U.S. patent application number 16/832553 was filed with the patent office on 2020-07-16 for bicyclic compounds as dual atx/ca inhibitors.
This patent application is currently assigned to Hoffmann-La Roche Inc.. The applicant listed for this patent is Hoffmann-La Roche Inc.. Invention is credited to Patrick DI GIORGIO, Jerome HERT, Daniel HUNZIKER, Patrizio MATTEI, Markus RUDOLPH, Petra SCHMITZ, Christoph ULLMER.
Application Number | 20200223854 16/832553 |
Document ID | / |
Family ID | 54199035 |
Filed Date | 2020-07-16 |
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United States Patent
Application |
20200223854 |
Kind Code |
A1 |
DI GIORGIO; Patrick ; et
al. |
July 16, 2020 |
BICYCLIC COMPOUNDS AS DUAL ATX/CA INHIBITORS
Abstract
The invention provides novel compounds having the general
formula (I) ##STR00001## wherein R.sup.1, R.sup.2, Y, W, m, n, p
and q are as defined herein, compositions including the compounds
and methods of using the compounds.
Inventors: |
DI GIORGIO; Patrick; (Basel,
CH) ; HERT; Jerome; (Basel, CH) ; HUNZIKER;
Daniel; (Basel, CH) ; MATTEI; Patrizio;
(Basel, CH) ; RUDOLPH; Markus; (Basel, CH)
; SCHMITZ; Petra; (Basel, CH) ; ULLMER;
Christoph; (Basel, CH) |
|
Applicant: |
Name |
City |
State |
Country |
Type |
Hoffmann-La Roche Inc. |
Little Falls |
NJ |
US |
|
|
Assignee: |
Hoffmann-La Roche Inc.
Little Falls
NJ
|
Family ID: |
54199035 |
Appl. No.: |
16/832553 |
Filed: |
March 27, 2020 |
Related U.S. Patent Documents
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Application
Number |
Filing Date |
Patent Number |
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15933701 |
Mar 23, 2018 |
10647719 |
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16832553 |
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PCT/EP2016/072347 |
Sep 21, 2016 |
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15933701 |
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Current U.S.
Class: |
1/1 |
Current CPC
Class: |
A61K 31/437 20130101;
A61K 31/407 20130101; A61P 27/02 20180101; A61K 31/5517 20130101;
C07D 471/04 20130101; C07D 487/04 20130101 |
International
Class: |
C07D 487/04 20060101
C07D487/04; A61K 31/5517 20060101 A61K031/5517; A61K 31/407
20060101 A61K031/407; C07D 471/04 20060101 C07D471/04; A61K 31/437
20060101 A61K031/437; A61P 27/02 20060101 A61P027/02 |
Foreign Application Data
Date |
Code |
Application Number |
Sep 24, 2015 |
EP |
15186633.2 |
Claims
1. Compounds of formula (I) ##STR00068## wherein R.sup.1 is
substituted phenyl, substituted phenyl-C.sub.1-6-alkyl, substituted
phenoxy-C.sub.1-6-alkyl, substituted phenyl-C.sub.2-6-alkenyl,
substituted phenyl-C.sub.2-6-alkynyl, substituted quinolinyl,
substituted quinolinyl-C.sub.1-6-alkyl, substituted
quinolinyl-C.sub.1-6-lalkenyl, substituted
quinolinyl-C.sub.1-6-alkynyl, substituted pyridinyl, substituted
pyridinyl-C.sub.1-6-alkyl, substituted pyridinyl-C.sub.2-6-alkenyl,
substituted pyridinyl-C.sub.2-6-alkynyl, substituted thiophenyl,
substituted thiophenyl-C.sub.1-6-alkyl, substituted
thiophenyl-C.sub.2-6-alkenyl or substituted
thiophenyl-C.sub.2-6-alkynyl, wherein substituted phenyl,
substituted phenyl-C.sub.1-6-alkyl, substituted
phenoxy-C.sub.1-6-alkyl, substituted phenyl-C.sub.2-6-alkenyl,
substituted phenyl-C.sub.2-6-alkynyl, substituted quinolinyl,
substituted quinolinyl-C.sub.1-6-alkyl, substituted
quinolinyl-C.sub.1-6-lalkenyl, substituted
quinolinyl-C.sub.1-6-alkynyl, substituted pyridinyl, substituted
pyridinyl-C.sub.1-6-alkyl, substituted pyridinyl-C.sub.2-6-alkenyl,
substituted pyridinyl-C.sub.2-6-alkynyl, substituted thiophenyl,
substituted thiophenyl-C.sub.1-6-alkyl, substituted
