U.S. patent application number 12/795323 was filed with the patent office on 2010-10-07 for large conductance calcium-activated k channel opener.
Invention is credited to Mitsuya Hongu, Toshihiro Hosaka, Toshihiko Kashiwagi, Hiroyuki Kobayashi, Rikako Kono.
Application Number | 20100256165 12/795323 |
Document ID | / |
Family ID | 26613619 |
Filed Date | 2010-10-07 |
United States Patent
Application |
20100256165 |
Kind Code |
A1 |
Hongu; Mitsuya ; et
al. |
October 7, 2010 |
LARGE CONDUCTANCE CALCIUM-ACTIVATED K CHANNEL OPENER
Abstract
A large conductance calcium-activated K channel opener
comprising as an active ingredient a nitrogen-containing 5-membered
heterocyclic compound represented by the following formula (I):
##STR00001## wherein X represents N--R.sup.4, O or S, R.sup.1 and
R.sup.2 each independently represent hydrogen, halogen, carboxyl,
amino, lower alkyl, lower alkoxycarbonyl, lower alkenyl,
cyclo-lower alkyl, carbamoyl, aryl, heterocyclic or
heterocyclic-substituted carbonyl group, R.sup.3 represents aryl,
heterocyclic or lower alkyl group, and R.sup.4 represents hydrogen
or lower alkyl group, or a pharmaceutically acceptable salt
thereof.
Inventors: |
Hongu; Mitsuya; (Saitama,
JP) ; Hosaka; Toshihiro; (Tokyo, JP) ;
Kashiwagi; Toshihiko; (Saitama, JP) ; Kono;
Rikako; (Saitama, JP) ; Kobayashi; Hiroyuki;
(Saitama, JP) |
Correspondence
Address: |
BIRCH STEWART KOLASCH & BIRCH
PO BOX 747
FALLS CHURCH
VA
22040-0747
US
|
Family ID: |
26613619 |
Appl. No.: |
12/795323 |
Filed: |
June 7, 2010 |
Related U.S. Patent Documents
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Application
Number |
Filing Date |
Patent Number |
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10474850 |
Feb 10, 2004 |
7759373 |
|
|
PCT/JP02/03723 |
Apr 15, 2002 |
|
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12795323 |
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Current U.S.
Class: |
514/255.05 ;
514/307; 514/341; 514/397; 544/333; 544/405; 546/144; 546/274.1;
548/315.1 |
Current CPC
Class: |
A61P 9/12 20180101; C07D
333/04 20130101; A61K 31/506 20130101; A61K 31/4178 20130101; A61K
31/427 20130101; C07D 333/52 20130101; A61P 39/00 20180101; C07D
233/68 20130101; A61K 31/4164 20130101; A61K 31/422 20130101; A61P
9/00 20180101; C07D 277/20 20130101; C07D 233/54 20130101; A61K
31/00 20130101; A61K 31/4439 20130101; A61P 3/10 20180101; A61P
13/00 20180101; C07D 333/28 20130101; A61P 43/00 20180101; C07D
263/32 20130101; C07D 263/34 20130101; A61K 31/421 20130101; A61P
13/02 20180101; A61P 13/12 20180101; A61P 13/06 20180101; A61P
25/22 20180101; A61P 9/04 20180101; A61P 13/04 20180101; A61P 13/10
20180101; A61P 15/08 20180101; A61P 9/10 20180101; A61P 15/10
20180101; C07D 263/30 20130101; A61K 31/426 20130101; A61P 11/06
20180101 |
Class at
Publication: |
514/255.05 ;
548/315.1; 514/397; 546/274.1; 514/341; 546/144; 514/307; 544/405;
544/333 |
International
Class: |
A61K 31/497 20060101
A61K031/497; C07D 233/64 20060101 C07D233/64; A61K 31/4178 20060101
A61K031/4178; C07D 401/14 20060101 C07D401/14; A61K 31/4439
20060101 A61K031/4439; C07D 217/14 20060101 C07D217/14; A61K
31/4725 20060101 A61K031/4725; C07D 403/04 20060101 C07D403/04;
A61P 13/00 20060101 A61P013/00; A61P 9/10 20060101 A61P009/10 |
Foreign Application Data
Date |
Code |
Application Number |
Apr 16, 2001 |
JP |
2001-116436 |
Aug 20, 2001 |
JP |
2001-249671 |
Claims
1. A nitrogen-containing 5-membered heterocyclic compound
represented by the following formula (I): ##STR00634## wherein X is
S or O; R.sup.1 is a heterocyclic group which is substituted by at
least one group selected from nitro group, hydroxyl group, formyl
group, carbamoyl group, cyano group, amino group, carboxyl group, a
lower alkoxycarbonyl group, a halogen atom, a lower alkyl group, a
hydroxy-lower alkyl group, a lower alkoxy group, a mono- or
di-lower alkylamino group, a mono- or di-lower alkanoylamino group,
a lower alkylthio group, a lower alkylsulfonyl group, a lower
alkylsulfinyl group, sulfamoyl group and a mono- or di-lower
alkylsulfamoyl group, where the heterocyclic group is a monocyclic,
dicyclic or tricyclic 6- to 14-membered aromatic hydrocarbon cyclic
group, containing 1 to 4 heteroatoms selected from nitrogen atom,
oxygen atom and sulfur atom, which may be partially or wholly
saturated; R.sup.2 is a lower alkyl group which may be substituted
by at least one group selected from a carboxyl group and a lower
alkoxycarbonyl; and R.sup.3 is (1) an aryl group which may be
substituted by at least one group selected from cyano group, nitro
group, amino group, a halogen atom, trifluoromethyl group, carboxyl
group, hydroxyl group, carbamoyl group, a mono- or di-lower
alkylamino group, a mono- or di-lower alkylamino-lower alkyl group,
a mono- or di-lower alkylcarbamoyl group, a lower alkyl group, a
hydroxy-lower alkyl group, a lower alkoxy group, a lower
alkoxycarbonyl group, a lower alkanoyl group, a lower alkanoyloxy
group, a lower alkanoyloxy-lower alkyl group, sulfo group, a lower
alkylthio group, a lower alkylthio-lower alkyl group, a lower
alkylsulfonyl group, a lower alkylsulfamoyl group and a lower
alkylsulfinyl group, where the aryl of R.sup.1, R.sup.2 or R.sup.3
is a monocyclic, dicyclic or tricyclic 6- to 14-membered aromatic
hydrocarbon cyclic group, or a pharmaceutically acceptable salt
thereof.
2. A nitrogen-containing 5-membered heterocyclic compound according
to claim 1, wherein R.sup.1 is a thienyl group which is substituted
by at least one group selected from a halogen atom and a lower
alkyl group; R.sup.2 is a carboxymethyl group; and R.sup.3 is a
phenyl group which is substituted by at least one group selected
from a halogen atom and a lower alkoxy group, or a pharmaceutically
acceptable salt thereof.
3. A pharmaceutical composition comprising a therapeutically
effective amount of a compound as set forth in claim 1 or 2 or a
pharmaceutically acceptable salt thereof in admixture with a
therapeutically acceptable carrier or diluent.
Description
[0001] This application is a Divisional application of and claims
priority to U.S. patent application Ser. No. 10/474,850, filed Feb.
10, 2004, which is the national phase under 35 U.S.C. .sctn.371 of
PCT International Application No. PCT/JP02/03723 which has an
International filing date of Apr. 15, 2002, which designated the
United States of America. This application also claims priority to
Japanese application 2001-116436, filed Apr. 16, 2001 in Japan, and
Japanese application 2001-249671, filed Aug. 20, 2001 in Japan. The
entire contents of all are herein incorporated by reference.
DESCRIPTION
Field of the Invention
[0002] This invention relates to an excellent large conductance
calcium-activated K channel opener containing a nitrogen-containing
5-membered heterocyclic compound as an active ingredient, which is
useful for treatment of disorders or diseases such as pollakiuria,
urinary incontinence, cerebral infarction, subarachnoid hemorrhage,
and the like.
Background of the Invention
[0003] Potassium is the most abundant intracelluar cation, and is
very important in maintaining physiological homeostasis. Potassium
channels are present in almost all vertebrate cells, and the
potassium influx through these channels is indispensable for
maintaining hyperpolarized resting membrane potential.
[0004] Large conductance calcium activated potassium channels (also
BK channels or maxi-K channels) are expressed especially in neurons
and smooth muscle cells. Because both of the increase of
intracellular calcium concentration and membrane depolarization can
activate maxi-K channels, maxi-K channels have been thought to play
a pivotal role in regulating voltage-dependent calcium influx.
Increase in the intracellular calcium concentration mediates many
processes such as release of neurotransmitters, contraction of
smooth muscles, cell growth and death, and the like. Actually, the
opening of maxi-K channels causes strong membrane
hyperpolarization, and inhibits these calcium-induced responses
thereby. Accordingly, by inhibiting various depolarization-mediated
physiological responses, a substance having an activity of opening
maxi-K channels is expected to have potential for the treatment of
diseases such as cerebral infarction, subarachnoid hemorrhage,
pollakiuria, urinary incontinence, and the like.
[0005] There have been various reports on a large conductance
calcium-activated potassium channel opener, and examples of such
channel opener are as follows; a pyrrole derivative disclosed in
International Publication WO96/40634, a furan derivative disclosed
in Japanese Provisional Patent Publication No. 2000-351773, and a
nitrogen-containing 5-membered derivative in which the nitrogen
atom is substituted by phenyl group or benzyl group disclosed in
International Publication WO98/04135.
[0006] Also, a compound having a similar structure to the
nitrogen-containing 5-membered heterocyclic compound which is an
active ingredient of the present invention has been disclosed. For
example, oxazole derivatives have been reported in Japanese
Provisional Patent Publications No. 36614/1984, No. 152382/1984 and
No. 172488/1984, but their uses are limited only to
antihypolipidemic agent. Also, in Japanese Provisional Patent
Publications No. 150591/1983, No. 34951/1985 and No. 54369/1988,
imidazole derivatives have been reported but their uses are limited
only to a cardiotonic, an antithrombosis, an antipyretic analgesic
or an anti-inflammation agent.
SUMMARY OF THE INVENTION
[0007] An object of the present invention is to provide an
excellent large conductance calcium-activated K channel opener
containing a nitrogen-containing 5-membered heterocyclic compound
as an active ingredient.
[0008] The present inventors have studied intensively to solve the
problems, and as a result, they have found that a certain kind of a
nitrogen-containing 5-membered heterocyclic compound has an
excellent large conductance calcium-activated K channel opening
activity, whereby they have accomplished the present invention.
[0009] That is, the present invention relates to a large
conductance calcium-activated K channel opener comprising a
nitrogen-containing 5-membered heterocyclic compound represented by
the following formula (I):
##STR00002## [0010] wherein X represents N--R.sup.4, O or S,
R.sup.1 and R.sup.2 are different from each other and each
independently represents hydrogen atom, a halogen atom, carboxyl
group, a substituted or unsubstituted amino group, a substituted or
unsubstituted lower alkyl group, a lower alkoxycarbonyl group, a
substituted or unsubstituted lower alkenyl group, a cyclo-lower
alkyl group, a substituted or unsubstituted carbamoyl group, a
substituted or unsubstituted aryl group, a substituted or
unsubstituted heterocyclic group or a substituted or unsubstituted
heterocyclic group-substituted carbonyl group, R.sup.3 represents a
substituted or unsubstituted aryl group, a substituted or
unsubstituted heterocyclic group or a substituted or unsubstituted
lower alkyl group, and R.sup.4 represents hydrogen atom or a
substituted or unsubstituted lower alkyl group, or a
pharmaceutically acceptable salt thereof as an active
ingredient.
BEST MODE FOR CARRYING OUT THE INVENTION
[0011] In the nitrogen-containing 5-membered heterocyclic compound
(I) which is an active ingredient of the present invention, the
aryl group is a monocyclic, dicyclic or tricyclic 6- to 14-membered
aromatic hydrocarbon cyclic group, and specific examples of the
aryl group may include a phenyl group, a naphthyl group and the
like. Of these, a phenyl group or a naphthyl group is
preferred.
[0012] The heterocyclic group or the heterocyclic group portion of
the heterocyclic group-substituted carbonyl group is a monocyclic,
dicyclic or tricyclic 6- to 14-membered aromatic hydrocarbon cyclic
group, containing 1 to 4 heteroatoms selected from nitrogen atom,
oxygen atom and sulfur atom, which may be partially or wholly
saturated.
[0013] As the monocyclic heterocyclic group, a 5- to 7-membered
heterocyclic group, containing 1 to 4 hetero atoms selected from
nitrogen atom, oxygen atom and sulfur atom, which may be partially
or wholly saturated is preferred, and specific examples of the
monocyclic heterocyclic group may include furyl group, thienyl
group, thiazolyl group, thiazolidinyl group, isoxazolyl group,
pyrrolidinyl group, pyrrolyl group, pyridyl group, pyrazinyl group,
pyrimidinyl group, tetrazolyl group, and the like.
[0014] As the dicyclic heterocyclic group, a dicyclic heterocyclic
group in which two of the above-mentioned monocyclic heterocyclic
groups are fused or a dicyclic heterocyclic group in which the
above monocyclic heterocyclic group and a benzene ring are fused is
preferred, and specific examples of the dicyclic heterocyclic group
may include indolyl group, quinolyl group, tetrahydroquinolyl
group, isoquinolyl group, quinoxalyl group, benzofuryl group,
dihydrobenzofuryl group, benzothienyl group, benzodioxanyl group,
trihydrocyclopentathienyl group, benzothianyl group, benzothiazolyl
group, imidazopyridyl group, indolyl group, indolinyl group,
chromanyl group, thiophenopyridyl group, furanopyridyl group, and
the like.
[0015] As the tricyclic heterocyclic group, a tricyclic
heterocyclic group in which the above-mentioned monocyclic
heterocyclic group and the above-mentioned dicyclic heterocyclic
group are fused or a tricyclic heterocyclic group in which the
above-mentioned monocyclic heterocyclic group and two benzene rings
are fused is preferred, and specific examples of the tricyclic
heterocyclic group may include carbazolyl group, carbolinyl group
and the like.
[0016] Of these heterocyclic groups, more specifically preferred
are furyl group, thienyl group, thiazolyl group, isoxazolyl group,
pyrrolidinyl group, pyrrolyl group, pyridyl group, pyrazinyl group,
pyrimidinyl group, tetrazolyl group, indolyl group, quinolyl group,
isoquinolyl group, benzofuryl group, benzothienyl group,
dihydrobenzofuryl group, thiophenopyridyl group and benzodioxanyl
group.
[0017] As a substituent for the amino group of R.sup.1 or R.sup.2,
there may be mentioned, for example, a group selected from formyl
group, a lower alkyl group, a lower alkanoyl group, a lower
alkylsulfonyl group and a lower alkoxycarbonyl group.
[0018] As a substituent for the lower alkyl group, there may be
mentioned, for example, a group selected from a halogen atom,
hydroxyl group, cyano group, carboxyl group, carbamoyl group, amino
group, aminosulfonyl group, a halogenosulfonyl group, amidinothio
group, a mono- or di-lower alkylamino group, a lower alkanoylamino
group, a lower alkylsulfonylamino group, hydroxyamino group, a
mono- or di-lower alkylcarbamoyl group, trifluoromethyl group, a
lower alkoxy group, a lower alkylthio group, a lower alkylsulfinyl
group, a lower alkylsulfonyl group, a lower alkylsulfonylamino
group, a lower alkoxycarbamoyl group, a lower
alkylsulfonylcarbamoyl group, sulfamoyl group, a mono- or di-lower
alkylsulfamoyl group, a lower alkoxycarbonyl group, a heterocyclic
group, a heterocyclic group-substituted carbamoyl group, a
heterocyclic group-substituted lower alkylcarbamoyl group and a
heterocyclic group-substituted sulfonylcarbamoyl group.
[0019] As a substituent for the lower alkenyl group, there may be
mentioned, for example, carboxyl group or a lower alkoxycarbonyl
group.
[0020] As a substituent for the carbamoyl group, there may be
mentioned, for example, a group selected from a lower alkyl group,
a lower alkoxy group and a lower alkylsulfonyl group.
[0021] As a substituent for the aryl group, there may be mentioned,
for example, a group selected from nitro group, amino group,
hydroxyl group, carbamoyl group, cyano group, carboxyl group,
trifluoromethyl group, a lower alkoxycarbonyl group, a halogen
atom, a lower alkyl group, a hydroxy-lower alkyl group, a lower
alkoxy group, a lower alkoxy-lower alkoxy group, a mono- or
di-lower alkylamino group, a mono- or di-lower alkanoylamino group,
a lower alkylthio group, a lower alkylsulfonyl group, a lower
alkylsulfinyl group, sulfamoyl group, a mono- or di-lower
alkylsulfamoyl group, a lower alkylsulfonylamino group and a
phenyl-lower alkoxy group.
[0022] As a substituent for the heterocyclic group, there may be
mentioned, for example, a group selected from nitro group, amino
group, hydroxyl group, formyl group, carbamoyl group, cyano group,
carboxyl group, a lower alkoxycarbonyl group, a halogen atom, a
lower alkyl group, a hydroxy-lower alkyl group, a lower alkoxy
group, a mono- or di-lower alkylamino group, a mono- or di-lower
alkanoylamino group, a lower alkylthio group, a lower alkylsulfonyl
group, a lower alkylsulfinyl group, sulfamoyl group and a mono- or
di-lower alkylsulfamoyl group.
[0023] As a substituent on the heterocyclic group for the
heterocyclic group-substituted carbonyl group, there may be
mentioned, for example, a group selected from nitro group, hydroxyl
group, carbamoyl group, cyano group, carboxyl group, a lower
alkoxycarbonyl group, a halogen atom, a lower alkyl group, a
hydroxy-lower alkyl group, a lower alkoxy group, a lower alkanoyl
group, a mono- or di-lower alkylamino group, a mono- or di-lower
alkanoylamino group, a lower alkylthio group, a lower alkylsulfonyl
group, a lower alkylsulfinyl group, sulfamoyl group and a mono- or
di-lower alkylsulfamoyl group.
[0024] The above-mentioned amino group, lower alkyl group,
carbamoyl group, aryl group, heterocyclic group and heterocyclic
group-substituted carbonyl group may be substituted by the same or
different 1 to 3 above-mentioned substituents.
[0025] As a substituent for the aryl group of R.sup.3, there may be
mentioned, for example, a group selected from cyano group, nitro
group, amino group, a halogen atom, trifluoromethyl group, carboxyl
group, hydroxyl group, carbamoyl group, a mono- or di-lower
alkylamino group, a mono- or di-lower alkylamino-lower alkyl group,
a mono- or di-lower alkylcarbamoyl group, a lower alkyl group, a
hydroxy-lower alkyl group, a lower alkoxy group, a lower
alkoxycarbonyl group, a lower alkanoyl group, a lower alkanoyloxy
group, a lower alkanoyloxy-lower alkyl group, sulfo group, a lower
alkylthio group, a lower alkylthio-lower alkyl group, a lower
alkylsulfonyl group, a lower alkylsulfamoyl group and a lower
alkylsulfinyl group.
[0026] As a substituent for the heterocyclic group, there may be
mentioned, for example, a group selected from oxo group, cyano
group, nitro group, amino group, a halogen atom, carboxyl group,
hydroxyl group, formyl group, carbamoyl group, a mono- or di-lower
alkylamino group, a N-lower alkyl-N-cyclo-lower alkylamino group, a
mono- or di-lower alkylamino-lower alkyl group, a mono- or di-lower
alkylcarbamoyl group, a lower alkyl group, a hydroxy-lower alkyl
group, a lower alkoxy group, a lower alkoxy-lower alkyl group, a
lower alkoxycarbonyl group, a lower alkanoyl group, sulfo group, a
lower alkylthio group, a lower alkylsulfonyl group, a lower
alkylsulfamoyl group, a lower alkylsulfinyl group and a
heterocyclic group.
[0027] As a substituent for the alkyl group, there may be
mentioned, for example, a group selected from hydroxyl group, cyano
group, carboxyl group, carbamoyl group, amino group, a mono- or
di-lower alkylamino group, a lower alkanoylamino group, a lower
alkylsulfonylamino group, hydroxyamino group, a mono- or di-lower
alkylcarbamoyl group, trifluoromethyl group, a halogen atom, a
lower alkoxy group, a lower alkylthio group, a lower alkylsulfinyl
group, a lower alkylsulfonyl group, sulfamoyl group, a mono- or
di-lower alkylsulfamoyl group, a lower alkoxycarbonyl group and a
heterocyclic group.
[0028] The above-mentioned aryl group, heterocyclic group and lower
alkyl group may be substituted by the same or different
above-mentioned 1 to 3 substituents.
[0029] As a substituent for the lower alkyl group of R.sup.4, there
may be mentioned a mono- or di-lower alkylamino group. The lower
alkyl group may be substituted by the same or different
above-mentioned 1 to 2 substituents.
[0030] Of the compounds (I) which are active ingredients of the
present invention, preferred compounds may be compounds wherein X
is N--R.sup.4, O or S; R.sup.1 or R.sup.2 is independently hydrogen
atom, a lower alkyl group, a lower alkyl group substituted by a
heterocyclic group, a di-lower alkylamino group, a carboxy-lower
alkyl group, a halogeno-lower alkyl group, a lower alkoxy-lower
alkyl group, a lower alkylsulfinyl-lower alkyl group, a lower
alkyl-sulfonyl-lower alkyl group, a lower alkylthio-lower alkyl
group, a trifluoromethyl-lower alkyl group, a cyclo-lower alkyl
group, an aryl group, a trifluoromethylaryl group, a cyanoaryl
group, a halogenoaryl group, a dihalogenoaryl group, a lower
alkylaryl group, a lower alkoxyaryl group, a mono- or di-lower
alkylaminoaryl group, a heterocyclic group, a lower
alkyl-heterocyclic group, a halogeno-hetero-cyclic group, or a
heterocyclic group substituted by a halogen atom and a lower alkyl
group; R.sup.3 is an aryl group, a halogenoaryl group, a
hydroxyaryl group, a cyanoaryl group, a nitroaryl group, a lower
alkylaryl group, a lower alkoxyaryl group, a lower alkylthioaryl
group, a heterocyclic group, a lower alkoxycarbonyl-heterocyclic
group, a cyano-heterocyclic group, a halogeno-heterocyclic group, a
lower alkyl-heterocyclic group, a di-lower alkyl-heterocyclic
group, a heterocyclic group substituted by a di-lower alkylamino
group, a heterocyclic group substituted by a halogen atom and a
lower alkyl group, or a heterocyclic group substituted by a halogen
atom and a hydroxy-lower alkyl group; and R.sup.4 is hydrogen
atom.
[0031] In another preferred embodiment of the present invention, X
is N--R.sup.4, O or S; R.sup.1 or R.sup.2 is independently hydrogen
atom, a lower alkyl group, a lower alkyl group substituted by a
heterocyclic group, a lower alkylamino group, a di-lower alkylamino
group, a cyano-lower alkyl group, a hydroxy-lower alkyl group, a
carboxy-lower alkyl group, a halogeno-lower alkyl group, a lower
alkoxy-lower alkyl group, a lower alkylsulfinyl-lower alkyl group,
a lower alkylthio-lower alkyl group, a cyclo-lower alkyl group, an
aryl group, a trifluoromethylaryl group, a hydroxyaryl group, a
halogenoaryl group, a dihalogenoaryl group, a lower alkylaryl
group, a di-lower alkoxyaryl group, a di-lower alkylaminoaryl
group, a lower alkylsulfonylaminoaryl group, an aryl group
substituted by hydroxyl group and a lower alkoxy group, an aryl
group substituted by hydroxy group and a halogen atom, an aryl
group substituted by a halogen atom and a di-lower alkoxy group, a
heterocyclic group, a halogeno-heterocyclic group, a lower
alkyl-heterocyclic group, a hydroxy-lower alkyl-heterocyclic group,
a heterocyclic group substituted by a halogen atom and a lower
alkyl group, a heterocyclic group substituted by a lower alkyl
group and a hydroxy-lower alkyl group, or a heterocyclic
group-substituted carbonyl group; R.sup.3 is a halogenoaryl group,
a hydroxyaryl group, a cyanoaryl group, a lower alkylaryl group, a
lower alkoxyaryl group, a lower alkylthioaryl group, an aryl group
substituted by a hydroxyl group and a lower alkoxy group, a
heterocyclic group, a cyano-heterocyclic group, a
halogeno-heterocyclic group, a lower alkyl-heterocyclic group, a
di-lower alkyl-heterocyclic group, a hydroxy-lower
alkyl-heterocyclic group, a di-lower aralkylamino-heterocyclic
group, a heterocyclic group substituted by a halogen atom and a
sulfo group, a heterocyclic group substituted by a halogen atom and
a sulfamoyl group, or a heterocyclic group substituted by a halogen
atom and a lower alkyl group; and R.sup.4 is hydrogen atom or a
lower alkyl group.
[0032] Of these, particularly preferred compounds are compounds
wherein X is O or S; R.sup.1 or R.sup.2 is independently a
carboxy-lower alkyl group, a lower alkyl group substituted by a
heterocyclic group, an aryl group, a halogenoaryl group, a
di-halogenoaryl group, a di-lower alkoxyaryl group, a lower
alkylthioaryl group, a heterocyclic group, a halogeno-heterocyclic
group, or a lower alkyl-heterocyclic group; and R.sup.3 is a
halogenoaryl group, a lower alkylaryl group, a di-lower
alkylaminoaryl group, a lower alkylthioaryl group, a lower
alkoxyaryl group, a heterocyclic group, a halogeno-heterocyclic
group, a lower alkyl-heterocyclic group, a lower
alkoxy-heterocyclic group, a lower alkylthio-hetero-cyclic group,
or a di-lower alkylamino-heterocyclic group.
[0033] Among the nitrogen-containing 5-membered heterocyclic
compounds (I), more preferred compounds in view of pharmaceutical
effects are compounds wherein R.sup.1 is (1) a lower alkyl group
which may be substituted by carboxyl group, a lower alkoxycarbonyl
group or a heterocyclic group, (2) an aryl group which may be
substituted by one or two halogen atoms, or (3) a heterocyclic
group which may be substituted by a halogen atom, R.sup.2 is (1) a
lower alkyl group which may be substituted by carboxyl group, a
lower alkoxycarbonyl group or a heterocyclic group, (2) a
heterocyclic group which may be substituted by a halogen atom, or
(3) an aryl group which may be substituted by one or two halogen
atoms; R.sup.3 is (1) a heterocyclic group which may be substituted
by one or two groups selected from amino group, a halogen atom, a
lower alkyl group, a lower alkoxy group, a mono- or di-lower
alkylamino group and a lower alkylthio group, or (2) an aryl group
which may be substituted by amino group, a halogen atom, a lower
alkyl group, a lower alkylthio group, a lower alkoxy group or a
mono- or di-lower alkylamino group; and R.sup.4 is hydrogen atom or
a lower alkyl group.
[0034] Of these, more preferred compounds are compounds wherein
R.sup.1 is (1) a carboxyl-lower alkyl group, (2) a lower
alkoxy-carbonyl-lower alkyl group, (3) a lower alkyl group
substituted by a tetrazolyl group, (4) a phenyl group which may be
substituted by one or two halogen atoms, or (5) a thienyl group
which may be substituted by a halogen atom; R.sup.2 is (1) a
carboxyl-lower alkyl group, (2) a lower alkoxycarbonyl-lower alkyl
group, (3) a lower alkyl group substituted by a tetrazolyl group,
(4) a thienyl group which may be substituted by a halogen atom, or
(5) a phenyl group which may be substituted by one or two halogen
atoms; and R.sup.3 is (1) a benzothienyl group which may be
substituted by a halogen atom, (2) a phenyl group which may be
substituted by a halogen atom, a lower alkylthio group, a lower
alkoxy group or a di-lower alkylamino group, (3) a pyridyl group
which may be substituted by a lower alkyl group, a lower alkoxy
group or a di-lower alkylamino group, (4) a pyrimidinyl group which
may be substituted by a di-lower alkylamino group or a lower
alkylthio group, (5) a thienyl group which may be substituted by
one or two lower alkyl groups, (6) thieno[3,2-b]pyridyl group, (7)
benzofuryl group, (8) dihydrobenzofuryl group or (9) an indolyl
group which may be substituted by a lower alkyl group.
[0035] Of these, particularly preferred compounds are compounds
wherein X is O or S; R.sup.1 is (1) a carboxyl-lower alkyl group,
(2) a lower alkoxycarbonyl-lower alkyl group, (3) a phenyl group
which may be substituted by one or two halogen atoms, or (4) a
thienyl group which may be substituted by a halogen atom; R.sup.2
is (1) a carboxyl-lower alkyl group, (2) a lower
alkoxycarbonyl-lower alkyl group, (3) a thienyl group which may be
substituted by a halogen atom, or (4) a phenyl group which may be
substituted by one or two halogen atoms; and R.sup.3 is (1) a
benzothienyl group which may be substituted by a halogen atom, (2)
a phenyl group which may be substituted by a halogen atom, a lower
alkylthio group, a lower alkoxy group or a di-lower alkylamino
group, (3) a pyridyl group which may be substituted by a lower
alkoxy group or a di-lower alkylamino group, (4) a pyrimidinyl
group which may be substituted by a di-lower alkylamino group, (5)
a thienyl group which may be substituted by two lower alkyl groups,
(6) thieno[3,2-b]pyridyl group, or (7) an indolyl group which may
be substituted by a lower alkyl group.
[0036] The most preferred compound in view of pharmaceutical
effects is the compound selected from the group consisting of:
[0037] 4-(5-chlorothiophen-2-yl)-2-(2-benzo[b]thienyl)thiazol-5-yl
acetic acid, [0038]
5-(4-chlorophenyl)-2-(2-N,N-dimethylaminopyrimidin-5-yl)-oxazol-4--
yl acetic acid, [0039]
4-(5-chlorothiophen-2-yl)-2-(4-methoxyphenyl)thiazol-5-yl acetic
acid, [0040]
5-(5-chlorothiophen-2-yl)-2-(4,5-dimethylthiophen-2-yl)-oxazol-4-y-
l acetic acid, [0041]
4-(5-chlorothiophen-2-yl)-2-(2-N,N-dimethylaminopyrimidin-5-yl)thiazol-5--
yl acetic acid, [0042]
4-(5-chlorothiophen-2-yl)-2-(2-N,N-dimethylaminopyridin-5-yl)thiazol-5-yl
acetic acid, [0043]
5-(4-chlorophenyl)-2-(4-fluorophenyl)oxazol-4-yl acetic acid,
[0044] 5-(4-chlorophenyl)-2-(2-benzo[b]thienyl)oxazol-4-yl acetic
acid, [0045]
4-(5-chlorothiophen-2-yl)-2-(2-benzo[b]thienyl)oxazol-5-yl acetic
acid, [0046]
5-(5-chlorothiophen-2-yl)-2-(2-N,N-dimethylaminopyrimidin-5-yl)oxa-
zol-4-yl acetic acid, [0047]
4-(4-chlorophenyl)-2-(2-N,N-dimethylaminopyrimidin-5-yl)-thiazol-5-yl
acetic acid, [0048]
5-(5-chlorothiophen-2-yl)-2-(2-benzo[b]thienyl)oxazol-4-yl acetic
acid, [0049] 4-(4-chlorophenyl)-2-(4-methoxyphenyl)thiazol-5-yl
acetic acid, [0050]
5-(5-chlorothiophen-2-yl)-2-(4-fluorophenyl)oxazol-4-yl acetic
acid, [0051]
5-(5-chlorothiophen-2-yl)-2-(6-fluorobenzo[b]thiophene-2-yl)oxazol-4-yl
acetic acid, [0052] 5-(3-thienyl)-2-(2-benzo[b]thienyl)oxazol-4-yl
acetic acid, [0053]
5-(5-chlorothiophen-2-yl)-2-(2-thieno[3,2-b]pyridyl)-oxazol-4-yl
acetic acid, [0054]
5-(3-fluoro-4-chlorophenyl)-2-(2-benzo[b]thienyl)oxazol-4-yl acetic
acid, [0055]
5-(5-chlorothiophen-2-yl)-2-(2-benzo[b]thienyl)thiazol-4-yl acetic
acid, [0056]
5-(5-chlorothiophen-2-yl)-2-(4-methylthiophenyl)oxazol-4-yl acetic
acid, [0057]
4-(5-chlorothiophen-2-yl)-2-(4-fluorophenyl)oxazol-5-yl acetic
acid, [0058]
5-(5-chlorothiophen-2-yl)-2-(4-chlorophenyl)oxazol-4-yl acetic
acid, [0059]
4-(3-fluoro-4-chlorophenyl)-2-(4-methoxyphenyl)thiazol-5-yl acetic
acid, [0060]
4-(5-chlorothiophen-2-yl)-2-(4,5-dimethylthiophen-2-yl)-thiazol-5-yl
acetic acid, [0061]
4-(3-fluoro-4-chlorophenyl)-2-(4-fluorophenyl)thiazol-5-yl acetic
acid, [0062]
4-(4-chlorophenyl)-2-(2-N,N-dimethylaminopyridin-5-yl)-thiazol-5-y-
l acetic acid, [0063]
4-(5-chlorothiophen-2-yl)-2-(4-N,N-dimethylaminophenyl)-thiazol-5-yl
acetic acid, [0064]
5-(5-chlorothiophen-2-yl)-2-(N-methylindol-2-yl)oxazol-4-yl acetic
acid, [0065]
5-(5-chlorothiophen-2-yl)-2-(4,5-dimethylthiophen-2-yl)-thiazol-4--
yl acetic acid; a lower alkyl ester of these compounds; and
[0066] a pharmaceutically acceptable salt of these compounds.
