride); phosphorus trichloride; phosphoryl diphenyl azide;
thionyl chloride; oxalyl chloride; ethyl chloroformate, isopropyl
chloroformate, and other lower alkyl haloformates;
triphenylphosphine; 2-ethyl-7-hydroxybenzisooxazolium salt;
2-ethyl-5-(m-sulfophenyl)isooxazolium hydroxide inner salts;
hexafluorophosphoric acid
benzotriazol-1-yl-oxy-tris(dimethylamino)phosphonium;
1-(p-chlorobenzenesulfonyloxy)-6-chloro-1H-benzotriazol; so-called
Vilsmeier reagents prepared by reacting N,N-dimethylformamide with
thionyl chloride, phosgene, trichloromethyl chloroformate,
phosphorus oxychloride, etc.; and the like. It is more preferable
to perform the reaction in the presence of such condensing agent(s)
and active esterifying agent(s) such as N-hydroxysuccinimide,
N-hydroxyphthalimide, 1-hydroxy-1H-benzotriazol, or the like.
[0068] Preferable examples of reactive derivatives of Compound (5)
include Schiff base imino- or enamine-type tautomers produced by
reacting Compound (5) with carbonyl compounds such as aldehydes,
ketones, etc.; silyl derivatives produced by reacting Compound (5)
with silyl compounds such as bis(trimethylsilyl)acetamide,
mono(trimethylsilyl)acetamide, bis(trimethylsilyl)urea, etc.;
derivatives produced by reacting Compound (5) with phosphorus
trichloride, phosgene, etc.; and the like.
[0069] The reaction is usually carried out in a known solvent that
does not adversely affect the reaction. Such solvents include, for
example, water; methanol, ethanol, isopropanol, n-butanol,
trifluoroethanol, ethylene glycol, and other alcohol solvents;
acetone, methyl ethyl ketone, and other ketone solvents;
tetrahydrofuran, dioxane, diethyl ether, diisopropyl ether,
diglyme, and other ether solvents; methyl acetate, ethyl acetate,
and other ester solvents; acetonitrile, N,N-dimethylformamide,
dimethyl sulfoxide, and other aprotic polar solvents; n-pentane,
n-hexane, n-heptane, cyclohexane, and other hydrocarbon solvents;
methylene chloride, ethylene chloride, and other halogenated
hydrocarbon solvents; other organic solvents; and mixed solvents
thereof.
[0070] The reaction may be performed in the presence of base(s). A
wide variety of known inorganic and organic bases are usable.
Inorganic bases include, for example, alkali metals (e.g., sodium,
potassium, etc.), alkali metal hydrogencarbonates (e.g., lithium
hydrogencarbonate, sodium hydrogencarbonate, potassium
hydrogencarbonate etc.), alkali metal hydroxides (e.g., lithium
hydroxide, sodium hydroxide, potassium hydroxide, cesium hydroxide,
etc.), alkali metal carbonates (e.g., lithium carbonate, sodium
carbonate, potassium carbonate, cesium carbonate, etc.), alkali
metal lower alkoxides (e.g., sodium methoxide, sodium ethoxide,
etc.), and alkali metal hydrides (e.g., sodium hydride, potassium
hydride, etc.). Organic bases include, for example, trialkylamines
[e.g., trimethylamine, triethylamine, N-ethyldiisopropylamine,
etc.], pyridine, quinoline, piperidine, imidazole, picoline,
dimethylaminopyridine, dimethylaniline, N-methylmorpholine,
1,5-diazabicyclo[4.3.0]non-5-ene (DBN),
1,4-diazabicyclo[2.2.2]octane (DABCO),
1,8-diazabicyclo[5.4.0]undec-7-ene (DBU), etc. When such bases are
liquid, they can also be used as solvents.
[0071] Such bases can be used singly or in combination.
[0072] The amount of base(s) is usually 0.1 to 10 moles, and
preferably 0.1 to 3 moles, per mole of Compound (4).
[0073] The proportion of Compound (4) to Compound (5) in Reaction
Scheme 1 is usually at least 1, and preferably about 1 to about 5
mol of the former per mol of the latter.
[0074] The reaction temperature is not limited, and the reaction
can usually be performed with cooling, at room temperature, or with
heating. It is suitable to perform the reaction in a temperature
range from room temperature to 100.degree. C., for 30 minutes to 30
hours, and preferably for 30 minutes to 5 hours.
[0075] In the above reaction, Compound (4) for use as a starting
material is an easily available known compound. Compound (5)
encompasses novel compounds. A production process for Compound (5)
is described hereinafter (Reaction Scheme 10).
[0076] Among the oxazole compounds represented by Formula (1),
those in which W is a divalent group represented by
--Y.sup.1-A.sup.1- wherein Y.sup.1 is --C(.dbd.O)-- and A.sup.1 is
a lower alkylene group having one lower alkoxycarbonyl group
(hereinafter referred to as "Compound (1b)") can be produced, for
example, by the process shown in Reaction Scheme 3.
##STR00010##
wherein R.sup.1 and R.sup.2 are as defined in Formula (1), R.sup.7
and R.sup.8 are each independently a lower alkyl group, and
A.sup.1a is a C.sub.1-5 alkylene group.
[0077] The --COOR.sup.8 group in Formula (1b) is the same as the
lower alkoxycarbonyl group defined as a substituent of A.sup.1 in
Formula (1). The lower alkyl group represented by R.sup.7 may be
the same as the lower alkyl group as defined above.
[0078] Examples of the C.sub.1-5 alkylene group represented by
A.sup.1a include ethylene, trimethylene, 2-methyltrimethylene,
2,2-dimethyltrimethylene, 1-methyltrimethylene, methylmethylene,
ethylmethylene, tetramethylene, pentamethylene, and other C.sub.1-5
straight- or branched-chain alkylene groups.
[0079] Compound (1b) is produced by reacting Compound (6) with
Compound (7).
[0080] The reaction is usually performed in a known solvent that
does not adversely affect the reaction. Such solvents include, for
example, water; methanol, ethanol, isopropanol, n-butanol,
trifluoroethanol, ethylene glycol, and other alcohol solvents;
acetone, methyl ethyl ketone, and other ketone solvents;
tetrahydrofuran, dioxane, diethyl ether, dimethoxyethane, diglyme,
and other ether solvents; methyl acetate, ethyl acetate, and other
ester solvents; acetonitrile, N,N-dimethylformamide, dimethyl
sulfoxide, N-methylpyrrolidone, and other aprotic polar solvents;
methylene chloride, ethylene chloride, and other halogenated
hydrocarbon solvents; other organic solvents; and mixed solvents
thereof.
[0081] The reaction can usually be performed in the presence of
suitable base(s). A wide variety of known inorganic and organic
bases are usable. Inorganic bases include, for example, alkali
metals (e.g., lithium, sodium, potassium, etc.), alkali metal
hydrogencarbonates (e.g., lithium hydrogencarbonate, sodium
hydrogencarbonate, potassium hydrogencarbonate, etc.), alkali metal
hydroxides (e.g., lithium hydroxide, sodium hydroxide, potassium
hydroxide, cesium hydroxide, etc.), alkali metal carbonates (e.g.,
lithium carbonate, sodium carbonate, potassium carbonate, cesium
carbonate, etc.), alkali metal lower alkoxides (e.g., sodium
methoxide, sodium ethoxide, potassium tert-butoxide, sodium
tert-butoxide, sodium tert-pentoxide, etc.), alkali metal hydrides
(e.g., sodium hydride, potassium hydride, etc.), and the like.
Organic bases include, for example, trialkylamines (e.g.,
trimethylamine, triethylamine, N-ethyldiisopropylamine, etc.),
pyridine, quinoline, piperidine, imidazole, picoline,
dimethylaminopyridine, dimethylaniline, N-methylmorpholine,
1,5-diazabicyclo[4.3.0]non-5-ene (DBN),
1,4-diazabicyclo[2.2.2]octane (DABCO),
1,8-diazabicyclo[5.4.0]undec-7-ene (DBU), etc. When such bases are
liquid, they can also be used as solvents. Such bases can be used
singly or in combination.
[0082] The amount of base(s) is usually 0.5 to 10 mol, and
preferably 0.5 to 6 mol, per mol of Compound (6).
[0083] The proportion of Compound (6) to Compound (7) is usually at
least 1 mol, and preferably about 1 to about 5 mol of the former,
per mol of the latter.
[0084] The reaction temperature is not limited, and the reaction
can usually be performed with cooling, at room temperature, or with
heating. It is suitable to perform the reaction in a temperature
range from room temperature to 150.degree. C., for 30 minutes to 60
hours, and preferably 1 to 30 minutes.
[0085] Compound (6) used as a starting material in the above
reaction is an easily available known compound. Compound (7)
encompasses novel compounds. A production process for Compound (7)
is described hereinafter (Reaction Scheme 11).
[0086] Among the oxazole compounds represented by Formula (1),
those in which W is a divalent group represented by
--Y.sup.1-A.sup.1- wherein A.sup.1 is a lower alkylene group
(hereinafter referred to as "Compound (1d)") are produced from the
corresponding compounds in which A.sup.1 is a lower alkylene group
having lower alkoxycarbonyl group(s) (hereinafter referred to as
"Compound (1c)"), by the process shown in Reaction Scheme 4.
##STR00011##
wherein R.sup.1, R.sup.2 and Y.sup.1 are as defined in Formula (1),
A.sup.1b is a lower alkylene group having lower alkoxycarbonyl
group(s), and A.sup.1c is a lower alkylene group.
[0087] Compound (1d) is produced by subjecting Compound (1c) to
hydrolysis-decarboxylation.
[0088] The reaction is usually performed in a known solvent that
does not adversely affect the reaction. Such solvents include, for
example, water; methanol, ethanol, isopropanol, n-butanol,
trifluoroethanol, ethylene glycol, and other alcohol solvents;
acetone, methyl ethyl ketone, and other ketone solvents;
tetrahydrofuran, dioxane, diethyl ether, dimethoxyethane, diglyme,
and other ether solvents; methyl acetate, ethyl acetate, and other
ester solvents; acetonitrile, N,N-dimethylformamide, dimethyl
sulfoxide, N-methylpyrrolidone, and other aprotic polar solvents;
methylene chloride, ethylene chloride, and other halogenated
hydrocarbon solvents; other organic solvents; and mixed solvents
thereof.
[0089] The hydrolysis-decarboxylation of Compound (1c) is usually
performed under acidic conditions. For example, an acid is added to
a suspension or solution of Compound (1c) in a suitable solvent,
and the resulting mixture is stirred at 0 to 120.degree. C. to
carry out the hydrolysis-decarboxylation.
[0090] Examples of usable acids include trifluoroacetic acid,
acetic acid, and other organic acids, hydrochloric acid, bromic
acid, hydrobromic acid, sulfuric acid, and other inorganic acids,
etc. Among such organic acids, organic acids can also be used as
reaction solvents.
[0091] The amount of acid(s) is usually 0.5 to 30 mol, and
preferably 0.5 to 10 mol, per mol of Compound (1c).
[0092] The reaction temperature is usually 0 to 120.degree. C., and
preferably room temperature to 110.degree. C. The reaction time is
usually 30 minutes to 24 hours, preferably 30 minutes to 12 hours,
and more preferably 1 to 8 hours.
[0093] Among the oxazole compounds represented by Formula (1),
those in which R.sup.1 is a phenyl group substituted on the phenyl
ring with hydroxy group(s) (hereinafter referred to as "Compound
(1f)") are produced from the corresponding compounds in which
R.sup.1 is a phenyl group substituted on the phenyl ring with
protected hydroxy group(s) (hereinafter referred to as "Compound
(1e)"), by the process shown in Reaction Scheme 5.
##STR00012##
wherein R.sup.2 and W are as defined in Formula (1); R.sup.9 is a
protected hydroxy group; R.sup.10 is the same group as the
substituent (1-2), (1-3), (1-4), (1-5), (1-6), (1-7), (1-8), (1-9)
or (1-10) of the aryl group represented by R.sup.1 in Formula (1);
m is 1 to 5; q is 0 to 4; m R.sup.9s may be the same or different;
and q R.sup.10s may be the same or different; with the proviso that
m+q 5.
[0094] Compound (1f) can be produced by subjecting Compound (1e) to
an elimination reaction of the hydroxy protecting group(s).
[0095] The elimination reaction can be carried out by hydrolysis,
hydrogenolysis, or other conventional methods.
[0096] The reaction is usually performed in a known solvent that
does not adversely affect the reaction. Such solvents include, for
example, water; methanol, ethanol, isopropanol, n-butanol,
trifluoroethanol, ethylene glycol, and other alcohol solvents;
acetone, methyl ethyl ketone, and other ketone solvents;
tetrahydrofuran, dioxane, diethyl ether, dimethoxyethane, diglyme,
and other ether solvents; methyl acetate, ethyl acetate, and other
ester solvents; acetonitrile, N,N-dimethylformamide, dimethyl
sulfoxide, N-methylpyrrolidone, and other aprotic polar solvents;
methylene chloride, ethylene chloride, and other halogenated
hydrocarbon solvents; and other organic solvents.
[0097] (i) Hydrolysis:
[0098] Hydrolysis is preferably carried out in the presence of
base(s) or acid(s) (including Lewis acids).
[0099] A wide variety of known inorganic and organic bases are
usable. Preferable examples of inorganic bases include alkali
metals (e.g., sodium, potassium, etc.), alkaline earth metals
(e.g., magnesium, calcium, etc.), hydroxides, carbonates and
hydrogencarbonates thereof, etc. Preferable examples of organic
bases include trialkylamines (e.g., trimethylamine, triethylamine,
etc.), picoline, 1,5-diazabicyclo[4,3,0]non-5-ene, etc.
[0100] A wide variety of known organic and inorganic acids are
usable. Preferable organic acids include, for example, formic acid,
acetic acid, propionic acid, and other fatty acids; trichloroacetic
acid, trifluoroacetic acid, and other trihaloacetic acids; and the
like. Preferable inorganic acids include, for example, hydrochloric
acid, hydrobromic acid, sulfuric acid, hydrogen chloride, hydrogen
bromide, etc. Examples of Lewis acids include boron trifluoride
ether complexes, boron tribromide, aluminium chloride, ferric
chloride, etc.
[0101] When using a trihaloacetic acid or Lewis acid, it is
preferable to carry out hydrolysis in the presence of a cation
scavenger (e.g., anisole, phenol, etc.).
[0102] The amount of base(s) or acid(s) is not limited as long as
it is an amount necessary for hydrolysis.
[0103] The reaction temperature is usually 0 to 120.degree. C.,
preferably room temperature to 100.degree. C., and more preferably
room temperature to 80.degree. C. The reaction time is usually 30
minutes to 24 hours, preferably 30 minutes to 12 hours, and more
preferably 1 to 8 hours.
[0104] (ii) Hydrogenolysis:
[0105] Hydrogenolysis can be carried out by a wide variety of known
methods including, for example, chemical reduction, catalytic
reduction, etc.
[0106] Examples of suitable reducing agents for chemical reduction
include hydrides (e.g., hydrogen iodide, hydrogen sulfide, lithium
aluminium hydride, sodium borohydride, sodium cyanoborohydride,
etc.); and combinations of metals (e.g., tin, zinc, iron, etc.) or
metallic compounds (e.g., chromium chloride, chromium acetate,
etc.), with organic or inorganic acids (e.g., formic acid, acetic
acid, propionic acid, trifluoroacetic acid, p-toluenesulfonic acid,
hydrochloric acid, hydrobromic acid, etc.).
[0107] Examples of suitable catalysts for catalytic reduction
include platinum catalysts (e.g., platinum plates, spongy platinum,
platinum black, colloidal platinum, platinum oxide, platinum wires,
etc.), palladium catalysts (e.g., spongy palladium, palladium
black, palladium oxide, palladium carbon, palladium/barium sulfate,
palladium/barium carbonate, etc.), nickel catalysts (e.g., reduced
nickel, nickel oxide, Raney nickel, etc.), cobalt catalysts (e.g.,
reduced cobalt, Raney cobalt, etc.), iron catalysts (e.g., reduced
iron and the like), etc.
[0108] When such acids used for chemical reduction are liquid, they
can also be used as solvents.
[0109] The amounts of reducing agent for chemical reduction and
catalyst for catalytic reduction are not limited and may be
conventional amounts.
[0110] The reaction temperature is usually 0 to 120.degree. C.,
preferably room temperature to 100.degree. C., and more preferably
room temperature to 80.degree. C. The reaction time is usually 30
minutes to 24 hours, preferably 30 minutes to 10 hours, and more
preferably 30 minutes to 4 hours.
[0111] Among the oxazole compounds represented by Formula (1),
those in which R.sup.1 is a phenyl group substituted on the phenyl
ring with R.sup.11O-- group(s) (hereinafter referred to as
"Compound (1g)") are produced from Compound (1f), by the process
shown in Reaction Scheme 6.
##STR00013##
wherein R.sup.2 and W are as defined in Formula (1); R.sup.10, m
and q are as defined above; X.sup.1 is a halogen atom or a group
that undergoes the same substitution reaction as that of a halogen
atom; R.sup.11O is the same group as the substituent (1-2), (1-3),
(1-4), (1-5), (1-6), (1-7), (1-8), (1-9) or (1-10) of the aryl
group represented by R.sup.1 in Formula (1); and m R.sup.11Os may
be the same or different.
[0112] In Compound (8), the halogen atom represented by X.sup.1 is
a fluorine atom, chlorine atom, bromine atom, or iodine atom.
[0113] Examples of the group that undergoes the same substitution
reaction as that of a halogen atom, the group being represented by
X.sup.1, include lower alkanesulfonyloxy groups, arylsulfonyloxy
groups, aralkylsulfonyloxy groups, etc.
[0114] Specific examples of lower alkanesulfonyloxy groups include
methanesulfonyloxy, ethanesulfonyloxy, isopropanesulfonyloxy,
n-propanesulfonyloxy, n-butanesulfonyloxy, tert-butanesulfonyloxy,
n-pentanesulfonyloxy, n-hexanesulfonyloxy, and other C.sub.1-6
straight- or branched-chain alkanesulfonyloxy groups, and the
like.
[0115] Arylsulfonyloxy groups include, for example,
phenylsulfonyloxy, naphthylsulfonyloxy, etc. The phenyl ring of
such arylsulfonyloxy groups may have, for example, 1 to 3
substituents selected from the group consisting of C.sub.1-6
straight- or branched-chain alkyl groups, C.sub.1-6 straight- or
branched-chain alkoxy groups, nitro groups, and halogen atoms.
Specific examples of such arylsulfonyloxy groups include
phenylsulfonyloxy, 4-methylphenylsulfonyloxy,
2-methylphenylsulfonyloxy, 4-nitrophenylsulfonyloxy,
4-methoxyphenylsulfonyloxy, 2-nitrophenylsulfonyloxy,
3-chlorophenylsulfonyloxy, etc. Specific examples of
naphthylsulfonyloxy groups include .alpha.-naphthylsulfonyloxy,
.beta.-naphthylsulfonyloxy, etc.
[0116] Aralkylsulfonyloxy groups include, for example,
phenyl-substituted C.sub.1-6 straight- or branched-chain
alkylsulfonyloxy groups which may have, on the phenyl ring, 1 to 3
substituents selected from the group consisting of C.sub.1-6
straight- or branched-chain alkyl groups, C.sub.1-6 straight- or
branched-chain alkoxy groups, nitro groups, and halogen atoms;
naphthyl-substituted C.sub.1-6 straight- or branched-chain
alkylsulfonyloxy groups; etc. Specific examples of
phenyl-substituted alkylsulfonyloxy groups as mentioned above
include benzylsulfonyloxy, 2-phenylethylsulfonyloxy,
4-phenylbutylsulfonyloxy, 2-methylbenzylsulfonyloxy,
4-methoxybenzylsulfonyloxy, 4-nitrobenzylsulfonyloxy,
3-chlorobenzylsulfonyloxy, etc. Specific examples of
naphthyl-substituted alkylsulfonyloxy groups as mentioned above
include .alpha.-naphthylmethylsulfonyloxy,
.beta.-naphthylmethylsulfonyloxy, etc.
[0117] Compound (1g) is produced by reacting Compound (1f) with
Compound (8), or by reacting Compound (1f) with Compound (8').
[0118] The reaction of Compound (1f) with Compound (8) is described
below.
[0119] The reaction of Compound (1f) with Compound (8) is usually
performed in a known solvent that does adversely affect the
reaction. Such solvents include, for example, water; methanol,
ethanol, isopropanol, n-butanol, trifluoroethanol, ethylene glycol,
and other alcohol solvents; acetone, methyl ethyl ketone, and other
ketone solvents; tetrahydrofuran, dioxane, diethyl ether, diglyme,
and other ether solvents; methyl acetate, ethyl acetate, and other
ester solvents; acetonitrile, N,N-dimethylformamide, dimethyl
sulfoxide, and other aprotic polar solvents; methylene chloride,
ethylene chloride, and other halogenated hydrocarbon solvents;
other organic solvents; mixed solvents thereof; etc.
[0120] The reaction of Compound (1f) with Compound (8) is usually
carried out in the presence of base(s). Usable bases include known
inorganic and organic bases. Inorganic bases include, for example,
alkali metals (e.g., sodium, potassium, etc.), alkali metal
hydrogencarbonates (e.g., lithium hydrogencarbonate, sodium
hydrogencarbonate, potassium hydrogencarbonate, etc.), alkali metal
hydroxides (e.g., lithium hydroxide, sodium hydroxide, potassium
hydroxide, cesium hydroxide, etc.), alkali metal carbonates (e.g.,
lithium carbonate, sodium carbonate, potassium carbonate, cesium
carbonate, etc.), alkali metal lower alkoxides (e.g., sodium
methoxide, sodium ethoxide, etc.), alkali metal hydrides (e.g.,
sodium hydride, potassium hydride, etc.), and the like. Organic
bases include, for example, trialkylamines (e.g., trimethylamine,
triethylamine, N-ethyldiisopropylamine, etc.), pyridine, quinoline,
piperidine, imidazole, picoline, dimethylaminopyridine,
dimethylaniline, N-methylmorpholine,
1,5-diazabicyclo[4.3.0]non-5-ene (DBN),
1,4-diazabicyclo[2.2.2]octane (DABCO),
1,8-diazabicyclo[5.4.0]undec-7-ene (DBU), etc. When such bases are
liquid, they can also be used as solvents. Such bases can be used
singly or in combination.
[0121] The amount of base(s) is usually 0.5 to 10 mol, and
preferably 0.5 to 6 mol, per mol of Compound (1f).
[0122] When performing the above reaction, alkali metals such as
potassium iodide, sodium iodide, etc. can be added as reaction
accelerators to the reaction system, as required.
[0123] The proportion of Compound (1f) to Compound (8) is usually
at least 1 mol, and preferably about 1 to about 5 mol of the
latter, per mol of the former.
[0124] The reaction temperature is not limited, and the reaction
can usually be performed with cooling, at room temperature, or with
heating. It is suitable to perform the reaction at about room
temperature for 1 to 30 hours.
[0125] Next, the reaction of Compound (1f) with Compound (8') is
described.
[0126] The reaction of Compound (1f) with Compound (8') is usually
performed in a known solvent that does not adversely affect the
reaction. Such solvents include, for example, water; methanol,
ethanol, isopropanol, n-butanol, trifluoroethanol, ethylene glycol,
and other alcohol solvents; acetone, methyl ethyl ketone, and other
ketone solvents; tetrahydrofuran, dioxane, diethyl ether, diglyme,
and other ether solvents; methyl acetate, ethyl acetate, and other
ester solvents; acetonitrile, N,N-dimethylformamide, dimethyl
sulfoxide, and other aprotic polar solvents; benzene, toluene,
xylene, and other aromatic hydrocarbon solvents; methylene
chloride, ethylene chloride, and other halogenated hydrocarbon
solvents; other organic solvents; mixed solvents thereof; etc.
[0127] The reaction is usually performed in the presence of dialkyl
azodicarboxylate(s) such as diisopropyl azodicarboxylate, diethyl
azodicarboxylate, etc., and phosphine ligand(s) such as triphenyl
phosphine, tri(n-butyl)phosphine, etc. The amount of dialkyl
azodicarboxylate(s) is usually 0.5 to 10 mol, and preferably 0.5 to
6 mol, per mole of Compound (1f). The amount of phosphine ligand(s)
is usually 0.5 to 10 mol, and preferably 0.5 to 6 mol, per mole of
Compound (1f).
[0128] The reaction of Compound (1f) with Compound (8') can be
carried out in the presence of suitable base(s). A wide variety of
known inorganic and organic bases are usable. Inorganic bases
include, for example, alkali metals (e.g., sodium, potassium,
etc.), alkali metal hydrogencarbonates (e.g., lithium
hydrogencarbonate, sodium hydrogencarbonate, potassium
hydrogencarbonate, etc.), alkali metal hydroxides (e.g., lithium
hydroxide, sodium hydroxide, potassium hydroxide, cesium hydroxide,
etc.), alkali metal carbonates (e.g., lithium carbonate, sodium
carbonate, potassium carbonate, cesium carbonate, etc.), alkali
metal lower alkoxides (e.g., sodium methoxide, sodium ethoxide,
etc.), alkali metal hydrides (e.g., sodium hydride, potassium
hydride, etc.), and the like. Organic bases include, for example,
trialkylamines (e.g., trimethylamine, triethylamine,
N-ethyldiisopropylamine, etc.), pyridine, quinoline, piperidine,
imidazole, picoline, dimethylaminopyridine, dimethylaniline,
N-methylmorpholine, 1,5-diazabicyclo[4.3.0]non-5-ene (DBN),
1,4-diazabicyclo[2.2.2]octane (DABCO),
1,8-diazabicyclo[5.4.0]undec-7-ene (DBU), etc. When such bases are
liquid, they can also be used as solvents. Such bases can be used
singly or in combination.
[0129] The amount of base(s) is usually 0.5 to 10 mol, and
preferably 0.5 to 6 mol, per mol of Compound (1f).
[0130] The proportion of Compound (1f) to Compound (8') is usually
at least 1 mol, and preferably about 1 to about 5 mol of the
latter, per mol of the former.
[0131] The reaction temperature is not limited, and the reaction
can usually be performed with cooling, at room temperature, or with
heating. It is suitable to perform the reaction at about room
temperature for 1 to 30 hours.
[0132] Compounds (8) and (8') used as starting materials in the
above reaction are easily available known compounds.
[0133] Among the oxazole compounds represented by Formula (1),
those in which W is a divalent group represented by
--Y.sup.1-A.sup.1- wherein Y.sup.1 is --C(.dbd.O) and A.sup.1 is a
lower alkenylene group (hereinafter referred to as "Compound (1h)")
can be produced by, for example, the process shown in Reaction
Scheme 7.
##STR00014##
wherein R.sup.1 and R.sup.2 are as defined in Formula (1), and
A.sup.1d is a C.sub.2-4 alkenylene group, a C.sub.1-4 alkylene
group, or a direct bond.
[0134] Each of the C.sub.2-4 alkenyl group and C.sub.1-4 alkylene
group may be straight- or branched-chain. --CH.dbd.CH-A.sup.1d
corresponds to the lower alkenylene group represented by A.sup.1 in
Formula (1).
[0135] Compound (1h) is produced by reacting Compound (9) with
Compound (10).
[0136] The reaction is usually performed in a known solvent that
does not adversely affect the reaction. Such solvents include, for
example, water; methanol, ethanol, isopropanol, n-butanol,
trifluoroethanol, ethylene glycol, and other alcohol solvents;
acetone, methyl ethyl ketone, and other ketone solvents;
tetrahydrofuran, dioxane, diethyl ether, dimethoxyethane, diglyme,
and other ether solvents; methyl acetate, ethyl acetate, and other
ester solvents; acetonitrile, N,N-dimethylformamide, dimethyl
sulfoxide, N-methylpyrrolidone, and other aprotic polar solvents;
methylene chloride, ethylene chloride, and other halogenated
hydrocarbon solvents; other organic solvents; mixed solvents
thereof; etc.
[0137] The reaction can be performed in the presence of base(s). A
wide variety of known inorganic and organic bases are usable.
Inorganic bases include, for example, alkali metals (e.g., lithium,
sodium, potassium, etc.), alkali metal hydrogencarbonates (e.g.,
lithium hydrogencarbonate, sodium hydrogencarbonate, potassium
hydrogencarbonate, etc.), alkali metal hydroxides (e.g., lithium
hydroxide, sodium hydroxide, potassium hydroxide, cesium hydroxide,
etc.), alkali metal carbonates (e.g., lithium carbonate, sodium
carbonate, potassium carbonate, cesium carbonate, etc.), alkali
metal lower alkoxides (e.g., sodium methoxide, sodium ethoxide,
potassium tert-butoxide, sodium tert-butoxide, etc.), alkali metal
hydrides (e.g., sodium hydride, potassium hydride, etc.), and the
like. Organic bases include, for example, trialkylamines (e.g.,
trimethylamine, triethylamine, N-ethyldiisopropylamine, etc.),
pyridine, quinoline, piperidine, imidazole, picoline,
dimethylaminopyridine, dimethylaniline, N-methylmorpholine,
1,5-diazabicyclo[4.3.0]non-5-ene (DBN),
1,4-diazabicyclo[2.2.2]octane (DABCO),
1,8-diazabicyclo[5.4.0]undec-7-ene (DBU), etc. When such bases are
liquid, they can also be used as solvents. Such bases can be used
singly or in combination.
[0138] The amount of base(s) is usually 0.5 to 10 mol, and
preferably 0.5 to 6 mol, per mol of Compound (9).
[0139] The proportion of Compound (9) to Compound (10) is usually
at least 1 mol, and preferably about 1 to about 5 mol of the
latter, per mol of the former.
[0140] The reaction temperature is not limited, and the reaction
can usually be performed with cooling, at room temperature, or with
heating. It is suitable to perform the reaction in a temperature
range from room temperature to 150.degree. C., for 30 minutes to 60
hours, and preferably for 1 to 30 hours.
[0141] Compound (9) used as a starting material in the above
reaction is an easily available known compound. Compound (10) used
as a starting material in the above reaction can be produced by the
process shown in Reaction Scheme 12.
[0142] Among the oxazole compounds represented by Formula (1),
those in which W is a divalent group represented by wherein A.sup.1
is a lower alkylene group (hereinafter referred to as "Compound
(1j)") can be produced from compounds in which A.sup.1 is a lower
alkenylene group (hereinafter referred to as "Compound (1i)"), by
the process shown in Reaction Scheme 8.
##STR00015##
wherein R.sup.1 and R.sup.2 are as defined in Formula (1), Y.sup.1
is as defined above, A.sup.1e is a lower alkenylene group, and
A.sup.1f is a lower alkylene group.
[0143] Compound (1j) is produced by subjecting Compound (1i) to
hydrogenolysis.
[0144] The reaction is performed under the same reaction conditions
as of the reaction shown in Reaction Scheme 5 for the
hydrogenolysis of Compound (1e) to obtain Compound (1f). Therefore,
the same reagent(s) and reaction conditions (e.g., solvent,
reaction temperature, etc.) as those used in the hydrogenolysis
shown in Reaction Scheme 5 can be used in the above reaction.
##STR00016##
wherein R.sup.2 and W are as defined in Formula (1), and X is as
defined above.
[0145] The halogenation reaction of Compound (11) is performed in a
suitable solvent in the presence of a halogenating agent. Usable
halogenating agents include, for example, Br.sub.2, Cl.sub.2, and
other halogen molecules; iodine chloride, sulfuryl chloride, cupric
bromide, and other copper compounds; N-bromosuccinimide,
N-chlorosuccinimide, and other N-halosuccinimides, etc. Usable
solvents include, for example, dichloromethane, dichloroethane,
chloroform, carbon tetrachloride, and other halogenated
hydrocarbons; acetic acid, propionic acid, and other fatty acids;
carbon disulfide; etc. The amount of halogenating agent is usually
1 to 10 mol, and preferably 1 to 5 mol, per mol of Compound (11).
The reaction is usually complete at 0.degree. C. to the boiling
point temperature of the solvent, and preferably about 0 to about
100.degree. C., in about 5 minutes to about 20 hours.
[0146] Among Compounds (5) for use as starting materials, those in
which R.sup.3 is a hydrogen atom (hereinafter referred to as
"Compound (5a)") are produced by the process shown in Reaction
Scheme 10.
##STR00017##
wherein R.sup.1 and A.sup.1 are as defined in Formula (1), X.sup.2
and X.sup.3 are each independently a halogen atom or a group that
undergoes the same substitution reaction as that of a halogen atom
as mentioned above, and M is an alkali metal.
[0147] Examples of the alkali metal represented by M include
sodium, potassium, etc.
[0148] Compound (14) is produced by reacting Compound (12) with
Compound (13).
[0149] The reaction of Compound (12) with Compound (13) is usually
performed in a known solvent that does not adversely affect the
reaction. Such solvents include, for example, water; methanol,
ethanol, isopropanol, n-butanol, trifluoroethanol, ethylene glycol,
and other alcohol solvents; acetone, methyl ethyl ketone, and other
ketone solvents; tetrahydrofuran, dioxane, diethyl ether,
dimethoxyethane, diglyme, and other ether solvents; methyl acetate,
ethyl acetate, and other ester solvents; acetonitrile,
N,N-dimethylformamide, dimethyl sulfoxide, N-methylpyrrolidone, and
other aprotic polar solvents; methylene chloride, ethylene
chloride, and other halogenated hydrocarbon solvents; and other
organic solvents; etc.
[0150] The proportion of Compound (12) to Compound (13) is usually
at least 1 mol, and preferably about 1 to about 5 mol of the
latter, per mol of the former. The reaction of Compound (12) with
Compound (13) is performed by continuing stirring usually in a
temperature range from room temperature to 200.degree. C., and
preferably from room temperature to 150.degree. C., usually for 30
minutes to 60 hours, and preferably 1 to 30 hours.
[0151] Compound (16) is produced by reacting Compound (15) with
Compound (14).
[0152] The reaction of Compound (15) with Compound (14) is usually
performed in a known solvent that does not adversely affect the
reaction. Such solvents include, for example, water; methanol,
ethanol, isopropanol, n-butanol, trifluoroethanol, ethylene glycol,
and other alcohol solvents; acetone, methyl ethyl ketone, and other
ketone solvents; tetrahydrofuran, dioxane, diethyl ether, diglyme,
and other ether solvents; methyl acetate, ethyl acetate, and other
ester solvents; acetonitrile, N,N-dimethylformamide, dimethyl
sulfoxide, and other aprotic polar solvents; methylene chloride,
ethylene chloride, and other halogenated hydrocarbon solvents;
other organic solvents; mixtures thereof; etc.
[0153] When performing the reaction of Compound (15) with Compound
(14), alkali metal iodides such as potassium iodide, sodium iodide,
etc. can be added as reaction accelerators to the reaction system,
as required.
[0154] The proportion of Compound (15) to Compound (14) is usually
at least 1 mol, and preferably about 1 to about 5 mol of the
latter, per mol of the former.
[0155] The temperature of the reaction of Compound (15) with
Compound (14) is not limited, and the reaction can usually be
performed with cooling, at room temperature, or with heating. It is
suitable to perform the reaction in a temperature range from room
temperature to 100.degree. C., for 1 to 60 hours, and preferably
for 1 to 30 hours.
[0156] In the reaction of Compound (15) with Compound (14),
phthalimide can be used in place of Compound (15) and the reaction
may be performed in the presence of base(s). A wide variety of
known inorganic and organic bases are usable. Examples of inorganic
bases include alkali metals (e.g., lithium, sodium, potassium,
etc.), alkali metal hydrogencarbonates (e.g., lithium
hydrogencarbonate, sodium hydrogencarbonate, potassium
hydrogencarbonate, etc.), alkali metal hydroxides (e.g., lithium
hydroxide, sodium hydroxide, potassium hydroxide, cesium hydroxide,
etc.), alkali metal carbonates (e.g., lithium carbonate, sodium
carbonate, potassium carbonate, cesium carbonate, etc.), alkali
metal lower alkoxides (e.g., sodium methoxide, sodium ethoxide,
potassium tert-butoxide, sodium tert-butoxide, etc.), alkali metal
hydrides (e.g., sodium hydride, potassium hydride, etc.), and the
like. Organic bases include, for example, trialkylamines (e.g.,
trimethylamine, triethylamine, N-ethyldiisopropylamine, etc.),
pyridine, quinoline, piperidine, imidazole, picoline,
dimethylaminopyridine, dimethylaniline, N-methylmorpholine,
1,5-diazabicyclo[4.3.0]non-5-ene (DBN),
1,4-diazabicyclo[2.2.2]octane (DABCO),
1,8-diazabicyclo[5.4.0]undec-7-ene (DBU), etc.
[0157] The amount of base(s) is usually 0.5 to 10 mol, and
preferably 0.5 to 6 mol, per mol of Compound (14).
[0158] Compound (5a) is produced by reacting Compound (16) with
Compound (17).
[0159] The reaction of Compound (16) with Compound (17) is usually
performed in a known solvent that does not adversely affect the
reaction. Such solvents include, for example, water; methanol,
ethanol, isopropanol, n-butanol, trifluoroethanol, ethylene glycol,
and other alcohol solvents; acetone, methyl ethyl ketone, and other
ketone solvents; tetrahydrofuran, dioxane, diethyl ether, diglyme,
and other ether solvents; methyl acetate, ethyl acetate, and other
ester solvents; acetonitrile, N,N-dimethylformamide, dimethyl
sulfoxide, and other aprotic polar solvents; methylene chloride,
ethylene chloride, and other halogenated hydrocarbon solvents;
other organic solvents; mixtures thereof; etc.
[0160] The proportion of Compound (16) to Compound (17) is usually
at least 1 mol, and preferably about 1 to about 5 mol of the
latter, per mol of the former.
[0161] The temperature of the reaction of Compound (16) with
Compound (17) is not limited, and the reaction can usually be
performed with cooling, at room temperature, or with heating. It is
suitable to perform the reaction at about room temperature for 1 to
30 hours.
##STR00018##
wherein R.sup.1 is as defined in Formula (1); R.sup.8 and A.sup.1a
are as defined above; X.sup.4 is a halogen atom or a group that
undergoes the same substitution reaction as that of a halogen atom
as mentioned above; and R.sup.12 is a lower alkyl group.
[0162] Compound (20) is produced by reacting Compound (18) with
Compound (19).
[0163] The reaction of Compound (18) with Compound (19) is usually
performed in a known solvent that does not adversely affect the
reaction. Such solvents include, for example, water; methanol,
ethanol, isopropanol, n-butanol, trifluoroethanol, ethylene glycol,
and other alcohol solvents; acetone, methyl ethyl ketone, and other
ketone solvents; tetrahydrofuran, dioxane, diethyl ether,
dimethoxyethane, diglyme, and other ether solvents; methyl acetate,
ethyl acetate, and other ester solvents; acetonitrile,
N,N-dimethylformamide, dimethyl sulfoxide, N-methylpyrrolidone, and
other aprotic polar solvents; methylene chloride, ethylene
chloride, and other halogenated hydrocarbon solvents; other organic
solvents; mixtures thereof; etc.
[0164] The reaction of Compound (18) with Compound (19) can usually
be performed in the presence of suitable base(s). A wide variety of
known inorganic and organic bases are usable. Inorganic bases
include, for example, alkali metals (e.g., lithium, sodium,
potassium, etc.), alkali metal hydrogencarbonates (e.g., lithium
hydrogencarbonate, sodium hydrogencarbonate, potassium
hydrogencarbonate, etc.), alkali metal hydroxides (e.g., lithium
hydroxide, sodium hydroxide, potassium hydroxide, cesium hydroxide,
etc.), alkali metal carbonates (e.g., lithium carbonate, sodium
carbonate, potassium carbonate, cesium carbonate, etc.), alkali
metal lower alkoxides (e.g., sodium methoxide, sodium ethoxide,
potassium tert-butoxide, sodium tert-butoxide, etc.), alkali metal
hydrides (e.g., sodium hydride, potassium hydride, etc.), and the
like. Organic bases include, for example, trialkylamines (e.g.,
trimethylamine, triethylamine, N-ethyldiisopropylamine, etc.),
pyridine, quinoline, piperidine, imidazole, picoline,
dimethylaminopyridine, dimethylaniline, N-methylmorpholine,
1,5-diazabicyclo[4.3.0]non-5-ene (DBN),
1,4-diazabicyclo[2.2.2]octane (DABCO),
1,8-diazabicyclo[5.4.0]undec-7-ene (DBU), etc. When such bases are
liquid, they can also be used as solvents.
[0165] Such bases can be used singly or in combination.
[0166] The amount of base(s) is usually 0.5 to 10 mol, and
preferably 0.5 to 6 mol, per mol of Compound (18).
[0167] The proportion of Compound (18) to Compound (19) in Reaction
Scheme 11 is usually at least 1 mol, and preferably about 1 to
about 5 mol of the latter, per mol of the former.
[0168] The reaction temperature is not limited, and the reaction
can usually be performed with cooling, at room temperature, or with
heating. It is suitable to perform the reaction in a temperature
range from room temperature to 100.degree. C., for 30 minutes to 60
hours, and preferably 1 to 30 hours.
[0169] Compound (7) is produced by subjecting Compound (20) to
hydrolysis-decarboxylation. The hydrolysis-decarboxylation of
Compound (20) can be carried out by the process shown in Reference
Example 48 given hereinafter, a process similar thereto, the
process shown in Reaction Scheme 4 above, or a process similar
thereto.
##STR00019##
wherein R.sup.1 is as defined in Formula (1), and X.sup.2 and
A.sup.1d are as defined above.
[0170] Compound (10) is produced by subjecting Compound (21) to an
oxidation reaction. The reaction can be carried out by the process
shown in Reference Example 64 given hereinafter, or a process
similar thereto, and is performed in the presence of a known
solvent that does not adversely affect the reaction. Such solvents
include, for example, water; methanol, ethanol, isopropanol,
n-butanol, trifluoroethanol, ethylene glycol, and other alcohol
solvents; acetone, methyl ethyl ketone, and other ketone solvents;
tetrahydrofuran, dioxane, diethyl ether, diglyme, and other ether
solvents; methyl acetate, ethyl acetate, and other ester solvents;
acetonitrile, N,N-dimethylformamide, dimethyl sulfoxide, and other
aprotic polar solvents; methylene chloride, ethylene chloride, and
other halogenated hydrocarbon solvents; other organic solvents;
mixtures thereof; etc.
[0171] The reaction is usually performed using oxidizing agent(s)
such as dimethyl sulfoxide, hexamethylenetetramine,
triethylamine-N-oxide, etc.
[0172] If necessary, the reaction can be performed in the presence
of suitable base(s). A wide variety of known inorganic and organic
bases are usable. Inorganic bases include, for example, alkali
metals (e.g., sodium, potassium, etc.), alkali metal
hydrogencarbonates (e.g., lithium hydrogencarbonate, sodium
hydrogencarbonate, potassium hydrogencarbonate, etc.), alkali metal
hydroxides (e.g., lithium hydroxide, sodium hydroxide, potassium
hydroxide, cesium hydroxide, etc.), alkali metal carbonates (e.g.,
lithium carbonate, sodium carbonate, potassium carbonate, cesium
carbonate, etc.), alkali metal lower alkoxides (e.g., sodium
methoxide, sodium ethoxide, etc.), alkali metal hydrides (e.g.,
sodium hydride, potassium hydride, etc.), and the like. Organic
bases include, for example, trialkylamines (e.g., trimethylamine,
triethylamine, N-ethyldiisopropylamine, etc.), pyridine, quinoline,
piperidine, imidazole, picoline, dimethylaminopyridine,
dimethylaniline, N-methylmorpholine,
1,5-diazabicyclo[4.3.0]non-5-ene (DBN),
1,4-diazabicyclo[2.2.2]octane (DABCO),
1,8-diazabicyclo[5.4.0]undec-7-ene (DBU), etc. When such bases are
liquid, they can also be used as solvents. Such bases can be used
singly or in combination.
[0173] The amount of oxidizing agent is usually 0.5 to 10 mol, and
preferably 0.5 to 6 mol, per mol of Compound (21).
[0174] The amount of base(s) is usually 0.5 to 10 mol, and
preferably 0.5 to 6 mol, per mol of Compound (21).
[0175] When performing the above reaction, alkali metals such as
potassium iodide, sodium iodide, etc. can be added as reaction
accelerators to the reaction system, as required.
[0176] The reaction temperature is not limited, and the reaction
can usually be performed with cooling, at room temperature, or with
heating. It is suitable to perform the reaction in a temperature
range from room temperature to 120.degree. C. for 30 minutes to 30
hours.
[0177] The starting material compounds used in the above reaction
schemes may be suitable salts, and the objective compounds obtained
by the above reactions may be in the form of suitable salts.
[0178] Each of the objective compounds obtained according to the
above reaction schemes can be isolated and purified from the
reaction mixture by, for example, cooling the reaction mixture,
separating the crude reaction product from the reaction mixture by
an isolation procedure such as filtration, concentration,
extraction and/or other isolation procedures, and then purifying
the crude reaction product by column chromatography,
recrystallization and/or other conventional purification
procedures.
[0179] Suitable salts of Compound (1) are pharmaceutically
acceptable salts including, for example, metal salts such as alkali
metal salts (e.g., sodium salt, potassium salt, etc.), alkaline
earth metal salts (e.g., calcium salt, magnesium salt, etc.), etc.,
ammonium salts, alkali metal carbonates (e.g., lithium carbonate,
potassium carbonate, sodium carbonate, cesium carbonate, etc.),
alkali metal hydrogencarbonates (e.g., lithium hydrogencarbonate,
sodium hydrogencarbonate, potassium hydrogencarbonate, etc.),
alkali metal hydroxides (e.g., lithium hydroxide, sodium hydroxide,
potassium hydroxide, cesium hydroxide, etc.), and other salts of
inorganic bases; tri(lower)alkylamines (e.g., trimethylamine,
triethylamine, N-ethyldiisopropylamine, etc.), pyridine, quinoline,
piperidine, imidazole, picoline, dimethylaminopyridine,
dimethylaniline, N-(lower)alkylmorpholines (e.g.,
N-methylmorpholine and the like), DBN, DBU, DABCO, and other salts
of organic bases; hydrochlorides, hydrobromides, hydroiodides,
sulfates, nitrates, phosphates, and other salts of inorganic acids;
formates, acetates, propionates, oxalates, malonates, succinates,
fumarates, maleates, lactates, malates, citrates, tartrates,
citrates, carbonates, picrates, methanesulfonates,
ethanesulfonates, p-toluenesulfonates, glutamates, and other salts
of inorganic acids; etc.
[0180] The starting material compounds and objective compounds
represented by the formulae in the above reaction schemes encompass
solvates (e.g. hydrates, ethanolates, etc.). Preferable solvates
include hydrates.
[0181] The compounds represented by Formula (1) of the present
invention of course encompass isomers such as geometrical isomers,
stereoisomer, optical isomers, etc.
Drug Efficacy and Use
[0182] Compounds represented by formula (1), optically active
isomers thereof, and salts thereof (hereinafter referred to as
"compounds of the present invention") have a specific inhibitory
action against PDE4, and are hence useful as active ingredients for
a PDE4 inhibitor.
[0183] Further, due to their PDE4-specific inhibitory action, the
compounds of the invention can be useful as active ingredients of
pharmaceutical compositions used as prophylactic and therapeutic
agents for various diseases. More specifically, diseases
efficiently preventable and treatable by the PED4-specific
inhibitory action include various origin-generated acute and
chronic (in particular, inflammatory and allergen induced)
respiratory tract diseases (e.g. bronchial asthma, chronic
obstructive pulmonary disease, etc.); dermatoses (in particular,
hyperplastic, inflammatory, and allergic diseases) (e.g. psoriasis
(vulgaris), toxic and allergic contact eczema, atopic dermatitis,
alopecia areata, and other hyperplastic, inflammatory and allergic
dermatoses); nervous function abnormality diseases such as
learning, memory, and/or cognition disorders associated with
Altzheimer's and Perkinson's diseases; diseases associated with
mental function abnormality (e.g. manic-depressive psychosis,
schizophrenia, anxiety disorder, etc.); systemic and local
arthritic disorders (e.g. knee osteoarthritis, articular
rheumatism, etc.); gastrointestinal diffuse inflammation (e.g.
Crohn's disease and ulcerative colitis); allergic and/or chronic
immune-mediated inflammatory diseases in the upper respiratory
tract (cavum pharynges, nose) and its vicinity (sinuses, eyes)
(e.g. allergic rhinitis/sinusitis, chronic rhinitis/sinusitis,
allergic conjunctivitis), and the like. Among these, the compounds
are particularly effective in preventing and treating atopic
dermatitis, making this diseases a suitable target disease for
prevention and treatment.
[0184] When used as a PDE4 inhibitor or as prophylactic or
therapeutic agent for the above-mentioned various diseases, the
compounds of the invention can be used as oral agents, injectable
solutions, external preparations, and the like.
[0185] For oral agents, for example, the compounds may be prepared
in any forms such as powders, tablets, granules, capsules, syrups,
films, troches, liquids, etc. Such oral agents can contain
pharmaceutically acceptable base materials and carriers, and
further optionally contain as necessary binders, disintegrators,
lubricants, humectants, buffers, preservatives, fragrances, and the
like.
[0186] For injectable solutions, the compounds may be prepared in
the form of solutions dissolved in physiological saline, grape
sugar solutions and the like, or aqueous suspensions.
[0187] For external preparations, the compounds may be prepared in
any forms, for example, such as liquid medicines, oily medicines,
lotions, liniments, emulsions, suspensions, creams, ointments, etc.
Such external preparations can optionally contain various carriers,
base materials, and additives as typically used in external
preparations, and examples include water, oils, surfactants,
solubilized components, emulsifiers, colorants (dyes and pigments),
fragrances, preservatives, disinfectants, thickeners, antioxidants,
chelators, pH adjusting agents, deodorants, etc.
[0188] When used as a PDE4 inhibitor, or as prophylactic or
therapeutic agent for the aforementioned various diseases,
effective dose and number of doses a day of the compound vary
depending on the purpose of use, kind of compound used, the age,
weight, symptoms, etc. of a subject, and cannot be uniformly
prescribed. For example, the inhibitor or agent can be administered
in a dose of 0.1 to 1000 mg of the compound(s) of the present
invention per day per adult, and may be administered in one to
several portions a day.
[0189] Further, in light of other viewpoints, the present invention
provides a method for treating or preventing the aforementioned
various diseases comprising the step of administrating an effective
dose of the compound(s) of the invention to a mammal, such as a
human.
[0190] Furthermore, since the compounds of the present invention
have inhibitory action against TNF-.alpha. production, they are
useful as active ingredients for TNF-.alpha. production
suppressants. Diseases that benefit from such TNF-.alpha.
production inhibitory action include those efficiently preventable
and treatable by the aforementioned PDE4-specific inhibitory
action. Preparation forms, administration routes and doses of
TNF-.alpha. production suppressant containing compounds of the
invention are the same as those of the aforementioned PDE4
inhibitor and prophylactic and therapeutic agents.
Effect of the Invention
[0191] The compounds of the present invention have an inhibitory
action specific against PDE4, and are hence useful as active
ingredients for a PDE 4 inhibitors.
[0192] Due to their specific PDE4 inhibitory activity, the
compounds of the invention are further useful as prophylactic and
therapeutic agents for various diseases including atopic
dermatitis.
BEST MODE FOR CARRYING OUT THE INVENTION
[0193] The present invention is described in more detail below with
reference to Examples; however, the present invention is not
limited thereto.
Reference Example 1
[0194] A 25 g quantity of isovanillic acid was suspended in 250 ml
of methanol, and 1.5 g of p-toluenesulfonic acid monohydrate was
added. The mixture was heated and refluxed overnight. After
completion of the reaction, methanol was distilled off under
reduced pressure. The residue was neutralized with saturated
aqueous sodium bicarbonate and then extracted with ethyl acetate.
After washing with saturated brine twice, the organic layer was
separated and concentrated under reduced pressure. The residue was
purified by silica gel column chromatography (n-hexane:ethyl
acetate=1:1) to give 24.5 g of white crystalline methyl
3-hydroxy-4-methoxybenzoate.
[0195] .sup.1H-NMR (CDCl.sub.3) .delta.: 7.63-7.58 (2H, m), 6.67
(1H, d, J=8.1 Hz), 5.63 (1H, s), 3.98 (3H, s), 3.90 (3H, s)
Reference Example 2
[0196] A 20 g quantity of methyl 3-hydroxy-4-methoxybenzoate
obtained in Reference Example 1 was dissolved in 200 ml of
methanol, and 24.6 ml of 1,8-diazabicyclo[5,4,0]undec-7-ene and 21
g of benzyl bromide were added. The mixture was heated and refluxed
overnight. After the reaction mixture was concentrated, water was
added to the residue and extraction with ethyl acetate was
performed. The extract was washed with saturated brine twice, and
the organic layer was separated and dried over magnesium sulfate.
After insolubles were removed by filtration, the filtrate was
concentrated under reduced pressure to give 25.5 g of white
crystalline methyl 3-benzyloxy-4-methoxybenzoate.
[0197] .sup.1H-NMR (CDCl.sub.3) .delta.: 7.68 (1H, dd, J=8.4, 1.8
Hz), 7.61 (1H, d, J=1.8 Hz), 7.48-7.28 (5H, m), 6.91 (1H, d, J=8.4
Hz), 5.17 (2H, s), 3.93 (3H, s), 3.87 (3H, s)
Reference Example 3
[0198] A 25 g quantity of the methyl 3-benzyloxy-4-methoxybenzoate
obtained in Reference Example 2 was dissolved in 100 ml of
acetonitrile, and a solution of 11 g of sodium hydroxide in 100 ml
of water was added. The mixture was stirred with heating at
40.degree. C. for 5 hours. The reaction mixture was cooled with
ice, and concentrated hydrochloric acid was added to give a pH of
about 3. The precipitated crystals were collected by filtration and
dried under reduced pressure to give 22.1 g of white crystalline
3-benzyloxy-4-methoxybenzoic acid.
[0199] .sup.1H-NMR (CDCl.sub.3) .delta.: 7.77 (1H, dd, J=8.4, 1.8
Hz), 7.65 (1H, d, J=1.8 Hz), 7.48-7.29 (5H, m), 6.94 (1H, d, J=8.4
Hz), 5.19 (2H, s), 3.95 (3H, s)
Reference Example 4
[0200] A 20 g quantity of the 3-benzyloxy-4-methoxybenzoic acid
obtained in Reference Example 3 was suspended in 200 ml of
dichloromethane, and one drop of dimethylformamide was added. A 8.1
ml quantity of oxalyl chloride was added dropwise with ice-cooling
and stirring. After 2 hours, the reaction mixture was concentrated
under reduced pressure. The residue was dissolved in 50 ml of
tetrahydrofuran and the resulting solution was added dropwise to
28% aqueous ammonia with ice-cooling and stirring. The obtained
mixture was stirred for 1 hour and the precipitated crystals were
collected by filtration and dried under reduced pressure to give
19.9 g of white powdery 3-benzyloxy-4-methoxybenzamide.
[0201] .sup.1H-NMR (CDCl.sub.3) .delta.: 7.85-7.28 (7H, m), 6.90
(1H, d, J=8.1 Hz), 5.67 (2H, br s), 5.18 (2H, s), 3.93 (3H, s)
Reference Example 5
[0202] A 15 g quantity of 3-benzyloxy-4-methoxybenzamide obtained
in Reference Example 4 was suspended in 450 ml of isopropanol, and
13.9 g of 1,3-dichloro-2-propanone was added. The mixture was
heated and refluxed overnight. After the reaction mixture was
concentrated to half its original volume under reduced pressure,
200 ml of n-hexane was added to the concentrate and the mixture was
stirred. The precipitated crystals were collected by filtration and
dried under reduced pressure to give 12.2 g of white powdery
2-(3-benzyloxy-4-methoxyphenyl)-4-chloromethyl oxazole.
[0203] .sup.1H-NMR (CDCl.sub.3) .delta.: 7.73-7.71 (3H, m),
7.50-7.29 (5H, m), 6.95 (1H, d, J=5.7 Hz), 5.20 (2H, s), 4.56 (2H,
s), 3.93 (3H, s)
Reference Example 6
[0204] A 11 g quantity of
2-(3-benzyloxy-4-methoxyphenyl)-4-chloromethyl oxazole obtained in
Reference Example 5 was suspended in 220 ml of ethanol, and 7.5 g
of sodium iodide and 9.3 g of potassium phthalimide were added. The
mixture was heated and refluxed overnight. The reaction mixture was
cooled with ice, and the precipitated crystals were collected by
filtration. The obtained crude crystals were suspended and washed
with 100 ml of water. The resulting crystals were dried under
reduced pressure to give 9.4 g of white powdery
2-[2-(3-benzyloxy-4-methoxyphenyl)oxazol-4-ylmethyl]isoindolin-1,3-dione.
[0205] .sup.1H-NMR (CDCl.sub.3) .delta.: 7.91-7.85 (2H, m)
7.76-7.69 (2H, m), 7.61-7.58 (3H, m) 7.46 (2H, d, J=6.6 Hz),
7.39-7.26 (3H, m), 6.91 (1H, d, J=9 Hz), 5.18 (2H, s), 4.85 (2H,
s), 3.90 (3H, s)
Reference Example 7
[0206] A 9 g quantity of the
2-[2-(3-benzyloxy-4-methoxyphenyl)oxazol-4-ylmethyl]isoindolin-1,3-dione
obtained in Reference Example 6 was suspended in 200 ml of ethanol,
and 3.1 ml of hydrazine monohydrate was added. The mixture was
heated and refluxed for 3 hours. After cooing the reaction mixture,
200 ml of dichloromethane was added and the mixture was stirred.
Insolubles were removed by filtration, and the filtrate was
concentrated under reduced pressure. The residue was purified by
silica gel column chromatography (NH silica, product of Fuji
Sylisia Chemical Ltd., dichloromethane:methanol=20:1) to give 4.5 g
of pale yellow powdery
[2-(3-benzyloxy-4-methoxyphenyl)oxazol-4-yl]methylamine.
[0207] .sup.1H-NMR (CDCl.sub.3) .delta.: 7.63-7.59 (2H, m)
7.53-7.46 (3H, m), 7.41-7.27 (3H, m) 6.94 (1H, d, J=9 Hz), 5.20
(2H, s), 3.89 (3H, s), 3.87 (2H, s), 2.14 (2H, br s)
Reference Example 8
[0208] A 15 g quantity of methyl 3-hydroxy-4-methoxybenzoate
obtained in Reference Example 1 was dissolved in 150 ml of
dimethylformamide, and 34 g of potassium carbonate and 22.2 g of
(bromomethyl)cyclopropane were added. The mixture was heated at
90.degree. C. overnight. Ice water was added to the reaction
mixture, and the precipitated crystals were collected by filtration
and washed with an excess of water. The obtained crystals were
dried under reduced pressure at room temperature to give 18.3 g of
white crystalline methyl
3-cyclopropylmethoxy-4-methoxybenzoate.
[0209] .sup.1H-NMR (CDCl.sub.3) .delta.: 7.67 (1H, dd, J=8.4, 1.8
Hz), 7.52 (1H, d, J=2.1 Hz), 6.89 (1H, d, J=8.4 Hz), 3.94-3.86 (8H,
m), 1.43-1.29 (1H, m), 0.70-0.58 (2H, m), 0.45-0.30 (2H, m)
Reference Example 9
[0210] Using 18 g of methyl 3-cyclopropylmethoxy-4-methoxybenzoate
obtained in Reference Example 8 and following the procedure of
Reference Example 3, 16.6 g of white crystalline
3-cyclopropylmethoxy-4-methoxybenzoic acid was obtained.
[0211] .sup.1H-NMR (CDCl.sub.3) .delta.: 7.76 (1H, dd, J=8.4, 1.8
Hz), 7.58 (1H, d, J=2.1 Hz), 6.92 (1H, d, J=8.4 Hz), 3.98-3.92 (8H,
m), 1.43-1.29 (1H, m), 0.70-0.58 (2H, m), 0.46-0.35 (2H, m)
Reference Example 10
[0212] Using 16.5 g of 3-cyclopropylmethoxy-4-methoxybenzoic acid
obtained in Reference Example 9 and following the procedure of
Reference Example 4, 16.2 g of pale yellow powdery
3-cyclopropylmethoxy-4-methoxybenzamide was obtained.
[0213] .sup.1H-NMR (CDCl.sub.3) .delta.: 7.43 (1H, d, J=2.1 Hz),
7.31 (1H, dd, J=8.4, 2.1 Hz), 6.88 (1H, d, J=8.1 Hz), 5.75 (2H, br
s), 3.97-3.89 (5H, m), 1.40-1.28 (1H, m), 0.69-0.62 (2H, m),
0.39-0.33 (2H, m)
Reference Example 11
[0214] Using 13 g of 3-cyclopropylmethoxy-4-methoxybenzamide
obtained in Reference Example 10 and following the procedure of
Reference Example 5, 10.5 g of pale yellow powdery
4-chloromethyl-2-(3-cyclopropylmethoxy-4-methoxyphenyl)oxazole was
obtained.
[0215] .sup.1H-NMR (CDCl.sub.3) .delta.: 7.65 (1H, d, J=0.9 Hz),
7.20 (1H, dd, J=8.7, 2.1 Hz), 7.53 (1H, d, J=2.1 Hz), 6.93 (1H, d,
J=8.4 Hz), 4.57 (2H, s), 3.97-3.90 (5H, m), 1.43-1.32 (1H, m),
0.71-0.63 (2H, m), 0.41-0.35 (2H, m)
Reference Example 12
[0216] Using 8 g of
4-chloromethyl-2-(3-cyclopropylmethoxy-4-methoxyphenyl)oxazole
obtained in Reference Example 11 and following the procedure of
Reference Example 6, 10 g of white crystalline
2-[2-(3-cyclopropylmethoxy-4-methoxyphenyl)oxazol-4-ylmethyl]isoindolin-1-
,3-dione was obtained.
[0217] .sup.1H-NMR (CDCl.sub.3) .delta.: 7.90-7.84 (2H, m),
7.76-7.69 (2H, m), 7.62 (1H, s), 7.57 (1H, dd, J=8.4, 2.1 Hz), 7.48
(1H, d, J=2.1 Hz), 6.89 (1H, d, J=8.4 Hz), 4.85 (2H, s), 3.95-3.90
(5H, m), 1.41-1.31 (1H, m), 0.69-0.62 (2H, m), 0.41-0.35 (2H,
m)
Reference Example 13
[0218] Using 9.5 g of
2-[2-(3-cyclopropylmethoxy-4-methoxyphenyl)oxazol-4-ylmethyl]isoindolin-1-
,3-dione obtained in Reference Example 12 and following the
procedure of Reference Example 7, 5.1 g of white powdery
[2-(3-cyclopropylmethoxy-4-methoxyphenyl)oxazol-4-yl]methylamine
was obtained.
[0219] .sup.1H-NMR (CDCl.sub.3) .delta.: 7.61-7.55 (1H, m),
7.53-7.50 (2H, m), 6.92 (1H, d, J=8.4 Hz), 3.96-3.87 (5H, m), 3.83
(2H, s), 1.41-1.33 (1H, m), 0.70-0.63 (2H, m), 0.41-0.35 (2H,
m)
Reference Example 14
[0220] A 5 g quantity of methyl 3-hydroxy-4-methoxybenzoate
obtained in Reference Example 1 was dissolved in 100 ml of
dimethylformamide, and 11.3 g of potassium carbonate and 5.64 g of
isobutyl bromide were added. The mixture was heated at 80.degree.
C. for 6 hours. Ice water was added to the reaction mixture, and
the precipitated crystals were collected by filtration and washed
with an excess of water. The resulting crystals were dried under
reduced pressure at room temperature to give 5.85 g of white
powdery methyl 3-isobutoxy-4-methoxybenzoate.
[0221] .sup.1H-NMR (CDCl.sub.3) .delta.: 7.65 (1H, dd, J=8.4, 2.1
Hz), 7.53 (1H, d, J=1.8 Hz), 6.88 (1H, d, J=8.1 Hz), 3.96 (3H, s),
3.91 (3H, s), 3.82 (2H, d, J=6.9 Hz), 2.20-2.11 (1H, m), 1.05 (6H,
d, J=6.6 Hz)
Reference Example 15
[0222] Using 5.85 g of methyl 3-isobutoxy-4-methoxybenzoate
obtained in Reference Example 14 and following the procedure of
Reference Example 3, 5.6 g of white powdery
3-isobutoxy-4-methoxybenzoic acid was obtained.
[0223] .sup.1H-NMR (CDCl.sub.3) .delta.: 7.75 (1H, dd, J=8.4, 1.8
Hz), 7.58 (1H, d, J=2.1 Hz), 6.91 (1H, d, J=8.7 Hz), 3.94 (3H, s),
3.83 (2H, d, J=6.6 Hz), 2.26-2.12 (1H, m), 1.05 (6H, d, J=6.6
Hz)
Reference Example 16
[0224] Using 5.5 g of 3-isobutoxy-4-methoxybenzoic acid obtained in
Reference Example 15 and following the procedure of Reference
Example 4, 5.1 g of pale yellow powdery
3-isobutoxy-4-methoxybenzamide was obtained.
[0225] .sup.1H-NMR (CDCl.sub.3) .delta.: 7.43 (1H, d, J=2.1 Hz),
7.31 (1H, dd, J=8.4, 2.1 Hz), 6.87 (1H, d, J=8.7 Hz), 5.78 (2H, br
s), 3.91 (3H, s), 3.83 (2H, d, J=6.6 Hz), 2.25-2.11 (1H, m), 1.04
(6H, d, J=6.6 Hz)
Reference Example 17
[0226] Using 5 g of 3-isobutoxy-4-methoxybenzamide obtained in
Reference Example 16 and following the procedure of Reference
Example 5, 3.4 g of pale yellow powdery
4-chloromethyl-2-(3-isobutoxy-4-methoxyphenyl)oxazole was
obtained.
[0227] .sup.1H-NMR (CDCl.sub.3) .delta.: 7.65 (1H, s), 7.60 (1H,
dd, J=8.4, 2.1 Hz), 7.53 (1H, d, J=2.1 Hz), 6.92 (1H, d, J=8.4 Hz),
4.57 (2H, s), 3.91 (3H, s), 3.85 (2H, d, J=6.9 Hz), 2.27-2.13 (1H,
m), 1.05 (6H, d, J=6.6 Hz)
Reference Example 18
[0228] Using 3.3 g of
4-chloromethyl-2-(3-isobutoxy-4-methoxyphenyl)oxazole obtained in
Reference Example 17 and following the procedure of Reference
Example 6, 4.4 g of white powdery
2-[2-(3-isobutoxy-4-methoxyphenyl)oxazol-4-ylmethyl]isoindolin-1,3-dione
was obtained.
[0229] .sup.1H-NMR (CDCl.sub.3) .delta.: 7.91-7.84 (2H, m),
7.76-7.71 (2H, m), 7.62 (1H, s), 7.55 (1H, dd, J=8.4, 2.1 Hz), 7.49
(1H, d, J=2.1 Hz), 6.88 (1H, d, J=8.4 Hz), 4.85 (2H, s), 3.89 (3H,
s), 3.83 (2H, d, J=6.6 Hz), 2.23-2.13 (1H, m), 1.05 (6H, d, J=6.6
Hz)
Reference Example 19
[0230] Using 4.4 g of
2-[2-(3-isobutoxy-4-methoxyphenyl)oxazol-4-ylmethyl]isoindolin-1,3-dione
obtained in Reference Example 18 and following the procedure of
Reference Example 7, 2 g of white solid
[2-(3-isobutoxy-4-methoxyphenyl)oxazol-4-yl]methylamine was
obtained.
[0231] .sup.1H-NMR (CDCl.sub.3) .delta.: 7.60-7.51 (3H, m), 6.92
(1H, d, J=8.4 Hz), 3.91 (3H, s), 3.87-3.84 (4H, m), 2.27-2.13 (1H,
m), 1.71 (2H, br s), 1.06 (6H, d, J=6.6 Hz)
Reference Example 20
[0232] Using 10 g of methyl 3-hydroxy-4-methoxybenzoate obtained in
Reference Example 1 and following the procedure of Reference
Example 14, 12.5 g of white powdery methyl
4-methoxy-3-(2,2,2-trifluoroethoxy)benzoate was obtained.
[0233] .sup.1H-NMR (CDCl.sub.3) .delta.: 7.79 (1H, dd, J=8.7, 1.8
Hz), 7.63 (1H, s), 6.94 (1H, d, J=8.7 Hz), 4.42 (2H, q, J=8.1 Hz),
3.94 (3H, s), 3.91 (3H, s)
Reference Example 21
[0234] Using 12 g of methyl 4-methoxy-3-(2,2,2-trifluoro
ethoxy)benzoate obtained in Reference Example 20 and following the
procedure of Reference Example 3, 11.5 g of white powdery
4-methoxy-3-(2,2,2-trifluoroethoxy)benzoic acid was obtained.
[0235] .sup.1H-NMR (CDCl.sub.3) .delta.: 7.86 (1H, dd, J=8.4, 1.8
Hz), 7.67 (1H, d, J=1.8 Hz), 6.97 (1H, d, J=8.4 Hz), 4.43 (2H, q,
J=8.4 Hz), 3.96 (3H, s)
Reference Example 22
[0236] Using 11.5 g of 4-methoxy-3-(2,2,2-trifluoroethoxy)benzoic
acid obtained in Reference Example 21 and following the procedure
of Reference Example 4, 10.8 g of white powdery
4-methoxy-3-(2,2,2-trifluoroethoxy)benzamide was obtained.
