U.S. patent application number 10/771847 was filed with the patent office on 2007-02-01 for novel substituted 2,3-benzodiazepine derivatives.
Invention is credited to Gizella Abraham, Fenrec Andrasi, Pal Berzsenyl, Tamas Hamori, Istvan Kurucz, Sandor Solyom.
Application Number | 20070027143 10/771847 |
Document ID | / |
Family ID | 32771128 |
Filed Date | 2007-02-01 |
United States Patent
Application |
20070027143 |
Kind Code |
A1 |
Solyom; Sandor ; et
al. |
February 1, 2007 |
Novel substituted 2,3-benzodiazepine derivatives
Abstract
The invention relates to new 2,3-benzodiazepine derivatives of
formula (I), isomers and acid addition salts thereof and to
pharmaceutical compositions containing the same, as well as to
pharmaceutical compositions and methods of using the same suitable
for treating conditions associated with muscle spasms, epilepsy,
acute and chronic forms of neurodegenerative diseases as well as
preventing, treating or alleviating the symptoms of acute and
chronic inflammatory disorders.
Inventors: |
Solyom; Sandor; (Budapest,
HU) ; Abraham; Gizella; (Budapest, HU) ;
Hamori; Tamas; (Budapest, HU) ; Berzsenyl; Pal;
(Budapest, HU) ; Andrasi; Fenrec; (Budapest,
HU) ; Kurucz; Istvan; (Budapest, HU) |
Correspondence
Address: |
LERNER, DAVID, LITTENBERG,;KRUMHOLZ & MENTLIK
600 SOUTH AVENUE WEST
WESTFIELD
NJ
07090
US
|
Family ID: |
32771128 |
Appl. No.: |
10/771847 |
Filed: |
February 3, 2004 |
Related U.S. Patent Documents
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Application
Number |
Filing Date |
Patent Number |
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10358053 |
Feb 4, 2003 |
6858605 |
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10771847 |
Feb 3, 2004 |
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Current U.S.
Class: |
514/220 ;
514/221; 540/560; 540/567 |
Current CPC
Class: |
A61P 3/10 20180101; A61P
25/16 20180101; A61P 13/02 20180101; C07D 491/04 20130101; A61P
11/08 20180101; A61P 11/06 20180101; A61P 43/00 20180101; A61P
21/04 20180101; A61P 13/10 20180101; A61P 11/02 20180101; A61P
11/00 20180101; A61P 25/00 20180101; A61P 25/08 20180101; A61P
29/00 20180101; A61P 25/28 20180101; A61P 37/08 20180101; C07D
243/02 20130101; C07D 417/04 20130101; A61P 19/08 20180101; A61P
21/02 20180101; A61P 27/16 20180101; A61P 25/14 20180101; A61P
27/06 20180101; A61P 9/10 20180101 |
Class at
Publication: |
514/220 ;
514/221; 540/567; 540/560 |
International
Class: |
A61K 31/5513 20070101
A61K031/5513; A61K 31/551 20070101 A61K031/551; C07D 491/02
20070101 C07D491/02 |
Claims
1. A compound of formula (I), wherein ##STR8## R.sup.3 represents a
substituted or unsubstituted 5- or 6-membered, aromatic, saturated
or partially saturated heterocyclic ring containing at least 2
hetero atoms, in which the hetero atom can be oxygen-, sulfur- or
nitrogen atom and in the case when the heterocyclic ring contains 2
heteroatoms one of them is different from nitrogen; R.sup.4,
R.sup.5, R.sup.6, and R.sup.7 independently from each other
represent hydrogen atom, halogen atom, C.sub.1-C.sub.3 alkyl group,
nitro group, amino group, wherein the amino group can be
substituted independently from each other with one or two
C.sub.1-C.sub.3 alkyl group, C.sub.2-C.sub.5 acyl group, or
C.sub.2-C.sub.5 alkoxycarbonyl group, or aminocarbonyl group, or
C.sub.2-C.sub.5alkylaminocarbonyl group, R.sup.9 represents
C.sub.1-C.sub.3 alkoxy group or halogen atom, R.sup.10 represents
hydrogen or halogen atom or R.sup.9 and R.sup.10 together can be
C.sub.1-C.sub.3 alkylendioxy group; and stereoisomers and
acid-addition salts of said compound.
2. The compound according to claim 1, wherein the heterocyclic ring
of R.sup.3 can be further substituted with one or more
C.sub.1-C.sub.5 alkyl group, a C.sub.2-C.sub.3 alkenyl, a
C.sub.3-C.sub.7 cycloalkyl, a trifluoromethyl, a C.sub.1-C.sub.3
alkoxy or a phenyl group, an oxo, a formyl, a carboxyl or a
C.sub.2-C.sub.4 alkoxycarbonyl group, a C.sub.1-C.sub.3
alkoxymethyl group, a halogen atom a hydroxymethyl group, wherein
the hydroxyl group can be alkylated or acylated, a C.sub.1-C.sub.3
alkylthiomethyl group, a cyanomethyl group or an aminomethyl group,
wherein the amino group can be alkylated or acylated.
3. The compound according to claim 1, wherein R.sup.3 is selected
from the group of substituted and unsubstituted isoxazole,
isothiazole, thiazole, thiazoline, 4-thiazolinone, oxazole,
oxazoline, 1,2,3-thiadiazole, 1,3,4-thiadiazole,
1,3,4-thiadiazolin-2-one, 1,2,4-thiadiazolin-3-one,
1,4,2-oxathiazoline, 1,3,4-oxadiazole, 1,2,3-triazole,
1,3,4-triazole, 1,2,3,4-thiatriazole, tetrazole, 1,3-thiazin-4-one
and 1,3,4-thiadiazin-4-one ring.
4. The compound according to claim 1, wherein R.sup.3 is a
substituted or unsubstituted 1,3,4-thiadiazol-2-yl,
4,5-dihydro-thiazol-2-yl, 2-thiazolyl or 1,3,4-oxadiazolyl group,
R.sup.5 is a hydrogen atom or methyl group, R.sup.6 substituent is
an amino group, and R.sup.9 and R.sup.10 represent together a
methylenedioxy group, or R.sup.9 is a chlorine atom or methoxy
group and R.sup.10 is a hydrogen or chlorine atom.
5. The compound according to claim 1 selected from the group
consisting of
(R)-5-(4-aminophenyl)-8-methyl-7-(5-methyl-1,3,4-thiadiazol-2-yl)-8,9--
dihydro-7H-1,3-dioxolo[4,5-h][2,3]benzodiazepine;
(R)-5-(4-aminophenyl)-8-methyl-7-(1,3,4-thiadiazol-2-yl)-8,9-dihydro-7H-1-
,3-dioxolo[4,5-h][2,3]benzodiazepine;
(R)-5-(4-aminophenyl)-8-methyl-7-(2-thiazolyl)-8,9-dihydro-7H-1,3-dioxolo-
[4,5-h][2,3]benzodiazepine;
(R)-5-(4-aminophenyl)-7-(4,5-dihydro-thiazol-2-yl)-8-methyl-8,9-dihydro-7-
H-1,3-dioxolo[4,5-h][2,3]benzodiazepine;
(R)-5-(4-aminophenyl)-7-(5-ethyl-1,3,4-thiadiazol-2-yl)-8-methyl-8,9-dihy-
dro-7H-1,3-dioxolo[4,5-h][2,3]benzodiazepine;
(R)-5-(4-aminophenyl)-8-methyl-7-(5-methyl-1,3,4-oxadiazol-2-yl)-8,9-dihy-
dro-7H-1,3-dioxolo[4,5-h][2,3]benzodiazepine;
(R)-5-(4-amino-3-methylphenyl)-8-methyl-7-(5-methyl-1,3,4-thiadiazol-2-yl-
)-8,9-dihydro-7H-1,3-dioxolo-[4,5-h][2,3]benzo-diazepine;
(R)-5-(4-Amino-3-methylphenyl)-7-(5-ethyl-1,3,4-thiadiazol-2-yl)-8-methyl-
-8,9-dihydro-7H-1,3-dioxolo-[4,5-h][2,3]benzodiazepine;
(R)-5-(4-amino-3-methylphenyl)-8-methyl-7-(5-propyl-1,3,4-thiadiazol-2-yl-
)-8,9-dihydro-7H-1,3-dioxolo[4,5-h][2,3]benzo-diazepine;
(R)-5-(4-amino-3-methylphenyl)-8-methyl-7-(1,3,4-thiadiazol-2-yl)-8,9-dih-
ydro-7H-1,3-dioxolo-[4,5-h][2,3]benzodiazepine;
(R)-5-(4-amino-3-methylphenyl-8-methyl-7-(5-methoxymethyl-1,3,4-thiadiazo-
l-2-yl)-8,9-dihydro-7H-1,3-dioxolo-[4,5-h][2,3]benzo-diazepine;
(R)-5-(4-amino-3-methylphenyl)-8-methyl-7-{5-[1-(1E)-propen-1-yl]-1,3,4-t-
hiadiazol-2-yl}-8,9-dihydro-7H-1,3-dioxolo[4,5-h][2,3]benzodiazepine;
(R)-5-(4-amino-3-chlorophenyl)-8-methyl-7-(5-methyl-1,3,4-thiadiazol-2-yl-
)-8,9-dihydro-7H-1,3-dioxolo-[4,5-h][2,3]benzodiazepine; and
(R)-5-(4-amino-3-chlorophenyl)-8-methyl-7-(5-methoxy-methyl-1,3,4-thiadia-
zol-2-yl)-8,9-dihydro-7H-1,3-dioxolo[4,5-h][2,3]benzodiazepine and
the acid addition salts thereof.
6. The compound according to claim 1, wherein the compound is
(R)-5-(4-amino-3-methylphenyl)-8-methyl-7-(5-methyl-1,3,4-thiadiazol-2-yl-
)-8,9-dihydro-7H-1,3-dioxolo-[4,5-h][2,3]benzodiazepine or the
addition salt thereof.
7. The compound according to claim 1, wherein the compound is
(R)-5-(4-amino-3-methylphenyl)-7-(5-ethyl-1,3,4-thiadiazol-2-yl)-8-methyl-
-8,9-dihydro-7H-1,3-dioxolo-[4,5-h][2,3]benzodiazepine or the acid
addition salt thereof.
8. The compound according to claim 1, wherein the compound is
(R)-5-(4-amino-3-methylphenyl)-8-methyl-7-(5-propyl-1,3,4-thiadiazol-2-yl-
)-8,9-dihydro-7H-1,3-dioxolo[4,5-h][2,3]benzodiazepine or the acid
addition salt thereof.
9. The compound according to claim 1, wherein the compound is
(R)-5-(4-amino-3-methylphenyl)-8-methyl-7-(1,3,4-thiadiazol-2-yl)-8,9-dih-
ydro-7H-1,3-dioxolo-[4,5-h][2,3]benzodiazepine or the acid addition
salt thereof.
10. The compound according to claim 1, wherein the compound is
(R)-5-(4-amino-3-methylphenyl)-8-methyl-7-(5-methoxymethyl-1,3,4-thiadiaz-
ol-2-yl)-8,9-dihydro-7H-1,3-dioxolo-[4,5-h][2,3]benzodiazepine or
the acid addition salt thereof.
11. The compound according to claim 1, wherein the compound is
(R)-5-(4-amino-3-methylphenyl)-8-methyl-7-{5-[1-(1E)-propen-1-yl]-1,3,4-t-
hiadiazol-2-yl}-8,9-dihydro-7H-1,3-dioxolo[4,5-h][2,3]benzodiazepine
or the acid addition salt thereof.
12. The compound according to claim 1, wherein the compound is
(R)-5-(4-amino-3-chlorophenyl)-8-methyl-7-(5-methyl-1,3,4-thiadiazol-2-yl-
)-8,9-dihydro-7H-1,3-dioxolo-[4,5-h][2,3]benzodiazepine or the acid
addition salt thereof.
13. The compound according to claim 1, wherein the compound is
(R)-5-(4-amino-3-chlorophenyl)-8-methyl-7-(5-methoxymethyl-1,3,4-thiadiaz-
ol-2-yl)-8,9-dihydro-7H-1,3-dioxolo[4,5-h][2,3]benzodiazepine or
the acid addition salts thereof.
14. A pharmaceutical composition, comprising a compound of formula
(I) according to any one of claims 1 to 14, or a stereoisomer or a
pharmaceutically acceptable salt thereof.
15. A method for treating glutamate dysfunction associated with an
acute or chronic neurodegenerative disease, comprising
administering to a subject in need of such treatment a
therapeutically effective amount of a compound of claim 1.
16. The method of claim 8, wherein the neurodegenerative disease is
selected from the group consisting of cerebral ischemia (stroke),
brain and spinal cord trauma, Alzheimer's disease, Huntington's
disease, amyotrophic lateral sclerosis, AIDS-induced dementia,
essential tremor, Parkinson's disease, multiple sclerosis and
urinary incontinence.
17. A method for treating epilepsy comprising administering to a
subject in need of such treatment a therapeutically effective
antiepileptic amount of a compound of claim 1.
18. A method for reducing muscle spasms comprising administering to
a subject in need of such treatment a therapeutically effective
muscle relaxing amount of a compound of claim 1.
19. A method for treating acute and chronic inflammatory disorders,
comprising administering to a mammal in need of such treatment a
therapeutically effective anti-inflammatory amount of a compound of
claim 1.
20. The method of claim 19 wherein the inflammatory disorder
treated is an allergic inflammatory disorder of the airways.
21. The method of claim 20 wherein the allergic inflammatory
disorders of the airways is selected from the group consisting of
allergic rhinitis, intrinsic or extrinsic asthma bronchiale, acute
or chronic bronchitis, chronic obstructive pulmonary disease and
pulmonary fibrosis.
22. A method for relief of pathological pain comprising
administering to a subject in need of such treatment a pain
reducing therapeutically effective amount of a compound of claim
1.
23. A method for treating glutamate dysfunction in acute or chronic
disease of the eyes associated with glutamate dysfunction,
comprising administering to a subject in need of such treatment a
therapeutically effective amount of a compound of claim 1.
24. The method of claim 23, wherein the disease treated is selected
from glaucoma or diabetic retinopathy.
Description
CROSS-REFERENCE TO RELATED APPLICATIONS
[0001] This application is a continuation-in-part of application
Ser. No. 10/358,053, filed Feb. 4, 2003.
BACKGROUND OF THE INVENTION
[0002] 1. Field of Invention
[0003] The invention relates to new 2,3-benzodiazepine derivatives
substituted by heterocycles, the acid addition salts thereof, as
well as the pharmaceutical compositions containing them. The
invention also relates to the use of said compounds as AMPA
receptor antagonists.
[0004] 2. Summary of Related Art
[0005] Over-activation of glutamate receptors has been associated
with several acute and chronic diseases of the central nervous
system ("CNS"). Various glutamate receptor antagonists have been
investigated as therapeutic modalities (see for example Parsons et
al., Drug News Perspect. 11:523 (1998) and Br{hacek over
(a)}uner-Osborne et al., J. Med. Chem. 43:2609 (2000)).
[0006] AMPA (2-amino-3-(3-hydroxy-5-methyl-4 isoxazolyl)-propionic
acid) type glutamate receptors play a major role in a variety of
central nervous system disorders. Inhibition of the activation of
AMPA type receptors has been shown to have neuroprotective,
antiepileptic and muscle-relaxant effects (see e.g., Cerebrovasc.
Brain Metab. Rev. 6:225 (1994); Neurology 44 Suppl. 8, S14 (1994);
J. Pharmacol. Exp. Ther. 260:742 (1992)).
[0007] Glutamate receptors have been found not only in the CNS but
also in peripheral tissues indicating therapeutic potential
opportunities beyond the CNS (see e.g., Skery et al, Trends in
Pharm. Sci., 22:74 (2001). Respiratory tract inflammation has been
postulated to be beneficially influenced by NMDA-type glutamate
antagonists (Said, Trends in Pharm. Sci. 20:132 (1999); and Said et
al., Trends in Pharm. Sci., 22:344 (2001)).
[0008] AMPA type receptors can be inhibited by various competitive
and non-competitive antagonists. The therapeutic potential of
non-competitive antagonists may be superior to that of competitive
ones insofar as their activity is not dependent on high
concentrations of endogenous glutamate (see e.g., Vizi et al., CNS
Drug Reu, 2:91 (1996)). One of the most prominent non-competitive
AMPA receptor antagonists is
5-(4-aminophenyl)-8-methyl-9H-1,3-dioxolo[4,5-h][2,3]benzodiazepine
(also designated as GYKI 52466) possessing remarkable
antiepileptic, muscle relaxant and neuroprotective activities.
(Tarnawa et al. Eur. J. Pharmacol., 167:193 (1989); Smith, et al,
Eur. J. Pharmacol., 187:131 (1990); Quardouz et al., Neurosci.
Lett., 125:5 (1991); Donevan et al., I. Neuron., 10:51 (1993)).
[0009] Several non-competitive AMPA antagonists have been described
in the literature including 3,4-dihydro-5H- or
4,5-dihydro-3H-2,3-benzodiazepines, containing an acyl group at
position 3 of the ring (see e.g., Hungarian Patent Nos. 206,719 B
and 219,777 B, U.S. Pat. No. 5,536,832, European Patent Publication
No. 0699 677 A1, and British Patent No. 2 311 779, as well as WO
96/04 283, WO 97/28 135, WO 99/07 707, WO 99/07 708 and WO 01/04
122). WO 96/06 606 (corresponding to U.S. Pat. No. 5,795,886)
describes several 2,3-benzodiazepine derivatives having aryl and
heteroaryl substituents (e.g., pyridyl, thienyl, furyl, phenyl,
imidazolyl, benzimidazolyl, etc.) at C3.
[0010] The compounds listed above have been found to be
particularly useful in diseases in which the over-function of the
glutamate system can be detected. Such acute disorders of the CNS
include for example stroke, brain ischemia, brain and spinal cord
injuries, perinatal hypoxia, hypoglycemic nervous damage, etc.
Additional chronic illnesses in which selected AMPA antagonists can
be applied include e.g., Alzheimer's disease, Huntington's disease,
amyotrophic lateral sclerosis, AIDS-induced dementia, glaucoma,
diabetic retinopathy as well as Parkinson's disease. Furthermore,
enhanced activity of the glutamate system has also been shown in
conditions associated with neural damage (e.g., epilepsy, migraine,
urinary bladder incontinence, psychosis--anxiety, schizophrenia
etc., drug-abuse, pathological pain, brain edema and tardive
dyskinesia) implying an impressive therapeutic potential for AMPA
antagonists.
[0011] Recently, experimental data suggested that selected AMPA
antagonists have beneficial effect on the autoimmune
encephalomyelitis elicited in rats, which is the accepted model of
multiple sclerosis (Smith et al., Nature Medicine 6:62 (2000)). In
addition, AMPA and NMDA receptors in the spinal cord have been
implicated in the contraction of the bladder and the urethra,
suggesting that AMPA antagonists may be useful in the treatment of
urinary incontinence (Nishizawa et al., A du in Exp. Med. &
Biol. 4:275 (1999)).
[0012] Two 2,3-benzodiazepine derivatives GYKI 52466 (supra), and
(R)-7-acetyl-5-(4-aminophenyl)-8,9-dihydro-8-methyl-7H-1,3-dioxolo[4,5-h]-
[2,3]benzodiazepine (GYKI 53773, also known as Talampanel) were
beneficial. The latter has proved to be active in clinical trials
on epilepsy patients (Bialer et al., Epilepsy Res. 43:11
(2001)).
[0013] In addition, GYKI 52466 has been reported to inhibit growth
of selected tumor cell types (colon adenocarcinoma, astrocytoma,
breast carcinoma, lung carcinoma and neuroblastoma) (Rzeski et al.,
Proc. Nat. Acad. Sci. 98:6372 (2001)).
SUMMARY OF THE INVENTION
[0014] The invention relates to new 2,3-benzodiazepine derivatives
of formula (I) below, isomers and acid addition salts thereof and
to pharmaceutical compositions containing the same, ##STR1##
wherein the substituent meanings are as follows:
[0015] R.sup.3 represents a substituted or unsubstituted 5- or
6-membered, aromatic, saturated or partially saturated heterocyclic
ring containing at least 2 heteroatoms, in which the heteroatom can
be oxygen-, sulfur- or nitrogen atom and in the case when the
heterocyclic ring contains 2 heteroatoms one of them is different
from nitrogen;
[0016] R.sup.4, R.sup.5, R.sup.6 and R.sup.7 independently from
each other represent hydrogen atom, halogen atom, C.sub.1-C.sub.3
alkyl group, nitro group or amino group, wherein the amino group
can be substituted independently from each other with one or two
C.sub.1-C.sub.3 alkyl group, C.sub.2-C.sub.5 acyl group, or
C.sub.2-C.sub.5 alkoxycarbonyl group, or aminocarbonyl group, or
C.sub.2-C.sub.5 alkylaminocarbonyl group; and
[0017] R.sup.9 represents C.sub.1-C.sub.3 alkoxy group or halogen
atom
[0018] R.sup.10 represents hydrogen or halogen atom or
[0019] R.sup.9 and R.sup.10 together can be C.sub.1-C.sub.3
alkylendioxy group.
[0020] Representative compounds include, without limitation,
(R)-5-(4-aminophenyl)-8-methyl-7-(5-methyl-1,3,4-thiadiazol-2-yl)-8,9-dih-
ydro-7H-1,3-dioxolo[4,5-h][2,3]benzodiazepine;
(R)-5-(4-aminophenyl)-8-methyl-7-(1,3,4-thiadiazol-2-yl)-8,9-dihydro-7H-1-
,3-dioxolo[4,5-h][2,3]benzodiazepine;
(R)-5-(4-aminophenyl)-8-methyl-7-(2-thiazolyl)-8,9-dihydro-7H-1,3-dioxolo-
[4,5-h][2,3]benzodiazepine;
(R)-5-(4-aminophenyl)-7-(4,5-dihydro-thiazol-2-yl)-8-methyl-8,9-dihydro-7-
H-1,3-dioxolo[4,5-h][2,3]benzodiazepine;
(R)-5-(4-aminophenyl)-7-(5-ethyl-1,3,4-thiadiazol-2-yl)-8-methyl-8,9-dihy-
dro-7H-1,3-dioxolo[4,5-h][2,3]benzodiazepine;
(R)-5-(4-aminophenyl)-8-methyl-7-(5-methyl-1,3,4-oxadiazol-2-yl)-8,9-dihy-
dro-7H-1,3-dioxolo[4,5-h][2,3]benzodiazepine;
(R)-5-(4-amino-3-methylphenyl-8-methyl-7-(5-methyl-1,3,4-thiadiazol-2-yl)-
-8,9-dihydro-7H-1,3-dioxolo-[4,5-h][2,3]benzodiazepine;
(R)-5-(4-amino-3-methylphenyl)-7-(5-ethyl-1,3,4-thiadiazol-2-yl)-8-methyl-
-8,9-dihydro-7H-1,3-dioxolo-[4,5-h][2,3]benzodiazepine;
(R)-5-(4-amino-3-methylphenyl)-8-methyl-7-(5-propyl-1,3,4-thiadiazol-2-yl-
)-8,9-dihydro-7H-1,3-dioxolo[4,5-h][2,3]benzo-diazepine;
(R)-5-(4-amino-3-methylphenyl)-8-methyl-7-(1,3,4-thiadiazol-2-yl)-8,9-dih-
ydro-7H-1,3-dioxolo-[4,5-h][2,3]benzodiazepine;
(R)-5-(4-amino-3-methylphenyl)-8-methyl-7-(5-methoxymethyl-1,3,4-thiadiaz-
ol-2-yl)-8,9-dihydro-7H-1,3-dioxolo-[4,5-h][2,3]benzodiazepine;
(R)-5-(4-amino-3-methylphenyl)-8-methyl-7-{5-[1-(1E)-propen-1-yl]-1,3,4-t-
hiadiazol-2-yl}-8,9-dihydro-7H-1,3-dioxolo[4,5-h][2,3]benzodiazepine;
(R)-5-(4-amino-3-chlorophenyl)-8-methyl-7-(5-methyl-1,3,4-thiadiazol-2-yl-
)-8,9-dihydro-7H-1,3-dioxolo-[4,5-h][2,3]benzodiazepine; and
(R)-5-(4-amino-3-chlorophenyl)-8-methyl-7-(5-methoxymethyl-1,3,4-thiadiaz-
ol-2-yl)-8,9-dihydro-7H-1,3-dioxolo[4,5-h][2,3]benzodiazepine and
the acid addition salts thereof.
[0021] The invention also discloses pharmaceutical compositions
comprising a compound of formula (I) as the active ingredient,
wherein the meaning of R.sup.3-R.sup.7, R.sup.9 and R.sup.10 is as
defined herein, or a steroisomer or a pharmaceutically acceptable
salt thereof together with pharmaceutically acceptable solvents,
diluents, carriers and filling materials.
[0022] The compounds are suitable for treating conditions
associated with muscle spasms, epilepsy, acute and chronic forms of
neurodegenerative diseases as well as preventing, treating or
alleviating the symptoms of acute and chronic inflammatory
disorders.
[0023] One of skill will appreciate, in light of the many
publications relating to the expanding therapeutic values of AMPA
type receptor antagonists, that the compounds of the invention are
useful in a very large number of unrelated conditions.
[0024] Hence, methods for treating glutamate dysfunction associated
with an acute or chronic neurodegenerative disease or in acute or
chronic disease of the eyes associated with glutamate dysfunction
are provided. Representative neurodegenerative disorders include,
for example, cerebral ischemia (stroke), brain and spinal cord
trauma, Alzheimer's disease, Huntington's disease, amyotrophic
lateral sclerosis, AIDS-induced dementia, essential tremor,
Parkinson's disease, multiple sclerosis and urinary incontinence.
Acute or chronic disorders of the eyes associated with glutamate
dysfunction include glaucoma or diabetic retinopathy. Disclosed
also are methods for treating epilepsy, reducing muscle spasms,
reducing pain, or inflammatory disorders which comprise
administering to the subject in need of such treatment a
therapeutically effective amount of the compounds of the invention.
Included among the inflammatory disorders are allergic inflammatory
disorders of the airways which can encompass allergic rhinitis,
intrinsic or extrinsic asthma bronchiale, acute or chronic
bronchitis, chronic obstructive pulmonary disease and pulmonary
fibrosis.
DETAILED DESCRIPTION OF THE INVENTION
[0025] The patents, published applications, and scientific
literature referred to herein establish the knowledge of those
skilled in the art and are hereby incorporated by reference in
their entirety to the same extent as if each was specifically and
individually indicated to be incorporated by reference. Any
conflict between any reference cited herein and the specific
teachings of this specifications shall be resolved in favor of the
latter. Likewise, any conflict between an art-understood definition
of a word or phrase and a definition of the word or phrase as
specifically taught in this specification shall be resolved in
favor of the latter.
[0026] The invention discloses novel substituted 2,3-benzodiazepine
derivative compounds and methods of making the same. Pharmaceutical
compositions employing the novel substituted 2,3-benzodiazepine
derivative compounds and their use for the treatment for a number
of disease conditions are also disclosed.
[0027] Technical and scientific terms used herein have the meaning
commonly understood by one of skill in the art to which the present
invention pertains, unless otherwise defined. Reference is made
herein to various methodologies and materials known to those of
skill in the art. Standard reference works setting forth the
general principles of pharmacology include Goodman and Gilman's The
Pharmacological Basis of Therapeutics, 10.sup.th Ed., McGraw Hill
Companies Inc., New York (2001). Any suitable materials and/or
methods known to those of skill can be utilized in carrying out the
present invention. However, preferred materials and methods are
described. Materials, reagents and the like to which reference are
made in the following description and examples are obtainable from
commercial sources, unless otherwise noted.
[0028] As used in this specification, the singular forms "a", "an"
and "the" specifically also encompass the plural forms of the terms
to which they refer, unless the content clearly dictates otherwise.
For example, reference to "an antagonist" includes mixtures of
antagonists.
[0029] As used in this specification, whether in a transitional
phrase or in the body of the claim, the terms "comprise(s)" and
"comprising" are to be interpreted as having an open-ended meaning.
That is, the terms are to be interpreted synonymously with the
phrases "having at least" or "including at least". When used in the
context of a process, the term "comprising" means that the process
includes at least the recited steps, but may include additional
steps. When used in the context of a compound or composition, the
term "comprising" means that the compound or composition includes
at least the recited features or components, but may also include
additional features or components.
[0030] The term "about" is used herein to mean approximately, in
the region of, roughly, or around. When the term "about" is used in
conjunction with a numerical range, it modifies that range by
extending the boundaries above and below the numerical values set
forth. In general, the term "about" is used herein to modify a
numerical value above and below the stated value by a variance of
20%.
[0031] As used herein, unless specifically indicated otherwise, the
word "or" is used in the "inclusive" sense of "and/or" and not the
"exclusive" sense of "either/or".
[0032] As used herein, the recitation of a numerical range for a
variable is intended to convey that the invention may be practiced
with the variable equal to any of the values within that range.
Thus, for a variable which is inherently discrete, the variable can
be equal to any integer value of the numerical range, including the
end-points of the range. Similarly, for a variable which is
inherently continuous, the variable can be equal to any real value
of the numerical range, including the end-points of the range. As
an example, a variable which is described as having values between
0 and 2, can be 0, 1 or 2 for variables which are inherently
discrete, and can be 0.0, 0.1, 0.01, 0.001, or any other real value
for variables which are inherently continuous.
[0033] The methods of the present invention are intended for use
with any mammal that may experience the benefits of the methods of
the invention. Foremost among such mammals are humans, although the
invention is not intended to be so limited, and is applicable to
veterinary uses. Thus, in accordance with the invention, "mammals"
or "mammal in need" include humans as well as non-human mammals,
particularly domesticated animals including, without limitation,
cats, dogs, and horses.
[0034] It will be understood that the subject to which a compound
of the invention is administered need not suffer from a specific
traumatic state. Indeed, the compounds of the invention may be
administered prophylactically, prior to any development of
symptoms. The term "therapeutic", "therapeutically", and
permutations of these terms are used to encompass therapeutic,
palliative as well as prophylactic uses. Hence, as used herein, by
"treating or alleviating the symptoms" is meant reducing,
preventing, and/or reversing the symptoms of the individual to
which a compound of the invention has been administered, as
compared to the symptoms of an individual receiving no such
administration.
[0035] Benzodiazepines of formula (II) below, and the isomers as
well as the acid addition salts thereof, are the subject of patent
application Ser. No. 10/358,053: ##STR2## wherein
[0036] R.sup.1 and R.sup.2 independently of each other represent
hydrogen atom or C.sub.1-C.sub.3 alkyl group,
[0037] R.sup.3 represents substituted or unsubstituted 5- or
6-membered, aromatic, saturated or partially saturated heterocyclic
ring containing at least 2 hetero atoms, in which the hetero atom
can be oxygen-, sulfur- or nitrogen atom and in the case when
R.sup.3 is a 5-membered ring one of the heteroatoms is different
from nitrogen;
[0038] R.sup.4, R.sup.5, R.sup.6, R.sup.7 and R.sup.8 independently
from each other represent hydrogen atom, halogen atom,
C.sub.1-C.sub.3 alkyl group, nitro group or amino group, wherein
the amino group can be substituted independently from each other
with one or two C.sub.1-C.sub.3 alkyl group, C.sub.2-C.sub.5 acyl
group, or C.sub.2-C.sub.5 alkoxycarbonyl group, or aminocarbonyl
group, or C.sub.2-C.sub.5 alkylaminocarbonyl group,
[0039] R.sup.9 represents C.sub.1-C.sub.3 alkoxy group or halogen
atom,
[0040] R.sup.10 represents hydrogen or halogen atom or
[0041] R.sup.9 and R.sup.10 together can be C.sub.1-C.sub.3
alkylendioxy group.