thiophenyl-C.sub.2-6-alkenyl and substituted
thiophenyl-C.sub.2-6-alkynyl are substituted by R.sup.3, R.sup.4
and R.sup.5; Y is a --OC(O)-- or --C(O)--; W is --C(O)--,
--S(O).sub.2-- or --CR.sup.6R.sup.7--; R.sup.2 is substituted
phenyl, substituted pyridinyl or substituted thiophenyl, wherein
substituted phenyl, substituted pyridinyl and substituted
thiophenyl are substituted by R.sup.6, R.sup.7 and R.sup.8; R.sup.3
is halogen, hydroxy, cyano, C.sub.1-6-alkyl, C.sub.1-6-alkoxy,
C.sub.1-6-alkoxy-C.sub.1-6-alkyl, halo-C.sub.1-6-alkoxy,
halo-C.sub.1-6-alkyl, hydroxy-C.sub.1-6-alkyl,
C.sub.3-8-cycloalkyl, C.sub.3-8-cycloalkyl-C.sub.1-6-alkyl,
C.sub.3-8-cycloalkyl-C.sub.1-6-alkoxy, C.sub.3-8-cycloalkoxy,
C.sub.3-8-cycloalkoxy-C.sub.1-6-alkyl, C.sub.1-6-alkylamino,
C.sub.1-6-alkylcarbonylamino, C.sub.3-8-cycloalkylcarbonylamino,
C.sub.1-6-alkyltetrazolyl,
C.sub.1-6-alkyltetrazolyl-C.sub.1-6-alkyl or
heterocycloalkyl-C.sub.1-6-alkoxy; R.sup.4 and R.sup.5 are
independently selected from H, halogen, hydroxy, cyano,
C.sub.1-6-alkyl, C.sub.1-6-alkoxy,
C.sub.1-6-alkoxy-C.sub.1-6-alkyl, halo-C.sub.1-6-alkoxy,
halo-C.sub.1-6-alkyl, hydroxy-C.sub.1-6-alkyl,
C.sub.3-8-cycloalkyl, C.sub.3-8-cycloalkyl-C.sub.1-6-alkyl,
C.sub.3-8-cycloalkyl-C.sub.1-6-alkoxy, C.sub.3-8-cycloalkoxy,
C.sub.3-8-cycloalkoxy-C.sub.1-6-alkyl,
C.sub.1-6-alkylcarbonylamino, C.sub.3-8-cycloalkylcarbonylamino,
C.sub.1-6-alkyltetrazolyl,
C.sub.1-6-alkyltetrazolyl-C.sub.1-6-alkyl or
heterocycloalkyl-C.sub.1-6-alkoxy; R.sup.6 is aminosulfonyl;
R.sup.7 and R.sup.8 are independently selected from H, halogen,
hydroxy, cyano, C.sub.1-6-alkyl, C.sub.1-6-alkoxy,
C.sub.1-6-alkoxy-C.sub.1-6-alkyl, halo-C.sub.1-6-alkoxy,
halo-C.sub.1-6-alkyl, hydroxy-C.sub.1-6-alkyl,
C.sub.3-8-cycloalkyl, C.sub.3-8-cycloalkyl-C.sub.1-6-alkyl,
C.sub.3-8-cycloalkyl-C.sub.1-6-alkoxy, C.sub.3-8-cycloalkoxy and
C.sub.3-8-cycloalkoxy-C.sub.1-6-alkyl; m, n, p and q are
independently selected from 1 or 2; and pharmaceutically acceptable
salts.
2. A compound according to claim 1, wherein ##STR00069## wherein
R.sup.1 is substituted phenyl, substituted phenyl-C.sub.1-6-alkyl,
substituted phenoxy-C.sub.1-6-alkyl, substituted
phenyl-C.sub.2-6-alkenyl, substituted phenyl-C.sub.2-6-alkynyl,
substituted pyridinyl, substituted pyridinyl-C.sub.1-6-alkyl,
substituted pyridinyl-C.sub.2-6-alkenyl, substituted
pyridinyl-C.sub.2-6-alkynyl, substituted thiophenyl, substituted
thiophenyl-C.sub.1-6-alkyl, substituted
thiophenyl-C.sub.2-6-alkenyl or substituted
thiophenyl-C.sub.2-6-alkynyl, wherein substituted phenyl,
substituted phenyl-C.sub.1-6-alkyl, substituted
phenoxy-C.sub.1-6-alkyl, substituted phenyl-C.sub.2-6-alkenyl,
substituted phenyl-C.sub.2-6-alkynyl, substituted pyridinyl,
substituted pyridinyl-C.sub.1-6-alkyl, substituted
pyridinyl-C.sub.2-6-alkenyl, substituted
pyridinyl-C.sub.2-6-alkynyl, substituted thiophenyl, substituted
thiophenyl-C.sub.1-6-alkyl, substituted
thiophenyl-C.sub.2-6-alkenyl and substituted
thiophenyl-C.sub.2-6-alkynyl are substituted by R.sup.3, R.sup.4
and R.sup.5; Y is a --OC(O)-- or --C(O)--; W is --C(O)--,
--S(O).sub.2-- or --CR.sup.6R.sup.7--; R.sup.2 is substituted
phenyl, substituted pyridinyl or substituted thiophenyl, wherein
substituted phenyl, substituted pyridinyl and substituted
thiophenyl are substituted by R.sup.6, R.sup.7 and R.sup.8; R.sup.3
is halogen, hydroxy, cyano, C.sub.1-6-alkyl, C.sub.1-6-alkoxy,
C.sub.1-6-alkoxy-C.sub.1-6-alkyl, halo-C.sub.1-6-alkoxy,
halo-C.sub.1-6-alkyl, hydroxy-C.sub.1-6-alkyl,
C.sub.3-8-cycloalkyl, C.sub.3-8-cycloalkyl-C.sub.1-6-alkyl,
C.sub.3-8-cycloalkyl-C.sub.1-6-alkoxy, C.sub.3-8-cycloalkoxy,