[0067] In still another preferred embodiment of the present
invention, X is O, one of R.sup.1 and R.sup.2 is a thienyl group
substituted by a chlorine atom, and the other is a carboxyl-lower
alkyl group, a lower alkoxycarbonyl-lower alkyl group or a lower
alkyl group substituted by a tetrazolyl group; and R.sup.3 is a
substituted or unsubstituted aryl group or a substituted or
unsubstituted heterocyclic group.
[0068] Of these, more preferred compounds are compounds wherein
R.sup.3 is (1) an aryl group which may be substituted by one or two
substituents selected from a halogen atom, a di-lower alkylamino
group, a lower alkylthio group and a lower alkoxy group, or (2) a
heterocyclic group which may be substituted by one or two
substituents selected from a halogen atom, a lower alkyl group, a
lower alkoxy group, a lower alkylthio group and a mono- or di-lower
alkylamino group.
[0069] Of these, particularly preferred compounds are compounds
wherein one of R.sup.1 and R.sup.2 is a thienyl group substituted
by a chlorine atom, and the other is a carboxyl-lower alkyl group
or a lower alkoxycarbonyl-lower alkyl group; the aryl group is
phenyl group; and the heterocyclic group is a thienyl group, a
pyridyl group, a pyrimidinyl group, a benzothienyl group, a
benzofuryl group, a dihydrobenzofuryl group, an indolyl group or a
thieno[3,2-b]pyridyl group.
[0070] Of these, further preferred compounds are compounds wherein
R.sup.3 is a phenyl group which is substituted by a halogen atom or
a lower alkylthio group; a thienyl group which is substituted by
one or two lower alkyl groups; a pyrimidinyl group which is
substituted by a di-lower alkylamino group; a benzothienyl group
which may be substituted by a halogen atom; an indolyl group which
may be substituted by a lower alkyl group; or a
thieno[3,2-b]pyridyl group.
[0071] In still another preferred embodiment of the present
invention, X is S, one of R.sup.1 and R.sup.2 is a thienyl group
substituted by a chlorine atom, and the other is a carboxyl-lower
alkyl group, a lower alkoxycarbonyl-lower alkyl group or a lower
alkyl group substituted by a tetrazolyl group, and R.sup.3 is a
substituted or unsubstituted heterocyclic group, where said
heterocyclic group is selected from a pyridyl group, a pyrimidinyl
group, a benzothienyl group, an indolyl group and a
thieno[3,2-b]-pyridyl group.
[0072] In a more preferred embodiment, R.sup.3 is a heterocyclic
group which may be substituted by one or two substituents selected
from a halogen atom, a lower alkoxy group, a lower alkyl group, a
lower alkylthio group and a mono- or di-lower alkylamino group,
where said heterocyclic group is selected from a pyridyl group, a
pyrimidinyl group, a benzothienyl group, and a thieno[3,2-b]pyridyl
group.
[0073] In a further preferred embodiment, one of R.sup.1 and
R.sup.2 is a thienyl group substituted by a chlorine atom, and the
other is a carboxyl-lower alkyl group or a lower
alkoxycarbonyl-lower alkyl group; R.sup.3 is a pyridyl group which
may be substituted by a di-lower alkylamino group; a pyrimidinyl
group which may be substituted by a mono- or di-lower alkylamino
group; or a benzothienyl group which may be substituted by a
halogen atom.
[0074] In the compound (I), an optical isomer based on an
asymmetric carbon may be present depending on a kind of a
substituent(s). Either of the optical isomer or a mixture thereof
may be used as the active ingredient of the present invention.
[0075] The active ingredient (I) of the present invention can be
used in the free form or in the form of a pharmaceutically
acceptable salt. Examples of pharmaceutically acceptable salts of
the compound (I) include inorganic acid salts such as
hydrochloride, sulfate, phosphate or hydrobromide, and organic acid
salts such as acetate, fumarate, oxalate, citrate,
methanesulfonate, benzenesulfonate, tosylate or maleate. In
addition, in case of a compound with substituents such as a
carboxyl group, salts with a base (for example, alkali metal salts
such as a sodium salt and a potassium salt or alkaline earth metal
salts such as a calcium salt) can be mentioned.
[0076] The compound (I) or pharmaceutically acceptable salts
thereof includes its internal salts, addition products, solvates
and hydrates.
[0077] The active ingredient (I) of the present invention or
pharmaceutically acceptable salts thereof can be administered
orally or parenterally and used as common pharmaceutical
preparations such as tablets, granules, capsules, powders,
injection solution and inhalants.
[0078] As a pharmaceutically acceptable carrier for a preparation
of oral administration, there may be mentioned a material commonly
used, for example, a binder (such as syrup, Gum Arabic, gelatin,
sorbit, tragacanth and polyvinyl pyrrolidone), an excipient (such
as lactose, sugar, corn starch, potassium phosphate, sorbit and
glycine), a lubricant (such as magnesium stearate, talc,
polyethylene glycol and silica), a disintegrator (such as potato
starch) and a humectant (such as lauryl sodium sulfate).
[0079] On the other hand, when the active ingredient of the present
invention is administered non-orally, it may be formulated into the
form of an injection or a drip infusion by using distilled water
for injection, physiological saline, an aqueous glucose solution
and the like, or a suppository.
[0080] A dose of the compound (I) or a pharmaceutically acceptable
salt thereof may vary depending on an administration method, an
age, weight, conditions or a kind or degree of disease of a
patient, and may be generally about 0.1 to 50 mg/kg per day, more
preferably about 0.3 to 30 mg/kg per day.
[0081] The compound (I) or a pharmaceutically acceptable salt
thereof has an excellent large conductance calcium-activated K
channel opening activity and hyperpolarizes a membrane electric
potential of cells, so that it may be used for a prophylactic,
relief and/or treatment agent of, for example, hypertension,
asthma, premature birth, irritable bowel syndrome, chronic heart
failure, angina, cardiac infarction, cerebral infarction,
subarachnoid hemorrhage, cerebral vasospasm, cerebral hypoxia,
peripheral blood vessel disorder, anxiety, male-pattern baldness,
erectile dysfunction, diabetes, diabetic peripheral nerve disorder,
other diabetic complication, sterility, urolithiasis and pain
accompanied thereby, pollakiuria, urinary incontinence, nocturnal
enuresis, and the like.
[0082] In the present specification, as the lower alkyl group, a
hydroxy lower alkyl group, a lower alkoxy group, a lower alkylthio
group, a lower alkylsulfinyl group, a lower alkoxysulfonyl group, a
lower alkylsulfamoyl group, a lower alkylcarbamoyl group, a lower
alkylamino group, or a lower alkylsulfonylamino group, there may be
mentioned those which are straight or branched and having 1 to 6
carbon atoms, particularly those which are straight or branched and
having 1 to 4 carbon atoms.
[0083] As a lower alkenyl group, a lower alkanoyl group, a lower
alkanoyloxy group, a lower alkanoylamino group or a lower
alkoxycarbonyl group, there may be mentioned those which are a
straight or branched and having 2 to 7 carbon atoms, particularly
those which are a straight or branched and having 2 to 5 carbon
atoms.
[0084] As a cyclo-lower alkyl group, there may be mentioned those
having 3 to 6 carbon atoms.
[0085] As a halogen atom, there may be mentioned fluorine atom,
chlorine atom, bromine atom or iodine atom.
[0086] The nitrogen-containing 5-membered heterocyclic compound (I)
which is an active ingredient of the present invention can be
prepared by the following Method A, Method B, Method C or Method D,
but the preparation methods are not limited to these methods.
(Method A)
[0087] ##STR00003## [0088] wherein X.sup.1 represents NH, O or S,
and other symbols have the same meanings as defined above.
[0089] Among the nitrogen-containing 5-membered heterocyclic
compound (I), a compound (I-a) can be prepared by reacting the
compound represented by the formula (II) or a salt thereof with a
condensation reagent.
[0090] As the condensation reagent, there may be suitably used,
when X.sup.1 is NH, for example, ammonia or an ammonium salt (such
as ammonium acetate, ammonium formate, ammonium carbonate, ammonium
benzoate and ammonium picolate), when X.sup.1 is O, for example,
phosphorus oxychloride, thionyl chloride, acetyl chloride,
triphenylphosphine-iodine, triphenylphosphine-phosgene, sulfuric
acid, polyphosphoric acid, p-toluenesulfonic acid, etc., and when
X.sup.1 is S, for example, phosphorus pentasulfide, Lawesson's
reagent
(2,4-bis(4-methoxyphenyl)-1,3-dithia-2,4-diphosphetan-2,4-disulfide),
and the like.
[0091] The present reaction can be carried out in a suitable
solvent or in the absence of a solvent. As the solvent, it is not
particularly limited so long as it does not disturb the reaction,
and there may be used, for example, acetic acid, dimethylformamide,
benzene, toluene, tetrahydrofuran, chloroform, methylene chloride,
acetonitrile or a mixed solvent of the above-mentioned solvents.
The present reaction proceeds suitably at 15 to 150.degree. C.,
particularly at room temperature to 120.degree. C.
(Method B)
[0092] ##STR00004## [0093] wherein Z.sup.1 represents a reactive
residue, and other symbols have the same meanings as defined
above.
[0094] Also, among the compound (I), a compound (I-b) can be
prepared by reacting a compound represented by the formula (III) or
a salt thereof with a compound represented by the formula (IV) or a
salt thereof in the presence of a base. As the base, there may be
suitably used, for example, an alkali metal carbonate, an alkali
metal hydride, an alkali metal alkoxide, an alkali metal hydroxide,
and the like.
[0095] The present reaction can be carried out in a suitable
solvent or in the absence of a solvent. As the solvent, it is not
particularly limited so long as it does not disturb the reaction,
and there may be used, for example, acetonitrile, methanol,
ethanol, chloroform, methylene chloride, dimethylformamide,
acetone, tetrahydrofuran or a mixed solvent of the above-mentioned
solvents. The present reaction proceeds suitably at 30 to
150.degree. C., particularly at 60 to 120.degree. C.
(Method C)
[0096] ##STR00005## [0097] wherein Z.sup.2 represents a reactive
residue, W.sup.1 represents hydrogen atom or a lower alkyl group,
W.sup.2 represents a lower alkyl group, and other symbols have the
same meanings as defined above.
[0098] The compound (I) can be also prepared by reacting a compound
represented by the formula (V) with a compound represented by the
formula (VI) or a compound represented by the formula (VII) in the
presence of a palladium catalyst. As the palladium catalyst, there
may be suitably used a zero-valent or divalent palladium catalyst,
for example, tetrakis(triphenylphosphine) palladium (0),
bis(triphenylphosphine)palladium(II) chloride, palladium (II)
acetate, etc.
[0099] When Method C is carried out by using the compound (VI), it
is preferably carried out in the presence of a base. As the base,
there may be suitably used, for example, an inorganic base such as
an alkali metal carbonate, an alkali metal hydroxide, an alkali
metal phosphate, an alkali metal fluoride, and the like, or an
organic base such as triethylamine, and the like.
[0100] The present reaction can be carried out in a suitable
solvent or in the absence of a solvent. As the solvent, it is not
particularly limited so long as it does not disturb the reaction,
and there may be used, for example, dimethoxyethane,
tetrahydrofuran, dimethylformamide, methanol, ethanol, toluene,
benzene, chloroform or a mixed solvent of the above-mentioned
solvents. The present reaction proceeds suitably at 60 to
150.degree. C., particularly at 80 to 120.degree. C.
(Method D)
[0101] ##STR00006## [0102] wherein the symbols have the same
meanings as defined above.
[0103] Also, among the compound (I), a compound (I-b) can be
prepared by reacting a compound represented by the formula (VIII)
or a salt thereof with a compound represented by the formula (IX)
and a salt thereof in the presence of ammonia or an ammonium
salt.
[0104] As the ammonium salt, there may be suitably used, for
example, ammonium acetate, ammonium formate, ammonium carbonate,
ammonium benzoate, ammonium picolate, and the like.
[0105] The present reaction can be carried out in a suitable
solvent or in the absence of a solvent. As the solvent, it is not
particularly limited so long as it does not disturb the reaction,
and there may be used, for example, acetic acid, methanol, ethanol,
dimethoxyethane, tetrahydrofuran, dimethylformamide or a mixed
solvent of the above-mentioned solvents. The present reaction
proceeds suitably at 0 to 150.degree. C., particularly at 30 to
120.degree. C.
[0106] In the above-mentioned Methods A to D, the compounds (II),
(III), (IV), (V), (VIII) or (IX) may be used as a salt of an
inorganic acid such as hydrochloride, sulfate, etc., or a salt of
an inorganic base such as an alkali metal salt, an alkaline earth
metal salt, etc.
[0107] As the reactive residue of Z.sup.1 and Z.sup.2, a halogen
atom is suitably used.
[0108] The nitrogen-containing 5-membered heterocyclic compound (I)
can be prepared by converting objective compounds obtained from one
of the above methods into other objective compounds. Such
conversion reactions may be suitably used depending on a
substituent(s) in a compound, and it can be carried out, for
example, by a conventional method as mentioned in the following
Methods (a) to (v).
Method (a):
[0109] A compound (I) wherein R.sup.1 or R.sup.2 is a halogen atom
can be prepared by reacting a compound (I) where corresponding
R.sup.1 or R.sup.2 is a hydrogen atom with a halogenating agent. As
the halogenating agent, there may be suitably used bromine,
chlorine, iodine, [bis(trifluoroacetoxy)iodo]benzene,
N-bromosuccinic imide and the like. This reaction proceeds suitably
at 0.degree. C. to 30.degree. C.
Method (b):
[0110] A compound (I) wherein R.sup.1 or R.sup.2 is a substituted
or unsubstituted aryl group, or a substituted or unsubstituted
heterocyclic group can be prepared by reaction of a compound (I)
where corresponding R.sup.1 or R.sup.2 is a halogen atom with a
(tri-lower alkyl) (a substituted or unsubstituted aryl) tin
compound, or (tri-lower alkyl) (a substituted or unsubstituted
heterocyclic) tin compound in the presence of a catalyst. As the
catalyst, there may be suitably used a zero-valent or divalent
palladium catalyst such as bis(triphenylphosphine) palladium (II)
chloride, palladium (II) acetate, tetrakis(triphenylphosphine)
palladium (0), etc. Also this reaction proceeds more suitably in
the presence of a zinc salt such as zinc chloride, zinc bromide,
zinc iodide, etc. This reaction proceeds suitably at 50.degree. C.
to 120.degree. C.
[0111] Also, this reaction may be carried out by using a
corresponding boric acid or its ester in place of the tin compound,
in the presence of a base. As the palladium catalyst and the base,
those as mentioned in the above Method C are suitably used. This
reaction proceeds suitably at 60.degree. C. to 120.degree. C.
Method (c):
[0112] A compound (I) wherein R.sup.1 or R.sup.2 is a substituted
or unsubstituted heterocyclic group-substituted carbonyl group can
be prepared by reacting a compound (I) where corresponding R.sup.1
or R.sup.2 is a substituted carbamoyl group with a substituted or
unsubstituted heterocyclyl lithium. This reaction proceeds suitably
at -78.degree. C. to 30.degree. C. The substituted or unsubstituted
heterocyclyl lithium can be prepared by lithiation of a
corresponding halogeno-heterocyclic compound with n-butyl lithium,
etc.
Method (d):
[0113] A compound (I) where X is N--R.sup.4 and R.sup.4 is a
substituted or unsubstituted alkyl group can be prepared by
reaction of a compound (I) where corresponding X is N--R.sup.4 and
R.sup.4 is hydrogen atom with a substituted or unsubstituted lower
alkyl halide (such as a lower alkyl iodide, a lower alkyl chloride
and a lower alkyl bromide) or a lower alkyl sulfonate (such as a
lower alkyl trifluoromethanesulfonate and a lower alkyl
methanesulfonate) in the presence of a base. As the base, there may
be suitably used an alkali metal hydride, an alkali metal
carbonate, an alkali metal alkoxide, an alkali metal hydroxide, and
the like. This reaction proceeds suitably at 30.degree. C. to
80.degree. C.
Method (e):
[0114] A compound (I) where R.sup.1 or R.sup.2 is a formylamino
group or an N-lower alkyl-N-formylamino group can be prepared by
reacting a compound (I) where corresponding R.sup.1 or R.sup.2 is
an amino group or an N-lower alkylamino group with a formic acid
lower alkyl ester (such as methyl ester and ethyl ester). This
reaction proceeds suitably at 60.degree. C. to 100.degree. C.
Method (f):
[0115] A compound (I) where R.sup.1 or R.sup.2 is an N-methylamino
group, an N-lower alkyl-N-methylamino group or an N-ethylamino
group can be prepared by reacting a compound (I) where
corresponding R.sup.1 or R.sup.2 is a formylamino group, an N-lower
alkyl-N-formylamino group or an N-acetylamino group with a reducing
agent. As the reducing agent, there may be suitably used a borane
complex (such as borane.dimethylsulfide complex), lithium aluminum
hydride, and the like. This reaction proceeds suitably at 0.degree.
C. to 60.degree. C.
Method (g):
[0116] A compound (I) where R.sup.1 or R.sup.2 is a lower
alkoxycarbonylamino group can be prepared by reacting a compound
(I) where corresponding R.sup.1 or R.sup.2 is an amino group with a
lower alkoxycarbonyl halide in the presence of a base. As the base,
there may be suitably used pyridine, triethylamine, an alkali metal
carbonate, an alkali metal lower alkoxide, an alkali metal hydride
and the like. This reaction proceeds suitably at 0.degree. C. to
30.degree. C.
Method (h):
[0117] A compound (I) where R.sup.1 or R.sup.2 is a hydroxy-lower
alkyl group can be prepared by reacting a compound (I) where
corresponding R.sup.1 or R.sup.2 is a hydrogen atom with
formaldehyde or a lower alkyl aldehyde in the presence of a base.
As the base, there may be suitably used an alkali metal carbonate,
an alkali metal lower alkoxide, triethylamine, and the like. This
reaction proceeds suitably at 60.degree. C. to 120.degree. C.
Method (i):
[0118] A compound (I) where R.sup.1 or R.sup.2 is a halogeno-lower
alkyl group can be prepared by reacting a compound (I) where
corresponding R.sup.1 or R.sup.2 is a hydroxy-lower alkyl group
with a halogenating agent. As the halogenating agent, there may be
suitably used thionyl chloride, thionyl bromide and the like. This
reaction proceeds suitably at 0.degree. C. to 50.degree. C.
Method (j):
[0119] A compound (I) where R.sup.1 or R.sup.2 is a lower
alkoxy-lower alkyl group can be prepared by reacting a compound (I)
where corresponding R.sup.1 or R.sup.2 is a halogeno-lower alkyl
group with a lower alkanol. As the lower alkanol, there may be
suitably used methanol, ethanol and the like. This reaction
proceeds suitably at 30.degree. C. to 80.degree. C.
Method (k):
[0120] A compound (I) where R.sup.1 or R.sup.2 is a lower
alkylthio-lower alkyl group can be prepared by reacting a compound
(I) where corresponding R.sup.1 or R.sup.2 is a halogeno-lower
alkyl group with a lower alkyl sulfide salt. As the lower alkyl
sulfide salt, there may be suitably used an alkali metal lower
alkyl sulfide such as sodium methyl sulfide and the like. This
reaction is preferably carried out in the presence of a base. As
the base, there may be suitably used triethylamine, pyridine, an
alkali metal carbonate, an alkali metal alkoxide and the like. This
reaction proceeds suitably at 0.degree. C. to 60.degree. C.
Method (l):
[0121] A compound (I) where R.sup.1 or R.sup.2 is a lower
alkylsulfinyl-lower alkyl group or a lower alkylsulfonyl-lower
alkyl group can be prepared by reacting a compound (I) where
corresponding R.sup.1 or R.sup.2 is a lower alkylthio-lower alkyl
group with an oxidizing agent. As the oxidizing agent, there may be
suitably used metachloroperbenzoic acid, aqueous hydrogen peroxide
solution and the like. This reaction proceeds suitably at
-20.degree. C. to 30.degree. C.
Method (m):
[0122] A compound (I) where R.sup.1 or R.sup.2 is a carboxy-lower
alkyl group or a carboxy-lower alkenyl group can be prepared by
hydrolysis of a compound (I) where corresponding R.sup.1 or R.sup.2
is a lower alkoxycarbonyl-lower alkyl or a cyano-lower alkyl group
or a lower alkoxycarbonyl-lower alkenyl or a cyano-lower alkeny
group with a base or an acid. As the base, an alkali metal
hydroxide and the like may be suitably used. As the acid,
hydrochloric acid or boron tribromide and the like may be suitably
used. This reaction proceeds suitably at 0.degree. C. to 80.degree.
C.
Method (n):
[0123] A compound (I) where R.sup.3 is a heterocyclic group
substituted by a sulfo group can be prepared by reaction of a
compound (I) where corresponding R.sup.3 is a heterocyclic group
(which may be substituted onto the other position of the
heterocyclic ring than that to which the sulfo group is to be
bonded) with halogenosulfonic acid (such as chlorosulfonic acid),
and then, treating with a basic aqueous solution (such as aqueous
ammonia). This reaction proceeds suitably at 0.degree. C. to
50.degree. C.
Method (o):
[0124] A compound (I) where R.sup.3 is a heterocyclic group
substituted by sulfamoyl group can be prepared by treating a
compound (I) where corresponding R.sup.3 is a heterocyclic group
substituted by chlorosulfonyl group with ammonia. This reaction
proceeds suitably at 0.degree. C. to 60.degree. C.
Method (p):
[0125] A compound (I) where R.sup.1, R.sup.2 or R.sup.3 is a
heterocyclic group substituted by a hydroxy-lower alkyl group or
R.sup.1 or R.sup.2 is a hydroxy-lower alkyl group can be prepared
by reacting a compound (I) where corresponding R.sup.1, R.sup.2 or
R.sup.3 is a heterocyclic group substituted by a lower
alkoxycarbonyl-lower alkyl group or corresponding R.sup.1 or
R.sup.2 is a lower alkoxycarbonyl-lower alkyl group with a reducing
agent. As the reducing agent, there may be suitably used lithium
aluminum hydride, lithium borohydride, a borane complex (such as
borane.dimethylsulfide complex) and the like. This reaction
proceeds suitably at 0.degree. C. to 60.degree. C.
Method (q):
[0126] A compound (I) where R.sup.1 or R.sup.2 is a substituted or
unsubstituted carbamoyl group can be prepared by reaction of a
compound (I) where corresponding R.sup.1 or R.sup.2 is a carboxyl
group with a corresponding substituted or unsubstituted amine in
the presence of a condensing agent. As the condensing agent, there
may be suitably used 3-ethyl-1-(3-dimethylaminopropyl)carbodiimide
hydrochloride, diethylcyanophosphate and the like. This reaction
proceeds suitably at 0.degree. C. to 50.degree. C.
Method (r):
[0127] A compound (I) where R.sup.3 is a pyridyl group substituted
with a mono- or di-lower alkylamino group or R.sup.3 is a pyrazinyl
group substituted with a mono- or di lower alkylamino group can be
prepared by reacting a compound (I) where corresponding R.sup.3 is
a halogenopyridyl group or a halogenopyrazinyl group with a
corresponding mono- or di-lower alkylamine. This reaction proceeds
suitably at 30.degree. C. to 120.degree. C.
Method (s):
[0128] A compound (I) where R.sup.3 is a pyrimidinyl group
substituted with a mono- or di-lower alkylamino group can be
prepared by reacting a compound (I) where corresponding R.sup.3 is
a pyrimidinyl group substituted with a lower alkylthio group with a
oxidizing agent, followed by reacting the resulting compound with
corresponding mono- or di-lower alkylamine. Examples of the
oxidizing agent may be m-chloroperbenzoic acid, hydrogen peroxide,
and the like. This reaction proceeds suitably at 0.degree. C. to
30.degree. C.
Method (t):
[0129] A compound (I) where R.sup.1 or R.sup.2 is a substituted or
unsubstituted carbamoyl-lower alkyl group can be prepared by
reacting a compound (I) where corresponding R.sup.1 or R.sup.2 is a
carboxy-lower alkyl group with a corresponding amine in the
presence of a condensing agent. Examples of the condensing agent
may be 3-ethyl-1-(3-dimethylaminopropyl)carbodiimide hydrochloride,
diethyl cyanophosphonate, and the like. This reaction proceeds
suitably at 0.degree. C. to 50.degree. C.
Method (u):
[0130] A compound (I) where R.sup.1 or R.sup.2 is a cyano-lower
alkyl group can be prepared by reacting a compound (I) where
corresponding R.sup.1 or R.sup.2 is a carbamoyl-lower alkyl group
with a dehydrating agent. Examples of the dehydrating agent may be
phosphorus oxychloride, acetic anhydride, thionyl chloride and the
like. This reaction proceeds suitably at 50.degree. C. to
100.degree. C.
Method (v):
[0131] A compound (I) where R.sup.1 or R.sup.2 is a
tetrazolyl-lower alkyl group can be prepared by reacting a compound
(I) where corresponding R.sup.1 or R.sup.2 is a cyano-lower alkyl
group with an azide compound.
[0132] Examples of the azide compound may be sodium azide, a
tri-alkyltin azide, a trialkylsilyl azide, and the like. This
reaction proceeds suitably at 80.degree. C. to 120.degree. C.
[0133] The reactions mentioned in the above Methods (a) to (v) can
be carried out in an inert solvent to the reaction or in the
absence of a solvent, which is not specifically limited, and the
solvent may be mentioned, for example, methylene chloride,
chloroform, tetrahydrofuran, methanol, ethanol, isopropanol,
dimethylformamide, dimethylsulfoxide, water, ethyl acetate,
dimethoxyethane, toluene, benzene, and the like, or a mixed solvent
of the above solvents.
[0134] Also, among the compounds (I), known compounds are included
and these known compounds have been reported in, for example,
Japanese Provisional Patent Publications No. 5832/1972, No.
29771/1973, 172488/1984, 34951/1985, No. 188371/1985 and No.
167676/1986, U.S. Pat. No. 3,470,195, U.S. Pat. No. 3,476,766, U.S.
Pat. No. 3,546,342, U.S. Pat. No. 3,574,228 and U.S. Pat. No.
3,905,961, International Publications No. WO95/04724 and No.
WO99/01128, Chem. Pharm. Bull., 34(8), 3111-3120 (1986), Chem.
Pharm. Bull., 36(11), 4435-4440 (1988), Chem. Pharm. Bull., 40(12),
3206-3213 (1992), Angew. Chem., 85(13), 584-585 (1973), J.
Heterocyclic Chem., 22(2), 569-574 (1985), J. Med. Chem., 29(3),
333-341 (1986), J. Med. Chem., 31(6), 1197-1204 (1988) and the
like. However, there is no description in these references that
these compounds have large conductance calcium-activated K channel
opening activity.
[0135] Incidentally, the starting compound (II) or (III) of the
present invention can be prepared, for example, according to the
method described in J. Med. Chem., 29, 333-341 (1986), Chem. Pharm.
Bull., 34(8), 3111-3120 (1986) or Japanese Provisional Patent
Publication No. 167676/1986.
[0136] The compound (II) can be prepared specifically by the
conventional method as mentioned below.
##STR00007## [0137] wherein the symbols have the same meanings as
defined above.
[0138] Also, among the compounds (V), a compound (V-a) wherein
R.sup.2 is a halogen atom can be prepared specifically by the
conventional method as mentioned below.
##STR00008## [0139] wherein Z.sup.3 represents a halogen atom, and
the other symbols have the same meaning as defined above.
[0140] The active ingredients of the present invention can be
exemplified by the following Preparation examples but they are not
limited thereto.
PREPARATION EXAMPLE
Preparation Example 1
[0141] A crude product of
2-(6-methylnicotinoylamino)-1-(3-pyridyl)-1-butanone (425 mg) was
dissolved in acetic acid (5 ml), and ammonium acetate (2.30 g) was
added to the solution. The resulting mixture was stirred under
reflux for one hour. After cooling, 28% of aqueous ammonia was
added to the reaction mixture and the mixture was extracted with
ethyl acetate. The organic layer was washed with brine, dried over
anhydrous sodium sulfate and the solvent was removed under reduced
pressure. To the residue was added hydrogen chloride-methanol
solution, and the solvent was again removed under reduced pressure.
The resulting residue was triturated with acetone to obtain
5-ethyl-2-(2-methyl-pyridin-5-yl)-4-(3-pyridyl)imidazole
trihydrochloride (369 mg) as pale yellowish crystalline powder.
[0142] Melting point: 270 to 273.degree. C. (decomposed)
[0143] MS.cndot.APCI (m/z) 265 (MH+)
Preparation Examples 2 to 42
[0144] The following compounds shown in Table 1 were prepared in a
manner similar to Preparation example 1 by using corresponding
starting materials.
TABLE-US-00001 TABLE 1 Preparation example No. Chemical structure
Salt Physical constant, etc. 2 ##STR00009## 2HCl Crystal Melting
point: 170-172.degree. C. MS.cndot.APCI (m/z): 312 (M + H)+ 3
##STR00010## 2HCl Crystal Melting point: 175-180.degree. C.
MS.cndot.APCI (m/z): 298 (M + H)+ 4 ##STR00011## 1HCl Crystal
Melting point: 234-237.degree. C. MS.cndot.APCI (m/z): 276 (M + H)+
5 ##STR00012## 1HCl Powder MS.cndot.APCI (m/z): 270 (M + H)+ 6
##STR00013## 2HCl Crystal Melting point: 275-280.degree. C.
MS.cndot.APCI (m/z): 270 (M + H)+ 7 ##STR00014## 2HCl Crystal
Melting point: 183-185.degree. C. MS.cndot.APCI (m/z): 284 (M + H)+
8 ##STR00015## 1HCl Crystal Melting point: 251-254.degree. C.
MS.cndot.APCI (m/z): 294 (M + H)+ 9 ##STR00016## 1HCl Crystal
Melting point: 278-281.degree. C. MS.cndot.APCI (m/z): 314 (M + H)+
10 ##STR00017## Free material Crystal Melting point:
127-129.degree. C. MS.cndot.APCI (m/z): 328 (M + H)+ 11
##STR00018## Free material Crystal Melting point: 187-189.degree.
C. MS.cndot.APCI (m/z): 328 (M + H)+ 12 ##STR00019## 2HCl Crystal
Melting point: 221-223.degree. C. MS.cndot.APCI (m/z): 284/286 (M +
H)+ 13 ##STR00020## 2HCl Crystal Melting point: 223-224.degree. C.
MS.cndot.APCI (m/z): 284/286 (M + H)+ 14 ##STR00021## 2HCl Powder
MS.cndot.APCI (m/z): 290 (M + H)+ 15 ##STR00022## 2HCl Powder
MS.cndot.APCI (m/z): 254 (M + H)+ 16 ##STR00023## 2HCl Powder
MS.cndot.APCI (m/z): 281 (M + H)+ 17 ##STR00024## 2HCl Powder
MS.cndot.APCI (m/z): 295 (M + H)+ 18 ##STR00025## 2HCl Crystal
Melting point: 250-253.degree. C. MS.cndot.APCI (m/z): 293 (M + H)+
19 ##STR00026## 2HCl Crystal Melting point: 214-216.degree. C.
MS.cndot.APCI (m/z): 334/336 (M + H)+ 20 ##STR00027## 2HCl Crystal
Melting point: 215-217.degree. C. MS.cndot.APCI (m/z): 256 (M + H)+
21 ##STR00028## Free material Powder MS.cndot.APCI (m/z): 308 (M +
H)+ 22 ##STR00029## 2HCl Crystal Melting point: 192-195.degree. C.
EI.cndot.MS (m/z): 239 (M+) 23 ##STR00030## 2HCl Crystal Melting
point: 325-328.degree. C. MS.cndot.APCI (m/z): 247 (M + H)+ 24
##STR00031## 2HCl Powder MS.cndot.APCI (m/z): 262 (M + H)+ 25
##STR00032## 2HCl Powder MS.cndot.APCI (m/z): 262/264 (M + H)+ 26
##STR00033## 3HCl Crystal Melting point: 269-273.degree. C.
MS.cndot.APCI (m/z): 237 (M + H)+ 27 ##STR00034## 2HCl Crystal
Melting point: 285-288.degree. C. MS.cndot.APCI (m/z): 274 (M + H)+
28 ##STR00035## 2HCl Crystal Melting point: 248-251.degree. C.
MS.cndot.APCI (m/z): 264 (M + H)+ 29 ##STR00036## 1HCl Crystal
Melting point: 202-204.degree. C. MS.cndot.APCI (m/z): 297 (M + H)+
30 ##STR00037## 1HCl Crystal Melting point: 192-193.degree. C.
MS.cndot.APCI (m/z): 281 (M + H)+ 31 ##STR00038## 1HCl Crystal
Melting point: 258-260.degree. C. MS.cndot.APCI (m/z): 288 (M + H)+
32 ##STR00039## 1HCl Crystal Melting point: 189-190.degree. C.
MS.cndot.APCI (m/z): 313 (M + H)+ 33 ##STR00040## 1HCl Crystal
Melting point: 215-217.degree. C. MS.cndot.APCI (m/z): 269 (M + H)+
34 ##STR00041## 1HCl Crystal Melting point: 194-196.degree. C.
MS.cndot.APCI (m/z): 303/305 (M + H)+ 35 ##STR00042## 1HCl Crystal
Melting point: 220-222.degree. C. MS.cndot.APCI (m/z): 252 (M + H)+
36 ##STR00043## 1HCl Foam MS.cndot.APCI (m/z): 313 (M + H)+ 37
##STR00044## 1HCl Powder MS.cndot.APCI (m/z): 314 (M + H)+ 38
##STR00045## 1HCl Crystal Melting point: 185-188.degree. C.
MS.cndot.APCI (m/z): 303 (M + H)+ 39 ##STR00046## 1HCl Crystal
Melting point: 233-236.degree. C. MS.cndot.APCI (m/z): 308 (M + H)+
40 ##STR00047## 1HCl Crystal Melting point: 188-190.degree. C.
