U.S. patent application number 11/798214 was filed with the patent office on 2007-09-13 for thiadiazoline derivative.
This patent application is currently assigned to Kyowa Hakko Kogyo Co., Ltd.. Invention is credited to Yoji Ino, Kazuhiko Kato, Chikara Murakata, Ryuichiro Nakai, Tomohisa Nakano, Yoshihisa Ohta, Takeshi Takahashi, Yoshinori Yamashita.
Application Number | 20070213380 11/798214 |
Document ID | / |
Family ID | 26624996 |
Filed Date | 2007-09-13 |
United States Patent
Application |
20070213380 |
Kind Code |
A1 |
Murakata; Chikara ; et
al. |
September 13, 2007 |
Thiadiazoline derivative
Abstract
##STR1## (wherein R.sup.1 and R.sup.4 are the same or different
and each represents a hydrogen atom, substituted or unsubstituted
lower alkyl, substituted or unsubstituted lower alkynyl,
substituted or unsubstituted lower alkenyl, or the like; R.sup.5
represents a substituted or unsubstituted heterocyclic group,
substituted or unsubstituted aryl, or the like; R.sup.2 represents
--C(.dbd.W)R.sup.6 or the like; R.sup.3 represents a hydrogen atom,
--C(.dbd.W.sup.A)R.sup.6A, or the like) Antitumor agents which
comprises a thiadiazoline derivative represented by the
aforementioned general formula (I) or a pharmacologically
acceptable salt thereof as an active ingredient are provided.
Inventors: |
Murakata; Chikara;
(Shizuoka, JP) ; Kato; Kazuhiko; (Shizuoka,
JP) ; Ohta; Yoshihisa; (Kanagawa, JP) ; Nakai;
Ryuichiro; (Shizuoka, JP) ; Yamashita; Yoshinori;
(Shizuoka, JP) ; Takahashi; Takeshi; (Shizuoka,
JP) ; Nakano; Tomohisa; (Shizuoka, JP) ; Ino;
Yoji; (Shizuoka, JP) |
Correspondence
Address: |
GREENBLUM & BERNSTEIN, P.L.C.
1950 ROLAND CLARKE PLACE
RESTON
VA
20191
US
|
Assignee: |
Kyowa Hakko Kogyo Co., Ltd.
Tokyo
JP
Fuji Photo Film Co., Ltd.
Kanagawa
JP
|
Family ID: |
26624996 |
Appl. No.: |
11/798214 |
Filed: |
May 11, 2007 |
Related U.S. Patent Documents
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Application
Number |
Filing Date |
Patent Number |
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10497531 |
Mar 28, 2005 |
|
|
|
PCT/JP02/12961 |
Dec 11, 2002 |
|
|
|
11798214 |
May 11, 2007 |
|
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|
Current U.S.
Class: |
514/363 ;
548/126 |
Current CPC
Class: |
A61K 31/433 20130101;
A61P 43/00 20180101; A61K 31/4439 20130101; A61P 7/00 20180101;
A61K 31/497 20130101; A61K 31/5377 20130101; C07D 285/135 20130101;
A61P 35/00 20180101 |
Class at
Publication: |
514/363 ;
548/126 |
International
Class: |
A61K 31/433 20060101
A61K031/433; C07D 285/135 20060101 C07D285/135 |
Foreign Application Data
Date |
Code |
Application Number |
Dec 11, 2001 |
JP |
2001-377456 |
Aug 16, 2002 |
JP |
2002-237399 |
Claims
1. A compound of formula ##STR78## wherein R.sup.2A is
--COC(CH.sub.3).sub.3, R.sup.3A is --OCH.sub.3 and R.sup.4A is
--H.sub.2NHSO.sub.2CH.sub.3; R.sup.2A is --COC(CH.sub.3).sub.3,
R.sup.3A is --COCH.sub.3 and R.sup.4A is
--CH.sub.2NHSO.sub.2CH.sub.2Cl; R.sup.2A is --COCH.sub.3, R.sup.3A
is --COCH.sub.3 and R.sup.4A is --CH.sub.2NHSO.sub.2CH.sub.2Cl;
R.sup.2A is--COC(CH.sub.3).sub.3, R.sup.3A is --COCH.sub.3 and
R.sup.4A is --CH.sub.2NHSO.sub.2CH.dbd.CH.sub.2; R.sup.2A is
--COC(CH.sub.3).sub.3, R.sup.3A is --COC(CH.sub.3).sub.3 and
R.sup.4A is --CH.sub.2NHSO.sub.2CH.dbd.CH.sub.2; R.sup.2A is
--COC(CH.sub.3).sub.3, R.sup.3A is --COCH.sub.3 and R.sup.4A is
##STR79## R.sup.2A is --COC(CH.sub.3).sub.3, R.sup.3A is
--COCH.sub.3 and R.sup.4A is
--CH.sub.2NHSO.sub.2(CH.sub.2).sub.2NHCH.sub.2CH.sub.3; R.sup.2A is
--COC(CH.sub.3).sub.3, R.sup.3A is --COCH.sub.3 and R.sup.4A is
--CH.sub.2NHSO.sub.2(CH.sub.2).sub.2N(CH.sub.3).sub.2; R.sup.2A is
--COC(CH.sub.3).sub.3, R.sup.3A is --COCH.sub.3 and R.sup.4A is
--CH.sub.2NHSO.sub.2(CH.sub.2).sub.2NH(CH.sub.2).sub.20H; R.sup.2A
is --COC(CH.sub.3).sub.3, R.sup.3A is --COC(CH.sub.3).sub.3 and
R.sup.4A is --CH.sub.2NHSO.sub.2(CH.sub.2).sub.2NHCH.sub.2CH.sub.3;
R.sup.2A is --COC(CH.sub.3).sub.3, R.sup.3A is
--COC(CH.sub.3).sub.3 and R.sup.4A is
--CH.sub.2NHSO.sub.2(CH.sub.2).sub.2N(CH.sub.3).sub.2; R.sup.2A is
--COC(CH.sub.3).sub.3, R.sup.3A is --COCH(CH.sub.3).sub.2 and
R.sup.4A is --CH.sub.2).sub.2 NHSO.sub.2CH.sub.3; R.sup.2A is
--COCH.sub.2CH.sub.3, R.sup.3A is --COCH.sub.2CH3 and R.sup.4A is
--CH(.sub.2).sub.2NHSO.sub.2CH.sub.3; or R.sup.2A is
--COC(CH.sub.3).sub.3, R.sup.3A is --COCH.sub.2CH.sub.3 and
R.sup.4A is --CH.sub.2).sub.2NHSO.sub.2CH.sub.3; or a
pharmacologically acceptable salt thereof.
2. A compound according to claim 1 of formula ##STR80## wherein
R.sup.2A is --COC(CH.sub.3).sub.3, R.sup.3A is --COCH.sub.3 and
R.sup.4A is --CH.sub.2NHSO.sub.2CH.dbd.CH.sub.2; R.sup.2A is
--COC(CH.sub.3).sub.3, R.sup.3A is --COC(CH.sub.3).sub.3 and
R.sup.4A is --CH.sub.2NHSO.sub.2CH.dbd.CH.sub.2; R.sup.2A is
--COC(CH.sub.3).sub.3, R.sup.3A is --COCH3 and R.sup.4A is
--CH.sub.2NHSO.sub.2(CH(.sub.2).sub.2NHCH.sub.2CH.sub.3; R.sup.2A
is --COC(CH.sub.3).sub.3, R.sup.3A is --COC(CH.sub.3).sub.3 and
R.sup.4A is --CH.sub.2NHSO.sub.2(CH.sub.2).sub.2NHCH.sub.2CH.sub.3;
or R.sup.2A is --OC(CH.sub.3).sub.3, R.sup.3A is
--COCH(CH.sub.3).sub.2 and R.sup.4A is
--CH.sub.2).sub.2NHSO.sub.2CH.sub.3; or a pharmacologically
acceptable salt thereof.
3. A compound according to claim 2 of formula ##STR81## wherein
R.sup.2A is --COC(CH.sub.3).sub.3, R.sup.3A is --OC(CH.sub.3).sub.3
and R.sup.4A is
--CH.sub.2NHSO.sub.2(CH.sub.2).sub.2NHCH.sub.2CH.sub.3; or a
pharmacologically acceptable salt thereof.
4. A compound according to claim 2 of formula ##STR82## wherein
R.sup.2A is --OC(CH.sub.3).sub.3, R.sup.3A is
--COCH(CH.sub.3).sub.2 and R.sup.4A is
--CH.sub.2).sub.2NHSO.sub.2CH.sub.3 or a pharmacologically
acceptable salt thereof.
5. A pharmaceutical composition comprising a compound of formula
##STR83## wherein R.sup.2A is --COC(CH.sub.3).sub.3, R.sup.3A is
--COC(CH.sub.3).sub.3 and R.sup.4A is
--CH.sub.2NHSO.sub.2(CH.sub.2).sub.2NHCH.sub.2CH.sub.3; or a
pharmacologically acceptable salt thereof.
6. A pharmaceutical composition comprising a compound of formula
##STR84## wherein R.sup.2A is --COC(CH.sub.3).sub.3, R.sup.3A is
--COCH(CH.sub.3).sub.2 and R.sup.4A is
--CH.sub.2).sub.2NHSO.sub.2CH.sub.3 or a pharmacologically
acceptable salt thereof.
7. A method of treating a human malignant tumor in a patient in
need thereof comprising administering a compound according to claim
3.
8. A method of treating a human malignant tumor in a patient in
need thereof comprising administering a compound according to claim
4.
Description
CROSS-REFERENCE TO RELATED APPLICATIONS
[0001] This application is a divisional of application Ser. No.
10/497,531, which is a National Stage Application of International
Application No. PCT/JP02/12961, filed Dec. 11, 2002, which was not
published in English under PCT Article 21(2), entering the National
Stage on Jun. 10, 2004, and which claims priority of Japanese
Application Nos. 2001-377456, filed Dec. 11, 2001 and 2002-237399,
filed Aug. 16, 2002. The entire disclosure of application Ser. No.
10/497,531 is considered as being part of this application, and the
entire disclosure of application Ser. No. 10/497,531 is expressly
incorporated by reference herein in its entirety.
TECHNICAL FIELD
[0002] The present invention relates to an antitumor agent
comprising a thiadiazoline derivative or a pharmacologically
acceptable salt thereof as an active ingredient, and a
thiadiazoline derivative or a pharmacologically acceptable salt
thereof which is useful for therapeutic treatment of a tumor.
BACKGROUND ART
[0003] In chemotherapies of cancers, a variety of anticancer agents
including antimitotic agents such as taxane and vinca alkaloid,
topoisomerase inhibitors, alkylating agents and the like have been
used. These agents have side effects such as bone marrow toxicity
and neuropathy, a problem of drug resistance and the like.
Therefore, novel anticancer agents which have improvement in the
above problems have so far been desired.
[0004] It is known that thiadiazoline derivatives have inhibitory
activity against transcription factor STAT6 activation,
antagonistic action of integrin, and the control of insect or
acarid pests (Japanese Published Unexamined Patent Application No.
2000-229959, WO01/56994, U.S. Pat. No. 6,235,762). In addition, it
is known-that the derivatives have antibacterial activity, ACE
inhibitory activity and the like [J. Bangladesh Chem. Soc., Vol. 5,
p. 127 (1992), WO93/22311, Japanese Published Unexamined Patent
Application No. 62-53976 (1987)].
DISCLOSURE OF THE INVENTION
[0005] An object of the present invention is to provide a
thiadiazoline derivative or a pharmacologically acceptable salt
thereof which is useful for therapeutic treatment of a human
malignant tumor, for example, breast cancer, gastric cancer,
ovarian cancer, colon cancer, lung cancer, brain tumor, laryngeal
cancer, hematological cancer, urinary or genital tumor including
bladder cancer and prostatic cancer, renal cancer, skin carcinoma,
hepatic carcinoma, pancreatic cancer, a uterine cancer, or the
like. Another object of the present invention is to provide an
antitumor agent comprising a thiadiazoline derivative or a
pharmacologically acceptable salt thereof as an active
ingredient.
[0006] The present invention relates to the following (1) to
(43).
[0007] (1) An antitumor agent which comprises a thiadiazoline
derivative represented by the general formula (I) or a
pharmacologically acceptable salt thereof as an active ingredient
##STR2## <wherein [0008] R.sup.1 and R.sup.4 are the same or
different and each represents [0009] a hydrogen atom, substituted
or unsubstituted lower alkyl, substituted or unsubstituted lower
alkynyl, substituted or unsubstituted lower alkenyl, substituted or
unsubstituted cycloalkyl, a substituted or unsubstituted
heterocyclic group, or substituted or unsubstituted aryl; [0010]
R.sup.2 represents [0011] a hydrogen atom, substituted or
unsubstituted lower alkyl, substituted or unsubstituted lower
alkynyl, substituted or unsubstituted lower alkenyl, substituted or
unsubstituted cycloalkyl, [0012] --C(.dbd.W)R.sup.6 [wherein [0013]
W represents [0014] an oxygen atom or a sulfur atom [0015] R.sup.6
represents [0016] a hydrogen atom, substituted or unsubstituted
lower alkyl, substituted or unsubstituted lower alkenyl,
substituted or unsubstituted cycloalkyl, a substituted or
unsubstituted aryl, a substituted or unsubstituted heterocyclic
group, [0017] --NR.sup.7R.sup.8 (wherein [0018] R.sup.7 and R.sup.8
are the same or different and each represents [0019] a hydrogen
atom, substituted or unsubstituted lower alkyl, substituted or
unsubstituted lower alkenyl, substituted or unsubstituted
cycloalkyl, substituted or unsubstituted aryl, or a substituted or
unsubstituted heterocyclic group, or [0020] R.sup.7 and R.sup.8 are
combined together with the adjacent nitrogen atom to form a
substituted or unsubstituted heterocyclic group), [0021] --OR.sup.9
(wherein [0022] R.sup.9 represents [0023] substituted or
unsubstituted lower alkyl, substituted or unsubstituted lower
alkenyl, substituted or unsubstituted cycloalkyl, or substituted or
unsubstituted aryl) or [0024] --SR.sup.10 (wherein [0025] R.sup.10
represents [0026] substituted or unsubstituted lower alkyl,
substituted or unsubstituted lower alkenyl, or substituted or
unsubstituted aryl)] [0027] --NR.sup.11R.sup.12 {wherein [0028]
R.sup.11 and R.sup.12 are the same or different and each represents
[0029] a hydrogen atom, substituted or unsubstituted lower alkyl,
substituted or unsubstituted lower alkenyl, substituted or
unsubstituted cycloalkyl, or [0030] --C(.dbd.O)R.sup.13 [wherein
[0031] R.sup.13 represents [0032] substituted or unsubstituted
lower alkyl, substituted or unsubstituted lower alkenyl,
substituted or unsubstituted aryl, a substituted or unsubstituted
heterocyclic group, [0033] --NR.sup.7AR.sup.8A (wherein R.sup.7A
and R.sup.8A have the same meanings as those of the aforementioned
R.sup.7 and R.sup.8, respectively), or [0034] --OR.sup.9A (wherein
R.sup.9A has the same meaning as that of the aforementioned
R.sup.9)]} or [0035] --SO.sub.2R.sup.14 (wherein [0036] R.sup.14
represents [0037] substituted or unsubstituted lower alkyl,
substituted or unsubstituted lower alkenyl, substituted or
unsubstituted aryl, or a substituted or unsubstituted heterocyclic
group), or [0038] R.sup.1 and R.sup.2 are combined together with
the adjacent nitrogen atom to form a substituted or unsubstituted
heterocyclic group, [0039] R.sup.5 represents [0040] substituted or
unsubstituted lower alkyl, substituted or unsubstituted lower
alkynyl, substituted or unsubstituted lower alkenyl, substituted or
unsubstituted cycloalkyl, a substituted or unsubstituted
heterocyclic group, or substituted or unsubstituted aryl, or [0041]
R.sup.4 and R.sup.5 are combined together to represent [0042]
--(CR.sup.28R.sup.29).sub.m1-Q-(CR.sup.28AR.sup.29A).sub.m2-
{wherein [0043] Q represents [0044] a single bond, substituted or
unsubstituted phenylene, or cycloalkylene, [0045] m1 and m2 are the
same or different and each represents [0046] an integer of from 0
to 4, with the proviso that m1 and m2 are not 0 at the same time,
[0047] R.sup.28, R.sup.29, R.sup.28A and R.sup.29A are the same or
different and each represents a hydrogen atom, substituted or
unsubstituted lower alkyl, --OR.sup.30 [wherein [0048] R.sup.30
represents [0049] a hydrogen atom, [0050] substituted or
unsubstituted lower alkyl, [0051] substituted or unsubstituted
lower alkenyl, --CONR.sup.31R.sup.32 (wherein [0052] R.sup.31 and
R.sup.32 are the same or different and each represents [0053] a
hydrogen atom, substituted or unsubstituted lower alkyl, a
substituted or unsubstituted heterocyclic group, or substituted or
unsubstituted aryl), [0054] --SO.sub.2NR.sup.33R.sup.34 (wherein
[0055] R.sup.33 and R.sup.34 are the same or different and each
represents [0056] a hydrogen atom, substituted or unsubstituted
lower alkyl, a substituted or unsubstituted heterocyclic group, or
substituted or unsubstituted aryl), or [0057] --COR.sup.35 (wherein
[0058] R.sup.35 represents [0059] a hydrogen atom, substituted or
unsubstituted lower alkyl, a substituted or unsubstituted
heterocyclic group, or substituted or unsubstituted aryl)], [0060]
--NR.sup.36R.sup.37 [wherein [0061] R.sup.36 and R.sup.37 are the
same or different and each represents [0062] a hydrogen atom,
[0063] substituted or unsubstituted lower alkyl, --COR.sup.38
(wherein [0064] R.sup.38 represents [0065] a hydrogen atom,
substituted or unsubstituted lower alkyl, a substituted or
unsubstituted heterocyclic group, substituted or unsubstituted
aryl, substituted or unsubstituted lower alkoxy, substituted or
unsubstituted aryloxy, amino, substituted or unsubstituted lower
alkylamino, substituted or unsubstituted di(lower alkyl)amino, or
substituted or unsubstituted arylamino), or [0066]
--SO.sub.2R.sup.39 (wherein [0067] R.sup.39 represents [0068]
substituted or unsubstituted lower alkyl, a substituted or
unsubstituted heterocyclic group, or substituted or unsubstituted
aryl)], or [0069] --CO.sub.2R.sup.40 (wherein [0070] R.sup.40
represents [0071] a hydrogen atom, substituted or unsubstituted
lower alkyl, or substituted or unsubstituted aryl), and [0072] when
m1 or m2 is an integer of 2 or more, each R.sup.28, R.sup.29,
R.sup.28A and R.sup.29A may be the same or different, respectively,
and any two of R.sup.28, R.sup.29, R.sup.28A and R.sup.29A which
are bound to the adjacent two carbon atoms may be combined to form
a bond}, and [0073] R.sup.3 represents [0074] a hydrogen atom or
[0075] --C(.dbd.W.sup.A)R.sup.6A (wherein W.sup.A and R.sup.6A have
the same meanings as those of the aforementioned W and R.sup.6,
respectively)>.
[0076] (2) The antitumor agent according to the aforementioned (1),
wherein R.sup.4 is substituted or unsubstituted lower alkyl,
substituted or unsubstituted lower alkynyl, substituted or
unsubstituted lower alkenyl, substituted or unsubstituted
cycloalkyl, a substituted or unsubstituted heterocyclic group, or
substituted or unsubstituted aryl, and R.sup.5 is substituted or
unsubstituted cycloalkyl, a substituted or unsubstituted
heterocyclic group, or substituted or unsubstituted aryl, or
R.sup.4 and R.sup.5 are combined to represent
--(CR.sup.28R.sup.29).sub.m1-Q-(CR.sup.28AR.sup.29A).sub.m2--.
[0077] (3) The antitumor agent according to the aforementioned (1),
wherein R.sup.5 is substituted or unsubstituted lower alkyl,
substituted or unsubstituted lower alkynyl, substituted or
unsubstituted lower alkenyl, or substituted or unsubstituted
cycloalkyl.
[0078] (4) The antitumor agent according to the aforementioned (1)
or (2), wherein R.sup.5 is substituted or unsubstituted aryl, or a
substituted or unsubstituted heterocyclic group.
[0079] (5) The antitumor agent according to the aforementioned (1)
or (2), wherein R.sup.5 is substituted or unsubstituted phenyl, or
substituted or unsubstituted thienyl.
[0080] (6) The antitumor agent according to any one of the
aforementioned (1) to (5), wherein R.sup.4 is substituted or
unsubstituted lower alkyl.
[0081] (7) The antitumor agent according to the aforementioned (1),
wherein R.sup.4 and R.sup.5 are combined to represent
--(CR.sup.28R.sup.29).sub.m1-Q-(CR.sup.28AR.sup.29A).sub.m2--.
[0082] (8) The antitumor agent according to the aforementioned (1),
wherein R.sup.4 and R.sup.5 are combined to represent
--(CH.sub.2).sub.m1-Q-(CH.sub.2).sub.m2--.
[0083] (9) The antitumor agent according to the aforementioned (7)
or (8), wherein Q is substituted or unsubstituted phenylene.
[0084] (10) The antitumor agent according to any one of the
aforementioned (1) to (9), wherein R.sup.1 is a hydrogen atom, or
substituted or unsubstituted lower alkyl.
[0085] (11) The antitumor agent according to any one of the
aforementioned (1) to (9), wherein R.sup.1 is a hydrogen atom.
[0086] (12) The antitumor agent according to any one of the
aforementioned (1) to (11), wherein R.sup.2 is
--C(.dbd.W)R.sup.6.
[0087] (13) The antitumor agent according to the aforementioned
(12), wherein R.sup.6 is substituted or unsubstituted lower alkyl,
substituted or unsubstituted lower alkynyl, substituted or
unsubstituted lower alkenyl, or substituted or unsubstituted
cycloalkyl.
[0088] (14) The antitumor agent according to the aforementioned
(12) or (13), wherein W is an oxygen atom.
[0089] (15) The antitumor agent according to any one of the
aforementioned (1) to (9), wherein R.sup.1 and R.sup.2 are combined
to form a substituted or unsubstituted heterocyclic group together
with the adjacent nitrogen atom.
[0090] (16) The antitumor agent according to any one of the
aforementioned (1) to (15), wherein R.sup.3 is
--C(.dbd.W.sup.A)R.sup.6A.
[0091] (17) The antitumor agent according to the aforementioned
(16), wherein R.sup.6A is substituted or unsubstituted lower alkyl,
substituted or unsubstituted lower alkynyl, substituted or
unsubstituted lower alkenyl, or substituted or unsubstituted
cycloalkyl.
[0092] (18) The antitumor agent according to the aforementioned
(16), wherein R.sup.6A is lower alkyl.
[0093] (19) The antitumor agent according to any one of the
aforementioned (16) to (18), wherein W.sup.A is an oxygen atom.
[0094] (20) A thiadiazoline derivative represented by the general
formula (IA) or a pharmacologically acceptable salt thereof:
##STR3## [0095] {wherein R.sup.1A, R.sup.2A, R.sup.3A, R.sup.4A and
R.sup.5A have the same meanings as those of the aforementioned
R.sup.1, R.sup.2, R.sup.3, R.sup.4 and R.sup.5, respectively, with
the proviso that when R.sup.2A and R.sup.3A are the same to be
--CONHR.sup.8B (wherein R.sup.8B represents a substituted or
unsubstituted lower alkyl, or substituted or unsubstituted aryl),
and [0096] (i) R.sup.4A is a hydrogen atom, or [0097] (ii) one of
R.sup.4A and R.sup.5A is substituted or unsubstituted lower alkyl,
then the other of R.sup.4A and R.sup.5A only represents substituted
or unsubstituted cycloalkyl, substituted or unsubstituted lower
alkenyl, or substituted or unsubstituted lower alkynyl [0098]
[provided that [0099] (a) when R.sup.1A, R.sup.2A and R.sup.3A are
hydrogen atoms, and [0100] one of R.sup.4A and R.sup.5A is methyl,
[0101] the other of R.sup.4A and R.sup.5A is not any of phenyl,
4-nitrophenyl, 4-aminophenyl, 4-bromophenyl, 3-nitrophenyl and
4-methoxy-3-nitrophenyl, [0102] (b) when R.sup.1A and R.sup.2A are
hydrogen atoms, R.sup.3A is acetyl, [0103] (i) and one of R.sup.4A
and R.sup.5A is methyl, [0104] the other of R.sup.4A and R.sup.5A
is not any of methyl, ethyl, phenyl, 4-methoxyphenyl,
2-naphthylsulfonylmethyl, 4-bromophenylsulfonylmethyl and
4-chlorophenylsulfonylmethyl, and [0105] (ii) and R.sup.4A is a
hydrogen atom, [0106] R.sup.5A is not any of phenyl, 4-nitrophenyl,
4-chlorophenyl, 4-methoxyphenyl, 4-dimethylaminophenyl and pyridyl,
[0107] (c) when R.sup.1A is a hydrogen atom, R.sup.2A and R.sup.3A
are acetyl, [0108] (i) and one of R.sup.4A and R.sup.5A is methyl,
[0109] the other of R.sup.4A and R.sup.5A is not any of methyl,
ethyl, propyl, butyl, hexyl, heptyl, phenyl, benzyl, acetylmethyl,
tert-butoxycarbonylmethyl, ethoxycarbonylmethyl,
4-bromophenylsulfonylmethyl, 4-bromophenylsulfonylethyl,
4-chlorophenylsulfonylmethyl, 3,4-dichlorophenylsulfonylmethyl,
3,4-dichlorophenylsulfonylethyl, 3,4-dimethylphenylsulfonylmethyl,
phenylsulfonylmethyl, 4-methylphenylsulfonylmethyl,
4-methylphenylsulfonyl ethyl, 4-(acetylamino)phenylsulfonylethyl,
4-bromophenylsulfonylethyl, 2-(4-methylphenyl
sulfonyl)-2-phenylethyl, 2-(4-methylphenylthio)-2-phenylethyl,
2-naphthylsulfonylethyl, 2-naphthylsulfonylmethyl, phenethyl,
3-benzoyloxyphenyl, 2-oxo-2H-1-benzopyran-3-yl, 2-furyl,
5-nitro-2-furyl, 5-methyl-2-furyl, 2-thienyl, 5-chloro-2-thienyl,
3-acetoxyphenyl, 3-nitrophenyl, 4-nitrophenyl, 4-fluorophenyl,
3-acetylaminophenyl, 4-methoxyphenyl, 3-methoxyphenyl,
4-ethylphenyl, 4-methylphenyl, 4-bromophenyl, 4-nonyloxyphenyl,
4-phenylphenyl, 3,4-dimethoxyphenyl, 1,3-benzodioxol-5-yl,
4-(benzimidazol-2-ylamino)phenyl,
4-(1-methylbenzimidazol-2-ylamino)phenyl, 3-pyridyl, 2-naphthyl,
2-acetylamino-4-acetyl-1,3,4-thiadiazolin-5-yl and
4-acetylaminophenylsulfonylmethyl, [0110] (ii) and one of R.sup.4A
and R.sup.5A is phenyl, [0111] the other of R.sup.4A and R.sup.5A
is not any of phenyl, 4-methoxyphenyl, 3,4-dimethoxyphenyl,
4-nitrophenyl, ethoxycarbonylmethyl, isobutyl, sec-butyl, n-butyl
and acetylaminomethyl, [0112] (iii) and one of R.sup.4A and
R.sup.5A is 2-acetoxyphenyl, [0113] the other of R.sup.4A and
R.sup.5A is not 2-phenylethenyl, [0114] (iv) and R.sup.4A is a
hydrogen atom or 4-methoxyphenyl, [0115] R.sup.5A is not
4-methoxyphenyl, [0116] (v) and R.sup.4A is a hydrogen atom, [0117]
R.sup.5A is not any of phenyl, 4-nitrophenyl, 4-chlorophenyl,
4-dimethylaminophenyl and pyridyl, [0118] (vi) and R.sup.4A and
R.sup.5A are combined to represent [0119]
--(CH.sub.2).sub.m1-Q-(CH.sub.2).sub.m2-- (wherein m1, m2 and Q
have the same meanings as those of the aforementioned,
respectively), [0120] --(CH(.sub.2).sub.m1-Q-(CH(.sub.2).sub.m2--
wherein Q is a single bond and the sum of m1 and m2 is 5, is
excluded [0121] (vii) and one of R.sup.4A and R.sup.5A is
1,2,3-triacetoxypropyl, [0122] the other of R.sup.4A and R.sup.5A
is not 3,4-dihydro-3-oxo-2-quinoxalinyl, and [0123] (viii) and one
of R.sup.4A and R.sup.5A is ethyl, [0124] the other of R.sup.4A and
R.sup.5A is not ethyl, [0125] (d) when R.sup.1A and R.sup.4A are
hydrogen atoms, and [0126] (i) R.sup.2A and R.sup.3A are the same
to be propionyl or benzoyl or [0127] (ii) R.sup.2A is propionyl and
R.sup.3A is acetyl, [0128] R.sup.5A is not phenyl, [0129] (e) when
R.sup.1A and R.sup.3A are hydrogen atoms, [0130] R.sup.2A is
acetyl, and [0131] one of R.sup.4A and R.sup.5A is methyl, [0132]
the other of R.sup.4A and R.sup.5A is not either of phenyl and
3,4-dichlorophenylsulfonylethyl, [0133] (f) when R.sup.1A is
phenyl, R.sup.2A and R.sup.3A are acetyl, [0134] (i) and one of
R.sup.4A and R.sup.5A is methyl, [0135] the other of R.sup.4A and
R.sup.5A is not either of 4-acetoxy-6-methyl-2-oxo-2H-pyran-3-yl
and 2-oxo-2H-1-benzopyran-3-yl, and [0136] (ii) and R.sup.4A is
phenyl, [0137] R.sup.5A is not phenyl, [0138] (g) when R.sup.1A is
methyl, R.sup.2A and R.sup.3A are acetyl, [0139] (i) and R.sup.4A
is a hydrogen atom, [0140] R.sup.5A is not phenyl, [0141] (ii) and
one of R.sup.4A and R.sup.5A is methyl, [0142] the other of
R.sup.4A and R.sup.5A is not either of ethoxycarbonylethyl and
ethoxycarbonylpropyl, [0143] (h) when R.sup.1A, R.sup.2A and
R.sup.4A are methyl, and [0144] R.sup.5A is pyridyl, [0145]
R.sup.5A is not --COR.sup.C (wherein R.sup.C represents methyl,
chloromethyl, methoxy, ethoxycarbonylmethyl or
ethoxycarbonylethenyl), [0146] (j) when one of R.sup.1A and
R.sup.2A is a hydrogen atom, [0147] the other of R.sup.1A and
R.sup.2A is ethyl, and [0148] R.sup.3A is a hydrogen atom or
acetyl, [0149] R.sup.4A and R.sup.5A are not methyl at the same
time, [0150] (k) when R.sup.1A is 4-chlorophenyl, [0151] R.sup.2A
is a hydrogen atom, and [0152] one of R.sup.4A and R.sup.5A is
methyl, [0153] the other of R.sup.4A and R.sup.5A is not
(1-methylbenzimidazol-2-ylamino)phenyl, and R.sup.3A is not acetyl,
[0154] (m) when R.sup.1A is phenyl, 4-chlorophenyl, 4-methylphenyl
or 4-methoxyphenyl, [0155] R.sup.2A is a hydrogen atom, and [0156]
R.sup.4A and R.sup.5A are methyl, [0157] R.sup.3A is not any of
acetyl, 4-chlorophenoxyacetyl, 2-chlorophenoxyacetyl,
3-methylphenoxyacetyl and phenylaminocarbonyl, [0158] (n) when
R.sup.2A and R.sup.3A are acetyl, [0159] one of R.sup.4A and
R.sup.5A is methyl, [0160] (i) and the other of R.sup.4A and
R.sup.5A is 1H-benzotriazol-1-ylmethyl, [0161] R.sup.1A is not any
of cyclohexyl, benzyl, phenyl, 2-methylphenyl and 4-methoxyphenyl,
[0162] (ii) and the other of R.sup.4A and R.sup.5A is
2-methylbenzimidazol-1-ylmethyl or 2-ethylbenzimidazol-1-ylmethyl,
[0163] R.sup.1A is not any of cyclohexyl, phenyl and 4-bromophenyl,
[0164] (o) when R.sup.1A is a hydrogen atom, [0165] R.sup.2A is
acetyl, and [0166] R.sup.4A and R.sup.5A are methyl, [0167]
R.sup.3A is not benzoyl, [0168] (p) when one of R.sup.1A and
R.sup.2A is hydrogen atom, [0169] the other of R.sup.1A and
R.sup.2A is methyl, and [0170] R.sup.4A and R.sup.5A are both
methyl or both ethyl, [0171] R.sup.3A is not any of acetyl,
benzoyl, pivaloyl, 3-nitrobenzoyl, 2-fluorobenzoyl,
4-fluorobenzoyl, 2-trifluoromethylbenzoyl and
3-trifluoromethylbenzoyl, and [0172] (q) when R.sup.1A is methyl,
[0173] R.sup.2A is methylaminocarbonyl, and [0174] R.sup.4A and
R.sup.5A are both methyl or both ethyl, [0175] R.sup.3A is not any
of acetyl, benzoyl, pivaloyl, 2-fluorobenzoyl, 4-fluorobenzoyl,
2-trifluoromethylbenzoyl, 3-trifluoromethylbenzoyl and
4-trifluoromethylbenzoyl]}.
[0176] (21) The thiadiazoline derivative according to the
aforementioned (20), wherein R.sup.4A is substituted or
unsubstituted lower alkyl, substituted or unsubstituted lower
alkynyl, or substituted or unsubstituted lower alkenyl, R.sup.5A is
substituted or unsubstituted cycloalkyl, a substituted or
unsubstituted heterocyclic group, or substituted or unsubstituted
aryl, or R.sup.4A and R.sup.5A are combined to represent
--(CR.sup.28R.sup.29).sub.m1-Q-(CR.sup.28AR.sup.29A).sub.m2--
(wherein R.sup.28, R.sup.29, R.sup.28A, R.sup.29A, m1, m2 and Q
have the same meanings as those of the aforementioned,
respectively), or the pharmacologically acceptable salt
thereof.
[0177] (22) The antitumor agent according to the aforementioned
(20), wherein R.sup.5A is substituted or unsubstituted lower alkyl,
substituted or unsubstituted lower alkynyl, substituted or
unsubstituted lower alkenyl, or substituted or unsubstituted
cycloalkyl.
[0178] (23) The thiadiazoline derivative according to the
aforementioned (20) or (21), wherein R.sup.5A is substituted or
unsubstituted aryl, or a substituted or unsubstituted heterocyclic
group, or the pharmacologically acceptable salt thereof.
[0179] (24) The thiadiazoline derivative according to the
aforementioned (20) or (21), wherein R.sup.5A is substituted or
unsubstituted phenyl or substituted or unsubstituted thienyl, or
the pharmacologically acceptable salt thereof.
[0180] (25) The thiadiazoline derivative according to any one of
the aforementioned (20) to (24), wherein R.sup.4A is substituted or
unsubstituted lower alkyl, or the pharmacologically acceptable salt
thereof.
[0181] (26) The thiadiazoline derivative according to any one of
the aforementioned (20) to (24), wherein R.sup.4A is substituted
lower alkyl, or the pharmacologically acceptable salt thereof.
[0182] (27) The thiadiazoline derivative according to the
aforementioned (20), wherein R.sup.4A and R.sup.5A combine together
to represent
--(CR.sup.28R.sup.29).sub.m1-Q-(CR.sup.28AR.sup.29A).sub.m2--
(wherein R.sup.28, R.sup.29, R.sup.28A, R.sup.29A, m1, m2, and Q
have the same meanings as those of the aforementioned,
respectively), or the pharmacologically acceptable salt
thereof.
[0183] (28) The thiadiazoline derivative according to the
aforementioned (20), wherein R.sup.4A and R.sup.5A are combined to
represent --(CH(.sub.2).sub.m1-Q-(CH(.sub.2).sub.m2-- (wherein m1,
m2 and Q have the same meanings as those of the aforementioned,
respectively), or the pharmacologically acceptable salt
thereof.
[0184] (29) The thiadiazoline derivative according to the
aforementioned (27) or (28), wherein Q is substituted or
unsubstituted phenylene, or the pharmacologically acceptable salt
thereof.
[0185] (30) The thiadiazoline derivative according to any one of
the aforementioned (20) to (29), wherein R.sup.1A is a hydrogen
atom, or substituted or unsubstituted lower alkyl, or the
pharmacologically acceptable salt thereof.
[0186] (31) The thiadiazoline derivative according to any one of
the aforementioned (20) to (29), wherein R.sup.1A is a hydrogen
atom, or the pharmacologically acceptable salt thereof.
[0187] (32) The thiadiazoline derivative according to any one of
the aforementioned (20) to (31), wherein R.sup.2A is
--C(.dbd.W)R.sup.6 (wherein W and R.sup.6 have the same meanings as
those of the aforementioned, respectively), or the
pharmacologically acceptable salt thereof.
[0188] (33) The thiadiazoline derivative according to the
aforementioned (32), wherein R.sup.6 is substituted or
unsubstituted lower alkyl, substituted or unsubstituted lower
alkynyl, substituted or unsubstituted lower alkenyl, or substituted
or unsubstituted cycloalkyl, or the pharmacologically acceptable
salt thereof.
[0189] (34) The thiadiazoline derivative according to the
aforementioned (32) or (33), wherein W is an oxygen atom, or the
pharmacologically acceptable salt thereof.
[0190] (35) The thiadiazoline derivative according to any one of
the aforementioned (20) to (29), wherein R.sup.1A and R.sup.2A are
combined together with the adjacent nitrogen atom to form a
substituted or unsubstituted heterocyclic group, or the
pharmacologically acceptable salt thereof.
[0191] (36) The thiadiazoline derivative according to any one of
the aforementioned (20) to (35), wherein R.sup.3A is
--C(.dbd.W.sup.A)R.sup.6A (wherein W.sup.A and R.sup.6A have the
same meanings as those of the aforementioned, respectively), or the
pharmacologically acceptable salt thereof.
[0192] (37) The thiadiazoline derivative according to the
aforementioned (36), wherein R.sup.6A is substituted or
unsubstituted lower alkyl, substituted or unsubstituted lower
alkynyl, substituted or unsubstituted lower alkenyl, or substituted
or unsubstituted cycloalkyl, or the pharmacologically acceptable
salt thereof.