[0042] The present invention is directed to 2,3-benzodiazepine
derivatives of formula (II) as shown below in formula (I): ##STR3##
wherein R.sup.1 and R.sup.8 are hydrogen, R.sup.2 is CH.sub.3, the
meaning of R.sup.4, R.sup.5, R.sup.6, R.sup.7, R.sup.9 and R.sup.10
is as defined above, R.sup.3 is a moiety selected from the group
consisting of substituted or unsubstituted isoxazole, isothiazole,
thiazole, thiazoline, 4-thiazolinone, oxazole, oxazoline,
1,2,3-thiadiazole, 1,3,4-thiadiazole, 1,3,4-thiadiazolin-2-one,
1,2,4-thiadiazolin-3-one, 1,4,2-oxathiazoline, 1,3,4-oxadiazole,
1,2,3-triazole, 1,3,4-triazole, 1,2,3,4-thiatriazole, tetrazole,
1,3-thiazin-4-one and 1,3,4-thiadiazin-4-one ring.
[0043] The heterocyclic substituent of the benzodiazepine ring as
R.sup.3 can be further substituted--among others--with one or more
C.sub.1-C.sub.6 alkyl group, C.sub.2-C.sub.3 alkenyl, a
C.sub.3-C.sub.7 cycloalkyl, a trifluoromethyl, a C.sub.1-C.sub.3
alkoxy or a phenyl group, an oxo, a formyl, a carboxyl or a
C.sub.2-C.sub.4 alkoxycarbonyl group, a C.sub.1-C.sub.3
alkoxymethyl group, a hydroxymethyl group, wherein the hydroxy
group can be alkylated or acylate, a C.sub.1-C.sub.3
alkylthiomethyl group, a cyanomethyl group or an aminomehtyl group,
wherein the amino group can be alkylated or acylated.
[0044] The meaning of alkyl group encompasses both straight and
branched chain alkyl groups. The meaning of alkenyl group can be
vinyl, 1-propenyl or 2-propenyl group. The meaning of halogen atom
can be fluorine, chlorine, bromine, or iodine atom. The amino group
can be unsubstituted or substituted with one or two alkyl groups,
as well as acylated with aliphatic or aromatic carboxylic acid or
any kind of carbonic acid esters.
[0045] In the case of compounds of formula (I), the term "isomers"
means both enantiomers, as well as the E and Z isomers if
applicable, furthermore, isomers shall include diastereomers,
tautomers and mixture of them, for example racemic mixture.
[0046] Salts of the compounds of formula (I) relate to
physiologically acceptable salts formed with inorganic or organic
acids. Suitable inorganic acids can be, for example, hydrochloric
acid, hydrobromic acid, phosphoric acid or sulfuric acid. Suitable
organic acids can be, for example, formic acid, acetic acid, maleic
and fumaric acid, succinic acid, lactic acid, tartaric acid, citric
acid or methanesulfonic acid.
[0047] Representative compounds of formula (a) include, without
limitation,
(R)-5-(4-aminophenyl)-8-methyl-7-(5-methyl-1,3,4-thiadiazol-2-yl)-8,9-dih-
ydro-7H-1,3-dioxolo[4,5-h][2,3]benzodiazepine;
(R)-5-(4-aminophenyl)-8-methyl-7-(1,3,4-thiadiazol-2-yl)-8,9-dihydro-7H-1-
,3-dioxolo[4,5-h][2,3]benzodiazepine;
(R)-5-(4-aminophenyl)-8-methyl-7-(2-thiazolyl)-8,9-dihydro-7H-1,3-dioxolo-
[4,5-h][2,3]benzodiazepine;
(R)-5-(4-aminophenyl)-7-(4,5-dihydro-thiazol-2-yl)-8-methyl-8,9-dihydro-7-
H-1,3-dioxolo[4,5-h][2,3]benzodiazepine;
(R)-5-(4-aminophenyl)-7-(5-ethyl-1,3,4-thiadiazol-2-yl)-8-methyl-8,9-dihy-
dro-7H-1,3-dioxolo[4,5-h][2,3]benzodiazepine;
(R)-5-(4-aminophenyl)-8-methyl-7-(5-methyl-1,3,4-oxadiazol-2-yl)-8,9-dihy-
dro-7H-1,3-dioxolo[4,5-h][2,3]benzodiazepine;
(R)-5-(4-amino-3-methylphenyl)-8-methyl-7-(5-methyl-1,3,4-thiadiazol-2-yl-
)-8,9-dihydro-7H-1,3-dioxolo-[4,5-h][2,3]benzo-diazepine;
(R)-5-(4-amino-3-methylphenyl)-7-(5-ethyl-1,3,4-thiadiazol-2-yl)-8-methyl-
-8,9-dihydro-7H-1,3-dioxolo-[4,5-h][2,3]benzodiazepine;
(R)-5-(4-amino-3-methylphenyl)-8-methyl-7-(5-propyl-1,3,4-thiadiazol-2-yl-
)-8,9-dihydro-7H-1,3-dioxolo[4,5-h][2,3]benzo-diazepine;
(R)-5-(4-amino-3-methylphenyl)-8-methyl-7-(1,3,4-thiadiazol-2-yl)-8,9-dih-
ydro-7H-1,3-dioxolo-[4,5-h][2,3]benzodiazepine;
(R)-5-(4-amino-3-methylphenyl)-8-methyl-7-(5-methoxymethyl-1,3,4-thiadiaz-
ol-2-yl)-8,9-dihydro-7H-1,3-dioxolo-[4,5-h][2,3]benzodiazepine;
(R)-5-(4-amino-3-methylphenyl)-8-methyl-7-{5-[1-(1E)-propen-1-yl]-1,3,4-t-
hiadiazol-2-yl}-8,9-dihydro-7H-1,3-dioxolo[4,5-h][2,3]benzodiazepine;
(R)-5-(4-amino-3-chlorophenyl)-8-methyl-7-(5-methyl-1,3,4-thiadiazol-2-yl-
)-8,9-dihydro-7H-1,3-dioxolo-[4,5-h][2,3]benzodiazepine; and
(R)-5-(4-amino-3-chlorophenyl)-8-methyl-7-(5-methoxymethyl-1,3,4-thiadiaz-
ol-2-yl)-8,9-dihydro-7H-1,3-dioxolo[4,5-h][2,3]benzodiazepine and
the acid addition salts thereof.
[0048] The compounds of formulas (I) and (II) can be prepared in
the following way. The heterocycle corresponding to R.sup.3 is
built up starting from a compound of formula (III) below: ##STR4##
wherein R.sup.1-R.sup.10 are defined for formulas (I) and (II)
above, by known methods or a compound having the following formula
(IV) or the following isochromenilium salt having formula (IVa)
which is formed from the compound of formula (IV), wherein the
meaning of R.sup.1, R.sup.2, R.sup.4, R.sup.5, R.sup.6, R.sup.7,
R.sup.8, R.sup.9 and R.sup.10 is as defined above: ##STR5## A
compound of formulas (IV) or (IVa) is reacted with a compound
having formula (V or (VI): H.sub.2N--NH--R.sup.3 (V)
H.sub.2N--NH--R.sup.11 (VI) wherein the meaning of R.sup.3 is as
defined above and the meaning of R.sup.11 is C.sub.2-C.sub.8
alkoxycarbonyl or aryl alkoxycarbonyl group to obtain the compounds
of formulas (VII) or (VIII). ##STR6##
[0049] The hydroxyl group of the compounds of formulas (VII) or
(VIII) is transformed into a sulfonate ester, and the latter
intermediate is submitted to ring-closure resulting in compounds of
formulas (I), (II) or (IX): ##STR7## by applying a strong base.
Alternatively, the compounds of formulas (VII) or (VIII) are
transformed into compounds of formulas (I), (II) or (IX) according
to Mitsunobu (Synthesis, I:1 (1988)). In the compound of formula
(IX), the R.sup.11 group is cleaved to give the compound of formula
(III), which is converted into the compound of formulas (I) or (II)
according to the method described in process as described above.
Then, if desired, in a compound of formula (I) or (II) obtained
according to any of the above processes, the nitro group is reduced
or the amino group is acylated, alkylated, or after diazotation, is
exchanged by a halogen atom or hydrogen atom, or a halogen atom is
exchanged by an amino group and in this way it is transformed into
another compound of formula (I) or (II) and/or the isomers are
separated and, if desired, salts are formed.
[0050] The compounds of formulas (III) and (IX) are chiral
compounds, and therefore formulas (III) and (IX) refers to either
of the individual enantiomers or mixtures thereof. The hemiketal
type compounds of formula (IV) as well as the hydrazone derivatives
of formulas (VII) and (VIII) represent different stereoisomers and
they refer to all of the individual stereoisomers and mixtures
thereof. The R.sup.11 group can be a C.sub.2-C.sub.8 alkoxycarbonyl
group, such as a tert-butoxycarbonyl or a benzyloxycarbonyl
group.
[0051] The starting materials of formula (III) are known in the
literature (U.S. Pat. No. 5,536,832 and British Patent No.
2,311,779, as well as WO 97/28 135 and WO 01/04 122). Hungarian
Patent No. 219,777 and British Patent No. 2,311,779 describe the
synthesis of optically active compounds of formula (III) as
well.
[0052] The optically active compounds of formula (III) can be
synthesized by reacting a hemiketal of formula (IV)--prepared for
example from an optically active substituted phenyl-isopropanol
according to Anderson et al. (J. Am. Chem. Soc. 117:12358
(1995))--with an alkoxycarbonyl-hydrazide containing an easily
removable alkoxycarbonyl group, such as a tert-butoxy-carbamate in
the presence of catalytic amount of an acid. The hydrazone of
formula (VIII) obtained after isolation then is transformed into a
mesyl ester e.g., with methanesulfonyl chloride in the presence of
triethylamine, and the latter is treated with base, for example
sodium hydroxide, in alcoholic solution to yield the benzodiazepine
derivative of formula (IX) in a ring closure reaction. Then the
substituent of the N-3 atom (numbering according to the
benzodiazepine ring) is cleaved, e.g., by hydrolysis or another
method, for example hydrogenolysis, to yield the desired compound
of formula (III). The cleavage of the tert-butoxycarbonyl group may
be carried out with trifluoroacetic acid, hydrogen bromide or zinc
bromide in dichloromethane.
[0053] The heterocyclic moiety--corresponding to the R.sup.3
substituent--of the compound of formula (I) or (II) is synthesized
starting from the compounds of formula (III) according to methods
known in the art relating to heterocyclic chemistry.
[0054] Some of the compounds of formula (I) or (II) can be
synthesized, for example, from the 4,5-dihydro-2,3-benzodiazepine
derivatives substituted with thiocarbamoyl group at position 3 of
the benzodiazepine ring. Latter compounds can be obtained from
4,5-dihydro-3H-2,3-benzodiazepine derivatives of formula (III), for
example with potassium thiocyanate in acetic acid medium. The thus
obtained 4,5-dihydro-3-thiocarbamoyl-3H-2,3-benzodiazepines are
reacted with .alpha.-halo ketones or .alpha.-halo aldehyde acetals
to yield 2,3-benzodiazepine derivatives having a substituted or
unsubstituted 2-thiazolyl group. In an analogous reaction, if
2-halo carboxylic acid esters are used instead of the .alpha.-halo
oxo-compound, the appropriate compounds containing a 3-thiazolinone
ring are formed.
[0055] When the above-mentioned 4,5-dihydro-2,3-benzodiazepines
containing thiocarbamoyl group in position 3 are reacted with
.beta.-halo carboxylic acid esters, for example ethyl
3-bromopropionate, then new 2,3-benzodiazepine derivatives
substituted with 5,6-dihydro-[1,3]thiazin-4-one ring are
obtained.
[0056] The compounds of formula (I) or (II) containing
1,3,4-thiadiazole group as R.sup.3 substituent can be synthesized
for example by the following way. First, a trimethylsilyl
derivative is prepared from a 4,5-dihydro-3H-[2,3]benzodiazepine of
formula (III), which is then reacted with thiophosgene to give
thiocarboxylic acid chloride. Finally, the latter is treated with
hydrazine to yield the thiocarboxylic acid hydrazide derivatives.
The 2,3-benzodiazepine derivatives substituted with
carbothiohydrazide group are reacted with an acid anhydride or
chloride and the thus-obtained partially occurring ring closure of
the carbothio-N-acylhydrazides is promoted by further acid
treatment to yield [1,3,4]thiadiazolyl-2,3-benzodiazepines. Another
procedure for the synthesis of the latter compounds is to react the
above-mentioned intermediate thiocarboxylic acid chloride with an
acid hydrazide, and then the resulting carbothiohydrazide
derivative containing an acyl group on the terminal N-atom is
treated with acid to give the cyclic product.
[0057] In an analogous reaction benzodiazepines of formula (I) or
(II) containing a [1,3,4]oxadiazole ring can be obtained, for
example, if the above mentioned N-acyl-thiocarboxylic acid
hydrazide derivative is treated with a sulfur binding reagent, for
example mercury (II) acetate.
[0058] The 4,5-dihydro-2,3-benzodiazepin-3-carbothiohydrazides can
serve as starting materials for further new compounds of formula
(a) or (II) substituted with a hetero-ring. For example, if the
N-methyl-carbamoyl-carbothiohydrazide obtained with methyl
isocyanate is heated with concentrated acid, for example
hydrochloric acid, then new compounds of formula (I) or (II)
substituted with (5-oxo-4,5-dihydro-[1,3,4]thiadiazol-2-yl) group
can be obtained. If the carbothiohydrazide derivative is reacted
with bromoacetic acid ester,
(5-oxo-5,6-dihydro-4H-[1,3,4]thiadiazin-2-yl)-[2,3]benzodiazepine
derivatives having a 6-membered ring as the R.sub.3 substituent are
obtained. If the carbothiohydrazide derivatives are reacted with
.alpha.-halo-ketones, for example chloroacetone, then e.g.,
(5-methyl-6H-[1,3,4]thiadiazin-2-yl)-[2,3]benzodiazepines are
formed.
[0059] The appropriate thiohydroxamic acids can be obtained from
[2,3]benzodiazepin-3-thiocarboxylic acid chlorides with
hydroxylamine, which can be transformed into heterocyclic compounds
by reacting with bifunctional alkylating agents. Among others,
[1,4,2]oxathiazol-3-yl-2,3-benzodiazepines can be synthesized for
example from thiohydroxamic acid derivatives with methylene
iodide.
[0060] The compounds of formula (I) or (II) containing
3-oxo-2,3-dihydro-[1,2,4]thiadiazol-5-yl group as R.sup.3
substituent can be prepared, for example, by reacting the
unsubstituted compounds of formula (III) with phenoxycarbonyl
isothiocyanate, then the resulting
phenoxycarbonyl-thiocarbamoyl-benzodiazepine transformed into
N-alkyl-carbamoyl-thiocarbamoyl-benzodiazepine with primary amines
and the latter is reacted e.g., with bromine to accomplish the ring
closure between the sulfur and the nitrogen atoms.
[0061] The compounds of formula (I) or (II) containing
4,5-dihydro-oxazol-2-yl group as an R.sup.3 substituent can be
synthesized by reacting the compounds of formula (III) with
chloroethyl isocyanate to give an urea derivative, which is heated
in the presence of sodium iodide and potassium carbonate in
dimethylformamide to accomplish the ring closure.
[0062] The compounds of formula (I) or (II) containing
2-alkyl-thiazol-4-yl group as R.sup.3 substituent can be
synthesized by reacting 3-bromo-acetyl-[2,3]benzodiazepines with
the appropriate carboxylic acid thioamide.
[0063] From 3-cyano-2,3-benzodiazepines--obtained from
2,3-benzodiazepines of formula (III) with cyanogen
bromide-2,3-benzodiazepines containing among others
(1H-tetrazol-5-yl) as well as (5-alkyl-[1,2,4]oxadiazol-3-yl)
groups as an R.sup.3 substituent can be synthesized. The tetrazolyl
compounds can be synthesized by reacting the nitrile derivative
with sodium azide in dimethylformamide in the presence of ammonium
chloride, while if the nitrile compound is first treated with
hydroxylamine and the thus obtained amidoxime is reacted with a
carboxylic acid anhydride or chloride, then the appropriate
1,2,4-oxadiazolyl compounds can be obtained.
[0064] The compounds of formula (I) or (II) containing
1,2,4-triazolyl group as R.sup.3 substituent can be synthesized
from a 3-thiocarbamoyl-[2,3]benzodiazepine derivative by reacting
first with methyl iodide, then the obtained S-methyl compound is
condensed with hydrazine and the so formed intermediate is treated
with a carboxylic acid anhydride or chloride.
[0065] Other illustrative processes for the synthesis of compounds
of formula (I) or (II) are those, where a hemiketal of formula (IV)
is reacted with a heterocyclic reagent substituted with a hydrazine
group in the presence of an acid as catalyst. The condensation
reaction can be carried out in the presence of hydrochloric acid as
catalyst by heating e.g., in isopropanol or toluene and possibly
with a Dean-Stark apparatus. It can be advantageous in some
instances to first transform the hemiketal into an isochromenilium
salt of formula (IVa) with a mineral acid e.g., perchloric acid and
the latter is reacted with a hydrazine reagent, for example in
isopropanol. The thus-obtained hydrazones of formula (VII) are
generally formed as a mixture of stereoisomers. They can be further
reacted e.g., with methanesulfonyl chloride in dichloromethane in
the presence of triethylamine, and the mesylate obtained after
isolation is treated with a concentrated solution of a base in an
alcohol or a mixture of alcohol-dichloromethane. The ring closure
reaction can be achieved for example, by the Mitsunobu reaction
(Mitsunobu Synthesis 1:1 (1981)) as well.
[0066] If desired, the compounds of formula (I) or (II) obtained by
different methods can be transformed into other compounds of
formula (I) or (II) with further reactions. For example, a reactive
halogen atom in the side chain of the heterocycle--the R.sup.3
substituent--can be exchanged for an amino group, for example by
heating with an excess of a proper amine, or the NH group of a
N-containing heterocyclic compound can be alkylated by known
methods. The latter transformation for example in the case of a
triazolyl compound, can be carried out with methyl iodide in the
presence of potassium tert-butoxide.
[0067] The reduction of the nitro group in the compounds of formula
(I) or (II) is generally carried out in polar solvents at room
temperature or at elevated temperature in the presence of catalysts
such as Raney-nickel, platinum or palladium. Besides gaseous
hydrogen, other hydrogen sources e.g., hydrazine hydrate, ammonium
formate, potassium formate or cyclohexene can also be applied. The
nitro group can be reduced, for example, with tin in the presence
of an acid, or with tin (II) chloride by heating in an alcohol as
well. The amino group can be further derivatised by known methods,
for example alkylation, acylation, or Sandmeyer reaction.
[0068] The AMPA antagonistic activity of the compounds of formula
(I) or (II) of the present invention is exemplified by the
following experiments. Reference to compounds by number refers to
compounds described in the numbered examples below.
Inhibition of the AMPA Receptors
[0069] Two experimental models were used for the demonstration of
the inhibition of the AMPA receptor activation of the compounds of
formula (I) or (II). In the first model the spreading depression
caused by glutamate agonists (i.e., AMPA or kainate) was studied,
while in the second one the transmembrane ion-current induced by
the activation of the AMPA/kainate receptors was measured
directly.
Inhibition of AMPA Induced "Spreading Depression" in Isolated
Chicken Retina--
[0070] The AMPA antagonistic effect of the compounds of formula (I)
or (II) was studied in the in vitro "spreading depression" model
(Sheardown Brain Res. 607:189 (1993)). The AMPA antagonists prolong
the latency of the development of the "spreading depression" caused
by AMPA (5 .mu.M). TABLE-US-00001 TABLE 1 Inhibition of the
"spreading depression" in chicken retina Compound (Number of
example)/IC.sub.50 .mu.M GYKI 52466 GYKI 53773 (reference)
(reference) 61 69 86 84 9.5 1.2 1-5 0.9 0.42 0.85
[0071] The data of Table 1 indicate that the compounds of the
present invention inhibit the AMPA-induced "spreading depression"
with an IC.sub.50 value of 0.4-5 .mu.M.
Inhibition of AMPA Induced Transmembrane Currents
[0072] The activity of the compounds of the present invention was
studied on acutely isolated cerebellar Purkinje cells by measuring
the whole-cell current induced by 5 .mu.M AMPA according for
example to the method described by Bleakman et al
(Neuropharmacology 12:1689 (1996)). According to the IC.sub.50
values obtained, the compounds of the present invention inhibit the
AMPA-induced ion-current by one to two magnitudes greater than the
internationally accepted reference compound GYKI 52466
(5-(4-aminophenyl)-9H-1,3-dioxolo[4,5-h][2,3]-benzodiazepine,
Hungarian patent No. 191 698), or GYKI 53773
((R)-7-acetyl-5-(4-aminophenyl)-8,9-dihydro-8-methyl-7H-1,3-dioxolo[4,5-h-
][2,3]benzodiazepine, U.S. Pat. No. 5,536,832), the IC.sub.50
values of which are 8.8 .mu.M, and 1.57 .mu.M, respectively. (See
Table 2). TABLE-US-00002 TABLE 2 Inhibition of the ion-currents
caused by 5 .mu.M AMPA determined by the whole cell patch clamp
method Compound (Number of example)/IC.sub.50 .mu.M GYKI 52466 GYKI
53773 (reference) (reference) 61 69 86 84 8.8 1.57 0.49 0.42 0.06
0.09
Anticonvulsant Activity
[0073] Although various drugs with different spectra of activity
are used in the therapy of epilepsy, they show severe side effects.
Furthermore, about 30% of epilepsy patients are refractory to these
drugs. Consequently, there is a need for such new antiepileptic
drugs, which act via a mechanism different from those in current
use. There are great expectations towards those compounds that
display their activity by diminishing the glutamate-induced
over-activation of the central nervous system (TIPS, 15:456
(1994)).
[0074] The anti-seizure activity of some of the compounds of the
present invention was measured using the electroshock test (J.
Pharmacol. Exp. Ther. 106:319 (1952)) and the results are shown in
Table 3. The spasmolytic activity of the compounds of the present
invention was investigated by using e.g., pentetrazole (J.
Pharmacol. Exp. Ther. 108:168 (1953)), strychnine (J. Pharmacol.
Exp. Ther. 129:75 (1960)), bemegrid, nicotine, bicuculline,
4-aminopyridine and mercapto-propionic acid for inducing the
clonic-tonic seizures and lethality. The investigated compounds
were administered orally in three doses using 10 male CD1
mice/dose, usually 60 min before the induction of seizures.
Non-limiting, illustrative results are summarized in Table 3.
TABLE-US-00003 TABLE 3 Investigation of the anticonvulsive activity
in mice Compound (Number of example)/ED.sub.50 mg/kg po. Method
GYKI 52466 GYKI 53773 61 69 86 84 89 102 MES 37.4 8.6 13.1 14.7 6.1
12.5 10.5 13.9 MES 30' 21.9 4.9 11.5 8.7 4.3 10-15 -- --
Pentetrazol 119.8 16.8 32.5 46.9 10.0 17.1 11.5 35.7 Strychnine
86.7 17.4 35.4 27.7 10.6 18.2 15.7 26.7 Bemegride 71.9 23.9 34.4
33.3 11.2 16.7 11.2 27.9 Bicuculline 35.0 14.6 31.0 18.1 4.6 17.0
17.1 25.8 Nicotine 71.8 22.7 59.3 16.8 16.5 77.2 45.9 31.7 4-AP
43.0 8.4 17.6 16.6 10.1 16.6 14.3 20.4 3-MPA 47.0 17.1 11.0 34.2
4.0 6.8 >50 >50 Abbreviations: MES = maximal electroshock
seizure; 4-AP = 4-aminopyridine; 3-MPA = 3-mercapto-propionic
acid
[0075] The data provided above indicate that the compounds of
formula (I) or (II) of the present invention showed significant
anticonvulsive activity in all of the eight tests studied. They
reveal both a broader spectrum and more significant anticonvulsive
efficacy compared to GYKI 52466 and GYKI 53773, both used as
reference compounds in the literature. The protective effect
displayed against the different convulsion inducing agents predicts
favorably for their potential use in the treatment of the different
kinds of epilepsy.
Muscle Relaxant Activity
[0076] Central muscle relaxants are used in such clinical
situations when the resting tone of the skeletal muscles is
increased as a consequence of a cerebral trauma or due to a chronic
neurodegenerative illness, resulting in muscle rigidity or tremor.
The muscle spasm is often painful and hinders normal motion.
[0077] The muscle relaxant activity of the compounds of formula (I)
or (II) of the present invention was determined in the inclined
screen test described by Randall (J. Pharmacol. Exp. Ther. 129:163
(60)) as well as in the rotarod test (Dunham et al, J. Am. Pharm.
Assoc. 46:208 (1957). The compounds were administered in three
doses intraperitoneally using 10 CD1-mice/dose. The muscle relaxant
activity of the compounds of the present invention was compared to
that of the reference compounds GYKI 52466 and GYKI 53773.
Representative, non-limiting results are summarized in Table 4.
From these data, it is evident, that the muscle relaxant activity
of the compounds of the present invention significantly exceeds
that of GYKI 53773, which is now in clinical phase-II studies.
TABLE-US-00004 TABLE 4 Muscle relaxant activity in mice Compound
Inclined screen Rotarod (Number of example) ED.sub.50 ip. (mg/kg)
ED.sub.50 ip. (mg/kg) GYKI 52466 (reference) 47.1 25.1 GYKI 53773
(reference) 13.4 2.3 61 10.7 5.4 69 12.2 1.2 86 3.9 0.8 84 12.8 1.4
89 4.3 1.7 102 14.8 2.9
[0078] The muscle relaxant activity of the compounds of formula (I)
or (I) determined in the above tests indicates potential
therapeutic use in the treatment of such illnesses in which the
increased muscle tone causes problems. Considering their skeletal
muscle relaxant and anti-tremor activity (discussed below), the
compounds may be useful in the treatment of essential tremor,
multiple sclerosis (spasms+tremor) and Parkinson's disease
(rigidity+tremor).
The Inhibition of Focal Ischemia
[0079] The focal anti-ischemic activity of the compounds of formula
(I) or (II) of the present invention was measured by the "middle
cerebral artery occlusion" (MCAO) test (Bartus Stroke 11:2265
(1994) and Sydserff et al, Brit. J. Pharmacol. 114:1631 (1995)).
The blood supply of the left middle cerebral artery of
anaesthetized rats was temporarily blocked (60 min) by an embolus
introduced intra-arterially following Halothane anesthesia, without
craniotomy, thereafter the perfusion was reestablished by removing
the embolus and thus a human "stroke-like" status was triggered in
an experimental animal model. After a histological process (TTC
staining) 24 h later, the infarcted area was determined by a
computer assisted scanner program and was compared to the results
obtained in a control group treated with the vehicle. Non-limiting,
representative results are summarized in Table 5. TABLE-US-00005
TABLE 5 Inhibition of focal ischemia in rats Decrease of the
infracted area in % compared to Dose that of the control Compound
mg/kg iv. 30 min 120 min 180 min (Number of (6x in every Time of
first treatment example) 30 min) after occlusion GYKI 52466 HCl 2
39* (reference) 5 34* 47** GYKI 53773 2 47* 49** 26 (reference) 61
1 63** 16 2 46* 69 2 28 86 1 35* *p < 0.05; **p < 0.01;
calculated with Dunnett test following ANOVA (Dunnett J. Amer.
Statist Ass. 50:1096 (1955))
[0080] The investigated compounds possess a strong neuroprotective
activity in this experimental model, which is considered the model
of the human stroke. Some of the compounds, egg, those described in
Example 61 and 86, show significant activity even when administered
3 h after the occlusion predicting a potential useful clinical
application.
Inhibition of Autoimmune Inflammation
[0081] Multiple sclerosis is a chronic autoimmune inflammation of
the central nervous system in which the axonal myelin coat,
assuring the safe impulse conduction, is damaged. The
oligodendrocytes forming the myelin coat express mainly
AMPA/kainate receptors. Thus, the neurodegenerative process is
further enhanced by glutamate, the excitatory neurotransmitter,
which is released by the activated immune cells in large quantities
which expresses its activity through AMPA/kainate receptors thereby
damaging myelin oligodendrocytes and axons of neurons (Steinman
Nature Medicare 6:15 (2000) and Werner et al., Neural Transmiss.
Suppl., 60: 375 (2000)). As a consequence of these processes, at
first mild neurological symptoms, such as visual, sensory, balance,
motion and urogenital problems develop which become increasingly
serious. The therapy of multiple sclerosis is still an unsolved
problem despite the intense research being pursued in this field
(Bjartmar et al., Drugs of Today 38:17 (2002)).
[0082] Muscle spasticity and intention tremor belong to the most
severe neurological symptoms of multiple sclerosis (Baker et al.,
Nature 404:84 (2000)). Moderation or cure of these symptoms by a
proper therapy would be very important.
[0083] The activity of the 2,3-benzodiazepine derivatives
possessing AMPA antagonistic activity was further investigated in
an autoimmune encephalomyelitis model (Smith et al., Nature
Medicine, 6:62 (2000)) in rats, using immunization with guinea pig
myelin basic protein (MBP) and complete Freund adjuvant. The
compounds were administered intraperitoneally twice a day for 8
days, starting on day 10 after immunization and with an observation
period until symptoms were present. 5-15 animals were used in each
group. Their weights were 160-180 g (Lewis rats, female) and
180-220 g (Lewis rats, male). The activity of the compounds was
determined according to the symptom score values, and compared to
those of the control group (see Table 6). Histopathological
investigations were carried out on the brain stem, the spinal cord,
and the sciatic nerve (Gijbels et al., J. Clin. Invest. 94:2177
(1994)) using 5-10 animal/group. Non-limiting, representative
results are presented in Table 7. TABLE-US-00006 TABLE 6 Effect of
2,3-benzodiazepines possessing AMPA antagonist activity on the
clinical symptoms of autoimmune encephalomyelitis in Lewis rats
Neurological symptoms Compound (change compared to controls, %)
(Number of Dose Female rats Male rats example) (mg/kg ip.) 0-8 day
0-14 day 0-8 day 0-14 day GYKI 53773 30 -38* -27 -43* -29
(reference) 15 -60* -63** -8 +7 GYKI 52466 30 -45 -4 -1 -1
(reference) 86 15 -97** -85** -93* -67 7.5 -62** -66** -65** -70**
3.75 -3 -18 -70** -77** 1.875 -40* -39* +5 -8 61 7.5 -56* -53* -60*
-63** 3.75 -44 -48 -44* -46* 1.875 -18 -7 +13 +5 69 7.5 -29 -24
-51* -50* 3.75 +43 +58* +35 -40* *p < 0.05; **p < 0.01
(Mann-Whitney test)
[0084] TABLE-US-00007 TABLE 7 Effect of 2,3-benzodiazepine
derivatives possessing AMPA antagonistic character on the
histological and clinical symptoms of autoimmune encephalomyelitis
in Lewis rats on day 24 after immunization. Neurological
Histological symptoms symptoms Compound (change, %) (change, %)
(Number of Dose rats rats example) (mg/kg ip.) Male female male
female GYKI 53773 30 +34 -16 -26 -41 (reference) 86 15 -66 -53 -67
-85 7.5 +1 -22 -66 -62 3.75 +4 -20 -72 -21 1.875 -25 -15 +54 -42 61
7.5 -20 -5 -54 -53
[0085] According to our histopathological and pharmacological
investigations the compounds described in, for example, Example 86
and 61 proved to be more active than the reference compound GYKI
53773.
[0086] The anti-tremor effect of the 2,3-benzodiazepine derivatives
of the present invention, possessing AMPA antagonistic character in
mouse models was studied using three tremorigen agents of different
mechanism of action, such as oxotremorine (Rathbun et al.,
Psychopharmacology; 4:114 (1963)), GYKI 20039
(3-(2,6-dichlorophenyl)-2-imino-thiazolidine; (Andrasi et al., Acta
Physiol. Acad. Sci. Hung. 37:183 (1970)) and harmaline. Number of
animals: 5/group. Weight of animals: 20-25 g (CD1 mice, male). The
activity of the investigated compounds was determined by their
score values compared to those of the control group. The ED.sub.50
values were calculated according to the Litchfield-Wilcoxon method
and are listed in Table 8. TABLE-US-00008 TABLE 8 Effect of
2,3-benzodiazepine derivatives possessing AMPA antagonistic
character on the tremor of CD1 mice induced by different chemical
agents. Compound ED.sub.50 (mg/kg po.) (Number of Dose range
Oxotremorin GYKI 20039 Harmaline example) (mg/kg p.o.) 1 mg/kg ip.