MS.cndot.APCI (m/z): 303 (M + H)+ 41 ##STR00048## 1HCl Crystal
Melting point: 250-255.degree. C. MS.cndot.APCI (m/z): 239 (M + H)+
42 ##STR00049## 1HCl Crystal Melting point: >300.degree. C.
MS.cndot.APCI (m/z): 246 (M + H)+
Preparation Example 43
[0145] 4-Cyano-2-(4-fluorobenzoylamino)-1-(3-pyridyl)-1-butanone
(500 mg) was dissolved in acetic acid (3 ml), and ammonium acetate
(2.99 g) was added to the solution and the resulting mixture was
refluxed overnight. After cooling, 28% of aqueous ammonia was added
to the reaction mixture and the mixture was extracted with ethyl
acetate. The organic layer was washed with brine, dried over
anhydrous sodium sulfate and the solvent was removed under reduced
pressure. The resulting residue was purified by silica gel flush
column chromatography (solvent: hexane:ethyl acetate=1:2) and
treated with hydrogen chloride-ethanol to obtain
5-(2-cyanoethyl)-2-(4-fluorophenyl)-4-(3-pyridyl)-imidazole
dihydrochloride (172 mg) as colorless powder.
[0146] MS.cndot.APCI (m/z): 293 (MH+)
Preparation Examples 44 to 62
[0147] The following compounds shown in Table 2 were prepared in a
manner similar to Preparation example 43 by using corresponding
starting materials.
TABLE-US-00002 TABLE 2 Preparation Chemical Physical constant,
example No. structure Salt etc. 44 ##STR00050## Free material
Crystal Melting point: 200-202.degree. C. (Decomposed) EI.cndot.MS
(m/z): 301 (M+) 45 ##STR00051## Free material Crystal Melting
point: 171-173.degree. C. EI.cndot.MS (m/z): 326 (M+) 46
##STR00052## 1HCl Powder MS.cndot.APCI (m/z): 298 (M + H)+ 47
##STR00053## 2HCl Crystal Melting point: 260-262.degree. C.
MS.cndot.APCI (m/z): 282 (M + H)+ 48 ##STR00054## 2HCl Powder
MS.cndot.APCI (m/z): 282 (M + H)+ 49 ##STR00055## 1HCl Crystal
Melting point: 241-243.degree. C. MS.cndot.APCI (m/z): 269 (M + H)+
50 ##STR00056## 1HCl Crystal Melting point: 190-192.degree. C.
MS.cndot.APCI (m/z): 269 (M + H)+ 51 ##STR00057## 1HCl Crystal
Melting point: 215-218.degree. C. MS.cndot.APCI (m/z): 274 (M + H)+
52 ##STR00058## 1HCl Crystal Melting point: 267-269.degree. C.
MS.cndot.APCI (m/z): 274 (M + H)+ 53 ##STR00059## 2HCl Powder
MS.cndot.APCI (m/z): 275 (M + H)+ 54 ##STR00060## 2HCl Crystal
Melting point: 198-201.degree. C. 55 ##STR00061## 2HCl Crystal
Melting point: 205-207.degree. C. MS.cndot.APCI (m/z): 290 (M + H)+
56 ##STR00062## 2HCl Powder MS.cndot.APCI (m/z): 284 (M + H)+ 57
##STR00063## 2HCl Powder MS.cndot.APCI (m/z): 275 (M + H)+ 58
##STR00064## 2HCl Powder MS.cndot.APCI (m/z): 348 (M + H)+ 59
##STR00065## Free material Crystal Melting point: 174-176.degree.
C. EI.cndot.MS (m/z): 282/284 (M+) 60 ##STR00066## Free material
Crystal Melting point: 147-149.degree. C. EI.cndot.MS (m/z):
297/299 (M+) 61 ##STR00067## Free material Crystal Melting point:
169-170.degree. C. EI.cndot.MS (m/z): 266 (M+) 62 ##STR00068## Free
material Crystal Melting point: 176-178.degree. C. EI.cndot.MS
(m/z): 291 (M+)
Preparation Example 63
[0148] Under ice-cooling, phosphorus oxychloride (0.24 ml) was
added dropwise to a solution of
2-(5-chlorothiophen-2-yl)amino-1-(3-pyridyl)-1-butanone (610 mg) in
N,N-dimethylformamide (7 ml), and the resulting mixture was stirred
at room temperature overnight and further at 60.degree. C.
overnight. After cooling, the reaction mixture was poured into ice
water, neutralized by a saturated aqueous sodium hydrogen carbonate
solution and extracted with ethyl acetate. The organic layer was
washed with water and brine, and then, dried over anhydrous
magnesium sulfate and the solvent was removed under reduced
pressure. The resulting residue was purified by silica gel column
chromatography (solvent: chloroform:ethyl acetate=2:1) and treated
with hydrogen chloride-ethanol solution to obtain
2-(5-chlorothiophen-2-yl)-4-ethyl-5-(3-pyridyl)oxazole
hydrochloride (466 mg) as pale yellowish powder.
[0149] Melting point: 201 to 204.degree. C.
[0150] MS.cndot.APCI (m/z): 291/293 (MH+)
Preparation Examples 64 and 65
[0151] The following compounds shown in Table 3 were prepared in a
manner similar to Preparation example 63 by using corresponding
starting materials.
TABLE-US-00003 TABLE 3 Preparation Chemical Physical constant,
example No. structure Salt etc. 64 ##STR00069## 1HCl Powder
MS.cndot.APCI (m/z): 343 (M + H)+ 65 ##STR00070## Free material
Powder MS.cndot.APCI (m/z): 349 (M + H)+
Preparation Example 66
[0152] A mixture of 2-bromo-2'-methoxy-acetophenone (514 mg),
4-fluorobenzamidine hydrochloride (392 mg) and potassium carbonate
(930 mg) in acetonitrile (5 ml) was refluxed for 2 hours. After
cooling, to the reaction mixture were added chloroform and water,
the organic layer was collected and dried over anhydrous sodium
sulfate, and the solvent was removed under reduced pressure. The
resulting residue was recrystallized from methanol to obtain
2-(4-fluorophenyl)-4-(2-methoxyphenyl)imidazole (1.54 g) as pale
yellowish crystal. This compound was treated with hydrogen
chloride-ethanol solution to be converted into a hydrochloride salt
form.
[0153] Melting point: 165 to 167.degree. C. (free material)
[0154] Melting point: 245 to 248.degree. C. (hydrochloride)
[0155] MS.cndot.APCI (m/z): 269 (MH+) (hydrochloride)
Preparation Example 67
[0156] A mixture of 5-ethyl-2-iodo-4-(3-pyridyl)-imidazole (150
mg), 3-hydroxymethylthiophene-2-boric acid (105 mg) and
tetrakis(triphenylphosphine)palladium (0) (58 mg) in an aqueous 2M
sodium carbonate solution (1 ml) and dimethoxyethane (3 ml) was
stirred under argon atmosphere at 100.degree. C. for 2.5 hours.
After cooling, to the reaction mixture were added water and ethyl
acetate. The organic layer was collected, and after washing with
brine, it was dried over anhydrous sodium sulfate and the solvent
was removed under reduced pressure. The resulting residue was
purified by NH silica gel flush column chromatography (solvent:
ethyl acetate) and treated with hydrogen chloride-dioxane solution
to obtain
5-ethyl-2-(3-hydroxymethylthiphen-2-yl)-4-(3-pyridyl)imidazole
dihydrochloride (110 mg) as colorless powder.
[0157] MS.cndot.APCI (m/z): 286 (MH+)
Preparation Examples 68
[0158] The following compounds shown in Table 4 were prepared in a
manner similar to Preparation example 67 by using corresponding
starting materials.
TABLE-US-00004 TABLE 4 Preparation Chemical Physical constant,
example No. structure Salt etc. 68 ##STR00071## 2HCl Powder
MS.cndot.APCI (m/z): 257 (M + H)
Preparation Example 69
[0159] A mixture of ethyl 2,3-diketovalerate (8.00 g),
4-fluoro-benzaldehyde (11.30 g) and ammonium acetate (35.00 g) in
acetic acid (120 ml) was stirred under argon atmosphere at 70 to
80.degree. C. for 40 minutes. After cooling, water was added to the
reaction mixture and the reaction mixture was extracted with a
mixed solution of ethyl acetate-diethyl ether. The organic layer
was washed successively with a saturated aqueous sodium hydrogen
carbonate solution and brine, dried over anhydrous sodium sulfate
and the solvent was removed under reduced pressure. The resulting
residue was purified by silica gel flush column chromatography
(solvent: hexane:ethyl acetate=3:1) and recrystallized from ethyl
acetate-diethyl ether to obtain ethyl
5-ethyl-2-(4-fluorophenyl)imidazol-4-carboxylate (5.16 g) as
colorless crystal.
[0160] Melting point: 197 to 198.degree. C.
[0161] MS.cndot.APCI (m/z): 263 (MH+)
Preparation Example 70
[0162] A mixture of ethyl
5-ethyl-2-(4-fluorophenyl)imidazol-4-carboxylate (2.81 g), 4N
aqueous sodium hydroxide solution (14 ml), ethanol (35 ml) and
tetrahydrofuran (15 ml) was stirred at room temperature overnight,
followed by refluxing for 3 hours. 4N aqueous sodium hydroxide
solution (28 ml) was added to the mixture and the mixture was
refluxed overnight. After cooling, the reaction mixture was
concentrated under reduced pressure and neutralized by 10%
hydrochloric acid, and precipitated solid was collected by
filtration. The solid was dissolved in tetrahydrofuran, dried over
anhydrous sodium sulfate and the solvent was removed under reduced
pressure. The resulting residue was triturated with diethyl ether
to obtain first crop of
5-ethyl-2-(4-fluorophenyl)imidazol-4-carboxylic acid (1.06 g) as
colorless powder. Moreover, the filtrate was purified by HP-20
resin (trade name, available from Nippon Rensui K.K.) (solvent:
water.fwdarw.methanol) to give second crop of
5-ethyl-2-(4-fluorophenyl)imidazol-4-carboxylic acid (1.60 g).
[0163] ESI.cndot.MS (m/z): 233 (M-H)
Preparation Example 71
[0164] A mixture of 5-ethyl-2-(4-fluorophenyl)imidazol-4-carboxylic
acid (600 mg), N,O-dimethylhydroxylamine hydrochloride (325 mg),
3-ethyl-1-(3-dimethylaminopropyl)carbodiimide hydrochloride (540
mg), 1-hydroxybenzotriazole (381 mg) and triethylamine (0.54 ml) in
N,N-dimethylformamide (9 ml) was stirred at room temperature
overnight. Water was added to the reaction mixture, and the
reaction mixture was extracted with ethyl acetate. The organic
layer was washed with water and brine and dried over anhydrous
sodium sulfate, and the solvent was removed under reduced pressure.
The resulting residue was purified by silica gel flush column
chromatography (solvent: hexane:ethyl acetate=2:1) to obtain
5-ethyl-2-(4-fluorophenyl)-4-(N-methoxy-N-methylcarbamoyl)imidazole
(656 mg) as colorless powder.
[0165] MS.cndot.APCI (m/z): 278 (MH+)
Preparation Example 72
[0166] To a solution of 2-bromopyridine (855 mg) in tetrahydrofuran
(16 ml) was added dropwise 1.6M n-butyl lithium (3.38 ml, hexane
solution) under argon gas atmosphere at -78.degree. C., and after
stirring the mixture at the same temperature for 30 minutes, a
solution of
5-ethyl-2-(4-fluorophenyl)-4-(N-methoxy-N-methylcarbamoyl)imidazole
(300 mg) in tetrahydrofuran (4 ml) was added dropwise to the
mixture. After the reaction mixture was stirred under ice-acetone
cooling for 30 minutes, a saturated aqueous ammonium chloride
solution was added to the mixture and the mixture was extracted
with ethyl acetate. The organic layer was washed with water and
brine, dried over anhydrous sodium sulfate, and the solvent was
removed under reduced pressure. The resulting residue was
triturated with diethyl ether-hexane to obtain
5-ethyl-2-(4-fluorophenyl)-imidazol-4-yl-(2-pyridyl) ketone (324
mg). 132 mg of the product was treated with hydrogen
chloride-dioxane solution to obtain the dihydro-chloride salt (73
mg) as colorless solid.
[0167] MS.cndot.APCI (m/z): 296 (MH+)
Preparation Example 73
[0168] The following compounds shown in Table 5 were prepared in a
manner similar to Preparation example 72 by using corresponding
starting materials.
TABLE-US-00005 TABLE 5 Physical Preparation Chemical constant,
example No. structure Salt etc. 73 ##STR00072## 2HCl Solid
MS.cndot.APCI (m/z): 296 (M + H)+
Preparation Example 74
[0169] In acetonitrile (80 ml) were dissolved 2,2-dichlorobutanal
(16.2 g) and 4-fluorobenzaldehyde (14.9 g). To the solution was
added dropwise 28% aqueous ammonia (135 ml) under ice-cooling, and
the resulting mixture was stirred at room temperature for 4 days.
Water was added to the reaction mixture and the mixture was
extracted with chloroform. The organic layer was washed with brine,
dried over anhydrous sodium sulfate and the solvent was removed
under reduced pressure. The resulting residue was crystallized from
methanol-diethyl ether to obtain
4-ethyl-2-(4-fluorophenyl)imidazole (9.36 g).
[0170] MS.cndot.APCI (m/z): 191 (MH+)
Preparation Examples 75 and 76
[0171] The following compounds shown in Table 6 were prepared in a
manner similar to Preparation example 74 by using corresponding
starting materials.
TABLE-US-00006 TABLE 6 Preparation Chemical Physical constant,
example No. structure Salt etc. 75 ##STR00073## 2HCl Solid
MS.cndot.APCI (m/z): 188 (M + H)+ 76 ##STR00074## Free material
Crystal Melting point: 168-170.degree. C. MS.cndot.APCI (m/z): 205
(M + H)+
Preparation Example 77
[0172] To a suspension of 4-ethyl-2-(4-fluorophenyl)imidazole (4.90
g) in chloroform (100 ml) was added bromine (4.53 g), and the
mixture was stirred at room temperature for 3 hours. To the
reaction mixture was added a saturated aqueous sodium hydrogen
carbonate solution, and the organic layer was collected. The
organic layer was washed with water and brine, dried over anhydrous
sodium sulfate, and the solvent was removed under reduced pressure.
The resulting residue was crystallized from chloroform to obtain
5-bromo-4-ethyl-2-(4-fluorophenyl)-imidazole (5.16 g) as colorless
crystal. 53 mg of the product was treated with 4N hydrogen
chloride-dioxane solution to obtain
5-bromo-4-ethyl-2-(4-fluorophenyl)imidazole (60 mg) as colorless
crystal.
[0173] Melting point: 192 to 193.degree. C. (Free material)
[0174] MS.cndot.APCI (m/z): 269/271 (MH+) (Free material)
[0175] Melting point: 219 to 221.degree. C. (decomposed)
(Hydrochloride)
[0176] MS.cndot.APCI (m/z): 269/271 (MH+) (Hydrochloride)
Preparation Examples 78 and 79
[0177] The following compounds shown in Table 7 were prepared in a
manner similar to Preparation example 77 by using corresponding
starting materials.
TABLE-US-00007 TABLE 7 Preparation Chemical Physical constant,
example No. structure Salt etc. 78 ##STR00075## 2HCl Solid
MS.cndot.APCI (m/z): 264/266 (M + H)+ 79 ##STR00076## 1HCl Crystal
Melting point: 178-180.degree. C. MS.cndot.APCI (m/z): 283/285 (M +
H)+
Preparation Example 80
[0178] A mixture of 5-bromo-4-ethyl-2-(4-fluorophenyl)imidazole
(100 mg), tributyl (3-pyridyl)tin (206 mg), zinc chloride (53 mg)
and bis(triphenylphosphine)palladium (II) dichloride (26 mg) in
N,N-dimethylformamide (3 ml) was refluxed under argon atmosphere
for 5 hours. After cooling, a 10% aqueous potassium fluoride
solution was added to the reaction mixture and the mixture was
extracted with ethyl acetate. The organic layer was washed with
brine, dried over anhydrous sodium sulfate, and the solvent was
removed under reduced pressure. The resulting residue was purified
by silica gel column chromatography (solvent: hexane:ethyl
acetate=1:4), and recrystallized from ethyl acetate-hexane and
treated with hydrogen chloride-methanol solution to obtain
5-ethyl-2-(4-fluorophenyl)-4-(3-pyridyl)imidazole dihydrochloride
(48 mg) as colorless powder.
[0179] MS.cndot.APCI (m/z): 268 (MH+)
Preparation Examples 81 to 101
[0180] The following compounds shown in Table 8 were prepared in a
manner similar to Preparation example 80 by using corresponding
starting materials.
TABLE-US-00008 TABLE 8 Preparation Chemical Physical constant,
example No. structure Salt etc. 81 ##STR00077## 2HCl Solid
MS.cndot.APCI (m/z): 270 (M + H)+ 82 ##STR00078## 2HCl Solid
MS.cndot.APCI (m/z): 300 (M + H)+ 83 ##STR00079## 2HCl Crystal
Melting point: 247-251.degree. C. MS.cndot.APCI (m/z): 271 (M + H)+
84 ##STR00080## 1HCl Crystal Melting point: 200-203.degree. C.
(Decomposed) MS.cndot.APCI (m/z): 297 (M + H)+ 85 ##STR00081## 1HCl
Crystal Melting point: 287-289.degree. C. MS.cndot.APCI (m/z): 269
(M + H)+ 86 ##STR00082## 1HCl Crystal Melting point:
254-256.degree. C. MS.cndot.APCI (m/z): 274 (M + H)+ 87
##STR00083## 1HCl Crystal Melting point: 233-235.degree. C.
MS.cndot.APCI (m/z): 299 (M + H)+ 88 ##STR00084## 1HCl Crystal
Melting point: 224-226.degree. C. MS.cndot.APCI (m/z): 281 (M + H)+
89 ##STR00085## 1HCl Crystal Melting point: 174-176.degree. C.
MS.cndot.APCI (m/z): 327 (M + H)+ 90 ##STR00086## 2HCl Powder
MS.cndot.APCI (m/z): 324 (M + H)+ 91 ##STR00087## 1HCl Crystal
Melting point: 220-222.degree. C. MS.cndot.APCI (m/z): 326 (M + H)+
92 ##STR00088## 1HCl Crystal Melting point: 262-264.degree. C.
MS.cndot.APCI (m/z): 331 (M + H)+ 93 ##STR00089## 2HCl Powder
MS.cndot.APCI (m/z): 282 (M + H)+ 94 ##STR00090## 2HCl Powder
MS.cndot.APCI (m/z): 282 (M + H)+ 95 ##STR00091## Free material
Crystal Melting point: 240-242.degree. C. MS.cndot.APCI (m/z): 306
(M + H)+ 96 ##STR00092## 1HCl Crystal Melting point:
120-122.degree. C. MS.cndot.APCI (m/z): 311 (M + H)+ 97
##STR00093## 2HCl Powder MS.cndot.APCI (m/z): 282 (M + H)+ 98
##STR00094## 2HCl Powder MS.cndot.APCI (m/z): 339 (M + H)+ 99
##STR00095## 1HCl Crystal Melting point: 228-230.degree. C.
MS.cndot.APCI (m/z): 299 (M + H)+ 100 ##STR00096## 2HCl Powder
MS.cndot.APCI (m/z): 340 (M + H)+ 101 ##STR00097## 1HCl Crystal
Melting point: 186-189.degree. C. MS.cndot.APCI (m/z): 324 (M +
H)+
Preparation Example 102
[0181] To a solution of
5-ethyl-2-(4-fluorophenyl)-4-(3-pyridyl)-imidazole (481 mg) in
N,N-dimethylformamide (7 ml) was added sodium hydride (79 mg, 60%
mineral oil) under ice-acetone cooling, and the mixture was stirred
for 15 minutes. To the mixture was added methyl iodide (307 mg) and
the mixture was stirred at room temperature for one hour. To the
reaction mixture was added a saturated aqueous ammonium chloride
solution, and the mixture was extracted with ethyl acetate. The
organic layer was washed with brine, dried over anhydrous sodium
sulfate, and the solvent was removed under reduced pressure. The
resulting residue was purified by silica gel flush column
chromatography (solvent: chloroform:methanol=95:5), and treated
with hydrogen chloride-methanol solution to obtain
5-ethyl-2-(4-fluoro-phenyl)-1-methyl-4-(3-pyridyl)imidazole
dihydrochloride (285 mg).
[0182] MS.cndot.APCI (m/z): 282 (MH+)
Preparation Examples 103 and 104
[0183] The following compounds shown in Table 9 were prepared in a
manner similar to Preparation example 102 by using corresponding
starting materials.
TABLE-US-00009 TABLE 9 Preparation Chemical Physical constant,
example No. structure Salt etc. 103 ##STR00098## 2HCl Powder
MS.cndot.APCI (m/z): 338 (M + H)+ 104 ##STR00099## 2HCl Powder
MS.cndot.APCI (m/z): 296 (M + H)+
Preparation Example 105
[0184] A mixture of 5-amino-2-(4-fluorophenyl)-4-phenylimidazole
(1.00 g) and ethyl formate (10 ml) was refluxed for 15 hours. After
cooling, the reaction mixture was concentrated under reduced
pressure and crystallized from diethyl ether to obtain
5-formylamino-2-(4-fluorophenyl)-4-phenylimidazole (1.17 g) as
colorless crystal.
[0185] Melting point: 245 to 247.degree. C.
[0186] MS.cndot.APCI (m/z): 282 (MH+)
Preparation Example 106
[0187] A mixture of
5-methylamino-2-(4-fluorophenyl)-4-phenyl-imidazole (560 mg) in
ethyl formate (20 ml) was refluxed overnight. After cooling, the
reaction mixture was concentrated under reduced pressure and
crystallized from diethyl ether-hexane to obtain
5-formylmethylamino-2-(4-fluorophenyl)-4-phenyl-imidazole (480 mg)
as colorless crystal.
[0188] Melting point: 256 to 258.degree. C.
[0189] MS.cndot.APCI (m/z): 296 (MH+)
Preparation Example 107
[0190] To a solution of
5-formylamino-2-(4-fluorophenyl)-4-phenylimidazole (1.06 g) in
tetrahydrofuran (15 ml) was added dropwise 10M
borane.dimethylsulfide complex (1.90 ml), and the mixture was
stirred under argon atmosphere at room temperature for 2.5 hours.
To the reaction mixture was slowly added 10% hydrochloric acid, and
the mixture was refluxed for one hour. After cooling, the mixture
was neutralized by adding a saturated aqueous sodium hydrogen
carbonate solution, and extracted with ethyl acetate. The organic
layer was washed with water and brine, dried over anhydrous sodium
sulfate and the solvent was removed under reduced pressure. The
resulting residue was purified by silica gel flush column
chromatography (solvent: hexane:ethyl acetate=5:1) to obtain
5-methylamino-2-(4-fluorophenyl)-4-phenylimidazole (702 mg) as
colorless powder. 88 mg of the product was treated with hydrogen
chloride-methanol solution to obtain the hydrochloride salt (84 mg)
as colorless powder.
[0191] Melting point: 253 to 255.degree. C.
[0192] MS.cndot.APCI (m/z): 268 (MH+)
Preparation Example 108
[0193] To a solution of
5-formylmethylamino-2-(4-fluorophenyl)-4-phenylimidazole (200 mg)
in tetrahydrofuran (5 ml) was added dropwise 10M
borane.dimethylsulfide complex (0.34 ml), and the mixture was
stirred under argon atmosphere at room temperature for overnight.
To the reaction mixture was slowly added 10% hydrochloric acid, and
the mixture was refluxed for one hour. After cooling, the mixture
was neutralized by adding a saturated aqueous sodium hydrogen
carbonate solution, and extracted with ethyl acetate. The organic
layer was washed with water and brine, dried over anhydrous sodium
sulfate and the solvent was removed under reduced pressure. The
resulting residue was purified by silica gel flush column
chromatography (solvent: hexane:ethyl acetate=5:1), and then,
treated with hydrogen chloride-methanol solution to obtain
5-dimethylamino-2-(4-fluorophenyl)-4-phenylimidazole hydrochloride
(174 mg) as colorless powder.
[0194] MS.cndot.APCI (m/z): 282 (MH+)
Preparation Example 109
[0195] To a solution of
5-amino-2-(4-fluorophenyl)-4-phenylimidazole (63 mg) and pyridine
(40 mg) in methylene chloride (5 ml) was added methyl
chlorocarbonate (28 mg) under ice-cooling and the mixture was
stirred at room temperature overnight. To the reaction mixture was
added diethyl ether, and the solvent was removed under reduced
pressure. The resulting residue was triturated with diethyl ether
and the powder was collected by filtration. The powder was treated
with hydrogen chloride-methanol solution to obtain
5-methoxycarbonylamino-2-(4-fluorophenyl)-4-phenylimidazole
hydrochloride (67 mg) as colorless powder.
[0196] MS.cndot.APCI (m/z): 312 (MH+)
Preparation Example 110
[0197] To a solution of
5-acetylamino-2-(4-fluorophenyl)-4-phenyl-imidazole (142 mg) in
tetrahydrofuran (7 ml) was added 10M borane.tetrahydrofuran complex
(12 ml, tetrahydrofuran solution), and the mixture was stirred
under argon atmosphere at room temperature for 2 days. To the
reaction mixture was slowly added 10% hydrochloric acid, and the
mixture was stirred at 60.degree. C. for 10 minutes. After cooling,
the mixture was neutralized by adding a saturated aqueous sodium
hydrogen carbonate solution, and extracted with ethyl acetate. The
organic layer was washed with water and brine, dried over anhydrous
sodium sulfate and the solvent was removed under reduced pressure.
The resulting residue was purified by silica gel flush column
chromatography (solvent: hexane:ethyl acetate=1:2), and then,
treated with hydrogen chloride-methanol solution to obtain
5-ethylamino-2-(4-fluorophenyl)-4-phenyl-imidazole hydrochloride
(89 mg) as colorless powder.
[0198] MS.cndot.APCI (m/z): 282 (MH+)
Preparation Example 111
[0199] A mixture of
5-ethylamino-2-(4-fluorophenyl)-4-phenyl-imidazole (145 mg) in
ethyl formate (8 ml) was refluxed for 8 hours. After cooling, the
mixture was concentrated under reduced pressure, and crystallized
from diethyl ether to obtain
5-formylethylamino-2-(4-fluorophenyl)-4-phenylimidazole (136 mg) as
colorless crystal.
[0200] Melting point: 201 to 202.degree. C.
[0201] MS.cndot.APCI (m/z): 310 (MH+)
Preparation Example 112
[0202] A mixture of
2-(5-chlorothiophen-2-yl)-4-(3-pyridyl)imidazole (1.07 g), 35%
formalin aqueous solution (35 ml), potassium carbonate (1.70 g),
isopropanol (30 ml) and N,N-dimethyl-formamide (10 ml) was stirred
at 90.degree. C. for 2 hours. After cooling, water was added to the
mixture and precipitated solid was collected by filtration. The
solid was dissolved in methanol and, after removing insolubles by
filtration, the solvent was removed under reduced pressure. The
resulting residue was triturated with ethyl acetate to obtain
2-(5-chlorothiophen-2-yl)-5-hydroxymethyl-4-(3-pyridyl)imidazole
(519 mg) as colorless powder.
[0203] MS.cndot.APCI (m/z): 292/294 (MH+)
Preparation Examples 113 and 118
[0204] The following compounds shown in Table 10 were prepared in a
manner similar to Preparation example 112 by using corresponding
starting materials.
TABLE-US-00010 TABLE 10 Preparation Chemical Physical constant,
example No. structure Salt etc. 113 ##STR00100## Free material
Crystal Melting point: 225-228.degree. C. MS.cndot.APCI (m/z): 270
(M + H)+ 114 ##STR00101## 3HCl Crystal Melting point:
266-269.degree. C. MS.cndot.APCI (m/z): 267 (M + H)+ 115
##STR00102## Free material Crystal Melting point: 232-234.degree.
C. MS.cndot.APCI (m/z): 269 (M + H)+ 116 ##STR00103## Free material
Powder MS.cndot.APCI (m/z): 277 (M + H)+ 117 ##STR00104## Free
material Crystal Melting point: 240-243.degree. C. MS.cndot.APCI
(m/z): 269 (M + H)+ 118 ##STR00105## Free material Powder
MS.cndot.APCI (m/z): 276 (M + H)+
Preparation Example 119
[0205] To a solution of
2-(5-chlorothiophen-2-yl)-5-hydroxymethyl-4-(3-pyridyl)imidazole
(200 mg) in methylene chloride (5 ml) was added thionyl chloride (5
ml), and the mixture was refluxed for one hour. After cooling, the
reaction mixture was concentrated under reduced pressure to obtain
a crude product of
2-(5-chlorothiophen-2-yl)-5-chloromethyl-4-(3-pyridyl)-imidazole
dihydrochloride (260 mg) as yellowish powder.
Preparation Example 120
[0206] In methanol (10 ml) was dissolved a crude product of
2-(5-chlorothiophen-2-yl)-5-chloromethyl-4-(3-pyridyl)-imidazole
dihydrochloride (260 mg) and the mixture was refluxed for 2 hours.
After cooling, a saturated aqueous sodium hydrogen carbonate
solution was added to the reaction mixture, and the mixture was
extracted with a mixed solution of ethyl acetate-tetrahydrofuran.
The organic layer was washed with brine, dried over anhydrous
magnesium sulfate and the solvent was removed under reduced
pressure. The resulting residue was purified by silica gel column
chromatography (solvent: chloroform: methanol=40:1), and then,
treated with hydrogen chloride-dioxane solution to obtain
2-(5-chlorothiophen-2-yl)-5-methoxymethyl-4-(3-pyridyl)imidazole
dihydrochloride (63 mg) as pale yellowish powder.
[0207] Melting point: 245 to 248.degree. C. (decomposed)
[0208] MS.cndot.APCI (m/z): 306/308 (MH+)
Preparation Examples 121 to 128
[0209] The following compounds shown in Table 11 were prepared in a
manner similar to Preparation example 112 or 120 by using
corresponding starting materials.
TABLE-US-00011 TABLE 11 Physical Preparation Chemical constant,
example No. structure Salt etc. 121 ##STR00106## 1HCl Crystal
Melting point: 204-207.degree. C. MS APCI (m/z): 283 (M + H)+ 122
##STR00107## 1HCl Powder MS.cndot.APCI (m/z): 289 (M + H)+ 123
##STR00108## 1HCl Crystal Melting point: 185-188.degree. C.
MS.cndot.APCI (m/z): 283 (M + H)+ 124 ##STR00109## 1HCl Powder
MS.cndot.APCI (m/z): 290 (M + H)+ 125 ##STR00110## 2HCl Powder
MS.cndot.APCI (m/z): 291 (M + H)+ 126 ##STR00111## 2HCl Powder
MS.cndot.APCI (m/z): 284 (M + H)+ 127 ##STR00112## 3HCl Crystal
Melting point: 251-255.degree. C. MS.cndot.APCI (m/z): 281 (M + H)+
128 ##STR00113## 1HCl Powder MS.cndot.APCI (m/z): 299 (M + H)+
Preparation Example 129
[0210] To a solution of
2-(3-fluorophenyl)-5-hydroxymethyl-4-(3-pyridyl)imidazole (389 mg)
in methylene chloride (10 ml) was added thionyl chloride (10 ml),
and the mixture was refluxed for one hour. After cooling, the
reaction mixture was concentrated under reduced pressure to obtain
a crude product of
2-(3-fluorophenyl)-5-chloromethyl-4-(3-pyridyl)imidazole
dihydrochloride (508 mg) as colorless powder.
Preparation Example 130
[0211] To a suspension of a crude product of
2-(3-fluorophenyl)-5-chloromethyl-4-(3-pyridyl)imidazole
dihydrochloride (268 mg) in tetrahydrofuran (10 ml) were added 15%
aqueous sodium methyl sulfide solution (0.95 ml) and triethylamine
(206 mg), and the mixture was stirred at room temperature for 1.5
hours. Water was added to the reaction mixture, and the reaction
mixture was extracted with ethyl acetate. The organic layer was
washed with brine and dried over anhydrous sodium sulfate, and the
solvent was removed under reduced pressure. The resulting residue
was purified by silica gel column chromatography (solvent:
chloroform:methanol=19:1) to obtain
2-(3-fluorophenyl)-5-methylthiomethyl-4-(3-pyridyl)imidazole (198
mg) as colorless powder.
[0212] MS.cndot.APCI (m/z): 300 (MH+)
Preparation Examples 131 to 134
[0213] The following compounds shown in Table 12 were prepared in a
manner similar to Preparation example 130 by using corresponding
starting materials.
TABLE-US-00012 TABLE 12 Prepara- tion example Chemical Physical
property, No. structure Salt etc. 131 ##STR00114## 1HCl Crystal
Melting point: 218-220.degree. C. MS APCI (m/z): 299 (M + H)+ 132
##STR00115## 1HCl Crystal Melting point: 256-259.degree. C. MS APCI
(m/z): 306 (M + H)+ 133 ##STR00116## Free material Crystal Melting
point: 172-174.degree. C. MS APCI (m/z): 300 (M + H)+ 134
##STR00117## Free material Crystal Melting point: 209-211.degree.
C. MS APCI (m/z): 307 (M + H)+
Preparation Example 135
[0214] To a solution of
2-(3-fluorophenyl)-5-methylthiomethyl-4-(3-pyridyl)imidazole (152
mg) in tetrahydrofuran (10 ml) was added metachloroperbenzoic acid
(97 mg, 70% purity) under ice-cooling, and the mixture was stirred
at room temperature for 5 hours. To the reaction mixture was added
a saturated aqueous sodium hydrogen carbonate solution, and the
mixture was extracted with ethyl acetate. The organic layer was
washed with brine and dried over anhydrous sodium sulfate, and the
solvent was removed under reduced pressure. The resulting residue
was purified by silica gel column chromatography (solvent:
chloroform:methanol=19:1), and then, treated with hydrogen
chloride-dioxane solution to obtain
2-(3-fluorophenyl)-5-methylsulfinylmethyl-4-(3-pyridyl)imidazole
hydrochloride (140 mg) as colorless powder.