[0193] (38) The thiadiazoline derivative according to the
aforementioned (36), wherein R.sup.6A is lower alkyl, or the
pharmacologically acceptable salt thereof.
[0194] (39) The thiadiazoline derivative according to any one of
the aforementioned (36) to (38), wherein W.sup.A is an oxygen atom,
or the pharmacologically acceptable salt thereof.
[0195] (40) A pharmaceutical composition which comprises the
thiadiazoline derivative according to any one of the aforementioned
(20) to (39) or a pharmacologically acceptable salt thereof as an
active ingredient.
[0196] (41) An antitumor agent which comprises the thiadiazoline
derivative according to any one of the aforementioned (20) to (39)
or a pharmacologically acceptable salt thereof as an active
ingredient.
[0197] (42) Use of the thiadiazoline derivative according to any
one of the aforementioned (20) to (39) or a pharmacologically
acceptable salt thereof for the manufacture of an antitumor
agent.
[0198] (43) A method for the treatment of malignant tumor
comprising administering an effective amount of the thiadiazoline
derivative according to any one of the aforementioned (20) to (39)
or a pharmacologically acceptable salt thereof.
[0199] Hereinafter, compounds represented by the general formulae
(I) and (IA) are referred to as Compound (I) and Compound (IA),
respectively. The compounds having the other formula numbers are
referred to in the same manner.
[0200] In the definition of each group of Compound (I) and Compound
(IA),
[0201] (i) examples of the lower alkyl moiety in the lower alkyl,
the lower alkoxy, the lower alkylamino and the di(lower alkyl)amino
include straight or branched chain alkyl having 1 to 10 carbon
atoms, for example, methyl, ethyl, propyl, isopropyl, butyl,
isobutyl, sec-butyl, tert-butyl, pentyl, isopentyl, neopentyl,
hexyl, heptyl, octyl, nonyl, decyl and the like.
[0202] The two lower alkyl moieties in the di(lower alkyl)amino may
be the same or different.
[0203] (ii) Examples of the cycloalkyl include cycloalkyl having 3
to 8 carbon atoms, for example, cyclopropyl, cyclobutyl,
cyclopentyl, cyclohexyl, cycloheptyl, cyclooctyl and the like.
[0204] Examples of the cycloalkylene include cycloalkylene having 3
to 8 carbon atoms, for example, cyclopropylene, cyclobutylene,
cyclopentylene, cyclohexylene, cycloheptylene, cyclooctylene and
the like.
[0205] (iii) Examples of the lower alkenyl include straight or
branched chain alkenyl having 2 to 8 carbon atoms, for example,
vinyl, allyl, butenyl, pentenyl, hexenyl, heptenyl, octenyl and the
like.
[0206] (iv) Examples of the lower alkynyl include straight or
branched chain alkynyl having 2 to 8 carbon atoms, for example,
ethynyl, propynyl, butynyl, pentynyl, hexynyl, heptynyl, octynyl
and the like.
[0207] (v) Examples of the aryl moiety in the aryl, the aryloxy and
the arylamino include phenyl, naphthyl and the like.
[0208] (vi) Examples of the heterocyclic group include an aliphatic
heterocyclic group, an aromatic heterocyclic group and the like.
Examples of the aliphatic heterocyclic group include a 5- or
6-membered monocyclic aliphatic heterocyclic group containing at
least one atom selected from a nitrogen atom, an oxygen atom and a
sulfur atom, and a bicyclic or tricyclic condensed aliphatic
heterocyclic group comprising 3- to 8-membered rings and containing
at least one atom selected from a nitrogen atom, an oxygen atom and
a sulfur atom, and the like, for example, pyrrolidinyl,
imidazolidinyl, piperidinyl, piperazinyl, morpholinyl,
thiomorpholinyl, piperidino, morpholino, oxazolinyl, dioxolanyl,
tetrahydropyranyl and the like. Examples of the aromatic
heterocyclic group include a 5- or 6-membered monocyclic aromatic
heterocyclic group containing at least one atom selected from a
nitrogen atom, an oxygen atom and a sulfur atom, and a bicyclic or
tricyclic condensed aromatic heterocyclic group comprising 3- to
8-membered rings and containing at least one atom selected from a
nitrogen atom, an oxygen atom and a sulfur atom, and the like, for
example, furyl, thienyl, benzothienyl, pyrrolyl, pyridyl,
pyrazinyl, imidazolyl, pyrazolyl, triazolyl, thiazolyl,
isothiazolyl, thiadiazolyl, oxazolyl, oxadiazolyl, pyrimidinyl,
indolyl, isoindolyl, benzothiazolyl, benzimidazolyl,
benzotriazolyl, quinolyl, isoquinolyl, quinazolinyl, pyranyl and
the like.
[0209] (vii) Examples of the heterocyclic group formed together
with the adjacent nitrogen atom include an aliphatic heterocyclic
group containing at least one nitrogen atom, and the like. Said
aliphatic heterocyclic group containing at least one nitrogen atom
may contain an oxygen atom, a sulfur atom or another nitrogen atom,
and examples thereof include, for example, pyrrolidinyl,
morpholino, thiomorpholino, pyrazolidinyl, piperidino, piperazinyl,
homopiperazinyl, aziridinyl, azetidinyl, azolidinyl,
perhydroazepinyl, perhydroazocinyl, succinimidyl, pyrrolidonyl,
glutarimidyl, piperidonyl and the like.
[0210] (viii) The substituents in the substituted lower alkyl, the
substituted lower alkoxy, the substituted lower alkenyl, the
substituted lower alkynyl, the substituted cycloalkyl, the
substituted lower alkylamino, and the substituted di(lower
alkyl)amino may be the same or different and include for example, 1
to 3 substituent(s), such as halogen, oxo, hydroxy, nitro, azide,
cycloalkyl, aryl, a heterocyclic group, substituted aryl (the
substituent in said substituted aryl has the same meaning as that
of the after-mentioned substituent (xii) in the substituted aryl),
a substituted heterocyclic group (the substituent in said
substituted heterocyclic group has the same meaning as that of the
after-mentioned substituent (xiii) in the substituted heterocyclic
group), --CONR.sup.15R.sup.16 <wherein [0211] R.sup.15 and
R.sup.16 are the same or different and each represents [0212] a
hydrogen atom, hydroxy, cycloalkyl, lower alkyl, [0213] lower
alkenyl, aryl, a heterocyclic group, [0214] substituted aryl (the
substituent in said substituted aryl has the same meaning as that
of the after-mentioned substituent (xii) in the substituted aryl),
[0215] a substituted heterocyclic group (the substituent in said
substituted heterocyclic group has the same meaning as that of the
after-mentioned substituent (xiii) in the substituted heterocyclic
group) or [0216] substituted lower alkyl {in said substituted lower
alkyl, the substituents are the same or different and 1 to 3
substituent(s), such as [0217] hydroxy, lower alkoxy, oxo, carboxy,
lower alkoxycarbonyl, an aryl, a heterocyclic group,
--CONR.sup.15AR.sup.16A [wherein [0218] R.sup.15A and R.sup.16A are
the same or different and each represents [0219] a hydrogen atom,
hydroxy, lower alkyl, or [0220] substituted lower alkyl (in said
substituted lower alkyl, the substituents (a) are the same or
different and 1 to 3 substituent(s), such as hydroxy, lower alkoxy,
oxo, carboxy, lower alkoxycarbonyl, aryl, a heterocyclic group,
amino, lower alkylamino, di(lower alkyl)amino and the like), or
[0221] R.sup.15A and R.sup.16A are combined to form a heterocyclic
group [0222] together with the adjacent nitrogen atom], [0223]
--NR.sup.41R.sup.42 [wherein [0224] R.sup.41 and R.sup.42 are the
same or different and each represents [0225] a hydrogen atom, lower
alkyl, [0226] lower alkanoyl, aroyl, aryl, [0227] a heterocyclic
group, [0228] substituted lower alkyl (the substituent in said
substituted lower alkyl has the same meaning as that of the
aforementioned substituent (a) in the substituted lower alkyl),
[0229] a substituted lower alkanoyl (in said substituted lower
alkanoyl, the substituents (b) are the same or different and 1 to 3
substituent(s), such as hydroxy, lower alkoxy, oxo, carboxy, lower
alkoxycarbonyl, amino, lower alkylamino, di(lower alkyl)amino and
the like), [0230] substituted aroyl (the substituent in said
substituted aroyl has the same meaning as that of the
aforementioned substituent (b) in the substituted lower alkanoyl),
[0231] substituted aryl (the substituent in said substituted aryl
has the same meaning as that of the after-mentioned substituent
(xii) in the substituted aryl) or [0232] a substituted heterocyclic
group (the substituent in said substituted heterocyclic group has
the same meaning as that of the after-mentioned substituent (xiii)
in the substituted heterocyclic group), or [0233] R.sup.41 and
R.sup.42 are combined to form a heterocyclic group or a substituted
heterocyclic group together with the adjacent nitrogen atom (the
substituent in said substituted heterocyclic group formed together
with the adjacent nitrogen atom has the same meaning as that of the
after-mentioned substituent (xiii) in the substituted heterocyclic
group formed together with the adjacent nitrogen atom)]}, or [0234]
R.sup.15 and R.sup.16 are combined to form a heterocyclic group or
a substituted heterocyclic group together with the adjacent
nitrogen atom (the substituent in said substituted heterocyclic
group formed together with the adjacent nitrogen atom has the same
meaning as that of the after-mentioned substituent (xiii) in the
substituted heterocyclic group formed together with the adjacent
nitrogen atom)>, [0235] --CO.sub.2R.sup.26 {wherein [0236]
R.sup.26 represents [0237] a hydrogen atom, lower alkyl,
cycloalkyl, lower alkenyl, lower alkynyl, aryl, [0238] substituted
aryl (the substituent in said substituted aryl has the same meaning
as that of the after-mentioned substituent (xii) in the substituted
aryl), or [0239] substituted lower alkyl [in said substituted lower
alkyl, the substituents (c) are the same or different and 1 to 3
substituent(s), such as [0240] hydroxy, halogen, lower alkoxy, oxo,
carboxy, lower alkoxycarbonyl, aryl, a heterocyclic group, [0241]
--CONR.sup.15BR.sup.16B (wherein R.sup.15B and R.sup.16B have the
same meanings as those of the aforementioned R.sup.15 and R.sup.16,
respectively), [0242] --NR.sup.41AR.sup.42A (wherein R.sup.41A and
R.sup.42A have the same meanings as those of the aforementioned
R.sup.41 and R.sup.42, respectively), and the like]}, [0243]
--COR.sup.26A (wherein R.sup.26A has the same meaning as that of
the aforementioned R.sup.26), [0244] --NR.sup.17R.sup.18
<wherein [0245] R.sup.17 and R.sup.18 are the same or different
and each represents [0246] a hydrogen atom, lower alkyl, lower
alkenyl, aroyl, aryl, a heterocyclic group, cycloalkyl,
aralkyloxycarbonyl, [0247] substituted lower alkyl {in said
substituted lower alkyl, the substituents (d) are the same or
different and 1 to 3 substituent(s), such as [0248] hydroxy, lower
alkoxy, oxo, carboxy, [0249] lower alkoxycarbonyl, aryl, a
heterocyclic group, [0250] substituted aryl (the substituent in
said substituted aryl has the same meaning as that of the
after-mentioned substituent (xii) in the substituted aryl), [0251]
a substituted heterocyclic group (the substituent in said
substituted heterocyclic group has the same meaning as that of the
after-mentioned substituent (xiii) in the substituted heterocyclic
group), [0252] --O(CH.sub.2CH.sub.2O).sub.nR.sup.19 (wherein n
represents an integer of from 1 to 15, and R.sup.19 represents
lower alkyl), [0253] --CONR.sup.15CR.sup.16C (wherein R.sup.15C and
R.sup.16C have the same meanings as those of the aforementioned
R.sup.15 and R.sup.16, respectively), [0254] --SO.sub.2R.sup.24
[wherein [0255] R.sup.24 represents [0256] lower alkyl, arylor
[0257] substituted aryl (the substituent in said substituted aryl
has the same meaning as that of the after-mentioned substituent
(xii) in the substituted aryl)], [0258] --NR.sup.41BR.sup.42B
(wherein R.sup.41B and R.sup.42B have the same meanings as those of
the aforementioned R.sup.41 and R.sup.42, respectively), and the
like}, [0259] substituted aryl (the substituent in said substituted
aryl has the same meaning as that of the after-mentioned
substituent (xii) in the substituted aryl), [0260] a substituted
heterocyclic group (the substituent in said substituted
heterocyclic group has the same meaning as that of the
after-mentioned substituent (xiii) in the substituted heterocyclic
group), [0261] --COR.sup.26B {wherein [0262] R.sup.26B represents
[0263] lower alkyl, lower alkenyl, lower alkynyl, aryl, [0264]
substituted lower alkyl (the substituent in said substituted lower
alkyl has the same meaning as that of the aforementioned
substituent (c) in the substituted lower alkyl), [0265] substituted
aryl (the substituent in said substituted aryl has the same meaning
as that of the after-mentioned substituent (xii) in the substituted
aryl), [0266] --NR.sup.26CR.sup.26D (wherein R.sup.26C and
R.sup.26D are the same or different, and each has the same meaning
as that of the aforementioned R.sup.26) or [0267] --OR.sup.27
[wherein [0268] R.sup.27 represents [0269] lower alkyl, aryl,
[0270] substituted lower alkyl (the substituent in said substituted
lower alkyl has the same meaning as that of the aforementioned
substituent (c) in the substituted lower alkyl) or [0271]
substituted aryl (the substituent in said substituted aryl has the
same meaning as that of the after-mentioned substituent (xii) in
the substituted aryl)]}, or [0272] --SO.sub.2R.sup.26E (wherein
R.sup.26E has the same meaning as that of the aforementioned
R.sup.26), or [0273] R.sup.17 and R.sup.18 are combined to form a
heterocyclic group or a substituted heterocyclic group together
with the adjacent nitrogen atom (the substituent in said
substituted heterocyclic group formed together with the adjacent
nitrogen atom has the same meaning as that of the after-mentioned
substituent (xiii) in the substituted heterocyclic group formed
together with the adjacent nitrogen atom)>, [0274]
--N+R.sup.20R.sup.21R.sup.22X-- (wherein [0275] R.sup.20 and
R.sup.21 are the same or different and each represents lower alkyl,
or R.sup.20 and R.sup.21 are combined to form a heterocyclic group
together with the adjacent nitrogen atom, [0276] R.sup.22
represents lower alkyl, and [0277] X represents each atom of
chlorine, bromine or iodine), [0278] --OR.sup.23 {wherein [0279]
R.sup.23 represents [0280] lower alkyl, cycloalkyl, aryl, a
heterocyclic group, [0281] substituted aryl (the substituent in
said substituted aryl has the same meaning as that of the
after-mentioned substituent (xii) in the substituted aryl), [0282]
a substituted heterocyclic group (the substituent in said
substituted heterocyclic group has the same meaning as that of the
after-mentioned substituent (xiii) in the substituted heterocyclic
group), [0283] substituted lower alkyl [in said substituted lower
alkyl, the substituents (e) are the same or different and 1 to 3
substituent(s), such as [0284] hydroxy, halogen, lower alkoxy, oxo,
carboxy, [0285] lower alkoxycarbonyl, aryl, a heterocyclic group,
[0286] substituted aryl (the substituent in said substituted aryl
has the same meaning as that of the after-mentioned substituent
(xii) in the substituted aryl), [0287] a substituted heterocyclic
group (the substituent in said substituted heterocyclic group has
the same meaning as that of the after-mentioned substituent (xiii)
in the substituted heterocyclic group), [0288]
--O(CH.sub.2CH.sub.2O).sub.nAR.sup.19A (wherein nA and R.sup.19A
have the same meanings as those of the aforementioned n and
R.sup.19, respectively), [0289] --CONR.sup.15DR.sup.16D (wherein
R.sup.15D and R.sup.16D have the same meanings as those of R.sup.15
and R.sup.16, respectively), [0290] --NR.sup.41CR.sup.42C (wherein
R.sup.41C and R.sup.42C have the same meanings as those of the
aforementioned R.sup.41 and R.sup.42, respectively) and the like],
[0291] --COR.sup.26F (wherein R.sup.26F has the same meaning as
that of the aforementioned R.sup.26) or [0292]
--CONR.sup.15ER.sup.16E (wherein R.sup.15E and R.sup.16E have the
same meanings as those of the aforementioned R.sup.15 and R.sup.16,
respectively)}, [0293] --SR.sup.23A (wherein R.sup.23A has the same
meaning as that of the aforementioned R.sup.23), --SO.sub.2R.sup.25
[wherein [0294] R.sup.25 represents [0295] lower alkyl, cycloalkyl,
aryl, [0296] substituted lower alkyl (the substituent in said
substituted lower alkyl has the same meaning as that of the
aforementioned substituent (c) in the substituted lower alkyl),
[0297] a substituted aryl (the substituent in the substituted aryl
has the same meaning as that of the after-mentioned substituent
(xii) in the substituted aryl), or [0298] --NR.sup.15FR.sup.16F
(wherein R.sup.15F and R.sup.16F have the same meanings as those of
the aforementioned R.sup.15 and R.sup.16, respectively)], [0299]
--OSO.sub.2R.sup.25A (wherein R.sup.25A has the same meaning as
that of the aforementioned R.sup.25), and the like.
[0300] Herein, the lower alkyl moiety in the lower alkyl, the lower
alkoxy, the lower alkoxycarbonyl, the lower alkylamino and the
di(lower alkyl)amino, the aryl moiety in the aryl and the aroyl,
the cycloalkyl, the lower alkenyl, the lower alkynyl, the
heterocyclic group, and the heterocyclic group formed together with
the adjacent nitrogen atom have the same meanings as those of the
aforementioned lower alkyl (i), aryl (v), cycloalkyl (ii), lower
alkenyl (iii), lower alkynyl (iv), heterocyclic group (vi) and a
heterocyclic group formed together with the adjacent nitrogen atom
(vii), respectively. Also, the lower alkyl moiety in the lower
alkanoyl mentioned here has the same meaning as that of the
aforementioned lower alkyl (i), the halogen (ix) represents each
atom of fluorine, chlorine, bromine and iodine, and examples of the
aralkyl moiety (xi) in the aralkyloxycarbonyl include aralkyl
having 7 to 15 carbon atoms, for example, benzyl, phenethyl,
benzhydryl, naphthylmethyl and the like.
[0301] (xii) The substituents in the substituted aryl, the
substituted aryloxy, the substituted arylamino and the substituted
phenylene may be the same or different and 1 to 3 substituent(s),
such as [0302] halogen, lower alkyl, nitro, oxo, hydroxy, lower
alkoxy, amino, lower alkylamino, di(lower alkyl)amino, lower
alkylaminocarbonyloxy, di(lower alkyl)aminocarbonyloxy, lower
alkanoyl, lower alkanoylamino, lower alkanoyloxy, aryl,
arylsulfonyl, heterocyclic amino, aroyl, carboxy, lower
alkoxycarbonyl, cyano, methylenedioxy, [0303] substituted lower
alkyl (in said substituted lower alkyl, the substituents (f) are
the same or different and 1 to 3 substituent(s), such as halogen,
oxo, carboxy, lower alkoxycarbonyl, amino, lower alkylamino,
di(lower alkyl)amino, hydroxy, lower alkoxy and the like), [0304]
substituted arylsulfonyl (the substituent in said substituted
arylsulfonyl has the same meaning as that of the aforementioned
substituent (f)), [0305] substituted heterocyclic amino (the
substituent in said substituted heterocyclic amino has the same
meaning as that of the aforementioned substituent (f)) and the
like. [0306] the lower alkyl moiety in the lower alkyl, the lower
alkylamino, the di(lower alkyl)amino, the lower
alkylaminocarbonyloxy, the di(lower alkyl)aminocarbonyloxy (the two
lower alkyl moieties in said di(lower alkyl)aminocarbonyloxy may be
the same or different), the lower alkoxycarbonyl and the lower
alkoxy, the heterocyclic moiety in the heterocyclic amino, the aryl
moiety in the aryl, the arylsulfonyl and the aroyl, and the halogen
have the same meanings as those of the aforementioned lower alkyl
(i), heterocyclic group (vi), aryl (v) and halogen (ix),
respectively. Also, examples of the lower alkanoyl moiety (x) in
the lower alkanoyl, the lower alkanoylamino and the lower
alkanoyloxy which are noted here include a straight or branched
chain alkanoyl having 2 to 9 carbon atoms, for example, acetyl,
propionyl, butyryl, isobutyryl, valeryl, isovaleryl, pivaloyl,
hexanoyl, heptanoyl, octanoyl, nonanoyl and the like.
[0307] (xiii) Examples of the substituent in the substituted
heterocyclic group and the substituted heterocyclic group formed
together with the adjacent nitrogen atom include oxo and the like
as well as the aforementioned groups mentioned in the definition of
the substituent (xii) in the substituted aryl.
[0308] Example of the pharmacologically acceptable salt of Compound
(I) and Compound (IA) include pharmacologically acceptable acid
addition salts, metal salts, ammonium salts, organic amine addition
salts, amino acid addition salts and the like. Examples of the acid
addition salt include an inorganic salt such as a hydrochloride, a
sulfate and a phosphate, an organic acid salt such as an acetate, a
maleate, a fumarate, a tartrate, a citrate, a lactate, an
aspartate, a glutamate, succinate and the like. Examples of the
metal salt include an alkali metal salt such as a sodium salt and a
potassium salt, an alkaline-earth metal salt such as a magnesium
salt and a calcium salt, an aluminium salt, a zinc salt and the
like. Examples of the ammonium salt include a salt of ammonium,
tetramethylammonium and the like. Examples of the organic amine
addition salt include an addition salt with morpholine, piperidine
or the like. Examples of the amino acid addition salt include an
addition salt with lysine, glycine, phenylalanine and the like.
[0309] Next, the methods of preparing the Compound (I) and the
Compound (IA) are described as follows.
[0310] In the preparing methods as shown below, when the defined
group changes under the conditions of the method carried out, or
the method is inappropriate for carrying out, the desired compound
can be obtained by using the protection and deprotection of the
groups which are ordinarily used in the synthetic organic chemistry
[e.g., Protective Groups in Organic Synthesis, T. W. Greene, John
Wiley & Sons Inc. (1981)] and the like. In addition, the order
of the steps for introducing a substituent and the like may be
changed, if necessary.
[0311] Compound (I) can be prepared according to the following
reaction steps.
[0312] Compound (IA) can also be prepared in the similar manner as
in the preparing methods of Compound (I) as shown below.
Preparing method 1
[0313] Among Compound (I), Compound (Ia) wherein R.sup.2 is a
hydrogen atom, substituted or unsubstituted lower alkyl,
substituted or unsubstituted lower alkynyl, substituted or
unsubstituted lower alkenyl, or substituted or unsubstituted
cycloalkyl, or R.sup.1 and R.sup.2 are combined to form a
substituted or unsubstituted heterocyclic group together with the
adjacent nitrogen atom, and R.sup.3 is --C(.dbd.O)R.sup.6A can be
obtained from Compound (II) and Compound (III),via Compound (IV),
in accordance with known methods [e.g., J. Heterocyclic Chem., Vol.
21, p. 599 (1984) and the like]: ##STR4## (wherein R.sup.1,
R.sup.4, R.sup.5, R.sup.6 and R.sup.6A have the same meanings as
those mentioned above, respectively, X.sup.1 has the same meaning
as that of the aforementioned X, and R.sup.2a represents a hydrogen
atom, substituted or unsubstituted lower alkyl, substituted or
unsubstituted lower alkynyl, substituted or unsubstituted lower
alkenyl, or substituted or unsubstituted cycloalkyl among the
definition of the aforementioned R.sup.2, or R.sup.1 and R.sup.2a
are combined to form a substituted or unsubstituted heterocyclic
group together with the adjacent nitrogen atom.) Preparing method
2
[0314] Among Compound (I), Compound (Ib) wherein R.sup.2 and
R.sup.3 are the same to be --C(.dbd.O)R.sup.6B (wherein R.sup.6B
has the same meaning as that of the aforementioned R.sup.6) can be
obtained from Compound (IVa) among Compound (IV) prepared by the
preparing method 1 wherein R.sup.2a is a hydrogen atom, and
Compound (Va) or Compound (Vb) in accordance with known methods
[e.g., J. Bangladesh Chem. Soc., Vol. 5, p. 127 (1992), J. Org.
Chem., Vol. 45, p. 1473 (1980), Patent of East Germany No. 243930,
and the like]: ##STR5## (wherein R.sup.1, R.sup.4, R.sup.5 and
R.sup.6B have the same meanings as those mentioned above,
respectively.) Preparing method 3
[0315] Among Compound (Ia), Compound (Ic) wherein R.sup.2 is a
hydrogen atom and R.sup.3 is --C(.dbd.O)R.sup.6A can be obtained by
the following step from Compound (Ib) prepared by the Preparing
method 2: ##STR6## (wherein R.sup.1, R.sup.4, R.sup.5, R.sup.6A and
R.sup.6B have the same meanings as those mentioned above,
respectively.)
[0316] Compound (Ic) can be obtained by treatment of Compound (Ib)
in an inert solvent, for example, N,N-dimethylformamide and the
like, in the presence of an appropriate base such as sodium hydride
and the like, at a temperature between 0.degree. C. and 80.degree.
C. for 10 minutes to 10 hours. The base is preferably used in an
amount of 1 to 5 equivalents to Compound (Ib).
[0317] Alternatively, Compound (Ic) can also be obtained by the
following method.
[0318] Compound (Ic) can be obtained by treatment of Compound (Ib)
in an inert solvent, for example, aqueous or anhydrous ethanol,
acetonitrile, chloroform and the like, in the presence of an
appropriate base such as hydrazine monohydrate, aqueous sodium
hydroxide and the like, at a temperature between 0.degree. C. and
50.degree. C. for 1 to 10 hours. The base is preferably used in an
amount of 2 to 10 equivalents to Compound (Ib).
[0319] Compound (Ic) can also be obtained by the following
method.
[0320] Compound (Ic) can be obtained by treatment of Compound (Ib)
in a solvent such as methanol, tert-butanol and the like, in the
presence of a reducing agent such as sodium borohydride and the
like, and if necessary, in the presence of cerium chloride
heptahydrate and the like, at a temperature between -10.degree. C.
and 100.degree. C. for 0.1 to 15 hours. The reducing agent is
preferably used in an amount of 1 to 200 equivalents to Compound
(Ib).
Preparing method 4
[0321] Among Compound (I), Compound (Ie) wherein R.sup.2 is
--C(.dbd.O)R.sup.6 and R.sup.3 is --C(.dbd.O)R.sup.6A can be
obtained by the following step from Compound (Ic) obtained by the
Preparing method 1 or 3. ##STR7## (wherein R.sup.1, R.sup.4,
R.sup.5, R.sup.6 and R.sup.6A have the same meanings as those
mentioned above, respectively, and X.sup.2 has the same meaning as
that of the aforementioned X.)
[0322] Compound (Ie) can be obtained by allowing Compound (Ic) to
react with Compound (VA) or Compound (VB) in an inert solvent, for
example, acetone, ethyl acetate, acetonitrile,
N,N-dimethylformamide, dichloromethane and the like, in the
presence of an appropriate base such as pyridine,
4-(dimethylamino)pyridine (DMAP), sodium hydride and the like, at a
temperature between 0.degree. C. and 120.degree. C. for 2 to 12
hours. The base and Compound (VA) or Compound (VB) are preferably
used, respectively, in an amount of 1 to 3 equivalents to Compound
(Ic).
Preparing method 5
[0323] Among Compound (I), Compound (If) wherein R.sup.2 is
--SO.sub.2R.sup.14 and R.sup.3 is --C(.dbd.O)R.sup.6A can be
obtained from Compound (Ic) prepared by the Preparing method 1 or 3
in accordance with the method described in for example,
Shin-Jikken-Kagaku-Koza (New Experiment Chemistry Lecture) Vol. 14,
p. 1803 (Maruzen, 1978): ##STR8## (wherein R.sup.1, R.sup.4,
R.sup.6, R.sup.6A and R.sup.14 have the same meanings as those
mentioned above, respectively, and X.sup.3 has the same meaning as
that of the aforementioned X.) Preparing method 6
[0324] Among Compound (I), Compound (Ig) wherein R.sup.2 is
--NR.sup.11R.sup.12 and R.sup.3 is --C(.dbd.O)R.sup.6A can be
obtained from Compound (VII) prepared in accordance with the method
described in Indian J. Chem., Section B, Vol. 31(B), p. 547 (1992)
in accordance with the methods described in for example, Indian J.
Chem., Section B, Vol. 31B(8), p. 547 (1992), Phosphorus Sulfur
& Silicon & the Related Elements, Vol. 122, p. 307 (1997)
and the like: ##STR9## (wherein R.sup.1, R.sup.4, R.sup.5,
R.sup.6A, R.sup.11 and R.sup.12 have the same meanings as those
mentioned above, respectively.) Preparing method 7
[0325] Among Compound (le), Compound (Ie-b) wherein R.sup.1 is
substituted or unsubstituted lower alkyl, substituted or
unsubstituted lower alkynyl, substituted or unsubstituted lower
alkenyl, or substituted or unsubstituted cycloalkyl can be obtained
by the following step from Compound (Ie-a) among Compound (Ie)
wherein R.sup.1 is a hydrogen atom prepared by the Preparing method
4: ##STR10## (wherein R.sup.4, R.sup.5, R.sup.6 and R.sup.6A have
the same meanings as those mentioned above, respectively, X.sup.4
has the same meaning as that of the aforementioned X, and R.sup.1a
represents substituted or unsubstituted lower alkyl, a substituted
or unsubstituted lower alkynyl, substituted or unsubstituted lower
alkenyl, or substituted or unsubstituted cycloalkyl among the
definition of the aforementioned R.sup.1.)
[0326] Compound (Ie-b) can be obtained by allowing Compound (Ie-a)
to react with Compound (VIII) in an inert solvent, for example,
N,N-dimethylformamide and the like, in the presence of an
appropriate base such as sodium hydroxide, at a temperature between
0.degree. C. and room temperature for 1 to 24 hours. The base and
Compound (VIII) are preferably used in amounts of 2 to 5
equivalents and 2 to 3 equivalents, respectively, to Compound
(Ie-a).
Preparing method 8
[0327] Among Compound (I), Compound (Ih) wherein R.sup.3 is a
hydrogen atom can be obtained by the methods described in for
example, Phosphorus, Sulfur and Silicone and the Related Elements,
Vol. 122, p. 307 (1997) and Chem. Ber., Vol. 123, p. 691 (1990) and
the like, or the methods similar to the aforementioned methods.
Preparing method 9
[0328] Among Compound (I), Compound (Ij) wherein R.sup.2 and/or
R.sup.3 is --C(.dbd.S)R.sup.6 and/or --C(.dbd.S)R.sup.6A,
respectively, can be obtained by thiocarbonylation of Compound (Ik)
wherein the corresponding R.sup.2 and/or R.sup.3 is
--C(.dbd.O)R.sup.6 and/or --C(.dbd.O)R.sup.6A, respectively, among
Compound (Ia) to Compound (Ih) obtained by the aforementioned the
Preparing methods 1 to 7.
[0329] For example, Compound (Ij) can be obtained by treatment of
Compound (Ik) in a solvent such as toluene and tetrahydrofuran,
with an appropriate thiocarbonylating agent such as
2,4-bis(4-methoxyphenyl)-1,3-dithia-2,4-diphophethane-2,4-disulfide
(Lawesson's reagent), phosphorus pentasulfide and the like, at a
temperature between room temperature and the boiling point of the
solvent for 1 to 24 hours. The thiocarbonylating agent is
preferably used in an amount of 2 to 10 equivalents to Compound
(Ik).
Preparing method 10
[0330] Among Compound (I), Compound (Im) wherein R.sup.3 is
--C(.dbd.O)R.sup.6A and R.sup.1 and R.sup.2f are combined to form a
substituted or unsubstituted heterocyclic group together with the
adjacent nitrogen atom can be obtained by the following step from
Compound (In) wherein R.sup.1 and R.sup.2a are hydrogen atoms among
Compound (Ia) prepared by the Preparing method 1, or from Compound
(In) wherein R.sup.1 is a hydrogen atom among Compound (Ic)
prepared by the Preparing method 3: ##STR11## (wherein R.sup.4,
R.sup.5 and R.sup.6A have the same meanings as those mentioned
above, respectively, X.sup.5 has the same meaning as that of the
aforementioned X, R.sup.1b and R.sup.2b represent a substituted or
unsubstituted heterocyclic group formed together with the adjacent
nitrogen atom, said heterocyclic group formed together with the
adjacent nitrogen atom has the same meaning as that of the
aforementioned heterocyclic group (vii) formed together with the
adjacent nitrogen atom, and the substituent in said substituted
heterocyclic group formed together with the adjacent nitrogen atom
has the same meaning as that of the aforementioned substituent
(xiii) in the heterocyclic group.)
[0331] Compound (Ip) can be obtained from Compound (In) by the
methods described in for example, Chem. Commun., Vol. 8, p. 873
(1998) and the like, or the methods similar to the aforementioned
methods.
[0332] Compound (Im) can be obtained by allowing Compound (Ip) to
react with Compound (IX) in an inert solvent, for example,
dichloromethane and the like, at a temperature between 0.degree. C.
and 60.degree. C. for 10 minutes to 24 hours. Compound (IX) is
preferably used in an amount of 2 to 50 equivalents to Compound
(Ip).
[0333] Alternatively, Compound (Im) can also be obtained from
Compound (Ie-c) wherein R.sup.1 is a hydrogen atom and R.sup.6 is
an alkyl group substituted with carboxyl group among Compound (Ie)
prepared by the Preparing method 4 by the method described in for
example, Synthesis-Stuttgart, Vol. 5, p. 420 (1991) or the methods
similar to the aforementioned method.
[0334] Moreover, Compound (Im) can also be obtained from Compound
(Ie-d) wherein R.sup.1 is a hydrogen atom and R.sup.6 is an alkyl
group substituted with halogen among Compound (Ie) by the method
described in for example, Shin-Jikken-Kagaku-Koza (New Experiment
Chemistry Lecture) Vol. 14, p. 1174 (Maruzen, 1978) and the like,
or the methods similar to the aforementioned methods.
[0335] Furthermore, among Compound (I), Compound (Ij-a) wherein
R.sup.3 is --C(.dbd.S)R.sup.6A and R.sup.1 and R.sup.2 are combined
to form a substituted or unsubstituted heterocyclic group together
with the adjacent nitrogen atom can be obtained from Compound (Im)
in the similar manner as the aforementioned the Preparing method
9.
[0336] In Compound (I), conversion of the functional group
contained in R.sup.1, R.sup.2, R.sup.3, R.sup.4 or R.sup.5 can also
be carried out by the aforementioned steps, or also by the other
known methods [e.g., Comprehensive Organic Transformations, R. C.
Larock (1989) and the like].
[0337] Compound (I) having the desired functional group at the
desired position can be obtained by carrying out the aforementioned
methods in appropriate combination.
[0338] The intermediates and the objective compounds in the
aforementioned preparation methods can be purified and isolated by
conducting a purification method ordinarily used in the synthetic
organic chemistry such as filtration, extraction, washing, drying,
concentration, recrystallization, various chromatography such as
high performance-liquid chromatography, thin layer chromatography,
silica gel chromatography and the like. The intermediates can also
be subjected to the next reaction without paticular
purification.
[0339] Some compounds among Compounds (I) may exist as position
isomers, geometrical isomers, optical isomers, tautomers and the
like. All possible isomers including the aforementioned isomers and
mixtures thereof can be used for the antitumor agent of the present
invention.
[0340] To obtain a salt of Compound (I), when Compound (I) obtained
as a salt form, it may be purified as it is. When Compound (I)
obtained as a free form, it may be dissolved or suspended in an
appropriate solvent, and added with an appropriate acid or base to
form a salt and then be isolated.
[0341] In addition, Compound (I) or a pharmacologically acceptable
salt thereof may exist in the form of adducts with water or variety
of solvents, which also can be used for the antitumor agent of the
present invention.
[0342] Specific examples of Compound (IA) obtained by the present
invention are shown in Tables 1 to 10. However, the compounds of
the present invention are not limited to these examples.
[0343] The compounds shown in Tables 1 to 10 are used for the
antitumor agent of the present invention, and other than the
compounds, specific examples of compounds used in the present
invention are shown in Tables 11 to 13. However, the compound used
in the present invention is not limited to these examples.