10 mg/kg ip. 40 mg/kg ip. GYKI 52466 6.25-75.0 20.5(14.9-28.3)
37.1(25.2-54.7) 38.5(25.7-57.9) (reference) GYKI 53773 3.125-20.0
5.6(3.6-8.5) 10.6(7.2-15.5) 9.0(-7.4-10.9) (reference) 86 3.125-9.0
4.3(3.5-5.4) 6.8(5.5-8.5) 6.0(4.9-7.4)
[0087] According to our investigations, the compound described in
Example 86 was more active than the reference compounds GYKI 53773
and GYKI 52466, respectively.
[0088] The 2,3-benzodiazepine derivatives with AMPA antagonistic
character, compensating for the harmful effect of glutamate by
blocking the corresponding receptors, are therapeutically
important. Their combined neuroprotective, muscle relaxant, tremor
inhibiting etc. properties beneficially influence the progression
of the pathological neurological disorders and diminish the
pathological neurological symptoms, respectively.
The Effect of the Compounds of the Present Intention on the Acute
and Chromic Inflammatory Disorders of the Airways
[0089] Bronchial hyperresponsiveness (BHR) and airway eosinophilia
(AEP) are characteristic features of bronchial asthma. BHR is
typified by an exaggerated response to a wide variety of stimuli
that can induce an increased resistance to airflow in the airways.
AEP is a result of prolonged eosinophil infiltration, mast cell,
and T cell activation in the airways. In actively (e.g., ovalbumin)
immunized rats (e.g., Brown Norway [BN] strain), repeated
sensitization followed by antigenic challenge results in lung
eosinophilia and bronchial hyperresponsiveness to different
spasmogens (e.g., acetylcholine). This is the most frequently
employed model for studying potential anti-asthmatic effects of new
chemical entities.
[0090] BN rats were actively immunized with allergen (ovalbumin).
On day one, rats were sensitized with the subcutaneous
administration of ovalbumin suspended in Al(OH).sub.3 (2.5 .mu.g
ovalbumin +20 mg Al(OH).sub.3 in 0.5 ml saline). Booster injections
(same dose and same route) were given at day 14 and 21.
Simultaneously at each occasion 0.25 ml of Bordatella pentussis
vaccine was injected intraperitoneally. On day 28, animals were
challenged by inhalation of the antigen (vaporized 1% OVA solution
for 1 hour). Test compounds were administered orally 2 hours
pre-challenge.
[0091] 48 hours following challenge, they were sacrificed by an
overdose of urethane (4-5 ml of 15% urethane given i.p.),
bronchoalveolar lavage fluid (BALF) was obtained, and tracheae
dissected from the animals. Eosinophil cell count (cells/ml BALF)
was determined manually using a selective stain for eosinophils and
counting the cells in a Buerker chamber. BHR was determined using
tracheal rings suspended in an organ bath. After an equilibration
period of 30 minutes, cumulative concentration response curves to
acetylcholine were determined. Maximal response of control
(unchallenged, non-treated) tracheal rings is obtained at 10.sup.-3
M acetylcholine. The height of this response is defined as 100%.
All other contractions are expressed as a percentage and related to
the control response.
[0092] Results TABLE-US-00009 TABLE 9 Effect of GYKI 52466
(reference), GYKI 53773 (reference) and the compound described in
Example 86 on the bronchial hypersensitivity and the eosinophilia
of the airways on BN-rats sensitized with ovalbumin and antigen
challenged by inhalation (mean .+-. SE, p determined by Student's
t-test). Compound (Number Experiment Parameter Control Challenge of
example) GYKI 52466 (reference) 3.0 mg/kg po 1 ED.sub.50* 5.63 .+-.
0.46 6.74 .+-. 1.45 5.60 .+-. 1.53 p 0.002 0.028 MAX** 100 .+-. 0
276 .+-. 217 135 .+-. 105 p 0.001 0.037 Eosinophil*** 0.17 .+-.
0.01 1.24 .+-. 0.23 0.91 .+-. 0.13 p 0.010 NS.sup..dagger-dbl. GYKI
53773 (reference) 3.0 mg/kg po 2 ED.sub.50* 5.22 .+-. 0.59 5.89
.+-. 0.66 4.64 .+-. 0.91 p 0.003 0.001 MAX** 100 .+-. 0 163 .+-. 65
85 .+-. 43 p <0.001 0.007 Eosinophil** 0.38 .+-. 0.11 1.24 .+-.
0.13 1.29 .+-. 0.11 p 0.004 NS.sup..dagger-dbl. 86 3.0 mg/kg po 3
ED.sub.50* 5.78 .+-. 0.17 6.99 .+-. 0.32 4.95 .+-. 0.59 p 0.001
0.008 MAX** 100 .+-. 0 255 .+-. 50 81 .+-. 14 p 0.001 0.003
Eosinophil*** 0.23 .+-. 0.08 1.43 .+-. 0.27 1.32 .+-. 0.32 p 0.005
NS.sup..dagger-dbl. *acetylcholine (Ach) concentration (-log M)
which causes a 50% contraction compared to the control **relative
contraction compared to the control at a maximal Ach concentration
***BALF eosinophil number (.times.10.sup.6/ml) .sup..dagger-dbl.not
significant (p > 0.05)
[0093] The representative results presented in Table 9 show that
representative compounds according to the present invention
diminished the bronchial hyperresponsiveness caused by the
allergen. The eosinophilia was not significantly influenced by the
applied doses.
[0094] The results of the different pharmacological investigations
mentioned above show that the compounds of formula (I) or (II) of
this invention are able to beneficially influence various diseases
and disorders in which glutamate (AMPA/kainate) receptors have been
implicated. Consequently the compounds according to the invention
are suitable for treating neurological and psychiatric disorders,
triggered by the extremely enhanced activity of the AMPA receptor.
Therefore, they have therapeutic utility as anticonvulsants, muscle
relaxants, as well as neuroprotective agents. They also display
therapeutic value for the treatment of epilepsy, as well as
different illnesses in which the spasm of skeletal-muscles is
involved, and in the treatment of neurodegenerative disorders such
as e.g., cerebral ischemia (stroke).
[0095] Exemplary neurological illnesses which can be beneficially
influenced or prevented include Parkinson's disease, Alzheimer's
disease, Huntington chorea, amyotrophic lateral sclerosis,
olivopontocerebellaric atrophy, AIDS dementia, senile dementia. A
similar beneficial effect can be achieved in the treatment of
neurodegenerative processes caused by cerebrovascular catastrophe
(stroke, brain, and spinal injuries) or hypoxia, anoxia or
hypoglycemia. The compounds of the invention can be advantageously
used for the treatment of different psychiatric diseases such as
anxiety, schizophrenia, sleep disorders, as well as alleviating the
withdrawal syndrome of alcohol and drug abuse. Furthermore they may
inhibit tolerance development in the case of sedatives or
analgesics.
[0096] It can be expected that they can be advantageously used in
epileptic disease entities, in the cure or palliation of muscle
spasms of central origin and in the relief of pathologic pain as
well as in the treatment of urinary incontinence.
[0097] In one aspect of the invention, a method of blocking the
activation of one or more excitatory amino acid receptors in
mammals is provided. This method includes administering to a mammal
in need of such treatment a pharmaceutically effective amount of a
compound of the formula (I) or (II).
[0098] In another aspect of the invention, a method of treating
epilepsy in mammals is provided. This method includes administering
to a mammal in need of such treatment an antiepileptic amount of a
compound of the formula (I) or (II).
[0099] In another aspect of the invention, a method of treating
spasms of the skeletal musculature in mammals is provided. This
method includes administering to a mammal in need of such treatment
a muscle-relaxing amount of a compound of the formula (I) or
(II).
[0100] In still another aspect of the invention, a method of
treating acute and chronic neurodegenerative disorders in mammals
is provided. This method includes administering to a mammal in need
of such treatment a pharmaceutically effective amount of a compound
of the formula (I) or (II).
[0101] In yet another aspect of the invention, a method for
treating inflammatory disorders in mammals is provided. This method
includes administering to a mammal in need of such treatment a
pharmaceutically effective amount of a compound of the formula (I)
or (II).
[0102] In other aspects of the invention, the compounds of formula
(I) or (II) can be advantageously used in the treatment of multiple
sclerosis. A further therapeutic field, in which the compounds of
formula (I) or (II) can be used, are illnesses that are caused by
the over-function of the periferic glutamate receptors. Such
illnesses include the acute and chronic inflammatory disorders of
the airways particularly allergic inflammations such as
asthma-related pathologies. This latter potential therapeutic use
is supported by the results obtained in ovalbumin sensitized
rats.
[0103] In one aspect of the invention, a pharmaceutical composition
is provided including a compound of formula (I) or (II), or a
stereoisomer, or a pharmaceutically acceptable salt thereof and a
pharmaceutically acceptable carrier, excipient or diluent.
[0104] The compounds of formula (I) or (II) are formulated in a
pharmaceutically acceptable vehicle with any of the well-known
pharmaceutically acceptable carriers, including diluents and
excipients (see Remington's Pharmaceutical Sciences, 18.sup.th Ed.,
Gennaro, Mack Publishing Co., Easton, Pa. 1990 and Remington: The
Science and Practice of Pharmacy, Lippincott, Williams &
Wilkins, 1995). While the type of pharmaceutically acceptable
carrier/vehicle employed in generating the compositions of the
invention will vary depending upon the mode of administration of
the composition to a mammal, generally pharmaceutically acceptable
carriers are physiologically inert and non-toxic. Formulations of
pharmaceutical compositions may contain more than one type of
compound of formula (I) or (II), as well as any other
pharmacologically active ingredient useful for the treatment of the
particular conditions, disease, or symptom being treated.
[0105] The compositions of the invention can be administered by
standard routes (e.g., oral, inhalation, rectal, nasal, topical,
including buccal and sublingual, or parenteral, including
subcutaneous, intramuscular, intravenous, intradermal, transdermal,
and intratracheal). In addition, polymers may be added according to
standard methodologies in the art for sustained release of a given
compound.
[0106] For oral administration, the compositions of the invention
may be presented as discrete units such as capsules, caplets,
gelcaps, cachets, pills, or tablets each containing a predetermined
amount of the active ingredient as a powder or granules; as a
solution or a suspension in an aqueous liquid or a non-aqueous
liquid; or as an oil-in-water liquid emulsion or a water-in-oil
emulsion and as a bolus, etc. Alternately, administration of a
composition including the compound of formula (I) or (II) may be
effected by liquid solutions, suspensions or elixirs, powders,
lozenges, micronized particles and osmotic delivery systems.
[0107] Formulations suitable for administration by inhalation
include formulations that can be dispensed by inhalation devices
known to those in the art. Such formulations may include carriers
such as powder and aerosols. Liquid and powdered compositions
suitable for nebulization and intrabronchial use, or aerosol
compositions administered via an aerosol unit dispensing metered
doses ("MDI") are contemplated.
[0108] The active ingredient may be formulated in an aqueous
pharmaceutically acceptable inhalant vehicle, such as, for example,
isotonic saline or bacterostatic water and other types of vehicles
that are well known in the art. The solutions are administered by
means of a pump or squeeze-actuated nebulized spray dispenser, or
by any other conventional means for causing or enabling the
requisite dosage amount of the liquid composition to be inhaled
into the patient's lungs.
[0109] Powder compositions include, by way of illustration,
pharmaceutically acceptable powdered preparations of the active
ingredient thoroughly intermixed with lactose or other inert
powders acceptable for intrabronchial administration. The powder
compositions can be administered via a dispenser, including, but
not limited to, an aerosol dispenser or encased in a breakable
capsule, which may be inserted by the patient into a device that
punctures the capsule and blows the powder out in a steady
stream.
[0110] Aerosol formulations for use in the subject method typically
include propellants, surfactants, and co-solvents and may be filled
into conventional aerosol containers that are closed by a suitable
metering valve.
[0111] Formulations suitable for nasal administration, wherein the
carrier is a solid, include a coarse powder having a particle size,
for example, in the range of 20 to 500 microns which is
administered in the manner in which snuff is administered, i.e. by
rapid inhalation through the nasal passage from a container of the
powder held close up to the nose. Suitable formulations, wherein
the carrier is a liquid, for administration, for example via a
nasal spray, aerosol, or as nasal drops, include aqueous or oily
solutions of the compound of formula (I) or (II).
[0112] Formulations suitable for parenteral administration include
aqueous and non-aqueous sterile injection solutions which may
contain antioxidants, stabilizers, buffers, bacteriostats and
solutes which render the formulation isotonic with the blood of the
intended recipient; and aqueous and non-aqueous sterile suspensions
which may include suspending agents and thickening agents.
[0113] The dosage of the active ingredient depends on the route of
administration, the type and severity of the disease as well as the
weight and age of the patient. The daily dose for adult patients
can be 0.1-500 mg, preferably 1-100 mg, in a single dose or divided
in several doses.
[0114] In another aspect of the present invention, a method is
provided for treating (a) an acute or chronic neurodegenerative
disease associated with glutamate dysfunction; (b) a method for
treating epilepsy; (c) a method for reducing muscle spasm in
mammals; (d) a method for preventing, treating or alleviating the
symptoms of acute or chronic inflammatory disorders of the airways;
(e) a method for relief of pathological pain in mammals. These
methods include administering to a mammal in need of such treatment
a therapeutically effective amount of a compound of formula (I) or
(II).
[0115] The term "therapeutically effective amount" is used to
denote treatments at dosages effective to achieve the therapeutic
result sought. Furthermore, one of skill will appreciate that the
therapeutically effective amount of the compound of the invention
may be lowered or increased by fine-tuning and/or by administering
more than one compound of the invention, or by administering a
compound of the invention with another pharmacologically active
compound. The invention therefore provides a method to tailor the
administration/treatment to the particular exigencies specific to a
given mammal. As illustrated in the following examples,
therapeutically effective amounts may be easily determined for
example empirically by starting at relatively low amounts and by
step-wise increments with concurrent evaluation of beneficial
effect.
[0116] It will be appreciated by those of skill in the art that the
number of administrations of the compounds according to the
invention will vary from patient to patient based on the particular
medical status of that patient at any given time.
[0117] The compounds according to the invention and the process for
their preparation are illustrated in detail by the following
Examples.
[0118] The following examples are intended to further illustrate
certain preferred embodiments of the invention and are not limiting
in nature. Those skilled in the art will recognize, or be able to
ascertain, using no more than routine experimentation, numerous
equivalents to the specific substances and procedures described
herein.
EXAMPLES
[0119] The starting materials of the examples were synthesized as
follows:
(.+-.)-8-Methyl-5-(4-nitrophenyl)-7-thiocarbamoyl-8,9-dihydro-7H-1,3-dioxo-
lo[4,5-h][2.3]benzodiazepine (I)
[0120] A mixture of 0.90 g (9.26 mmol) of potassium thiocyanate,
2.00 g (6.15 mmol) of
(.+-.)-8-methyl-5-(4-nitrophenyl)-8,9-dihydro-7H-1,3-dioxolo[4,5-h][2,3]b-
enzodiazepine and 40 ml of acetic acid was stirred at
100-110.degree. C. for 6 h. After cooling, the precipitated
crystals were filtered off, washed with water and dried to yield
1.80 g (76%) of the title compound. Mp.: 242-243.degree. C.
[0121] The thiocarbamoyl compounds II-X were synthesized from the
corresponding dihydro-[2,3]benzodiazepine according to the above
procedure.
(R)-8-Methyl-5-(4-nitrophenyl)-7-thiocarbamoyl-8,9-dihydro-7H-1,3-dioxolo[-
4,5-h][2,3]benzodiazepine (II)
[0122] Mp.: 213-215.degree. C. Yield: 73%, [.alpha.].sub.D:
-251.degree. (c=0.5; CHCl.sub.3).
(S)-8-Methyl-5-(4-nitrophenyl)-7-thiocarbamoyl-8,9-dihydro-7H-1,3-dioxolo[-
4,5-h][2.3]benzodiazepine (III)
[0123] Mp.: 213-214.degree. C. Yield: 76%, [.alpha.].sub.D:
+252.degree. (c=1; CHCl.sub.3).
(.+-.)-8-Methyl-5-(3-methyl-4-nitrophenyl)-7-thiocarbamoyl-8,9-dihydro-7H--
1,3-dioxolo[4,5-h][2.3]benzodiazepine (IV)
[0124] Mp.: 230-236.degree. C. Yield: 86%.
(.+-.)-8-Chloro-4-methyl-(4-nitrophenyl)-3-thiocarbamoyl-4,5-dihydro-3H-[2-
,3]benzodiazepine (V)
[0125] Mp.: 261-265.degree. C. Yield: 72%.
(.+-.)-7,8-Dichloro-4-methyl-1-(4-nitrophenyl)-3-thiocarbamoyl-4,5-dihydro-
-3H-[2,3]benzodiazepine (VI)
[0126] Mp.: amorphous. Yield: 59%.
(.+-.)-8-Methyl-5-phenyl-7-thiocarbamoyl-8,9-dihydro-7H-1,3-dioxolo[4,5-h]-
[2,3]benzodiazepine
[0127] Mp.: 225-235.degree. C. Yield: 86%.
5-(4-Nitrophenyl)-7-thiocarbamoyl-8,9-dihydro-7H-1,3-dioxolo[4,5-h][2,3]be-
nzodiazepine (VIII)
[0128] Mp.: 235-238.degree. C. Yield: 62%.
(.+-.)-8-Methyl-5-(4-methyl-3-nitrophenyl)-7-thiocarbamoyl-8,9-dihydro-7H--
1,3-dioxolo[4,5-h][2,3]benzodiazepine (IX)
[0129] Mp.: 201-202.degree. C. Yield: 84%.
(.+-.)-7-Bromo-4-methyl-8-methoxy-1-(4-nitrophenyl)-3-thiocarbamoyl-3,4-di-
hydro-3H-[2,3]benzodiazepine (X)
[0130] Mp.: 250-253.degree. C. Yield: 94%.
(.+-.)-8-Methyl-5-(4-nitrophenyl)-8,9-dihydro-7H-1,3-dioxolo[4,5-h][2,3]be-
nzodiazepine-7-carbothioyl chloride (XI)
[0131] 3.25 g (10.0 mmol) of
(.+-.)-8-methyl-8,9-dihydro-7H-1,3-dioxolo[4,5-h][2,3]benzodiazepine
was dissolved in 90 ml of dry toluene by warming and after adding
2.17 ml (15.5 mmol) of triethylamine, was reacted with 1.90 ml
(15.0 mmol) of trimethylsilyl chloride at about 28-30.degree. C.
After stirring at room temperature for 16 h this reaction mixture
was added dropwise over a period of about 2 h to the solution of
1.38 g (12.0 mmol) of thiophosgene in 30 ml of dry toluene. This
mixture was stirred at room temperature for 5 h, and then diluted
with 30 ml of toluene. It was then decomposed by addition of 30 ml
of water. After separation, the toluene phase was washed twice with
30 ml of water, followed by a 10% aqueous sodium chloride solution.
After drying, the solvent was evaporated and the residue was
treated with diisopropyl ether to yield 3.27 g (81%) of the crude
product.
[0132] The crude product was recrystallized from chloroform,
petroleum ether.
[0133] Yield: 3.05 g. Mp.: about 185.degree. C. it recrystallizes,
then it melts at 210.degree. C.
[0134] The carbothioyl chloride type compounds XII-XVII were
synthesized by analogous methods from racemic or optically active
dihydro-[2,3]benzodiazepine derivatives:
(R)-8-Methyl-5-(4-nitrophenyl)-8,9-dihydro-7H-1,3-dioxolo[4,5-h][2,3]benzo-
diazepine-7-carbothioyl chloride (XII)
[0135] Mp.: 187-188.degree. C. Yield: 80%, [.alpha.].sub.D:
-610.degree. (c=0.5; CHCl.sub.3).
(.+-.)-8-Methyl-5-(3-nitrophenyl)-8,9-dihydro-7H-1,3-dioxolo[4,5-h][2,3]be-
nzodiazepine-7-carbothioyl chloride (XIII)
[0136] Mp.: 198-199.degree. C. Yield: 79%.
(.+-.)-8-Methyl-5-(3-methyl-4-nitrophenyl)-8,9-dihydro-7H-1,3-dioxolo[4,5--
h][2,3]benzodiazepine-7-carbothioyl chloride (XIV)
[0137] Mp.: 210-215.degree. C. Yield: 79%.
(.+-.)-8-Methyl-5-(4-methyl-3-nitrophenyl-8,9-dihydro-7H-1,3-dioxolo[4,5-h-
][2,3]benzodiazepine-7-carbothioyl chloride (XV)
[0138] Mp.: 201-202.degree. C. Yield: 84%.
(.+-.)-8-Chloro-4-methyl-1-(4-nitrophenyl)-4,5-dihydro-3H-[2.3]benzodiazep-
ine-3-carbothioyl chloride (XVI)
[0139] Mp.: 210-214.degree. C. (DMF). Yield: 70%.
(.+-.)-7-Bromo-4-methyl-8-methoxy-1-(4-nitrophenyl)-4,5-dihydro-3H-[2,3]be-
nzodiazepine-3-carbothioyl chloride (XVII)
[0140] Mp.: 199-204.degree. C. Yield: 82%.
(.+-.)-8-Methyl-5-(4-nitrophenyl)-8,9-dihydro-7H-1,3-dioxolo[4,5-h][2,3]be-
nzodiazepine-7-carbothiohydrazide (XVIII)
[0141] 1.0 g (2.47 mmol) of carbothioyl chloride XI was added to a
stirred solution of 0.37 g (7.42 mmol) of hydrazine hydrate in 15
ml of tetrahydrofuran at 5-10.degree. C. over a period of about 0.5
h, then after 1 h stirring, the mixture was poured into water and
the precipitated product was filtered off to yield 0.89 g (90%) of
the crude product. After drying, it was used in the further
reaction steps. The melting point of the product after
recrystallization from ethanol was 196.degree. C.
[0142] The carbothiohydrazide derivatives XIX-XXII were synthesized
by analogous methods:
(R)-8-Methyl-5-(4-nitrophenyl-8,9-dihydro-7H-1,3-dioxolo[4,5-h][2,3]benzod-
iazepine-7-carbothiohydrazide (XIX)
[0143] Mp.: 140-142.degree. C. Yield: 99%, [.alpha.].sub.D:
-201.degree. (c=0.5; CHCl.sub.3).
(.+-.)-8-Chloro-4-methyl-1-(4-nitrophenyl)-4,5-dihydro-3H-[2,3]benzodiazep-
ine-3-carbothiohydrazide (XX)
[0144] Mp.: 210-211.degree. C. Yield: 61%.
(.+-.)-7-Bromo-4-methyl-8-methoxy
1-(4-nitrophenyl)-4,5-dihydro-3H-[2,3]benzodiazepine-3-carbothiohydrazide
(XXI)
[0145] Mp.: 196-201.degree. C. Yield: 98%.
(.+-.)-8-Methyl-5-(3-methyl-4-nitrophenyl)-8,9-dihydro-7H-1,3-dioxolo[4,5--
h][2,3]benzodiazepine-7-carbothiohidrazide (XXII)
[0146] Mp.: 188-190.degree. C. Yield: 98%.
(.+-.)-8-Methyl-5-(4-nitrophenyl)-8,9-dihydro-7H-1,3-dioxolo[4,5-h][2,3]be-
nzodiazepine-7-carbonitrile (XXII)
[0147] A mixture of 3.25 g (10 mmol) of
(.+-.)-8-methyl-5-(4-nitrophenyl)-8,9-dihydro-7H-1,3-dioxolo[4,5-h][2,3]b-
enzodiazepine, 20 ml of dimethylformamide, 2.76 g (20 mmol) of
potassium chloride and 1.80 g (17 mmol) of cyanogen bromide was
stirred at room temperature for 20 h. After pouring into water, the
precipitated crystals were filtered off, and washed with water to
yield 3.34 g (95%) of the title compound, Mp.: 172-176.degree.
C.
(.+-.)-8-Methyl-5-(4-nitrophenyl)-8,9-dihydro-7H-1,3-dioxolo[4,5-h][2,3]be-
nzodiazepine-7-carbamidoxime (XXIV)
[0148] A mixture of 2.80 g (8.0 mmol) of compound XXIII, 30 ml of
2-methoxyethanol, 0.84 g (10 mmol) of sodium acetate and 0.60 g
(8.8 mmol) of hydroxylamine hydrochloride was stirred for 0.5 h,
then concentrated in vacuum. The residue was treated with water,
the precipitated crystals were filtered off and washed with water
to yield 3.05 g (100%) of the title compound, Mp.: 138-145.degree.
C.
(.+-.)-8-Methyl-5-(4-nitrophenyl)-8,9-dihydro-7H-1,3-dioxolo[4,5-h][2,3]be-
nzodiazepine-7-carboxylic acid (2-chloroethyl)-amide (XXV)
[0149] A mixture of 1.0 g (3.07 mmol) of
(.+-.)-8-methyl-5-(4-nitrophenyl)-8,9-dihydro-7H-1,3-dioxolo[4,5-h][2,3]b-
enzodiazepine, 25 ml of dry dichloromethane and 0.62 g (5.88 mmol)
of 2-chloroethyl isocyanate was stirred at room temperature for 24
h, then concentrated. The residue was purified by refluxing in
ethanol to yield 1.25 g (94%) of the title compound, Mp.:
222-223.degree. C.
(.+-.)-Phenyl(8-methyl-5-(4-nitrophenyl)-8,9-dihydro-7H-1,3-dioxolo[4,5-h]-
[2,3]benzodiazepine-3-carbothioyl)-carbamate (XXVI)
[0150] 0.37 g (3.80 mmol) of potassium thiocyanate was dissolved in
8 ml of acetone, then 0.48 ml (3.80 mmol) of phenyl chloroformate
was added dropwise to the mixture at room temperature. The reaction
mixture was stirred at room temperature for 0.5 h, then at
40.degree. C. for 0.25 h. Then the mixture was cooled with
ice-water and a solution of 1.04 g (3.20 mmol) of
(.+-.)-8-methyl-5-(4-nitrophenyl)-8,9-dihydro-7H-1,3-dioxolo[4,5-
-h][2,3]benzodiazepine in 15 ml of acetone was added dropwise over
a period of 0.5 h. After stirring for 0.5 h the bulk of the solvent
was evaporated and the residue was treated with water, the crystals
were filtered and washed with water to yield 1.73 g, (90%) of the
title compound. Mp.: 160.degree. C.
(.+-.)-1-Methyl-3-{8-methyl-5-(4-nitrophenyl)-8,9-dihydro-7H-1,3-dioxolo[4-
,5-h][2.3]benzodiazepine-7-carbothioyl}-urea (XXVII)
[0151] 1.57 g (3.11 mmol) of compound XXVI was dissolved in 8 ml of
methylformamide and 0.35 ml (4.04 mmol of 40% aqueous methylamine
solution was added dropwise to the ice cooled stirred solution.
After stirring for 2 h the mixture was poured into water, the
precipitated crystals were filtered off and washed with water to
yield 1.56 g of the crude product, which was recrystallized from
ethanol. Yield: 1.01 g (73%). Mp.: 192-193.degree. C.
[0152] The compounds XXVIII and XXIX were synthesized
analogously.
[0153]
(.+-.)-1-Cyclopropyl-3-{8-methyl-5-(4-nitrophenyl)-8,9-dihydro-7H--
1,3-dioxolo[4,5-h][2,3]benzodiazepine-7-carbothioyl}-urea
(XXVIII)
[0154] Mp.: 281-283.degree. C. (ethyl acetate). Yield: 80%
(.+-.)-1-Ethyl-3-{8-methyl-5-(4-nitrophenyl)-8,9-dihydro-7H-1,3-dioxolo[4,-
5-h][2,3]benzodiazepine-7-carbothioyl}-urea (XXIX)
[0155] Mp.: 176-177.degree. C. (methanol). Yield: 73%.
(.+-.)-1-{8-Methyl-5-(4-nitrophenyl)-8,9-dihydro-7H-1,3-dioxolo[4,5-h][2,3-
]benzodiazepine-7-carbothioyl}-4-methyl-semicarbazide (XXX)
[0156] To a stirred solution of 0.40 g (1.0 mmol) of compound XVIII
in 15 ml of chloroform 0.07 ml (1.2 mmol) of methyl isocyanate was
added. After 1 h the reaction mixture was washed with sodium
hydrogen carbonate solution and water and after concentration the
obtained solid material was purified by refluxing in ethanol. The
desired product was 0.36 g, yield: 88%. Mp.: 200.degree. C.
(R)-8-Methyl-5-(3-methyl-4-nitrophenyl)-8,9-dihydro-7H-1,3-dioxolo[4,5-h][-
2,3]benzodiazepine (XXXI)
[0157] The title compound was prepared based on the procedures
described in the literature (Ling et al., J. Chem. Soc. Perkin
Trans. 1:1423 (1995)) and the British patent specification No.
2,311,779.
[0158] Mp.: 159-160.degree. C. (ethanol). [.alpha.].sub.D:
+172.degree. (c=1; CHCl.sub.3).
(R)-7-(tert-Butoxycarbonyl-8-methyl-5-(4-nitrophenyl)-8,9-dihydro-7H-1,3-d-
ioxolo[4,5-h][2,3]benzodiazepine (XXXII)
[0159] The compound was prepared according to a synthesis described
in literature (Anderson et al., J. Am. Chem. Soc. 117: 12358(1995))
with the exception that tert-butyl carbamate was used instead of
acetic hydrazide.
[0160] Mp.: 168-169.degree. C. (isopropanol). [.alpha.].sub.D:
-444.degree. (c=0.6; CHCl.sub.3).
Example 1
[0161]
(.+-.)-8-Methyl-5-(4-nitrophenyl)-7-(2-thiazolyl)-8,9-dihydro-7H-1-
,3-dioxolo[4,5-h][2,3]benzodiazepine
[0162] A mixture of 1.00 g (2.60 mmol) of the starting material I,
2.54 g (12.89 mmol) of bromoacetaldehyde diethyl acetal and 10 ml
of dimethylformamide was stirred at 80.degree. C. for 40 min. Then
the reaction mixture was diluted with water and the crude product
obtained was recrystallized from ethanol to yield 0.85 g (80%) of
the title compound. Mp.: 145-150.degree. C.
Example 2
(R)-8-Methyl-5-(4-nitrophenyl)-7-(2-thiazolyl)-8,9-dihydro-7H-1,3-dioxolo[-
4,5-h][2,3]benzodiazepine
[0163] The title compound was obtained from the starting material
II according to the method described in Example 1. Mp.:
108-110.degree. C., yield: 89%, [.alpha.].sub.D: +514.degree.
(c=0.5; CHCl.sub.3)
Example 3
(S)-8-Methyl-5-(4-nitrophenyl)-7-(2-thiazolyl)-8,9-dihydro-7H-1,3-dioxolo[-
4,5-h][2,3]benzodiazepine
[0164] The title compound was obtained from the starting material
III according to the method described in Example 1. Mp.:
114-116.degree. C., yield: 83%, [.alpha.].sub.D: -522.degree.
(c=0.6; CHCl.sub.3)
Example 4
(.+-.)-8-Methyl-7-(4-methyl-thiazol-2-yl)-5-(4-nitrophenyl)-8,9-dihydro-7H-
-1,3-dioxolo[4,5-h][2.3]benzodiazepine
[0165] A mixture of 0.76 g (1.98 mmol) of the starting material I,
1.10 g (11.88 mmol) of chloroacetone and 15 ml of dimethylformamide
was stirred at 80-90.degree. C. for 40 min. Then the reaction
mixture was diluted with water, the precipitated crystals were
filtered off, dried and purified by refluxing in ethanol to yield
0.69 g (82%) of the title compound; Mp.: 188-189.degree. C.
Example 5
(.+-.)-8-Methyl-7-(5-methyl-thiazol-2-yl)-5-(4-nitrophenyl)-8,9-dihydro-7H-
-1,3-dioxolo[4,5-h][2,3]benzodiazepine
[0166] A mixture of 1.50 g (3.90 mmol) of starting material I, 3.57
g (19.50 mmol) of 2-bromopropionaldehyde dimethyl acetal and 15 ml
of dimethylformamide was stirred at 90.degree. C. for 1.5 h. Then
the reaction mixture was diluted with water and the crude product
obtained was purified by column chromatography using silica gel (MN
Kieselgel 60; Macherey-Nagel, Duren, Germany) as adsorbent and a
mixture of toluene--ethyl acetate (16:1) as eluent to yield 1.08 g
(66%) of the title compound; Mp.: 193-195.degree. C.