[0237] .sup.1H-NMR (CDCl.sub.3) .delta.: 7.50 (1H, br s), 7.49 (1H,
dd, J=8.4, 2.4 Hz), 6.94 (1H, d, J=8.4 Hz), 4.43 (2H, q, J=8.4 Hz),
3.93 (3H, s)
Reference Example 23
[0238] Using 10.5 g of 4-methoxy-3-(2,2,2-trifluoroethoxy)benzamide
obtained in Reference Example 22 and following the procedure of
Reference Example 5, 7.1 g of pale yellow powdery
4-chloromethyl-2-[4-methoxy-3-(2,2,2-trifluoroethoxy)phenyl]oxazole
was obtained.
[0239] .sup.1H-NMR (CDCl.sub.3) .delta.: 7.75 (1H, dd, J=8.4, 2.1
Hz), 7.66 (1H, br s), 7.64 (1H, d, J=2.1 Hz), 6.98 (1H, d, J=8.4
Hz), 4.56 (2H, s), 4.45 (2H, q, J=8.4 Hz), 3.94 (3H, s)
Reference Example 24
[0240] Using 3 g of
4-chloromethyl-2-[4-methoxy-3-(2,2,2-trifluoroethoxy)phenyl]oxazole
obtained in Reference Example 23 and following the procedure of
Reference Example 6, 3.6 g of white powdery
2-{2-[4-methoxy-3-(2,2,2-trifluoroethoxy)phenyl]oxazol-4-ylmethyl}isoindo-
lin-1,3-dione was obtained.
[0241] .sup.1H-NMR (CDCl.sub.3) .delta.: 7.91-7.85 (2H, m),
7.76-7.64 (3H, m), 7.60 (1H, s), 7.59 (1H, d, J=2.1 Hz), 6.94 (1H,
d, J=8.7 Hz), 4.85 (2H, s), 4.43 (2H, q, J=8.4 Hz), 3.91 (3H,
s)
Reference Example 25
[0242] Using 3.6 g of 2-{2-[4-methoxy-3-(2,2,2-trifluoro
ethoxy)phenyl]oxazol-4-ylmethyl}isoindolin-1,3-dione obtained in
Reference Example 24 and following the procedure of Reference
Example 7, 1.93 g of white powdery
{2-[4-methoxy-3-(2,2,2-trifluoroethoxy)phenyl]oxazol-4-yl}methylamine
was obtained.
[0243] .sup.1H-NMR (CDCl.sub.3) .delta.: 7.73 (1H, dd, J=8.4, 2.1
Hz), 7.63 (1H, d, J=2.1 Hz), 7.52 (1H, s), 6.98 (1H, d, J=8.4 Hz),
4.46 (2H, q, J=8.4 Hz), 3.93 (3H, s), 3.83 (2H, s), 1.55 (2H, br
s)
Reference Example 26
[0244] Using 9.5 g of ethyl vanillate and following the procedure
of Reference Example 14, 11 g of white powdery ethyl
3-methoxy-4-(2,2,2-trifluoroethoxy)benzoate was obtained.
[0245] .sup.1H-NMR (CDCl.sub.3) .delta.: 7.65 (1H, dd, J=8.4, 2.1
Hz), 7.60 (1H, d, J=2.1 Hz), 6.96 (1H, d, J=8.4 Hz), 4.49-4.33 (4H,
m), 3.93 (3H, s), 1.39 (3H, t, J=6.9 Hz)
Reference Example 27
[0246] A 12 g quantity of ethyl
3-methoxy-4-(2,2,2-trifluoroethoxy)benzoate obtained in Reference
Example 26 was suspended in 120 ml of 47% hydrobromic acid, and the
suspension was heated and refluxed overnight. The reaction mixture
was poured into ice water, and the precipitated crystals were
collected by filtration, washed with an excess of water, and then
dried under reduced pressure to give 8.4 g of pale red powdery
3-hydroxy-4-(2,2,2-trifluoroethoxy)benzoic acid.
[0247] .sup.1H-NMR (CDCl.sub.3) .delta.: 7.71-7.66 (2H, m), 6.91
(1H, d, J=5.1 Hz), 5.55 (1H, br s), 4.50 (2H, q, J=7.8 Hz)
Reference Example 28
[0248] An 8.4 g quantity of 3-hydroxy-4-(2,2,2-trifluoro
ethoxy)benzoic acid obtained in Reference Example 27 was suspended
in 150 ml of ethanol, and 0.5 ml of concentrated sulfuric acid was
added. The mixture was heated and refluxed overnight. After
completion of the reaction, ethanol was distilled off under reduced
pressure. The residue was neutralized with saturated aqueous sodium
bicarbonate and then extracted with ethyl acetate. After washing
with saturated brine twice, the organic layer was separated and
concentrated under reduced pressure. The residue was purified by
silica gel column chromatography (n-hexane:ethyl acetate=1:1) to
give 7.2 g of white crystalline ethyl
3-hydroxy-4-(2,2,2-trifluoroethoxy)benzoate.
[0249] .sup.1H-NMR (CDCl.sub.3) .delta.: 7.66-7.60 (2H, m), 6.87
(1H, d, J=8.1 Hz), 5.54 (1H, s), 4.48 (2H, q, J=7.8 Hz), 4.35 (2H,
q, J=7.2 Hz), 1.38 (3H, t, J=7.2 Hz)
Reference Example 29
[0250] Using 7 g of ethyl 3-hydroxy-4-(2,2,2-trifluoro
ethoxy)benzoate obtained in Reference Example 28 and following the
procedure of Reference Example 14, 8.5 g of white powdery ethyl
3-cyclopropylmethoxy-4-(2,2,2-trifluoroethoxy)benzoate was
obtained.
[0251] .sup.1H-NMR (CDCl.sub.3) .delta.: 7.63 (1H, dd, J=8.7, 2.1
Hz), 7.58 (1H, d, J=2.1 Hz), 7.00 (1H, d, J=8.7 Hz), 4.48 (2H, q,
J=8.1 Hz), 4.35 (2H, q, J=6.9 Hz), 3.92 (2H, d, J=7.2 Hz),
1.41-1.25 (4H, m), 0.69-0.60 (2H, m), 0.40-0.32 (2H, m)
Reference Example 30
[0252] Using 8.5 g of ethyl
3-cyclopropylmethoxy-4-(2,2,2-trifluoroethoxy)benzoate obtained in
Reference Example 29 and following the procedure of Reference
Example 3, 7.5 g of white powdery
3-cyclopropylmethoxy-4-(2,2,2-trifluoroethoxy)benzoic acid was
obtained.
[0253] .sup.1H-NMR (CDCl.sub.3) .delta.: 7.71 (1H, dd, J=8.4, 1.8
Hz), 7.63 (1H, d, J=2.1 Hz), 7.02 (1H, d, J=8.1 Hz), 4.51 (2H, q,
J=8.1 Hz), 3.93 (2H, d, J=7.2 Hz), 1.37-1.25 (1H, m), 0.69-0.60
(2H, m), 0.41-0.35 (2H, m)
Reference Example 31
[0254] Using 7 g of 3-cyclopropylmethoxy-4-(2,2,2-trifluoro
ethoxy)benzoic acid obtained in Reference Example 30 and following
the procedure of Reference Example 4, 7.35 g of white solid
3-cyclopropylmethoxy-4-(2,2,2-trifluoroethoxy)benzamide was
obtained.
[0255] .sup.1H-NMR (CDCl.sub.3) .delta.: 7.48 (1H, d, J=2.1 Hz),
7.28-7.25 (1H, m), 7.01 (1H, d, J=8.4 Hz), 4.48 (2H, q, J=8.4 Hz),
3.93 (2H, d, J=6.9 Hz), 1.37-1.25 (1H, m), 0.69-0.60 (2H, m),
0.41-0.35 (2H, m)
Reference Example 32
[0256] Using 5 g of 3-cyclopropylmethoxy-4-(2,2,2-trifluoro
ethoxy)benzamide obtained in Reference Example 31 and following the
procedure of Reference Example 5, 3.1 g of white powdery
4-chloromethyl-2-[3-cyclopropylmethoxy-4-(2,2,2-trifluoroethoxy)phenyl]ox-
azole was obtained.
[0257] .sup.1H-NMR (CDCl.sub.3) .delta.: 7.67 (1H, s), 7.59-7.56
(2H, m), 7.05 (1H, d, J=9.0 Hz), 4.56 (2H, s), 4.48 (2H, q, J=8.4
Hz), 1.35-1.26 (1H, m), 0.70-0.63 (2H, m), 0.41-0.35 (2H, m)
Reference Example 33
[0258] Using 0.85 g of
4-chloromethyl-2-[3-cyclopropylmethoxy-4-(2,2,2-trifluoroethoxy)phenyl]ox-
azole obtained in Reference Example 32 and following the procedure
of Reference Example 6, 0.6 g of white powdery
2-{2-[3-cyclopropylmethoxy-4-(2,2,2-trifluoroethoxy)phenyl]oxazol-4-ylmet-
hyl}isoindolin-1,3-dione was obtained.
[0259] .sup.1H-NMR (CDCl.sub.3) .delta.: 7.91-7.84 (2H, m),
7.76-7.69 (2H, m), 7.64 (1H, s), 7.60-7.51 (2H, m), 7.01 (1H, d,
J=8.7 Hz), 4.85 (2H, s), 4.46 (2H, q, J=8.4 Hz), 3.93 (2H, d, J=6.9
Hz), 1.35-1.24 (1H, m), 0.68-0.61 (2H, m), 0.40-0.34 (2H, m)
Reference Example 34
[0260] Using 0.55 g of
2-{2-[3-cyclopropylmethoxy-4-(2,2,2-trifluoroethoxy)phenyl]oxazol-4-ylmet-
hyl}isoindolin-1,3-dione obtained in Reference Example 33 and
following the procedure of Reference Example 7, 0.32 g of white
powdery {2-[3-cyclopropyl
methoxy-4-(2,2,2-trifluoroethoxy)phenyl]oxazol-4-yl}methylamine was
obtained.
[0261] .sup.1H-NMR (CDCl.sub.3) .delta.: 7.61-7.52 (3H, m), 7.05
(1H, d, J=8.7 Hz), 4.48 (2H, q, J=8.4 Hz), 3.95 (2H, d, J=7.2 Hz),
3.84 (2H, s), 1.56 (2H, br s), 1.35-1.24 (1H, m), 0.70-0.61 (2H,
m), 0.41-0.35 (2H, m)
Reference Example 35
[0262] Using 20 g of 3,4-diethoxybenzamide and following the
procedure of Reference Example 5, 24.5 g of white powdery
4-chloromethyl-2-(3,4-diethoxyphenyl)oxazole was obtained.
[0263] .sup.1H-NMR (CDCl.sub.3) .delta.: 7.65 (1H, s), 7.58 (1H,
dd, J=8.4, 1.8 Hz), 7.54 (1H, d, J=1.8 Hz), 6.92 (1H, d, J=8.4 Hz),
4.56 (2H, s), 4.18 (2H, q, J=6.9 Hz), 4.15 (2H, q, J=6.9 Hz), 1.48
(6H, t, J=6.9 Hz)
Reference Example 36
[0264] Using 8 g of 4-chloromethyl-2-(3,4-diethoxyphenyl) oxazole
obtained in Reference Example 35 and following the procedure of
Reference Example 6, 10 g of white powdery
2-[2-(3,4-diethoxyphenyl)oxazol-4-ylmethyl]isoindolin-1,3-dione was
obtained.
[0265] .sup.1H-NMR (CDCl.sub.3) .delta.: 7.88 (2H, m), 7.72 (2H,
m), 7.62 (1H, s), 7.54 (1H, d, J=8.4, 2.1 Hz), 7.50 (1H, d, J=2.1
Hz), 6.88 (1H, d, J=8.4 Hz), 4.85 (2H, s), 4.16 (2H, q, J=6.9 Hz),
4.11 (2H, q, J=6.9 Hz), 1.47 (6H, t, J=6.9 Hz)
Reference Example 37
[0266] Using 10 g of
2-[2-(3,4-diethoxyphenyl)oxazol-4-ylmethyl]isoindolin-1,3-dione
obtained in Reference Example 36 and following the procedure of
Reference Example 7, 5.7 g of white powdery
[2-(3,4-diethoxyphenyl)oxazol-4-yl]methylamine was obtained.
[0267] .sup.1H-NMR (CDCl.sub.3) .delta.: 7.56 (1H, d, J=8.4, 1.8
Hz), 7.54 (1H, d, J=1.8 Hz), 7.51 (1H, s), 6.91 (1H, d, J=8.4 Hz),
4.18 (2H, q, J=6.9 Hz), 4.14 (2H, q, J=6.9 Hz), 1.80 (1H, br s),
3.84 (2H, s), 1.48 (3H, t, J=6.9 Hz), 1.48 (3H, t, J=6.9 Hz)
Reference Example 38
[0268] Using 2.0 g of 3,4-dimethoxybenzamide and following the
procedure of Reference Example 5, 2.4 g of white powdery
4-chloromethyl-2-(3,4-dimethoxyphenyl)oxazole was obtained.
[0269] .sup.1H-NMR (CDCl.sub.3) .delta.: 7.66 (1H, s), 7.62 (1H,
dd, J=8.4, 1.8 Hz), 7.55 (1H, d, J=1.8 Hz), 6.93 (1H, d, J=8.4 Hz),
4.52 (2H, s), 3.95 (3H, s), 3.91 (3H, s)
Reference Example 39
[0270] Using 2.4 g of 4-chloromethyl-2-(3,4-dimethoxyphenyl)
oxazole obtained in Reference Example 38 and following the
procedure of Reference Example 6, 2.3 g of white powdery
2-[2-(3,4-dimethoxyphenyl)oxazol-4-ylmethyl]isoindolin-1,3-dione
was obtained.
Reference Example 40
[0271] Using 2.3 g of the
2-[2-(3,4-dimethoxyphenyl)oxazol-4-ylmethyl]isoindolin-1,3-dione
obtained in Reference Example 39 and following the procedure of
Reference Example 7, 1.3 g of white powdery
[2-(3,4-dimethoxyphenyl)oxazol-4-yl]methylamine was obtained.
.sup.1H-NMR (CDCl.sub.3) .delta.: 7.60 (1H, d, J=8.1, 2.1 Hz), 7.54
(1H, d, J=2.1 Hz), 6.92 (1H, d, J=8.1 Hz), 3.96 (3H, s), 3.93 (3H,
s), 3.85 (2H, s), 1.81 (2H, br s)
Reference Example 41
[0272] A 9 g quantity of 4-difluoromethoxy-3-hydroxy benzaldehyde
was dissolved in 180 ml of acetonitrile, and 13.1 g of potassium
carbonate and 8.6 ml of benzyl bromide were added. The mixture was
stirred at room temperature for 4 hours. After insolubles were
removed by filtration, the filtrate was concentrated and the
residue was purified by silica gel column chromatography
(n-hexane:ethyl acetate=1:1) to give 11.9 g of colorless oily
3-benzyloxy-4-difluoromethoxybenzaldehyde.
[0273] .sup.1H-NMR (CDCl.sub.3) .delta.:10.21 (1H, s), 7.56 (1H, t,
J=74.1 Hz), 7.53-7.28 (7H, m), 6.68 (1H, d, J=8.4 Hz), 5.20 (2H,
s)
Reference Example 42
[0274] A 6 g quantity of 3-benzyloxy-4-difluoromethoxybenzaldehyde
obtained in Reference Example 41 was dissolved in 500 ml of
acetone, and 17 g of potassium permanganate was added. The mixture
was heated and refluxed overnight. After distilling off acetone
from the reaction mixture, 100 ml of 5N sodium hydroxide was added
to the residue, and insolubles were removed by filtration.
Concentrated hydrochloric acid was added to the filtrate to give a
pH of about 3, and the precipitated crystals were collected by
filtration. The obtained crystals were dried under reduced pressure
to give 2.1 g of brownish powdery
3-benzyloxy-4-difluoromethoxybenzoic acid.
[0275] .sup.1H-NMR (CDCl.sub.3) .delta.: 7.78-7.72 (2H, m),
7.73-7.32 (5H, m), 7.33-7.24 (1H, m), 6.67 (1H, t, J=74.1 Hz), 5.20
(2H, s)
Reference Example 43
[0276] A 2 g quantity of 3-benzyloxy-4-difluoromethoxybenzoic acid
obtained in Reference Example 42 was suspended in 40 ml of
dichloromethane, and one drop of dimethylformamide was added. A 0.7
ml quantity of oxalyl chloride was added dropwise with ice-cooling
and stirring. After 2 hours, the reaction mixture was concentrated
under reduced pressure. The residue was dissolved in 5 ml of
acetone and the resulting solution was added dropwise to 28%
aqueous ammonia with ice-cooling and stirring. The obtained mixture
was stirred for 1 hour and the precipitated crystals were collected
by filtration and dried under reduced pressure to give 1.9 g of
white powdery 3-benzyloxy-4-difluoromethoxybenzamide.
[0277] .sup.1H-NMR (CDCl.sub.3) .delta.: 7.62 (1H, d, J=1.8 Hz),
7.45-7.20 (7H, m), 6.63 (1H, t, J=74.4 Hz), 5.19 (2H, s), 4.73 (2H,
br s)
Reference Example 44
[0278] A 1.8 g quantity of 3-benzyloxy-4-difluoromethoxybenzamide
obtained in Reference Example 43 was suspended in 50 ml of
isopropanol, and 1.17 g of 1,3-dichloro-2-propanone was added. The
mixture was heated and refluxed overnight. The reaction mixture was
concentrated, and the resulting residue was purified by silica gel
column chromatography (dichloromethane). The obtained crude
crystals were recrystallized from isopropanol to give 0.7 g of
white powdery
2-(3-benzyloxy-4-difluoromethoxyphenyl)-4-chloromethyloxazole.
[0279] .sup.1H-NMR (CDCl.sub.3) .delta.: 7.44 (1H, d, J=1.8 Hz),
7.70 (1H, s), 7.48-7.32 (5H, m), 7.28-7.24 (1H, m), 6.63 (1H, t,
J=74.7 Hz), 5.21 (2H, s), 4.57 (2H, s)
Reference Example 45
[0280] A 0.37 g quantity of 2-(3-benzyloxy-4-difluoromethoxy
phenyl)-4-chloromethyloxazole obtained in Reference Example 44 was
dissolved in 20 ml of ethanol, and 0.23 g of sodium iodide and 0.27
g of potassium phthalimide were added. The mixture was heated and
refluxed for 4 hours. After the reaction mixture was concentrated,
water was added to the residue and extraction with ethyl acetate
was performed. The organic layer was washed with water twice and
concentrated by removing the solvent and the residue was purified
by silica gel column chromatography (dichloromethane:methanol=20:1)
to give 0.3 g of white powdery
2-[2-(3-benzyloxy-4-difluoromethoxyphenyl)oxazol-4-ylmethyl]isoindolin-1,-
3-dione.
[0281] .sup.1H-NMR (CDCl.sub.3) .delta.: 7.90-7.84 (2H, m),
7.76-7.71 (4H, m), 7.59 (1H, dd, J=8.4, 2.1 Hz), 7.47-7.30 (5H, m),
7.22 (1H, d, J=2.4 Hz), 6.60 (1H, t, J=74.7 Hz), 5.20 (2H, s), 4.87
(2H, s)
Reference Example 46
[0282] A 0.3 g quantity of
2-[2-(3-benzyloxy-4-difluoromethoxyphenyl)oxazol-4-ylmethyl]isoindolin-1,-
3-dione obtained in Reference Example 45 was suspended in 10 ml of
ethanol, and 0.1 ml of hydrazine monohydrate was added. The mixture
was heated and refluxed for 2 hours. After cooling the reaction
mixture, the precipitated insolubles were removed by filtration.
The filtrate was concentrated under reduced pressure to give 0.13 g
of colorless oily
[2-(3-benzyloxy-4-difluoromethoxyphenyl)oxazol-4-yl]methylamine.
[0283] .sup.1H-NMR (CDCl.sub.3) .delta.: 7.74 (1H, d, J=1.8 Hz),
7.61 (1H, dd, J=7.8, 1.8 Hz), 7.47 (1H, d, J=1.8 Hz), 7.45-7.31
(5H, m), 7.26-7.20 (1H, m), 6.62 (1H, t, J=74.7 Hz), 5.21 (2H, s),
3.85 (2H, br s).
Reference Example 47
[0284] A 5.25 g quantity of sodium hydride was suspended in 150 ml
of tetrahydrofuran, and a solution of 14.4 g of dimethyl malonate
in 75 ml of tetrahydrofuran was added dropwise with ice-cooling
over 15 minutes. After stirring for 30 minutes, a solution of 25 g
of the 2-(3-benzyloxy-4-methoxyphenyl)-4-chloromethyloxazole
obtained in Reference Example 5 in 150 ml of dimethylformamide was
added dropwise over 15 minutes. After the dropwise addition, the
mixture was stirred at 50 to 60.degree. C. for 4 hours, and an
aqueous saturated ammonium chloride solution was added with
ice-cooling. After stirring the mixture for 30 minutes, water was
added and extraction with ethyl acetate was performed. The extract
was dried over anhydrous magnesium sulfate, and the solvent was
distilled off. The residue was recrystallized from a mixture of
ethyl acetate and diisopropyl ether to give 26.5 g of white powdery
dimethyl
2-[2-(3-benzyloxy-4-methoxyphenyl)oxazol-4-ylmethyl]malonate.
[0285] .sup.1H-NMR (DMSO-d.sub.6) .delta.: 7.89 (1H, s), 7.59-7.31
(7H, m), 7.15 (1H, d, J=7.8 Hz), 5.16 (2H, s), 3.90-3.84 (4H, m),
3.71 (6H, s), 3.04 (2H, d, J=7.8 Hz)
Reference Example 48
[0286] A 26.52 g quantity of the dimethyl
2-[2-(3-benzyloxy-4-methoxyphenyl)oxazol-4-ylmethyl]malonate
obtained in Reference Example 47 was suspended in 53 ml of dimethyl
sulfoxide, and 2.62 g of lithium chloride and 1.12 ml of purified
water were added. The mixture was stirred at 130.degree. C. for 4
hours. After the reaction mixture was allowed to cool, water was
added and extraction with ethyl acetate was performed. The extract
was dried over anhydrous magnesium sulfate, and the solvent was
distilled off. The residue was purified by silica gel column
chromatography (n-hexane:ethyl acetate=3:1) to give 16 g of white
powdery methyl
3-[2-(3-benzyloxy-4-methoxyphenyl)oxazol-4-yl]propionate.
[0287] .sup.1H-NMR (CDCl.sub.3) .delta.: 7.62-7.59 (2H, m), 7.47
(2H, d, J=6.9 Hz), 7.40-7.31 (4H, m), 6.93 (1H, d, J=8.4 Hz), 5.20
(2H, s), 3.92 (3H, s), 3.69 (3H, s), 2.91 (2H, t, J=7.2 Hz), 2.72
(2H, t, J=7.2 Hz)
Reference Example 49
[0288] A 0.48 g quantity of sodium hydride was suspended in 15 ml
of tetrahydrofuran, and a solution of 1.31 g of dimethyl malonate
in 7.5 ml of tetrahydrofuran was added dropwise over 15 minutes.
After the mixture was stirred for 30 minutes, a solution of 3.0 g
of
4-chloromethyl-2-[3-cyclopropylmethoxy-4-(2,2,2-trifluoroethoxy)phenyl]ox-
azole obtained in Reference Example 32 dissolved in 15 ml of
dimethylformamide was added over 15 minutes. After the dropwise
addition, the mixture was heated at 50 to 60.degree. C. with
stirring for 4 hours. An aqueous saturated ammonium chloride
solution was added to the reaction mixture with ice-cooling and
stirred was continued for 30 minutes. Water was added and
extraction with ethyl acetate was performed. The extract was dried
over anhydrous magnesium sulfate, and the solvent was distilled
off. A 8.0 ml quantity of dimethylsulfoxide, 0.35 g of lithium
chloride, and 0.15 ml of purified water were added to the residue,
and the mixture was heated with stirring at 130.degree. C. for 4
hours. After the reaction mixture was allowed to cool, water was
added and extraction with ethyl acetalte was performed. The extract
was dried over anhydrous magnesium sulfate and the solvent was
distilled off. The residue was purified by silica gel column
chromatography (n-hexane:ethyl acetate=4:1) to give 1.63 g of
colorless oily methyl
3-{2-[3-cyclopropylmethoxy-4-(2,2,2-trifluoroethoxy)phenyl]oxazol-4-yl}pr-
opionate.
[0289] .sup.1H-NMR (CDCl.sub.3) .delta.: 7.56-7.53 (2H, m), 7.43
(1H, s), 7.04 (1H, d, J=8.4 Hz), 4.47 (2H, q, J=8.4 Hz), 3.94 (2H,
d, J=6.6 Hz), 3.69 (3H, s), 2.91 (2H, t, J=7.2 Hz), 2.72 (2H, t,
J=7.2 Hz), 0.88 (1H, t, J=6.6 Hz), 0.69-0.65 (2H, m), 0.40-0.35
(2H, m)
Reference Example 50
[0290] A 0.5 g quantity of 2-cyclopropylethanol and 3.1 ml of
triethylamine were dissolved in 10 ml of ethyl acetate, and 0.75 ml
of methanesulfonyl chloride was added with ice-cooling and
stirring. After stirring for 30 minutes, water was added to the
reaction mixture and extraction was performed. The organic layer
was washed with water twice and concentrated by removing the
solvent under reduced pressure to give 1 g of pale yellow oily
2-cyclopropylethyl methanesulfonate.
[0291] .sup.1H-NMR (CDCl.sub.3) .delta.: 4.29 (2H, t, J=6.6 Hz),
3.03 (3H, s), 1.66 (2H, q, J=6.6 Hz), 0.84-0.70 (1H, m), 0.54-0.47
(2H, m), 0.20-0.10 (2H, m)
Reference Example 51
[0292] Using 2 g of 2-cyclopentylethanol and following the
procedure of Reference Example 50, 3.4 g of pale yellow oily
2-cyclopentylethyl methanesulfonate was obtained.
[0293] .sup.1H-NMR (CDCl.sub.3) .delta.: 4.24 (2H, t, J=6.6 Hz),
3.03 (3H, s), 1.95-1.73 (5H, m), 1.70-1.48 (4H, m), 1.29-1.06 (2H,
m)
Reference Example 52
[0294] Using 0.5 g of cyclopentylmethanol and following the
procedure of Reference Example 50, 0.7 g of pale yellow oily
cyclopentylmethyl methanesulfonate was obtained.
[0295] .sup.1H-NMR (CDCl.sub.3) .delta.: 4.11 (2H, d, J=6.9 Hz),
3.04 (3H, s), 2.38-2.23 (1H, m), 1.86-1.76 (2H, m), 1.74-1.53 (4H,
m), 1.36-1.24 (2H, m)
Reference Example 53
[0296] A 25 g quantity of 1-(2-hydroxyphenyl)ethanone and 76 g of
potassium carbonate were suspended in 500 ml of acetonitrile, and
31 ml of allyl bromide was added. The mixture was stirred at room
temperature for 48 hours. The reaction mixture was filtered to
remove insolubles, and the filtrate was concentrated under reduced
pressure. The obtained residue was purified by silica gel column
chromatography (n-hexane:ethyl acetate=4:1) to give 34 g of pale
yellow oily 1-(2-allyloxyphenyl)ethanone.
[0297] .sup.1H-NMR (CDCl.sub.3) .delta.: 7.73 (1H, dd, J=7.8, 1.8
Hz), 7.46-7.40 (1H, m), 7.02-6.93 (2H, m), 6.15-6.02 (1H, m),
5.47-5.30 (2H, m), 4.66-4.61 (2H, m), 2.64 (3H, s)
Reference Example 54
[0298] A 40 g quantity of 3,4-diethoxybenzamide and 80 g of methyl
5-bromo-4-oxopentanoate (containing about 35% of methyl
3-bromo-4-oxopentanoate) were added to 400 ml of dimethylformamide,
and the mixture was stirred at 130.degree. C. for 16 hours. The
reaction mixture was concentrated under reduced pressure and
diluted with ethyl acetate. Ethyl acetate (500 ml) and saturated
sodium bicarbonate solution (500 ml) were gradually added with
stirring, and stirring was continued. The organic layer was dried
over anhydrous magnesium sulfate and then concentrated under
reduced pressure. The residue was purified by silica gel column
chromatography (ethyl acetate:n-hexane=1:8 to 1:4) to give 18 g of
white powdery methyl
3-[2-(3,4-diethoxyphenyl)oxazol-4-yl]propionate.
[0299] .sup.1H-NMR (CDCl.sub.3) .delta.: 7.65-7.55 (2H, m), 7.51
(1H, s), 6.93 (1H, d, J=8.1 Hz), 4.19 (2H, q, J=6.9 Hz), 4.15 (2H,
q, J=6.9 Hz), 3.80 (3H, s), 3.00-2.90 (2H, m), 2.70-2.60 (2H, m),
1.50 (3H, t, J=6.9 Hz), 1.49 (3H, t, J=6.9 Hz)
Reference Example 55
[0300] A 37.9 g quantity of 3,4-dibenzyloxybenzamide and 28.8 g of
1,3-dichloro-2-propanone were suspended in 500 ml of propanol, and
the suspension was heated and refluxed for 3 days. After cooling,
the reaction mixture was concentrated to half its original volume
under reduced pressure and 300 ml of diisopropyl ether was added.
The precipitated crystals were collected by filtration and
recrystallized from acetone-methanol-diisopropyl ether. The
obtained crystals were dried under reduced pressure to give 20.1 g
of colorless powdery
2-(3,4-bis(benzyloxy)phenyl)-4-chloromethyloxazole.
[0301] .sup.1H-NMR (CDCl.sub.3) .delta.: 7.66 (1H, d, J=2.1 Hz),
7.64 (1H, s), 7.59 (1H, dd, J=8.4, 2.1 Hz), 7.50-7.28 (10H, m),
6.99 (1H, d, J=8.4 Hz), 5.22 (2H, s), 5.21 (2H, s), 4.55 (2H,
s)
Reference Example 56
[0302] Using 10 g of
2-(3,4-bis(benzyloxy)phenyl)-4-chloromethyloxazole obtained in
Reference Example 55 and following the procedure of Reference
Example 47, 12.3 g of colorless oily dimethyl
2-[2-(3,4-bis(benzyloxy)phenyl)oxazol-4-ylmethyl]malonate was
obtained.
[0303] .sup.1H-NMR (CDCl.sub.3) .delta.: 7.61 (1H, d, J=2.1 Hz),
7.58-7.27 (12H, m), 6.97 (1H, d, J=8.4 Hz), 5.23-5.20 (4H, m), 3.89
(1H, t, J=7.5 Hz), 3.75 (3H, s), 3.73 (3H, s), 3.18 (2H, d, J=7.5
Hz)
Reference Example 57
[0304] Using 12.3 g of dimethyl
2-[2-(3,4-bis(benzyloxy)phenyl)oxazol-4-ylmethyl]malonate obtained
in Reference Example 56 and following the procedure of Reference
Example 48, 4 g of pale red powdery methyl
3-[2-(3,4-bis(benzyloxy)phenyl)oxazol-4-yl]propionate was
obtained.
[0305] .sup.1H-NMR (CDCl.sub.3) .delta.: 7.63 (1H, d, J=2.1 Hz),
7.57-7.27 (12H, m), 6.97 (1H, d, J=8.4 Hz), 5.21 (2H, d, J=7.2 Hz),
3.69 (3H, s), 2.90 (2H, t, J=7.2 Hz), 2.72 (2H, d, J=7.2 Hz)
Reference Example 58
[0306] Using 29.4 g of 3-ethoxy-4-methoxybenzamide and 57 g of
1,3-dichloro-2-propanone and following the procedure of Reference
Example 55, 19.9 g of white powdery
4-chloromethyl-2-(3-ethoxy-4-methoxyphenyl)oxazole was
obtained.
[0307] .sup.1H-NMR (CDCl.sub.3) .delta.: 7.65 (1H, s), 7.61 (1H,
dd, J=8.1, 2.1 Hz), 7.55 (1H, d, J=2.1 Hz), 6.92 (1H, d, J=8.1 Hz),
4.56 (2H, s), 4.18 (2H, q, J=6.9 Hz), 3.93 (3H, s), 1.50 (3H, t,
J=6.9 Hz)
Reference Example 59
[0308] A 25 g quantity of ethyl 3,4-dihydroxybenzoate was dissolved
in 250 ml of dimethylformamide, and 5.5 g of sodium hydride was
added with ice-cooling and stirring. The mixture was stirred, and a
solution of 16.3 ml of benzylbromide in 10 ml of dimethylformamide
was added dropwise. After the dropwise addition, the mixture was
stirred at room temperature overnight. Water was added to the
reaction mixture and extraction with ethyl acetate was performed.
The organic layer was washed with water twice and concentrated by
removing the solvent under reduced pressure. The obtained residue
was purified by silica gel column chromatography (n-hexane:ethyl
acetate=2:1) to give 15 g of crude crystals. The crude crystals
were recrystallized from a mixture of 30 ml of n-hexane and 15 ml
of ethyl acetate to give 8.6 g of colorless plate crystalline ethyl
4-benzyloxy-3-hydroxybenzonate.
[0309] .sup.1H-NMR (CDCl.sub.3) .delta.: 7.67-7.47 (2H, m),
7.41-7.30 (5H, m), 6.94 (1H, d, J=8.7 Hz), 5.67 (1H, s), 5.16 (2H,
s), 4.34 (2H, q, J=7.2 Hz), 1.37 (3H, t, J=7.2 Hz)
Reference Example 60
[0310] Using ethyl 4-benzyloxy-3-hydroxybenzonate obtained in
Reference Example 59 and following the procedure of Reference
Example 2, ethyl 4-benzyloxy-3-ethoxybenzoate was obtained.
[0311] .sup.1H-NMR (CDCl.sub.3) .delta.: 7.61-7.55 (2H, m),
7.45-7.27 (5H, m), 6.90 (1H, d, J=8.1 Hz), 5.21 (2H, s), 4.34 (2H,
q, J=6.9 Hz), 4.17 (2H, q, J=6.9 Hz), 1.48 (3H, t, J=6.9 Hz), 1.37
(3H, t, J=6.9 Hz)
Reference Example 61
[0312] Using ethyl 4-benzyloxy-3-ethoxybenzoate obtained in
Reference Example 60 and following the procedure of Reference
Example 3, 4-benzyloxy-3-ethoxybenzoic acid was obtained.
[0313] .sup.1H-NMR (CDCl.sub.3) .delta.: 7.68 (1H, dd, J=8.4, 1.2
Hz), 7.61 (1H, d, J=1.2 Hz), 7.45-7.28 (5H, m), 6.92 (1H, d, J=8.4
Hz), 5.23 (2H, s), 4.17 (2H, q, J=6.9 Hz), 1.48 (3H, t, J=6.9
Hz)
Reference Example 62
[0314] Using 4-benzyloxy-3-ethoxybenzoic acid obtained in Reference
Example 61 and following the procedure of Reference Example 4,
colorless needle crystalline 4-benzyloxy-3-ethoxybenzamide was
obtained.
[0315] .sup.1H-NMR (CDCl.sub.3) .delta.: 7.47-7.21 (7H, m), 6.88
(1H, d, J=8.1 Hz), 5.21 (2H, s), 4.18 (2H, q, J=7.2 Hz), 1.48 (3H,
t, J=7.2 Hz)
Reference Example 63
[0316] Using 4-benzyloxy-3-ethoxybenzamide obtained in Reference
Example 62 and following the procedure of Reference Example 5,
colorless powdery 4-chloromethyl-2-(4-benzyloxy-3-ethoxyphenyl)
oxazole was obtained.
[0317] .sup.1H-NMR (CDCl.sub.3) .delta.: 7.64 (1H, s), 7.57-7.30
(7H, m), 6.94 (1H, d, J=8.4 Hz), 5.20 (2H, s), 4.56 (2H, s), 4.20
(2H, q, J=7.2 Hz), 1.49 (3H, t, J=7.2 Hz)
Reference Example 64
[0318] A 6.81 g quantity of sodium iodide and 5.09 g of sodium
bicarbonate were added to a suspension of 10 g of
2-(3-benzyloxy-4-methoxyphenyl)-4-chloromethyloxazole obtained in
Reference Example 5 in 60 ml of dimethylsulfoxide. The mixture was
heated at 120.degree. C. with stirring for 30 minutes. After the
reaction mixture was allowed to cool, saturated brine was added and
extraction with ethyl acetate was performed. The organic layer was
washed with saturated brine and dried over anhydrous magnesium
sulfate, and the solvent was then distilled off under reduced
pressure. The obtained residue was purified by silica gel column
chromatography (n-hexane:ethyl acetate=3:1) to give 2.98 g of
yellow oily
2-(3-benzyloxy-4-methoxyphenyl)oxazole-4-carbaldehyde.
[0319] .sup.1H-NMR (CDCl.sub.3) .delta.: 9.98 (1H, s), 8.26 (1H,
s), 7.71 (1H, dd, J=8.1, 2.1 Hz), 7.69 (1H, br s), 7.48 (2H, br d,
J=8.4 Hz), 7.42-7.31 (3H, m), 6.98 (1H, d, J=8.1 Hz), 5.21 (2H, s),
3.95 (3H, s)
Reference Example 65
[0320] Using
4-chloromethyl-2-[4-methoxy-3-(2,2,2-trifluoroethoxy)phenyl]oxazole
obtained in Reference Example 23 and following the procedure of
Reference Example 64, colorless powdery
2-[4-methoxy-3-(2,2,2-trifluoroethoxy)phenyl]oxazole-4-carbaldehyde
was obtained.
[0321] .sup.1H-NMR (CDCl.sub.3) .delta.: 9.99 (1H, s), 8.28 (1H,
s), 7.82 (1H, dd, J=8.4, 2.1 Hz), 7.71 (1H, d, J=2.1 Hz), 7.01 (1H,
d, J=8.4 Hz), 4.46 (2H, q, J=8.4 Hz), 3.95 (3H, s)
Reference Example 66
[0322] Using 4-chloromethyl-2-(3,4-diethoxyphenyl)oxazole obtained
in Reference Example 35 and following the procedure of Reference
Example 64, pale yellow powdery
2-(3,4-diethoxyphenyl)oxazole-4-carbaldehyde was obtained.
[0323] .sup.1H-NMR (CDCl.sub.3) .delta.: 9.99 (1H, s), 8.26 (1H,
s), 7.65 (1H, dd, J=8.4, 2.1 Hz), 7.62 (1H, d, J=2.1 Hz), 6.94 (1H,
d, J=8.4 Hz), 4.19 (2H, q, J=7.2 Hz), 4.17 (2H, q, J=7.2 Hz), 1.50
(6H, t, J=7.2 Hz)
Reference Example 67
[0324] Using 12.7 g of 3-isopropoxy-4-methoxybenzoic acid and
following the procedure of Reference Example 4, white powdery
3-isopropoxy-4-methoxybenzamide was obtained.
[0325] .sup.1H-NMR (CDCl.sub.3) .delta.: 7.46 (1H, d, J=2.1 Hz),
7.34 (1H, dd, J=8.4, 2.1 Hz), 6.87 (1H, d, J=8.4 Hz), 5.93 (1H, br
s), 4.62 (1H, m), 3.90 (3H, s), 1.38 (6H, d, J=6.0 Hz).
Reference Example 68
[0326] Using 11.4 g of 3-isopropoxy-4-methoxybenzamide obtained in
Reference Example 67 and 25 g of 1,3-dichloro-2-propanone and
following the procedure of Reference Example 5, 12.2 g of white
powdery 4-chloromethyl-2-(3-isopropoxy-4-methoxyphenyl) oxazole was
obtained.
[0327] .sup.1H-NMR (CDCl.sub.3) .delta.: 7.65 (1H, s), 7.61 (1H,
dd, J=8.4, 2.1 Hz), 7.57 (1H, d, J=2.1 Hz), 6.93 (1H, d, J=8.4 Hz),
4.64 (1H, m), 4.53 (2H, s), 3.90 (3H, s), 1.40 (6H, d, J=6.0
Hz)
Reference Example 69
[0328] Using 4-chloromethyl-2-(3-isopropoxy-4-methoxyphenyl)
oxazole obtained in Reference Example 68 and following the
procedure of Reference Example 64, pale yellow powdery
2-(3-isopropoxy-4-methoxyphenyl)oxazole-4-carbaldehyde was
obtained.
[0329] .sup.1H-NMR (CDCl.sub.3) .delta.: 9.99 (1H, s), 8.27 (1H,
s), 7.68 (1H, dd, J=8.1, 2.1 Hz), 7.64 (1H, d, J=2.1 Hz), 6.95 (1H,
d, J=8.1 Hz), 4.67 (1H, sept., J=6.3 Hz), 3.92 (3H, s), 1.41 (6H,
d, J=6.3 Hz)
Reference Example 70
[0330] A 10 g quantity of 1-(2-hydroxyphenyl)ethanone was dissolved
in 100 ml of dimethylformamide, and 11.2 ml of chloromethyl methyl
ether and 25.4 g of potassium carbonate were added. The mixture was
stirred at 50.degree. C. for 6 hours and then at room temperature
for 4 days. After insolubles were removed from the reaction mixture
by filtration, ice water was added to the filtrate and extraction
with ethyl acetate was performed. The organic layer was washed with
water and dried over anhydrous magnesium sulfate. The organic layer
was concentrated under reduced pressure, and the residue was
purified by silica gel column chromatography (n-hexane:ethyl
acetate=5:1) to give 6.26 g of colorless oily
1-(2-methoxymethoxyphenyl)ethanone.
[0331] .sup.1H-NMR (CDCl.sub.3) .delta.: 7.71 (1H, dd, J=7.8, 1.8
Hz), 7.43 (1H, td, J=7.8, 1.8 Hz), 7.18 (1H, d, J=7.8 Hz), 7.05
(1H, t, J=7.8 Hz), 5.28 (2H, s), 3.52 (3H, s), 2.64 (3H, s)
Reference Example 71
[0332] A 3 g quantity of methyl 3-[2-(3,4-diethoxyphenyl)
oxazol-4-yl]propionate obtained in Reference Example 54 was
suspended in 5 ml of methanol, and 5 ml of a 20% aqueous sodium
hydroxide solution was added. The mixture was heated and refluxed
for 4 hours. After cooling the reaction mixture to room
temperature, extraction with dichloromethane was performed. The
dichloromethane layer was washed with water and dried over
anhydrous magnesium sulfate. The solvent was distilled off and the
obtained crystals were dried to give 2.8 g of white powdery
3-[2-(3,4-dimethoxyphenyl)oxazol-4-yl]propionic acid.
[0333] .sup.1H-NMR (CDCl.sub.3) .delta.: 7.65-7.55 (3H, m), 7.51
(1H, d, J=2.1 Hz), 6.91 (1H, d, J=8.4 Hz), 4.17 (2H, q, J=6.9 Hz),
4.15 (2H, q, J=6.9 Hz), 3.00-2.90 (2H, m), 2.90-2.80 (2H, m), 1.48
(3H, t, J=6.9 Hz), 1.48 (3H, t, J=6.9 Hz)
Reference Example 72
[0334] Using 10 g of 4-benzyloxy-3-methoxybenzamide and following
the procedure of Reference Example 54, 2 g of white powdery methyl
3-[2-(4-benzyloxy-3-methoxyphenyl)oxazol-4-yl]propionate was
obtained.
[0335] .sup.1H-NMR (CDCl.sub.3) .delta.: 7.54-7.28 (8H, m) 6.93
(1H, d, J=8.1 Hz), 5.20 (2H, s), 3.97 (3H, s), 3.68 (3H, s), 2.91
(2H, t, J=7.5 Hz), 2.64 (2H, t, J=7.5 Hz)
Reference Example 73
[0336] Using 2 g of methyl 3-[2-(4-benzyloxy-3-methoxyphenyl)
oxazol-4-yl]propionate obtained in Reference Example 72 and
following the procedure of Reference Example 71, 1.03 g of white
powdery 3-[2-(4-benzyloxy-3-methoxyphenyl)oxazol-4-yl]propionic
acid was obtained.
[0337] .sup.1H-NMR (CDCl.sub.3) .delta.:12.20 (1H, s), 7.86 (1H,
s), 7.51-7.31 (7H, m) 7.17 (1H, d, J=8.4 Hz), 5.15 (2H, s), 3.85
(3H, s), 2.75 (2H, t, J=7.5 Hz), 2.59 (2H, t, J=7.5 Hz)
Reference Example 74
[0338] A 0.4 g quantity of 4-chloromethyl-2-(3,4-diethoxy
phenyl)oxazole obtained in Reference Example 35 was dissolved in 15
ml of methylamine (40% methanol solution), and was heated and
refluxed for 1 hour. The reaction mixture was concentrated and the
obtained residue was dried under reduced pressure to give 0.23 g of
yellow oily
[2-(3,4-dimethoxyphenyl)oxazol-4-ylmethyl]methylamine.
[0339] .sup.1H-NMR (CDCl.sub.3) .delta.: 8.00 (1H, s), 7.58-7.50
(2H, m), 6.90 (1H, d, J=8.4 Hz), 4.21-4.10 (6H, m), 2.76 (3H, s),
1.51-1.45 (6H, m)
Reference Example 75
[0340] Using ethyl 2-chloroacetoacetate and 16 g of
3,4-diethoxybenzamide and following the procedure of Reference
Example 5, 3.8 g of ethyl
[2-(3,4-dimethoxyphenyl)oxazol-4-yl]acetate was obtained.
[0341] .sup.1H-NMR (CDCl.sub.3) .delta.: 7.64 (1H, s), 7.60-7.50
(2H, m), 6.91 (1H, d, J=8.1 Hz), 4.25-4.10 (6H, m), 3.58 (2H, s),
1.50-1.40 (6H, m), 1.29 (3H, t, J=6.9 Hz)
Reference Example 76
[0342] A 0.35 g quantity of lithium aluminum hydride was added to
30 ml of tetrahydrofuran with ice-cooling and stirring, and ethyl
[2-(3,4-dimethoxyphenyl)oxazol-4-yl]acetate obtained in Reference
Example 75 was slowly added with stirring. After stirring at room
temperature for 3 hours, the mixture was stirred with ice-cooling
for 3 hours, and 0.35 ml of water, 0.35 ml of a 15% aqueous sodium
hydroxide solution, and 1.05 ml of water were added in that order.
The reaction mixture was dried over anhydrous magnesium sulfate,
and insolubles were then removed by filtration. The filtrate was
concentrated under reduced pressure to give 2.5 g of colorless
crystalline 2-[2-(3,4-dimethoxyphenyl)oxazol-4-yl]ethanol.
[0343] .sup.1H-NMR (CDCl.sub.3) .delta.: 7.56 (1H, d, J=8.4, 2.1
Hz), 7.52 (1H, d, J=2.1 Hz), 7.46 (1H, s), 6.91 (1H, d, J=8.4 Hz),
4.17 (2H, q, J=7.2 Hz), 4.15 (2H, q, J=7.2 Hz), 3.94 (2H, q, J=5.4
Hz), 2.94 (1H, t, J=5.4 Hz), 2.81 (2H, t, J=5.4 Hz), 1.48 (3H, t,
J=7.2 Hz), 1.48 (3H, t, J=7.2 Hz)
Reference Example 77
[0344] A 2.0 g quantity of
2-[2-(3,4-dimethoxyphenyl)oxazol-4-yl]ethanol obtained in Reference
Example 76 and 2.3 g of triphenylphosphine were added to 20 ml of
dichloromethane, and 2.9 g of carbon tetrabromide was slowly added
with ice-cooling and stirring. After the temperature of the mixture
had reached room temperature, stirring was continued for 1.5 hours.
The reaction mixture was concentrated, and the residue was purified
by silica gel column chromatography (n-hexane:ethyl acetate=8:1) to
give 1.9 g of colorless crystalline
4-(2-bromoethyl)-2-(3,4-diethoxyphenyl)oxazole.
[0345] .sup.1H-NMR (CDCl.sub.3) .delta.: 7.60-7.50 (3H, m), 6.91
(1H, d, J=8.4 Hz), 4.18 (2H, q, J=7.2 Hz), 4.14 (2H, q, J=7.2 Hz),
3.67 (2H, t, J=6.9 Hz), 3.14 (2H, t, J=6.9 Hz), 1.48 (3H, t, J=7.2
Hz), 1.48 (3H, t, J=7.2 Hz)
Reference Example 78
[0346] Using 1.5 g of 4-(2-bromoethyl)-2-(3,4-diethoxyphenyl)
oxazole obtained in Reference Example 77 and following the
procedures of Reference Examples 6 and 7, 0.8 g of yellow oily
2-[2-(3,4-diethoxyphenyl)oxazol-4-yl]ethylamine was obtained.
[0347] .sup.1H-NMR (CDCl.sub.3) .delta.: 7.60-7.50 (3H, m), 6.91
(1H, d, J=8.4 Hz), 4.17 (2H, q, J=7.2 Hz), 4.15 (2H, q, J=7.2 Hz),
3.90-3.80 (2H, m), 3.00-2.90 (2H, m), 1.85 (2H, brs), 1.48 (3H, t,
J=7.2 Hz), 1.48 (3H, t, J=7.2 Hz)
Reference Example 79
[0348] Using 10.4 g of 3,4-diethoxybenzamide and 19.5 g of ethyl
3-bromo-2-oxopropionate and following the procedure of Reference
Example 5, 12.9 g of white powdery ethyl
2-(3,4-diethoxyphenyl)oxazole-4-carboxylate was obtained.
[0349] .sup.1H-NMR (CDCl.sub.3) .delta.: 8.21 (1H, d, J=0.9 Hz),
7.64 (1H, dd, J=8.1, 0.9 Hz), 7.63 (1H, s), 6.92 (1H, d, J=8.1 Hz),
4.42 (2H, q, J=7.2 Hz), 4.17 (2H, q, J=6.9 Hz), 4.15 (2H, q, J=6.9
Hz), 1.48 (3H, t, J=6.9 Hz), 1.41 (3H, t, J=7.2 Hz)
Reference Example 80
[0350] Using 10 g of the ethyl
2-(3,4-diethoxyphenyl)oxazole-4-carboxylate obtained in Reference
Example 79 and following the procedure of Reference Example 71, 8.6
g of white powdery 2-(3,4-diethoxyphenyl)oxazole-4-carboxylic acid
was obtained.
[0351] .sup.1H-NMR (CDCl.sub.3) .delta.: 8.24 (1H, s), 7.60-7.50
(3H, m), 6.02 (1H, brs), 4.13 (4H, q, J=6.9 Hz), 1.46 (3H, t, J=6.9
Hz), 1.39 (3H, t, J=6.9 Hz)
Reference Example 81
[0352] Using 0.4 g of ethyl
[2-(3,4-diethoxyphenyl)oxazol-4-yl]acetate obtained in Reference
Example 75 and following the procedure of Reference Example 71,
0.35 g of white powdery [2-(3,4-diethoxyphenyl)oxazol-4-yl]acetic
acid was obtained.
[0353] .sup.1H-NMR (CDCl.sub.3) .delta.: 7.65-7.55 (3H, m), 7.51
(1H, d, J=2.1 Hz), 6.91 (1H, d, J=8.4 Hz), 4.17 (2H, q, J=6.9 Hz),
4.15 (2H, q, J=6.9 Hz), 3.73 (2H, s), 1.49 (6H, t, J=6.9 Hz)
Reference Example 82
[0354] Using 3 g of
4-chloromethyl-2-[4-methoxy-3-(2,2,2-trifluoroethoxy)phenyl]oxazole
obtained in Reference Example 23 and following the procedure of
Reference Example 47, 1.91 g of colorless oily dimethyl
2-{2-[4-methoxy-3-(2,2,2-trifluoroethoxy)phenyl]oxazol-4-ylmethyl}malonat-
e was obtained.
[0355] .sup.1H-NMR (CDCl.sub.3) .delta.: 7.70 (1H, dd, J=8.4, 2.1
Hz), 7.60 (1H, d, J=2.1 Hz), 7.42 (1H, s), 6.96 (1H, d, J=8.4 Hz),
4.44 (2H, q, J=6.9 Hz), 3.93 (3H, s), 3.89 (1H, t, J=7.5 Hz), 3.18
(2H, d, J=7.5 Hz)
Reference Example 83
[0356] Using 1.9 g of dimethyl
2-{2-[4-methoxy-3-(2,2,2-trifluoroethoxy)phenyl]oxazol-4-ylmethyl}malonat-
e obtained in Reference Example 82 and following the procedure of
Reference Example 48, 1.44 g of colorless oily methyl
3-{2-[4-methoxy-3-(2,2,2-trifluoroethoxy)phenyl]oxazol-4-yl}propionate
was obtained.
[0357] .sup.1H-NMR (CDCl.sub.3) .delta.: 7.70 (1H, dd, J=8.4, 2.1
Hz), 7.60 (1H, d, J=2.1 Hz), 7.42 (1H, s), 6.96 (1H, d, J=8.4 Hz),
4.45 (2H, q, J=6.9 Hz), 3.92 (3H, s), 3.75 (3H, s), 2.91 (2H, t,
J=7.5 Hz), 2.72 (2H, t, J=7.5 Hz)
Example 1
[0358] A 3.5 g quantity of the [2-(3-benzyloxy-4-methoxy
phenyl)oxazol-4-yl]methylamine obtained in Reference Example 7 was
suspended in 70 ml of acetone. To the obtained suspension were
added 2.3 g of 1-hydroxybenzotriazole, 3.3 g of
1-ethyl-3-(3-dimethylaminopropyl)carbodiimide hydrochloride and 3.8
g of 2-ethoxybenzoic acid, and the mixture was heated and refluxed
for one hour. The reaction mixture was cooled, and acetone was
distilled off under reduced pressure. Water was added to the
residue, and extraction was then performed with ethyl acetate. The
organic layer was washed with water twice, and concentrated under
reduced pressure. The obtained residue was purified by silica gel
column chromatography (dichloromethane:methanol=20:1) to give 4.6 g
of white powdery
N-[2-(3-benzyloxy-4-methoxyphenyl)oxazol-4-ylmethyl]-2-ethoxybenzamide.
[0359] .sup.1H-NMR (CDCl.sub.3) .delta.: 8.55 (1H, br s) 8.23 (1H,
dd, J=7.8, 1.8 Hz), 7.65-7.61 (3H, m), 7.49-7.29 (6H, m), 7.09 (1H,
t, J=7.5 Hz), 7.04-6.92 (2H, m), 5.20 (2H, s), 4.61 (2H, d, J=5.4
Hz), 4.16 (2H, q, J=6.9 Hz), 3.93 (3H, s), 1.26 (3H, t, J=6.9
Hz)
Example 2
[0360] A 4.65 g quantity of the
N-[2-(3-benzyloxy-4-methoxyphenyl)oxazol-4-ylmethyl]-2-ethoxybenzamide
obtained in Example 1 was dissolved in 90 ml of ethanol, and 0.45 g
of 10% palladium carbon powder was added thereto. The mixture was
stirred in a hydrogen atmosphere at room temperature for one hour.
The catalyst was removed by filtration, and the filtrate was then
concentrated under reduced pressure to give 3.7 g of white
crystalline
N-[2-(3-hydroxy-4-methoxyphenyl)oxazol-4-ylmethyl]-2-ethoxybenzamide.
[0361] .sup.1H-NMR (CDCl.sub.3) .delta.: 8.58 (1H, br s) 8.23 (1H,
dd, J=7.8, 1.8 Hz), 7.62-7.55 (3H, m), 7.41 (1H, td, J=7.5 Hz, 1.8
Hz), 7.06 (1H, t, J=7.2 Hz), 6.95-6.88 (2H, m), 5.74 (1H, s), 4.62
(2H, d, J=5.1 Hz), 4.17 (2H, q, J=6.9 Hz), 3.95 (3H, s), 1.47 (3H,
t, J=6.9 Hz)
Example 3
[0362] A 0.2 g quantity of the N-[2-(3-hydroxy-4-methoxy
phenyl)oxazol-4-ylmethyl]-2-ethoxybenzamide obtained in Example 2
and 0.3 ml of 1,8-diazabicyclo[5,4,0]undec-7-ene were dissolved in
4 ml of ethanol, and 0.14 g of (bromomethyl)cyclopropane was added
thereto. The mixture was heated and refluxed overnight. The
reaction mixture was allowed to cool, water was then added thereto,
and extraction was performed with ethyl acetate. After washing with
water twice, the organic layer was concentrated under reduced
pressure. The obtained residue was purified by silica gel column
chromatography (n-hexane:ethyl acetate=3:1) to give 0.18 g of white
powdery
N-[2-(3-cyclopropylmethoxy-4-methoxyphenyl)oxazol-4-ylmethyl]-2-ethoxyben-
zamide.
[0363] .sup.1H-NMR (CDCl.sub.3) .delta.: 8.55 (1H, br s) 8.24 (1H,
dd, J=7.8, 2.1 Hz), 7.62-7.59 (2H, m), 7.53 (1H, d, J=2.1 Hz),
7.45-7.39 (1H, m), 7.07 (1H, td, J=8.1 Hz, 1.2 Hz), 6.95-6.91 (2H,
m), 4.62 (2H, d, J=5.4 Hz), 4.18 (2H, q, J=6.9 Hz), 3.94-3.92 (5H,
m), 1.49 (3H, t, J=6.9 Hz), 1.42-1.34 (1H, m), 0.71-0.64 (2H, m),
0.41-0.35 (2H, m)
Example 4
[0364] A 0.3 g quantity of the N-[2-(3-hydroxy-4-methoxy
phenyl)oxazol-4-ylmethyl]-2-ethoxybenzamide obtained in Example 2
and 0.22 g of potassium carbonate were dissolved in 10 ml of
dimethylformamide, and 0.34 g of 1,1,1-trifluoro-2-iodoethane was
added thereto. The mixture was stirred with heating at 50.degree.
C. overnight. The reaction mixture was allowed to cool, water was
then added thereto, and extraction was performed with ethyl
acetate. After washing with water twice, the organic layer was
concentrated under reduced pressure. The obtained residue was
purified by silica gel column chromatography (n-hexane:ethyl
acetate=3:1) to give 0.14 g of white powdery
N-{2-[4-methoxy-3-(2,2,2-trifluoroethoxy)phenyl]oxazol-4-ylmethyl}-2-etho-
xybenzamide.
[0365] .sup.1H-NMR (CDCl.sub.3) .delta.: 8.56 (1H, br s) 8.24 (1H,
dd, J=7.8, 2.1 Hz), 7.73 (1H, dd, J=8.4, 2.1 Hz), 7.65-7.63 (2H,
m), 7.45-7.39 (1H, m), 7.09-7.01 (1H, m), 6.99-6.90 (2H, m), 4.62
(2H, d, J=5.4 Hz), 4.55 (2H, q, J=8.4 Hz), 4.32 (2H, q, J=6.9 Hz),
3.93 (3H, s), 1.49 (3H, t, J=6.9 Hz)
[0366] Using 0.2 g of the N-[2-(3-hydroxy-4-methoxyphenyl)
oxazol-4-ylmethyl]-2-ethoxybenzamide obtained in Example 2,
compounds of Examples 5 to 14 were obtained in the same manner as
in Example 3.
Example 5
N-[2-(3-butoxy-4-methoxyphenyl)oxazol-4-ylmethyl]-2-ethoxy
benzamide
Yield 0.2 g
White Powder
[0367] .sup.1H-NMR (CDCl.sub.3) .delta.: 8.56 (1H, br s) 8.24 (1H,
dd, J=7.8, 2.1 Hz), 7.62-7.54 (3H, m), 7.45-7.39 (1H, m), 7.07 (1H,
t, J=8.1 Hz), 6.96-6.90 (2H, m), 4.62 (2H, d, J=5.4 Hz), 4.18 (2H,
q, J=6.9 Hz), 4.10 (2H, t, J=6.9 Hz), 3.92 (3H, s), 1.92-1.82 (2H,
m), 1.59-1.47 (5H, m) 1.00 (3H, t, J=7.5 Hz)
Example 6
N-[2-(3-cyclopentyloxy-4-methoxyphenyl)oxazol-4-ylmethyl]-2-ethoxybenzamid-
e
Yield 0.22 g
Colorless Oily Substance
[0368] .sup.1H-NMR (CDCl.sub.3) .delta.: 8.57 (1H, br s) 8.24 (1H,
dd, J=7.8, 2.1 Hz), 7.62-7.54 (3H, m), 7.45-7.39 (1H, m), 7.07 (1H,
t, J=8.1 Hz), 6.96-6.90 (2H, m), 4.91-4.86 (1H, m), 4.62 (2H, d,
J=5.4 Hz), 4.17 (2H, q, J=6.9 Hz), 3.90 (3H, s), 2.02-1.60 (8H, m),
1.49 (3H, t, J=6.9 Hz)
Example 7
N-{2-[3-(3-hydroxypropoxy)-4-methoxyphenyl]oxazol-4-ylmethyl}-2-ethoxybenz-
amide
Yield 0.12 g
White Powder
[0369] .sup.1H-NMR (CDCl.sub.3) .delta.: 8.56 (1H, br s) 8.24 (1H,
d, J=7.8 Hz), 7.62-7.54 (3H, m), 7.45-7.39 (1H, m), 7.09-7.06 (1H,
m), 6.96-6.90 (2H, m), 4.62 (2H, d, J=5.4 Hz), 4.29-4.16 (4H, m),
3.92-3.79 (5H, m), 2.57 (1H, br s), 2.12 (2H, t, J=5.4 Hz), 1.49
(3H, t, J=6.9 Hz)
Example 8
N-[2-(4-methoxy-3-(2-propynyloxy)phenyl)oxazol-4-ylmethyl]-2-ethoxybenzami-
de
Yield 0.19 g
White Powder
[0370] .sup.1H-NMR (CDCl.sub.3) .delta.: 8.58 (1H, br s) 8.24 (1H,
dd, J=7.8, 1.8 Hz), 7.70-7.63 (3H, m), 7.45-7.39 (1H, m), 7.07 (1H,
td, J=8.4, 0.9 Hz), 6.98-6.93 (2H, m), 4.84 (2H, d, J=2.4 Hz), 4.63
(2H, dd, J=5.4, 0.9 Hz), 4.19 (2H, q, J=7.2 Hz), 3.94 (3H, s), 2.54
(1H, t, J=2.4 Hz), 1.50 (3H, t, J=7.2 Hz)
Example 9
N-[2-(3-ethoxy-4-methoxyphenyl)oxazol-4-ylmethyl]-2-ethoxy
benzamide
Yield 0.22 g
White Powdery
[0371] .sup.1H-NMR (CDCl.sub.3) .delta.: 8.55 (1H, br s) 8.24 (1H,
dd, J=7.8, 1.8 Hz), 7.62-7.54 (3H, m), 7.44-7.39 (1H, m), 7.07 (1H,
t, J=8.1 Hz), 6.96-6.91 (2H, m), 4.62 (2H, d, J=5.4 Hz), 4.23-4.14
(4H, m), 3.93 (3H, s), 1.53-1.46 (6H, m)
Example 10
N-[2-(4-methoxy-3-(2-oxiranylmethoxy)phenyl)oxazol-4-ylmethyl]-2-ethoxyben-
zamide
Yield 27 mg
White Powder
[0372] .sup.1H-NMR (CDCl.sub.3) .delta.: 8.54 (1H, br s) 8.24 (1H,
dd, J=7.8, 1.8 Hz), 7.67-7.58 (3H, m), 7.45-7.38 (1H, m), 7.07 (1H,
t, J=7.8 Hz), 6.95 (2H, d, J=8.4 Hz), 4.62 (2H, d, J=5.1 Hz),
4.36-4.07 (4H, m), 3.93 (3H, s), 3.46-3.41 (1H, m), 2.92 (1H, t,
J=4.5 Hz), 2.80-2.76 (1H, m), 1.48 (3H, t, J=7.2 Hz)
Example 11
N-[2-(4-methoxy-3-propoxyphenyl)oxazol-4-ylmethyl]-2-ethoxy
benzamide
Yield 0.19 g
White Powder
[0373] .sup.1H-NMR (CDCl.sub.3) .delta.: 8.56 (1H, br s) 8.24 (1H,
dd, J=7.8, 1.8 Hz), 7.63-7.54 (3H, m), 7.45-7.39 (1H, m), 7.07 (1H,
td, J=8.4, 1.2 Hz), 6.96-6.91 (2H, m), 4.63 (2H, dd, J=5.1, 0.9
Hz), 4.18 (2H, q, J=6.9 Hz), 4.06 (2H, t, J=6.9 Hz), 3.92 (3H, s),
1.97-1.85 (2H, m), 1.49 (3H, t, J=6.9 Hz), 1.07 (3H, t, J=7.2
Hz)
Example 12
N-[2-(3-isopropoxy-4-methoxyphenyl)oxazol-4-ylmethyl]-2-ethoxy
benzamide
Yield 0.17 g
White Powder
[0374] .sup.1H-NMR (CDCl.sub.3) .delta.: 8.57 (1H, br s) 8.24 (1H,
dd, J=7.8, 1.8 Hz), 7.62-7.55 (3H, m), 7.45-7.38 (1H, m), 7.07 (1H,
t, J=7.8 Hz), 6.96-6.91 (2H, m), 4.72-4.59 (3H, m), 4.18 (2H, q,
J=6.9 Hz), 3.91 (3H, s), 1.49 (3H, t, J=6.9 Hz), 1.41 (6H, d, J=6.3
Hz)
Example 13
N-[2-(3-(3-butenyloxy)-4-methoxyphenyl)oxazol-4-ylmethyl]-2-ethoxybenzamid-
e
Yield 0.21 g
White Powder
[0375] .sup.1H-NMR (CDCl.sub.3) .delta.: 8.56 (1H, br s) 8.23 (1H,
dd, J=7.8, 1.8 Hz), 7.63-7.55 (3H, m), 7.45-7.38 (1H, m), 7.07 (1H,
t, J=7.8 Hz), 6.96-6.91 (2H, m), 5.97-5.88 (1H, m), 5.23-5.10 (2H,
m), 4.62 (2H, dd, J=5.1, 0.9 Hz), 4.21-4.12 (4H, m), 3.92 (3H, s),
2.68-2.60 (2H, m), 1.49 (3H, t, J=6.9 Hz)
Example 14
N-[2-(3-isobutoxy-4-methoxyphenyl)oxazol-4-ylmethyl]-2-ethoxy
benzamide
Yield 84 mg
White Powder
[0376] .sup.1H-NMR (CDCl.sub.3) .delta.: 8.54 (1H, br s), 8.23 (1H,
dd, J=7.8, 1.8 Hz) 7.62-7.53 (2H, m), 7.44 (1H, d, J=1.8 Hz), 7.41
(2H, td, J=7.8, 1.8 Hz), 7.06 (1H, t, J=7.8 Hz), 6.95-6.90 (2H, m),
4.62 (2H, d, J=5.4 Hz), 4.18 (2H, q, J=6.9 Hz), 3.91 (3H, s), 3.85
(2H, d, J=6.9 Hz), 2.20 (1H, qt, J=6.9, 6.6 Hz), 1.49 (3H, t, J=6.9
Hz), 1.06 (6H, d, J=6.6 Hz)
Example 15
[0377] Using 0.2 g of the N-[2-(3-hydroxy-4-methoxyphenyl)
oxazol-4-ylmethyl]-2-ethoxybenzamide obtained in Example 2,
N-{2-[4-methoxy-3-(3,3,3-trifluoropropoxy)phenyl]oxazol-4-ylmethyl}-2-eth-
oxybenzamide was obtained in the same manner as in Example 4.
Yield 60 mg
White Powder
[0378] .sup.1H-NMR (CDCl.sub.3) .delta.: 8.55 (1H, br s) 8.23 (1H,
dd, J=7.8, 1.8 Hz), 7.68-7.63 (2H, m), 7.56 (1H, d, J=2.1 Hz),
7.45-7.39 (1H, m), 7.07 (1H, t, J=7.2 Hz), 6.97-6.93 (2H, m), 4.62
(2H, d, J=5.4 Hz), 4.32 (2H, t, J=6.9 Hz), 4.18 (2H, q, J=6.9 Hz),
3.92 (3H, s), 2.78-2.67 (2H, m), 1.49 (3H, t, J=6.9 Hz)
Example 16
[0379] A 1.5 g quantity of the [2-(3-benzyloxy-4-methoxy
phenyl)oxazol-4-yl]methylamine obtained in Reference Example 7 was
suspended in 30 ml of acetone. To the obtained suspension were
added 1.0 g of 1-hydroxybenzotriazole, 1.4 g of
1-ethyl-3-(3-dimethylaminopropyl)carbodiimide hydrochloride and 0.8
g of 3-methylpicolinic acid, and the mixture was heated and
refluxed for 30 minutes. The reaction mixture was cooled, and
acetone was distilled off under reduced pressure. Water was added
to the residue, and extraction was then performed with ethyl
acetate. The organic layer was washed with water twice, and the
solvent was concentrated under reduced pressure. The obtained
residue was purified by silica gel column chromatography
(dichloromethane:methanol=20:1) to give 1.5 g of white powdery
N-[2-(3-benzyloxy-4-methoxyphenyl)oxazol-4-ylmethyl]-3-methylpicolinamide-
.