[0215] MS.cndot.APCI (m/z): 316 (MH+)
Preparation Examples 136 to 140
[0216] The following compounds shown in Table 13 were prepared in a
manner similar to Preparation example 135 by using corresponding
starting materials.
TABLE-US-00013 TABLE 13 Prepara- tion example Physical constant,
No. Chemical structure Salt etc. 136 ##STR00118## 1HCl Crystal
Melting point: 198-200.degree. C. MS APCI (m/z): 315 (M + H)+ 137
##STR00119## 1HCl Powder MS APCI (m/z): 322 (M + H)+ 138
##STR00120## 2HCl Powder MS APCI (m/z): 316 (M + H)+ 139
##STR00121## 2HCl Powder MS APCI (m/z): 323 (M + H)+ 140
##STR00122## 1HCl Crystal Melting point: 278-280.degree. C. MS APCI
(m/z): 351 (M + H)+
Preparation Example 141
[0217] A mixture of ethyl
2-(5-chlorothiophen-2-yl)-5-(3-pyridyl)-oxazole-4-yl acetate (68
mg), lithium hydroxide (9 mg), ethanol (4 ml) and water (4 ml) was
stirred at room temperature for 2.5 hours. The reaction mixture was
concentrated under reduced pressure, acidified to pH 4 with 10%
hydrochloric acid, and precipitated solid was collected by
filtration. This solid was treated with hydrogen chloride-dioxane
solution to obtain
2-(5-chlorothiophen-2-yl)-5-(3-pyridyl)oxazole-4-yl acetic acid
hydrochloride (50 mg) as pale yellowish powder.
[0218] Melting point: 234 to 238.degree. C. (decomposed)
[0219] MS.cndot.APCI (m/z): 321/323 (MH+)
Preparation Example 142
[0220] The following compounds shown in Table 14 were prepared in a
manner similar to Preparation example 141 by using corresponding
starting materials.
TABLE-US-00014 TABLE 14 Preparation Physical example No. Chemical
structure Salt constant, etc. 142 ##STR00123## 1HCl Powder MS APCI
(m/z): 313 (M - H)
Preparation Examples 143 and 144
[0221] A mixture of
2-(5-chlorothiophen-3-yl)-5-ethyl-4-(3-pyridyl)-imidazole (2.00 g)
in chlorosulfonic acid (15 ml) was stirred at room temperature for
one week. The mixture was slowly added dropwise to 28% aqueous
ammonia (500 ml), and the resulting mixture was stirred for 30
minutes and then concentrated under reduced pressure. The resulting
residue was dissolved in methanol-tetrahydrofuran (5:1), dried over
anhydrous sodium sulfate and the solvent was removed under reduced
pressure. The residue was purified by silica gel flush column
chromatography (solvent: chloroform:methanol=10:1.fwdarw.2.5:1),
and then, by NH silica gel flush column chromatography (solvent:
chloroform:methanol=10:1.fwdarw.4:1) to obtain
2-(5-chloro-2-sulfothiophen-3-yl)-5-ethyl-4-(3-pyridyl)imidazole
and
2-(5-chloro-2-sulfamoylthiophen-3-yl)-5-ethyl-4-(3-pyridyl)imidazole.
Each product was treated with hydrogen chloride-dioxane solution to
obtain
2-(5-chloro-2-sulfothiophen-3-yl)-5-ethyl-4-(3-pyridyl)imidazole
dihydrochloride (741 mg) and
2-(5-chloro-2-sulfamoylthiophen-3-yl)-5-ethyl-4-(3-pyridyl)imidazole
dihydrochloride (105 mg) each as colorless powder.
2-(5-Chloro-2-sulfothiophen-3-yl)-5-ethyl-4-(3-pyridyl)-imidazole
dihydrochloride
Preparation Example 143
[0222] ESI.cndot.MS (m/z): 368 (M-H)
2-(5-Chloro-2-sulfamoylthiophen-3-yl)-5-ethyl-4-(3-pyridyl)
imidazole dihydrochloride
Preparation Example 144
[0223] MS.cndot.APCI (m/z): 369 (MH+)
Preparation Example 145
[0224] To a solution of
2-(2-ethoxycarbonylthiophen-3-yl)-5-ethyl-4-(3-pyridyl)imidazole
(879 mg) in tetrahydrofuran (20 ml) was added lithium aluminum
hydride (204 mg) under ice-cooling, and the mixture was stirred
under argon atmosphere at the same temperature for 1.5 hours. Under
ice-cooling, an aqueous potassium sodium tartarate solution and
ethyl acetate were added to the mixture and the organic layer was
collected. The organic layer was washed with water and brine, dried
over anhydrous magnesium sulfate, and the solvent was removed under
reduced pressure. The resulting residue was purified by silica gel
column chromatography (solvent: chloroform:methanol=19:1), and
then, treated with hydrogen chloride-ethanol solution to obtain
2-(2-hydroxymethylthiophen-3-yl)-5-ethyl-4-(3-pyridyl)imidazole
dihydrochloride (788 mg) as colorless powder.
[0225] MS.cndot.APCI (m/z): 286 (MH+)
Preparation Example 146
[0226] To a solution of ethyl
2-(5-chlorothiophen-2-yl)-4-(3-pyridyl)imidazol-5-yl acetate (122
mg) in tetrahydrofuran (3.5 ml) was added lithium aluminum hydride
(15 mg) under ice-cooling, and the mixture was stirred under
ice-cooling for 2.5 hours. Under ice-cooling, an aqueous sodium
hydroxide solution and ethyl acetate were added to the mixture, and
the organic layer was collected. The organic layer was washed with
water and brine, dried over anhydrous sodium sulfate, and the
solvent was removed under reduced pressure. The resulting residue
was purified by preparative thin-layer chromatography (TLC) (silica
gel; solvent: chloroform:methanol=20:1) to obtain
2-(5-chlorothiophen-2-yl)-5-hydroxyethyl-4-(3-pyridyl)imidazole
(109 mg) as colorless crystalline powder. 27 mg of the product was
treated with hydrogen chloride-dioxane solution to obtain the
dihydrochloride salt (26 mg) as colorless powder.
[0227] Melting point: 179 to 180.degree. C. (free material)
[0228] MS.cndot.APCI (m/z): 306 (MH+) (hydrochloride)
Preparation Example 147
[0229] A mixture of ethyl
4-(4-fluorobenzoylamino)-4-(2-thienyl)-3-ketobutyrate (349 mg), and
phosphorus oxychloride (0.12 ml) in N,N-dimethylformamide (5 ml)
was stirred at room temperature for 2.5 hours. The reaction mixture
was poured into water, neutralized with a saturated aqueous sodium
hydrogen carbonate solution and extracted with ethyl acetate. The
organic layer was washed with water and brine, dried over anhydrous
sodium sulfate and the solvent was removed under reduced pressure.
The resulting residue was purified by silica gel flush column
chromatography (solvent: hexane:ethyl acetate=20:1) to obtain ethyl
2-(4-fluorophenyl)-4-(2-thienyl)oxazol-5-yl acetate (95 mg) as pale
yellowish powder.
[0230] MS.cndot.APCI (m/z): 332 (MH+)
Preparation Example 148
[0231] To a solution of ethyl
2-(4-fluorophenyl)-4-(2-thienyl)-oxazol-5-yl acetate (94 mg) in
tetrahydrofuran (3 ml) and ethanol (3 ml) was added 1N aqueous
sodium hydroxide solution (1 ml) and the mixture was stirred at
room temperature for one hour. To the reaction mixture was added
10% hydrochloric acid, and the mixture was extracted with ethyl
acetate. The organic layer was washed with brine, dried over
anhydrous sodium sulfate and the solvent was removed under reduced
pressure. The resulting residue was dissolved in methanol (5 ml),
0.5M sodium methoxide (556 .mu.l, methanol solution) was added to
the solution and the solvent was removed under reduced pressure to
obtain sodium 2-(4-fluorophenyl)-4-(2-thienyl)oxazol-5-yl acetate
(90 mg) as pale brownish powder.
[0232] ESI.cndot.MS (m/z): 302 (M-H)
Preparation Example 149
[0233] To a solution of ethyl 2-(4-fluorophenyl)oxazol-4-yl acetate
(11.10 g) in chloroform (110 ml) was added bromine (2.47 ml) at
room temperature and the mixture was stirred at room temperature
for one hour. To the reaction mixture was added a saturated aqueous
sodium hydrogen carbonate solution and a saturated aqueous sodium
thiosulfate solution, and the organic layer was collected. The
organic layer was washed with brine and dried over anhydrous sodium
sulfate, and the solvent was removed under reduced pressure. The
resulting residue was crystallized from hexane-diethyl ether to
obtain ethyl 5-bromo-2-(4-fluorophenyl)oxazol-4-yl acetate (7.47 g)
as colorless crystal. Further, the filtrate was purified by silica
gel flush column chromatography (solvent: n-hexane:ethyl
acetate=10:1) to obtain ethyl
5-bromo-2-(4-fluorophenyl)-oxazol-4-yl acetate (3.57 g) as pale
yellowish crystal.
[0234] Melting point: 84 to 85.degree. C.
[0235] MS.cndot.APCI (m/z): 323/330 (MH+)
Preparation Example 150
[0236] A mixture of ethyl 2-(4-fluorophenyl)oxazol-4-yl acetate
(249 mg), iodine (127 mg) and [bis(trifluoroacetoxy)]iodo]benzene
(244 mg) in chloroform (3 ml) was stirred at room temperature for 4
hours. To the reaction mixture were added a saturated aqueous
sodium hydrogen carbonate solution and a saturated aqueous sodium
thiosulfate solution, and the organic layer was collected. The
organic layer was washed with brine and dried over anhydrous sodium
sulfate, and the solvent was removed under reduced pressure. The
resulting residue was purified by silica gel flush column
chromatography (solvent: n-hexane:ethyl acetate=8:1) to obtain
ethyl 2-(4-fluorophenyl)-5-iodoxazol-4-yl acetate (300 mg) as
colorless crystal.
[0237] Melting point: 120 to 122.degree. C.
[0238] MS.cndot.APCI (m/z): 376 (MH+)
Preparation Example 151
[0239] A mixture of ethyl 5-bromo-2-(4-fluorophenyl)oxazol-4-yl
acetate (328 mg), 5-chlorothiophen-2-boric acid (244 mg),
bis(triphenylphosphine)palladium (II) dichloride (35 mg) in 2M
aqueous sodium carbonate solution (1.5 ml) and dimethoxyethane (5
ml) was refluxed for one hour. After cooling, to the reaction
mixture were added water and ethyl acetate, the organic layer was
collected, dried over anhydrous sodium sulfate, and the solvent was
removed under reduced pressure. The resulting residue was purified
by silica gel flush column chromatography (solvent: n-hexane:ethyl
acetate=6:1) to obtain ethyl
5-(5-chlorothiophen-2-yl)-2-(4-fluorophenyl)oxazol-4-yl acetate
(181 mg) as pale yellowish crystal.
[0240] Melting point: 129 to 130.degree. C.
[0241] MS.cndot.APCI (m/z): 366/368 (MH+)
Preparation Example 152
[0242] To a solution of ethyl
5-(5-chlorothiophen-2-yl)-2-(4-fluorophenyl)oxazol-4-yl acetate
(115 mg) in methanol (5 ml) was added 4N aqueous sodium hydroxide
solution (1 ml), and the mixture was refluxed for 30 minutes. After
cooling, ethyl acetate and 10% hydrochloric acid were added to the
reaction mixture, and the organic layer was collected. The organic
layer was washed with brine, dried over anhydrous sodium sulfate,
and the solvent was removed under reduced pressure. The resulting
residue was dissolved in methanol (5 ml), 0.5M sodium methoxide
(605 .mu.l, methanol solution) was added to the solution and the
solvent was removed under reduced pressure. The resulting residue
was triturated with acetone to obtain
5-(5-chlorothiophen-2-yl)-2-(4-fluorophenyl)oxazol-4-yl acetic acid
sodium salt (100 mg) as pale yellowish powder.
[0243] ESI.cndot.MS (m/z): 336 (M-H)
Preparation Examples 153 to 166
[0244] The following compounds shown in Table 15 were prepared in a
manner similar to Preparation example 63, 151 or 152 by using
corresponding starting materials.
TABLE-US-00015 TABLE 15 Preparation example No. Chemical structure
Salt Physical property, etc. 153 ##STR00124## Na Crystal Melting
point: >300.degree. C. MS APCI (m/z): 396 (M - Na) 154
##STR00125## Free material Crystal Melting point: 105-107.degree.
C. MS APCI (m/z): 344 (M + H)+ 155 ##STR00126## Na Powder ESI MS
(m/z): 314 (M - Na) 156 ##STR00127## Na Powder ESI MS (m/z): 298 (M
- Na) 157 ##STR00128## Free material Powder MS APCI (m/z): 382 (M +
H)+ 158 ##STR00129## Na Powder MS APCI (m/z): 352 (M - Na) 159
##STR00130## Free material Powder MS APCI (m/z): 386 (M + H)+ 160
##STR00131## Na Powder MS APCI (m/z): 356 (M - Na) 161 ##STR00132##
Free material Crystal Melting point: 88-89.degree. C. MS APCI
(m/z): 344 (M + H)+ 162 ##STR00133## Na Powder MS APCI (m/z): 314
(M - Na) 163 ##STR00134## Free material Crystal Melting point:
138-139.degree. C. MS APCI (m/z): 346 (M + H)+ 164 ##STR00135## Na
Powder MS APCI (m/z): 316 (M - Na) 165 ##STR00136## Free material
Powder MS APCI (m/z): 362 (M + H)+ 166 ##STR00137## Na Powder MS
APCI (m/z): 332 (M - Na)
Preparation Examples 167 to 202
[0245] The following compounds shown in Table 16 were prepared in a
manner similar to one of the above-mentioned Preparation examples,
or conventionally known preparation processes as described in
Japanese Provisional Patent Publications No. 5832/1972, No.
29771/1973 and the like.
TABLE-US-00016 TABLE 16 Physical Preparation property, example No.
Chemical structure Salt etc. 167 ##STR00138## Free material MS EI
(m/z): 268 (M+) 168 ##STR00139## Free material MS EI (m/z): 258
(M+) 169 ##STR00140## Free material MS EI (m/z): 286 (M+) 170
##STR00141## Free material 171 ##STR00142## Free material MS EI
(m/z): 272 (M+) 172 ##STR00143## Free material MS EI (m/z): 286
(M+) 173 ##STR00144## Free material MS EI (m/z): 326 (M+) 174
##STR00145## Free material MS EI (m/z): 252 (M+) 175 ##STR00146##
Free material MS EI (m/z): 320 (M+) 176 ##STR00147## Free material
177 ##STR00148## Free material MS EI (m/z): 332/334/336 (M+) 178
##STR00149## 2HCl Powder MS APCI (m/z): 254 (M + H)+ 179
##STR00150## 1HCl Powder MS APCI (m/z): 296 (M + H)+ 180
##STR00151## 1HCl Powder MS APCI (m/z): 263 (M + H)+ 181
##STR00152## 1HCl Powder MS APCI (m/z): 321 (M + H)+ 182
##STR00153## 1HCl Powder MS APCI (m/z): 285 (M + H)+ 183
##STR00154## 1HCl Powder MS APCI (m/z): 329 (M + H)+ 184
##STR00155## 1HCl Powder MS APCI (m/z): 343 (M + H)+ 185
##STR00156## 1HCl Powder MS APCI (m/z): 345 (M + H)+ 186
##STR00157## 1HCl Powder MS APCI (m/z): 345 (M + H)+ 187
##STR00158## 2HCl Powder MS APCI (m/z): 254 (M + H)+ 188
##STR00159## Free material 189 ##STR00160## Free material Crystal
Melting point: 208-209.degree. C. 190 ##STR00161## Free material
Powder MS EI (m/z): 285 (M+) 191 ##STR00162## Free material Crystal
Melting point: 109-111.degree. C. MS APCI (m/z): 332 (M + H)+ 192
##STR00163## Free material Crystal Melting point: 214-215.degree.
C. 193 ##STR00164## Free material 194 ##STR00165## Free material
Powder MS EI (m/z): 319/321 (M+) 195 ##STR00166## Free material MS
EI (m/z): 334/336 (M+) 196 ##STR00167## Free material Crystal
Melting point: 125-127.degree. C. MS APCI (m/z): 328 (M + H)+ 197
##STR00168## Na Powder MS ESI (m/z): 302 (M - Na) 198 ##STR00169##
Na Powder MS ESI (m/z): 298 (M - Na) 199 ##STR00170## Na Powder MS
ESI (m/z): 314 (M - Na) 200 ##STR00171## Free material Crystal
Melting point: 198-199.degree. C. 201 ##STR00172## Na Powder MS
APCI (m/z): 302 (M - Na) 202 ##STR00173## Free material Crystal
Melting point: 123-125.degree. C. MS APCI (m/z): 327 (M + H)+
Preparation Example 203
[0246] A mixture of ethyl
3-amino-4-(5-chlorothiophen-2-yl)-4-oxobutyrate hydrochloride (300
mg), benzo[b]furan-5-carboxylic acid (245 mg),
3-ethyl-1-(3-dimethylamino-propyl)carbodiimide hydrochloride (289
mg), 1-hydroxy-benzotriazole (204 mg) and triethylamine (0.35 ml)
in methylene chloride (4.5 ml) was stirred at room temperature for
overnight. A saturated aqueous sodium hydrogen carbonate solution
was added to the reaction mixture, and the mixture was extracted
with chloroform. The organic layer was dried over anhydrous sodium
sulfate and the solvent was removed under reduced pressure. The
resulting residue was purified by silica gel column chromatography
(solvent: hexane:ethyl acetate=4:1), and then, triturated with
diisopropyl ether to obtain ethyl
3-[(5-benzo[b]furoyl)amino-4-(5-chlorothiophen-2-yl)-4-oxo-butyrate
(352 mg) as colorless powder.
[0247] To a solution of the resulting ethyl
3-[(5-benzo[b]furoyl)-amino-4-(5-chlorothiophen-2-yl)-4-oxobutyrate
(331 mg) in N,N-dimethylformamide (4.08 ml) was added phosphoryl
chloride (0.23 ml) under ice-cooling, and the mixture was stirred
at 60.degree. C. overnight. To the reaction mixture was added a
saturated aqueous sodium hydrogen carbonate solution, the mixture
was extracted with ethyl acetate, dried over anhydrous sodium
sulfate and the solvent was removed under reduced pressure. The
resulting residue was purified by silica gel column chromatography
(solvent: chloroform:ethyl acetate=20:1), and then, triturated with
diisopropyl ether to obtain ethyl
2-(5-benzo[b]furyl)-5-(5-chlorothiophen-2-yl)oxazol-4-yl acetate
(257 mg) as colorless powder.
[0248] MS.cndot.APCI (m/z): 388/390 (MH+)
Preparation Examples 204 to 226
[0249] The following compounds shown in Table 17 were prepared in a
manner similar to Preparation example 203 by using corresponding
starting materials.
TABLE-US-00017 TABLE 17 Preparation Physical property, example No.
Chemical structure Salt etc. 204 ##STR00174## Free material Powder
MS APCI (m/z): 344 (M + H)+ 205 ##STR00175## Free material Powder
MS APCI (m/z): 356 (M + H)+ 206 ##STR00176## Free material Powder
MS APCI (m/z): 354 (M + H)+ 207 ##STR00177## Free material Powder
MS APCI (m/z): 370 (M + H)+ 208 ##STR00178## Free material Powder
MS APCI (m/z): 365 (M + H)+ 209 ##STR00179## Free material Powder
MS APCI (m/z): 354 (M + H)+ 210 ##STR00180## Free material Powder
MS APCI (m/z): 334 (M + H)+ 211 ##STR00181## Free material Powder
MS APCI (m/z): 382/384 (M + H)+ 212 ##STR00182## Free material
Powder MS APCI (m/z): 355/357 (M + H)+ 213 ##STR00183## Free
material Powder MS APCI (m/z): 348 (M + H)+ 214 ##STR00184## Free
material Powder MS APCI (m/z): 412 (M + H)+ 215 ##STR00185## Free
material Powder MS APCI (m/z): 404/406 (M + H)+ 216 ##STR00186##
Free material Powder MS APCI (m/z): 436/438 (M + H)+ 217
##STR00187## Free material Powder MS APCI (m/z): 436/438 (M + H)+
218 ##STR00188## Free material Powder MS APCI (m/z): 390/392 (M +
H)+ 219 ##STR00189## Free material Powder MS APCI (m/z): 406/408 (M
+ H)+ 220 ##STR00190## Free material Powder MS APCI (m/z): 399/401
(M + H)+ 221 ##STR00191## Free material Powder MS APCI (m/z):
353/355 (M + H)+ 222 ##STR00192## Free material Powder MS APCI
(m/z): 383/385 (M + H)+ 223 ##STR00193## Free material Powder MS
APCI (m/z): 349/351 (M + H)+ 224 ##STR00194## Free material Powder
MS APCI (m/z): 372 (M + H)+ 225 ##STR00195## Free material Powder
MS APCI (m/z): 394 (M + H)+ 226 ##STR00196## Free material Powder
MS APCI (m/z): 392/394 (M + H)+
Preparation Example 227
[0250] To a solution of
4-[(5-benzo[b]furoyl)aminoacetyl]-2-chlorothiophene (543 mg) in
N,N-dimethylformamide (10 ml) was added sodium hydride (71.3 mg,
60% mineral oil) under ice-cooling, and the mixture was stirred at
room temperature for 20 minutes. After ice-cooling, ethyl
bromoacetate (0.21 ml) was added dropwise to the mixture, and the
resulting mixture was stirred at room temperature for 40 minutes.
After cooling, 5% aqueous citric acid solution was added to the
reaction mixture and the mixture was extracted with ethyl acetate.
The organic layer was washed with water and brine, dried over
anhydrous sodium sulfate and the solvent was removed under reduced
pressure to obtain a crude product of ethyl
3-[(5-benzo[b]furoyl)amino]-4-(5-chlorothiophen-3-yl)-4-oxobutyrate
(896 mg).
[0251] To a solution of the resulting crude product of ethyl
3-[(5-benzo[b]furoyl)amino]-4-(5-chlorothiophen-3-yl)-4-oxobutyrate
(896 mg) in N,N-dimethylformamide (7 ml) was added phosphoryl
chloride (0.48 ml) at room temperature, and the mixture was stirred
at the same temperature overnight. To the reaction mixture was
added water, the mixture was extracted with ethyl acetate, dried
over anhydrous sodium sulfate and the solvent was removed under
reduced pressure. The resulting residue was purified by silica gel
column chromatography (solvent: hexane:acetone=7:1), and then,
triturated with diethyl ether to obtain ethyl
2-(5-benzo[b]furyl)-5-(5-chlorothiophen-3-yl)oxazol-4-ylacetate
(349 mg) as colorless powder.
[0252] MS.cndot.APCI (m/z): 388 (MH+)
Preparation Examples 228 to 232
[0253] The following compounds shown in Table 18 were prepared in a
manner similar to Preparation example 227 by using corresponding
starting materials.
TABLE-US-00018 TABLE 18 Preparation Physical example No. Chemical
structure Salt constant, etc. 228 ##STR00197## Free material Powder
MS APCI (m/z): 366 (M + H)+ 229 ##STR00198## Free material Powder
MS APCI (m/z): 366 (M + H)+ 230 ##STR00199## Free material Powder
MS APCI (m/z): 388 (M + H)+ 231 ##STR00200## Free material 232
##STR00201## Free material Powder MS APCI (m/z): 349/351 (M +
H)+
Preparation Examples 233 to 293
[0254] The following compounds shown in Table 19 were prepared in a
manner similar to Preparation example 148 or 152 by using
corresponding starting materials.
TABLE-US-00019 TABLE 19 Preparation Physical property, example No.
Chemical structure Salt etc. 233 ##STR00202## Na Powder ESI MS
(m/z): 346 (M - Na) 234 ##STR00203## Na Powder ESI MS (m/z): 346 (M
- Na) 235 ##STR00204## Na Powder ESI MS (m/z): 314 (M - Na) 236
##STR00205## Na Powder ESI MS (m/z): 314 (M - Na) 237 ##STR00206##
Na Powder ESI MS (m/z): 312 (M - Na) 238 ##STR00207## Na Powder ESI
MS (m/z): 389 (M - Na) 239 ##STR00208## Na Powder ESI MS (m/z): 347
(M - Na) 240 ##STR00209## Na Powder ESI MS (m/z): 364 (M - Na) 241
##STR00210## Na Powder ESI MS (m/z): 330 (M - Na) 242 ##STR00211##
Na Powder ESI MS (m/z): 346 (M - Na) 243 ##STR00212## Na Powder ESI
MS (m/z): 330 (M - Na) 244 ##STR00213## Na Powder ESI MS (m/z): 364
(M - Na) 245 ##STR00214## Na Powder ESI MS (m/z): 396 (M - Na) 246
##STR00215## Na Powder ESI MS (m/z): 344 (M - Na) 247 ##STR00216##
Na Powder ESI MS (m/z): 326 (M - Na) 248 ##STR00217## Na Powder ESI
MS (m/z): 338 (M - Na) 249 ##STR00218## Na Powder ESI MS (m/z): 349
(M - Na) 250 ##STR00219## Na Powder ESI MS (m/z): 344 (M - Na) 251
##STR00220## Na Powder ESI MS (m/z): 388 (M - Na) 252 ##STR00221##
Na Powder ESI MS (m/z) 322 (M - Na) 253 ##STR00222## Na Powder ESI
MS (m/z): 348 (M - Na) 254 ##STR00223## Na Powder ESI MS (m/z): 336
(M - Na) 255 ##STR00224## Na Powder ESI MS (m/z): 324 (M - Na) 256
##STR00225## Na Powder ESI MS (m/z): 382 (M - Na) 257 ##STR00226##
Na Powder ESI MS (m/z): 350 (M - Na) 258 ##STR00227## Na Powder ESI
MS (m/z): 312 (M - Na) 259 ##STR00228## Na Powder ESI MS (m/z): 328
(M - Na) 260 ##STR00229## Na Powder ESI MS (m/z): 362/364 (M - Na)
261 ##STR00230## Na Powder ESI MS (m/z): 328 (M - Na) 262
##STR00231## Na Powder ESI MS (m/z): 292 (M - Na) 263 ##STR00232##
Na Powder ESI MS (m/z): 314 (M - Na) 264 ##STR00233## Na Powder ESI
MS (m/z): 286 (M - Na) 265 ##STR00234## Na Powder ESI MS (m/z): 304
(M - Na) 266 ##STR00235## Na Powder ESI MS (m/z): 324 (M - Na) 267
##STR00236## Na Powder ESI MS (m/z): 340 (M - Na) 268 ##STR00237##
Na Powder ESI MS (m/z): 304 (M - Na) 269 ##STR00238## Na Powder ESI
MS (m/z): 324 (M - Na) 270 ##STR00239## Na Powder ESI MS (m/z): 286
(M - Na) 271 ##STR00240## Na Powder ESI MS (m/z): 374/376 (M - Na)
272 ##STR00241## Na Powder ESI MS (m/z): 358/360 (M - Na) 273
##STR00242## Na Powder ESI MS (m/z): 360 (M - Na) 274 ##STR00243##
Na Powder ESI MS (m/z): 325 (M - Na) 275 ##STR00244## Na Powder ESI
MS (m/z): 352/354 (M - Na) 276 ##STR00245## Na Powder ESI MS (m/z):
335 (M - Na) 277 ##STR00246## Na Powder ESI MS (m/z): 300 (M - Na)
278 ##STR00247## Na Powder ESI MS (m/z): 323/325 (M - Na) 279
##STR00248## Na Powder ESI MS (m/z): 318 (M - Na) 280 ##STR00249##
Na Powder ESI MS (m/z): 382 (M - Na) 281 ##STR00250## Na Powder ESI
MS (m/z): 364 (M - Na) 282 ##STR00251## Na Powder ESI MS (m/z):
360/362 (M - Na) 283 ##STR00252## Na Powder ESI MS (m/z): 376/378
(M - Na) 284 ##STR00253## Na Powder ESI MS (m/z): 369/371 (M - Na)
285 ##STR00254## Na Powder ESI MS (m/z): 336 (M - Na) 286
##STR00255## Na Powder ESI MS (m/z): 336/338 (M - Na) 287
##STR00256## Na Powder ESI MS (m/z): 358 (M - Na) 288 ##STR00257##
Na Powder ESI MS (m/z): 358 (M - Na) 289 ##STR00258## Na Powder ESI
MS (m/z): 364/366 (M - Na) 290 ##STR00259## Na Powder ESI MS (m/z):
364/366 (M - Na) 291 ##STR00260## Na Powder ESI MS (m/z): 326 (M -
Na) 292 ##STR00261## Na Powder ESI MS (m/z): 384 (M - Na) 293
##STR00262## Na Powder ESI MS (m/z): 342 (M - Na)
Preparation Examples 294 and 295
[0255] The following compounds shown in Table 20 were prepared in a
manner similar to Preparation example 149 by using corresponding
starting materials.
TABLE-US-00020 TABLE 20 Prepara- tion example Physical No. Chemical
structure Salt property, etc. 294 ##STR00263## Free ma- terial
Powder MS APCI (m/z): 340/342 (M + H)+ 295 ##STR00264## Free ma-
terial Crystal Melting point: 120-122.degree. C. MS APCI (m/z): 376
(MH)+
Preparation Example 296
[0256] A mixture of ethyl 5-bromo-2-(4-fluorophenyl)oxazol-4-yl
acetate (164 mg), phenylboric acid (91 mg) and
bis(triphenylphosphine) palladium (II) chloride (18 mg) in 2M
aqueous sodium carbonate solution (0.75 ml) and dimethoxyethane (3
ml) was stirred under argon atmosphere at 100.degree. C. for one
hour. After cooling, to the reaction mixture were added water and
ethyl acetate, the organic layer was collected, washed with brine
and dried over anhydrous sodium sulfate, and the solvent was
removed under reduced pressure. The resulting residue was purified
by silica gel column chromatography (solvent: hexane:ethyl
acetate=6:1) to obtain ethyl
2-(4-fluoro-phenyl)-5-phenyloxazol-4-yl acetate (144 mg) as
colorless powder.
[0257] Melting point: 118 to 120.degree. C.
[0258] MS.cndot.APCI (m/z): 326 (MH+)
Preparation Examples 297 to 320
[0259] The following compounds shown in Table 21 were prepared in a
manner similar to Preparation example 296 by using corresponding
starting materials.
TABLE-US-00021 TABLE 21 Preparation Physical example no. Chemical
structure Salt constant, etc. 297 ##STR00265## Free material Powder
MS APCI (m/z): 344 (M + H)+ 298 ##STR00266## Free material Powder
MS APCI (m/z): 344 (M + H)+ 299 ##STR00267## Free material Powder
MS APCI (m/z): 419 (M + H)+ 300 ##STR00268## Free material Powder
MS APCI (m/z): 377 (M + H)+ 301 ##STR00269## Free material Powder
MS APCI (m/z): 432 (M + H)+ 302 ##STR00270## Free material Powder
MS APCI (m/z): 342 (M + H)+ 303 ##STR00271## Free material Powder
MS APCI (m/z): 376 (M + H)+ 304 ##STR00272## Free material Powder
MS APCI (m/z): 360 (M + H)+ 305 ##STR00273## Free material Powder
MS APCI (m/z): 394 (M + H)+ 306 ##STR00274## Free material Powder
MS APCI (m/z): 394/396 (M + H)+ 307 ##STR00275## Free material
Powder MS APCI (m/z): 360/362 (M + H)+ 308 ##STR00276## Free
material Powder MS APCI (m/z): 374 (M + H)+ 309 ##STR00277## Free
material Powder MS APCI (m/z): 356 (M + H)+ 310 ##STR00278## Free
material Powder MS APCI (m/z): 368 (M + H)+ 311 ##STR00279## Free
material Powder MS APCI (m/z): 379 (M + H)+ 312 ##STR00280## Free
material Powder MS APCI (m/z): 366 (M + H)+ 313 ##STR00281## Free
material Powder MS APCI (m/z): 374 (M + H)+ 314 ##STR00282## Free
material Powder MS APCI (m/z): 418 (M + H)+ 315 ##STR00283## Free
material Powder MS APCI (m/z): 378 (M + H)+ 316 ##STR00284## Free
material Powder MS APCI (m/z): 362 (M + H)+ 317 ##STR00285## Free
material Powder MS APCI (m/z): 416 (M + H)+ 318 ##STR00286## Free
material Powder MS APCI (m/z): 468 (M + H)+ 319 ##STR00287## Free
material Powder MS APCI (m/z): 374 (M + H)+ 320 ##STR00288## Free
material Powder MS APCI (m/z): 374 (M + H)+
Preparation Example 321
[0260] To a suspension of ethyl
2-(4-fluorophenyl)-5-(2-thienyl)-oxazol-4-yl acetate (166 mg) in
chloroform (1.5 ml) and acetic acid (1.5 ml) was added
N-bromosuccinimide (94 mg), and the mixture was stirred at room
temperature overnight. To the reaction mixture were added a
saturated aqueous sodium hydrogen carbonate solution and ethyl
acetate, and the organic layer was collected. The organic layer was
washed with water and brine, dried over anhydrous sodium sulfate,
and the solvent was removed under reduced pressure. The resulting
residue was crystallized from diethyl ether-n-hexane to obtain
ethyl 2-(4-fluorophenyl)-5-(5-bromothiophen-2-yl)oxazol-4-yl
acetate (147 mg).