TABLE-US-00001 TABLE 1 ##STR12## Example Compound R.sup.1A R.sup.2A
R.sup.4A No. No. 2 2 --H --COCH.sub.3 --CH.sub.2CH.sub.3 4 4 --H
--COCH.sub.3 --CH(CH.sub.3).sub.2 5 5 --H --COCH.sub.3 ##STR13## 7
7 --CH.sub.3 --COCH.sub.3 --CH.sub.3 8 8 --CH.sub.2CH.sub.3
--CH.sub.2CH.sub.3 --CH.sub.3 8 9 --CH.sub.2CH.sub.3 --COCH.sub.3
--CH.sub.3 9 10 --(CH.sub.2).sub.2CH.sub.3
--(CH.sub.2).sub.2CH.sub.3 -CH3 9 11 --(CH.sub.2).sub.2CH.sub.3
--COCH.sub.3 --CH.sub.3 129 136 --H --CO.sub.2C(CH.sub.3).sub.3
--CH.sub.3 130 137 --H --CON(CH.sub.3).sub.2 --CH.sub.3 131 138
##STR14## --CH.sub.3 132 139 ##STR15## --CH.sub.3 133 140 --H
--CO(CH.sub.2).sub.4CH.sub.3 --CH.sub.2NHSO.sub.2CH.sub.3 134 141
--H --COCH.dbd.CHCH.sub.3 --CH.sub.2NHSO.sub.2CH.sub.3 135 142 --H
##STR16## --CH.sub.2NHSO.sub.2CH.sub.3 136 143 --H
--COC(CH.sub.3).sub.2OCOCH.sub.3 --CH.sub.2NHSO.sub.2CH.sub.3 137
144 --H --COC(CH.sub.3).sub.2OH --CH.sub.2NHSO.sub.2CH.sub.3 138
145 --H --COCH.sub.2OCH.sub.3 --CH.sub.2NHSO.sub.2CH.sub.3 139 146
--H --COCH.sub.2Cl --CH.sub.2NHSO.sub.2CH.sub.3 140 147 --H
--COCH.sub.2N(CH.sub.3).sub.2 --CH.sub.2NHSO.sub.2CH.sub.3 141 148
--H --CO(CH.sub.2).sub.3CO.sub.2CH.sub.3
--CH.sub.2NHSO.sub.2CH.sub.3 142 149 --H
--CO(CH.sub.2).sub.3CO.sub.2H --CH.sub.2NHSO.sub.2CH.sub.3 143 150
##STR17## --CH.sub.2NHSO.sub.2CH.sub.3 144 151 --H
--CO(CH.sub.2).sub.3Br --CH.sub.2NHSO.sub.2CH.sub.3 145 152
##STR18## --CH.sub.2NHSO.sub.2CH.sub.3 146 153 --H
--CO(CH.sub.2).sub.4Br --CH.sub.2NHSO.sub.2CH.sub.3 147 154
##STR19## --CH.sub.2NHSO.sub.2CH.sub.3 148 155 --H
--CO(CH.sub.2).sub.5Br --CH.sub.2NHSO.sub.2CH.sub.3 149 156
##STR20## --CH.sub.2NHSO.sub.2CH.sub.3
[0344] TABLE-US-00002 TABLE 2 ##STR21## Example Compound R.sup.1A
R.sup.2A R.sup.3A No. No. 10 12 --CH.sub.2Ph --CH.sub.2Ph
--COCH.sub.3 10 13 --CH.sub.2Ph --COCH.sub.3 --COCH.sub.3 12 15
--CH.sub.3 --H --COCH.sub.3 13 16 --CH.sub.3 --CH.sub.3
--COCH.sub.3 14 17 --CH.sub.3 --H --COCH.sub.2CH.sub.3 15 18
--CH.sub.3 --COCH.sub.3 --COCH.sub.2CH.sub.3 16 19 --CH.sub.3
--COCH.sub.2CH.sub.3 --COCH.sub.2CH.sub.3 17 20 --CH.sub.3
--CO(CH.sub.2).sub.2CH.sub.3 --CO(CH.sub.2).sub.2CH.sub.3 18 21
--CH.sub.3 --COCH(CH.sub.3).sub.2 --COCH(CH.sub.3).sub.2 76 79
--CH.sub.2CH.dbd.CH.sub.2 --COCH.sub.3 --COCH.sub.3 77 80
--CH.sub.2CH.dbd.CH.sub.2 --H --COCH(CH.sub.3).sub.2 77 81
--CH.sub.2CH.dbd.CH.sub.2 --COCH.sub.3 --COCH(CH.sub.3).sub.2 78 82
--H --COC(CH.sub.3).sub.3 --COC(CH.sub.3).sub.3 79 83 --CH.sub.3
--H --COCH(CH.sub.3).sub.2 79 84 --CH.sub.3 --COCH.sub.3
--COCH(CH.sub.3).sub.2 80 85 --H --COCH(CH.sub.3).sub.2
--COCH(CH.sub.3).sub.2 81 86 --H --H --COCH(CH.sub.3).sub.2 81 87
--H --COCH.sub.3 --COCH(CH.sub.3).sub.2 82 88 --H
--COCH(CH.sub.3).sub.2 --COCH.sub.3 83 89 --H ##STR22##
--COCH.sub.3 84 90 --H --H --COCH.sub.2CH(CH.sub.3).sub.2 84 91 --H
--COCH(CH.sub.3).sub.2 --COCH.sub.2CH(CH.sub.3).sub.2 85 92 --H
--COCH.sub.3 --COC(CH.sub.3).sub.3 86 93 --H --COC(CH.sub.3).sub.3
--COCH.sub.3 * Ph: phenyl
[0345] TABLE-US-00003 TABLE 3 ##STR23## Example Compound R.sup.1A
R.sup.4A R.sup.5A No. No. 22 25 --H --CH.sub.3 --CH.dbd.CHPh 23 26
--H --(CH.sub.2).sub.3CH.sub.3 --(CH.sub.2).sub.3CH.sub.3 24 27 --H
##STR24## 25 28 --H ##STR25## 26 29 --H ##STR26## 28 31 --H
##STR27## 29 32 --H --CH.sub.3 ##STR28## 30 33 --H --CH.sub.3
##STR29## 31 34 --H --CH.sub.3 ##STR30## 32 35 --H --CH.sub.3
##STR31## 33 36 --H --CH.sub.3 ##STR32## 34 37 --H --CH.sub.3
##STR33## 35 38 --H --CH.sub.3 ##STR34## 38 41 --CH.sub.2CH.sub.3
--CH.sub.3 ##STR35## 39 42 --H --CH.sub.3 ##STR36## 40 43 --H
--CH.sub.3 ##STR37## 41 44 --H --CH.sub.3 ##STR38## 42 45 --H
--CH.sub.3 ##STR39## 125 132 --H --CH.sub.3 ##STR40## 126 133 --H
--CH.sub.3 ##STR41## 127 134 --H --CH.sub.3 ##STR42## * Ph:
Phenyl
[0346] TABLE-US-00004 TABLE 4 ##STR43## Example Compound R.sup.1A
R.sup.4A Y.sup.1A No. No. (Substituting position) 43 46 --H
--CH.sub.3 --CH.sub.3(2) 44 47 --H --CH.sub.3 --CH.sub.3(3) 45 48
--H --CH.sub.3 --CH.sub.3(4) 46 49 --H --CH.sub.2CH.sub.3
--CH.sub.2CH.sub.3(2) 47 50 --H --CH.sub.3 --OCH.sub.3(2) 48 51 --H
--CH.sub.3 --OCH.sub.3(3) 50 53 --H --CH.sub.3 --F (2) 51 54 --H
--CH.sub.3 --F (3) 52 55 --H --CH.sub.3 --F (4) 53 56 --H
--CH.sub.3 --Cl (2) 54 57 --CH.sub.2CH.sub.3 --CH.sub.3 --Cl (2) 55
58 --H --CH.sub.3 --Cl (3) 56 59 --H --CH.sub.3 --Cl (4) 57 60 --H
--CH.sub.3 --Br (2) 58 61 --H --CH.sub.3 --OCOCH.sub.3(2) 60 63 --H
--H --OCOCH.sub.3(3) 61 64 --H --CH.sub.3 --OCOCH.sub.3(4) 62 65
--H --CH.sub.3 --NO.sub.2(2) 65 68 --H --CH.sub.3 --OH (2) 66 69
--H --CH.sub.3 --OH (3) 67 70 --H --CH.sub.3 --OH (4) 68 71 --H
--CH.sub.3 --CN (3) 69 72 --H --CH.sub.3 --CN (4) 70 73 --H
--CH.sub.3 --CF.sub.3(3) 71 74 --H --CH.sub.3 --COOH (2) 118 125
--CH.sub.2CH.sub.3 --CH.sub.3 --OCOCH.sub.3(3) 119 126
--CH.sub.2CH.sub.3 --CH.sub.3 --OH (3) 120 127 --H --CH.sub.3
--OCONHCH.sub.2CH.sub.3(3)
[0347] TABLE-US-00005 TABLE 5 ##STR44## Example Compound Y.sup.1A
Y.sup.2A No. No. (Substituting position) (Substituting position) 72
75 --OCH.sub.3(2) --OCH.sub.3(6) 73 76 --OH (3) --OH (5) 74 77 --OH
(3) --OH (4) 75 78 --CH.sub.3(2) --CH.sub.3(4)
[0348] TABLE-US-00006 TABLE 6 ##STR45## Example Compound R.sup.1A
R.sup.4A R.sup.5A No. No. 87 94 --H --CH.sub.2CH.sub.3 -Ph 88 95
--H --CH.sub.2NHSO.sub.2CH.sub.3 -Ph 89 96 --CH.sub.3
--CH.sub.2NHSO.sub.2CH.sub.3 -Ph 90 97 --H
--CH.sub.2NHSO.sub.2CH.sub.2CH.sub.3 -Ph 91 98 --H
--CH.sub.2OCH.sub.3 -Ph 92 99 --H
--(CH.sub.2).sub.2NHSO.sub.2CH.sub.3 -Ph 94 101 --H
--CH.sub.2NHCOCF.sub.3 -Ph 97 104 --H
--(CH.sub.2).sub.2N(CH.sub.3).sub.2 -Ph 98 105 --H
--(CH.sub.2)COOCH.sub.3 -Ph 99 106 --H --(CH.sub.2).sub.2COOH -Ph
100 107 --H --(CH.sub.2).sub.2CONH.sub.2 -Ph 101 108 --H
--(CH.sub.2).sub.2CONHOH -Ph 102 109 --H
--(CH.sub.2).sub.2CONHCH.sub.3 -Ph 103 110 --H
--(CH.sub.2).sub.2CON(CH.sub.3).sub.2 -Ph 104 111 --H
--(CH.sub.2).sub.2CONH(CH.sub.2).sub.2OH -Ph 105 112 --H
--(CH.sub.2).sub.2CONH(CH.sub.2).sub.3CH.sub.3 -Ph 106 113 --H
##STR46## -Ph 107 114 --H --(CH.sub.2).sub.3COOCH.sub.3 -Ph 108 115
--H --(CH.sub.2).sub.3COOH -Ph 109 116 --H
--(CH.sub.2).sub.3CONHCH.sub.3 -Ph 110 117 --H
--(CH.sub.2).sub.3CONH.sub.2 -Ph 123 130 --H --CH.sub.3 ##STR47##
128 135 --H --CH.sub.3 ##STR48## 154 161 --H ##STR49## -Ph 155 162
--H ##STR50## -Ph 156 163 --H ##STR51## -Ph 156 164 --H ##STR52##
-Ph 157 165 --H ##STR53## -Ph 158 166 --H --(CH.sub.2).sub.3OH -Ph
159 167 --H --(CH.sub.2).sub.3OSO.sub.2NH.sub.2 -Ph * Ph: phenyl *
Ph: phenyl, Compound 164: an isomer of Compound 163
[0349] TABLE-US-00007 TABLE 7 ##STR54## Example Compound R.sup.1A
R.sup.4A R.sup.5A No. No. 93 100 --H
--(CH.sub.2).sub.2NHSO.sub.2CH.sub.3 -Ph 95 102
--COCH(CH.sub.3).sub.2 --CH.sub.2NHSO.sub.2CH.sub.3 -Ph 96 103 --H
--CH.sub.2NHSO.sub.2CH.sub.3 -Ph 121 128 --H --CH.sub.3 ##STR55##
122 129 --H --CH.sub.3 ##STR56## 124 131 --H --CH.sub.3 ##STR57## *
Ph: phenyl
[0350] TABLE-US-00008 TABLE 8 ##STR58## Example Compound R.sup.2A
R.sup.3A R.sup.4A No. No. 111 118 --H --COCH.sub.3
--CH.sub.2NHSO.sub.2CH.sub.3 112 119 --COC(CH.sub.3).sub.3
--COCH.sub.3 --CH.sub.2NHSO.sub.2CH.sub.3 113 120 --H
--COC(CH.sub.3).sub.3 --CH.sub.2NHSO.sub.2CH.sub.3 114 121
--CO(CH.sub.2).sub.5Br --COC(CH.sub.3).sub.3
--CH.sub.2NHSO.sub.2CH.sub.3 115 122 --CO(CH.sub.2).sub.5N.sub.3
--COC(CH.sub.3).sub.3 --CH.sub.2NHSO.sub.2CH.sub.3 116 123
--CO(CH.sub.2).sub.5NH.sub.2 --COC(CH.sub.3).sub.3
--CH.sub.2NHSO.sub.2CH.sub.3 117 124
--CO(CH.sub.2).sub.5NHCOCH.sub.3 --COC(CH.sub.3).sub.3
--CH.sub.2NHSO.sub.2CH.sub.3 150 157 --H --COC(CH.sub.3).sub.3
--(CH.sub.2).sub.2NH.sub.2CH.sub.3 151 158 --CO(CH.sub.2).sub.3Br
--COC(CH.sub.3).sub.3 --(CH.sub.2).sub.2NHSO.sub.2CH.sub.3 153 160
--COC(CH.sub.3).sub.3 --CSCH.sub.3 --CH.sub.2NHSO.sub.2CH.sub.3 160
168 --COC(CH.sub.3).sub.3 --COCH.sub.3
--CH.sub.2NHSO.sub.2CH.sub.2Cl 160 169 --COCH.sub.3 --COCH.sub.3
--CH.sub.2NHSO.sub.2CH.sub.2Cl 161 170 --COC(CH.sub.3).sub.3
--COCH.sub.3 --CH.sub.2NHSO.sub.2CH.dbd.CH.sub.2 161 171
--COC(CH.sub.3).sub.3 --COC(CH.sub.3).sub.3
--CH.sub.2NHSO.sub.2CH.dbd.CH.sub.2 162 172 --COC(CH.sub.3).sub.3
--COCH.sub.3 ##STR59## 163 173 --COC(CH.sub.3).sub.3 --COCH.sub.3
--CH.sub.2NHSO.sub.2(CH.sub.2).sub.2NHCH.sub.2CH.sub.3 164 174
--COC(CH.sub.3).sub.3 --COCH.sub.3
--CH.sub.2NHSO.sub.2(CH.sub.2).sub.2N(CH.sub.3).sub.2 165 175
--COC(CH.sub.3).sub.3 --COCH.sub.3
--CH.sub.2NHSO.sub.2(CH.sub.2).sub.2NH(CH.sub.2).sub.2 OH 166 176
--COC(CH.sub.3).sub.3 --COC(CH.sub.3).sub.3
--CH.sub.2NHSO.sub.2(CH.sub.2).sub.2NHCH.sub.2CH.sub.3 167 177
--COC(CH.sub.3).sub.3 --COC(CH.sub.3).sub.3
--CH.sub.2NHSO.sub.2(CH.sub.2).sub.2N(CH.sub.3).sub.2 168 178 --H
--COCH.sub.3 --(CH.sub.2).sub.2CO.sub.2CH.sub.3 169 179
--COC(CH.sub.3).sub.3 --COCH.sub.3
--(CH.sub.2).sub.2CO.sub.2CH.sub.3 170 180 --H
--COCH(CH.sub.3).sub.2 --(CH.sub.2).sub.2NHSO.sub.2CH.sub.3 171 181
--COC(CH.sub.3).sub.3 --COCH(CH.sub.3).sub.2
--(CH.sub.2).sub.2NHSO.sub.2CH CH.sub.3 174 184 ##STR60##
--COCH(CH.sub.3).sub.2 --(CH.sub.2).sub.2NHSO.sub.2CH.sub.3 175 185
--COCH.sub.2CH.sub.3 --COCH.sub.2CH.sub.3
--(CH.sub.2).sub.2NHSO.sub.2CH.sub.3 176 186 --H
--COCH.sub.2.sub.CH.sub.3 --(CH.sub.2).sub.2NHSO.sub.2CH.sub.3 177
187 --COC(CH.sub.3).sub.3 --COCH.sub.2CH.sub.3
--(CH.sub.2).sub.2NHSO.sub.2CH.sub.3 180 190 --H
--COC(CH.sub.3).sub.3 --(CH.sub.2).sub.2COOCH.sub.3 181 191
##STR61## --COC(CH.sub.3).sub.3 --(CH.sub.2).sub.2COOCH.sub.3
[0351] TABLE-US-00009 TABLE 9 ##STR62## Example Compound R.sup.1A
R.sup.2A R.sup.3A R.sup.4A No. No. 152 159 ##STR63##
--COC(CH.sub.3).sub.3 --(CH.sub.2).sub.2NHSO.sub.2CH.sub.3 172 182
##STR64## --COCH(CH.sub.3).sub.2
--(CH.sub.2).sub.2NHSO.sub.2CH.sub.3 173 183 ##STR65##
--COCH(CH.sub.3).sub.2 --(CH.sub.2).sub.2NHSO.sub.2CH.sub.3 178 188
##STR66## --COCH.sub.2CH.sub.3 --(CH.sub.2).sub.2NHSO.sub.2CH.sub.3
179 189 ##STR67## --COCH.sub.2CH.sub.3
--(CH.sub.2).sub.2NHSO.sub.2CH.sub.3 182 192 ##STR68##
--COC(CH.sub.3).sub.3 --(CH.sub.2).sub.2COOCH.sub.3 183 193
##STR69## --COC(CH.sub.3).sub.3 --(CH.sub.2).sub.2COOH 184 194
##STR70## --COC(CH.sub.3).sub.3
--(CH.sub.2).sub.2CONH(CH.sub.2).sub.2OH
[0352] TABLE-US-00010 TABLE 10 ##STR71## Example Compound R.sup.2A
R.sup.28 Y.sup.3A No. No. 185 195 --COC(CH.sub.3).sub.3
--OCOCH.sub.3 --H 186 196 --COC(CH.sub.3).sub.3 --OH --H 187 197
--H --H --OCOCH.sub.3 188 198 --COC(CH.sub.3).sub.3 --H
--OCOCH.sub.3 189 199 --COC(CH.sub.3).sub.3 --H --OH
[0353] TABLE-US-00011 TABLE 11 (I-ix) ##STR72## Example Compound
No. No. R.sup.2 R.sup.4 1 1 --COCH.sub.3 --CH.sub.3 3 3
--COCH.sub.3 --(CH.sub.2).sub.3CH.sub.3 6 6 --COCH.sub.3 --Ph 11 14
--H --CH.sub.3 *Ph: phenyl
[0354] TABLE-US-00012 TABLE 12 (I-x) ##STR73## Example Compound No.
No. R.sup.1 R.sup.4 R.sup.5 19 22 --H --CH.sub.3 --CH.sub.3 20 23
--H --CH.sub.3 --(CH.sub.2).sub.3CH.sub.3 21 24 --H --CH.sub.3
--(CH.sub.2).sub.2Ph 27 30 --H ##STR74## 36 39 --H --CH.sub.3
##STR75## 37 40 --H --CH.sub.3 ##STR76## *Ph: phenyl
[0355] TABLE-US-00013 TABLE 13 (I-xi) ##STR77## Example Compound
Y.sup.1 No. No. R.sup.1 R.sup.4 (Substituting position) 49 52 --H
--CH.sub.3 --OCH.sub.3 (4) 59 62 --H --CH.sub.3 --OCOCH.sub.3 (3)
63 66 --H --CH.sub.3 --NO.sub.2 (3) 64 67 --H --CH.sub.3 --NO.sub.2
(4)
[0356] Next, the pharmacological activity of typical Compounds (I)
will be explained by the following test example. [0357] Test
example 1: Antiproliferative activity in HCT 116 human colon cancer
cells
[0358] HCT 116 cells (ATCC No.: CCL-247) were placed on a 96-well
microtiter plate (Nunc, 167008) at a density of 1.times.10.sup.3
cells/well. The plate was incubated in a 5% CO.sub.2 incubator at
37.degree. C. for 24 hours, and then to the plate was added test
compounds diluted stepwise to 100 mL/well in total, and the plate
was further incubated in a 5% CO.sub.2 incubator at 37.degree. C.
for 72 hours. To the culture medium, the XTT (sodium
3'-[1-(phenylaminocarbonyl)-3,4-tetrazolium]-bis(4-methoxy-6-nitro)benzen-
esulfonic acid hydrate) labeling mixture (Roche Diagnostics,
1465015) was dispensed in 50 mL/well portions, then the plate was
incubated in a 5% CO.sub.2 incubator at 37.degree. C. for 1 hour,
and the absorbance was measured at 490 nm and 655 nm with a
microplate spectrophotometer (Bio-Rad, Model 550). The inhibitory
activity against cell proliferation was shown as a concentration of
50% proliferation inhibition, GI.sub.50. [0359] GI.sub.50
calculation method: The value (difference in absorbance) was
calculated by subtracting the absorbance at 655 nm from the
absorbance at 490 nm of each well. The difference in absorbance
obtained from the cells untreated with a test compound was defined
as 100%, and compared with the difference in absorbance obtained
from the cells treated with the solution of the compound in the
known concentration, and thereby the concentration of the compound
of 50% inhibition against cell proliferation was calculated to
obtain GI.sub.50.
[0360] The results of the typical compounds obtained in Test
example 1 are shown in Table 14. Compounds 138, 152, 165, 170, 173,
and 199 showed the GI.sub.50 value less than 10 .mu.mol/L.
TABLE-US-00014 TABLE 14 Compound No. GI.sub.50 (.mu.mol/L) 1 1.0 7
0.48 18 0.62 41 0.60 46 0.57 57 0.53 69 0.23 82 0.18 99 0.063 104
0.074 107 0.061 134 0.40
[0361] Compound (I) or Compound (IA), or a pharmacologically
acceptable salt thereof, per se, can be administered, however, is
generally desired to be provided as a form of various
pharmaceutical preparations. Also, the pharmaceutical preparations
are used for animals or human.
[0362] The pharmaceutical preparations according to the present
invention can comprise as an active ingredient Compound (I) or
Compound (IA), or a pharmacologically acceptable salt thereof,
solely or as a mixture with any other effective ingredient for the
treatment. The pharmaceutical preparations are manufactured by
mixing the active ingredient with one or more of pharmacologically
acceptable carriers using any method well known in the technical
field of pharmaceutical science.
[0363] As for administration routes, it is preferred to chose the
most effective route for the treatment such as oral administration
or parenteral administration, for example, intravenous
administration and the like.
[0364] Examples of formulations for administration include tablets,
injections and the like.
[0365] Examples of the pharmaceutical carrier used include lactose,
mannitol, glucose, hydroxypropyl cellulose, starch, magnesium
stearate, sorbitan fatty acid ester, glyceric acid ester, polyvinyl
alcohol, distilled water for injection, physiological saline,
propylene glycol, polyethylene glycol, ethanol and the like. The
pharmaceutical preparation according to the present invention may
comprise other various additives such as excipients, lubricants,
binders, disintegrator, isotonicities and emulsifiers.
[0366] Compound (I) or Compound (IA), or a pharmacologically
acceptable salt thereof is generally administered systemically or
locally in the form of an oral or parenteral preparation when used
for the aforementioned purpose. The dose and the frequency of
administration may vary depending on the administration form, the
age and body weight of a patient, nature and severity of the
condition to be treated, and the like. Generally, 0.1 to 1,000
mg/kg, preferably 0.5 to 500 mg/kg per single administration for an
adult may be administered orally or parenterally, once a day or a
few times a day, or may be continuously administered intravenously
for 1 to 24 hours a day. However, the dose and the frequency of
administration may vary depending on the aforementioned various
conditions and the like.
BEST MODE FOR CARRYING OUT THE INVENTION
[0367] The present invention will be explained in detail with
reference to the following examples.
[0368] The spectra of proton nuclear magnetic resonance (.sup.1H
NMR) used in Examples were measured at 270 or 300 MHz, and
exchangeable hydrogen may not always be clearly observed depending
on the compound and the measurement conditions. For the
descriptions of the multiplicity of signals, those generally
applied are used, and the symbol "br" represents an apparent broad
signal.
EXAMPLE 1
Compound 1
[0369] Step 1: Acetophenone (4.00 g, 33.3 mmol) and
thiosemicarbazide (3.15 g, 34.6 mmol) were dissolved in methanol
(30 mL). To the solution was added hydrochloric acid (0.1 mL) and
the mixture was vigorously stirred at room temperature for 15
hours. To the reaction mixture was added water (30 mL), and the
deposited crystals were collected by filtration. The collected
crystals were washed with water and diisopropyl ether, and then
dried to obtain acetophenone=thiosemicarbazone (5.64 g, 88%).
[0370] .sup.1H NMR (270 MHz, DMSO-d.sub.6) .delta.(ppm): 2.30 (S,
3H), 7.37-7.40 (m, 3H), 7.91-7.94 (m, 3H), 8.27 (br s, 1H), 10.21
(br S, 1H) [0371] Step 2: Acetophenone=thiosemicarbazone (300 mg,
0.889 mmol) obtained above was dissolved in acetic anhydride (1.0
mL, 11 mmol). After being refluxing under heating, the solution was
cooled to room temperature with vigorous stirring. To the reaction
mixture was added diisopropyl ether (3 mL), and the deposited
crystals were collected by filtration. After the collected crystals
were suspended in diisopropyl ether and stirred for 3 hours, the
crystals were collected by filtration and dried to obtain Compound
1 (195 mg, 72%). [0372] .sup.1H NMR (270 MHz, CDCl.sub.3)
.delta.(ppm): 2.01 (s, 3H), 2.19 (s, 3H), 2.28 (s, 3H), 7.24-7.36
(br s, 5H), 11.63 (br s, 1H)
EXAMPLE 2
Compound 2
[0372] [0373] Step 1: In a manner similar to that in Step 1 of
Example 1, propiophenone=thiosemicarbazone (759 mg, 88%) was
obtained from propiophenone (541 mg, 3.92 mmol) and
thiosemicarbazide (382 mg, 4.18 mmol). [0374] .sup.1H NMR (270 MHz,
DMSO-d.sub.6) .delta.(ppm): 1.01 (t, J=7.4 Hz, 3H), 2.85 (br q,
J=7.4 Hz, 2H), 7.39 (m, 3H), 7.89 (m, 3H), 8.24 (br s, 1H), 10.30
(br s, 1H) [0375] Step 2: In a manner similar to that in Step 2 of
Example 1, Compound 2 (601 mg, 76%) was obtained from
propiophenone=thiosemicarbazone (559 mg, 2.70 mmol) obtained above.
[0376] .sup.1H NMR (270 MHz, DMSO-d.sub.6) .delta.(ppm): 1.02 (t,
J=7.1 Hz, 3H), 2.00 (s, 3H), 2.21 (s, 3H), 2.38 (dt, J=7.1, 7.3 Hz,
1H), 2.85 (dt, J=7.1, 7.3 Hz, 1H), 7.23-7.38 (m, 5H), 11.59 (br s,
1H)
EXAMPLE 3
Compound 3
[0376] [0377] Step 1: In a manner similar to that in Step 1 of
Example 1, n-butyl(phenyl)methanone=thiosemicarbazone (589 mg, 63%)
was obtained from n-butyl(phenyl)methanone (649 mg, 4.00 mmol) and
thiosemicarbazide (367 mg, 4.03 mmol). [0378] .sup.1H NMR (270 MHz,
DMSO-d.sub.6) .delta.(ppm): 0.99 (t, J=7.3 Hz, 3H), 1.38-1.49 (m,
4H), 2.96-2.99 (m, 2H), 7.37-7.39 (m, 3H), 7.87-7.91 (m, 3H), 8.26
(br s, 1H), 10.36 (br s, 1H) [0379] Step 2: In a manner similar to
that in Step 2 of Example 1, Compound 3 (168 mg, 62%) was obtained
from n-butyl(phenyl)methanone=thiosemicarbazone (200 mg, 0.850
mmol) obtained above. [0380] .sup.1H NMR (270 MHz, CDCL.sub.3)
.delta.(ppm): 0.96 (t, J=7.3 Hz, 3H), 1.25-1.34 (m, 1H), 1.36-1.54
(m, 2H), 1.68-1.80 (m, 1H), 2.18 (s, 3H), 2.20-2.26 (m, 1H), 2.26
(s, 3H), 2.99-3.10 (m, 1H), 7.22-7.40 (m, 5H), 8.22 (br s, 1H)
EXAMPLE 4
Compound 4
[0380] [0381] Step 1: In a manner similar to that in Step 1 of
Example 1, isopropyl(phenyl)methanone=thiosemicarbazone (613 mg,
68%) was obtained from isopropyl(phenyl)methanone (608 mg, 4.10
mmol) and thiosemicarbazide (364 mg, 3.99 mmol). [0382] .sup.1H NMR
(270 MHz, DMSO-d.sub.6) .delta.(ppm): 1.07 (d, J=6.9 Hz, 6H), 2.82
(m, 1H), 7.28 (br d, J=6.3 Hz, 2H), 7.51-7.60 (m, 3H), 7.78 (br s,
1H), 8.23 (br s, 1H), 8.43 (br s, 1H) [0383] Step 2: In a manner
similar to that in Step 2 of Example 1, Compound 4 (217 mg, 52%)
was obtained from isopropyl(phenyl)methanone=thiosemicarbazone (300
mg, 1.36 mmol) obtained above. [0384] .sup.1H NMR (270 MHz,
CDCl.sub.3) .delta.(ppm): 1.04 (d, J=6.9 Hz, 3H), 1.13 (d, J=6.9
Hz, 3H), 2.09 (s, 3H), 2.19 (s, 3H), 3.86 (m, 1H), 7.25-7.36 (m,
3H), 7.75 (br d, J=7.3 Hz, 2H), 8.08 (br s, 1H)
EXAMPLE 5
Compound 5
[0385] In a manner similar to that in Step 1 and 2 of Example 1,
Compound 5 (130 mg, 10%) was obtained from
cyclopropyl(phenyl)methanone (649 mg, 4.00 mmol) and
thiosemicarbazide (367 mg, 4.03 mmol). [0386] .sup.1H NMR (270 MHz,
CDCl.sub.3) .delta.(ppm): 0.60-0.98 (m, 4H), 1.84 (s, 3H), 2.34 (s,
3H), 2.45 (m, 1H), 7.20-7.35 (m, 3H), 7.54 (br d, J=8.7 Hz, 2H),
9.40 (br s, 1H)
EXAMPLE 6
Compound 6
[0387] In a manner similar to that in Step 1 and 2 of Example 1,
Compound 6 (150 mg, 29%) was obtained from benzophenone (0.20 g,
2.19 mmol) and thiosemicarbazide (400 mg, 2.20 mmol). [0388]
.sup.1H NMR (270 MHz, CDCl.sub.3) .delta.(ppm): 1.89 (s, 3H), 2.32
(s, 3H), 7.25-7.52 (m, 10H), 9.13 (br s, 1H)
EXAMPLE 7
Compound 7
[0388] [0389] Step 1: In a manner similar to that in Step 1 of
Example 1, acetophenone=4-methylthiosemicarbazone (1.51 g, 77%) was
obtained from 4-methylthiosemicarbazide (1.00 g, 9.51 mmol) and
acetophenone (1.33 mL, 11.4 mmol). [0390] Step 2: In a manner
similar to that in Step 2 of Example 1, Compound 7 (1.03 g, 47%)
was obtained from acetophenone=4-methylthiosemicarbazone (1.00 g,
9.51 mmol) obtained above. [0391] .sup.1H NMR (270 MHz,
DMSO-d.sub.6) .delta.(ppm): 2.21 (s, 3H), 2.23 (s, 3H), 2.26 (s,
3H), 3.41(s, 3H), 7.28-7.36 (m, 5H)
EXAMPLE 8
Compounds 8 and 9
[0392] To a solution of 60% sodium hydride (110 mg, 2.70 mmol) in
N,N-dimethylformamide (10.0 mL) was added Compound 1 (50.0 mg, 1.80
mmol) prepared in Example 1, and the mixture was stirred at room
temperature for 30 minutes. To the reaction mixture was added ethyl
iodide (0.22 mL, 2.70 mmol) and the reaction mixture was further
stirred at room temperature for 12 hours. To the reaction mixture
was added 5% aqueous ammonium chloride and the mixture was
extracted with ethyl acetate. The organic layer was washed with
saturated aqueous sodium chloride and then dried over anhydrous
sodium sulfate, and the solvent was evaporated under reduced
pressure. The residue was purified by silica gel column
chromatography (ethyl acetate/n-hexane=1/1) to obtain Compound 8
(120 mg, 22%) and Compound 9 (330 mg, 60%).
Compound 8
[0393] .sup.1H NMR (270 MHz, CDCl.sub.3) .delta.(ppm): 1.19 (t,
J=7.0 Hz, 6H), 2.23 (s, 3H), 2.41 (s, 3H), 3.26 (q, J=7.0 Hz, 4H),
7.21-7.45 (m, 5H)
Compound 9
[0393] [0394] .sup.1H NMR (270 MHz, CDCl.sub.3) .delta.(ppm): 1.36
(t, J=7.2 Hz, 3H), 2.24 (s, 6H), 2.37 (s, 3H), 3.91 (q, J=7.2 Hz,
2H), 7.22-7.41 (m, 5H)
EXAMPLE 9
Compounds 10 and 11
[0395] In a manner similar to that in Example 8, Compound 10 (0.15
g, 26%) and compound 11 (0.27 g, 48%) were obtained from Compound 1
(0.50 g, 1.80 mmol) prepared in Example 1 and n-propyl iodide (0.26
mL, 2.70 mmol).
Compound 10
[0396] .sup.1H NMR (270 MHz, CDCl.sub.3) .delta.(ppm): 0.89 (t,
J=7.6 Hz, 6H), 1.61 (br q, J=7.6 Hz, 4H), 2.27 (s, 3H), 2.40 (s,
3H), 3.14 (br t, J=7.3 Hz, 4H), 7.21-7.47 (m, 5H)
Compound 11
[0396] [0397] .sup.1H NMR (270 MHz, CDCl.sub.3) .delta.(ppm): 1.00
(t, J=7.3 Hz, 3H), 1.74-1.82 (m, 2H), 2.28 (s, 6H), 2.36 (s, 3H),
3.75-3.86 (m, 2H), 7.21-7.44 (m, 5H)
EXAMPLE 10
Compounds 12 and 13
[0398] In a manner similar to that in Example 8, Compound 12 (120
mg, 16%) and Compound 13 (0.22 g, 33%) were obtained from Compound
1 (500 mg, 1.80 mmol) prepared in Example 1 and benzyl bromide
(0.32 mL, 2.70 mmol).
Compound 12
[0399] .sup.1H NMR (270 MHz, CDCl.sub.3) .delta.(ppm): 2.24 (s,
3H), 2.46 (s, 3H), 4.43 (s, 4H), 7.14-7.49 (m, 15H)
Compound 13
[0400] .sup.1H NMR (270 MHz, CDCl.sub.3) .delta.(ppm): 2.16 (s,
3H), 2.26 (s, 3H), 2.36 (s, 3H), 5.11 (br s, 2H), 7.22-7.38 (m,
10H)
EXAMPLE 11
Compound 14
[0401] To acetophenone=thiosemicarbazone (10.0 g, 51.8 mmol)
prepared in Step 1 of Example 1 was added acetic anhydride (4.90
mL, 51.9 mmol) and pyridine (8.40 mL, 104 mmol), and the mixture
was stirred at room temperature for 12 hours. After the reaction
mixture was concentrated under reduced pressure, ethyl acetate and
2 mol/L aqueous sodium hydroxide was added, and the mixture was
subjected to separation. The organic layer was washed with
saturated aqueous ammonium chloride and saturated aqueous sodium
chloride, and dried over anhydrous sodium sulfate, and then the
solvent was evaporated under reduced pressure. The residue was
purified by silica gel column chromatography (ethyl
acetate/n-hexane=1/1) to obtain Compound 14 (9.22 g, 76%). [0402]
.sup.1H NMR (270 MHz, DMSO-d.sub.6) .delta.(ppm): 2.12 (s, 3H),
2.31 (s, 3H), 6.49 (br s, 2H), 7.21-7.41 (m, 5H)
EXAMPLE 12
Compound 15
[0403] Compound 7 (550 mg, 1.89 mmol) prepared in Example 7 was
dissolved in N,N-dimethylformamide (10.0 mL). To the solution was
added 60% sodium hydride (0.23 g, 5.75 mmol) and the mixture was
stirred at room temperature for 30 minutes. To the reaction mixture
was added water and the mixture was extracted with ethyl acetate.