C.sub.3-8-cycloalkoxy-C.sub.1-6-alkyl, C.sub.1-6-alkylamino,
C.sub.1-6-alkylcarbonylamino, C.sub.3-8-cycloalkylcarbonylamino,
C.sub.1-6-alkyltetrazolyl,
C.sub.1-6-alkyltetrazolyl-C.sub.1-6-alkyl or
heterocycloalkyl-C.sub.1-6-alkoxy; R.sup.4 and R.sup.5 are
independently selected from H, halogen, hydroxy, cyano,
C.sub.1-6-alkyl, C.sub.1-6-alkoxy,
C.sub.1-6-alkoxy-C.sub.1-6-alkyl, halo-C.sub.1-6-alkoxy,
halo-C.sub.1-6-alkyl, hydroxy-C.sub.1-6-alkyl,
C.sub.3-8-cycloalkyl, C.sub.3-8-cycloalkyl-C.sub.1-6-alkyl,
C.sub.3-8-cycloalkyl-C.sub.1-6-alkoxy, C.sub.3-8-cycloalkoxy,
C.sub.3-8-cycloalkoxy-C.sub.1-6-alkyl,
C.sub.1-6-alkylcarbonylamino, C.sub.3-8-cycloalkylcarbonylamino,
C.sub.1-6-alkyltetrazolyl,
C.sub.1-6-alkyltetrazolyl-C.sub.1-6-alkyl or
heterocycloalkyl-C.sub.1-6-alkoxy; R.sup.6 is aminosulfonyl;
R.sup.7 and R.sup.8 are independently selected from H, halogen,
hydroxy, cyano, C.sub.1-6-alkyl, C.sub.1-6-alkoxy,
C.sub.1-6-alkoxy-C.sub.1-6-alkyl, halo-C.sub.1-6-alkoxy,
halo-C.sub.1-6-alkyl, hydroxy-C.sub.1-6-alkyl,
C.sub.3-8-cycloalkyl, C.sub.3-8-cycloalkyl-C.sub.1-6-alkyl,
C.sub.3-8-cycloalkyl-C.sub.1-6-alkoxy, C.sub.3-8-cycloalkoxy and
C.sub.3-8-cycloalkoxy-C.sub.1-6-alkyl; m, n, p and q are
independently selected from 1 or 2; and pharmaceutically acceptable
salts.
3. A compound according to claim 1, wherein R.sup.1 is substituted
phenyl-C.sub.1-6-alkyl, substituted phenoxy-C.sub.1-6-alkyl,
substituted phenyl-C.sub.2-6-alkenyl, substituted
quinolinyl-C.sub.1-6-alkyl, substituted pyridinyl or substituted
pyridinyl-C.sub.1-6-alkyl, wherein substituted
phenyl-C.sub.1-6-alkyl, substituted phenoxy-C.sub.1-6-alkyl,
substituted phenyl-C.sub.2-6-alkenyl, substituted
quinolinyl-C.sub.1-6-alkyl, substituted pyridinyl and substituted
pyridinyl-C.sub.1-6-alkyl are substituted by R.sup.3, R.sup.4 and
R.sup.5; Y is a --OC(O)-- or --C(O)--; W is --C(O)--; R.sup.2 is
substituted phenyl or substituted pyridinyl, wherein substituted
phenyl and substituted pyridinyl are substituted by R.sup.6,
R.sup.7 and R.sup.8; R.sup.3 is halo-C.sub.1-6-alkoxy,
C.sub.1-6-alkylcarbonylamino,
C.sub.1-6-alkyltetrazolyl-C.sub.1-6-alkyl,
C.sub.1-6-alkylpiperidinyl-C.sub.1-6-alkoxy or
tetrahydropyranyl-C.sub.1-6-alkoxy; R.sup.4 is H, cyano, halogen,
C.sub.1-6-alkyl, halo-C.sub.1-6-alkyl or C.sub.3-8-cycloalkyl;
R.sup.5 is H; R.sup.6 is aminosulfonyl; R.sup.7 and R.sup.8 are
independently selected from H or halogen; m and q are 1; n and p
are independently selected from 1 or 2; and pharmaceutically
acceptable salts.
4. A compound according to anyone of claims 1 to 3, wherein R.sup.1
is substituted phenyl-C.sub.1-6-alkyl, substituted
phenoxy-C.sub.1-6-alkyl, substituted phenyl-C.sub.2-6-alkenyl,
substituted pyridinyl or substituted pyridinyl-C.sub.1-6-alkyl,
wherein substituted phenyl-C.sub.1-6-alkyl, substituted
phenoxy-C.sub.1-6-alkyl, substituted phenyl-C.sub.2-6-alkenyl,
substituted pyridinyl and substituted pyridinyl-C.sub.1-6-alkyl are
substituted by R.sup.3, R.sup.4 and R.sup.5; Y is a --OC(O)-- or
--C(O)--; W is --C(O)--; R.sup.2 is substituted phenyl or
substituted pyridinyl, wherein substituted phenyl and substituted
pyridinyl are substituted by R.sup.6, R and R.sup.8; R.sup.3 is
halo-C.sub.1-6-alkoxy, C.sub.1-6-alkylcarbonylamino,
C.sub.1-6-alkyltetrazolyl-C.sub.1-6-alkyl or
tetrahydropyranyl-C.sub.1-6-alkoxy; R.sup.4 is H, cyano, halogen,
C.sub.1-6-alkyl, halo-C.sub.1-6-alkyl or C.sub.3-8-cycloalkyl;
R.sup.5 is H; R.sup.6 is aminosulfonyl; R.sup.7 and R.sup.8 are
independently selected from H or halogen; m and q are 1; n and p
are independently selected from 1 or 2; and pharmaceutically
acceptable salts.