[0261] MS.cndot.APCI (m/z): 410/412 (MH+)
Preparation Example 322
[0262] The following compound shown in Table 22 was prepared in a
manner similar to Preparation example 321 by using corresponding
starting materials.
TABLE-US-00022 TABLE 22 Preparation Physical example No. Chemical
structure Salt constant, etc. 322 ##STR00289## Free material Powder
MS APCI (m/z): 380/382 (M + H)+
Preparation Example 323
[0263] A mixed solution of ethyl
2-(4-fluorophenyl)-5-[3-(2-methylpropyloxy)-4-methoxymethoxyphenyl]oxazol-
-4-yl acetate (300 mg), 4N hydrogen chloride-dioxane solution (5
ml) and ethanol (5 ml) was stirred at room temperature overnight.
After the solvent was removed under reduced pressure, the residue
was triturated with diethyl ether and washed with n-hexane to
obtain ethyl
2-(4-fluorophenyl)-5-[3-(2-methylpropyloxy)-4-hydroxyphenyl]oxazol-4-yl
acetate (269 mg).
[0264] MS.cndot.APCI (m/z): 414 (MH+)
Preparation Example 324
[0265] The following compound shown in Table 23 was prepared in a
manner similar to Preparation example 323 by using corresponding
starting materials.
TABLE-US-00023 TABLE 23 Preparation Physical example No. Chemical
structure Salt constant, etc. 324 ##STR00290## Free material Powder
MS.cndot.APCI (m/z): 372 (M + H)+
Preparation Example 325
[0266] To a mixed solution of ethyl
2-(4-fluorophenyl)-5-(5-formyl-4-methylthiophen-2-yl)oxazol-4-yl
acetate (175 mg) in ethanol (5 ml) and tetrahydrofuran (5 ml) was
added sodium borohydride (54 mg), and the mixture was stirred at
room temperature for 30 minutes. To the reaction mixture were added
water and ethyl acetate, the organic layer was collected, washed
with brine and dried over anhydrous magnesium sulfate, and the
solvent was removed under reduced pressure. The resulting residue
was purified by silica gel column chromatography (solvent:
hexane:ethyl acetate=2:1) to obtain ethyl
2-(4-fluorophenyl)-5-(5-hydroxymethyl-4-methylthiophen-2-yl)oxazol-4-yl
acetate (125 mg) as pale yellowish powder.
[0267] MS.cndot.APCI (m/z): 376 (MH+)
Preparation Example 326
[0268] The following compound shown in Table 24 was prepared in a
manner similar to Preparation example 325 by using corresponding
starting materials.
TABLE-US-00024 TABLE 24 Preparation Physical example No. Chemical
structure Salt constant, etc. 326 ##STR00291## Free material Powder
MS.cndot.APCI (m/z): 376 (M + H)+
Preparation Example 327
[0269] To a solution of ethyl
5-(3-benzyloxyphenyl)-2-(4-fluorophenyl)oxazol-4-ylacetate (349 mg)
in methanol (20 ml) was added 10% palladium-carbon (350 mg), and
the mixture was stirred under hydrogen atmosphere at room
temperature for 2 hours. After the reaction, palladium-carbon was
removed by filtration, the residue was washed with methanol and the
filtrate was concentrated under reduced pressure. The resulting
residue was crystallized from diisopropyl ether to obtain ethyl
2-(4-fluorophenyl)-5-(3-hydroxyphenyl)oxazol-4-ylacetate (195 mg)
as colorless crystal.
[0270] Melting point: 175 to 177.degree. C.
[0271] MS.cndot.APCI (m/z): 342 (MH+)
Preparation Example 328
[0272] To a solution of ethyl
2-(2-(4-fluorophenyl)-5-(3-thienyl)-oxazol-4-yl-2-methylpropionate
(54 mg) in methylene chloride (3 ml) was added boron tribromide
(0.45 ml, 1.0M methylene chloride solution) under ice-cooling, and
the mixture was allowed to warm to room temperature. To the
mixture, another portion of boron tribromide (1.05 ml, 1.0M
methylene chloride solution) was added to the mixture, and the
resulting mixture was stirred at room temperature for 18 hours. To
the reaction mixture were added water and ethyl acetate, the
organic layer was collected, washed with brine and dried over
anhydrous sodium sulfate, and the solvent was removed under reduced
pressure. The resulting residue was purified by silica gel column
chromatography (solvent: chloroform:methanol=15:1) to obtain
2-[(2-(4-fluorophenyl)-5-(3-thienyl)oxazol-4-yl]-2-methylpropionic
acid (32 mg). The product was dissolved in methanol, sodium
methoxide (0.19 ml, 0.5M methanol solution) was added to the
solution and after the mixture was stirred for 10 minutes, the
solvent was removed under reduced pressure. The resulting residue
was triturated with acetone to obtain sodium
2-[2-(4-fluorophenyl)-5-(3-thienyl)oxazol-4-yl]-2-methyl-propionat-
e (30 mg) as pale brownish powder.
[0273] MS.cndot.ESI (m/z): 330 (M-Na)
Preparation Example 329
[0274] To a solution of ethyl
2-(4-fluorophenyl)-5-(3-thienyl)-oxazol-4-yl acetate (130 mg) in
N,N-dimethylformamide (5 ml) was added sodium hydride (47 mg, 60%
mineral oil) under ice-cooling, and the mixture was stirred at room
temperature under argon atmosphere for 20 minutes. To the mixture
was added methyl iodide (0.06 ml) in an ice bath, and the resulting
mixture was stirred at room temperature for 14 hours. To the
reaction mixture were added a saturated aqueous ammonium chloride
solution and ethyl acetate, the organic layer was collected. The
organic layer was washed with water and brine, dried over anhydrous
sodium sulfate, and the solvent was removed under reduced pressure.
The resulting residue was purified by silica gel column
chromatography (solvent: n-hexane:diisopropyl ether=5:1) to obtain
ethyl
2-[2-(4-fluorophenyl)-5-(3-thienyl)oxazol-4-yl]-2-methylpropionate
(62 mg) as colorless oil.
[0275] MS.cndot.APCI (m/z): 360 (MH+)
Preparation Example 330
[0276] A solution of ethyl
2-(6-chloropyridin-3-yl)-5-(5-chlorothiophen-2-yl)oxazol-4-yl
acetate (150 mg) in 50% aqueous dimethylamine solution (656 mg) and
ethanol (3 ml) was refluxed for 16 hours. After cooling, water and
ethyl acetate were added to the reaction mixture, and the organic
layer was collected, dried over anhydrous sodium sulfate, and the
solvent was removed under reduced pressure. The resulting residue
was purified by silica gel column chromatography (solvent:
chloroform:ethyl acetate=7:1) to obtain ethyl
2-(6-dimethylaminopyridin-3-yl)-5-(5-chlorothiophen-2-yl)oxazol-4-yl
acetate (54 mg) as pale yellowish solid.
[0277] MS.cndot.APCI (m/z): 392/394 (MH+)
Preparation Examples 331 and 332
[0278] The following compounds shown in Table 25 were prepared in a
manner similar to Preparation example 330 by using corresponding
starting materials.
TABLE-US-00025 TABLE 25 Preparation Physical example constant, No.
Chemical structure Salt etc. 331 ##STR00292## Free material Powder
MS.cndot.APCI (m/z): 358 (M + H)+ 332 ##STR00293## Free material
Powder MS.cndot.APCI (m/z): 358 (M + H)+
Preparation Example 333
[0279] A mixture of methyl
3-(5-benzo[b]furoylamino)-4-(3-thienyl)-4-oxobutyrate (240 mg) and
phosphorus oxychloride (0.19 ml) in N,N-dimethylformamide (4.8 ml)
was stirred at room temperature for 2 hours. The reaction mixture
was poured into water, neutralized by a saturated aqueous sodium
hydrogen carbonate solution and extracted with ethyl acetate. The
organic layer was washed with water and brine, dried over anhydrous
sodium sulfate and the solvent was removed under reduced pressure.
The resulting residue was purified by silica gel column
chromatography (solvent: hexane:ethyl acetate=20:1) to obtain
methyl 2-(5-benzo[b]furyl)-5-(3-thienyl)oxazole-4-yl acetate (121
mg) as colorless powder.
[0280] MS.cndot.APCI (m/z): 340 (MH+)
Preparation Examples 334 to 336
[0281] The following compounds shown in Table 26 were prepared in a
manner similar to one of the above-mentioned Preparation examples,
or conventionally known preparation processes as described in U.S.
Pat. No. 3,470,195 and the like.
TABLE-US-00026 TABLE 26 Preparation Physical example No. Chemical
structure Salt constant, etc. 334 ##STR00294## Free material 335
##STR00295## Free material 336 ##STR00296## Free material Powder
MS.cndot.APCI (m/z): 250 (M + H)+
Preparation Example 337
[0282] To a solution of 2-[(4-fluorobenzoylamino)acetyl]thiophene
(527 mg) in N,N-dimethylformamide (10 ml) was added sodium hydride
(88 mg, 60% mineral oil) under ice-cooling, and the mixture was
stirred under argon atmosphere at room temperature for one hour.
After ice-cooling, acrylonitrile (127 ml) was added to the mixture
and the mixture was stirred at room temperature for 3 hours. After
addition of ice-water, the mixture was extracted with ethyl
acetate. The organic layer was washed with water and brine, dried
over anhydrous sodium sulfate and the solvent was removed under
reduced pressure. The resulting residue was dissolved in
N,N-dimethylformamide (10 ml), and phosphoryl chloride (240 .mu.l)
was added to the solution under ice-cooling. The mixture was
stirred under argon atmosphere at room temperature for 3 hours. To
the reaction mixture was added a saturated aqueous sodium hydrogen
carbonate solution, the mixture was extracted with ethyl acetate
and dried over anhydrous sodium sulfate, and the solvent was
removed under reduced pressure. The resulting residue was purified
by silica gel column chromatography (solvent: hexane:ethyl
acetate=9:1.fwdarw.7:1), and triturated with hexane and ethyl
acetate to obtain
4-(2-cyanoethyl)-2-(4-fluorophenyl)-5-(2-thienyl)oxazole (132 mg)
as colorless powder.
[0283] MS.cndot.APCI (m/z): 299 (MH+)
Preparation Example 338
[0284] A mixture of
4-(2-cyanoethyl)-2-(4-fluorophenyl)-5-(2-thienyl)oxazole (95 mg),
conc. hydrochloric acid (3 ml) and formic acid (4 ml) was stirred
at 60.degree. C. overnight. After addition of conc. hydrochloric
acid (1 ml), the mixture was stirred at 70.degree. C. for 6 hours.
After cooling, water was added to the reaction mixture, and the
mixture was extracted with ethyl acetate. The organic layer was
washed with water and brine, dried over anhydrous sodium sulfate
and the solvent was removed under reduced pressure. The resulting
residue was purified by silica gel column chromatography (solvent:
chloroform:methanol=19:1). The resulting colorless powder was
dissolved in methanol (5 ml), 0.5M sodium methoxide (600 .mu.l,
methanol solution) was added to the solution and the solvent was
removed under reduced pressure. The resulting residue was
triturated with acetone to obtain
2-(4-fluorophenyl)-5-(2-thienyl)oxazole-4-yl propionic acid sodium
salt (103 mg) as pale brownish powder.
[0285] MS.cndot.ESI (m/z): 316 (M-Na)
Preparation Example 339
[0286] (1) To a suspension of tellurium powder (153 mg) in ethanol
(3 ml) was added sodium borohydride (108 mg), and the mixture was
refluxed under argon atmosphere for 15 minutes. Under ice-cooling,
acetic acid (160 .mu.l) and a solution of ethyl
5-(5-chlorothiophen-2-yl)-2-(4-fluorophenyl)oxazole-4-yl acrylate
(302 mg) in tetrahydrofuran (4 ml) were added to the mixture, and
the resulting mixture was stirred at room temperature for one hour.
The reaction mixture was filtered through Cellite and the residue
was washed with ethyl acetate. The filtrate was washed with water
and brine, dried over anhydrous sodium sulfate and the solvent was
removed under reduced pressure. The resulting reside was purified
by silica gel column chromatography (solvent: hexane:ethyl
acetate=30:1), and triturated with hexane to obtain a crude product
of ethyl 5-(5-chlorothiophen-2-yl)-2-(4-fluorophenyl)oxazole-4-yl
propionate (263 mg) as colorless powder.
[0287] (2) To a solution of the product obtained in the
above-mentioned (1) (63 mg) in tetrahydrofuran (1 ml) and ethanol
(2 ml) was added 1N aqueous sodium hydroxide solution (170 .mu.l)
and the resulting mixture was refluxed for 1.5 hours. After
cooling, the reaction mixture was concentrated under reduced
pressure. The resulting residue was triturated with acetone to
obtain 5-(5-chlorothiophen-2-yl)-2-(4-fluorophenyl)oxazole-4-yl
propionic acid sodium salt (60 mg) as colorless powder.
[0288] MS.cndot.ESI (m/z): 350/352 (M-Na)
Preparation Example 340
[0289] (1) A mixture of
5-(5-chlorothiophen-2-yl)-2-(4-fluorophenyl)-4-hydroxymethyloxazole
(1.44 g) and manganese dioxide (4.76 g) in tetrahydrofuran (20 ml)
was refluxed for 3 hours. The reaction mixture was filtered through
Cellite and the filtrate was concentrated under reduced pressure.
The resulting reside was triturated with diethyl ether to obtain
5-(5-chlorothiophen-2-yl)-2-(4-fluorophenyl)-4-formyloxazole (943
mg) as colorless powder.
[0290] MS.cndot.APCI (m/z): 308 (MH+)
[0291] (2) To a solution of ethyl diethylphosphonoacetate (740
.mu.l) in tetrahydrofuran (12 ml) was added sodium hydride (153 mg,
60% mineral oil) in an ice-acetone bath, and the resulting mixture
was stirred at the same temperature for 15 minutes.
5-(5-Chlorothiophen-2-yl)-2-(4-fluorophenyl)-4-formyloxazole (400
mg) was added to the mixture and the mixture was allowed to warm to
room temperature for one hour. After cooling, the reaction mixture
was neutralized by a saturated aqueous ammonium chloride solution
and extracted with ethyl acetate. The organic layer was washed with
water and brine, dried over anhydrous sodium sulfate and the
solvent was removed under reduced pressure. The resulting residue
was purified by silica gel column chromatography (solvent:
hexane:ethyl acetate=30:1), and then, triturated with diethyl ether
and hexane to obtain 404 mg of ethyl
5-(5-chlorothiophen-2-yl)-2-(4-fluorophenyl)oxazole-4-yl acrylate
as colorless powder.
[0292] MS.cndot.APCI (m/z): 378 (MH+)
Preparation Example 341
[0293] A mixture of
5-(5-chlorothiophen-2-yl)-2-(4-fluorophenyl)-4-methoxycarbonyloxazole
(1.8 g) and lithium borohydride (580 mg) in tetrahydrofuran (40 ml)
was stirred at room temperature for one hour, and then, refluxed
for 1.5 hours. After cooling, water and 10% hydrochloric acid were
added to the reaction mixture, and the mixture was extracted with
ethyl acetate. The organic layer was washed with water and brine,
dried over anhydrous sodium sulfate and the solvent was removed
under reduced pressure. The resulting residue was triturated with
diethyl ether-ethyl acetate to obtain
5-(5-chlorothiophen-2-yl)-2-(4-fluorophenyl)-4-hydroxymethyloxazol-
e (1.48 g) as colorless powder.
[0294] MS.cndot.APCI (m/z): 310/312 (MH+)
Preparation Example 342
[0295] In a manner similar to Preparation example 341 by using the
corresponding starting materials,
5-(4-chloro-3-fluorophenyl)-2-(4-fluorophenyl)-4-hydroxymethyloxazole
was obtained.
[0296] MS.cndot.APCI (m/z): 322/324 (MH+)
Preparation Example 343
[0297] To a solution of ethyl
2-(4-fluorophenyl)oxazole-4-carboxylate (7.44 g) in chloroform (100
ml) was added dropwise bromine (8.1 ml) at room temperature, and
the resulting mixture was stirred at room temperature for 30
minutes and then refluxed for 8 hours. After cooling the reaction
mixture, 10% aqueous sodium thiosulfate solution was added to the
mixture and the mixture was extracted with chloroform. The organic
layer was washed with a saturated aqueous sodium hydrogen carbonate
solution and brine, dried over anhydrous sodium sulfate and the
solvent was removed under reduced pressure. The residue was
purified by silica gel column chromatography (solvent: ethyl
acetate:n-hexane=1:9) to obtain ethyl
5-bromo-2-(4-fluorophenyl)-oxazol-4-carboxylate (9.21 g) as pale
yellowish powder.
[0298] MS.cndot.APCI (m/z): 314/316 (MH+)
Preparation Example 344
[0299] To a solution of methyl
3-(5-chlorothiophen-2-yl)-2-(4-fluorobenzoylamino)-3-oxopropionate
(7.25 g) in N,N-dimethyl-formamide (80 ml) was added dropwise
phosphorus oxychloride (5.7 ml) under ice-cooling, and the mixture
was then stirred at room temperature for 3 days. After cooling,
water was added to the reaction mixture and the mixture was
extracted with ethyl acetate. The organic layer was washed with
water and brine, dried over anhydrous sodium sulfate and the
solvent was removed under reduced pressure. The resulting residue
was purified by silica gel column chromatography (solvent:
hexane:ethyl acetate=100:1), and then, triturated with diethyl
ether-hexane to obtain methyl
5-(5-chlorothiophen-2-yl)-2-(4-fluorophenyl)oxazol-4-carboxylate
(2.8 g) as colorless powder.
[0300] MS.cndot.APCI (m/z): 338/340 (MH+)
Preparation Example 345
[0301] In a manner similar to Preparation example 344 by using the
corresponding starting materials, methyl
5-(3-thienyl)-2-(4-fluorophenyl)oxazol-4-carboxylate was
obtained.
Preparation Example 346
[0302] A mixture of ethyl
5-bromo-2-(4-fluorophenyl)oxazol-4-carboxylate (600 mg), 0.05M
(4-chloro-3-fluorophenyl) zinc bromide (6 ml, tetrahydrofuran
solution), and tetrakis-(triphenylphosphine) palladium (231 mg) in
tetrahydrofuran (5 ml) was stirred under argon atmosphere at room
temperature for 2 hours, followed by refluxing for 40 minutes. The
reaction mixture was cooled and concentrated under reduced
pressure, and water was added to the residue and the mixture was
extracted with ethyl acetate. The organic layer was successively
washed with 10% hydrochloric acid, a saturated aqueous sodium
hydrogen carbonate solution and brine, dried over anhydrous sodium
sulfate and the solvent was removed under reduced pressure. The
residue was purified by silica gel column chromatography (solvent:
ethyl acetate:n-hexane=1:8) to obtain ethyl
5-(4-chloro-3-fluorophenyl)-2-(4-fluorophenyl)oxazol-4-carboxylate
(580 mg) as pale reddish solid.
[0303] MS.cndot.APCI (m/z): 364/366 (MH+)
Preparation Example 347
[0304] A mixture of p-fluorobenzamide (5 g), ethyl bromopyruvate
(9.92 ml), and sodium hydrogen carbonate (15 g) in tetrahydrofuran
(150 ml) was refluxed for 20 hours. After cooling the reaction
mixture, insoluble material was removed by filtration through
Cellite and the filtrate was concentrated under reduced pressure.
The residue was dissolved in tetrahydrofuran (30 ml) and
trifluoroacetic anhydride (30 ml) was added to the mixture in an
ice bath. After stirring at room temperature for one hour, a
saturated aqueous sodium hydrogen carbonate solution was added to
the mixture in an ice bath, and the mixture was extracted with
ethyl acetate. The organic layer was washed with brine, dried over
anhydrous sodium sulfate and the solvent was removed under reduced
pressure. The resulting residue was purified by silica gel column
chromatography (solvent: ethyl acetate:n-hexane=1:9) to obtain
ethyl 2-(4-fluorophenyl)oxazol-4-carboxylate (7.44 g) as colorless
solid.
[0305] MS.cndot.APCI (m/z): 236 (MH+)
Preparation Example 348
[0306] (1) Chlorine gas was bubbled through a suspension of
2-[5-(4-chloro-3-fluorophenyl)-2-(4-fluorophenyl)oxazol-4-yl]methylthiour-
ea (200 mg) in water (15 ml) under ice-cooling for 5 minutes. The
mixture was stirred at the same temperature for 30 minutes followed
by stirring at room temperature for 30 minutes. Water was added to
the reaction mixture, and the mixture was extracted with
chloroform. The organic layer was washed with water and brine,
dried over anhydrous sodium sulfate and the solvent was removed
under reduced pressure to obtain a crude product of
5-(4-chloro-3-fluorophenyl)-2-(4-fluorophenyl)-oxazol-4-yl
methanesulfonyl chloride.
[0307] (2) The product obtained in (1) was dissolved in
tetrahydrofuran (3 ml), 28% aqueous ammonia (2 ml) was added to the
solution, and the mixture was stirred at room temperature for 3
hours. The reaction mixture was concentrated under reduced pressure
and the residue was purified by silica gel column chromatography
(solvent: chloroform:methanol=20:1) to obtain
5-(4-chloro-3-fluorophenyl)-2-(4-fluorophenyl)oxazol-4-ylmethanesu-
lfonamide (164 mg) as pale yellowish solid.
[0308] MS.cndot.APCI (m/z): 385/387 (MH+)
[0309] (3) To a solution of
5-(4-chloro-3-fluorophenyl)-2-(4-fluorophenyl)oxazol-4-ylmethanesulfonami-
de obtained in (2) (125 mg) in methanol was added 0.5M sodium
methoxide (0.64 ml, methanol solution). The solvent was removed
under reduced pressure, and the resulting residue was triturated
with acetone to obtain
5-(4-chloro-3-fluorophenyl)-2-(4-fluorophenyl)oxazol-4-yl
methanesulfonamide sodium salt (80 mg).
[0310] MS.cndot.APCI (m/z): 383/385 (MH+)
Preparation Example 349
[0311] (1) A solution of
5-(4-chloro-3-fluorophenyl)-2-(4-fluorophenyl)-4-hydroxymethyloxazole
(965 mg) and thionyl chloride (1.1 ml) in tetrahydrofuran (30 ml)
was stirred at 0.degree. C. for 30 minutes, followed by stirring at
room temperature for 2 hours. Additional thionyl chloride (1.1 ml)
was added to the mixture and the mixture was refluxed for one hour.
The reaction mixture was concentrated under reduced pressure. The
remaining volatiles were removed by evaporation with toluene, and
further dried under reduced pressure to obtain a crude product of
5-(4-chloro-3-fluorophenyl)-4-chloromethyl-2-(4-fluorophenyl)oxazole
(925 mg).
[0312] (2) A solution of the crude product obtained in (1) (925 mg)
and thiourea (269 mg) in tetrahydrofuran (50 ml) was refluxed for
15 hours. The reaction mixture was concentrated under reduced
pressure to one-third volume, and the residue was triturated with
adding diethyl ether to obtain
2-[5-(4-chloro-3-fluorophenyl)-2-(4-fluorophenyl)-oxazol-4-yl]-met-
hylthiourea hydrochloride (954 mg).
[0313] MS.cndot.APCI (m/z): 380/382 (MH+)
Preparation Example 350
[0314] To a solution of
5-(2-cyanoethyl)-2-(4-fluorophenyl)-4-(2-methoxyphenyl)imidazole
(40 mg) in dichloromethane (10 ml) was added dropwise boron
tribromide (94 mg) under ice-cooling, and the mixture was stirred
at room temperature overnight. To the reaction mixture was added
dropwise a saturated aqueous sodium hydrogen carbonate solution
under ice-cooling, and then, the mixture was extracted with
chloroform. The organic layer was dried over anhydrous sodium
sulfate, and the solvent was removed under reduced pressure. The
residue was purified by preparative TLC (solvent: hexane:ethyl
acetate=1:1), and further purified by NH silica gel column
chromatography (solvent: hexane:ethyl acetate=1:1). To the product
was added hydrogen chloride-ethanol solution and the mixture was
concentrated to obtain
5-(2-cyanoethyl)-2-(4-fluorophenyl)-4-(2-hydroxyphenyl)-imidazo- le
hydrochloride (6 mg) as colorless solid.
[0315] MS.cndot.APCI (m/z): 308 (MH+)
Preparation Examples 351 to 355
[0316] The following compounds shown in Table 27 were prepared in a
manner similar to Preparation examples 43 and Preparation example
152 by using the corresponding starting materials.
TABLE-US-00027 TABLE 27 Physical Preparation constant, example No.
Chemical structure Salt etc. 351 ##STR00297## Na Powder
ESI.cndot.MS (m/z): 373/375 (M - Na)- 352 ##STR00298## Na Powder
ESI.cndot.MS (m/z): 361/363 (M - H) 353 ##STR00299## Na Powder
ESI.cndot.MS (m/z): 347/349 (M - Na) 354 ##STR00300## Na Powder
ESI.cndot.MS (m/z): 362/364 (M - Na) 355 ##STR00301## Na Powder
ESI.cndot.MS (m/z): 367/369 (M - H)
Preparation Example 356
[0317] A mixture of ethyl
2-(6-aminopyridin-3-yl)-5-(5-chlorothiophen-2-yl)oxazol-4-yl
acetate (70 mg) and 40% aqueous chloroacetaldehyde solution (47 p.
1) in ethanol (2.1 ml) was refluxed for 3 hours, and 40% aqueous
chloroacetaldehyde solution (16 .mu.l) was added to the mixture and
the resulting mixture was refluxed for one hour. After cooling, a
saturated aqueous sodium hydrogen carbonate solution was added to
the reaction mixture, the mixture was extracted with ethyl acetate,
dried over anhydrous sodium sulfate and the solvent was removed
under reduced pressure. The resulting residue was purified by
silica gel column chromatography (solvent:
chloroform:methanol=49:1.fwdarw.97:3) to obtain ethyl
2-(imidazo[a,1]pyridin-5-yl)-5-(5-chlorothiophen-2-yl)oxazol-4-yl
acetate (65 mg).
[0318] MS.cndot.APCI (m/z): 388/390 (MH+)
Preparation Example 357
[0319] (1) To a solution of ethyl
2-(6-chloropyridin-3-yl)-5-(5-chlorothiophen-2-yl)oxazol-4-yl
acetate (1 g) in N,N-di-methylformaldehyde (10 ml) was added sodium
azide (1.7 g), and the mixture was refluxed overnight. After
cooling, water was added to the reaction mixture and the mixture
was extracted with ethyl acetate, the organic layer was dried over
anhydrous sodium sulfate and the solvent was removed under reduced
pressure. The resulting residue was purified by silica gel column
chromatography (solvent: chloroform:ethyl acetate=8:1) to obtain
ethyl 2-(6-azidopyridin-3-yl)-5-(5-chlorothiophen-2-yl)oxazol-4-yl
acetate (401 mg) as yellowish powder.
[0320] (2) A mixture of ethyl
2-(6-azidopyridin-3-yl)-5-(5-chlorothiophen-2-yl)oxazol-4-yl
acetate (401 mg) and 540 mg of triphenylphosphine (540 mg) in water
(2 ml) and acetic acid (8 ml) was refluxed for 2 hours. After
cooling, water was added to the reaction mixture and the mixture
was extracted with ethyl acetate. The organic layer was washed with
water and brine, dried over anhydrous sodium sulfate and the
solvent was removed under reduced pressure. The resulting residue
was purified by silica gel column chromatography (solvent:
chloroform:ethyl acetate=5:1.fwdarw.2:3.fwdarw.1:2), and then,
triturated with diethyl ether to obtain ethyl
2-(6-aminopyridin-3-yl)-5-(5-chlorothiophen-2-yl)oxazol-4-yl
acetate (177 mg) as yellowish powder.
[0321] MS.cndot.APCI (m/z): 364/366 (MH+)
Preparation Example 358
[0322] A mixture of ethyl
5-(5-chlorothiophen-2-yl)-2-(1-formyl-indolin-5-yl)oxazol-4-yl
acetate (160 mg) and 6N hydrochloric acid (2 ml) in ethanol (4 ml)
was stirred at 60.degree. C. for 4 days. Water was added to the
reaction mixture and the mixture was extracted with ethyl acetate.
The organic layer was washed with brine, dried over anhydrous
sodium sulfate, and the solvent was removed under reduced pressure.
The residue was purified by preparative TLC (solvent:
chloroform:methanol=20:1) to obtain ethyl
5-(5-chlorothiophen-2-yl)-2-(5-indolinyl)oxazol-4-yl acetate (53
mg) as colorless powder.
[0323] MS.cndot.APCI (m/z): 389/391 (MH+)
Preparation Example 359
[0324] To a suspension of ethyl
2-(2-methylthiopyrimidin-5-yl)-5-(5-chlorothiophen-2-yl)oxazol-4-yl
acetate (156 mg) in tetrahydrofuran (3.12 ml) was added
metachloroperbenzoic acid (88 mg, 70% purity) under ice-cooling,
and the mixture was stirred at room temperature for one hour. After
ice-cooling again, 70% metachloroperbenzoic acid (40 mg) was added
to the mixture and the resulting mixture was stirred at room
temperature for one hour. To the mixture was added 50% aqueous
dimethylamine solution (1 ml) and the mixture was stirred at room
temperature for 30 minutes. Water was added to the reaction mixture
and the mixture was extracted with chloroform. The organic layer
was washed with brine, dried over anhydrous sodium sulfate and the
solvent was removed under reduced pressure. The resulting residue
was purified by silica gel column chromatography (solvent:
chloroform:ethyl acetate=8:1) to obtain ethyl
2-(2-dimethylaminopyrimidin-5-yl)-5-(5-chlorothiophen-2-yl)
oxazol-4-yl acetate (139 mg) as colorless powder.
[0325] MS.cndot.APCI (m/z): 393/395 (MH+)
Preparation Examples 360 and 361
[0326] The following compounds shown in Table 28 were prepared in a
manner similar to Preparation examples 359 by using the
corresponding starting materials.
TABLE-US-00028 TABLE 28 Preparation Physical example No. Chemical
structure Salt constant, etc. 360 ##STR00302## Free material Powder
MS.cndot.APCI (m/z): 407/409 (M + H)+ 361 ##STR00303## Free
material Powder MS.cndot.APCI (m/z): 405/407 (M + H)+
Preparation Examples 362 to 364
[0327] The compounds obtained in Preparation examples 359 to 361
were subjected to hydrolysis according to the conventional manner
to obtain the compounds shown in Table 29.
TABLE-US-00029 TABLE 29 Physical Preparation constant, example No.
Chemical structure Salt etc. 362 ##STR00304## Na Powder
ESI.cndot.MS (m/z): 363/365 (M - Na)- 363 ##STR00305## Na Powder
ESI.cndot.MS (m/z): 377/379 (M - Na)- 364 ##STR00306## Na Powder
ESI.cndot.MS (m/z): 375/377 (M - Na)-
Preparation Example 365
[0328] To a suspension of ethyl
2-(6-chloropyridin-3-yl)-5-(3-thienyl)oxazol-4-yl acetate (150 mg)
in ethanol (3 ml) was added 15% aqueous sodium methyl sulfide
solution (2 ml), and the mixture was refluxed for 3 days. After
cooling, the reaction mixture was neutralized by 10% hydrochloric
acid, and extracted with ethyl acetate. The organic layer was dried
over anhydrous sodium sulfate and the solvent was removed under
reduced pressure. The resulting residue was washed with diethyl
ether and dissolved in methanol (5 ml), and 0.5M sodium methoxide
(495 .mu.l, methanol solution) was added to the solution and the
solvent was removed under reduced pressure. The resulting residue
was triturated with acetone to obtain
2-(6-methylthiopyridin-3-yl)-5-(3-thienyl)oxazol-4-yl acetic acid
sodium salt (74 mg) as pale yellowish powder.
[0329] MS.cndot.ESI (m/z): 331 (M-Na)
Preparation Example 366
[0330] In a manner similar to Preparation example 365 and using
corresponding starting materials,
2-(6-methylthiopyridin-3-yl)-5-(2-thienyl)oxazol-4-yl acetic acid
sodium salt was obtained.
[0331] MS.cndot.ESI (m/z): 331 (M-Na)
Preparation Example 367
[0332] To a suspension of ethyl
2-(6-chloropyridin-3-yl)-5-(5-chlorothiophen-2-yl)oxazol-4-yl
acetate (192 mg) in ethanol (5 ml) was added sodium hydride (100
mg, 60% mineral oil), and the mixture was refluxed for 6 hours, and
then, water (1 ml) was added to the mixture and the mixture was
further refluxed for 30 minutes. After cooling, the reaction
mixture was neutralized by 10% hydrochloric acid, and extracted
with ethyl acetate. The organic layer was dried over anhydrous
sodium sulfate and the solvent was removed under reduced pressure.
The resulting residue was washed with hexane and dissolved in
methanol (5 ml), and 0.5M sodium methoxide (867 .mu.l, methanol
solution) was added to the solution and the solvent was removed
under reduced pressure. The resulting residue was triturated with
acetone to obtain
2-(6-ethoxypyridin-3-yl)-5-(5-chlorothiophen-2-yl)oxazol-4-yl
acetic acid sodium salt (169 mg) as pale yellowish powder.
[0333] MS.cndot.ESI (m/z): 363/365 (M-Na)
Preparation Examples 368 and 369
[0334] The following compounds shown in Table 30 were prepared in a
manner similar to Preparation examples 367 by using the
corresponding starting materials.
TABLE-US-00030 TABLE 30 Physical Preparation constant, example No.
Chemical structure Salt etc. 368 ##STR00307## Na Powder
ESI.cndot.MS (m/z): 349/351 (M - Na)- 369 ##STR00308## Na Powder
ESI.cndot.MS (m/z): 315 (M - Na)-
Preparation Example 370
[0335] To a mixture of 2-(4-fluorophenyl)-5-(3-thienyl)oxazol-4-yl
acetic acid (130 mg) in N,N-dimethylformamide (5 ml) was added
N,N-carbonyldiimidazole (347 mg), and the mixture was stirred at
room temperature for 2 hours. Methanesulfonamide (204 mg) and
1,8-diazabicyclo[5.4.0]undecene (0.32 ml) were added to the mixture
and the resulting mixture was stirred at 100.degree. C. overnight.