[0380] .sup.1H-NMR (CDCl.sub.3) .delta.: 8.57 (1H, br s), 8.39 (1H,
d, J=7.5 Hz), 7.65-7.28 (10H, m), 6.94 (1H, d, J=9.0 Hz), 5.21 (2H,
s), 4.58 (2H, dd, J=5.7, 0.9 Hz), 3.93 (3H, s), 2.76 (3H, s)
Example 17
[0381] A 1.5 g quantity of the N-[2-(3-benzyloxy-4-methoxy
phenyl)oxazol-4-ylmethyl]-3-methylpicolinamide obtained in Example
16 was dissolved in 50 ml of ethanol, and 0.1 g of 10% palladium
carbon powder was added thereto. The mixture was stirred in a
hydrogen atmosphere at 50.degree. C. for two hours. The catalyst
was removed by filtration, and the filtrate was then concentrated
to give 1.3 g of white crystalline
N-[2-(3-hydroxy-4-methoxyphenyl)oxazol-4-ylmethyl]-3-methylpicolinamide.
[0382] .sup.1H-NMR (CDCl.sub.3) .delta.: 8.58 (1H, br s), 8.38 (1H,
dd, J=4.5, 0.9 Hz), 7.63 (1H, s), 7.62-7.54 (3H, m), 7.32-7.27 (1H,
m), 6.90 (1H, d, J=8.4 Hz), 5.75 (1H, br s), 4.58 (2H, dd, J=6.0,
0.9 Hz), 3.94 (3H, s), 2.75 (3H, s)
Example 18
[0383] A 0.15 g quantity of the
N-[2-(3-hydroxy-4-methoxyphenyl)oxazol-4-ylmethyl]-3-methylpicolinamide
obtained in Example 17 and 0.5 ml of
1,8-diazabicyclo[5,4,0]undec-7-ene were dissolved in 4 ml of
ethanol, and 0.13 g of bromocyclopentane was added thereto. The
mixture was heated and refluxed for 3 hours. The reaction mixture
was allowed to cool, water was then added thereto, and extraction
was performed with ethyl acetate. The extract was washed with water
twice, and the organic layer was concentrated under reduced
pressure. The obtained residue was purified by silica gel column
chromatography (n-hexane:ethyl acetate=3:1) to give 0.11 g of white
powdery
N-[2-(3-cyclopentyloxy-4-methoxyphenyl)oxazol-4-ylmethyl]-3-methy-
lpicolinamide.
[0384] .sup.1H-NMR (CDCl.sub.3) .delta.: 8.57 (1H, br s), 8.39 (1H,
dd, J=4.8, 0.9 Hz), 7.62-7.53 (4H, m), 7.32-7.27 (1H, m), 6.91 (1H,
d, J=8.4 Hz), 4.88 (1H, tt, J=3.3 Hz), 4.59 (2H, dd, J=5.7, 0.9
Hz), 3.89 (3H, s), 2.76 (3H, s), 2.07-1.79 (6H, m), 1.70-1.60 (2H,
m)
Example 19
[0385] A 0.15 g quantity of the N-[2-(3-hydroxy-4-methoxy
phenyl)oxazol-4-ylmethyl]-3-methylpicolinamide obtained in Example
17 and 0.18 g of potassium carbonate were dissolved in 4 ml of
dimethylformamide, and 0.19 g of 1,1,1-trifluoro-2-iodoethane was
added thereto. The mixture was stirred with heating at 80.degree.
C. overnight. The reaction mixture was allowed to cool, water was
then added thereto, and extraction was performed with ethyl
acetate. The extract was washed with water twice, and the organic
layer was concentrated under reduced pressure. The obtained residue
was purified by silica gel column chromatography (n-hexane:ethyl
acetate=3:1) to give 0.11 g of white powdery
N-{2-[4-methoxy-3-(2,2,2-trifluoroethoxy)phenyl]oxazol-4-ylmethyl-
}-3-methylpicolinamide.
[0386] .sup.1H-NMR (CDCl.sub.3) .delta.: 8.58 (1H, br s), 8.39 (1H,
dd, J=4.5, 1.2 Hz), 7.73 (1H, dd, J=8.7, 2.1 Hz), 7.63-7.57 (3H,
m), 7.32-7.27 (1H, m), 6.97 (1H, d, J=8.4 Hz), 4.59 (2H, dd, J=5.7,
0.9 Hz), 4.46 (2H, q, J=8.4 Hz), 3.93 (3H, s), 2.76 (3H, s)
Example 20
[0387] Using 0.2 g of the N-[2-(3-hydroxy-4-methoxyphenyl)
oxazol-4-ylmethyl]-3-methylpicolinamide obtained in Example 17,
0.11 g of
N-[2-(3-ethoxy-4-methoxyphenyl)oxazol-4-ylmethyl]-3-methylpicolinamide
was obtained in the same manner as in Example 3.
Colorless Crystals
[0388] .sup.1H-NMR (CDCl.sub.3) .delta.: 8.57 (1H, br s), 8.39 (1H,
dd, J=4.8, 1.5 Hz), 7.65-7.50 (4H, m), 7.30 (1H, dd, J=7.8, 4.8
Hz), 6.92 (1H, d, J=8.1 Hz), 4.59 (1H, dd, J=6.0, 0.6 Hz), 4.19
(2H, q, J=6.9 Hz), 4.17 (2H, q, J=6.9 Hz), 3.92 (3H, s), 2.76 (3H,
s), 1.50 (3H, t, J=6.9 Hz)
Example 21
[0389] Using 0.15 g of the N-[2-(3-hydroxy-4-methoxyphenyl)
oxazol-4-ylmethyl]-3-methylpicolinamide obtained in Example 17, mg
of
N-[2-(3-allyloxy-4-methoxyphenyl)oxazol-4-ylmethyl]-3-methylpicolinamide
was obtained in the same manner as in Example 3.
Colorless Crystal
[0390] .sup.1H-NMR (CDCl.sub.3) .delta.: 8.58 (1H, br s), 8.39 (1H,
dd, J=4.5, 1.5 Hz), 7.65-7.50 (4H, m), 7.30 (1H, dd, J=7.8, 4.5
Hz), 6.93 (1H, d, J=8.4 Hz), 6.12 (1H, m), 5.45 (1H, m), 5.32 (1H,
dd, J=9.6, 1.5 Hz), 4.70 (2H, d, J=5.4 Hz), 4.59 (1H, d, J=6.0 Hz),
3.92 (3H, s), 2.76 (3H, s).
Example 22
[0391] A 170 mg quantity of the N-[2-(3-hydroxy-4-methoxy
phenyl)oxazol-4-ylmethyl]-3-methylpicolinamide obtained in Example
17 was dissolved in 10 ml of tetrahydrofuran. To the obtained
solution were added 134 mg of 2-hydroxyindane, 0.5 ml of
diisopropyl azodicarboxylate (40% toluene solution) and 202 mg of
tri(n-butyl)phosphine, and the mixture was stirred at room
temperature overnight, and at 50.degree. C. for 2.5 hours. To the
reaction mixture were added 100 mg of 2-hydroxyindane, 0.5 ml of
diisopropyl azodicarboxylate (40% toluene solution) and 200 mg of
tri(n-butyl)phosphine, and the mixture was stirred at 50.degree. C.
for 5 hours, and at room temperature overnight. The reaction
mixture was concentrated under reduced pressure. The residue was
purified by silica gel column chromatography (n-hexane:ethyl
acetate:methylene chloride=1:1:1) to give 92 mg of
N-{2-[3-(indan-2-yloxy)-4-methoxyphenyl]oxazol-4-ylmethyl}-3-methylpicoli-
namide.
Pale Yellow Oily Substance
[0392] .sup.1H-NMR (CDCl.sub.3) .delta.: 8.59 (1H, br s), 8.39 (1H,
d, J=3.3 Hz), 7.65-7.16 (9H, m), 6.93 (1H, d, J=8.1 Hz), 5.30 (1H,
tt, J=6.6, 3.9 Hz), 4.60 (2H, d, J=5.7 Hz), 3.86 (3H, s), 3.46 (2H,
dd, J=16.8, 6.6 Hz), 3.27 (2H, dd, J=16.8, 3.9 Hz), 2.76 (3H,
s)
Example 23
[0393] Using 0.88 g of the [2-(3-benzyloxy-4-methoxyphenyl)
oxazol-4-yl]methylamine obtained in Reference Example 7, 1.03 g of
white powdery
N-[2-(3-benzyloxy-4-methoxyphenyl)oxazol-4-ylmethyl]-2-trifluorom-
ethylbenzamide was obtained in the same manner as in Example 1.
[0394] .sup.1H-NMR (CDCl.sub.3) .delta.: 7.72-7.46 (9H, m),
7.40-7.27 (3H, m), 6.95 (1H, d, J=8.4 Hz) 6.34 (1H, br s), 5.20
(2H, s), 4.59 (2H, d, J=5.4 Hz), 3.93 (3H, s)
Example 24
[0395] Using 1.0 g of the N-[2-(3-benzyloxy-4-methoxyphenyl)
oxazol-4-ylmethyl]-2-trifluoromethylbenzamide obtained in Example
23, 0.66 g of white powdery N-[2-(3-hydroxy-4-methoxyphenyl)
oxazol-4-ylmethyl]-2-trifluoromethylbenzamide was obtained in the
same manner as in Example 2.
[0396] .sup.1H-NMR (CDCl.sub.3) .delta.: 7.71-7.50 (7H, m), 6.90
(1H, d, J=8.4 Hz), 6.39 (1H, br s), 5.76 (1H, s), 4.59 (2H, d,
J=5.4 Hz), 3.94 (3H, s)
Example 25
[0397] Using 0.2 g of the N-[2-(3-hydroxy-4-methoxyphenyl)
oxazol-4-ylmethyl]-2-trifluoromethylbenzamide obtained in Example
24, 0.18 g of white powdery
N-[2-(3-cyclopropylmethoxy-4-methoxyphenyl)oxazol-4-ylmethyl]-2-trifluoro-
methylbenzamide was obtained in the same manner as in Example
3.
[0398] .sup.1H-NMR (CDCl.sub.3) .delta.: 7.72-7.50 (7H, m), 6.93
(1H, d, J=8.4 Hz), 6.34 (1H, s), 4.60 (2H, d, J=5.4 Hz), 3.93 (3H,
s), 1.42-1.32 (1H, m), 0.70-0.63 (2H, m), 0.41-0.35 (2H, m)
Example 26
[0399] Using 0.2 g of the N-[2-(3-hydroxy-4-methoxyphenyl)
oxazol-4-ylmethyl]-2-trifluoromethylbenzamide obtained in Example
24, 40 mg of white powdery
N-{2-[3-(3-hydroxypropoxy)-4-methoxyphenyl]oxazol-4-ylmethyl}-2-trifluoro-
methylbenzamide was obtained in the same manner as in Example
3.
[0400] .sup.1H-NMR (CDCl.sub.3) .delta.: 7.71-7.50 (7H, m), 6.92
(1H, d, J=8.4 Hz), 6.34 (1H, br s), 4.60 (2H, d, J=5.4 Hz), 4.28
(2H, q, J=5.7 Hz), 3.98-3.86 (5H, m), 2.47 (1H, t, J=5.7 Hz),
2.15-2.07 (3H, m)
Example 27
[0401] Using 0.5 g of the 2-(3-benzyloxy-4-methoxyphenyl)
oxazol-4-yl]methylamine obtained in Reference Example 7, 0.62 g of
white powdery
N-[2-(3-benzyloxy-4-methoxyphenyl)oxazol-4-ylmethyl]-3-ethoxypico-
linamide was obtained in the same manner as in Example 1.
[0402] .sup.1H-NMR (CDCl.sub.3) .delta.: 8.24-8.22 (2H, m),
7.64-7.60 (3H, m), 7.50-7.46 (2H, m), 7.41-7.28 (5H, m), 6.94 (1H,
d, J=9.0 Hz), 5.20 (2H, s), 4.61 (2H, d, J=5.7 Hz), 4.17 (2H, q,
J=6.9 Hz), 3.93 (3H, s), 1.50 (3H, t, J=6.9 Hz)
Example 28
[0403] Using 0.6 g of the N-[2-(3-benzyloxy-4-methoxyphenyl)
oxazol-4-ylmethyl]-3-ethoxypicolinamide obtained in Example 27, 0.5
g of white amorphous
N-[2-(3-hydroxy-4-methoxyphenyl)oxazol-4-ylmethyl]-3-ethoxypicolinamide
was obtained in the same manner as in Example 2.
[0404] .sup.1H-NMR (CDCl.sub.3) .delta.: 8.25-8.22 (2H, m), 7.64
(1H, d, J=1.8 Hz), 7.60-7.54 (2H, m), 7.39-7.28 (2H, m), 6.91 (1H,
d, J=8.1 Hz), 5.71 (1H, br s), 4.61 (2H, dd, J=5.4, 0.9 Hz), 4.17
(2H, q, J=6.9 Hz), 3.94 (3H, s), 1.52 (3H, t, J=6.9 Hz)
Example 29
[0405] Using 0.5 g of the N-[2-(3-hydroxy-4-methoxyphenyl)
oxazol-4-ylmethyl]-3-ethoxypicolinamide obtained in Example 28,
0.18 g of white amorphous
N-[2-(3-cyclopentyloxy-4-methoxyphenyl)oxazol-4-ylmethyl]-3-ethoxypicolin-
amide was obtained in the same manner as in Example 3.
[0406] .sup.1H-NMR (CDCl.sub.3) .delta.: 8.25-8.22 (2H, m), 7.64
(1H, s), 7.58 (1H, dd, J=8.4, 2.1 Hz), 7.53 (1H, d, J=1.8 Hz),
7.39-7.32 (2H, m), 6.91 (1H, d, J=8.4 Hz), 4.91-4.86 (1H, m), 4.62
(2H, dd, J=5.4, 0.9 Hz), 4.17 (2H, q, J=6.9 Hz), 3.89 (3H, s),
2.05-1.79 (6H, m), 1.66-1.60 (2H, m), 1.51 (3H, t, J=6.9 Hz)
Example 30
[0407] Using 0.31 g of the 2-(3-benzyloxy-4-methoxyphenyl)
oxazol-4-yl]methylamine obtained in Reference Example 7, 0.16 g of
white powdery
N-[2-(3-benzyloxy-4-methoxyphenyl)oxazol-4-ylmethyl]-2-(2,2,2-tri-
fluoroethoxy)benzamide was obtained in the same manner as in
Example 1.
[0408] .sup.1H-NMR (CDCl.sub.3) .delta.: 8.22 (1H, dd, J=7.8, 1.8
Hz), 7.82 (1H, br s), 7.63-7.60 (3H, m), 7.49-7.27 (6H, m), 7.19
(1H, t, J=7.2 Hz), 6.96-6.88 (2H, m), 5.19 (2H, s), 4.62 (2H, d,
J=5.4 Hz), 4.47 (2H, q, J=7.8 Hz), 3.92 (3H, s)
Example 31
[0409] Using 0.16 g of the N-[2-(3-benzyloxy-4-methoxyphenyl)
oxazol-4-ylmethyl]-2-(2,2,2-trifluoroethoxy)benzamide obtained in
Example 30, 0.11 g of white powdery N-[2-(3-hydroxy-4-methoxy
phenyl)oxazol-4-ylmethyl]-2-(2,2,2-trifluoroethoxy)benzamide was
obtained in the same manner as in Example 2.
[0410] .sup.1H-NMR (CDCl.sub.3) .delta.: 8.21 (1H, dd, J=7.8, 1.8
Hz), 7.84 (1H, br s), 7.62-7.54 (3H, m), 7.49-7.43 (1H, m), 7.19
(1H, td, J=7.8, 0.9 Hz), 5.71 (1H, s), 4.62 (2H, dd, J=5.4, 0.9
Hz), 4.48 (2H, q, J=7.8 Hz), 3.94 (3H, s)
Example 32
[0411] Using 0.11 g of the
N-[2-(3-hydroxy-4-methoxyphenyl)oxazol-4-ylmethyl]-2-(2,2,2-trifluoroetho-
xy)benzamide obtained in Example 31, 78 mg of white amorphous
N-[2-(3-cyclopropylmethoxy-4-methoxyphenyl)oxazol-4-ylmethyl]-2-(2,2,2-tr-
ifluoroethoxy)benzamide was obtained in the same manner as in
Example 3.
[0412] .sup.1H-NMR (CDCl.sub.3) .delta.: 8.22 (1H, dd, J=7.8, 2.1
Hz), 7.83 (1H, br s), 7.61-7.57 (3H, m), 7.53 (1H, d, J=2.1 Hz),
7.50-7.43 (1H, m), 7.19 (1H, td, J=7.8, 0.9 Hz), 6.94-6.88 (2H, m),
4.63 (2H, dd, J=5.4, 0.9 Hz), 4.48 (2H, q, J=7.8 Hz), 1.42-1.32
(1H, m), 0.70-0.63 (2H, m), 0.41-0.35 (2H, m)
Example 33
[0413] Using 0.5 g of the 2-(3-benzyloxy-4-methoxyphenyl)
oxazol-4-yl]methylamine obtained in Reference Example 7, 0.68 g of
pale yellow powdery
N-[2-(3-benzyloxy-4-methoxyphenyl)oxazol-4-ylmethyl]-2-methoxybenzamide
was obtained in the same manner as in Example 1.
[0414] .sup.1H-NMR (CDCl.sub.3) .delta.: 8.39 (1H, br s), 8.23 (1H,
dd, J=4.8, 1.8 Hz), 7.65-7.60 (3H, m), 7.50-7.28 (6H, m), 7.08 (1H,
t, J=7.2 Hz), 6.98-6.93 (2H, m), 5.21 (2H, s), 4.61 (2H, dd, J=5.4,
0.9 Hz), 3.95 (3H, s), 3.93 (3H, s)
Example 34
[0415] Using 0.67 g of the N-[2-(3-benzyloxy-4-methoxyphenyl)
oxazol-4-ylmethyl]-2-methoxybenzamide obtained in Example 33, 0.52
g of white amorphous
N-[2-(3-hydroxy-4-methoxyphenyl)oxazol-4-ylmethyl]-2-methoxybenzamide
was obtained in the same manner as in Example 2.
[0416] .sup.1H-NMR (CDCl.sub.3) .delta.: 8.43 (1H, br s), 8.23 (1H,
dd, J=7.8, 2.1 Hz), 7.63 (1H, s), 7.60-7.54 (2H, m), 7.47-7.41 (1H,
m), 7.10-7.05 (1H, m), 6.97 (1H, d, J=8.4 Hz), 6.91 (1H, d, J=8.1
Hz), 5.74 (1H, br s), 4.62 (2H, dd, J=5.4, 0.9 Hz), 3.97 (3H, s),
3.95 (3H, s)
Example 35
[0417] Using 0.5 g of the N-[2-(3-hydroxy-4-methoxyphenyl)
oxazol-4-ylmethyl]-2-methoxybenzamide obtained in Example 34, 0.39
g of white powdery N-[2-(3-cyclopentyloxy-4-methoxyphenyl)
oxazol-4-ylmethyl]-2-methoxybenzamide was obtained in the same
manner as in Example 3.
[0418] .sup.1H-NMR (CDCl.sub.3) .delta.: 8.41 (1H, br s), 8.23 (1H,
dd, J=7.8, 1.8 Hz), 7.63 (1H, s), 7.59 (1H, dd, J=8.4, 1.8 Hz),
7.54 (1H, d, J=1.8 Hz), 7.48-7.42 (1H, m), 7.08 (1H, t, J=7.8 Hz),
6.98 (1H, d, J=8.1 Hz), 6.92 (1H, d, J=8.4 Hz), 4.91-4.87 (1H, m),
4.62 (2H, dd, J=5.4, 0.9 Hz), 3.97 (3H, s), 3.90 (3H, s), 2.05-1.80
(6H, m), 1.66-1.59 (2H, m)
Example 36
[0419] A 0.2 g quantity of the
[2-(3-cyclopropylmethoxy-4-methoxyphenyl)oxazol-4-yl]methylamine
obtained in Reference Example 13 was suspended in 4 ml of acetone.
To the obtained suspension were added 0.2 g of
1-hydroxybenzotriazole, 0.29 g of
1-ethyl-3-(3-dimethylaminopropyl)carbodiimide hydrochloride and
0.14 g of 3-methylpicolinic acid, and the mixture was heated and
refluxed for 30 minutes. The reaction mixture was cooled, water was
then added thereto, and extraction was performed with ethyl
acetate. The organic layer was washed with water twice, and the
solvent was concentrated under reduced pressure. The obtained
residue was purified by silica gel column chromatography
(n-hexane:ethyl acetate=1:1) to give 0.16 g of white powdery
N-[2-(3-cyclopropylmethoxy-4-methoxyphenyl)oxazol-4-ylmethyl]-3-m-
ethylpicolinamide.
[0420] .sup.1H-NMR (CDCl.sub.3) .delta.: 8.58 (1H, br s) 8.39 (1H,
dd, J=4.5, 1.2 Hz), 7.63-7.57 (3H, m), 7.52 (1H, d, J=2.1 Hz),
7.33-7.28 (1H, m), 6.92 (1H, d, J=8.4 Hz), 4.59 (2H, dd, J=6.0, 0.9
Hz), 3.97-3.90 (5H, m), 2.76 (3H, s), 1.41-1.31 (1H, m), 0.70-0.63
(2H, m), 0.41-0.35 (2H, m)
[0421] Using 0.2 g of the [2-(3-cyclopropylmethoxy-4-methoxy
phenyl)oxazol-4-yl]methylamine obtained in Reference Example 13,
compounds of Examples 37 to 43 were obtained in the same manner as
in Example 1.
Example 37
N-[2-(3-cyclopropylmethoxy-4-methoxyphenyl)oxazol-4-ylmethyl]-2-isopropoxy-
benzamide
Yield 0.17 g
White Powder
[0422] .sup.1H-NMR (CDCl.sub.3) .delta.: 8.62 (1H, br s) 8.23 (1H,
dd, J=7.8, 1.8 Hz), 7.62-7.58 (2H, m), 7.54 (1H, d, J=2.1 Hz),
7.43-7.38 (1H, m), 7.05 (1H, td, J=8.1, 0.9 Hz), 6.97-6.91 (2H, m),
4.76-4.67 (1H, m), 4.61 (2H, dd, J=5.4, 0.9 Hz), 3.94-3.90 (5H, m),
1.41-1.38 (7H, m), 0.69-0.64 (2H, m), 0.41-0.35 (2H, m)
Example 38
N-[2-(3-cyclopropylmethoxy-4-methoxyphenyl)oxazol-4-ylmethyl]-2-methylbenz-
amide
Yield 0.16 g
White Powder
[0423] .sup.1H-NMR (CDCl.sub.3) .delta.: 7.64 (1H, s) 7.59 (1H, dd,
J=8.4, 2.1 Hz), 7.50 (1H, d, J=2.1 Hz), 7.41-7.16 (3H, m), 6.93
(1H, d, J=8.4 Hz), 6.31 (1H, br s), 4.58 (2H, dd, J=5.4, 0.9 Hz),
3.95-3.92 (5H, m), 2.46 (3H, s), 1.42-1.32 (1H, m), 0.70-0.63 (2H,
m), 0.41-0.35 (2H, m)
Example 39
N-[2-(3-cyclopropylmethoxy-4-methoxyphenyl)oxazol-4-ylmethyl]-2-ethylbenza-
mide
Yield 0.15 g
White Powder
[0424] .sup.1H-NMR (CDCl.sub.3) .delta.: 7.64 (1H, s) 7.59 (1H, dd,
J=8.4, 2.1 Hz), 7.50 (1H, d, J=1.8 Hz), 7.41-7.16 (3H, m), 6.93
(1H, d, J=8.1 Hz), 6.31 (1H, br s), 4.57 (2H, d, J=5.4 Hz),
3.95-3.92 (5H, m), 2.81 (2H, q, J=7.5 Hz), 1.42-1.32 (1H, m), 1.23
(3H, t, J=7.5 Hz), 0.70-0.63 (2H, m), 0.41-0.35 (2H, m)
Example 40
N-[2-(3-cyclopropylmethoxy-4-methoxyphenyl)oxazol-4-ylmethyl]-2-chlorobenz-
amide
Yield 0.17 g
White Powder
[0425] .sup.1H-NMR (CDCl.sub.3) .delta.: 7.71-7.66 (2H, m), 7.59
(1H, dd, J=8.4, 1.8 Hz), 7.50 (1H, d, J=2.1 Hz), 7.42-7.29 (3H, m),
6.93 (1H, d, J=8.4 Hz), 6.75 (1H, br s), 4.62 (2H, dd, J=5.4, 0.9
Hz), 3.95-3.92 (5H, m), 1.41-1.32 (1H, m), 0.70-0.63 (2H, m),
0.41-0.35 (2H, m)
Example 41
N-[2-(3-cyclopropylmethoxy-4-methoxyphenyl)oxazol-4-ylmethyl]-5-fluoro-2-m-
ethoxybenzamide
Yield 0.19 g
White Powder
[0426] .sup.1H-NMR (CDCl.sub.3) .delta.: 8.45 (1H, br s), 7.94 (1H,
dd, J=9.6, 3.3 Hz), 7.63 (1H, s), 7.61 (1H, dd, J=8.1, 1.8 Hz),
7.51 (1H, d, J=1.8 Hz), 7.17-7.10 (1H, m), 6.95-6.90 (2H, m), 4.61
(2H, d, J=5.4 Hz), 3.96-3.92 (8H, m), 1.40-1.30 (1H, m), 0.70-0.64
(2H, m), 0.41-0.35 (2H, m)
Example 42
N-[2-(3-cyclopropylmethoxy-4-methoxyphenyl)oxazol-4-ylmethyl]-4-fluoro-2-m-
ethoxybenzamide
Yield 0.19 g
White Powder
[0427] .sup.1H-NMR (CDCl.sub.3) .delta.: 8.27-8.21 (2H, m),
7.63-7.58 (2H, m), 7.52 (1H, d, J=2.1 Hz), 6.93 (1H, d, J=8.4 Hz),
6.81-6.74 (1H, m), 6.69 (1H, dd, J=10.2, 2.1 Hz), 4.60 (2H, dd,
J=5.4, 0.9 Hz), 3.97-3.90 (8H, m), 1.40-1.30 (1H, m), 0.70-0.64
(2H, m), 0.41-0.35 (2H, m)
Example 43
N-[2-(3-cyclopropylmethoxy-4-methoxyphenyl)oxazol-4-ylmethyl]-2-fluoro-6-m-
ethoxybenzamide
Yield 0.17 g
White Powder
[0428] .sup.1H-NMR (CDCl.sub.3) .delta.: 7.65 (1H, s), 7.59 (1H,
dd, J=8.4, 2.1 Hz), 7.50 (1H, d, J=2.1 Hz), 7.34-7.27 (1H, m), 6.92
(1H, d, J=8.4 Hz), 6.76-6.70 (2H, m), 6.51 (1H, br s), 4.61 (2H, d,
J=5.7 Hz), 3.94-3.91 (5H, m), 3.85 (3H, s), 1.42-1.31 (1H, m),
0.70-0.63 (2H, m), 0.41-0.35 (2H, m)
Example 44
[0429] Using 0.4 g of the [2-(3-cyclopropylmethoxy-4-methoxy
phenyl)oxazol-4-yl]methylamine obtained in Reference Example 13,
N-[2-(3-cyclopropylmethoxy-4-methoxyphenyl)oxazol-4-ylmethyl]-2-methylsul-
fanylbenzamide was obtained in the same manner as in Example 1.
Yield 0.4 g
White Powder
[0430] .sup.1H-NMR (CDCl.sub.3) .delta.: 7.68 (1H, s), 7.61-7.56
(2H, m), 7.50 (1H, d, J=1.8 Hz), 7.34-7.17 (3H, m), 6.95-6.90 (2H,
m), 4.61 (2H, dd, J=5.4, 0.9 Hz), 3.95-3.92 (5H, m), 2.46 (3H, s),
1.42-1.31 (1H, m), 0.70-0.63 (2H, m), 0.41-0.35 (2H, m)
Example 45
[0431] Using 0.7 g of the [2-(3-cyclopropylmethoxy-4-methoxy
phenyl)oxazol-4-yl]methylamine obtained in Reference Example 13,
N-[2-(3-cyclopropylmethoxy-4-methoxyphenyl)oxazol-4-ylmethyl]-3-hydroxypi-
colinamide was obtained in the same manner as in Example 1.
Yield 0.6 g
White Powder
[0432] .sup.1H-NMR (CDCl.sub.3) .delta.:12.02 (1H, s), 8.45 (1H, br
s), 8.06 (1H, dd, J=4.2, 1.8 Hz), 7.63-7.59 (2H, m), 7.52 (1H, s),
7.37-7.29 (3H, m), 6.93 (1H, d, J=8.4 Hz), 4.60 (2H, d, J=6.0 Hz),
3.96-3.93 (5H, m), 1.56-1.33 (1H, m), 0.70-0.64 (2H, m), 0.42-0.36
(2H, m)
[0433] Using 0.1 g of the [2-(3-cyclopropylmethoxy-4-methoxy
phenyl)oxazol-4-yl]methylamine obtained in Reference Example 13,
compounds of Examples 46 to 56 were obtained in the same manner as
in Example 1.
Example 46
N-[2-(3-cyclopropylmethoxy-4-methoxyphenyl)oxazol-4-ylmethyl]-2-methoxyben-
zamide
Yield 0.1 g
White Powder
[0434] .sup.1H-NMR (CDCl.sub.3) .delta.: 8.40 (1H, br s), 8.23 (1H,
dd, J=7.8, 2.1 Hz) 7.64-7.58 (2H, m), 7.52 (1H, d, J=2.1 Hz),
7.48-7.42 (1H, m), 7.08 (1H, td, J=7.8, 0.9 Hz), 6.99-6.91 (2H, m),
4.62 (2H, dd, J=5.4, 0.9 Hz), 3.97-3.91 (8H, m), 1.40-1.32 (1H, m),
0.70-0.63 (2H, m), 0.41-0.35 (2H, m)
Example 47
N-[2-(3-cyclopropylmethoxy-4-methoxyphenyl)oxazol-4-ylmethyl]-2-trifluorom-
ethoxybenzamide
Yield 43 mg
White Powder
[0435] .sup.1H-NMR (CDCl.sub.3) .delta.: 8.02 (1H, dd, J=7.8, 1.8
Hz), 7.64-7.27 (6H, m), 7.10 (1H, br s), 6.93 (1H, d, J=8.4 Hz),
4.62 (2H, dd, J=5.4, 0.9 Hz), 3.95-3.92 (5H, m), 1.43-1.28 (1H, m),
0.69-0.63 (2H, m), 0.41-0.36 (2H, m)
Example 48
N-[2-(3-cyclopropylmethoxy-4-methoxyphenyl)oxazol-4-ylmethyl]-2-propoxyben-
zamide
Yield 0.1 g
White Powder
[0436] .sup.1H-NMR (CDCl.sub.3) .delta.: 8.50 (1H, br s), 8.24 (1H,
dd, J=7.8, 1.8 Hz) 7.61-7.58 (2H, m), 7.53 (1H, d, J=1.8 Hz),
7.44-7.38 (1H, m), 7.06 (1H, t, J=7.8 Hz), 6.95-6.91 (2H, m), 4.62
(2H, d, J=5.1 Hz), 4.06 (2H, t, J=6.6 Hz), 3.95-3.68 (5H, m), 1.86
(2H, td, J=7.5, 6.6 Hz), 1.41-1.31 (1H, m), 0.96 (3H, t, J=7.5 Hz),
0.70-0.61 (2H, m), 0.41-0.35 (2H, m)
Example 49
N-[2-(3-cyclopropylmethoxy-4-methoxyphenyl)oxazol-4-ylmethyl]pyrazine-2-ca-
rboxamide
Yield 90 mg
White Powder
[0437] .sup.1H-NMR (CDCl.sub.3) .delta.: 9.42 (1H, s), 8.75 (1H, d,
J=2.4 Hz), 8.52 (1H, dd, J=2.7, 1.5 Hz), 8.25 (1H, br s), 7.64 (1H,
s), 7.60 (1H, dd, J=8.4, 1.8 Hz), 7.52 (1H, d, J=1.8 Hz), 6.92 (1H,
d, J=8.4 Hz), 4.63 (2H, dd, J=5.4, 0.9 Hz), 4.11-3.92 (5H, m),
1.40-1.32 (1H, m), 0.70-0.63 (2H, m), 0.41-0.35 (2H, m)
Example 50
N-[2-(3-cyclopropylmethoxy-4-methoxyphenyl)oxazol-4-ylmethyl]-3-ethoxypico-
linamide
Yield 85 mg
White Powder
[0438] .sup.1H-NMR (CDCl.sub.3) .delta.: 8.24-8.22 (2H, m) 7.64
(1H, s), 7.60 (1H, dd, J=8.4, 1.8 Hz), 7.51 (1H, d, J=2.1 Hz),
7.39-7.32 (2H, m), 6.92 (1H, d, J=8.4 Hz), 4.62 (2H, dd, J=5.4, 0.9
Hz), 4.17 (2H, q, J=6.9 Hz), 3.98-3.92 (5H, m), 1.52 (3H, t, J=6.9
Hz), 1.43-1.32 (1H, m), 0.71-0.63 (2H, m), 0.41-0.35 (2H, m)
Example 51
N-[2-(3-cyclopropylmethoxy-4-methoxyphenyl)oxazol-4-ylmethyl]-2-butoxybenz-
amide
Yield 70 mg
White Powder
[0439] .sup.1H-NMR (CDCl.sub.3) .delta.: 8.48 (1H, br s) 8.23 (1H,
dd, J=7.8, 1.8 Hz), 7.63-7.59 (2H, m), 7.53 (1H, d, J=2.1 Hz),
7.45-7.38 (1H, m), 7.06 (1H, td, J=8.4, 0.9 Hz), 6.96-6.91 (2H, m),
4.61 (2H, d, J=5.1 Hz), 4.09 (2H, t, J=6.6 Hz), 3.94-3.91 (5H, m),
1.84-1.75 (2H, m), 1.46-1.33 (3H, m), 0.84 (3H, t, J=7.2 Hz),
0.70-0.63 (2H, m), 0.41-0.35 (2H, m)
Example 52
N-[2-(3-cyclopropylmethoxy-4-methoxyphenyl)oxazol-4-ylmethyl]-2-isobutoxyb-
enzamide
Yield 0.12 g
White Powder
[0440] .sup.1H-NMR (CDCl.sub.3) .delta.: 8.46 (1H, br s) 8.24 (1H,
dd, J=7.8, 1.8 Hz), 7.62-7.58 (2H, m), 7.52 (1H, d, J=1.8 Hz), 7.41
(1H, t, J=7.2 Hz), 7.06 (1H, t, J=7.2 Hz), 6.95-6.91 (2H, m), 4.62
(2H, d, J=5.1 Hz), 3.95-3.92 (5H, m), 3.86 (2H, d, J=6.3 Hz),
2.20-2.10 (1H, m), 1.40-1.31 (1H, m), 0.95 (6H, d, J=6.6 Hz),
0.70-0.63 (2H, m), 0.41-0.37 (2H, m)
Example 53
N-[2-(3-cyclopropylmethoxy-4-methoxyphenyl)oxazol-4-ylmethyl]-3-isopropoxy-
picolinamide
Yield 0.1 g
White Powder
[0441] .sup.1H-NMR (CDCl.sub.3) .delta.: 8.28-8.25 (2H, m) 7.63
(1H, s), 7.60 (1H, dd, J=8.4, 2.1 Hz), 7.52 (1H, d, J=2.1 Hz),
7.38-7.31 (2H, m), 6.93 (1H, d, J=8.4 Hz), 4.70-4.61 (3H, m),
3.98-3.90 (5H, m), 1.42-1.31 (7H, m), 0.70-0.61 (2H, m), 0.41-0.35
(2H, m)
Example 54
N-[2-(3-cyclopropylmethoxy-4-methoxyphenyl)oxazol-4-ylmethyl]-2-ethylsulfa-
nylbenzamide
Yield 85 mg
White Powder
[0442] .sup.1H-NMR (CDCl.sub.3) .delta.: 7.70-7.66 (2H, m), 7.59
(1H, dd, J=8.4, 1.8 Hz), 7.51 (1H, d, J=2.1 Hz), 7.43-7.32 (2H, m),
7.27-7.22 (2H, m), 6.92 (1H, d, J=8.7 Hz), 4.61 (2H, dd, J=5.4, 0.6
Hz), 3.95-3.92 (5H, m), 2.90 (2H, q, J=7.5 Hz), 1.40-1.34 (1H, m),
1.26 (3H, t, J=7.2 Hz), 0.70-0.63 (2H, m), 0.41-0.35 (2H, m)
Example 55
N-[2-(3-cyclopropylmethoxy-4-methoxyphenyl)oxazol-4-ylmethyl]-1-oxidepicol-
inamide
Yield 53 mg
Pale Yellow Powder
[0443] .sup.1H-NMR (CDCl.sub.3) .delta.:11.64 (1H, br s), 8.44 (1H,
dd, J=7.8, 2.1 Hz), 8.25 (1H, d, J=6.3 Hz), 7.63-7.35 (5H, m), 6.91
(1H, d, J=8.7 Hz), 4.65 (2H, d, J=5.7 Hz), 3.97-3.88 (5H, m),
1.43-1.32 (1H, m), 0.70-0.63 (2H, m), 0.41-0.36 (2H, m)
Example 56
N-[2-(3-cyclopropylmethoxy-4-methoxyphenyl)oxazol-4-ylmethyl]-2,6-dimethox-
ybenzamide
Yield 46 mg
White Powder
[0444] .sup.1H-NMR (CDCl.sub.3) .delta.: 7.67 (1H, s), 7.59 (1H,
dd, J=8.4, 1.8 Hz), 7.50 (1H, d, J=2.1 Hz), 7.30-7.24 (1H, m), 6.92
(1H, d, J=8.4 Hz), 6.56 (2H, d, J=8.4 Hz), 6.24 (1H, br s), 4.62
(2H, dd, J=5.7, 0.9 Hz), 3.95-3.92 (5H, m), 3.81 (6H, s), 1.41-1.32
(1H, m), 0.70-0.63 (2H, m), 0.41-0.35 (2H, m)
[0445] Using 0.13 g of [2-(3-cyclopropylmethoxy-4-methoxy
phenyl)oxazol-4-yl]methylamine, compounds of Examples 57 to 59 were
obtained in the same manner as in Example 1.
Example 57
N-[2-(3-cyclopropylmethoxy-4-methoxyphenyl)oxazol-4-ylmethyl]-3-methoxypic-
olinamide
Yield 24 mg
White Powder
[0446] .sup.1H-NMR (CDCl.sub.3) .delta.: 8.23-8.19 (2H, m) 7.65
(1H, s), 7.59 (1H, dd, J=8.4, 2.1 Hz), 7.51 (1H, d, J=1.8 Hz),
7.43-7.34 (2H, m), 6.92 (1H, d, J=8.7 Hz), 4.60 (2H, d, J=5.4 Hz),
3.96-3.93 (8H, m), 1.43-1.30 (1H, m), 0.70-0.63 (2H, m), 0.41-0.35
(2H, m)
Example 58
N-[2-(3-cyclopropylmethoxy-4-methoxyphenyl)oxazol-4-ylmethyl]-3-isobutoxyp-
icolinamide
Yield 0.11 g
White Powder
[0447] .sup.1H-NMR (CDCl.sub.3) .delta.: 8.24 (1H, dd, J=3.9, 1.8
Hz), 8.17 (1H, br s), 7.63 (1H, s), 7.59 (1H, dd, J=8.4, 1.8 Hz),
7.38-7.31 (2H, m), 6.92 (1H, d, J=8.4 Hz), 4.62 (2H, dd, J=5.4, 0.9
Hz), 3.95-3.92 (5H, m), 3.84 (2H, d, J=6.3 Hz), 2.20 (1H, qt, J=6.6
Hz), 1.40-1.34 (1H, m), 1.03 (6H, d, J=6.6 Hz), 0.70-0.63 (2H, m),
0.41-0.35 (2H, m)
Example 59
N-[2-(3-cyclopropylmethoxy-4-methoxyphenyl)oxazol-4-ylmethyl]-2-methylnico-
tinamide
Yield 71 mg
White Powder
[0448] .sup.1H-NMR (CDCl.sub.3) .delta.: 8.55 (1H, dd, J=7.8, 1.8
Hz), 7.71 (1H, dd, J=7.5, 1.8 Hz), 7.65 (1H, s), 7.59 (1H, dd,
J=8.4, 2.1 Hz), 7.17-7.13 (1H, m), 6.93 (2H, d, J=8.4 Hz), 6.35
(1H, br s), 4.58 (2H, dd, J=5.4, 0.9 Hz), 3.96-3.91 (5H, m), 2.69
(3H, s), 1.41-1.31 (1H, m), 0.70-0.63 (2H, m), 0.41-0.35 (2H,
m)
Example 60
[0449] 0.4 g of N-[2-(3-cyclopropylmethoxy-4-methoxyphenyl)
oxazol-4-ylmethyl]-2-methylsulfanylbenzamide obtained in Example 44
was dissolved in 20 ml of dichloromethane, and 0.67 g of
metachloroperbenzoic acid was added thereto while the solution was
cooled with ice with stirring. The mixture was then stirred for an
hour. The reaction mixture was concentrated under reduced pressure,
the residue was purified by silica gel column chromatography (NH
silica, n-hexane:ethyl acetate=1:1), and 50 mg of white powdery
N-[2-(3-cyclopropylmethoxy-4-methoxyphenyl)
oxazol-4-ylmethyl]-2-methanesulfonylbenzamide was obtained.
[0450] .sup.1H-NMR (CDCl.sub.3) .delta.: 8.11 (1H, dd, J=7.8, 0.9
Hz), 7.76 (1H, s), 7.69-7.55 (4H, m), 7.50 (1H, d, J=2.1 Hz), 6.93
(1H, d, J=8.4 Hz), 6.50 (1H, br s), 4.62 (2H, d, J=5.4 Hz),
3.95-3.90 (5H, m), 3.93-3.67 (1H, m), 3.37 (3H, s), 1.40-1.32 (1H,
m), 1.27-1.18 (3H, m), 0.70-0.63 (2H, m), 0.41-0.35 (2H, m)
Example 61
[0451] 0.1 g of N-[2-(3-cyclopropylmethoxy-4-methoxyphenyl)
oxazol-4-ylmethyl]-3-hydroxypicolinamide obtained in Example 45 and
0.16 g of cesium carbonate were dissolved in 4 ml of acetonitorile,
and 0.2 g of 1-bromopropane was added thereto and stirred overnight
at room temperature. Water was added to the reaction mixture and
extraction was performed with ethyl acetate. The extract was washed
with water once, and further washed with saturated aqueous citric
acid once. The organic layer was concentrated under reduced
pressure, and the obtained residue was purified by silica gel
column chromatography, yielding 72 mg of white powdery
N-2-(3-cyclopropylmethoxy-4-methoxyphenyl)oxazol-4-ylmethyl]-3-pr-
opoxypicolinamide.
[0452] .sup.1H-NMR (CDCl.sub.3) .delta.: 8.25-8.20 (2H, m) 7.64
(1H, s), 7.60 (1H, dd, J=8.4, 1.8 Hz), 7.52 (1H, d, J=1.8 Hz),
7.39-7.32 (2H, m), 6.92 (1H, d, J=8.4 Hz), 4.62 (2H, dd, J=5.7, 0.9
Hz), 4.05 (2H, t, J=6.6 Hz), 3.94-3.92 (5H, m), 1.90 (2H, t, J=7.5,
6.6 Hz), 1.40-1.33 (1H, m), 1.04 (3H, t, J=7.5 Hz), 0.70-0.63 (2H,
m), 0.41-0.35 (2H, m)
Example 62
[0453] Using 0.18 g of
[2-(3-isobutoxy-4-methoxyphenyl)oxazol-4-yl]methylamine obtained in
Reference Example 19, 0.16 g of white powdery
N-[2-(3-isobutoxy-4-methoxyphenyl)oxazol-4-ylmethyl]-3-methylpicolinamide
was obtained in the same manner as in Example 1.
[0454] .sup.1H-NMR (CDCl.sub.3) .delta.: 8.58 (1H, br s) 8.39 (1H,
dd, J=4.5, 1.8 Hz), 7.63 (1H, s), 7.62-7.59 (2H, m), 7.57 (1H, d,
J=0.9 Hz), 7.32-7.27 (1H, m), 6.92 (1H, d, J=8.4 Hz), 4.59 (2H, dd,
J=6.0, 0.9 Hz), 3.91 (3H, s), 3.86 (2H, d, J=6.9 Hz), 2.76 (3H, s),
2.20 (1H, qt, J=6.9, 6.6 Hz), 1.06 (6H, d, J=6.6 Hz)
[0455] Using 0.15 g of
[2-(3-isobutoxy-4-methoxyphenyl)oxazol-4-yl]methylamine obtained in
Reference Example 19, compounds of Examples 63 to 75 were obtained
in the same manner as in Example 1.
Example 63
N-[2-(3-isobutoxy-4-methoxyphenyl)oxazol-4-ylmethyl]-2-methoxybenzamide
Yield 0.12 g
White Powder
[0456] .sup.1H-NMR (CDCl.sub.3) .delta.: 8.41 (1H, br s) 8.23 (1H,
dd, J=7.8, 1.8 Hz), 7.64 (1H, s), 7.59 (1H, dd, J=8.4, 2.1 Hz),
7.53 (1H, d, J=2.1 Hz), 7.48-7.42 (1H, m), 7.11-6.90 (3H, m), 4.63
(2H, dd, J=5.4, 0.9 Hz), 3.97 (3H, s), 3.91 (3H, s), 3.86 (2H, d,
J=6.9 Hz), 2.21 (1H, qt, J=6.6 Hz), 1.06 (6H, d, J=6.6 Hz)
Example 64
N-[2-(3-isobutoxy-4-methoxyphenyl)oxazol-4-ylmethyl]-2-methyl
sulfanylbenzamide
Yield 0.15 g
White Powder
[0457] .sup.1H-NMR (CDCl.sub.3) .delta.: 7.69 (1H, s), 7.61-7.56
(2H, m), 7.51 (1H, d, J=1.8 Hz), 7.45-7.15 (3H, m) 6.94-6.90 (2H,
m), 4.61 (2H, d, J=5.7 Hz), 3.91 (3H, s), 3.85 (2H, d, J=6.9 Hz),
2.46 (3H, s), 2.20 (1H, qt, J=6.9 Hz), 1.06 (6H, d, J=6.9 Hz)
Example 65
N-[2-(3-isobutoxy-4-methoxyphenyl)oxazol-4-ylmethyl]-3-ethoxy
picolinamide
Yield 80 mg
White Powder
[0458] .sup.1H-NMR (CDCl.sub.3) .delta.: 8.25-8.22 (2H, m) 7.65
(1H, s), 7.58 (1H, dd, J=8.4, 1.8 Hz), 7.52 (1H, d, J=1.8 Hz),
7.40-7.32 (2H, m), 6.92 (1H, d, J=8.4 Hz), 4.62 (2H, dd, J=5.4, 0.9
Hz), 4.18 (2H, q, J=6.9 Hz), 3.91 (3H, s), 3.86 (2H, d, J=6.9 Hz),
2.20 (1H, qt, J=6.9 Hz), 1.52 (3H, t, J=6.9 Hz), 1.06 (6H, d, J=6.6
Hz)
Example 66
N-[2-(3-isobutoxy-4-methoxyphenyl)oxazol-4-ylmethyl]-2-methoxy-4-fluoroben-
zamide
Yield 0.11 g
White Powder
[0459] .sup.1H-NMR (CDCl.sub.3) .delta.: 8.27-8.21 (2H, m), 7.63
(1H, s), 7.59 (1H, dd, J=8.4, 2.1 Hz), 7.52 (1H, d, J=2.1 Hz), 6.93
(1H, d, J=8.4 Hz), 6.81-6.74 (1H, m), 6.69 (1H, dd, J=10.5, 2.4
Hz), 4.61 (2H, dd, J=5.4, 0.9 Hz), 3.96 (3H, s), 3.91 (3H, s), 3.85
(2H, d, J=6.6 Hz), 2.20 (1H, qt, J=6.9, 6.6 Hz), 1.06 (6H, d, J=6.6
Hz)
Example 67
N-[2-(3-isobutoxy-4-methoxyphenyl)oxazol-4-ylmethyl]-2-isopropoxy
benzamide
Yield 0.15 g
Colorless Oily Substance
[0460] .sup.1H-NMR (CDCl.sub.3) .delta.: 8.64 (1H, br s) 8.24 (1H,
dd, J=7.8, 1.8 Hz), 7.62-7.57 (2H, m), 7.54 (1H, d, J=1.8 Hz),
7.44-7.37 (1H, m), 7.08-7.02 (1H, m), 6.98-6.91 (2H, m), 4.72 (1H,
q, J=6.0 Hz), 4.62 (2H, dd, J=5.1, 0.9 Hz), 3.92 (3H, s), 3.85 (2H,
d, J=6.6 Hz), 2.20 (1H, qt, J=6.6 Hz), 1.40 (6H, d, J=6.0 Hz), 1.06
(6H, d, J=6.6 Hz)
Example 68
N-[2-(3-isobutoxy-4-methoxyphenyl)oxazol-4-ylmethyl]-2-fluoro-6-methoxyben-
zamide
Yield 0.13 g
White Powder
[0461] .sup.1H-NMR (CDCl.sub.3) .delta.: 7.65 (1H, d, J=0.9 Hz),
7.58 (1H, dd, J=8.4, 2.1 Hz), 7.51 (1H, d, J=2.1 Hz), 7.34-7.24
(1H, m), 6.92 (1H, d, J=8.4 Hz), 6.77-6.70 (2H, m), 6.52 (1H, br
s), 4.62 (2H, dd, J=5.7, 0.9 Hz), 3.91 (3H, s), 3.90-3.82 (5H, m),
2.20 (1H, qt, J=6.9 Hz), 1.06 (6H, d, J=6.9 Hz)
Example 69
N-[2-(3-isobutoxy-4-methoxyphenyl)oxazol-4-ylmethyl]-3-methoxy
picolinamide
Yield 0.14 g
White Powder
[0462] .sup.1H-NMR (CDCl.sub.3) .delta.: 8.19-8.22 (2H, m), 7.65
(1H, s), 7.58 (1H, dd, J=8.4, 1.8 Hz), 7.52 (1H, d, J=2.1 Hz),
7.43-7.34 (1H, m), 6.92 (1H, d, J=8.4 Hz), 4.61 (2H, dd, J=5.7, 0.9
Hz), 3.96 (3H, s), 3.91 (3H, s), 3.86 (2H, d, J=6.6 Hz), 2.20 (1H,
qt, J=6.9, 6.6 Hz), 1.06 (6H, d, J=6.9 Hz)
Example 70
N-[2-(3-isobutoxy-4-methoxyphenyl)oxazol-4-ylmethyl]-3-isobutoxy
picolinamide
Yield 68 mg
White Powder
[0463] .sup.1H-NMR (CDCl.sub.3) .delta.: 8.24 (1H, dd, J=3.9, 2.1
Hz), 8.17 (1H, br s), 7.64 (1H, s), 7.58 (1H, dd, J=8.4, 2.1 Hz),
7.52 (1H, d, J=1.8 Hz), 7.38-7.28 (2H, m), 6.92 (2H, d, J=8.4 Hz),
4.63 (2H, dd, J=5.4, 0.9 Hz), 3.91 (3H, s), 3.87-3.82 (4H, m),
2.27-2.13 (2H, m), 1.07-1.02 (2H, m)
Example 71
N-[2-(3-isobutoxy-4-methoxyphenyl)oxazol-4-ylmethyl]-2-propoxy
benzamide
Yield 75 mg
White Powder
[0464] .sup.1H-NMR (CDCl.sub.3) .delta.: 8.52 (1H, br s), 8.23 (1H,
dd, J=7.8, 1.8 Hz), 7.62-7.58 (2H, m), 7.53 (1H, s), 7.42 (1H, td,
J=7.2, 1.8 Hz), 7.06 (1H, t, J=7.8 Hz), 6.95-6.91 (2H, m), 4.62
(2H, d, J=5.1 Hz), 4.06 (2H, t, J=6.6 Hz), 3.94 (3H, s), 3.85 (2H,
d, J=6.6 Hz), 2.24-2.16 (1H, m), 1.93-1.81 (2H, m), 1.06 (6H, d,
J=6.6 Hz), 0.97 (3H, t, J=7.2 Hz)
Example 72
N-[2-(3-isobutoxy-4-methoxyphenyl)oxazol-4-ylmethyl]-2-butoxy
benzamide
Yield 47 mg
White Powder
[0465] .sup.1H-NMR (CDCl.sub.3) .delta.: 8.48 (1H, br s), 8.23 (1H,
dd, J=7.8, 1.8 Hz), 7.62-7.58 (2H, m), 7.53 (1H, s), 7.42 (1H, td,
J=7.2, 1.8 Hz), 7.06 (1H, t, J=7.8 Hz), 6.95-6.91 (2H, m), 4.61
(2H, d, J=5.1 Hz), 4.10 (2H, t, J=6.6 Hz), 3.91 (3H, s), 3.85 (2H,
d, J=6.6 Hz), 2.24-2.16 (1H, m), 1.85-1.75 (2H, m), 1.43-1.36 (2H,
m), 1.05 (6H, d, J=6.6 Hz), 0.84 (3H, t, J=7.2 Hz)
Example 73
N-[2-(3-isobutoxy-4-methoxyphenyl)oxazol-4-ylmethyl]-2-isobutoxy
benzamide
Yield 90 mg
White Powder
[0466] .sup.1H-NMR (CDCl.sub.3) .delta.: 8.52 (1H, br s), 8.23 (1H,
dd, J=7.8, 1.8 Hz), 7.62-7.58 (2H, m), 7.53 (1H, s), 7.42 (1H, td,
J=7.2, 1.8 Hz), 7.06 (1H, t, J=7.8 Hz), 6.93-6.90 (2H, m), 4.62
(2H, d, J=5.1 Hz), 3.91 (3H, s), 3.87-3.83 (4H, m), 2.24-2.16 (2H,
m), 1.06 (6H, d, J=6.6 Hz), 0.95 (6H, d, J=6.6 Hz)
Example 74
N-[2-(3-isobutoxy-4-methoxyphenyl)oxazol-4-ylmethyl]-3-isopropoxy
picolinamide
Yield 0.11 g
White Powder
[0467] .sup.1H-NMR (CDCl.sub.3) .delta.: 8.52 (1H, br s), 8.27 (1H,
br s), 7.63 (1H, s), 7.58 (1H, dd, J=7.8, 1.8 Hz), 7.53 (1H, s),
7.35-7.34 (2H, m), 6.92 (1H, d, J=8.4 Hz), 4.67-4.61 (3H, m), 3.91
(3H, s), 3.85 (2H, d, J=6.6 Hz), 2.22-2.17 (1H, m), 1.42 (6H, d,
J=6.6 Hz), 1.06 (6H, d, J=6.6 Hz)
Example 75
N-[2-(3-isobutoxy-4-methoxyphenyl)oxazol-4-ylmethyl]-2-methyl
nicotinamide
Yield 0.13 g
White Powder
[0468] .sup.1H-NMR (CDCl.sub.3) .delta.: 8.52 (1H, br s), 7.86 (1H,
d, J=7.5 Hz), 7.76 (1H, d, J=7.5 Hz), 7.69 (1H, s), 7.59 (1H, d,
J=4.2 Hz), 7.56 (1H, s), 6.92 (1H, d, J=8.7 Hz), 4.58 (2H, d, J=5.1
Hz), 3.91 (3H, s), 3.84 (2H, d, J=6.9 Hz), 2.69 (3H, s), 2.23-2.15
(1H, m), 1.05 (6H, d, J=5.1 Hz)
Example 76
[0469] Using 0.2 g of {2-[4-methoxy-3-(2,2,2-trifluoroethoxy)
phenyl]oxazol-4-yl}methylamine obtained in Reference Example 25,
0.24 g of white powdery
N-{2-[4-methoxy-3-(2,2,2-trifluoroethoxy)phenyl]oxazol-4-ylmethyl}-3-meth-
oxypicolinamide was obtained in the same manner as in Example
1.
[0470] .sup.1H-NMR (CDCl.sub.3) .delta.: 8.24-8.19 (2H, m), 7.72
(1H, dd, J=8.4, 1.8 Hz), 7.65 (1H, d, J=0.9 Hz), 7.62 (1H, d, J=1.8
Hz), 7.43-7.35 (2H, m), 6.98 (1H, d, J=8.4 Hz), 4.60 (2H, dd,
J=5.7, 0.9 Hz), 4.46 (2H, q, J=5.4 Hz), 3.95 (3H, s), 3.93 (3H,
s)
[0471] Using 0.2 g of
{2-[4-methoxy-3-(2,2,2-trifluoroethoxy)phenyl]oxazol-4-yl}methylamine
obtained in Reference Example 25, compounds of Example 77 to 79
were obtained in the same manner as in Example 1.
Example 77
N-{2-[4-methoxy-3-(2,2,2-trifluoroethoxy)phenyl]oxazol-4-ylmethyl}-3-ethox-
ypicolinamide
Yield 0.24 g
White Powder
[0472] .sup.1H-NMR (CDCl.sub.3) .delta.: 8.26-8.22 (2H, m), 7.72
(1H, dd, J=8.4, 2.1 Hz), 7.65 (1H, s), 7.63 (1H, d, J=1.8 Hz),
7.40-7.32 (2H, m), 6.98 (1H, d, J=8.1 Hz), 4.62 (2H, dd, J=5.7, 0.9
Hz), 4.46 (2H, q, J=8.4 Hz), 4.18 (2H, q, J=6.9 Hz), 1.52 (3H, t,
J=6.9 Hz)
Example 78
N-{2-[4-methoxy-3-(2,2,2-trifluoroethoxy)phenyl]oxazol-4-ylmethyl}-2-metho-
xybenzamide
Yield 0.18 g
White Powder
[0473] .sup.1H-NMR (CDCl.sub.3) .delta.: 8.42 (1H, br s), 8.23 (1H,
dd, J=7.5, 1.8 Hz), 7.73 (1H, dd, J=8.4, 2.1 Hz), 7.65-7.60 (2H,
m), 7.48-7.42 (1H, m), 7.08 (1H, td, J=8.4, 0.9 Hz), 6.98 (1H, d,
J=8.4 Hz), 4.62 (2H, dd, J=5.4, 0.9 Hz), 4.46 (2H, q, J=8.4 Hz),
3.98 (3H, s), 3.93 (3H, s)
Example 79
N-{2-[4-methoxy-3-(2,2,2-trifluoroethoxy)phenyl]oxazol-4-ylmethyl}-2-methy-
lbenzamide
Yield 0.15 g
White Powder
[0474] .sup.1H-NMR (CDCl.sub.3) .delta.: 7.72 (1H, dd, J=8.4, 2.1
Hz), 7.66 (1H, s), 7.61 (1H, d, J=2.1 Hz), 7.41-7.14 (4H, m), 6.98
(1H, d, J=8.4 Hz), 6.31 (1H, br s), 4.58 (2H, dd, J=5.4, 0.9 Hz),
4.45 (2H, q, J=8.4 Hz), 3.93 (3H, s), 2.46 (3H, s)
[0475] Using 0.15 g of
{2-[4-methoxy-3-(2,2,2-trifluoroethoxy)phenyl]oxazol-4-yl}methylamine
obtained Reference Example 25, compounds of Examples 80 to 82 were
obtained in the same manner as in Example 1.
Example 80
N-{2-[4-methoxy-3-(2,2,2-trifluoroethoxy)phenyl]oxazol-4-ylmethyl}-2-propo-
xybenzamide
Yield 0.15 g
White Powder
[0476] .sup.1H-NMR (CDCl.sub.3) .delta.: 8.53 (1H, br s), 8.24 (1H,
dd, J=7.8, 1.8 Hz), 7.73 (1H, dd, J=8.4, 2.1 Hz), 7.65-7.60 (2H,
m), 7.45-7.38 (1H, m), 7.09-6.93 (3H, m), 4.62 (2H, d, J=5.1 Hz),
4.45 (2H, q, J=8.1 Hz), 4.07 (2H, t, J=6.6 Hz), 3.94 (3H, s), 1.88
(2H, qt, J=7.5, 6.6 Hz), 0.98 (3H, t, J=7.5 Hz)
Example 81
N-{2-[4-methoxy-3-(2,2,2-trifluoroethoxy)phenyl]oxazol-4-ylmethyl}-2-isopr-
opoxybenzamide
Yield 0.18 g
White Powder
[0477] .sup.1H-NMR (CDCl.sub.3) .delta.: 8.64 (1H, br s), 8.23 (1H,
dd, J=7.8, 1.8 Hz), 7.74 (1H, dd, J=8.4, 2.1 Hz), 7.65 (1H, d,
J=2.1 Hz), 7.63 (1H, s), 7.44-7.37 (1H, m), 7.08-6.94 (3H, m), 4.73
(1H, tt, J=6.0 Hz), 4.62 (2H, dd, J=5.1, 0.9 Hz), 4.46 (2H, q,
J=8.4 Hz), 3.94 (3H, s), 1.41 (6H, d, J=6.0 Hz)
Example 82
N-{2-[4-methoxy-3-(2,2,2-trifluoroethoxy)phenyl]oxazol-4-ylmethyl}-4-chlor-
o-2-methoxybenzamide
Yield 0.21 g
White Powder
[0478] .sup.1H-NMR (CDCl.sub.3) .delta.: 8.29 (1H, br s), 8.17 (1H,
d, J=8.4 Hz), 7.73 (1H, dd, J=8.4, 1.8 Hz), 7.64 (1H, d, J=1.5 Hz),
7.07 (1H, dd, J=8.4, 1.8 Hz), 7.00-6.96 (2H, m), 4.60 (2H, dd,
J=5.4, 0.9 Hz), 4.46 (2H, q, J=8.4 Hz), 3.98 (3H, s), 3.93 (3H,
s)
Example 83
[0479] Using 0.1 g of
{2-[3-cyclopropylmethoxy-4-(2,2,2-trifluoroethoxy)phenyl]oxazol-4-yl}meth-
ylamine obtained in Reference Example 34, 0.11 g of white powdery
N-{2-[3-cyclopropylmethoxy-4-(2,2,2-trifluoroethoxy)phenyl]oxazol-4-ylmet-
hyl}-2-ethoxybenzamide was obtained in the same manner as in
Example 1.
[0480] .sup.1H-NMR (CDCl.sub.3) .delta.: 8.54 (1H, br s), 8.23 (1H,
dd, J=7.8, 1.8 Hz) 7.64 (1H, s), 7.60-7.55 (2H, m), 7.45-7.38 (1H,
m), 7.10-7.04 (2H, m), 6.94 (1H, d, J=8.1 Hz), 4.62 (2H, dd, J=5.4,
0.9 Hz), 4.48 (2H, q, J=8.4 Hz), 4.18 (2H, q, J=6.9 Hz), 3.95 (2H,
d, J=7.2 Hz), 1.48 (3H, t, J=7.2 Hz), 1.35-1.29 (1H, m), 0.70-0.63
(2H, m), 0.41-0.35 (2H, m)
Example 84
[0481] Using 0.18 g of
{2-[3-cyclopropylmethoxy-4-(2,2,2-trifluoroethoxy)phenyl]oxazol-4-yl}meth-
ylamine obtained in Reference Example 34, 0.2 g of white powdery
N-{2-[3-cyclopropylmethoxy-4-(2,2,2-trifluoroethoxy)phenyl]oxazol-4-ylmet-
hyl}-3-methylpicolinamide was obtained in the same manner as in
Example 1.
[0482] .sup.1H-NMR (CDCl.sub.3) .delta.: 8.57 (1H, br s), 8.39 (1H,
dd, J=4.5, 1.2 Hz) 7.64 (1H, s), 7.60-7.55 (3H, m), 7.32-7.26 (1H,
m), 7.06-7.03 (1H, m), 4.59 (2H, dd, J=5.7, 0.9 Hz), 4.48 (2H, q,
J=8.4 Hz), 3.95 (2H, d, J=6.9 Hz), 2.76 (3H, s), 1.38-1.28 (1H, m),
0.69-0.62 (2H, m), 0.40-0.35 (2H, m)
Example 85
[0483] Using 0.3 g of
[2-(3,4-diethoxyphenyl)oxazol-4-yl]methylamine obtained in
Reference Example 37, 0.11 g of white powdery
N-[2-(3,4-diethoxyphenyl)oxazol-4-ylmethyl]-2-propoxy benzamide was
obtained in the same manner as in Example 1.
[0484] .sup.1H-NMR (CDCl.sub.3) .delta.: 8.51 (1H, br s), 8.24 (1H,
dd, J=7.8, 1.8 Hz), 7.60-7.50 (3H, m), 7.41 (1H, m), 7.06 (1H, m),
7.00-6.90 (2H, m), 4.61 (2H, d, J=5.1 Hz), 4.06 (2H, t, J=6.6 Hz),
1.87 (2H, tq, J=7.2, 6.6 Hz), 1.49 (6H, t, J=6.9 Hz), 0.96 (3H, t,
J=7.2 Hz)
[0485] Using 0.3 g of
[2-(3,4-diethoxyphenyl)oxazol-4-yl]methylamine obtained in
Reference Example 37, compounds of Examples 86 to 91 were obtained
in the same manner as in Example 1.
Example 86
N-[2-(3,4-diethoxyphenyl)oxazol-4-ylmethyl]-2-trifluoromethyl
benzamide
Yield 0.11 g
White Powder
[0486] .sup.1H-NMR (CDCl.sub.3) .delta.: 7.75-7.50 (7H, m), 6.91
(1H, d, J=8.4 Hz), 6.32 (1H, br s), 4.59 (2H, d, J=5.4 Hz), 4.17
(2H, q, J=6.9 Hz), 4.14 (2H, q, J=6.9 Hz), 1.48 (6H, t, J=6.9
Hz)
Example 87
N-[2-(3,4-diethoxyphenyl)oxazol-4-ylmethyl]picolinamide
Yield 0.34 g
White Powder
[0487] .sup.1H-NMR (CDCl.sub.3) .delta.: 8.55 (1H, m), 8.47 (1H, br
s), 8.21 (1H, d, J=7.8 Hz), 7.85 (1H, m), 7.57 (1H, dd, J=8.4, 1.8
Hz), 7.55 (1H, d, J=1.8 Hz), 7.42 (1H, m), 6.91 (1H, d, J=8.4 Hz),
6.32 (1H, br s), 4.63 (2H, d, J=6.0 Hz), 4.18 (2H, q, J=6.9 Hz),
4.15 (2H, q, J=6.9 Hz), 1.48 (3H, t, J=6.9 Hz), 1.48 (3H, t, J=6.9
Hz)
Example 88
N-[2-(3,4-diethoxyphenyl)oxazol-4-ylmethyl]-2-ethoxybenzamide
Yield 0.23 g
White Powder
[0488] .sup.1H-NMR (CDCl.sub.3) .delta.: 8.55 (1H, m), 8.47 (1H, br
s), 8.21 (1H, d, J=7.8 Hz), 7.85 (1H, m), 7.57 (1H, dd, J=8.4, 1.8
Hz), 7.55 (1H, d, J=1.8 Hz), 7.42 (1H, m), 6.91 (1H, d, J=8.4 Hz),
6.32 (1H, br s), 4.63 (2H, d, J=6.0 Hz), 4.18 (2H, q, J=6.9 Hz),
4.15 (2H, q, J=6.9 Hz), 1.48 (3H, t, J=6.9 Hz), 1.48 (3H, t, J=6.9
Hz)
Example 89
N-[2-(3,4-diethoxyphenyl)oxazol-4-ylmethyl]-4-ethoxybenzamide
Yield 0.32 g
White Powder
[0489] .sup.1H-NMR (CDCl.sub.3) .delta.: 7.80-7.70 (2H, m), 7.63
(1H, s), 7.60-7.50 (2H, m), 6.95-6.85 (3H, m), 6.66 (1H, br s),
4.57 (2H, q, J=6.0 Hz), 4.17 (2H, q, J=6.9 Hz), 4.15 (2H, q, J=6.9
Hz), 4.06 (2H, q, J=6.9 Hz), 1.48 (3H, t, J=6.9 Hz), 1.48 (3H, t,
J=6.9 Hz), 1.42 (3H, t, J=6.9 Hz).
Example 90
N-[2-(3,4-diethoxyphenyl)oxazol-4-ylmethyl]-5-methoxy-2-trifluoro
methoxybenzamide
Yield 0.34 g
White Powder
[0490] .sup.1H-NMR (CDCl.sub.3) .delta.: 7.95 (1H, br s), 7.73 (1H,
d, J=3.0 Hz), 7.70-7.50 (3H, m), 6.99 (1H, dd, J=9.0, 3.0 Hz),
6.90-6.80 (2H, m), 4.61 (2H, d, J=6.0 Hz), 4.18 (2H, q, J=6.9 Hz),
4.15 (2H, q, J=6.9 Hz), 3.82 (3H, s), 1.48 (3H, t, J=6.9 Hz), 1.46
(3H, t, J=6.9 Hz)
Example 91
N-[2-(3,4-diethoxyphenyl)oxazol-4-ylmethyl]-3-ethoxybenzamide
Yield 0.12 g
White Powder
[0491] .sup.1H-NMR (CDCl.sub.3) .delta.: 7.57 (1H, dd, J=8.1, 2.1
Hz), 7.53 (1H, d, J=2.1 Hz), 7.35-7.25 (3H, m), 7.01 (1H, m), 6.92
(1H, d, J=8.1 Hz), 6.68 (1H, br s), 4.58 (2H, d, J=5.4 Hz), 4.18
(2H, q, J=6.9 Hz), 4.15 (2H, q, J=6.9 Hz), 4.07 (2H, q, J=6.9 Hz),
1.49 (3H, t, J=6.9 Hz), 1.48 (3H, t, J=6.9 Hz), 1.42 (3H, t, J=6.9
Hz)
Example 92
[0492] Using 0.3 g of
[2-(3,4-dimethoxyphenyl)oxazol-4-yl]methylamine obtained in
Reference Example 40, 0.27 g of white powdery
N-[2-(3,4-dimethoxyphenyl)oxazol-4-ylmethyl]-2-ethoxy benzamide was
obtained in the same manner as in Example 1.