The organic layer was washed with saturated aqueous ammonium
chloride and then dried over anhydrous sodium sulfate, and the
solvent was evaporated under reduced pressure. The residue was
purified by silica gel column chromatography (ethyl
acetate/n-hexane=1/1) to obtain Compound 15 (0.31 g, 66%). [0404]
.sup.1H NMR (270 MHz, CDCl.sub.3) .delta.(ppm): 2.17 (s, 3H), 2.41
(s, 3H), 2.91 (br d, J=5.0 Hz, 3H), 3.92 (br s, 1H), 7.25-7.47 (m,
5H)
EXAMPLE 13
Compound 16
[0405] To a solution of 60% sodium hydride (50.0 mg, 1.20 mmol) in
N,N-dimethylformamide (2.0 mL) was added Compound 14 (100 mg, 0.41
mmol) prepared in Example 11, and the mixture was stirred at room
temperature for 30 minutes. To the reaction mixture was added
methyl iodide (0.08 mL, 1.24 mmol), and the mixture was further
stirred at room temperature for 12 hours. To the reaction mixture
was added 5% aqueous ammonium chloride and the mixture was
extracted with ethyl acetate. The organic layer was washed with
saturated aqueous sodium chloride and then dried over anhydrous
sodium sulfate, and the solvent was evaporated under reduced
pressure. The residue was purified by silica gel column
chromatography (ethyl acetate/n-hexane=1/1) to obtain Compound 16
(70.0 mg, 67%). [0406] .sup.1H NMR (270 MHz, CDCl.sub.3)
.delta.(ppm): 2.26 (s, 3H), 2.41 (s, 3H), 2.91 (s, 6H), 7.23-7.48
(m, 5H)
EXAMPLE 14
Compound 17
[0407] In a manner similar to that in Example 12, Compound 17 (580
mg, 71%) was obtained from Compound 19 (1.00 g, 3.13 mmol) obtained
in the after-mentioned Example 16. [0408] .sup.1H NMR (270 MHz,
CDCl.sub.3) .delta.(ppm): 1.13 (t, J=7.2 Hz, 3H), 2.39 (s, 3H),
2.61 (q, J=7.2 Hz, 2H), 2.88 (d, J=6.3 Hz, 3H), 4.02 (br d, J=6.3
Hz, 1H), 7.22-7.38 (m, 5H)
EXAMPLE 15
Compound 18
[0409] Compound 17 (100 mg, 0.38 mmol) prepared in Example 14 was
dissolved in acetone (2.0 mL). To the solution was added acetyl
chloride (0.15 mL, 2.11 mmol) and pyridine (0.15 mL, 1.85 mmol),
and the mixture was stirred at room temperature for 2 hours. To the
reaction mixture was added ethyl acetate and 2 mol/L aqueous sodium
hydroxide, and the solution was subjected to separation. The
organic layer was washed with saturated aqueous ammonium chloride
and saturated aqueous sodium chloride, and dried over anhydrous
sodium sulfate, and then the solvent was evaporated under reduced
pressure. The residue was purified by silica gel column
chromatography (ethyl acetate/n-hexane=1/2) to obtain Compound 18
(0.07 g, 59%). [0410] .sup.1H NMR (270 MHz, CDCl.sub.3)
.delta.(ppm): 1.12 (t, J=7.6 Hz, 3H), 2.27 (s, 3H), 2.35 (s, 3H),
2.65 (q, J=7.6 Hz, 2H), 3.45 (s, 3H), 7.23-7.42 (m, 5H)
EXAMPLE 16
Compound 19
[0411] To acetophenone=4-methylthiosemicarbazone (2.00 g, 9.66
mmol) prepared in Step 1 of Example 7 was added propionic anhydride
(8.67 mL, 67.6 mmol), and the mixture was heated and stirred at
100.degree. C. for 3 hours. To the reaction mixture was added ethyl
acetate and 2 mol/L aqueous sodium hydroxide. After the mixture was
stirred at room temperature for 30 minutes, the mixture was
subjected to separation. The organic layer was washed with
saturated aqueous ammonium chloride and saturated aqueous sodium
chloride, and dried over anhydrous sodium sulfate, and then the
solvent was evaporated under reduced pressure. The residue was
purified by silica gel column chromatography (ethyl
acetate/n-hexane=1/2) to obtain Compound 19 (1.39 g, 45%). [0412]
.sup.1H NMR (270 MHz, CDCl.sub.3) .delta.(ppm): 1.12 (t, J 7.3 Hz,
3H), 1.17 (t, J=7.5 Hz, 3H), 2.36 (s, 3H), 2.54 (q, J=7.3 Hz, 2H),
2.66 (q, J=7.5 Hz, 2H), 3.45 (s, 3H), 7.21-7.42 (m, 5H)
EXAMPLE 17
Compound 20
[0413] In a manner similar to that in Example 16, Compound 20 (1.55
g, 46%) was obtained from acetophenone=4-methylthiosemicarbazone
(2.00 g, 9.66 mmol) prepared in Step 1 of Example 7 and butyric
anhydride (11.1 mL, 67.8 mmol). [0414] .sup.1H NMR (270 MHz,
CDCl.sub.3) .delta.(ppm): 0.95 (t, J=7.3 Hz, 3H), 0.98 (t, J=7.4
Hz, 3H), 1.15-1.78 (m, 4H), 2.35 (s, 3H), 2.49 (t, J=7.3 Hz, 2H),
2.61 (t, J=7.4 Hz, 2H), 3.45 (s, 3H), 7.21-7.42 (m, 5H)
EXAMPLE 18
Compound 21
[0415] In a manner similar to that in Example 16, Compound 21 (1.43
g, 43%) was obtained from acetophenone=4-methylthiosemicarbazone
(2.00 g, 9.66 mmol) prepared in Step 1 of Example 7 and isobutyric
anhydride (11.2 mL, 67.5 mmol). [0416] .sup.1H NMR (270 MHz,
CDCl.sub.3) .delta.(ppm): 1.05-1.25 (m, 12H), 2.34 (s, 3H), 2.99
(q, J=7.3 Hz, 1H), 3.25 (q, J=7.5 Hz, 1H), 3.50 (s, 3H), 7.21-7.45
(m, 5H)
EXAMPLE 19
Compound 22
[0416] [0417] Step 1: In a manner similar to that in Step 1 of
Example 1, acetone=thiosemicarbazone (215 mg, 41%) was obtained
from acetone (4.8 g, 40 mmol) and thiosemicarbazide (364 mg, 3.99
mmol). [0418] .sup.1H NMR (270 MHz, DMSO-d.sub.6) .delta.(ppm):
1.89 (s, 3H), 1.91 (s, 3H), 7.51 (br s, 1H), 7.98 (br s, 1H), 9.90
(br s, 1H) [0419] Step 2: In a manner similar to that in Step 2 of
Example 1, Compound 22 (151 mg, 61%) was obtained from
acetone=thiosemicarbazone (150 mg, 1.14 mmol) prepared above.
[0420] .sup.1H NMR (270 MHz, CDCl.sub.3) .delta.(ppm): 1.98 (s,
6H), 2.19 (s, 3H), 2.20 (s, 3H), 9.06 (br s, 1H)
EXAMPLE 20
Compound 23
[0420] [0421] Step 1: In a manner similar to that in Step 1 of
Example 1, 2-hexanone=thiosemicarbazone (671 mg, 97%) was obtained
from 2-hexanone (401 mg, 4.00 mmol) and thiosemicarbazide (364 mg,
3.99 mmol). [0422] .sup.1H NMR (270 MHz, DMSO-d.sub.6)
.delta.(ppm): 0.88 (t, J=6.9 Hz, 3H), 1.23-1.31 (m, 2H), 1.41-1.50
(m, 2H), 1.88 (s, 3H), 2.17-2.23 (m, 2H), 7.44 (br s, 1H), 8.02 (br
s, 1H), 9.88 (br s, 1H) [0423] Step 2: In a manner similar to that
in Step 2 of Example 1, Compound 23 (255 mg, 57%) was obtained from
2-hexanone=thiosemicarbazone (300 mg, 1.73 mmol) prepared above.
[0424] .sup.1H NMR (270 MHz, CDCl.sub.3) .delta.(ppm): 0.90 (t,
J=6.9 Hz, 3H), 1.23-1.38 (m, 3H), 1.52-1.56 (m, 1H), 1.84-2.18 (m,
1H), 1.97 (s, 3H), 2.18 (s, 3H), 2.19 (s, 3H), 2.44-2.55 (m, 1H),
8.68 (br s, 1H)
EXAMPLE 21
Compound 24
[0424] [0425] Step 1: In a manner similar to that in Step 1 of
Example 1, benzylacetone=thiosemicarbazone (788 mg, 89%) was
obtained from benzylacetone (593 mg, 4.00 mmol) and
thiosemicarbazide (367 mg, 4.03 mmol). [0426] .sup.1H NMR (270 MHz,
DMSO-d.sub.6) .delta.(ppm): 1.92 (s, 3H), 2.52 (m, 2H), 2.84 (m,
2H), 7.14-7.30 (m, 5H), 7.43 (br s, 1H), 8.03 (br s, 1H), 9.94 (br
s, 1H) [0427] Step 2: In a manner similar to that in Step 2 of
Example 1, Compound 24 (382 mg, 92%) was obtained from
benzylacetone=thiosemicarbazone (300 mg, 1.36 mmol) prepared above.
[0428] .sup.1H NMR (270 MHz, CDCl.sub.3) .delta.(ppm): 2.00 (s,
3H), 2.17 (s, 3H), 2.13 (dd, J=2.3, 10.2 Hz, 1H), 2.19 (s, 3H),
2.59 (dd, J=2.2, 10.2 Hz, 1H), 2.87 (br d, J=12.2 Hz, 1H), 2.95 (br
s, J=11.8 Hz, 1H), 7.14-7.29 (m, 5H), 8.39 (br s, 1H)
EXAMPLE 22
Compound 25
[0428] [0429] Step 1: In a manner similar to that in Step 1 of
Example 1, benzylideneacetone=thiosemicarbazone (730 mg, 80%) was
obtained 1 from benzylideneacetone (610 mg, 4.17 mmol) and
thiosemicarbazide (371 mg, 4.07 mmol). [0430] .sup.1H NMR (300 MHz,
CDCl.sub.3) .delta.(ppm): 2.13 (s, 3H), 6.89 (d, J=16.8 Hz, 1H),
7.10 (d, J=16.8 Hz, 1H), 7.27-7.41 (m, 3H), 7.43-7.56 (m, 2H), 7.78
(br s, 1H), 8.26 (br s, 1H), 10.27 (br s, 1H) [0431] Step 2: In a
manner similar to that in Step 2 of Example 1, Compound 25 (195 mg,
72%) was obtained from benzylideneacetone=thiosemicarbazone (300
mg, 0.889 mmol) prepared above. [0432] .sup.1H NMR (300 MHz,
DMSO-d.sub.6) .delta.(ppm): 2.13 (s, 3H), 2.15 (s, 3H), 2.23 (s,
3H), 6.62 (d, J=12.2 Hz, 1H), 6.65 (d, J=12.2 Hz, 1H), 7.20-7.39
(m, 5H), 8.57 (br s, 1H)
EXAMPLE 23
Compound 26
[0432] [0433] Step 1: In a manner similar to that in Step 1 of
Example 1, 5-Nonanone=thiosemicarbazone (553 mg, 64%) was obtained
from 5-nonanone (569 mg, 4.00 mmol) and thiosemicarbazide (364 mg,
3.99 mmol). [0434] .sup.1H NMR (270 MHz, DMSO-d.sub.6)
.delta.(ppm): 0.87 (t, J=6.9 Hz, 6H), 1.20-1.53 (m, 8H), 2.17-2.22
(m, 2H), 2.31-2.37 (m, 2H), 7.40 (br s, 1H), 8.00 (br s, 1H), 10.03
(br s, 1H) [0435] Step 2: In a manner similar to that in Step 2 of
Example 1, Compound 26 (245 mg, 59%) was obtained from
5-nonanone=thiosemicarbazone (300 mg, 1.39 mmol) prepared above.
[0436] .sup.1H NMR (270 MHz, CDCl.sub.3) .delta.(ppm): 0.90 (t,
J=6.9 Hz, 6H), 1.18-1.37 (m, 6H), 1.55-1.63 (m, 2H), 1.77-1.88 (m,
2H), 2.18 (s, 3H), 2.19 (s, 3H), 2.45-2.56 (m, 2H), 8.90 (br s,
1H)
EXAMPLE 24
Compound 27
[0436] [0437] Step 1: In a manner similar to that in Step 1 of
Example 1, a-tetralone=thiosemicarbazone (797 mg, 88%) was obtained
from a-tetralone (604 mg, 4.13 mmol) and thiosemicarbazide (368 mg,
4.04 mmol). [0438] .sup.1H NMR (270 MHz, DMSO-d.sub.6)
.delta.(ppm): 1.78-1.82 (m, 2H), 2.65-2.75 (m, 4H), 7.15-7.27 (m,
3H), 7.97 (br s, 1H), 8.20-8.40 (m, 2H), 10.10 (br s, 1H) [0439]
Step 2: In a manner similar to that in Step 2 of Example 1,
Compound 27 (324 mg, 78%) was obtained from
a-tetralone=thiosemicarbazone (300 mg, 1.37 mmol) prepared above.
[0440] .sup.1H NMR (270 MHz, CDCL.sub.3) .delta.(ppm): 1.89 (s,
3H), 2.09-2.22 (m, 2H), 2.28 (s, 3H), 2.36-2.41 (m, 1H), 2.80-2.86
(m, 2H), 2.97-3.08 (m, 1H), 7.01 (br d, J=8.6 Hz, 1H), 7.08-7.18
(m, 2H), 7.40 (br d, J=7.3 Hz, 1H), 9.24.(br s,,1H)
EXAMPLE 25
Compound 28
[0440] [0441] Step 1: In a manner similar to that in Step 1 of
Example 1, .beta.-tetralone=thiosemicarbazone (684 mg, 75%) was
obtained from .beta.-tetralone (607 mg, 4.15 mmol) and
thiosemicarbazide (379 mg, 4.16 mmol). [0442] Step 2: In a manner
similar to that in Step 2 of Example 1, Compound 28 (301 mg, 65%)
was obtained from .beta.-tetralone=thiosemicarbazone (334 mg, 1.53
mmol) prepared above. [0443] .sup.1H NMR (270 MHz, DMSO-d.sub.6)
.delta.(ppm): 2.12 (s, 3H), 2.15-2.30 (m, 1H), 2.24 (s, 3H),
3.05-3.09 (m, 2H), 3.14 (br d, J=15.8 Hz, 1H), 3.23-3.41 (m, 1H),
4.38 (br d, J=15.8 Hz, 1H), 6.99-7.00 (m, 1H), 7.02-7.25 (m, 3H),
8.42 (br s, 1H)
EXAMPLE 26
Compound 29
[0443] [0444] Step 1: In a manner similar to that in Step 1 of
Example 1, 1-indanone=thiosemicarbazone (1.54 g, 94%) was obtained
from 1-indanone (1.06 g, 8.00 mmol) and thiosemicarbazide (740 mg,
8.12 mmol). [0445] .sup.1H NMR (270 MHz, DMSO-d.sub.6)
.delta.(ppm): 2.85-2.89 (m, 2H), 3.03-3.08 (m, 2H), 7.28-7.38 (m,
3H), 7.87 (br d, J=7.6 Hz, 1H), 7.92 (br s, 1H), 8.17 (br s, 1H),
10.2 (br s, 1H) [0446] Step 2: In a manner similar to that in Step
2 of Example 1, Compound 29 (184 mg, 44%) was obtained from
1-indanone=thiosemicarbazone (300 mg, 1.46 mmol) prepared above.
[0447] .sup.1H NMR (270 MHz, CDCl.sub.3) .delta.(ppm): 2.17 (s,
3H), 2.24 (s, 3H), 2.58-2.65 (m, 1H), 2.96-3.07 (m, 1H), 3.13-3.21
(m, 2H), 7.15-7.27 (m, 3H), 7.32-7.37 (m, 1H), 9.60 (br s, 1H)
EXAMPLE 27
Compound 30
[0447] [0448] Step 1: In a manner similar to that in Step 1 of
Example 1, cyclohexanone=thiosemicarbazone (479 mg, 70%) was
obtained from cyclohexanone (393 mg, 4.00 mmol) and
thiosemicarbazide (364 mg, 3.99 mmol). [0449] .sup.1H NMR (270 MHz,
DMSO-d.sub.6) .delta. (ppm): 1.55 (br s, 6H), 2.19-2.23 (m, 2H),
2.38 (br s, 2H), 7.50 (br s, 1H), 7.93 (br s, 1H), 10.13 (br s, 1H)
[0450] Step 2: In a manner similar to that in Step 2 of Example 1,
Compound 30 (214 mg, 72%) was obtained from
cyclohexanone=thiosemicarbazone (200 mg, 1.17 mmol) prepared above.
[0451] .sup.1H NMR (300 MHz, CDCl.sub.3) .delta.(ppm): 1.25-1.53
(m, 3H), 1.58-1.68 (m, 1H), 1.81-1.86 (m, 2H), 2.03-2.08 (m, 2H),
2.16 (s, 3H), 2.17 (s, 3H), 2.90-3.01 (m, 2H), 7.95 (br s, 1H)
EXAMPLE 28
Compound 31
[0452] In a manner similar to that in Step 1 and 2 of Example 1,
Compound 31 (214 mg, 20%) was obtained from 2-norbornanone (452 mg,
4.10 mmol) and thiosemicarbazide (377 mg, 4.14 mmol). [0453]
.sup.1H NMR (270 MHz, CDCl.sub.3) .delta.(ppm): 1.32-1.67 (m, 5H),
1.76-1.89 (m, 2H), 2.18 (s, 3H), 2.19 (br s, 1H), 2.21 (s, 3H),
2.26 (br s, 1H), 3.60 (br d, J=13.9 Hz, 1H), 8.20 (br s, 1H)
EXAMPLE 29
Compound 32
[0454] In a manner similar to that in Step 1 and 2 of Example 1,
Compound 32 (214 mg, 32%) was obtained from 1'-acetonaphthone (344
mg, 2.02 mmol) and thiosemicarbazide (190 mg, 2.08 mmol). [0455]
.sup.1H NMR (270 MHz, CDCl.sub.3) .delta.(ppm): 2.06 (s, 3H), 2.07
(s, 3H), 2.33 (s, 3H), 7.45-7.65 (m, 4H), 7.89-7.99 (m, 3H), 11.50
(br s, 1H)
EXAMPLE 30
Compound 33
[0455] [0456] Step 1: In a manner similar to that in Step 1 of
Example 1, 2'-acetonaphthone=thiosemicarbazone (448 mg, 92%) was
obtained from 2'-acetonaphthone (342 mg, 2.10 mmol) and
thiosemicarbazide (189 mg, 2.07 mmol). [0457] .sup.1H NMR (270 MHz,
DMSO-d.sub.6) .delta.(ppm): 2.42 (s, 3H), 7.53 (m, 2H), 7.86-8.05
(m, 4H), 8.28-8.34 (m, 3H), 10.28 (br s, 1H) [0458] Step 2: In a
manner similar to that in Step 2 of Example 1, Compound 33 (302 mg,
90%) was obtained from 2'-acetonaphthone=thiosemicarbazone (250 mg,
1.03 mmol) prepared above. [0459] .sup.1H NMR (270 MHz,
DMSO-d.sub.6) .delta.(ppm): 2.02 (s, 3H), 2.22 (s, 3H), 2.38 (s,
3H), 7.51-7.55 (m, 3H), 7.85-7.95 (m, 4H), 11.68 (br s, 1H)
EXAMPLE 31
Compound 34
[0459] [0460] Step 1: In a manner similar to that in Step 1 of
Example 1, 1-(2-pyridyl)ethanone=thiosemicarbazone (694 mg, 88%)
was obtained from 2-acetylpyridine (485 mg, 4.00 mmol) and
thiosemicarbazide (369 mg, 4.05 mmol). [0461] .sup.1H NMR (270 MHz,
DMSO-d.sub.6) .delta.(ppm): 2.38 (s, 3H), 7.37 (br t, J=6.3 Hz,
1H), 7.78 (br t, J=7.2 Hz, 1H), 8.13 (br s, 1H), 8.40 (br s, 1H),
8.41 (br d, J=8.2 Hz, 1H), 8.56 (br d, J=6.6 Hz, 1H), 10.31 (br s,
1H) [0462] Step 2: In a manner similar to that in Step 2 of Example
1, Compound 34 (160 mg, 37%) was obtained from
1-(2-pyridyl)ethanone=thiosemicarbazone (304 mg, 1.56 mmol)
prepared above. [0463] .sup.1H NMR (270 MHz, CDCl.sub.3)
.delta.(ppm): 2.09 (s, 3H), 2.26 (s, 3H), 2.42 (s, 3H), 7.17 (br t,
J=6.9 Hz, 1H), 7.38 (br d, J=8.2 Hz, 1H), 7.68 (br t, J=7.7 Hz,
1H), 8.44 (br s, 1H), 8.58 (br d, J=6.3 Hz, 1H)
EXAMPLE 32
Compound 35
[0463] [0464] Step 1: In a manner similar to that in Step 1 of
Example 1, 1-(3-pyridyl)ethanone=thiosemicarbazone (722 mg, 93%)
was obtained from 3-acetylpyridine (484 mg, 4.00 mmol) and
thiosemicarbazide (388 mg, 4.00 mmol). [0465] .sup.1H NMR (270 MHz,
DMSO-d.sub.6) .delta.(ppm): 2.32 (s, 3H), 7.32-7.42 (m, 1H), 8.07
(br s, 1H), 8.29-8.34 (m, 2H), 8.54-8.57 (m, 1H), 9.09 (br s, 1H),
10.32 (br s, 1H) [0466] Step 2: In a manner similar to that in Step
2 of Example 1, Compound 35 (213 mg, 72%) was obtained from
1-(3-pyridyl)ethanone=thiosemicarbazone (205 mg, 1.05 mmol)
prepared above. [0467] .sup.1H NMR (270 MHz, CDCl.sub.3)
.delta.(ppm): 2.14 (s, 3H), 2.21 (s, 3H), 2.39 (s, 3H), 7.31 (br
dd, J=5.4, 7.9 Hz, 1H), 7.75 (br d, J=7.9 Hz, 1H), 8.52 (br d,
J=5.4 Hz, 1H), 8.72 (br s, 1H), 9.08 (br s, 1H)
EXAMPLE 33
Compound 36
[0467] [0468] Step 1: In a manner similar to that in Step 1 of
Example 1, 1-(4-pyridyl)ethanone=thiosemicarbazone (722 mg, 95%)
was obtained from 4-acetylpyridine (507 mg, 4.19 mmol) and
thiosemicarbazide (408 mg, 4.46 mmol). [0469] Step 2: In a manner
similar to that in Step 2 of Example 1, Compound 36 (389 mg, 85%)
was obtained from 1-(4-pyridyl)ethanone=thiosemicarbazone (318 mg,
1.64 mmol) prepared above. [0470] .sup.1H NMR (270 MHz, CDCl.sub.3)
.delta.(ppm): 2.16 (s, 3H), 2.25 (s, 3H), 2.35 (s, 3H), 7.30 (d,
J=6.3 Hz, 2H), 8.46 (br s, 1H), 8.60 (d, J=6.3 Hz, 2H)
EXAMPLE 34
Compound 37
[0470] [0471] Step 1: In a manner similar to that in Step 1 of
Example 1, 1-pyrazinylethanone=thiosemicarbazone (714 mg, 92%) was
obtained from acetylpyrazine (489 mg, 4.00 mmol) and
thiosemicarbazide (366 mg, 4.00 mmol). [0472] Step 2: In a manner
similar to that in Step 2 of Example 1, Compound 37 (489 mg, 85%)
was obtained from 1-pyrazinylethanone=thiosemicarbazone (400 mg,
2.05 mmol) prepared above. [0473] .sup.1H NMR (270 MHz, CDCl.sub.3)
.delta.(ppm): 2.16 (s, 3H), 2.26 (s, 3H), 2.42 (s, 3H), 8.06 (br s,
1H), 8.46 (d, J=2.7 Hz, 1H), 8.52 (dd, J=1.7, 2.7 Hz, 1H), 8.71 (d,
J=1.7 Hz, 1H)
EXAMPLE 35
Compound 38
[0473] [0474] Step 1: In a manner similar to that in Step 1 of
Example 1, 1-(2-pyrrolyl)ethanone=thiosemicarbazone (408 mg, 55%)
was obtained from 2-acetylpyrrole (437 mg, 4.00 mmol) and
thiosemicarbazide (374 mg, 4.09 mmol). [0475] Step 2: In a manner
similar to that in Step 2 of Example 1, Compound 38 (504 mg, 95%)
was obtained from 1-(2-pyrrolyl)ethanone=thiosemicarbazone (314 mg,
1.72 mmol) prepared above. [0476] .sup.1H NMR (270 MHz, CDCl.sub.3)
.delta.(ppm): 2.12 (s, 3H), 2.21 (s, 3H), 2.38 (s, 3H), 2.55 (s,
3H), 6.17-6.22(m, 2H), 7.11 (br s, 1H), 8.13 (br s, 1H)
EXAMPLE 36
Compound 39
[0476] [0477] Step 1: In a manner similar to that in Step 1 of
Example 1, 1-(2-furyl)ethanone=thiosemicarbazone (441 mg, 60%) was
obtained from 2-acetylfuran (444 mg, 4.00 mmol) and
thiosemicarbazide (368 mg, 4.03 mmol). [0478] Step 2: In a manner
similar to that in Step 2 of Example 1, Compound 39 (217 mg, 83%)
was obtained from 1-(2-furyl)ethanone=thiosemicarbazone (180 mg,
0.982 mmol) prepared above. [0479] .sup.1H NMR (270 MHz,
CDCl.sub.3) .delta.(ppm): 2.13 (s, 3H), 2.22 (s, 3H), 2.30 (s, 3H),
6.31 (m, 2H), 7.36 (br s, 1H), 8.43 (br s, 1H)
EXAMPLE 37
Compound 40
[0479] [0480] Step 1: In a manner similar to that in Step 1 of
Example 1, 1-(2-thienyl)ethanone=thiosemicarbazone (636 mg, 78%)
was obtained from 2-acetylthiophene (521 mg, 4.13 mmol) and
thiosemicarbazide (376 mg, 4.11 mmol). [0481] Step 2: In a manner
similar to that in Step 2 of Example 1, Compound 40 (549 mg, 78%)
was obtained from 1-(2-thienyl)ethanone=thiosemicarbazone (498 mg,
2.50 mmol) prepared above. [0482] .sup.1H NMR (300 MHz, CDCl.sub.3)
.delta.(ppm): 2.07 (s, 3H), 2.24 (s, 3H), 2.42 (s, 3H), 6.89 (br t,
J=7.2 Hz, 1H), 7.06 (dd, J=6.9, 7.2 Hz 1H), 7.24 (br d, J=6.9 Hz,
1H), 8.81 (br s, 1H)
EXAMPLE 38
Compound 41
[0483] In a manner similar to that in Example 8, Compound 41 (148
mg, 52%) was obtained in from Compound 40 (260 mg, 0.918 mmol)
prepared in Example 37. [0484] .sup.1H NMR (270 MHz, CDCl.sub.3)
.delta.(ppm): 1.36 (t, J=7.0 Hz, 3H), 2.25 (s, 3H), 2.30 (s, 3H),
2.43 (s, 3H), 3.92 (br q, J=7.0 Hz, 2H), 6.91 (br t, J=5.2 Hz, 1H),
7.06 (br d, J=5.2 Hz, 1H), 7.24 (br d, J=5.2 Hz, 1H)
EXAMPLE 39
Compound 42
[0484] [0485] Step 1: In a manner similar to that in Step 1 of
Example 1, 1-(3-methyl-2-thienyl)ethanone=thiosemicarbazone (410
mg, 48%) was obtained from 2-acetyl-3-methylthiophene (561 mg, 4.00
mmol) and thiosemicarbazide (374 mg, 4.09 mmol). [0486] Step 2: In
a manner similar to that in Step 2 of Example 1, Compound 42 (335
mg, 93%) was obtained from
1-(3-methyl-2-thienyl)ethanone=thiosemicarbazone (260 mg, 1.22
mmol) prepared above. [0487] .sup.1H NMR (270 MHz, CDCl.sub.3)
.delta.(ppm): 2.02 (s, 3H), 2.19 (s, 3H), 2.24 (s, 3H), 2.38 (s,
3H) 6.78 (d, J=5.0 Hz, 1H), 7.07 (d, J=5.0 Hz, 1H), 9.37 (br s,
1H)
EXAMPLE 40
Compound 43
[0487] [0488] Step 1: In a manner similar to that in Step 1 of
Example 1, 1-(benzo[b]thiophen-2-yl)ethanone=thiosemicarbazone (990
mg, 99%) was obtained from 1-(benzo[b]thiophen-2-yl)ethanone (705
mg, 4.00 mmol) and thiosemicarbazide (370 mg, 4.05 mmol). [0489]
.sup.1H NMR (270 MHz, DMSO-d.sub.6) .delta.(ppm): 2.40 (s, 3H),
7.36-7.41 (m, 2H), 7.45 (br s, 1H), 7.81-7.90 (m, 3H), 8.42 (br s,
1H), 10.56 (br s, 1H) [0490] Step 2: In a manner similar to that in
Step 2 of Example 1, Compound 43 (599 mg, 90%) was obtained from
1-(benzo[b]thiophen-2-yl)ethanone=thiosemicarbazone (500 mg, 2.01
mmol) prepared above. [0491] .sup.1H NMR (270 MHz, DMSO-d.sub.6)
.delta.(ppm): 2.04 (s, 3H), 2.17 (s, 3H), 2.38 (s, 3H), 7.31-7.40
(m, 3H), 7.79 (br d, J=7.6 Hz, 1H), 7.89 (br d, J=7.8 Hz, 1H),
11.75 (br s, 1H)
EXAMPLE 41
Compound 44
[0491] [0492] Step 1: In a manner similar to that in Step 1 of
Example 1, 1-(3-thienyl)ethanone=thiosemicarbazone (839 mg, 98%)
was obtained from 3-acetylthiophene (520 mg, 4.12 mmol) and
thiosemicarbazide (366 mg, 4.00 mmol). [0493] .sup.1H NMR (270 MHz,
DMSO-d.sub.6) .delta.(ppm): 2.27 (s, 3H), 7.52 (br d, J=5.3 Hz,
1H), 7.83 (br d, J=5.3 Hz, 1H), 7.95 (br s, 1H), 8.22 (br s, 1H),
10.08 (br s, 1H) [0494] Step 2: In a manner similar to that in Step
2 of Example 1, Compound 44 (540 mg, 83%) was obtained from
1-(3-thienyl)ethanone=thiosemicarbazone (458 mg, 2.30 mmol)
prepared above. [0495] .sup.1H NMR (270 MHz, DMSO-d.sub.6)
.delta.(ppm): 2.02 (s, 3H), 2.15 (s, 3H), 2.25 (s, 3H), 7.05 (br d,
J=6.0 Hz, 1H), 7.37 (br s, 1H), 7.47 (br d, J=6.0 Hz, 1H)
EXAMPLE 42
Compound 45
[0495] [0496] Step 1: In a manner similar to that in Step 1 of
Example 1, 1-(2-thiazolyl)ethanone=thiosemicarbazone (711 mg, 90%)
was obtained from 2-acetylthiazole (379 mg, 4.15 mmol) and
thiosemicarbazide (366 mg, 4.00 mmol). [0497] 1H NMR (270 MHz,
DMSO-d.sub.6) .delta.(ppm): 2.42 (s, 3H), 7.67 (br s, 1H), 7.79 (br
d, J=4.3 Hz, 1H), 7.87 (br d, J=4.3 Hz, 1H), 8.51 (br s, 1H), 10.65
(br s, 1H) [0498] Step 2: In a manner similar to that in Step 2 of
Example 1, Compound 45 (374 mg, 45%) was obtained from
1-(2-thiazolyl)ethanone=thiosemicarbazone (374 mg, 1.87 mmol)
prepared above. [0499] .sup.1H NMR (270 MHz, DMSO-d.sub.6)
.delta.(ppm): 2.03 (s, 3H), 2.18 (s, 3H), 2.31 (s, 3H), 7.74-7.79
(m, 2H), 11.70 (br s, 1H)
EXAMPLE 43
Compound 46
[0500] In a manner similar to that in Step 1 and 2 of Example 1,
Compound 46 (141 mg, 10%) was obtained from 2'-methylacetophenone
(627 mg, 4.67 mmol) and thiosemicarbazide (374 mg, 4.09 mmol).