The reaction mixture was poured into 10% hydrochloric acid, and
extracted with ethyl acetate. The organic layer was washed with
water and brine, and dried over anhydrous sodium sulfate, and the
solvent was removed under the reduced pressure. The resulting
residue was purified by silica gel column chromatography (solvent:
hexane:ethyl acetate=1:1), and then, the resulting product was
dissolved in methanol (10 ml), and 0.5M sodium methoxide (68 .mu.l,
methanol solution) was added to the solution and the solvent was
removed under reduced pressure to obtain
N-[2-(4-fluorophenyl)-5-(3-thienyl)oxazol-4-yl
acetyl]methanesulfonamide sodium salt (42 mg) as colorless
powder.
[0336] MS.cndot.ESI (m/z): 379 (M-Na)
Preparation Example 371
[0337] Corresponding starting compounds are treated in a manner
similar to Preparation example 370 to obtain the compound shown in
Table 31.
TABLE-US-00031 TABLE 31 Physical Preparation constant, example No.
Chemical structure Salt etc. 371 ##STR00309## Na Powder
ESI.cndot.MS (m/z): 442 (M - H)
Preparation Example 372
[0338] To a mixture of ethyl
2-(4-fluorophenyl)-5-(5-chlorothiophen-2-yl)oxazol-4-yl acetate
(1.01 g) in ethanol (5 ml), diethyl ether (5 ml) and
tetrahydrofuran (6 ml) was added sodium hydride (110 mg, 60%
mineral oil) under argon atmosphere, and the mixture was stirred
for 10 minutes under ice-cooling. After addition of isoamyl nitrite
(647 mg), the mixture was stirred at room temperature for 1.5
hours. 10% Hydrochloric acid was added to the mixture and the
resulting mixture was extracted with ethyl acetate. The organic
layer was washed with water and brine, dried over anhydrous sodium
sulfate and the solvent was removed under reduced pressure. The
resulting crude product (395 mg) was taken up into formic acid (4
ml) and ethanol (3 ml). To the mixture zinc powder (291 mg) was
added at room temperature, and the mixture was stirred for 10
minutes followed by stirring at 70.degree. C. for 20 minutes. After
cooling, the reaction mixture was filtered through glass filter,
the residue was washed with ethanol and the filtrate was
concentrated under reduced pressure. To the resulting residue was
added a saturated aqueous sodium hydrogen carbonate solution, the
mixture was extracted with ethyl acetate and the organic layer was
washed with water and brine, dried over anhydrous sodium sulfate,
and the solvent was removed under reduced pressure. The resulting
residue was triturated with diethyl ether-hexane to obtain ethyl
2-amino-2-[5-(5-chlorothiophen-2-yl)-2-(4-fluorophenyl)-oxazol-4-yl-
]acetate (307 mg) as colorless powder.
[0339] MS.cndot.APCI (m/z): 381/383 (MH+)
Preparation Example 373
[0340] A mixture of 2-(4-fluorophenyl)-5-(3-thienyl)oxazol-4-yl
acetic acid (100 mg), methoxyamine hydrochloride (37.6 mg),
3-ethyl-1-(3-dimethylaminopropyl)carbodiimide hydrochloride (95
mg), 1-hydroxybenzotriazole (67 mg) and triethylamine (0.14 ml) in
N,N-dimethylformamide (3 ml) was stirred at room temperature
overnight. Water was added to the reaction mixture, the mixture was
extracted with chloroform. The organic layer was washed with water
and brine, dried over anhydrous sodium sulfate and the solvent was
removed under reduced pressure. The resulting residue was purified
by silica gel column chromatography (solvent:
chloroform:methanol=20:1), and triturated with diethyl ether-hexane
to obtain
N-methoxy-[2-(4-fluorophenyl)-5-(3-thienyl)oxazol-4-yl]acetamide
(75 mg) as colorless powder.
[0341] MS.cndot.APCI (m/z): 333 (MH+)
Preparation Examples 374 to 377
[0342] The corresponding starting materials were treated in a
manner similar to Preparation example 373 to obtain the compounds
shown in Table 32 below.
TABLE-US-00032 TABLE 32 Preparation Physical example No. Chemical
structure Salt constant, etc. 374 ##STR00310## Free material Powder
MS.cndot.APCI (m/z): 317 (M + H) 375 ##STR00311## HCl Powder
MS.cndot.APCI (m/z): 394 (M + H) 376 ##STR00312## HCl Powder
MS.cndot.APCI (m/z): 380 (M + H) 377 ##STR00313## Free material
Crystal Melting point: 183-184.degree. C. MS.cndot.APCI (m/z): 347
(M + H)
Preparation Example 378
[0343] (1) Under argon atmosphere, to a solution of
2-(4-fluorophenyl)-4-(2-hydroxyethyl)-5-(3-thienyl)oxazole (300 mg)
in methylene chloride (10 ml) were successively added
methane-sulfonyl chloride (96 .mu.l) and triethylamine (188 .mu.l)
under ice-cooling, and the mixture was stirred at room temperature
for 3 hours. The reaction mixture was poured into water and
extracted with methylene chloride. The organic layer was washed
with water and brine, dried over anhydrous sodium sulfate and the
solvent was removed under reduced pressure to obtain a crude
product of
2-(4-fluorophenyl)-4-(2-methanesulfonyloxyethyl)-5-(3-thienyl)oxazole.
[0344] (2) To a solution of methanesulfonamide (136 mg) in
N,N-di-methylformamide (10 ml) was added sodium hydride (57 mg, 60%
mineral oil) under ice-cooling, and the mixture was stirred at room
temperature for one hour. After the mixture was ice-cooled again,
an N,N-dimethylformamide solution of the crude product obtained in
(1) was added to the mixture and the resulting mixture was stirred
at room temperature for one hour and then stirred at 60.degree. C.
overnight. The reaction mixture was ice-cooled, and then, poured
into an aqueous ammonium chloride solution and extracted with ethyl
acetate. The organic layer was washed with water and brine, dried
over anhydrous sodium sulfate and the solvent was removed under
reduced pressure. After the resulting residue was purified by
silica gel column chromatography (solvent: hexane:ethyl
acetate=4:1), the obtained product was dissolved in methanol (5
ml), and 0.5M sodium methoxide (562 .mu.l, methanol solution) was
added to the solution and the solvent was removed under reduced
pressure to obtain
2-(4-fluorophenyl)-4-methanesulfonylaminoethyl-5-(3-thienyl)oxazole
sodium salt (143 mg) as colorless powder.
[0345] MS.cndot.ESI (m/z): 365 (M-Na)
Preparation Example 379
[0346] (1) A mixture of 2-(4-fluorophenyl)-5-(3-thienyl)oxazol-4-yl
acetic acid (1.5 g), diphenylphosphoryl azide (1.28 ml) and
triethylamine (0.83 ml) in t-butanol (30 ml) was refluxed for one
day. After cooling the reaction mixture, the solvent was removed
under reduced pressure. Water was added to the residue and the
mixture was extracted with chloroform. The organic layer was washed
with a saturated aqueous sodium hydrogen carbonate solution and
brine, dried over anhydrous sodium sulfate, and the solvent was
removed under reduced pressure. Chloroform was added to the
residue, the mixture was heated and insoluble material was removed
by filtration, and the filtrate was concentrated under reduced
pressure. The residue was purified by silica gel column
chromatography (solvent: ethyl acetate: n-hexane=1:9.fwdarw.1:7) to
obtain
4-(t-butoxycarbonylamino)methyl-2-(4-fluorophenyl-5-(3-thienyl)oxazole
(501 mg).
[0347] MS.cndot.APCI (m/z): 375 (MH+)
[0348] (2) A solution of
4-(t-butoxycarbonylamino)methyl-2-(4-fluorophenyl)-5-(3-thienyl)oxazole
(455 mg) in 4N hydrogen chloride-dioxane solution was stirred at
room temperature for 13 hours. The reaction mixture was
concentrated under reduced pressure and the remaining volatiles
were removed by evaporation with toluene, and the resulting residue
was triturated with diethyl ether to obtain
4-aminomethyl-2-(4-fluorophenyl)-5-(3-thienyl)oxazole hydrochloride
(288 mg) as colorless powder.
[0349] MS.cndot.APCI (m/z): 275 (MH+)
Preparation Example 380
[0350] (1) To a suspension of
4-aminomethyl-2-(4-fluorophenyl)-5-(3-thienyl)oxazole (110 mg) in
dichloromethane (5 ml) were successively added dropwise under
acetone-ice cooling methane sulfonyl chloride (0.036 ml) and
triethylamine (0.15 ml). The reaction mixture was stirred at
0.degree. C. for one hour, and further stirred at room temperature
for 2 hours. To the reaction mixture was added a saturated aqueous
ammonium chloride solution and extracted with chloroform. The
organic layer was washed with water and brine, dried over anhydrous
sodium sulfate, and the solvent was removed under reduced pressure.
The residue was purified by silica gel column chromatography
(solvent: chloroform:methanol=100:0.fwdarw.95:5) to obtain a crude
product of
N-[2-(4-fluorophenyl)-5-(3-thienyl)oxazol-4-yl]-methanesulfonamide
(140 mg).
[0351] (2) Crude
N-(2-(4-fluorophenyl)-5-(3-thienyl)oxazol-4-yl)-methanesulfonamide
(133 mg) was dissolved in methanol (5 ml) and tetrahydrofuran (5
ml), and 0.5M sodium methoxide (0.72 ml, methanol solution) was
added to the solution and the mixture was stirred at room
temperature for 10 minutes. The reaction mixture was concentrated
under reduced pressure and the resulting residue was triturated
with acetone to obtain
N-[2-(4-fluorophenyl)-5-(3-thienyl)oxazol-4-yl]methanesulfonamide
sodium salt (112 mg).
[0352] MS.cndot.APCI (m/z): 353 (MH+)
Preparation Examples 381 to 429
[0353] The following compounds shown in Table 33 were prepared in a
manner similar to Preparation example 63 by using corresponding
starting materials.
TABLE-US-00033 TABLE 33 Preparation example No. Chemical structure
Salt Physical property, etc. 381 ##STR00314## Free material Crystal
Melting point: 108.5-109.degree. C. MS.cndot.APCI (m/z): 381 (M +
H) 382 ##STR00315## Free material Crystal Melting point:
117-117.5.degree. C. MS.cndot.APCI (m/z): 362 (M + H) 383
##STR00316## Free material Crystal Melting point: 67-68.degree. C.
MS.cndot.APCI (m/z): 382 (M + H) 384 ##STR00317## Free material
Crystal Melting point: 118-119.degree. C. MS.cndot.APCI (m/z): 391
(M + H) Preparation example No. Chemical structure Salt Physical
constant, etc. 385 ##STR00318## Free material Powder MS.cndot.APCI
(m/z): 405/407 (M + H)+ 386 ##STR00319## Free material Powder
MS.cndot.APCI (m/z): 396/398 (M + H)+ 387 ##STR00320## Free
material Powder MS.cndot.APCI (m/z): 399/401 (M + H) 388
##STR00321## Free material Powder MS.cndot.APCI (m/z): 391/393 (M +
H)+ 389 ##STR00322## Free material Powder MS.cndot.APCI (m/z):
405/407 (M + H)+ 390 ##STR00323## Free material Powder
MS.cndot.APCI (m/z): 401/403 (M + H)+ 391 ##STR00324## Free
material Powder MS.cndot.APCI (m/z): 382/384 (M + H)+ 392
##STR00325## Free material Powder MS.cndot.APCI (m/z): 417/419 (M +
H)+ 393 ##STR00326## Free material Powder MS.cndot.APCI (m/z):
387/389 (M + H)+ 394 ##STR00327## Free material Powder
MS.cndot.APCI (m/z): 368/370 (M + H)+ 395 ##STR00328## Free
material Powder MS.cndot.APCI (m/z): 359 (M + H)+ 396 ##STR00329##
Free material Powder MS.cndot.APCI (m/z): 372/374 (M + H)+ 397
##STR00330## Free material Powder MS.cndot.APCI (m/z): 387/389 (M +
H)+ 398 ##STR00331## Free material Powder MS.cndot.APCI (m/z):
376/378 (M + H)+ 399 ##STR00332## Free material Powder
MS.cndot.APCI (m/z): 394/396 (M + H)+ 400 ##STR00333## Free
material Powder MS.cndot.APCI (m/z): 400/402 (M + H)+ 401
##STR00334## Free material Powder MS.cndot.APCI (m/z): 403/405 (M +
H)+ 402 ##STR00335## Free material Powder ESI.cndot.MS (m/z):
333/335 (M - Na)- 403 ##STR00336## Free material Powder
MS.cndot.APCI (m/z): 393/395 (M + H)+ 404 ##STR00337## Free
material Powder MS.cndot.APCI (m/z): 406/408 (M + H)+ 405
##STR00338## Free material Powder MS.cndot.APCI (m/z): 327 (M + H)
406 ##STR00339## Free material Powder MS.cndot.APCI (m/z): 418/420
(M + H)+ 407 ##STR00340## Free material Powder MS.cndot.APCI (m/z):
388/390 (M + H) 408 ##STR00341## Free material Crystal Melting
point: 155-156.5.degree. C. MS.cndot.APCI (m/z): 370 (M + H)+ 409
##STR00342## Free material Crystal Melting point: 77-78.degree. C.
MS.cndot.APCI (m/z): 360 (M + H)+ 410 ##STR00343## Free material
Crystal Melting point: 84-86.degree. C. MS.cndot.APCI (m/z): 358 (M
+ H)+ 411 ##STR00344## Free material Crystal Melting point:
130-133.degree. C. MS.cndot.APCI (m/z): 365 (M + H)+ 412
##STR00345## Free material Oil MS.cndot.APCI (m/z): 370 (M + H)+
413 ##STR00346## Free material Powder MS.cndot.APCI (m/z): 418/420
(M + H)+ 414 ##STR00347## Free material Powder MS.cndot.APCI (m/z):
422/424 (M + H)+ 415 ##STR00348## Free material Powder
MS.cndot.APCI (m/z): 408/410 (M + H)+ 416 ##STR00349## Free
material Powder MS.cndot.APCI (m/z): 408/410 (M + H)+ 417
##STR00350## Free material Powder MS.cndot.APCI (m/z): 394/396 (M +
H)+ 418 ##STR00351## Free material Powder MS.cndot.APCI (m/z):
420/422 (M + H)+ 419 ##STR00352## Free material Powder
MS.cndot.APCI (m/z): 392/394 (M + H)+ 420 ##STR00353## Free
material Powder MS.cndot.APCI (m/z): 405/407 (M + H)+ 421
##STR00354## Free material Powder MS.cndot.APCI (m/z): 401/403 (M +
H)+ 422 ##STR00355## Free material Powder MS.cndot.APCI (m/z): 359
(M + H)+ 423 ##STR00356## Free material Powder MS.cndot.APCI (m/z):
368/370 (M + H)+ 424 ##STR00357## Free material Powder
MS.cndot.APCI (m/z): 417/419 (M + H)+ 425 ##STR00358## Free
material Powder MS.cndot.APCI (m/z): 384/386 (M + H)+ 426
##STR00359## Free material Crystal Melting point: 112-113.degree.
C. MS.cndot.APCI (m/z): 420 (M + H)+ 427 ##STR00360## Free material
Crystal Melting point: 80-81.degree. C. MS.cndot.APCI (m/z): 328 (M
+ H)+ 428 ##STR00361## Free material Crystal Melting point:
168.5-169.5.degree. C. MS.cndot.APCI (m/z): 365 (M + H)+ 429
##STR00362## Free material Crystal Melting point: 145-146.degree.
C. MS.cndot.APCI (m/z): 389/391 (M + H)+
Preparation Examples 430 to 479
[0354] The following compounds shown in Table 34 were prepared in a
manner similar to Preparation example 148 or 152 by using
corresponding starting materials.
TABLE-US-00034 TABLE 34 Physical Preparation constant, example No.
Chemical structure Salt etc. 430 ##STR00363## Na Powder
ESI.cndot.MS (m/z): 352 (M - Na) 431 ##STR00364## Na Powder
ESI.cndot.MS (m/z): 332 (M - Na) 432 ##STR00365## Na Powder
ESI.cndot.MS (m/z): 298 (M - Na) 433 ##STR00366## Na Powder
ESI.cndot.MS (m/z): 298 (M - Na) 434 ##STR00367## Na Powder
ESI.cndot.MS (m/z): 369 (M - Na) 435 ##STR00368## Na Powder
ESI.cndot.MS (m/z): 358/360 (M - Na) 436 ##STR00369## Na Powder
ESI.cndot.MS (m/z): 348 (M - Na) 437 ##STR00370## Na Powder
ESI.cndot.MS (m/z): 340 (M - Na)- 438 ##STR00371## Na Powder
ESI.cndot.MS (m/z): 328 (M - Na)- 439 ##STR00372## Na Powder
ESI.cndot.MS (m/z): 335 (M - Na)- 440 ##STR00373## Na Powder
ESI.cndot.MS (m/z): 330 (M - Na)- 441 ##STR00374## Na Powder
ESI.cndot.MS (m/z): 361/363 (M - Na)- 442 ##STR00375## Na Powder
ESI.cndot.MS (m/z): 335 (M - Na)- 443 ##STR00376## Na Powder
ESI.cndot.MS (m/z): 340 (M - Na)- 444 ##STR00377## Na Powder
ESI.cndot.MS (m/z): 366/368 (M - Na)- 445 ##STR00378## Na Powder
ESI.cndot.MS (m/z): 366/368 (M - Na)- 446 ##STR00379## Na Powder
ESI.cndot.MS (m/z): 375/377 (M - Na)- 447 ##STR00380## Na Powder
ESI.cndot.MS (m/z): 386/388 (M - Na)- 448 ##STR00381## Na Powder
ESI.cndot.MS (m/z): 378/380 (M - Na)- 449 ##STR00382## Na Powder
ESI.cndot.MS (m/z): 378/380 (M - Na)- 450 ##STR00383## Na Powder
ESI.cndot.MS (m/z): 388/390 (M - Na)- 451 ##STR00384## Na Powder
ESI.cndot.MS (m/z): 392/394 (M - Na)- 452 ##STR00385## Na Powder
ESI.cndot.MS (m/z): 333/335 (M - Na)- 453 ##STR00386## Na Powder
ESI.cndot.MS (m/z): 373/375 (M - Na)- 454 ##STR00387## Na Powder
ESI.cndot.MS (m/z): 368/370 (M - Na)- 455 ##STR00388## Na Powder
ESI.cndot.MS (m/z): 358/360 (M - Na)- 456 ##STR00389## Na Powder
ESI.cndot.MS (m/z): 390/392 (M - Na)- 457 ##STR00390## Na Powder
ESI.cndot.MS (m/z): 364/366 (M - Na)- 458 ##STR00391## Na Powder
ESI.cndot.MS (m/z): 338/340 (M - Na)- 459 ##STR00392## Na Powder
ESI.cndot.MS (m/z): 389/391 (M - Na)- 460 ##STR00393## Na Powder
ESI.cndot.MS (m/z): 370/372 (M - Na)- 461 ##STR00394## Na Powder
ESI.cndot.MS (m/z): 362/364 (M - Na)- 462 ##STR00395## Na Powder
ESI.cndot.MS (m/z): 378/380 (M - Na)- 463 ##STR00396## Na Powder
ESI.cndot.MS (m/z): 376/378 (M - Na)- 464 ##STR00397## Na Powder
ESI.cndot.MS (m/z): 363/365 (M - Na)- 465 ##STR00398## Na Powder
ESI.cndot.MS (m/z): 387/389 (M - Na)- 466 ##STR00399## Na Powder
ESI.cndot.MS (m/z): 357/359 (M - Na)- 467 ##STR00400## Na Powder
ESI.cndot.MS (m/z): 352/354 (M - Na)- 468 ##STR00401## Na Powder
ESI.cndot.MS (m/z): 375/377 (M - Na)- 469 ##STR00402## Na Powder
ESI.cndot.MS (m/z): 371/373 (M - Na)- 470 ##STR00403## Na Powder
ESI.cndot.MS (m/z): 375/377 (M - Na)- 471 ##STR00404## Na Powder
ESI.cndot.MS (m/z): 361/363 (M - Na)- 472 ##STR00405## Na Powder
ESI.cndot.MS (m/z): 371/373 (M - Na)- 473 ##STR00406## Na Powder
ESI.cndot.MS (m/z): 357/359 (M - Na)- 474 ##STR00407## Na Powder
ESI.cndot.MS (m/z): 346/348 (M - Na)- 475 ##STR00408## Na Powder
ESI.cndot.MS (m/z): 342/344 (M - Na)- 476 ##STR00409## Na Powder
ESI.cndot.MS (m/z): 329 (M - Na)- 477 ##STR00410## Na Powder
ESI.cndot.MS (m/z): 329 (M - Na)- 478 ##STR00411## Na Powder
ESI.cndot.MS (m/z): 338/340 (M - Na)- 479 ##STR00412## Na Powder
ESI.cndot.MS (m/z): 364/366 (M - Na)-
Preparation Example 480
[0355] A mixture of ethyl
3-(4-chlorobenzoylamino)-4-phenyl-4-oxobutyrate (25 g) in acetic
acid (150 ml) was heated to 130.degree. C., and a largely excessive
amount of ammonium acetate was added to the mixture. After
confirming completion of the reaction by TLC, the reaction mixture
was cooled. Ice-water was added to the mixture and the mixture was
extracted with ethyl acetate. The organic layer was washed with an
aqueous sodium hydrogen carbonate solution and brine, and dried
over anhydrous sodium sulfate, and the solvent was removed under
reduced pressure. The residue was crystallized from diisopropyl
ether to obtain 2-(4-chlorophenyl)-4-phenylimidazol-5-yl acetamide
(10.42 g).
[0356] MS.cndot.EI (m/z): 311 (M+)
Preparation Example 481
[0357] To a solution of 2-(4-chlorophenyl)-4-phenylimidazol-5-yl
acetamide (10.00 g) in N,N-dimethylformamide (50 ml) was added
dropwise 8.9 ml of phosphorus oxychloride (8.9 ml) below 20.degree.
C., and the mixture was stirred at room temperature for one hour.
To the reaction mixture were added ice-water and ethyl acetate, and
the mixture was neutralized by sodium hydrogen carbonate. The
organic layer was collected, washed with brine, and dried over
anhydrous sodium sulfate and the solvent was removed under reduced
pressure. The residue was crystallized from diisopropyl ether to
obtain 2-(4-chlorophenyl)-5-cyano-methyl-4-phenylimidazole (6.85
g).
[0358] MS.cndot.EI (m/z): 293 (M+)
Preparation Example 482
[0359] The corresponding starting materials were treated in a
manner similar to Preparation example 112 to obtain
2-(5-chlorothiophen-3-yl)-5-hydroxymethyl-4-(3-pyridyl)imidazole.
[0360] MS.cndot.APCI (m/z): 292 (MH+)
Preparation Example 483
[0361] The corresponding starting materials were treated in a
manner similar to Preparation example 130 to obtain
2-(4-fluorophenyl)-5-methylthiomethyl-4-phenylimidazole
hydrochloride.
[0362] MS.cndot.APCI (m/z): 298 (M+)
Preparation Example 484
[0363] The corresponding starting materials were treated in a
manner similar to Preparation example 141 to obtain
2-(4-fluorophenyl)-5-(3-pyridyl)oxazol-4-yl acetic acid
hydrochloride.
[0364] MS.cndot.APCI (m/z): 299 (M+)
Preparation Example 485
[0365] A mixture of
2-(2-hydroxymethylthiophen-3-yl)-5-ethyl-4-(3-pyridyl)imidazole
dihydrochloride (212 mg) and manganese oxide (2 g) in
tetrahydrofuran (15 ml) was refluxed for one hour. The reaction
mixture was filtered and washed with tetrahydrofuran, and the
filtrate was concentrated under reduced pressure. The residue was
purified by silica gel column chromatography (solvent:
chloroform:methanol=30:1.fwdarw.20:1) to obtain
2-(2-formylthiophen-3-yl)-5-ethyl-4-(3-pyridyl)imidazole (93 mg) as
orange crystal.
[0366] MS.cndot.APCI (m/z): 284 (MH+)
Preparation Example 486
[0367] To a solution of
2-(2-formylthiophen-3-yl)-5-ethyl-4-(3-pyridyl)imidazole (68 mg) in
tetrahydrofuran (5 ml) was added dropwise 3M methyl magnesium
bromide (0.24 ml, diethyl ether solution) under argon atmosphere in
an ice bath, and the mixture was stirred at the same temperature
for 30 minutes. To the reaction mixture was added a saturated
aqueous ammonium chloride solution, and the mixture was extracted
with ethyl acetate. The organic layer was washed with brine, dried
over anhydrous magnesium sulfate and the solvent was removed under
reduced pressure. The residue was purified by silica gel column
chromatography (solvent: chloroform:methanol=20:1) to obtain
2-[2-(1-hydroxyethyl)thiophen-3-yl]-5-ethyl-4-(3-pyridyl)-imida-
zole dihydrochloride (60 mg) as orange brownish powder.
[0368] MS.cndot.APCI (m/z): 300 (MH+)
Preparation Example 487
[0369] (1) A mixture of ethyl
4-(2-thienyl)-2-(4-fluorophenyl)oxazol-5-yl acetate (140 mg),
N-chlorosuccinic imide (62 mg) and a catalytic amount of 70%
aqueous perchloric acid solution in carbon tetrachloride (7 ml) was
stirred at room temperature overnight. The reaction mixture was
poured into water, neutralized by a saturated aqueous sodium
hydrogen carbonate solution and extracted with ethyl acetate. The
organic layer was washed with water and brine and dried over
anhydrous sodium sulfate, and the solvent was removed under reduced
pressure. The resulting residue was purified by silica gel column
chromatography (solvent: hexane:ethyl acetate=95:5) to obtain ethyl
4-(5-chlorothiophen-2-yl)-2-(4-fluorophenyl)oxazol-5-yl acetate
(39.6 mg) as colorless powder.
[0370] MS.cndot.APCI (m/z): 366/368 (MH+)
[0371] (2) The compound obtained in the above (1) was hydrolyzed
according to the conventional manner to obtain
4-(5-chlorothiophen-2-yl)-2-(4-fluorophenyl)oxazol-5-yl acetic acid
sodium salt.
[0372] ESI.cndot.MS (m/z): 336/338 (M-Na)--
Preparation Examples 488 to 502
[0373] The corresponding starting materials were treated in a
manner similar to Preparation example 147 to obtain the compounds
shown in Table 35 below.
TABLE-US-00035 TABLE 35 Preparation Physical constant, example No.
Chemical structure Salt etc. 488 ##STR00413## Free material Powder
MS.cndot.APCI (m/z): 392/394 (M + H)+ 489 ##STR00414## Free
material Powder MS.cndot.APCI (m/z): 359 (M + H)+ 490 ##STR00415##
Free material Oil MS.cndot.APCI (m/z): 358 (M + H)+ 491
##STR00416## Free material Powder MS.cndot.APCI (m/z): 370 (M + H)+
492 ##STR00417## Free material Oil MS.cndot.APCI (m/z): 344 (M +
H)+ 493 ##STR00418## Free material Powder MS.cndot.APCI (m/z): 370
(M + H)+ 494 ##STR00419## Free material Oil MS.cndot.APCI (m/z):
372/374 (M + H)+ 495 ##STR00420## Free material Oil MS.cndot.APCI
(m/z): 378/380 (M + H)+ 496 ##STR00421## Free material Powder
MS.cndot.APCI (m/z): 393/395 (M + H)+ 497 ##STR00422## Free
material Powder MS.cndot.APCI (m/z): 386/388 (M + H)+ 498
##STR00423## Free material Powder MS.cndot.APCI (m/z): 387/389 (M +
H)+ 499 ##STR00424## Free material Powder MS.cndot.APCI (m/z):
398/400 (M + H)+ 500 ##STR00425## Free material Powder
MS.cndot.APCI (m/z): 360/362 (M + H)+ 501 ##STR00426## Free
material Powder MS.cndot.APCI (m/z): 404/406 (M + H)+ 502
##STR00427## Free material Powder MS.cndot.APCI (m/z): 359 (M +
H)+
Preparation Examples 503 to 517
[0374] The corresponding starting materials were treated in a
manner similar to Preparation example 148 to obtain the compounds
shown in Table 36 below.
TABLE-US-00036 TABLE 36 Prep- aration ex- Physical ample constant,
No. Chemical structure Salt etc. 503 ##STR00428## Na Powder
ESI.cndot.MS (m/z): 374/376 (M + Na)+ 504 ##STR00429## Na Powder
ESI.cndot.MS (m/z): 362/364 (M - Na)- 505 ##STR00430## Na Powder
ESI.cndot.MS (m/z): 329 (M - Na)- 506 ##STR00431## Na Powder
ESI.cndot.MS (m/z): 328 (M - Na)- 507 ##STR00432## Na Powder
ESI.cndot.MS (m/z): 314 (M - Na)- 508 ##STR00433## Na Powder
ESI.cndot.MS (m/z): 329 (M - Na)- 509 ##STR00434## Na Powder
ESI.cndot.MS (m/z): 681 (2 M - Na + H)- 510 ##STR00435## Na Powder
ESI.cndot.MS (m/z): 340 (M - H)- 511 ##STR00436## Na Powder
ESI.cndot.MS (m/z): 330/332 (M - Na)- 512 ##STR00437## Na Powder
ESI.cndot.MS (m/z): 363/365 (M - Na)- 513 ##STR00438## Na Powder
ESI.cndot.MS (m/z): 357/359 (M - Na)- 514 ##STR00439## Na Powder
ESI.cndot.MS (m/z): 356/358 (M - Na)- 515 ##STR00440## Na Powder
ESI.cndot.MS (m/z): 368/370 (M - Na)- 516 ##STR00441## Na Powder
ESI.cndot.MS (m/z): 348/350 (M - Na)- 517 ##STR00442## Na Powder
ESI.cndot.MS (m/z): 342/344 (M - Na)-
Preparation Examples 518 to 521
[0375] The corresponding starting materials were treated in a
manner similar to Preparation example 151 or 296 to obtain the
compounds shown in Table 37 below.
TABLE-US-00037 TABLE 37 Preparation Physical constant, example No.
Chemical structure Salt etc. 518 ##STR00443## Free material Powder
MS.cndot.APCI (m/z): 351 (M + H) 519 ##STR00444## Free material
Powder MS.cndot.APCI (m/z): 415 (M + H) 520 ##STR00445## Free
material Powder MS.cndot.APCI (m/z): 378 (M + H) 521 ##STR00446##
Free material Powder MS.cndot.APCI (m/z): 390/392 (M + H)+
Preparation Examples 522 to 525
[0376] The corresponding starting materials were treated in a
manner similar to Preparation example 152 to obtain the compounds
shown in Table 38 below.
TABLE-US-00038 TABLE 38 Preparation Physical constant, example No.
Chemical structure Salt etc. 522 ##STR00447## Na Powder
ESI.cndot.MS (m/z): 321 (M - Na) 523 ##STR00448## Na Powder
ESI.cndot.MS (m/z): 348 (M - Na) 524 ##STR00449## Na Powder
ESI.cndot.MS (m/z): 285 (M - Na) 525 ##STR00450## Na Powder
ESI.cndot.MS (m/z): 360/362 (M - Na)-
Preparation Examples 526 to 528
[0377] The corresponding starting materials were treated in a
manner similar to Preparation example 330 to obtain the compounds
shown in Table 39 below.
TABLE-US-00039 TABLE 39 Prep- aration Physical example constant,
No. Chemical structure Salt etc. 526 ##STR00451## Free material
Powder MS.cndot.APCI (m/z): 402 (M + H)+ 527 ##STR00452## Free
material Powder MS.cndot.APCI (m/z): 386 (M + H)+ 528 ##STR00453##
Free material Powder MS.cndot.APCI (m/z): 418/420 (M + H)+
Preparation Examples 529 to 531
[0378] The corresponding starting materials were hydrolyzed in the
conventional method to obtain the compounds shown in Table 40
below.
TABLE-US-00040 TABLE 40 Prep- aration Physical example constant,
No. Chemical structure Salt etc. 529 ##STR00454## Na Powder
ESI.cndot.MS (m/z): 372 (M - 2Na + H)- 530 ##STR00455## Na Powder
ESI.cndot.MS (m/z): 356 (M - Na)- 531 ##STR00456## Na Powder
ESI.cndot.MS (m/z): 388/390 (M - Na)-
Preparation Examples 532 to 536
[0379] The corresponding starting materials were treated in a
manner similar to Preparation example 227 to obtain the compounds
shown in Table 41 below.
TABLE-US-00041 TABLE 41 Preparation Physical constant, example No.
Chemical structure Salt etc. 532 ##STR00457## HCl Powder
MS.cndot.APCI (m/z): 269 (M + H) 533 ##STR00458## Free material
Powder MS.cndot.APCI (m/z): 388/390 (M + H)+ 534 ##STR00459## Free
material Powder MS.cndot.APCI (m/z): 398/400 (M + H)+ 535
##STR00460## Free material Powder MS.cndot.APCI (m/z): 416/418 (M +
H) 536 ##STR00461## Free material Powder MS.cndot.APCI (m/z):
408/410 (M + H)+
Preparation Example 537
[0380] A mixture of ethyl
3-bromo-4-(5-chlorothiophen-2-yl)-4-oxo-butyrate (651 mg) and
4-fluorothiobenzamide (310 mg) in N,N-dimethylformamide (10 ml) was
stirred at 70.degree. C. for 2 hours. After cooling, water was
added to the reaction mixture, and extracted with ethyl acetate.