[0493] .sup.1H-NMR (CDCl.sub.3) .delta.: 8.56 (1H, br s), 8.24 (1H,
dd, J=8.1, 1.8 Hz), 7.65-7.60 (2H, m), 7.55 (1H, d, J=1.5 Hz), 7.42
(1H, m), 7.07 (1H, m), 6.95-6.90 (2H, m), 4.63 (2H, d, J=5.1 Hz),
4.18 (2H, q, J=6.9 Hz), 3.98 (3H, s), 3.97 (3H, s), 1.26 (3H, t,
J=6.9 Hz)
Example 93
[0494] Using 0.25 g of
[2-(3,4-dimethoxyphenyl)oxazol-4-yl]methylamine obtained in
Reference Example 40, 0.23 g of white powdery
N-[2-(3,4-dimethoxyphenyl)oxazol-4-ylmethyl]-2-ethyl benzamide was
obtained in the same manner as in Example 1.
[0495] .sup.1H-NMR (CDCl.sub.3) .delta.: 7.66 (1H, s), 7.60 (1H,
dd, J=8.4, 1.8 Hz), 7.52 (1H, d, J=1.8 Hz), 7.40-7.20 (4H, m), 6.93
(1H, d, J=8.4 Hz), 6.34 (1H, br s), 4.58 (2H, d, J=5.4 Hz), 3.96
(3H, s), 3.94 (3H, s), 2.82 (2H, q, J=7.5 Hz), 1.20 (3H, t, J=7.5
Hz)
Example 94
[0496] Using 0.2 g of
[2-(3,4-dimethoxyphenyl)oxazol-4-yl]methylamine obtained in
Reference Example 40, 0.16 g of white powdery
N-[2-(3,4-dimethoxyphenyl)oxazol-4-ylmethyl]-3-methyl picolinamide
was obtained in the same manner as in Example 1.
[0497] .sup.1H-NMR (CDCl.sub.3) .delta.: 8.58 (1H, br s), 8.39 (1H,
m), 7.65-7.55 (4H, m), 7.30 (1H, m), 6.92 (1H, d, J=8.4 Hz), 4.59
(2H, d, J=6.0 Hz), 3.97 (3H, s), 3.93 (3H, s), 2.76 (3H, s), 1.58
(3H, s)
Example 95
[0498] Using 0.2 g of
[2-(3,4-dimethoxyphenyl)oxazol-4-yl]methylamine obtained in
Reference Example 40, 0.12 g of white powdery
N-[2-(3,4-dimethoxyphenyl)oxazol-4-ylmethyl]-3-methoxy picolinamide
was obtained in the same manner as in Example 1.
[0499] .sup.1H-NMR (CDCl.sub.3) .delta.: 8.21 (1H, br s), 8.20 (1H,
dd, J=3.9, 1.8 Hz), 7.65 (1H, s), 7.61 (1H, dd, J=8.4, 1.8 Hz),
7.54 (1H, d, J=1.8 Hz), 7.45-7.30 (2H, m), 6.92 (1H, d, J=8.4 Hz),
4.61 (2H, d, J=6.0 Hz), 3.97 (3H, s), 3.96 (3H, s), 3.93 (3H,
s)
Example 96
[0500] 0.13 g of
[2-(3-benzyloxy-4-difluoromethoxyphenyl)oxazol-4-yl]methylamine
obtained in Reference Example 46 was suspended in 10 ml of acetone.
Then 0.14 g of 1-hydroxybenzotriazole and 0.19 g of
1-ethyl-3-(3-dimethylaminopropyl)carbodiimide hydrochloride and
0.14 g of 3-methyl picolinate were added to the obtained suspension
and the mixture was refluxed for 30 minutes. The reaction mixture
was concentrated under reduced pressure, and water was added to the
residue. Ethyl acetate extraction was performed. The organic layer
was washed twice with water, and concentrated. The residue was
purified by silica gel column chromatography(n-hexane:ethyl
acetate=1:1), yielding 0.16 g of white powdery
N-[2-(3-benzyloxy-4-difluoromethoxyphenyl)oxazol-4-ylmethyl]-3-me-
thylpicolinamide.
[0501] .sup.1H-NMR (CDCl.sub.3) .delta.: 8.56 (1H, br s), 8.40 (1H,
d, J=3.9 Hz), 7.74-7.58 (4H, m), 7.47-7.23 (7H, m), 6.62 (1H, t,
J=74.7 Hz), 5.21 (2H, s), 4.60 (2H, d, J=5.7 Hz), 2.76 (3H, s)
Example 97
[0502] 0.16 g of N-[2-(3-benzyloxy-4-difluoromethoxyphenyl)
oxazol-4-ylmethyl]-3-methylpicolinamide obtained in Example 96 was
dissolved in 5 ml of ethanol, 20 mg of 10% palladium carbon powder
was added thereto, and the mixture was stirred at room temperature
for 30 minutes under a hydrogen atmosphere. The catalyst was
filtered off, and the filtrate was concentrated to obtain 0.12 g of
white powdery
N-[2-(4-difluoromethoxy-3-hydroxyphenyl)oxazol-4-ylmethyl]-3-methylpicoli-
namide.
[0503] .sup.1H-NMR (CDCl.sub.3) .delta.: 8.60-8.54 (1H, m), 8.39
(1H, d, J=3.3 Hz), 7.69-7.55 (4H, m), 7.37-7.28 (1H, m), 7.18 (1H,
d, J=8.4 Hz), 6.59 (1H, t, J=73.2 Hz), 5.79 (1H, br s), 4.59 (2H,
dd, J=6.0, 0.9 Hz), 2.76 (3H, s)
Example 98
[0504] 0.12 g of
N-[2-(4-difluoromethoxy-3-hydroxyphenyl)oxazol-4-ylmethyl]-3-methylpicoli-
namide obtained in Example 97 and 0.15 ml of
1,8-diazabicyclo[5,4,0]undec-7-ene were dissolved in 4 ml of
ethanol. 0.15 ml of (bromomethyl)cyclopropane was added thereto and
refluxed with heating for 3 hours. The solvent was distilled off,
and water was added to the residue. Ethyl acetate extraction was
performed. The organic layer was washed twice with water, and
concentrated. The residue was purified by silica gel column
choromatography (n-hexane:ethyl acetate=1:1). The obtained crude
crystals were recrystalized using an ethanol-n-hexane mixture, and
60 mg of white powdery
N-[2-(3-cyclopropylmethoxy-4-difluoromethoxyphenyl)oxazol-4-ylmethyl]-3-m-
ethylpicolinamide was obtained.
[0505] .sup.1H-NMR (CDCl.sub.3) .delta.: 8.59-8.54 (1H, m), 8.39
(1H, dd, J=4.5, 1.2 Hz), 7.67 (1H, s), 7.63-7.56 (3H, m), 7.37-7.28
(1H, m), 7.22 (1H, d, J=8.1 Hz), 6.69 (1H, t, J=75.0 Hz), 4.59 (2H,
dd, J=5.7, 0.9 Hz), 3.98 (2H, d, J=6.9 Hz), 2.76 (3H, s), 1.35-1.20
(1H, m), 0.70-0.63 (2H, m), 0.41-0.35 (2H, m)
Example 99
[0506] Using 0.2 g of [2-(3-cyclopropylmethoxy-4-methoxyphenyl)
oxazol-4-yl]methylamine obtained in Reference Example 13, 0.11 g of
white powdery N-[2-(3-cyclopropylmethoxy-4-methoxyphenyl)
oxazol-4-ylmethyl]isoquinoline-1-carboxamide was obtained in the
same manner as in Example 1.
[0507] .sup.1H-NMR (CDCl.sub.3) .delta.: 9.60 (1H, m), 8.67 (1H, br
s), 8.47 (1H, d, J=2.4 Hz), 7.90-7.80 (2H, m), 7.75-7.65 (3H, m),
7.61 (1H, dd, J=8.4, 1.8 Hz), 7.53 (1H, d, J=1.8 Hz), 6.92 (1H, d,
J=8.4 Hz), 4.68 (2H, d, J=6.0 Hz), 3.94 (2H, d, J=7.5 Hz), 3.92
(3H, s), 1.39 (1H, m), 0.70-0.60 (2H, m), 0.40-0.35 (2H, m)
Example 100
[0508] 4.42 g of sodium hydroxide was suspended in 160 ml of
dimethoxyethane. The suspension was stirred with ice cooling while
16 g of 3-[2-(3-benzyloxy-4-methoxyphenyl)oxazol-4-yl]methyl
propionate obtained in Reference Example 48 and 39.23 g of
2-ethoxyperbenzoic acid were separately added, and then heating and
refluxing were conducted for 7 hours. After cooling with ice,
saturated ammonium chloride solution was added to the mixture and
stirred for 30 minutes. Water was then added thereto, and ethyl
acetate extraction was performed, followed by drying over anhydrous
magnesium sulfate, and the solvent was then distilled off. The
residue was subjected to silica gel column purification
(n-hexane:ethyl acetate=3:1), and 13.4 g of yellow oily substance,
methyl 2-[2-(3-benzyloxy-4-methoxyphenyl)
oxazol-4-ylmethyl]-3-(2-ethoxyphenyl)-3-oxopropionate was
obtained.
[0509] .sup.1H-NMR (CDCl.sub.3) .delta.: 7.71 (1H, d, J=7.8 Hz),
7.57-7.54 (3H, m), 7.48-7.28 (6H, m), 6.99-6.90 (3H, m), 5.16 (2H,
s), 4.98 (1H, t, J=6.9 Hz), 4.14 (2H, q, J=6.9 Hz), 3.91 (3H, s),
3.70 (3H, s), 3.27-3.19 (2H, m), 1.45 (3H, t, J=6.9 Hz)
Example 101
[0510] A 13.4 g quantity of methyl
2-[2-(3-benzyloxy-4-methoxyphenyl)oxazol-4-ylmethyl]-3-(2-ethoxyphenyl)-3-
-oxopropionate obtained in Example 100 was suspended in 67 ml of
ethanol, 67 ml of 47% hydrobromic acid was added thereto, and the
suspension was heated and refluxed overnight. After standing to
cool, the crystals generated were collected by filtration, washed
with water and diisopropyl ether, and dried, thereby yielding 8.1 g
of white powdery
1-(2-ethoxyphenyl)-3-[2-(3-hydroxy-4-methoxyphenyl)oxazol-4-yl]propan-1-o-
ne.
[0511] .sup.1H-NMR (CDCl.sub.3) .delta.: 8.30 (1H, d, J=8.7 Hz),
7.84 (1H, d, J=1.8 Hz), 7.83-7.71 (2H, m), 7.45 (1H, t, J=8.4 Hz),
7.06 (1H, d, J=8.7 Hz), 6.99-6.93 (2H, m), 4.17 (2H, q, J=6.9 Hz),
4.00 (3H, s), 3.67 (2H, t, J=6.6 Hz), 3.35 (2H, t, J=6.6 Hz), 1.55
(3H, t, J=6.9 Hz)
Example 102
[0512] A 8.1 g quantity of
1-(2-ethoxyphenyl)-3-[2-(3-hydroxy-4-methoxyphenyl)oxazol-4-yl]propan-1-o-
ne obtained in Example 101 was suspended in 220 ml of ethanol, 10 g
of 1,8-diazabicyclo[5,4,0]undec-7-ene and 5.96 g of (bromomethyl)
cyclopropane were added thereto, and stirring was conducted for 5
hours while heating and refluxing. After distilling off ethanol
under reduced pressure, water was added, ethyl acetate extraction
was performed, followed by drying over anhydrous magnesium sulfate
and distilling the solvent off. The residue was subjected to silica
gel column purification (n-hexane:ethyl acetate=4:1), and the
obtained crude crystals were recrystalized using ethanol, thereby
yielding 4.4 g of white powdery
3-[2-(3-cycropropylmethoxy-4-methoxyphenyl)oxazol-4-yl]-1-(2-ethoxy
phenyl)propan-1-one.
[0513] .sup.1H-NMR (CDCl.sub.3) .delta.: 7.70 (1H, dd, J=7.5, 1.8
Hz), 7.56 (1H, dd, J=8.4, 2.1 Hz), 7.50 (1H, s), 7.45-7.39 (2H, m),
7.00-6.89 (3H, m), 4.13 (2H, q, J=7.2 Hz), 3.93-3.91 (5H, m), 3.41
(2H, t, J=6.6 Hz), 2.99 (2H, t, J=6.6 Hz), 1.51 (3H, t, J=7.2 Hz),
1.47 (1H, m), 0.67-0.64 (2H, m), 0.40-0.36 (2H, m)
Example 103
[0514] A 0.3 g quantity of
1-(2-ethoxyphenyl)-3-[2-(3-hydroxy-4-methoxyphenyl)oxazol-4-yl]propan-1-o-
ne obtained in Example 101 was suspended in 10 ml of ethanol, 0.37
g of 1,8-diazabicyclo[5,4,0]undec-7-ene and 0.26 g of ethyl iodide
were added thereto, and the suspension was stirred for 4 hours
while heating and refluxing. After distilling off ethanol under
reduced pressure, water was added, ethyl acetate extraction was
performed, followed by drying over anhydrous magnesium sulfate and
distilling the solvent off. The residue was subjected to silica gel
column purification (n-hexane:ethyl acetate=3:1), thereby yielding
0.15 g of white powdery 3-[2-(3-ethoxy-4-methoxyphenyl)
oxazol-4-yl]-1-(2-ethoxyphenyl)propan-1-one.
[0515] .sup.1H-NMR (CDCl.sub.3) .delta.: 7.70 (1H, dd, J=7.5, 1.8
Hz), 7.56 (1H, dd, J=8.4, 1.8 Hz), 7.52-7.40 (2H, m), 6.99-6.89
(3H, m), 4.21-4.09 (4H, m), 3.91 (3H, s), 3.42 (2H, t, J=6.9 Hz),
2.99 (2H, t, J=6.9 Hz), 1.51-1.45 (6H, m)
Example 104
[0516] A 0.3 g quantity of
1-(2-ethoxyphenyl)-3-[2-(3-hydroxy-4-methoxyphenyl)oxazol-4-yl]propan-1-o-
ne obtained in Example 101 was suspended in 10 ml of ethanol, 0.37
g of 1,8-diazabicyclo[5,4,0]undec-7-ene and 0.14 ml of allyl
bromide were added thereto, and stirring was conducted for 3 hours
while heating and refluxing. After distilling off ethanol under
reduced pressure, water was added, ethyl acetate extraction was
performed, followed by drying over anhydrous magnesium sulfate and
distilling the solvent off. The residue was subjected to silica gel
column purification (n-hexane:ethyl acetate=3:1), thereby yielding
0.2 g of white powdery
3-[2-(3-allyloxy-4-methoxyphenyl)oxazol-4-yl]-1-(2-ethoxyphenyl)propan-1--
one.
[0517] .sup.1H-NMR (CDCl.sub.3) .delta.: 7.70 (1H, dd, J=7.8, 1.8
Hz), 7.58 (1H, dd, J=8.4, 1.8 Hz), 7.52 (1H, d, J=1.8 Hz),
7.45-7.40 (2H, m), 7.00-6.90 (3H, m), 6.18-6.05 (1H, m), 5.47-5.29
(2H, m), 4.67 (2H, d, J=5.1 Hz), 4.13 (2H, q, J=6.9 Hz), 3.92 (3H,
s), 3.42 (2H, t, J=7.2 Hz), 2.99 (2H, t, J=7.2 Hz), 1.47 (3H, t,
J=6.9 Hz).
[0518] Using 1-(2-ethoxyphenyl)-3-[2-(3-hydroxy-4-methoxy
phenyl)oxazol-4-yl]propan-1-one obtained in Example 101, compounds
of Examples 105 to 110 were obtained in the same manner as in
Examples 102.
Example 105
[0519]
3-[2-(3-cyclopentyloxy-4-methoxyphenyl)oxazol-4-yl]-1-(2-ethoxyphen-
yl)propan-1-one
[0520] .sup.1H-NMR (CDCl.sub.3) .delta.: 7.70 (1H, dd, J=7.5, 1.8
Hz), 7.57-7.51 (2H, m), 7.45-7.39 (2H, m), 6.99-6.88 (3H, m), 4.88
(1H, br s), 4.12 (2H, q, J=6.9 Hz), 3.88 (3H, s), 3.42 (2H, t,
J=6.9 Hz), 2.99 (2H, t, J=6.9 Hz), 2.04-1.87 (6H, m), 1.65-1.60
(2H, m), 1.47 (3H, t, J=6.9 Hz)
Example 106
3-[2-(3-isobutoxy-4-methoxyphenyl)oxazol-4-yl]-1-(2-ethoxyphenyl)
propan-1-one
[0521] .sup.1H-NMR (CDCl.sub.3) .delta.: 7.70 (1H, dd, J=7.5, 1.8
Hz), 7.55 (1H, dd, J=8.4, 1.8 Hz), 7.50 (1H, d, J=2.1 Hz),
7.45-7.40 (2H, m), 4.13 (2H, q, J=6.9 Hz), 3.90 (3H, s), 3.84 (2H,
d, J=6.9 Hz), 3.42 (2H, t, J=7.2 Hz), 3.00 (2H, t, J=7.2 Hz),
2.23-2.14 (1H, m), 1.48 (3H, t, J=6.9 Hz), 1.05 (6H, d, J=6.9
Hz)
Example 107
1-(2-ethoxyphenyl)-3-[2-(4-methoxy-3-propoxyphenyl)oxazol-4-yl]propan-1-on-
e
[0522] .sup.1H-NMR (CDCl.sub.3) .delta.: 7.70 (1H, dd, J=7.5, 1.8
Hz), 7.56 (1H, dd, J=8.1, 1.8 Hz), 7.52 (1H, s), 7.45-7.40 (2H, m),
7.00-6.89 (3H, m), 4.13 (2H, q, J=6.9 Hz), 4.05 (2H, t, J=6.9 Hz),
3.90 (3H, s), 3.42 (2H, t, J=7.5 Hz), 3.00 (2H, t, J=7.5 Hz),
1.95-1.84 (2H, m), 1.47 (3H, t, J=6.9 Hz), 1.05 (3H, t, J=6.9
Hz)
Example 108
3-[2-(3-(3-butenyloxy)-4-methoxyphenyl)oxazol-4-yl]-1-(2-ethoxy
phenyl)propan-1-one
[0523] .sup.1H-NMR (CDCl.sub.3) .delta.: 7.70 (1H, dd, J=7.5, 1.8
Hz), 7.57 (1H, dd, J=8.4, 1.8 Hz), 7.52 (1H, s), 7.45-7.40 (2H, m),
6.97-6.89 (3H, m), 6.00-5.90 (1H, m), 5.22-5.10 (2H, m), 4.17-4.11
(4H, m), 3.90 (3H, s), 3.42 (2H, t, J=7.5 Hz), 3.00 (2H, t, J=7.5
Hz), 2.67-2.62 (2H, m), 1.47 (3H, t, J=6.9 Hz)
Example 109
3-[2-(3-butoxy-4-methoxyphenyl)oxazol-4-yl]-1-(2-ethoxyphenyl)
propan-1-one
[0524] .sup.1H-NMR (CDCl.sub.3) .delta.: 7.70 (1H, dd, J=7.5, 1.8
Hz), 7.57 (1H, dd, J=8.4, 1.8 Hz), 7.53 (1H, d, J=2.1 Hz),
7.45-7.39 (2H, m), 7.00-6.89 (3H, m), 4.16-4.07 (4H, m), 3.98 (3H,
s), 3.42 (2H, t, J=7.2 Hz), 3.00 (2H, t, J=7.2 Hz), 1.90-1.86 (2H,
m), 1.57-1.42 (5H, m), 0.99 (3H, t, J=7.2 Hz)
Example 110
1-(2-ethoxyphenyl)-3-[2-(4-methoxy-3-(2-propenyloxy)phenyl)
oxazol-4-yl]propan-1-one
[0525] .sup.1H-NMR (CDCl.sub.3) .delta.: 7.70 (1H, dd, J=7.8, 1.8
Hz), 7.66-7.63 (2H, m), 7.46-7.39 (2H, m), 7.00-6.92 (3H, m), 4.83
(2H, d, J=2.1 Hz), 4.13 (2H, q, J=6.9 Hz), 3.92 (3H, s), 3.42 (2H,
t, J=7.2 Hz), 2.99 (2H, t, J=7.2 Hz), 2.52 (1H, t, J=2.1 Hz), 1.47
(3H, t, J=6.9 Hz)
Example 111
[0526] A 5.0 g quantity of
1-(2-ethoxyphenyl)-3-[2-(3-hydroxy-4-methoxyphenyl)oxazol-4-yl]propan-1-o-
ne obtained in Example 101 was dissolved in 50 ml of
dimethylformamide, 3.35 g of 2-bromopropane and 5.63 g of potassium
carbonate were added thereto, and stirring was conducted overnight
at room temperature. Water was added to the obtained mixture, ethyl
acetate extraction was performed, followed by drying over anhydrous
magnesium sulfate and distilling the solvent off. The residue was
subjected to silica gel column purification (n-hexane:ethyl
acetate=4:1), and the obtained crude crystals were recrystalized
using ethanol, thereby yielding 2.99 g of white powdery
1-(2-ethoxyphenyl)-3-[2-(3-isopropoxy-4-methoxyphenyl)
oxazol-4-yl]propan-1-one.
[0527] .sup.1H-NMR (CDCl.sub.3) .delta.: 7.70 (1H, dd, J=7.5, 1.8
Hz), 7.59-7.54 (2H, m), 7.45-7.39 (2H, m), 7.00-6.89 (3H, m),
4.68-4.60 (1H, m), 4.13 (2H, q, J=6.9 Hz), 3.89 (3H, s), 3.42 (2H,
t, J=7.5 Hz), 2.99 (2H, t, J=7.5 Hz), 1.47 (3H, t, J=6.9 Hz), 1.39
(6H, d, J=6.3 Hz)
[0528] Using 1-(2-ethoxyphenyl)-3-[2-(3-hydroxy-4-methoxy
phenyl)oxazol-4-yl]propane-1-one obtained in Example 101, compounds
of Examples 112 to 122 were obtained in the same manner as in
Example 111.
Example 112
1-(2-ethoxyphenyl)-3-{2-[4-methoxy-3-(2,2,2-trifluoroethoxy)phenyl]oxazol--
4-yl}propan-1-one
[0529] .sup.1H-NMR (CDCl.sub.3) .delta.: 7.72-7.68 (2H, m), 7.60
(1H, d, J=1.8 Hz), 7.45-7.39 (2H, m), 7.00-6.92 (3H, m), 4.44 (2H,
q, J=8.4 Hz), 4.13 (2H, q, J=6.6 Hz), 3.90 (3H, s), 3.42 (2H, t,
J=6.9 Hz), 2.99 (2H, t, J=6.9 Hz), 1.48 (3H, t, J=6.6 Hz)
Example 113
3-[2-(3-cyclohexylmethoxy-4-methoxyphenyl)oxazol-4-yl]-1-(2-ethoxyphenyl)p-
ropan-1-one
[0530] .sup.1H-NMR (CDCl.sub.3) .delta.: 7.70 (1H, dd, J=7.5, 1.8
Hz), 7.55 (1H, dd, J=8.4, 1.8 Hz), 7.50 (1H, d, J=1.8 Hz),
7.45-7.40 (2H, m), 7.00-6.88 (3H, m), 4.14 (2H, q, J=6.9 Hz), 3.90
(3H, s), 3.86 (2H, d, J=6.0 Hz), 3.42 (2H, t, J=7.2 Hz), 2.99 (2H,
t, J=7.2 Hz), 2.00-1.86 (3H, m), 1.79-1.63 (3H, m), 1.45 (3H, t,
J=6.9 Hz), 1.40-1.22 (2H, m), 1.10-1.02 (2H, m)
Example 114
3-[2-(3-cyclopentylmethoxy-4-methoxyphenyl)oxazol-4-yl]-1-(2-ethoxyphenyl)-
propan-1-one
[0531] .sup.1H-NMR (CDCl.sub.3) .delta.: 7.70 (1H, dd, J=7.5, 1.8
Hz), 7.55 (1H, dd, J=8.4, 1.8 Hz), 7.50 (1H, d, J=1.8 Hz),
7.45-7.40 (2H, m), 7.00-6.88 (3H, m), 4.14 (2H, q, J=6.9 Hz), 3.95
(2H, d, J=7.2 Hz), 3.90 (3H, s), 3.42 (2H, t, J=7.2 Hz), 3.00 (2H,
t, J=7.2 Hz), 2.48-2.44 (1H, m), 2.04-1.86 (2H, m), 1.63-1.50 (4H,
m), 1.45 (3H, s), 1.39-1.35 (2H, m)
Example 115
1-(2-ethoxyphenyl)-3-[2-(4-methoxy-3-(4-pentenyloxy)phenyl)
oxazol-4-yl]propan-1-one
[0532] .sup.1H-NMR (CDCl.sub.3) .delta.: 7.70 (1H, dd, J=7.5, 2.1
Hz), 7.56 (1H, dd, J=8.1, 2.1 Hz), 7.51 (1H, d, J=2.1 Hz),
7.45-7.39 (2H, m), 7.00-6.89 (3H, m), 5.87-5.81 (1H, m), 5.10-4.99
(2H, m), 4.17-4.08 (4H, m), 3.91 (3H, s), 3.42 (2H, t, J=7.2 Hz),
2.99 (2H, t, J=7.2 Hz), 2.27-2.22 (2H, m), 2.04-1.95 (2H, m), 1.47
(3H, t, J=7.2 Hz)
Example 116
3-[2-(3-cyclobutylmethoxy-4-methoxyphenyl)oxazol-4-yl]-1-(2-ethoxyphenyl)p-
ropan-1-one
[0533] .sup.1H-NMR (CDCl.sub.3) .delta.: 7.70 (1H, dd, J=7.5, 2.1
Hz), 7.56 (1H, dd, J=8.1, 2.1 Hz), 7.51 (1H, d, J=2.1 Hz),
7.45-7.39 (2H, m), 7.00-6.80 (3H, m), 4.13 (2H, q, J=7.2 Hz), 4.07
(2H, d, J=7.2 Hz), 3.90 (3H, s), 3.42 (2H, t, J=7.2 Hz), 3.00 (2H,
t, J=7.2 Hz), 2.96-2.85 (1H, m), 2.20-2.14 (2H, m), 1.91-1.80 (2H,
m), 1.45 (3H, t, J=7.2 Hz)
Example 117
1-(2-ethoxyphenyl)-3-{2-[4-methoxy-3-(3-methyl-2-butenyloxy)phenyl]oxazol--
4-yl}propan-1-one
[0534] .sup.1H-NMR (CDCl.sub.3) .delta.: 7.70 (1H, dd, J=7.5, 1.8
Hz), 7.57 (1H, dd, J=8.1, 1.8 Hz), 7.51 (1H, d, J=1.8 Hz),
7.00-6.89 (3H, m), 5.55 (1H, t, J=6.6 Hz), 4.64 (2H, d, J=6.6 Hz),
4.13 (2H, q, J=6.9 Hz), 3.91 (3H, s), 3.42 (2H, t, J=7.2 Hz), 3.00
(2H, t, J=7.2 Hz), 1.77 (6H, d, J=6.6 Hz), 1.45 (3H, t, J=6.9
Hz)
Example 118
3-{2-[3-(2-cyclohexenyloxy)-4-methoxyphenyl]oxazol-4-yl}-1-(2-ethoxyphenyl-
)propan-1-one
[0535] .sup.1H-NMR (CDCl.sub.3) .delta.: 7.70 (1H, dd, J=7.5, 1.8
Hz), 7.60-7.57 (2H, m), 7.42-7.39 (2H, m), 7.00-6.89 (3H, m),
6.00-5.92 (2H, m), 4.88 (1H, br s), 4.15 (2H, q, J=7.2 Hz), 3.89
(3H, s), 3.42 (2H, t, J=7.2 Hz), 2.99 (2H, t, J=7.2 Hz), 2.04-1.80
(4H, m), 1.72-1.53 (2H, m), 1.45 (3H, t, J=7.2 Hz)
Example 119
1-(2-ethoxyphenyl)-3-[2-(4-methoxy-3-phenethyloxyphenyl)oxazol-4-yl]propan-
-1-one
[0536] .sup.1H-NMR (CDCl.sub.3) .delta.: 7.69 (1H, dd, J=7.8, 1.8
Hz), 7.59 (1H, dd, J=8.4, 1.8 Hz), 7.56 (1H, d, J=1.8 Hz),
7.51-6.98 (7H, m), 6.95-6.90 (3H, m), 4.27 (2H, t, J=7.2 Hz), 4.11
(2H, q, J=6.9 Hz), 3.91 (3H, s), 3.41 (2H, t, J=7.2 Hz), 3.20 (2H,
t, J=7.2 Hz), 2.98 (2H, t, J=7.2 Hz), 1.54 (3H, t, J=6.9 Hz)
Example 120
1-(2-ethoxyphenyl)-3-{2-[4-methoxy-3-(3-phenylpropoxy)phenyl]oxazol-4-yl}p-
ropan-1-one
[0537] .sup.1H-NMR (CDCl.sub.3) .delta.: 7.70 (1H, dd, J=7.5, 1.8
Hz), 7.58 (1H, dd, J=8.4, 1.8 Hz), 7.56 (1H, d, J=1.8 Hz),
7.49-7.39 (2H, m), 7.30-7.15 (5H, m), 6.99-6.90 (3H, m), 4.16-4.08
(4H, m), 3.92 (3H, s), 3.42 (2H, t, J=7.2 Hz), 2.98 (2H, t, J=7.2
Hz), 2.84 (2H, t, J=8.1 Hz), 2.24-2.15 (2H, m), 1.46 (3H, t, J=6.9
Hz)
Example 121
3-{2-[3-(2-cyclopropylethoxy)-4-methoxyphenyl]oxazol-4-yl}-1-(2-ethoxyphen-
yl)propan-1-one
[0538] .sup.1H-NMR (CDCl.sub.3) .delta.: 7.70 (1H, dd, J=7.8, 1.8
Hz), 7.57-7.55 (2H, m), 7.43-7.39 (2H, m), 7.00-6.89 (3H, m),
4.19-4.10 (4H, m), 3.91 (3H, s), 3.42 (2H, t, J=6.9 Hz), 3.01 (2H,
t, J=6.9 Hz), 1.81-1.74 (2H, m), 1.48 (3H, t, J=6.9 Hz), 0.88-0.83
(1H, m), 0.52-0.47 (2H, m), 0.16-0.12 (2H, m)
Example 122
3-{2-[3-(2-cyclopentylethoxy)-4-methoxyphenyl]oxazol-4-yl}-1-(2-ethoxyphen-
yl)propan-1-one
[0539] .sup.1H-NMR (CDCl.sub.3) .delta.: 7.70 (1H, dd, J=7.8, 1.8
Hz), 7.56 (1H, dd, J=8.4, 1.8 Hz), 7.51 (1H, d, J=2.1 Hz),
7.45-7.39 (2H, m), 7.00-6.89 (3H, m), 4.17-4.07 (4H, m), 3.90 (3H,
s), 3.42 (2H, t, J=6.9 Hz), 3.00 (2H, t, J=6.9 Hz), 2.00-1.81 (5H,
m), 1.66-1.62 (4H, m), 1.45 (3H, t, J=6.9 Hz), 1.28-1.15 (2H,
m)
Example 123
[0540] A 1.0 g quantity of methyl
3-{2-[3-cyclopropylmethoxy-4-(2,2,2-trifluoroethoxy)phenyl]oxazol-4-yl}pr-
opionate obtained in Reference Example 49 and 0.54 g of methyl
3-methoxypicolinate were added to 5 ml of dimethylformamide, and
the mixture was stirred with ice cooling for 10 minutes. A 0.83 g
of sodium t-pentoxide was added to the obtained mixture, which was
then stirred with ice cooling for an hour, followed by further
stirring at room temperature for 1 hour. The reaction mixture was
stirred with ice cooling, saturated ammonium chloride solution was
added thereto, and further stirred for 30 minutes. Water was added
to the mixture, ethyl acetate extraction was performed, followed by
drying over anhydrous magnesium sulfate and distilling the solvent
off. A 5.0 ml quantity of dimethylsulfoxide, 84 mg of lithium
chloride and 41 .mu.l of purified water were added to the residue,
and the mixture was stirred with heating at 110.degree. C.
overnight. After standing to cool, water was added to the obtained
mixture, ethyl acetate extraction was performed, followed by drying
over anhydrous magnesium sulfate and distilling the solvent off.
The obtained residue was subjected to silica gel column
purification (n-hexane:ethyl acetate=4:1), and the obtained crude
crystals were recrystalized from a mixture of ethyl acetate and
diisopropyl ether, thereby yielding 0.11 g white powdery
3-{2-[3-cyclopropyl
methoxy-4-(2,2,2-trifluoroethoxy)phenyl]oxazol-4-yl}-1-(3-methoxy
pyridin-2-yl)propan-1-one.
[0541] .sup.1H-NMR (CDCl.sub.3) .delta.: 8.24 (1H, d, J=4.2 Hz),
7.55-7.47 (2H, m), 7.43 (1H, s), 7.40-7.35 (2H, m), 7.03 (1H, d,
J=8.4 Hz), 4.46 (2H, q, J=7.2 Hz), 3.94 (2H, d, J=6.6 Hz), 3.90
(3H, s), 3.51 (2H, d, J=7.2 Hz), 3.01 (2H, d, J=7.2 Hz), 1.31-1.26
(1H, m), 0.68-0.62 (2H, m), 0.39-0.34 (2H, m)
Example 124
[0542] A 2 g quantity of methyl 3-[2-(3-benzyloxy-4-methoxy
phenyl)oxazol-4-yl]propionate obtained in Reference Example 48 and
1.1 g of methyl 3-methoxypicolinate were dissolved in 10 ml of
dimethylformamide, and while stirring the solution with ice cooling
1.81 g of sodium t-pentoxide was added thereto and stirred for 30
minutes. The mixture was further stirred for 5 hours at room
temperature, ice was added to the reaction mixture, followed by
addition of saturated aqueous ammonium chloride solution, and the
mixture was further stirred. After stirring the reaction mixture
for 30 minutes, water was added thereto and ethyl acetate
extraction was performed. The organic layer was washed twice with
water, and concentrated under reduced pressure. The obtained
residue was purified by silica gel column chromatography
(n-hexane:ethyl acetate=1:1), thereby yielding 1.55 g of white
amorphous methyl 2-[2-(3-benzyloxy-4-methoxy
phenyl)oxazol-4-ylmethyl]-3-(3-methoxypyridin-2-yl)-3-oxopropionate.
[0543] .sup.1H-NMR (CDCl.sub.3) .delta.: 8.24 (1H, dd, J=4.5, 1.8
Hz), 7.57-7.28 (10H, m), 6.91 (1H, d, J=9.0 Hz), 5.18-5.13 (3H, m),
3.91-3.90 (6H, m), 3.64 (3H, s), 3.36-3.18 (2H, m)
Example 125
[0544] A 1.5 g quantity of methyl
2-[2-(3-benzyloxy-4-methoxyphenyl)oxazol-4-ylmethyl]-3-(3-methoxypyridin--
2-yl)-3-oxopropionate obtained in Example 124 was dissolved in 22.5
ml of ethanol, 7.5 ml of 47% hydrobromic acid was added threreto,
and the mixture was stirred with heating at 80.degree. C. for 7.5
hours. While stirring with ice cooling, the reaction mixture was
neutralized with a 5N sodium hydroxide solution, and ethyl acetate
extraction was performed. The organic layer was washed twice with
water, and concentrated under reduced pressure, and the obtained
residue was purified by silica gel column chromatography
(dichloromethane:methanol=20:1), thereby yielding 0.65 g of pale
yellow oily substance,
3-[2-(3-hydroxy-4-methoxyphenyl)oxazol-4-yl]-3-(3-methoxypyridin-2-yl)pro-
pan-1-one.
[0545] .sup.1H-NMR (CDCl.sub.3) .delta.: 8.24 (1H, dd, J=7.2, 1.5
Hz), 7.55-7.27 (5H, m), 6.88 (1H, d, J=8.7 Hz), 5.72 (1H, s),
3.92-3.89 (6H, m), 3.51 (2H, t, J=7.5 Hz), 3.03 (2H, t, J=7.5
Hz)
Example 126
[0546] Using 0.24 g of
3-[2-(3-hydroxy-4-methoxyphenyl)oxazol-4-yl]-3-(3-methoxypyridine-2-yl)pr-
opan-1-one obtained in Example 125, 0.11 g of white powdery
3-[2-(3-cyclopropylmethoxy-4-methoxyphenyl)oxazol-4-yl]-3-(3-methoxypyrid-
in-2-yl)propan-1-one was obtained in the same manner as in Example
102.
[0547] .sup.1H-NMR (CDCl.sub.3) .delta.: 8.24 (1H, dd, J=4.2, 1.2
Hz), 7.59-7.32 (5H, m), 6.91 (1H, d, J=8.4 Hz), 3.94-3.90 (8H, m),
3.51 (2H, t, J=7.2 Hz), 3.01 (2H, t, J=7.2 Hz), 1.40-1.30 (1H, m),
0.69-0.62 (2H, m), 0.41-0.35 (2H, m)
[0548] Using
3-[2-(3-hydroxy-4-methoxyphenyl)oxazol-4-yl]-3-(3-methoxypyridin-2-yl)pro-
pan-1-one obtained in Example 125, compounds of Examples 127 and
128 were obtained in the same manner as in Example 102.
Example 127
3-[2-(3-isobutoxy-4-methoxyphenyl)oxazol-4-yl]-3-(3-methoxy
pyridin-2-yl)propan-1-one
[0549] .sup.1H-NMR (CDCl.sub.3) .delta.: 8.24 (1H, dd, J=4.2, 1.5
Hz), 7.58-7.30 (5H, m), 6.91 (1H, d, J=8.4 Hz), 3.92-3.90 (6H, m),
3.84 (2H, d, J=6.9 Hz), 3.52 (2H, t, J=7.2 Hz), 3.01 (2H, t, J=7.2
Hz), 2.20 (1H, q, J=6.9 Hz), 1.06 (6H, d, J=6.9 Hz)
Example 128
3-[2-(3-cyclopentyloxy-4-methoxyphenyl)oxazol-4-yl]-1-(3-methoxy
pyridin-2-yl)propan-1-one
[0550] .sup.1H-NMR (CDCl.sub.3) .delta.: 8.24 (1H, dd, J=4.5, 1.5
Hz), 7.60-7.30 (5H, m), 6.90 (1H, d, J=8.7 Hz), 4.90-4.85 (1H, m),
3.90-3.88 (6H, m), 3.51 (2H, d, J=6.9 Hz), 3.01 (2H, t, J=6.9 Hz),
2.00-1.81 (6H, m), 1.64-1.60 (2H, m)
Example 129
[0551] Using 0.15 g of 3-[2-(3-hydroxy-4-methoxyphenyl)
oxazol-4-yl]-3-(3-methoxypyridin-2-yl)propan-1-one obtained in
Example 125, 44 mg of white powdery
1-(3-methoxypyridin-2-yl)-3-{2-[4-methoxy-3-(2,2,2-trifluoroethoxy)phenyl-
]oxazol-4-yl}propan-1-one was obtained in the same manner as in
Example 111.
[0552] .sup.1H-NMR (CDCl.sub.3) .delta.: 8.24 (1H, dd, J=4.2, 1.2
Hz), 7.70 (1H, dd, J=8.4, 1.8 Hz), 7.60 (1H, d, J=1.8 Hz), 7.51
(1H, d, J=1.8 Hz), 7.47-7.32 (2H, m), 6.96 (1H, d, J=8.4 Hz), 4.45
(2H, q, J=8.4 Hz), 3.95-3.88 (6H, m), 3.52 (2H, t, J=7.2 Hz), 3.01
(2H, t, J=7.2 Hz)
Example 130
[0553] A 2 g quantity of methyl 3-[2-(3-benzyloxy-4-methoxy
phenyl)oxazol-4-yl]propionate obtained in Reference Example 48 and
1 g of methyl 3-ethoxypicolinate were dissolved in 10 ml of
dimethylformamide, and while stirring the solution with ice cooling
1.81 g of sodium t-pentoxide was added thereto and stirred for 30
minutes. The mixture was further stirred for 4 hours at room
temperature, and ice was added to the reaction mixture, followed by
addition of saturated aqueous ammonium chloride solution for
further stirring. After stirring the reaction mixture for 30
minutes, water was added thereto and ethyl acetate extraction was
performed. The organic layer was washed twice with water, and
concentrated under reduced pressure. The obtained residue was
purified by silica gel column chromatography (n-hexane:ethyl
acetate=1:1), thereby yielding 1.5 g of colorless oily substance
methyl
2-[2-(3-benzyloxy-4-methoxyphenyl)oxazol-4-ylmethyl]-3-(3-ethoxypyridin-2-
-yl)-3-oxopropionate.
[0554] .sup.1H-NMR (CDCl.sub.3) .delta.: 8.22 (1H, dd, J=4.2, 1.2
Hz), 7.57-7.27 (10H, m), 6.91 (1H, d, J=9.0 Hz), 5.18-5.12 (3H, m),
4.12 (2H, q, J=6.9 Hz), 3.92 (3H, s), 3.65 (3H, s), 3.30-3.23 (2H,
m), 1.46 (3H, t, J=6.9 Hz)
Example 131
[0555] Using 1.5 g of methyl 2-[2-(3-benzyloxy-4-methoxyphenyl)
oxazol-4-ylmethyl]-3-(3-ethoxypyridin-2-yl)-3-oxopropionate
obtained in Example 130, 0.7 g of pale yellow oily substance,
1-(3-ethoxypyridin-2-yl)-3-[2-(3-hydroxy-4-methoxyphenyl)oxazol-4-yl]prop-
an-1-one, was obtained in the same manner as in Example 125.
[0556] .sup.1H-NMR (CDCl.sub.3) .delta.: 8.23 (1H, dd, J=4.2, 1.2
Hz), 7.55-7.49 (2H, m), 7.45 (1H, s), 7.42-7.28 (2H, m), 6.88 (1H,
d, J=8.7 Hz), 5.70 (1H, s), 4.11 (2H, q, J=6.9 Hz), 3.49 (2H, t,
J=7.2 Hz), 3.01 (2H, t, J=6.9 Hz), 1.46 (3H, t, J=6.9 Hz)
Example 132
[0557] Using 0.2 g of
1-(3-ethoxypyridin-2-yl)-3-[2-(3-hydroxy-4-methoxyphenyl)oxazol-4-yl]prop-
an-1-one obtained in Example 131, 0.2 g of pale yellow oily
substance,
3-[2-(3-cyclopentyloxy-4-methoxyphenyl)oxazol-4-yl]-1-(3-ethoxypyridin-2--
yl)propan-1-one, was obtained in the same manner as in Example
102.
[0558] .sup.1H-NMR (CDCl.sub.3) .delta.: 8.23 (1H, dd, J=4.5, 1.5
Hz), 7.57-7.45 (2H, m), 7.44 (1H, d, J=0.9 Hz), 7.38-7.28 (2H, m),
6.89 (1H, d, J=8.7 Hz), 4.89-4.87 (1H, m), 4.12 (2H, q, J=6.9 Hz),
3.94-3.91 (5H, m), 3.88 (3H, s), 3.49 (2H, t, J=7.2 Hz), 3.01 (2H,
t, J=7.2 Hz), 2.01-1.81 (6H, m), 1.65-1.58 (2H, m), 1.47 (3H, t,
J=6.9 Hz)
[0559] Using 1-(3-ethoxypyridin-2-yl)-3-[2-(3-hydroxy-4-methoxy
phenyl)oxazol-4-yl]propan-1-one obtained in Example 131, compounds
of Examples 133 and 134 were obtained in the same manner as in
Example 102.
Example 133
3-[2-(3-cyclopropylmethoxy-4-methoxyphenyl)oxazol-4-yl]-1-(3-ethoxypyridin-
-2-yl)propan-1-one
[0560] .sup.1H-NMR (CDCl.sub.3) .delta.: 8.23 (1H, dd, J=4.2, 1.5
Hz), 7.57 (1H, dd, J=8.4, 1.8 Hz), 7.50 (1H, d, J=1.8 Hz), 7.45
(1H, d, J=1.8 Hz), 7.38-7.28 (2H, m), 6.91 (1H, d, J=8.4 Hz), 4.12
(2H, q, J=6.9 Hz), 3.94-3.91 (5H, m), 3.49 (2H, t, J=7.2 Hz), 3.02
(2H, t, J=7.2 Hz), 1.46 (3H, t, J=6.9 Hz), 1.42-1.32 (1H, m),
0.69-0.62 (2H, m), 0.40-0.35 (2H, m)
Example 134
1-(3-ethoxypyridin-2-yl)-3-[2-(3-isobutoxy-4-methoxyphenyl)oxazol-4-yl]pro-
pan-1-one
[0561] .sup.1H-NMR (CDCl.sub.3) .delta.: 8.23 (1H, dd, J=4.5, 1.5
Hz), 7.56 (1H, dd, J=8.4, 2.1 Hz), 7.50 (1H, d, J=2.1 Hz), 7.45
(1H, s), 7.38-7.28 (2H, m), 6.90 (1H, d, J=8.4 Hz), 4.12 (2H, q,
J=6.9 Hz), 3.90 (3H, s), 3.85 (2H, d, J=6.6 Hz), 3.50 (2H, t, J=6.9
Hz), 3.02 (2H, t, J=6.9 Hz), 2.19 (2H, qt, J=6.6 Hz), 1.47 (3H, t,
J=6.9 Hz), 1.05 (6H, d, J=6.6 Hz)
Example 135
[0562] A 5 g quantity of methyl 3-[2-(3-benzyloxy-4-methoxy
phenyl)oxazol-4-yl]propionate obtained in Reference Example 48 and
3.2 g of methyl 3-methylpicolinate were dissolved in 150 ml of
dimethoxyethane. While stirring the solution with ice cooling 1.2 g
of sodium hydride was added thereto and further stirred. The
reaction mixture was heated and refluxed for 4 hours. At the
completion of the reaction, a saturated aqueous ammonium chloride
solution was added to the mixture while stirring with ice cooling,
and the mixture was further stirred. After stirring the reaction
mixture for 30 minutes, water was added thereto and ethyl acetate
extraction was performed. The organic layer was washed twice with
water, and concentrated under reduced pressure. The obtained
residue was purified by silica gel column chromatography
(n-hexane:ethyl acetate=2:1), thereby yielding 5.5 g of colorless
oily substance methyl
2-[2-(3-benzyloxy-4-methoxyphenyl)oxazol-4-ylmethyl]-3-(3-methylpyridin-2-
-yl)-3-oxopropionate.
[0563] .sup.1H-NMR (CDCl.sub.3) .delta.: 8.49 (1H, dd, J=4.8, 1.2
Hz), 7.59-7.28 (10H, m), 6.91 (1H, d, J=9.0 Hz), 5.23-5.16 (3H, m),
3.91 (3H, s), 3.65 (3H, s), 3.37-3.18 (2H, m,) 2.59 (3H, s)
Example 136
[0564] A 5.5 g quantity of methyl 2-[2-(3-benzyloxy-4-methoxy
phenyl)oxazol-4-ylmethyl]-3-(3-methylpyridin-2-yl)-3-oxopropionate
obtained in Example 135 was dissolved in 20 ml of ethanol, 80 ml of
a 5N aqueous hydrochloric acid solution was added thereto, and the
mixture was stirred with heating at 80.degree. C. for 1.5 hours.
While stirring with ice cooling, the reaction mixture was
neutralized with 5 N aqueous sodium hydroxide solution, and ethyl
acetate extraction was performed. The organic layer was washed
twice with water, concentrated under reduced pressure, and the
obtained crude crystals were recrystalized with a mixture of 20 ml
of ethanol and 40 ml of n-hexane, thereby yielding 1.92 g of pale
yellow powdery 3-[2-(3-hydroxy-4-methoxy
phenyl)oxazol-4-yl]-1-(3-methylpyridin-2-yl)propan-1-one.
[0565] .sup.1H-NMR (CDCl.sub.3) .delta.: 8.49 (1H, dd, J=4.5, 1.2
Hz), 7.60-7.51 (3H, m), 7.44 (1H, d, J=0.9 Hz), 7.41-7.29 (1H, m),
6.89 (1H, dd, J=7.8, 1.2 Hz), 5.68 (1H, s), 3.93 (3H, s), 3.58 (2H,
t, J=7.5 Hz), 3.00 (2H, t, J=7.5 Hz), 2.57 (3H, s)
Example 137
[0566] A 0.3 g quantity of 3-[2-(3-hydroxy-4-methoxyphenyl)
oxazol-4-yl]-1-(3-methylpyridin-2-yl)propan-1-one obtained in
Example 136 and 0.4 ml of 1,8-diazabicyclo[5,4,0]undec-7-ene were
dissolved in 5 ml of ethanol, 0.24 g of (bromomethyl)cyclopropane
was added thereto, and the mixture was heated and refluxed for 4.5
hours. After standing to cool, water was added to the reaction
mixture, and ethyl acetate extraction was performed. The extract
was washed twice with water, the organic layer was then
concentrated under reduced pressure, and the obtained residue was
purified by silica gel column chromatography (n-hexane:ethyl
acetate=2:1), thereby yielding 0.2 g of white powdery
3-[2-(3-cyclopropylmethoxy-4-methoxyphenyl)oxazol-4-yl]-1-(3-methyl
pyridin-2-yl)propan-1-one.
[0567] .sup.1H-NMR (CDCl.sub.3) .delta.: 8.50 (1H, dd, J=4.5, 1.2
Hz), 7.60-7.54 (2H, m), 7.49 (1H, d, J=1.8 Hz), 7.45 (1H, s),
7.34-7.29 (1H, m), 6.91 (1H, d, J=8.7 Hz), 3.94-3.91 (5H, m), 3.60
(2H, t, J=7.5 Hz), 3.00 (2H, t, J=7.5 Hz), 2.57 (3H, s), 1.40-1.32
(1H, m), 0.69-0.62 (2H, m), 0.41-0.35 (2H, m)
Example 138
[0568] A 0.23 g quantity of 3-[2-(3-hydroxy-4-methoxy
phenyl)oxazol-4-yl]-1-(3-methylpyridin-2-yl)propan-1-one obtained
in Example 136 and 0.3 ml of 1,8-diazabicyclo[5,4,0]undec-7-ene
were dissolved in 5 ml of ethanol, 0.21 g of ethyl iodide was added
thereto, and the mixture was heated and refluxed for 4 hours. After
standing to cool, water was added to the reaction mixture, and
ethyl acetate extraction was performed. The extract was washed
twice with water, the organic layer was then concentrated under
reduced pressure, and the obtained residue was purified by silica
gel column chromatography (n-hexane:ethyl acetate=2:1), thereby
yielding 0.17 g of white powdery
3-[2-(3-ethoxy-4-methoxyphenyl)oxazol-4-yl]-1-(3-methylpyridin-2-yl)
propan-1-one.
[0569] .sup.1H-NMR (CDCl.sub.3) .delta.: 8.24 (1H, d, J=4.2 Hz),
7.58-7.55 (2H, m), 7.51 (1H, d, J=2.1 Hz), 7.45 (1H, s), 6.90 (1H,
d, J=8.4 Hz), 4.19 (2H, q, J=7.2 Hz), 3.91 (3H, s), 3.59 (2H, t,
J=7.2 Hz), 3.00 (2H, t, J=7.2 Hz), 2.57 (3H, s), 1.49 (3H, t, J=7.2
Hz)
Example 139
[0570] A 0.3 g quantity of 3-[2-(3-hydroxy-4-methoxyphenyl)
oxazol-4-yl]-1-(3-methylpyridin-2-yl)propan-1-one obtained in
Example 136 and 0.4 ml of 1,8-diazabicyclo[5,4,0]undec-7-ene were
dissolved in 5 ml of ethanol, 0.23 g of 2-bromopropane was added
thereto, and the mixture was heated and refluxed for 4.5 hours.
After standing to cool, water was added to the reaction mixture,
and ethyl acetate extraction was performed. The extract was washed
twice with water, the organic layer was then concentrated under
reduced pressure, and the obtained residue was purified by silica
gel column chromatography (n-hexane:ethyl acetate=2:1), thereby
yielding 0.16 g of white powdery
3-[2-(3-isopropoxy-4-methoxyphenyl)oxazol-4-yl]-1-(3-methylpyridin-2-yl)p-
ropan-1-one.
[0571] .sup.1H-NMR (CDCl.sub.3) .delta.: 8.50 (1H, dd, J=4.5, 1.2
Hz), 7.59-7.53 (3H, m), 7.45 (1H, s), 7.34-7.31 (1H, m), 6.91 (1H,
d, J=8.7 Hz), 4.65 (1H, sept., J=6.0 Hz), 3.89 (3H, s), 3.59 (2H,
t, J=7.5 Hz), 3.00 (2H, t, J=7.5 Hz), 2.62 (3H, s), 1.39 (6H, d,
J=6.0 Hz)
Example 140
[0572] A 0.3 g quantity of 3-[2-(3-hydroxy-4-methoxyphenyl)
oxazol-4-yl]-1-(3-methylpyridin-2-yl)propan-1-one obtained in
Example 136 and 0.3 ml of 1,8-diazabicyclo[5,4,0]undec-7-ene were
dissolved in 6 ml of ethanol, 0.22 g of allyl bromide was added
thereto, and the mixture was heated and refluxed for 4 hours. After
standing to cool, water was added to the reaction mixture, and
ethyl acetate extraction was performed. The extract was washed
twice with water, the organic layer was then concentrated under
reduced pressure, and the obtained residue was purified by silica
gel column chromatography (n-hexane:ethyl acetate=2:1), thereby
yielding 0.18 g of white powdery
3-[2-(3-allyloxy-4-methoxyphenyl)oxazol-4-yl]-1-(3-methylpyridin-2-yl)pro-
pan-1-one.
[0573] .sup.1H-NMR (CDCl.sub.3) .delta.: 8.51-8.48 (1H, m),
7.60-7.56 (2H, m), 7.52 (1H, d, J=2.1 Hz), 7.45 (1H, s), 7.34-7.29
(1H, m), 6.92 (1H, d, J=8.7 Hz), 6.16-6.05 (1H, m), 5.48-5.28 (2H,
m), 4.69-4.66 (2H, m), 3.92 (3H, s), 3.60 (2H, t, J=7.2 Hz), 3.00
(2H, t, J=7.2 Hz), 2.57 (3H, s)
Example 141
[0574] A 0.15 g quantity of 3-[2-(3-hydroxy-4-methoxy
phenyl)oxazol-4-yl]-1-(3-methylpyridin-2-yl)propan-1-one obtained
in Example 136 and 0.15 ml of 1,8-diazabicyclo[5,4,0]undec-7-ene
were dissolved in 5 ml of ethanol, 0.13 g of (bromomethyl)
cyclobutane was added thereto, and the mixture was heated and
refluxed overnight. After standing to cool, water was added to the
reaction mixture, and ethyl acetate extraction was performed. The
extract was washed twice with water, the organic layer was then
concentrated under reduced pressure, and the obtained residue was
purified by silica gel column chromatography (n-hexane:ethyl
acetate=2:1), thereby yielding 90 mg of white powdery
3-[2-(3-cyclobutylmethoxy-4-methoxyphenyl)oxazol-4-yl]-1-(3-methylpyridin-
-2-yl)propan-1-one.
[0575] .sup.1H-NMR (CDCl.sub.3) .delta.: 8.50 (1H, dd, J=4.5, 1.2
Hz), 7.60-7.51 (3H, m), 7.45 (1H, d, J=2.1 Hz), 7.34-7.29 (1H, m),
6.89 (1H, d, J=8.7 Hz), 4.07 (2H, d, J=6.9 Hz), 3.89 (3H, s), 3.60
(2H, t, J=7.5 Hz), 3.01 (2H, t, J=7.5 Hz), 2.89-2.83 (1H, m), 2.57
(3H, s), 2.22-2.13 (2H, m), 2.00-1.84 (4H, m)
[0576] Using
3-[2-(3-hydroxy-4-methoxyphenyl)oxazol-4-yl]-1-(3-methylpyridin-2-yl)prop-
an-1-one obtained in Example 136, compounds of Examples 142 to 154
were obtained in the same manner as in Example 137.
Example 142
3-[2-(3-isobutoxy-4-methoxyphenyl)oxazol-4-yl]-1-(3-methyl
pyridin-2-yl)propan-1-one
[0577] .sup.1H-NMR (CDCl.sub.3) .delta.: 8.50 (1H, dd, J=4.5, 1.2
Hz), 7.60-7.53 (2H, m), 7.50 (1H, d, J=1.8 Hz), 7.45 (1H, s),
7.34-7.28 (1H, m), 6.90 (1H, d, J=8.4 Hz), 3.90 (3H, s), 3.84 (2H,
d, J=6.9 Hz), 3.60 (2H, t, J=7.8 Hz), 3.01 (2H, t, J=7.8 Hz), 2.57
(3H, s), 2.20 (1H, qt, J=6.9 Hz), 1.05 (6H, d, J=6.9 Hz)
Example 143
3-[2-(4-methoxy-3-propoxyphenyl)oxazol-4-yl]-1-(3-methylpyridin-2-yl)propa-
n-1-one
[0578] .sup.1H-NMR (CDCl.sub.3) .delta.: 8.50 (1H, dd, J=4.5, 1.2
Hz), 7.59-7.54 (2H, m), 7.51 (1H, d, J=1.8 Hz), 7.50 (1H, s),
7.34-7.29 (1H, m), 6.90 (1H, d, J=8.4 Hz), 4.05 (2H, t, J=6.9 Hz),
3.91 (3H, s), 3.60 (2H, t, J=7.5 Hz), 3.01 (2H, t, J=7.5 Hz), 2.57
(3H, s), 1.90 (2H, qt, J=6.9 Hz), 1.24 (3H, t, J=6.9 Hz)
Example 144
3-[2-(3-cyclopentyloxy-4-methoxyphenyl)oxazol-4-yl]-1-(3-methyl
pyridine-2-yl)propane-1-one
[0579] .sup.1H-NMR (CDCl.sub.3) .delta.: 8.50 (1H, dd, J=4.5, 1.2
Hz), 7.59-7.50 (3H, m), 7.44 (1H, d, J=1.2 Hz), 7.34-7.31 (1H, m),
6.89 (1H, d, J=8.4 Hz), 4.90-4.84 (1H, m), 3.88 (3H, s), 3.59 (2H,
t, J=7.2 Hz), 3.00 (2H, t, J=7.2 Hz), 2.57 (3H, s), 2.03-1.80 (6H,
m), 1.64-1.58 (2H, m)
Example 145
3-[2-(4-methoxy-3-(2-propenyloxy)phenyl)oxazol-4-yl]-1-(3-methylpyridin-2--
yl)propan-1-one
[0580] .sup.1H-NMR (CDCl.sub.3) .delta.: 8.50 (1H, d, J=4.5 Hz),
7.67-7.63 (2H, m), 7.58 (1H, d, J=8.1 Hz), 7.46 (1H, s), 7.34-7.30
(1H, m), 6.93 (1H, dd, J=6.6, 2.4 Hz), 4.82 (2H, d, J=2.4 Hz), 3.92
(3H, s), 3.60 (2H, t, J=7.2 Hz), 3.01 (2H, t, J=7.2 Hz), 2.58 (3H,
s), 2.53 (1H, t, J=2.4 Hz)
Example 146
3-[2-(3-(3-butenyloxy)-4-methoxyphenyl)oxazol-4-yl]-1-(3-methylpyridin-2-y-
l)propan-1-one
[0581] .sup.1H-NMR (CDCl.sub.3) .delta.: 8.50 (1H, dd, J=4.2, 1.5
Hz), 7.59-7.55 (2H, m), 7.52 (1H, d, J=2.1 Hz), 7.45 (1H, d, J=2.1
Hz), 7.34-7.29 (1H, m), 5.97-5.85 (1H, m), 5.23-5.09 (2H, m), 4.14
(2H, t, J=6.9 Hz), 3.91 (3H, s), 3.60 (2H, t, J=7.5 Hz), 3.00 (2H,
t, J=7.5 Hz), 2.68-2.57 (5H, m)
Example 147
3-[2-(3-butoxy-4-methoxyphenyl)oxazol-4-yl]-1-(3-methylpyridin-2-yl)propan-
-1-one
[0582] .sup.1H-NMR (CDCl.sub.3) .delta.: 8.50 (1H, d, J=4.8 Hz),
7.59-7.51 (3H, m), 7.45 (1H, s), 7.34-7.30 (1H, m), 6.90 (1H, d,
J=8.7 Hz), 4.09 (2H, t, J=6.6 Hz), 3.90 (3H, s), 3.60 (2H, t, J=7.2
Hz), 3.01 (2H, t, J=7.2 Hz), 2.57 (3H, s), 1.86 (2H, td, J=7.2, 6.6
Hz), 1.56-1.45 (2H, m), 0.99 (3H, t, J=7.2 Hz)
Example 148
3-[2-(3-cyclohexylmethoxy-4-methoxyphenyl)oxazol-4-yl]-1-(3-methylpyridin--
2-yl)propan-1-one
[0583] .sup.1H-NMR (CDCl.sub.3) .delta.: 8.50 (1H, d, J=4.5 Hz),
7.61-7.53 (2H, m), 7.49 (1H, d, J=1.8 Hz), 7.45 (1H, s), 7.34-7.28
(1H, m), 6.89 (1H, d, J=8.7 Hz), 3.90-3.86 (5H, m), 3.60 (2H, t,
J=7.5 Hz), 3.01 (2H, t, J=7.5 Hz), 2.57 (3H, s), 1.94-1.85 (3H, m),
1.79-1.57 (3H, m), 1.38-0.88 (5H, m)
Example 149
3-[2-(4-methoxy-3-(4-pentenyloxy)phenyl)oxazol-4-yl]-1-(3-methylpyridin-2--
yl)propan-1-one
[0584] .sup.1H-NMR (CDCl.sub.3) .delta.: 8.50 (1H, dd, J=4.5, 1.2
Hz), 7.59-7.54 (2H, m), 7.51 (1H, d, J=2.1 Hz), 7.45 (1H, s),
7.34-7.29 (1H, m), 6.91 (1H, d, J=8.4 Hz), 5.91-5.80 (1H, m),
5.11-4.97 (2H, m), 4.10 (2H, d, J=6.6 Hz), 3.91 (3H, s), 3.60 (2H,
t, J=7.5 Hz), 3.01 (2H, t, J=7.5 Hz), 2.57 (3H, s), 2.30-2.22 (2H,
m), 2.05-1.92 (2H, m)
Example 150
3-[2-(4-methoxy-3-phenethyloxyphenyl)oxazol-4-yl]-1-(3-methyl
pyridin-2-yl)propan-1-one
[0585] .sup.1H-NMR (CDCl.sub.3) .delta.: 8.48 (1H, dd, J=4.5, 0.9
Hz), 7.60-7.49 (3H, m), 7.43 (1H, s), 7.35-7.20 (6H, m), 6.91 (1H,
d, J=8.7 Hz), 4.27 (2H, t, J=7.5 Hz), 3.91 (3H, s), 3.58 (2H, t,
J=7.2 Hz), 3.19 (2H, t, J=7.5 Hz), 3.00 (2H, t, J=7.2 Hz), 2.55
(3H, s)
Example 151
3-{2-[4-methoxy-3-(3-phenylpropoxy)phenyl]oxazol-4-yl}-1-(3-methylpyridin--
2-yl)propan-1-one
[0586] .sup.1H-NMR (CDCl.sub.3) .delta.: 8.50 (1H, dd, J=4.5, 1.2
Hz), 7.58 (1H, d, J=2.1 Hz), 7.55 (1H, d, J=2.1 Hz), 7.49 (1H, d,
J=2.1 Hz), 7.44 (1H, s), 7.34-7.15 (6H, m), 6.91 (1H, d, J=8.4 Hz),
4.11 (2H, t, J=6.6 Hz), 3.92 (3H, s), 3.60 (2H, t, J=7.5 Hz), 3.00
(2H, t, J=7.5 Hz), 2.84 (2H, t, J=7.5 Hz), 2.57 (3H, s), 2.20 (2H,
tt, J=7.5, 6.6 Hz)
Example 152
[0587] Using 0.5 g of cyclopentylmethyl methanesulfonate obtained
in Reference Example 52 and 0.2 g of
3-[2-(3-hydroxy-4-methoxyphenyl)oxazol-4-yl]-1-(3-methylpyridin-2-yl)prop-
an-1-one obtained in Example 136, 90 mg of white powdery
3-[2-(3-cyclopentylmethoxy-4-methoxyphenyl)oxazol-4-yl]-1-(3-methyl
pyridin-2-yl)propan-1-one was obtained in the same manner as in
Example 137.
[0588] .sup.1H-NMR (CDCl.sub.3) .delta.: 8.49 (1H, d, J=3.9 Hz),
7.59-7.50 (3H, m), 7.45 (1H, s), 7.34-7.29 (1H, m), 6.90 (1H, d,
J=8.4 Hz), 3.95 (2H, d, J=7.2 Hz), 3.90 (3H, s), 3.60 (2H, t, J=7.5
Hz), 3.01 (2H, t, J=7.5 Hz), 2.57 (3H, s), 2.54-2.41 (1H, m),
1.91-1.82 (2H, m), 1.68-1.56 (4H, m), 1.42-1.24 (2H, m)
Example 153
[0589] Using 0.16 g of 2-cyclopropylethyl methanesulfonate obtained
in Reference Example 50 and 0.15 g of
3-[2-(3-hydroxy-4-methoxyphenyl)oxazol-4-yl]-1-(3-methylpyridin-2-yl)prop-
an-1-one obtained in Example 136, 0.1 g of white powdery
3-{2-[3-(2-cyclopropylethoxy)-4-methoxyphenyl]oxazol-4-yl}-1-(3-methyl
pyridin-2-yl)propan-1-one was obtained in the same manner as in
Example 137.
[0590] .sup.1H-NMR (CDCl.sub.3) .delta.: 8.50 (1H, dd, J=4.5, 1.5
Hz), 7.60-7.54 (3H, m), 7.46 (1H, s), 7.35-7.27 (1H, m), 6.91 (1H,
d, J=8.1 Hz), 4.18 (2H, t, J=6.9 Hz), 3.91 (3H, s), 3.61 (2H, t,
J=7.5 Hz), 3.02 (2H, t, J=7.5 Hz), 2.58 (3H, s), 1.78 (2H, q, J=6.9
Hz), 0.91-0.80 (1H, m), 0.53-0.46 (2H, m), 0.16-0.11 (2H, m)
Example 154
[0591] Using 0.19 g of 2-cyclopentylethyl methanesulfonate obtained
in Reference Example 51 and 0.15 g of
3-[2-(3-hydroxy-4-methoxyphenyl)oxazol-4-yl]-1-(3-methylpyridin-2-yl)prop-
an-1-one obtained in Example 136, 0.13 g of white powdery
3-{2-[3-(2-cyclopentylethoxy)-4-methoxyphenyl]oxazol-4-yl}-1-(3-methyl
pyridin-2-yl)propan-1-one was obtained in the same manner as in
Example 137.
[0592] .sup.1H-NMR (CDCl.sub.3) .delta.: 8.50 (1H, dd, J=4.5, 1.2
Hz), 7.60-7.50 (3H, m), 7.45 (1H, s), 7.34-7.30 (1H, m), 6.90 (1H,
d, J=8.4 Hz), 4.10 (2H, t, J=6.9 Hz), 3.92 (3H, s), 3.60 (2H, t,
J=7.5 Hz), 3.01 (2H, t, J=7.5 Hz), 2.57 (3H, s), 2.01-1.79 (5H, m),
1.67-1.50 (5H, m), 1.24-1.12 (2H, m)
Example 155
[0593] A 0.23 g quantity of 3-[2-(3-hydroxy-4-methoxyphenyl)
oxazol-4-yl]-1-(3-methylpyridin-2-yl)propan-1-one obtained in
Example 136 and 0.28 g of potassium carbonate were dissolved in 5
ml of dimethylformamide. A 0.29 g quantity of
1,1,1-trifluoro-2-iodoethane was added thereto, and the mixture was
stirred with heating at 80.degree. C. overnight. The reaction
mixture was allowed to cool, water was then added thereto, and
extraction was performed with ethyl acetate. After washing with
water twice, the organic layer was concentrated under reduced
pressure. The obtained residue was purified by silica gel column
chromatography (dichloromethane:ethyl acetate=1:1) to give 0.14 g
of white powdery
3-{2-[4-methoxy-3-(2,2,2-trifluoroethoxy)phenyl]oxazol-4-yl}-1-(3-methylp-
yridin-2-yl)propan-1-one.