5. A compound according to anyone of claim 1 to 4, wherein R.sup.1
is substituted phenyl-C.sub.1-6-alkyl, substituted
phenoxy-C.sub.1-6-alkyl, substituted phenyl-C.sub.2-6-alkenyl,
substituted quinolinyl-C.sub.1-6-alkyl, substituted pyridinyl or
substituted pyridinyl-C.sub.1-6-alkyl, wherein substituted
phenyl-C.sub.1-6-alkyl, substituted phenoxy-C.sub.1-6-alkyl,
substituted phenyl-C.sub.2-6-alkenyl, substituted
quinolinyl-C.sub.1-6-alkyl, substituted pyridinyl and substituted
pyridinyl-C.sub.1-6-alkyl are substituted by R.sup.3, R.sup.4 and
R.sup.5.
6. A compound according to anyone of claim 1 to 5, wherein R.sup.1
is substituted phenyl-C.sub.1-6-alkyl, substituted
phenoxy-C.sub.1-6-alkyl, substituted phenyl-C.sub.2-6-alkenyl,
substituted pyridinyl or substituted pyridinyl-C.sub.1-6-alkyl,
wherein substituted phenyl-C.sub.1-6-alkyl, substituted
phenoxy-C.sub.1-6-alkyl, substituted phenyl-C.sub.2-6-alkenyl,
substituted pyridinyl and substituted pyridinyl-C.sub.1-6-alkyl are
substituted by R.sup.3, R.sup.4 and R.sup.5.
7. A compound according to any one of claims 1 to 6, wherein
R.sup.1 is pyridinyl-C.sub.1-6-alkyl substituted by R.sup.3,
R.sup.4 and R.sup.5.
8. A compound according to any one of claims 1 to 7, wherein Y is
--OC(O)--.
9. A compound according to any one of claims 1 to 8, wherein
R.sup.2 is substituted phenyl or substituted pyridinyl, wherein
substituted phenyl and substituted pyridinyl are substituted by
R.sup.6, R.sup.7 and R.sup.8.
10. A compound according to any one of claims 1 to 9, wherein
R.sup.2 is phenyl substituted by R.sup.6, R.sup.7 and R.sup.8.
11. A compound according to any one of claims 1 to 10, wherein
R.sup.3 is halo-C.sub.1-6-alkoxy, C.sub.1-6-alkylcarbonylamino,
C.sub.1-6-alkyltetrazolyl-C.sub.1-6-alkyl,
C.sub.1-6-alkylpiperidinyl-C.sub.1-6-alkoxy or
tetrahydropyranyl-C.sub.1-6-alkoxy.
12. A compound according to any one of claims 1 to 11, wherein
R.sup.3 is halo-C.sub.16-alkoxy, C.sub.1-6-alkylcarbonylamino,
C.sub.1-6-alkyltetrazolyl-C.sub.1-6-alkyl or
tetrahydropyranyl-C.sub.1-6-alkoxy.
13. A compound according to any one of claims 1 to 12, wherein
R.sup.3 is C.sub.1-6-alkylcarbonylamino.
14. A compound according to any one of claims 1 to 13, wherein
R.sup.4 is H, cyano, halogen, C.sub.1-6-alkyl, halo-C.sub.1-6-alkyl
or C.sub.3-8-cycloalkyl.
15. A compound according to any one of claims 1 to 14, wherein
R.sup.4 is halo-C.sub.16-alkyl.
16. A compound according to any one of claims 1 to 15, wherein
R.sup.5 is H.
17. A compound according to any one of claims 1 to 16, wherein
R.sup.7 and R.sup.8 are independently selected from H or
halogen.
18. A compound according to any one of claims 1 to 17, wherein
R.sup.7 is halogen.
19. A compound according to any one of claims 1 to 18, wherein
R.sup.8 is H.
20. A compound according to any one of claims 1 to 19, wherein m
and q are 1 and n and p are independently selected from 1 or 2.
21. A compound according to any one of claims 1 to 20, wherein m,
n, p and q are 1.
22. A compound according to any one of claims 1 to 21, wherein
R.sup.1 is pyridinyl-C.sub.1-6-alkyl substituted by R.sup.3,
R.sup.4 and R.sup.5; Y is --OC(O)--; W is --C(O)--; R.sup.2 is
phenyl substituted by R.sup.6, R.sup.7 and R.sup.8; R.sup.3 is
C.sub.1-6-alkylcarbonylamino; R.sup.4 is halo-C.sub.1-6-alkyl;
R.sup.5 is H; R.sup.7 is halogen; R.sup.8 is H; m, n, p and q are 1
and pharmaceutically acceptable salts.