[0501] .sup.1H NMR (270 MHz, CDCl.sub.3) .delta.(ppm): 1.99 (br s,
1H), 2.21 (s, 3H), 2.33 (s, 3H), 2.38 (s, 3H), 7.15-7.20 (m, 3H),
7.38 (m, 1H), 8.90 (br s, 1H)
EXAMPLE 44
Compound 47
[0501] [0502] Step 1: In a manner similar to that in Step 1 of
Example 1, 3'-methylacetophenone=thiosemicarbazone (791 mg, 89%)
was obtained from 3'-methylacetophenone (540 mg, 4.02 mmol) and
thiosemicarbazide (369 mg, 4.04 mmol). [0503] Step 2: In a manner
similar to that in Step 2 of Example 1, Compound 47 (316 mg, 79%)
was obtained from 3'-methylacetophenone=thiosemicarbazone (300 mg,
1.36 mmol) prepared above. [0504] .sup.1H NMR (270 MHz, CDCl.sub.3)
.delta.(ppm): 2.15 (s, 3H), 2.23 (s, 3H), 2.34 (s, 3H), 2.37 (s,
3H), 7.01-7.09 (m, 1H), 7.19-7.30 (m, 3H), 7.90 (br s, 1H)
EXAMPLE 45
Compound 48
[0504] [0505] Step 1: In a manner similar to that in Step 1 of
Example 1, 4'-methylacetophenone=thiosemicarbazone (767 mg, 93%)
was obtained from 4'-methylacetophenone (536 mg, 3.99 mmol) and
thiosemicarbazide (382 mg, 4.19 mmol). [0506] .sup.1H NMR (270 MHz,
DMSO-d.sub.6) .delta.(ppm): 2.27 (s, 3H), 2.32 (s, 3H), 7.18 (d,
J=7.9 Hz, 2H), 7.82 (d, J=7.9 Hz, 2H), 7.88 (br s, 1H), 8.23 (br s,
1H), 10.15 (br s, 1H) [0507] Step 2: In a manner similar to that in
Step 2 of Example 1, Compound 48 (224 mg, 80%) was obtained from
4'-methylacetophenone=thiosemicarbazone (200 mg, 0.965 mmol)
prepared above. [0508] .sup.1H NMR (270 MHz, DMSO-d.sub.6)
.delta.(ppm): 2.06 (s, 3H), 2.24 (s, 3H), 2.31 (s, 3H), 2.36 (s,
3H), 7.13 (d, J=8.3 Hz, 2H), 7.31 (d, J=8.3 Hz, 2H), 8.40 (br s,
1H)
EXAMPLE 46
Compound 49
[0508] [0509] Step 1: In a manner similar to that in Step 1 of
Example 1, 2'-ethylpropiophenone=thiosemicarbazone (672 mg, 71%)
was obtained from 2'-ethylpropiophenone (649 mg, 4.00 mmol) and
thiosemicarbazide (378 mg, 4.14 mmol). [0510] Step 2: In a manner
similar to that in Step 2 of Example 1, Compound 49 (759 mg, 88%)
was obtained from 2'-ethylpropiophenone=thiosemicarbazone (300 mg,
1.27 mmol) prepared above. [0511] .sup.1H NMR (270 MHz, CDCl.sub.3)
.delta.(ppm): 1.13 (t, J=6.9 Hz, 3H), 1.24 (t, J=7.3 Hz, 3H), 1.96
(s, 3H), 2.20 (m, 1H), 2.24 (s, 3H), 2.71 (m, 2H), 3.14 (m, 1H),
7.13 (br t, J=7.1 Hz, 1H), 7.21-7.26 (m, 2H), 7.51 (br d, J=7.9 Hz,
1H), 8.87 (br s, 1H)
EXAMPLE 47
Compound 50
[0511] [0512] Step 1: In a manner similar to that in Step 1 of
Example 1, 2'-methoxyacetophenone=thiosemicarbazone (891 mg, 92%)
was obtained from 2'-methoxyacetophenone (601 mg, 4.00 mmol) and
thiosemicarbazide (366 mg, 4.00 mmol). [0513] Step 2: In a manner
similar to that in Step 2 of Example 1, Compound 50 (64.0 mg, 93%)
was obtained from 2'-methoxyacetophenone=thiosemicarbazone (50.0
mg, 0.224 mmol) prepared above. [0514] .sup.1H NMR (270 MHz,
CDCl.sub.3) .delta.(ppm): 2.08 (s, 3H), 2.29 (s, 3H), 2.45 (s, 3H),
3.87 (s, 3H), 6.90 (br t, J=7.3 Hz, 1H), 6.91 (br d, J=7.3 Hz, 1H),
7.06 (br d, J=7.3 Hz, 1H), 7.27 (br t, J=7.3 Hz, 1H), 8.31 (br s,
1H)
EXAMPLE 48
Compound 51
[0514] [0515] Step 1: In a manner similar to that in Step 1 of
Example 1, 3'-methoxyacetophenone=thiosemicarbazone (713 mg, 58%)
was obtained from 3'-methoxyacetophenone (601 mg, 4.00 mmol) and
thiosemicarbazide (377 mg, 4.12 mmol). [0516] .sup.1H NMR (270 MHz,
DMSO-d.sub.6) .delta.(ppm): 2.29 (s, 3H), 3.80 (s, 3H), 6.96 (br d,
J=7.9 Hz, 1H), 7.30 (br t, J=7.9 Hz, 1H), 7.44 (br s, 1H), 7.46 (br
d, J=7.9 Hz, 1H), 7.94 (br s, 1H), 8.28 (br s, 1H), 10.18 (br s,
1H) [0517] Step 2: In a manner similar to that in Step 2 of Example
1, Compound 51 (419 mg, 71%) was obtained from
3'-methoxyacetophenone=thiosemicarbazone (500 mg, 2.24 mmol)
prepared above. [0518] .sup.1H NMR (270 MHz, CDCl.sub.3)
.delta.(ppm): 2.10 (s, 3H), 2.30 (s, 3H), 2.34 (s, 3H), 3.78 (s,
3H), 6.78 (br d, J=7.9 Hz, 1H), 6.94 (br s, 1H), 7.01 (br d, J=7.9
Hz, 1H), 7.25 (br t, J=7.9 Hz, 1H), 9.48 (br s, 1H)
EXAMPLE 49
Compound 52
[0518] [0519] Step 1: In a manner similar to that in Step 1 of
Example 1, 4'-methoxyacetophenone=thiosemicarbazone (448 mg, 83%)
was obtained from 4'-methoxyacetophenone (362 mg, 2.41 mmol) and
thiosemicarbazide (225 mg, 2.46 mmol). [0520] Step 2: In a manner
similar to that in Step 2 of Example 1, Compound 52 (248 mg, 90%)
was obtained from 4'-methoxyacetophenone=thiosemicarbazone (200 mg,
0.896 mmol) prepared above. [0521] .sup.1H NMR (270 MHz,
CDCl.sub.3) .delta.(ppm): 2.06 (s, 3H), 2.24 (s, 3H), 2.35 (s, 3H),
3.78 (s, 3H), 6.84 (d, J=8.6 Hz, 2H), 7.36 (d, J=8.6 Hz, 2H), 8.56
(br s, 1H)
EXAMPLE 50
Compound 53
[0521] [0522] Step 1: In a manner similar to that in Step 1 of
Example 1, 2'-fluoroacetophenone=thiosemicarbazone (704 mg, 83%)
was obtained from 2'-fluoroacetophenone (558 mg, 4.04 mmol) and
thiosemicarbazide (385 mg, 4.12 mmol). [0523] .sup.1H NMR (270 MHz,
DMSO-d.sub.6) .delta.(ppm): 2.29 (s, 3H), 7.19-7.28 (m, 2H),
7.40-7.48 (m, 1H), 7.74-7.80 (m, 2H), 8.30 (br s, 1H), 10.34 (br s,
1H) [0524] Step 2: In a manner similar to that in Step 2 of Example
1, Compound .53 (199 mg, 71%) was obtained from
2'-fluoroacetophenone=thiosemicarbazone (200 mg, 0.948 mmol)
prepared above. [0525] .sup.1H NMR (270 MHz, CDCl.sub.3)
.delta.(ppm): 2.05 (s, 3H), 2.26 (s, 3H), 2.40 (s, 3H), 7.01-7.12
(m, 2H), 7.23-7.31 (m, 2H), 8.68 (br s, 1H)
EXAMPLE 51
Compound 54
[0525] [0526] Step 1: In a manner similar to that in Step 1 of
Example 1, 3'-fluoroacetophenone=thiosemicarbazone (772 mg, 92%)
was obtained from 3'-fluoroacetophenone (553 mg, 4.00 mmol) and
thiosemicarbazide (372 mg, 4.07 mmol). [0527] .sup.1H NMR (270 MHz,
DMSO-d.sub.6) .delta.(ppm): 2.29 (s, 3H), 7.17-7.24 (m, 1H),
7.38-7.46 (m, 1H), 7.69 (br d, J=8.9 Hz, 1H), 7.88 (br d, J=11.2
Hz, 1H), 8.09 (br s, 1H), 8.31 (br s, 1H), 10.24 (br s, 1H) [0528]
Step 2: In a manner similar to that in Step 2 of Example 1,
Compound 54 (242 mg, 74%) was obtained from
3'-fluoroacetophenone=thiosemicarbazone (233 mg, 1.10 mmol)
prepared above. [0529] .sup.1H NMR (270 MHz, CDCl.sub.3)
.delta.(ppm): 2.08 (s, 3H), 2.26 (s, 3H), 2.35 (s, 3H), 6.92-6.99
(m, 1H), 7.07-7.13 (m, 1H), 7.18-7.22 (m, 1H), 7.28-7.34 (m, 1H),
8.54 (br s, 1H)
EXAMPLE 52
Compound 55
[0529] [0530] Step 1: In a manner similar to that in Step 1 of
Example 1, 4'-fluoroacetophenone=thiosemicarbazone (769 mg, 91%)
was obtained from 4'-fluoroacetophenone (553 mg, 4.00 mmol) and
thiosemicarbazide (376 mg, 4.11 mmol). [0531] Step 2: In a manner
similar to that in Step 2 of Example 1, Compound 55 (251 mg, 86%)
was obtained from 4'-fluoroacetophenone=thiosemicarbazone (208 mg,
0.986 mmol) prepared above. [0532] .sup.1H NMR (270 MHz,
CDCl.sub.3) .delta.(ppm): 2.14 (s, 3H), 2.22 (s, 3H), 2.36 (s, 3H),
6.98-7.05 (m, 2H), 7.38-7.44 (m, 2H), 8.09 (br s, 1H)
EXAMPLE 53
Compound 56
[0532] [0533] Step 1: In a manner similar to that in Step 1 of
Example 1, 2'-chloroacetophenone=thiosemicarbazone (362 mg, 58%)
was obtained from 2'-chloroacetophenone (344 mg, 2.23 mmol) and
thiosemicarbazide (194 mg, 2.12 mmol). [0534] Step 2: In a manner
similar to that in Step 2 of Example 1, Compound 56 (347 mg, 97%)
was obtained from 2'-chloroacetophenone=thiosemicarbazone (200 mg,
1.14 mmol) prepared above. [0535] .sup.1H NMR (270 MHz, CDCl.sub.3)
.delta.(ppm): 1.98 (s, 3H), 2.23 (s, 3H), 2.38 (s, 3H), 7.22-7.27
(m, 2H), 7.37-7.45 (m, 2H), 9.05 (br s, 1H)
EXAMPLE 54
Compound 57
[0536] In a manner similar to that in Example 8, Compound 57 (347
mg, 97%) was obtained from Compound 56 (200 mg, 1.14 mmol) prepared
in Example 53. [0537] .sup.1H NMR (270 MHz, CDCl.sub.3)
.delta.(ppm): 1.35 (t, J=6.9 Hz, 3H), 2.25 (s, 3H), 2.30 (s, 3H),
2.40 (s, 3H), 3.91-3.93 (br s, 2H), 7.22-7.28 (m, 2H), 7.38-7.42
(m, 2H)
EXAMPLE 55
Compound 58
[0537] [0538] Step 1: In a manner similar to that in Step 1 of
Example 1, 3'-chloroacetophenone=thiosemicarbazone (211 mg, 45%)
was obtained from 3'-chloroacetophenone (319 mg, 2.06 mmol) and
thiosemicarbazide (188 mg, 2.06 mmol). [0539] Step 2: In a manner
similar to that in Step 2 of Example 1, Compound 58 (347 mg, 97%)
was obtained from 3'-chloroacetophenone=thiosemicarbazone (200 mg,
1.14 mmol) prepared above. [0540] .sup.1H NMR (270 MHz, CDCl.sub.3)
.delta.(ppm): 2.01 (s, 3H), 2.19 (s, 3H), 2.25 (s, 3H), 7.29-7.41
(m, 4H), 11.68 (br s, 1H)
EXAMPLE 56
Compound 59
[0540] [0541] Step 1: In a manner similar to that in Step 1 of
Example 1, 4'-chloroacetophenone=thiosemicarbazone (362 mg, 58%)
was obtained from 4'-chloroacetophenone (344 mg, 2.23 mmol) and
thiosemicarbazide (194 mg, 2.06 mmol). [0542] Step 2: In a manner
similar to that in Step 2 of Example 1, Compound 59 (193 mg, 86%)
was obtained from 4'-chloroacetophenone=thiosemicarbazone (164 mg,
0.720 mmol) prepared above. [0543] .sup.1H NMR (270 MHz,
CDCl.sub.3) .delta.(ppm): 2.11 (s, 3H), 2.23 (s, 3H), 2.24 (s, 3H),
7.30 (d, J=8.6 Hz, 2H), 7.36 (d, J=8.6 Hz, 2H), 8.34 (br s, 1H)
EXAMPLE 57
Compound 60
[0543] [0544] Step 1: In a manner similar to that in Step 1 of
Example 1, 2'-bromoacetophenone=thiosemicarbazone (392 mg, 69%) was
obtained from 2'-bromoacetophenone (415 mg, 2.08 mmol) and
thiosemicarbazide (190 mg, 2.08 mmol). [0545] .sup.1H NMR (270 MHz,
DMSO-d.sub.6) .delta.(ppm): 2.28 (s, 3H), 7.29-7.76 (m, 5H), 8.25
(br s, 1H), 10.35 (br s, 1H) [0546] Step 2: In a manner similar to
that in Step 2 of Example 1, Compound 60 (328 mg, 99%) was obtained
from 2'-bromoacetophenone=thiosemicarbazone (254 mg, 0.933 mmol)
prepared above. [0547] .sup.1H NMR (270 MHz, CDCl.sub.3)
.delta.(ppm): 2.01 (s, 3H), 2.23 (s, 3H), 2.38 (s, 3H), 7.13 (br t,
J=7.6 Hz, 1H), 7.30 (br t, J=7.6 Hz, 1H), 7.47 (br d, J=7.6 Hz,
1H), 7.62 (br s, J=7.6 Hz, 1H), 8.86 (br s, 1H)
EXAMPLE 58
Compound 61
[0547] [0548] Step 1: In a manner similar to that in Step 1 of
Example 1, 2'-hydroxyacetophenone=thiosemicarbazone (649 mg, 78%)
was obtained from 2'-hydroxyacetophenone (544 mg, 4.00 mmol) and
thiosemicarbazide (377 mg, 4.12 mmol). [0549] .sup.1H NMR (270 MHz,
DMSO-d.sub.6) .delta.(ppm): 2.31 (s, 3H), 6.85 (br t, J=7.0 Hz,
1H), 6.88 (br d, J=7.0 Hz, 1H), 7.25 (br t, J=7.0 Hz, 1H), 7.50 (br
s, 1H), 7.53 (br d, J=7.0 Hz, 1H), 7.81 (br s, 1H), 8.10 (br s,
1H), 10.35 (br s, 1H) [0550] Step 2: In a manner similar to that in
Step 2 of Example 1, Compound 61 (322 mg, 70%) was obtained from
2'-hydroxyacetophenone=thiosemicarbazone (233 mg, 1.10 mmol)
prepared above. [0551] .sup.1H NMR (270 MHz, DMSO-d.sub.6)
.delta.(ppm): 2.04 (s, 3H), 2.06 (s, 3H), 2.23 (s, 3H), 2.24 (s,
3H), 7.12 (br d, J=7.6 Hz, 1H), 7.23 (br t, J=7.6 Hz, 1H), 7.35 (br
t, J=7.6 Hz, 1H), 7.39 (br d, J=7.6 Hz, 1H), 10.20 (br s, 1H)
EXAMPLE 59
Compound 62
[0551] [0552] Step 1: In a manner similar to that in Step 1 of
Example 1, 3'-hydroxyacetophenone=thiosemicarbazone (654 mg, 78%)
was obtained from 3'-hydroxyacetophenone (546 mg, 4.01 mmol) and
thiosemicarbazide (379 mg, 4.15 mmol). [0553] Step 2: In a manner
similar to that in Step 2 of Example 1, Compound 62 (351 mg, 84%)
was obtained from 3'-hydroxyacetophenone=thiosemicarbazone (262 mg,
1.25 mmol) prepared above. [0554] .sup.1H NMR (270 MHz,
DMSO-d.sub.6) .delta.(ppm): 1.96 (s, 3H), 2.27 (s, 3H), 2.28 (s,
3H), 2.34 (s, 3H), 7.07 (br d, J=8.4 Hz, 1H), 7.15 (br s, 1H), 7.32
(br d, J=8.4 Hz, 1H), 7.33 (br t, J=8.4 Hz, 1H), 9.24 (br s,
1H)
EXAMPLE 60
Compound 63
[0554] [0555] Step 1: In a manner similar to that in Step 1 of
Example 1, 3'-hydroxybenzaldehyde=thiosemicarbazone (732 mg, 88%)
was obtained from 3'-hydroxybenzaldehyde (488 mg, 4.00 mmol) and
thiosemicarbazide (378 mg, 4.15 mmol). [0556] .sup.1H NMR (270 MHz,
DMSO-d.sub.6) .delta.(ppm): 6.80 (m, 1H), 7.13 (br s, 1H), 7.19 (m,
2H), 7.87 (br s, 1H), 7.96 (s, 1H), 8.14 (br s, 1H), 9.56 (br s,
1H), 11.35 (br s, 1H) [0557] Step 2: In a manner similar to that in
Step 2 of Example 1, Compound 63 (322 mg, 70%) was obtained from
3'-hydroxybenzaldehyde=thiosemicarbazone (300 mg, 1.43 mmol)
prepared above. [0558] .sup.1H NMR (270 MHz, DMSO-d.sub.6)
.delta.(ppm): 2.18 (s, 3H), 2.25 (s, 3H), 2.28 (s, 3H), 6.86 (s,
1H), 7.04 (br d, J=7.4 Hz, 1H), 7.05 (s, 1H), 7.19 (br d, J=7.4 Hz,
1H), 7.31 (br t, J=7.4 Hz, 1H), 8.16 (br s, 1H)
EXAMPLE 61
Compound 64
[0558] [0559] Step 1: In a manner similar to that in Step 1 of
Example 1, 4'-hydroxyacetophenone=thiosemicarbazone (830 mg, 99%)
was obtained from 4'-hydroxyacetophenone (544 mg, 4.00 mmol) and
thiosemicarbazide (387 mg, 4.25 mmol). [0560] .sup.1H NMR (270 MHz,
DMSO-d.sub.6) .delta.(ppm): 2.23 (s, 3H), 6.75 (d, J=8.5 Hz, 2H),
7.76 (d, J=8.5 Hz, 2H), 7.78 (br s, 1H), 8.14 (br s, 1H), 9.75 (s,
1H), 10.05 (s, 1H) [0561] Step 2: In a manner similar to that in
Step 2 of Example 1, Compound 64 (199 mg, 61%) was obtained from
4'-hydroxyacetophenone=thiosemicarbazone (202 mg, 0.965 mmol)
prepared above. [0562] .sup.1H NMR (270 MHz, CDCl.sub.3)
.delta.(ppm): 2.15 (s, 3H), 2.22 (s, 3H), 2.23 (s, 3H), 2.29 (s,
3H), 7.07 (br d, J=8.6 Hz, 2H), 7.43 (br d, J=8.6 Hz, 2H), 7.99 (br
s, 1H)
EXAMPLE 62
Compound 65
[0562] [0563] Step 1: In a manner similar to that in Step 1 of
Example 1, 2'-nitroacetophenone=thiosemicarbazone (785 mg, 81%) was
obtained from 2'-nitroacetophenone (673 mg, 4.08 mmol) and
thiosemicarbazide (365 mg, 3.99 mmol). [0564] .sup.1H NMR (270 MHz,
DMSO-d.sub.6) .delta.(ppm): 2.27 (s, 3H), 7.32 (br s, 1H),
7.60-7.68 (m, 1H), 7.72-7.79 (m, 2H), 7.96 (br d, J=7.9 Hz, 1H),
8.31 (br s, IH), 10.52 (br s, 1H) [0565] Step 2: In a manner
similar to that in Step 2 of Example 1, Compound 65 (548 mg, 94%)
was obtained from 2'-nitroacetophenone=thiosemicarbazone (431 mg,
1.81 mmol) prepared above. [0566] .sup.1H NMR (270 MHz, CDCl.sub.3)
.delta.(ppm): 2.04 (s, 3H), 2.07 (s, 3H), 2.23 (s, 3H), 7.49-7.71
(m, 4H), 11.73 (br s, 1H)
EXAMPLE 63
Compound 66
[0566] [0567] Step 1: In a manner similar to that in Step 1 of
Example 1, 3'-nitroacetophenone=thiosemicarbazone (910 mg, 75%) was
obtained from 3'-nitroacetophenone (661 mg, 4.00 mmol) and
thiosemicarbazide (370 mg, 4.05 mmol). [0568] .sup.1H NMR (270 MHz,
DMSO-d.sub.6) .delta.(ppm): 2.37 (s, 3H), 7.67 (br t, J=7.9 Hz,
1H), 8.16 (br s, 1H), 8.23 (br d, J=7.9 Hz, 1H), 8.40 (br s, 1H),
8.43 (br S, J=7.9 Hz, 1H), 8.61 (br s, 1H), 10.40 (br s, 1H) [0569]
Step 2: In a manner similar to that in Step 2 of Example 1,
Compound 66 (409 mg, 60%) was obtained from
3'-nitroacetophenone=thiosemicarbazone (506 mg, 2.12 mmol) prepared
above. [0570] .sup.1H NMR (270 MHz, CDCl.sub.3) .delta.(ppm): 2.15
(s, 3H), 2.25 (s, 3H), 2.40 (s, 3H), 7.53 (br t, J=8.3 Hz, 1H),
7.73 (br d, J=8.3 Hz, 1H), 8.15 (br d, J=8.3 Hz, 1H), 8.30 (br s,
2H)
EXAMPLE 64
Compound 67
[0570] [0571] Step 1: In a manner similar to that in Step 1 of
Example 1, 4'-nitroacetophenone=thiosemicarbazone (475 mg, 94%) was
obtained from 4'-nitroacetophenone (350 mg, 2.12 mmol) and
thiosemicarbazide (195 mg, 2.13 mmol). [0572] Step 2: In a manner
similar to that in Step 2 of Example 1, Compound 67 (216 mg, 40%)
was obtained from 4'-nitroacetophenone=thiosemicarbazone (397 mg,
1.67 mmol) prepared above. [0573] .sup.1H NMR (270 MHz, CDCl.sub.3)
.delta.(ppm): 2.15 (s, 3H), 2.24 (s, 3H), 2.38 (s, 3H), 7.59 (d,
J=8.6 Hz, 2H), 8.20 (d, J=8.6 Hz, 2H), 8.30 (br s, 1H)
EXAMPLE 65
Compound 68
[0574] Compound 61 (118 mg, 0.352 mmol) prepared in Example 58 was
dissolved in methanol (5 mL), and to the solution was added
potassium carbonate (200 mg, 1.48 mmol) and the mixture was stirred
at room temperature for 10 minutes. The reaction mixture was
filtered, and the filtrate was concentrated under reduced pressure.
After the residue was dissolved in ethyl acetate, to the solution
was added water and 1 mol/L hydrochloric acid, and the mixture was
subjected to separation. The organic layer was washed with
saturated aqueous sodium chloride and dried over anhydrous sodium
sulfate, and then the solvent was evaporated under reduced
pressure. The resulting yellow oil was dissolved in methanol (3
mL). To the solution was added diisopropyl ether (10 mL), and the
deposited crystals were collected by filtration and dried to obtain
Compound 68 (96.9 mg, 94%). [0575] .sup.1H NMR (270 MHz,
DMSO-d.sub.6) .delta.(ppm): 1.98 (s, 3H), 2.23 (s, 3H), 2.35 (s,
3H), 6.72 (br t, J=7.6 Hz, 1H), 6.83 (br d, J=7.6 Hz, 1H), 6.88 (br
d, J=7.6 Hz, 1H), 7.10 (br t, J=7.6 Hz, 1H), 9.95 (br s, 1H), 11.45
(br s, 1H)
EXAMPLE 66
Compound 69
[0576] In a manner similar to that in Example 65, Compound 69 (101
mg, 82%) was obtained from Compound 62 (140 mg, 0.417 mmol)
prepared in Example 59. [0577] .sup.1H NMR (270 MHz, DMSO-d.sub.6)
.delta.(ppm): 2.01 (s, 3H), 2.18 (s, 3H), 2.23 (s, 3H), 6.66 (br t,
J=7.9 Hz, 1H), 6.69 (br s, 1H), 6.76 (br d, J=7.9 Hz, 1H), 7.13 (br
t, J=7.9 Hz, 1H), 9.46 (br s, 1H), 11.60 (br s, 1H)
EXAMPLE 67
Compound 70
[0578] In a manner similar to that in Example 65, Compound 70 (88
mg, 91%) was obtained from Compound 64 (110 mg, 0.328 mmol)
prepared in Example 61. [0579] .sup.1H NMR (270 MHz, CDCl.sub.3)
.delta.(ppm): 2.00 (s, 3H), 2.16 (s, 3H), 2.23 (s, 3H), 6.71 (d,
J=8.6 Hz, 2H), 7.15 (d, J=8.6 Hz, 2H), 9.48 (br s, 1H), 11.6 (br s,
1H)
EXAMPLE 68
Compound 71
[0579] [0580] Step 1: In a manner similar to that in Step 1 of
Example 1, 3'-cyanoacetophenone=thiosemicarbazone (863 mg, 99%) was
obtained from 3-acetylbenzonitrile (581 mg, 4.00 mmol) and
thiosemicarbazide (370 mg, 4.05 mmol). [0581] Step 2: In a manner
similar to that in Step 2 of Example 1, Compound 71 (274 mg, 68%)
was obtained from 3'-cyanoacetophenone=thiosemicarbazone (300 mg,
1.34 mmol) prepared above. [0582] .sup.1H NMR (270 MHz, CDCl.sub.3)
.delta.(ppm): 2.08 (s, 3H), 2.26 (s, 3H), 2.36 (s, 3H), 7.46 (m,
1H), 7.56 (m, 1H), 7.68 (m, 1H), 7.71 (br s, 1H), 8.73 (br s,
1H)
EXAMPLE 69
Compound 72
[0582] [0583] Step 1: In a manner similar to that in Step 1 of
Example 1, 4'-cyanoacetophenone=thiosemicarbazone (430 mg, 98%) was
obtained from 4-acetylbenzonitrile (290 mg, 2.0 mmol) and
thiosemicarbazide (185 mg, 2.02 mmol). [0584] .sup.1H NMR (270 MHz,
DMSO-d.sub.6) .delta.(ppm): 2.30 (s, 3H), 7.82 (d, J=8.4 Hz, 2H),
8.12 (br s, 1H), 8.14 (d, J=8.4 Hz, 2H), 8.40 (br s, 1H), 10.51 (br
s, 1H) [0585] Step 2: In a manner similar to that in Step 2 of
Example 1, Compound 72 (494 mg, 94%) was obtained from
4'-cyanoacetophenone=thiosemicarbazone (380 mg, 1.74 mmol) prepared
above. [0586] .sup.1H NMR (270 MHz, DMSO-d.sub.6) .delta.(ppm):
2.01 (s, 3H), 2.18 (s, 3H), 2.31 (s, 3H), 7.54 (d, J=11.7 Hz, 2H),
7.81 (d, J=11.7 Hz, 2H), 11.73 (br s, 1H)
EXAMPLE 70
Compound 73
[0586] [0587] Step 1: In a manner similar to that in Step 1 of
Example 1, 3'-trifluoromethylacetophenone=thiosemicarbazone (888
mg, 63%) was obtained from 3'-trifluoromethylacetophenone (765 mg,
4.07 mmol) and thiosemicarbazide (370 mg, 4.05 mmol). [0588] Step
2: In a manner similar to that in Step 2 of Example 1, Compound 73
(270 mg, 68%) was obtained from
3'-trifluoromethylacetophenone=thiosemicarbazone (300 mg, 1.15
mmol) prepared above. [0589] .sup.1H NMR (270 MHz, CDCl.sub.3)
.delta.(ppm): 2.01 (s, 3H), 2.27 (s, 3H), 2.37 (s, 3H), 7.43 (br t,
J=7.6 Hz, 1H), 7.52 (br d, J=7.6 Hz, 1H), 7.63 (br d, J=7.6 Hz,
1H), 7.65 (br s, 1H), 8.89 (br s, 1H)
EXAMPLE 71
Compound 74
[0589] [0590] Step 1: In a manner similar to that in Step 1 of
Example 1, 2'-carboxyacetophenone=thiosemicarbazone (489 mg, 52%)
was obtained from 2-acetylbenzoic acid (381 mg, 4.17 mmol) and
thiosemicarbazide (381 mg, 4.17 mmol). [0591] Step 2: In a manner
similar to that in Step 2 of Example 1, Compound 74 (313 mg, 64%)
was obtained from 2'-carboxyacetophenone=thiosemicarbazone (363 mg,
1.53 mmol) prepared above. [0592] .sup.1H NMR (270 MHz, CDCl.sub.3)
.delta.(ppm): 2.04 (s, 3H), 2.29 (s, 3H), 2.38 (s, 3H), 3.20-3.30
(br s, 1H), 7.88-8.15 (m, 3H), 8.32-8.33 (br m, 1H)
EXAMPLE 72
Compound 75
[0592] [0593] Step 1: In a manner similar to that in Step 1 of
Example 1, 2',6'-dimethoxyacetophenone=thiosemicarbazone (747 mg,
83%) was obtained from 2',6'-dimethoxyacetophenone (606 mg, 3.98
mmol) and thiosemicarbazide (374 mg, 4.09 mmol). [0594] .sup.1H NMR
(270 MHz, DMSO-d.sub.6) .delta.(ppm): 2.09 (s, 3H), 3.77 (s, 6H),
6.80 (d, J=8.2 Hz, 2H), 7.44 (t, J=8.2 Hz, 1H), 7.83 (br s, 1H),
8.04 (br s, 1H), 8.31 (br s, 1H) [0595] Step 2: In a manner similar
to that in Step 2 of Example 1, Compound 75 (441 mg, 89%) was
obtained from 2',6'-dimethoxyacetophenone=thiosemicarbazone (363
mg, 1.61 mmol) prepared above. [0596] .sup.1H NMR (270 MHz,
CDCl.sub.3) .delta.(ppm): 2.02 (s, 3H), 2.21 (s, 3H), 2.51 (s, 3H),
3.78 (s, 6H), 6.53 (d, J=8.5 Hz, 2H), 7.15 (t, J=8.5 Hz, 1H), 8.70
(br s, 1H)
EXAMPLE 73
Compound 76
[0596] [0597] Step 1: In a manner similar to that in Step 1 of
Example 1, 3',5'-dihydroxyacetophenone=thiosemicarbazone (707 mg,
78%) was obtained from 3',5'-dihydroxyacetophenone (613 mg, 4.03
mmol) and thiosemicarbazide (376 mg, 4.11 mmol). [0598] .sup.1H NMR
(270 MHz, DMSO-d.sub.6) .delta.(ppm): 2.20 (s, 3H), 6.25 (br s,
1H), 6.69 (br s, 2H), 7.64 (br s, 1H), 8.26 (br s, 1H), 9.29 (br s,
2H), 10.19 (br s, 1H) [0599] Step 2: In a manner similar to that in
Step 2 of Example 1, Compound 76 (591 mg, 69%) was obtained from
3',5'-dihydroxyacetophenone=thiosemicarbazone (622 mg, 2.76 mmol)
prepared above. [0600] .sup.1H NMR (270 MHz, CDCl.sub.3)
.delta.(ppm): 2.01 (s, 3H), 2.17 (s, 3H), 2.18 (s, 3H), 6.10 (br s,
1H), 6.16 (br s, 2H), 9.27 (br s, 2H), 11.59 (br s, 1H)
EXAMPLE 74
Compound 77
[0600] [0601] Step 1: In a manner similar to that in Step 1 of
Example 1, 3',4'-dihydroxyacetophenone=thiosemicarbazone (747 mg,
83%) was obtained from 3',4'-dihydroxyacetophenone (606 mg, 3.98
mmol) and thiosemicarbazide (374 mg, 4.09 mmol). [0602] .sup.1H NMR
(270 MHz, DMSO-d.sub.6) .delta.(ppm): 2.20 (s, 3H), 6.72 (br d,
J=8.3 Hz, 1H), 7.18 (br d, J=8.3 Hz, 1H), 7.29 (br s, 1H), 7.65 (br
s, 1H), 8.18 (br s, 2H), 9.09 (br s, 2H), 10.09 (br s, 1H) [0603]
Step 2: In a manner similar to that in Step 2 of Example 1,
Compound 77 (441 mg, 89%) was obtained from
3',4'-dihydroxyacetophenone=thiosemicarbazone (363 mg, 1.61 mmol)
prepared above. [0604] .sup.1H NMR (270 MHz, CDCl.sub.3)
.delta.(ppm): 2.01 (s, 3H), 2.06 (s, 3H), 2.20 (s, 3H), 6.62 (br t,
J=7.6 Hz, 1H), 6.66 (br d, J=8.2 Hz, 1H), 6.71 (br s, 1H), 8.93 (s,
1H), 8.97 (s, 1H), 11.56 (br s, 1H)
EXAMPLE 75
Compound 78
[0604] [0605] Step 1: In a manner similar to that in Step 1 of
Example 1, 2',4'-dimethylacetophenone=thiosemicarbazone (110 mg,
12%) was obtained from 2',4'-dimethylacetophenone (598 mg, 4.04
mmol) and thiosemicarbazide (366 mg, 4.00 mmol). [0606] Step 2: In
a manner similar to that in Step 2 of Example 1, Compound 78 (107
mg, 77%) was obtained from
2',4'-dimethylacetophenone=thiosemicarbazone (100 mg, 0.452 mmol)
prepared above. [0607] .sup.1H NMR (270 MHz, CDCl.sub.3)
.delta.(ppm): 2.16 (s, 3H), 2.21 (s, 3H), 2.35 (s, 3H), 6.92 (d,
J=7.9 Hz, 1H), 7.07 (d, J=7.9 Hz, 1H), 8.22 (br s, 1H)
EXAMPLE 76
Compound 79
[0607] [0608] Step 1: To a solution of hydrazine monohydrate (1.00
mL, 20.6 mmol) in acetonitrile (5.00 mL) was added allyl
isothiocyanate (2.00 mL, 20.4 mmol), and the mixture was stirred at
60.degree. C. for 30 minutes. To the reaction mixture was added
diethyl ether (50 mL), and the deposited solid was collected by
filtration. The collected solid was dried to obtain
4-allylthiosemicarbazide (1.22 g, 46%). [0609] .sup.1H NMR (270
MHz, DMSO-d.sub.6) .delta.(ppm): 4.11 (t, J=5.3 Hz, 2H), 4.47 (br
s, 2H), 5.03 (d, J=12.3 Hz, 1H), 5.08 (d, J=19.1 Hz, 1H), 5.86 (m,
1H), 7.88 (br s, 1H), 8.70 (br s, 1H) [0610] Step 2: In a manner
similar to that in Step 1 of Example 1,
acetophenone=4-allylthiosemicarbazone (1.74 g, 80%) was obtained
from acetophenone (1.09 mL, 9.34 mmol) and 4-allylthiosemicarbazide
(1.22 g, 9.31 mmol) prepared above. [0611] .sup.1H NMR (270 MHz,
DMSO-d.sub.6) .delta.(ppm): 2.31 (s, 3H), 4.25 (t, J=5.8 Hz, 2H),
5.10 (d, J=10.5 Hz, 1H), 5.18 (d, J=17.5 Hz, 1H), 5.91 (m, 1H),
7.37-7.42 (m, 3H), 7.91-7.94 (m, 2H), 8.61 (t, J=6.0 Hz, 1H), 10.3
(br s, 1H) [0612] Step 3: Acetophenone=4-allylthiosemicarbazone (30
mg, 0.11 mmol) prepared above was dissolved in chloroform (0.5 mL),
and to the solution was added acetyl chloride (0.17 mL, 2.32 mmol)
and pyridine (0.190 mL, 2.31 mmol), and the solution was stirred at
room temperature for 5 hours. To the reaction mixture was added 2
mol/L aqueous sodium hydroxide, then the mixture was extracted with
ethyl acetate. The organic layer was washed with saturated aqueous
ammonium chloride and saturated aqueous sodium chloride, and then
dried over anhydrous sodium sulfate, and the solvent was
evaporated. The residue was purified by silica gel column
chromatography (ethyl acetate/n-hexane=1/2) to obtain Compound 79
(25 mg, 89%). [0613] .sup.1H NMR (270 MHz, CDCl.sub.3)
.delta.(ppm): 2.26 (s, 3H), 2.27 (s, 3H), 2.36 (s, 3H), 4.47-4.53
(m, 2H), 5.24 (d, J=17.3 Hz, 1H), 5.29 (d, J=10.5 Hz, 1H), 5.91 (m,
1H), 7.20-7.45 (m, 5H) [0614] FAB-MS (m/z): 318 (M.sup.++1)
EXAMPLE 77
Compounds 80 and 81
[0614] [0615] Step 1: In a manner similar to that in Step 3 of
Example 76, Compound 80 (42 mg, 5%) was obtained from
acetophenone=4-allylthiosemicarbazone (694 mg, 2.97 mmol) prepared
in Step 2 of Example 76, isobutyryl chloride (0.63 mL, 5.97 mmol)
and pyridine (0.43 mL, 5.26,mmol). [0616] .sup.1H NMR (270 MHz,
CDCl.sub.3) .delta.(ppm): 1.10 (d, J=6.8 Hz, 3H), 1.13 (d, J=6.9
Hz, 3H), 2.39 (s, 3H), 3.25 (quin., J=7.0 Hz, 1H), 3.84-4:00 (m,
3H), 5.19 (d, J=10.2 Hz, 1H), 5.26 (d, J=17.2 Hz, 1H), 5.93 (m,
1H), 7.20-7.49 (m, 5H) [0617] Step 2: In a manner similar to that
in Example 15, Compound 81 (527 mg, 74%) was obtained from Compound
80 (623 mg, 2.05 mmol) prepared above, acetyl chloride (0.59 mL,
8.30 mmol) and pyridine (0.77 mL, 8.28 mmol). [0618] .sup.1H NMR
(270 MHz, CDCl.sub.3) .delta.(ppm): 1.10 (d, J=6.9 Hz, 3H), 1.12
(d, J=6.9 Hz, 3H), 2.27 (s, 3H), 2.34 (s, 3H), 3.21 (quin., J=6.9
Hz, 1H), 4.51 (br s, 2H), 5.25 (d, J=17.2 Hz, 1H), 5.30 (d, J=10.7
Hz, 1H), 5.93 (m, 1H), 7.20-7.42 (m, 5H) [0619] AP-MS (m/z): 346
(M.sup.++1)
EXAMPLE 78
Compound 82
[0620] In a manner similar to that in Step 3 of Example 76,
Compound 82 (269 mg, 47%) was obtained from
acetophenone=thiosemicarbazone (306 mg, 1.59 mmol) prepared in Step
1 of Example 1, pivaloyl chloride (0.40 mL, 3.21 mmol) and pyridine
(0.26 mL, 3.22 mmol). [0621] .sup.1H NMR (270 MHz, CDCl.sub.3)
.delta.(ppm): 1.29 (s, 9H), 1.30 (s, 9H), 2.35 (s, 3H), 7.20-7.46
(m, 5H), 7.90 (m, 1H) [0622] AP-MS (m/z): 360 (M.sup.+-1)
EXAMPLE 79
Compounds 83 and 84
[0622] [0623] Step 1: In a manner similar to that in Example 12,
Compound 83 (537 mg, 67%) was obtained from Compound 21 (1.00 g,
2.88 mmol) prepared in Example 18. [0624] .sup.1H NMR (270 MHz,
CDCl.sub.3) .delta.(ppm): 1.12 (d, J=6.9 Hz, 3H), 1.14 (d, J=6.9
Hz, 3H), 2.39 (s, 3H), 2.91 (d, J=4.9 Hz, 3H), 3.30 (m, 1H), 3.90
(br, 1H), 7.20-7.43 (m, 5H) [0625] Step 2: In a manner similar to
that in Example 15, Compound 84 (233 mg, 38%) was obtained from
Compound 83 (536 mg, 1.93 mmol) prepared above, acetyl chloride
(0.28 mL, 3.87 mmol) and pyridine (0.32 mL, 3.90 mmol). [0626]
.sup.1H NMR (270 MHz, CDCl.sub.3) .delta.(ppm): 1.12 (d, J=6.9 Hz,
3H), 1.14 (d, J=6.9 Hz, 3H), 2.28 (s, 3H), 2.34 (s, 3H), 3.28
(quin., J=6.9 Hz, 1H), 3.46 (br s, 3H), 7.20-7.43 (m, 5H) [0627]
FAB-MS (m/z): 320 (M.sup.+30 1) [0628] Elemental analysis
(C.sub.16H.sub.21N.sub.3O.sub.2S): Found (%) C; 60.16, H; 6.63, N;
13.15, Calcd. (%) C; 60.27, H; 6.73, N; 13.20
EXAMPLE 80
Compound 85
[0629] In a manner similar to that in Step 2 of Example 1, Compound
85 (176 mg, 20%) was obtained from acetophenone=thiosemicarbazone
(517 mg, 2.68 mmol) prepared in Step 1 of Example 1 and isobutyric
anhydride (2.22 mL, 13.4 mmol). [0630] .sup.1H NMR (270 MHz,
CDCl.sub.3) .delta. ppm): 1.09 (d, J=2.6 Hz, 3H), 1.12 (d, J=2.6
Hz, 3H), 1.21 (d, J=2.6 Hz, 3H), 1.23 (d, J=2.6 Hz, 3H), 2.37 (s,
3H), 2.50 (quin., J=6.9 Hz, 1H), 3.20 (quin., J=6.9 Hz, 1H),
7.20-7.48 (m, 5H), 7.98 (br s, 1H) [0631] AP-MS (m/z): 334
(M.sup.++1) [0632] Elemental analysis
(C.sub.17H.sub.23N.sub.3O.sub.2S): Found (%) C; 61.23, H; 6.95, N;
12.60, Calcd. (%) C; 61.22, H; 6.93, N; 12.63
EXAMPLE 81
Compounds 86 and 87
[0632] [0633] Step 1: In a manner similar to that in Example 11,
Compound 86 (588 mg, 43%) was obtained from
acetophenone=thiosemicarbazone (1.01 g, 5.22 mmol) prepared in Step
1 of Example 1, isobutyric anhydride (1.73 mL, 10.4 mmol) and
pyridine (0.84 mL, 10.4 mmol). [0634] .sup.1H NMR (270 MHz,
CDCl.sub.3) .delta.(ppm): 1.09 (d, J=6.9 Hz, 3H), 1.11 (d, J=6.9
Hz, 3H), 2.40 (s, 3H), 3.21 (quin., J=6.9 Hz, 1H), 4.12 (br s, 2H),
7.20-7.40 (m, 5H) [0635] Step 2: In a manner similar to that in
Example 15, Compound 87 (47 mg, 16%) was obtained from Compound 86
(256 mg, 0.97 mmol) prepared above and acetic anhydride (0.46 mL,
4.88 mmol). [0636] .sup.1H NMR (270 MHz, CDCl.sub.3) .delta.(ppm):
1.19 (d, J=6.9 Hz, 3H), 1.20 (d, J=6.9 Hz, 3H), 2.25 (s, 3H), 2.38
(s, 3H), 2.47 (quin., J=6.9 Hz, 1H), 7.20-7.50 (m, 5H)
EXAMPLE 82
Compound 88
[0637] In a manner similar to that in Example 15, Compound 88 (53
mg, 8%) was obtained from Compound 14 (502 mg, 2.14 mmol) prepared
in Example 11 and isobutyric anhydride (1.77 mL, 10.7 mmol). [0638]
.sup.1H NMR (270 MHz, CDCl.sub.3) .delta.(ppm): 1.20 (d, J .=6.9
Hz, 3H), 1.22 (d, J=6.9 Hz, 3H), 2.24 (s, 3H), 2.38 (s, 3H), 2.48
(quin., J=6.9 Hz, 1H), 7.20-7.46 (m, 5H), 8.08 (br s, 1H) [0639]
AP-MS (m/z): 306 (M.sup.+30 1)
EXAMPLE 83
Compound 89
[0640] In a manner similar to that in Example 15, Compound 89 (274
mg, 64%) was obtained from Compound 14 (303 mg, 1.29 mmol) prepared
in Example 11, cyclopentanecarbonyl chloride (0.32 mL, 2.59 mmol)
and pyridine (0.21 mL, 2.60 mmol). [0641] .sup.1H NMR (270 MHz,
CDCl.sub.3) .delta.(ppm): 1.50-1.95 (m, 8H), 2.24 (s, 3H), 2.38 (s,
3H), 2.65 (quin., J=7.9 Hz, 1H), 7.20-7.45 (m, 5H), 8.04 (br s, 1H)
[0642] AP-MS (m/z): 330 (M.sup.+-1) [0643] Elemental analysis
(C.sub.17H.sub.21N.sub.3O.sub.2S.0.4H.sub.2O): Found (%) C; 60.30,
H; 6.49, N; 12.41, Calcd. (%) C; 60.45, H; 6.49, N; 12.05
EXAMPLE 84
Compounds 90 and 91
[0643] [0644] Step 1: In a manner similar to that in Example 11,
Compound 90 (123 mg, 13%) was obtained from
acetophenone=thiosemicarbazone (507 mg, 2.63 mmol) prepared in Step
1 of Example 1, isovaleric anhydride (1.05 mL, 5.30 mmol) and
pyridine (0.43 mL, 5.26 mmol). [0645] .sup.1H NMR (270 MHz,
CDCl.sub.3) .delta.(ppm): 0.82-1.00 (m, 6H), 2.12 (quin., J=6.6 Hz,
1H), 2.38 (s, 3H), 2.45 (d, J=7.7 Hz, 2H), 4.34 (br, 2H), 7.20-7.48
(m, 5H) [0646] Step 2: In a manner similar to that in Example 15,
Compound 91 (128 mg, 98%) was obtained from Compound 91 (105 mg,
0.38 mmol) prepared above, isobutyryl chloride (0.08 mL, 0.76 mmol)
and pyridine (0.06 mL, 0.80 mmol). [0647] .sup.1H NMR (270 MHz,
CDCl.sub.3) .delta.(ppm): 0.92 (d, J=6.6 Hz, 1H), 0.93 (d, J=6.6
Hz, 1H), 1.18 (d, J=3.3 Hz, 1H), 1.21 (d, J=3.3 Hz, 1H), 2.13
(quin., J=6.6 Hz, 1H), 2.38 (s, 3H), 2.39-2.56 (m, 4H), 7.20-7.48
(m, 5H), 8.15 (br s, 1H)
EXAMPLE 85
Compound 92
[0647] [0648] Step 1: To a solution of acetophenone (4.00 mL, 34.3
mmol) in ethanol (15 mL) was added hydrazine monohydrate (6.67 mL,
138 mmol), and the mixture was heated under reflux for 4 hours.