[0594] .sup.1H-NMR (CDCl.sub.3) .delta.: 8.50 (1H, dd, J=4.5, 0.9
Hz), 7.70 (1H, dd, J=8.4, 2.1 Hz), 7.60-7.56 (2H, m), 7.46 (1H, d,
J=2.1 Hz), 7.35-7.30 (1H, m), 6.96 (1H, d, J=8.4 Hz), 4.45 (2H, q,
J=8.4 Hz), 3.92 (3H, s), 3.60 (2H, t, J=7.5 Hz), 3.00 (2H, t, J=7.5
Hz), 2.57 (3H, s)
Example 156
[0595] Using 0.1 g of
3-[2-(3-hydroxy-4-methoxyphenyl)oxazol-4-yl]-1-(3-methylpyridin-2-yl)prop-
an-1-one obtained in Example 136, 45 mg of pale yellow powdery
3-{2-[4-methoxy-3-(3-methyl-2-butenyloxy)phenyl]oxazol-4-yl}-1-(3-methylp-
yridin-2-yl)propan-1-one was obtained in the same manner as in
Example 155.
[0596] .sup.1H-NMR (CDCl.sub.3) .delta.: 8.50 (1H, dd, J=4.5, 1.2
Hz), 7.59-7.52 (3H, m), 7.45 (1H, s), 7.34-7.29 (1H, m), 6.90 (1H,
d, J=8.4 Hz), 5.58-5.52 (1H, m), 4.64 (2H, d, J=6.9 Hz), 3.91 (3H,
s), 3.60 (2H, t, J=7.5 Hz), 3.01 (2H, t, J=7.5 Hz), 2.57 (3H, s),
1.78 (3H, d, J=0.9 Hz), 1.77 (3H, s)
Example 157
[0597] Using 0.6 g of
3-[2-(3-hydroxy-4-methoxyphenyl)oxazol-4-yl]-1-(3-methylpyridin-2-yl)prop-
an-1-one obtained in Example 136, 0.31 g of white powdery
3-{2-[3-(2-cyclohexenyloxy)-4-methoxyphenyl]oxazol-4-yl}-1-(3-methylpyrid-
in-2-yl)propan-1-one was obtained in the same manner as in Example
155.
[0598] .sup.1H-NMR (CDCl.sub.3) .delta.: 8.50 (1H, dd, J=4.5, 1.2
Hz), 7.60-7.56 (3H, m), 7.45 (1H, s), 7.34-7.29 (1H, m), 6.91 (1H,
d, J=9.0 Hz), 5.99-5.88 (2H, m), 4.88 (1H, br s), 3.89 (3H, s),
3.60 (2H, t, J=7.2 Hz), 3.01 (2H, t, J=7.2 Hz), 2.57 (3H, s),
2.17-1.84 (5H, m), 1.71-1.61 (1H, m)
Example 158
[0599] A 0.3 g quantity of
3-{2-[3-(2-cyclohexenyloxy)-4-methoxyphenyl]oxazol-4-yl}-1-(3-methylpyrid-
in-2-yl)propan-1-one obtained in Example 157 was dissolved in 20 ml
of ethanol. A 50 mg quantity of 10% palladium-carbon powder was
added thereto, and the mixture was stirred at room temperature for
2 hours. The catalyst was removed by filtration, and the filtrate
was then concentrated. The obtained residue was purified by silica
gel column chromatography (n-hexane:ethyl acetate=3:1) to give 0.2
g of pale yellow oily
3-[2-(3-cyclohexyloxy-4-methoxyphenyl)oxazol-4-yl]-1-(3-methylpyridi-
n-2-yl)propan-1-one.
[0600] .sup.1H-NMR (CDCl.sub.3) .delta.: 8.50 (1H, d, J=4.5 Hz),
7.59-7.54 (3H, m), 7.45 (1H, s), 7.34-7.30 (1H, m), 6.91 (1H, d,
J=8.1 Hz), 4.35-4.25 (1H, m), 3.89 (3H, s), 3.60 (2H, t, J=7.5 Hz),
3.01 (2H, t, J=7.5 Hz), 2.57 (3H, s), 2.07-2.02 (2H, m), 1.84-1.80
(2H, m), 1.60-1.51 (4H, m), 1.43-1.23 (2H, m)
Example 159
[0601] A 0.26 g quantity of 3-[2-(3-hydroxy-4-methoxyphenyl)
oxazol-4-yl]-1-(3-methylpyridin-2-yl)propan-1-one obtained in
Example 136 was dissolved in 10 ml of tetrahydrofuran. To the
obtained solution were added 0.2 g of 2-hydroxyindane, 0.75 ml of
diisopropyl azodicarboxylate (40% toluene solution) and 0.31 g of
tri(n-butyl)phosphine, and the mixture was stirred at 50.degree. C.
After hours, 0.2 g of 2-hydroxyindan, 0.75 ml of diisopropyl
azodicarboxylate (40% toluene solution) and 0.31 g of
tri(n-butyl)phosphine were further added thereto, and the mixture
was stirred at 50.degree. C. overnight. The reaction mixture was
concentrated under reduced pressure. The residue was purified by
silica gel column chromatography (n-hexane:ethyl
acetate:dichloromethane=1:1:1), and recrystallized from
acetone/diisopropyl ether to give 0.13 g of colorless powdery
3-{2-[3-(indan-2-yloxy)-4-methoxyphenyl]oxazol-4-yl}-1-(3-methylpyridin-2-
-yl)propan-1-one.
[0602] .sup.1H-NMR (CDCl.sub.3) .delta.: 8.51 (1H, br d, J=4.8 Hz),
7.62-7.16 (9H, m), 6.91 (1H, d, J=8.7 Hz), 5.29 (1H, tt, J=6.6, 3.9
Hz), 3.85 (3H, s), 3.63 (2H, t, J=7.2 Hz), 3.45 (2H, dd, J=16.8,
6.6 Hz), 3.26 (2H, dd, J=16.8, 3.9 Hz), 3.01 (2H, t, J=7.2 Hz),
2.58 (3H, s)
Example 160
[0603] A 2 g quantity of methyl
3-[2-(3-benzyloxy-4-methoxyphenyl)oxazol-4-yl]propionate obtained
in Reference Example 48 and 1.5 g of methyl picolinate were
dissolved in 40 ml of dimethoxyethane. A 0.33 g quantity of sodium
hydride was added thereto with ice-cooling and stirring, and
stirring was further continued. The reaction mixture was heated and
refluxed for 2 hours. After the reaction, an aqueous saturated
ammonium chloride solution was added thereto with ice-cooling and
stirring, and the mixture was stirred. The reaction mixture was
stirred for 30 minutes, water was then added thereto, and
extraction was performed with ethyl acetate. The organic layer was
washed twice with water and concentrated by removing the solvent
under reduced pressure. The obtained residue was purified by silica
gel column chromatography (n-hexane:ethyl acetate=3:1) to give 2 g
of colorless oily methyl
2-[2-(3-benzyloxy-4-methoxyphenyl)oxazol-4-ylmethyl]-3-oxo-3-pyridin-2-yl-
propionate.
[0604] .sup.1H-NMR (CDCl.sub.3) .delta.: 8.67 (1H, dd, J=4.2, 0.9
Hz), 8.07 (1H, dd, J=7.8, 2.1 Hz), 7.83 (1H, td, J=7.8, 1.8 Hz),
7.55-7.30 (9H, m), 6.90 (1H, d, J=9.0 Hz), 5.29 (1H, t, J=7.8 Hz),
5.16 (2H, s), 3.91 (3H, s), 3.66 (3H, s), 3.36-3.28 (2H, m)
Example 161
[0605] Using 2 g of methyl 2-[2-(3-benzyloxy-4-methoxyphenyl)
oxazol-4-ylmethyl]-3-oxo-3-(pyridin-2-yl)propionate obtained in
Example 160, 0.48 g of white powdery
3-[2-(3-hydroxy-4-methoxyphenyl)oxazol-4-yl]-1-(pyridin-2-yl)propan-1-one
was obtained in the same manner as in Example 136.
[0606] .sup.1H-NMR (CDCl.sub.3) .delta.: 8.67 (1H, dd, J=4.2, 0.9
Hz), 8.05 (1H, dd, J=7.8, 2.1 Hz), 7.83 (1H, td, J=7.8, 1.8 Hz),
7.55-7.43 (4H, m), 6.88 (1H, dd, J=7.8, 2.1 Hz), 5.72 (1H, s), 3.93
(3H, s), 3.64 (2H, t, J=7.5 Hz), 3.03 (2H, t, J=7.5 Hz)
Example 162
[0607] A 0.15 g quantity of
3-[2-(3-hydroxy-4-methoxyphenyl)oxazol-4-yl]-1-(pyridin-2-yl)propan-1-one
obtained in Example 161 and 0.2 ml of
1,8-diazabicyclo[5,4,0]undec-7-ene were dissolved in 5 ml of
ethanol. A 0.14 g quantity of (bromomethyl)cyclobutane was added
thereto, and the mixture was heated and refluxed overnight. The
reaction mixture was allowed to cool, water was then added thereto,
and extraction was performed with ethyl acetate. After washing with
water twice, the organic layer was concentrated under reduced
pressure. The obtained residue was purified by silica gel column
chromatography (dichloromethane:ethyl acetate=5:1) to give 50 mg of
white powdery
3-[2-(3-cyclobutylmethoxy-4-methoxyphenyl)oxazol-4-yl]-1-(pyridin-
-2-yl)propan-1-one.
[0608] .sup.1H-NMR (CDCl.sub.3) .delta.: 8.68 (1H, d, J=4.5 Hz),
8.05 (1H, d, J=7.8 Hz), 7.83 (1H, td, J=7.8, 1.8 Hz), 7.58-7.44
(4H, m), 6.90 (1H, d, J=8.4 Hz), 4.07 (2H, d, J=6.9 Hz), 3.89 (3H,
s), 3.65 (2H, t, J=7.5 Hz), 3.05 (2H, t, J=7.5 Hz), 2.94-2.81 (1H,
m), 2.24-2.04 (2H, m), 2.00-1.81 (4H, m)
Example 163
[0609] Using 0.3 g of
3-[2-(3-hydroxy-4-methoxyphenyl)oxazol-4-yl]-1-(pyridin-2-yl)propan-1-one
obtained in Example 161, 0.28 g of white powdery
3-[2-(4-methoxy-3-(4-pentenyloxy)phenyl)
oxazol-4-yl]-1-(pyridin-2-yl)propan-1-one was obtained in the same
manner as in Example 102.
[0610] .sup.1H-NMR (CDCl.sub.3) .delta.: 8.69 (1H, dd, J=4.2, 1.5
Hz), 8.05 (1H, d, J=7.8 Hz), 7.85 (1H, t, J=7.8 Hz), 7.60-7.46 (4H,
m), 6.91 (1H, d, J=8.4 Hz), 5.92-5.83 (1H, m), 5.11-4.99 (2H, m),
4.11 (2H, d, J=6.9 Hz), 3.91 (3H, s), 3.65 (2H, t, J=7.5 Hz), 3.05
(2H, t, J=7.5 Hz), 2.28-2.23 (2H, m), 1.98 (2H, t, J=7.5 Hz)
Example 164
[0611] A 10 g quantity of
2-(3-benzyloxy-4-methoxyphenyl)-4-chloromethyloxazole obtained in
Reference Example 5 and 10.7 g of 1-(2-allyloxyphenyl)ethanone
obtained in Reference Example 53 were dissolved in 200 ml of
tetrahydrofuran. A 1.82 g quantity of sodium hydride was added
thereto with ice-cooling and stirring, and stirring was further
continued. The reaction mixture was heated and refluxed for 4
hours. After the reaction, an aqueous saturated ammonium chloride
solution was added thereto with ice-cooling and stirring, and the
mixture was stirred. After stirring for 30 minutes, water was added
thereto, and extraction was performed with ethyl acetate. The
organic layer was washed with water twice and concentrated by
removing the solvent under reduced pressure. The obtained residue
was purified by silica gel column chromatography (n-hexane:ethyl
acetate=3:1) to give 1.4 g of white powdery
1-(2-allyloxyphenyl)-3-[2-(3-benzyloxy-4-methoxyphenyl)oxazol-4-yl]propan-
-1-one.
[0612] .sup.1H-NMR (CDCl.sub.3) .delta.: 7.70 (1H, dd, J=7.8, 1.8
Hz), 7.62-7.58 (2H, m), 7.49-7.30 (7H, m), 7.02-6.91 (3H, m),
6.12-6.02 (1H, m), 5.42 (1H, dd, J=17.4, 1.5 Hz), 5.30 (1H, dd,
J=10.5, 1.5 Hz), 5.19 (2H, s), 4.65-4.62 (2H, m), 3.92 (3H, s),
3.42 (2H, t, J=7.2 Hz), 2.99 (2H, t, J=7.2 Hz)
Example 165
[0613] Using 1.4 g of
1-(2-allyloxyphenyl)-3-[2-(3-benzyloxy-4-methoxyphenyl)oxazol-4-yl]propan-
-1-one obtained in Example 164, 0.55 g of pale yellow oily
3-[2-(3-hydroxy-4-methoxyphenyl)
oxazol-4-yl]-1-(2-hydroxyphenyl)propan-1-one was obtained in the
same manner as in Example 101.
[0614] .sup.1H-NMR (CDCl.sub.3) .delta.: 12.5 (1H, s), 7.81 (1H,
dd, J=7.8, 1.5 Hz), 7.57-7.30 (4H, m), 6.98 (1H, d, J=8.1 Hz),
6.92-6.86 (2H, m), 5.73 (1H, br s), 3.94 (3H, s), 3.44 (2H, t,
J=7.5 Hz), 3.02 (2H, t, J=7.5 Hz)
Example 166
[0615] Using 0.5 g of
3-[2-(3-hydroxy-4-methoxyphenyl)oxazol-4-yl]-1-(2-hydroxyphenyl)propan-1--
one obtained in Example 165, 0.61 g of white powdery
3-[2-(3-allyloxy-4-methoxyphenyl)oxazol-4-yl]-1-(2-allyloxyphenyl)propan--
1-one was obtained in the same manner as in Example 111.
[0616] .sup.1H-NMR (CDCl.sub.3) .delta.: 7.70 (1H, dd, J=7.5, 2.1
Hz), 7.58 (1H, dd, J=8.1, 2.1 Hz), 7.52 (1H, d, J=2.1 Hz),
7.45-7.40 (2H, m), 7.02-6.90 (3H, m), 6.16-6.03 (2H, m), 5.47-5.27
(4H, m), 4.68-4.62 (4H, m), 3.92 (3H, s), 3.42 (2H, t, J=6.9 Hz),
2.99 (2H, t, J=6.9 Hz)
Example 167
[0617] Using 1.1 g of methyl
3-[2-(3-benzyloxy-4-methoxyphenyl)oxazol-4-yl]propionate obtained
in Reference Example 48, 1 g of yellow oily methyl
2-[2-(3-benzyloxy-4-methoxyphenyl)oxazol-4-ylmethyl]-3-(2-methoxyphenyl)--
3-oxopropionate was obtained in the same manner as in Example
100.
[0618] .sup.1H-NMR (CDCl.sub.3) .delta.: 7.71 (1H, dd, J=7.8, 1.8
Hz), 7.57-7.53 (3H, m), 7.48-7.30 (6H, m), 6.97 (1H, t, J=7.2 Hz),
6.91 (2H, d, J=7.8 Hz), 5.17 (2H, s), 4.99 (1H, t, J=6.9 Hz), 3.92
(3H, s), 3.90 (3H, s), 3.69 (3H, s), 3.27-3.19 (2H, m)
Example 168
[0619] Using 1 g of methyl 2-[2-(3-benzyloxy-4-methoxyphenyl)
oxazol-4-ylmethyl]-3-(2-methoxyphenyl)-3-oxopropionate obtained in
Example 167, 0.63 g of white powdery
3-[2-(3-hydroxy-4-methoxyphenyl)oxazol-4-yl]-1-(2-methoxyphenyl)propan-1--
one was obtained in the same manner as in Example 101.
[0620] .sup.1H-NMR (CDCl.sub.3) .delta.: 7.70 (1H, dd, J=8.4, 2.1
Hz), 7.56-7.52 (2H, m), 7.44-7.41 (2H, m), 6.99-6.87 (3H, m), 3.95
(3H, s), 3.89 (3H, s), 3.38 (2H, t, J=7.2 Hz), 2.98 (2H, t, J=7.2
Hz)
Example 169
[0621] Using 0.22 g of
3-[2-(3-hydroxy-4-methoxyphenyl)oxazol-4-yl]-1-(2-methoxyphenyl)propan-1--
one obtained in Example 168, 90 mg of colorless oily
3-[2-(3-isopropoxy-4-methoxyphenyl)oxazol-4-yl]-1-(2-methoxyphenyl)propan-
-1-one was obtained in the same manner as in Example 102.
[0622] .sup.1H-NMR (CDCl.sub.3) .delta.: 7.70 (1H, d, J=7.5 Hz),
7.57 (1H, d, J=8.1 Hz), 7.54 (1H, s), 7.47-7.40 (2H, m), 7.01-6.89
(3H, m), 4.67-4.62 (1H, m), 3.91 (6H, s), 3.38 (2H, t, J=7.2 Hz),
3.00 (2H, t, J=7.2 Hz), 1.39 (6H, d, J=6.3 Hz)
[0623] Using
3-[2-(3-hydroxy-4-methoxyphenyl)oxazol-4-yl]-1-(2-methoxyphenyl)propan-1--
one obtained in Example 168, compounds of Examples 170 to 173 were
obtained in the same manner as in Example 102.
Example 170
3-[2-(3-cyclopropylmethoxy-4-methoxyphenyl)oxazol-4-yl]-1-(2-methoxyphenyl-
)propan-1-one
[0624] .sup.1H-NMR (CDCl.sub.3) .delta.: 7.69-7.40 (4H, m),
6.99-6.89 (4H, m), 3.94-3.89 (8H, m), 3.37 (2H, t, J=7.2 Hz), 3.01
(2H, t, J=7.2 Hz), 1.40-1.35 (1H, m), 0.67-0.65 (2H, m), 0.38-0.36
(2H, m)
Example 171
[0625]
3-[2-(3-cyclopentyloxy-4-methoxyphenyl)oxazol-4-yl]-1-(2-methoxyphe-
nyl)propan-1-one
[0626] .sup.1H-NMR (CDCl.sub.3) .delta.: 7.70 (1H, dd, J=7.5, 1.8
Hz), 7.56 (1H, dd, J=8.4, 2.1 Hz), 7.51 (1H, s), 7.43 (1H, td,
J=8.4, 1.8 Hz), 6.99-6.88 (3H, m), 4.48 (1H, br s), 3.89 (3H, s),
3.88 (3H, s), 3.38 (2H, t, J=6.6 Hz), 2.98 (2H, t, J=6.6 Hz),
2.04-1.85 (4H, m), 1.63-1.55 (4H, m)
Example 172
3-[2-(3-ethoxy-4-methoxyphenyl)oxazol-4-yl]-1-(2-methoxyphenyl)
propan-1-one
[0627] .sup.1H-NMR (CDCl.sub.3) .delta.: 7.70 (1H, dd, J=7.5, 1.8
Hz), 7.57 (1H, dd, J=8.1, 2.1 Hz), 7.51 (1H, d, J=1.8 Hz),
7.47-7.41 (2H, m), 7.01-6.89 (3H, m), 4.18 (2H, q, J=7.8 Hz), 3.94
(3H, s), 3.90 (3H, s), 3.38 (2H, t, J=6.6 Hz), 2.99 (2H, t, J=6.6
Hz), 1.49 (3H, t, J=7.8 Hz)
Example 173
3-[2-(3-isobutoxy-4-methoxyphenyl)oxazol-4-yl]-1-(2-methoxy
phenyl)propan-1-one
[0628] .sup.1H-NMR (CDCl.sub.3) .delta.: 7.70 (1H, dd, J=7.5, 1.8
Hz), 7.58-7.36 (4H, m), 7.01-6.89 (3H, m), 3.90 (6H, s), 3.84 (2H,
d, J=6.6 Hz), 3.38 (2H, t, J=6.9 Hz), 2.99 (2H, t, J=6.9 Hz),
2.22-2.10 (1H, m), 1.05 (6H, d, J=6.6 Hz)
[0629] Using
3-[2-(3-hydroxy-4-methoxyphenyl)oxazol-4-yl]-1-(2-methoxyphenyl)propan-1--
one obtained in Example 168, compounds of Examples 174 to 175 were
obtained in the same manner as in Example 111.
Example 174
3-[2-(3-allyloxy-4-methoxyphenyl)oxazol-4-yl]-1-(2-methoxyphenyl)
propan-1-one
[0630] .sup.1H-NMR (CDCl.sub.3) .delta.: 7.70 (1H, dd, J=7.5, 1.8
Hz), 7.59 (1H, dd, J=8.4, 1.8 Hz), 7.52 (1H, d, J=1.8 Hz),
7.48-7.41 (2H, m), 7.02-6.90 (3H, m), 6.12-6.07 (1H, m), 5.43 (1H,
dd, J=17, 1.5 Hz), 5.31 (1H, d, J=10 Hz), 4.68 (2H, d, J=5.4 Hz),
3.92 (3H, s), 3.90 (3H, s), 3.38 (2H, t, J=7.2 Hz), 2.99 (2H, t,
J=7.2 Hz)
Example 175
1-(2-methoxyphenyl)-3-{2-[4-methoxy-3-(2,2,2-trifluoroethoxy)phenyl]oxazol-
-4-yl}propan-1-one
[0631] .sup.1H-NMR (CDCl.sub.3) .delta.: 7.69 (1H, dd, J=7.5, 1.8
Hz), 7.60 (1H, d, J=1.8 Hz), 7.48-7.42 (2H, m), 7.02-6.95 (3H, m),
4.43 (2H, q, J=8.1 Hz), 3.92 (3H, s), 3.90 (3H, s), 3.38 (2H, t,
J=6.9 Hz), 2.99 (2H, t, J=6.9 Hz)
Example 176
[0632] A 0.4 g quantity of sodium hydride was suspended in 20 ml of
tetrahydrofuran, and 1.13 g of 1-(2-benzyloxy)ethanone and 1.46 g
of 4-chloromethyl-2-(3-cyclopropylmethoxy-4-methoxyphenyl) oxazole
obtained in Reference Example 11 were successively added thereto
with ice-cooling. The mixture was stirred for 4 hours with heating
and refluxing. An aqueous saturated ammonium chloride solution was
added to the reaction mixture with ice cooling. After stirring for
15 minutes, water was added thereto, and extraction was performed
with ethyl acetate. Drying was performed with anhydrous magnesium
sulfate, and the solvent was removed. Purification was performed
using a silica gel column (n-hexane:ethyl acetate=4:1), and the
obtained compound was dissolved in 12 ml of ethanol. A 35 mg
quantity of 10% palladium-carbon powder was added thereto, and
stirring was performed under a hydrogen atmosphere overnight. The
catalyst was removed by filtration and the obtained filtrate was
concentrated. The residue was purified using a silica gel column
(n-hexane:ethyl acetate=4:1) to give 0.43 g of white powdery
3-[2-(3-cyclopropylmethoxy-4-methoxyphenyl)oxazol-4-yl]-1-(2-hydroxy
phenyl)propan-1-one.
[0633] .sup.1H-NMR (CDCl.sub.3) .delta.:12.2 (1H, s), 7.83 (1H, d,
J=1.5 Hz), 7.80-7.44 (4H, m), 7.00-6.87 (3H, m), 3.94-3.92 (5H, m),
3.44 (2H, t, J=7.2 Hz), 3.03 (2H, t, J=7.2 Hz), 1.37-1.26 (1H, m),
0.70-0.65 (2H, m), 0.41-0.37 (2H, m)
Example 177
[0634] A 2 g quantity of 4-chloromethyl-2-(3-cyclopropyl
methoxy-4-methoxyphenyl)oxazole obtained in Reference Example 11
and 3.6 g of 1-(2-allyloxyphenyl)ethanone obtained in Reference
Example 53 were dissolved in 40 ml of tetrahydrofuran. A 0.55 g
quantity of sodium hydride was added thereto with ice-cooling and
stirring, and the mixture was stirred. The reaction mixture was
heated and refluxed for 6 hours. After the reaction completion, an
aqueous saturated ammonium chloride solution was added thereto with
ice-cooling, and the mixture was stirred. The reaction mixture was
stirred for 30 minutes, water was then added thereto, and
extraction was performed with ethyl acetate. The organic layer was
washed with water twice and concentrated by removing the solvent
under reduced pressure. The obtained residue was purified by silica
gel column chromatography (n-hexane:ethyl acetate=3:1) to give 0.5
g of while powdery
1-(2-allyloxyphenyl)-3-[2-(3-cyclopropylmethoxy-4-methoxyphenyl)
oxazol-4-yl]propan-1-one.
[0635] .sup.1H-NMR (CDCl.sub.3) .delta.: 7.70 (1H, dd, J=7.8, 1.8
Hz), 7.57 (1H, dd, J=8.4, 2.1 Hz), 7.49 (1H, d, J=2.1 Hz),
7.45-7.39 (2H, m), 7.02-6.89 (3H, m), 6.09-6.02 (1H, m), 5.45-5.26
(2H, m), 4.65-4.62 (2H, m), 3.94-3.91 (5H, m), 3.42 (2H, t, J=7.2
Hz), 2.99 (2H, t, J=7.2 Hz), 1.45-1.35 (1H, m), 0.68-0.62 (2H, m),
0.40-0.36 (2H, m)
Example 178
[0636] Using 1.4 g of 4-chloromethyl-2-(3,4-diethoxyphenyl) oxazole
obtained in Reference Example 35 and 0.88 g of
1-(2-allyloxyphenyl)ethanone obtained in Reference Example 53, 0.42
g of white powdery 1-(2-allyloxyphenyl)-3-[2-(3,4-diethoxyphenyl)
oxazol-4-yl]propan-1-one was obtained in the same manner as in
Example 177.
[0637] .sup.1H-NMR (CDCl.sub.3) .delta.: 7.69 (1H, dd, J=7.5, 2.1
Hz), 7.56-7.51 (2H, m), 7.45-7.39 (2H, m), 7.02-6.89 (3H, m),
6.14-6.01 (1H, m), 5.42 (1H, dd, J=17, 1.5 Hz), 5.29 (1H, dd,
J=10.5, 1.5 Hz), 4.65-4.62 (2H, m), 4.20-4.10 (4H, m), 3.42 (2H, t,
J=7.2 Hz), 2.99 (2H, t, J=7.2 Hz), 1.50 (6H, t, J=7.2 Hz)
Example 179
[0638] Using 0.31 g of 1-(2-chlorophenyl)ethanone and 0.59 g of
4-chloromethyl-2-(3-cyclopropylmethoxy-4-methoxyphenyl)oxazole
obtained in Reference Example 11, 0.11 g of colorless oily
1-(2-chlorophenyl)-3-[2-(3-cyclopropylmethoxy-4-methoxyphenyl)oxazol-4-yl-
]propan-1-one was obtained in the same manner as in Example
177.
[0639] .sup.1H-NMR (CDCl.sub.3) .delta.: 7.60-7.55 (2H, m),
7.49-7.43 (2H, m), 7.40 (1H, s), 7.39-7.30 (2H, m), 6.91 (1H, d,
J=8.7 Hz), 3.94-3.91 (5H, m), 3.36 (2H, t, J=6.9 Hz), 3.01 (2H, t,
J=6.9 Hz), 1.37-1.29 (1H, m), 0.69-0.63 (2H, m), 0.40-0.37 (2H,
m)
Example 180
[0640] Using 2 g of methyl
3-[2-(3,4-diethoxyphenyl)oxazol-4-yl]propionate obtained in
Reference Example 54 and 1.3 g of ethyl 3-methylpicolinate, 0.8 g
of yellow oily methyl
2-[2-(3,4-diethoxyphenyl)oxazol-4-ylmethyl]-3-(3-methylpyridin-2-yl)-3-ox-
opropionate was obtained in the same manner as in Example 124.
[0641] .sup.1H-NMR (CDCl.sub.3) .delta.: 8.50 (1H, m), 7.60-7.40
(4H, m), 7.30 (1H, m), 6.88 (1H, d, J=8.4 Hz), 5.20 (1H, t, J=7.2
Hz), 4.20-4.05 (4H, m), 2.99 (3H, s), 3.35-3.20 (2H, m), 2.59 (3H,
s), 1.47 (3H, t, J=6.9 Hz), 1.47 (3H, t, J=6.9 Hz)
Example 181
[0642] A 0.8 g quantity of methyl
2-[2-(3,4-diethoxyphenyl)oxazol-4-ylmethyl]-3-(3-methylpyridin-2-yl)-3-ox-
opropionate obtained in Example 180 was added to a mixture of 5 ml
acetic acid and 1.5 ml of concentrated hydrochloric acid, and the
resulting mixture was stirred at 110.degree. C. for 4 hours. After
cooling the obtained solution to room temperature, 30 ml of ethyl
acetate and 30 ml of saturated sodium hydrogen carbonate solution
were gradually added thereto with stirring, and stirring was
further continued. The organic layer was dried over anhydrous
magnesium sulfate, and concentrated under reduced pressure. The
residue was purified by silica gel column chromatography (ethyl
acetate:n-hexane=3:1), and further recrystallized from ethyl
acetate/n-hexane to give 0.28 g of white powdery
3-[2-(3,4-diethoxyphenyl)oxazol-4-yl]-1-(3-methylpyridin-2-yl)propan-1-on-
e.
[0643] .sup.1H-NMR (CDCl.sub.3) .delta.: 8.49 (1H, m), 7.60-7.50
(3H, m), 7.44 (1H, s), 7.32 (1H, m), 6.90 (1H, d, J=8.1 Hz), 4.17
(2H, q, J=6.9 Hz), 4.13 (2H, q, J=6.9 Hz), 3.51 (2H, t, J=7.2 Hz),
3.00 (2H, t, J=7.2 Hz), 2.57 (3H, s), 1.48 (3H, t, J=6.9 Hz), 1.47
(3H, t, J=6.9 Hz)
Example 182
[0644] A 2 g quantity of methyl 3-[2-(3,4-diethoxyphenyl)
oxazol-4-yl]propionate obtained in Reference Example 54 and 1.5 g
of ethyl 2-ethoxybenzoate were dissolved in 10 ml of
dimethylformamide. A 1.81 g quantity of sodium t-pentoxide was
added thereto with ice-cooling and stirring, and the mixture was
stirred for 30 minutes. The reaction mixture was further stirred at
room temperature for 5 hours, and ice was added thereto. An aqueous
saturated ammonium chloride solution was added thereto, and the
mixture was stirred. The reaction mixture was stirred for 30
minutes, water was then added thereto, and extraction was performed
with ethyl acetate. The organic layer was washed with water twice
and concentrated by removing the solvent under reduced pressure.
The obtained residue was purified by silica gel column
chromatography (n-hexane:ethyl acetate=1:1). The obtained yellow
oily substance was added to a mixture of 5 ml of acetic acid and
1.5 ml of concentrated hydrochloric acid, and the resulting mixture
was stirred at 110.degree. C. for 4 hours. After cooling the
mixture to room temperature, 30 ml of ethyl acetate and 30 ml of
saturated sodium hydrogen carbonate solution were gradually added
thereto with stirring, and stirring was further continued. The
organic layer was dried over anhydrous magnesium sulfate, and
concentrated under reduced pressure. The residue was purified by
silica gel column chromatography (ethyl acetate:n-hexane=3:1), and
the obtained crude crystals were recrystallized from ethyl
acetate/n-hexane to give 0.46 g of white powdery
3-[2-(3,4-diethoxyphenyl)oxazol-4-yl]-1-(2-ethoxyphenyl)propan-1-one.
[0645] .sup.1H-NMR (CDCl.sub.3) .delta.: 7.70 (1H, dd, J=7.5, 2.1
Hz), 7.60-7.50 (2H, m), 7.45-7.35 (2H, m), 7.00-6.80 (2H, m), 4.17
(2H, q, J=7.2 Hz), 4.13 (2H, q, J=7.2 Hz), 3.42 (2H, t, J=7.2 Hz),
2.99 (2H, t, J=7.2 Hz), 1.48 (3H, t, J=7.2 Hz), 1.48 (3H, t, J=7.2
Hz), 1.48 (3H, t, J=7.2 Hz)
[0646] Using methyl 3-[2-(3,4-diethoxyphenyl)oxazol-4-yl]propionate
obtained in Reference Example 54, compounds of Example 183 to 185
were obtained in the same manner as in Example 182.
Example 183
3-[2-(3,4-diethoxyphenyl)oxazol-4-yl]-1-(3-ethoxypyridin-2-yl)propan-1-one
[0647] .sup.1H-NMR (CDCl.sub.3) .delta.: 8.23 (1H, dd, J=4.5, 1.2
Hz), 7.55-7.50 (2H, m), 7.40-7.25 (2H, m), 7.45 (1H, s), 6.90 (1H,
d, J=8.1 Hz), 4.20-4.05 (6H, m), 3.49 (2H, t, J=7.2 Hz), 3.02 (2H,
t, J=7.2 Hz), 1.47 (3H, t, J=7.2 Hz), 1.47 (3H, t, J=7.2 Hz), 1.46
(3H, t, J=7.2 Hz)
Example 184
3-[2-(3,4-diethoxyphenyl)oxazol-4-yl]-1-(3-ethoxyphenyl)propan-1-one
[0648] .sup.1H-NMR (CDCl.sub.3) .delta.: 8.00-7.95 (2H, m),
7.60-7.50 (2H, m), 7.43 (1H, s), 6.95-6.85 (3H, m), 4.17 (2H, q,
J=7.2 Hz), 4.17 (2H, q, J=7.2 Hz), 4.09 (2H, q, J=7.2 Hz), 3.34
(2H, t, J=7.2 Hz), 3.01 (2H, t, J=7.2 Hz), 1.48 (3H, t, J=7.2 Hz),
1.48 (3H, t, J=7.2 Hz), 1.44 (3H, t, J=7.2 Hz).
Example 185
3-[2-(3,4-diethoxyphenyl)oxazol-4-yl]-1-(4-ethoxyphenyl)propan-1-one
[0649] .sup.1H-NMR (CDCl.sub.3) .delta.: 7.60-7.50 (4H, m), 7.44
(1H, s), 7.35 (1H, t, J=7.8 Hz), 7.09 (1H, dd, J=9.0, 2.4 Hz), 6.10
(1H, d, J=5.4 Hz), 4.16 (2H, q, J=7.2 Hz), 4.15 (2H, q, J=7.2 Hz),
4.08 (2H, q, J=7.2 Hz), 3.38 (2H, t, J=7.2 Hz), 3.02 (2H, t, J=7.2
Hz), 1.48 (3H, t, J=7.2 Hz), 1.48 (3H, t, J=7.2 Hz), 1.40 (3H, t,
J=7.2 Hz).
Example 186
[0650] Using 2 g of dimethyl 2-[2-(3,4-bis(benzyloxy)phenyl)
oxazol-4-ylmethyl]malonate obtained in Reference Example 56, 2.2 g
of pale yellow oily methyl
2-[2-(3,4-bisbenzyloxyphenyl)oxazol-4-ylmethyl]-3-(3-methylpyridin-2-yl)--
3-oxopropionate was obtained in the same manner as in Example
100.
[0651] .sup.1H-NMR (CDCl.sub.3) .delta.: 8.49 (1H, dd, J=4.5, 1.2
Hz), 7.59-7.28 (15H, m), 6.94 (1H, d, J=8.4 Hz), 5.23-5.17 (5H, m),
3.69 (3H, s), 3.32-3.23 (2H, m), 2.59 (3H, s)
Example 187
[0652] Using 2.2 g of methyl 2-[2-(3,4-bisbenzyloxyphenyl)
oxazol-4-ylmethyl]-3-(3-methylpyridin-2-yl)-3-oxopropionate
obtained in Example 186, 0.24 g of white powdery
3-[2-(3,4-dihydroxyphenyl)oxazol-4-ylmethyl]-1-(3-methylpyridin-2-yl)prop-
an-1-one was obtained in the same manner as in Example 136.
[0653] .sup.1H-NMR (CDCl.sub.3) .delta.: 9.46 (1H, br s), 9.32 (1H,
br s), 8.54 (1H, d, J=3.0 Hz), 7.80-7.76 (2H, m), 7.54-7.49 (1H,
m), 7.32 (1H, d, J=2.1 Hz), 7.23 (1H, dd, J=8.4, 2.1 Hz), 6.82 (1H,
d, J=8.4 Hz), 3.47 (2H, t, J=7.5 Hz), 2.83 (2H, t, J=7.5 Hz), 2.51
(3H, s)
Example 188
[0654] Using 0.12 g of
3-[2-(3,4-dihydroxyphenyl)oxazol-4-ylmethyl]-1-(3-methylpyridin-2-yl)prop-
an-1-one obtained in Example 187, 35 mg of white powdery
3-{2-[3,4-bis-(2,2,2-trifluoroethoxy)phenyl]oxazol-4-yl}-1-(3-methylpyrid-
in-2-yl) propan-1-one was obtained in the same manner as in Example
111.
[0655] .sup.1H-NMR (CDCl.sub.3) .delta.: 8.50 (1H, d, J=4.5 Hz),
7.68 (1H, dd, J=8.4, 1.8 Hz), 7.63 (1H, d, J=1.8 Hz), 7.58 (1H, d,
J=8.4 Hz), 7.49 (1H, s), 7.35-7.28 (1H, m), 7.04 (1H, d, J=8.4 Hz),
4.50-4.39 (4H, m), 3.60 (2H, t, J=7.2 Hz), 3.01 (2H, t, J=7.2 Hz),
2.59 (3H, s)
Example 189
[0656] Using 0.76 g of
4-chloromethyl-2-(3-ethoxy-4-methoxyphenyl)oxazole obtained in
Reference Example 58 and 0.5 g of 1-(2-allyloxyphenyl)ethanone
obtained in Reference Example 53, 0.13 g of white powdery
1-(2-allyloxyphenyl)-3-[2-(3-ethoxy-4-methoxyphenyl)oxazol-4-yl]propan-1--
one was obtained in the same manner as in Example 177.
[0657] .sup.1H-NMR (CDCl.sub.3) .delta.: 7.70 (1H, dd, J=7.5, 2.1
Hz), 7.56 (1H, dd, J=8.4, 2.1 Hz), 7.51 (1H, d, J=2.1 Hz),
7.45-7.40 (2H, m), 7.02-6.89 (3H, m), 6.12-6.01 (1H, m), 5.42 (1H,
dd, J=17, 1.5 Hz), 5.28 (1H, dd, J=17, 1.5 Hz), 4.65-4.62 (2H, m),
4.18 (2H, q, J=6.9 Hz), 3.92 (3H, s), 3.42 (2H, t, J=7.2 Hz), 2.99
(2H, t, J=7.2 Hz), 1.49 (3H, t, J=6.9 Hz)
Example 190
[0658] A 2 g quantity of
4-chloromethyl-2-(4-benzyloxy-3-ethoxyphenyl)oxazole obtained in
Reference Example 63 and 0.96 g of 1-(2-ethoxyphenyl)ethanone were
dissolved in 20 ml of tetrahydrofuran, and 0.47 g sodium hydride
was added thereto. After foaming, the reaction mixture was heated
and refluxed for 3 hours. After cooling, the reaction mixture was
added to ice water, and extraction was performed with ethyl
acetate. The organic layer was washed with water, dried over
magnesium sulfate, and concentrated under reduced pressure. The
residue was purified by silica gel column chromatography
(n-hexane:ethyl acetate=3:1) to give 0.4 g of colorless powdery
3-[2-(4-benzyloxy-3-ethoxyphenyl)oxazol-4-yl]-1-(2-ethoxyphenyl)propan-1--
one.
[0659] .sup.1H-NMR (CDCl.sub.3) .delta.: 7.70 (1H, dd, J=7.5, 1.8
Hz), 7.55-7.30 (8H, m), 6.97 (2H, t, J=7.5 Hz), 6.93 (1H, d, J=7.5
Hz), 5.19 (2H, s), 4.18 (2H, q, J=6.9 Hz), 4.13 (2H, q, J=6.9 Hz),
3.41 (2H, t, J=6.9 Hz), 2.99 (2H, t, J=6.9 Hz), 1.48 (3H, t, J=6.9
Hz), 1.47 (3H, t, J=6.9 Hz)
Example 191
[0660] Using
3-[2-(4-benzyloxy-3-ethoxyphenyl)oxazol-4-yl]-1-(2-ethoxyphenyl)propan-1--
one obtained in Example 190, colorless oily
3-[2-(3-ethoxy-4-hydroxyphenyl)oxazol-4-yl]-1-(2-ethoxy
phenyl)propan-1-one was obtained in the same manner as in Example
2.
[0661] .sup.1H-NMR (CDCl.sub.3) .delta.: 7.70 (1H, dd, J=7.5, 1.8
Hz), 7.52 (1H, dd, J=8.1, 2.1 Hz), 7.49 (1H, d, J=2.1 Hz),
7.45-7.38 (2H, m), 6.97 (1H, t, J=7.5 Hz), 6.95 (1H, d, J=7.5 Hz),
6.93 (1H, d, J=8.1 Hz), 5.89 (1H, s), 4.20 (2H, q, J=7.2 Hz), 4.13
(2H, q, J=7.2 Hz), 3.41 (2H, t, J=7.2 Hz), 2.98 (2H, t, J=7.2 Hz),
1.47 (3H, t, J=7.2 Hz), 1.47 (3H, t, J=7.2 Hz)
Example 192
[0662] Using
3-[2-(3-ethoxy-4-hydroxyphenyl)oxazol-4-yl]-1-(2-ethoxyphenyl)propan-1-on-
e obtained in Example 191, colorless needle crystalline
3-[2-(3-ethoxy-4-isopropoxyphenyl)oxazol-4-yl]-1-(2-ethoxyphenyl)propan-1-
-one was obtained in the same manner as in Example 111.
[0663] .sup.1H-NMR (CDCl.sub.3) .delta.: 7.70 (1H, dd, J=7.5, 1.8
Hz), 7.54-7.51 (2H, m), 7.45-7.39 (2H, m), 6.97 (2H, br t, J=7.5
Hz), 6.93 (1H, d, J=7.5 Hz), 4.55 (1H, sept, J=6.0 Hz), 4.14 (2H,
q, J=6.9 Hz), 4.13 (2H, q, J=6.9 Hz), 3.42 (2H, t, J=7.5 Hz), 2.99
(2H, t, J=7.5 Hz), 1.47 (3H, t, J=6.9 Hz), 1.45 (3H, t, J=6.9 Hz),
1.37 (6H, d, J=6.0 Hz)
Example 193
[0664] A 2.98 g quantity of 2-(3-benzyloxy-4-methoxyphenyl)
oxazole-4-carbaldehyde obtained in Reference Example 64 and 1.72 g
of 1-(2-propoxyphenyl)ethanone were dissolved in 50 ml of pyridine.
A 2.66 g quantity of potassium carbonate was added thereto, and the
mixture was heated and stirred at 120.degree. C. for 22 hours.
After cooling, the reaction mixture was added to saturated brine,
and extraction was performed with ethyl acetate. The organic layer
was washed with water and then dried over anhydrous magnesium
sulfate, and the solvent was removed under reduced pressure. The
residue was purified by silica gel column chromatography
(n-hexane:ethyl acetate=3:1) to give 1.82 g of colorless oily
(E)-3-[2-(3-benzyloxy-4-methoxyphenyl)oxazol-4-yl]-1-(2-propoxypheny-
l)-2-propen-1-one.
[0665] .sup.1H-NMR (CDCl.sub.3) .delta.: 7.80 (1H, s), 7.79 (1H, d,
J=15.3 Hz), 7.69-7.66 (3H, m), 7.51-7.32 (7H, m), 7.04-6.95 (3H,
m), 5.21 (2H, s), 4.05 (2H, t, J=6.3 Hz), 3.94 (3H, s), 1.88 (2H,
sext., J=6.3 Hz), 1.08 (3H, t, J=6.3 Hz)
Example 194
[0666] A 1.82 g quantity of
(E)-3-[2-(3-benzyloxy-4-methoxyphenyl)oxazol-4-yl]-1-(2-propoxyphenyl)-2--
propen-1-one obtained in Example 193 was dissolved in 50 ml of
methanol. A 200 mg quantity of 5% palladium-carbon powder was added
thereto, and the mixture was stirred under a hydrogen atmosphere at
room temperature for 2 hours. The catalyst was then removed by
filtration. The filtrate was diluted with 100 ml of methanol, and
500 mg of 10% palladium-carbon powder was added thereto. The
mixture was stirred under a hydrogen atmosphere at room temperature
for 3 hours. The catalyst was removed by filtration, and the
solvent was removed under reduced pressure. Diisopropyl ether was
added to the residue for crystallization to give 0.78 g of
colorless powdery
3-[2-(3-hydroxy-4-methoxyphenyl)oxazol-4-yl]-1-(2-propoxyphenyl)propan-1--
one.
[0667] .sup.1H-NMR (CDCl.sub.3) .delta.: 7.70 (1H, dd, J=7.5, 1.8
Hz), 7.55 (1H, d, J=2.1 Hz), 7.53 (1H, dd, J=8.1, 2.1 Hz), 7.42
(1H, ddd, J=8.1, 7.5, 1.8 Hz), 7.40 (1H, s), 6.97 (1H, td, J=7.5,
0.9 Hz), 6.93 (1H, br d, J=8.1 Hz), 6.89 (1H, d, J=8.1 Hz), 4.02
(2H, t, J=6.6 Hz), 3.94 (3H, s), 3.43 (2H, t, J=7.2 Hz), 2.99 (2H,
t, J=7.2 Hz), 1.88 (2H, sext., J=6.6 Hz), 1.06 (3H, t, J=6.6
Hz)
Example 195
[0668] Using 0.15 g of
3-[2-(3-hydroxy-4-methoxyphenyl)oxazol-4-yl]-1-(2-propoxyphenyl)propan-1--
one obtained in Example 194, 67 mg of colorless powdery
3-[2-(3-ethoxy-4-methoxyphenyl)oxazol-4-yl]-1-(2-propoxyphenyl)propan-1-o-
ne was obtained in the same manner as in Example 102.
[0669] .sup.1H-NMR (CDCl.sub.3) .delta.: 7.71 (1H, dd, J=7.8, 1.8
Hz), 7.59-7.40 (4H, m), 6.97 (1H, t, J=7.8 Hz), 6.94 (1H, d, J=7.8
Hz), 6.91 (1H, d, J=7.8 Hz), 4.18 (2H, q, J=6.6 Hz), 4.02 (2H, t,
J=6.6 Hz), 3.92 (3H, s), 3.43 (2H, t, J=7.2 Hz), 3.00 (2H, t, J=7.2
Hz), 1.87 (2H, sext., J=6.6 Hz), 1.49 (3H, t, J=6.6 Hz), 1.06 (3H,
t, J=6.6 Hz)
Example 196
[0670] Using 0.15 g of
3-[2-(3-hydroxy-4-methoxyphenyl)oxazol-4-yl]-1-(2-propoxyphenyl)propan-1--
one obtained in Example 194, 67 mg of colorless oily
3-[2-(3-cyclopentyloxy-4-methoxyphenyl)
oxazol-4-yl]-1-(2-propoxyphenyl)propan-1-one was obtained in the
same manner as in Example 102.
[0671] .sup.1H-NMR (CDCl.sub.3) .delta.: 7.71 (1H, dd, J=7.5, 1.8
Hz), 7.55 (1H, dd, J=8.4, 1.8 Hz), 7.51 (1H, d, J=1.8 Hz), 7.42
(1H, br t, J=7.5 Hz), 7.39 (1H, s), 6.97 (1H, t, J=7.5 Hz), 6.93
(1H, d, J=7.5 Hz), 6.89 (1H, d, J=8.4 Hz), 4.90-4.84 (1H, m), 4.02
(2H, t, J=6.6 Hz), 3.88 (3H, s), 3.43 (2H, t, J=7.2 Hz), 2.99 (2H,
t, J=7.2 Hz), 2.03-1.60 (10H, m), 1.05 (3H, t, J=7.2 Hz)
Example 197
[0672] Using
3-[2-(3-hydroxy-4-methoxyphenyl)oxazol-4-yl]-1-(2-propoxyphenyl)propan-1--
one obtained in Example 194, colorless oily
3-[2-(3-isopropoxy-4-methoxyphenyl)oxazol-4-yl]-1-(2-propoxy
phenyl)propan-1-one was obtained in the same manner as in Example
102.
[0673] .sup.1H-NMR (CDCl.sub.3) .delta.: 7.71 (1H, dd, J=7.8, 1.8
Hz), 7.57 (1H, dd, J=8.4, 2.1 Hz), 7.54 (1H, d, J=2.1 Hz), 7.42
(1H, ddd, J=8.4, 7.2, 1.8 Hz), 7.39 (1H, s), 6.97 (1H, br t, J=7.2
Hz), 6.96 (1H, br d, J=8.4 Hz), 6.91 (1H, d, J=8.4 Hz), 4.65 (1H,
sept., J=6.0 Hz), 4.02 (2H, t, J=7.2 Hz), 3.90 (3H, s), 3.43 (2H,
t, J=7.2 Hz), 2.99 (2H, t, J=7.2 Hz), 1.87 (2H, sext., J=7.2 Hz),
1.40 (6H, d, J=6.0 Hz), 1.06 (3H, t, J=7.2 Hz)
Example 198
[0674] Using
3-[2-(3-hydroxy-4-methoxyphenyl)oxazol-4-yl]-1-(2-propoxyphenyl)propan-1--
one obtained in Example 194, colorless powdery
3-[2-(3-cyclopropylmethoxy-4-methoxyphenyl)oxazol-4-yl]-1-(2-propoxypheny-
l)propan-1-one was obtained in the same manner as in Example
102.
[0675] .sup.1H-NMR (CDCl.sub.3) .delta.: 7.70 (1H, dd, J=7.5, 1.8
Hz), 7.57 (1H, dd, J=8.4, 1.8 Hz), 7.50 (1H, d, J=1.8 Hz),
7.45-7.39 (2H, m), 6.97 (1H, br t, J=7.5 Hz), 6.93 (1H, br d, J=7.5
Hz), 6.91 (1H, br d, J=8.4 Hz), 4.02 (2H, t, J=6.6 Hz), 3.92 (2H,
d, J=7.2 Hz), 3.92 (3H, s), 3.43 (2H, t, J=7.2 Hz), 2.99 (2H, t,
J=7.2 Hz), 1.87 (2H, sext., J=6.6 Hz), 1.41-1.32 (1H, m), 1.06 (3H,
t, J=6.6 Hz), 0.69-0.63 (2H, m), 0.40-0.35 (2H, m)
Example 199
[0676] Using
3-[2-(3-hydroxy-4-methoxyphenyl)oxazol-4-yl]-1-(2-propoxyphenyl)propan-1--
one obtained in Example 194, colorless needle crystalline
3-[2-(3-(3-butenyloxy)-4-methoxyphenyl)oxazol-4-yl]-1-(2-propoxyphenyl)pr-
opan-1-one was obtained in the same manner as in Example 102.
[0677] .sup.1H-NMR (CDCl.sub.3) .delta.: 7.71 (1H, dd, J=7.7, 1.5
Hz), 7.58 (1H, dd, J=8.5, 2.0 Hz), 7.52 (1H, d, J=2.0 Hz), 7.42
(1H, ddd, J=7.7, 7.5, 1.8 Hz), 7.40 (1H, s), 6.97 (1H, ddd, J=7.7,
7.5, 0.9 Hz), 6.93 (1H, br d, J=7.7 Hz), 6.91 (1H, d, J=8.5 Hz),
5.92 (1H, ddt, J=17.3, 10.3, 6.8 Hz), 5.19 (1H, ddd, J=17.3, 3.3,
1.5 Hz), 5.11 (1H, ddd, J=10.3, 3.3, 0.6 Hz), 4.14 (2H, t, J=7.2
Hz), 4.02 (2H, t, J=7.2 Hz), 3.91 (3H, s), 3.43 (2H, t, J=7.2 Hz),
2.99 (2H, t, J=7.2 Hz), 2.63 (2H, br q, J=6.9 Hz), 1.87 (2H, sext.,
J=7.2 Hz), 1.06 (3H, t, J=7.2 Hz)
Example 200
[0678] Using
3-[2-(3-hydroxy-4-methoxyphenyl)oxazol-4-yl]-1-(2-propoxyphenyl)propan-1--
one obtained in Example 194, colorless needle crystalline
3-[2-(3-allyloxy-4-methoxyphenyl)oxazol-4-yl]-1-(2-propoxyphenyl)propan-1-
-one was obtained in the same manner as in Example 102.
[0679] .sup.1H-NMR (CDCl.sub.3) .delta.: 7.71 (1H, dd, J=7.7, 1.8
Hz), 7.59 (1H, dd, J=8.5, 1.8 Hz), 7.52 (1H, d, J=1.8 Hz), 7.42
(1H, ddd, J=8.3, 7.7, 1.8 Hz), 7.40 (1H, s), 6.97 (1H, td, J=7.7,
1.1 Hz), 6.93 (1H, br d, J=8.3 Hz), 6.91 (1H, d, J=8.5 Hz), 6.12
(1H, ddt, J=17.3, 10.5, 5.5 Hz), 5.44 (1H, ddd, J=17.3, 3.0, 1.5
Hz), 5.31 (1H, ddd, J=10.5, 3.0, 1.5 Hz), 4.67 (2H, dt, J=5.5, 1.5
Hz), 4.02 (2H, t, J=6.3 Hz), 3.92 (3H, s), 3.43 (2H, t, J=7.2 Hz),
2.99 (2H, t, J=7.2 Hz), 1.87 (2H, sext., J=6.3 Hz), 1.06 (3H, t,
J=6.3 Hz)
Example 201
[0680] Using 0.1 g of
3-[2-(3-hydroxy-4-methoxyphenyl)oxazol-4-yl]-1-(2-propoxyphenyl)propan-1--
one obtained in Example 194, 67 mg of colorless powdery
3-[2-(3-cyclobutylmethoxy-4-methoxy
phenyl)oxazol-4-yl]-1-(2-propoxyphenyl)propan-1-one was obtained in
the same manner as in Example 111.
[0681] .sup.1H-NMR (CDCl.sub.3) .delta.: 7.71 (1H, dd, J=7.8, 1.8
Hz), 7.56 (1H, dd, J=7.8, 1.8 Hz), 7.52 (1H, d, J=1.8 Hz),
7.45-7.40 (2H, m), 6.98 (1H, t, J=7.8 Hz), 6.94 (1H, d, J=7.8 Hz),
6.90 (1H, d, J=7.8 Hz), 4.07 (2H, d, J=6.9 Hz), 4.02 (2H, t, J=6.6
Hz), 3.90 (3H, s), 3.44 (2H, t, J=7.2 Hz), 3.00 (2H, t, J=7.2 Hz),
2.86 (1H, quint, J=7.2 Hz), 2.21-2.16 (2H, m), 1.96-1.84 (6H, m),
1.06 (3H, t, J=7.5 Hz)
Example 202
[0682] Using
2-[4-methoxy-3-(2,2,2-trifluoroethoxy)phenyl]oxazole-4-carbaldehyde
obtained in Reference Example 65, pale yellow oily
(E)-3-{2-[4-methoxy-3-(2,2,2-trifluoroethoxy)phenyl]oxazol-4-yl}-1-(2-pro-
poxyphenyl)-2-propen-1-one was obtained in the same manner as in
Example 193.
[0683] .sup.1H-NMR (CDCl.sub.3) .delta.: 7.83 (1H, d, J=15.0 Hz),
7.81 (1H, s), 7.76 (1H, dd, J=8.4, 2.1 Hz), 7.69 (1H, dd, J=7.8,
1.8 Hz), 7.69 (1H, d, J=2.1 Hz), 7.50 (1H, d, J=15.0 Hz), 7.45 (1H,
ddd, J=8.4, 7.8, 1.8 Hz), 7.01 (1H, br t, J=8.4 Hz), 6.99 (1H, d,
J=8.4 Hz), 6.98 (1H, br d, J=7.8 Hz), 4.46 (2H, q, J=8.4 Hz), 4.06
(2H, t, J=6.3 Hz), 3.94 (3H, s), 1.90 (2H, sext., J=6.3 Hz), 1.09
(3H, t, J=6.3 Hz)
Example 203
[0684] Using (E)-3-{2-[4-methoxy-3-(2,2,2-trifluoroethoxy)
phenyl]oxazol-4-yl}-1-(2-propoxyphenyl)-2-propen-1-one obtained in
Example 202, colorless powdery
3-{2-[4-methoxy-3-(2,2,2-trifluoroethoxy)phenyl]oxazol-4-yl}-1-(2-propoxy-
phenyl)propan-1-one was obtained in the same manner as in Example
194.
[0685] .sup.1H-NMR (DMSO-d.sub.6) .delta.: 7.83 (1H, s), 7.62 (1H,
dd, J=7.8, 1.8 Hz), 7.57 (1H, dd, J=7.8, 1.5 Hz), 7.55 (1H, d,
J=1.5 Hz), 7.51 (1H, br t, J=7.8 Hz), 7.17 (1H, d, J=7.8 Hz), 7.15
(1H, d, J=7.8 Hz), 7.01 (1H, t, J=7.8 Hz), 4.80 (2H, q, J=9.0 Hz),
4.06 (2H, t, J=6.6 Hz), 3.86 (3H, s), 3.33 (2H, t, J=7.2 Hz), 2.84
(2H, t, J=7.2 Hz), 1.79 (2H, sext., J=6.6 Hz), 0.99 (3H, t, J=6.6
Hz)
Example 204
[0686] Using 2-(3,4-diethoxyphenyl)oxazole-4-carbaldehyde obtained
in Reference Example 66, pale yellow powdery
(E)-3-[2-(3,4-diethoxyphenyl)oxazol-4-yl]-1-(2-propoxyphenyl)-2-propen-1--
one was obtained in the same manner as in Example 193.
[0687] .sup.1H-NMR (CDCl.sub.3) .delta.: 7.81 (1H, d, J=15.0 Hz),
7.79 (1H, br d, J=7.5 Hz), 7.68 (1H, dd, J=7.8, 1.8 Hz), 7.62 (1H,
d, J=1.8 Hz), 7.59 (1H, br s), 7.49 (1H, d, J=15.0 Hz), 7.44 (1H,
br t, J=7.5 Hz), 7.01 (1H, br t, J=7.5 Hz), 6.97 (1H, br d, J=7.5
Hz), 6.93 (1H, d, J=7.8 Hz), 4.18 (2H, q, J=6.9 Hz), 4.16 (2H, q,
J=6.9 Hz), 4.05 (2H, t, J=6.3 Hz), 1.89 (1H, br sext., J=6.9 Hz),
1.50 (3H, t, J=6.9 Hz), 1.49 (3H, t, J=6.9 Hz), 1.09 (3H, t, J=7.2
Hz)
Example 205
[0688] Using
(E)-3-[2-(3,4-diethoxyphenyl)oxazol-4-yl]-1-(2-propoxyphenyl)-2-propen-1--
one obtained in Example 204, colorless powdery
3-[2-(3,4-diethoxyphenyl)oxazol-4-yl]-1-(2-propoxyphenyl)
propan-1-one was obtained in the same manner as in Example 194.
[0689] .sup.1H-NMR (CDCl.sub.3) .delta.: 7.60 (1H, dd, J=7.8, 1.8
Hz), 7.54 (1H, dd, J=8.4, 2.1 Hz), 7.52 (1H, d, J=2.1 Hz), 7.42
(1H, ddd, J=7.8, 7.2, 1.8 Hz), 7.39 (1H, s), 6.97 (1H, td, J=7.8,
1.2 Hz), 6.93 (1H, br d, J=7.2 Hz), 6.90 (1H, d, J=8.4 Hz), 4.17
(2H, q, J=6.9 Hz), 4.14 (2H, q, J=6.9 Hz), 4.02 (2H, t, J=6.6 Hz),
3.43 (2H, t, J=7.2 Hz), 2.99 (2H, t, J=7.2 Hz), 1.87 (2H, sept.,
J=6.6 Hz), 1.48 (6H, t, J=6.9 Hz), 1.05 (3H, t, J=6.6 Hz)
Example 206
[0690] Using 2-(3-benzyloxy-4-methoxyphenyl)oxazole-4-carbaldehyde
obtained in Reference Example 64, pale yellow powdery
(E)-3-[2-(3-benzyloxy-4-methoxyphenyl)oxazol-4-yl]-1-(2-isopropoxyphenyl)-
-2-propen-1-one was obtained in the same manner as in Example
193.
[0691] .sup.1H-NMR (CDCl.sub.3) .delta.: 7.79 (1H, s), 7.79 (1H, d,
J=15.3 Hz), 7.69-7.65 (3H, m), 7.50-7.32 (7H, m), 7.03-6.95 (3H,
m), 5.21 (2H, s), 4.66 (1H, sept, J=6.0 Hz), 3.94 (3H, s), 1.41
(6H, d, J=6.0 Hz)
Example 207
[0692] Using
(E)-3-[2-(3-benzyloxy-4-methoxyphenyl)oxazol-4-yl]-1-(2-isopropoxyphenyl)-
-2-propen-1-one obtained in Example 206, colorless powdery
3-[2-(3-hydroxy-4-methoxyphenyl)oxazol-4-yl]-1-(2-isopropoxyphenyl)propan-
-1-one was obtained in the same manner as in Example 194.
[0693] .sup.1H-NMR (CDCl.sub.3) .delta.: 7.67 (1H, dd, J=7.5, 1.8
Hz), 7.55 (1H, br s), 7.54 (1H, dd, J=7.5, 1.8 Hz), 7.40 (1H, td,
J=7.5, 1.8 Hz), 7.40 (1H, s), 6.95 (1H, br t, J=7.5 Hz), 6.93 (1H,
br d, J=7.5 Hz), 6.89 (1H, d, J=7.5 Hz), 5.64 (1H, s), 4.68 (1H,
sept., J=6.0 Hz), 3.94 (3H, s), 3.40 (2H, t, J=7.2 Hz), 2.98 (2H,
t, J=7.2 Hz), 1.40 (6H, d, J=6.0 Hz)
[0694] The above compound was also obtained by the following
method. A 10 g quantity of
2-(3-benzyloxy-4-methoxyphenyl-4-chloromethyloxazole obtained in
Reference Example 5 and 5.4 g of 1-(2-isopropoxyphenyl)ethanone
were dissolved in 100 ml of tetrahydrofuran, and 2.42 g of sodium
hydride was added thereto. After foaming, the reaction mixture was
heated and refluxed for 3 hours. After cooling, the reaction
mixture was added to ice water, and extraction was performed with
ethyl acetate. The organic layer was washed with water, dried over
magnesium sulfate, and then concentrated under reduced pressure.
The residue was purified by silica gel column chromatography
(n-hexane:ethyl acetate=3:1) to give 4.30 g of pale yellow oily
3-[2-(3-benzyloxy-4-methoxyphenyl)oxazol-4-yl]-1-(2-isopropoxyphenyl)prop-
an-1-one. Subsequently, 1.84 g of the obtained
3-[2-(3-benzyloxy-4-methoxyphenyl)oxazol-4-yl]-1-(2-isopropoxyphenyl)prop-
an-1-one was dissolved in 100 ml of methanol.
[0695] An 800 mg quantity of 10% palladium-carbon powder was added
thereto. The mixture was stirred under a hydrogen atmosphere at
room temperature for 1 hour. The catalyst was removed by
filtration, and the solvent was removed. The residue was then
recrystallized from acetone/diisopropyl ether to give 1.15 g of
3-[2-(3-hydroxy-4-methoxyphenyl)oxazol-4-yl]-1-(2-isopropoxyphenyl)propan-
-1-one.
Example 208
[0696] Using 0.15 g of
3-[2-(3-hydroxy-4-methoxyphenyl)oxazol-4-yl]-1-(2-isopropoxyphenyl)propan-
-1-one obtained in Example 207, 0.12 g of pale yellow oily
3-[2-(3-cyclopropylmethoxy-4-methoxyphenyl)oxazol-4-yl]-1-(2-isopropoxyph-
enyl)propan-1-one was obtained in the same manner as in Example
102.
[0697] .sup.1H-NMR (CDCl.sub.3) .delta.: 7.67 (1H, dd, J=7.8, 1.8
Hz), 7.57 (1H, dd, J=8.4, 2.1 Hz), 7.50 (1H, d, J=2.1 Hz), 7.41
(1H, td, J=7.8, 1.8 Hz), 7.39 (1H, s), 6.95 (1H, br t, J=7.8 Hz),
6.93 (1H, br d, J=7.8 Hz), 6.91 (1H, d, J=8.4 Hz), 4.68 (1H, sept.,
J=6.0 Hz), 3.92 (2H, d, J=6.9 Hz), 3.92 (3H, s), 3.41 (2H, t, J=7.2
Hz), 2.98 (2H, t, J=7.2 Hz), 1.40 (6H, d, J=6.0 Hz), 1.46-1.32 (1H,
m), 0.69-0.62 (2H, m), 0.40-0.35 (2H, m)
Example 209
[0698] Using 0.15 g of
3-[2-(3-hydroxy-4-methoxyphenyl)oxazol-4-yl]-1-(2-isopropoxyphenyl)propan-
-1-one obtained in Example 207, 42 mg of colorless powdery
3-[2-(3-ethoxy-4-methoxyphenyl)oxazol-4-yl]-1-(2-isopropoxyphenyl)propan--
1-one was obtained in the same manner as in Example 102.
[0699] .sup.1H-NMR (CDCl.sub.3) .delta.: 7.68 (1H, dd, J=7.7, 1.8
Hz), 7.57 (1H, dd, J=8.5, 2.0 Hz), 7.52 (1H, d, J=2.0 Hz), 7.41
(1H, td, J=7.7, 1.8 Hz), 7.40 (1H, s), 6.95 (1H, br t, J=7.7 Hz),
6.94 (1H, br d, J=7.7 Hz), 6.91 (1H, d, J=8.5 Hz), 4.69 (1H, sept.,
J=6.0 Hz), 4.18 (2H, q, J=6.9 Hz), 3.92 (3H, s), 3.41 (2H, t, J=6.9
Hz), 2.99 (2H, t, J=6.9 Hz), 1.49 (3H, t, J=6.9 Hz), 1.40 (6H, d,
J=6.0 Hz)
Example 210
[0700] Using
3-[2-(3-hydroxy-4-methoxyphenyl)oxazol-4-yl]-1-(2-isopropoxyphenyl)propan-
-1-one obtained in Example 207, pale yellow oily
3-[2-(3-isopropoxy-4-methoxyphenyl)oxazol-4-yl]-1-(2-isopropoxyphenyl)pro-
pan-1-one was obtained in the same manner as in Example 102.
[0701] .sup.1H-NMR (CDCl.sub.3) .delta.: 7.68 (1H, dd, J=7.5, 1.8
Hz), 7.57 (1H, dd, J=7.5, 1.8 Hz), 7.54 (1H, d, J=1.8 Hz),
7.44-7.38 (2H, m), 6.95 (1H, br t, J=7.5 Hz), 6.94 (1H, d, J=7.5
Hz), 6.91 (1H, d, J=7.5 Hz), 4.67 (2H, sept., J=6.0 Hz), 3.90 (3H,
s), 3.40 (2H, t, J=7.2 Hz), 2.98 (2H, t, J=7.2 Hz), 1.40 (12H, d,
J=6.0 Hz)
Example 211
[0702] Using
3-[2-(3-hydroxy-4-methoxyphenyl)oxazol-4-yl]-1-(2-isopropoxyphenyl)propan-
-1-one obtained in Example 207, colorless oily
3-[2-(3-allyloxy-4-methoxyphenyl)oxazol-4-yl]-1-(2-isopropoxyphenyl)propa-
n-1-one was obtained in the same manner as in Example 102.
[0703] .sup.1H-NMR (CDCl.sub.3) .delta.: 7.68 (1H, dd, J=7.7, 1.8
Hz), 7.58 (1H, dd, J=8.3, 1.8 Hz), 7.53 (1H, d, J=1.8 Hz), 7.41
(1H, ddd, J=7.9, 7.7, 1.8 Hz), 7.40 (1H, s), 6.98 (1H, td, J=7.9,
1.8 Hz), 6.94 (1H, br d, J=7.7 Hz), 6.92 (1H, d, J=8.3 Hz), 6.12
(1H, ddt, J=17.3, 10.5, 5.3 Hz), 5.44 (1H, ddd, J=17.3, 3.0, 1.7
Hz), 5.31 (1H, ddd, J=10.5, 3.0, 1.5 Hz), 4.75-4.60 (3H, m), 3.92
(3H, s), 3.41 (2H, t, J=7.2 Hz), 2.99 (2H, t, J=7.2 Hz), 1.40 (6H,
d, J=6.0 Hz).
Example 212
[0704] Using
3-[2-(3-hydroxy-4-methoxyphenyl)oxazol-4-yl]-1-(2-isopropoxyphenyl)propan-
-1-one obtained in Example 207, colorless needle crystalline
3-[2-(3-(3-butenyloxy)-4-methoxyphenyl)oxazol-4-yl]-1-(2-isopropoxyphenyl-
)propan-1-one was obtained in the same manner as in Example
102.