23. A compound according to claim 1 and of formula I(a),
##STR00070## wherein R.sup.1 is substituted phenyl-C.sub.1-6-alkyl,
substituted phenoxy-C.sub.1-6-alkyl, substituted
phenyl-C.sub.2-6-alkenyl, substituted pyridinyl or substituted
pyridinyl-C.sub.1-6-alkyl, wherein substituted
phenyl-C.sub.1-6-alkyl, substituted phenoxy-C.sub.1-6-alkyl,
substituted phenyl-C.sub.2-6-alkenyl, substituted pyridinyl and
substituted pyridinyl-C.sub.1-6-alkyl are substituted by R.sup.3,
R.sup.4 and R.sup.5; Y is a --OC(O)-- or --C(O)--; W is --C(O)--;
R.sup.3 is halo-C.sub.1-6-alkoxy, C.sub.1-6-alkylcarbonylamino,
C.sub.1-6-alkyltetrazolyl-C.sub.1-6-alkyl or
tetrahydropyranyl-C.sub.1-6-alkoxy; R.sup.4 is H, cyano, halogen,
C.sub.1-6-alkyl, halo-C.sub.1-6-alkyl or C.sub.3-8-cycloalkyl;
R.sup.5 is H; R.sup.7 and R.sup.8 are independently selected from H
or halogen; m and q are 1; n and p are independently selected from
1 or 2; and pharmaceutically acceptable salts.
24. A compound according to claim 1 and of formula I(b),
##STR00071## wherein R.sup.1 is pyridinyl-C.sub.1-6-alkyl
substituted by R.sup.3, R.sup.4 and R.sup.5; Y is --OC(O)--; W is
--C(O)--; R.sup.3 is C.sub.1-6-alkylcarbonylamino; R.sup.4 is
halo-C.sub.1-6-alkyl; R.sup.5 is H; R.sup.7 is halogen; R.sup.8 is
H; m, n, p and q are 1 and pharmaceutically acceptable salts.
25. A compound according to any one of claims 1 to 24, selected
from
[3-(2,2-dimethylpropanoylamino)-5-(trifluoromethyl)pyridin-2-yl]methyl
2-(4-sulfamoylbenzoyl)-1,3,4,6-tetrahydropyrrolo[3,4-c]pyrrole-5-carboxyl-
ate;
[3-(2,2-dimethylpropanoylamino)-5-(trifluoromethyl)pyridin-2-yl]methy-
l
2-(2,5-difluoro-4-sulfamoylbenzoyl)-1,3,4,6-tetrahydropyrrolo[3,4-c]pyrr-
ole-5-carboxylate;
[3-(2,2-dimethylpropanoylamino)-5-(trifluoromethyl)pyridin-2-yl]methyl
2-(3-chloro-4-sulfamoylbenzoyl)-1,3,4,6-tetrahydropyrrolo[3,4-c]pyrrole-5-
-carboxylate;
[3-(2,2-dimethylpropanoylamino)-5-(trifluoromethyl)pyridin-2-yl]methyl
2-(3-fluoro-4-sulfamoylbenzoyl)-1,3,4,6-tetrahydropyrrolo[3,4-c]pyrrole-5-
-carboxylate;
[3-(2,2-dimethylpropanoylamino)-5-(trifluoromethyl)pyridin-2-yl]methyl
2-(2-fluoro-4-sulfamoylbenzoyl)-1,3,4,6-tetrahydropyrrolo[3,4-c]pyrrole-5-
-carboxylate;
[3-(2,2-dimethylpropanoylamino)-5-(trifluoromethyl)pyridin-2-yl]methyl
2-(5-sulfamoylpyridine-2-carbonyl)-1,3,4,6-tetrahydropyrrolo[3,4-c]pyrrol-
e-5-carboxylate; 4-(trifluoromethoxy)benzyl
5-(4-sulfamoylbenzoyl)-3,4,5,6-tetrahydropyrrolo[3,4-c]pyrrole-2(1H)-carb-
oxylate;
6-[5-[2-cyclopropyl-6-(oxan-4-ylmethoxy)pyridine-4-carbonyl]-1,3,-
4,6-tetrahydropyrrolo[3,4-c]pyrrole-2-carbonyl]pyridine-3-sulfonamide;
4-[5-[2-cyclopropyl-6-(oxan-4-ylmethoxy)pyridine-4-carbonyl]-1,3,4,6-tetr-
ahydropyrrolo[3,4-c]pyrrole-2-carbonyl]-3-fluorobenzenesulfonamide;
[3-(2,2-dimethylpropanoylamino)-5-(trifluoromethyl)pyridin-2-yl]methyl
2-(2,3-difluoro-4-sulfamoylbenzoyl)-1,3,4,6-tetrahydropyrrolo[3,4-c]pyrro-
le-5-carboxylate;
3-fluoro-4-(5-(3-(2-((5-methyl-2H-tetrazol-2-yl)methyl)-4-(trifluoromethy-
l)phenyl)propanoyl)-1,2,3,4,5,6-hexahydropyrrolo[3,4-c]pyrrole-2-carbonyl)-
benzenesulfonamide;
[3-(2,2-dimethylpropanoylamino)-5-(trifluoromethyl)pyridin-2-yl]methyl
2-(2,6-difluoro-4-sulfamoylbenzoyl)-1,3,4,6-tetrahydropyrrolo[3,4-c]pyrro-