The organic layer was washed with water and brine, dried over
anhydrous sodium sulfate, and the solvent was removed under reduced
pressure. The resulting residue was purified by NH silica gel
column chromatography (solvent: hexane:ethyl acetate=10:1) to
obtain ethyl
4-(5-chlorothiophen-2-yl)-2-(4-fluorophenyl)thiazol-5-yl acetate
(471 mg).
[0381] MS.cndot.APCI (m/z): 382/284 (MH+)
Preparation Examples 538 to 567
[0382] The corresponding starting materials were treated in a
manner similar to Preparation example 537 to obtain the compounds
shown in Table 42 below.
TABLE-US-00042 TABLE 42 Preparation Physical constant, example No.
Chemical structure Salt etc. 538 ##STR00462## Free material Powder
.sup.1H-NMR 300 MHz (DMSO-d.sub.6) .delta. 3.11 (6H, s), 3.70 (3H,
s), 4.05 (2H, s), 6.74 (1H, dd), 7.52-7.58 (2H, m), 7.64-7.77 (2H,
m), 8.00 (1H, dd), 8.63-8.65 (2H, m) 539 ##STR00463## Free material
Powder MS.cndot.APCI (m/z): 374/376 (M + H)+ 540 ##STR00464## Free
material Powder MS.cndot.APCI (m/z): 400/402 (M + H)+ 541
##STR00465## Free material Powder MS.cndot.APCI (m/z): 362/364 (M +
H)+ 542 ##STR00466## Free material Powder MS.cndot.APCI (m/z):
410/412(M + H)+ 543 ##STR00467## Free material Powder MS.cndot.APCI
(m/z): 407/409 (M + H)+ 544 ##STR00468## Free material Powder
MS.cndot.APCI (m/z): 398/400 (M + H)+ 545 ##STR00469## Free
material Powder MS.cndot.APCI (m/z): 398/400 (M + H)+ 546
##STR00470## Free material Powder MS.cndot.APCI (m/z): 409/411 (M +
H)+ 547 ##STR00471## Free material Powder MS.cndot.APCI (m/z):
395/397 (M + H)+ 548 ##STR00472## Free material Oil MS.cndot.APCI
(m/z): 374 (M + H)+ 549 ##STR00473## Free material Powder
MS.cndot.APCI (m/z): 375 (M + H)+ 550 ##STR00474## Free material
Oil MS.cndot.APCI (m/z): 348 (M + H)+ 551 ##STR00475## Free
material Powder MS.cndot.APCI (m/z): 386 (M + H)+ 552 ##STR00476##
Free material Powder MS.cndot.APCI (m/z): 360 (M + H)+ 553
##STR00477## Free material Oil MS.cndot.APCI (m/z): 360 (M + H)+
554 ##STR00478## Free material Powder MS.cndot.APCI (m/z): 420/422
(M + H)+ 555 ##STR00479## Free material Powder MS.cndot.APCI (m/z):
421/423 (M + H)+ 556 ##STR00480## Free material Powder
MS.cndot.APCI (m/z): 394/396 (M + H)+ 557 ##STR00481## Free
material Powder MS.cndot.APCI (m/z): 432/434 (M + H)+ 558
##STR00482## Free material Powder MS.cndot.APCI (m/z): 406/408 (M +
H)+ 559 ##STR00483## Free material Powder MS.cndot.APCI (m/z):
420/422 (M + H)+ 560 ##STR00484## Free material Powder
MS.cndot.APCI (m/z): 412/414 (M + H)+ 561 ##STR00485## Free
material Powder MS.cndot.APCI (m/z): 374 (M + H)+ 562 ##STR00486##
Free material Powder MS.cndot.APCI (m/z): 375 (M + H)+ 563
##STR00487## Free material Powder MS.cndot.APCI (m/z): 348 (M + H)+
564 ##STR00488## Free material Powder MS.cndot.APCI (m/z): 386 (M +
H)+ 565 ##STR00489## Free material Powder MS.cndot.APCI (m/z):
392/394 (M + H)+ 566 ##STR00490## Free material Powder
MS.cndot.APCI (m/z): 394/396 (M + H)+ 567 ##STR00491## Free
material Powder MS.cndot.APCI (m/z): 408/410 (M + H)+
Preparation Examples 568 to 597
[0383] The corresponding starting materials were hydrolyzed in the
conventional manner to obtain the compounds shown in Table 43
below.
TABLE-US-00043 TABLE 43 Physical constant, Preparation example No.
Chemical structure Salt etc. 568 ##STR00492## Na Powder ESI MS
(m/z): 352/354 (M - Na)- 569 ##STR00493## Na Powder ESI MS (m/z):
390/392 (M - Na)- 570 ##STR00494## Na Powder ESI MS (m/z): 364/366
(M - Na)- 571 ##STR00495## Na Powder ESI MS (m/z): 378/380 (M -
Na)- 572 ##STR00496## Na Powder ESI MS (m/z): 384/386 (M - Na)- 573
##STR00497## Na Powder ESI MS (m/z): 346 (M - Na)- 574 ##STR00498##
Na Powder ESI MS (m/z): 384/386 (M - Na)- 575 ##STR00499## Na
Powder ESI MS (m/z): 358/360 (M - Na)- 576 ##STR00500## Na Powder
ESI MS (m/z): 372/374 (M - Na)- 577 ##STR00501## Na Powder ESI MS
(m/z): 318 (M - Na)- 578 ##STR00502## Na Powder ESI MS (m/z): 330
(M - Na)- 579 ##STR00503## Na Powder ESI MS(m/z): 344 (M - Na)- 580
##STR00504## Na Powder ESI MS (m/z): 345 (M - Na)- 581 ##STR00505##
Na Powder ESI MS (m/z): 391/393 (M - Na)- 582 ##STR00506## Na
Powder ESI MS (m/z): 376/378 (M - Na)- 583 ##STR00507## Na Powder
ESI MS (m/z): 358/360 (M - Na)- 584 ##STR00508## Na Powder ESI MS
(m/z): 364/366 (M - Na)- 585 ##STR00509## Na Powder ESI MS (m/z):
390/392 (N - Na)- 586 ##STR00510## Na Powder ESI MS (m/z): 379/381
(M - Na)- 587 ##STR00511## Na Powder ESI MS (m/z): 368/370 (M -
Na)- 588 ##STR00512## Na Powder ESI MS (m/z): 368/370 (M - Na)- 589
##STR00513## Na Powder ESI MS (m/z): 377/379 (M - Na)- 590
##STR00514## Na Powder ESI MS (m/z): 380/382 (M - Na)- 591
##STR00515## Na Powder ESI MS (m/z): 365/367 (M - Na)- 592
##STR00516## Na Powder ESI MS (m/z): 356 (M - Na)- 593 ##STR00517##
Na Powder ESI MS (m/z): 356 (M - Na)- 594 ##STR00518## Na Powder
ESI MS (m/z): 318 (M - Na)- 595 ##STR00519## Na Powder ESI MS
(m/z): 345 (M - Na)- 596 ##STR00520## Na Powder ESI MS (m/z): 344
(M - Na)- 597 ##STR00521## Na Powder ESI MS (m/z): 330 (M -
Na)-
Preparation Examples 598 to 599
[0384] The corresponding starting materials were treated in a
manner similar to Preparation example 359 to obtain the compounds
shown in Table 44 below.
TABLE-US-00044 TABLE 44 Preparation Chemical Physical example No.
structure Salt constant, etc. 598 ##STR00522## Free material Powder
MS APCI (m/z): 389/391 (M + H)+ 599 ##STR00523## Free material
Powder MS APCI (m/z): 409/411 (M + H)+
Preparation Examples 600 to 601
[0385] The corresponding starting materials were hydrolyzed in the
conventional manner to obtain the compounds shown in Table 45
below.
TABLE-US-00045 TABLE 45 Physical constant, Preparation example No.
Chemical structure Salt etc. 600 ##STR00524## Na Powder ESI MS
(m/z): 379/381 (M - Na) 601 ##STR00525## Na Powder ESI MS (m/z):
373/375 (M -Na)-
Preparation Example 602
[0386] A mixture of ethyl
3-amino-4-(5-chlorothiophen-2-yl)-4-oxobutyrate hydrochloride (596
mg), 4-fluorobenzoyl chloride (380 mg) and sodium hydrogen
carbonate (1.0 g) in ethyl acetate (10 ml) and water (10 ml) was
stirred at room temperature for 2 hours. To the reaction mixture
were added ethyl acetate (30 ml) and water (30 ml), and the organic
layer was collected. The organic layer was washed with water and
brine, dried over anhydrous magnesium sulfate and the solvent was
removed under reduced pressure. The resulting residue was
triturated with hexane to obtain a crude product of ethyl
4-(5-chlorothiophen-2-yl)-3-[(4-fluorobenzoyl)amino]-4-oxobutyrate
(732 mg) as colorless powder.
[0387] A mixture of ethyl
4-(5-chlorothiophen-2-yl)-3-[(4-fluorobenzoyl)amino]-4-oxobutyrate
(720 mg) and
2,4-bis(4-methoxyphenyl)-1,3-dithia-2,4-diphosphetan-2,4-disulfid-
e (1.14 g) in tetrahydrofuran (20 ml) was refluxed for 2.5 hours.
The reaction mixture was cooled and purified by silica gel column
chromatography (solvent: hexane:ethyl acetate=20:1), and triturated
with hexane to obtain ethyl
5-(5-chlorothiophen-2-yl)-2-(4-fluorophenyl)thiazol-4-yl acetate
(667 mg) as yellowish powder.
[0388] MS.cndot.APCI (m/z): 382/284 (MH+)
Preparation Examples 603 to 607
[0389] The corresponding starting materials were treated in a
manner similar to Preparation example 602 to obtain the compounds
shown in Table 46 below.
TABLE-US-00046 TABLE 46 Preparation Chemical Physical example No.
structure Salt constant, etc. 603 ##STR00526## Free material Powder
MS APCI (m/z): 398/400 (M + H)+ 604 ##STR00527## Free material
Powder MS APCI (m/z): 420/422 (M + H)+ 605 ##STR00528## Free
material Powder MS APCI (m/z): 394/396 (M + H)+ 606 ##STR00529##
Free material Powder MS APCI (m/z): 409/411 (M + H)+ 607
##STR00530## Free material Powder MS APCI (m/z): 408/410 (M +
H)+
Preparation Examples 608 to 612
[0390] The corresponding starting materials were hydrolyzed in the
conventional manner to obtain the compounds shown in Table 47
below.
TABLE-US-00047 TABLE 47 Physical Preparation example No. Chemical
structure Salt constant, etc. 608 ##STR00531## Na Powder ESI MS
(m/z): 378/380 (M - Na)- 609 ##STR00532## Na Powder ESI MS (m/z):
364/366 (M - Na)- 610 ##STR00533## Na Powder ESI MS (m/z): 390/392
(M - Na)- 611 ##STR00534## Na Powder ESI MS (m/z): 379/381 (M -
Na)- 612 ##STR00535## Na Powder ESI MS (m/z): 368/370 (M - Na)-
Preparation Examples 613 to 622
[0391] In accordance with the above-mentioned preparation examples
or the conventionally known preparation processes, the compounds
shown in Table 48 below were obtained.
[0392] 10
TABLE-US-00048 TABLE 48 Physical Preparation example No. Chemical
structure Salt constant, etc. 613 ##STR00536## Free material 614
##STR00537## Na Powder ESI MS (m/z): 302 (M - Na) 615 ##STR00538##
Free material 616 ##STR00539## Free material 617 ##STR00540## Free
material 618 ##STR00541## Free material Crystal Melting point:
207-209.degree. C. 619 ##STR00542## Free material Crystal Melting
point: 110-111.degree. C. 620 ##STR00543## Na Powder ESI MS (m/z):
328/330 (M - Na)- 621 ##STR00544## Free material Powder 622
##STR00545## Free material Crystal Melting point: 213-214.degree.
C.
Preparation Examples 623 to 631
[0393] According to the preparation example 129, 130, 135, 148, 152
or 330 mentioned above, the compounds shown in Table 49 below were
obtained.
TABLE-US-00049 TABLE 49 Preparation Chemical Physical example No.
structure Salt constant, etc. 623 ##STR00546## Free material
Crystal Melting point: 208-210.degree. C. MS APCI (m/z): 338 (M +
H) 624 ##STR00547## Free material Crystal Melting point:
173-174.5.degree. C. MS APCI (m/z): 322 (M + H) 625 ##STR00548##
Free material Crystal Melting point: 111-112.degree. C. MS APCI
(m/z): 486 (M + H) 626 ##STR00549## Na Powder ESI MS (m/z): 348/350
(M - Na)- 627 ##STR00550## Na Powder ESI MS (m/z): 351/353 (M -
Na)- 628 ##STR00551## Na Powder MS APCI (m/z): 363 /365 (M - Na)-
629 ##STR00552## Free material Solid MS APCI (m/z): 393/395 (M + H)
630 ##STR00553## Na Powder ESI MS (m/z): 358/360 (M - Na)- 631
##STR00554## Na Powder ESI MS (m/z): 359/361 (M - Na)-
Preparation Example 632
[0394] (1) Ethyl 2-(4-chlorophenyl)-5-phenylthiazol-4-ylacetate
(4.5 g) was dissolved in methanol (50 ml), and ammonia was
saturated in the solution at 0.degree. C. and the resulting mixture
was allowed to stand at room temperature for 3 days. After removing
the solvent, methanol was added to the residue. The resulting
precipitate was collected and dried to obtain
2-(4-chlorophenyl)-5-phenylthiazol-4-yl acetamide (4.2 g).
[0395] Melting point: 202-203.degree. C.
[0396] MS.cndot.EI (m/z): 328 (M+)
[0397] (2) To a solution of 2-(4-chlorophenyl)-5-phenylthiazol-4-yl
acetamide (3.4 g) and phosphorus oxychloride (3 ml) in chloroform
(50 ml) was added one drop of pyridine, and the mixture was
refluxed for 8 hours. Cold diluted aqueous ammonia was poured into
the mixture and the organic layer was collected. After removing the
solvent under reduced pressure, ethanol was added to the residue
and crystal was collected by filtration to obtain
2-(4-chlorophenyl)-5-phenylthiazol-4-yl acetonitrile (3.1 g).
[0398] Melting point: 118-120.degree. C.
[0399] MS.cndot.EI (m/z): 310 (M+)
[0400] (3) To a solution of 2-(4-chlorophenyl)-5-phenylthiazol-4-yl
acetonitrile (2.33 g) in N,N-dimethylformamide (30 ml) were added
sodium azide (1.40 g) and ammonium chloride (1.3 g), and the
mixture was stirred at 90.degree. C. for 12 hours. After removing
the solvent under reduced pressure, ethyl acetate and water were
added to the residue. The organic layer was collected, dried and
the solvent was removed under reduced pressure. The residue was
recrystallized from chloroform and methanol to obtain
5-[2-(4-chlorophenyl)-5-phenyl-thiazol-4-ylmethyl]tetrazole (1.75
g).
[0401] Melting point: 213-214.degree. C.
[0402] MS.cndot.EI (m/z): 353 (M+)
Preparation Examples 633 to 641
[0403] The corresponding starting materials were treated in a
manner similar to Preparation example 43, 135, 608 or the
conventionally known processes to obtain the compounds shown in
Table 50 below.
TABLE-US-00050 TABLE 50 Preparation Physical example No. Chemical
structure Salt constant, etc. 633 ##STR00555## Free material Solid
MS.cndot.APCI (m/z): 397/399 (M + H)+ 634 ##STR00556## Free
material Powder MS.cndot.APCI (m/z): 392/394 (M + H)+ 635
##STR00557## Free material Powder MS.cndot.APCI (m/z): 377/379 (M +
H)+ 636 ##STR00558## Free material Powder MS.cndot.APCI (m/z):
391/393 (M + H)+ 637 ##STR00559## Free material Powder
MS.cndot.APCI (m/z): 402/404 (M + H)+ 638 ##STR00560## Free
material Powder MS.cndot.APCI (m/z): 308 (MH+) 639 ##STR00561##
1HCl Crystal Melting point: 203-204.degree. C. EI.cndot.MS (m/z):
298 (M.sup.+ - 16)+ 640 ##STR00562## Na Powder ESI.cndot.MS (m/z):
352 (M - Na) 641 ##STR00563## Free material
Reference Examples 642 to 644
[0404] The following compounds listed in Table 50a were prepared in
a manner similar to Example 608 or 632, or similar to that
described in Japanese Provisional Patent Publication No.
167685/1986.
TABLE-US-00051 TABLE 50a Preparation Physical example No. Chemical
structure Salt constant, etc. 642 ##STR00564## Free Powder
ESI.cndot.MS (m/z): 414/416 (M - H)- 643 ##STR00565## Na Powder
ESI.cndot.MS (m/z): 334 (M - Na)- 644 ##STR00566## Free
Reference Example 1
[0405] (1) A mixture of 2-acetylpyrimidine (2.90 g), hydroxylamine
hydrochloride (2.48 g) and triethylamine (5.3 ml) in ethanol (40
ml) was stirred at room temperature overnight. The reaction mixture
was poured into water, and extracted with methylene chloride. The
organic layer was washed with a saturated aqueous ammonium sulfate
solution and brine, dried over anhydrous sodium sulfate, and the
solvent was removed under reduced pressure to obtain
2-acetylpyrimidine oxime (4.44 g) as colorless powder.
[0406] MS.cndot.APCI (m/z): 138 (MH+)
[0407] (2) A mixture of 2-acetylpyrimidine oxime (4.40 g) and
p-toluenesulfonyl chloride (6.79 g) in pyridine (40 ml) was stirred
at room temperature overnight. The reaction mixture was poured into
ice-water and precipitated crude product was collected by
filtration. The filtrate was neutralized by 10% hydrochloric acid
and extracted with ethyl acetate. The organic layer was washed with
water and brine, dried over anhydrous sodium sulfate and the
solvent was removed under reduced pressure. The resulting residue
and the crude product previously obtained were combined and
triturated with diethyl ether to obtain
O-p-toluenesulfonyl-2-acetylpyrimidine oxime (4.53 g) as colorless
powder.
[0408] (3) To ice-cooled ethanol (19 ml) was added sodium hydride
(681 mg, 60% mineral oil) and the mixture was stirred at room
temperature for 30 minutes. To the solution was added dropwise a
solution of O-p-toluenesulfonyl-2-acetylpyrimidine oxime (4.51 g)
in ethanol (16 ml) and of tetrahydrofuran (10 ml) under
ice-cooling, and the resulting mixture was stirred at room
temperature for 1.5 hours. To the reaction mixture was added
diethyl ether (150 ml) and precipitated insoluble material was
removed by filtration. The filtrate was extracted with 2N
hydrochloric acid and the aqueous layer was concentrated under
reduced pressure. The resulting residue was triturated with
acetone-ethanol to obtain 2-(2-aminoacetyl)pyrimidine hydrochloride
(2.87 g) as pale brownish powder.
[0409] MS.cndot.APCI (m/z): 138 (MH+)
Reference Examples 2 to 4
[0410] Corresponding starting compounds were treated in a manner
similar to Reference example 1 to obtain the compounds shown in
Table 51 below.
TABLE-US-00052 TABLE 51 Reference Physical constant, example No.
Chemical structure Salt etc. 2 ##STR00567## 1HCl Powder
MS.cndot.APCI (m/z): 143 (M + H)+ 3 ##STR00568## 1HCl Powder
MS.cndot.APCI (m/z): 143 (M + H)+ 4 ##STR00569## 1HCl Powder
MS.cndot.APCI (m/z): 138 (M + H)+
Reference Example 5
[0411] (1) To a solution of 1-(3-pyridyl)-1-butanone (20.0 g) in
47% aqueous hydrobromic acid (40 ml) and acetic acid (40 ml) was
added bromine (15.2 ml), and the mixture was stirred at 60.degree.
C. for 30 minutes. The reaction mixture was poured into ice-water,
and after adding a saturated aqueous sodium thiosulfate solution,
potassium carbonate was added to the mixture to adjust pH to 4. The
reaction mixture was extracted with ethyl acetate, washed
successively with a saturated aqueous sodium hydrogen carbonate
solution and brine, and dried over anhydrous sodium sulfate. The
solvent was removed under reduced pressure to obtain a crude
product of 2-bromo-1-(3-pyridyl)-1-butanone (30.15 g) as brownish
oil.
[0412] (2) The crude product obtained in the above (1) was
dissolved in N,N-dimethylformamide (100 ml), and sodium azide (9.50
g) was added to the solution under ice-cooling and the resulting
mixture was stirred at room temperature for one hour. Water was
added to the reaction mixture, the mixture was extracted with ethyl
acetate three times, and combined organic layers was washed with
brine, and dried over anhydrous sodium sulfate. The solvent was
removed under reduced pressure and the residue was purified by
silica gel flush column chromatography (solvent: n-hexane:ethyl
acetate=2:1) to obtain 2-azido-1-(3-pyridyl)-1-butanone (18.65 g)
as yellowish oil.
[0413] MS.cndot.APCI (m/z): 191 (MH+)
[0414] (3) A mixture of 2-azido-1-(3-pyridyl)-1-butanone (18.60 g),
di-t-butyldicarbonate (23.50 g) and 10% palladium-carbon (2.70 g)
in methanol (200 ml) was stirred under hydrogen atmosphere at room
temperature for one hour. After removing the palladium-carbon by
filtration, the solvent was removed under reduced pressure and the
residue was purified by silica gel flush column chromatography
(solvent: hexane:ethyl acetate=2:1.fwdarw.1:1) to obtain
2-(t-butoxycarbonylamino)-1-(3-pyridyl)-1-butanone (20.53 g) as
yellowish red oil.
[0415] (4) A mixture of
2-(t-butoxycarbonylamino)-1-(3-pyridyl)-1-butanone (20.50 g) and 6N
hydrochloric acid (38.8 ml) in ethanol (100 ml) was refluxed for
one hour. After cooling, the reaction mixture was concentrated
under reduced pressure and the resulting residue was triturated
with ethanol-ethylacetate (1:1) to obtain
2-amino-1-(3-pyridyl)-1-butanone dihydrochloride (13.40 g) as pale
reddish purple crystalline powder.
[0416] Melting point: 199 to 201.degree. C. (decomposed)
Reference Examples 6 to 8
[0417] Corresponding starting compounds were treated in a manner
similar to Reference example 5 to obtain the compounds shown in
Table 52 below.
TABLE-US-00053 TABLE 52 Reference example Physical No. Chemical
structure Salt constant, etc. 6 ##STR00570## 1HCl Powder
MS.cndot.APCI (m/z): 184 (M + H) + 7 ##STR00571## 1HCl Crystal
Melting point: 156-158.degree. C. MS.cndot.APCI (m/z): 178 (M + H)+
8 ##STR00572## 1HCl Powder MS.cndot.APCI (m/z): 164 (M + H)+
Reference Example 9
[0418] To a solution of an acid chloride product prepared from
6-methyl nicotinic acid (245 mg) in chloroform (10 ml) were added
2-amino-1-(3-pyridyl)-1-butanone dihydrochloride (356 mg) and
triethylamine (1.05 ml), and the mixture was stirred for 30
minutes. The mixture was poured into water and extracted with ethyl
acetate. The organic layer was collected, washed with brine and
dried over anhydrous sodium sulfate. The solvent was removed under
reduced pressure to obtain a crude product of
2-(6-methylnicotynoylamino)-1-(3-pyridyl)-1-butanone (425 mg).
Reference Example 10
[0419] (1) A mixture of 3-(2-aminoacetyl)pyridine dihydrochloride
(50.00 g), 4-fluorobenzoyl chloride (41.71 g) and sodium hydrogen
carbonate (100.44 g) in ethyl acetate (1 liter) and water (0.6
liter) was stirred at room temperature for 2 hours. To the reaction
mixture were added tetrahydrofuran (0.5 liter) and water (1 liter),
and the organic layer was collected. The organic layer was washed
with water and brine, dried over anhydrous magnesium sulfate and
the solvent was removed under reduced pressure. The resulting
residue was triturated with ethyl acetate to obtain
3-[2-(4-fluorobenzoyl)aminoacetyl]pyridine (40.87 g) as pale
yellowish powder.
[0420] Melting point: 164.5 to 165.5.degree. C.
[0421] MS.cndot.APCI (m/z): 259 (MH+)
[0422] (2) To a solution of
3-[2-(4-fluorobenzoyl)aminoacetyl]-pyridine (500 mg) in
N,N-dimethylformamide (10 ml) were added sodium hydride (81.3 mg,
60% mineral oil) and acrylonitrile (113 mg) under dry ice-acetone
cooling, and the mixture was stirred at the same temperature under
argon atmosphere for 10 minutes. The mixture was warmed slowly to
0.degree. C. and stirred at the same temperature for 30 minutes. To
the reaction mixture was added a saturated aqueous ammonium
chloride solution and the mixture was extracted with ethyl acetate.
The organic layer was washed with brine, dried over anhydrous
sodium sulfate and the solvent was removed under reduced pressure
to obtain a crude product of
4-cyano-2-(4-fluorobenzoylamino)-1-(3-pyridyl)-1-butanone (500
mg).
Reference Example 11
[0423] (1) To acetic anhydride (2.39 ml) was added dropwise formic
acid (0.97 ml) under ice-cooling, and the mixture was stirred at
50.degree. C. for 30 minutes. The mixture was ice-cooled again, and
diluted with tetrahydrofuran (9 ml). To the mixture were added
2-amino-1-(3-pyridyl)-1-butanone dihydrochloride (600 mg) and
triethylamine (1.41 ml), and the mixture was stirred under
ice-cooling for 1.5 hours. To the reaction mixture was added a
saturated aqueous sodium hydrogen carbonate solution, and the
mixture was extracted with ethyl acetate. The organic layer was
washed with brine, dried over anhydrous sodium sulfate and the
solvent was removed under reduced pressure. The resulting residue
was triturated with ethyl acetate-diethyl ether to obtain
2-formylamino-1-(3-pyridyl)-1-butanone (440 mg) as colorless
powder.
[0424] MS.cndot.APCI (m/z): 193 (MH+)
[0425] (2) A mixture of 2-formylamino-1-(3-pyridyl)-1-butanone (640
mg) and ammonium acetate (5.13 g) in acetic acid (5 ml) was stirred
at 100.degree. C. for 1.5 hours. After cooling, 28% aqueous ammonia
was added to the reaction mixture and the mixture was extracted
with chloroform. The organic layer was washed with brine, dried
over anhydrous sodium sulfate and the solvent was removed under
reduced pressure. The resulting residue was triturated with ethyl
acetate-diethyl ether to obtain 5-ethyl-4-(3-pyridyl)imidazole (520
mg) as colorless powder.
[0426] MS.cndot.APCI (m/z): 174 (MH+)
[0427] (3) To a solution of 5-ethyl-4-(3-pyridyl)imidazole (1.50 g)
and potassium acetate (2.55 g) in methanol (40 ml) was added iodine
(2.86 g), and the mixture was stirred at room temperature
overnight. To the reaction mixture were added water and ethyl
acetate, and the organic layer was collected, washed with a
saturated aqueous sodium thiosulfate solution and brine and dried
over anhydrous sodium sulfate, and the solvent was removed under
reduced pressure. The resulting residue was purified by NH silica
gel flush column chromatography (solvent: ethyl acetate) to obtain
5-ethyl-2-iodo-4-(3-pyridyl)imidazole (1.75 g).
[0428] MS.cndot.APCI (m/z): 300 (MH+)
Reference Example 12
[0429] (1) A mixture of methyl .alpha.-amino-2-thiophene acetate
(1.48 g), 4-fluorobenzoyl chloride (1.64 g) and sodium hydrogen
carbonate (2.89 g) in methylene chloride (20 ml) and water (20 ml)
was stirred at room temperature overnight. The organic layer was
collected, washed with water and brine, and the solvent was removed
under reduced pressure. The resulting residue was triturated with
ethyl acetate-hexane to obtain methyl
.alpha.-(4-fluorobenzoylamino)-2-thiophene acetate (2.40 g) as
colorless powder.
[0430] MS.cndot.APCI (m/z): 294 (MH+)
[0431] (2) To a solution of diisopropylamine (2.48 g) in
tetrahydrofuran (45 ml) was added dropwise 1.6M n-butyl lithium
(15.71 ml, n-hexane solution) under argon atmosphere at -78.degree.
C., and after stirring for 30 minutes, a solution of ethyl acetate
(2.16 g) in tetrahydrofuran (5 ml) was added dropwise to the
mixture and the resulting mixture was further stirred for 30
minutes. To the mixture was slowly added a solution of methyl
.alpha.-(4-fluorobenzoylamino)-2-thiophene acetate (2.40 g) in
tetrahydrofuran (15 ml), and the mixture was stirred for one hour.
To the reaction mixture were added a saturated aqueous ammonium
chloride solution and the mixture was extracted with ethyl acetate.
The organic layer was washed with water and brine, dried over
anhydrous sodium sulfate and the solvent was removed under reduced
pressure. The resulting residue was purified by silica gel flush
column chromatography (solvent: chloroform:ethanol=100:1) to obtain
ethyl 4-(4-fluorobenzoylamino)-4-(2-thienyl)acetoacetate (2.53 g)
as yellowish oil.
[0432] MS.cndot.APCI (m/z): 350 (MH+)
Reference Example 13
[0433] (1) To a solution of benzo[b]furan-5-carboxylic acid (1.30
g) and of methyl isocyanoacetate (834 mg) in N,N-dimethylformamide
(10 ml) were added diethyl cyanophosphate (1.33 ml) and
triethylamine (3.6 ml) at room temperature, and the mixture was
stirred overnight. After removing the solvent under reduced
pressure, an aqueous citric acid solution and ethyl acetate were
added to the residue, the organic layer was collected, washed
successively with an aqueous citric acid solution, water, a
saturated aqueous sodium hydrogen carbonate solution and brine,
dried over anhydrous sodium sulfate, and the solvent was removed
under reduced pressure. The resulting residue was purified by
silica gel column chromatography (solvent: n-hexane:ethyl
acetate=1:1) to obtain a crude product of methyl
5-(5-benzo[ID]furyl)oxazol-4-carboxylate (1.14 g).
[0434] (2) To a solution of the crude product of methyl
5-(5-benzo[b]furyl) oxazol-4-carboxylate (1.14 g) in methanol (20
ml) and tetrahydrofuran (5 ml) was added conc. hydrochloric acid (8
ml), and the mixture was stirred overnight. The reaction mixture
was concentrated under reduced pressure and the resulting residue
was triturated with methanol-diethyl ether-acetone to obtain
5-(aminoacetyl)benzo[ID]furan hydrochloride (600 mg).
[0435] MS.cndot.APCI (m/z): 176 (MH+)
Reference Example 14
[0436] Corresponding starting compounds were treated in a manner
similar to Reference example 13(1) and (2) to obtain the compounds
shown in Table 53 below.
TABLE-US-00054 TABLE 53 Reference example Physical No. Chemical
structure Salt constant, etc. 14 (1) ##STR00573## Free material
Solid MS.cndot.APCI (m/z): 244 (M + H)+ 14 (2) ##STR00574## 1HCl
Powder MS.cndot.APCI (m/z): 176 (M + H)+
Reference Examples 15 to 19
[0437] Corresponding starting compounds were treated in a manner
similar to Reference example 10 (1) to obtain the compounds shown
in Table 54 below.
TABLE-US-00055 TABLE 54 Reference example Physical No. Chemical
structure Salt constant, etc. 15 ##STR00575## Free material Powder
MS.cndot.APCI (m/z): 298 (M + H)+ 16 ##STR00576## Free material
Powder MS.cndot.APCI (m/z): 298 (M + H)+ 17 ##STR00577## Free
material Powder MS.cndot.APCI (m/z): 320 (M + H)+ 18 ##STR00578##
Free material Powder MS.cndot.APCI (m/z): 320 (M + H)+ 19
##STR00579## Free material Powder MS.cndot.APCI (m/z): 281/283 (M +
H)+
Reference Example 20
[0438] (1) To a solution of 2-chloro-5-(bromoacetyl)thiophene
(28.04 g) in acetonitrile (150 ml) was added sodium diformylimide
(13.35 g), and the mixture was stirred at room temperature for 45
minutes followed by stirring at 50.degree. C. for 2.5 hours. The
reaction mixture was filtered through Celite, insoluble material
was washed with tetrahydrofuran, the filtrate and the washed
solution were combined and the solvent was removed under reduced
pressure. The residue was crystallized from diisopropyl ether to
obtain a crude crystal of 2-chloro-5-(diformylaminoacetyl)thiophene
(20.63 g).
[0439] (2) To the crude crystal of
2-chloro-5-(diformylaminoacetyl)-thiophene were added potassium
hydroxide (0.60 g), ethanol (70 ml) and tetrahydrofuran (40 ml),
and the mixture was stirred at room temperature for one hour. After
removing the solvent under reduced pressure, tetrahydrofuran (150
ml) and anhydrous magnesium sulfate were added to the residue, and
insoluble material was removed by filtration and washed with
tetrahydrofuran. The filtrate and the washed solution were combined
and the solvent was removed under reduced pressure. The residue was
crystallized from diisopropyl ether-ethyl acetate to obtain
2-chloro-5-(formylaminoacetyl)thiophene (14.81 g) as pale brownish
crystal.
[0440] Melting point: 111 to 113.degree. C.
[0441] MS.cndot.APCI (m/z): 204 (MH+)
[0442] (3) To a solution of 2-chloro-5-(formylaminoacetyl)thiophene
(20.1 g) in N,N-dimethylformamide (400 ml) was added sodium hydride
(4.44 g, 60% mineral oil) under ice-cooling, and the mixture was
stirred under argon atmosphere at room temperature for one hour.