Example 6
(.+-.)-7-(4,5-Dimethyl-thiazol-2-yl)-8-methyl-5-(4-nitrophenyl)-8,9-dihydr-
o-7H-1,3-dioxolo[4,5-h][2,3]benzodiazepine
[0167] A mixture of 0.60 g (1.56 mmol) of the starting material I,
1.02 g (9.57 mmol) of 3-chloro-2-butanone and 8 ml of
dimethylformamide was stirred at 90.degree. C. for 3 h. After
cooling the precipitated crystals were filtered off, dried and
purified by recrystallization from dimethylformamide and water to
yield 0.49 g (76%) of the title compound; Mp.: >260.degree. C.
(dec.).
Example 7
(.+-.)-8-Methyl-5-(4-nitrophenyl)-7-(4-phenyl-thiazol-2-yl)-8,9-dihydro-7H-
-1,3-dioxolo[4,5-h][2,3]benzodiazepine
[0168] A mixture of 0.45 g (1.17 mmol) of the starting material I,
0.35 g (1.76 mmol) of phenacyl bromide and 7 ml of
dimethylformamide was stirred at 80.degree. C. for 30 min. After
cooling the precipitated crystals were filtered off, washed with
ethanol and dried to yield 0.50 g (88%) of the title compound; Mp.:
>260.degree. C. (dec.).
Example 8
(.+-.)-7-(4-Ethoxycarbonyl-thiazol-2-yl)-8-methyl-5-(4-nitrophenyl)-8,9-di-
hydro-7H-1,3-dioxolo[4,5-h][2.3]benzodiazepine
[0169] A mixture of 0.45 g (1.17 mmol) of the starting material I,
0.46 g (2.36 mmol) of ethyl bromopyruvate and 7 ml of
dimethylformamide was stirred at 80.degree. C. for 30 min. After
cooling the precipitated crystals were filtered off, washed with
ethanol and dried to yield 0.41 g (85%) of the title compound; Mp.:
242-243.degree. C.
Example 9
(.+-.)-7-(4,5-Dihydro-thiazol-2-yl)-8-methyl-5-(4-nitrophenyl)-8,9-dihydro-
-7H-1,3-dioxolo[4,5-h][2.3]benzodiazepine
[0170] A mixture of 1.00 g (2.6 mmol) of the starting material I,
2.13 g (10.40 mmol) of 2-bromoethylamine hydrobromide and 10 ml of
dimethylformamide was stirred at 90-100.degree. C. for 4 h. After
diluting with water the precipitated crystals were filtered off,
dissolved in dichloromethane and washed several times with 10%
sodium hydrogen carbonate solution. After drying the product was
purified by column chromatography using silica gel (Kieselgel 60)
as adsorbent and a mixture of hexane--ethyl acetate (1:1) as eluent
to yield 0.80 g (75%) of the title compound; Mp.: 185-187.degree.
C.
Example 10
(R)-7-(4,5-Dihydro-thiazol-2-yl)-8-methyl-5-(4-nitrophenyl)-8,9-dihydro-7H-
-1,3-dioxolo[4,5-h][2,3]benzodiazepine
[0171] The title compound was obtained from the starting material
II according to the method described in Example 9.
[0172] Mp.: 118-124.degree. C. Yield: 73%, [.alpha.].sub.D:
+575.degree. (c=0.4; CHCl.sub.3).
Example 11
(S)-7-(4,5-Dihydro-thiazol-2-yl)-8-methyl-5-(4-nitrophenyl)-8,9-dihydro-7H-
-1,3-dioxolo[4,5-h][2,3]benzodiazepine
[0173] The title compound was obtained from the starting material
III according to the method described in Example 9.
[0174] Mp.: 120-125.degree. C. Yield: 71%. [.alpha.].sub.D:
-594.degree. (c=0.4; CHCl.sub.3).
Example 12
(.+-.)-7-(4,5-Dihydro-4-oxo-thiazol-2-yl)-8-methyl-5-(4-nitrophenyl)-8,9-d-
ihydro-7H-1,3-dioxolo[4,5-h][2,3]benzodiazepine
[0175] A mixture of 1.00 g (2.6 mmol) of the starting material I,
1.19 g (7.78 mmol) of methyl bromoacetate and 10 ml of
dimethylformamide was stirred at 80-90.degree. C. for 1 h. After
diluting with water the obtained crude product was purified by
refluxing in methanol to yield 1.00 g (91%) of the title compound;
Mp.: 218-220.degree. C.
Example 13
(.+-.)-7-(4,5-Dihydro-5-methyl-4-oxo-thiazol-2-yl)-8-methyl-5-(4-nitrophen-
yl)-8,9-dihydro-7H-1,3-dioxolo[4,5-h][2,3]benzodiazepine
[0176] A mixture of 1.00 g (2.60 mmol) of the starting material I,
0.94 g (5.19 mmol) of ethyl 2-bromopropionate and 10 ml of
dimethylformamide was stirred at 80-90.degree. C. for 2 h. After
diluting with water the obtained crude product was purified by
refluxing in 15 ml of ethanol to yield 1.08 g (95%) of the title
compound; Mp.: 213-214.degree. C.
Example 14
(.+-.)-7-(5,6-Dihydro-4-oxo-4H-1,3-thiazin-2-yl)-8-methyl-5-(4-nitrophenyl-
)-8,9-dihydro-7H-1,3-dioxolo[4,5-h][2,3]benzodiazepine
[0177] A mixture of 2.00 g (5.20 mmol) of the starting material I,
1.89 g (10.44 mmol) of ethyl 3-bromopropionate and 20 ml of
dimethylformamide was stirred at 80-90.degree. C. for 3 h. The
reaction mixture was diluted with 25% sodium chloride solution and
extracted with dichloromethane. After drying and concentration the
crude product was purified by column chromatography using silica
gel (MN Kieselgel 60) as adsorbent and a mixture of ethyl
acetate-methanol (2:1) as eluent to yield 1.34 g (59%) of the title
compound; Mp.: 220-221.degree. C.
Example 15
5-(4-Nitrophenyl)-7-(2-thiazolyl)-8,9-dihydro-7H-1,3-dioxolo[4,5-h][2,3]be-
nzodiazepine
[0178] The title compound was obtained from the starting material
VIII and bromoacetaldehyde diethyl acetal according to the method
described in Example 1. Mp.: 203-215.degree. C. Yield: 77%.
Example 16
(.+-.)-8-Methyl-5-(3-methyl-4-nitrophenyl)-7-(2-thiazolyl)-8,9-dihydro-7H--
1,3-dioxolo[4,5-h][2,3]benzodiazepine
[0179] The title compound was obtained from the starting material
IV according to the method described in Example 1. Mp.:
171-175.degree. C. Yield: 46%.
Example 17
(.+-.)-8-Methyl-5-phenyl-7-(2-thiazolyl)-8,9-dihydro-7H-1,3-dioxolo[4,5-h]-
[2,3]benzodiazepine
[0180] The title compound was obtained from the starting material
VII according to the method described in Example 1. Mp.:
180-184.degree. C. Yield: 51%.
Example 18
(.+-.)-7-Bromo-4-methyl-8-methoxy-1-(4-nitrophenyl)-3-(2-thiazolyl)-4,5-di-
hydro-3H-[2,3]benzodiazepine
[0181] The title compound was obtained from the starting material X
according to the method described in Example 1. Mp.:
184-190.degree. C. Yield: 54%.
Example 19
(.+-.)-8-Chloro-4-methyl-1-(4-nitrophenyl)-3-(2-thiazolyl)-4,5-dihydro-3H--
[2,3]benzodiazepine
[0182] The title compound was obtained from the starting material V
according to the method described in Example 1. Mp.:
213-216.degree. C. Yield: 67%.
Example 20
(.+-.)-8-Chloro-4-methyl-3-(4-methyl-thiazol-2-yl)-1-(4-nitrophenyl)-4,5-d-
ihydro-3H-[2,3]benzodiazepine
[0183] The title compound was obtained from the starting material V
according to the method described in Example 4. Mp.:
209-216.degree. C. Yield: 94%.
Example 21
(.+-.)-3-(4,5-Dihydro-thiazol-2-yl)-8-chloro-4-methyl-1-(4-nitrophenyl)-4,-
5-dihydro-3H-[2,3]benzodiazepine
[0184] The title compound was obtained from the starting material V
according to the method described in Example 9. Mp.:
225-227.degree. C. Yield: 69%.
Example 22
(.+-.)-3-(4,5-Dihydro-3-oxo-thiazol-2-yl)-8-chloro-4-methyl-1-(4-nitrophen-
yl)-4,5-dihydro-3H-[2.3]benzodiazepine
[0185] The title compound was obtained from the starting material V
according to the method described in Example 12. Mp.:
226-228.degree. C. Yield: 96%.
Example 23
(.+-.)-7,8-Dichloro-4-methyl-3-(4-methyl-thiazol-2-yl)-1-(4-nitrophenyl)-4-
,5-dihydro-3H-[2,3]benzodiazepine
[0186] The title compound was obtained from the starting material
VI according to the method described in Example 4. Mp.:
240-242.degree. C. Yield: 77%.
Example 24
(.+-.)-7-(4,5-Dihydro-oxazol-2-yl)-8-methyl-5-(4-nitrophenyl)-8,9-dihydro--
7H-1,3-dioxolo[4,5-h][2.3]benzodiazepine
[0187] A mixture of 1.43 g (3.32 mmol) of the starting material
XXV, 1.38 g (9.98 mmol) of anhydrous potassium carbonate, 0.24 g
(1.60 mmol) of sodium iodide and 24 ml of dimethylformamide was
stirred at 100-110.degree. C. for 4 h. Then the mixture was diluted
with water and the precipitated crude product was recrystallized
from ethanol to yield 1.00 g (76%) of the title compound; Mp.:
194-196.degree. C.
Example 25
(.+-.)-8-Methyl-5-(4-nitrophenyl)-7-(1,3,4-thiadiazol-2-yl)-8,9-dihydro-7H-
-1,3-dioxolo[4,5-h][2,3]benzodiazepine
[0188] A mixture of 0.57 g (1.43 mmol) of the starting material
XVIII, 6 ml of triethyl orthoformate and a catalytic amount of
hydrochloric acid was stirred at 80.degree. C. for 1 h. After
cooling the precipitated crystals were filtered off, washed with
ethanol and dried to yield 0.45 g (77%) of the title compound; Mp.:
212-213.degree. C.
Example 26
(R)-8-Methyl-5-(4-nitrophenyl)-7-(1,3,4-thiadiazol-2-yl)-8,9-dihydro-7H-1,-
3-dioxolo[4,5-h][2,3]benzodiazepine
[0189] The title compound was obtained from the starting material
XIX according to the method described in Example 25. Mp.:
144-147.degree. C. (ethanol-water). Yield: 88%, [.alpha.].sub.D:
+428.degree. (c=0.2; CHCl.sub.3)
Example 27
(.+-.)-8-Methyl-7-(5-methyl-1,3,4-thiadiazol-2-yl)-5-(4-nitrophenyl)-8,9-d-
ihydro-7H-1,3-dioxolo[4,5-h][2.3]benzodiazepine
[0190] To an ice cooled stirred mixture of 1.0 g (2.50 mmol) of the
starting material XVIII, 35 ml of dichloromethane, 0.40 ml (2.75
mmol) of triethylamine and 0.22 ml (2.80 mmol) of acetyl chloride
was added. The so obtained solution was left at room temperature
for 16 h, then 0.6 g of p-toluenesulfonic acid was added and the
mixture was stirred at 40.degree. C. for 2 h. Then the reaction
mixture was washed with sodium hydrogen carbonate solution and
water until neutrality, dried and concentrated. The crude product
was treated with methanol, then recrystallized from ethanol to
yield 0.99 g (91%) of the title compound. Mp.: 213-215.degree.
C.
Example 28
(R)-8-Methyl-7-(5-methyl-1,3,4-thiadiazol-2-yl)-5-(4-nitrophenyl)-8,9-dihy-
dro-7H-1,3-dioxolo[4,5-h][2,3]benzodiazepine
Method A.
[0191] The title compound was obtained from the starting material
XIX by carrying out the acylation with acetic anhydride according
to the method described in Example 27. The obtained crude product
was purified by column chromatography using silica gel (MN
Kieselgel 60) as adsorbent and a mixture of n-hexane-ethyl acetate
(1:1) as eluent. After concentration of the fractions containing
the title compound, the residue was treated with isopropyl ether to
yield 0.95 g of a solid foam (polymorph). Yield: 89%.
Method B.
[0192] To a solution of 4.04 g (10.0 mmol) of the starting material
XII, 3 ml of dimethylformamide, 1.40 ml (10.0 mmol) of
triethylamine and 0.06 g (0.5 mmol) of 4-dimethylaminopyridine 1.48
g (20.0 mmol) of acetic hydrazide was added. The reaction mixture
was stirred at 50.degree. C. for 5 h, then diluted with water, the
precipitated crystals were filtered off and washed with water. The
so obtained 4.5 g of
(R)--N'-{8-methyl-5-(4-nitrophenyl)-8,9-dihydro-7H-1,3-dioxolo[4,5-h][2,3-
]benzodiazepine-7-carbothioyl}-acetic hydrazide according to its
.sup.1H-NMR spectrum was a mixture of rotation isomers. (The
analyzed sample was purified by column chromatography using a
mixture of n-hexane-ethyl acetate (1:1) as eluent and it was
crystallized with 0.5 mol of ethyl acetate, Mp.: 118.degree.
C.).
[0193] To a suspension of the above intermediate in 50 ml of
ethanol 0.75 ml of concentrated hydrochloric acid was added, and
the so obtained solution was refluxed for 2 h. After concentration
and treatment with water 4.2 g of a crude product was obtained.
Purification by column chromatography using silica gel (MN
Kieselgel 60) as adsorbent and a mixture of n-hexane-ethyl acetate
as eluent and drying at 60.degree. C. in vacuum yielded the title
compound with a melting point of 101-102.degree. C.
[.alpha.].sub.D: +453.degree. (c=0.5; CHCl.sub.3).
[0194] The compounds of Examples 29-34 were obtained according to
the method described in Example 27 using the appropriate acid
chlorides.
Example 29
(.+-.)-7-(5-Cyclopropyl-1,3,4-thiadiazol-2-yl)-8-methyl-5-(4-nitrophenyl)--
8,9-dihydro-7H-1,3-dioxolo[4,5-h][2.3]benzodiazepine
[0195] Mp.: 142-145.degree. C.; yield: 49%.
Example 30
(.+-.)-7-(5-Ethyl-1,3,4-thiadiazol-2-yl)-8-methyl-5-(4-nitrophenyl)
8,9-dihydro-7H-1,3-dioxolo[4,5-h][2,3]benzodiazepine
[0196] Mp.: 163-164.degree. C.; yield: 84%.
Example 31
(R)-7-(5-Ethyl-1,3,4-thiadiazol-2-yl)-8-methyl-5-(4-nitrophenyl)-8,9-dihyd-
ro-7H-1,3-dioxolo[4,5-h][2,3]benzodiazepine
[0197] Mp.: 105.degree. C.; yield: 63%. [.alpha.].sub.D:
+418.degree. (c=0.5; CHCl.sub.3).
Example 32
(.+-.)-8-Methyl-5-(4-nitrophenyl)-7-(5-trifluoromethyl-1,3,4-thiadiazol-2--
yl)-8,9-dihydro-7H-1,3-dioxolo[4,5-h][2.3]benzodiazepine
[0198] Mp.: 184-185.degree. C.; yield: 67%.
Example 33
(.+-.)-8-Methyl-5-(4-nitrophenyl)-7-(5-phenyl-1,3,4-thiadiazol-2-yl)-8,9-d-
ihydro-7H-1,3-dioxolo[4,5-h][2,3]benzodiazepine
[0199] Mp.: 210-212.degree. C.; yield: 56%.
Example 34
(.+-.)-7-(5-Chloromethyl-1,3,4-thiadiazol-2-yl)-8-methyl-5-(4-nitrophenyl)-
-8,9-dihydro-7H-1,3-dioxolo[4,5-h][2,3]benzodiazepine
[0200] Mp.: 210-211.degree. C. yield: 64%.
Example 35
(.+-.)-7-(5-Cyclopropylaminomethyl-1,3,4-thiadiazol-2-yl)-8-methyl-5-(4-ni-
trophenyl)-8,9-dihydro-7H-1,3-dioxolo[4,5-h][2,3]benzodiazepine
[0201] A mixture of 5 ml of dimethylformamide, 0.44 g (0.96 mmol)
of
(.+-.)-7-(5-chloromethyl-1,3,4-thiadiazol-2-yl)-8-methyl-5-(4-nitrophenyl-
)-8,9-dihydro-7H-1,3-dioxolo
[0202] [4,5-h][2,3]benzodiazepine (Example 34) and 0.37 ml (5.31
mmol) of cyclopropylamine was stirred at 70-80.degree. C. for 1 h.
Then the reaction mixture was poured into 20% sodium chloride
solution and, the precipitated crude product was extracted into
ethyl acetate. The solution was washed with water, dried and after
evaporation yielded 0.39 g (85%) of the title compound, as solid
foam.
Example 36
(.+-.)-8-Chloro-4-methyl-1-(4-nitrophenyl)-3-(1,3,4-thiadiazol-2-yl)-4,5-d-
ihydro-3H-[2,3]benzodiazepine
[0203] The title compound was obtained from the starting material
XX according to the method described in Example 25. Mp.:
188.degree. C.; yield: 86%
Example 37
(.+-.)-8-Chloro-4-methyl-3-(5-methyl-1,3,4-thiadiazol-2-yl)-1-(4-nitrophen-
yl)-4,5-dihydro-3H-[2,3]benzodiazepine
[0204] The title compound was obtained from the starting material
XX according to the method described in Example 27. Mp.:
162-164.degree. C.; yield: 52%.
Example 38
(.+-.)-8-Methyl-5-(3-methyl-4-nitrophenyl)-7-(5-methyl-1,3,4-thiadiazol-2--
yl)-8,9-dihydro-7H-1,3-dioxolo[4,5-h][2,3]benzodiazepine
[0205] The title compound was obtained from the starting material
XXI according to the process described in method A of Example
28.
[0206] Mp.: 228-240.degree. C.; yield: 74%.
Example 39
(.+-.)-8-Methyl-5-(4-methyl-3-nitrophenyl)-7-(5-methyl-1,3,4-thiadiazol-5--
yl)-8,9-dihydro-7H-1,3-dioxolo[4,5-h][2,3]benzodiazepine
[0207] The title compound was obtained from the starting material
XV according to the process described in method B of Example
28.
[0208] Mp.: 220.degree. C. (ethanol); yield: 57%.
Example 40
(.+-.)-8-Methyl-7-(5-methyl-1,3,4-thiadiazol-2-yl)-5-(3-nitrophenyl)-8,9-d-
ihydro-7H-1,3-dioxolo[4,5-h][2,3]benzodiazepine
[0209] The title compound was obtained from the starting material
XII according to the process described in method B of Example
28.
[0210] Mp.: 118-119.degree. C., yield: 67%.
Example 41
(.+-.)-7-Bromo-4-methyl-3-(5-methyl-1,3,4-thiadiazol-2-yl)-8-methoxy-1-(4--
nitrophenyl)-4,5-dihydro-3H-[2.3]benzodiazepine
[0211] The title compound was obtained from the starting material
XXI according to the process described in method A of Example
28.
[0212] Mp.: 229-233.degree. C., yield: 76%.
Example 42
(.+-.)-8-Methyl-7-(5-methyl-6H-1,3,4-thiadiazin-2-yl)-5-(4-nitrophenyl)-8,-
9-dihydro-7H-1,3-dioxolo[4,5-h][2,3]benzodiazepine
[0213] A mixture of 1.00 g (2.50 mmol) of the starting material
XVIII, 20 ml of dimethylformamide and 0.57 g (6.16 mmol) of
chloroacetone was stirred at room temperature for 2 h. After
dilution with water the precipitated crystals were filtered off and
purified by refluxing in ethyl acetate to yield 0.73 g (67%) of the
title compound; Mp.: 203-204.degree. C.
Example 43
(.+-.)-7-(5,6-Dihydro-5-oxo-4H-1,3,4-thiadiazin-2-yl)-8-methyl-5-(4-nitrop-
henyl)-8,9-dihydro-7H-1,3-dioxolo[4,5-h][2,3]benzodiazepine
[0214] A mixture of 1.00 g (2.50 mmol) of the starting material
XVIII, 20 ml of dimethylformamide and 0.94 g (6.14 mmol) of methyl
bromoacetate was stirred at 70.degree. C. for 1.5 h. After dilution
with water the precipitated crystals were filtered off and purified
by refluxing in ethyl acetate to yield 0.41 g (37%) of the title
compound; Mp.: 294-295.degree. C. (dec.).
Example 44
(.+-.)-8-Methyl-5-(4-nitrophenyl)-7-(5-oxo-4,5-dihydro-1,3,4-thiadiazol-2--
yl)-8,9-dihydro-7H-1,3-dioxolo[4,5-h][2,3]benzodiazepine
[0215] A mixture of 2.14 g (4.69 mmol) of the starting material XXX
and 122 ml of concentrated hydrochloric acid was stirred at
80.degree. C. A solid material precipitated from the starting
solution. The reaction mixture was concentrated to about half of
its volume, diluted with 40 ml of water and made alkaline with
sodium hydrogen carbonate solution. The precipitated product was
filtered off and washed with water to yield 1.40 g (70%) of the
tide compound. Mp.: 288.degree. C.
Example 45
(R)-8-Methyl-5-(4-nitrophenyl)-7-(5-methyl-1,3,4-oxadiazol-2-yl)-8,9-dihyd-
ro-7H-1,3-dioxolo[4,5-h][2,3]benzodiazepine
[0216] A stirred mixture of 2.2 g (5.15 mmol) of
(R)--N'-(8-methyl-5-(4-nitrophenyl)-8,9-dihydro-7H-1,3-dioxolo[4,5-h][2,3-
]benzodiazepin-7-carbothioyl)-acetic hydrazide (an intermediate of
method B of Example 28), 44 ml of ethanol and 1.72 g (5.39 mmol) of
mercury (II) acetate was refluxed for 2 h. The residue obtained on
concentration was dissolved in dichloromethane and filtered through
a neutral aluminum oxide column. After washing the column the
filtrate was concentrated and the residue was purified by column
chromatography using silica gel (MN Kieselgel 60) as adsorbent and
a mixture of n-hexane-ethyl acetate (1:2.5) as eluent to yield 1.07
g (51%) of the title compound. Mp.: 202-204.degree. C. after
recrystallization from ethanol. [.alpha.]: -249.degree. (c=0.22;
CHCl.sub.3).
Example 46
(.+-.)-8-Methyl-7-(2-methyl-3-oxo-2,3-dihydro-1,2,4-thiadiazol-5-yl)-5-(4--
nitrophenyl)-8,9-dihydro-7H-1,3-dioxolo[4,5-h][2,3]benzodiazepine
[0217] To an ice cooled stirred solution of 0.44 g (1.0 mmol) of
the starting material XXVII in 8 ml of chloroform a solution of
0.19 g (1.2 mmol) of bromine in 3 ml of chloroform was added. After
0.5 h the reaction mixture was diluted with 15 ml of chloroform and
washed with sodium hydrogen carbonate solution and water. The
residue obtained on concentration was stirred with methanol and
filtered to yield 0.36 g (82%) of the title compound. Mp.:
296.degree. C. after recrystallization from ethyl acetate.
[0218] The compounds of Example 47 and 48 were obtained analogously
from the starting materials XXVIII and XXIX, respectively.
Example 47
(.+-.)-7-(2-Cyclopropyl-3-oxo-2,3-dihydro-1,2,4-thiadiazol-5-yl)-8-methyl--
5-(4-nitrophenyl)-8,9-dihydro-7H-1,3-dioxolo[4,5-h][2,3]benzodiazepine
[0219] Mp.: 246-247.degree. C. (ethyl acetate), yield: 64%.
Example 48
(.+-.)-7-(2-Ethyl-3-oxo-2,3-dihydro-1,2,4
thiadiazol-5-yl)-8-methyl-5-(4-nitrophenyl)-8,9-dihydro-7H-1,3-dioxololo[-
4,5-h][2,3]benzodiazepine
[0220] Mp.: 250-256.degree. C., yield: 60%.
Example 49
(.+-.)-7-(4-Carboxythiazol-2-yl)-8-methyl-5-(4-nitrophenyl)-8,9-dihydro-7H-
-1,3-dioxolo[4,5-h][2,3]benzodiazepine
[0221] A mixture of 9 ml of ethanol, 0.85 g (1.89 mmol) of
(.+-.)-7-(4-ethoxycarbonyl-thiazol-2-yl)-8-methyl-5-(4-nitrophenyl)-8,9-d-
ihydro-7H-1,3-dioxolo[4,5-h][2,3]benzodiazepine Example 8) and 7 ml
of 1N sodium hydroxide solution was stirred at 90.degree. C. After
cooling, it was acidified with acetic acid, diluted with water and
the precipitated crystals were filtered off, washed with water and
dried to yield 0.78 g (98%) of the title compound; Mp.:
>260.degree. C.
Example 50
(.+-.)-8-Methyl-5-(4-nitrophenyl)-7-(5-tetrazolyl)-8,9-dihydro-7H-1,3-diox-
olo[4,5-h][2,3]benzodiazepine
[0222] A mixture of 0.60 g (1.70 mmol) of the starting material
XXIII, 3 ml of dimethylformamide, 0.12 g (1.87 mmol) of sodium
azide and 0.10 g (1.87 mmol) of ammonium chloride was stirred at
140.degree. C. for 30 min. The cooled reaction mixture was diluted
with water and the precipitated crystals were filtered off. The so
obtained product was purified by column chromatography using silica
gel (MN Kieselgel 60) as adsorbent and a mixture of
chloroform-methanol (99:1) as eluent to yield 0.68 g (54%) of the
title compound; Mp.: 263-264.degree. C.
Example 51
(.+-.)-8-Methyl-5-(4-nitrophenyl)-7-(1,2,4-oxadiazol-3-yl)-8,9-dihydro-7H--
1,3-dioxolo[4,5-h][2,3]benzodiazepine
[0223] A mixture of 1.50 g (3.91 mmol) of the starting material
XXIV and 15 ml of triethyl orthoformate in the presence of 0.05 ml
of 36% hydrochloric acid was stirred at 110.degree. C. for 30 min,
then concentrated in vacuum. The residue was stirred with water,
the precipitated crystals were filtered off, washed with water and
recrystallized from 2-methoxyethanol to yield 1.15 g (75%) of the
title compound; Mp.: 190-196.degree. C.
Example 52
(.+-.)-8-Methyl-7-(5-methyl-1,2,4-oxadiazol-3-yl)-5-(4-nitrophenyl)-8,9-di-
hydro-7H-1,3-dioxolo[4,5-h][2,3]benzodiazepine
[0224] A mixture of 3.0 g (7.82 mmol) of the starting material XXIV
and 15 ml of acetic anhydride was stirred at 110.degree. C. for 1
h, then after cooling it was diluted with water and extracted with
dichloromethane. The organic layer was concentrated and the residue
was purified by column chromatography using silica gel (MN
Kieselgel 60) as adsorbent and a mixture of n-hexane-ethyl acetate
(2:1) as eluent to yield 1.58 g (50%) of the tide compound; Mp.:
191-200.degree. C.
Example 53
(.+-.)-8-Methyl-7-(2-methylthiazol-4-yl)-5-(4-nitrophenyl)-8,9-dihydro-7H--
1,3-dioxolo[4,5-h][2,3]benzodiazepine
Step A
(.+-.)-7-Bromoacetyl-8-methyl-5-(4-nitrophenyl)-8,9-dihydro-7H-1,3-dioxolo-
[4,5-h][2,3]benzodiazepine
[0225] A mixture of 4.80 g (14.7 mmol) of the starting material I,
24 ml of dimethylformamide, 2.16 g (15.5 mmol) of bromoacetic acid
and 4.56 g (22 mmol) of dicyclohexylcarbodiimide was stirred for 20
h. The reaction mixture was filtered and the filtrate was
concentrated. The residue was taken up in ethyl acetate, washed
with water, concentrated and recrystallized from ethanol to yield
4.83 g (73%) of the title compound; Mp.: 183-186.degree. C.
Step B
[0226] The product obtained in Step A was dissolved in 45 ml of
dimethylformamide and after adding 4.96 g (65 mmol) of
thioacetamide it was stirred at 80.degree. C. for 1 h, then cooled
and poured into water. The precipitated crude product was filtered
off, washed with water and purified by column chromatography using
silica gel (MN Kieselgel 60) as adsorbent and a mixture of
hexane-ethyl acetate (9:1) as eluent to yield 1.67 g (37%) of the
tide compound; Mp.: 178-190.degree. C.
Example 54
(.+-.)-8-Methyl-5-(4-nitrophenyl)-7-(2-pyrimidinyl)-8,9-dihydro-7H-1,3-dio-
xolo[4,5-h][2,3]benzodiazepine
Step A
1-{6-[(4-Nitrophenyl)-(pyrimidinyl-2-yl-hydrazono)-methyl]-benzo-1,3-dioxo-
lo-5-yl}-propan-2-ol
[0227] A stirred mixture of 3.29 g (9.99 mmol) of
(.+-.)-7-methyl-5-(4-nitrophenyl)-7,8-dihydro-5H-[1,3]dioxolo[4,5-g]isoch-
roman-5-ol, 40 ml of ethyl acetate and 1.0 ml (1.15 mmol) of
perchloric acid was refluxed for 1 h. After cooling the
precipitated
(.+-.)-7-methyl-5-(4-nitrophenyl)-7,8-dihydro-[1,3]dioxolo[4,5-g]isochrom-
en-6-ylium perchlorate was filtered off, and it was stirred at
reflux temperature with 1.6 g (14.55 mmol) of 2-hydrazinopyrimidine
in 50 ml of isopropanol for 2 h, then concentrated. The residue was
dissolved in dichloromethane and washed several times with water.
After drying and evaporation the crude product was purified by
column chromatography using silica gel (MN Kieselgel 60) as
adsorbent and a mixture of toluene-ethyl acetate (0.1:4) as eluent
to yield 2.71 g (64%) of the title compound; Mp.: 125-127.degree.
C.
Step B
1-{6-[(4-Nitrophenyl)-(pyrimidin-2-yl-hydrazono)-methyl]-benzo-1,3-dioxolo-
-5-yl}-propan-2-ol mesylate
[0228] 2.35 g (5.58 mmol) of the compound prepared in Step A was
dissolved in 50 ml of dry dichloromethane. The solution was cooled
to 0.degree. C. and after addition of 2.1 ml (15.07 mmol) of
triethylamine 0.87 ml (11.22 mmol) of methanesulfonyl chloride was
added over a period of 20 min, then the mixture was stirred at room
temperature for 3 h. After washing with water it was dried and
concentrated to yield 2.69 g (54%) of the title compound as an
intermediate; Mp.: 122-124.degree. C.
Step C
[0229] A mixture of 3.13 g (6.27 mmol) of the compound obtained in
Step B, 60 ml of a 1:1 mixture of dichloromethane-methanol and 0.52
ml (6.90 mmol) of 50% sodium hydroxide solution was stirred at room
for 1.5 h. After filtration the reaction mixture was concentrated,
the residue was treated with water and recrystallized from three
fold dimethylformamide containing 10% water to yield 1.96 g (77%)
of the title compound; Mp.: 261-263.degree. C.