le-5-carboxylate;
[5-chloro-3-(2,2-dimethylpropanoylamino)pyridin-2-yl]methyl
2-(2-fluoro-4-sulfamoylbenzoyl)-1,3,4,6-tetrahydropyrrolo[3,4-c]pyrrole-5-
-carboxylate;
[5-chloro-3-(2,2-dimethylpropanoylamino)pyridin-2-yl]methyl
2-(3-fluoro-4-sulfamoylbenzoyl)-1,3,4,6-tetrahydropyrrolo[3,4-c]pyrrole-5-
-carboxylate;
[5-chloro-3-(2,2-dimethylpropanoylamino)pyridin-2-yl]methyl
2-(2,3-difluoro-4-sulfamoylbenzoyl)-1,3,4,6-tetrahydropyrrolo[3,4-c]pyrro-
le-5-carboxylate;
[5-chloro-3-(2,2-dimethylpropanoylamino)pyridin-2-yl]methyl
2-(2,6-difluoro-4-sulfamoylbenzoyl)-1,3,4,6-tetrahydropyrrolo[3,4-c]pyrro-
le-5-carboxylate;
[5-chloro-3-(2,2-dimethylpropanoylamino)pyridin-2-yl]methyl
2-(2,5-difluoro-4-sulfamoylbenzoyl)-1,3,4,6-tetrahydropyrrolo[3,4-c]pyrro-
le-5-carboxylate;
[3-(2,2-dimethylpropanoylamino)-6-methylpyridin-2-yl]methyl
2-(2-fluoro-4-sulfamoylbenzoyl)-1,3,4,6-tetrahydropyrrolo[3,4-c]pyrrole-5-
-carboxylate;
[6-chloro-3-(2,2-dimethylpropanoylamino)pyridin-2-yl]methyl
2-(2-fluoro-4-sulfamoylbenzoyl)-1,3,4,6-tetrahydropyrrolo[3,4-c]pyrrole-5-
-carboxylate; [3-(2,2-dimethylpropanoylamino)pyridin-2-yl]methyl
2-(2-fluoro-4-sulfamoylbenzoyl)-1,3,4,6-tetrahydropyrrolo[3,4-c]pyrrole-5-
-carboxylate;
[6-chloro-3-(2,2-dimethylpropanoylamino)pyridin-2-yl]methyl
2-(2,5-difluoro-4-sulfamoylbenzoyl)-1,3,4,6-tetrahydropyrrolo[3,4-c]pyrro-
le-5-carboxylate;
[6-chloro-3-(2,2-dimethylpropanoylamino)pyridin-2-yl]methyl
2-(3-fluoro-4-sulfamoylbenzoyl)-1,3,4,6-tetrahydropyrrolo[3,4-c]pyrrole-5-
-carboxylate;
[6-chloro-3-(2,2-dimethylpropanoylamino)pyridin-2-yl]methyl
2-(2,3-difluoro-4-sulfamoylbenzoyl)-1,3,4,6-tetrahydropyrrolo[3,4-c]pyrro-
le-5-carboxylate;
[6-chloro-3-(2,2-dimethylpropanoylamino)pyridin-2-yl]methyl
2-(2,6-difluoro-4-sulfamoylbenzoyl)-1,3,4,6-tetrahydropyrrolo[3,4-c]pyrro-
le-5-carboxylate;
[5-cyano-3-(2,2-dimethylpropanoylamino)pyridin-2-yl]methyl
2-(2-fluoro-4-sulfamoylbenzoyl)-1,3,4,6-tetrahydropyrrolo[3,4-c]pyrrole-5-
-carboxylate;
[5-cyano-3-(2,2-dimethylpropanoylamino)pyridin-2-yl]methyl
2-(2,6-difluoro-4-sulfamoylbenzoyl)-1,3,4,6-tetrahydropyrrolo[3,4-c]pyrro-
le-5-carboxylate;
[5-cyano-3-(2,2-dimethylpropanoylamino)pyridin-2-yl]methyl
2-(2,3-difluoro-4-sulfamoylbenzoyl)-1,3,4,6-tetrahydropyrrolo[3,4-c]pyrro-
le-5-carboxylate;
[5-cyano-3-(2,2-dimethylpropanoylamino)pyridin-2-yl]methyl
2-(2,5-difluoro-4-sulfamoylbenzoyl)-1,3,4,6-tetrahydropyrrolo[3,4-c]pyrro-
le-5-carboxylate;
[3-(2,2-dimethylpropanoylamino)-5-(trifluoromethyl)pyridin-2-yl]methyl
6-(2-fluoro-4-sulfamoylbenzoyl)-1,3,4,5,7,8-hexahydro-2,6-naphthyridine-2-
-carboxylate;
[5-chloro-4-cyano-2-(2,2-dimethylpropanoylamino)phenyl]methyl
2-(5-sulfamoylpyridine-2-carbonyl)-1,3,4,6-tetrahydropyrrolo[3,4-c]pyrrol-
e-5-carboxylate; [4-(trifluoromethoxy)phenyl]methyl
6-(2-fluoro-4-sulfamoylbenzoyl)-1,3,4,5,7,8-hexahydro-2,6-naphthyridine-2-
-carboxylate; [4-(trifluoromethoxy)phenyl]methyl
2-(5-sulfamoylpyridine-2-carbonyl)-1,3,4,6-tetrahydropyrrolo[3,4-c]pyrrol-
e-5-carboxylate; [4-(trifluoromethoxy)phenyl]methyl
2-(2-fluoro-4-sulfamoylbenzoyl)-1,3,4,6-tetrahydropyrrolo[3,4-c]pyrrole-5-
-carboxylate;
3-fluoro-4-[2-[(E)-3-[4-(trifluoromethoxy)phenyl]prop-2-enoyl]-1,3,4,6-te-