After ice-cooling, to the mixture was added dropwise ethyl
bromoacetate (20.8 g), and the mixture was stirred at room
temperature for 2 hours. After cooling, ice was added to the
reaction mixture, and then water and ethyl acetate were also added
to the mixture. The organic layer was collected, washed with water
and brine, dried over anhydrous sodium sulfate and the solvent was
removed under reduced pressure. The resulting residue was purified
by silica gel column chromatography (solvent: n-hexane:ethyl
acetate-6:1) to obtain ethyl
4-(5-chlorothiophen-2-yl)-3-formylamino-4-oxobutyrate (17.8 g) as
yellowish oil.
[0443] MS.cndot.APCI (m/z): 290/292 (MH+)
[0444] (4) To a solution of
4-(5-chlorothiophen-2-yl)-3-formyl-amino-4-oxobutyrate (17.8 g) in
ethanol (178 ml) was added 4N hydrogen chloride-dioxane solution
(178 ml) under ice-cooling, and the mixture was stirred at room
temperature for 18 hours. After completion of the reaction, the
solvent was removed under reduced pressure, and the resulting
residue was triturated with ethyl acetate to obtain ethyl
4-(5-chlorothiophen-2-yl)-3-amino-4-oxobutyrate hydrochloride (14.2
g) as colorless powder.
[0445] MS.cndot.APCI (m/z): 262/264 (MH+)
Reference Example 21
[0446] Corresponding starting compounds were treated in a manner
similar to Reference example 20 (1) to (4) to obtain the compounds
shown in Table 55 below.
TABLE-US-00056 TABLE 55 Reference example Physical No. Chemical
structure Salt constant, etc. 21 (1) ##STR00580## Free material
Powder MS.cndot.APCI (m/z): 170 (M + H)+ 21 (2) ##STR00581## Free
material Powder MS.cndot.APCI (m/z): 256 (M + H)+ 21 (3)
##STR00582## 1HCl Powder MS.cndot.APCI (m/z): 228 (M + H)+
Reference Example 22
[0447] (1) A mixed solution of (3-methyl N-(5-benzo[b]furoyl)
aspartate (1.0 g) and acetic anhydride (10 ml) was stirred at
85.degree. C. for one hour. The reaction mixture was cooled to room
temperature and the solvent was removed under reduced pressure. The
resulting residue was crystallized from n-hexane-diethyl ether to
obtain
2-(5-benzo[b]furyl)-4-methoxycarbonylmethyl-5-oxo-2-oxazoline (751
mg) as colorless powder.
[0448] (2) To a mixture of
2-(5-benzo[b]furyl)-4-methoxycarbonyl-methyl-5-oxo-2-oxazoline (410
mg) and 3-thenoyl chloride (242 mg) in ethyl acetate (8 ml) was
added triethyl amine (0.23 ml) under ice-cooling, and the mixture
was stirred at room temperature for 0.5 hour. Ethyl acetate was
added to the mixture, the mixture was filtered and the resulting
filtrate was concentrated under reduced pressure. A mixture of the
resulting residue and pyridine (3.6 ml) was stirred at room
temperature for 10 minutes followed by stirring at 60.degree. C.
for 2 hours. Then, acetic acid (1.35 ml) was added to the mixture
and the resulting mixture was stirred at 80.degree. C. for 1.5
hours. After cooling, to the reaction mixture were added water and
ethyl acetate, the organic layer was collected, washed successively
with a 10% aqueous hydrochloric acid solution, a saturated aqueous
sodium hydrogen carbonate solution and brine, dried over anhydrous
sodium sulfate, and the solvent was removed under reduced pressure.
The resulting residue was purified by silica gel column
chromatography (solvent: hexane:ethyl acetate=5:1) to obtain methyl
3-(5-benzo[b]furoylamino)-4-(3-thienyl)-4-oxobutyrate (253 mg) as
colorless powder.
[0449] MS.cndot.APCI (m/z): 358 (MH+)
Reference Example 23
[0450] Corresponding starting compounds were treated in a manner
similar to Reference example 10(1) to obtain
2-[2-(4-fluorobenzoyl-amino)acetyl]thiophene.
Reference Example 24
[0451] (1) To a solution of methyl
5-(5-chlorothiophen-2-yl)oxazol-4-carboxylate (12.6 g) in methanol
(150 ml) was added 4N hydrogen chloride-dioxane solution (100 ml)
under argon atmosphere, and the mixture was stirred at 70.degree.
C. for overnight. The reaction mixture was cooled and the solvent
was removed under reduced pressure, and the resulting residue was
triturated with acetone to obtain methyl
2-amino-3-(5-chlorothiophen-2-yl)-3-oxo-propionate hydrochloride
(13.9 g) as colorless powder.
[0452] MS.cndot.APCI (m/z): 234 (MH+)
[0453] (2) A mixture of methyl
2-amino-3-(5-chlorothiophen-2-yl)-3-oxopropionate hydrochloride
(6.0 g), 4-fluorobenzoyl chloride (4.23 g) and sodium hydrogen
carbonate (11.2 g) in ethyl acetate (100 ml) and water (10 ml) was
stirred at room temperature for 2 hours. The organic layer was
collected, washed with water and brine, dried over anhydrous
magnesium sulfate and the solvent was removed under reduced
pressure. The resulting residue was triturated with diethyl ether
to obtain methyl
3-(5-chlorothiophen-2-yl)-2-(4-fluorobenzoylamino)-3-oxopropionate
(7.3 g) as colorless powder.
[0454] MS.cndot.APCI (m/z): 356/358 (MH+)
Reference Example 25
[0455] A mixture of 1,2,3,4-tetrahydroquinolin-6-carboxylic acid (2
g), 32% aqueous formalin solution (2 ml) and 10% palladium-carbon
(400 mg) in N,N-dimethylformamide (10 ml) was stirred under
hydrogen atmosphere at room temperature for one hour. After
removing the palladium-carbon by filtration, the solvent was
removed under reduced pressure and the resulting residue was
triturated with diethyl ether to obtain
1-methyl-1,2,3,4-tetrahydroquinolin-6-carboxylic acid (1.98 g) as
yellowish powder.
[0456] ESI.cndot.MS (m/z): 190 (M-H).
Reference Example 26
[0457] Corresponding starting compounds were treated in a manner
similar to Reference example 25 to obtain
1-methylindolin-5-carboxylic acid.
[0458] ESI.cndot.MS (m/z): 176 (M-H)--
Reference Example 27
[0459] A mixture of methyl 6-methoxymethylnicotinate (737 mg) in a
2N aqueous sodium hydroxide solution (2 ml) and methanol (15 ml)
was refluxed overnight. After cooling, the reaction mixture was
concentrated under reduced pressure, and the resulting residue was
triturated with diethyl ether to obtain 6-methoxymethylnicotinic
acid sodium salt (754 .mu.g) as colorless powder.
[0460] ESI.cndot.MS (m/z): 166 (M-Na)
Reference Example 28
[0461] (1) To a solution of methyl 6-bromomethylnicotinate (350 mg)
in tetrahydrofuran (5 ml) was added a 50% aqueous dimethylamine
solution (3 ml), and the mixture was vigorously stirred at room
temperature for 10 minutes. To the reaction mixture was added water
and the mixture was extracted with ethyl acetate. The organic layer
was washed with water and brine, dried over anhydrous sodium
sulfate, and the solvent was removed under reduced pressure. The
resulting residue was purified by silica gel column chromatography
(solvent: chloroform:methanol=100:1) to obtain methyl
6-(dimethylamino)methylnicotinate (276 mg) as brownish powder.
[0462] MS.cndot.APCI (m/z): 195 (MH+)
[0463] (2) A mixture of methyl 6-(dimethylamino)methylnicotinate
(256 mg) and 10N hydrochloric acid was refluxed overnight. After
cooling, the reaction mixture was concentrated under reduced
pressure to obtain 6-(dimethylamino)methylnicotinic acid
hydrochloride (329 mg) as colorless powder.
[0464] MS.cndot.APCI (m/z): 181 (MH+)
Reference Example 29
[0465] To a suspension of 3-(2-aminoacetyl) pyridine
dihydrochloride (5.23 g) in chloroform (50 ml) were added
di-t-butyl dicarbonate (5.73 g) and triethylamine (10.5 ml), and
the mixture was stirred for one hour. Water was added to the
reaction mixture and the mixture was extracted with chloroform. The
organic layer was washed with water and brine, dried over anhydrous
sodium sulfate, and active charcoal was added thereto and insoluble
material was removed by filtration. The filtrate was concentrated
under reduced pressure, and the residue was purified by medium
pressure column chromatography (solvent: chloroform:
methanol=30:1.fwdarw.20:1), and triturated with diisopropyl ether
to obtain 3-(2-t-butoxycarbonylaminoacetyl)pyridine (3.20 g).
[0466] Melting point: 98 to 99.degree. C.
[0467] MS.cndot.APCI (m/z): 237 (MH+)
Reference Example 30
[0468] (1) A mixture of (2-methoxy) phenacyl bromide (550 mg) and
sodium diformylimide (274 mg) in acetonitrile (2.5 ml) was stirred
at room temperature for 30 minutes, and then, stirred at 70.degree.
C. for 24 hours. Insoluble material was removed by filtration,
washed with acetonitrile and the filtrate was concentrated under
reduced pressure. The residue was purified by silica gel column
chromatography (solvent: hexane:ethyl acetate=2:1), and triturated
with hexane-ethyl acetate to obtain
2-(diformyl-amino)-2'-methoxyacetophenone (4.40 g) as colorless
powder.
[0469] (2) A mixture of 2-(diformyl-amino)-2'-methoxyacetophenone
(3.28 g) and 5% hydrogen chloride-ethanol solution (37 ml) was
stirred at room temperature for 17 hours. The reaction mixture was
concentrated under reduced pressure and the residue was triturated
with diethyl ether. To the powder was again added 5% hydrogen
chloride-ethanol solution and the mixture was stirred at room
temperature for one day, and the mixture was concentrated under
reduced pressure. The residue was washed with diethyl ether and
ethyl acetate to obtain 2-amino-2'-methoxyaceto-phenone
hydrochloride (2.91 g) as colorless solid.
[0470] MS.cndot.APCI (m/z): 166 (MH+)
Reference Example 31
[0471] A mixture of methyl dl-.alpha.-amino-2-thiophene acetate
(5.59 g), N-chlorosuccinimide (4.67 g) and acetic acid (60 ml) was
stirred at room temperature overnight. The reaction mixture was
concentrated under reduced pressure, to the residue obtained was
added water, and the mixture was extracted with ethyl acetate. The
organic layer was washed with water and brine, dried over anhydrous
sodium sulfate, and the solvent was removed under reduced pressure.
To the resulting residue were added methanol (40 ml) and 4N
hydrogen chloride-dioxane solution (30 ml), the solvent was removed
under reduced pressure and the residue was triturated with using
diethyl ether and methanol to obtain methyl
dl-.alpha.-amino-2-(5-chlorothiophene)acetate hydrochloride (4.24
g) as pale brownish powder.
[0472] MS.cndot.APCI (m/z): 206/208 (MH+)
Reference Examples 32 to 46
[0473] Corresponding starting compounds were treated in a manner
similar to Reference example 12(1) to obtain the compounds shown in
Table 56 below.
TABLE-US-00057 TABLE 56 Reference example Physical No. Chemical
structure Salt constant, etc. 32 ##STR00583## Free material Powder
MS.cndot.APCI (m/z): 360/362 (M + H)+ 33 ##STR00584## Free material
Powder MS.cndot.APCI (m/z): 349/351 (M + H)+ 34 ##STR00585## Free
material Powder MS.cndot.APCI (m/z): 348/350 (M + H)+ 35
##STR00586## Free material Powder MS.cndot.APCI (m/z): 360/362 (M +
H)+ 36 ##STR00587## Free material Powder MS.cndot.APCI (m/z):
355/357 (M + H)+ 37 ##STR00588## Free material Powder MS.cndot.APCI
(m/z): 340/342 (M + H)+ 38 ##STR00589## Free material Powder
MS.cndot.APCI (m/z): 335/336 (M + H)+ 39 ##STR00590## Free material
Powder MS.cndot.APCI (m/z): 321 (M + H)+ 40 ##STR00591## Free
material Powder MS.cndot.APCI (m/z): 332 (M + H)+ 41 ##STR00592##
Free material Powder MS.cndot.APCI (m/z): 321 (M + H)+ 42
##STR00593## Free material Powder MS.cndot.APCI (m/z): 306 (M + H)+
43 ##STR00594## Free material Powder MS.cndot.APCI (m/z): 320 (M +
H)+ 44 ##STR00595## Free material Powder MS.cndot.APCI (m/z): 332
(M + H)+ 45 ##STR00596## Free material Powder MS.cndot.APCI (m/z):
366/368 (M + H) 46 ##STR00597## Free material Oil MS.cndot.APCI
(m/z): 354/356 (M + H)+
Reference Examples 47 to 61
[0474] Corresponding starting compounds were treated in a manner
similar to Reference example 12(2) to obtain the compounds shown in
Table 57 below.
TABLE-US-00058 TABLE 57 Reference example Physical No. Chemical
structure Salt constant, etc. 47 ##STR00598## Free material Powder
MS.cndot.APCI (m/z): 390/392 (M + H)+ 48 ##STR00599## Free material
Powder MS.cndot.APCI (m/z): 396/398 (M + H)+ 49 ##STR00600## Free
material Powder MS.cndot.APCI (m/z): 377 (M + H)+ 50 ##STR00601##
Free material Powder MS.cndot.APCI (m/z): 388 (M + H)+ 51
##STR00602## Free material Powder MS.cndot.APCI (m/z): 377 (M + H)+
52 ##STR00603## Free material Powder MS.cndot.APCI (m/z): 376 (M +
H)+ 53 ##STR00604## Free material Powder MS.cndot.APCI (m/z): 388
(M + H)+ 54 ##STR00605## Free material Oil MS.cndot.APCI (m/z): 362
(M + H)+ 55 ##STR00606## Free material Powder MS.cndot.APCI (m/z):
422/424 (M + H)+ 56 ##STR00607## Free material Crystal Melting
point: 126-128.degree. C. MS.cndot.APCI (m/z): 410/412 (M + H)+ 57
##STR00608## Free material Powder MS.cndot.APCI (m/z): 416/418 (M +
H)+ 58 ##STR00609## Free material Powder MS.cndot.APCI (m/z):
411/413 (M + H)+ 59 ##STR00610## Free material Powder MS.cndot.APCI
(m/z): 405/407 (M + H)+ 60 ##STR00611## Free material Powder
MS.cndot.APCI (m/z): 404/406 (M + H)+ 61 ##STR00612## Free material
Powder MS.cndot.APCI (m/z): 378/380 (M + H)+
Reference Examples 62 to 66
[0475] Corresponding starting compounds were treated in a manner
similar to Reference example 10 (1) to obtain the compounds shown
in Table 58 below.
TABLE-US-00059 TABLE 58 Reference Physical example constant, No.
Chemical structure Salt etc. 62 ##STR00613## Free material Powder
MS.cndot.APCI (m/z): 259 (M + H) 63 ##STR00614## Free material
Powder MS.cndot.APCI (m/z): 340/342 (M + H)+ 64 ##STR00615## Free
material Powder MS.cndot.APCI (m/z): 348/350 (M + H)+ 65
##STR00616## Free material Powder MS.cndot.APCI (m/z): 320/322 (M +
H)+ 66 ##STR00617## Free material Powder MS.cndot.APCI (m/z):
330/332 (M + H)+
Reference Example 67
[0476] Under argon atmosphere, to a solution of
4-chloro-3-fluoro-benzaldehyde (10 g) in N,N-dimethylformamide (50
ml) was added sodium cyanide (620 mg) at room temperature, and the
mixture was stirred at the same temperature for 3 hours. Then, to
the mixture was added dropwise a solution of ethyl acrylate (5.2
ml) in N,N-dimethylformamide (25 ml), and the resulting mixture was
stirred at the room temperature for 3 hours. The reaction mixture
was poured into water and extracted with diethyl ether. The organic
layer was washed with water and brine, dried over anhydrous sodium
sulfate and the solvent was removed under reduced pressure. The
resulting residue was purified by silica gel column chromatography
(solvent: hexane:ethyl acetate=20:1) to obtain ethyl
4-(4-chloro-3-fluorophenyl)-4-oxobutyrate (9.4 g) as pale yellowish
powder.
[0477] MS.cndot.APCI (m/z): 259/261 (MH+)
Reference Example 68
[0478] Under argon atmosphere, a mixture of succinic acid monoethyl
ester monochloride (2.0 g), tributyl(3-thienyl) tin (5.44 g) and
bis(triphenylphosphine) palladium chloride (853 mg) in dioxane (40
ml) was refluxed for 3 hours. After cooling, to the residue was
added a saturated aqueous sodium hydrogen carbonate solution, and
the mixture was extracted with ethyl acetate. The organic layer was
washed with brine, dried over anhydrous sodium sulfate and the
solvent was removed under reduced pressure. The resulting residue
was purified by silica gel column chromatography (solvent:
hexane:ethyl acetate=6:1), and recrystallized from ethyl
acetate-hexane to obtain ethyl 4-(3-thienyl)-4-oxobutyrate (1.4 g)
as pale yellowish powder.
[0479] MS.cndot.APCI (m/z): 213 (MH+)
Reference Example 69
[0480] To a solution of ethyl
4-(5-chlorothiophen-2-yl)-4-oxobutyrate (900 mg) in dichloromethane
(9 ml) was added bromine (200 .mu.l) under ice-cooling, and after
stirring at the same temperature for 30 minutes, the reaction
mixture was warmed to room temperature and the mixture was stirred
for one hour. The reaction mixture was poured into ice-water, and
ethyl acetate and diethyl ether were added thereto. The organic
layer was collected, washed with water and brine, dried over
anhydrous sodium sulfate and the solvent was removed under reduced
pressure to obtain ethyl
3-bromo-4-(5-chlorothiophen-2-yl)-4-oxo-butyrate (1.22 g) as pale
brownish liquid.
[0481] MS.cndot.APCI (m/z): 326/328 (MH+)
Reference Examples 70 and 71
[0482] Corresponding starting compounds were treated in a manner
similar to Reference example 69 to obtain the compounds shown in
Table 59 below.
TABLE-US-00060 TABLE 59 Reference Physical example constant, No.
Chemical structure Salt etc. 70 ##STR00618## Free material Oil
MS.cndot.APCI (m/z): 337/339 (M + H)+ 71 ##STR00619## Free material
Oil MS.cndot.APCI (m/z): 291/293 (M + H)+
Reference Example 72
[0483] to a mixture of (2-methylthio)pyrimidin-5-carboxylic acid
sodium salt (1.50 g), ammonium chloride (2.09 g) and
1-hydroxybenzotriazole (1.27 g) in N,N-dimethylformamide (20 ml)
were successively added
3-ethyl-1-(3-dimethylamino-propyl)carbodiimide hydrochloride (1.80
g) and triethylamine (6.5 ml) under ice-cooling, and the mixture
was stirred at room temperature overnight. To the reaction mixture
was added an aqueous ammonium chloride solution and the mixture was
extracted with ethyl acetate, washed with water and brine, dried
over anhydrous sodium sulfate and the solvent was removed under
reduced pressure. The resulting residue was digested with diethyl
ether-ethyl acetate. Then, the suspension was cooled and the
precipitate was filtered, and washed with diethyl ether-n-hexane to
obtain (2-methylthio)pyrimidin-5-carboxamide (927 mg).
[0484] MS.cndot.APCI (m/z): 170 (MH+)
Reference Example 73
[0485] Corresponding starting compounds were treated in a manner
similar to Reference example 72 to obtain
4,5-dimethylthiophen-2-carboxamide.
[0486] MS.cndot.APCI (m/z): 156 (MH+)
Reference Example 74
[0487] To a suspension of 6-chloronicotinamide (1.50 g) in ethanol
(30 ml) was added sodium hydride (1.88 g, 60% mineral oil), and the
mixture was stirred at room temperature for 24 hours. Another
portion of sodium hydride (940 mg, 60% mineral oil) was added to
the mixture, and the resulting mixture was stirred at room
temperature for 24 hours followed by refluxing for 4.5 hours. Then,
the reaction mixture was cooled, a saturated aqueous ammonium
chloride solution was added thereto and the mixture was extracted
with ethyl acetate. The organic layer was washed with brine, dried
over anhydrous sodium sulfate and the solvent was removed under
reduced pressure. The residue was triturated with diethyl ether to
obtain 6-ethoxynicotinamide (1.05 g) as colorless powder.
[0488] MS.cndot.APCI (m/z): 167 (MH+)
Reference Example 75
[0489] A mixture of (2-methylthio)pyrimidin-5-carboxamide (569 mg)
and Lawesson's reagent (2.72 g) in chloroform (20 ml) was refluxed
overnight. After cooling the reaction mixture, it was purified by
NH silica gel column chromatography (solvent: ethyl acetate). The
residue was triturated with diethyl ether and washed with n-hexane
to obtain (2-methylthio)pyrimidin-5-carbothioamide (247 mg) as
yellowish powder.
[0490] MS.cndot.APCI (m/z): 186 (MH+)
Reference Examples 76 to 80
[0491] Corresponding starting compounds were treated in a manner
similar to Reference example 75 to obtain the compounds shown in
Table 60 below.
TABLE-US-00061 TABLE 60 Reference Physical example No. Chemical
structure Salt constant, etc. 76 ##STR00620## Free material Crystal
Melting point: 227.5-228.5.degree. C. MS.cndot.APCI (m/z): 183 (M +
H)+ 77 ##STR00621## Free material Powder MS.cndot.APCI (m/z): 182
(M + H)+ 78 ##STR00622## Free material Powder MS.cndot.APCI (m/z):
183 (M + H)+ 79 ##STR00623## Free material Powder MS.cndot.APCI
(m/z): 194 (M + H)+ 80 ##STR00624## Free material Powder
ESI.cndot.MS (m/z): 170 (M - H)
Reference Example 81
[0492] Corresponding starting compounds were treated in a manner
similar to Reference example 13(1) to obtain methyl
5-(3-chloro-4-fluorphenyl)oxazol-4-yl carboxylate.
[0493] MS.cndot.APCI (m/z): 256/258 (MH+)
Reference Examples 82 and 83
[0494] Corresponding starting compounds were treated in a manner
similar to Reference example 13(2) to obtain the compounds shown in
Table 61 below.
TABLE-US-00062 TABLE 61 Reference Physical example constant, No.
Chemical structure Salt etc. 82 ##STR00625## HCl Powder
MS.cndot.APCI (m/z): 136 (M + H)+ 83 ##STR00626## HCl Powder
MS.cndot.APCI (m/z): 188/190 (M + H)+
Reference Examples 84 to 87
[0495] Corresponding starting compounds were treated in a manner
similar to Reference example 10 (1) or Reference example 20 (4) to
obtain the compounds shown in Table 62 below.
TABLE-US-00063 TABLE 62 Reference example Physical No. Chemical
structure Salt constant, etc. 84 ##STR00627## HCl Powder
MS.cndot.APCI (m/z): 256/258 (M + H)+ 85 ##STR00628## HCl Powder
MS.cndot.APCI (m/z): 228 (M + H)+ 86 ##STR00629## HCl Powder
MS.cndot.APCI (m/z): 223 (M + H) 87 ##STR00630## Free Crystal
Melting point: 158-159.degree. C.
Reference Examples 88 to 90
[0496] Corresponding starting compounds were treated in a manner
similar to Reference example 20(3) to obtain the compounds shown in
Table 63 below.
TABLE-US-00064 TABLE 63 Reference example Physical No. Chemical
structure Salt constant, etc. 88 ##STR00631## Free material Oily
state MS.cndot.APCI (m/z): 284/286 (M + H)+ 89 ##STR00632## Free
material Oily state MS.cndot.APCI (m/z): 256 (M + H)+ 90
##STR00633## Free material Oily state MS.cndot.APCI (m/z): 323 (M +
H)
Experimental Example 1
[0497] Relaxation effect on potassium-induced contraction of
isolated rabbit urinary bladder
[0498] Urinary bladder was isolated from Male NZW rabbits (2.0-3.5
kg) and immersed in ice-cold Krebs-bicarbonate solution (in mM:
118
[0499] NaCl, 4.7 KCl, 1.2, 2.5 CaCl.sub.2, MgSO.sub.4, 1.2
KH.sub.2PO.sub.4, 11 glucose, 25 NaHCO.sub.3). The urinary bladder
was cut into longitudinal strips (5 mm length, 3-4 mm width) after
mucosal layer was removed. Preparations were mounted in organ baths
containing 10 ml of Krebs solution maintained at 37.degree. C. and
gassed with 95% O.sub.2/5% CO.sub.2. Accordingly, preparations were
stretched with an initial tension of 2.0.+-.1.0 g, and changes in
isometric tension were measured by force-displacement transducer.
The preparations were pre-contracted by changing organ-bath
solution into high-K.sup.+ (30 mM) Krebs solution (in mM: 92.7
NaCl, 30 KCl, 1.2, 2.5 CaCl.sub.2, MgSO.sub.4, 1.2
KH.sub.2PO.sub.4, 11 glucose, 25 NaHCO.sub.3)
[0500] After stable tension was obtained, compounds were added into
organ baths cumulatively (10.sup.-8M-10.sup.-4M). The effects of
compounds were expressed as a percentage of the maximum relaxation
produced by 0.1 mM papaverine. 50% relaxation concentration
(EC.sub.50 was calculated and EC.sub.50 value range (.mu.M) of the
compounds of the present invention was shown in the following Table
64 with a rank of A, B or C. These ranges are as mentioned below.
3.gtoreq.C.gtoreq.1.gtoreq.B.gtoreq.0.5.gtoreq.A
TABLE-US-00065 TABLE 64 Preparation EC.sub.50 value example No.
range 5 C 10 C 13 A 14 C 16 C 19 A 25 A 30 C 33 A 34 C 35 C 36 C 38
C 39 C 49 B 50 C 51 A 52 A 53 B 54 C 55 C 56 B 57 C 59 C 60 C 61 C
81 C 84 A 86 B 87 C 88 C 90 C 95 C 96 C 97 B 99 B 104 B 108 C 120 A
121 C 131 C 132 B 136 B 140 C 152 C 155 C 158 C 168 B 169 C 170 C
171 C 172 C 173 C 180 C 181 B 182 A 187 B 197 C 235 B 240 B 243 A
244 C 245 C 246 B 247 C 248 C 249 C 252 B 253 B 255 C 256 A 257 A
262 C 265 C 267 A 268 A 269 A 271 B 272 A 273 C 275 A 277 B 278 B
279 A 280 A 281 A 282 B 283 A 284 C 285 C 286 A 287 A 288 A 339 C
350 C 355 A 362 C 363 C 364 C 365 C 366 A 367 B 372 C 373 C 374 C
377 C 378 C 431 B 432 A 434 B 435 B 437 A 438 C 441 C 444 C 445 C
446 A 451 C 452 A 453 B 454 C 455 C 458 A 459 C 462 B 464 C 469 C
473 B 478 A 479 A 486 C 487 B 503 C 504 C 506 B 507 A 511 A 512 B
514 B 517 A 524 C 531 C 572 C 574 C 575 A 576 B 578 B 579 B 584 C
586 A 587 B 590 A 594 A 596 C 597 A 600 A 601 B 609 B 610 A 612 A
616 C 623 C 626 C 639 C
Experimental Example 2
[0501] Inhibitory effect on the rhythmic bladder contractions
induced by substance P in anesthetized rats
[0502] For the experiments, Sprague-Dawley female rats (9 to 12
weeks old) weighing between 200 to 300 g were used. After urethane
anesthetization (subcutaneously administered with a dose of 1.2
g/kg), cannulae were placed in both right and left femoral veins.
One intravenous catheter was used for administration of compounds,
and the other was for the substance P (0.33 .mu.g/kg/min) infusion.
We also cannulated into ureter to pass urine. Polyethylene
catheters were inserted into carotid artery for continuous
monitoring of arterial blood pressure and heart rate. For
continuous infusion, transurethral bladder catheter was inserted
into the bladder through the urethra and tied in place by a
ligature around the urethral orifice. One end of the catheter was
attached to a pressure transducer in order to measure intravesical
pressure. The other end of the catheter was used for infusion of
saline into the bladder. After stabilization of blood pressure and
heart rate and after the bladder was emptied, cystometry was
performed by filling the bladder slowly with about 0.6 ml of
saline. After about 10 minutes, intravenous infusion of substance P
(0.33 .mu.g/kg/min) was started for stabilization of the
micturition reflex. Compounds were administered after stable
rhythmic bladder contraction was obtained over 15 minutes. All
compounds were dissolved or suspended in saline containing 0.5%
Tween 80 for intravenous administration (0.1 ml/kg). The rhythmic
contraction frequency and the intravesical pressure were observed
for 35 minutes after administration of the test compound.
[0503] As a result, the compounds of the present invention
decreased the frequency of bladder rhythmic contraction without
changing the amplitude of contraction. Also, we determined a time
(minute) during which the frequency of the rhythmic contraction had
been completely inhibited by administering 0.25 mg/kg of the
compound. A 100% inhibition time (minute) of the selected compounds
of the present invention is shown in the following Table 65 with a
rank of A, B or C. These ranges are as mentioned below.
[0504] A.gtoreq.20>B.gtoreq.10>C (minute)
TABLE-US-00066 TABLE 65 100% Preparation inhibition example No.
time range 13 C 14 A 16 B 24 C 25 B 27 B 28 B 30 B 31 A 34 A 43 C
46 B 47 B 48 C 50 C 53 C 54 B 55 B 56 B 59 B 61 A 62 C 63 C 67 B 72
C 80 B 83 B 85 C 86 B 87 B 88 B 90 B 93 B 99 B 102 C 104 A 107 B
108 B 120 C 122 B 123 C 124 B 125 C 132 B 133 C 136 C 137 C 142 C
143 C 144 C 152 B 153 B 155 B 156 B 158 C 160 C 162 C 164 B 166 B
168 B 171 B 172 C 176 C 181 B 182 B 187 B 189 C 197 C 198 C 201 C
233 C 234 C 235 B 236 C 237 C 238 C 239 C 240 C 241 C 242 C 243 A
244 B 245 C 246 B 247 C 248 B 249 B 250 B 251 C 252 C 253 A 254 C
255 B 256 C 257 B 258 C 259 B 260 A 262 C 263 C 267 C 268 C 269 B
270 B 271 C 272 B 273 C 274 B 275 A 276 C 277 C 278 B 279 C 280 C
281 C 282 B 283 C 284 B 285 B 286 C 287 B 288 C 289 B 290 B 291 C
292 C 293 C 295 B 296 C 331 A 337 C 338 C 348 C 350 B 351 C 362 A
363 C 364 B 365 B 366 C 367 A 368 B 369 B 370 C 371 C 373 C 374 C
375 C 376 C 377 C 378 C 380 C 430 B 431 B 432 C 433 C 434 B 435 B
436 C 437 B 438 C 439 C 440 C 441 B 442 C 443 C 444 B 445 A 446 C
447 B 448 C 449 B 450 B 451 B 452 B 453 C 454 A 455 B 456 C 457 B
458 B 459 C 462 C 464 C 466 B 467 A 469 B 470 B 472 A 473 A 474 C
475 B 476 B 478 B 479 C 482 C 484 B 486 B 487 C 503 A 504 C 505 B
511 C 512 B 513 C 514 B 516 B 517 C 522 B 523 B 524 B 525 A 529 B
530 C 531 C 532 C 568 A 569 A 570 A 571 A 572 C 573 B 574 B 575 B
576 A 577 B 578 B 579 C 580 C 582 A 583 B 584 A 585 C 586 B 587 A
588 C 589 A 590 B 591 B 594 C 596 B 600 A 601 A
608 B 609 B 610 B 611 B 612 A 613 C 614 C 615 B 616 B 617 B 622 B
623 C 624 C 626 C 627 C 628 C 630 C 639 C
Experimental Example 3
[0505] Large conductance calcium-activated K channel opening action
in isolated rabbit bladder
[0506] The urinary bladder strips were prepared according to the
same manner as described in Experimental example 1. Briefly, the
isolated urinary bladder was cut into longitudinal strips in
ice-cold Krebs-bicarbonate solution, and mounted in organ baths.
The initial tension was 2.0+/-1.0 g. The preparations were
contracted by high-K.sup.+ (20 mM or 60 mM) Krebs solution.
[0507] Active ingredients of the present invention showed
relaxation effect on 20 mM K.sup.+-contracted preparation and the
effect was blocked by iberiotoxin, a selective large conductance
calcium-activated K channel blocker.
[0508] Also in in vivo animal study, pre-administration of
iberiotoxin (0.15 mg/kg, intravenous administration) reduced
inhibitory effect of active ingredients in the present invention on
the rhythmic bladder contraction.
[0509] It is suggested from the results that the active ingredients
of the present invention have a detrusor relaxing activity through
the large conductance calcium-activated K channel.
[0510] Thus, it was shown that the compounds which are active
ingredients of the present invention were effective for prophylaxis
and treatment of diseases such as pollakiuria, urinary incontinence
and the like through the large conductance calcium-activated K
channel opening activity.
[0511] The nitrogen-containing 5-membered heterocyclic compound (I)
or a pharmaceutically acceptable salt which is an active ingredient
of the present invention has an excellent large conductance
calcium-activated K channel opening activity and hyperpolarizes a
membrane electric potential of cells, so that it is useful for a
prophylactic, relief and/or treatment agent of, for example,
hypertension, asthma, premature birth, irritable bowel syndrome,
chronic heart failure, angina, cardiac infarction, cerebral
infarction, subarachnoid hemorrhage, cerebral vasospasm, cerebral
hypoxia, peripheral blood vessel disorder, anxiety, male-pattern
baldness, erectile dysfunction, diabetes, diabetic peripheral nerve
disorder, other diabetic complication, sterility, urolithiasis and
pain accompanied thereby, pollakiuria, urinary incontinence,
nocturnal enuresis, and the like.
[0512] Also, the nitrogen-containing 5-membered heterocyclic
compound (I) or a pharmaceutically acceptable salt has a low
toxicity, so that it has high safety as a medicine.
* * * * *