After cooling, to the mixture was added water, and the mixture was
extracted with ethyl acetate. The organic layer was washed with
saturated aqueous sodium chloride, and then dried over anhydrous
sodium sulfate, and the solvent was evaporated. The residue was
purified by silica gel column chromatography (ethyl
acetate/n-hexane=1/2) to obtain acetophenone=hydrazone (5.39 g,
.about.100%). [0649] .sup.1H NMR (300 MHz, CDCl.sub.3)
.delta.(ppm): 2.00 (s, 3H), 5.34 (br s, 2H), 7.22-7.60 (m, 5H)
[0650] .sup.13C NMR (300 MHz, CDCl.sub.3) .delta.(ppm): 11.3,
125.1, 127.7, 127.9, 139.1, 146.7 [0651] Step 2: To a solution of
ammonium thiocyanate (3.40 g, 44.6 mmol) in acetone (20 mL) was
added acetyl chloride (2.80 mL, 37.1 mmol), and the mixture was
stirred at 70.degree. C. for 10 minutes. To the reaction mixture
was added acetophenone=hydrazone (5.36 g, 40.0 mmol) prepared
above, and the mixture was heated under reflux for 20 minutes.
After the reaction mixture was cooled, saturated aqueous ammonium
chloride was added to the mixture, and the mixture was extracted
with chloroform. The organic layer was washed with saturated
aqueous sodium chloride, and then dried over anhydrous sodium
sulfate, and the solvent was evaporated. The residue was purified
by silica gel column chromatography (ethyl acetate/n-hexane=1/2) to
obtain acetophenone=4-acetylthiosemicarbazone (148 mg, 2%). [0652]
.sup.1H NMR (300 MHz, DMSO-d.sub.6) .delta.(ppm): 2.15 (s, 3H),
2.28 (s, 3H), 7.47-7.51 (m, 3H), 7.56-7.59 (m, 2H), 11.6 (br s,
1H), 13.6 (br s, 1H) [0653] Step 3: In a manner similar to that in
Step 3 of Example 76, Compound 92 (36 mg, 88%) was obtained from
acetophenone=4-acetylthiosemicarbazone (30 mg, 0.13 mmol) prepared
above, pivaloyl chloride (32 .mu.L, 0.26 mmol) and pyridine (20
.mu.L, 0.26 mmol). [0654] .sup.1H NMR (300 MHz, CDCl.sub.3)
.delta.(ppm): 1.27 (s, 9H), 2.25 (s, 3H), 2.38 (s, 3H), 7.23-7.46
(m, 5H), 8.13 (br s, 1H) [0655] .sup.13C NMR (300 MHz, CDCl.sub.3)
.delta.(ppm): 24.0, 27.2, 39.4, 80.5, 125.1, 128.0, 128.6, 143.0,
143.1, 169.0, 176.7 [0656] AP-MS (m/z): 318 (M.sup.++1)
EXAMPLE 86
Compound 93
[0657] In a manner similar to that in Step 2 of Example 1, Compound
93 (123 mg, 45%) was obtained from Compound 14 (201 mg, 0.853 mmol)
prepared in Example 11 and pivaloyl chloride (0.21 mL, 1.71 mmol).
[0658] .sup.1H NMR (270 MHz, CDCl.sub.3) .delta.(ppm): 1.26 (s,
9H), 2.24 (s, 3H), 2.38 (s, 3H), 7.20-7.51 (m, 5H), 8.10 (br s, 1H)
[0659] AP-MS (m/z): 319 (M.sup.++1)
EXAMPLE 87
Compound 94
[0659] [0660] Step 1: In a manner similar to that in Step 1 of
Example 1, propiophenone=thiosemicarbazone (759 mg, 88%) was
obtained from propiophenone (382 mg, 4.18 mmol) and
thiosemicarbazide (541 mg, 3.92 mmol). [0661] Step 2: In a manner
similar to that in Step 3 of Example 76, Compound 94 (270 mg, 58%)
was obtained from propiophenone=thiosemicarbazone (256 mg, 1.24
mmol) prepared above, pivaloyl chloride (597 .mu.L, 4.84 mmol) and
pyridine (391 .mu.L, 4.84 mmol). [0662] .sup.1H NMR (270 MHz,
CDCl.sub.3) .delta.(ppm): 1.15 (dd, J=7.1, 7.3 Hz, 3H), 1.29 (s,
9H), 1.34 (s, 9H), 2.29 (qd, J=7.3, 14.6 Hz, 1H), 3.10 (qd, J=7.1,
14.6 Hz, 1H), 7.21-7.40 (m, 5H), 8.31 (br s, 1H) [0663] AP-MS
(m/z): 377 (M.sup.++1)
EXAMPLE 88
Compound 95
[0663] [0664] Step 1: 2-Aminoacetophenone hydrochloride (6.10 g,
35.5 mmol) was dissolved in dichloromethane (60 mL), and to the
solution was added triethylamine (7.56 g, 74.9 mmol). The solution
was cooled to 0.degree. C., and to the solution was added
methanesulfonyl chloride (2.84 mL, 36.5 mmol). The solution was
stirred at the same temperature for 5 minutes, and then at room
temperature for 2 hours. To the reaction mixture was added water
and 1 mol/L hydrochloric acid, and the mixture was extracted with
chloroform. After the organic layer was dried over anhydrous sodium
sulfate, the solvent was evaporated under reduced pressure. The
residue was suspended in chloroform (5 mL) and the suspension was
stirred, and then, the resulted crystals were collected by
filtration to obtain 2-(methylsulfonylamino)acetophenone (4.58 g,
57%). [0665] Step 2: In a manner similar to that in Step 1 of
Example 1, 2-(methylsulfonylamino)acetophenone=thiosemicarbazone
(3.08 g, 51%) was obtained from 2-(methylsulfonylamino)acetophenone
(4.58 g, 20.2 mmol) prepared above and thiosemicarbazide (1.84 g,
20.2 mmol). [0666] Step 3: In a manner similar to that in Step 3 of
Example 76, Compound 95 (1.81 g, 91%) was obtained from
2-(methylsulfonylamino)acetophenone=thiosemicarbazone (1.31 g, 4.36
mmol) prepared above, pivaloyl chloride (2.10 g, 17.4 mmol) and
pyridine (1.38 g, 17.4 mmol). [0667] .sup.1H NMR (270 MHz,
CDCl.sub.3) .delta.(ppm): 1.30 (s, 9H), 1.36 (s, 9H), 2.97 (s, 3H),
3.98 (dd, J=5.3, 13.8 Hz, 1H), 4.64 (dd, J=8.5, 13.8 Hz, 1H), 5.10
(br dd, J=5.3, 8.5 Hz, 1H), 7.25-7.39 (m, 5H), 7.93 (br s, 1H)
[0668] AP-MS (m/z): 453 (M.sup.+-1)
EXAMPLE 89
Compound 96
[0668] [0669] Step 1: In a manner similar to that in Step 1 of
Example 1,
2-(methylsulfonylamino)acetophenone=4-methylthiosemicarbazone (122
mg) was obtained from 2-(methylsulfonylamino)acetophenone (209 mg,
0.98 mmol) prepared in [0670] Step 1 of Example 88 and
4-methylthiosemicarbazide (106 mg, 1.00 mmol). [0671] Step 2: In a
manner similar to that in Step 3 of Example 76, Compound 96 (68 mg,
15%) was obtained from
2-(methylsulfonylamino)acetophenone=4-methylthiosemicarbazone (122
mg, 0.41 mmol) obtained above, pivaloyl chloride. (128 .mu.L, 1.04
mmol) and pyridine (80 .mu.L, 1.04 mmol). [0672] .sup.1H NMR (300
MHz, DMSO-d.sub.6) .delta.(ppm): 1.27 (s, 3H), 1.28 (s, 3H), 2.95
(s, 3H), 3.53 (s, 3H), 3.94 (dd, J=13.9, 6.4 Hz, 1H), 4.27 (dd,
J=13.9, 7.9 Hz, 1H), 7.11 (t, J=7.2 Hz, 1H), 7.21-7.38 (m, 5H)
[0673] AP-MS (m/z): 467 (M.sup.+-1)
EXAMPLE 90
Compound 97
[0673] [0674] Step 1: In a manner similar to that in Step 1 of
Example 88, 2-(ethylsulfonylamino)acetophenone (367 mg, 39%) was
obtained from 2-aminoacetophenone hydrochloride (714 mg, 4.16
mmol), triethylamine (1.45 mL, 10.4 mmol) and ethanesulfonyl
chloride (0.434 mL, 4.58 mmol). [0675] Step 2: In a manner similar
to that in Step 1 of Example 1,
2-(ethylsulfonylamino)acetophenone=thiosemicarbazone (327 mg, 43%)
was obtained from 2-(ethylsulfonylamino)acetophenone (367 mg, 1.61
mmol) prepared above and thiosemicarbazide (147 mg, 1.61 mmol).
[0676] Step 3: In a manner similar to that in Step 2 of Example 1,
Compound 97 (39 mg, 25%) was obtained from
2-(ethylsulfonylamino)acetophenone=thiosemicarbazone (99 mg, 0.330
mmol), pivaloyl chloride (162 .mu.L, 1.32 mmol) and pyridine (130
.mu.L, 1.58 mmol). [0677] .sup.1H NMR (270 MHz, CDCl.sub.3)
.delta.(ppm): 1.26 (s, 9H), 1.28 (t, J=7.8 Hz, 3H), 1.29 (s, 9H),
3.09 (m, 2H), 3.97 (dd, J=5.1, 13.5 Hz, 1H), 4.60 (dd, J=8.1, 13.5
Hz, 1H), 4.99 (br dd, J=5.1, 8.1 Hz, 1H), 7.25-7.38 (br s, 5H),
7.93 (br s, 1H)
EXAMPLE 91
Compound 98
[0677] [0678] Step 1: In a manner similar to that in Step 1 of
Example 1, 2-methoxyacetopbenone=thiosemicarbazone (367 mg, 62%)
was obtained from 2-methoxyacetophenone (288 mg, 1.92 mmol) and
thiosemicarbazide (179 mg, 1.96 mmol). [0679] Step 2: In a manner
similar to that in Step 2 of Example 1, Compound 98 (132 mg, 59%)
was obtained from 2-methoxyacetophenone=thiosemicarbazone (128 mg,
0.573 mmol) prepared above, pivaloyl chloride (211 .mu.L, 1.72
mmol) and pyridine (152 .mu.L, 1.88 mmol). [0680] .sup.1H NMR (270
MHz, CDCl.sub.3) .delta.(ppm): 1.28 (s, 9H), 1.32 (s, 9H), 3.51 (s,
3H), 4.36 (d, J=9.6 Hz, 1H), 4.48 (d, J=9.6 Hz, 1H), 7.24-7.38 (m,
5H), 7.88 (s, 1H) [0681] AP-MS (m/z): 392 (M.sup.++1)
EXAMPLE 92
Compound 99
[0681] [0682] Step 1: Methane sulfonamide (0.476 g, 5.00 mmol) was
dissolved in N,N-dimethylformamide (10 mL), and to the solution was
added 60% sodium hydride (0.275 g, 5.00 mmol) and the mixture was
stirred in a water bath for 20 minutes. To the reaction mixture was
added 3-chloropropiophenone (843 mg, 5.00 mol). The mixture was
stirred in a water bath for one hour, and further stirred at room
temperature for 15 hours. To the reaction mixture was added water,
and the mixture was extracted with ethyl acetate. The organic layer
was washed with saturated aqueous sodium chloride and dried over
anhydrous sodium sulfate, and then the solvent was evaporated under
reduced pressure. The residue was purified by silica gel column
chromatography (chloroform/methanol=20/1) to obtain
3-(methylsulfonylamino)propiophenone (240 mg, 21%). [0683] Step 2:
In a manner similar to that in Step 1 of Example 1,
3-(methylsulfonylamino)propiophenone=thiosemicarbazone (219 mg,
45%) was obtained from 3-(methylsulfonylamino)propiophenone (388
mg, 1.71 mmol) prepared above and thiosemicarbazide (156 mg, 1.71
mmol). [0684] Step 3: In a manner similar to that in Step 2 of
Example 1, Compound 99 (218 mg, 86%) was obtained from
3-(methylsulfonylamino)propiophenone=thiosemicarbazone (200 mg,
0.696 mmol) obtained above, pivaloyl chloride (342 .mu.L, 2.78
mmol) and pyridine (219 .mu.L, 2.78 mmol). [0685] .sup.1H NMR (300
MHz, CDCl.sub.3) .delta.(ppm): 1.30 (s, 9H), 1.34 (s, 9H),
2.56-2.65 (m, 1H), 2.94 (s, 3H), 3.21-3.44 (m, 2H), 3.58-3.70 (m,
1H), 4.45 (br s, 1H), 7.28-7.37 (m, 5H), 7.97 (br s, 1H) [0686]
AP-MS (m/z): 467 (M.sup.--1)
EXAMPLE 93
Compound 100
[0687] In a manner similar to that in Step 3 of Example 76, an oily
compound was obtained from
3-(methylsulfonylamino)propiophenone=thiosemicarbazone (173 mg,
0.604 mmol) prepared in Step 2 of Example 92, isobutyryl chloride
(316 .mu.L 3.02 mmol) and pyridine (292 .mu.L, 3.62 mmol). The oily
compound was dissolved in methanol (10 mL). To the solution was
added potassium carbonate (1.00 g, 7.24 mmol), and the mixture was
vigorously stirred for 1 hour. The reaction mixture was filtered,
and the filtrate was concentrated. And then, to the concentrate was
added chloroform, water and 1.0 mol/L hydrochloric acid, and the
solution was extracted with chloroform. The organic layer was
washed with saturated aqueous sodium chloride, and dried over
anhydrous sodium sulfate. The solvent was evaporated under reduced
pressure, and the residue was purified by preparative thin layer
chromatography (chloroform/methanol=20/1) to obtain Compound 100
(111 mg, 41%). [0688] .sup.1H NMR (270 MHz, DMSO-d.sub.6)
.delta.(ppm): 0.99-1.07 (m, 12H), 2.55-2.66 (m, 2H), 2.80-3.00 (m,
1H), 2.89 (s, 3H), 3.05-3.17 (m, 1H), 3.24-3.38 (m, 2H), 7.15 (br
t, J=5.9 Hz, 1H), 7.24-7.39 (m, 5H), 11.6 (br s, 1H)
EXAMPLE 94
Compound 101
[0688] [0689] Step 1: In a manner similar to that in Step 1 of
Example 88, 2-(trifluoroacetylamino)acetophenone (4.38 g, 59%) was
obtained from 2-aminoacetophenone hydrochloride (5.47 g, 31.9
mmol), triethylamine (11.1 mL, 80.0 mmol) and trifluoroacetic
anhydride (4.96 mL, 35.1 mmol). [0690] Step 2: In a manner similar
to that in Step 1 of Example 1,
2-(trifluoroacetylamino)acetophenone=thiosemicarbazone was obtained
from 2-(trifluoroacetylamino)acetophenone (3.00 g, 13.0 mmol)
prepared above and thiosemicarbazide (1.18 g, 13.0 mmol). [0691]
Step 3: In a manner similar to that in Step 3 of Example 76,
Compound 101 (1.72 g, 28%) was obtained from
2-(trifluoroacetylamino)acetophenone=thiosemicarbazone prepared
above, pivaloyl chloride (50 mmol, 6.16 mL) and pyridine (60.0
mmol, 4.85 mL). [0692] .sup.1H NMR (270 MHz, CDCl.sub.3)
.delta.(ppm): 1.27 (s, 9H), 1.38 (s, 9H), 3.95 (dd, J=3.0, 13.5 Hz,
1H), 4.89 (dd, J=3.7, 13.5 Hz, 1H), 7.15 (br d, J=7.3 Hz, 2H),
7.30-7.40 (m, 3H), 7.92 (br s, 1H), 8.27 (br s, 1H) [0693] AP-MS
(m/z): 471 (M.sup.--1)
EXAMPLE 95
Compound 102
[0694] In a manner similar to that in Step 3 of Example 76,
Compound 102 (64.6 mg, 39%) was obtained from
2-(methylsulfonylamino)acetophenone=thiosemicarbazone (100 mg,
0.333 mmol) prepared in Step 2 of Example 88, isobutyryl chloride
(140 .mu.L, 1.33 mmol) and pyridine (108 .mu.L, 1.33 mmol). [0695]
.sup.1H NMR (270 MHz, CDCl.sub.3) .delta.(ppm): 1.17 (d, J=6.9 Hz,
3H), 1.19 (d, J=6.9 Hz, 3H), 1.25 (d, J=6.9 Hz, 6H), 1.29 (d, J=6.9
Hz, 6H), 3.05 (s, 3H), 3.10-3.30 (m, 3H), 4.01 (dd, J=4.8, 14.2 Hz,
1H), 4.74 (dd, J=7.8, 14.2 Hz, 1H), 5.37 (br s, 1H), 7.26-7.40 (m,
5H)
EXAMPLE 96
Compound 103
[0695] [0696] Compound 102 (40.0 mg, 0.0805 mg) prepared in Example
95 was dissolved in methanol (10 mL). To the solution was added
potassium carbonate (1.00 g, 7.24 mmol), and the mixture was
vigorously stirred for 1 hour. The reaction mixture was filtered,
and the filtrate was concentrated. Then, to the residue was added
chloroform, 1 mol/L hydrochloric acid and water, and the mixture
was extracted with chloroform. The organic layer was washed with
saturated aqueous sodium chloride, and dried over anhydrous sodium
sulfate. The solvent was evaporated under reduced pressure, and the
residue was purified by preparative thin layer chromatography
(chloroform/methanol=20/1) to obtain Compound 103 (24.2 mg, 84%).
[0697] .sup.1H NMR (270 MHz, CDCl.sub.3) .delta.(ppm): 1.13 (d,
J=6.9 Hz, 3H), 1.18 (d, J=6.9 Hz, 3H), 1.21 (d, J=6.9 Hz, 3H), 1.23
(d, J=6.9 Hz, 3H), 2.50 (m, 1H), 2.90 (s, 3H), 3.27 (m, 1H), 3.98
(dd, J=5.0, 13.9 Hz, 1H), 4.60 (dd, J=8.2, 13.9 Hz, 1H), 5.35 (br
dd, J=5.0, 8.2 Hz, 1H), 7.26-7.40 (m, 5H), 8.02 (br s, 1H)
EXAMPLE 97
Compound 104
[0697] [0698] Step 1: In a manner similar to that in Step 1 of
Example 1, 3-(dimethylamino)propiophenone=thiosemicarbazone (491mg,
46%) was obtained from 3-(dimethylamino)propiophenone (910 mg, 4.26
mmol) and thiosemicarbazide (387 mg, 4.25 mmol). [0699] Step 2: In
a manner similar to that in Step 3 of Example 76, Compound 104 (116
mg, 33%) was obtained from
3-(dimethylamino)propiophenone=thiosemicarbazone (210 mg, 0.839
mmol) prepared above, pivaloyl chloride (496 .mu.L, 3.78 mmol) and
pyridine (326 .mu.L, 3.78 mmol). [0700] .sup.1H NMR (270 MHz,
CDCl.sub.3) .delta.(ppm): 1.29 (s, 9H), 1.31 (s, 9H), 2.23-2.29 (m,
1H), 2.26 (br s, 3H), 2.27 (br s, 3H), 2.46 (ddd, J=8.8, 4.3, 11.3
Hz, 1H), 2.87 (m, 1H), 3.31 (m, 1H), 7.20-7.36 (m, 5H), 7.90 (br s,
1H)
EXAMPLE 98
Compound 105
[0700] [0701] Step 1: In a manner similar to that in Step 2 of
Example 1, 3-carbomethoxypropiophenone=thiosemicarbazone (10.6 g,
94%) was obtained from 3-carbomethoxypropiophenone (8.13 g, 42.3
mmol) and thiosemicarbazide (3.86 g, 42.3 mmol). [0702] Step 2: In
a manner similar to that in Step 3 of Example 76, Compound 105
(9.70 g, 77%) was obtained from
3-carbomethoxypropiophenone=thiosemicarbazone (7.76 g, 29.2 mmol)
prepared above, pivaloyl chloride (14.4 mL, 117 mmol) and pyridine
(11.3 mL, 140 mmol). [0703] .sup.1H NMR (270 MHz, CDCl.sub.3)
.delta.(ppm): 1.29 (s, 9H), 1.32 (s, 9H), 2.37 (m, 1H), 2.67 (m,
1H), 2.79 (m, 1H), 3.42 (m, 1H), 3.70 (s, 3H), 7.22-7.40 (m, 5H),
7.89 (br s, 1H)
EXAMPLE 99
Compound 106
[0704] Sodium hydroxide (2.7g,.67 mmol) was dissolved in water (23
mL). Subsequently, to the solution was added methanol (30 mL) and
the solution was stirred. To the solution was added Compound 105
(9.65 g, 22.3 mmol) prepared in Example 98, and the mixture was
stirred at room temperature for 5 hours. To the reaction mixture
was added 1 mol/L hydrochloric acid (20 mL) and water (30 mL), and
the deposited white crystals were collected by filtration. The
resulting crystals were washed with water and diisopropyl ether,
and then, dried under reduced pressure to obtain Compound 106 (8.92
g, 96%). [0705] .sup.1H NMR (270 MHz, CDCl.sub.3) .delta.(ppm):
1.30 (s, 9H), 1.33 (s, 9H), 2.00-2.51 (br s, 1H), 2.44 (m, 1H),
2.66 (m, 1H), 2.88 (m, 1H), 3.44 (m, 1H), 7.23-7.40 (m, 5H), 7.92
(br s, 1H)
EXAMPLE 100
Compound 107
[0706] Compound 106 (1.21 g, 2.88 mmol) prepared in Example 99 was
cooled to 0.degree. C. Oxalyl chloride (5 mL) was added to the
compound, and the solution was allowed to react at 0.degree. C. for
1 hour. The solvent was evaporated under reduced pressure, and the
residue was dried in vacuo. To the residue was added
tetrahydrofuran, and the mixture was stirred at 0.degree. C. Then,
to the reaction mixture was added 4 mol/L ammonia-methanol solution
(5 mL, 20 mmol), and the mixture was stirred at room temperature
for 3 hours. To the reaction mixture was added 1 mol/L hydrochloric
acid (20 mL) and water (30 mL), and extracted with chloroform. The
organic layer was washed with saturated aqueous sodium chloride,
and dried over anhydrous sodium sulfate. After the solvent was
evaporated under reduced pressure, to the resulting residue was
added diisopropyl ether, and then the deposited white crystals were
collected by filtration. The resulting crystals were washed with
water and diisopropyl ether, and then dried under reduced pressure
to obtain Compound 107 (8.92 g, 96%). [0707] .sup.1H NMR (270 MHz,
DMSO-d.sub.6) .delta.(ppm): 1.17 (s, 9H), 1.28 (s, 9H), 1.81-2.03
(m, 1H), 2.15-2.30 (m, 1H), 2.49-2.75 (m, 1H), 2.95-3.20 (m, 1H),
6.80 (br s, 1H), 7.20-7.41 (m, 5H), 10.93 (br s, 2H)
EXAMPLE 101
Compound 108
[0708] In a manner similar to that in Example 100, Compound 108 (65
mg, 60%) was obtained from Compound 106 (0.104 g, 0.248 mmol)
prepared in Example 99, oxalyl chloride (5 mL), hydroxylamine
hydrochloride (0.017 g, 0.245 mmol) and triethylamine (0.062 g,
0.614 mmol). [0709] APCI-MS (m/z): 433 (M.sup.--1)
EXAMPLE 102
Compound 109
[0710] In a manner similar to that in Example 100, Compound 109
(1.08 g, 87%) was obtained from Compound 106 (1.20 g, 2.86 mmol)
prepared in Example 99, oxalyl chloride (5 mL) and 4 mol/L
methylamine-methanol solution (10 mL, 40 mmol). [0711] AP-MS (m/z):
431 (M.sup.--1)
EXAMPLE 103
Compound 110
[0711] [0712] Step 1: In a manner similar to that in Step 1 of
Example 1, 3-(dimethylaminocarbonyl)propiophenone=thiosemicarbazone
(3.67 g, 79%) was obtained from
3-(dimethylaminocarbonyl)propiophenone (4.00 g, 18.7 mmol) and
thiosemicarbazide (1.70 g, 18.7 mmol). [0713] Step 2: In a manner
similar to that in Step 3 of Example 76, Compound 110 (1.64 g, 49%)
was obtained from
3-(dimethylaminocarbonyl)propiophenone=thiosemicarbazone (2.00 g,
7.99 mmol) prepared above, pivaloyl chloride (3.94 mL, 32.0 mmol)
and pyridine (3.11 mL, 38.4 mmol). [0714] AP-MS (m/z): 447
(M.sup.++1)
EXAMPLE 104
Compound 111
[0715] In a manner similar to that in Example 100, Compound 111
(480 mg, 84%) was obtained from Compound 106 (51.8 mg, 0.124 mmol)
prepared in Example 99, oxalyl chloride (0.5 mL), ethanolamine
(7.58 mg, 0.248 mmol) and triethylamine (18.8 mg, 0.186 mmol).
[0716] .sup.1H NMR (270 MHz, CDCl.sub.3) .delta.(ppm): 1.29 (s,
9H), 1.33 (s, 9H), 2.16-2.25 (m, 1H), 2.65-2.79 (m, 2H), 3.33-3.44
(m, 3H), 3.72 (m, 2H), 6.18 (br s, 1H), 7.22-7.35 (m, 6H), 8.01 (br
s, 1H)
EXAMPLE 105
Compound 112
[0717] In a manner similar to that in Example 100, Compound 112
(400 mg, 68%) was obtained from Compound 106 (51.8 mg, 0.124 mmol)
prepared in Example 99, oxalyl chloride (0.5 mL), n-butylamine
(18.14 mg, 0.248 mmol) and triethylamine (18.8 mg, 0.186 mmol).
[0718] .sup.1H NMR (300 MHz, CDCl.sub.3) .delta.(ppm): 0.92 (t,
J=7.1 Hz, 3H), 1.25-1.60 (m, 4H), 1.29 (s, 9H), 1.33 (s, 9H), 2.16
(m, 1H), 2.69 (m, 2H), 3.25 (m, 2H), 3.67 (m, 1H), 5.62 (br s, 1H),
7.23-7.34 (m, 5H), 7.94 (br s, 1H)
EXAMPLE 106
Compound 113
[0719] In a manner similar to that in Example 100, Compound 113 (50
mg, 81%) was obtained from Compound 106 (51.8 mg, 0.124 mmol)
prepared in Example 99, oxalyl chloride (0.5 mL), cyclohexylamine
(24.6 mg, 0.248 mmol) and triethylamine (18.8 mg, 0.186 mmol).
[0720] .sup.1H NMR (270 MHz, CDCl.sub.3) .delta.(ppm): 1.05-1.50
(m, 6H), 1.28 (s, 9H), 1.33 (s, 9H), 1.65-1.80 (m, 2H), 1.85-1.95
(m, 2H), 2.14 (m, 1H), 2.65 (m, 2H), 3.37 (m, 1H), 3.38 (m, 1H),
5.50 (br s, 1H), 7.10-7.38 (m, 5H), 7.93 (br s, 1H)
EXAMPLE 107
Compound 114
[0720] [0721] Step 1: In a manner similar to that in Step 1 of
Example 1, 4-carbomethoxybutyrophenone=thiosemicarbazone (0.700 g,
88%) was obtained from 4-carbomethoxybutyrophenone (0.588 g, 2.85
mmol) and thiosemicarbazide (0.260 g, 2.85 mmol). [0722] Step 2: In
a manner similar to that in Step 3 of Example 76, Compound 114 (318
mg, 64%) was obtained from
4-carbomethoxybutyrophenone=thiosemicarbazone prepared above,
pivaloyl chloride (0.549 mL, 4.45 mmol) and pyridine (0.431 mL,
5.34 mmol). [0723] .sup.1H NMR (300 MHz, CDCl.sub.3) .delta.(ppm):
1.29 (s, 9H), 1.32 (s, 9H), 1.51-1.60 (m, 1H), 2.10-2.30 (m, 2H),
2.44 (m, 2H), 3.03-3.17 (m, 1H), 3.68 (s, 3H), 7.20-7.36 (m, 5H),
7.95 (br s, 1H)
EXAMPLE 108
Compound 115
[0724] In a manner similar to that in Example 99, Compound 115 (234
mg, 95%) was obtained from Compound 114 (254 mg, 0.567 mmol)
prepared in Example 107, sodium hydroxide (70.0 mg, 1.75 mmol),
water (2 mL) and ethanol (4 mL). [0725] .sup.1H NMR (270 MHz,
CDCl.sub.3) .delta.(ppm): 1.29 (s, 9H), 1.32 (s, 9H), 1.65-1.75 (m,
1H), 2.10-2.35 (m, 2H), 2.50 (m, 2H), 3.10-3.20 (m, 1H), 7.23-7.35
(m, 6H), 7.92 (br s, 1H)
EXAMPLE 109
Compound 116
[0726] In a manner similar to that in Example 100, Compound 116
(0.028 g, 55%) was obtained from Compound 115 (50.0 mg, 0.115 mmol)
prepared in Example 108, oxalyl chloride (0.5 mL) and 40%
methylamine-methanol solution (5 mL). [0727] .sup.1H NMR (270 MHz,
CDCl.sub.3) .delta.(ppm): 1.29 (s, 9H), 1.32 (s, 9H), 1.50-1.65 (m,
1H), 2.21-2.35 (m, 4H), 2.80 (d, J=4.8 Hz, 3H), 3.13 (m, 1H), 5.71
(br s, 1H), 7.20-7.35 (m, 5H), 7.97 (br s, 1H)
EXAMPLE 110
Compound 117
[0728] In a manner similar to that in Example 100, Compound 117
(0.024 g, 47%) was obtained from Compound 115 (51.5 mg, 0.119 mmol)
prepared in Example 108, oxalyl chloride (0.5 mL) and 4 mol/L
ammonia-methanol solution (5 mL). [0729] AP-MS (m/z): 431
(M.sup.--1)
EXAMPLE 111
Compound 118
[0730] In a manner similar to that in Step 3 of Example 76,
Compound 118 (302 mg, 26%) was obtained from
2-(methylsulfonylamino)acetophenone=thiosemicarbazone (1.00 g, 3.49
mmol) prepared in Step 2 of Example 88, acetic anhydride (659
.mu.L, 6.98 mmol) and pyridine (565 .mu.L, 6.98 mmol). [0731]
.sup.1H NMR (270 MHz, CDCl.sub.3) .delta.(ppm): 2.29 (s, 3H), 2.99
(s, 3H), 4.04 (d, J=14.0 Hz, 1H), 4.55 (d, J=14.0 Hz, 1H),
7.30-7.41 (m, 5H) [0732] AP-MS (m/z): 329 (M.sup.++1)
EXAMPLE 112
Compound 119
[0733] Compound 118 (10.6 mg, 0.0323 mmol) prepared in Example 111
was dissolved in tetrahydrofuran (80 mL). To the solution was added
dimethylaminopyridine (7.9 mg, 0.0646 mmol) and pyridine (7.8
.mu.L, 0.0969 mmol), and the mixture was cooled to 0.degree. C. To
the solution was added pivaloyl chloride (20 .mu.L, 0.162 mmol),
and the misture was stirred at 0.degree. C. for 5 minutes, and
further stirred at room temperature for 4 hours. To the reaction
mixture was added water and 1 mol/L hydrochloric acid, and
extracted with ethyl acetate. The organic layer was dried over
anhydrous sodium sulfate, and the solvent was evaporated under
reduced pressure. The residue was purified by preparative thin
layer chromatography (chloroform/methanol=12/1) to obtain Compound
119 (5.3 mg, 40%). [0734] .sup.1H-NMR (270 MHz, CDCl.sub.3)
.delta.(ppm): 1.27 (s, 9H), 2.32 (s, 3H), 2.95 (s, 3H), 3.98 (dd,
J=5.2, 14.0 Hz, 1H), 4.60 (dd, J=8.1, 13.9 Hz, 1H), 5.40 (m, 1H),
7.29-7.40 (m, 5H), 8.11 (br s, 1H)
EXAMPLE 113
Compound 120
[0735] 2-(Methylsulfonylamino)acetophenone=thiosemicarbazone (300
mg, 1.05 mmol) prepared in Step 2 of Example 88 was dissolved in
tetrahydrofuran (18 mL). To the solution was added
4-dimethylaminopyridine (641 mg, 5.25 mmol) and pivaloyl chloride
(0.13 mL, 1.1 mmol), and the mixture was stirred at room
temperature. To the mixture was further added, after 1 hour and
after 2 hours each, pivaloyl chloride (0.065 mL, 0.53 mmol), and
the mixture was stirred for 3.6 hours in total. To the reaction
mixture was added water, and the mixture was extracted with ethyl
acetate. The organic layer was washed with saturated aqueous sodium
chloride, and then dried over anhydrous sodium sulfate. The solvent
was evaporated under reduced pressure, and the residue was purified
by preparative thin layer chromatography (chloroform/methanol=20/1)
to obtain Compound 120 (88 mg, yield 22%). [0736] .sup.1H NMR (270
MHz, CDCl.sub.3) .delta.(ppm): 1.34 (s, 9H), 2.96 (s, 3H), 4.06
(dd, J=6.2, 13.7 Hz, 1H), 4.19 (br s, 2H), 4.58 (dd, J=7.0, 13.7
Hz, 1H), 5.20 (t, J=6.4 Hz, 1H), 7.27-7.55 (m, 5H) [0737] AP-MS
(m/z): 371 (M.sup.++1)
EXAMPLE 114
Compound 121
[0738] 6-Bromohexanoic acid (469 mg, 2.41 mmol) was dissolved in
dichloromethane (15 mL). To the solution was added oxalyl chloride
(0.28 mL, 3.2 mmol), and the mixture was stirred at room
temperature for 2 hours. The solvent was evaporated from the
reaction mixture under reduced pressure, and the resulting residue
was dissolved in dichloromethane (15 mL). To the solution was added
Compound 120 (297 mg, 0.802 mmol) prepared in Example 113 and
pyridine (0.20 mL, 2.4 mmol), and the mixture was stirred at room
temperature for 1 hour. After the reaction mixture -was
concentrated under reduced pressure, water was added to the
residue, and the solution was extracted with ethyl acetate. The
organic layer was washed with saturated aqueous sodium chloride,
and then dried over anhydrous sodium sulfate. The solvent was
evaporated under reduced pressure, and the residue was purified by
preparative thin layer chromatography (chloroform/methanol=30/1) to
obtain Compound 121 (315 mg, yield 72%). [0739] .sup.1H NMR (270
MHz, CDCl.sub.3) .delta.(ppm): 1.32 (s, 9H), 1.50 (m, 2H), 1.67 (m,
2H), 1.86 (q, J=6.7 Hz, 2H), 2.34 (t, J=7.3 Hz, 2H), 2.98 (s, 3H),
3.40 (t, J=6.6 Hz, 2H), 3.99 (dd, J=5.2, 13.6 Hz, 1H), 4.63 (dd,
J=8.2, 13.6 Hz, 1H), 5.24 (dd, J=5.5, 7.9 Hz, 1H), 7.26-7.38 (m,
5H), 8.40 (br s, 1H) [0740] AP-MS (m/z): 547 (M.sup.++1)
EXAMPLE 115
Compound 122
[0741] Compound 121 (315 mg, 0.575 mmol) prepared in Example 114
was dissolved in N,N-diethylformamide (9.5 mL). To the solution was
added sodium azide (187 mg, 2.88 mmol), and the mixture was stirred
at 80.degree. C. for 2 hours. To the reaction mixture was added
water and the mixture was extracted with ethyl acetate. The organic
layer was washed with saturated aqueous sodium chloride, and then
dried over anhydrous sodium sulfate. The solvent was evaporated
under reduced pressure, and the residue was purified by preparative
thin layer chromatography (hexane/ethyl acetate=1/2) to obtain
Compound 122 (211 mg, yield 72%). [0742] .sup.1H NMR (270 MHz,
CDCl.sub.3) .delta.(ppm): 1.32 (s, 9H), 1.42 (m, 2H), 1.55-1.74 (m,
4H), 2.35 (t, J=7.3 Hz, 2H), 2.97 (s, 3H), 3.28 (t, J=6.7 Hz, 2H),
4.13 (dd, J=7.2, 14.3 Hz, 1H), 4.63 (dd, J=8.3, 13.5 Hz, 1H), 5.21
(dd, J=5.2, 8.0 Hz, 1H), 7.26-7.38 (m, 5H), 8.37 (s, 1H) [0743]
AP-MS (m/z): 510 (M.sup.++1)
EXAMPLE 116
Compound 123
[0744] Compound 122 (23.6 mg, 0.0463 mmol) prepared in Example 115
was dissolved in tetrahydrofuran (1.0 mL). To the solution was
added triphenylphosphine (36.4 mg, 0.139 mmol), and the mixture was
stirred at room temperature for 25 minutes. To the reaction mixture
was added water, and the mixture was extracted with ethyl acetate.