trahydropyrrolo[3,4-c]pyrrole-5-carbonyl]benzenesulfonamide;
6-[2-[3-[4-(trifluoromethoxy)phenyl]propanoyl]-1,3,4,6-tetrahydropyrrolo[-
3,4-c]pyrrole-5-carbonyl]pyridine-3-sulfonamide;
3-fluoro-4-[2-[3-[4-(trifluoromethoxy)phenyl]propanoyl]-1,3,4,6-tetrahydr-
opyrrolo[3,4-c]pyrrole-5-carbonyl]benzenesulfonamide;
6-[2-[(E)-3-[4-(trifluoromethoxy)phenyl]prop-2-enoyl]-1,3,4,6-tetrahydrop-
yrrolo[3,4-c]pyrrole-5-carbonyl]pyridine-3-sulfonamide;
6-[2-[2-[4-(trifluoromethoxy)phenoxy]acetyl]-1,3,4,6-tetrahydropyrrolo[3,-
4-c]pyrrole-5-carbonyl]pyridine-3-sulfonamide;
3-fluoro-4-[2-[2-[4-(trifluoromethoxy)phenoxy]acetyl]-1,3,4,6-tetrahydrop-
yrrolo[3,4-c]pyrrole-5-carbonyl]benzenesulfonamide;
4-[2-[3-[4-cyano-2-[(5-methyltetrazol-2-yl)methyl]phenyl]propanoyl]-1,3,4-
,6-tetrahydropyrrolo[3,4-c]pyrrole-5-carbonyl]-3-fluorobenzenesulfonamide;
4-[2-[3-[4-chloro-2-[(5-methyltetrazol-2-yl)methyl]phenyl]propanoyl]-1,3,-
4,6-tetrahydropyrrolo[3,4-c]pyrrole-5-carbonyl]-3-fluorobenzenesulfonamide-
;
3-fluoro-4-[2-[3-[2-[(4-methyltriazol-2-yl)methyl]-4-(trifluoromethyl)ph-
enyl]propanoyl]-1,3,4,6-tetrahydropyrrolo[3,4-c]pyrrole-5-carbonyl]benzene-
sulfonamide;
3-fluoro-4-[2-[3-[2-[(4-methyltriazol-1-yl)methyl]-4-(trifluoromethyl)phe-
nyl]propanoyl]-1,3,4,6-tetrahydropyrrolo[3,4-c]pyrrole-5-carbonyl]benzenes-
ulfonamide; and pharmaceutically acceptable salts thereof.
26. A compound according to any one of claims 1 to 25, selected
from
[5,6-dichloro-3-(2,2-dimethylpropanoylamino)pyridin-2-yl]methyl
2-(2-fluoro-4-sulfamoylbenzoyl)-1,3,4,6-tetrahydropyrrolo[3,4-c]pyrrole-5-
-carboxylate;
[5,6-dichloro-3-(2,2-dimethylpropanoylamino)pyridin-2-yl]methyl
2-(2,3-difluoro-4-sulfamoylbenzoyl)-1,3,4,6-tetrahydropyrrolo[3,4-c]pyrro-
le-5-carboxylate;
[5,6-dichloro-3-(2,2-dimethylpropanoylamino)pyridin-2-yl]methyl
2-(2,6-difluoro-4-sulfamoylbenzoyl)-1,3,4,6-tetrahydropyrrolo[3,4-c]pyrro-
le-5-carboxylate;
[3-(2,2-dimethylpropanoylamino)-5-(trifluoromethyl)pyridin-2-yl]methyl
2-(3-fluoro-5-sulfamoylpyridine-2-carbonyl)-1,3,4,6-tetrahydropyrrolo[3,4-
-c]pyrrole-5-carboxylate;
4-[5-[2-cyclopropyl-6-(oxan-4-ylmethoxy)pyridine-4-carbonyl]-1,3,4,6-tetr-
ahydropyrrolo[3,4-c]pyrrole-2-carbonyl]-2,3-difluorobenzenesulfonamide;
4-[5-[2-cyclopropyl-6-[(1-methylpiperidin-4-yl)methoxy]pyridine-4-carbony-
l]-1,3,4,6-tetrahydropyrrolo[3,4-c]pyrrole-2-carbonyl]-2,3-difluorobenzene-
sulfonamide;
[5-chloro-3-[(5-methyltetrazol-2-yl)methyl]pyridin-2-yl]methyl
2-(2-fluoro-4-sulfamoylbenzoyl)-1,3,4,6-tetrahydropyrrolo[3,4-c]pyrrole-5-
-carboxylate;
3-fluoro-4-[2-[3-[3-[(5-methyltetrazol-2-yl)methyl]-5-(trifluoromethyl)py-
ridin-2-yl]propanoyl]-1,3,4,6-tetrahydropyrrolo[3,4-c]pyrrole-5-carbonyl]b-
enzenesulfonamide;
5-fluoro-6-[2-[3-[2-[(5-methyltetrazol-2-yl)methyl]-4-(trifluoromethyl)ph-
enyl]propanoyl]-1,3,4,6-tetrahydropyrrolo[3,4-c]pyrrole-5-carbonyl]pyridin-
e-3-sulfonamide;
[3-(2,2-dimethylpropanoylamino)quinolin-2-yl]methyl
2-(2-fluoro-4-sulfamoylbenzoyl)-1,3,4,6-tetrahydropyrrolo[3,4-c]pyrrole-5-
-carboxylate;
[3-(2,2-dimethylpropanoylamino)-5-(trifluoromethyl)pyridin-2-yl]methyl
5-(2-fluoro-4-sulfamoylphenyl)sulfonyl-1,3,4,6-tetrahydropyrrolo[3,4-c]py-
rrole-2-carboxylate; and pharmaceutically acceptable salts
thereof.