Example 55
(.+-.)-7-(3-Chloropyridazin-6-yl)-8-methyl-5-(4-nitrophenyl)-8,9-dihydro-7-
H-1,3-dioxolo[4,5-h][2,3]benzodiazepine
Step A
1-{6-[(6-Chloropyridazin-3-yl)-hydrazono-(4-nitrophenyl)-methyl]-(benzo-1,-
3-dioxolo-5-yl)}-propan-2-ol
[0230] A stirred mixture of 2.00 g (6.07 mmol) of
(.+-.)-7-methyl-5-(4-nitrophenyl)-7,8-dihydro-5H-[1,3]dioxolo[4,5-g]isoch-
roman-5-ol, 32 ml of isopropanol, 0.3 ml of hydrochloric acid and
1.04 g (7.28 mmol) of 4-hydrazino-6-chloropyridazine was refluxed
for 3 h. After diluting with water, the precipitated crystals were
filtered off, dried and recrystallized first from ethyl acetate,
then from dimethylformamide containing 10% water to yield 1.53 g
(55%) of the title compound; Mp.: 135-137.degree. C.
Step B
[0231] A mixture of 0.3 g (0.66 mmol) of the compound prepared in
Step A, 10 ml of dimethylformamide and 0.34 g (1.30 mmol) of
triphenylphosphine was stirred at room temperature for 5 min, then
0.20 ml (1.27 mmol) of diethyl azodicarboxylate was added and
stirring was continued for 24 h. After dilution with sodium
chloride solution the precipitated product was filtered off, dried
and purified by column chromatography using silica gel (MN
Kieselgel 60) as adsorbent and a mixture of chloroform-methanol
(99:1) as eluent. The residue obtained on concentration was
crystallized by refluxing in ethanol to yield 0.12 g (42%) of the
title compound; Mp.: 254-255.degree. C.
Example 56
(.+-.)-8-Methyl-5-(4-nitrophenyl)-7-(1H(2H)-1,2,4-triazol-3-yl)-8,9-dihydr-
o-7H-1,3-dioxolo[4,5-h][2,3]benzodiazepine
Step A
(.+-.)-8-Methyl-5-(4-nitrophenyl)-8,9-dihydro-7H-1,3-dioxolo[4,5-h][2,3]be-
nzodiazepin-7-S-methyl-thiocarboximidate
[0232] The title compound was obtained from the starting material I
in dimethylformamide with methyl iodide in the presence of
potassium carbonate at room temperature. Mp.: 191-192.degree. C.,
yield: 94%.
Step B
[0233] A mixture of 3.0 g (7.53 mmol) of the compound obtained in
Step A, 110 ml of 2-methoxyethanol and 4.50 g (74.93 mmol) of
formic hydrazide was stirred at 110.degree. C. in the presence of
catalytic amount of p-toluenesulfonic acid for 16 h. The residue
obtained on concentration was treated with 10% sodium carbonate
solution, the obtained crude product was filtered, dried and
purified by column chromatography using silica gel WIN Kieselgel
60) as adsorbent and a mixture of hexane-ethyl acetate (1:2) as
eluent to yield 1.86 g (63%) of the title compound; Mp.:
154-156.degree. C.
Example 57
(.+-.)-8-Methyl-7-(5-methyl-2(1)H-1,2,4-triazol-3-yl)-5-(4-nitrophenyl)-8,-
9-dihydro-7H-1,3-dioxolo[4,5-h][2,3]benzodiazepine
[0234] A mixture of 15 ml of 2-methoxyethanol, 0.41 g (1.03 mmol)
of
(.+-.)-8-methyl-5-(4-nitrophenyl)-8,9-dihydro-7H-1,3-dioxolo[4,5-h][2,3]b-
enzodiazepine-7-5-methyl-thiocarboximidate (Step A of Example 56)
and 0.35 g (4.68 mmol) of acetic hydrazide was stirred at
110.degree. C. in the presence of catalytic amount of
p-toluenesulfonic acid for 16 h. The residue obtained on
concentration was treated with 10% sodium carbonate solution, the
obtained crude product was filtered, dried and purified by column
chromatography using silica gel (MN Kieselgel 60) as adsorbent and
a mixture of hexane-ethyl acetate (1:2) as eluent to yield 0.32 g
(78%) of the title compound; Mp.: 144-147.degree. C. (solid
foam).
Example 58
(.+-.)-7-(1,5-Dimethyl-1H-1,2,4-triazol-3-yl)-8-methyl-5-(4-nitrophenyl)-8-
,9-dihydro-7H-1,3-dioxolo[4,5-h][2.3]benzodiazepine (isomer I) and
(.+-.)-7-(2,5-dimethyl-2H-1,2,4-triazol-3-yl)-8-methyl-5-(4-nitrophenyl)--
8,9-dihydro-7H-1,3-dioxolo[4,5-h][2.3]benzodiazepine (isomer
II)
[0235] A mixture of 0.57 g (5.08 mmol) of potassium tert-butoxide,
2.05 g (5.04 mmol) of
(.+-.)-8-methyl-7-(5-methyl-2(1)H-1,2,4-triazol-3-yl)-5-(4-nitrophenyl)-8-
,9-dihydro-7H-1,3-dioxolo[4,5-h][2,3]benzodiazepine (Example 57),
40 ml of tetrahydrofuran and 0.32 ml (5.14 mmol) of methyl iodide
was stirred at room temperature for 16 h. then the reaction mixture
was diluted with water, extracted with ethyl acetate, the organic
layer was dried and concentrated. The two products formed in the
reaction were separated by column chromatography using silica gel
(MN Kieselgel 60) as adsorbent and ethyl acetate as eluent. Isomer
II, having R.sub.F: 0.55 was first obtained, which was refluxed in
ethanol to yield 0.30 g (14%), Mp.: 185-187.degree. C. Then isomer
I was collected, having R.sub.F: 0.26, which after refluxing in
ethanol weighed 0.67 g (32%), Mp.: 193-195.degree. C.
Example 59
[0236]
(.+-.)-8-Methyl-7-(1-methyl-1H-1,2,4-triazol-3-yl)-5-(4-nitropheny-
l)-8,9-dihydro-7H-1,3-dioxolo[4,5-h][2,3]benzodiazepine (isomer I)
and
(.+-.)-8-methyl-7-(2-methyl-2H-1,2,4-triazol-3-yl)-5-(4-nitrophenyl)-8,9--
dihydro-7H-1,3-dioxolo[4,5-h][2,3]benzodiazepine (isomer II)
[0237] A mixture of 0.41 g (3.65 mmol) of potassium tert-butoxide,
1.4 g (3.57 mmol) of
(.+-.)-8-methyl-5-(4-nitrophenyl)-7-(1H(2H)-1,2,4-triazol-3-yl)-8,9-dihyd-
ro-7H-1,3-dioxolo[4,5-h][2,3]benzodiazepine (Example 56), 35 ml of
tetrahydrofuran and 0.23 ml (3.69 mmol) of methyl iodide was
stirred at room temperature for 16 h. After dilution with water the
reaction mixture was extracted with ethyl acetate, the organic
layer was dried and concentrated. The two products formed in the
reaction were separated by column chromatography using silica gel
(MN Kieselgel 60) as adsorbent and ethyl acetate as eluent. Isomer
I, having R.sub.F: 0.22, weighed 0.37 g, yield: 26%, Mp.:
115-117.degree. C. Isomer II, having R.sub.F: 0.63, was 0.35 g,
yield: 24%, Mp.: 92-94.degree. C.
Examples 60-119
General Procedures for Reduction of the Nitro Groups of the
Compounds Obtained in the Above Examples
Method A
[0238] 2.0 mmol of nitro compound was dissolved in a mixture of
methanol-dichloromethane and after adding 6-10 mmol of 85-98%
hydrazine hydrate and 0.1-2 g RaNi catalyst the mixture was stirred
at 20-40.degree. C. for 1-5 h. After filtration of the catalyst the
filtrate was concentrated, the residue was treated with water and
the product was filtered off.
Method B
[0239] 5.5 g of RaNi catalyst was prehydrogenated in 250 ml of a
2:1 mixture of methanol-dichloromethane, then 20.0 mmol of nitro
compound was added in 250 ml of the above solvent mixture and the
so obtained mixture was hydrogenated at atmospheric pressure. After
filtration of the catalyst the filtrate was concentrated, the
residue was treated with water, the product was filtered, washed
and dried.
Method C
[0240] A stirred mixture of 1.82 mmol of nitro compound, 30 ml of
ethanol and 2.46 g (10.91 mmol) of tin (II) chloride dihydrate was
refluxed for 3 h. The reaction mixture was concentrated, then
aqueous sodium hydrogen carbonate and ethyl acetate were added to
the residue. After separation the water phase was extracted with
ethyl acetate, the combined organic layers were washed with sodium
chloride solution, dried and concentrated. If necessary the residue
was purified either by column chromatography or by
recrystallization.
Method D
[0241] 3.4 mmol of nitro compound was dissolved in 35 ml of a
mixture of methanol-dichloromethane (1:1), 0.4 g of a 10% palladium
on activated carbon catalyst and 0.47 g of potassium carbonate were
added and the so obtained mixture was hydrogenated in the presence
of 1 ml of water. After completion of the reaction the catalyst was
filtered off, the filtrate was concentrated, the residue was
treated with water and filtered.
Method E
[0242] 4.0 mmol of nitro compound was dissolved in 48 ml of
methanol containing 5% water, then after addition of 0.20 g of the
catalyst 10% palladium on activated carbon 3.5 equivalent of a
concentrated aqueous solution of potassium formate was added
dropwise at room temperature and the mixture was stirred at the
above temperature. After completion of the reaction the catalyst
was filtered off, the filtrate was concentrated, the residue is
treated with water and filtered. TABLE-US-00010 TABLE 10
2,3-Benzodiazepines containing aminophenyl group (The .sup.1H NMR
spectra were recorded at 250 MHz unless stated otherwise)
Mp.(.degree. C.) Number of Solvent of Yield (%) Example Name
recrystall. [.alpha.].sub.D 60
(.+-.)-5-(4-Aminophenyl)-8-methyl-7-(2-thiazolyl)-8,9-dihydro-
187-190 78 7H-1,3-dioxolo[4,5-h][2,3]benzodiazepine Method A
.sup.1H NMR(CDCl.sub.3) .delta. 1.32(3H, d, 6.5 Hz), 2.78(1H, dd,
14.0 Hz, 9.7 Hz), 2.97(1H, dd, 14.0 Hz, 4.9 Hz), 3.80(2H, br),
5.26(1H, m), 5.98(2H, m), 6.65(1H, s), 6.67(1H, d, 4.0 Hz),
6.73(2H, dm), 6.80(1H, s), 7.37(1H, d, 4.0 Hz), 7.55(2H, dm) MS:
EI(70eV): [M].sup.+.: 378, m/z: 363, 279, 278, 253, 252 61
(R)-5-(4-Aminophenyl)-8-methyl-7-(2-thiazolyl)-8,9-dihydro- 125-130
84 7H-1,3-dioxolo[4,5-h][2,3]benzodiazepine -578.degree.(c=1,
CHCl.sub.3) Method A .sup.1H NMR(CDCl.sub.3) .delta. 1.29(3H, d,
6.5 Hz), 2.77(1H dd, 14.0 Hz, 9.7 Hz), 3.00(1H, dd, 14.0 Hz, 4.9
Hz), 3.92(2H, br), 5.23(1H, m), 5.98(2H, m), 6.62(1H, d, 4.0 Hz),
6.65(1H, s), 6.72(2H, dm), 6.80(1H, s), 7.32(1H, d, 4.0 Hz),
7.55(2H, dm) 62 (S)-5-(4-Aminophenyl)-8-methyl-7-(2-thiazolyl)-8,9-
124-128 94 dihydro-7H-1,3-dioxolo[4,5-h][2,3]benzodiazepine
+546.degree.(c=0.34, CHCl.sub.3) Method A .sup.1H NMR(DMSO-d.sub.6)
.delta. 1.15(3H, d, 6.5 Hz), 2.60(1H, dd, 13.6 Hz, 10.5 Hz),
2.94(1H, dd, 13.6 Hz, 4.8 Hz), 4.99(1H, m), 5.72(2H, br), 6.03(2H,
m), 6.60(2H, dm), 6.62(1H, s), 6.81(1H, d, 4.0 Hz), 7.04(1H, s),
7.27(1H, d, 4.0 Hz), 7.55(2H, dm) MS: EI(70eV): [M].sup.+.: 378,
m/z: 377, 363, 279, 278, 253, 252 CI: [M+H].sup.+: 379, [M].sup.+.:
378, m/z: 363 63
(.+-.)-5-(4-Aminophenyl)-8-methyl-7-(4-methyl-thiazol-2- 190-191 65
yl)-8,9-dihydro-7H-1,3-dioxolo-[4,5-h][2,3]benzodiazepine (EtOH)
Method A .sup.1H NMR(CDCl.sub.3) .delta. 1.30(3H, d, 6.5 Hz),
2.29(3H, s), 2.77(1H, dd, 14.0 Hz, 10.0 Hz), 2.92(1H, dd, 14.0 Hz,
5.1 Hz), 3.94(2H, br), 5.27(1H, m), 5.97(2H, m), 6.20(1H, s),
6.53(2H, dm), 6.70(1H, s), 6.88(1H, s), 7.53(2H, dm) 64
(.+-.)-5-(4-Aminophenyl)-8-methyl-7-(5-methyl-thiazol-2- 165-167 47
yl)-8,9-dihydro-7H-1,3-dioxolo-[4,5-h][2,3]benzodiazepine Method A
.sup.1H NMR(DMSO-d.sub.6) .delta. 1.17(3H, d, 6.5 Hz), 225(3H, s),
2.60(1H, dd, 13.9 Hz, 10.3 Hz), 2.94(1H, dd, 13.9 Hz, 5.1 Hz),
4.95(1H, m), 5.70(2H, br), 6.05(2H, dm), 6.57(1H, s), 6.62(2H, dm),
6.93(1H, s), 7.04(1H, s), 7.36(2H, dm) 65
(.+-.)-5-(4-Aminophenyl)-8-methyl-7-(4,5-dimethyl-thiazol- 240-242
83 2-yl)-8,9-dihydro-7H-1,3-dioxolo-[4,5-h][2,3]benzodiazepine
(EtOH) Method A .sup.1H NMR(DMSO-d.sub.6) .delta. 1.16(3H, d, 6.5
Hz), 2.06(3H, s), 2.13(3H, s), 2.62(1H, dd, 14.0 Hz, 10.0 Hz),
2.92(1H, dd, 14.0 Hz, 5.0 Hz), 4.97(1H, m), 5.70(2H, br), 6.04(2H,
dm), 6.60(1H,s), 6.62(2H, dm), 7.02(1H, s), 7.34(2H, dm) 66
(.+-.)-5-(4-Aminophenyl)-7-(4-phenyl-thiazol-2-yl)-8-methyl-
221-223 89 8,9-dihydro-7H-1,3-dioxolo-[4,5-h][2,3]benzodiazepine
(EtOH) Method A .sup.1H NMR(CDCl.sub.3) .delta. 1.29(3H, d, 6.5
Hz), 2.80(1H, dd, 14.0 Hz, 9.4 Hz), 3.00(1H, dd, 14.0 Hz, 4.8 Hz),
3.93(2H, br), 5.40(1H, m), 5.98(2H, m), 6.62(1H, s), 6.70(2H, dm),
6.78(1H,s), 7.29(1H, t), 7.39(1H, t), 7.50(1H, s), 7.57(2H, dm),
7.86(2H, d) 67
(.+-.)-5-(4-Aminophenyl)-7-(4-ethoxycarbonyl-thiazol-2-yl)-8-
251-252 83
methyl-8,9-dihydro-7H-1,3-dioxolo-[4,5-h][2,3]benzodiazepine (EtOH)
Method A .sup.1H NMR(CDCl.sub.3) .delta. 1.29(3H, d, 6.5 Hz),
1.38(3H, t), 2.76(1H, dd, 14.0 Hz, 10.0 Hz), 2.92(1H, dd, 14.0 Hz,
5.0 Hz), 3.98(2H, br), 4.33(2H, q), 5.40(1H, m), 6.00(2H, m),
6.68(1H,s), 6.69(2H, dm), 6.82(1H, s), 6.86(1H, s), 7.51(2H, dm) 68
(.+-.)-5-(4-Aminophenyl)-7-(4,5-dihydro-thiazol-2-yl)-8- 145-150 84
methyl-8,9-dihydro-7H-1,3-dioxolo-[4,5-h][2,3]benzodiazepine (EtOH)
Method A .sup.1H NMR(CDCl.sub.3) .delta. 1.21(3H, d, 6.5 Hz),
2.70(1H, dd, 14.0 Hz, 10.0 Hz), 2.96(1H, dd, 14.0 Hz, 5.0 Hz),
3.20(1H, m), 3.70(1H, m), 3.90(2H, br), 4.17(2H, m), 5.09(1H, m),
5.98(2H, dm), 6.60(1H, s), 6.66(2H, dm), 6.73(1H, s), 7.47(2H, dm)
MS: EI(70eV): [M].sup.+.: 380, m/z: 365, 339, 279, 264, 253, 252 69
(R)-5-(4-Aminophenyl)-7-(4,5-dihydro-thiazol-2-yl)-8-methyl-
148-150 82 8,9-dihydro-7H-1,3-dioxolo- (EtOH) -239.degree.
[4,5-h][2,3]benzodiazepine (c=0.5, CHCl.sub.3) Method A .sup.1H
NMR(DMSO-d.sub.6) .delta. 1.16(3H, d, 6.5 Hz), 2.60(1H, dd, 14.0
Hz, 10.0 Hz), 2.90(1H, dd, 14.0 Hz, 4.0 Hz), 3.25(2H, m), 4.00(2H,
m), 4.82(1H, m), 5.73(2H, br), 6.07(2H, dm), 6.64(s), 6.64(2H, dm),
7.02(1H, s), 7.30(2H, dm) MS: EI(70eV): [M].sup.+.: 380, m/z: 365,
339, 279, 278, 264, 253, 252 CI: [M+H].sup.+: 381, [M].sup.+.: 380,
m/z: 279 70 (S)-5-(4-Aminophenyl)-7-(4,5-dihydro-thiazol-2-yl)-8-
150-152 92 methyl-8,9-dihydro-7H-1,3-dioxolo- +175.degree.(c=0.51,
CHCl.sub.3) [4,5-h][2,3]benzodiazepine Method A MS: EI(70eV):
[M].sup.+.: 380, m/z: 365, 339, 279, 278, 264, 253, 252 CI:
[M+H].sup.+: 381, [M].sup.+.: 380, m/z: 279 71
(.+-.)-5-(4-Aminophenyl)-7-(4,5-dihydro-4-oxo-thiazol-2-yl)-8-
218-220 85
methyl-8,9-dihydro-7H-1,3-dioxolo-[4,5-h][2,3]benzodiazepine (EtOH)
Method A .sup.1H NMR(DMSO-d.sub.6).delta. 1.29(3H, d, 6.5Hz),
2.61(1H, dd, 13.0Hz, 12.0Hz), 2.96(1H, dd, 13.0Hz, 5.0Hz), 3.72(2H,
m), 5.08(1H, m), 6.01(2H, br), 6.06(2H, dm), 6.60(2H, dm), 6.62(1H,
s), 7.10(1H, s), 7.40(2H, dm) 72
(.+-.)-5-(4-Aminophenyl)-7-(4,5-dihydro-5-methyl-4-oxo- 200-204 63
thiazol-2-yl)-8-methyl-8,9-dihydro-7H-1,3-dioxolo- (EtOH)
[4,5-h][2,3]benzodiazepine Method A .sup.1H
NMR(DMSO-d.sub.6).delta. 1.32(d) and 1.45(d, overlapping,
diastereomers), 2.60(1H, dd, 13.0Hz, 12.0Hz), 2.94(1H, dd, 13.0Hz,
5.0Hz), 3.96 and 4.05(1H, q), 5.08(1H, m), 6.0(2H, br), 6.07(2H,
dm), 6.60(2H, dm), 6.62(1H, s), 7.08(1H, s), 7.40(2H, dm) MS:
EI(70eV): [M].sup.+.: 408, m/z: 393, 279, 265, 253, 252 73
(.+-.)-5-(4-Aminophenyl)-7-(5,6-dihydro-4-oxo-4H-1,3- 226-228 90
thiazin-2-yl)-8-methyl-8,9-dihydro-7H-1,3-dioxolo- (EtOH)
[4,5-h][2,3]benzodiazepine Method A .sup.1H
NMR(DMSO-d.sub.6).delta. 1.25(3H, d, 6.5 Hz), 2.35(2H, m), 2.57(1H,
dd, 13.0 Hz, 12.0 Hz), 2.88(1H, dd, 13.0 Hz, 4.0 Hz), 3.05(2H, m),
5.21(1H, m), 5.97(2H, br), 6.09(2H, dm), 6.60(1H, s), 6.62(2H, dm),
7.04(1H, s), 7.42(2H, dm) MS: EI(70eV): [M].sup.+.: 408, m/z: 295,
279, 253, 252 74
5-(4-Aminophenyl)-7-(2-thiazolyl)-8,9-dihydro-7H-1,3-dioxolo
200-204 52 [4,5-h][2,3]benzodiazepine Method A .sup.1H
NMR(DMSO-d.sub.6) .delta. 2.88(2H, t), 4.21(2H, t), 5.70(2H, s),
6.08(2H, s), 6.60(1H, s), 6.62(2H, dm), 6.89(1H, d, 4.0 Hz),
7.08(1H, s), 728(1H, d, 4.0 Hz), 7.37(2H, dm) 75
(.+-.)-5-(4-Amino-3-methylphenyl)-8-methyl-7-(2-thiazolyl)-8,9-
225-227 78 dihydro-7H-1,3-dioxolo-[4,5-h][2,3]benzodiazepine Method
B MS: EI(70eV): [M].sup.+.: 392, m/z: 377, 293, 266 CI:
[M+H].sup.+: 393, [M].sup.+.: 392, m/z: 266 76
(.+-.)-1-(4-Aminophenyl)-4-methyl-8-methoxy-3-(2-thiazolyl)-4,5-
105-107 57 dihydro-3H-[2,3]benzodiazepine Method D MS: EI(70eV):
[M].sup.+.: 364, m/z: 349, 265, 223 CI: [M+H].sup.+: 365,
[M].sup.+.: 364 77
(.+-.)-1-(4-Aminophenyl)-8-chloro-4-methyl-3-(2-thiazolyl)-4,5-
104-107 72 dihydro-3H-[2,3]benzodiazepine Method A .sup.1H
NMR(CDCl.sub.3) .delta. 1.31(3H, d, 6.5 Hz), 2.96(1H, dd, 13.0 Hz,
10.0Hz), 3.10(1H, dd, 13.0 Hz, 5.0 Hz), 5.35(1H, m), 6.68(1H, d,
4.0 Hz), 6.72(2H, dm), 7.21(1H, d, 4.0 Hz), 7.25(1H, d, 1.0Hz),
7.27(1H, d, 7.0 Hz), 7.34(1H, dd), 7.53(2H, dm) 78
(.+-.)-1-(4-Aminophenyl)-8-chloro-4-methyl-3-(4-methyl-thiazol-2-
173-175 90 yl)-4,5-dihydro-3H-[2,3]benzodiazepine Method A .sup.1H
NMR(CDCl.sub.3) .delta. 1.26(3H, d, 6.5 Hz), 227(3H, d, 1.0 Hz),
2.81(1H, dd, 14.0 Hz, 9.7 Hz), 3.02(1H, dd, 14.0 Hz, 5.0 Hz),
3.95(2H, br), 5.28(1H, m), 6.20(1H, q, 1.0 Hz), 6.70(2H, dm),
7.17(1H, d, 2.2 Hz), 7.22(1H, d, 8.2 Hz), 7.33(1H, dd, 8.2 Hz, 2.2
Hz), 7.51(2H, dm) 79
(.+-.)-1-(4-Aminophenyl)-3-(4,5-dihydro-thiazol-2-yl)-8- 213-216 79
chloro-4-methyl-4,5-dihydro-3H-[2,3]benzodiazepine (MeOH) Method A
.sup.1H NMR(DMSO-d.sub.6) .delta. 1.08(3H, d, 6.5 Hz), 2.68(1H, dd,
14.0 Hz, 10.0 Hz), 3.06(1H, dd, 14.0 Hz, 5.0 Hz), 3.20(2H, m),
4.02(2H, m), 5.68(2H, s), 4.92(1H, m), 6.60(2H, dm), 7.09(1H, d,
1.0 Hz), 7.28(2H, dm), 7.41(1H, d, 7.0 Hz), 7.48(1H, dd) 80
(.+-.)-1-(4-Aminophenyl)-3-(4,5-dihydro-4-oxo-thiazol-2- 226-228 75
yl)-8-chloro-4-methyl-4,5-dihydro-3H-[2,3]benzodiazepine (iPrOH)
Method A .sup.1H NMR(DMSO-d.sub.6) .delta. 1.32(3H, d, 6.5 Hz),
2.68(1H, dd, 13.8 Hz, 12.0 Hz), 3.08(1H, dd, 13.8 Hz, 4.8 Hz),
3.77(2H, m), 5.10(1H, m), 6.12(2H, br), 6.66(2H, dm), 7.17(1H, d,
2.0 Hz), 7.41(2H, dm), 7.52(1H, d, 8.0 Hz), 7.54(1H, dd, 8.0 Hz,
2.0 Hz) 81
(.+-.)-1-(4-Aminophenyl)-7,8-dichloro-3-(4-methyl-thiazol-2-
182-184 48 yl)-4-methyl-4,5-dihydro-3H-[2,3]benzodiazepine (EtOH)
Method A .sup.1H NMR(CDCl.sub.3) .delta. 1.28(3H, d, 6.5 Hz),
2.30(3H, s), 2.80(1H, dd, 14.0 Hz, 9.6 Hz), 3.02(1H, dd, 14.0 Hz,
4.9 Hz), 3.96(2H, br), 5.31(1H, m), 6.22(1H, q, 1.0 Hz), 6.69(2H,
dm), 7.28(1H, s), 7.39(1H, s), 7.50(2H, dm) 82
(.+-.)-5-(4-Aminophenyl)-7-(4,5-dihydro-oxazol-2-yl)-8- 166-167 87
methyl-8,9-dihydro-7H-1,3-dioxolo-[4,5-h][2,3]benzodiazepine (EtOH)
Method A .sup.1H NMR(DMSO-d.sub.6) .delta. 1.20(3H, d, 6.5 Hz),
2.31(1H, dd, 13.8 Hz, 12.0 Hz), 2.78(1H, dd, 13.8 Hz, 5.8 Hz),
3.61(2H, m), 4.18(2H, m), 4.51(1H, m), 5.66(2H, br), 6.03(2H, dm),
6.51(1H, s), 6.53(2H, dm), 6.98(1H, s), 7.30(2H, dm) MS: EI(70eV):
[M].sup.+.: 364, m/z: 349, 323, 279, 278, 252 CI: [M+H].sup.+: 365,
[M].sup.+.: 364 83
(.+-.)-5-(4-Aminophenyl)-8-methyl-7-(1,3,4-thiadiazol-2- 192-194 77
yl)-8,9-dihydro-7H-1,3-dioxolo- (50% [4,5-h][2,3]benzodiazepine
EtOH--H.sub.2O) Method A .sup.1H NMR(DMSO-d.sub.6) .delta. 1.20(3H,
d, 6.5 Hz), 2.62(1H, dd, 13.9 Hz, 10.8 Hz), 2.99(1H, dd, 13.9 Hz,
5.2 Hz), 5.01(1H, m), 5.78(2H, br), 6.03(2H, dm), 6.58(1H, s),
6.60(2H, dm), 7.07(1H, s), 7.32(2H, dm,) 84
(R)-5-(4-Aminophenyl)-8-methyl-7-(1,3,4-thiadiazol-2- 219-220 67
yl)-8,9-dihydro-7H-1,3-dioxolo-[4,5-h][2,3]benzodiazepine (ethyl
formate) -490.degree. (c=0.9, CHCl.sub.3) Method C .sup.1H
NMR(CDCl.sub.3) .delta. 1.33(3H, d, 6.5 Hz), 2.80(1H, dd, 14.0 Hz,
9.9 Hz), 2.97(1H, dd, 14.0 Hz, 5.0 Hz), 4.02(2H, br), 5.30(1H, m),
5.98(2H, dm), 6.65(1H, s), 6.68(2H, dm), 6.80(1H,s), 7.51(2H, dm,),
8.50(1H, s) 85
(.+-.)-5-(4-Aminophenyl)-8-methyl-7-(5-methyl-1,3,4-thiadiazol-2-
143-148 89
yl)-8,9-dihydro-7H-1,3-dioxolo-[4,5-h][2,3]benzodiazepine Method A
.sup.1H NMR(CDCl.sub.3) .delta. 1.32(3H, d, 6.5 Hz), 2.56(3H, s),
2.76(1H, dd, 14.0 Hz, 10.0 Hz), 2.93(1H, dd, 14.0 Hz, 5.0 Hz),
4.00(2H, br), 5.19(1H, m), 5.98(2H, dm), 6.64(1H, s), 6.70(2H,dm),
6.79(1H, s), 7.48(2H, dm,) MS: EI(70eV): [M].sup.+.: 393, m/z: 378,
279, 278, 253, 252 CI: [M+H].sup.+: 394, [M].sup.+.: 393, m/z: 252
86 (R)-5-(4-Aminophenyl)-8-methyl-7-(5-methyl-1,3,4-thiadiazol-2-
168-170 78
yl)-8,9-dihydro-7H-1,3-dioxolo-[4,5-h][2,3]benzodiazepine (50%
EtOH-- -482.degree. H.sub.2O) (c=0.5, CHCl.sub.3) Method .sup.1H
NMR(DMSO-d.sub.6) .delta. 1.23(3H, d, 6.5 Hz), 2.50(3H, s),
2.60(1H, dd, 13.8 Hz, 9.6 Hz), 2.97(1H, B, C dd, 13.8 Hz, 4.9 Hz),
4.93(1H, m), 5.78(2H, br), 6.03(2H, dm), 6.58(1H, s), 6.60(2H, dm),
7.09 (1H, s), 7.31(2H, dm) 87
(.+-.)-5-(4-Aminophenyl)-7-(5-cyclopropyl-1,3,4-thiadiazol-2-
145-148 75 yl)-8-methyl-8,9-dihydro-7H-1,3-dioxolo[4,5-h][2,3]
(precipit. benzodiazepine with water) Method A .sup.1H
NMR(DMSO-d.sub.6) .delta. 0.88(2H, m), 1.05(2H, m), 1.22(3H, d, 6.5
Hz), 2.22(1H, m), 2.61(1H, dd, 14.0 Hz, 10.0 Hz), 2.99(1H, dd, 14.0
Hz, 5.0 Hz), 4.97(1H, m), 5.78(2H, br), 6.05(2H, dm), 6.60(1H, s),
6.63(2H, dm), 7.06(1H, s), 7.36(2H, dm) 88
(.+-.)-5-(4-Aminophenyl)-7-(5-ethyl-1,3,4-thiadiazol-2-yl)-8-
135-138 67 methyl-8,9-dihydro-7H-1,3-dioxolo-[4,5-h][2,3] Method A
.sup.1H NMR(CDCl.sub.3) .delta. 1.35(3H, t), 1.36(3H, d, 6.5 Hz),
2.79(1H, dd, 14.0 Hz, 10.0 Hz), 2.98(2H, q), 2.99(1H, dd, 14.0 Hz,
5.0 Hz), 3.98(2H, br), 5.25(1H, m), 6.02(2H, dm), 6.63(1H, s),
6.73(2H, dm), 6.82(1H, s), 7.51(2H, dm,)
89 (R)-5-(4-Aminophenyl)-7-(5-ethyl-1,3,4-thiadiazol-2- 142-144 47
yl)-8-methyl-8,9-dihydro-7H-1,3-dioxolo- (precipit. -602.degree.
[4,5-h][2,3]benzodiazepine with water) (c=0.5, EtOH) Method E MS:
EI(70eV): [M].sup.+.: 407, m/z: 392, 279, 278, 253, 252 CI:
[M+H].sup.+: 408, [M].sup.+.: 407 90
(.+-.)-5-(4-Aminophenyl)-8-methyl-7-(5-trifluoromethyl- 216-218 33
1,3,4-thiadiazol-2-yl)-8,9-dihydro-7H-1,3-dioxolo-
[4,5-h][2,3]benzodiazepine Method A .sup.1H NMR(CDCl.sub.3) .delta.