[0705] .sup.1H-NMR (CDCl.sub.3) .delta.: 7.67 (1H, dd, J=7.9, 1.8
Hz), 7.57 (1H, dd, J=8.5, 2.0 Hz), 7.53 (1H, d, J=2.0 Hz), 7.40
(1H, ddd, J=7.9, 7.5, 1.8 Hz), 7.40 (1H, s), 6.95 (1H, br t, J=7.5
Hz), 6.93 (1H, br d, J=7.5 Hz), 6.91 (1H, d, J=8.5 Hz), 5.92 (1H,
ddt, J=17.1, 10.3, 6.8 Hz), 5.19 (1H, ddd, J=17.3, 3.3, 1.5 Hz),
5.10 (1H, ddd, J=10.3, 3.3, 1.3 Hz), 4.68 (1H, sept., J=6.0 Hz),
4.14 (2H, t, J=7.2 Hz), 3.91 (3H, s), 3.41 (2H, t, J=7.2 Hz), 3.01
(2H, t, J=7.2 Hz), 2.63 (2H, br q, J=7.2 Hz), 1.40 (6H, d, J=6.0
Hz)
Example 213
[0706] Using 0.15 g of
3-[2-(3-hydroxy-4-methoxyphenyl)oxazol-4-yl]-1-(2-isopropoxyphenyl)propan-
-1-one obtained in Example 207, mg of colorless powdery
1-(2-isopropoxyphenyl)-3-{2-[4-methoxy-3-(2,2,2-trifluoroethoxy)phenyl]ox-
azol-4-yl}propan-1-one was obtained in the same manner as in
Example 111.
[0707] .sup.1H-NMR (CDCl.sub.3) .delta.: 7.70-7.60 (2H, m),
7.44-7.38 (2H, m), 6.98-6.91 (4H, m), 4.69 (1H, sept., J=6.0 Hz),
4.48-4.41 (2H, m), 3.93 (3H, s), 3.42 (2H, t, J=7.2 Hz), 3.00 (2H,
t, J=7.2 Hz), 1.41 (6H, d, J=6.0 Hz)
Example 214
[0708] Using
3-[2-(3-hydroxy-4-methoxyphenyl)oxazol-4-yl]-1-(2-isopropoxyphenyl)propan-
-1-one obtained in Example 207, colorless powdery
3-[2-(3-cyclobutylmethoxy-4-methoxyphenyl)
oxazol-4-yl]-1-(2-isopropoxyphenyl)propan-1-one was obtained in the
same manner as in Example 111.
[0709] .sup.1H-NMR (CDCl.sub.3) .delta.: 7.68 (1H, dd, J=8.4, 1.8
Hz), 7.56 (1H, dd, J=8.4, 1.8 Hz), 7.52 (1H, d, J=1.8 Hz),
7.44-7.38 (2H, m), 6.95 (1H, br t, J=8.4 Hz), 6.94 (1H, br d, J=8.4
Hz), 6.90 (1H, d, J=8.4 Hz), 4.69 (1H, sept., J=6.0 Hz), 4.07 (2H,
d, J=6.9 Hz), 3.90 (3H, s), 3.41 (2H, t, J=7.2 Hz), 2.99 (2H, t,
J=7.2 Hz), 2.86 (1H, quint, J=7.2 Hz), 2.22-2.14 (2H, m), 1.99-1.84
(4H, m), 1.40 (6H, d, J=6.0 Hz)
Example 215
[0710] Using 2-(3,4-diethoxyphenyl)oxazole-4-carbaldehyde obtained
in Reference Example 66, yellow oily
(E)-3-[2-(3,4-diethoxyphenyl)oxazol-4-yl]-1-(2-isopropoxyphenyl)-2-propen-
-1-one was obtained in the same manner as in Example 193.
[0711] .sup.1H-NMR (CDCl.sub.3) .delta.: 7.81 (1H, d, J=15.3 Hz),
7.79 (1H, br s), 7.69-7.53 (3H, m), 7.46 (1H, d, J=15.3 Hz), 7.43
(1H, td, J=7.8, 1.2 Hz), 7.00 (1H, br t, J=7.8 Hz), 6.93 (1H, br d,
J=7.8 Hz), 6.91 (1H, br d, J=7.8 Hz), 4.67 (1H, sept, J=6.0 Hz),
4.22-4.11 (4H, m), 1.52-1.45 (6H, m), 1.41 (6H, d, J=6.0 Hz)
Example 216
[0712] Using
(E)-3-[2-(3,4-diethoxyphenyl)oxazol-4-yl]-1-(2-isopropoxyphenyl)-2-propen-
-1-one obtained in Example 215, pale yellow oily
3-[2-(3,4-diethoxyphenyl)oxazol-4-yl]-1-(2-isopropoxy
phenyl)propan-1-one was obtained in the same manner as in Example
194.
[0713] .sup.1H-NMR (CDCl.sub.3) .delta.: 7.67 (1H, dd, J=7.5, 1.5
Hz), 7.60-7.38 (4H, m), 6.97-6.89 (3H, m), 4.68 (1H, sept, J=6.0
Hz), 4.21-4.10 (4H, m), 3.41 (2H, t, J=7.2 Hz), 2.98 (2H, t, J=7.2
Hz), 1.48 (6H, br t, J=7.2 Hz), 1.40 (6H, d, J=6.0 Hz)
Example 217
[0714] Using 2-(3,4-diethoxyphenyl)oxazole-4-carbaldehyde obtained
in Reference Example 66, colorless powdery
(E)-3-[2-(3,4-diethoxyphenyl)oxazol-4-yl]-1-o-tolyl-2-propen-1-one
was obtained in the same manner as in Example 193.
[0715] .sup.1H-NMR (CDCl.sub.3) .delta.: 7.81 (1H, s), 7.64-7.28
(8H, m), 6.93 (1H, d, J=8.1 Hz), 4.20 (2H, q, J=6.9 Hz), 4.16 (2H,
q, J=6.9 Hz), 2.47 (3H, s), 1.50 (3H, t, J=6.9 Hz), 1.49 (3H, t,
J=6.9 Hz)
Example 218
[0716] Using
(E)-3-[2-(3,4-diethoxyphenyl)oxazol-4-yl]-1-o-tolyl-2-propen-1-one
obtained in Example 217, colorless needle crystalline
3-[2-(3,4-diethoxyphenyl)oxazol-4-yl]-1-o-tolyl propan-1-one was
obtained in the same manner as in Example 194.
[0717] .sup.1H-NMR (CDCl.sub.3) .delta.: 7.68 (1H, dd, J=7.5, 1.8
Hz), 7.55 (1H, dd, J=8.1, 1.8 Hz), 7.51 (1H, d, J=1.8 Hz), 7.43
(1H, br s), 7.36 (1H, td, J=7.5, 1.5 Hz), 7.27-7.22 (2H, m), 6.90
(1H, d, J=8.1 Hz), 4.17 (2H, q, J=6.9 Hz), 4.14 (2H, q, J=6.9 Hz),
3.32 (2H, t, J=7.2 Hz), 3.00 (2H, t, J=7.2 Hz), 2.49 (3H, s), 1.48
(6H, t, J=6.9 Hz)
Example 219
[0718] Using 2-(3-benzyloxy-4-methoxyphenyl)oxazole-4-carbaldehyde
obtained in Reference Example 64, pale yellow powdery
(E)-3-[2-(3-benzyloxy-4-methoxyphenyl)oxazol-4-yl]-1-o-tolyl-2-propen-1-o-
ne was obtained in the same manner as in Example 193.
[0719] .sup.1H-NMR (CDCl.sub.3) .delta.: 7.81 (1H, s), 7.69-7.26
(13H, m), 6.96 (1H, d, J=9.0 Hz), 5.23 (2H, s), 3.94 (3H, s), 2.47
(3H, s)
Example 220
[0720] Using
(E)-3-[2-(3-benzyloxy-4-methoxyphenyl)oxazol-4-yl]-1-o-tolyl-2-propen-1-o-
ne obtained in Example 219, colorless powdery
3-[2-(3-hydroxy-4-methoxyphenyl)oxazol-4-yl]-1-o-tolyl propan-1-one
was obtained in the same manner as in Example 194.
[0721] .sup.1H-NMR (CDCl.sub.3) .delta.: 7.67 (1H, dd, J=7.2, 1.8
Hz), 7.56 (1H, d, J=1.8 Hz), 7.53 (1H, dd, J=8.1, 1.8 Hz), 7.43
(1H, s), 7.35 (1H, td, J=7.2, 1.8 Hz), 7.26-7.22 (2H, m), 6.89 (1H,
d, J=8.1 Hz), 5.69 (1H, s), 3.94 (3H, s), 3.31 (2H, t, J=7.2 Hz),
3.00 (2H, t, J=7.2 Hz), 2.49 (3H, s)
Example 221
[0722] A 0.15 g quantity of
3-[2-(3-hydroxy-4-methoxyphenyl)oxazol-4-yl]-1-o-tolylpropan-1-one
obtained in Example 220 was dissolved in 10 ml of isopropyl
alcohol. An 86 .mu.l quantity of (bromomethyl)cyclopropane and 200
.mu.l of 1,8-diazabicyclo[5,4,0]undec-7-ene were added thereto, and
the mixture was heated and refluxed for 24 hours. Water was added
to the reaction mixture, and extraction was then performed with
ethyl acetate. The organic layer was washed with saturated brine,
dried over anhydrous magnesium sulfate, and concentrated under
reduced pressure. The residue was purified by silica gel column
chromatography (n-hexane:ethyl acetate=3:1), and recrystallized
from acetone/diisopropyl ether/n-hexane to give 71 mg of colorless
needle crystalline
3-[2-(3-cyclopropylmethoxy-4-methoxyphenyl)oxazol-4-yl]-1-o-tolylpropan-1-
-one.
[0723] .sup.1H-NMR (CDCl.sub.3) .delta.: 7.68 (1H, dd, J=7.5, 1.5
Hz), 7.57 (1H, dd, J=8.1, 2.1 Hz), 7.49 (1H, d, J=2.1 Hz), 7.43
(1H, t, J=0.9 Hz), 7.36 (1H, td, J=7.5, 1.5 Hz), 7.25-7.22 (2H, m),
6.91 (1H, d, J=8.1 Hz), 3.93 (2H, d, J=6.9 Hz), 3.92 (3H, s), 3.32
(2H, t, J=7.2 Hz), 3.00 (2H, t, J=7.2 Hz), 2.49 (3H, s), 1.41-1.32
(1H, m), 0.69-0.63 (2H, m), 0.40-0.35 (2H, m)
Example 222
[0724] Using 2-(3-isopropoxy-4-methoxyphenyl)oxazole-4-carbaldehyde
obtained in Reference Example 69, yellow powdery
(E)-3-[2-(3-isopropoxy-4-methoxyphenyl)oxazol-4-yl]-1-(2-benzyloxyphenyl)-
-2-propen-1-one was obtained in the same manner as in Example
193.
[0725] .sup.1H-NMR (CDCl.sub.3) .delta.: 7.76 (1H, s), 7.69-6.92
(14H, m), 5.20 (2H, s), 4.63 (1H, sept., J=6.0 Hz), 1.38 (6H, d,
J=6.0 Hz)
Example 223
[0726] Using
(E)-3-[2-(3-isopropoxy-4-methoxyphenyl)oxazol-4-yl]-1-(2-benzyloxyphenyl)-
-2-propen-1-one obtained in Example 222, colorless plate
crystalline
1-(2-hydroxyphenyl)-3-[2-(3-isopropoxy-4-methoxyphenyl)oxazol-4-yl]propan-
-1-one was obtained in the same manner as in Example 194.
[0727] .sup.1H-NMR (CDCl.sub.3) .delta.:12.25 (1H, s), 7.82 (1H,
dd, J=8.4, 1.5 Hz), 7.58 (1H, dd, J=8.4, 1.8 Hz), 7.54 (1H, d,
J=1.8 Hz), 7.46 (1H, ddd, J=8.4, 7.2, 1.5 Hz), 7.45 (1H, s), 6.98
(1H, dd, J=8.4, 1.2 Hz), 6.92 (1H, d, J=8.4 Hz), 6.89 (1H, ddd,
J=8.4, 7.2, 1.2 Hz), 4.65 (1H, sept., J=6.0 Hz), 3.90 (3H, s), 3.44
(2H, t, J=7.5 Hz), 3.03 (2H, t, J=7.5 Hz), 1.40 (6H, d, J=6.0
Hz)
Example 224
[0728] A 67 mg quantity of
1-(2-hydroxyphenyl)-3-[2-(3-isopropoxy-4-methoxyphenyl)oxazol-4-yl]propan-
-1-one obtained in Example 223 was dissolved in 5 ml of
dimethylformamide. A 31 .mu.l quantity of allyl bromide and 73 mg
of potassium carbonate were added thereto, and the mixture was
stirred at room temperature overnight. A 50 .mu.l quantity of allyl
bromide was further added thereto, and the mixture was stirred at
50.degree. C. for 8 hours, and at room temperature overnight. The
reaction mixture was added to water, and extraction was then
performed with ethyl acetate. The organic layer was washed with
saturated brine, dried over anhydrous magnesium sulfate, and the
solvent was removed under reduced pressure. The residue was
purified by silica gel column chromatography (n-hexane:ethyl
acetate=3:1), and crystallized from n-hexane to give 33 mg of
colorless powdery
1-(2-allyloxyphenyl)-3-[2-(3-isopropoxy-4-methoxyphenyl)oxazol-4-yl]propa-
n-1-one.
[0729] .sup.1H-NMR (CDCl.sub.3) .delta.: 7.70 (1H, dd, J=7.8, 1.8
Hz), 7.57 (1H, dd, J=8.4, 2.1 Hz), 7.54 (1H, d, J=2.1 Hz), 7.44
(1H, ddd, J=7.8, 7.5, 1.8 Hz), 7.40 (1H, br s), 6.99 (1H, td,
J=7.8, 1.2 Hz), 6.94 (1H, br d, J=7.5 Hz), 6.91 (1H, d, J=8.4 Hz),
6.08 (1H, ddt, J=17.1, 10.5, 5.4 Hz), 5.42 (1H, ddd, J=17.1, 3.0,
1.5 Hz), 5.29 (1H, ddd, J=10.5, 2.7, 1.5 Hz), 4.69-4.61 (3H, m),
3.89 (3H, s), 3.42 (2H, t, J=7.2 Hz), 2.99 (2H, t, J=7.2 Hz), 1.39
(6H, d, J=6.3 Hz)
Example 225
[0730] Using 0.3 g of
3-[2-(3-hydroxy-4-methoxyphenyl)oxazol-4-yl]-1-o-tolylpropan-1-one
obtained in Example 220, 0.15 g of white powdery
3-[2-(3-ethoxy-4-methoxyphenyl)oxazol-4-yl]-1-o-tolylpropan-1-one
was obtained in the same manner as in Example 3.
[0731] .sup.1H-NMR (CDCl.sub.3) .delta.: 7.68 (1H, m), 7.57 (1H,
dd, J=8.1, 2.1 Hz), 7.51 (1H, d, J=2.1 Hz), 7.44 (1H, d, J=0.9 Hz),
7.36 (1H, m), 7.30-7.20 (3H, m), 6.91 (1H, d, J=8.4 Hz), 4.18 (2H,
q, J=6.9 Hz), 3.92 (3H, s), 3.35-3.25 (2H, m), 3.05-2.95 (2H, m),
2.50 (3H, s), 1.50 (3H, t, J=6.9 Hz)
Example 226
[0732] Using 0.3 g of
3-[2-(3-hydroxy-4-methoxyphenyl)oxazol-4-yl]-1-o-tolylpropan-1-one
obtained in Example 220, 0.1 g of white powdery
3-[2-(3-allyloxy-4-methoxyphenyl)oxazol-4-yl]-1-o-tolylpropan-1-one
was obtained in the same manner as in Example 3.
[0733] .sup.1H-NMR (CDCl.sub.3) .delta.: 7.68 (1H, m), 7.59 (1H,
dd, J=8.4, 2.1 Hz), 7.52 (1H, d, J=2.1 Hz), 7.43 (1H, s), 7.38 (1H,
m), 7.35-7.25 (2H, m), 6.92 (1H, d, J=8.4 Hz), 6.13 (1H, ddd,
J=17.1, 10.5, 5.4 Hz), 5.44 (1H, ddd, J=17.1, 2.7, 1.5 Hz), 5.31
(1H, ddd, J=10.5, 2.7, 1.5 Hz), 4.68 (1H, dt, J=5.4, 1.5 Hz), 3.92
(3H, s), 3.32 (2H, t, J=7.2 Hz), 3.00 (2H, t, J=7.2 Hz), 2.50 (3H,
s)
Example 227
[0734] Using 0.2 g of
3-[2-(3-hydroxy-4-methoxyphenyl)oxazol-4-yl]-1-o-tolylpropan-1-one
obtained in Example 220, 0.1 g of pale yellow oily
3-[2-(3-isopropoxy-4-methoxyphenyl)oxazol-4-yl]-1-o-tolylpropan-1-one
was obtained in the same manner as in Example 3.
[0735] .sup.1H-NMR (CDCl.sub.3) .delta.: 7.69 (1H, m), 7.60-7.50
(2H, m), 7.50-7.30 (3H, m), 7.24 (1H, m), 6.91 (1H, dd, J=5.1, 3.0
Hz), 4.65 (1H, m), 3.90 (3H, s), 3.35-3.25 (2H, m), 3.05-2.95 (2H,
m), 2.49 (3H, s), 1.40 (6H, d, J=6.0 Hz)
Example 228
[0736] A 65 mg quantity of sodium hydride was suspended in 5 ml of
tetrahydrofuran. A 0.27 g quantity of 1-(2-ethoxyphenyl)ethanone
and 0.3 g of 2-(3-benzyloxy-4-difluoro
methoxyphenyl)-4-chloromethyloxazole obtained in Reference Example
44 was successively added thereto with ice-cooling and stirring,
and the mixture was stirred for 3 hours with heating and refluxing.
An aqueous saturated ammonium chloride solution was added to the
reaction mixture with ice-cooling and stirring. After stirring for
15 minutes, water was added thereto, and extraction was performed
with ethyl acetate. The mixture was dried over anhydrous magnesium
sulfate, and the solvent was removed. The obtained residue was
purified by silica gel column chromatography (n-hexane:ethyl
acetate=4:1) to give 75 mg of colorless oily
3-[2-(3-benzyloxy-4-difluoromethoxyphenyl)
oxazol-4-yl]-1-(2-ethoxyphenyl)propan-1-one.
[0737] .sup.1H-NMR (CDCl.sub.3) .delta.: 7.72-7.69 (2H, m), 7.59
(1H, dd, J=8.1, 1.8 Hz), 7.47-7.32 (7H, m), 7.00-6.92 (3H, m), 6.61
(1H, t, J=74.7 Hz), 5.20 (2H, s), 4.15 (2H, q, J=7.2 Hz), 3.43 (2H,
t, J=7.2 Hz), 3.00 (2H, t, J=7.2 Hz), 1.48 (3H, t, J=7.2 Hz)
Example 229
[0738] A 75 mg quantity of
3-[2-(3-benzyloxy-4-difluoromethoxyphenyl)oxazol-4-yl]-1-(2-ethoxyphenyl)-
propan-1-one obtained in Example 228 was dissolved in 1 ml of
ethanol. A 7 mg quantity of 10% palladium-carbon powder was added
thereto, and the mixture was stirred under a hydrogen atmosphere at
room temperature for 45 minutes. The catalyst was removed by
filtration, the filtrate was concentrated, and the obtained residue
was purified by silica gel column chromatography
(dichloromethane:ethanol=100:1) to give 32 mg of white powdery
3-[2-(4-difluoromethoxy-3-hydroxyphenyl)oxazol-4-yl]-1-(2-ethoxyp-
henyl)propan-1-one.
[0739] .sup.1H-NMR (CDCl.sub.3) .delta.: 7.70 (1H, dd, J=7.5, 1.8
Hz), 7.65 (1H, d, J=1.8 Hz), 7.56-7.43 (3H, m), 7.16 (1H, d, J=6.0
Hz), 6.98-6.92 (2H, m), 6.57 (1H, t, J=74.7 Hz), 5.57 (1H, s), 4.13
(2H, q, J=7.2 Hz), 3.42 (2H, t, J=7.2 Hz), 3.00 (2H, t, J=7.2 Hz),
1.48 (3H, t, J=7.2 Hz)
Example 230
[0740] A 30 mg quantity of
3-[2-(4-difluoromethoxy-3-hydroxyphenyl)oxazol-4-yl]-1-(2-ethoxyphenyl)pr-
opan-1-one obtained in Example 229 was dissolved in 0.5 ml of
dimethylformamide. An 18 mg quantity of 2-bromopropane and 30 mg of
potassium carbonate were added thereto, and the mixture was stirred
at room temperature overnight. Water was added to the reaction
mixture, and extraction was performed with ethyl acetate. Drying
was performed with anhydrous magnesium sulfate, and the solvent was
removed. The obtained residue was purified by silica gel column
chromatography (n-hexane:ethyl acetate=4:1) to give 23 mg of white
powdery
3-[2-(4-difluoromethoxy-3-isopropoxyphenyl)oxazol-4-yl]-1-(2-ethoxyphenyl-
)propan-1-one.
[0741] .sup.1H-NMR (CDCl.sub.3) .delta.: 7.70 (1H, dd, J=7.8, 1.8
Hz), 7.61 (1H, d, J=1.8 Hz), 7.55 (1H, dd, J=8.4, 1.8 Hz),
7.50-7.38 (2H, m), 7.19 (1H, d, J=8.1 Hz), 7.00-6.70 (2H, m), 6.60
(1H, t, J=74.7 Hz), 4.72-4.64 (1H, m), 4.13 (2H, q, J=7.2 Hz), 3.42
(2H, t, J=7.2 Hz), 3.00 (2H, t, J=7.2 Hz), 1.48 (3H, t, J=7.2 Hz),
1.39 (6H, d, J=6.0 Hz)
Example 231
[0742] Using 2-(3-benzyloxy-4-methoxyphenyl)-4-chloromethyl oxazole
obtained in Reference Example 5 and 1-(2-methoxymethoxy
phenyl)ethanone obtained in Reference Example 70, yellow oily
3-[2-(3-benzyloxy-4-methoxyphenyl)oxazol-4-yl]-1-(2-methoxymethoxy
phenyl)propan-1-one was obtained in the same manner as in Example
190.
[0743] .sup.1H-NMR (CDCl.sub.3) .delta.: 7.66 (1H, dd, J=7.8, 1.8
Hz), 7.59 (1H, dd, J=7.8, 1.8 Hz), 7.51 (1H, br s), 7.49-7.27 (7H,
m), 7.17 (1H, br d, J=7.8 Hz), 7.04 (1H, td, J=7.5, 1.2 Hz), 6.93
(1H, br d, J=7.8 Hz), 5.25 (2H, s), 5.19 (2H, s), 3.92 (3H, s),
3.48 (3H, s), 3.39 (2H, t, J=7.2 Hz), 3.00 (2H, t, J=7.2 Hz)
Example 232
[0744] Using
3-[2-(3-benzyloxy-4-methoxyphenyl)oxazol-4-yl]-1-(2-methoxymethoxyphenyl)-
propan-1-one obtained in Example 231,
3-[2-(3-hydroxy-4-methoxyphenyl)oxazol-4-yl]-1-(2-methoxymethoxy
phenyl)propan-1-one was obtained in the same manner as in Example
194.
[0745] .sup.1H-NMR (CDCl.sub.3) .delta.: 7.66 (1H, dd, J=7.8, 1.8
Hz), 7.55 (1H, d, J=2.1 Hz), 7.53 (1H, dd, J=8.1, 2.1 Hz), 7.41
(1H, s), 7.41 (1H, ddd, J=7.8, 7.5, 1.8 Hz), 7.17 (1H, br d, J=7.8
Hz), 7.04 (1H, td, J=7.5, 0.8 Hz), 6.89 (1H, d, J=8.1 Hz), 5.64
(1H, s), 5.26 (2H, s), 3.94 (3H, s), 3.49 (3H, s), 3.40 (2H, t,
J=7.2 Hz), 2.99 (2H, t, J=7.2 Hz)
Example 233
[0746] Using
3-[2-(3-hydroxy-4-methoxyphenyl)oxazol-4-yl]-1-(2-methoxymethoxyphenyl)pr-
opan-1-one obtained in Example 232, colorless oily
3-[2-(3-isopropoxy-4-methoxyphenyl)oxazol-4-yl]-1-(2-methoxymethoxyphenyl-
)propan-1-one was obtained in the same manner as in Example
102.
[0747] .sup.1H-NMR (CDCl.sub.3) .delta.: 7.66 (1H, dd, J=7.5, 1.8
Hz), 7.57 (1H, dd, J=8.4, 1.8 Hz), 7.53 (1H, d, J=1.8 Hz), 7.42
(1H, ddd, J=8.4, 7.5, 1.8 Hz), 7.41 (1H, s), 7.17 (1H, dd, J=8.4,
1.2 Hz), 7.04 (1H, td, J=7.5, 1.2 Hz), 6.91 (1H, d, J=8.4 Hz), 5.26
(2H, s), 4.64 (1H, sept, J=6.0 Hz), 3.90 (3H, s), 3.49 (3H, s),
3.40 (2H, t, J=7.2 Hz), 3.00 (2H, t, J=7.2 Hz), 1.39 (6H, d, J=6.0
Hz)
Example 234
[0748] Using 0.76 g of
4-chloromethyl-2-(3-ethoxy-4-methoxyphenyl)oxazole obtained in
Reference Example 58, 60 mg of white powdery
3-[2-(3-ethoxy-4-methoxyphenyl)oxazol-4-yl]-1-[2-(2,2,2-trifluoroethoxy)p-
henyl]propan-1-one was obtained in the same manner as in Example
228.
[0749] .sup.1H-NMR (CDCl.sub.3) .delta.: 7.76 (1H, dd, J=7.8, 2.1
Hz), 7.58-7.48 (3H, m), 7.39 (1H, s), 7.12 (1H, t, J=7.5 Hz),
6.92-6.88 (2H, m), 4.46 (2H, q, J=7.8 Hz), 4.18 (2H, q, J=7.2 Hz),
3.92 (3H, s), 3.40 (2H, t, J=7.5 Hz), 3.00 (2H, t, J=7.5 Hz), 1.49
(3H, t, J=7.2 Hz)
Example 235
[0750] Using 0.76 g of
4-chloromethyl-2-(3-ethoxy-4-methoxyphenyl)oxazole obtained in
Reference Example 58 and 0.58 g of
1-(2-trifluoromethoxyphenyl)ethanone, 0.18 g of pale yellow oily
3-[2-(3-ethoxy-4-methoxyphenyl)oxazol-4-yl]-1-(2-trifluoro
methoxyphenyl)propan-1-one was obtained in the same manner as in
Example 228.
[0751] .sup.1H-NMR (CDCl.sub.3) .delta.: 7.71 (1H, dd, J=7.5, 1.8
Hz), 7.58-7.50 (3H, m), 7.42 (1H, s), 7.38-7.30 (2H, m), 6.91 (1H,
d, J=8.4 Hz), 4.17 (2H, q, J=6.6 Hz), 3.91 (3H, s), 3.45 (2H, t,
J=7.2 Hz), 3.01 (2H, t, J=7.2 Hz), 1.49 (3H, t, J=6.6 Hz)
Example 236
[0752] Using 0.5 g of
3-[2-(3,4-dimethoxyphenyl)oxazol-4-yl]propionic acid obtained in
Reference Example 71, 0.32 g of white powdery
3-[2-(3,4-diethoxyphenyl)oxazol-4-yl]-1-pyrrolidin-1-yl-propan-1-one
was obtained in the same manner as in Example 1.
[0753] .sup.1H-NMR (CDCl.sub.3) .delta.: 7.55 (1H, dd, J=6.75, 1.8
Hz), 7.52 (1H, d, J=1.8 Hz), 7.44 (1H, s), 6.91 (1H, d, J=8.1 Hz),
4.20-4.10 (4H, m), 3.50-3.40 (4H, m), 3.00-2.90 (2H, m), 2.70-2.60
(2H, m), 1.95-1.75 (4H, m), 1.48 (3H, t, J=7.2 Hz), 1.48 (3H, t,
J=7.2 Hz)
Example 237
[0754] Using 0.3 g of
3-[2-(3,4-dimethoxyphenyl)oxazol-4-yl]propionic acid obtained in
Reference Example 71, 0.28 g of white powdery
3-[2-(3,4-diethoxyphenyl)oxazol-4-yl]-1-(3-hydroxy
pyrrolidin-1-yl)propan-1-one was obtained in the same manner as in
Example 1.
[0755] .sup.1H-NMR (CDCl.sub.3) .delta.: 7.55 (1H, dd, J=6.75, 1.8
Hz), 7.52 (1H, d, J=1.8 Hz), 7.44 (1H, s), 6.91 (1H, d, J=8.1 Hz),
4.20-4.10 (4H, m), 3.50-3.40 (4H, m), 3.00-2.90 (2H, m), 2.70-2.60
(2H, m), 2.10-1.90 (3H, m), 1.48 (3H, t, J=6.9 Hz), 1.48 (3H, t,
J=6.9 Hz)
Example 238
[0756] Using 1 g of
3-[2-(4-benzyloxy-3-methoxyphenyl)oxazol-4-yl]propionic acid
obtained in Reference Example 73, 1.03 g of pale yellow powdery
3-[2-(4-benzyloxy-3-methoxyphenyl)oxazol-4-yl]-1-pyrrolidin-1-ylpropan-1--
one was obtained in the same manner as in Example 1.
[0757] .sup.1H-NMR (CDCl.sub.3) .delta.: 7.61-7.27 (8H, m), 6.93
(1H, d, J=8.4 Hz), 5.20 (2H, s), 3.97 (3H, s), 3.49-3.39 (4H, m),
2.94 (2H, t, J=7.5 Hz), 2.65 (2H, t, J=7.5 Hz), 1.95-1.78 (4H,
m)
Example 239
[0758] Using 1 g of
3-[2-(4-benzyloxy-3-methoxyphenyl)oxazol-4-yl]-1-pyrrolidin-1-yl-propan-1-
-one obtained in Example 238, 0.59 g of white powdery
3-[2-(4-hydroxy-3-methoxyphenyl)oxazol-4-yl]-1-pyrrolidin-1-ylpropan-1-on-
e was obtained in the same manner as in Example 2.
[0759] .sup.1H-NMR (CDCl.sub.3) .delta.: 7.56-7.51 (2H, m), 7.44
(1H, s), 6.90 (1H, d, J=8.4 Hz), 5.97 (1H, s), 3.97 (3H, s),
3.49-3.39 (4H, m), 2.94 (2H, t, J=7.5 Hz), 2.66 (2H, t, J=7.5 Hz),
1.97-1.79 (4H, m)
Example 240
[0760] Using 0.15 g of
3-[2-(4-hydroxy-3-methoxyphenyl)oxazol-4-yl]-1-pyrrolidin-1-yl-propan-1-o-
ne obtained in Example 239, 0.13 g of white powdery
3-[2-(4-ethoxy-3-methoxyphenyl)oxazol-4-yl]-1-pyrrolidin-1-ylpropan-1-one
was obtained in the same manner as in Example 3.
[0761] .sup.1H-NMR (CDCl.sub.3) .delta.: 7.57 (1H, dd, J=8.1, 2.1
Hz), 7.52 (1H, d, J=1.8 Hz), 7.45 (1H, s), 6.91 (1H, d, J=8.1 Hz),
4.15 (2H, q, J=6.9 Hz), 3.96 (3H, s), 3.49-3.40 (4H, m), 2.94 (2H,
t, J=7.2 Hz), 2.66 (2H, t, J=7.2 Hz), 1.97-1.79 (4H, m), 1.49 (3H,
t, J=6.9 Hz)
Example 241
[0762]
N-[2-(3-cyclopropylmethoxy-4-methoxyphenyl)oxazol-4-ylmethyl]-2-tri-
fluoromethylbenzamide obtained in Example 25 was dissolved in 1 ml
of dimethylformamide. A 30 mg quantity of sodium hydride was added
thereto with ice-cooling and stirring, and the mixture was stirred
for 30 minutes. A 30 mg quantity of methyl iodide was added
thereto, and the reaction mixture was stirred at room temperature
for 2 hours. Water and ethyl acetate were then added thereto, and
extraction was performed. The organic layer was washed with water
twice and concentrated by removing the solvent under reduced
pressure. The residue was purified by silica gel chromatography
(n-hexane:ethyl acetate=3:1) to give 35 mg of colorless oily
N-[2-(3-cyclopropylmethoxy-4-methoxyphenyl)oxazol-4-ylmethyl]-N-methyl-2--
trifluoromethylbenzamide.
[0763] .sup.1H-NMR (CDCl.sub.3) .delta.: 7.72-7.34 (7H, m), 6.94
(1H, dd, J=8.4, 1.8 Hz), 4.88-4.11 (1H, m), 3.98-3.89 (5H, m),
3.17-2.88 (3H, m), 1.43-1.34 (1H, m), 0.71-0.64 (2H, m), 0.42-0.36
(2H, m)
Example 242
[0764] Using 0.14 g of
[2-(3,4-diethoxyphenyl)oxazol-4-ylmethyl]methylamine obtained in
Reference Example 74, 70 mg of colorless oily
N-[2-(3,4-dimethoxyphenyl)oxazol-4-ylmethyl]-2-ethoxy-N-methylbenzamide
was obtained in the same manner as in Example 1.
[0765] .sup.1H-NMR (CDCl.sub.3) .delta.: 7.60-7.26 (5H, m),
7.00-6.87 (3H, m), 4.23-4.02 (8H, m), 3.19-2.96 (3H, m), 1.52-1.40
(6H, m), 1.36 (3H, t, J=6.9 Hz)
Example 243
[0766] Using 0.2 g of
2-[2-(3,4-diethoxyphenyl)oxazol-4-yl]ethylamine obtained in
Reference Example 78 and 0.18 g of 2-ethoxy benzoic acid, 0.14 g of
white powdery
N-{2-[2-(3,4-dimethoxyphenyl)oxazol-4-yl]ethyl}-2-ethoxybenzamide
was obtained in the same manner as in Example 1.
[0767] .sup.1H-NMR (CDCl.sub.3) .delta.: 8.22 (1H, dd, J=7.5, 4.8
Hz), 7.60-7.50 (2H, m), 7.47 (1H, s), 7.39 (1H, m), 7.06 (1H, m),
6.95-6.85 (2H, m), 4.30-4.05 (6H, m), 4.09 (2H, q, J=6.9 Hz), 3.85
(2H, q, J=6.6 Hz), 2.91 (2H, t, J=6.6 Hz), 1.48 (6H, t, J=6.9 Hz),
1.28 (6H, t, J=6.9 Hz)
Example 244
[0768] Using 0.3 g of 2-(3,4-diethoxyphenyl)oxazole-4-carboxylic
acid obtained in Reference Example 80 and 0.28 g of
1-(2-amino)ethanone, 0.32 g of white powdery
N-(2-oxo-2-phenylethyl)-2-(3,4-diethoxyphenyl)oxazole-4-carboxamide
was obtained in the same manner as in Example 1.
[0769] .sup.1H-NMR (DMSO-d.sub.6) .delta.: 8.67 (1H, d, J=0.9 Hz),
8.49 (1H, t, J=5.7 Hz), 8.10-8.00 (2H, m), 7.70-7.50 (5H, m), 7.16
(1H, m), 4.81 (2H, d, J=5.7 Hz), 4.13 (4H, q, J=6.9 Hz), 1.38 (6H,
t, J=6.9 Hz), 1.37 (3H, t, J=6.9 Hz)
Example 245
[0770] Using 2-(3,4-diethoxyphenyl)oxazole-4-carboxylic acid
obtained in Reference Example 80, 0.32 g of white powdery
1-(4-{4-[2-(3,4-diethoxyphenyl)oxazole-4-carbonyl]piperazin-1-yl}phenyl)e-
thanone was obtained in the same manner as in Example 1.
[0771] .sup.1H-NMR (CDCl.sub.3) .delta.: 8.20 (1H, s), 7.95-7.85
(2H, m), 7.62 (1H, dd, J=8.4, 2.1 Hz), 7.54 (1H, d, J=2.1 Hz),
7.00-6.85 (3H, m), 4.40-4.20 (2H, m), 4.19 (2H, q, J=6.9 Hz), 4.16
(2H, q, J=6.9 Hz), 4.00-3.80 (2H, m), 3.50-3.45 (4H, m), 2.53 (3H,
s), 1.50 (3H, t, J=6.9 Hz), 1.50 (3H, t, J=6.9 Hz)
Example 246
[0772] Using 0.28 g of 2-(3,4-diethoxyphenyl)oxazole-4-carboxylic
acid obtained in Reference Example 80 and 0.2 g of
1-(4-methoxyphenyl)piperazine, 0.36 g of white powdery
4-(2-(3,4-diethoxyphenyl)oxazol-4-yl)-1-(4-methoxyphenyl)piperazine
was obtained in the same manner as in Example 1.
[0773] .sup.1H-NMR (CDCl.sub.3) .delta.: 8.16 (1H, s), 7.61 (1H,
dd, J=8.7, 2.1 Hz), 7.54 (1H, s), 6.95-6.84 (5H, m), 4.40-4.30 (2H,
m), 4.21-4.12 (4H, m), 4.00-3.93 (2H, m), 3.78 (3H, s), 3.14 (4H,
t, J=4.8 Hz), 1.47 (6H, t, J=7.2 Hz)
Example 247
[0774] Using 0.28 g of 2-(3,4-diethoxyphenyl)oxazole-4-carboxylic
acid obtained in Reference Example 80 and
1-(4-hydroxyphenyl)piperazine, white powdery
4-(2-(3,4-diethoxyphenyl)
oxazol-4-yl)-1-(4-hydroxyphenyl)piperazine was obtained in the same
manner as in Example 1.
[0775] .sup.1H-NMR (CDCl.sub.3) .delta.: 8.16 (1H, s), 7.61 (1H,
dd, J=8.7, 2.1 Hz), 7.54 (1H, s), 6.95-6.78 (5H, m), 4.40-4.30 (2H,
m), 4.21-4.12 (4H, m), 4.00-3.93 (2H, m), 3.14 (4H, t, J=4.8 Hz),
1.49 (6H, t, J=7.2 Hz)
Example 248
[0776] Using 0.28 g of 2-(3,4-diethoxyphenyl)oxazole-4-carboxylic
acid obtained in Reference Example 80 and 0.14 g of
2-phenylethylamine, 0.21 g of white powdery
N-phenethyl-2-(3,4-dimethoxyphenyl)oxazole-4-carboxamide was
obtained in the same manner as in Example 1.
[0777] .sup.1H-NMR (CDCl.sub.3) .delta.: 8.17 (1H, s), 7.56 (1H,
dd, J=8.4, 2.1 Hz), 7.50 (1H, d, J=2.1 Hz), 7.36-7.21 (5H, m), 7.12
(1H, br s), 6.93 (1H, d, J=8.4 Hz), 4.22-4.12 (4H, m), 3.74-3.66
(2H, m), 2.95 (2H, t, J=7.2 Hz), 1.57-1.46 (6H, m)
Example 249
[0778] Using 0.28 g of 2-(3,4-diethoxyphenyl)oxazole-4-carboxylic
acid obtained in Reference Example 80 and 0.13 g of
1-(2-aminoethyl)pyrrolidine, 0.15 g of pale yellow powdery
N-(2-(pyrrolidin-1-yl)ethyl)-2-(3,4-dimethoxyphenyl)oxazole-4-carboxamide
was obtained in the same manner as in Example 1.
[0779] .sup.1H-NMR (CDCl.sub.3) .delta.: 8.17 (1H, s), 7.60 (1H,
dd, J=8.4, 1.8 Hz), 7.55 (1H, d, J=1.8 Hz), 7.44 (1H, br s), 6.92
(1H, d, J=8.4 Hz), 4.23-4.12 (4H, m), 3.65-3.58 (2H, m), 2.79 (2H,
t, J=6.6 Hz), 2.70-2.58 (4H, m), 1.87-1.75 (4H, m), 1.53-1.46 (6H,
m)
Example 250
[0780] Using 0.15 g of [2-(3,4-diethoxyphenyl)oxazol-4-yl]acetic
acid obtained in Reference Example 81 and 0.11 g of o-phenetidine,
0.12 g of white powdery 2-[2-(3,4-diethoxyphenyl)
oxazol-4-yl]-N-(2-ethoxyphenyl)acetamide was obtained in the same
manner as in Example 1.
[0781] .sup.1H-NMR (CDCl.sub.3) .delta.: 8.74 (1H, br s), 8.37 (1H,
dd, J=7.2, 1.8 Hz), 7.70-7.65 (2H, m), 7.61 (1H, d, J=1.8 Hz),
7.00-6.90 (3H, m), 6.80 (1H, dd, J=7.8, 1.2 Hz), 4.18 (2H, q, J=6.9
Hz), 4.16 (2H, q, J=6.9 Hz), 3.97 (2H, q, J=7.2 Hz), 3.74 (2H, s),
1.49 (3H, t, J=6.9 Hz), 1.49 (3H, t, J=6.9 Hz), 1.18 (3H, t, J=7.2
Hz)
Example 251
[0782] Using 0.15 g of [2-(3,4-diethoxyphenyl)oxazol-4-yl]acetic
acid obtained in Reference Example 81 and 85 mg of
2-amino-3-hydroxypyridine, 0.11 g of white powdery
2-[2-(3,4-diethoxyphenyl)oxazol-4-yl]-N-(3-hydroxypyridin-2-yl)acetamide
was obtained in the same manner as in Example 1.
[0783] .sup.1H-NMR (CDCl.sub.3) .delta.:10.37 (1H, brs), 9.88 (1H,
brs), 7.84 (1H, dd, J=4.8, 1.2 Hz), 7.65-7.60 (3H, m), 7.31 (1H,
dd, J=4.2, 1.2 Hz), 6.94 (1H, d, J=9.0 Hz), 4.22 (2H, q, J=6.9 Hz),
4.16 (2H, q, J=6.9 Hz), 1.51 (3H, t, J=6.9 Hz), 1.49 (3H, t, J=6.9
Hz)
Example 252
[0784] A 0.5 g quantity of
4-chloromethyl-2-(3,4-diethoxyphenyl)oxazole obtained in Reference
Example 35, 0.36 g of piperazin-2-one and 0.28 g of potassium
carbonate were added to 10 ml of acetonitrile, and the mixture was
heated and refluxed for 7 hours. The residue was diluted with ethyl
acetate, and washed with water and then with saturated brine. The
organic layer was dried over anhydrous magnesium sulfate and
concentrated by removing the solvent under reduced pressure. The
residue was purified by silica gel column chromatography
(dichloromethane:methanol=1:0 to 50:1), and the obtained crude
crystals were recrystallized from ethyl acetate to give 0.25 g of
colorless crystalline
4-[2-(3,4-diethoxyphenyl)oxazol-4-ylmethyl]piperazin-2-one.
[0785] .sup.1H-NMR (CDCl.sub.3) .delta.: 7.59 (1H, d, J=8.1, 2.1
Hz), 7.56 (1H, d, J=2.1 Hz), 6.91 (1H, d, J=8.1 Hz), 6.03 (1H,
brs), 4.17 (2H, q, J=6.9 Hz), 4.15 (2H, q, J=6.9 Hz), 3.61 (2H, s),
3.45-3.35 (2H, m), 3.27 (2H, s), 2.80-2.75 (2H, m), 1.48 (6H, t,
J=6.9 Hz)
Example 253
[0786] Using 0.5 g of 4-chloromethyl-2-(3,4-diethoxyphenyl) oxazole
obtained in Reference Example 35 and 0.5 g of morpholine, 0.31 g of
white powdery 4-[2-(3,4-diethoxyphenyl)oxazol-4-ylmethyl]morpholine
was obtained in the same manner as in Example 252.
[0787] .sup.1H-NMR (CDCl.sub.3) .delta.: 7.70-7.50 (2H, m), 7.54
(1H, s), 6.91 (1H, d, J=8.4 Hz), 4.25-4.10 (4H, m), 3.80-3.70 (4H,
m), 3.51 (2H, s), 2.60-2.50 (4H, m), 1.48 (6H, t, J=6.9 Hz)
Example 254
[0788] A 0.5 g quantity of 4-chloromethyl-2-(3,4-diethoxy
phenyl)oxazole obtained in Reference Example 35, 0.28 g of
2-mercaptopyridine and 0.28 g of potassium carbonate were added to
10 ml of dimethylformamide, and the mixture was stirred at room
temperature for 24 hours. The reaction mixture was diluted with
ethyl acetate, and washed with water and then with saturated brine.
The organic layer was dried over anhydrous magnesium sulfate and
concentrated by removing the solvent under reduced pressure. The
residue was purified by silica gel column chromatography (ethyl
acetate:n-hexane=1:4 to 1:2), and the obtained crude crystals were
recrystallized from a mixture of ethyl acetate and n-hexane to give
0.63 g of colorless crystalline
2-[2-(3,4-diethoxyphenyl)oxazol-4-ylmethylsulfanyl]pyridine.
[0789] .sup.1H-NMR (CDCl.sub.3) .delta.: 8.45 (3H, m), 7.60-7.50
(3H, m), 7.47 (1H, m), 7.18 (1H, d, J=8.1 Hz), 6.99 (1H, m), 6.89
(1H, d, J=8.1 Hz), 4.38 (2H, s), 4.17 (2H, q, J=6.9 Hz), 4.14 (2H,
q, J=6.9 Hz), 1.47 (6H, t, J=6.9 Hz)
Example 255
[0790] A 0.58 g quantity of
2-[2-(3,4-diethoxyphenyl)oxazol-4-ylmethylsulfanyl]pyridine
obtained in Example 254 was added to 20 ml of dichloromethane. A
0.55 g quantity of m-chloroperbenzoic acid was gradually added
thereto with ice-cooling, and the mixture was then stirred. The
reaction mixture was diluted with 30 ml of dichloromethane, and
washed with an aqueous 10% sodium hydroxide solution and then with
saturated brine. The organic layer was dried over anhydrous
magnesium sulfate and concentrated by removing the solvent under
reduced pressure. The residue was purified by silica gel column
chromatography (ethyl acetate:n-hexane=2:1 to 3:1), and the
obtained crude crystals was recrystallized from a mixture of ethyl
acetate and n-hexane to give 0.49 g of colorless crystalline
2-[2-(3,4-diethoxyphenyl)oxazol-4-ylmethanesulfonyl]pyridine.
[0791] .sup.1H-NMR (CDCl.sub.3) .delta.: 8.81 (1H, m), 8.00 (1H,
m), 7.91 (1H, m), 7.61 (1H, s), 7.55 (1H, m), 7.50-7.40 (2H, m),
6.87 (1H, d, J=8.4 Hz), 4.71 (2H, s), 4.13 (4H, q, J=6.9 Hz), 1.47
(6H, t, J=6.9 Hz)
Example 256
[0792] A 0.27 g quantity of
[2-(3,4-diethoxyphenyl)oxazol-4-yl]methylamine obtained in
Reference Example 37 and 0.3 ml of triethylamine were dissolved in
10 ml of acetonitrile. A 0.19 g quantity of
o-toluenesulfonylchloride was added thereto, and the mixture was
stirred at room temperature for 1 hour. Water was added to the
reaction mixture, and extraction was performed with ethyl acetate.
The organic layer was washed with water twice, and the solvent was
removed. The obtained residue was purified using a silica gel
column (n-hexane:ethyl acetate=1:1). The obtained crude crystals
were recrystallized from a mixture of n-hexane and ethyl acetate to
give 0.3 g of white powdery
N-[2-(3,4-diethoxyphenyl)oxazol-4-ylmethyl]-2-methylbenzenesulfonamide.
[0793] .sup.1H-NMR (CDCl.sub.3) .delta.: 7.96 (1H, dd, J=7.5, 1.5
Hz), 7.48-7.16 (6H, m), 6.90 (1H, d, J=8.4 Hz), 5.11 (1H, br s),
4.21-4.11 (6H, m), 2.64 (3H, s), 1.52-1.46 (6H, m)
Example 257
[0794] A 0.5 g quantity of
3-[2-(3-cyclopropylmethoxy-4-methoxyphenyl)oxazol-4-yl]-1-(2-ethoxyphenyl-
)propan-1-one obtained in Example 102 and 0.18 ml of hydrazine
monohydrate were added to diethylene glycol. A 0.14 g quantity of
potassium hydroxide was added thereto, and the mixture was stirred
at 150.degree. C. for 1 hour. The reaction mixture was allowed to
cool, water was then added thereto, and extraction was performed
with ethyl acetate. Drying was performed with anhydrous magnesium
sulfate, and the solvent was removed. The residue was purified by
silica gel column chromatography (n-hexane:ethyl acetate=4:1) to
give 0.1 g of colorless oily
2-(3-cyclopropylmethoxy-4-methoxyphenyl)-4-[3-(2-ethoxyphenyl)propyl]oxaz-
ole.
[0795] .sup.1H-NMR (CDCl.sub.3) .delta.: 7.58 (1H, dd, J=8.4, 1.8
Hz), 7.51 (1H, d, J=1.8 Hz), 7.39 (1H, s), 7.17-7.12 (2H, m),
6.93-6.81 (3H, m), 4.03 (2H, q, J=6.9 Hz), 3.94-3.92 (5H, m), 2.72
(2H, t, J=7.5 Hz), 2.62 (2H, t, J=7.5 Hz), 2.03-1.96 (2H, m),
1.43-1.25 (4H, m), 0.69-0.63 (2H, m), 0.40-0.35 (2H, m)
Example 258
[0796] A 1.6 g quantity of sodium hydride was suspended in 100 ml
of tetrahydrofuran. A 2.68 g quantity of 1-(2-methylphenyl)
ethanone and 6.58 g of 2-(3-benzyloxy-4-methoxyphenyl)-4-chloro
methyloxazole obtained in Reference Example 5 were successively
added thereto with ice-cooling and stirring, and the mixture was
heated and refluxed for 4 hours. An aqueous saturated ammonium
chloride solution was added thereto with ice-cooling. After
stirring for 15 minutes, water was added thereto, and extraction
was performed with ethyl acetate. Drying was then performed with
anhydrous magnesium sulfate, and the solvent was removed. The
residue was purified by silica gel column chromatography
(n-hexane:ethyl acetate=4:1), and 1.6 g of the obtained crude
product was dissolved in 20 ml of ethanol. A 0.16 g quantity of 10%
palladium-carbon powder was added thereto, and the mixture was
stirred under a hydrogen atmosphere for 18 hours. The reaction
mixture was filtered, and the obtained filtrate was concentrated.
The residue was purified by silica gel column chromatography
(dichloromethane:ethanol=100:1) to give 0.47 g of yellow oily
2-(3-hydroxy-4-methoxyphenyl)-4-(3-o-tolyl propyl) oxazole.
[0797] .sup.1H-NMR (CDCl.sub.3) .delta.: 7.60-7.54 (2H, m), 7.38
(1H, s), 7.15-7.08 (4H, m), 6.90 (1H, d, J=8.4 Hz), 5.65 (1H, s),
3.94 (3H, s), 2.72-2.62 (4H, m), 2.37 (3H, s)
Example 259
[0798] Using 0.47 g of
2-(3-hydroxy-4-methoxyphenyl)-4-(3-o-tolylpropyl)oxazole obtained
in Example 258, 0.37 g of colorless oily
2-(3-cyclopropylmethoxy-4-methoxyphenyl)-4-(3-o-tolylpropyl)
oxazole was obtained in the same manner as in Example 111.
[0799] .sup.1H-NMR (CDCl.sub.3) .delta.: 7.58 (1H, dd, J=8.1, 2.1
Hz), 7.51 (1H, d, J=2.1 Hz), 7.38 (1H, s), 7.15-7.08 (4H, m), 6.92
(1H, d, J=8.1 Hz), 3.94-3.92 (5H, m), 2.72-2.62 (4H, m), 2.31 (3H,
s), 2.04-1.92 (2H, m), 1.40-1.35 (1H, m), 0.69-0.63 (2H, m),
0.40-0.35 (2H, m)
Example 260
[0800] A 0.21 g quantity of
3-[2-(3-cyclopropylmethoxy-4-methoxyphenyl)oxazol-4-yl]-1-(2-ethoxyphenyl-
)propan-1-one obtained in Example 102 was added to 5 ml of ethanol,
and the mixture was stirred with ice-cooling. A 37 mg quantity of
sodium borohydride was gradually added thereto. After the
temperature of the reaction mixture had reached room temperature,
stirring was performed for 2 hours. An aqueous 5N hydrochloric acid
solution was added to the reaction mixture, and solvent was then
removed. Extraction was performed with dichloromethane, and the
extract was washed with saturate brine. The extract was then dried
over anhydrous magnesium sulfate, the solvent was removed, and the
residue was purified by silica gel column chromatography
(n-hexane:ethyl acetate=3:1) to give 0.18 g of colorless oily
3-[2-(3-cyclopropylmethoxy-4-methoxyphenyl)oxazol-4-yl]-1-(2-ethoxyphenyl-
)propan-1-ol.
[0801] .sup.1H-NMR (CDCl.sub.3) .delta.: 7.58 (1H, dd, J=8.4, 2.1
Hz), 7.50 (1H, d, J=1.8 Hz), 7.39-7.35 (2H, m), 7.23-7.18 (1H, m),
6.97-6.84 (3H, m), 5.00 (1H, br s), 4.07 (2H, q, J=6.6 Hz),
3.94-3.92 (5H, m), 3.44 (1H, br s), 2.80-2.60 (2H, m), 2.20-2.15
(2H, m), 1.43-1.37 (4H, m), 0.69-0.63 (2H, m), 0.40-0.37 (2H,
m)
Example 261
[0802] An 80 mg quantity of 3-[2-(3-isopropoxy-4-methoxy
phenyl)oxazol-4-yl]-1-(3-methylpyridin-2-yl)propan-1-one obtained
in Example 139 was dissolved in 3 ml of dimethylformamide. A 0.2 g
quantity of sodium hydride was added thereto with ice-cooling and
stirring, and the mixture was stirred for 30 minutes. A 75 mg
quantity of methyl iodide was added thereto, and the reaction
mixture was stirred at room temperature for 8 hours. Water was
added to the reaction mixture, and extraction was performed with
ethyl acetate. The organic layer was washed with water twice, and
the solvent was removed. The obtained residue was purified using a
silica gel column (n-hexane:ethyl acetate=3:1) to give 35 mg of
colorless oily 3-[2-(3-isopropoxy-4-methoxyphenyl)
oxazol-4-yl]-2,2-dimethyl-1-(3-methylpyridin-2-yl)propan-1-one.
[0803] .sup.1H-NMR (CDCl.sub.3) .delta.: 8.41 (1H, dd, J=4.5, 1.2
Hz), 7.38-7.60 (3H, m), 7.34 (1H, s), 7.21-7.24 (1H, m), 6.90 (1H,
d, J=8.7 Hz), 4.63 (1H, sept., J=6.0 Hz), 3.94 (3H, s), 3.15 (2H,
s), 2.28 (3H, s), 1.38-1.49 (12H, m)
Example 262
[0804] Using 0.9 g of methyl
3-{2-[4-methoxy-3-(2,2,2-trifluoroethoxy)phenyl]oxazol-4-yl}propionate
obtained in Reference Example 83, 1.05 g of yellow oily methyl
3-(3-methoxypyridin-2-yl)-2-{2-[4-methoxy-3-(2,2,2-trifluoroethoxy)phenyl-
]oxazol-4-ylmethyl}-3-oxopropinate was obtained in the same manner
as in Example 100.
[0805] .sup.1H-NMR (CDCl.sub.3) .delta.: 8.25 (1H, dd, J=4.5, 1.5
Hz), 7.65 (1H, dd, J=8.4, 2.1 Hz), 7.55 (1H, d, J=2.1 Hz),
7.47-7.33 (3H, m), 6.94 (1H, d, J=8.4 Hz), 5.17 (1H, t, J=6.9 Hz),
4.43 (2H, q, J=8.4 Hz), 3.93 (3H, s), 3.92 (3H, s), 3.65 (3H, s),
3.32-3.23 (2H, m)
Example 263
[0806] Using 0.7 g of methyl
3-(3-methoxypyridin-2-yl)-2-{2-[4-methoxy-3-(2,2,2-trifluoroethoxy)phenyl-
]oxazol-4-ylmethyl}-3-oxopropionate obtained in Example 262, 0.42 g
of colorless oily methyl
2-{2-[4-methoxy-3-(2,2,2-trifluoroethoxy)phenyl]oxazol-4-ylmethyl}-2-meth-
yl-3-(3-methylpyridin-2-yl)-3-oxopropinate was obtained in the same
manner as in Example 261.
[0807] .sup.1H-NMR (CDCl.sub.3) .delta.: 8.18 (1H, dd, J=6.9, 1.8
Hz), 7.64 (1H, dd, J=8.4, 2.1 Hz), 7.54 (1H, d, J=2.1 Hz),
7.42-7.34 (3H, m), 6.93 (1H, d, J=8.7 Hz), 4.43 (2H, q, J=8.4 Hz),
3.93 (3H, s), 3.91 (3H, s), 3.64 (3H, s), 3.40 (1H, d, J=15 Hz),
3.26 (1H, d, J=15 Hz)
Example 264
[0808] Using 0.42 g of methyl
2-{2-[4-methoxy-3-(2,2,2-trifluoroethoxy)phenyl]oxazol-4-ylmethyl}-2-meth-
yl-3-(3-methyl pyridin-2-yl)-3-oxopropinate obtained in Example
263, 0.25 g of colorless oily
1-(3-methoxypyridin-2-yl)-3-{2-[4-methoxy-3-(2,2,2-trifluoroethoxy)phenyl-
]oxazol-4-yl}-2-methylpropan-1-one was obtained in the same manner
as in Example 136.
[0809] .sup.1H-NMR (CDCl.sub.3) .delta.: 8.24 (1H, dd, J=4.5, 1.5
Hz), 7.67 (1H, dd, J=8.4, 2.1 Hz), 7.57 (1H, d, J=2.1 Hz),
7.43-7.28 (3H, m), 6.94 (1H, d, J=8.7 Hz), 4.45 (1H, q, J=8.4 Hz),
4.21 (1H, q, J=6.9 Hz), 3.91 (3H, s), 3.88 (3H, s), 3.15-3.06 (1H,
m), 2.73-2.64 (1H, m), 1.23 (3H, d, J=7.2 Hz)
Example 265
[0810] Using 0.2 g of
1-(3-methoxypyridin-2-yl)-3-{2-[4-methoxy-3-(2,2,2-trifluoroethoxy)phenyl-
]oxazol-4-yl}-2-methyl propan-1-one obtained in Example 264, 80 mg
of colorless oily
1-(3-methoxypyridin-2-yl)-3-{2-[4-methoxy-3-(2,2,2-trifluoroethoxy)phenyl-
]oxazol-4-yl}-2,2-dimethylpropan-1-one was obtained in the same
manner as in Example 261.
[0811] .sup.1H-NMR (CDCl.sub.3) .delta.: 8.17 (1H, dd, J=4.5, 1.5
Hz), 7.70 (1H, dd, J=8.4, 1.8 Hz), 7.60 (1H, d, J=1.8 Hz),
7.31-7.21 (2H, m), 6.96 (1H, d, J=8.4 Hz), 4.45 (2H, q, J=8.4 Hz),
3.92 (3H, s), 3.78 (3H, s), 3.05 (2H, s), 1.34 (6H, s)
Example 266
[0812] A 60 ml quantity of trifluoroacetic acid was stirred with
ice cooling, 12.3 g of the compound obtained in Example 231 was
added thereto, and stirring was conducted for one hour. At the
completion of the reaction, the reaction mixture was neutralized by
addition of an aqueous saturated sodium bicarbonate solution, and
ethyl acetate was added to the obtained mixture. The organic layer
was washed twice with water, separated, concentrated under reduced
pressure, and the obtained crude crystals were recrystallized from
ethanol, thereby yielding 5.9 g of white powdery
3-[2-(3-benzyloxy-4-methoxyphenyl)oxazol-4-yl]-1-(2-hydroxyphenyl)propan--
1-one.
[0813] .sup.1H-NMR (CDCl.sub.3) .delta.:12.2 (1H, s), 7.81 (1H, d,
J=8.1 Hz), 7.62-7.26 (9H, m), 6.99-6.85 (3H, m), 5.19 (2H, s), 3.92
(3H, s), 3.43 (2H, t, J=7.5 Hz), 3.02 (2H, t, J=7.5 Hz)
Example 267
[0814] Using the compound obtained in Example 266 and
chlorodifluoromethane, white powdery 3-[2-(3-benzyloxy-4-methoxy
phenyl)oxazol-4-yl]-1-(2-difluoromethoxyphenyl)propan-1-one was
obtained following the procedure of Example 19.
[0815] .sup.1H-NMR (CDCl.sub.3) .delta.: 7.71 (1H, dd, J=7.8, 1.8
Hz), 7.90-6.60 (7H, m), 6.34 (1H, t, J=73.8 Hz), 5.20 (2H, s), 3.92
(3H, s), 3.36 (2H, t, J=7.2 Hz), 2.29 (2H, t, J=7.2 Hz)
Reference Example 84
[0816] Using 2-fluoroethanol, a colorless oily 2-fluoroethyl
methanesulfonate was obtained following the procedure of Reference
Example 50.
[0817] .sup.1H-NMR (CDCl.sub.3) .delta.: 4.76-4.73 (1H, m),
4.60-4.58 (1H, m), 4.53-4.50 (1H, m), 4.43-4.41 (1H, m), 3.08 (3H,
s)
Reference Example 85
[0818] Using 2,2-difluoroethanol, colorless oily 2,2-difluoro
ethylmethanesulfonate was obtained following the procedure of
Reference Example 50
[0819] .sup.1H-NMR (CDCl.sub.3) .delta.: 6.01 (1H, tt, J=54.3, 3.9
Hz), 4.38 (2H, td, J=12.9, 3.9 Hz), 3.12 (3H, s)
Example 268
[0820] Using the compound obtained in Example 266 and the compound
obtained in Reference Example 84, white powdery
3-[2-(3-benzyloxy-4-methoxyphenyl)oxazol-4-yl]-1-[2-(2-fluoroethoxy)pheny-
l]propan-1-one was obtained following the procedure of Example
3.
[0821] .sup.1H-NMR (CDCl.sub.3) .delta.: 7.74 (1H, dd, J=7.8, 1.8
Hz), 7.61-7.59 (2H, m), 7.49-7.31 (7H, m), 7.07 (1H, t, J=7.8 Hz),
6.92 (2H, d, J=8.7 Hz), 5.20 (2H, s), 4.90-4.87 (1H, m), 4.74-4.71
(1H, m), 4.37-4.35 (1H, m), 4.28-4.26 (1H, m), 3.92 (3H, s), 3.44
(2H, t, J=7.5 Hz), 2.99 (2H, t, J=7.5 Hz)
Example 269
[0822] Using the compound obtained in Example 266 and the compound
obtained in Reference Example 85, white powdery
3-[2-(3-benzyloxy-4-methoxyphenyl)oxazol-4-yl]-1-[2-(2,2-difluoroethoxy)p-
henyl]propan-1-one was obtained following the procedure of Example
3.
[0823] .sup.1H-NMR (CDCl.sub.3) .delta.: 7.74 (1H, dd, J=7.8, 1.8
Hz), 7.61-7.28 (9H, m), 7.08 (1H, t, J=7.8 Hz), 6.95-6.89 (2H, m),
6.22 (1H, tt, J=54.9, 3.9 Hz), 5.19 (2H, s), 4.29 (1H, td, J=12.9,
3.9 Hz), 3.92 (3H, s), 3.38 (2H, t, J=7.5 Hz), 2.98 (2H, t, J=7.5
Hz)
Example 270
[0824] Using the compound obtained in Example 267, white powdery
1-(2-difluoromethoxyphenyl)-3-[2-(3-hydroxy-4-methoxy
phenyl)oxazol-4-yl]propan-1-one was obtained following the
procedure of Example 2.
[0825] .sup.1H-NMR (CDCl.sub.3) .delta.: 7.71 (1H, t, J=7.5 Hz),
7.54-7.41 (4H, m), 7.38-7.16 (2H, m), 6.89 (1H, d, J=8.1 Hz), 6.59
(1H, t, J=74.7 Hz), 5.69 (1H, s), 3.93 (3H, s), 3.36 (2H, t, J=7.2
Hz), 2.99 (2H, t, J=7.2 Hz)
Example 271
[0826] Using the compound obtained in Example 268, white powdery
1-[2-(2-fluoroethoxy)phenyl]-3-[2-(3-hydroxy-4-methoxy
phenyl)oxazol-4-yl]propan-1-one was obtained following the
procedure of Example 2.
[0827] .sup.1H-NMR (CDCl.sub.3) .delta.: 7.73 (1H, dd, J=7.8, 1.8
Hz), 7.55-7.42 (4H, m), 7.05 (1H, t, J=7.8 Hz), 6.91 (2H, d, J=8.7
Hz), 4.91-4.88 (1H, m), 4.75-4.72 (1H, m), 4.38-4.35 (1H, m),
4.29-4.26 (1H, m), 3.94 (3H, s), 3.43 (2H, t, J=7.5 Hz), 2.99 (2H,
t, J=7.5 Hz)
Example 272
[0828] Using the compound obtained in Example 269, white powdery
1-[2-(2,2-difluoroethoxy)phenyl]-3-[2-(3-hydroxy-4-methoxyphenyl)oxazol-4-
-yl]propan-1-one was obtained following the procedure of Example
2.
[0829] .sup.1H-NMR (CDCl.sub.3) .delta.: 7.73 (1H, dd, J=7.8, 1.8
Hz), 7.56-7.41 (4H, m), 7.08 (1H, t, J=7.8 Hz), 6.92-6.87 (2H, m),
6.21 (1H, tt, J=54.9, 3.9 Hz), 5.67 (1H, s), 4.29 (1H, td, J=12.9,
3.9 Hz), 3.94 (3H, s), 3.38 (2H, t, J=7.2 Hz), 2.98 (2H, t, J=7.2
Hz)
Example 273
[0830] Using the compound obtained in Example 270 and
2-bromopropane, white powdery
1-(2-difluoromethoxyphenyl)-3-[2-(3-isopropoxy-4-methoxyphenyl)oxazol-4-y-
l]propan-1-one was obtained following the procedure of Example
3.
[0831] .sup.1H-NMR (CDCl.sub.3) .delta.: 7.70-7.25 (5H, m),
7.20-6.80 (2H, m), 6.59 (1H, t., J=73.5 Hz), 4.64 (1H, m), 3.93
(3H, s), 1.39 (3H, d, J=6.0 Hz)
Example 274
[0832] Using the compound obtained in Example 270 and ethyl iodide,
white powdery
1-(2-difluoromethoxyphenyl)-3-[2-(3-ethoxy-4-methoxyphenyl)oxazol-
-4-yl]propan-1-one was obtained following the procedure of Example
3.
[0833] .sup.1H-NMR (CDCl.sub.3) .delta.: 7.71 (1H, dd, J=7.8, 1.8
Hz), 7.60-7.46 (3H, m), 7.42 (1H, s), 7.31-7.16 (2H, m), 6.91 (1H,
d, J=8.1 Hz), 6.59 (1H, t, J=73.5 Hz), 4.18 (2H, q, J=7.2 Hz), 3.92
(3H, s), 3.37 (2H, t, J=7.2 Hz), 3.00 (2H, t, J=7.2 Hz), 1.49 (3H,
t, J=7.2 Hz)
Example 275
[0834] Using the compound obtained in Example 271 and
2-bromopropane, white powdery
1-(2-fluoroethoxyphenyl)-3-[2-(3-isopropoxy-4-methoxyphenyl)oxazol-4-yl]p-
ropan-1-one was obtained following the procedure of Example 3.
[0835] .sup.1H-NMR (CDCl.sub.3) .delta.: 7.73 (1H, d, J=7.2 Hz),
7.58-7.54 (2H, m), 7.45-7.41 (2H, m), 7.04 (1H, t, J=7.2 Hz), 6.92
(2H, t, J=8.1 Hz), 4.81 (2H, dt, J=47.4, 4.2 Hz), 4.64-4.60 (1H,
m), 4.32 (2H, dt, J=23.1, 4.2 Hz), 3.89 (3H, s), 3.43 (2H, t, J=7.2
Hz), 3.00 (2H, t, J=7.2 Hz), 1.39 (6H, d, J=5.7 Hz)
Example 276
[0836] Using the compound obtained in Example 271 and
4-bromo-1-butene, white powdery
3-[2-(3-but-3-enyloxy-4-methoxyphenyl)
oxazol-4-yl]-1-[2-(2-fluoroethoxy)phenyl]propan-1-one was obtained
following the procedure of Example 3.
[0837] .sup.1H-NMR (CDCl.sub.3) .delta.: 7.73 (1H, d, J=7.5 Hz),
7.58-7.53 (2H, m), 7.45-7.42 (2H, m), 7.03 (1H, t, J=7.8 Hz), 6.92
(2H, t, J=8.4 Hz), 6.00-5.84 (1H, m), 5.21-5.09 (2H, m) 4.81 (2H,
dt, J=47.4, 4.2 Hz), 4.32 (2H, dt, J=23.1, 4.2 Hz), 4.14 (2H, t,
J=7.2 Hz), 3.90 (3H, s), 3.43 (2H, t, J=7.5 Hz), 3.00 (2H, t, J=7.5
Hz), 2.64-2.61 (2H, m)
Example 277
[0838] Using the compound obtained in Example 271 and isobutyl
bromide, white powdery
1-[2-(2-fluoroethoxy)phenyl]-3-[2-(3-isobutoxy-4-methoxyphenyl)oxazol-4-y-
l]propan-1-one was obtained following the procedure of Example
3.