The organic layer was washed with saturated aqueous sodium
chloride, and then dried over anhydrous sodium sulfate. The solvent
was evaporated under reduced pressure, and the residue was purified
by preparative thin layer chromatography
(chloroform/methanol/ammonia=5/0.8/0.2) to obtain Compound 123 (7.1
mg, yield 32%). [0745] .sup.1H-NMR (270 MHz, CDCl.sub.3)
.delta.(ppm): 1.31 (s, 9H), 1.47 (m, 2H), 1.57 (m, 2H), 1.70 (m,
2H), 2.39 (m, 2H), 2.82 (m, 2H), 2.97 (s, 3H), 3.95 (d, J=13.7 Hz,
1H), 4.14 (br s, 3H), 4.65 (d, J=13.5 Hz, 1H), 7.24-7.35 (m, 5H)
[0746] AP-MS (m/z): 484 (M.sup.++1)
EXAMPLE 117
Compound 124
[0747] Compound 123 (5.0 mg, 0.010 mmol) prepared in Example 116
was dissolved in dichloromethane (0.4 mL). To the solution was
added pyridine (0.0025 mL, 0.031 mmol) and acetyl chloride (0.0015
mL, 0.021 mmol), and the mixture was stirred at room temperature
for 0.8 hour. To the reaction mixture was added water and the
mixture was extracted with ethyl acetate. The organic layer was
washed with saturated aqueous sodium chloride, and then dried over
anhydrous sodium sulfate. The solvent was evaporated under reduced
pressure, and the residue was purified by preparative thin layer
chromatography (chloroform/methanol=20/1) to obtain Compound 124
(3.9 mg, yield 72%). [0748] .sup.1H NMR (270 MHz, CDCl.sub.3)
.delta.(ppm): 1.32 (s, 9H), 1.37 (m, 2H), 1.53 (m, 2H), 1.69 (m,
2H), 1.98 (s, 3H), 2.39 (t, J=7.4 Hz, 2H), 2.97 (s, 3H), 3.24 (m,
2H), 3.98 (dd, J=5.2, 13.6 Hz, 1H), 4.64 (dd, J=8.2, 13.5 Hz, 1H),
5.22 (dd, J=5.4, 8.2 Hz, 1H), 5.68 (m, 1H), 7.24-7.38 (m, 5H), 9.08
(s, 1H) [0749] FAB-MS (m/z): 526 (M.sup.++1)
EXAMPLE 118
Compound 125
[0749] [0750] Step 1: In a manner similar to that in Step 1 of
Example 1, 3'-hydroxyacetophenone=4-ethylthiosemicarbazone (342 mg,
70%) was obtained from 3'-hydroxyacetophenone (279 mg, 2.05 mmol)
and 4-ethylthiosemicarbazide (242 mg, 2.03 mmol). [0751] Step 2: In
a manner similar to that in Step 2 of Example 1, Compound 125 (90
mg, 60%) was obtained from
3'-hydroxyacetophenone=4-ethylthiosemicarbazone (200 mg, 0.843
mmol) prepared above, acetic anhydride (260 mg, 2.53 mmol) and
pyridine (108 .mu.L, 1.34 mmol). [0752] .sup.1H NMR (270 MHz,
CDCl.sub.3) .delta.(ppm): 2.02 (s, 3H), 2.20 (s, 3H), 2.28 (s, 3H),
2.30 (t, J=8.4 Hz, 3H), 2.36 (s,-3H), 3.30-3.47 (br s, 2H),
7.20-7.40 (m, 5H)
EXAMPLE 119
Compound 126
[0753] In a manner similar to that in Example 65, Compound 126 (81
mg, 49%) was obtained from Compound 125 (187 mg, 0.515 mg) prepared
in Example 118, methanol (10 mL) and potassium carbonate (1.00 g,
7.24 mmol). [0754] .sup.1H NMR (270 MHz, DMSO-d.sub.6)
.delta.(ppm): 2.01 (s, 3H), 2.18 (s, 3H), 2.23 (s, 3H), 2.29 (t,
J=8.4 Hz, 3H), 3.40 (br s, 2H), 6.65-6.80 (m, 3H), 7.13 (m, 1H),
11.6 (br s, 1H)
EXAMPLE 120
Compound 127
[0755] Compound 69 (50.5 mg, 0.172 mmol) prepared in Example 66 was
dissolved in dichloromethane (0.5 mL). To the solution was added
triethylamine (17.4 mg, 0.172 mmol) and ethyl isocyanate (13.6
.mu.L, 0.172 mmol), and the mixture was stirred at room temperature
for 12 hours. To the reaction mixture was added 1 mol/L
hydrochloric acid and water, and the mixture was subjected to
separation. The organic layer was washed with saturated aqueous
sodium chloride and dried over anhydrous sodium sulfate. The
solvent was evaporated under reduced pressure, and the residue was
purified by preparative thin layer chromatography
(chloroform/methanol/water=90/10/1) to obtain Compound 127 (53.3
mg, 85%). [0756] .sup.1H NMR (270 MHz, CDCl.sub.3) .delta.(ppm):
1.21 (t, J=7.0 Hz, 3H), 2.09 (s, 3H), 2.22 (s, 3H), 2.35 (s, 3H),
3.31 (m, 2H), 5.03 (br s, 1H), 7.06 (br d, J=8.4 Hz, 1H), 7.24-7.35
(m, 3H), 8.41 (br s, 1H)
EXAMPLE 121
Compound 128
[0757] In a manner similar to that in Step 3 of Example 76,
Compound 128 (500 mg, 63%) was obtained from
3'-hydroxyacetophenone=thiosemicarbazone (398 mg, 1.90 mmol)
prepared in Step 1 of Example 59, isobutyryl chloride (1.56 mL,
7.60 mmol) and pyridine (721 mg, 9.12 mmol). [0758] .sup.1H NMR
(270 MHz, CDCl.sub.3) .delta.(ppm): 1.09 (d, J=6.8 Hz, 3H), 1.10
(d, J=6.8 Hz, 3H), 1.21 (d, J=6.8 Hz, 3H), 1.22 (d, J=6.8 Hz, 3H),
1.29 (d, J=7.3 Hz, 6H), 2.34 (s, 3H), 2.51 (m, 1H), 2.78 (m, 1H),
3.18 (m, 1H), 7.00 (br d, J=7.3 Hz, 1H), 7.13 (br s, 1H), 7.25-7.33
(m, 2H), 7.93 (br s, 1H)
EXAMPLE 122
Compound 129
[0759] In a manner similar to that in Example 65, Compound 129 (298
mg, 85%) was obtained from Compound 128 (420 mg, 1.00 mmol)
prepared in Example 121 and potassium carbonate (1.00 g, 7.24
mmol). [0760] .sup.1H NMR (270 MHz, CDCl.sub.3) .delta.(ppm): 1.11
(d, J=7.0 Hz, 3H), 1.12 (d, J=7.0 Hz, 3H), 1.22 (d, J=7.0 Hz, 3H),
1.23 (d, J=7.0 Hz, 3H), 2.23 (s, 3H), 2.51 (m, 1H), 3.20 (m, 1H),
5.60 (br s, 1H), 6.63 (br d, J=7.3 Hz, 1H), 6.85 (br s, 1H), 6.94
(br d, J=7.9 Hz, 1H), 7.15 (br t, J=7.9 Hz, 1H), 8.00 (br s,
1H)
EXAMPLE 123
Compound 130
[0761] In a manner similar to that in Step 3 of Example 76,
Compound 130 (389 mg, 88%) was obtained from
2'-chloroacetophenone=thiosemicarbazone (253 mg, 1.11 mmol)
prepared in Step 1 of Example 53, pivaloyl chloride (546 .mu.L,
4.44 mmol) and pyridine (389 .mu.L, 4.80 mmol). [0762] .sup.1H NMR
(270 MHz, CDCl.sub.3) .delta.(ppm): 1.29 (s, 9H), 1.30 (s, 9H),
2.35 (s, 3H), 7.20-7.27 (m, 2H), 7.35-7.43 (m, 2H), 7.95 (br s,
1H)
EXAMPLE 124
Compound 131
[0763] In a manner similar to that in Step 3 of Example 76,
Compound 131 (389 mg, 86%) was obtained from
2'-chloroacetophenone=thiosemicarbazone (400 mg, 1.89 mmol)
prepared in Step 1 of Example 53, isobutyryl chloride (594 .mu.L,
5.67 mmol) and pyridine (538 mg, 6.80 mmol). [0764] .sup.1H NMR
(270 MHz, CDCl.sub.3) .delta.(ppm): 1.10 (d, J=6.6 Hz, 3H), 1.12
(d, J=6.6 Hz, 3H), 1.23 (d, J=6.9 Hz, 2H), 1.25 (d, J=6.9 Hz, 3H),
2.39 (s, 3H), 2.52 (m, 1H), 3.18 (m, 1H), 7.22-7.28 (m, 2H),
7.37-7.45 (m, 2H), 7.96 (br s, 1H)
EXAMPLE 125
Compound 132
[0764] [0765] Step 1: In a manner similar to that in Step 1 of
Example 1, 1-(5-bromo-2-thienyl)ethanone=thiosemicarbazone (7.33
mg, 86%) was obtained from 1-(5-bromo-2-thienyl)ethanone (630 mg,
3.07 mmol) and thiosemicarbazide (281 mg, 3.07 mmol). [0766] Step
2: In a manner similar to that in Step 2 of Example 1, Compound 132
(158 mg, 58%) was obtained from
1-(5-bromo-2-thienyl)ethanone=thiosemicarbazone (2.11 mg, 0.758
mmol) prepared above and acetic anhydride (10 mL). [0767] .sup.1H
NMR (270 MHz, CDCl.sub.3) .delta.(ppm): 2.15 (s, 3H), 2.19 (s, 3H),
2.36 (s, 3H), 6.84 (br s, 1H), 6.86 (br s, 1H), 8.29 (br s, 1H)
EXAMPLE 126
Compound 133
[0767] [0768] Step 1: In a manner similar to that in Step 1 of
Example 1, 1-(3-bromo-2-thienyl)ethanone=thiosemicarbazone was
obtained from 1-(3-bromo-2-thienyl)ethanone (108 mg, 0.388 mmol)
and thiosemicarbazide (36.5 mg, 0.399 mmol). [0769] Step 2: In a
manner similar to that in Step 2 of Example 1, Compound 133 (139
mg, 99%) was obtained from
1-(3-bromo-2-thienyl)ethanone=thiosemicarbazone prepared above and
acetic anhydride (10 mL). [0770] .sup.1H NMR (270 MHz, CDCl.sub.3)
.delta.(ppm): 2.04 (s, 3H), 2.14 (s, 3H), 2.23 (s, 3H), 2.41 (s,
3H), 6.96 (br s, 1H), 7.17 (br s, 1H), 9.08 (br s, 1H)
EXAMPLE 127
Compound 134
[0770] [0771] Step 1: In a manner similar to that in Step 1 of
Example 1, 1-(3-chloro-2-thienyl)ethanone=thiosemicarbazone was
obtained from 1-(3-chloro-2-thienyl)ethanone (137 mg, 0.853 mmol)
and thiosemicarbazide (78 mg, 0.853 mmol). [0772] Step 2: In a
manner similar to that in Step 2 of Example 1, Compound 134 (158
mg, 58%) was obtained from
1-(3-chloro-2-thienyl)ethanone=thiosemicarbazone prepared above and
acetic anhydride (10 mL). [0773] .sup.1H NMR (270 MHz, CDCl.sub.3)
.delta.(ppm): 2.14 (s, 3H), 2.21 (s, 3H), 2.43 (s, 3H), 6.89 (d,
J=5.3 Hz, 1H), 7.18 (d, J=5.3 Hz, 1H), 8.28 (br S, 1H)
EXAMPLE 128
Compound 135
[0773] [0774] Step 1: In a manner similar to that in Step 1 of
Example 1, 1-(3-chloro-2-thienyl)ethanone=thiosemicarbazone (96.1
mg, 71%) was obtained from 1-(3-chloro-2-thienyl)ethanone (92.9 mg,
0.578 mmol) and thiosemicarbazide (52.9 mg, 0.578 mmol). [0775]
Step 2: In a manner similar to that in Step 3 of Example 76,
Compound 134 (90 mg, 60%) was obtained from
1-(3-chloro-2-thienyl)ethanone=thiosemicarbazone (86.9 mg, 0.372
mmol) prepared above, pivaloyl chloride (138 .mu.L, 1.12 mmol) and
pyridine (108 .mu.L, 1.34 mmol). [0776] .sup.1H NMR (270 MHz,
CDCl.sub.3) .delta.(ppm): 1.33 (s, 9H), 1.35 (s, 9H), 2.43 (s, 3H),
6.90 (d, J=6.3 Hz, 1H), 7.20 (d, J=6.3 Hz, 1H), 7.97 (br s, 1H)
EXAMPLE 129
Compound 136
[0777] Compound 14 (41 mg, 0.17 mmol) prepared in Example 11 was
dissolved in acetonitrile (0.5 mL). To the solution was added
di-tert-butyl dicarbonate (0.114 mg, 0.522 mmol) and DMAP (43 mg,
0.35 mmol), and the mixture was stirred at room temperature for 1
hour. To the reaction mixture was added water, and the mixture was
extracted with ethyl acetate. The organic layer was washed with
saturated aqueous sodium chloride, and then dried over anhydrous
sodium sulfate, and the solvent was evaporated under reduced
pressure. The residue was purified by preparative thin layer
chromatography (chloroform/methanol=20/1) to obtain Compound 136
(24 mg, 41%). [0778] .sup.1H NMR (270 MHz, CDCl.sub.3)
.delta.(ppm): 1.47 (s, 9H), 2.21 (s, 3H), 2.40 (s, 3H), 7.14-7.48
(m, 6H) [0779] AP-MS (m/z): 334 (M.sup.--1)
EXAMPLE 130
Compound 137
[0780] Compound 14 (74 mg, 0.31 mmol) prepared in Example 11 was
dissolved in N,N-dimethylformamide (2 mL). To the solution was
added 60% sodium hydride (50 mg, 1.3 mmol) and dimethylcarbamoyl
chloride (0.116 mL, 1.26 mmol), and the mixture was stirred at room
temperature for 1 hour. To the reaction mixture was added water,
and the mixture was extracted with ethyl acetate. The organic layer
was washed with saturated aqueous sodium chloride, and then dried
over anhydrous sodium sulfate, and the solvent was evaporated under
reduced pressure. The residue was purified by preparative thin
layer chromatography (chloroform/methanol=40/1, then ethyl
acetate/n-hexane=3/1) to obtain Compound 137 (44 mg, 46%). [0781]
.sup.1H NMR (270 MHz, CDCl.sub.3) .delta.(ppm): 2.23 (s, 3H), 2.37
(s, 3H), 3.00 (s, 6H), 7.20-7.45 (m, 5H) [0782] AP-MS (m/z): 307
(M.sup.++1)
EXAMPLE 131
Compound 138
[0782] [0783] Step 1: Copper (II) bromide (130 mg, 0.583 mmol) was
dissolved in acetonitrile (5.4 mL). To the solution was added
tert-butyl nitrite (0.093 mL, 0.78 mmol) under ice cooling. After
being stirred for 10 minutes, to the mixture was added Compound 14
(180 mg, 0.486 mmol) prepared in Example 11, and the mixture was
stirred for 1 hour with gradually raising the temperature up to
room temperature. To the reaction mixture was added water, and the
mixture was extracted with ethyl acetate. The organic layer was
washed with saturated aqueous sodium chloride, and then dried over
anhydrous sodium sulfate, and the solvent was evaporated under
reduced pressure. The residue was purified by silica gel column
chromatography (ethyl acetate/n-hexane=1/18) to obtain
3-acetyl-5-bromo-2-methyl-2-phenyl-1,3,4-thiadialine (145 mg, 84%).
[0784] Step 2: 3-Acetyl-5-bromo-2-methyl-2-phenyl-1,3,4-thiadialine
(50 mg, 0.17 mmol) prepared above was dissolved in dichloromethane
(0.5 mL). To the solution was added piperidine (0.033 mL, 0.33
mmol), and the mixture was stirred at room temperature for 20
minutes. To the reaction mixture was further added piperidine
(0.165 mL, 1.67 mmol), and the mixture was stirred at the same
temperature for 5.5 hours. To the reaction mixture was added water,
and the mixture was extracted with ethyl acetate. The organic layer
was washed with saturated aqueous sodium chloride, and then dried
over anhydrous sodium sulfate, and the solvent was evaporated under
reduced pressure. The residue was purified by preparative thin
layer chromatography (chloroform) to obtain Compound 138 (12 mg,
24%). [0785] .sup.1H NMR (270 MHz, CDCl.sub.3) .delta.(ppm): 1.60
(m, 6H), 2.25 (s, 3H), 2.40 (s, 3H), 3.24 (m, 4H), 7.20-7.39 (m,
3H), 7.45 (m, 2H) [0786] AP-MS (m/z): 304 (M.sup.++1)
EXAMPLE 132
Compound 139
[0787] In a manner similar to that in Step 2 of Example 131,
Compound 139 (38 mg, 59%) was obtained from
3-acetyl-5-bromo-2-methyl-2-phenyl-1,3,4-thiadiallyn (61 mg, 0.20
mmol) prepared in Step 1 of Example 131 and 4-methylpiperidine
(0.483 mL, 4.08 mmol). [0788] .sup.1H NMR (270 MHz, CDCl.sub.3)
.delta.(ppm): 0.96 (d, J=6.4 Hz, 3H), 1.25 (m, 2H), 1.44-1.71 (m,
3H), 2.25 (s, 3H), 2.40 (s, 3H), 2.88 (m, 2H), 3.61 (m, 2H),
7.20-7.49 (m, 3H), 7.46 (m, 2H) [0789] AP-MS (m/z): 318
(M.sup.++1)
EXAMPLE 133
Compound 140
[0790] Compound 118 (50 mg, 0.15 mmol) prepared in Example 111 was
dissolved in dichloromethane (2 mL). To the solution was added
pyridine (0.031 mL, 0.38 mmol) and hexanoyl chloride (0.053 mL,
0.38 mmol), and the mixture was stirred at room temperature for 2.5
hours. To the reaction mixture was further added pyridine (0.012
mL, 0.15 mmol) and hexanoyl chloride (0.021 mL, 0.15 mmol), and the
mixture was stirred at the same temperature for 1 hour. To the
reaction mixture was added water, and the mixture was extracted
with ethyl acetate. The organic layer was washed with saturated
aqueous sodium chloride, and then dried over anhydrous sodium
sulfate, and the solvent was evaporated under reduced pressure. The
residue was purified by preparative thin layer chromatography
(chloroform/methanol=15/1) to obtain Compound 140 (52 mg, 80%).
[0791] .sup.1H NMR (270 MHz, CDCl.sub.3) .delta.(ppm): 0.90 (t,
J=6.6 Hz, 3H), 1.22-1.41 (m, 4H), 1.64 (m, 2H), 2.31 (s, 3H), 2.32
(t, J=7.5 Hz, 2H), 2.96 (s, 3H), 3.98 (dd, J=5.4, 13.9 Hz, 1H),
4.60 (dd, J=8.1, 13.9 Hz, 1H), 5.38 (dd, J=5.4, 8.1 Hz, 1H),
7.20-7.44 (m, 5H), 8.02 (s, 1H) [0792] AP-MS (m/z): 427
(M.sup.++1)
EXAMPLE 134
Compound 141
[0793] In a manner similar to that in Example 133, Compound 141 (22
mg, 18%) was obtained from Compound 118 (100 mg, 0.305 mmol)
prepared in Example 111, pyridine (0.062 mL, 0.78 mmol) and
crotonoyl chloride (0.075 mL, 0.78 mmol). [0794] .sup.1H NMR (270
MHz, CDCl.sub.3) .delta.(ppm): 1.91 (dd, J=1.7, 7.0 Hz, 3H), 2.32
(s, 3H), 2.97 (s, 3H), 3.99 (dd, J=5.6, 13.9 Hz, 1H), 4.61 (dd,
J=7.6, 13.9 Hz, 1H), 5.51 (dd, J=5.6, 7.6 Hz, 1H), 5.86 (dd, J=1.7,
15.2 Hz, 1H), 7.03 (dd, J=7.0, 15.2 Hz, 1H), 7.22-7.41 (m, 5H),
8.49 (s, 1H) [0795] AP-MS (m/z): 397 (M.sup.++1)
EXAMPLE 135
Compound 142
[0796] In a manner similar to that in Example 133, Compound 142 (42
mg, 70%) was obtained from Compound 118 (50 mg, 0.15 mmol) prepared
in Example 111, pyridine (0.062 mL, 0.76 mmol) and
cyclopropanecarbonyl chloride (0.070 mL, 0.76 mmol). [0797] .sup.1H
NMR (270 MHz, CD.sub.3OD) .delta.(ppm): 0.87-0.98 (m, 4H), 1.77 (m,
1H), 2.28 (s, 3H), 3.01 (s, 3H), 3.97 (d, J=14.0 Hz, 1H), 4.55 (d,
J=14.0 Hz, 1H), 7.22-7.42 (m, 5H) [0798] AP-MS (m/z): 397
(M.sup.++1)
EXAMPLE 136
Compound 143
[0799] In a manner similar to that in Example 133, Compound 143 (24
mg, 22%) was obtained from Compound 118 (80 mg, 0.24 mmol) prepared
in Example 111, pyridine (0.069 mL, 0.85 mmol) and
2-acetoxyisobutyryl chloride (0.12 mL, 0.85 mmol). [0800] .sup.1H
NMR (270 MHz, CDCl.sub.3) .delta.(ppm): 1.65 (s, 3H), 1.67 (s, 3H),
2.15 (s, 3H), 2.32 (s, 3H), 2.97 (s, 3H), 3.99 (dd, J=5.5, 14.0 Hz,
1H), 4.61 (dd, J=8.1, 14.0 Hz, 1H), 5.39 (dd, J=5.5, 8.1 Hz, 1H),
7.29-7.46 (m, 5H), 8.53 (s, 1H) [0801] AP-MS (m/z): 457
(M.sup.++1)
EXAMPLE 137
Compound 144
[0802] Compound 143 (21 mg, 0.045 mmol) prepared in Example 136 was
dissolved in a mixed solvent of methanol (1.6 mL) and water (0.8
mL). To the solution was added lithium hydroxide (11 mg, 0.45
mmol), and the mixture was stirred at room temperature for 3.5
hours. To the reaction mixture was added water, and the mixture was
extracted with ethyl acetate. The organic layer was washed with
saturated aqueous sodium chloride, and then dried over anhydrous
sodium sulfate, and the solvent was evaporated under reduced
pressure. The residue was purified by preparative thin layer
chromatography (chloroform/methanol=9/1) to obtain Compound 144 (11
mg, 56%). [0803] .sup.1H NMR (270 MHz, CDCl.sub.3) .delta.(ppm):
1.44 (s, 3H), 1.48 (s, 3H), 2.32 (s, 3H), 2.85 (br s, 1H), 2.97 (s,
3H), 3.98 (dd, J=5.6, 13.9 Hz, 1H), 4.63 (dd, J=7.8, 13.9 Hz, 1H),
5.53 (dd, J=5.6, 7.8 Hz, 1H), 7.25-7.42 (m, 5H), 9.36 (s, 1H)
[0804] AP-MS (m/z): 415 (M.sup.++1)
EXAMPLE 138
Compound 145
[0805] In a manner similar to that in Example 133, Compound 145 (53
mg, 86%) was obtained from Compound 118 (50 mg, 0.15 mmol) prepared
in Example 111, pyridine (0.031 mL, 0.38 mmol) and methoxyacetyl
chloride (0.035 mL, 0.38 mmol). [0806] .sup.1H NMR (270 MHz,
CDCl.sub.3) .delta.(ppm): 2.32 (s, 3H), 2.96 (s, 3H), 3.49 (s, 3H),
4.00 (s, 2H), 4.00 (dd, J=5.8, 13.9 Hz, 1H), 4.61 (dd, J=7.8, 13.9
Hz, 1H), 5.46 (dd, J=5.8, 7.8 Hz, 1H), 7.25-7.44 (m, 5H), 8.94 (s,
1H) [0807] AP-MS (m/z): 401 (M.sup.++1)
EXAMPLE 139
Compound 146
[0808] In a manner similar to that in Example 133, Compound 146
(105 mg, 85%) was obtained from Compound 118 (100 mg, 0.305 mmol)
prepared in Example 111, pyridine (0.062 mL, 0.76 mmol) and
chloroacetyl chloride (0.061 mL, 0.76 mmol). [0809] .sup.1H NMR
(270 MHz, CDCl.sub.3) .delta.(ppm): 2.34 (s,3H), 2.97 (s, 3H), 4.02
(dd, J=5.6, 14.0 Hz, 1H), 4.11 (d, J=15.9 Hz, 1H), 4.18 (d, J=15.9
Hz, 1H), 4.62 (dd, J=7.8, 14.0 Hz, 1H), 5.28 (dd, J=5.6, 7.8 Hz,
1H), 7.22-7.43 (m, 5H), 8.87 (s, 1H) [0810] AP-MS (m/z): 405
(M.sup.++1)
EXAMPLE 140
Compound 147
[0811] Compound 146 (50 mg, 0.12 mmol) prepared in Example 139 was
dissolved in methanol (1 mL). To the solution was added 50% aqueous
dimethylamine (0.033 mL), and the mixture was stirred at room
temperature for 1 hour. To the reaction mixture was further added
50% aqueous dimethylamine (0.033 mL), and the mixture was stirred
at the same temperature for 1.5 hours. To the reaction mixture was
added water, and the mixture was extracted with ethyl acetate. The
organic layer was washed with saturated aqueous sodium chloride,
and then dried over anhydrous sodium sulfate, and the solvent was
evaporated under reduced pressure. The residue was purified by
preparative thin layer chromatography (chloroform/acetone=1/1) to
obtain Compound 147 (20 mg, 39%). [0812] .sup.1H NMR (270 MHz,
CDCl.sub.3) .delta.(ppm): 2.34 (s, 3H), 2.38 (s, 6H), 2.96 (s, 3H),
3.06 (d, J=17.3 Hz, 1H), 3.10 (d, J=17.3 Hz, 1H), 4.00 (d, J=13.9
Hz, 1H), 4.61 (d, J=13.9 Hz, 1H), 5.36 (br, 1H), 7.25-7.41 (m, 5H)
[0813] AP-MS (m/z): 414 (M.sup.++1)
EXAMPLE 141
Compound 148
[0814] In a manner similar to that in Example 133, Compound 148
(304 mg, 74%) was obtained from Compound 118 (297 mg, 0.903 mmol)
prepared in Example 111, pyridine (0.183 mL, 2.26 mmol) and methyl
4-(chloroformyl)butyrate (0.312 mL, 2.26 mmol). [0815] .sup.1H NMR
(270 MHz, CDCl.sub.3) .delta.(ppm): 2.00 (m, 2H), 2.32-2.56 (m,
4H), 2.34 (s, 3H), 2.99 (s, 3H), 3.71 (s, 3H), 4.01 (dd, J=5.4,
13.9 Hz, 1H), 4.63 (dd, J=7.9, 13.9 Hz, 1H), 5.45 (m, 1H),
7.21-7.49 (m, 5H), 8.54 (s, 1H) [0816] AP-MS (m/z): 457
(M.sup.++1)
EXAMPLE 142
Compound 149
[0817] In a manner similar to that in Example 137, after Compound
148 (262 mg, 0.573 mmol) prepared in Example 141 was treated with
lithium hydroxide monohydrate (206 mg, 4.91 mmol), to the reaction
mixture was added ice and 0.5 mol/L hydrochloric acid, and the
mixture was extracted with a mixed solvent of chloroform and
methanol. After the extract was concentrated, the residue was
purified by silica gel column chromatography
(chloroform/methanol=43/7) to obtain Compound 149 (222 mg, 88%).
[0818] .sup.1H NMR (270 MHz, CD.sub.3OD) .delta.(ppm): 1.89 (m,
2H), 2.28 (s, 3H), 2.33 (t, J=7.3 Hz, 2H), 2.43 (t, J=7.5 Hz, 2H),
3.01 (s, 3H), 3.99 (d, J=14.0 Hz, 1H), 4.56 (d, J=14.0 Hz, 1H),
7.20-7.45 (m, 5H) [0819] AP-MS (m/z): 441 (M.sup.--1)
EXAMPLE 143
Compound 150
[0820] Compound 149 (83 mg, 0.19 mmol) prepared in Example 142 was
dissolved in 1,2-dichloroethane (3.2 mL). To the solution was added
thionyl chloride (3.2 mL), and the mixture was stirred at
60.degree. C. for 2.5 hours. The reaction mixture was concentrated
under reduced pressure, and then the residue was purified by
preparative thin layer chromatography (chloroform/methanol=20/1) to
obtain Compound 150 (61 mg, 76%). [0821] .sup.1H NMR (270 MHz,
CDCl.sub.3) .delta.(ppm): 2.09 (m, 2H), 2.29 (s, 3H), 2.80 (t,
J=6.5 Hz, 4H), 3.05 (s, 3H), 3.95 (dd, J=3.7, 13.9 Hz, 1H), 4.82
(dd, J=9.6, 13.9 Hz, 1H), 5.70 (dd, J=3.7, 9.6 Hz, 1H), 7.29-7.47
(m, 3H), 7.58 (m, 2H) [0822] AP-MS (m/z): 425 (M.sup.++1)
EXAMPLE 144
Compound 151
[0823] In a manner similar to that in Example 133, Compound 151
(113 mg, 78%) was obtained from Compound 118 (100 mg, 0.305 mmol)
prepared in Example 111, pyridine (0.062 mL, 0.76 mmol) and
4-bromobutyryl chloride (0.088 mL, 0.76 mmol). [0824] .sup.1H NMR
(270 MHz, CDCl.sub.3) .delta.(ppm): 2.20 (m, 2H), 2.31 (s, 3H),
2.55 (t, J=6.9 Hz, 2H), 2.96 (s, 3H),.3.47 (t, J=6.2 Hz, 2H), 3.99
(dd, J=5.5, 13.9 Hz, 1H), 4.61 (dd, J=7.9, 13.9 Hz, 1H), 5.37 (dd,
J=5.5, 7.9 Hz, 1H), 7.23-7.42 (m, 5H), 8.18 (s, 1H) [0825] AP-MS
(m/z): 476 (M.sup.--1)
EXAMPLE 145
Compound 152
[0826] Compound 151 (70 mg, 0.15 mmol) prepared in Example 144 was
dissolved in N,N-dimethylformamide (1.8 mL). To the solution was
added 60% sodium hydride (9 mg, 0.2 mmol), and the mixture was
stirred at room temperature for 2 hours. To the reaction mixture
was added water, and the mixture was extracted with ethyl acetate.
The organic layer was washed with saturated aqueous sodium
chloride, and then dried over anhydrous sodium sulfate, and the
solvent was evaporated under reduced pressure. The residue was
purified by preparative thin layer chromatography
(chloroform/methanol=9/1) to obtain Compound 152 (51 mg, 88%).
[0827] .sup.1H NMR (270 MHz, CDCl.sub.3) .delta.(ppm): 2.20 (m,
2H), 2.35 (s, 3H), 2.57 (m, 2H), 2.95 (s, 3H), 3.93 (m, 2H), 3.99
(dd, J=5.5, 13.9 Hz, 1H), 4.61 (dd, J=8.1, 13.9 Hz, 1H), 5.33 (dd,
J=5.5, 8.1 Hz, 1H), 7.25-7.44 (m, 5H) [0828] AP-MS (m/z): 397
(M.sup.++1)
EXAMPLE 146
Compound 153
[0829] In a manner similar to that in Example 133, Compound 153
(120 mg, 80%) was obtained from Compound 118 (100 mg, 0.305 mmol)
prepared in Example 111, pyridine (0.087 mL, 1.1 mmol) and
5-bromovaleryl chloride (0.143 mL, 1.07 mmol). [0830] .sup.1H NMR
(270 MHz, CDCl.sub.3) .delta.(ppm): 1.75-1.98 (m, 4H), 2.31 (s,
3H), 2.36 (t, J.=7.0 Hz, 2H), 2.96 (5, 3H), 3.40 (t, J=6.2 Hz, 2H),
3.99 (dd, J=5.5, 13.9 Hz, 1H), 4.61 (dd, J=7.9, 13.9 Hz, 1H), 5.40
(dd, J=5.5, 7.9 Hz, 1H), 7.23-7.42 (m, 5H), 8.22 (s, 1H) [0831]
AP-MS (m/z): 491, 493 (M.sup.++1)
EXAMPLE 147
Compound 154
[0832] In a manner similar to that in Example 145, Compound 154 (36
mg, 72%) was obtained from Compound 153 (60 mg, 0.12 mmol) prepared
in Example 146 and 60% sodium hydride (7 mg, 0.2 mmol). [0833]
.sup.1H NMR (270 MHz, CDCl.sub.3) .delta.(ppm): 1.81-2.02 (m, 4H),
2.36 (s, 3H), 2.54 (m, 2H), 2.94 (s, 3H), 3.85 (m, 2H), 3.95 (dd,
J=4.8, 13.8 Hz, 1H), 4.56 (dd, J=8.4, 13.8 Hz, 1H), 5.41 (dd,
J=4.8, 8.4 Hz, 1H), 7.25-7.41 (m, 5H) [0834] AP-MS (m/z): 411
(M.sup.++1)
EXAMPLE 148
Compound 155
[0835] In a manner similar to that in Example 133, Compound 155
(122 mg, 80%) was obtained from Compound 118 (99 mg, 0.30 mmol)
prepared in Example 111, pyridine (0.061 mL, 0.75 mmol) and
6-bromohexanoyl chloride (0.115 mL, 0.754 mmol). [0836] .sup.1H NMR
(270 MHz, CDCl.sub.3) .delta.(ppm): 1.40-1.77 (m, 4H), 1.87 (m,
2H), 2.31 (s, 3H), 2.35 (t, J=7.4 Hz, 2H), 2.96 (s, 3H), 3.40 (t,
J=6.6 Hz, 2H), 3.99 (dd, J=5.4, 14.0 Hz, 1H), 4.60 (dd, J=7.9, 14.0
Hz, 1H), 5.36 (dd, J=5.4, 7.9 Hz, 1H), 7.20-7.43 (m, 5H), 8.06 (s,
1H) [0837] AP-MS (m/z): 505, 507 (M.sup.++1)
EXAMPLE 149
Compound 156
[0838] In a manner similar to that in Example 145, Compound 156 (17
mg, 32%) was obtained from Compound 155 (63 mg, 0.12 mmol) prepared
in Example 148 and 60% sodium hydride (7 mg, 0.2 mmol). [0839]
.sup.1H NMR (270 MHz, DMSO-d.sub.6) .delta.(ppm): 1.55-1.78 (m,
6H), 2.19 (s, 3H), 2.68 (m, 2H), 2.95 (s, 3H), 3.87 (dd, J=7.9,
13.7 Hz, 1H), 4.12 (m, 2H), 4.29 (dd, J=5.6, 13.7 Hz, 1H),
7.20-7.41 (m, 6H) [0840] AP-MS (m/z): 425 (M.sup.++1)
EXAMPLE 150
Compound 157
[0841] Compound 99 (1.50 g, 3.21 mmol) prepared in Example 92 was
dissolved in methanol (30 mL). To the solution was gradually added
sodium borohydride (1.21 g, 32.0 mmol) at 50.degree. C., and the
mixture was stirred at the same temperature for 1.5 hours. To the
reaction mixture was added water, and the mixture was extracted
with ethyl acetate. The organic layer was washed with saturated
aqueous sodium chloride, and then dried over anhydrous sodium
sulfate, and the solvent was evaporated under reduced pressure. The
residue was purified by silica gel column chromatography
(chloroform/methanol=20/1) to obtain Compound 157 (0.26 g, 21%).
[0842] .sup.1H NMR (270 MHz, CDCl.sub.3) .delta.(ppm): 1.31 (s,
9H), 2.62 (m, 1H), 2.94 (s, 3H), 3.22 (m, 1H), 3.41 (m, 1H), 3.61
(m, 1H), 4.21 (s, 2H), 4.79 (m, 1H), 7.19-7.38 (m, 5H) [0843] AP-MS
(m/z): 385 (M.sup.++1)
EXAMPLE 151
Compound 158
[0844] In a manner similar to that in Example 133, Compound 158
(114 mg, 85%) was obtained from Compound 157 (97 mg, 0.25 mmol)
prepared in Example 150, pyridine (0.051 mL, 0.63 mmol) and
4-bromobutyryl chloride (0.073 mL, 0.63 mmol). [0845] .sup.1H NMR
(270 MHz, CDCl.sub.3) .delta.(ppm): 1.32 (s, 9H), 2.22 (m, 2H),
2.58 (t, J=7.4 Hz, 2H), 2.65 (m, 1H), 2.97 (s, 3H), 3.27 (m, 1H),
3.39 (m, 1H), 3.49 (t, J=6.2 Hz, 2H), 3.62 (m, 1H), 4.45 (br t,
1H), 7.21-7.39 (m, 5H), 8.00 (s, 1H) [0846] AP-MS (m/z): 533, 535
(M.sup.++1)
EXAMPLE 152
Compound 159
[0847] In a manner similar to that in Example 145, Compound 159 (64
mg, 68%) was obtained from Compound 158 (110 mg, 0.206 mmol)
prepared in Example 151 and 60% sodium hydride (12 mg, 0.31 mmol).
[0848] .sup.1H NMR (270 MHz, CDCl.sub.3) .delta.(ppm): 1.34 (s,
9H), 2.23 (m, 2H), 2.56 (m, 2H), 2.61 (m, 1H), 2.97 (s, 3H), 3.27
(m, 1H), 3.40 (m, 1H), 3.63 (m, 1H), 3.98 (m, 2H), 4.01 (br t,
J=3.5 Hz, 1H), 7.20-7.37 (m, 5H) [0849] AP-MS (m/z): 453
(M.sup.++1)
EXAMPLE 153
Compound 160
[0850] Compound 119 (21 mg, 0.052 mmol) prepared in Example 112 was
dissolved in a mixed solvent of toluene (1 mL) and tetrahydrofuran
(1 mL). To the solution was added
2,4-bis(4-methoxyphenyl)-1,3-dithia-2,4-diphosphethane-2,4-disulfide
(Lawesson's reagent) (43 mg, 0.11 mmol), and the mixture was
stirred at 90.degree. C. for 5 hours. The reaction mixture was
purified by preparative thin layer chromatography
(chloroform/methanol=20/1) to obtain Compound 160 (15 mg, 67%).