1.39(3H, d, 6.5 Hz), 2.80(1H, dd, 14.0 Hz, 10.0 Hz), 2.93(1H, dd,
14.0 Hz, 5.0 Hz), 4.06(2H, br), 5.28(1H, dm), 6.00(2H, dm),
6.61(1H, s), 6.69(2H, dm), 6.81(1H, s), 7.48 (2H, dm,) MS:
EI(70eV): [M].sup.+.: 447, m/z: 432, 279, 253, 252 CI: [M+H].sup.+:
448, [M].sup.+.: 447, m/z: 252 91
(.+-.)-5-(4-Aminophenyl)-7-(5-phenyl-1,3,4-thiadiazol-2- 228-230 84
yl)-8-methyl-8,9-dihydro-7H-1,3-dioxolo-[4,5-h][2,3] (50%
benzodiazepine EtOH--H.sub.2O) Method A .sup.1H NMR(DMSO-d.sub.6)
.delta. 1.28(3H, d, 6.5 Hz), 2.67(1H, dd, 14.0 Hz, 10.0 Hz),
3.01(1H, dd, 14.0 Hz, 5.0 Hz), 5.02(1H, m), 5.81(2H, br), 6.07(2H,
dm), 6.59(1H, s), 6.61(2H, dm), 7.08(1H, s), 7.40(2H, dm), 7.45(3H,
m), 7.81(2H, d) MS: EI(70eV): [M].sup.+.: 455, m/z: 440, 295, 279,
253, 252 CI: [M+H].sup.+: 456, [M].sup.+.: 455, m/z: 295 92
(.+-.)-5-(4-Aminophenyl)-7-(5-cyclopropylamino-methyl-1,3,4-
135-138 35
thiadiazol-2-yl)-8-methyl-8,9-dihydro-7H-1,3-dioxolo[4,5-h]
[2,3]benzodiazepine Method A .sup.1H NMR(CDCl.sub.3) .delta.
0.45(4H, m), 1.33(3H, d, 6.5 Hz), 2.28(1H, m), 2.75(1H, dd, 14.0
Hz, 9.9 Hz), 2.85(1H, dd, 14.0 Hz, 4.9 Hz), 4.0(2H, br), 4.10(2H,
s), 5.26(1H, m), 6.00(2H, m), 6.60(1H, s), 6.68(2H, dm), 6.80(1H,
s), 7.49(2H, dm) 93
(.+-.)-1-(4-Aminophenyl)-8-chloro-4-methyl-3-(1,3,4-thiadiazol-2-
125-128 79 yl)-4,5-dihydro-3H-[2,3]benzodiazepine Method A .sup.1H
NMR(DMSO-d.sub.6) .delta. 1.18(3H, d, 6.5 Hz), 2.69(1H, dd, 14.0
Hz, 10.8 Hz), 3.14(1H, dd, 14.0 Hz, 5.1 Hz), 5.05(1H, m), 5.83(2H,
s), 6.62(2H, dm), 7.10(1H, s), 7.33(2H, dm), 7.51(2H, m) 94
(.+-.)-1-(4-Aminophenyl)-8-chloro-4-methyl-3-(5-methyl- 131-133 88
1,3,4-thiadiazol-2-yl)-4,5-dihydro-3H-[2,3]benzodiazepine Method A
.sup.1H NMR(DMSO-d.sub.6) .delta. 1.18(3H, d, 6.5 Hz), 2.70(1H, dd,
14.0 Hz, 10.3 Hz), 3.11(1H, dd, 14.0 Hz, 5.3 Hz), 2.50(3H, s),
4.96(1H, m), 5.80(2H, s), 6.62(2H, dm), 7.10(1H, s), 7.32(2H, dm),
7.51 (2H, m) 95
(.+-.)-5-(4-Amino-3-methylphenyl)-8-methyl-7-(5-methyl- 140-144 72
1,3,4-thiadiazol-2-yl)-8,9-dihydro-7H-1,3-dioxolo-[4,5-h][2,3]
benzodiazepine Method B MS: EI(70eV): [M].sup.+.: 407, m/z: 392,
293, 266 CI: [M+H].sup.+: 408, [M].sup.+.: 407, m/z: 266 96
(.+-.)-5-(3-Amino-4-methylphenyl)-8-methyl-7-(5-methyl- 125 70
1,3,4-thiadiazol-2-yl)-7H-1,3-dioxolo-[4,5-h][2,3] benzodiazepine
Method B .sup.1H NMR(500 MHz)(DMSO-d.sub.6) .delta. 1.17(3H, d, 6.5
Hz), 2.10(3H, s), 2.51(3H, s), 2.72(1H, dd, 14.1 Hz, 9.1 Hz),
3.05(1H, dd, 14.1 Hz, 4.5 Hz), 5.01(2H, s), 5.03(1H, m), 6.07(2H,
dm), 6.55(1H, s), 6.70(1H, dd), 6.83(1H, d, 1.2 Hz), 7.00(1H, d,
7.8 Hz), 7.06(1H, s) 97
(.+-.)-5-(3-Aminophenyl)-8-methyl-7-(5-methyl-1,3,4-thiadiazol-2-
197-198 77
yl)-8,9-dihydro-7H-1,3-dioxolo-[4,5-h][2,3]benzodiazepine (iPrOH)
Method .sup.1H NMR(500 MHz)(DMSO-d.sub.6) .delta. 1.17(3H, d, 6.5
Hz), 2.51(3H, s), 2.77(1H, dd, 14.2 Hz, B, C 8.6 Hz), 3.08(1H, dd,
14.2 Hz, 4.3 Hz), 5.06(1H, m), 5.24(2H, s), 6.07(2H, dm), 6.54(1H,
s), 6.67(1H, d), 6.71(1H, d), 6.74(1H, d), 7.06(1H, s) 98
(.+-.)-1-(4-Aminophenyl)-4-methyl-3-(5-methyl-1,3,4-thiadiazol-2-
180-184 84 yl)-8-methoxy-4,5-dihydro-3H-[2,3]benzodiazepine Method
D MS: EI(70eV): [M].sup.+.: 379, m/z: 364, 265, 238, 223 CI:
[M+H].sup.+: 380, [M].sup.+.: 379, m/z: 223 99
(.+-.)-5-(4-Aminophenyl)-8-methyl-7-(5-methyl-6H-1,3,4- 154-157 85
thiadiazin-2-yl)-8,9-dihydro-7H-1,3-dioxolo-[4,5-h][2,3]
benzodiazepine Method A .sup.1H NMR(DMSO-d.sub.6) .delta. 1.20(3H,
d, 6.5 Hz), 2.10(3H, s), 2.55(1H, dd, 14.0Hz, 11 Hz), 2.92(1H, dm),
2.92(1H, dd, 14.5 Hz), 3.28(1H, d, 14.5 Hz), 5.10(1H, m), 5.70(2H,
s), 6.02(2H, dm), 6.55 (2H, dm), 7.01(1H, s), 7.38(2H, dm),
7.60(1H, s) 100
(.+-.)-5-(4-Aminophenyl)-7-(5,6-dihydro-5-oxo-4H-1,3,4- 172-176 83
thiadiazin-2-yl)-8-methyl-8,9-dihydro-7H-1,3-dioxolo[4,5-
h][2,3]benzodiazepine Method A .sup.1H NMR(DMSO-d.sub.6) .delta.
1.16(3H, d, 6.5 Hz), 2.49(1H, dd, 14.0 Hz, 10.0 Hz), 2.87(1H, dd,
14.0 Hz, 5.2 Hz), 3.31(2H, s), 4.78(1H, m), 5.68(2H, s), 6.05(2H,
dm), 6.65(1H, s), 6.66(2H, dm), 7.00(1H, s), 7.32(2H, dm), 10.5(1H,
s) 101 (.+-.)-5-(4-Aminophenyl)-8-methyl-7-(5-oxo-4,5-dihydro-
263-264 47 1,3,4-thiadiazol-2-yl)-8,9-dihydro-7H-1,3-dioxolo-
[4,5-h][2,3]benzodiazepine Method C .sup.1H NMR(DMSO-d.sub.6)
.delta. 1.17(3H, d, 6.5 Hz), 2.58(1H, dd, 14.0 Hz, 10.4 Hz),
2.97(1H, dd, 14.0 Hz, 5.4 Hz), 4.71(1H, m), 5.65(2H, s), 6.04(2H,
dm), 6.61(2H, dm), 6.62(1H, s), 7.01(1H, s), 7.23(2H, dm),
11.81(1H, brs) MS: EI(70eV): [M].sup.+.: 395, m/z: 394, 306, 252
CI: [M+H].sup.+: 396, [M].sup.+.: 395, m/z: 280 102
(R)-5-(4-Aminophenyl)-8-methyl-7-(5-methyl-1,3,4-oxadiazol-2-
145-149 86
yl)-8,9-dihydro-7H-1,3-dioxolo-[4,5-h][2,3]benzodiazepine
-663.degree.(c=0.5, EtOH Method A MS: EI(70eV): [M].sup.+.: 377,
m/z: 252 CI: [M+H].sup.+: 378, [M].sup.+.: 377, m/z: 252 103
(.+-.)-5-(4-Aminophenyl)-8-methyl-7-(2-methyl-3-oxo-2,3- 213 67
dihydro-1,2,4-thiadiazol-5-yl)-8,9-dihydro-7H-1,3-dioxolo (EtOH)
[4,5-h][2,3]benzodiazepine Method A .sup.1H NMR(DMSO-d.sub.6)
.delta. 1.23(3H, d, 6.5 Hz), 2.70(1H, dd, 13.8 Hz, 10.2 Hz),
3.03(1H, dd, 13.8 Hz, 4.2 Hz), 3.06(3H, s), 4.91(1H, m), 5.90(2H,
s), 6.08(2H, dm), 6.61(1H, s), 6.61(2H, dm), 7.06(1H, s), 7.30(2H,
dm) 104
(.+-.)-5-(4-Aminophenyl)-7-(2-cyclopropyl-3-oxo-2,3-dihydro-
265-267 82
1,2,4-thiadiazol-2-yl)-8-methyl-8,9-dihydro-7H-1,3-dioxolo
[4,5-h][2,3]benzodiazepine Method A .sup.1H NMR(DMSO-d.sub.6)
.delta. 0.85(4H, m), 1.22(3H, d, 6.5 Hz), 2.75(1H, dd, 14.0 Hz,
10.0 Hz), 2.75(1H, m), 3.02(1H, dd, 14.0 Hz, 4.7 Hz), 4.92(1H, m),
5.90(2H, s), 6.07(2H, dm), 6.60(1H, s), 6.63(2H, dm), 7.04(1H, s),
7.30(2H, dm) 105
(.+-.)-5-(4-Aminophenyl)-7-(2-ethyl-3-oxo-2,3-dihydro-1,2,4-
212-214 59 thiadiazol-2-yl)-8-methyl-8,9-dihydro-7H-1,3-dioxolo
[4,5-h][2,3]benzodiazepine Method A .sup.1H NMR(CDCl.sub.3) .delta.
1.25(3H, t), 1.27(3H, d, 6.5 Hz), 2.80(1H, dd, 14.0 Hz, 9.0 Hz),
3.01(1H, dd, 14.0 Hz, 4.0 Hz), 3.72(2H, q), 4.07(2H, br), 5.13(1H,
m), 6.03(2H, dm), 6.65(1H, s), 6.67(2H, dm), 6.80(1H, s), 7.37(2H,
dm) MS: EI(70eV): [M].sup.+.: 423, m/z: 408, 279, 252, 160 CI:
[M+H].sup.+: 424, [M].sup.+.: 423 106
(.+-.)-5-(4-Aminophenyl)-7-(4-carboxy-thiazol-2-yl)-8-methyl-
>260 97 8,9-dihydro-7H-1,3-dioxolo-[4,5-h][2,3]benzodiazepine
(dec.) Method A MS: EI(70eV): [M].sup.+.: 422, m/z: 407, 279, 253
107 (.+-.)-5-(4-Aminophenyl)-8-methyl-7-(5-tetrazolyl)-8,9-dihydro-
>360 68 7H-1,3-dioxolo[4,5-h][2,3]benzodiazepine Method A MS:
EI(70eV): [M].sup.+.: 363, m/z: 295, 294, 252 CI: [M+H].sup.+: 364,
[M].sup.+.: 363, m/z: 295 108
(.+-.)-5-(4-Aminophenyl)-8-methyl-7-(1,2,4-oxadiazol-3-yl)- 124-126
48 7H-1,3-dioxolo-[4,5-h][2,3]benzodiazepine hydrochloride Method A
MS: EI(70eV): [M].sup.+.: 363, m/z: 348, 253, 252 CI: [M+H].sup.+:
364, [M].sup.+.: 363, m/z: 252 109
(.+-.)-5-(4-Aminophenyl)-8-methyl-7-(5-methyl-1,2,4-oxadiazol-
130-135 74
3-yl)-8,9-dihydro-7H-1,3-dioxolo-[4,5-h][2,3]benzodiazepine Method
A MS: EI(70eV)(of the hydrochloride salt): [M].sup.+.: 377, m/z:
362, 278, 252 CI: [M+H].sup.+: 378, [M].sup.+.: 377, m/z: 252 110
(.+-.)-5-(4-Aminophenyl)-8-methyl-7-(2-methyl-thiazol-4- 132-135 22
yl)-8,9-dihydro-7H-1,3-dioxolo-[4,5-h][2,3]benzodiazepine Method C
MS: EI(70eV): [M].sup.+.: 392, m/z: 377, 279, 253, 252 CI:
[M+H].sup.+: 393, [M].sup.+.: 392 111
(.+-.)-5-(4-Aminophenyl)-8-methyl-7-(2-pyrimidinyl)-8,9- 233-235 96
dihydro-7H-1,3-dioxolo[4,5-h][2,3]benzodiazepine (EtOH) Method A
.sup.1H NMR(DMSO-d.sub.6) .delta. 1.23(3H, d, 6.5 Hz), 2.50(1H, dd,
14.0 Hz, 10.0 Hz), 2.89(14.0 Hz, 4.8 Hz), 5.18(1H, m), 5.71(2H, s),
6.03(2H, dm), 6.58(2H, dm), 6.60(1H, s), 6.60(1H, t, 4.8 Hz),
7.43(1H, s), 7.30(2H, dm), 8.33(2H, d, 4.8 Hz) 112
(.+-.)-5-(4-Aminophenyl)-7-(3-chloropyridazin-6-yl)-8-methyl-
164-166 94 8,9-dihydro-7H-1,3-dioxolo-[4,5-h][2,3]benzodiazepine
(EtOH) Method A MS: EI(70eV): [M].sup.+.: 407/409, m/z: 392/394,
355, 279, 278, 253, 252 CI: [M+H].sup.+: 408/410, [M].sup.+.:
407/409, m/z: 279 113
(.+-.)-5-(4-Aminophenyl)-8-methyl-7-(1H(2H)1,2,4-triazol-3- 178-181
64 yl)-8,9-dihydro-7H-1,3-dioxolo-[4,5-h][2,3]benzodiazepine Method
A MS: EI(70eV): [M].sup.+.: 362, m/z: 347, 279, 252 114
(.+-.)-5-(4-Aminophenyl)-8-methyl-7-(5-methyl-1H(2H)-1,2,4- 166-169
72 triazol-3-yl)-8,9-dihydro-7H-1,3-dioxolo-[4,5-h][2,3]
benzodiazepine Method A MS: EI(70eV): [M].sup.+.: 376, m/z: 361,
279, 252 115
(.+-.)-5-(4-Aminophenyl)-8-methyl-7-(2-methyl-2H-1,2,4- 182-183 83
triazol-3-yl)-8,9-dihydro-7H-1,3-dioxolo-[4,5-h][2,3]
benzodiazepine Method A MS: EI(70eV): [M].sup.+.: 376, m/z: 361,
279, 252 116
(.+-.)-5-(4-Aminophenyl)-8-methyl-7-(1-methyl-1H-1,2,4- 165-168 83
triazol-3-yl)-8,9-dihydro-7H-1,3-dioxolo-[4,5-h][2,3]
benzodiazepine Method A MS: EI(70eV): [M].sup.+.: 376, m/z: 361,
253, 252 117 (.+-.)-5-(4-Aminophenyl)-8-methyl-7-(2,5-dimethyl-2H-
185-187 78
1,2,4-triazol-3-yl)-8,9-dihydro-7H-1,3-dioxolo-[4,5-h][2,3]
benzodiazepine Method A MS: EI(70eV): [M].sup.+.: 390, m/z: 375,
279, 265, 252 118
(.+-.)-5-(4-Aminophenyl)-8-methyl-7-(1,5-dimethyl-1H-1,2,4- 197-200
85 triazol-3-yl)-8,9-dihydro-7H-1,3-dioxol[4,5-h][2,3]
benzodiazepine Method C MS: EI(70eV): [M].sup.+.: 390, m/z: 375,
253, 252 119 (R)-5-(4-amino-3-methylphenyl)-8-methyl-7-(5-methyl-
158-160 83 1,3,4-thiadiazol-2-yl)-8,9-dihydro-7H-1,3-dioxolo-
-515.degree.(c=0.38, CHCl.sub.3) [4,5-h][2,3]benzodiazepine Method
B .sup.1H NMR(DMSO-d.sub.6).delta. 1.18(3H, d, 5.4 Hz), 2.07(s,
3H), 2.47(s, 3H), 2.57(dd, 1H, 13.7 Hz, 10.3 Hz), 2.95(dd, 1H, 13.7
Hz, 4.9 Hz), 4.92(m, 1H), 5.2-5.8(br, 2H), 6.01(s, br, 1H), 6.06(s,
br, 1H), 6.55(s, 1H), 6.64(d, 1H, 8.2 Hz), 7.04(s, 1H), 7.17(d, 1H,
8.2 Hz), 7.25(s, br, 1H) MS: EI(70eV): [M].sup.+.: 407, m/z: 392,
293, 278, 266 CI: [M+H].sup.+: 408, [M].sup.+.: 407
Examples 120-131
General Procedure for the Synthesis of 2,3-benzodiazepines
Containing Acteylamino-Phenyl Group
[0243] 2,3-benzodiazepines containing an aminophenyl group were
dissolved in dichloromethane and stirred at room temperature with
an excess of acetic anhydride. After completion of the reaction the
mixture was washed with sodium hydrogen carbonate solution and
water, then dried and concentrated. TABLE-US-00011 TABLE 11
2,3-benzodiazepine derivatives substituted with acetylaminophenyl
group Mp. (.degree. C.) Number of Solvent of Yield (%) Example Name
recrystall. [.alpha.].sub.D 120
(.+-.)-5-(4-Acetylaminophenyl)-8-methyl-7-(5-methyl- 176-179 65
thiazol-2-yl)-8,9-dihydro-7H-1,3-dioxolo-
[4,5-h][2,3]benzodiazepine 121
(.+-.)-5-(4-Acetylaminophenyl)-8-methyl-7-(4-methyl- 236-238 65
thiazol-2-yl)-8,9-dihydro-7H-1,3-dioxolo- (50%
[4,5-h][2,3]benzodiazepine EtOH--H.sub.2O) 122
(.+-.)-5-(4-Acetylaminophenyl)-7-(4,5-dihydro-thiazol-2-
211-213(EtOH) 96 yl)-8-methyl-8,9-dihydro-7H-1,3-dioxolo-
[4,5-h][2,3]benzodiazepine 123
(R)-5-(4-Acetylaminophenyl)-8-methyl-7-(2-thiazolyl)-
126(rearrangement) 95
8,9-dihydro-7H-1,3-dioxolo[4,5-h][2,3]benzodiazepine 172-174(EtOH)
-140.degree.(c=0.44, CHCl.sub.3) 124
(S)-5-(4-Acetylaminophenyl)-8-methyl-7-(2-thiazolyl)- 124-128 95
8,9-dihydro-7H-1,3-dioxolo- +134.degree. [4,5-h][2,3]benzodiazepine
(c=0.48, CHCl.sub.3) 125
(R)-5-(4-Acetylaminophenyl)-7-(4,5-dihydro-thiazol-2- 143-145 95
yl)-8-methyl-8,9-dihydro-7H-1,3-dioxolo- +108.degree.
[4,5-h][2,3]benzodiazepine (c=0.45, CHCl.sub.3) 126
(S)-5-(4-Acetylaminophenyl)-7-(4,5-dihydro-thiazol-2- 148-154 91
yl)-8-methyl-8,9-dihydro-7H-1,3-dioxolo- -111.degree.
[4,5-h][2,3]benzodiazepine (c=048, CHCl.sub.3) 127
(.+-.)-5-(4-Acetylaminophenyl)-7-(4,5-dihydro-oxazol-2- 124-128 44
yl)-8-methyl-8,9-dihydro-7H-1,3-dioxolo- [4,5-h][2,3]benzodiazepine
128 (.+-.)-5-(4-Acetylaminophenyl)-8-methyl-7-(2- 162-163 96
pyrimidinyl)-8,9-dihydro-7H-1,3-dioxolo- (EtOH)
[4,5-h][2,3]benzodiazepine 129
(.+-.)-5-(4-Acetylaminophenyl)-7-(3-chloro-pyridazin-6- 164-170 78
yl)-8-methyl-8,9-dihydro-7H-1,3-dioxolo- [4,5-h][2,3]benzodiazepine
130 (R)-5-(4-Acetylaminophenyl)-8-methyl-7-(5-methyl- 276-277 73
1,3,4-thiadiazol-2-yl)-8,9-dihydro-7H-1,3-dioxolo- (MeOH)
-114.degree. [4,5-h][2,3]benzodiazepine (c=0.5, CHCl.sub.3) 131
(.+-.)-5-(4-Acetylamino-3-methylphenyl)-8-methyl-7-(5- 258-262 63
methyl-1,3,4-thiadiazol-2-yl)-8,9-dihydro-7H-1,3-
dioxolo[4,5-h][2,3]benzodiazepine
Example 132
(.+-.)-8-Methyl-5-(3-methyl-4-nitrophenyl)-7-(4,5-dihydro-thiazol-2-yl)-8,-
9-dihydro-7H-1,3-dioxolo[4,5-h][2,3]benzodiazepine
Step A
(R)-8-Methyl-5-(3-methyl-4-nitrophenyl)-7-thiocarbamoyl-8,9-dihydro-7H-1,3-
-dioxolo[4,5-h][2,3]benzodiazepine
[0244] This compound was prepared from starting compound XXXI
according to the process described for starting compound I. Mp.:
123-125.degree. C. Yield: 70%.
Step B
[0245] The product of Step A was transformed into the title
compound according to the procedure described in Example 9. Mp.:
130-135.degree. C. Yield: 81%.
Example 133
(R)-8-Methyl-5-(3-methyl-4-nitrophenyl)-7-(thiazol-2-yl)-8,9-dihydro-7H-1,-
3-dioxolo[4,5-h][2,3]benzodiazepine
[0246] The title compound was obtained from the intermediate
described under Step A of Example 132 according to a method
described in Example 1. Mp.: 138-142.degree. C. Yield: 55%.
Example 134
(R)-7-(5-Ethyl-1,3,4-thiadiazol-2-yl)-8-methyl-5-(3-methyl-4-nitrophenyl)--
8,9-dihydro-7H-1,3-dioxolo[4,5-h][2,3]benzodiazepine
Step A
(R)-8-Methyl-5-(3-methyl-4-nitrophenyl)-8,9-dihydro-7H-1,3-dioxolo[4,5-h][-
2,3]benzodiazepine-7-carbothioyl chloride
[0247] This compound was prepared from starting compound XXXI
according to the method described for starting compound XI. Mp.:
193-196.degree. C. Yield: 85%. [.alpha.].sub.D: -500.0.degree.
(c=0.5; CHCl.sub.3).
Step B
[0248] 2.50 g (6.0 mmol) of the compound obtained in Step A was
reacted with 1.28 g (21.3 mmol) of propionyl hydrazide in 10 ml of
dimethylformamide at 70.degree. C. for 2 h. The cooled reaction
mixture was poured onto water and the resulting precipitate was
collected by filtration. This wet substance was further reacted in
24 ml of ethanol with 0.5 ml conc. hydrochloric acid at boiling
point for 1 h. Solvent was evaporated and the residue was dissolved
in dichloromethane and extracted with sodium bicarbonate solution
and water. Evaporation of the solvent gave the crude title product
which was purified by column chromatography using a mixture of
n-hexane-ethyl acetate (1:1) as eluent, giving 1.15 g (yield: 49%)
of the product. Mp.: 129-130.degree. C.
Example 135
(R)-8-Methyl-5-(3-methyl-4-nitrophenyl)-7-(5-propyl-1,3,4-thiadiazol-2-yl)-
-8,9-dihydro-7H-1,3-dioxolo[4,5-h][2,3]benzodiazepine
[0249] The title compound was obtained according to the method
described in Example 134 but using butyric hydrazide. Mp.:
143-145.degree. C. Yield: 73%. [.alpha.].sub.D: +343.3.degree.
(c=0.5; CHCl.sub.3).
Example 136
(R)-8-Methyl-5-(3-methyl-4-nitrophenyl)-7-(1,3,4-thiadiazol-2-yl)-8,9-dihy-
dro-7H-1,3-dioxolo[4,5-h][2.3]benzodiazepine
Step A
(R)-8-Methyl-5-(3-methyl-4-nitrophenyl)-8,9-dihydro-7H-1,3-dioxolo[4,5-h][-
2,3]benzodiazepin-7-carbothiohydrazide
[0250] The Step A intermediate of Example 134 was transformed into
the carbothiohydrazide according to a method described for starting
material XVIII. Mp.: 109-115.degree. C. Yield: 91%.
[.alpha.].sub.D: -276.5.degree.(c=0.5; CHCl.sub.3).
Step B
[0251] The compound of Step A was reacted with triethyl
orthoformate and a catalytic amount of hydrochloric acid similarly
to a method described in Example 25, to give the title product.
Mp.: 182-189.degree. C. Yield: 92%. [.alpha.].sub.D: +356.0.degree.
(c=0.5; CHCl.sub.3).
Example 137
(R)-8-Methyl-5-(3-methyl-4
nitrophenyl)-7-(5-methoxymethyl-1,3,4-thiadiazol-2-yl)-8,9-dihydro-7H-1,3-
-dioxolo[4,5-h][2,3]benzodiazepine
[0252] The compound of Step A of Example 136 (2.07 g, 5.0 mmol) was
reacted in 10 ml of dimethylformamide with 1.86 g (5.5 mmol) of
pentachlorophenol methoxyacetate at 50.degree. C. for 2 h. The
reaction mixture was diluted with water and the resulting
precipitate was isolated by filtration. This wet intermediate was
taken up in ethanol (24 ml), 0.50 ml of conc. hydrochloric acid was
added and it was boiled for 1 h. Evaporation of the solvent gave a
residue, which was dissolved in methylene chloride and the solution
was washed with a 5% sodium carbonate solution and water.
Evaporation of the solvent resulted in the crude title product that
was purified with column chromatography, a mixture of
n-hexane-ethyl acetate (2:1) was used as eluent to give 2.21 g of
the pure product. Mp.: 153-155.degree. C. Yield: 91%.
[.alpha.].sub.D: +317.5.degree. (c=0.5; CHCl.sub.3).
[0253] The compounds of Examples 138-148 were prepared analogously
to the method described in Example 137 using the appropriate
activated carboxylic acid derivatives as reagents (e.g.: acyl
chloride, acid anhydride, pentachlorophenol ester,
N-hydroxysuccinimide ester of the corresponding carboxylic
acids).
Example 138
(R)-8-Methyl-5-(3-methyl-4-nitrophenyl)-7-(5-isopropyl-1,3,4-thiadiazol-2--
yl)-8,9-dihydro-7H-1,3-dioxolo[4,5-h][2.3]benzodiazepine
[0254] Mp.: 130-133.degree. C. Yield: 90%.
Example 139
(R)-7-(5-Cyclopropyl-1,3,4-thiadiazol-2-yl)-8-methyl-5-(3-methyl-4-nitroph-
enyl)-8,9-dihydro-7H-1,3-dioxolo[4,5-h][2,3]benzodiazepine
[0255] Mp.: 126-130.degree. C. Yield: 93%.
Example 140
(R)-7-(5-Hydroxymethyl-1,3,4-thiadiazol-2-yl)-8-methyl-5-(3-methyl-4-nitro-
phenyl)-8,9-dihydro-7H-1,3-dioxolo[4,5-h][2,3]benzodiazepine
[0256] Mp.: 142-145.degree. C. Yield: 67%.
Example 141
(R)-7-(5-Acetoxymethyl-1,3,4-thiadiazol-2-yl)-8-methyl-5-(3-methyl-4-nitro-
phenyl)-8,9-dihydro-7H-1,3-dioxolo[4,5-h][2,3]benzodiazepine
[0257] Mp.: 110-115.degree. C. Yield: 97%.
Example 142
(R)-7-(5-Cyanomethyl-1,3,4-thiadiazol-2-yl)-8-methyl-5-(3-methyl-4-nitroph-
enyl)-8,9-dihydro-7H-1,3-dioxolo[4,5-h][2,3]benzodiazepine
[0258] Mp.: 118-122.degree. C. Yield: 98%.
Example 143
(R)-8-Methyl-5-(3-methyl-4-nitrophenyl)-7-(5-methylthiomethyl-1,3,4-thiadi-
azol-2-yl)-8,9-dihydro-7H-1,3-dioxolo[4,5-h][2,3]benzodiazepine
[0259] Mp.: 132-134.degree. C. Yield: 96%.
Example 144
(R)-7-(5-Ethoxycarbonyl-1,3,4-thiadiazol-2-yl)-8-methyl-5-(3-methyl-4-nitr-
ophenyl)-8,9-dihydro-7H-1,3-dioxolo[4,5-h][2,3]benzodiazepine
[0260] Mp.: 115-118.degree. C. Yield: 80%. [.alpha.].sub.D:
+140.3.degree.(c=0.5; CHCl.sub.3).
Example 145
(R)-7-(5-Benzyloxycarbonyl-aminomethyl-1,3,4-thiadiazol-2-yl)-8-methyl-5-(-
3-methyl-4-nitrophenyl)-8,9-dihydro-7H-1,3-dioxolo[4,5-h][2,3]benzodiazepi-
ne
[0261] Mp.: 240-243.degree. C. Yield: 95%.
Example 146
(R)-8-Methyl-5-(3-methyl-4-nitrophenyl)-7-{5-[1-(1E)-propen-1-yl]-1,3,4-th-
iadiazol-2-yl}-8,9-dihydro-7H-1,3-dioxolo[4,5-h][2,3]benzodiazepine
[0262] Mp.: 232-237.degree. C. Yield: 28%. [.alpha.].sub.D:
-359.2.degree.(c=0.4; CHCl.sub.3).
Example 147
(R)-7-(5-Hexyl-1,3,4-thiadiazol-2-yl)-8-methyl-5-(3-methyl-4-nitrophenyl)--
8,9-dihydro-7H-1,3-dioxolo[4,5-h][2,3]benzodiazepine
[0263] Mp.: 217-224.degree. C. Yield: 66%.
Example 148
(R)-7-(5,6-Dihydro-5-oxo-4H-1,3,4-thiadiazin-2-yl)-8-methyl-5-(3-methyl-4--
nitrophenyl)-8,9-dihydro-7H-1,3-dioxolo[4,5-h][2,3]benzodiazepine
[0264] The title compound was prepared from the compound obtained
in Step A of Example 136 applying the method described in Example
43, however pentachlorophenol chloroacetate was used as alkylating
agent. Mp.: 207-211.degree. C. Yield: 70%. [.alpha.].sub.D:
+378.5.degree.(c=0.5; CHCl.sub.3).
Example 149
(R)-8-Methyl-5-(4-nitrophenyl)-7-(1,3,4-oxadiazol-2-yl)-8,9-dihydro-7H-1,3-
-dioxolo[4,5-h][2,3]benzodiazepine
[0265] The title compound was obtained from
(R)--N'-{8-methyl-5-(4-nitrophenyl)-8,9-dihydro-7H-1,3-dioxolo[4,5-h][2,3-
]benzodiazepine-7-carbothioyl}-formic hydrazide, according to the
method described in Example 45. Mp.: 145-147.degree. C. Yield: 35%,
[.alpha.].sub.D: -604.0.degree. (c=0.5; CHCl.sub.3).