[0839] .sup.1H-NMR (CDCl.sub.3) .delta.: 7.73 (1H, dd, J=7.8, 1.8
Hz), 7.57-7.51 (2H, m), 7.48-7.42 (2H, m), 7.40 (1H, t, J=7.5 Hz),
6.92 (2H, t, J=8.7 Hz), 4.81 (2H, dt, J=47.4, 4.2 Hz), 4.32 (2H,
dt, J=23.1, 4.2 Hz), 3.90 (3H, s), 3.84 (2H, d, J=6.9 Hz), 3.43
(2H, t, J=7.5 Hz), 3.00 (2H, t, J=7.5 Hz), 2.23-2.14 (1H, m), 1.04
(6H, d, J=5.7 Hz)
Example 278
[0840] Using the compound obtained in Example 272 and
2-bromopropane, white powdery
1-[2-(2,2-difluoroethoxy)phenyl]-3-[2-(3-isopropoxy-4-methoxyphenyl)oxazo-
l-4-yl]propan-1-one was obtained following the procedure of Example
3.
[0841] .sup.1H-NMR (CDCl.sub.3) .delta.: 7.74 (1H, dd, J=7.5, 1.8
Hz), 7.59-7.44 (3H, m), 7.41 (1H, s), 7.08 (1H, t, J=7.5 Hz), 6.91
(1H, d, J=8.4 Hz), 6.22 (1H, tt, J=54.6, 3.9 Hz) 4.65 (1H, sept.,
J=6.0 Hz), 4.29 (2H, td, J=12.9, 3.9 Hz), 3.90 (3H, s) 3.38 (2H, t,
J=7.5 Hz) 2.99 (2H, t, J=7.5 Hz) 1.40 (6H, d, J=6.0 Hz)
Example 279
[0842] Using the compound obtained in Example 272 and
1-bromopropane, white powdery
1-[2-(2,2-difluoroethoxy)phenyl]-3-[2-(3-propoxy-4-methoxyphenyl)oxazol-4-
-yl]propan-1-one was obtained following the procedure of Example
3.
[0843] .sup.1H-NMR (CDCl.sub.3) .delta.: 7.74 (1H, dd, J=7.8, 1.8
Hz), 7.61-7.43 (3H, m), 7.41 (1H, s), 7.08 (1H, t, J=7.5 Hz),
6.92-6.89 (2H, m), 6.23 (1H, tt, J=54.6, 3.9 Hz), 4.29 (2H, td,
J=12.9, 3.9 Hz), 4.06 (2H, t, J=6.9 Hz), 3.91 (3H, s), 3.38 (2H, t,
J=7.5 Hz), 2.99 (2H, t, J=7.5 Hz), 1.90 (2H, qt, J=7.2 Hz), 1.06
(3H, t, J=7.2 Hz)
Example 280
[0844] Using the compound obtained in Example 272 and ethyl iodide,
white powdery
1-[2-(2,2-difluoroethoxy)phenyl]-3-[2-(3-ethoxy-4-methoxyphenyl)o-
xazol-4-yl]propan-1-one was obtained following the procedure of
Example 3.
[0845] .sup.1H-NMR (CDCl.sub.3) .delta.: 7.74 (1H, dd, J=7.8, 1.8
Hz), 7.61-7.44 (3H, m), 7.41 (1H, s), 7.08 (1H, t, J=7.8 Hz),
6.93-6.90 (2H, m), 6.23 (1H, tt, J=54.6, 3.9 Hz) 4.29 (2H, td,
J=12.9, 3.9 Hz), 4.18 (2H, q, J=6.9 Hz), 3.92 (3H, s), 3.38 (2H, t,
J=7.5 Hz), 2.99 (2H, t, J=7.5 Hz), 1.50 (3H, t, J=6.9 Hz)
Example 281
[0846] Using the compound obtained in Example 272 and ally bromide,
white powdery
3-[2-(3-allyloxy-4-methoxyphenyl)oxazol-4-yl]-1-[2-(2,2-difluoroe-
thoxy)phenyl]propan-1-one was obtained following the procedure of
Example 3.
[0847] .sup.1H-NMR (CDCl.sub.3) .delta.: 7.74 (1H, dd, J=7.8, 1.8
Hz), 7.60-7.44 (3H, m), 7.41 (1H, s), 7.08 (1H, t, J=7.5 Hz),
6.94-6.89 (2H, m), 6.41-6.04 (2H, m), 5.44 (1H, dd, J=17.4, 1.5
Hz), 5.31 (1H, dd, J=10.2, 1.5 Hz), 4.29 (2H, td, J=12.9, 3.9 Hz),
3.92 (3H, s), 3.38 (2H, t, J=7.2 Hz), 2.99 (2H, t, J=7.2 Hz)
Example 282
[0848] Using the compound obtained in Example 272 and
4-bromo-1-butene, white powdery
3-[2-(3-but-3-enyloxy-4-methoxyphenyl)
oxazol-4-yl]-1-[2-(2,2-difluoroethoxy)phenyl]propan-1-one was
obtained following the procedure of Example 3.
[0849] .sup.1H-NMR (CDCl.sub.3) .delta.: 7.75 (1H, dd, J=7.8, 1.8
Hz), 7.60-7.44 (3H, m), 7.42 (1H, s), 7.09 (1H, t, J=7.5 Hz),
6.93-6.89 (2H, m), 6.23 (1H, tt, J=54.6, 3.9 Hz), 5.99-5.85 (1H,
m), 5.23-5.10 (2H, m), 4.29 (2H, td, J=12.9, 3.9 Hz), 4.14 (2H, t,
J=7.2 Hz), 3.91 (3H, s), 3.39 (2H, t, J=7.2 Hz), 2.99 (2H, t, J=7.2
Hz), 2.68-2.60 (2H, m)
Example 283
[0850] Using the compound obtained in Example 272 and
(bromomethyl)cyclopropane, white powdery 3-[2-(3-cyclopropyl
methoxy-4-methoxyphenyl)oxazol-4-yl]-1-[2-(2,2-difluoroethoxy)phenyl]prop-
an-1-one was obtained following the procedure of Example 3.
[0851] .sup.1H-NMR (CDCl.sub.3) .delta.: 7.75 (1H, dd, J=7.8, 1.8
Hz), 7.58-7.44 (3H, m), 7.41 (1H, s), 7.09 (1H, t, J=7.5 Hz),
6.93-6.90 (2H, m), 6.24 (1H, tt, J=54.6, 3.9 Hz), 4.29 (2H, td,
J=12.9, 3.9 Hz), 3.94-3.91 (5H, m), 3.39 (2H, t, J=7.2 Hz), 2.99
(2H, t, J=7.2 Hz), 1.43-1.33 (1H, m), 0.70-0.63 (2H, m), 0.41-0.35
(2H, m)
Example 284
[0852] Using the compound obtained in Example 272 and the compound
obtained in Reference Example 85, white powdery
3-{2-[3-(2,2-difluoroethoxy)-4-methoxyphenyl]oxazol-4-yl}-1-[2-(2,2-diflu-
oroethoxy)phenyl]propan-1-one was obtained following the procedure
of Example 3.
[0853] .sup.1H-NMR (CDCl.sub.3) .delta.: 7.74 (1H, dd, J=7.8, 1.8
Hz), 7.65 (1H, dd, J=7.8, 1.8 Hz), 7.50 (1H, d, J=2.1 Hz),
7.50-7.42 (1H, m), 7.42 (1H, s), 7.08 (1H, t, J=7.5 Hz), 6.96-6.89
(2H, m), 6.42-5.95 (2H, m), 4.35-4.23 (4H, m), 3.92 (3H, s), 3.39
(2H, t, J=7.5 Hz), 3.00 (2H, t, J=7.5 Hz)
Example 285
[0854] Using the compound obtained in Example 272 and isobutyl
bromide, white powdery
1-[2-(2,2-difluoroethoxy)phenyl]-3-[2-(3-isobutoxy-4-methoxyphenyl)oxazol-
-4-yl]-propan-1-one was obtained following the procedure of Example
3.
[0855] .sup.1H-NMR (CDCl.sub.3) .delta.: 7.74 (1H, d, J=7.5 Hz),
7.57-7.44 (3H, m), 7.41 (1H, s), 7.08 (1H, t, J=7.5 Hz), 6.92-6.89
(2H, m), 6.23 (1H, tt, J=54.6, 3.9 Hz), 4.29 (2H, td, J=12.9, 3.9
Hz), 3.90 (3H, s), 3.85 (2H, d, J=6.6 Hz), 3.38 (2H, t, J=7.5 Hz),
2.99 (2H, t, J=7.5 Hz), 2.19 (1H, qt, J=6.6 Hz), 1.05 (6H, d, J=6.6
Hz)
Example 286
[0856] Using the compound obtained in Reference Example 35 and the
compound obtained in Reference Example 70, pale yellow oily
3-[2-(3,4-diethoxyphenyl)oxazol-4-yl]-1-(2-methoxymethoxyphenyl)
propan-1-one was obtained following the procedure of Example
190.
[0857] .sup.1H-NMR (CDCl.sub.3) .delta.: 7.66 (1H, dd, J=7.8, 1.8
Hz), 7.56-7.38 (3H, m), 7.17 (1H, d, J=8.4 Hz), 7.04 (1H, t, J=7.5
Hz), 6.92-6.88 (2H, m), 5.26 (2H, s), 4.21-4.08 (4H, m), 3.49 (3H,
s), 3.40 (2H, t, J=7.2 Hz), 3.00 (2H, t, J=7.2 Hz), 1.51-1.45 (6H,
m)
Example 287
[0858] Using the compound obtained in Example 286, white powdery
3-[2-(3,4-diethoxyphenyl)oxazol-4-yl]-1-(2-hydroxyphenyl)
propan-1-one was obtained following the procedure of Example
266.
[0859] .sup.1H-NMR (CDCl.sub.3) .delta.:12.25 (1H, s), 7.82 (1H,
dd, J=8.1, 1.5 Hz), 7.60-7.43 (4H, m), 6.98 (1H, d, J=8.4 Hz),
6.92-6.86 (2H, m), 4.21-4.10 (4H, m), 3.44 (2H, t, J=7.2 Hz), 3.03
(2H, t, J=7.2 Hz), 1.51-1.43 (6H, m)
Example 288
[0860] Using the compound obtained in Example 287 and
chlorodifluoromethane, white powdery 3-[2-(3,4-diethoxyphenyl
oxazol-4-yl)-1-(2-difluoromethoxyphenyl)propan-1-one was obtained
following the procedure of Example 19.
[0861] .sup.1H-NMR (CDCl.sub.3) .delta.: 7.51 (1H, d, J=8.7 Hz),
7.60-7.45 (3H, m), 7.30 (1H, s), 7.28-7.19 (2H, m), 6.90 (1H, d,
J=8.7 Hz), 6.58 (1H, t, J=75 Hz), 4.15 (4H, q, J=7.2 Hz) 3.36 (2H,
t, J=7.2 Hz), 3.00 (2H, t, J=7.2 Hz), 1.47 (6H, t, J=7.2 Hz)
Example 289
[0862] Using the compound obtained in Example 287 and the compound
obtained in Reference Example 84, white powdery
3-[2-(3,4-diethoxyphenyl)oxazol-4-yl]-1-[2-(2-fluoroethoxy)phenyl]propan--
1-one was obtained following the procedure of Example 3.
[0863] .sup.1H-NMR (CDCl.sub.3) .delta.: 7.74 (1H, dd, J=7.8, 1.8
Hz), 7.56-7.41 (4H, m), 7.04 (1H, td, J=7.5, 0.9 Hz), 6.95-6.88
(2H, m), 4.81 (2H, dt, J=47.1, 4.2 Hz), 4.32 (2H, dt, J=27.3, 4.2
Hz), 4.21-4.10 (4H, m), 3.43 (2H, t, J=7.2 Hz) 3.00 (2H, t, J=7.2
Hz) 1.50-1.45 (6H, m)
Example 290
[0864] Using the compound obtained in Example 287 and the compound
obtained in Reference Example 85, white powdery
3-[2-(3,4-diethoxyphenyl)oxazol-4-yl]-1-[2-(2,2-difluoroethoxy)phenyl]pro-
pan-1-one was obtained following the procedure of Example 3.
[0865] .sup.1H-NMR (CDCl.sub.3) .delta.: 7.74 (1H, dd, J=7.5, 1.8
Hz), 7.56-7.43 (3H, m), 7.41 (1H, s), 7.08 (1H, t, J=7.5 Hz), 6.90
(1H, d, J=7.8 Hz), 6.23 (1H, tt, J=54.9, 3.9 Hz), 4.29 (2H, td,
J=13.2, 3.9 Hz), 4.21-4.10 (4H, m), 3.38 (2H, t, J=7.5 Hz) 2.98
(2H, t, J=7.5 Hz), 1.50-1.45 (6H, m)
Example 291
[0866] A 0.2 g quantity of the compound obtained in Example 223 and
0.1 ml of triethylamine were dissolved in 5 ml of dichloromethane,
0.1 ml of acetyl chloride was added to the obtained solution, and
the mixture was stirred for 6 hours at room temperature. At the
completion of the reaction, water was added to the reaction
mixture, and the obtained mixture was extracted with ethyl acetate.
The organic layer was washed twice with water, and the solvent was
distilled off. The residue was purified using a silica gel column
(n-hexane:ethyl acetate=2:1), and the obtained crude crystals were
recrystallized with ethanol, thereby yielding 15 mg of white
powdery
2-{3-[2-(3-isopropoxy-4-methoxyphenyl)oxazol-4-yl]propionyl}phenyl
acetate.
[0867] .sup.1H-NMR (CDCl.sub.3) .delta.: 7.83 (1H, dd, J=7.8, 1.5
Hz), 7.60-7.50 (3H, m), 7.42 (1H, s), 7.34-7.28 (1H, m), 7.12 (1H,
dd, J=8.1, 0.9 Hz), 6.92 (1H, d, J=8.4 Hz), 4.69-4.61 (1H, m), 3.90
(3H, s), 3.32 (2H, t, J=7.2 Hz), 2.97 (2H, t, J=7.2 Hz), 2.35 (3H,
s), 1.40 (6H, d, J=6.0 Hz)
Example 292
[0868] Using the compound obtained in Reference Example 35 and
1-(2-trifluoromethoxyphenyl)ethanone, white powdery
3-[2-(3,4-diethoxyphenyl)oxazol-4-yl]-1-(2-trifluoromethoxyphenyl)propan--
1-one was obtained following the procedure of Example 190.
[0869] .sup.1H-NMR (CDCl.sub.3) .delta.: 7.70 (1H, dd, J=7.8, 1.8
Hz), 7.58-7.41 (3H, m), 7.38 (1H, s), 7.35-7.29 (2H, m), 6.90 (1H,
d, J=8.4 Hz), 4.20-4.10 (4H, m), 3.34 (2H, t, J=6.9 Hz), 3.00 (2H,
t, J=6.9 Hz), 1.48 (6H, t, J=6.9 Hz)
Example 293
[0870] Using the compound obtained in Reference Example 11 and
1-(2-trifluoromethoxyphenyl)ethanone, white powdery
3-[2-(3-cyclopropylmethoxy-4-methoxyphenyl)oxazol-4-yl]-1-(2-trifluoro
methoxyphenyl)propan-1-one was obtained following the procedure of
Example 190.
[0871] .sup.1H-NMR (CDCl.sub.3) .delta.: 7.70 (1H, d, J=8.7 Hz),
7.57-7.53 (3H, m), 7.49 (1H, s), 7.42-7.30 (2H, m), 6.90 (1H, d,
J=8.7 Hz), 3.94-3.91 (5H, m), 3.34 (2H, t, J=7.2 Hz) 3.00 (2H, t,
J=7.2 Hz), 1.42-1.30 (1H, m), 0.67-0.64 (2H, m), 0.40-0.36 (2H,
m)
[0872] Using the compound obtained in Reference Example 35 and the
corresponding acetophenone derivatives, compounds of Examples 294
to 299 were obtained following the procedure of Example 190.
Example 294
3-[2-(3,4-diethoxyphenyl)oxazol-4-yl]-1-(2,5-dimethoxyphenyl)
propan-1-one
White Powder
[0873] 1H-NMR (CDCl.sub.3) .delta.: 7.57-7.52 (2H, m), 7.40 (1H,
s), 7.01 (1H, dd, J=9.0, 3.3 Hz), 6.90 (2H, t, J=8.4 Hz), 4.20-4.10
(4H, m), 3.85 (3H, s), 3.78 (3H, s), 3.39 (2H, t, J=7.2 Hz), 2.98
(2H, t, J=7.2 Hz), 1.47 (6H, t, J=6.9 Hz)
Example 295
3-[2-(3,4-diethoxyphenyl)oxazol-4-yl]-1-(2-ethoxy-5-methylphenyl)
propan-1-one
White Powder
[0874] .sup.1H-NMR (CDCl.sub.3) .delta.: 7.61-7.49 (3H, m), 7.40
(1H, s), 7.25-7.20 (2H, m), 6.90 (1H, d, J=8.1 Hz), 6.83 (1H, d,
J=8.4 Hz), 4.21-4.06 (6H, m), 3.41 (2H, t, J=7.5 Hz), 2.99 (2H, t,
J=7.5 Hz), 2.28 (3H, s), 1.53-1.40 (9H, m)
Example 296
3-[2-(3,4-diethoxyphenyl)oxazol-4-yl]-1-(2,4-dimethylphenyl)
propan-1-one
Colorless Powder
[0875] .sup.1H-NMR (CDCl.sub.3) .delta.: 7.63 (1H, d, J=8.4 Hz),
7.54 (1H, dd, J=8.4, 1.8 Hz), 7.51 (1H, d, J=1.8 Hz), 7.42 (1H, s),
7.06-7.02 (2H, m), 6.90 (1H, d, J=8.4 Hz), 4.17 (2H, q, J=6.9 Hz),
4.14 (2H, q, J=6.9 Hz), 3.30 (2H, t, J=7.2 Hz), 2.99 (2H, t, J=7.2
Hz), 2.49 (3H, s), 2.34 (3H, s), 1.48 (6H, t, J=6.9 Hz)
Example 297
3-[2-(3,4-diethoxyphenyl)oxazol-4-yl]-1-(2,5-dimethylphenyl)
propan-1-one
Colorless Needle Crystals
[0876] .sup.1H-NMR (CDCl.sub.3) .delta.: 7.55 (1H, br s, J=8.7 Hz),
7.52 (1H, br s), 7.44 (1H, br d, J=8.7 Hz), 7.17-7.09 (2H, m), 6.90
(1H, d, J=8.7 Hz), 4.17 (2H, q, J=6.9 Hz), 4.14 (2H, q, J=6.9 Hz),
3.29 (2H, t, J=7.2 Hz), 2.99 (2H, t, J=7.2 Hz), 2.44 (3H, s), 2.33
(3H, s), 1.47 (6H, t, J=6.9 Hz)
Example 298
3-[2-(3,4-diethoxyphenyl)oxazol-4-yl]-1-(2-ethoxy-4-methylphenyl)
propan-1-one
White Powder
[0877] .sup.1H-NMR (CDCl.sub.3) .delta.: 7.66 (1H, d, J=7.8 Hz),
7.60-7.51 (2H, m), 7.39 (1H, s), 6.90 (1H, d, J=8.4 Hz), 6.79 (1H,
d, J=8.4 Hz), 6.73 (1H, s), 4.21-4.08 (6H, m), 3.40 (2H, t, J=7.2
Hz), 2.98 (2H, t, J=7.2 Hz), 2.36 (3H, s), 1.53-1.45 (9H, m)
Example 299
3-[2-(3,4-diethoxyphenyl)oxazol-4-yl]-1-(2-ethoxy-4-fluorophenyl)
propan-1-one
Colorless Needle Crystals
[0878] .sup.1H-NMR (CDCl.sub.3) .delta.: 7.78 (1H, dd, J=8.7, 7.2
Hz), 7.54 (1H, dd, J=8.4, 2.1 Hz), 7.51 (1H, d, J=2.1 Hz), 7.39
(1H, br s), 6.90 (1H, d, J=8.4 Hz), 6.71-6.61 (2H, m), 4.16 (2H, q,
J=6.9 Hz), 4.14 (2H, q, J=6.9 Hz), 4.11 (2H, q, J=6.9 Hz), 3.39
(2H, t, J=7.2 Hz), 2.98 (2H, t, J=7.2 Hz), 1.49 (3H, t, J=6.9 Hz),
1.47 (6H, t, J=6.9 Hz)
Example 300
[0879] The compound obtained in Reference Example 54 and methyl
(2-methoxymethyl)benzoate were used and treated following the
procedure of Example 100, followed by treatment according to
Reference Example 48, yielding white powdery 3-[2-(3,4-diethoxy
phenyl)oxazol-4-yl]-1-(2-methoxymethylphenyl)propan-1-one.
[0880] .sup.1H-NMR (CDCl.sub.3) .delta.: 7.74 (1H, dd, J=7.8, 1.2
Hz), 7.64-7.27 (6H, m), 6.91 (1H, d, J=8.4 Hz), 4.73 (2H, s),
4.21-4.10 (4H, m), 3.43 (3H, s), 3.34 (2H, t, J=7.2 Hz), 3.00 (2H,
t, J=7.2 Hz), 1.51-1.43 (6H, m)
[0881] Using the compound obtained in Reference Example 54 and the
corresponding methyl benzoate derivatives, compounds of Examples
301 to 303 were obtained following the procedure of the Example
300.
Example 301
3-[2-(3,4-diethoxyphenyl)oxazol-4-yl]-1-(2-ethylphenyl)propan-1-one
[0882] .sup.1H-NMR (CDCl.sub.3) .delta.: 7.62-7.51 (4H, m), 7.43
(1H, s), 7.38-7.30 (2H, m), 6.90 (1H, d, J=8.7 Hz), 4.18-4.13 (4H,
m), 3.31 (2H, t, J=7.2 Hz), 3.00 (2H, t, J=7.2 Hz), 2.81 (2H, q,
J=7.5 Hz), 1.48 (6H, t, J=6.9 Hz), 1.20 (3H, t, J=7.5 Hz)
Example 302
3-[2-(3,4-diethoxyphenyl)oxazol-4-yl]-1-(2,3-dimethoxyphenyl)
propan-1-one
[0883] .sup.1H-NMR (CDCl.sub.3) .delta.: 7.56-7.51 (2H, m), 7.41
(1H, s), 7.18-7.01 (3H, m), 6.90 (1H, d, J=8.4 Hz), 4.21-4.10 (4H,
m), 3.89 (6H, s), 3.38 (2H, t, J=7.2 Hz), 2.99 (2H, t, J=7.2 Hz),
1.48 (6H, t, J=6.9 Hz)
Example 303
3-[2-(3,4-diethoxyphenyl)oxazol-4-yl]-1-(2-ethoxy-3-methylphenyl)
propan-1-one
[0884] .sup.1H-NMR (CDCl.sub.3) .delta.: 7.55-7.51 (2H, m), 7.40
(1H, s), 7.36-7.29 (2H, m), 7.04 (1H, t, J=7.2 Hz), 6.90 (1H, d,
J=8.1 Hz), 4.20-4.11 (4H, m), 3.83 (2H, q, J=7.5 Hz), 3.39 (2H, t,
J=7.2 Hz), 2.98 (2H, t, J=7.2 Hz), 2.30 (3H, s), 1.48 (6H, t, J=6.9
Hz), 1.26 (3H, t, J=6.9 Hz)
Example 304
[0885] Using the compound obtained in Reference Example 58 and
1-(2-ethoxy-4-fluorophenyl)ethanone, pale yellow powdery
1-(2-ethoxy-4-fluorophenyl)-3-[2-(3-ethoxy-4-methoxyphenyl)oxazol-4-yl]pr-
opan-1-one was obtained following the procedure of Example 190.
[0886] .sup.1H-NMR (CDCl.sub.3) .delta.: 7.77 (1H, t, J=7.8 Hz),
7.56 (1H, dd, J=8.4, 1.8 Hz), 7.51 (1H, d, J=1.8 Hz), 7.40 (1H, s),
6.91 (1H, d, J=8.4 Hz), 6.71-6.61 (2H, m), 4.21-4.07 (4H, m), 3.92
(3H, s), 3.39 (2H, t, J=7.2 Hz), 2.98 (2H, t, J=7.2 Hz), 1.52-1.47
(6H, m)
Example 305
[0887] Using the compound obtained in Reference Example 58 and
1-(4-fluoro-2-isopropoxyphenyl)ethanone, colorless oily
3-[2-(3-ethoxy-4-methoxyphenyl)oxazol-4-yl]-1-(4-fluoro-2-isopropoxy
phenyl)propan-1-one was obtained following the procedure of Example
190.
[0888] .sup.1H-NMR (CDCl.sub.3) .delta.: 7.77 (1H, t, J=7.8 Hz),
7.57 (1H, dd, J=8.4, 1.8 Hz), 7.51 (1H, d, J=1.8 Hz), 7.40 (1H, s),
6.91 (1H, d, J=8.4 Hz), 6.71-6.61 (2H, m), 4.63 (1H, sept, J=6.0
Hz), 4.18 (2H, q, J=6.9 Hz), 3.92 (3H, s), 3.38 (2H, t, J=7.2 Hz),
2.98 (2H, t, J=7.2 Hz), 1.50 (3H, t, J=6.9 Hz), 1.42 (6H, d, J=6.0
Hz)
Example 306
[0889] Using the compound obtained in Reference Example 68 and
1-(2-ethoxy-5-methylphenyl)ethanone, white powdery
1-(2-ethoxy-5-methylphenyl)-3-[2-(3-isopropoxy-4-methoxyphenyl)oxazol-4-y-
l]propan-1-one was obtained following the procedure of Example
190.
[0890] .sup.1H-NMR (CDCl.sub.3) .delta.: 7.60-7.40 (3H, m), 7.39
(1H, s), 7.24-7.19 (1H, m), 6.91 (1H, d, J=8.1 Hz), 6.83 (1H, d,
J=8.4 Hz), 4.69-4.58 (1H, m), 4.10 (2H, q, J=6.9 Hz), 3.89 (3H, s),
3.41 (2H, t, J=7.2 Hz), 2.98 (2H, t, J=7.2 Hz), 2.29 (3H, s),
1.48-1.38 (9H, m)
Example 307
[0891] Using the compound obtained in Reference Example 68 and
1-(2-ethoxy-4-methylphenyl)ethanone, white powdery
1-(2-ethoxy-4-methylphenyl)-3-[2-(3-isopropoxy-4-methoxyphenyl)oxazol-4-y-
l]propan-1-one was obtained following the procedure of Example
190.
[0892] .sup.1H-NMR (CDCl.sub.3) .delta.: 7.66 (1H, d, J=8.1 Hz),
7.59-7.53 (2H, m), 7.39 (1H, s), 6.91 (1H, d, J=8.4 Hz), 6.79 (1H,
d, J=8.1 Hz), 6.73 (1H, s), 4.58-4.71 (1H, m), 4.12 (2H, q, J=6.9
Hz), 3.90 (1H, s) 3.40 (2H, t, J=7.5 Hz), 2.98 (2H, t, J=7.5 Hz),
2.36 (3H, s), 1.48 (3H, t, J=6.9 Hz), 1.40 (6H, d, J=6.0 Hz)
Example 308
[0893] Using the compound obtained in Example 136 and
chlorodifluoromethane, white powdery
3-[2-(3-difluoromethoxy-4-methoxyphenyl)oxazol-4-yl]-1-(3-methylpyridin-2-
-yl)propan-1-one was obtained following the procedure of Example
4.
[0894] .sup.1H-NMR (CDCl.sub.3) .delta.: 8.50 (1H, m), 7.83 (1H,
dd, J=8.4, 2.1 Hz), 7.78 (1H, d, J=2.1 Hz), 7.58 (1H, d, J=7.8 Hz),
7.47 (1H, s), 7.32 (1H, m), 7.00 (1H, d, J=8.4 Hz), 6.58 (1H, t,
J=74.7 Hz), 3.93 (3H, s), 3.59 (2H, t, J=7.2 Hz), 3.00 (2H, t,
J=7.2 Hz), 2.57 (3H, s)
Example 309
[0895] Using the compound obtained in Example 136 and the compound
obtained in Reference Example 85, white powdery
3-{2-[3-(2,2-difluoroethoxy)-4-methoxyphenyl]oxazol-4-yl}-1-(3-methyl
pyridin-2-yl)propan-1-one was obtained following the procedure of
Example 3.
[0896] .sup.1H-NMR (CDCl.sub.3) .delta.: 8.50 (1H, dd, J=4.5, 0.9
Hz), 7.66 (1H, dd, J=8.4, 2.1 Hz), 7.60-7.54 (2H, m), 7.46 (1H, s),
7.35-7.31 (1H, m), 6.94 (1H, d, J=8.7 Hz), 6.16 (1H, tt, J=54.9,
1.2 Hz) 4.29 (2H, td, J=12.9, 1.2 Hz), 3.92 (3H, s), 3.61 (2H, t,
J=6.9 Hz), 3.01 (2H, t, J=6.9 Hz), 2.58 (3H, s)
Example 310
[0897] Using the compound obtained in Example 136 and the compound
obtained in Reference Example 84, white powdery
3-{2-[3-(2-fluoroethoxy)-4-methoxyphenyl]oxazol-4-yl}-1-(3-methylpyridin--
2-yl)propan-1-one was obtained following the procedure of Example
3.
[0898] .sup.1H-NMR (CDCl.sub.3) .delta.: 8.50-8.49 (1H, m),
7.63-7.54 (3H, m), 7.45 (1H, s), 7.34-7.27 (1H, m), 6.93 (1H, d,
J=8.7 Hz), 4.88 (1H, t, J=4.2 Hz), 4.72 (1H, t, J=4.2 Hz) 4.39 (1H,
t, J=4.2 Hz), 4.30 (1H, t, J=4.2 Hz), 3.92 (3H, s), 3.60 (2H, t,
J=7.2 Hz), 3.00 (2H, t, J=7.2 Hz), 2.57 (3H, s)
Example 311
[0899] Using the compound obtained in Example 136 and
2-bromobutane, yellow oily 3-[2-(3-sec-butoxy-4-methoxyphenyl)
oxazol-4-yl]-1-(3-methylpyridin-2-yl)propan-1-one was obtained
following the procedure of Example 3.
[0900] .sup.1H-NMR (CDCl.sub.3) .delta.: 8.50 (1H, dd, J=4.5, 1.2
Hz), 7.59-7.55 (3H, m), 7.54 (1H, s), 7.45-7.30 (1H, m), 6.91 (1H,
d, J=8.4 Hz), 4.43-4.37 (1H, m), 3.89 (3H, s), 3.60 (2H, t, J=7.5
Hz), 3.01 (2H, t, J=7.5 Hz), 2.57 (3H, s), 1.86-1.62 (2H, m), 1.34
(3H, d, J=6.6 Hz), 1.00 (3H, t, J=6.6 Hz)
Example 312
[0901] Using the compound obtained in Example 136 and
3-bromopentane, white powdery 3-{2-[3-(1-ethylpropoxy)-4-methoxy
phenyl]oxazol-4-yl}-1-(3-methylpyridin-2-yl)propan-1-one was
obtained following the procedure of Example 3.
[0902] .sup.1H-NMR (CDCl.sub.3) .delta.: 8.50 (1H, dd, J=4.5, 1.2
Hz), 7.61-7.53 (3H, m), 7.45 (1H, s), 7.34-7.30 (1H, m), 6.91 (1H,
d, J=8.1 Hz), 4.28-4.20 (1H, m), 3.89 (3H, s), 3.60 (2H, t, J=7.5
Hz), 3.01 (2H, t, J=7.5 Hz), 2.57 (3H, s), 1.78-1.68 (4H, m), 0.98
(6H, t, J=6.6 Hz)
Example 313
[0903] Using the compound obtained in Example 101 and
chlorodifluoromethane, white powdery
3-[2-(3-difluoromethoxy-4-methoxyphenyl)oxazol-4-yl]-1-(2-ethoxyphenyl)pr-
opan-1-one was obtained following the procedure of Example 4.
[0904] .sup.1H-NMR (CDCl.sub.3) .delta.: 7.85-7.80 (2H, m), 7.70
(1H, m), 7.50-7.40 (2H, m), 7.0-6.9 (3H, m), 6.58 (1H, t, J=74.4
Hz), 4.14 (2H, q, J=6.9 Hz), 3.93 (3H, s), 3.42 (2H, t, J=7.2 Hz),
2.99 (2H, t, J=7.2 Hz), 1.48 (3H, t, J=6.9 Hz)
Example 314
[0905] Using the compound obtained in Example 101 and the compound
obtained in Reference Example 85, white powdery
3-{2-[3-(2,2-difluoroethoxy)-4-methoxyphenyl]oxazol-4-yl}-1-(2-ethoxy
phenyl)propan-1-one was obtained following the procedure of Example
3.
[0906] .sup.1H-NMR (CDCl.sub.3) .delta.: 7.73-7.63 (2H, m), 7.55
(1H, d, J=2.1 Hz), 7.46-7.39 (2H, m), 7.01-6.91 (3H, m), 6.16 (1H,
tt, J=54.9, 1.2 Hz), 4.29 (2H, td, J=12.9, 1.2 Hz), 4.14 (2H, q,
J=6.9 Hz), 3.91 (3H, s), 3.43 (2H, t, J=7.2 Hz), 3.00 (2H, t, J=7.2
Hz), 1.48 (3H, t, J=7.2 Hz)
Example 315
[0907] Using the compound obtained in Example 101 and the compound
obtained in Reference Example 84, white powdery
1-(2-ethoxyphenyl)-3-{2-[3-(2-fluoroethoxy)-4-methoxyphenyl]oxazol-4-yl}p-
ropan-1-one was obtained following the procedure of Example 3.
[0908] .sup.1H-NMR (CDCl.sub.3) .delta.: 7.69 (1H, dd, J=7.8, 1.8
Hz), 7.61 (1H, dd, J=8.4, 1.8 Hz), 7.55 (1H, s), 7.44-7.39 (2H, m),
7.00-6.91 (3H, m), 4.81 (2H, dt, J=47.4, 4.2 Hz), 4.32 (2H, dt,
J=23.1, 4.2 Hz), 4.17-4.10 (2H, m), 3.90 (3H, s), 3.41 (2H, t,
J=7.2 Hz), 2.99 (2H, t, J=7.2 Hz), 1.46 (3H, t, J=5.7 Hz)
Reference Example 86
[0909] Using the compound obtained in Reference Example 59 and the
compound obtained in Reference Example 85, white powdery ethyl
4-benzyloxy-3-(2,2-difluoroethoxy)benzoate was obtained following
the procedure of Example 4.
[0910] .sup.1H-NMR (CDCl.sub.3) .delta.: 7.71 (1H, dd, J=8.4, 2.1
Hz), 7.61 (1H, d, J=2.1 Hz), 7.44-7.29 (5H, m), 6.95 (1H, d, J=8.4
Hz), 6.11 (1H, tt, J=54.9, 4.2 Hz), 5.19 (2H, s), 4.38-4.21 (4H,
m), 1.39 (3H, t, J=7.2 Hz)
Reference Example 87
[0911] Using the compound obtained in Reference Example 86, white
powdery 4-benzyloxy-3-(2,2-difluoroethoxy)benzoic acid was obtained
following the procedure of Reference Example 3.
[0912] .sup.1H-NMR (DMSO d.sub.6) .delta.: 7.61 (1H, dd, J=8.4, 1.8
Hz), 7.54 (1H, d, J=1.8 Hz), 7.50-7.30 (5H, m), 7.18 (1H, d, J=8.4
Hz), 6.38 (1H, tt, J=54.3, 3.6 Hz), 5.22 (2H, s), 4.37 (2H, td,
J=14.7, 3.6 Hz)
Reference Example 88
[0913] Using the compound obtained in Reference Example 87, white
powdery 4-benzyloxy-3-(2,2-difluoroethoxy)benzamide was obtained
following the procedure of Reference Example 4.
[0914] .sup.1H-NMR (DMSO d.sub.6) .delta.: 7.86 (1H, br s),
7.56-7.29 (7H, m), 7.25 (1H, br s), 7.14 (1H, d, J=8.4 Hz), 6.40
(1H, tt, J=54.3, 3.6 Hz), 5.20 (2H, s), 4.34 (2H, td, J=14.7, 3.6
Hz)
Reference Example 89
[0915] Using the compound obtained in Reference Example 88, white
powdery
2-[4-benzyloxy-3-(2,2-difluoroethoxy)phenyl]-4-chloromethyloxazole
was obtained following the procedure of Reference Example 5.
[0916] .sup.1H-NMR (CDCl.sub.3) .delta.: 7.68-7.60 (3H, m),
7.45-7.30 (5H, m), 7.01 (1H, d, J=8.4 Hz), 6.12 (1H, tt, J=54.9,
4.2 Hz) 5.18 (2H, s), 4.56 (2H, s), 4.30 (2H, td, J=13.2, 4.2
Hz)
Reference Example 90
[0917] Using the compound obtained in Reference Example 89, white
powdery dimethyl
2-{2-[4-benzyloxy-3-(2,2-difluoroethoxy)phenyl]oxazol-4-ylmethyl-
}malonate was obtained following the procedure of Reference Example
47.
[0918] .sup.1H-NMR (CDCl.sub.3) .delta.: 7.63-7.57 (2H, m),
7.45-7.30 (6H, m), 6.99 (1H, d, J=8.1 Hz), 6.12 (1H, tt, J=54.9,
4.2 Hz), 5.18 (2H, s), 4.29 (2H, td, J=13.2, 4.2 Hz), 3.89 (2H, t,
J=7.5 Hz), 3.75 (6H, s), 3.18 (2H, t, J=7.5 Hz)
Reference Example 91
[0919] Using the compound obtained in Reference Example 90,
brownish oily methyl 3-{2-[4-benzyloxy-3-(2,2-difluoro
ethoxy)phenyl]oxazol-4-yl}-propionate was obtained following the
procedure of Reference Example 48.
[0920] .sup.1H-NMR (CDCl.sub.3) .delta.: 7.64-7.59 (2H, m),
7.42-7.33 (6H, m), 6.99 (1H, d, J=8.1 Hz), 6.12 (1H, tt, J=54.9,
4.2 Hz), 5.18 (2H, s), 4.29 (2H, td, J=13.2, 4.2 Hz), 3.68 (3H, s),
2.91 (2H, t, J=7.5 Hz), 2.72 (2H, t, J=7.5 Hz)
Example 316
[0921] Using the compound obtained in Reference Example 91, pale
yellow oily methyl
2-{2-[4-benzyloxy-3-(2,2-difluoroethoxy)-phenyl]oxazol-4-ylmethyl}-3-(3-m-
ethylpyridin-2-yl)-3-oxopropionate was obtained following the
procedure of Example 100.
[0922] .sup.1H-NMR (CDCl.sub.3) .delta.: 8.50 (1H, d, J=4.5 Hz),
7.60-7.52 (3H, m), 7.46-7.30 (7H, m), 6.97 (1H, d, J=8.1 Hz), 6.11
(1H, tt, J=54.9, 4.2 Hz), 5.24-5.16 (3H, m), 4.27 (2H, td, J=13.2,
4.2 Hz), 3.66 (3H, s), 3.34-3.22 (2H, m), 2.60 (3H, s)
Example 317
[0923] Using the compound obtained in Example 316, white powdery
3-{2-[3-(2,2-difluoroethoxy)-4-hydroxyphenyl]oxazol-4-yl}-1-(3-methylpyri-
din-2-yl)propan-1-one was obtained following the procedure of
Example 136.
[0924] .sup.1H-NMR (CDCl.sub.3) .delta.: 8.50 (1H, d, J=4.5 Hz),
7.61-7.57 (2H, m), 7.52 (1H, s), 7.45 (1H, s), 7.34-7.30 (1H, m),
7.00 (1H, d, J=8.1 Hz), 6.11 (1H, tt, J=54.9, 4.2 Hz), 6.07 (1H,
s), 4.32 (2H, td, J=13.2, 4.2 Hz), 3.59 (2H, t, J=7.5 Hz), 3.00
(2H, t, J=7.5 Hz), 2.57 (3H, s)
Example 318
[0925] Using the compound obtained in Example 317 and methyl
iodide, white powdery
3-{2-[3-(2,2-difluoroethoxy)-4-ethoxyphenyl]oxazol-4-yl}-1-(3-met-
hylpyridin-2-yl)-propan-1-one was obtained following the procedure
of Example 3.
[0926] .sup.1H-NMR (CDCl.sub.3) .delta.: 8.51 (1H, d, J=4.5 Hz),
7.66-7.57 (3H, m), 7.46 (1H, s), 7.34-7.30 (1H, m), 6.94 (1H, d,
J=8.4 Hz), 6.14 (1H, tt, J=54.6, 3.9 Hz), 4.28 (2H, td, J=12.9, 3.9
Hz), 4.13 (2H, q, J=6.9 Hz), 3.60 (2H, t, J=7.5 Hz), 3.02 (2H, t,
J=7.5 Hz), 2.57 (3H, s), 1.47 (3H, t, J=6.9 Hz)
Example 319
[0927] Using the compound obtained in Example 317 and
2-bromopropane, white powdery
3-{2-[3-(2,2-difluoroethoxy)-4-isopropoxyphenyl]oxazol-4-yl}-1-(3-methylp-
yridin-2-yl)propan-1-one was obtained following the procedure of
Example 3.
[0928] .sup.1H-NMR (CDCl.sub.3) .delta.: 8.51 (1H, d, J=4.5 Hz),
7.65-7.57 (3H, m), 7.46 (1H, s), 7.34-7.30 (1H, m), 6.95 (1H, d,
J=8.4 Hz), 6.12 (1H, tt, J=54.6, 3.9 Hz), 4.62-4.54 (1H, m), 4.26
(2H, td, J=12.9, 3.9 Hz), 3.60 (2H, t, J=7.5 Hz), 3.01 (2H, t,
J=7.5 Hz), 2.57 (3H, s), 1.37 (6H, d, J=6.0 Hz)
Example 320
[0929] Using the compound obtained in Reference Example 7 and
2-difluoromethoxy benzoic acid, white powdery
N-[2-(3-benzyloxy-4-methoxyphenyl)oxazol-4-ylmethyl]-2-difluoromethoxyben-
zamide was obtained following the procedure of Example 1.
[0930] .sup.1H-NMR (CDCl.sub.3) .delta.: 8.10 (1H, dd, J=7.8, 1.8
Hz), 7.64-7.57 (3H, m), 7.51-7.45 (4H, m), 7.40-7.26 (4H, m), 7.15
(1H, d, J=8.4 Hz), 6.95 (1H, d, J=9.0 Hz), 6.59 (1H, t, J=72.9 Hz),
5.20 (2H, s), 4.61 (2H, d, J=5.4 Hz), 3.93 (3H, s)
Example 321
[0931] Using the compound obtained in Example 320, white powdery
2-difluoromethoxy-N-[2-(3-hydroxy-4-methoxyphenyl)oxazol-4-ylmethyl]-benz-
amide was obtained following the procedure of Example 2.
[0932] .sup.1H-NMR (CDCl.sub.3) .delta.: 8.09 (1H, d, J=7.8 Hz),
7.64-7.45 (5H, m), 7.32 (1H, t, J=7.8 Hz), 7.15 (1H, d, J=7.8 Hz),
6.91 (1H, d, J=8.4 Hz), 6.60 (1H, t, J=72.9 Hz), 5.77 (1H, s), 4.61
(2H, d, J=5.1 Hz), 3.94 (3H, s)
Example 322
[0933] Using the compound obtained in Example 321 and allyl
bromide, white powdery
N-[2-(3-allyloxy-4-methoxyphenyl)-oxazol-4-ylmethyl]-2-difluorome-
thoxybenzamide was obtained following the procedure of Example
3.
[0934] .sup.1H-NMR (CDCl.sub.3) .delta.: 8.10 (1H, d, J=7.8 Hz),
7.64-7.30 (6H, m), 7.15 (1H, d, J=8.4 Hz), 6.94 (1H, d, J=8.1 Hz),
6.61 (1H, t, J=75 Hz), 6.17-6.08 (1H, m), 5.45 (1H, dd, J=17.1, 1.5
Hz), 5.32 (1H, dd, J=10.5, 1.5 Hz), 4.70 (2H, t, J=5.4 Hz), 4.62
(2H, t, J=5.4 Hz), 3.93 (3H, s)
Example 323
[0935] Using the compound obtained in Example 321 and
2-bromopropane, white powdery
2-difluoromethoxy-N-[2-(3-isopropoxy-4-methoxyphenyl)oxazol-4-ylmethyl]be-
nzamide was obtained following the procedure of Example 3.
[0936] .sup.1H-NMR (CDCl.sub.3) .delta.: 8.10 (1H, d, J=7.8 Hz),
7.64-7.30 (6H, m), 7.15 (1H, d, J=8.4 Hz), 6.94 (1H, d, J=8.1 Hz),
6.61 (1H, t, J=75 Hz), 4.70-4.61 (5H, m), 3.91 (3H, s), 1.39 (6H,
d, J=6.0 Hz)
Example 324
[0937] Using the compound obtained in Example 17 and
3-bromopentane, white powdery N-{2-[3-(1-ethylpropoxy)-4-methoxy
phenyl]oxazol-4-ylmethyl}-3-methylpicolinamide was obtained
following the procedure of Example 3.
[0938] .sup.1H-NMR (CDCl.sub.3) .delta.: 8.58 (1H, br s), 8.39 (1H,
d, J=4.5 Hz), 7.63-7.55 (4H, m), 7.32-7.28 (1H, m), 6.92 (1H, d,
J=8.4 Hz), 4.59 (2H, d, J=6.0 Hz), 4.28-4.20 (1H, m), 3.90 (3H, s),
2.76 (3H, s), 1.82-1.68 (4H, m), 0.99 (6H, t, J=7.5 Hz)
Example 325
[0939] Using the compound obtained in Example 2 and 3-bromopentane,
white powdery
2-ethoxy-N-{2-[3-(1-ethylpropoxy)-4-methoxyphenyl]oxazol-4-ylmeth-
yl}benzamide was obtained following the procedure of Example 3.
[0940] .sup.1H-NMR (CDCl.sub.3) .delta.: 8.57 (1H, br s), 8.24 (1H,
dd, J=8.1, 1.8 Hz), 7.62-7.56 (3H, m), 7.45-7.39 (1H, m), 7.07 (1H,
t, J=8.1 Hz), 6.96-6.91 (2H, m), 4.63 (2H, dd, J=5.4, 0.9 Hz),
4.26-4.14 (3H, m), 3.90 (3H, s), 1.79-1.69 (4H, m), 1.49 (3H, t,
J=7.2 Hz), 1.00 (6H, t, J=7.2 Hz)
Reference Example 92
[0941] Using the compound obtained in Reference Example 44,
colorless oily dimethyl 2-[2-(3-benzyloxy-4-difluoromethoxy
phenyl)oxazol-4-ylmethyl]malonate was obtained following the
procedure of Reference Example 47.
[0942] .sup.1H-NMR (CDCl.sub.3) .delta.: 7.70 (1H, s), 7.59 (1H, d,
J=7.8 Hz), 7.48-7.22 (6H, m), 6.62 (1H, t, J=74.7 Hz), 5.21 (2H,
s), 3.90 (1H, t, J=7.5 Hz), 3.73 (6H, s), 3.20 (2H, t, J=7.5
Hz)
Reference Example 93
[0943] Using the compound obtained in Reference Example 92, pale
yellow oily methyl 3-[2-(3-benzyloxy-4-difluoromethoxy
phenyl)oxazol-4-yl]propionate was obtained following the procedure
of Reference Example 48.
[0944] .sup.1H-NMR (CDCl.sub.3) .delta.: 7.71 (1H, d, J=1.8 Hz),
7.48-7.31 (6H, m), 7.24 (1H, d, J=8.4 Hz), 6.62 (1H, t, J=74.7 Hz),
5.21 (2H, s), 3.70 (3H, s), 2.93 (2H, t, J=7.2 Hz), 2.71 (2H, t,
J=7.2 Hz)
Example 326
[0945] Using the compound obtained in Reference Example 93,
colorless oily methyl 2-[2-(3-benzyloxy-4-difluoromethoxy
phenyl)oxazol-4-ylmethyl]-3-(3-methylpyridin-2-yl)-3-oxo propionate
was obtained following the procedure of Example 100.
[0946] .sup.1H-NMR (CDCl.sub.3) .delta.: 8.50 (1H, dd, J=4.8, 1.2
Hz), 7.67-7.30 (10H, m), 7.21 (1H, d, J=8.4 Hz), 6.60 (1H, t,
J=74.7 Hz), 5.18 (2H, s), 4.11 (1H, t, J=7.2 Hz), 3.65 (3H, s),
3.45-3.20 (2H, m), 2.60 (3H, s)
Example 327
[0947] The compound obtained in Example 326 was used and treated
following the procedure of Example 125, followed by treatment
according to the procedure of Example 2, yielding white powdery
3-[2-(4-difluoromethoxy-3-hydroxyphenyl)oxazol-4-yl]-1-(3-methylpyridin-2-
-yl)propan-1-one.
[0948] .sup.1H-NMR (CDCl.sub.3) .delta.: 8.50 (1H, dd, J=4.5, 1.2
Hz), 7.67-7.45 (4H, m), 7.33-7.30 (1H, m), 7.16 (1H, d, J=8.1 Hz),
6.58 (1H, t, J=75 Hz), 5.76 (1H, s), 3.60 (2H, t, J=7.5 Hz), 3.01
(2H, t, J=7.5 Hz), 2.57 (3H, s)
Example 328
[0949] A 0.15 quantity of the compound obtained in Example 327 and
0.18 ml of 1,8-diazabicyclo[5,4,0]undec-7-ene were dissolved in 3
ml of ethanol, 0.15 g of (bromomethyl)cyclopropane was then added
to the obtained solution, and the obtained mixture was heated and
refluxed overnight. After cooling, water was added to the obtained
reaction mixture, and ethyl acetate extraction was performed. The
organic layer was washed twice with water and concentrated under
reduced pressure, and the obtained residue was purified by silica
gel column chromatography (n-hexane:ethyl acetate=3:1). The
obtained crystals were recrystallized from aqueous 80% ethanol,
thereby yielding 42 mg of white powdery
3-[2-(3-cyclopropylmethoxy-4-difluoromethoxyphenyl)oxazol-4-yl]-1-(3-meth-
ylpyridin-2-yl)propan-1-one.
[0950] .sup.1H-NMR (CDCl.sub.3) .delta.: 8.51 (1H, dd, J=4.8, 1.2
Hz), 7.60-7.53 (3H, m), 7.50 (1H, s), 7.35-7.31 (1H, m), 7.21 (1H,
d, J=8.1 Hz), 6.68 (1H, t, J=75.3 Hz), 3.95 (2H, d, J=6.9 Hz), 3.60
(2H, t, J=7.5 Hz), 3.02 (2H, t, J=7.5 Hz), 2.58 (3H, s), 1.37-1.25
(1H, m), 0.69-0.63 (2H, m), 0.40-0.34 (2H, m)
Example 329
[0951] A 80 mg quantity of the compound obtained in Example 327 and
0.09 ml of 1,8-diazabicyclo[5,4,0]undec-7-ene were dissolved in 2
ml of ethanol, 80 mg of 1-bromopropane was then added to the
obtained solution, and heated and refluxed overnight. After
cooling, water was added to the obtained reaction mixture, and
ethyl acetate extraction was performed. The organic layer was
washed twice with water, concentrated under reduced pressure, and
the obtained residue was purified by silica gel column
chromatography (n-hexane:ethyl acetate=3:1). The obtained crystals
were recrystallized from aqueous 80% ethanol, thereby yielding 25
mg of white powdery
3-[2-(4-difluoromethoxy-3-propoxyphenyl)oxazol-4-yl]-1-(3-methylp-
yridin-2-yl)propan-1-one.
[0952] .sup.1H-NMR (CDCl.sub.3) .delta.: 8.51 (1H, dd, J=4.8, 1.2
Hz), 7.61-7.53 (3H, m), 7.50 (1H, s), 7.35-7.31 (1H, m), 7.20 (1H,
d, J=8.1 Hz), 6.61 (1H, t, J=75 Hz), 4.07 (2H, t, J=6.6 Hz), 3.60
(2H, t, J=7.5 Hz), 3.02 (2H, t, J=7.5 Hz), 2.58 (3H, s), 1.87 (2H,
td, J=7.5, 6.6 Hz), 1.07 (3H, t, J=7.5 Hz)
Example 330
[0953] A 0.15 g quantity of the compound obtained in Example 327
and 0.18 ml of 1,8-diazabicyclo[5,4,0]undec-7-ene were dissolved in
3 ml of ethanol, 0.15 g of allyl bromide was then added to the
obtained solution, and heating and refluxing were conducted for 2
hours. After cooling, water was added to the obtained reaction
mixture, and ethyl acetate was performed. The organic layer was
washed twice with water, concentrated, and the obtained residue was
purified by silica gel column chromatography (n-hexane:ethyl
acetate=3:1). The obtained crystals were recrystallized from
aqueous 80% ethanol, thereby yielding 70 mg of white powdery
3-[2-(3-allyloxy-4-difluoromethoxyphenyl)oxazol-4-yl]-1-(3-methylpyridin--
2-yl)propan-1-one.
[0954] .sup.1H-NMR (CDCl.sub.3) .delta.: 8.51 (1H, dd, J=4.5, 1.2
Hz), 7.62-7.56 (3H, m), 7.50 (1H, s), 7.50-7.31 (1H, m), 7.22 (1H,
d, J=8.4 Hz), 6.62 (1H, t, J=75 Hz), 6.12-6.02 (1H, m), 5.46 (1H,
dd, J=17.4, 1.5 Hz), 5.33 (1H, dd, J=10.8, 1.5 Hz), 4.68 (2H, d,
J=8.1 Hz), 3.61 (2H, t, J=7.2 Hz), 3.02 (2H, t, J=7.2 Hz), 2.58
(3H, s)
Example 331
[0955] An 80 mg quantity of the compound obtained in Example 327
and 0.09 ml of 1,8-diazabicyclo[5,4,0]undec-7-ene were dissolved in
2 ml of ethanol, and 80 mg of 4-bromo-1-butene was then added to
the obtained solution, and heating and refluxing were conducted
overnight. After cooling, water was added to the obtained reaction
mixture, and ethyl acetate extraction was performed. The organic
layer was washed twice with water, concentrated under reduced
pressure, and the obtained residue was purified by silica gel
column chromatography (n-hexane:ethyl acetate=3:1). The obtained
crystals were recrystallized from aqueous 80% ethanol, thereby
yielding 22 mg of white powdery
3-[2-(3-but-3-enyloxy-4-difluoromethoxyphenyl)-oxazol-4-yl]-1-(3-methylpy-
ridin-2-yl)propan-1-one .sup.1H-NMR (CDCl.sub.3) .delta.: 8.51 (1H,
dd, J=4.8, 1.2 Hz), 7.61-7.54 (3H, m), 7.50 (1H, s), 7.35-7.31 (1H,
m), 7.20 (1H, d, J=8.4 Hz), 6.62 (1H, t, J=75 Hz), 5.98-5.83 (1H,
m), 5.24-5.12 (2H, m), 4.16 (2H, t, J=6.6 Hz), 3.61 (2H, t, J=7.2
Hz), 3.03 (2H, t, J=7.2 Hz), 2.64-2.58 (5H, m)
Example 332
[0956] A 0.15 g quantity of the compound obtained in Example 327
and 0.18 ml of DBU were dissolved in 3 ml of ethanol, 0.15 g of
2-bromopropane was then added to the obtained solution, and heating
and refluxing were conducted overnight. After cooling, water was
added to the reaction mixture, and ethyl acetate extraction was
performed. The organic layer was washed twice with water,
concentrated under reduced pressure, and the obtained residue was
purified by silica gel column chromatography (n-hexane:ethyl
acetate=3:1). The obtained crystals were recrystallized from
aqueous 80% ethanol, thereby yielding 70 mg of white powdery
3-[2-(4-difluoromethoxy-3-isopropoxyphenyl)
oxazol-4-yl]-1-(3-methylpyridin-2-yl)propan-1-one
[0957] .sup.1H-NMR (CDCl.sub.3) .delta.: 8.51 (1H, dd, J=4.8, 0.9
Hz), 7.63-7.53 (3H, m), 7.50 (1H, s), 7.35-7.31 (1H, m), 7.20 (1H,
d, J=8.1 Hz), 6.61 (1H, t, J=75 Hz), 4.73-4.65 (1H, m), 3.61 (2H,
t, J=7.2 Hz), 3.02 (2H, t, J=7.2 Hz), 2.58 (3H, s), 1.39 (6H, d,
J=6.0 Hz)
Example 333
[0958] Using the compound obtained in Example 327 and ethyl iodide,
white powdery 3-[2-(4-difluoromethoxy-3-ethoxyphenyl)
oxazol-4-yl]-1-(3-methylpyridin-2-yl)propan-1-one was obtained
following the procedure of Example 330.
[0959] .sup.1H-NMR (CDCl.sub.3) .delta.: 8.50 (1H, dd, J=4.5, 1.2
Hz), 7.61-7.49 (4H, m), 7.35-7.30 (1H, m), 7.20 (1H, d, J=8.4 Hz),
6.62 (1H, t, J=75 Hz), 4.18 (2H, q, J=6.9 Hz), 3.61 (2H, t, J=7.2
Hz), 3.02 (2H, t, J=7.2 Hz), 2.58 (3H, s), 1.47 (3H, t, J=6.9
Hz)
Example 334
[0960] A 60 mg quantity of the compound obtained in Example 229 and
0.2 ml of DBU were dissolved in 4 ml of ethanol, 0.2 ml of ethyl
iodide was then added to the obtained solution, and heating and
refluxing were conducted for 2 hours. After cooling, water was
added to the reaction mixture, and ethyl acetate extraction was
performed. The organic layer was washed twice with water,
concentrated under reduced pressure, and the obtained residue was
purified by silica gel column chromatography (n-hexane:ethyl
acetate=3:1). The obtained crystals were recrystallized from
ethanol, thereby yielding 36 mg of white powdery
3-[2-(4-difluoromethoxy-3-ethoxyphenyl)oxazol-4-yl]-1-(2-ethoxyphenyl)
propan-1-one.
[0961] .sup.1H-NMR (CDCl.sub.3) .delta.: 7.71 (1H, dd, J=7.5, 1.8
Hz), 7.60-7.34 (4H, m), 7.01-6.91 (2H, m), 7.20 (1H, d, J=8.1 Hz),
6.62 (1H, t, J=75 Hz), 4.22-4.07 (4H, m), 3.43 (2H, t, J=7.2 Hz),
3.00 (2H, t, J=7.2 Hz), 1.50-1.40 (6H, m)
Example 335
[0962] A 0.15 g quantity of the compound obtained in Example 229
and 0.17 ml of DBU were dissolved in 4 ml of ethanol, 0.14 g of
ally bromide was then added to the obtained solution, and heating
and refluxing were conducted for 2 hours. After cooling, water was
added to the obtained reaction mixture, and ethyl acetate
extraction was performed. The organic layer was washed twice with
water, concentrated under reduced pressure, and the obtained
residue was purified by silica gel column chromatography
(n-hexane:ethyl acetate=3:1). The obtained crystals were
recrystallized from aqueous 80% ethanol, thereby yielding 90 mg of
white powdery
3-[2-(3-allyloxy-4-difluoromethoxyphenyl)oxazol-4-yl]-1-(2-ethoxyphenyl)p-
ropan-1-one.
[0963] .sup.1H-NMR (CDCl.sub.3) .delta.: 7.71 (1H, dd, J=7.5, 1.8
Hz), 7.62-7.56 (2H, m), 7.46-7.40 (2H, m), 7.22 (1H, d, J=8.1 Hz),
7.01-6.92 (2H, m), 6.62 (1H, t, J=75 Hz), 6.15-6.00 (1H, m), 5.45
(1H, dd, J=17.1, 1.5 Hz), 5.32 (1H, dd, J=10.5, 1.5 Hz), 4.67 (2H,
d, J=8.1 Hz), 4.14 (2H, q, J=6.9 Hz), 3.42 (2H, t, J=7.5 Hz), 3.00
(2H, t, J=7.5 Hz), 1.48 (3H, t, J=6.9 Hz)
Example 336
[0964] A 0.12 g quantity of the compound obtained in Example 229
and 0.14 ml of DBU were dissolved in 3 ml of ethanol, 0.12 g of
(bromomethyl)cyclopropane was then added to the obtained solution,
and heating and refluxing were conducted overnight. After cooling,
water was added to the obtained reaction mixture, and ethyl acetate
extraction was performed. The organic layer was washed twice with
water, concentrated under reduced pressure, and the obtained
residue was purified by silica gel column chromatography
(n-hexane:ethyl acetate=3:1). The obtained crystals were
recrystallized from ethanol, thereby yielding 80 mg of white
powdery 3-[2-(3-cyclopropylmethoxy-4-difluoromethoxy
phenyl)oxazol-4-yl]-1-(2-ethoxyphenyl)propan-1-one.
[0965] .sup.1H-NMR (CDCl.sub.3) .delta.: 7.71 (1H, dd, J=7.8, 1.8
Hz), 7.59-7.54 (2H, m), 7.46-7.40 (2H, m), 7.21 (1H, d, J=8.1 Hz),
7.01-6.95 (2H, m), 6.68 (1H, t, J=75 Hz), 4.14 (2H, q, J=6.9 Hz),
3.95 (2H, d, J=6.9 Hz), 3.42 (2H, t, J=7.2 Hz), 3.00 (2H, t, J=7.2
Hz), 1.47 (3H, t, J=6.9 Hz), 1.34-1.28 (1H, m), 0.69-0.63 (2H, m),
0.40-0.34 (2H, m).
Example 337
[0966] A 0.12 g quantity of the compound obtained in Example 229
and 0.14 ml of DBU were dissolved in 3 ml of ethanol, 0.12 g of
4-bromo-1-butene was then added to the obtained solution, and
heating and refluxing were conducted overnight. After cooling,
water was added to the obtained reaction mixture, and ethyl acetate
extract was performed. The organic layer was washed twice with
water, concentrated under reduced pressure, and the obtained
residue was purified by silica gel column chromatography
(n-hexane:ethyl acetate=3:1). The obtained crystals were
recrystallized from ethanol, thereby yielding 80 mg of white
powdery
3-[2-(3-but-3-enyloxy-4-difluoromethoxyphenyl)oxazol-4-yl]-1-(2-ethoxyphe-
nyl)propan-1-one.
[0967] .sup.1H-NMR (CDCl.sub.3) .delta.: 7.70 (1H, dd, J=7.8, 1.8
Hz), 7.61-7.54 (2H, m), 7.45-7.40 (2H, m), 7.20 (1H, d, J=8.1 Hz),
7.00-6.92 (2H, m), 6.62 (1H, t, J=75 Hz), 5.97-5.83 (1H, m),
5.23-5.12 (2H, m), 4.18-4.10 (4H, m), 3.42 (2H, t, J=7.2 Hz), 3.00
(2H, t, J=7.2 Hz), 2.63-2.56 (4H, m), 1.47 (3H, t, J=6.9 Hz)
Example 338
[0968] Using the compound obtained in Example 97 and ethyl iodide,
white powdery
N-[2-(4-difluoromethoxy-3-ethoxyphenyl)-oxazol-4-ylmethyl]-3-meth-
ylpicolinamide was obtained following the procedure of Example
3.
[0969] .sup.1H-NMR (CDCl.sub.3) .delta.: 8.60 (1H, br s), 8.39 (1H,
d, J=3.6 Hz), 7.67-7.57 (4H, m), 7.33-7.20 (2H, m), 6.63 (1H, t,
J=75 Hz), 4.60 (2H, d, J=5.7 Hz), 4.20 (2H, q, J=6.9 Hz), 2.76 (3H,
s), 1.48 (3H, t, J=6.9 Hz)
Example 339
[0970] Using the compound obtained in Example 97 and allyl bromide,
white solid N-[2-(3-allyloxy-4-difluoromethoxy
phenyl)oxazol-4-ylmethyl]-3-methylpicolinamide was obtained
following the procedure of Example 3.
[0971] .sup.1H-NMR (CDCl.sub.3) .delta.: 8.60 (1H, br s), 8.40-8.39
(1H, m), 7.67 (1H, s), 7.65-7.58 (3H, m), 7.33-7.22 (3H, m), 6.63
(1H, t, J=75 Hz), 6.13-6.03 (1H, m), 5.50-5.32 (2H, m), 4.70-4.68
(2H, m), 4.60 (2H, d, J=8.7 Hz), 2.76 (3H, s)
Example 340
[0972] Using the compound obtained in Example 97 and
1-bromopropane, white powdery
N-[2-(4-difluoromethoxy-3-propoxyphenyl)oxazol-4-ylmethyl]-3-meth-
ylpicolinamide was obtained following the procedure of Example
3.
[0973] .sup.1H-NMR (CDCl.sub.3) .delta.: 8.58 (1H, br s), 8.39 (1H,
d, J=7.8, Hz), 7.67-7.57 (4H, m), 7.33-7.20 (2H, m), 6.62 (1H, t,
J=75 Hz), 4.60 (2H, d, J=6.0 Hz), 4.08 (2H, t, J=6.6 Hz), 2.76 (3H,
s), 1.94-1.82 (2H, m), 1.07 (3H, t, J=7.5 Hz)
Example 341
[0974] Using the compound obtained in Example 97 and
2-bromopropane, white solid
N-[2-(4-difluoromethoxy-3-isopropoxyphenyl)oxazol-4-ylmethyl]-3-met-
hylpicolinamide was obtained following the procedure of Example
3.
[0975] .sup.1H-NMR (CDCl.sub.3) .delta.: 8.58 (1H, br s), 8.39-8.38
(1H, m), 7.67-7.57 (4H, m), 7.33-7.19 (2H, m), 6.62 (1H, t, J=75
Hz), 4.74-4.67 (1H, m), 4.59 (2H, d, J=6.0 Hz), 2.76 (3H, s), 1.39
(6H, d, J=6.0 Hz)
Example 342
[0976] Using the compound obtained in Example 97 and
3-bromopentane, colorless oily
N-{2-[4-difluoromethoxy-3-(1-ethylpropoxy)phenyl]oxazol-4-ylmethyl}-3-met-
hylpicolinamide was obtained following the procedure of Example
3.
[0977] .sup.1H-NMR (CDCl.sub.3) .delta.: 8.58 (1H, br s), 8.40-8.38
(1H, m), 7.67 (1H, s), 7.63-7.55 (3H, m), 7.33-7.20 (3H, m), 6.61
(1H, t, J=75 Hz), 4.59 (2H, d, J=6.0 Hz), 4.33 (1H, qt, J=6.0 Hz),
2.76 (3H, s), 1.79-1.70 (4H, m), 0.98 (6H, t, J=7.2 Hz)
Example 343
[0978] Using the compound obtained in Example 97 and
4-bromo-1-butene, colorless oily
N-[2-(3-but-3-enyloxy-4-difluoromethoxy
phenyl)oxazol-4-ylmethyl]-3-methylpicolinamide was obtained
following the procedure of Example 3.
[0979] .sup.1H-NMR (CDCl.sub.3) .delta.: 8.58 (1H, br s), 8.40-8.38
(1H, m), 7.67 (1H, s), 7.64-7.58 (3H, m), 7.33-7.20 (2H, m), 6.63
(1H, t, J=75 Hz), 5.95-5.84 (1H, m), 5.23-5.13 (2H, m), 4.61-4.59
(2H, m), 4.18 (2H, t, J=6.6 Hz), 2.76 (3H, s), 2.64-2.58 (2H,
m)
Example 344
[0980] Using the compound obtained in Example 97 and isobutyl
bromide, colorless oily N-[2-(4-difluoromethoxy-3-isobutoxy
phenyl)oxazol-4-ylmethyl]-3-methylpicolinamide was obtained
following the procedure of Example 3.
[0981] .sup.1H-NMR (CDCl.sub.3) .delta.: 8.60 (1H, br s), 8.39 (1H,
br s), 7.68 (1H, s), 7.62-7.57 (3H, m), 7.33-7.20 (2H, m), 6.61
(1H, t, J=75 Hz), 4.60 (2H, d, J=6.0 Hz), 3.88 (2H, d, J=6.3 Hz),
2.76 (3H, s), 2.19-2.04 (1H, m), 1.06 (6H, d, J=6.3 Hz)
Example 345
[0982] Using the compound obtained in Example 97 and
(bromomethyl)cyclobutane, colorless oily N-[2-(3-cyclobutyl
methoxy-4-difluoromethoxyphenyl)oxazol-4-ylmethyl]-3-methyl
picolinamide was obtained following the procedure of Example 3.
[0983] .sup.1H-NMR (CDCl.sub.3) .delta.: 8.60 (1H, br s), 8.40 (1H,
br s), 7.68 (1H, s), 7.64-7.59 (3H, m), 7.33-7.20 (2H, m), 6.61
(1H, t, J=75 Hz), 4.60 (2H, d, J=6.0 Hz), 4.08 (2H, d, J=6.6 Hz),
2.89-2.76 (4H, m), 2.25-2.12 (2H, m), 2.04-1.92 (4H, m)
Example 346
[0984] Using the compound obtained in Reference Example 46 and
2-ethoxybenzoic acid, white powdery N-[2-(3-benzyloxy-4-difluoro
methoxyphenyl)oxazol-4-ylmethyl]-2-ethoxybenzamide was obtained
following the procedure of Example 96.
[0985] .sup.1H-NMR (CDCl.sub.3) .delta.: 8.56 (1H, br s), 8.24 (1H,
dd, J=7.8, 1.8 Hz), 7.73 (1H, d, J=1.8 Hz), 7.68-7.61 (2H, m),
7.48-7.24 (7H, m), 7.07 (1H, t, J=8.1 Hz), 6.95 (1H, d, J=8.4 Hz),
6.63 (1H, t, J=75 Hz), 5.21 (2H, s), 4.63 (2H, d, J=5.4 Hz), 4.18
(2H, q, J=6.9 Hz), 1.48 (3H, t, J=6.9 Hz)
Example 347
[0986] Using the compound obtained in Example 346, white powdery
N-[2-(4-difluoromethoxy-3-hydroxyphenyl)oxazol-4-ylmethyl]-2-ethoxybenzam-
ide was obtained following the procedure of Example 97.