[0851] .sup.1H NMR (270 MHz, CDCl.sub.3) .delta.(ppm): 1.30 (s,
9H), 2.76 (s, 3H), 3.08 (s, 3H), 4.08 (dd, J=7.3, 13.8 Hz, 1H),
5.03 (t, J=7.3 Hz, 1H), 5.54 (dd, J=7.3, 13.8 Hz, 1H), 7.26-7.42
(m, 5H), 8.16 (s, 1H) [0852] AP-MS (m/z): 429 (M.sup.++1)
EXAMPLE 154
Compound 161
[0853] In a manner similar to that in Example 100, Compound 161 (70
mg, 37%) was obtained from Compound 106 (0.165 g, 0.393 mmol)
prepared in Example 99, oxalyl chloride (2 mL),
2-(methylamino)ethanol (295 mg, 3.93 mmol) and triethylamine (476
mg, 4.72 mmol). [0854] AP-MS (m/z): 475 (M.sup.--1)
EXAMPLE 155
Compound 162
[0855] In a manner similar to that in Example 100, Compound 162
(135 mg, 68%) was obtained from Compound 106 (0.165 g, 0.393 mmol)
prepared in Example 99, oxalyl chloride (2 mL) and diethanolamine
(413 mg, 3.93 mmol). [0856] AP-MS (m/z) : 507 (M.sup.++1)
EXAMPLE 156
Compounds 163 and 164
[0857] In a manner similar to that in Example 100, Compound 163
(6.2 mg, 5%) and Compound 164 (36.1 mg, 31%) were obtained from
Compound 106 (0.099 g, 0.237 mmol) prepared in Example 99, oxalyl
chloride (1.25 mL) and 3-amino-1,2-propanediol (92 .mu.L, 1.19
mmol).
Compound 163
[0858] AP-MS (m/z): 493 (M.sup.++1)
Compound 164
[0858] [0859] AP-MS (m/z): 493 (M.sup.++1)
EXAMPLE 157
Compound 165
[0860] In a manner similar to that in Example 100, Compound 165 (37
mg, 33%) was obtained from Compound 115 (0.102 g, 0.236 mmol)
prepared in Example 108, oxalyl chloride (1.25 mL) and
2-aminoethanol (144 mg, 2.36 mmol). [0861] AP-MS (m/z): 477
(M.sup.++1)
EXAMPLE 158
Compound 166
[0862] Compound 105 (0.200 g, 0.461 mmol) prepared in Example 98
was dissolved in tetrahydrofuran (2 mL). To the solution was added
lithium aluminium hydride (30 mg, 0.791 mmol) at 0.degree. C., and
the mixture was stirred at room temperature for 2 hours. To the
reaction mixture was added water and 30% aqueous sodium hydroxide.
The insoluble precipitate was removed by filtration, and the
filtrate was concentrated under reduced pressure. The residue was
purified by preparative thin layer chromatography
(chloroform/methanol=9/1) to obtain Compound 166 (64.0 mg, 34%).
[0863] .sup.1H NMR (270 MHz, CDCl.sub.3) .delta.(ppm): 1.29 (s,
9H), 1.32 (s, 9H), 1.65 (m, 1H), 2.08 (m, 1H), 2.33 (m, 1H), 3.16
(m, 1H), 3.78 (m, 2H), 7.21-7.38 (m, 5H), 7.95 (br s, 1H) [0864]
AP-MS (m/z): 404 (M.sup.--1)
EXAMPLE 159
Compound 167
[0865] Compound 166 (0.0448 g, 0.110 mmol) prepared in Example 158
was dissolved in N,N-dimethylacetamide (0.5 mL). To the solution
was added sulfamoyl chloride (51.1 mg, 0.442 mmol) at 0.degree. C.
with stirring, and the mixture was stirred at 0.degree. for 20
minutes. After to the reaction mixture was added water, and the
mixture was stirred. The deposited solid was collected by
filtration, and dried under reduced pressure. The resulting solid
was purified by preparative thin layer chromatography
(chloroform/methanol=30/1) to obtain Compound 167 (30.2 mg, 57%).
[0866] .sup.1H NMR (270 MHz, CDCl.sub.3) .delta.(ppm): 1.29 (s,
9H), 1.33 (s, 9H), 1.89 (m, 1H), 2.14 (m, 1H), 2.38 (m, 1H), 3.32
(m, 1H), 4.28 (m, 1H), 4.43 (m, 1H), 5.08 (br s, 1H), 7.29 (m, 5H),
7.93 (br s, 1H) [0867] AP-MS (m/z): 483 (M.sup.--1)
EXAMPLE 160
Compounds 168 and 169
[0867] [0868] Step 1: 2-Aminoacetophenone hydrochloride (4.56 g,
26.6 mmol) was dissolved in dichloromethane (250 mL). To the
solution was added triethylamine (9.30 mL, 66.7 mmol), and the
mixture was stirred at room temperature for 10 minutes. After the
reaction mixture was cooled to 0.degree. C., chloromethanesulfonyl
chloride (purity 90%, 3.60 mL, 36.3 mmol) was added to the mixture,
and the mixture was stirred at the same temperature for 1 hour. To
the reaction mixture was added 2 mol/L hydrochloric acid, and the
mixture was extracted with chloroform. The organic layer was washed
with saturated aqueous sodium chloride, and then dried over
anhydrous sodium sulfate, and the solvent was evaporated under
reduced pressure. To the residue was added diethyl ether, and the
deposited crystals were collected by filtration and dried to obtain
2-(chloromethylsulfonylamino)acetophenone (5.00 g, 76%). [0869]
.sup.1H NMR (300 MHz, DMSO-d.sub.6) .delta.(ppm): 4.67 (s, 2H),
4.94 (s, 2H), 7.54 (t, J=8.1 Hz, 2H), 7.67 (t, J=7.5 Hz, 1H), 7.97
(d, J=8.1 Hz, 2H), 8.01 (br s, 1H) [0870] AP-MS (m/z): 247
(M.sup.+) [0871] Step 2: 2-(Chloromethylsulfonylamino)acetophenone
(1.00 g, 4.05 mmol) prepared above and thiosemicarbazide
hydrochloride (1.03 g, 8.07 mmol) were dissolved in methanol (60
mL). To the solution was added concentrated hydrochloric acid (1.00
mL), and the mixture was stirred at 60.degree. C. for 2 hours. The
reaction mixture was concentrated, and to the residue was added
ethyl acetate and saturated aqueous sodium hydrogencarbonate, and
the mixture was subjected to separation. The organic layer was
washed with saturated aqueous sodium chloride, and then dried over
anhydrous sodium sulfate, and the solvent was evaporated under
reduced pressure. The residue was purified by silica gel column
chromatography (ethyl acetate/n-hexane=1/1 and 2/1) to obtain
2-(chloromethylsulfonylamino)acetophenone=thiosemicarbazone (0.51
g, 40%). [0872] .sup.1H NMR (300 MHz, DMSO-d.sub.6) .delta.(ppm):
4.17 (s, 2H), 4.93 (s, 2H), 7.37-7.42 (m, 3H), 7.52-7.56 (m, 2H),
8.13 (br s, 1H), 8.48 (br, 2H), 8.85 (br s, 1H) [0873] AP-MS (m/z):
319 (M.sup.+) [0874] Step 3:
2-(Chloromethylsulfonylamino)acetophenone=thiosemicarbazone (7.48
g, 23.4 mmol) prepared above was dissolved in chloroform (250 mL).
To the solution was added pyridine (11.4 mL, 141 mmol) and pivaloyl
chloride (8.70 mL, 70.6 mmol), and the mixture was stirred at room
temperature for 30 minutes. To the reaction mixture was added
acetic anhydride (4.40 mL, 46.6 mmol), and the mixture was further
stirred at room temperature for 15 hours. To the reaction mixture
was added 2 mol/L hydrochloric acid, and the mixture was extracted
with chloroform. The organic layer was washed with saturated
aqueous sodium chloride, and then dried over anhydrous sodium
sulfate, and the solvent was evaporated under reduced pressure. The
residue was purified by silica gel column chromatography (ethyl
acetate/n-hexane=1/1 and 2/1) to obtain Compound 168 (3.56 g, 25%)
and Compound 169 (1.77 g, 14%).
Compound 168
[0874] [0875] .sup.1H NMR (300 MHz, DMSO-d.sub.6) .delta.(ppm):
1.16 (s, 9H), 2.23 (s,3H),4.00 (dd, J=11.3, 8.0 Hz, 1H), 4.47 (dd,
J=11.3, 2.5 Hz, 1H), 4.91 (d, J=12.0 Hz, 1H), 4.97 (d, J=12.0 Hz,
1H), 7.28-7.39 (m, 5H), 8.10 (br s, 1H), 11.2 (br s, 1H) [0876]
AP-MS (m/z): 446 (M.sup.+)
Compound 169
[0877] .sup.1H NMR (300 MHz, DMSO-d.sub.6) .delta.(ppm): 2.01 (s,
3H), 2.18 (s, 3H), 3.95 (d, J=14.3 Hz, 1H), 4.45 (d, J=14.3 Hz,
1H), 4.91 (d, J=12.0 Hz, 1H), 4.97 (d, J=12.0 Hz, 1H), 7.25-7.39
(m, 5H), 8.08 (br s, 1H), 11.6 (br s, 1H) [0878] AP-MS (m/z): 404
(M.sup.+)
EXAMPLE 161
Compounds 170 and 171
[0879] Step 1: 2-Aminoacetophenone hydrochloride (1.00 g, 5.85
mmol) was dissolved in dichloromethane (50 mL). To the solution was
added triethylamine (2.50 mL, 17.9 mmol), and the mixture was
stirred at room temperature for 10 minutes. After the reaction
mixture was cooled to 0.degree. C., chloroethanesulfonyl chloride
(0.92 mL, 8.80 mmol) was added to the mixture, and the mixture was
stirred at the same temperature for 15 minutes. To the reaction
mixture was added 2 mol/L hydrochloric acid and the mixture was
extracted with chloroform. The organic layer was washed with
saturated aqueous sodium chloride, and then dried over anhydrous
sodium sulfate, and the solvent was evaporated under reduced
pressure. To the residue was added a mixed solvent of ethyl acetate
and n-hexane for crystallization to obtain
2-(vinylsulfonylamino)acetophenone (0.42 g, 32%). [0880] .sup.1H
NMR (300 MHz, CDCl.sub.3) .delta.(ppm): 4.54 (d, J=4.5 Hz, 2H),
5.42 (br s, 1H), 5.94 (d, J=9.9 Hz, 1H), 6.28 (d, J=16.5 Hz, 1H),
6.53 (br dd, J=16.2, 9.9 Hz, 1H), 7.52 (t, J=7.5 Hz, 3H), 7.65 (t,
J=7.8 Hz, 1H), 7.93 (t, J=5.1 Hz, 1H) [0881] AP-MS (m/z): 225
(M.sup.+) [0882] Step 2: 2-(Vinylsulfonylamino)acetophenone (0.32
g, 1.42 mmol) prepared above and thiosemicarbazide hydrochloride
(0.27 g, 2.13 mmol) were dissolved in methanol (20 mL). To the
solution was added concentrated hydrochloric acid (2 drops), and
the mixture was stirred at room temperature for 3 hours. The
reaction mixture was concentrated. To the residue was added ethyl
acetate and saturated aqueous sodium hydrogencarbonate, and the
mixture was subjected to separation. The organic layer was washed
with saturated aqueous sodium chloride, and then dried over
anhydrous sodium sulfate, and the solvent was evaporated under
reduced pressure. The residue was purified by silica gel column
chromatography (ethyl acetate/n-hexane=1/1) to obtain
2-(vinylsulfonylamino)acetophenone=thiosemicarbazone (0.25 g, 58%).
[0883] .sup.1H NMR (300 MHz, CDCl.sub.3) .delta.(ppm): 4.10 (s,
2H), 5.97 (d, J=9.9 Hz, 1H), 6.25 (d, J=16.8 Hz, 1H), 6.54 (dd,
J=16.8, 9.9 Hz, 1H), 7.24-7.27 (m, 2H), 7.42 (br s, 1H), 7.52-7.53
(m, 3H), 7.81 (br s, 1H), 8.70 (m, 1H) [0884] AP-MS (m/z): 297
(M.sup.+) [0885] Step 3:
2-(Vinylsulfonylamino)acetophenone=thiosemicarbazone (0.25 g, 0.83
mmol) prepared above was dissolved in acetone (10 mL). To the
solution was added pyridine (0.34 mL, 4.17 mmol) and pivaloyl
chloride (0.31 mL, 2.50 mmol), and the mixture was stirred at room
temperature for 30 minutes. To the reaction mixture was added
acetic anhydride (0.16 mL, 1.66 mmol), and the mixture was further
stirred for 3 days at room temperature. The reaction mixture was
concentrated, and to the residue was added ethyl acetate and 2
mol/L hydrochloric acid, and the mixture was subjected to
separation. The organic layer was washed with saturated aqueous
sodium chloride, and then dried over anhydrous sodium sulfate, and
the solvent was evaporated under reduced pressure. The residue was
purified by silica gel column chromatography (ethyl
acetate/n-hexane=1/1) to obtain Compound 170 (0.18 g, 52%) and
Compound 171 (0.10 g, 26%).
Compound 170
[0886] .sup.1H NMR (300 MHz, CDCl.sub.3) .delta.(ppm): 1.27 (s,
9H),2.31 (s,3H),3.87 (dd, J=13.4, 5.0 Hz, 1H), 4.45 (dd, J=13.4,
7.9 Hz, 1H), 5.57 (br s, 1H), 5.92 (d, J=9.9 Hz, 1H), 6.25 (d,
J=16.5 Hz, 1H), 6.49 (dd, J=16.5, 9.9 Hz, 1H), 7.27-7.34 (m, 5H),
8.22 (br s, 1H) [0887] AP-MS (m/z): 424 (M.sup.+)
Compound 171
[0887] [0888] .sup.1H NMR (300 MHz, CDCl.sub.3) .delta.(ppm): 1.29
(s, 9H), 1.33 (s, 9H), 3.85 (dd, J=13.5, 4.8 Hz, 1H), 4.49 (dd,
J=13.5, 8.1 Hz, 1H), 5.29 (br s, 1H), 5.93 (br d, J=9.9 Hz, 1H),
6.27 (br d, J=16.5 Hz, 1H), 6.53 (br dd, J=16.4, 9.6 Hz, 1H),
7.27-7.34 (m, 5H), 8.06 (br s, 1H) [0889] AP-MS (m/z): 466
(M.sup.+)
EXAMPLE 162
Compound 172
[0890] Compound 170 (0.05 g, 0.11 mmol) prepared in Step 3 of
Example 161 was dissolved in acetonitrile (3 mL). To the solution
was added morpholine (0.10 mL), and the mixture was stirred at
80.degree. C. for 2 hours. The reaction mixture was concentrated,
and the residue was purified by silica gel column chromatography
(chloroform/methanol=10/1) to obtain Compound 172 (0.04 g, 77%).
[0891] .sup.1H NMR (300 MHz, CDCl.sub.3) .delta.(ppm): 1.27 (s,
9H), 2.33 (s, 3H), 2.42-2.45 (m, 4H), 2.78 (dquin, J=16.5, 6.0 Hz,
2H), 3.19 (t, J=6.6 Hz, 2H), 3.65-3.68 (m, 4H), 4.04 (dd, J=14.1,
4.8 Hz, 1H), 4.55 (dd, J=14.1, 7.5 Hz, 1H), 5.73 (br s, 1H),
7.30-7.38 (m, 5H), 8.05 (br s, 1H) [0892] AP-MS (m/z): 511
(M.sup.+)
EXAMPLE 163
Compound 173
[0893] In a manner similar to that in Example 162, Compound 173
(0.03 g, 66%) was obtained from Compound 170 (0.05 g, 0.11 mmol)
prepared in Step 3 of Example 161 and 70% aqueous ethylamine (0.10
mL). [0894] .sup.1H NMR (300 MHz, CDCl.sub.3) .delta.(ppm): 1.10
(t, J=6.9 Hz, 3H), 1.27 (s, 9H), 2.32 (s, 3H), 2.65 (quin, J=7.2
Hz, 2H), 3.05-3.09 (m, 2H), 3.18-3.20 (m, 2H), 4.00 (d, J=13.5 Hz,
1H), 4.55 (d, J=13.8 Hz, 1H), 7.30-7.37 (m, 5H), 8.07 (br s, 1H)
[0895] AP-MS (m/z): 470 (M.sup.++1)
EXAMPLE 164
Compound 174
[0896] In a manner similar to that in Example 162, Compound 174
(0.03 g, 67%) was obtained from Compound 170 (0.05 g, 0.11 mmol)
prepared in Step 3 of Example 161 and 2 mol/L dimethylamine
methanol solution (0.10 mL). [0897] .sup.1H NMR (300 MHz,
CDCl.sub.3) .delta.(ppm): 1.26 (s, 9H), 2.24 (s, 6H), 2.31 (s, 3H),
2.71-2.81 (m, 2H), 3.12-3.19 (m, 2H), 4.00 (d, J=13.5 Hz, 1H), 4.56
(d, J=13.5 Hz, 1H), 6.00 (br s, 1H), 7.31-7.36 (m, 5H), 8.06 (br s,
1H) [0898] AP-MS (m/z): 469 (M.sup.+)
EXAMPLE 165
Compound 175
[0899] In a manner similar to that in Example 162, Compound 175
(0.03 g, 52%) was obtained from Compound 170 (0.05 g, 0.11 mmol)
prepared in Step 3 of Example 161 and 2-aminoethanol (0.10 mL).
[0900] .sup.1H NMR (300 MHz, CDCl.sub.3) .delta.(ppm): 1.26 (s,
9H), 2.35 (s, 3H), 2.65-2.78 (m, 2H), 3.08-3.30 (m, 4H), 3.64 (t,
J=5.1 Hz, 2H), 3.98 (d, J=13.5 Hz, 1H), 4.54 (d, J=13.5 Hz, 1H),
7.26-7.38 (m, 5H), 8.25 (br s, 1H) [0901] AP-MS (m/z): 485
(M.sup.+)
EXAMPLE 166
Compound 176
[0902] In a manner similar to that in Example 162, Compound 176
(0.01 g, 26%) was obtained from Compound 171 (0.05 g, 0.11 mmol)
prepared in Step 3 of Example 161 and 70% aqueous ethylamine (0.10
mL). [0903] .sup.1H NMR (300 MHz, CDCl.sub.3) .delta.(ppm): 1.18
(m, 3H), 1.28 (s, 9H), 1.34 (s, 9H), 2.63 (quin, J=7.0 Hz, 2H),
2.73 (br q, J=6.3 Hz, 1H), 2.84 (br q, J=6.2 Hz, 1H), 3.18 (br t,
J=6.6 Hz, 2H), 4.02 (d, J=13.2 Hz, 1H), 4.58 (d, J=13.2 Hz, 1H),
5.85 (br s, 1H), 7.27-7.35 (m, 5H), 8.02 (br s, 1H) [0904] AP-MS
(m/z): 512 (M.sup.++1)
EXAMPLE 167
Compound 177
[0905] In a manner similar to that in Example 162, Compound 177
(0.02 g, 39%) was obtained from Compound 171 (0.05 g, 0.11 mmol)
prepared in Step 3 of Example 161 and 2 mol/L dimethylamine
methanol solution (0.10 mL). [0906] .sup.1H NMR (300 MHz,
CDCl.sub.3) .delta.(ppm): 1.28 (s, 9H), 1.34 (s, 9H), 2.25 (s, 6H),
2.73 (br q, J=6.3 Hz, 1H), 2.84 (br q, J=6.2 Hz, 1H), 3.18 (br t,
J=6.6 Hz, 2H), 4.02 (d, J=13.2 Hz, 1H), 4.58 (d, J=13.2 Hz, 1H),
5.85 (br s, 1H), 7.27-7.35 (m, 5H), 8.02 (br s, 1H) [0907] AP-MS
(m/z): 512 (M.sup.++1)
EXAMPLE 168
Compound 178
[0908] In a manner similar to that in Example 11, Compound 178
(64.0 mg, 38%) was obtained from
carbomethoxypropiophenone=thiosemicarbazone (0.144 g, 0.543 mol)
prepared in Step 1 of Example 98, acetic anhydride (77 .mu.L, 0.814
mmol) and pyridine (79 .mu.L, 0.977 mmol). [0909] .sup.1H NMR (270
MHz, CDCl.sub.3) .delta.(ppm): 2.13 (s, 3H), 2.20-2.70 (m, 4H),
3.61 (s, 3H), 6.52 (br s, 2H), 7.20-7.35 (m, 5H)
EXAMPLE 169
Compound 179
[0910] In a manner similar to that in Example 15, Compound 179
(24.0 mg, 94%) was obtained from Compound 178 (0.0200 g, 0.0650
mol) prepared in Example 168, pivaloyl chloride (16 .mu.L, 0.130
mmol) and pyridine (15 .mu.L, 0.182 mmol). [0911] .sup.1H NMR (270
MHz, CDCl.sub.3) .delta.(ppm): 1.30 (s, 9H), 2.10 (s, 3H),
2.17-2.75 (m, 4H), 3.57 (s, 3H), 7.18-7.32 (m, 5H), 8.02 (br s, 1H)
[0912] AP-MS (m/z): 390 (M.sup.--1)
EXAMPLE 170
Compound 180
[0913] Compound 100 (304 mg, 0.0690 mmol) prepared in Example 93
and cerium chloride heptahydrate (257 mg, 0.690 mmol) were
dissolved in methanol (800 mL). To the solution was gradually added
sodium borohydride (522 mg, 13.8 mmol), and the mixture was stirred
at room temperature for 20 minutes. The reaction mixture was
concentrated under reduced pressure. To the residue was added 1
mol/L hydrochloric acid (100 mL), and the mixture was extracted
with chloroform. The organic layer was dried over anhydrous sodium
sulfate, and the solvent was evaporated under reduced pressure. The
residue was purified by silica gel column chromatography
(chloroform/acetone/ethyl acetate/n-hexane=9/1/1/1) to obtain
Compound 180 (217 mg, 85%). [0914] .sup.1H NMR (270 MHz,
CDCl.sub.3) .delta.(ppm): 1.14 (t, J=7.0 Hz, 6H), 2.68 (m, 1H),
2.98 (s, 3H), 3.27 (m, 2H), 3.44 (m, 1H), 3.63 (m, 1H), 4.18 (br s,
2H), 4.51 (br s, 1H), 7.30 (m, 5H) [0915] AP-MS (m/z): 371
(M.sup.++1)
EXAMPLE 171
Compound 181
[0916] In a manner similar to that in Example 15, Compound 181
(87.3 mg, 71%) was obtained from Compound 180 (100 mg, 0.270 mmol)
prepared in Example 170, pyridine (65.4 .mu.L, 0.810 mmol) and
pivaloyl chloride (83.4 .mu.L, 0.676 mmol). [0917] AP-MS (m/z): 455
(M.sup.++1)
EXAMPLE 172
Compound 182
[0918] Compound 180 (60.6 mg, 0.170 mmol) obtained in Example 170
was dissolved in dichloromethane. To the solution was added
pyridine (63.2 .mu.L, 0.788 mmol) and 5-bromovaleryl chloride (23.0
.mu.L, 0.172 mmol), and the mixture was stirred at room temperature
for 5 hours. To the reaction mixture was added 1 mol/L hydrochloric
acid and the mixture was extracted with chloroform. The organic
layer was dried over anhydrous sodium sulfate, and the solvent was
evaporated under reduced pressure. The residue was dissolved in
dimethyl sulfoxide (0.3 mL). To the solution was added sodium
acetate (58.7 mg), and the mixture was stirred at 100.degree. C.
for 5 minutes. To the reaction mixture was added water (20 mL) and
1 mol/L hydrochloric acid (20 mL), and the mixture was extracted
with chloroform. And then, the organic layer was dried over
anhydrous sodium sulfate, and the solvent was evaporated under
reduced pressure. The residue was purified by preparative thin
layer chromatography (chloroform/acetone/ethyl
acetate/n-hexane=9/1/1/1) to obtain Compound 182 (42.5 mg, 45%).
[0919] AP-MS (m/z): 453 (M.sup.++1)
EXAMPLE 173
Compound 183
[0920] Compound 180 (100 mg, 0.270 mmol) prepared in Example 170
and pyridine (31.5 .mu.L, 0.389 mmol) were dissolved in
dichloromethane (2 mL). To the solution was added 4-bromobutyryl
chloride (37.5 .mu.L, 0.324 mmol) at 0.degree. C., and the mixture
was stirred at room temperature for 5 hours. To the reaction
mixture was added 1 mol/L hydrochloric acid, and the mixture was
extracted with chloroform. The organic layer was dried over
anhydrous sodium sulfate, and the solvent was evaporated under
reduced pressure. To the residue was added methanol (20 mL) and
potassium carbonate (1.0 g), and the mixture was vigorously stirred
at room temperature for 20 minutes. To the reaction mixture was
added water and 1 mol/L hydrochloric acid, and the mixture was
extracted with chloroform. The organic layer was dried over
anhydrous sodium sulfate, and the solvent was evaporated. The
residue was purified by silica gel column chromatography
(chloroform/acetone/ethyl acetate/n-hexane=9/1/1/1) to obtain
Compound 183 (27.6 mg, 37%). [0921] .sup.1H NMR (270 MHz,
CDCl.sub.3) .delta.(ppm): 1.15 (d, J=6.6 Hz, 6H), 2.22 (m, 2H),
2.55-2.67 (m, 3H), 2.94 (s, 3H), 3.31-3.47 (m, 3H), 3.61 (m, 1H),
3.91-3.98 (m, 2H), 5.0 (br s, 1H), 7.20-7.35 (m, 5H) [0922] AP-MS
(m/z): 437 (M.sup.--1)
EXAMPLE 174
Compound 184
[0923] In a manner similar to that in Example 173, Compound 180
(84.1 mg, 0.227 mmol) prepared in Example 170 was treated with
pyridine (88.0 .mu.L, 1.09 mmol) and 5-bromovaleryl chloride (121
.mu.L, 0.908 mmol), and then treated with methanol and potassium
carbonate (1.0 g) to obtain Compound 184 (89.1 mg, 81%). [0924]
AP-MS (m/z): 485 (M.sup.++1)
EXAMPLE 175
Compound 185
[0925] In a manner similar to that in Step 3 of Example 92,
Compound 185 (16.7 g, 85%) was obtained from
3-(methylsulfonylamino)propiophenone=thiosemicarbazone (14.4 g,
47.9 mmol), propionyl chloride (16.7 mL, 192 mmol) and pyridine
(18.6 mL, 230 mmol). [0926] .sup.1H NMR (270 MHz, CDCl.sub.3)
.delta.(ppm): 1.12 (t, J=7.5 Hz, 3H), 1.19 (t, J=7.3 Hz, 3H), 2.37
(m, 2H), 2.63 (m, 3H), 2.96 (s, 3H), 3.35 (m, 2H), 3.58 (m, 1H),
4.55 (br s, 1H), 7.20-7.35 (m, 5H), 8.01 (br s, 1H)
EXAMPLE 176
Compound 186
[0927] In a manner similar to that in Example 170, Compound 186
(11.7 g, 81%) was obtained from Compound 185 (16.7 g, 40.5 mmol)
prepared in Example 175, cerium chloride heptahydrate (15.1 g, 40.5
mol) and sodium borohydride (12.8 g, 338 mol). [0928] .sup.1H NMR
(270 MHz, CDCl.sub.3) .delta.(ppm): 1.13 (t, J=8.7 Hz, 3H),
2.61-2.71 (m, 3H), 2.97 (s, 3H), 3.27-3.47 (m, 2H), 3.60-3.67 (m,
1H), 4.21 (br s, 2H), 4.65 (br s, 1H), 7.26-7.36 (m, 5H)
EXAMPLE 177
Compound 187
[0929] In a manner similar to that in Example 15, Compound 187
(90.3 mg, 76%) was obtained from Compound 186 (96.0 mg, 0.269 mmol)
prepared in Example 176, pyridine (65.4 .mu.L, 0.810 mmol) and
pivaloyl chloride (83.4 .mu.L, 0.676 mmol). [0930] .sup.1H NMR (270
MHz, CDCl.sub.3) .delta.(ppm): 1.13 (t, J=6.0 Hz, 3H), 1.28 (s,
9H), 2.66 (m, 3H), 2.97 (s, 3H), 3.35 (m, 2H), 3.61 (m, 1H), 4.58
(br s, 1H), 7.32 (m, 5H), 8.08 (br s, 1H) AP-MS (m/z): 441
(M++1)
EXAMPLE 178
Compound 188
[0931] In a manner similar to that in Example 172, Compound 188
(42.5 mg, 45%) was obtained from Compound 186 (100 mg, 0.221 mmol)
prepared in Example 176, pyridine (85 .mu.L, 1.05 mmol),
4-bromobutyryl chloride (110 .mu.L, 0.949 mmol) and potassium
carbonate (1.0 g). [0932] .sup.1H NMR (270 MHz, CDCl.sub.3)
.delta.(ppm): 1.14 (t, J=7.5 Hz, 3H), 2.19 (m, 2H), 2.50-2.81 (m,
5H), 2.96 (s, 3H), 3.35 (m, 2H), 3.59 (m, 1H), 3.93 (m, 2H), 4.52
(br s, 1H), 7.20-7.34 (m, 5H) [0933] AP-MS (m/z): 424
(M.sup.--1)
EXAMPLE 179
Compound 189
[0934] In a manner similar to that in Example 172, Compound 189
(27.6 mg, 37%) was obtained from Compound 186 (60.6 mg, 0.170 mmol)
prepared in Example 176, pyridine (63.2 .mu.L, 0.788 mmol),
5-bromovaleryl chloride (110 .mu.L, 0.949 mmol) and potassium
carbonate (1.0 g).
[0935] .sup.1H NMR (270 MHz, CDCl3) .delta.(ppm): 1.14 (t, J=7.5
Hz, 3H), 1.79-1.99 (m, 4H), 2.54-2.75 (m, 5H), 2.96 (s. 3H),
3.19-3.27 (m, 2H), 3.57-3.68 (m, 1H), 3.83-3.95 (m, 2H), 4.36 (br
s, 1H), 7.20-7.37 (m, 5H) [0936] AP-MS (m/z): 439 (M.sup.++1)
EXAMPLE 180
Compound 190
[0937] In a manner similar to that in of Example 170, Compound 190
(86.5 mg, 0.248 mmol) was obtained from Compound 105 (1.01 g, 2.33
mmol) prepared in Example 98 and sodium borohydride (2.20 g, 58.2
mmol).
[0938] .sup.1H NMR (270 MHz, CDCl.sub.3) .delta.(ppm): 1.30 (s,
9H), 2.37-2.46 (m, 1H), 2.63-2.86 (m, 2H), 3.41-3.51 (m, 1H), 3.71
(s, 3H), 4.09 (br s, 2H), 7.22-7.43 (m, 5H)
EXAMPLE 181
Compound 191
[0939] Compound 191 (89.5 mg, 29%) was obtained in the same manner
as that in Example 133 from Compound 190 (86.5 mg, 0.248 mmol)
obtained in Example 180 and 4-bromobutyryl chloride (57 .mu.L,
0.495 mmol). [0940] AP-MS (m/z): 496 (M.sup.--1)
EXAMPLE 182
Compound 192
[0941] Compound 191 (89.5 mg, 0.18 mmol) prepared in Example 181
was dissolved in N,N-dimethylformamide (2.0 mL). To the solution
was added 60% sodium hydride (14 mg, 0.359 mmol), and the mixture
was stirred at room temperature for 1 hour. To the reaction mixture
was added acetic acid and water, and the mixture was extracted with
ethyl acetate. The organic layer was washed with saturated saline,
and then dried over anhydrous sodium sulfate, and the solvent was
evaporated under reduced pressure. The residue was purified by
silica gel column chromatography (ethyl acetate/n-hexane=2/1) to
obtain Compound 192 (30.2 mg, 40%). [0942] .sup.1H NMR (270 MHz,
CDCl.sub.3) .delta.(ppm): 1.36 (s, 9H), 2.17-2.42 (m, 3H),
2.53-2.84 (m, 4H), 3.38-3.50 (s, 1H), 3.72 (s, 3H), 3.97 (m, 2H),
7.22-7.39 (m, 5H)
EXAMPLE 183
Compound 193
[0943] In a manner similar to that in Example 99, Compound 193
(21.7mg, 74%) was obtained from Compound 192 (30.2 mg, 0.723 mmol)
prepared in Example 182 and sodium hydroxide (8.7 mg,0.217 mmol).
[0944] AP-MS (m/z): 402 (M.sup.--1)
EXAMPLE 184
Compound 194
[0945] n a manner similar to that in Example 100, Compound 194 (7.3
mg, 30%) was obtained from Compound 193 (21.7 mg, 0.054 mmol)
prepared in Example 183, oxalyl chloride (0.25 ml) and
2-aminoethanol (16 .mu.L, 26.9 mmol). [0946] .sup.1H NMR (270 MHz,
CDCl.sub.3) .delta.(ppm): 1.34 (s, 9H), 2.17-2.28 (m, 3H),
2.54-2.82 (m, 2H), 3.34-3.46(m, 3H), 3.72 (dd, J=4.0, 6.0 Hz, 2H),
3.96 (br q, J=7.0 Hz, 2H), 7.32-7.34 (m, 5H)
EXAMPLE 185
Compound 195
[0946] [0947] Step 1: In a manner similar to that in Step 1 of
Example 1, 2-acetoxy-1-indanone=thiosemicarbazone (3.23 g, 57%) was
obtained from 2-acetoxy-1-indanone (4.1 g, 21.6 mmol) and
thiosemicarbazide hydrochloride (3.0 g, 23.7 mmol). [0948] Step 2:
In a manner similar to that in Step 2 of Example 1,
3-acetyl-5-aminospiro[1,3,4-thiadiazolin-2,1'-indan]-2'-yl acetate
(187.4 mg, 48%) was obtained from
2-acetoxy-1-indanone=thiosemicarbazone (335.5 mg, 1.27 mmol)
prepared above, pyridine (13 mL) and acetic anhydride (136 .mu.L,
1.53 mmol). [0949] Step 3:
3-Acetyl-5-aminospiro[1,3,4-thiadiazolin-2,1'-indan]-2'-yl acetate
(163.8 mg) prepared above was dissolved in dichloromethane (2.0
mL). To the solution was added pyridine (520 .mu.L, 6.44 mmol) and
pivaloyl chloride (661 .mu.L, 5.36 mmol), and the mixture was
stirred at room temperature for 24 hours. To the reaction mixture
was added water and chloroform, and the mixture was extracted with
chloroform. The organic layer was washed with saturated aqueous
sodium chloride, and then dried over anhydrous sodium sulfate, and
the solvent was evaporated under reduced pressure. The residue was
purified by silica gel column chromatography (chloroform/ethyl
acetate=3/2) to obtain Compound 195 (118.0 mg, 57%) as a
diastereoisomer mixture. [0950] AP-MS (m/z): 390 (M.sup.++1)
EXAMPLE 186
Compound 196
[0951] Compound 195 (90.3 mg, 0.233 mmol) prepared in Example 185
was dissolved in methanol solution of 10% ammonia (4.8 mL), and the
solution was allowed to stand at room temperature for 6 hours. The
reaction mixture was concentrated, and then the residue was
purified by silica gel column chromatography (chloroform/ethyl
acetate=3/2) to obtain Compound 196 (16.6 mg, 20%) as a
diastereoisomer mixture. [0952] FAB-MS (m/z): 348 (M.sup.++1)
EXAMPLE 187
Compound 197
[0952] [0953] Step 1: In a manner similar to that in Step 1 of
Example 1, 4-acetoxy-1-indanone=thiosemicarbazone (2.78 g, 80%) was
obtained from 4-acetoxy-1-indanone (2.51 g, 13.2 mmol) and
thiosemicarbazide hydrochloride (1.85 g; 14.5 mmol). [0954] Step 2:
In a manner similar to that in Example 11, Compound 197 (193.9 mg,
39%) was obtained from 4-acetoxy-1-indanone=thiosemicarbazone
(364.5 mg, 1.38 mmol) prepared above, acetic anhydride (123 .mu.L,
1.38 mmol) and pyridine (112 .mu.L, 1.38 mmol). [0955] .sup.1H NMR
(300 MHz, CDCl.sub.3) .delta.(ppm): 2.18 (s, 3H), 2.30 (s, 3H),
2.59-2.68 (m, 1H), 2.76-2.86 (m, 1H), 3.09-3.30 (m, 2H), 4.17 (br
s, 2H), 6.99 (dd, J=7.7, 1.5 Hz, 1H), 7.31 (m, 2H)
EXAMPLE 188
Compound 198
[0956] In a manner similar to that in Example 15, Compound 198 (136
mg, 98%) was obtained from Compound 197 (108.8 mg, 0.356 mmol)
prepared in Example 187, pyridine (346 .mu.L, 4.28 mmol) and
pivaloyl chloride (439 .mu.L, 3.56 mmol). [0957] .sup.1H NMR (270
MHz, CDCl.sub.3) .delta.(ppm): 1.34 (s, 9H), 2.18 (s, 3H), 2.29 (s,
3H), 2.56-2.63 (m, 1H), 2.79-2.92 (m, 1H), 3.08-3.22 (m, 2H),
6.98-7.03 (m, 1H), 7.28-7.31 (m, 2H), 8.08 (br s, 1H)
EXAMPLE 189
Compound 199
[0958] In a manner similar to that in Example 186, Compound 199
(70.0 mg, 94%) was obtained from Compound 198 (83.1 mg,0.214 mmol)
prepared in Example 188 and methanol solution of 10% ammonia (4.2
mL). [0959] .sup.1H NMR (300 MHz, CDCl.sub.3) .delta.(ppm): 1.34
(s, 9H), 2.21 (s, 3H), 2.58-2.67 (m, 1H), 2.81-2.91 (m, 1H),
3.07-3.27 (m, 2H), 5.25 (br s, 1H), 6.62 (d, J=7.7 Hz, 1H), 6.94
(d, J=7.7 Hz, 1H), 7.10 (t, J=7.7 Hz, 1H), 7.99 (br s, 1H)
EXAMPLE 190
Tablets
[0960] Tablets comprising the following composition are obtained
according to the conventional method. TABLE-US-00015 Compound 1 5
mg Lactose 60 mg Potato starch 30 mg Polyvinyl alcohol 2 mg
Magnesium stearate 1 mg Tar dye trace
INDUSTRIAL APPLICABILITY
[0961] The present invention provides a thiadiazoline derivative or
a pharmacologically acceptable salt thereof which is useful for
therapeutic treatment of a human malignant tumor, for example,
breast cancer, gastric cancer, ovarian cancer, colon cancer, lung
cancer, brain tumor, laryngeal cancer, hematological cancer,
urinary or genital tumor including bladder cancer and prostatic
cancer, renalcancer, skin carcinoma, hepatic carcinoma, pancreatic
cancer, or uterine cancer, or the like. In addition, the present
invention provides an antitumor agent comprising a thiadiazoline
derivative or a pharmacologically acceptable salt thereof as an
active ingredient.
* * * * *