Example 150
(.+-.)-8-Methyl-5-(4-nitrophenyl)-7-(1,2,3,4-thiatriazol-5-yl)-8,9-dihydro-
-7H-1,3-dioxolo[4,5-h][2,3]benzodiazepine
[0266] A solution of 1.00 g (2.5 mmol) of starting material XVIII,
0.37 ml (4.6 mmol) of trifluoroacetic acid in 10 ml of formamid was
stirred at 25.degree. C. for 5 min. Then a solution of 0.16 g (2.5
mmol) of sodium nitrite in 0.30 ml of water was added dropwise.
After 0.5 h the reaction mixture was diluted with water and the
precipitate formed was filtered off, washed with water and dried to
yield 0.92 g (90%) of the title compound. Mp.: 109-110.degree.
C.
Example 151
(.+-.)-8-Methyl-5-(4-nitrophenyl)-7-(2-methyl-1,3-oxazol-5-yl)-8,9-dihydro-
-7H-1,3-dioxolo[4,5-h][2,3]benzodiazepine
Step A
(.+-.)-N'-{2-[8-methyl-5-(4-nitrophenyl)-8,9-dihydro-7H-1,3-dioxolo[4,5-h]-
[2,3]benzodiazepin-7-yl]-2-oxoethyl}-acetamide
[0267] A solution of 1.5 g (4.6 mmol) of
(.+-.)-8-methyl-5-(4-nitrophenyl)-8,9-dihydro-7H-1,3-dioxolo[4,5-h][2,3]b-
enzodiazepine, 0.5 g (4.6 mmol) of N-acetylglycine and 1.0 g (5.0
mmol) of 1,3-dicyclohexylcarbodiimid was stirred in 15 ml of
dichloromethane at 25.degree. C. for 3 h. The precipitated
1,3-dicyclohexylurea was filtered off and the filtrate was
evaporated to dryness. The crude product was purified by column
chromatography using a mixture of ethyl acetate-hexane (1:1) as
eluent to yield 1.1 g (58%) of the title compound.
Step B
[0268] 0.74 g (2.8 mmol) of triphenylphosphine was dissolved in 10
ml of dichloromethane and a solution of 0.2 ml (2.8 mmol) of
bromine in 1 ml of dichloromethane was added. After 30 min a
solution of 1.0 g (2.4 mmol) of the compound prepared in Step A and
1.0 ml (7.1 mmol) of triethylamine in 5 ml of dichloromethane was
added and the mixture was boiled under nitrogen for 3 h. The
resulting solution was washed with water, dried and concentrated to
dryness. The crude product was purified by column chromatography
using a mixture of ethyl acetate-hexane (1:1) as eluent to yield
0.6 g (62%) of the title compound. Mp.: 203-205.degree. C.
Example 152
(.+-.)-7-(2,4-dimethyl-1,3-oxazol-5-yl)-8-methyl-5-(4-nitrophenyl)-8,9-dih-
ydro-7H-1,3-dioxolo[4,5-h][2,3]benzodiazepine
[0269] The title compound was obtained according to the method
described in Example 151, but using
(.+-.)-N-{2-[8-methyl-5-(4-nitrophenyl)-8,9-dihydro-7H-1,3-dioxolo[4,5-h]-
[2,3]benzodiazepine-7-yl]-1-methyl-2-oxoethyl}-acetamide as
intermediate. Mp.: 76-78.degree. C.; yield: 68%.
Example 153
(R)-5-(3-Chloro-4-nitrophenyl)-8-methyl-7-(5-methyl-1,3,4-thiadiazol-2-yl)-
-8,9-dihydro-7H-1,3-dioxolo[4,5-h][2,3]benzodiazepine
Step A
(R)-7-(tert-Butoxycarbonyl)-5-(3-chloro-4-nitrophenyl)-8-methyl-7H-1,3-dio-
xolo[4,5-h][2,3]benzodiazepin
[0270] The compound was prepared according to a synthesis described
in literature (Anderson et al., J. Am. Chem. Soc. 117: 12358
(1995)) using 3-chloro-4-nitrobenzaldehyde and tert-butyl carbazate
as key reagents. Mp.: 160-162.degree. C.
Step B
(R)-5-(3-Chloro-4-nitrophenyl)-8-methyl-8,9-dihydro-7H-1,3-dioxolo[4,5-h][-
2,3]benzodiazepin
[0271] The compound obtained in Step A (8.2 g; 18.2 mmol) was
dissolved in ethyl acetate, containing 12% hydrochloric acid (82
ml). The solution was maintained at RT for 3 h. Then the solvent
was evaporated and the residue was dissolved in ethyl acetate and
washed with saturated sodium hydrogencarbonate solution and water.
Evaporation yielded 5.3 g (81%) of the title product. Mp.:
165-170.degree. C. [.alpha.].sub.D: +65.0.degree. (c=0.5;
CHCl.sub.3).
Step C
(R)-5-(3-Chloro-4-nitrophenyl)-8-methyl-8,9-dihydro-7H-1,3-dioxolo[4,5-h][-
2,3]benzodiazepine-7-carbothioyl
[0272] The compound was prepared from the intermediate obtained in
Step B according to the method described for starting material XI.
Mp.: 132-134.degree. C. Yield: 88%. [.alpha.].sub.D:
-533.0.degree.(c=0.5; CHCl.sub.3).
Step D
[0273] The title compound was obtained from the compound prepared
in Step C according to a method described in Method B of Example
28. Mp.: 151-152.degree. C. Yield: 89%. [.alpha.].sub.D:
+284.1.degree. (c=0.5; CHCl.sub.3).
Example 154
(R)-5-(3-Chloro-4-nitrophenyl)-8-methyl-7-(5-methoxymethyl-1,3,4-thiadiazo-
l-2-yl)-8,9-dihydro-7H-1,3-dioxolo[4,5-h][2,3]benzodiazepine
Step A
(R)-5-(3-Chloro-4-nitrophenyl)-8-methyl-8,9-dihydro-7H-1,3-dioxolo[4,5-h][-
2,3]benzodiazepine-7-carbothiohydrazide
[0274] The compound obtained in Step C of Example 153 was
transformed into the title compound according to a method described
for starting material XVIII. Mp.: 126-127.degree. C.; yield:
85%.
Step B
[0275] The compound obtained in Step A was used to prepare the
title compound according to the method described in Example 137.
Mp.: 208-210.degree. C.; yield: 65%. [.alpha.].sub.D:
+470.6.degree. (c=0.5; CHCl.sub.3).
Example 155
(.+-.)-8-Methyl-7-(3-methyl-isoxazol-5-yl)-5-(4-nitrophenyl)-8,9-dihydro-7-
H-1,3-dioxolo[4,5-h][2,3]benzodiazepine
Step A
(.+-.)-1-{8-methyl-5-(4-nitrophenyl)-8,9-dihydro-7H-1,3-dioxolo[4,5-h][2,3-
]benzodiazepin-7-yl}-butane-1,3-dione
[0276] A solution of 4.0 g (12.3 mmol) of
(.+-.)-8-methyl-5-(4-nitrophenyl)-8,9-dihydro-7H-1,3-dioxolo[4,5-h][2,3]b-
enzodiazepine, 0.52 ml (13.5 mmol) of diketene in 80 ml of toluene
was stirred at 80.degree. C. for 3 h. The reaction mixture was
washed with water, dried and concentrated. The residue was
triturated with diisopropyl ether to yield 4.0 g (80%) of the title
compound. Mp.: 169-171.degree. C.
Step B
(.+-.)-4-{8-Methyl-5-(4-nitrophenyl)-8,9-dihydro-7H-1,3-dioxolo[4,5-h][2,3-
]benzodiazepin-7-yl}-4-thioxo butan-2-one
[0277] A solution of 3.0 g (7.2 mmol) of a compound of Step A 2.4 g
(5 mmol) of Lawesson's reagent in 500 ml of toluene was stirred at
reflux temperature for 4 h. Then the reaction mixture was filtered
and the solvent evaporated. The crude product was purified by
column chromatography using a mixture of ethyl acetate-hexane (1:3)
as eluent to yield 2.1 g (70%) of the title compound. Mp.:
178-185.degree. C.
Step C
[0278] A solution of 1.9 g (4.5 mmol) of the compound obtained in
Step B and 0.6 g (9.0 mmol) hydroxylamine hydrochloride was stirred
in 20 ml of ethanol and heated at reflux for 3 h. The reaction
mixture was diluted with water and the precipitate formed was
filtered off. The crude product was purified by column
chromatography using a mixture of ethyl acetate-hexane (1:3) as
eluent to yield 0.60 g (32%) of the title compound. Mp.:
179-182.degree. C.
Example 156
(R)-5-(3,5-Dimethyl-4-nitrophenyl)-8-methyl-7-(5-methyl-1,3,4-thiadiazol-2-
-yl)-7H-1,3-dioxolo[4,5-h][2,3]benzodiazepine
Step A
(R)-7-(tert-Butoxycarbonyl)-5-(3,5-dimethyl-4-nitrophenyl)-8-methyl-8,9-di-
hydro-7H-1,3-dioxolo[4,5-h][2,3]benzodiazepine
[0279] The compound was prepared according to a synthesis described
in literature (Anderson et al., J. Am. Chem. Soc. 117: 12358
(1995)), however as key reagents 3,5-dimethyl-4-nitrobenzaldehyde
and tert-butyl carbazate were used. Mp.: 222-223.degree. C.
[.alpha.].sub.D: -443.0.degree. (c=0.5; CHCl.sub.3).
Step B
(R)-5-(3,5-Dimethyl-4-nitrophenyl)-8-methyl-8,9-dihydro-7H-1,3-dioxolo[4,5-
-h][2,3]benzodiazepine
[0280] The compound obtained in Step A was subjected to hydrolysis
according to a method described in Example 153 under Step B. Mp.:
193.degree. C.; yield: 88%. [.alpha.].sub.D: +181.degree. (c=0.5;
CHCl.sub.3).
Step C
(R)-5-(3,5-Dimethyl-4-nitrophenyl)-8-methyl-8,9-dihydro-7H-1,3-dioxolo[4,5-
-h][2,3]benzodiazepine-7-carbothioyl chloride
[0281] The compound obtained in Step B was transformed into the
title carbothioyl derivative according to a method described for
starting compound XI. Mp.: 216.degree. C.; yield: 82%.
[.alpha.].sub.D: -389.degree. (c=0.5; CHCl.sub.3).
Step D
[0282] The title compound of this example was prepared from
compound obtained in Step C according to Method B described in
Example 28. Mp.: 235.degree. C.; yield: 86%. [.alpha.].sub.D:
+221.degree. (c=0.5; CHCl.sub.3).
Example 157
(R)-5-(3,5-Dimethyl-4-nitrophenyl)-8-methyl-7-(5-methyl-1,3,4-oxadiazol-2--
yl)-8,9-dihydro-7H-1,3-dioxolo[4,5-h][2,3]benzodiazepine
[0283] The thiosemicarbazide type intermediate of Step D of Example
156 was treated with mercury(II)acetate for 16 h according to a
procedure described in Example 45. Mp.: 132-133.degree. C.; yield:
90%. [.alpha.].sub.D: -436.degree. (c=0.5; CHCl.sub.3).
Example 158
(R)-5-(3,5-Dimethyl-4-nitrophenyl)-8-methyl-7-(2-thiazolyl)-8,9-dihydro-7H-
-1,3-dioxolo[4,5-h][2,3]benzodiazepine
Step A
(R)-5-(3,5-Dimethyl-4-nitrophenyl)-8-methyl-7-thiocarbamoyl-8,9-dihydro-7H-
-1,3-dioxolo[4,5-h][2,3]benzodiazepine
[0284] This intermediate was prepared from the compound obtained in
Step B of Example 156 by a method described for starting material
I, however, during the reaction significant hydrolysis of the title
product to the corresponding urea derivative was noticed as well.
Title compound was isolated by column chromatography using a
mixture of hexane-ethyl acetate (3:1) as eluent. Mp.:
228-230.degree. C.; yield: 18%.
Step B
[0285] Intermediate compound obtained in Step A was reacted with
bromoacetaldehyde diethyl acetal as described in Example 1. Mp.:
167.degree. C.; yield: 46%.
Example 159
(R)-8-Methyl-7-(2-methyl-3-oxo-2,3-dihydro-1,2,4-thiadiazol-5-yl)-5-(4-nit-
rophenyl)-8,9-dihydro-7H-1,3-dioxolo[4,5-h][2,3]benzodiazepine
Step A
(R)-Phenyl-(8-methyl-5-(4-nitrophenyl)-8,9-dihydro-7H-1,3-dioxolo[4,5-h][2-
,3]benzodiazepine-3-carbothioyl)-carbamate
[0286] Prepared according to the procedure described for starting
compound XXVI, however, from
(R)-8-methyl-5-(4-nitrophenyl)-8,9-dihydro-7H-1,3-dioxolo[4,5-h][2,3]benz-
odiazepine. The crude product was used without further
purification.
Step B
(R)-1-Methyl-3-{8-methyl-5-(4-nitrophenyl)-8,9-dihydro-7H-1,3-dioxolo[4,5--
h][2,3]benzodiazepin-7-carbothioyl}-urea
[0287] Intermediate of Step A was reacted with methylamine
according to the method described for the racemic starting compound
XXVII. Mp.: 164.degree. C.; yield: 63%. [.alpha.].sub.D:
-526.degree. (c=0.5; CHCl.sub.3).
Step C
[0288] The compound of Step B was reacted with bromine according to
a procedure described in Example 46 to give the title product. Mp.:
177-180.degree. C.; yield: 98%. [.alpha.].sub.D: +438.degree.
(c=0.5; CHCl.sub.3).
Example 160
(.+-.)-7-(5,5-Dimethyl-4-oxo-4,5-dihydro-thiazol-2-yl)-8-methyl-5-(4-nitro-
phenyl)-1,3-dioxolo[4,5-h][2,3]benzodiazepine
[0289] To a suspension of 1.20 g (2.86 mmol) of starting material I
in 10 ml of dimethylformamide 1.67 g (8.58 mmol) of
ethyl-.alpha.-bromoisobutyrate were added. The mixture was stirred
at 80.degree. C. for 1 h and at 100-110.degree. C. for 23 h. The
solution was diluted with water and the separated oily substance
was extracted into dichloromethane. After washing and drying the
solvent was evaporated and the residue was purified by column
chromatography, using a mixture of hexane-ethyl acetate (1:1) as
eluent. Evaporation of the fractions containing the main product
gave 0.80 g of the title compound as a gum.
Example 161
(R)-8-Methyl-5-(4-nitrophenyl)-7-(1,2,3-thiadiazol-5-yl)-8,9-dihydro-7H-1,-
3-dioxolo[4,5-h][2,3]benzodiazepine
[0290] To an ethereal solution containing diazomethane in high
excess, a solution of 2.42 g (3.0 mmol) of starting material XII in
40 ml of tetrahydrofurane was added dropwise at -15.degree. C. The
solution was kept at room temperature for 5 days, when TLC showed
full conversion. Evaporation gave a residue which was purified by
column chromatography, using a mixture of hexane-ethyl acetate
(3:1) as eluent. 2.13 g of the title product was resulted. Mp.:
175-176.degree. C. [.alpha.].sub.D: -96.degree. (c=0.5;
CHCl.sub.3).
Example 162
(R)-5-(2-Bromo-3-methyl-4-nitrophenyl)-8-methyl-7-(5-methyl-1,3,4-thiadiaz-
ol-2-yl)-8,9-dihydro-7H-1,3-dioxolo[4,5-h][2,3]benzodiazepine
Step A
(R)-5-(2-Bromo-3-methyl-4-nitrophenyl)-7-(tert-butoxycarbonyl)-8-methyl-8,-
9-dihydro-7H-1,3-dioxolo[4,5-h][2,3]benzodiazepine
[0291] The compound was prepared using 2-bromo-3-methylbenzaldehyde
and tert-butylcarbazate according to a method published in the
literature (Anderson et al., J. Am. Chem. Soc. 117:12358
(1995)).
[0292] Ms:EI (70 eV):[M].sup.+: 517/519, m/z: 417/419, 376/378,
57
[0293] CI:[M+H].sup.+: 518/520
Step B
(R)-5-(2-Bromo-3-methyl-4-nitrophenyl)-8-methyl-8,9-dihydro-7H-1,3-dioxolo-
[4,5-h][2,3]benzodiazepine
[0294] Compound obtained in Step A was hydrolyzed according to
method disclosed in Example 153, Step B.
[0295] Ms:EI (70 eV):[M].sup.+: 417/419, m/z: 402/404, 374/376,
338, 160
[0296] CI:[M+H].sup.+: 418/420, [M].sup.+: 417/419
Step C
(R)-5-(2-Bromo-3-methyl-4-nitrophenyl)-8-methyl-8,9-dihydro-7H-1,3-dioxolo-
[4,5-h][2,3]benzodiazepine-7-carbothioyl chloride
[0297] The compound obtained in Step B was transformed into the
title compound according to a method described for starting
material XI.
[0298] Ms:EI (70 eV):[M].sup.+: 495/497, m/z: 460/462, 401/403,
355/357
[0299] CI:[M+H].sup.+: 496/498/500, m/z: 460/462
Step D
[0300] The title compound obtained in Step C was further reacted
with acetic hydrazide according to a method described in Method B
of Example 28 to give the title compound as a foam.
[0301] MS:EI (70 eV)[M].sup.+: 515/517, m/z: 500/502, 401/403,
59
[0302] CI:[M+H].sup.+: 516/518 TABLE-US-00012 TABLE 12
2,3-Benzodiazepines containing aminophenyl group (The .sup.1H NMR
spectra were recorded at 500 MHz unless stated otherwise) Mp.
(.degree. C.) Number of Solvent of Yield (%) Example Name
recrystall. [.alpha.].sub.D 163
(R)-5-(4-Amino-3-methylphenyl)-8-methyl-7-(4,5- 125-128 53
dihydro-thiazol-2-yl)-8,9-dihydro-7H-1,3-dioxolo-
-282.0.degree.(c=0.5, CHCl.sub.3) [4,5-h][2,3]benzodiazepine
Method* B .sup.1H NMR(DMSO-d.sub.6) d 1.10(3H, d, 6.0 Hz), 2.06(3H,
s), 2.53(1H, dd, 14.0 Hz, 10.0 Hz), 2.86(1H, dd, 14.0 Hz, 4.5 Hz),
3.0-3.2(2H, m), 3.93(1H, m), 4.05(1H, m), 4.85(1H, m), 5.35(2H, s),
6.04(1H, s), 6.07(1H, s), 6.55(1H, s), 6.61(1H, d, 8.5 Hz),
6.98(1H, s), 7.13(1H, d, br, 8.5 Hz), 7.22(1H, s, br) 164
(R)-5-(4-Amino-3-methylphenyl)-8-methyl-7-(thiazol-2- 124-127 86
yl)-8,9-dihydro-7H-1,3-dioxolo- -619.5.degree.(c=0.5, CHCl.sub.3)
[4,5-h][2,3]benzodiazepine Method B .sup.1H NMR(DMSO-d.sub.6) d
1.16(3H, d, 6.0 Hz), 2.09(3H, s), 2.59(1H, dd, 14.0 Hz, 10.5 Hz),
2.95(1H, dd, 14.0 Hz, 5.5 Hz), 5.01(1H, m), 5.47(2H, s, br),
6.03(1H, d, 1.1 Hz), 6.08(1H, d, 1.1 Hz), 6.58(1H, s), 6.64(1H, d,
8.0 Hz), 6.83(1H, d, 3.5 Hz), 7.05(1H, s), 7.21(1H, dd, 8.0 Hz, 2.0
Hz), 7.28(1H, d, 3.5 Hz), 7.31(1H, d, 2.0 Hz) 165
(R)-5-(4-Amino-3-methylphenyl)-7-(5-ethyl-1,3,4- 129-133(EtOH) 90
thiadiazol-2-yl)-8-methyl-8,9-dihydro-7H-1,3-dioxolo-
-534.9.degree.(c=0.5, CHCl.sub.3) [4,5-h][2,3]benzodiazepine Method
B .sup.1H NMR(DMSO-d.sub.6) d 1.20(3H, d, 6.1 Hz), 1.23(3H, t, 7.6
Hz), 2.07(3H, s), 2.58(1H, dd, 14.0 Hz, 10.6 Hz), 2.85(2H, q, 7.6
Hz), 2.95(1H, dd, 14.0 Hz, 5.4 Hz), 4.93(1H, m), 5.50(2H, s, br),
6.03(1H, d, 1.0 Hz), 6.08(1H, d, 1.0 Hz), 6.57(1H, s), 6.63(1H, d,
8.4 Hz), 7.06(1H, s), 7.20(1H, dd, 8.4 Hz, 2.1 Hz), 7.25(1H, d, 2.1
Hz) MS: EI(70eV): [M].sup.+.: 421, m/z: 406, 293, 266 CI:
[M+H].sup.+: 422, [M].sup.+.: 421 166
(R)-5-(4-Amino-3-methylphenyl)-8-methyl-7-(5-propyl- 150-154(EtOH)
56 1,3,4-thiadiazol-2-yl)-8,9-dihydro-7H-1,3-dioxolo[4,5-
-516.0.degree.(c=0.5, CHCl.sub.3) h][2,3]benzodiazepine Method B
.sup.1H NMR(DMSO-d.sub.6) d 0.91(t, 7.5 Hz), 1.20(3H, d, 6.1 Hz),
1.66(2H, m), 2.08(3H, s), 2.58(1H, dd, 13.8 Hz, 10.6 Hz), 2.80(2H,
t, 7.2 Hz), 2.96(1H, dd, 13.8 Hz, 5.1 Hz), 4.94(1H, m), 5.50(2H,
s), 6.03(1H, s), 6.08(1H, s), 6.57(1H, s), 6.64(1H, d, 8.3 Hz),
7.05(1H, s), 7.19(1H, dd, 8.3 Hz, 2.1 Hz), 7.25(1H, d, 2.1 Hz) 167
(R)-5-(4-Amino-3-methylphenyl)-8-methyl-7-(1,3,4- 143-148(EtOAc) 63
thiadiazol-2-yl)-8,9-dihydro-7H-1,3-dioxolo- -527.3.degree.(c=0.5,
CHCl.sub.3) [4,5-h][2,3]benzodiazepine Method B .sup.1H
NMR(DMSO-d.sub.6) d 1.21(3H, d, 6.1 Hz), 2.08(3H, s), 2.61(1H, dd,
13.6 Hz, 10.6 Hz), 3.00(1H, dd, 13.6 Hz, 5.0 Hz), 5.00(1H, m),
5.52(2H, s, br), 6.03(1H, d, 0.7 Hz), 6.08(1H, d, 0.7 Hz), 6.58(1H,
s), 6.64(1H, d, 8.3 Hz), 7.07(1H, s), 7.20(1H, dd, 8.3 Hz, 2.1 Hz),
7.28(1H, d, 2.1 Hz), 8.78(1H, s) MS: EI(70eV): [M].sup.+.: 393,
m/z: 378, 266 CI: [M+H].sup.+: 394, [M].sup.+.: 393 168
(R)-5-(4-Amino-3-methylphenyl)-8-methyl-7-(5- 171-172(EtOH) 86
methoxymethyl-1,3,4-thiadiazol-2-yl)-8,9-dihydro-7H-
-540.0.degree.(c=0.5, CHCl.sub.3)
1,3-dioxolo-[4,5-h][2,3]benzodiazepine Method B .sup.1H
NMR(DMSO-d.sub.6) d 1.21(3H, d, 6.1 Hz), 2.08(3H, s), 2.60(1H, dd,
14.0 Hz, 11.0 Hz), 2.97(1H, dd, 14.0 Hz, 5.4 Hz), 4.57(1H, d, 12.7
Hz), 4.60(1H, d, 12.7 Hz), 4.98(1H, m), 5.3-5.8(2H), 6.03(1H, s),
6.08(1H, s), 6.58(1H, s), 6.65(1H, d, 8.6 Hz), 7.06(1H, s),
7.21(1H, dd, 8.6Hz, 2.2 Hz), 7.26(1H, d, 2.2 Hz) 169
(R)-5-(4-Amino-3-methylphenyl)-7-(5-isopropyl-1,3,4- 134-140 83
thiadiazol-2-yl)-8-methyl-8,9-dihydro-7H-1,3- -518.8.degree.(c=0.5,
CHCl.sub.3) dioxolo[4,5-h][2,3]benzodiazepine Method B .sup.1H
NMR(DMSO-d.sub.6) d 1.20(3H, d, 6.2Hz), 1.26(3H, d, 6.9Hz), 128(3H,
d, 6.9Hz), 2.07(3H, s), 2.58(1H, dd, 13.8 Hz, 10.8 Hz), 2.95(1H,
dd, 13.8 Hz, 5.5 Hz), 3.18(1H, m), 4.94(1H, m), 5.51(2H, s, br),
6.03(1H, s), 6.08(1H, s), 6.57(1H, s), 6.64(1H, d, 8.4 Hz),
7.06(1H, s), 721(1H, dd, 8.4 Hz, 2.1 Hz), 7.24(1H, d, 2.1 Hz) 170
(R)-5-(4-Amino-3-methylphenyl)-7-(5-cyclopropyl- 124-128 47
1,3,4-thiadiazo1-2-yl)-8-methyl-8,9-dihydro-7H-1,3-
-504.1.degree.(c=0.5, CHCl.sub.3) dioxolo[4,5-h][2,3]benzodiazepine
Method B .sup.1H NMR(DMSO-d.sub.6) d 0.86(2H, m), 1.03(2H, m),
1.16(3H, d, 6.2 Hz), 2.07(3H, s), 2.23(1H, m), 2.57(1H, dd, 14.0
Hz, 10.8 Hz), 2.95(1H, dd, 14.0 Hz, 5.5 Hz), 4.92(1H, m), 5.50(2H,
s), 6.03(1H, s), 6.08(1H, s), 6.55(1H, s), 6.64(1H, d, 8.3 Hz),
7.05(1H, s), 7.19(1H, dd, 8.3 Hz, 2.1 Hz), 7.23(1H, d, 2.1 Hz) 171
(R)-5-(4-Amino-3-methylphenyl)-7-(5-hydroxymethyl- 184-186 75
1,3,4-thiadiazol-2-yl)-8-methyl-8,9-dihydro-7H-1,3-
-540.0.degree.(c=0.5, CHCl.sub.3) dioxolo[4,5-h][2,3]benzodiazepine
Method A .sup.1H NMR(DMSO-d.sub.6) d 1.20(3H, d, 6.1 Hz), 2.08(3H,
s), 2.60(1H, dd, 13.9 Hz, 10.6 Hz), 2.97(1H, dd, 13.9 Hz, 5.3 Hz),
4.61(2H, d, 5.8 Hz), 4.95(1H, m), 5.52(2H, s), 5.81(1H, t, 5.8 Hz),
6.03(1H, s), 6.08(1H, s), 6.58(1H, s), 6.65(1H, d, 8.5 Hz),
7.06(1H, s), 7.19(1H, dd, 8.5 Hz, 2.0 Hz), 7.26(1H, d, 2.0 Hz) 172
(R)-7-(5-Acetoxymethyl-1,3,4-thiadiazol-2-yl)-5-(4- 204-206(EtOH)
45 amino-3-methylphenyl)-8-methyl-8,9-dihydro-7H-1,3-
-560.0.degree.(c=0.5, CHCl.sub.3) dioxolo[4,5-h][2,3]benzodiazepine
Method E .sup.1H NMR(DMSO-d.sub.6) d 1.21(3H, d, 6.2 Hz), 2.07(3H,
s), 2.08(3H, s), 2.60(1H, dd, 14.0 Hz, 11.0 Hz), 2.97(1H, dd, 14.0
Hz, 5.4 Hz), 4.99(1H, m), 5.20(1H, d, 13.1 Hz), 5.24(1H, d, 13.1
Hz), 5.55(2H, s), 6.03(1H, s), 6.09(1H, s), 6.59(1H, s), 6.65(1H,
d, 8.4 Hz), 7.06(1H, s), 7.21(1H, dd, 8.4 Hz, 2.1 Hz), 7.26(1H, d,
2.1 Hz) 173 (R)-5-(4-Amino-3-methylphenyl)-7-(5-cyanomethyl-
135-140 25 1,3,4-thiadiazol-2-yl)-8-methyl-8,9-dihydro-7H-1,3-
-517.9.degree.(c=0.5, CHCl.sub.3) dioxolo[4,5-h][2,3]benzodiazepine
Method A .sup.1H NMR(DMSO-d.sub.6) d 1.21(3H, d, 6.2 Hz), 2.08(3H,
s), 2.61(1H, dd, 13.9 Hz, 11.0 Hz), 2.99(1H, dd, 13.9 Hz, 5.5 Hz),
4.40(2H, s), 4.96(1H, m), 5.55(2H, s), 6.03(1H, d, 0.7 Hz),
6.09(1H, d, 0.7 Hz), 6.59(1H, s), 6.65(1H, d, 8.3 Hz), 7.06(1H, s),
7.21(1H, dd, 8.3 Hz, 1.8 Hz), 7.26(1H, d, 1.8 Hz) 174
(R)-5-(4-Amino-3-methylphenyl)-8-methyl-7-(5- 177-180(EtOH) 57
methylthiomethyl-1,3,4-thiadiazol-2-yl)-8,9-dihydro-
-496.0.degree.(c=0.5, CHCl.sub.3)
7H-1,3-dioxolo[4,5-h][2,3]benzodiazepine Method A .sup.1H
NMR(DMSO-d.sub.6) d 1.21(3H, d, 6.1 Hz), 2.03(3H, s), 2.08(3H, s),
2.60(1H, dd, 13.8 Hz, 10.6 Hz), 2.97(1H, dd, 13.8 Hz, 5.3 Hz),
3.91(1H, d, 14.7 Hz), 3.95(1H, d, 14.7 Hz), 4.96(1H, m), 5.52(2H,
s), 6.03(1H, d, 0.9 Hz), 6.09(1H, d, 0.9 Hz), 6.59(1H, s), 6.65(1H,
d, 8.4 Hz), 7.06(1H, s), 7.21(1H, dd, 8.4 Hz, 2.0 Hz), 7.25(1H, d,
2.0 Hz) 175 (R)-5-(4-Amino-3-methylphenyl)-7-(5-ethoxycarbonyl-
135-140 86 1,3,4-thiadiazol-2-yl)-8-methyl-8,9-dihydro-7H-1,3-
-606.3.degree.(c=0.5, CHCl.sub.3) dioxolo[4,5-h][2,3]benzodiazepine
Method E .sup.1H NMR(DMSO-d.sub.6) d 1.15(3H, d, 6.2 Hz), 1.30(3H,
t, 7.1 Hz), 2.09(3H, s), 2.64(1H, dd, 13.8 Hz, 11.3 Hz), 2.99(1H,
dd, 13.8 Hz, 5.4 Hz), 4.30(2H, m), 5.11(1H, m), 5.65(2H, s),
6.04(1H, s), 6.09(1H, s), 6.61(1H, s), 6.65(1H, d, 8.3 Hz),
7.08(1H, s), 7.25(1H, dd, 8.3 Hz, 2.0 Hz), 7.26(1H, d, 2.0 Hz) 176
(R)-5-(4-Amino-3-methylphenyl)-7-(5-aminomethyl- 139-140(EtOH) 31
1,3,4-thiadiazol-2-yl)-8-methyl-8,9-dihydro-7H-1,3-
-482.2.degree.(c=0.5, CHCl.sub.3) dioxolo[4,5-h][2,3]benzodiazepine
Method B .sup.1H NMR(DMSO-d.sub.6) d 1.21(3H, d, 6.0 Hz), 2.08(3H,
s), 2.59(1H, dd, 13.9 Hz, 13.9 Hz), 2.95(1H, dd, 13.9 Hz, 5.1 Hz),
3.87(2H, s), 4.95(1H, m), 5.50(2H, s), 6.03(1H, s), 6.07(1H, s),