[0987] .sup.1H-NMR (CDCl.sub.3) .delta.: 8.60 (1H, br s), 8.23 (1H,
dd, J=7.8, 1.8 Hz), 7.71-7.60 (2H, m), 7.57 (1H, dd, J=8.4, 1.8
Hz), 7.46-7.39 (1H, m), 7.19 (1H, d, J=8.4 Hz), 7.07 (1H, t, J=8.1
Hz), 6.95 (1H, d, J=8.4 Hz), 6.61 (1H, t, J=73.2 Hz), 6.02 (1H, br
s), 4.64 (2H, dd, J=5.4, 0.9 Hz), 4.19 (2H, q, J=6.9 Hz), 1.49 (3H,
t, J=6.9 Hz)
Example 348
[0988] A 80 mg quantity of the compound obtained in Example 347 and
0.1 ml of DBU were dissolved in 2 ml of ethanol, 80 mg of isobutyl
bromide was then added to the obtained solution, and heating and
refluxing were conducted overnight. After cooling, water was added
to the obtained reaction mixture, and ethyl acetate extraction was
performed. The organic layer was washed twice with water,
concentrated under reduced pressure, and the obtained residue was
purified by silica gel column chromatography (n-hexane:ethyl
acetate=3:1). The obtained crystals were recrystallized from
aqueous 80% ethanol, thereby yielding 30 mg of white powdery
N-[2-(4-difluoromethoxy-3-isobutoxyphenyl)
oxazol-4-ylmethyl]-2-ethoxybenzamide.
[0989] .sup.1H-NMR (CDCl.sub.3) .delta.: 8.54 (1H, br s), 8.24 (1H,
dd, J=7.8, 1.8 Hz), 7.67 (1H, s), 7.66-7.57 (2H, m), 7.45-7.39 (1H,
m), 7.23 (1H, d, J=8.1 Hz), 7.07 (1H, t, J=8.1 Hz), 6.95 (1H, d,
J=7.5 Hz), 6.62 (1H, t, J=75 Hz), 4.64 (2H, d, J=5.1 Hz), 4.19 (2H,
q, J=6.9 Hz), 3.87 (2H, d, J=6.6 Hz), 2.17 (1H, qt, J=6.6 Hz), 1.49
(3H, t, J=6.9 Hz), 1.07 (6H, d, J=6.9 Hz)
Example 349
[0990] Using the compound obtained in Example 347 and ethyl iodide,
white powdery N-[2-(4-difluoromethoxy-3-ethoxyphenyl)
oxazol-4-ylmethyl]-2-ethoxybenzamide was obtained following the
procedure of Example 348.
[0991] .sup.1H-NMR (CDCl.sub.3) .delta.: 8.56 (1H, br s), 8.24 (1H,
dd, J=7.8, 1.8 Hz), 7.67-7.58 (3H, m), 7.46-7.40 (1H, m), 7.24-7.21
(1H, m), 7.08 (1H, t, J=7.8 Hz), 6.95 (1H, d, J=7.8 Hz), 6.64 (1H,
t, J=75 Hz) 4.63 (1H, d, J=5.1 Hz), 4.23-4.15 (4H, m), 1.52-1.46
(6H, m)
Example 350
[0992] Using the compound obtained in Example 347 and
1-bromopropane, white powdery N-[2-(4-difluoromethoxy-3-propoxy
phenyl)oxazol-4-ylmethyl]-2-ethoxybenzamide was obtained following
the procedure of Example 348.
[0993] .sup.1H-NMR (CDCl.sub.3) .delta.: 8.56 (1H, br s), 8.24 (1H,
dd, J=7.5, 1.8 Hz), 7.67 (1H, s), 7.64-7.57 (2H, m), 7.46-7.40 (1H,
m), 7.23 (1H, d, J=7.8 Hz), 7.07 (1H, t, J=7.5 Hz), 6.95 (1H, d,
J=8.4 Hz), 6.63 (1H, t, J=75 Hz), 4.64 (2H, d, J=5.4 Hz), 4.19 (2H,
q, J=7.2 Hz), 4.07 (2H, t, J=6.6 Hz), 1.90 (2H, qt, J=7.2, 6.6 Hz),
1.49 (3H, t, J=6.9 Hz), 1.08 (3H, t, J=7.2 Hz)
Example 351
[0994] Using the compound obtained in Example 347 and allyl
bromide, white powdery N-[2-(3-allyloxy-4-difluoromethoxy
phenyl)oxazol-4-ylmethyl]-2-ethoxybenzamide was obtained following
the procedure of Example 348.
[0995] .sup.1H-NMR (CDCl.sub.3) .delta.: 8.55 (1H, br s), 8.24 (1H,
dd, J=7.8, 1.8 Hz), 7.68 (1H, s), 7.65-7.60 (2H, m), 7.46-7.40 (1H,
m), 7.25-7.23 (1H, m), 7.08 (1H, t, J=7.8 Hz), 6.96 (1H, d, J=8.4
Hz), 6.64 (1H, t, J=74.7 Hz), 6.10-6.03 (1H, m), 5.47 (1H, dd,
J=17.4, 1.5 Hz), 5.34 (1H, dd, J=10.5, 1.5 Hz), 4.69 (2H, dt,
J=5.1, 1.5 Hz), 4.63 (2H, dd, J=5.4, 1.2 Hz), 4.19 (2H, q, J=6.9
Hz), 1.49 (3H, t, J=6.9 Hz)
Example 352
[0996] Using the compound obtained in Example 347 and
2-bromopropane, white powdery
N-[2-(4-difluoromethoxy-3-isopropoxyphenyl)oxazol-4-ylmethyl]-2-ethoxyben-
zamide was obtained following the procedure of Example 348.
[0997] .sup.1H-NMR (CDCl.sub.3) .delta.: 8.57 (1H, br s), 8.24 (1H,
dd, J=7.5, 1.8 Hz), 7.67 (1H, s), 7.65-7.57 (2H, m), 7.46-7.40 (1H,
m), 7.26-7.21 (1H, m), 7.08 (1H, t, J=7.5 Hz), 6.95 (1H, d, J=8.4
Hz), 6.63 (1H, t, J=75 Hz), 4.74-4.62 (3H, m), 4.19 (2H, q, J=6.9
Hz), 1.49 (3H, t, J=6.9 Hz), 1.40 (6H, d, J=6.3 Hz)
Example 353
[0998] Using the compound obtained in Example 347 and
(bromomethyl)cyclopropane, white powdery N-[2-(3-cyclopropyl
methoxy-4-difluoromethoxyphenyl)oxazol-4-ylmethyl]-2-ethoxy
benzamide was obtained following the procedure of Example 348.
[0999] .sup.1H-NMR (CDCl.sub.3) .delta.: 8.55 (1H, br s), 8.24 (1H,
dd, J=8.1, 1.8 Hz), 7.67 (1H, s), 7.61-7.58 (2H, m), 7.46-7.39 (1H,
m), 7.26-7.21 (1H, m), 7.07 (1H, t, J=7.5 Hz), 6.95 (1H, d, J=8.4
Hz), 6.70 (1H, t, J=75 Hz) 4.63 (2H, dd, J=5.4, 0.9 Hz), 4.19 (2H,
q, J=6.9 Hz), 1.49 (3H, t, J=6.9 Hz), 1.35-1.30 (1H, m), 0.71-0.64
(2H, m), 0.41-0.35 (2H, m)
Example 354
[1000] Using the compound obtained in Example 347 and
4-bromo-1-butene, white powdery
N-[2-(3-but-3-enyloxy-4-difluoromethoxy
phenyl)oxazol-4-ylmethyl]-2-ethoxybenzamide was obtained following
the procedure of Example 348.
[1001] .sup.1H-NMR (CDCl.sub.3) .delta.: 8.56 (1H, br s), 8.24 (1H,
dd, J=7.5, 1.8 Hz), 7.67 (1H, s), 7.64-7.58 (2H, m), 7.46-7.40 (1H,
m), 7.26-7.21 (1H, m), 7.08 (1H, t, J=7.5 Hz), 6.95 (1H, d, J=8.4
Hz), 6.64 (1H, t, J=75 Hz), 5.92-5.86 (1H, m), 5.24-5.13 (2H, m),
4.64 (2H, d, J=5.1 Hz), 4.22-4.14 (4H, m), 2.65-2.58 (2H, m), 1.49
(3H, t, J=6.9 Hz)
Example 355
[1002] Using the compound obtained in Example 347 and
3-bromopentane, white powdery
N-{2-[4-difluoromethoxy-3-(1-ethylpropoxy)phenyl]oxazol-4-ylmethyl}-2-eth-
oxybenzamide was obtained following the procedure of Example
348.
[1003] .sup.1H-NMR (CDCl.sub.3) .delta.: 8.57 (1H, br s), 8.24 (1H,
dd, J=7.8, 1.8 Hz), 7.67 (1H, s), 7.63-7.58 (2H, m), 7.46-7.40 (1H,
m), 7.23 (1H, d, J=8.4 Hz), 7.07 (1H, t, J=8.1 Hz), 6.95 (1H, d,
J=8.1 Hz), 6.63 (1H, t, J=75 Hz), 4.64 (2H, d, J=5.1 Hz), 4.33 (1H,
qt, J=6.0, 5.1 Hz), 4.19 (2H, q, J=6.9 Hz), 1.79-1.70 (4H, m), 1.49
(3H, t, J=6.9 Hz), 0.99 (6H, t, J=7.5 Hz)
Reference Example 94
[1004] Using the compound obtained in Reference Example 59 and
chlorodifluoromethane, white powdery ethyl
4-benzyloxy-3-difluoromethoxybenzoate was obtained following the
procedure of Example 4.
[1005] .sup.1H-NMR (CDCl.sub.3) .delta.: 7.90-7.80 (2H, m),
7.45-7.30 (5H, m), 7.03 (1H, d, J=8.4 Hz), 6.59 (1H, t, J=74.4 Hz),
5.23 (2H, s), 4.35 (2H, q, J=7.2 Hz), 1.38 (3H, t, J=7.2 Hz)
Reference Example 95
[1006] Using the compound obtained in Reference Example 94, white
powdery
2-(4-benzyloxy-3-difluoromethoxyphenyl)-4-chloromethyloxazole was
obtained following the procedures of Reference Examples 3 to 5.
[1007] .sup.1H-NMR (CDCl.sub.3) .delta.: 7.90-7.80 (2H, m), 7.65
(1H, s), 7.45-7.30 (5H, m), 7.06 (1H, d, J=7.2 Hz), 6.60 (1H, t,
J=74.7 Hz), 5.20 (2H, s), 4.56 (2H, s)
Example 356
[1008] Using the compound obtained in Reference Example 95, white
powdery
3-{2-(3-difluoromethoxy-4-hydroxyphenyl)oxazol-4-yl}-1-(3-methylpyridin-2-
-yl)propan-1-one was obtained following the procedures of Reference
Examples 92 and 93 and Examples 326 and 327.
[1009] .sup.1H-NMR (CDCl.sub.3) .delta.: 8.49 (1H, d, J=4.5 Hz),
7.76-7.72 (2H, m), 7.59 (1H, d, J=8.4 Hz), 7.57 (1H, s), 7.37-7.30
(1H, m), 7.02 (1H, d, J=8.4 Hz), 6.59 (1H, t, J=75 Hz), 3.59 (2H,
t, J=7.5 Hz), 3.01 (2H, t, J=7.5 Hz), 2.57 (3H, s)
Example 357
[1010] Using the compound obtained in Example 356 and
2-bromopropane, white powdery 3-[2-(3-difluoromethoxy-4-isopropoxy
phenyl)oxazol-4-yl]-1-(3-methylpyridin-2-yl)propan-1-one was
obtained following the procedure of Example 3.
[1011] .sup.1H-NMR (CDCl.sub.3) .delta.: 8.50 (1H, d, J=4.5 Hz),
7.83-7.78 (2H, m), 7.58 (1H, d, J=8.4 Hz), 7.47 (1H, s), 7.34-7.30
(1H, m), 7.01 (1H, d, J=8.4 Hz), 6.58 (1H, t, J=75 Hz), 4.67-4.57
(1H, m), 3.59 (2H, t, J=7.5 Hz), 3.01 (2H, t, J=7.5 Hz), 2.57 (3H,
s), 1.39 (6H, d, J=6.0 Hz)
Example 358
[1012] Using the compound obtained in Example 356 and allyl
bromide, white powdery 3-[2-(4-allyloxy-3-difluoromethoxy
phenyl)oxazol-4-yl]-1-(3-methylpyridin-2-yl)propan-1-one was
obtained following the procedure of Example 3.
[1013] .sup.1H-NMR (CDCl.sub.3) .delta.: 8.50 (1H, dd, J=4.8, 1.2
Hz), 7.84-7.80 (2H, m), 7.60-7.56 (1H, m), 7.47 (1H, d, J=1.2 Hz),
7.34-7.30 (1H, m), 7.01 (1H, d, J=8.4 Hz), 6.60 (1H, t, J=74.7 Hz),
6.10-6.00 (1H, m), 5.44 (1H, dd, J=17.4, 1.5 Hz), 5.33 (1H, dd,
J=10.5, 1.5 Hz), 4.65 (2H, dt, J=5.1, 1.5 Hz), 3.60 (2H, t, J=7.5
Hz), 3.01 (2H, t, J=7.5 Hz), 2.58 (3H, s)
Example 359
[1014] Using the compound obtained in Example 356 and
4-bromo-1-butene, white powdery
3-[2-(4-but-3-enyloxy-3-difluoromethoxy
phenyl)oxazol-4-yl]-1-(3-methylpyridin-2-yl)propan-1-one was
obtained following the procedure of Example 3.
[1015] .sup.1H-NMR (CDCl.sub.3) .delta.: 8.50 (1H, dd, J=4.8, 1.2
Hz), 7.84-7.78 (2H, m), 7.58 (1H, d, J=7.5 Hz), 7.46 (1H, s),
7.34-7.30 (1H, m), 7.00 (1H, d, J=8.4 Hz), 6.59 (1H, t, J=75 Hz),
5.94-5.85 (1H, m), 5.23-5.12 (2H, m), 4.12 (2H, t, J=6.6 Hz), 3.60
(2H, t, J=7.2 Hz), 3.00 (2H, t, J=7.2 Hz), 2.63-2.56 (5H, m)
Example 360
[1016] Using the compound obtained in Example 356 and
(bromomethyl)cyclopropane, white powdery 3-[2-(4-cyclopropyl
methoxy-3-difluoromethoxyphenyl)oxazol-4-yl]-1-(3-methylpyridin-2-yl)prop-
an-1-one was obtained following the procedure of Example 3.
[1017] .sup.1H-NMR (CDCl.sub.3) .delta.: 8.50 (1H, dd, J=4.8, 1.2
Hz), 7.83-7.79 (2H, m), 7.57 (1H, d, J=7.5 Hz), 7.46 (1H, s),
7.34-7.30 (1H, m), 6.98 (1H, d, J=8.1 Hz), 6.65 (1H, t, J=75 Hz),
3.92 (2H, d, J=7.2 Hz), 3.59 (2H, t, J=7.2 Hz), 3.00 (2H, t, J=7.2
Hz), 2.57 (3H, s), 1.33-1.27 (1H, m), 0.69-0.63 (2H, m), 0.40-0.34
(2H, m)
Example 361
[1018] Using the compound obtained in Example 356 and
1-bromopropane, white powdery 3-[2-(3-difluoromethoxy-4-propoxy
phenyl)oxazol-4-yl]-1-(3-methylpyridin-2-yl)propan-1-one was
obtained following the procedure of Example 3.
[1019] .sup.1H-NMR (CDCl.sub.3) .delta.: 8.50 (1H, dd, J=4.8, 1.2
Hz), 7.84-7.78 (2H, m), 7.58 (1H, d, J=8.1 Hz), 7.47 (1H, s),
7.43-7.30 (1H, m), 7.00 (1H, d, J=8.4 Hz), 6.59 (1H, t, J=75 Hz),
4.03 (2H, t, J=6.6 Hz), 3.59 (2H, t, J=7.5 Hz), 3.01 (2H, t, J=7.5
Hz), 2.58 (3H, s), 1.87 (2H, qt, J=7.2 Hz), 1.06 (3H, t, J=7.2
Hz)
Example 362
[1020] Using the compound obtained in Example 356 and ethyl iodide,
white powdery 3-[2-(3-difluoromethoxy-4-ethoxyphenyl)
oxazol-4-yl]-1-(3-methylpyridin-2-yl)propan-1-one was obtained
following the procedure of Example 3.
[1021] .sup.1H-NMR (CDCl.sub.3) .delta.: 8.50 (1H, d, J=4.5 Hz),
7.84-7.78 (2H, m), 7.59 (1H, d, J=8.4 Hz), 7.47 (1H, s), 7.34-7.30
(1H, m), 6.99 (1H, d, J=8.4 Hz), 6.60 (1H, t, J=75 Hz), 4.15 (2H,
q, J=6.9 Hz), 3.59 (2H, t, J=7.2 Hz), 3.01 (2H, t, J=7.2 Hz), 2.57
(3H, s), 1.47 (3H, t, J=6.9 Hz)
Example 363
[1022] The compound obtained in Reference Example 95 was used and
treated following the procedure of Example 228, followed by
treatment according to the procedure of Example 229, yielding white
powdery
3-[2-(3-difluoromethoxy-4-hydroxyphenyl)oxazol-4-yl]-1-(2-ethoxyphenyl)pr-
opan-1-one.
[1023] .sup.1H-NMR (CDCl.sub.3) .delta.: 7.80-7.75 (2H, m), 7.71
(1H, dd, J=7.8, 1.8 Hz), 7.46-7.40 (2H, m), 7.22-6.69 (3H, m), 6.59
(1H, t, J=75 Hz), 5.91 (1H, br s), 4.14 (2H, q, J=7.2 Hz), 3.42
(2H, t, J=7.5 Hz), 2.99 (2H, t, J=7.5 Hz), 1.48 (3H, t, J=7.2
Hz)
Example 364
[1024] Using the compound obtained in Example 363 and
4-bromo-1-butene, white powdery
3-[2-(4-but-3-enyloxy-3-difluoromethoxy
phenyl)oxazol-4-yl]-1-(2-ethoxyphenyl)propan-1-one was obtained
following the procedure of Example 3.
[1025] .sup.1H-NMR (CDCl.sub.3) .delta.: 7.84-7.79 (2H, m), 7.71
(1H, dd, J=7.8, 1.8 Hz), 7.46-7.39 (2H, m), 7.01-6.92 (3H, m), 6.59
(1H, t, J=75 Hz), 5.91-5.85 (1H, m), 5.23-5.12 (2H, m), 4.18-4.09
(4H, m), 3.42 (2H, t, J=6.9 Hz), 2.99 (2H, t, J=6.9 Hz), 2.60 (2H,
m), 1.48 (3H, t, J=6.9 Hz)
Example 365
[1026] Using the compound obtained in Example 363 and allyl
bromide, white powdery 3-[2-(4-allyloxy-3-difluoromethoxy
phenyl)oxazol-4-yl]-1-(2-ethoxyphenyl)propan-1-one was obtained
following the procedure of Example 3.
[1027] .sup.1H-NMR (CDCl.sub.3) .delta.: 7.83-7.79 (2H, m), 7.70
(1H, dd, J=7.8, 1.8 Hz), 7.46-7.39 (2H, m), 7.02-6.92 (3H, m), 6.60
(1H, t, J=74.7 Hz), 6.06-6.00 (1H, m), 5.47-5.30 (2H, m), 4.66-4.63
(2H, m), 4.14 (2H, q, J=6.9 Hz), 3.42 (2H, t, J=6.9 Hz), 2.99 (2H,
t, J=6.9 Hz), 1.48 (3H, t, J=6.9 Hz)
Example 366
[1028] Using the compound obtained in Example 363 and ethyl iodide,
white powdery 3-[2-(3-difluoromethoxy-4-ethoxyphenyl)
oxazol-4-yl]-1-(2-ethoxyphenyl)propan-1-one was obtained following
the procedure of Example 3.
[1029] .sup.1H-NMR (CDCl.sub.3) .delta.: 7.84-7.80 (2H, m), 7.71
(1H, dd, J=7.8, 1.8 Hz), 7.45-7.39 (2H, m), 7.00-6.91 (3H, m), 6.60
(1H, t, J=75 Hz) 4.18-4.10 (4H, m), 3.42 (2H, t, J=7.5 Hz), 2.99
(2H, t, J=7.5 Hz), 1.50-1.44 (6H, m)
Reference Example 96
[1030] The compound obtained in Reference Example 95 was used and
treated following the procedure of Reference Example 45, followed
by treatment according to the procedure of Reference Example 46,
yielding pale yellow oily
[2-(4-benzyloxy-3-difluoromethoxyphenyl)oxazol-4-yl]methylamine was
obtained.
[1031] .sup.1H-NMR (CDCl.sub.3) .delta.: 7.89-7.82 (2H, m), 7.61
(1H, s), 7.56-7.31 (5H, m), 7.07 (1H, d, J=8.1 Hz), 6.62 (1H, t,
J=75 Hz), 5.19 (2H, s), 3.83 (2H, s)
Example 367
[1032] The compound obtained in Reference Example 96 was used and
treated following the procedure of Example 96, followed by
treatment according to the procedure of Example 97, yielding white
powdery
N-[2-(3-difluoromethoxy-4-hydroxyphenyl)oxazol-4-ylmethyl]-3-methylpicoli-
namide.
[1033] .sup.1H-NMR (CDCl.sub.3) .delta.: 8.59 (1H, br s), 8.39 (1H,
d, J=4.5 Hz), 7.79-7.76 (2H, m), 7.63-7.58 (2H, m), 7.37-7.28 (1H,
m), 7.07 (1H, d, J=8.1 Hz), 6.61 (1H, t, J=75 Hz), 6.16 (1H, s),
4.58 (2H, d, J=5.4 Hz), 2.76 (3H, s)
Example 368
[1034] Using the compound obtained in Example 367 and allyl
bromide, white powdery N-[2-(4-allyloxy-3-difluoromethoxy
phenyl)oxazol-4-ylmethyl]-3-methylpicolinamide was obtained
following the procedure of Example 98.
[1035] .sup.1H-NMR (CDCl.sub.3) .delta.: 8.60 (1H, br s), 8.39 (1H,
d, J=4.5 Hz), 7.87-7.83 (2H, m), 7.65 (1H, s), 7.60-7.57 (1H, m),
7.33-7.29 (1H, m), 7.10 (1H, d, J=8.4 Hz), 6.61 (1H, t, J=75 Hz),
6.10-5.99 (1H, m), 5.55 (1H, dd, J=17.1, 1.5 Hz), 5.34 (1H, dd,
J=10.5, 1.5 Hz), 4.65 (2H, d, J=5.4 Hz), 4.58 (2H, d, J=5.4 Hz),
2.76 (3H, s)
Example 369
[1036] Using the compound obtained in Example 367 and
(bromomethyl)cyclobutane, white powdery N-[2-(4-cyclobutyl
methoxy-3-difluoromethoxyphenyl)oxazol-4-ylmethyl]-3-methyl
picolinamide was obtained following the procedure of Example
98.
[1037] .sup.1H-NMR (CDCl.sub.3) .delta.: 8.58 (1H, br s), 8.39 (1H,
d, J=4.5 Hz), 7.87-7.82 (2H, m), 7.64 (1H, s), 7.59 (1H, d, J=8.4
Hz), 7.33-7.29 (2H, m), 7.01 (1H, d, J=8.4 Hz), 6.59 (1H, t, J=75
Hz), 4.59 (1H, d, J=5.4 Hz), 4.03 (2H, d, J=6.9 Hz), 2.90-2.82 (1H,
m), 2.76 (3H, s), 2.22-2.13 (2H, m), 2.00-1.84 (4H, m)
Example 370
[1038] Using the compound obtained in Example 367 and isobutyl
bromide, white powdery N-[2-(3-difluoromethoxy-4-isobutoxy
phenyl)oxazol-4-ylmethyl]-3-methylpicolinamide was obtained
following the procedure of Example 98.
[1039] .sup.1H-NMR (CDCl.sub.3) .delta.: 8.58 (1H, br s), 8.39 (1H,
d, J=4.5 Hz), 7.87-7.83 (2H, m), 7.64 (1H, s), 7.60-7.57 (1H, m),
7.33-7.28 (1H, m), 7.00 (1H, d, J=8.4 Hz), 6.59 (1H, t, J=75 Hz),
4.59 (1H, d, J=5.4 Hz), 3.81 (2H, d, J=6.9 Hz), 2.76 (3H, s),
2.22-2.09 (1H, m), 1.06 (6H, d, J=6.6 Hz)
Example 371
[1040] Using the compound obtained in Example 367 and
4-bromo-1-butene, white powdery
N-[2-(4-but-3-enyloxy-3-difluoromethoxy
phenyl)oxazol-4-ylmethyl]-3-methylpicolinamide was obtained
following the procedure of Example 98.
[1041] .sup.1H-NMR (CDCl.sub.3) .delta.: 8.59 (1H, br s), 8.39 (1H,
d, J=4.5 Hz), 7.88-7.83 (2H, m), 7.65 (1H, s), 7.60-7.57 (1H, m),
7.33-7.29 (1H, m), 7.01 (1H, d, J=8.4 Hz), 6.61 (1H, t, J=75 Hz),
5.94-5.83 (1H, m), 5.24-5.12 (2H, m), 4.59 (1H, d, J=5.4 Hz), 4.13
(2H, t, J=6.6 Hz), 2.76 (3H, s), 2.63-2.57 (2H, m)
Example 372
[1042] Using the compound obtained in Example 367 and
(bromomethyl)cyclopropane, white powdery N-[2-(4-cyclopropyl
methoxy-3-difluoromethoxyphenyl)oxazol-4-ylmethyl]-3-methyl
picolinamide was obtained following the procedure of Example
98.
[1043] .sup.1H-NMR (CDCl.sub.3) .delta.: 8.58 (1H, br s), 8.39 (1H,
d, J=4.5 Hz), 7.86-7.83 (2H, m), 7.65 (1H, s), 7.59 (1H, d, J=8.4
Hz), 7.33-7.28 (1H, m), 7.00 (1H, d, J=8.4 Hz), 6.66 (1H, t, J=75
Hz), 4.59 (2H, d, J=5.4 Hz), 3.93 (2H, d, J=6.9 Hz), 2.76 (3H, s),
1.33-1.24 (1H, m), 0.70-0.64 (2H, m), 0.41-0.35 (2H, m)
Example 373
[1044] The compound obtained in Reference Example 96 was used and
treated following the procedure of Example 96, followed by
treatment according to the procedure of Example 97, yielding white
powdery
N-[2-(3-difluoromethoxy-4-hydroxyphenyl)oxazol-4-ylmethyl]-2-ethoxybenzam-
ide.
[1045] .sup.1H-NMR (CDCl.sub.3) .delta.: 8.59 (1H, br s), 8.24 (1H,
dd, J=7.8, 1.2 Hz), 7.81-7.78 (2H, m), 7.63 (1H, s), 7.46-7.40 (1H,
m), 7.11-7.05 (2H, m), 6.96 (1H, d, J=8.4 Hz), 6.62 (1H, t, J=75
Hz), 5.87 (1H, br s), 4.62 (2H, d, J=5.4 Hz), 4.19 (2H, q, J=6.9
Hz), 1.50 (3H, t, J=6.9 Hz)
Example 374
[1046] Using the compound obtained in Example 373 and
2-bromopropane, white powdery N-[2-(3-difluoromethoxy-4-isopropoxy
phenyl)oxazol-4-ylmethyl]-2-ethoxybenzamide was obtained following
the procedure of Example 98.
[1047] .sup.1H-NMR (CDCl.sub.3) .delta.: 8.60 (1H, br s), 8.24 (1H,
dd, J=7.8, 2.1 Hz), 7.85-7.82 (2H, m), 7.64 (1H, s), 7.45-7.39 (1H,
m), 7.09-7.01 (2H, m), 6.95 (1H, d, J=8.1 Hz), 6.59 (1H, t, J=75
Hz), 4.71-4.61 (5H, m), 4.19 (2H, q, J=6.9 Hz), 1.51 (3H, t, J=6.9
Hz), 1.40 (6H, d, J=6.9 Hz)
Example 375
[1048] Using the compound obtained in Example 373 and
(bromomethyl)cyclopropane, white powdery N-[2-(4-cyclopropyl
methoxy-3-difluoromethoxyphenyl)oxazol-4-ylmethyl]-2-ethoxy
benzamide was obtained following the procedure of Example 98.
[1049] .sup.1H-NMR (CDCl.sub.3) .delta.: 8.59 (1H, br s), 8.24 (1H,
dd, J=7.8, 2.1 Hz), 7.85-7.82 (2H, m), 7.64 (1H, s), 7.45-7.39 (1H,
m), 7.09-6.94 (3H, m), 6.66 (1H, t, J=75 Hz), 4.62 (2H, d, J=5.4
Hz), 4.19 (2H, q, J=6.9 Hz), 3.93 (2H, d, J=8.4 Hz), 1.50 (3H, t,
J=6.9 Hz), 1.34-1.24 (1H, m), 0.71-0.64 (2H, m), 0.41-0.35 (2H,
m)
Example 376
[1050] Using the compound obtained in Example 373 and
1-bromopropane, white powdery N-[2-(3-difluoromethoxy-4-propoxy
phenyl)oxazol-4-ylmethyl]-2-ethoxybenzamide was obtained following
the procedure of Example 98.
[1051] .sup.1H-NMR (CDCl.sub.3) .delta.: 8.60 (1H, br s), 8.23 (1H,
dd, J=7.8, 1.8 Hz), 7.87-7.83 (2H, m), 7.64 (1H, s), 7.42 (1H, t,
J=7.5 Hz), 7.09-6.85 (3H, m), 6.35 (1H, t, J=75 Hz), 4.62 (2H, d,
J=6.0 Hz), 4.19 (2H, q, J=6.6 Hz), 4.04 (2H, t, J=6.0 Hz),
1.91-1.84 (2H, m), 1.50 (3H, t, J=6.9 Hz), 1.07 (3H, t, J=6.9
Hz)
Example 377
[1052] Using the compound obtained in Example 373 and allyl
bromide, white powdery N-[2-(4-allyloxy-3-difluoromethoxyphenyl)
oxazol-4-ylmethyl]-2-ethoxybenzamide was obtained following the
procedure of Example 98.
[1053] .sup.1H-NMR (CDCl.sub.3) .delta.: 8.60 (1H, br s), 8.23 (1H,
dd, J=7.8, 1.8 Hz), 7.86-7.83 (2H, m), 7.64 (1H, s), 7.42 (1H, t,
J=7.5 Hz), 7.10-6.97 (3H, m), 6.61 (1H, t, J=75 Hz), 6.07-6.01 (1H,
m), 5.49-5.32 (2H, m), 4.68-4.61 (4H, m), 4.19 (2H, q, J=6.9 Hz),
1.50 (3H, t, J=6.9 Hz)
Reference Example 97
[1054] Using ethyl 3,4-dihydroxybenzoate and chlorodifluoro
methane, white powdery ethyl 3,4-bis-difluoromethoxybenzoate was
obtained following the procedure of Example 4.
[1055] .sup.1H-NMR (CDCl.sub.3) .delta.: 8.00-7.90 (2H, m), 7.31
(1H, d, J=8.1 Hz), 6.60 (1H, t, J=72.9 Hz), 6.57 (1H, t, J=72.9
Hz), 4.39 (2H, q, J=7.2 Hz), 1.40 (3H, t, J=7.2 Hz)
Reference Example 98
[1056] Using the compound obtained in Reference Example 97, white
powdery 2-(3,4-bis-difluoromethoxyphenyl)-4-chloromethyl oxazol was
obtained following the procedures of Reference Examples 3 to 5.
[1057] .sup.1H-NMR (CDCl.sub.3) .delta.: 7.95-7.90 (2H, m), 7.73
(1H, s), 7.35 (1H, d, J=8.4 Hz), 6.60 (1H, t, J=72.9 Hz), 6.59 (1H,
t, J=72.9 Hz), 4.57 (2H, s)
Example 378
[1058] Using the compound obtained in Reference Example 98, white
powdery
3-[2-(3,4-bis-difluoromethoxyphenyl)oxazol-4-yl]-1-(2-ethoxyphenyl)propan-
-1-one was obtained following the procedure of Example 190.
[1059] .sup.1H-NMR (CDCl.sub.3) .delta.: 7.89-7.84 (2H, m), 7.71
(1H, dd, J=7.5, 1.8 Hz), 7.48-7.41 (2H, m), 7.32 (1H, d, J=8.4 Hz),
7.01-6.93 (2H, m), 6.58 (1H, t, J=75 Hz), 6.57 (1H, t, J=75 Hz),
4.14 (2H, q, J=6.9 Hz), 3.43 (2H, t, J=6.9 Hz), 3.00 (2H, t, J=6.9
Hz), 1.48 (3H, t, J=6.9 Hz)
Reference Example 99
[1060] The compound obtained in Reference Example 98 was used and
treated following the procedure of Reference Example 45, followed
by treatment according to the procedure of Reference Example 46,
yielding pale yellow oily [2-(3,4-bis-difluoromethoxy
phenyl)oxazol-4-yl]-methylamine.
[1061] .sup.1H-NMR (CDCl.sub.3) .delta.: 7.92-7.88 (2H, m), 7.58
(1H, s), 7.34 (1H, d, J=8.4 Hz), 6.60 (1H, t, J=75 Hz), 6.59 (1H,
t, J=75 Hz), 3.85 (2H, s)
Example 379
[1062] Using the compound obtained in Reference Example 99, white
powdery
N-[2-(3,4-bis-difluoromethoxyphenyl)oxazol-4-ylmethyl]-3-methylpicolinami-
de was obtained following the procedure of Example 96.
[1063] .sup.1H-NMR (CDCl.sub.3) .delta.: 8.61 (1H, br s), 8.40 (1H,
dd, J=7.5, 1.5 Hz), 7.93-7.88 (2H, m), 7.70 (1H, s), 7.60 (1H, d,
J=1.5 Hz), 7.58-7.31 (2H, m), 6.60 (1H, t, J=75 Hz), 6.58 (1H, t,
J=75 Hz), 4.60 (2H, dd, J=6.0, 1.2 Hz), 2.77 (3H, s)
Example 380
[1064] Using the compound obtained in Reference Example 99, white
powdery
N-[2-(3,4-bis-difluoromethoxyphenyl)oxazol-4-ylmethyl]-2-ethoxybenzamide
was obtained following the procedure of in Example 1.
[1065] .sup.1H-NMR (CDCl.sub.3) .delta.: 8.59 (1H, br s), 8.23 (1H,
dd, J=7.5, 1.8 Hz), 7.94-7.88 (2H, m), 7.70 (1H, s), 7.46-7.33 (2H,
m), 7.07 (1H, t, J=7.5 Hz), 6.95 (1H, d, J=8.4 Hz), 6.60 (1H, t,
J=75 Hz), 6.59 (1H, t, J=75 Hz), 4.63 (2H, d, J=6.0 Hz), 4.19 (2H,
q, J=6.9 Hz), 1.50 (3H, t, J=6.9 Hz)
Example 381
[1066] Using the compound obtained in Reference Example 98, white
powdery
3-[2-(3,4-bis-difluoromethoxyphenyl)oxazol-4-yl]-1-(3-methylpyridin-2-yl)-
propan-1-one was obtained following the procedure of Example
356.
[1067] .sup.1H-NMR (CDCl.sub.3) .delta.: 8.51 (1H, br s), 7.88-7.85
(2H, m), 7.59 (1H, d, J=8.4 Hz), 7.53 (1H, s), 7.35-7.30 (2H, m),
6.58 (1H, t, J=75 Hz), 6.57 (1H, t, J=75 Hz), 3.60 (2H, t, J=6.3
Hz), 3.02 (2H, t, J=6.3 Hz), 2.58 (3H, s)
Example 382
[1068] Using the compound obtained in Example 347 and the compound
obtained in Reference Example 85, white powdery N-{2-[4-difluoro
methoxy-3-(2,2-difluoroethoxy)phenyl]-oxazol-4-ylmethyl}-2-ethoxy
benzamide was obtained following the procedure of Example 348.
[1069] .sup.1H-NMR (CDCl.sub.3) .delta.: 8.55 (1H, br s), 8.24 (1H,
dd, J=7.8, 1.8 Hz), 7.71-7.65 (3H, m), 7.46-7.41 (1H, m), 7.29 (1H,
s), 7.08 (1H, t, J=8.1 Hz), 6.96 (1H, d, J=8.1 Hz), 6.59 (1H, t,
J=74.1 Hz), 6.15 (1H, tt, J=54.9, 4.2 Hz) 4.64 (2H, d, J=5.4 Hz),
4.32 (2H, td, J=12.9, 4.2 Hz), 4.20 (2H, q, J=6.9 Hz) 1.50 (3H, t,
J=6.9 Hz)
Example 383
[1070] Using the compound obtained in Example 347 and
1,1,1-trifluoro-2-iodoethane, white powdery
N-{2-[4-difluoromethoxy-3-(2,2,2-trifluoroethoxy)phenyl]-oxazol-4-ylmethy-
l}-2-ethoxy benzamide was obtained following the procedure of
Example 348.
[1071] .sup.1H-NMR (CDCl.sub.3) .delta.: 8.56 (1H, br s), 8.24 (1H,
dd, J=7.8, 1.8 Hz), 7.75-7.68 (3H, m), 7.46-7.40 (1H, m), 7.30 (1H,
d, J=8.4 Hz), 7.08 (1H, t, J=8.1 Hz), 6.96 (1H, d, J=8.1 Hz), 6.60
(1H, t, J=74.1 Hz), 4.63 (2H, d, J=5.4 Hz), 4.49 (2H, q, J=8.1 Hz),
4.20 (2H, q, J=6.9 Hz) 1.50 (3H, t, J=6.9 Hz)
Example 384
[1072] Using the compound obtained in Example 17 and 2-bromo
propane, colorless oily N-[2-(4-methoxy-3-isopropoxyphenyl)
oxazol-4-ylmethyl]-3-methylpicolinamide was obtained following the
procedure of Example 19.
[1073] .sup.1H-NMR (CDCl.sub.3) .delta.: 8.58 (1H, br s), 8.39 (1H,
dd, J=4.8, 1.2 Hz), 7.63-7.57 (4H, m), 7.33-7.28 (1H, m), 6.93 (1H,
d, J=8.4 Hz), 4.68 (1H, sept., J=6.3 Hz), 4.59 (2H, d, J=5.7 Hz),
3.89 (3H, s), 2.76 (3H, s), 1.41 (6H, d, J=6.3 Hz)
Example 385
[1074] Using the compound obtained in Example 347 and
(bromomethyl)cyclobutane, white powdery
N-[2-(3-Cyclobutylmethoxy-4-difluoromethoxyphenyl)oxazol-4-ylmethyl]-2-et-
hoxybenzamide was obtained following the procedure of Example
348.
[1075] .sup.1H-NMR (CDCl.sub.3) .delta.: 8.56 (1H, br s), 8.24 (1H,
dd, J=7.8, 1.8 Hz), 7.67-7.58 (3H, m), 7.50-7.40 (1H, m), 7.23 (1H,
d, J=8.4 Hz), 7.08 (1H, t, J=8.1 Hz), 6.96 (1H, d, J=8.1 Hz), 6.63
(1H, t, J=75 Hz), 4.64 (2H, d, J=5.1 Hz), 4.19 (2H, q, J=6.9 Hz),
4.08 (2H, d, J=6.6 Hz) 2.86-2.82 (1H, m), 2.19-2.12 (2H, m),
2.04-1.87 (4H, m), 1.50 (3H, t, J=6.9 Hz)
[1076] The chemical structures of the compounds obtained above in
the Reference Examples and Examples are shown below in Tables 1 to
40.
TABLE-US-00001 TABLE 1 ##STR00020## Ref. Ex. No. R.sup.a R.sup.b 5
Methyl Benzyl 11 Methyl ##STR00021## 17 Methyl ##STR00022## 23
Methyl --CH.sub.2CF.sub.3 32 --CH.sub.2CF.sub.3 ##STR00023## 35
Ethyl Ethyl 38 Methyl Methyl 44 --CHF.sub.2 Benzyl 55 Benzyl Benzyl
58 Methyl Ethyl 63 Benzyl Ethyl 68 Methyl iso-Propyl
TABLE-US-00002 TABLE 2 ##STR00024## --OEt: Ethoxy Ex. No. R.sup.c 1
Benzyl 2 H 3 ##STR00025## 4 --CH.sub.2CF.sub.3 5 n-Butyl 6
Cyclopentyl 7 ##STR00026## 8 ##STR00027## 9 Ethyl 10 ##STR00028##
11 n-propyl 12 iso-propyl 13 ##STR00029## 14 iso-Butyl 15
--CH.sub.2CH.sub.2CF.sub.3 92 Methyl
TABLE-US-00003 TABLE 3 ##STR00030## Ex. No. Ar.sup.a 25
2-Trifluoromethylphenyl 32 2-(2,2,2-Trifluoroethoxy)phenyl 37
2-iso-Propoxyphenyl 38 2-Methylphenyl 39 2-Ethylphenyl 40
2-Chlorophenyl 41 5-Fluoro-2-methoxyphenyl 42
4-Fluoro-2-methoxyphenyl 43 6-Fluoro-2-methoxyphenyl 44
2-Methylthiophenyl 46 2-Methoxyphenyl 47 2-Trifluoromethoxyphenyl
48 2-n-Propoxyphenyl 51 2-n-Butoxyphenyl 52 2-iso-Butoxyphenyl 54
2-Ethylthiophenyl 56 2,6-Dimethoxyphenyl 60
2-Methanesulfonylphenyl
TABLE-US-00004 TABLE 4 ##STR00031## Ex. No. Ar.sub.b 63
2-Methoxyphenyl 64 2-Methylthiophenyl 66 4-Fluoro-2-methoxyphenyl
67 2-iso-Propoxyphenyl 68 6-Fluoro-2-methoxyphenyl 71
2-n-Propoxyphenyl 72 2-n-Butoxyphenyl 73 2-iso-Butoxyphenyl
TABLE-US-00005 TABLE 5 ##STR00032## Ex. No. Ar.sup.c 78
2-Methoxyphenyl 79 2-Methylphenyl 80 2-n-Propoxyphenyl 81
2-iso-Propoxyphenyl 82 4-Chloro-2-methoxyphenyl
TABLE-US-00006 TABLE 6 ##STR00033## Ex. No. Ar.sup.d 85
2-n-Propoxyphenyl 86 2-Trifluoromethylphenyl 88 2-Ethoxyphenyl 89
4-Ethoxyphenyl 90 5-Methoxy-2-trifluoromethoxyphenyl 91
3-Ethoxyphenyl
TABLE-US-00007 TABLE 7 ##STR00034## Ex. No. Ar.sup.e R.sup.d
R.sup.e 23 2-Trifluoromethylphenyl Methyl Benzyl 24
2-Trifluoromethylphenyl Methyl H 26 2-Trifluoromethylphenyl Methyl
##STR00035## 30 2-(2,2,2- Methyl Benzyl Trifluoroethoxy)phenyl 31
2-(2,2,2- Methyl H Trifluoroethoxy)phenyl 33 2-Methoxyphenyl Methyl
Benzyl 34 2-Methoxyphenyl Methyl H 35 2-Methoxyphenyl Methyl
cyclo-Pentyl 83 2-Ethoxyphenyl --CH.sub.2CF.sub.3 ##STR00036## 93
2-Ethoxyphenyl Methyl Methyl
TABLE-US-00008 TABLE 8 ##STR00037## Ex. No. R.sup.f R.sup.g 16
Methyl Benzyl 17 Methyl H 18 Methyl Cyclopentyl 19 Methyl
--CH.sub.2CF.sub.3 20 Methyl Ethyl 21 Methyl Allyl 22 Methyl
##STR00038## 36 Methyl ##STR00039## 62 Methyl iso-Butyl 84
--CH.sub.2CF.sub.3 ##STR00040## 94 Methyl Methyl 96 --CHF.sub.2
Benzyl 97 --CHF.sub.2 H 98 --CHF.sub.2 ##STR00041## 384 Methyl
iso-Propyl
TABLE-US-00009 TABLE 9 ##STR00042## Ex. No. R.sup.h R.sup.i 27
Ethyl Benzyl 28 Ethyl H 29 Ethyl Cyclopentyl 45 H ##STR00043## 50
Ethyl ##STR00044## 53 iso-Propyl ##STR00045## 57 Methyl
##STR00046## 58 iso-Butyl ##STR00047## 61 n-Propyl ##STR00048## 65
Ethyl iso-Butyl 69 Methyl iso-Butyl 70 iso-Butyl iso-Butyl 74
iso-Propyl iso-Butyl 76 Methyl --CH.sub.2CF.sub.3 77 Ethyl
--CH.sub.2CF.sub.3 95 Methyl Methyl
TABLE-US-00010 TABLE 10 ##STR00049## Ex. No. Ar.sup.f R.sup.j
R.sup.k 49 ##STR00050## Methyl ##STR00051## 55 ##STR00052## Methyl
##STR00053## 59 ##STR00054## Methyl ##STR00055## 75 ##STR00056##
Methyl iso-Butyl 87 ##STR00057## Ethyl Ethyl 99 ##STR00058## Methyl
##STR00059##
TABLE-US-00011 TABLE 11 ##STR00060## --OEt: Ethoxy Ex. No. R.sup.l
R.sup.m 101 Methyl H 102 Methyl ##STR00061## 103 Methyl Ethyl 104
Methyl Allyl 105 Methyl Cyclopentyl 106 Methyl iso-Butyl 107 Methyl
n-Propyl 108 Methyl ##STR00062## 109 Methyl n-Butyl 110 Methyl
##STR00063## 111 Methyl iso-Propyl 112 Methyl --CH.sub.2CF.sub.3
113 Methyl ##STR00064## 114 Methyl ##STR00065## 115 Methyl
##STR00066## 116 Methyl ##STR00067## 117 Methyl ##STR00068## 118
Methyl ##STR00069## 119 Methyl ##STR00070## 120 Methyl ##STR00071##
121 Methyl ##STR00072## 122 Methyl ##STR00073## 182 Ethyl Ethyl 190
Benzyl Ethyl 191 H Ethyl 192 iso- Ethyl Propyl 228 --CHF.sub.2
Benzyl 229 --CHF.sub.2 H 230 --CHF.sub.2 iso-Propyl
TABLE-US-00012 TABLE 12 ##STR00074## --OMe: Methoxy Ex. No. R.sup.n
169 iso-Propyl 170 ##STR00075## 171 Cyclopentyl 172 Ethyl 173
iso-Butyl 174 Allyl 175 --CH.sub.2CF.sub.3
TABLE-US-00013 TABLE 13 ##STR00076## Ex. No. R.sup.o 194 H 195
Ethyl 196 Cyclopentyl 197 iso-Propyl 198 ##STR00077## 199
##STR00078## 200 Allyl 201 ##STR00079## 203 --CH.sub.2CF.sub.3
TABLE-US-00014 TABLE 14 ##STR00080## Ex. No. R.sup.p 207 H 208
##STR00081## 209 Ethyl 210 iso-Propyl 211 Allyl 212 ##STR00082##
213 --CH.sub.2CF.sub.3 214 ##STR00083##
TABLE-US-00015 TABLE 15 ##STR00084## Ex. No. R.sup.q 164 Benzyl 166
Allyl 177 ##STR00085## 189 Ethyl 224 iso-Propyl
TABLE-US-00016 TABLE 16 ##STR00086## Ex. No. R.sup.r 220 H 221
##STR00087## 225 Ethyl 226 Allyl 227 iso-Propyl
TABLE-US-00017 TABLE 17 ##STR00088## --OEt: Ethoxy Ex. No. Ar.sup.g
178 2-Allyloxyphenyl 184 3-Ethoxyphenyl 185 4-Ethoxyphenyl 205
2-n-Propoxyphenyl 216 2-iso-Propoxyphenyl 218 2-Methylphenyl
TABLE-US-00018 TABLE 18 Ex. No. Chemical Structure 165 ##STR00089##
168 ##STR00090## 176 ##STR00091## 179 ##STR00092## 223 ##STR00093##
231 ##STR00094## 232 ##STR00095## 233 ##STR00096## 234 ##STR00097##
235 ##STR00098##
TABLE-US-00019 TABLE 19 ##STR00099## Ex. No. R.sup.s 136 H 137
##STR00100## 138 Ethyl 139 iso-Propyl 140 Allyl 141 ##STR00101##
142 iso-Butyl 143 n-Propyl 144 Cyclopentyl 145 ##STR00102## 146
##STR00103## 147 n-Butyl 148 ##STR00104## 149 ##STR00105## 150
--CH.sub.2CH.sub.2Ph 151 --CH.sub.2CH.sub.2CH.sub.2Ph 152
##STR00106## 153 ##STR00107## 154 ##STR00108## 155
--CH.sub.2CF.sub.3 156 ##STR00109## 157 ##STR00110## 158 Cyclohexyl
159 ##STR00111## Ph: Phenyl
TABLE-US-00020 TABLE 20 ##STR00112## Ex. No. R.sup.t R.sup.u 125
Methyl H 126 Methyl ##STR00113## 127 Methyl iso-Butyl 128 Methyl
Cyclopentyl 129 Methyl --CH.sub.2CF.sub.3 131 Ethyl H 132 Ethyl
Cyclopentyl 133 Ethyl ##STR00114## 134 Ethyl iso-Butyl
TABLE-US-00021 TABLE 21 Ex. No. Chemical Structure 123 ##STR00115##
161 ##STR00116## 162 ##STR00117## 163 ##STR00118## 181 ##STR00119##
183 ##STR00120## 187 ##STR00121## 188 ##STR00122##
TABLE-US-00022 TABLE 22 ##STR00123## Ex. No. Ar.sup.h R.sup.v
R.sup.w 193 2-n-Propoxyphenyl Methyl Benzyl 202 2-n-Propoxyphenyl
Methyl --CH.sub.2CF.sub.3 204 2-n-Propoxyphenyl Ethyl Ethyl 206
2-iso-Propoxyphenyl Methyl Benzyl 215 2-iso-Propoxyphenyl Ethyl
Ethyl 217 2-Methylphenyl Ethyl Ethyl 219 2-Methylphenyl Methyl
Benzyl 222 2-Benzyloxyphenyl Methyl iso-Propyl
TABLE-US-00023 TABLE 23 ##STR00124## Ex. No. Ar.sup.i R.sup.x
R.sup.y 100 2-Ethoxyphenyl Methyl Benzyl 124 3-Methoxypyridyl
Methyl Benzyl 130 3-Ethoxypyridyl Methyl Benzyl 135 3-Methylpyridyl
Methyl Benzyl 160 2-Pyridyl Methyl Benzyl 167 2-MethoxyPhenyl
Methyl Benzyl 180 3-MethylPyridyl Ethyl Ethyl 186 3-MethylPyridyl
Benzyl Benzyl
TABLE-US-00024 TABLE 24 Ex. No. Chemical Structure 236 ##STR00125##
237 ##STR00126## 238 ##STR00127## 239 ##STR00128## 240
##STR00129##
TABLE-US-00025 TABLE 25 Ex. No. Chemical Structure 241 ##STR00130##
242 ##STR00131## 243 ##STR00132## 244 ##STR00133## 245
##STR00134##
TABLE-US-00026 TABLE 26 Ex. No. Chemical Structure 246 ##STR00135##
247 ##STR00136## 248 ##STR00137## 249 ##STR00138## 250
##STR00139##
TABLE-US-00027 TABLE 27 Ex. No. Chemical Structure 251 ##STR00140##
252 ##STR00141## 253 ##STR00142## 254 ##STR00143## 255 ##STR00144##
256 ##STR00145##
TABLE-US-00028 TABLE 28 Ex. No. Chemical Structure 257 ##STR00146##
258 ##STR00147## 259 ##STR00148## 260 ##STR00149## 261
##STR00150##
TABLE-US-00029 TABLE 29 Ex. No. Chemical Structure 262 ##STR00151##
263 ##STR00152## 264 ##STR00153## 265 ##STR00154##
TABLE-US-00030 TABLE 30 Ref. Ex. No. Chemical Structure 89
##STR00155## 90 ##STR00156## 91 ##STR00157## 92 ##STR00158## 93
##STR00159## 95 ##STR00160##
TABLE-US-00031 TABLE 31 Ref. Ex. No. Chemical Structure 96
##STR00161## 98 ##STR00162## 99 ##STR00163##
TABLE-US-00032 TABLE 32 ##STR00164## --OEt: Ethoxy Ex. No. R.sub.A
R.sub.B 325 Methyl 1-Ethylpropyl 346 Difluoromethyl Benzyl 347
Difluoromethyl H 348 Difluoromethyl iso-Butyl 349 Difluoromethyl
Ethyl 350 Difluoromethyl n-Propyl 351 Difluoromethyl Allyl 352
Difluoromethyl iso-Propyl 353 Difluoromethyl Cyclopropylmethyl 354
Difluoromethyl 3-Butenyl 355 Difluoromethyl 1-Ethylpropyl 373 H
Difluoromethyl 374 iso-Propyl Difluoromethyl 375 Cyclopropylmethyl
Difluoromethyl 376 n-Propyl Difluoromethyl 377 Allyl Difluoromethyl
380 Difluoromethyl Difluoromethyl 382 Difluoromethyl
2,2-Difluoroethyl 383 Difluoromethyl 2,2,2-Trifluoroethyl 385
Difluoromethyl Cyclobutylmethyl
TABLE-US-00033 TABLE 33 ##STR00165## Ex. No. R.sub.C R.sub.D 324
Methyl 1-Ethylpropyl 338 Difluoromethyl Ethyl 339 Difluoromethyl
Allyl 340 Difluoromethyl n-Propyl 341 Difluoromethyl iso-Propyl 342
Difluoromethyl 1-Ethylpropyl 343 Difluoromethyl 3-Butenyl 344
Difluoromethyl iso-Butyl 345 Difluoromethyl Cyclobutylmethyl 367 H
Difluoromethyl 368 Allyl Difluoromethyl 369 Cyclobutylmethyl
Difluoromethyl 370 iso-Butyl Difluoromethyl 371 3-Butenyl
Difluoromethyl 379 Difluoromethyl Difluoromethyl
TABLE-US-00034 TABLE 34 ##STR00166## --OEt: Ethoxy Ex. No. R.sub.E
R.sub.F 313 Methyl Difluoromethyl 314 Methyl 2,2-Difluoroethyl 315
Methyl 2-Fluoroethyl 334 Difluoromethyl Ethyl 335 Difluoromethyl
Allyl 336 Difluoromethyl Cyclopropylmethyl 337 Difluoromethyl
3-Butenyl 363 H Difluoromethyl 364 3-Butenyl Difluoromethyl 365
Allyl Difluoromethyl 366 Ethyl Difluoromethyl 378 Difluoromethyl
Difluoromethyl
TABLE-US-00035 TABLE 35 ##STR00167## Ex. No. R.sub.G R.sub.H 308
Methyl Difluoromethyl 309 Methyl 2,2-Difluoroethyl 310 Methyl
2-Fluoroethyl 311 Methyl sec-Butyl 312 Methyl 1-Ethylpropyl 317 H
2,2-Difluoroethyl 318 Ethyl 2,2-Difluoroethyl 319 iso-Propyl
2,2-Difluoroethyl 327 Difluoromethyl H 328 Difluoromethyl
Cyclopropylmethyl 329 Difluoromethyl n-Propyl 330 Difluoromethyl
Allyl 331 Difluoromethyl 3-Butenyl 332 Difluoromethyl iso-Propyl
333 Difluoromethyl Ethyl 356 H Difluoromethyl 357 iso-Propyl
Difluoromethyl 358 Allyl Difluoromethyl 359 3-Butenyl
Difluoromethyl 360 Cyclopropylmethyl Difluoromethyl 361 n-Propyl
Difluoromethyl 362 Ethyl Difluoromethyl 381 Difluoromethyl
Difluoromethyl
TABLE-US-00036 TABLE 36 ##STR00168## Ex. No. R.sub.I R.sub.J
R.sub.K 267 Methyl Benzyl Difluoromethyl 268 Methyl Benzyl
2-Fluoroethyl 269 Methyl Benzyl 2,2-Difluoroethyl 270 Methyl H
Difluoromethyl 271 Methyl H 2-Fluoroethyl 272 Methyl H
2,2-Difluoroethyl 273 Methyl iso-Propyl Difluoromethyl 274 Methyl
Ethyl Difluoromethyl 275 Methyl iso-Propyl 2-Fluoroethyl 276 Methyl
3-Butenyl 2-Fluoroethyl 277 Methyl iso-Butyl 2-Fluoroethyl 278
Methyl iso-Propyl 2,2-Difluoroethyl 279 Methyl n-Propyl
2,2-Difluoroethyl 280 Methyl Ethyl 2,2-Difluoroethyl 281 Methyl
Allyl 2,2-Difluoroethyl 282 Methyl 3-Butenyl 2,2-Difluoroethyl 283
Methyl Cyclopropylmethyl 2,2-Difluoroethyl 284 Methyl
2,2-Difluoroethyl 2,2-Difluoroethyl 285 Methyl iso-Butyl
2,2-Difluoroethyl 288 Ethyl Ethyl Difluoromethyl 289 Ethyl Ethyl
2-Fluoroethyl 290 Ethyl Ethyl 2,2-Difluoroethyl 292 Ethyl Ethyl
Trifluoromethyl 293 Methyl Cyclopropylmethyl Trifluoromethyl
TABLE-US-00037 TABLE 37 Ex. No. Chemical Structure 266 ##STR00169##
286 ##STR00170## 287 ##STR00171## 291 ##STR00172## 294 ##STR00173##
295 ##STR00174##
TABLE-US-00038 TABLE 38 Ex. No. Chemical Structure 296 ##STR00175##
297 ##STR00176## 298 ##STR00177## 299 ##STR00178## 300 ##STR00179##
301 ##STR00180## 302 ##STR00181## 303 ##STR00182##
TABLE-US-00039 TABLE 39 Ex. No. Chemical Structure 304 ##STR00183##
305 ##STR00184## 306 ##STR00185## 307 ##STR00186## 316 ##STR00187##
320 ##STR00188## 321 ##STR00189##
TABLE-US-00040 TABLE 40 Ex. No. Chemical Structure 322 ##STR00190##
323 ##STR00191## 326 ##STR00192##
Test Example 1
Phosphodiesterase(PDE)4 Inhibitory Activity Evaluation Test
(1) Large Scale Plasmid Preparation
[1077] Plasmid containing genes (HPDE4D) coding for human PDE4D3
cDNA (stored in Otsuka America Pharmaceutical, Inc., Maryland
Research Laboratories) was transformed in E. coli, cultured on a
large scale, and purified using an EndoFree.TM. Plasmid Maxi Kit
(Qiagen).
(2) Abundant Expression and Purification of PDE4D
[1078] COS-7 cells derived from African green monkey kidneys were
passage cultured in D-MEM media containing 100 units/ml penicillin,
100 .mu.g/ml streptomycin, and 10% FBS. The cells were transfected
with the plasmid prepared in (1) above using Lipofectamine.TM. 2000
(hereinafter referred to as "LF2000", Invitrogen), following the
manufacturer's protocol. The COS-7 cells were inoculated in a 10 cm
culture dish on the previous day so as to be 90% confluent on the
day of transfection. Culture dishes each containing a plasmid
solution (solution A) in which 24 .mu.g of plasmid was diluted in
1.5 ml Opti-MEM I Reduced Serum Medium (Invitrogen) and an LF2000
solution (solution B) in which 60 .mu.l of LF2000 was diluted in
1.5 ml Opti-MEM I Reduced Serum Medium were separately allowed to
stand for 5 minutes at room temperature. Solutions A and B were
then mixed and the mixture was allowed to stand for 20 minutes at
room temperature. The mixture was added to the cultured cells, and
incubated at 37.degree. C. (5% CO.sub.2) overnight. On the
following day, the medium was replaced, and the mixture was further
incubated overnight to harvest the cells in the following manner.
The cells were washed with PBS (Sigma) once, and 10 ml of a
Trypsin-EDTA solution (Sigma) was added to each culture dish. After
the solution was distributed to each of the culture dishes, the
cells were detached, and the dishes were allowed to stand for about
5 minutes at 37.degree. C. The detached cells from the dishes were
suspended in media, collected into centrifuge tubes, and
centrifuged at 1200 rpm for 5 minutes at 4.degree. C., and
supernatants were removed. The cells were further washed with PBS,
and stored at -80.degree. C. KHEM buffer (100 mM Hepes, 50 mM KCl,
10 mM EGTA, 1.92 mM MgCl.sub.2, pH 7.4) containing 1 mM DTT, 1
.mu.g/ml antipain, 1 .mu.g/ml aprotinin, 1 .mu.g/ml leupeptin, 1
.mu.g/ml pepstatin A, 157 .mu.g/ml benzamidine, and 120 .mu.g/ml
Pefabloc SC was added to the stored cells, and the contents were
moved to a glass homogenizer to be homogenized on ice. The cell
suspension was centrifuged at 1000 rpm for 5 minutes at 4.degree.
C., and the supernatant was further centrifuged at 14000 rpm for
one hour. After centrifugation, the supernatant was dispensed into
new tubes as PDE4D enzyme solutions, and stored in a deep
freezer.
(3) Determination on Dilution Ratio of PDE4D Enzyme Solutions
[1079] The PDE4D enzyme solutions prepared in (2) above were
dissolved in 20 mM Tris-HCl solution (pH 7.4) to give 10-, 25-,
50-, 100-, 200-, 400-, and 800-fold dilutions of the enzyme
solutions. PDE4D activities were measured according to (4) below.
The percentage of catalyzed cAMP to total cAMP was calculated, and
such a dilution, in which the percentage was between 10% and 30%,
was adopted in the inhibitory study below.
(4) Measurement of PDE4D Inhibitory Activity
[1080] Necessary amounts of test compounds were weighed, and 100%
dimethylsulfoxide (DMSO) was added thereto to adjust the
concentration to 10 mM. The solutions were stored in a freezer as
stock solutions of each test compound. After being thawed when
required, the solutions were diluted 20-fold with 100% DMSO to give
a 500 .mu.M concentration. Further, 10-fold serial dilutions were
made with 100% DMSO to prepare test compounds of different
concentrations. 2 .mu.l of solutions containing one of each of the
test compound were separately added into 1.2 ml tubes in which 23
.mu.l of 20 mM Tris-HCl (pH 7.4) had been placed beforehand. 25
.mu.l of a PDE4D enzyme solution diluted at an optimal ratio
determined in (3) above were added on ice to each of the tubes, and
50 .mu.l of a substrate solution containing 2 .mu.M[.sup.3H]cAMP
prepared by dilution with a 20 mM Tris-HCl (pH 7.4) containing 10
mM MgCl.sub.2 was added thereto. The final DMSO concentration in
the reaction liquid was 2%. After mixing, the mixture was incubated
for 10 minutes at 30.degree. C. At the completion of the
incubation, the tubes were placed in a bath containing boiling
water for 3 minutes, and the reaction was stopped. After cooling
the tubes in ice, 25 .mu.l solution of 0.2 mg/ml snake venom was
added thereto, and after mixing the mixture was incubated for 10
minutes at 30.degree. C. At the completion of the incubation, 0.4
ml of a Dowex 1.times.8 resin solution prepared in an EtOH:H.sub.2O
(1:1) solution was added thereto. After mixing, the tubes were
allowed to stand at room temperature for at least an hour. 50 .mu.l
of the supernatant in one of each of the tubes was moved to one of
the wells of a topCount plate, and the plate was dried overnight.
.sup.3H radioactivity (cpm) was measured using a lopCount.TM..
[1081] The IC.sub.50 values (concentration which produced 50%
inhibition of substrate hydrolysis) for the test compounds were
determined with the Excel (Microsoft Excel 2000 SR-1) statistical
package using regression analysis function.
[1082] The results are shown in Table 41. The table demonstrates
that compounds represented by formula (I) have the outstanding PDE4
inhibitory activities.
[1083] In the structural formulae shown in the following table,-Me
is a methyl group, -Et is an ethyl group, --OMe is a methoxy group,
-OEt is an ethoxy group, and --SMe is a methylthio group.
TABLE-US-00041 TABLE 41 PDE 4 Ex. No. Chemical Structure
(IC.sub.50: nM) 3 ##STR00193## <50 14 ##STR00194## <50 18
##STR00195## <50 19 ##STR00196## <50 21 ##STR00197## <50
22 ##STR00198## <50 29 ##STR00199## <50 32 ##STR00200##
<50 35 ##STR00201## <50 36 ##STR00202## <50 42
##STR00203## <50 43 ##STR00204## <50 44 ##STR00205## <50
61 ##STR00206## <50 62 ##STR00207## <50 63 ##STR00208##
<50 76 ##STR00209## <50 98 ##STR00210## <50 99
##STR00211## <50 102 ##STR00212## <50 103 ##STR00213## <50
104 ##STR00214## <50 108 ##STR00215## <50 111 ##STR00216##
<50 112 ##STR00217## <50 116 ##STR00218## <50 126
##STR00219## <50 129 ##STR00220## <50 132 ##STR00221## <50
133 ##STR00222## <50 137 ##STR00223## <50 138 ##STR00224##
<50 139 ##STR00225## <50 140 ##STR00226## <50 141
##STR00227## <50 143 ##STR00228## <50 146 ##STR00229## <50
153 ##STR00230## <50 155 ##STR00231## <50 157 ##STR00232##
<50 159 ##STR00233## <50 166 ##STR00234## <50 169
##STR00235## <50 170 ##STR00236## <50 172 ##STR00237## <50
174 ##STR00238## <50 177 ##STR00239## <50 181 ##STR00240##
<50 182 ##STR00241## <50 195 ##STR00242## <50 208
##STR00243## <50 224 ##STR00244## <50 232 ##STR00245## <50
274 ##STR00246## <50 275 ##STR00247## <50 276 ##STR00248##
<50 278 ##STR00249## <50 280 ##STR00250## <50 281
##STR00251## <50 283 ##STR00252## <50 284 ##STR00253## <50
285 ##STR00254## <50 289 ##STR00255## <50 290 ##STR00256##
<50 299 ##STR00257## <50 304 ##STR00258## <50 305
##STR00259## <50 309 ##STR00260## <50 311 ##STR00261## <50
312 ##STR00262## <50 314 ##STR00263## <50 315 ##STR00264##
<50 318 ##STR00265## <50 324 ##STR00266## <50 328
##STR00267## <50 329 ##STR00268## <50 330 ##STR00269## <50
331 ##STR00270## <50 332 ##STR00271## <50 333 ##STR00272##
<50 334 ##STR00273## <50 335 ##STR00274## <50 336
##STR00275## <50 337 ##STR00276## <50 338 ##STR00277## <50
339 ##STR00278## <50 340 ##STR00279## <50 341 ##STR00280##
<50 342 ##STR00281## <50 343 ##STR00282## <50 344
##STR00283## <50 345 ##STR00284## <50 348 ##STR00285## <50
349 ##STR00286## <50 350 ##STR00287## <50 351 ##STR00288##
<50 352 ##STR00289## <50 353 ##STR00290## <50 354
##STR00291## <50 355 ##STR00292## <50 382 ##STR00293## <50
383 ##STR00294## <50 384 ##STR00295## <50
Test Example 2
Inhibitory Activity Measurement on TNF-.alpha. Production
[1084] TNF-.alpha. production inhibitory activity was evaluated
according to the following tests.
(1) Isolation of Mononuclear Cells from Mouse Peripheral Blood
[1085] Mononuclear cells were isolated from heparinized blood
obtained from male BALB/c mice (Charles River Laboratories, Japan)
by density gradient centrifugation using Lympholyte-M (Cedarlane
Laboratories). Viable cell numbers in the peripheral blood
mononuclear cells were counted using trypan blue dye, and prepared
in cell culture medium (RPMI 1640 medium containing 10% FCS) to
1.25.times.10.sup.6 cells/ml.
(2) Induction of TNF-.alpha. Production
[1086] Test compounds were dissolved in DMSO, and test compound
solutions were diluted for use in cell culture media. 20 .mu.l test
compound solutions of different concentrations and 160 .mu.l
peripheral blood mononuclear cell suspensions were placed in a
96-well plate, and cultured for 30 minutes. 20 .mu.l (final
concentration 1 .mu.g/ml) lipopolysaccharide (LPS) derived from E.
coli (serotype 055:B5) was added thereto to induce TNF-.alpha.
production. The mixtures were then cultured at 37.degree. C. for 5
hours, and the culture supernatant was removed from each well.
(3) Measurement of TNF-.alpha. Concentration
[1087] TNF-.alpha. concentrations in the culture supernatants were
measured by ELISA (OptEIA.TM. Set Mouse TNF-.alpha., BD
Pharmingen). The IC.sub.50 values (concentration which produced 50%
inhibition of TNF-.alpha. production) for the test compounds were
determined with the Excel (Microsoft Excel 2000 SR-1) statistical
package using regression analysis function.
[1088] The results obtained are shown in table 42.
TABLE-US-00042 TABLE 42 Test compounds TNF-.alpha. (IC.sub.50: nM)
Compound of Ex. 18 <50 Compound of Ex. 43 <50 Compound of Ex.
126 <50 Compound of Ex. 157 <50 Compound of Ex. 177
<50
* * * * *