6.57(1H, s), 6.65(1H, d, 8.1 Hz), 7.05(1H, s), 7.21(1H, d, br, 8.1
Hz), 7.26(1H, s, br) 177
(R)-5-(4-Amino-3-methylphenyl)-8-methyl-7-{5-[1- 139-143 65
(1E)-propen-1-yl]-1,3,4-thiadiazol-2-yl}-8,9-dihydro-
-498.9.degree.(c=0.5, CHCl.sub.3)
7H-1,3-dioxolo[4,5-h][2,3]benzodiazepine Method B .sup.1H
NMR(DMSO-d.sub.6) d 1.21(3H, d, 6.2 Hz), 1.86(1H, dd, 6.8 Hz, 1.8
Hz), 2.08(3H, s), 2.59(1H, dd, 14.0 Hz, 10.8 Hz), 2.98(1H, dd, 14.0
Hz, 5.4 Hz), 4.98(1H, m), 5.53(2H, s, br), 6.03(1H, s), 6.08(1H,
s), 6.32(1H, dq, 15.7 Hz, 6.8 Hz), 6.55(1H, dq, 15.7 Hz, 1.8 Hz),
6.57(1H, s), 6.44(1H, d, 8.4 Hz), 7.06(1H, s), 7.22(1H, dd, 8.4 Hz,
2.1 Hz), 7.26(1H, d, 2.1 Hz) 178
(R)-5-(4-Amino-3-methylphenyl)-7-(5-hexyl-1,3,4- 180-181 75
thiadiazol-2-yl)-8-methyl-8,9-dihydro-7H-1,3- -485.2.degree.(c=0.5,
CHCl.sub.3) dioxolo[4,5-h][2,3]benzodiazepine Method B .sup.1H
NMR(DMSO-d.sub.6) d 0.84(3H, t, 7.0 Hz), 1.20(3H, d, 6.1 Hz),
1.2-1.3(6H, m), 1.62(2H, m), 2.07(3H, s), 2.58(1H, dd, 13.9 Hz,
10.5 Hz), 2.82(2H, t, 7.5 Hz), 2.95(1H, dd, 13.9 Hz, 5.4 Hz),
4.94(1H, m), 5.49(2H, s), 6.03(1H, s), 6.08(1H, s), 6.57(1H, s),
6.64(1H, d, 8.4 Hz), 7.05(1H, s), 7.19(1H, dd, 8.4 Hz, 2.2 Hz),
7.25(1H, d, 2.2 Hz) 179
(R)-5-(4-Amino-3-methylphenyl)-8-methyl-(5,6- 175-180 61
dihydro-5-oxo-4H-1,3,4-thiadiazin-2-yl)-8,9-dihydro-
-686.0.degree.(c=0.5, CHCl.sub.3)
7H-1,3-dioxolo[4,5-h][2,3]benzodiazepine Method B .sup.1H
NMR(DMSO-d.sub.6) d 1.15(3H, d, 6.4 Hz), 2.05(3H, s), 2.48(1H, dd,
13.8 Hz, 10.4 Hz), 2.85(1H, dd, 13.8 Hz, 5.3 Hz), 3.32(2H, s),
4.75(1H, m), 5.42(2H, s), 6.04(1H, s), 6.07(1H, s), 6.55(1H, s),
6.61(1H, d, 8.4 Hz), 6.99(1H, s), 7.15(1H, dd, 8.4 Hz, 1.8 Hz),
7.26(1H, d, 1.8 Hz), 10.47(1H, s) 180
(R)-5-(4-Aminophenyl)-8-methyl-7-(1,3,4-oxadiazol-2- 187-190 78
yl)-8,9-dihydro-7H-1,3-dioxolo[4,5- -604.0.degree.(c=0.5,
CHCl.sub.3) h][2,3]benzodiazepine Method A .sup.1H NMR(CDCl.sub.3)
d 1.45(3H, d, 6.0 Hz), 2.73(1H, dd, 14.0 Hz, 10.5 Hz), 2.86(1H, dd,
14.0 Hz, 5.5 Hz), 3.99(2H, s, br), 4.94(1H, m), 5.98(1H, d, 1.0
Hz), 6.02(1H, d, 1.0 Hz), 6.64(1H, s), 6.68(2H, d, 8.0 Hz),
6.82(1H, s), 7.56(2H, d, 8.0 Hz), 7.99(1H, s) 181
(R)-5-(4-Amino-3-methylphenyl)-8-methyl-7-(5- 140-145 85
methyl-1,3,4-oxadiazol-2-yl)-8,9-dihydro-7H-1,3-
-554.8.degree.(c=0.5, CHCl.sub.3) dioxolo[4,5-h][2,3]benzodiazepine
Method B MS: EI(70eV): [M].sup.+.: 391, m/z: 266 CI: [M+H].sup.+:
392 182 (R)-5-(4-Amino-3-chlorophenyl)-8-methyl-7-(5-methyl- 98-100
92 1,3,4-thiadiazol-2-yl)-8,9-dihydro-7H-1,3-dioxolo-
-266.0.degree.(c=0.5, CHCl.sub.3) [4,5-h][2,3]benzodiazepine Method
C .sup.1H NMR(DMSO-d.sub.6) d 1.18(3H, d, 6.0 Hz), 2.50(3H, s),
2.65(1H, dd, 14.0 Hz, 9.9 Hz), 2.98(1H, dd, 14.0 Hz, 4.9 Hz),
4.95(1H, m), 5.95(2H, s), 6.05(1H, s), 6.09(1H, s), 6.63(1H, s),
6.83(1H, d, 8.6 Hz), 7.07(1H, s), 7.24(1H, dd, 8.6 Hz, 2.0 Hz),
7.44(1H, d, 2.0 Hz) MS: EI(70eV): [M].sup.+.: 427/429, m/z:
412/414, 313/315, 286/288, 160 CI: [M+H].sup.+: 428/30, [M].sup.+.:
427/429 183 (R)-5-(4-Amino-3-chlorophenyl)-8-methyl-7-(5- 105-109
91 methoxymethyl-1,3,4-thiadiazol-2-yl)-8,9-dihydro-7H-
-350.0.degree.(c=0.5, CHCl.sub.3)
1,3-dioxolo[4,5-h][2,3]benzodiazepine Method C .sup.1H
NMR(DMSO-d.sub.6) d 1.20(3H, d, 6.1 Hz), 2.67(1H, dd, 14.1 Hz, 10.3
Hz), 3.00(1H, dd, 14.1 Hz, 5.4 Hz), 3.32(3H, s), 4.58(1H, d, 13.0
Hz), 4.62(1H, d, 13.0 Hz), 5.01(1H, m), 5.98(2H, s, br), 6.05(1H,
s), 6.09(1H, s), 6.64(1H, s), 6.84(1H, d, 8.4 Hz), 7.07(1H, s),
7.29(1H, dd, 8.4 Hz, 1.8 Hz), 7.44(1H, d, 1.8 Hz) MS: EI(70eV):
[M].sup.+.: 457/459, m/z: 442/444, 313/315, 286/288, 160 CI:
[M+H].sup.+: 458/60, [M].sup.+: 457/459 184
(R)-5-(4-Amino-2-bromo-3-methylphenyl)-8-methyl-7- foam 98
(5-methyl-1,3,4-thiadiazol-2-yl)-8,9-dihydro-7H-1,3-
dioxolo[4,5-h][2,3]benzodiazepine Method A .sup.1H NMR(CDCl.sub.3)
d 1.25(3H, d, 6.2 Hz), 2.25(3H, s), 2.53(3H, s), 2.93(1H, dd, 14.6
Hz, 7.3 Hz), 3.25(1H, dd, 14.6 Hz, 3.1 Hz), 3.4-4.3(2H), 5.43(1H,
m), 5.92(1H, d, 1.4 Hz), 5.93(1H, d, 1.4 Hz), 6.36(1H, s), 6.69(1H,
d, 8.1 Hz), 6.72(1H, s), 7.12(1H, d, 8.1 Hz) MS: EI(70eV):
[M].sup.+.: 485/487, m/z: 470/472, 406, 265, 219
CI: [M+H].sup.+: 486/488 185
(.+-.)-5-(4-Aminophenyl)-8-methyl-7-(3-methyl-isoxazol- 100-103 87
5-yl)-8,9-dihydro-7H-1,3-dioxolo- [4,5-h][2,3]benzodiazepine Method
C .sup.1H NMR(DMSO-d.sub.6) d 1.16(3H, d, 6.5 Hz), 2.07(3H, s),
2.45(1H, dd, 14.0 Hz, 11.5 Hz), 2.88(1H, dd, 14.0 Hz, 6.0 Hz),
4.58(1H, m), 5.26(1H, s), 5.70(2H, s), 6.02(1H, s), 6.07(1H, s),
6.56(1H, s), 6.58(2H, d, 8.5 Hz), 7.03(1H, s), 7.36(2H, d, 8.5 Hz)
MS: EI(70eV): [M].sup.+.: 376, m/z: 306, 265, 252, 82, 54 CI:
[M+H].sup.+: 377, [M].sup.+: 376 186
(R)-5-(4-Aminophenyl)-8-methyl-7-(1,2,3-thiadiazol-5- 220-221 33
yl)-8,9-dihydro-7H-1,3-dioxolo- -705.0.degree.(c=0.5, CHCl.sub.3)
[4,5-h][2,3]benzodiazepine Method A .sup.1H NMR(DMSO-d.sub.6) d
1.18(3H, d, 6.1 Hz), 2.60(1H, dd, 13.8 Hz, 11.4 Hz), 2.95(1H, dd,
13.8 Hz, 5.1 Hz), 4.75(1H, m), 5.81(2H, s, br), 6.03(1H, s),
6.08(1H, s), 6.59(1H, s), 6.61(2H, d, 8.4 Hz), 7.08(1H, s),
7.35(2H, d, 8.4 Hz), 8.10(1H, s) MS: EI(70eV): [M].sup.+.: 379,
m/z: 351, 336, 279, 252 CI: [M+H].sup.+: 380, m/z: 352 187
(.+-.)-5-(4-Aminophenyl)-8-methyl-7-(2-methyl-1,3- 148-150 88
oxazol-5-yl)-8,9-dihydro-7H-1,3-dioxolo- [4,5-h][2,3]benzodiazepine
Method A .sup.1H NMR(DMSO-d.sub.6) d 1.07(3H, d, 5.3 Hz), 2.23(3H,
br), 2.40(1H, dd, 13.7 Hz, 7.7 Hz), 2.83(1H, dd, 13.7 Hz, 5.6 Hz),
4.31(1H, m), 5.58(s, br), 6.03(1H, s), 6.05(1H, s), 6.54(2H, d, 8.2
Hz), 6.57(1H, s), 7.00(1H, s), 7.28(2H, d, 8.2 Hz) MS: EI(70eV):
[M].sup.+.: 376, m/z: 335, 306, 265, 252 CI: [M+H].sup.+: 377 188
(.+-.)-5-(4-Aminophenyl)-8-methyl-7-(2,4,dimethyl-1,3- 180-182 92
oxazol-5-yl)-8,9-dihydro-7H-1,3-dioxolo- [4,5-h][2,3]benzodiazepine
Method A .sup.1H NMR(DMSO-d.sub.6) d 0.94(3H, d, 6.1 Hz), 1.76(3H,
s), 2.29(3H, s), 2.43(1H, dd, 13.8 Hz, 3.3 Hz), 2.79(1H, dd, 13.8
Hz, 6.6 Hz), 4.13(1H, m), 5.53(s, br), 6.07(1H, s), 6.08(1H, s),
6.52(2H, d, 8.4 Hz), 6.58(1H, s), 6.99(1H, s), 7.18(2H, d, 8.4 Hz)
MS: EI(70eV): [M].sup.+.: 390, m/z: 349, 334, 306, 279, 265, 252
CI: [M+H].sup.+: 391, [M].sup.+.: 390 189
(R)-5-(4-Amino-3,5-dimethylphenyl)-8-methyl-7- 202-203 75
(thiazol-2-yl)-8,9-dihydro-7H-1,3-dioxolo- -686.0.degree.(c=0.3,
CHCl.sub.3) [4,5-h][2,3]benzodiazepine Method A MS: EI(70eV):
[M].sup.+: 406, m/z: 391, 307, 280 190
(R)-5-(4-Amino-3,5-dimethylphenyl)-8-methyl-7-(5- 280-281 74
methyl-1,3,4-thiadiazol-2-yl)-8,9-dihydro-7H-1,3-
-538.0.degree.(c=0.5, CHCl.sub.3) dioxolo[4,5-h][2,3]benzodiazepine
Method A .sup.1H NMR(DMSO-d.sub.6) d 1.18(3H, d, 6.1 Hz), 2.11(6H,
s), 2.49(3H, s), 2.57(1H, dd, 13.9 Hz, 10.8 Hz), 2.95(1H, dd, 13.9
Hz, 5.1 Hz), 4.93(1H, m), 5.19(2H, s, br), 6.03(1H, d, 0.5 Hz),
6.08(1H, d, 0.5 Hz), 6.56(1H, s), 7.05(1H, s), 7.12(2H, s) MS:
EI(70eV): [M].sup.+.: 421, m/z: 406, 307, 306, 280 CI: [M+H].sup.+:
422 191 (R)-5-(4-Amino-3,5-dimethylphenyl)-8-methyl-7-(5- 148-150
87 methyl-1,3,4-oxadiazol-2-yl)-8,9-dihydro-7H-1,3-
-705.0.degree.(c=0.5, CHCl.sub.3) dioxolo[4,5-h][2,3]benzodiazepine
Method A MS: EI(70eV): [M].sup.+: 405, m/z: 280, 245, 134, 83, 77
CI: [M+H].sup.+: 406 192
(R)-5-(4-Aminophenyl)-8-methyl-7-(2-methyl-3-oxo- 185-190 60
2,3-dihydro-1,2,4-thiadiazol-2-yl)-8,9-dihydro-7H-1,3-
-45.0.degree.(c=0.47, CHCl.sub.3)
dioxolo-[4,5-h][2,3]benzodiazepine Method A .sup.1H
NMR(DMSO-d.sub.6) d 1.19(3H, d, 6.5 Hz), 2.69(1H, dd, 14.0 Hz, 10.0
Hz), 3.00(1H, dd, 14.0 Hz, 4.5 Hz), 3.05(3H, s), 4.89(1H, m),
5.81(2H, s, br), 6.05(1H, s), 6.08(1H, s), 6.58(2H, d, 8.5 Hz),
6.59(1H, s), 7.06(1H, s), 7.26(2H, d, 8.5 Hz) MS: EI(70eV):
[M].sup.+.: 409, m/z: 279, 252 CI: [M+H].sup.+: 410, [M].sup.+.:
409 193 (.+-.)-5-(4-Aminophenyl)-8-methyl-7-(5,5-dimethyl-4-
124-130 75 oxo-4,5-dihydrothiazol-2-yl)-8,9-dihydro-7H-1,3-
amorphous dioxolo-[4,5-h][2,3]benzodiazepine Method A MS: EI(70eV):
[M].sup.+.: 422, m/z: 407, 279, 252 CI: [M+H].sup.+: 423 *See the
general procedures given before Examples 60-118 for reduction of
the nitro groups of various 2,3-benzodiazepines.
Example 194
(R)-7-(4,5-Dihydro-thiazol-2-yl)-5-(4-chlorophenyl)-8-methyl-8,9-dihydro-7-
H-1,3-dioxolo[4,5-h][2,3]benzodiazepine
Step A
(R)-7-(tert-Butoxycarbonyl)-5-(4-chlorophenyl)-8-methyl-8,9-dihydro-7H-1,3-
-dioxolo[4,5-h][2,3]benzodiazepine
[0303] The compound was prepared according to a synthesis described
in literature (Anderson et al., J. Am. Chem. Soc. 117: 12358
(1995)) with the exception that tert-butylcarbazate and
4-chlorobenzaldehide were used instead of acetic hydrazide and
4-nitrobenzaldehide, respectively. The title product was isolated
as a foam and used for the next step.
Step B
(R)-5-(4-Chlorophenyl)-8-methyl-8,9-dihydro-7H-1,3-dioxolo[4,5-g][2,3]benz-
odiazepine
[0304] 11.0 g (28.2 mmol) of the product obtained in Step A was
dissolved in 120 ml of ethyl acetate containing 10% hydrochloric
acid and stirred for 3 h, then the solution was washed with sodium
carbonate and water. After drying and evaporation the crude product
was recrystallized from ethyl acetate to yield 5.07 g (57.degree.%)
of the title compound. Mp.: 185-187.degree. C.; [.alpha.].sub.D:
+241.0.degree. (c=0.5; CHCl.sub.3).
Step C
(R)-5-(4-Chlorophenyl)-8-methyl-7-thiocarbamoyl-8,9-dihydro-7H-1,3-dioxolo-
[4,5-g][2,3]benzodiazepine
[0305] A mixture containing 1.57 g (5.0 mmol) of the product
obtained in Step B, 0.73 g (7.5 mmol) of potassium thiocyanate and
16 ml of acetic acid was stirred at 110.degree. C. for 3 h. After
cooling water was added and the precipitated crystals were filtered
off, washed with water and dried to yield 1.73 g (92%) of the title
compound. Mp.: 208-212.degree. C.
Step D
[0306] The compound obtained in Step C (1.0 g, 2.66 mM) was reacted
with 2.20 g (10.7 mmol) of 2-bromoethylamine hydrobromide in 5 ml
of dimethylformamide according to the method described in Example
9. The product was isolated by column chromatography and an
additional recrystallization from ethyl acetate to yield 0.26 g
(25%) of the title compound. Mp.: 216-219.degree. C.;
[.alpha.].sub.D: +326.7.degree.(c=0.5; CHCl.sub.3).
[0307] .sup.1HNMR (DMSO-d.sub..alpha.) .delta. 1.11 (3H, d, 5.7
Hz), 2.79 (1H, dd, 14.7 Hz, 6.4H), 3.16 (1H, dd, 14.7 Hz, 1.7 Hz),
3.25 (2H, m), 4.16 (2H, m), 4.28 (2H, m), 5.25 (1H, m), 5.99 (2H,
s), 6.59 (1H, s), 6.71 (1H, s) 7.34 (2H, d, 8.0 Hz), 7.53 (2H, d,
8.0 Hz)
Example 195
(R)-5-(4-Chlorophenyl)-8-methyl-7-(2-thiazolyl)-8,9-dihydro-7H-1,3-dioxolo-
[4,5-h][2.3]benzodiazepine
[0308] The compound obtained in Step C of Example 194 (0.55 g, 1.47
mmol) was reacted with 0.22 ml (1.47 mmol) of bromoacetaldehyde
diethyl acetal according to the method described in Example 1. The
crude product was purified by column chromatography using a mixture
of n-hexane-ethyl acetate (2:1) as eluent. After concentration of
the fractions containing the title compound the residue was treated
with water to yield 0.40 g (68%) of the title compound. Mp.:
116-117.degree. C.; [.alpha.].sub.D: +118.6.degree. (c=0.5;
CHCl.sub.3).
[0309] .sup.1H NMR (CDCl.sub.3) .delta. 1.22 (3H, d, 6.4 Hz), 2.83
(1H, dd, 14.6 Hz, 7.2 Hz), 3.18 (1H, dd, 14.6 Hz, 3.4 Hz), 5.38
(1H, m), 6.01 (2H, s), 6.61 (1H, s), 6.69 (1H d, 3.7 Hz), 6.78 (1H,
s), 7.32 (1H, d, 3.7 Hz), 7.38 (2H d, 8.6H), 7.58 (2H, d, 8.6
Hz)
Example 196
(R)-5-(4-Chlorophenyl)-8-methyl-7-(5-methyl-1,3,4-thiadiazol-2-yl)-8,9-dih-
ydro-7H-1,3-dioxolo[4,5-h][2,3]benzodiazepine
Step A
(R)-5-(4-Chlorophenyl)-8-methyl-8,9-dihydro-7H-1,3-dioxolo[4,5-h][2,3]benz-
odiazepine-7-carbothioyl chloride
[0310] The compound obtained in Step B of Example 194 (2.20 g, 7.0
mmol was reacted according to the method described for starting
compound XI. The crude product was purified by column
chromatography using a mixture of n-hexane-ethyl acetate (4:1) as
eluent to yield 1.38 g (49%) of the title compound as a solid
foam.
Step B
[0311] 1.0 g (2.48 mmol) of the product obtained in Step A was used
to prepare the title compound according to a method described in
Example 28, Method B. The product, isolated by column
chromatography, was solidified by water to give 0.42 g (52%), Mp.:
105-108.degree. C.; [.alpha.].sub.D: +103.2.degree. (c=0.5;
CHCl.sub.3).
[0312] .sup.1H NMR (CDCl.sub.3) .delta. 1.25 (3H, d, 6.2 Hz), 2.61
(3H, s), 2.84 (1H, dd, 14.3H, 7.1 Hz), 3.18 (1H, dd, 14.3 Hz, 3.6
Hz), 5.35 (1H, m), 6.02 (2H, s), 6.57 (1H, s), 6.79 (1H, s), 7.38
(2H, d, 8.2 Hz), 7.52 (2H, d, 8.2H)
Example 197
(R)-5-(4-Acetylamino-3-methylphenyl)-8-methyl-7-(5-methyl-1,3,4-thiadiazol-
-2-yl)-8,9-dihydro-7H-1,3-dioxolo[4,5-h][2,3]benzodiazepine
[0313] The compound of Example 119 was acetylated according to the
general method described for Examples 120-131. Mp.: 267-269.degree.
C. Yield: 67%; [.alpha.].sub.D: -121.0.degree. (c=0.5;
CHCl.sub.3).
[0314] .sup.1H NMR (DMSO-d.sub.6) .delta. 1.16 (3H, d, 6.1H), 2.10
(3H, s), 2.25 (1H, s), 2.50 (3H, s), 2.79 (1H, dd, 14.0H, 8.2 Hz),
3.09 (1H, dd, 14.0 Hz, 4.0 Hz), 5.08 (1H, m), 6.07 (1H, s), 6.09
(1H, s), 6.55 (1H, s), 7.07 (1H, s), 7.31 (1H, d, 8.3 Hz), 7.38
(1H, s, br), 7.59 (1H, d, br, 8.3H), 9.36 (1H, s)
Example 198
(R)-1-Methyl-3{2-methyl-4-[8-methyl-7-(5-methyl-1,3,4-thiadiazol-2-yl)-8,9-
-dihydro-7H-1,3-dioxolo[4,5-h][2,3]benzodiazepin-5-yl}phenylurea
[0315] The substance (1.03 g, 2.53 mmol) obtained in Example 119
was reacted with 0.75 ml (12.6 mmol) of methyl isocyanate in 20 ml
of dichloromethane for 6 days at RT. Evaporation of the solvent
gave a crude product which was purified by column chromatography,
using a mixture of hexane-ethyl acetate (2:1) as eluent to give
0.67 g (57%) of the title compound. Mp.: 237-242.degree. C.;
[.alpha.].sub.D: -140.0.degree. (c=0.5; CHCl.sub.3).
[0316] .sup.1H NMR (DMSO-d.sub.6) .delta. 1.17 (3H, d, 6.4 Hz),
2.21 (3H, s), 2.51 (3H, s), 2.66 (3H, d, 4.6 Hz), 2.71 (1H, dd,
14.2 Hz, 9.4 Hz), 3.04 (1H, dd, 14.2 Hz, 4.5 Hz), 5.02 (1H, m),
6.05 (1H, d, 0.9 Hz), 6.08 (1H, d, 0.9H), 6.55 (1H, s), 6.56 (1H,
q, 4.6 H), 7.07 (1H, s), 7.30 (1H, dd, 8.4 Hz, 2.0 Hz), 7.34 (1H,
d, 2.0 Hz), 7.82 (1H, s), 8.00 (1H, d, 8.4 Hz)
Example 199
(R)-2-Methyl-4-[8-methyl-7-(5-methyl-1,3,4-thiadiazol-2-yl)-8,9-dihydro-7H-
-1,3-dioxolo[4,5-h][2,3]benzodiazepin-5-yl]-phenylcarbamic acid
ethyl ester
[0317] The substance (0.90 g, 2.21 mmol) obtained in Example 119
was reacted with ethyl chloroformate (0.30 ml, 3.15 mmol) in
dichloromethane in the presence of 0.40 ml (2.88 mmol) of
triethylamine for 6 h at RT. The solution was washed with diluted
hydrochloric acid and sodium hydrogen carbonate solution, dried and
evaporated to dryness. The residue was purified by column
chromatography using a mixture of hexane-ethyl acetate (2:1) as
eluent to give 0.45 g (42%) of the title product. Mp.:
241-244.degree. C.; [.alpha.].sub.D: -180.0.degree. (c=0.5;
CHCl.sub.3).
[0318] .sup.1H NMR (DMSO-d.sub.6) .delta. 1.15 (3H, d, 6.1 Hz),
1.25 (3H, t, 7.0 Hz), 2.25 (3H, s), 2.51 (3H, s), 2.78 (1H, dd,
14.3 Hz, 8.7 Hz), 3.05 (1H, dd, 14.3 Hz, 4.3 Hz), 4.13 (2H, q, 7.0
Hz), 5.07 (1H, m), 6.06 (1H, d, 0.7 Hz), 6.08 (1H, d, 0.7 Hz), 6.55
(1H, s), 7.07 (1H, s), 7.31 (1H, dd, 8.3 Hz, 2.0 Hz), 7.36 (1H, d,
2.0 Hz), 7.53 (1H, d, 8.3 Hz), 8.96 (1H, s)
[0319] Further results with compounds of the present invention are
collected in the following tables, exemplifying the AMPA
antagonistic activity of compounds of formula (I). (The
corresponding in vitro and in vivo investigational methods and
related references were described and cited earlier in this
application.) TABLE-US-00013 TABLE 13 (Supplement to Table 1)
Inhibition of the "spreading depression" in chicken retina Compound
(Number of example)/IC.sub.50 .mu.M 119 165 166 167 168 182 0.069
0.113 0.201 0.064 0.082 0.020
[0320] TABLE-US-00014 TABLE 14 (Supplement to Table 2) Inhibition
of ion-currents caused by 5 .mu.M AMPA determined by the whole cell
patch clamp method Compound (Number of example)/IC.sub.50 .mu.M 119
165 166 167 168 182 0.026 0.024 0.028 0.070 0.011 0.031
[0321] TABLE-US-00015 TABLE 15 (Supplement to Table 3)
Investigation of the anticonvulsive activity in mice Compound
(Number of example)/ED.sub.50 mg/kg po. Method 119 165 166 167 168
182 MES 60' 2.87 3.99 4.01 5.85 4.49 6.17 MES 30' 2.15 2.39 4.54
4.78 2.21 5.08 Pentetrazol 5.00 10.10 9.18 9.66 6.90 8.37
Strychnine 8.40 10.20 7.29 10.50 10.00 5.90 Bemegride 5.70 10.00
7.77 8.33 6.70 7.94 Bicuculline 2.50 5.79 13.30 12.70 10.60 8.44
Nicotine 6.30 18.60 21.80 10.80 17.70 24.20 4-AP 2.68 8.60 6.81
10.80 4.60 5.44 3-MPA 3.37 8.53 9.92 10.30 4.62 7.57 Abbreviations:
MES = maximal electroshock seizure; 4-AP = 4-aminopyridine; 3-MPA =
3-mercapto-propionic acid
[0322] TABLE-US-00016 TABLE 16 (Supplement to Table 4) Muscle
relaxant activity in mice Compound Inclined screen Rotarod (Number
of example) ED.sub.50 ip. (mg/kg) ED.sub.50 ip. (mg/kg) 119 2.49
0.51 165 2.94 0.91 166 3.27 0.86 167 4.24 0.80 168 3.58 0.80 182
5.84 2.61
[0323] TABLE-US-00017 TABLE 17 (Supplement to Table 5) Inhibition
of focal ischemia in rats Dose Decrease of the infracted area in %
Compound mg/kg iv. compared to that of the control (Number of
(6.times.in every 30 min 120 min 180 min 240 min example) 30 min)
Time of first treatment after occlusion 119 0.5 7 1.0 38 1.5 51* 21
2.0 56* 44** 21 *p < 0.05; **p < 0.01; calculated with
Dunnett test following ANOVA (Dunnett J. Amer. Statist. Ass. 50:
1096 (1955))
[0324] Compounds of the invention were further investigated in the
autoimmune encephalomyelitis model in rats as outlined in this
description before, with the variance that 10 animals were used in
each group, of weights 140-160 g (Lewis rats, female). The results
are shown in Tables 19 and 20. TABLE-US-00018 TABLE 18 (Supplement
to Table 6) Effect of 2,3-benzodiazepines possessing AMPA
antagonist activity on the clinical symptoms of autoimmune
encephalomyelitis in Lewis rats Neurological symptoms (change
compared Compound to controls, %) (Number of Dose Female rats
example) mg/kg i.p. mg/kg p.o. 0-8 day 0-14 day 119 3.75 -97***
-90** 1.875 -72* -71** 1.0 -75** -72** 0.5 -33 -35 0.2 -36 -37 3.75
-64*** -61*** 1.875 -50** -50** 1.0 -20 -23 0.5 +2 -1 166 7.5 -51*
-53* 3.75 -6 -9 168 7.5 -55* -56* 3.75 -16 -23 For statistics see
Table 20.
[0325] TABLE-US-00019 TABLE 19 (Supplement to Table 7) Effect of
2,3-benzodiazepine derivatives possessing AMPA antagonistic
character on the histological and clinical symptoms of autoimmune
encephalomyelitis in Lewis rats on day 24 after immunization.
Histopathological Neurological Compound symptoms symptoms (Number
of Dose (change %) (change %) example) mg/kg i.p. mg/kg p.o. Female
rats 119 3.75 +3 -90** 1.875 -8 -71** 1.0 -3 -72** 0.5 -13 -35 0.2
+2 -37 3.75 -32 -61*** 1.875 -42 -50** 1.0 -21 -23 0.5 -16 -1 *p
< 0.05; **p < 0.01; ***p < 0.001 (Mann-Whitney test).
[0326] TABLE-US-00020 TABLE 20 (Supplement to Table 8) Effect of
2,3-benzodiazepine derivatives possessing AMPA antagonistic
character on the tremor of CD1 mice induced by different chemical
agents. Compound ED.sub.50 (mg/kg po.) (Number of Oxotremorin GYKI
20039 example) 1 mg/kg ip. 10 mg/kg ip. 119 1.38(0.80-2.38)
2.21(1.37-3.56) 165 4.63(3.66-5.85) 5.34(3.90-7.31) 166
2.74(1.97-3.00) 4.54(3.69-5.58) 167 4.81(3.45-6.72)
7.73(4.99-11.98) 168 3.29(2.63-4.12) 4.11(3.22-5.45) 182
2.66(1.24-5.72) 3.64(2.37-5.57)
[0327] TABLE-US-00021 TABLE 21 (Supplement to Table 9) Effect of
the compound described in Example 119 on the bronchial
hypersensitivity and the eosinophilia of the airways of BN-rats
sensitized with ovalbumin and antigen challenged by inhalation
(mean .+-. SE, N = 10, p determined by Student's t-test). Compound
(Number of example) 119 Parameter Control Challenge 3.0 mg/kg po
ED.sub.50* 5.19 .+-. 0.07 5.97 .+-. 0.29 4.35 .+-. 0.36 p 0.001
0.001 MAX** 100 .+-. 0 154 .+-. 21 82 .+-. 7 p 0.001 0.009
Eosinophil*** 0.15 .+-. 0.03 1.17 .+-. 0.18 1.16 .+-. 0.24 p 0.001
NS.sup..dagger-dbl. *acetylcholine (Ach) concentration (-log M)
which causes a 50% contraction compared to the control **relative
contraction compared to the control at a maximal Ach concentration
***BALF eosinophil number (.times.10.sup.6/ml) .sup..dagger-dbl.not
significant (p > 0.05)
EQUIVALENTS
[0328] While the claimed invention has been described in detail and
with reference to specific embodiments thereof, it will be apparent
to one of ordinary skill in the art that various changes and
modifications can be made to the claimed invention without
departing from the spirit and scope thereof. Thus, for example,
those skilled in the art will recognize, or be able to ascertain,
using no more than routine experimentation, numerous equivalents to
the specific substances and procedures described herein. Such
equivalents are considered to be within the scope of this
invention, and are covered by the following claims.
* * * * *