27. A compound according to any one of claims 1 to 26, selected
from
[3-(2,2-dimethylpropanoylamino)-5-(trifluoromethyl)pyridin-2-yl]methyl
2-(3-chloro-4-sulfamoylbenzoyl)-1,3,4,6-tetrahydropyrrolo[3,4-c]pyrrole-5-
-carboxylate;
[3-(2,2-dimethylpropanoylamino)-5-(trifluoromethyl)pyridin-2-yl]methyl
2-(3-fluoro-4-sulfamoylbenzoyl)-1,3,4,6-tetrahydropyrrolo[3,4-c]pyrrole-5-
-carboxylate;
[3-(2,2-dimethylpropanoylamino)-5-(trifluoromethyl)pyridin-2-yl]methyl
2-(2-fluoro-4-sulfamoylbenzoyl)-1,3,4,6-tetrahydropyrrolo[3,4-c]pyrrole-5-
-carboxylate;
[5-chloro-3-(2,2-dimethylpropanoylamino)pyridin-2-yl]methyl
2-(2,3-difluoro-4-sulfamoylbenzoyl)-1,3,4,6-tetrahydropyrrolo[3,4-c]pyrro-
le-5-carboxylate; and pharmaceutically acceptable salts
thereof.
28. A process to prepare a compound according to any one of claims
1 to 27 comprising the reaction of a compound of formula (II) in
the presence of a compound of formula (III), wherein R.sup.1,
R.sup.2, m, n, p and q are as defined in any one of claim 1 to 24
and W is --C(O)--. ##STR00072##
29. A compound according to any one of claims 1 to 27 for use as
therapeutically active substance.
30. A pharmaceutical composition comprising a compound according to
any one of claims 1 to 27 and a therapeutically inert carrier.
31. The use of a compound according to any one of claims 1 to 27
for the treatment or prophylaxis of ocular conditions.
32. A compound according to any one of claims 1 to 27 for the
treatment or prophylaxis of ocular conditions.
33. The use of a compound according to any one of claims 1 to 27
for the preparation of a medicament for the treatment or
prophylaxis of ocular conditions.
34. A method for the treatment or prophylaxis ocular conditions,
which method comprises administering an effective amount of a
compound according to any one of claims 1 to 27.
35. A compound according to any one of claims 1 to 27, when
manufactured according to a process of claim 28.
36. The invention as hereinbefore described.
Description
CROSS-REFERENCE TO RELATED APPLICATIONS
[0001] This application is a continuation of U.S. application Ser.
No. 15/933,701, filed Mar. 23, 2018, which is a continuation of
International Application No. PCT/EP2016/072347, filed Sep. 21,
2016, which claims priority to EP Application No. 15186633.2, filed
Sep. 24, 2015, the disclosure of each of which is incorporated
herein by reference in its entirety.
[0002] The present invention relates to organic compounds useful
for therapy or prophylaxis in a mammal, and in particular to dual
autotaxin (ATX)/carbonic anhydrase inhibitors which are inhibitors
of lysophosphatidic acid (LPA) production and thus modulators of
LPA levels and associated signaling, for the treatment or
prophylaxis of inflammatory conditions, conditions of the nervous
system, vascular and cardiovascular conditions, cancer, and ocular
conditions.
[0003] The present invention provides novel compounds of formula
(I)
##STR00002## [0004] wherein [0005] R.sup.1 is substituted phenyl,
substituted phenyl-C.sub.1-6-alkyl, substituted
phenoxy-C.sub.1-6-alkyl, substituted phenyl-C.sub.2-6-alkenyl,
substituted phenyl-C.sub.2-6-alkynyl, substituted quinolinyl,
substituted quinolinyl-C.sub.1-6-alkyl, substituted
quinolinyl-C.sub.1-6-lalkenyl, substituted
quinolinyl-C.sub.1-6-alkynyl, substituted pyridinyl, substituted
pyridinyl-C.sub.1-6-alkyl, substituted pyridinyl-C.sub.2-6-alkenyl,
substituted pyridinyl-C.sub.2-6-alkynyl, substituted thiophenyl,
substituted thiophenyl-C.sub.1-6-alkyl, substituted
thiophenyl-C.sub.2-6-alkenyl or substituted
thiophenyl-C.sub.2-6-alkynyl, wherein substituted phenyl,
substituted phenyl-C.sub.1-6-alkyl, substituted
phenoxy-C.sub.1-6-alkyl, substituted phenyl-C.sub.2-6-alkenyl,
substituted phenyl-C.sub.2-6-alkynyl, substituted quinolinyl,
substituted quinolinyl-C.sub.1-6-alkyl, substituted
quinolinyl-C.sub.1-6-lalkenyl, substituted
quinolinyl-C.sub.1-6-alkynyl, substituted pyridinyl, substituted
pyridinyl-C.sub.1-6-alkyl, substituted pyridinyl-C.sub.2-6-alkenyl,
substituted pyridinyl-C.sub.2-6-alkynyl, substituted thiophenyl,
substituted thiophenyl-C.sub.1-6-alkyl, substituted
thiophenyl-C.sub.2-6-alkenyl and substituted
thiophenyl-C.sub.2-6-alkynyl are substituted by R.sup.3, R.sup.4
and R.sup.5; [0006] Y is a --OC(O)-- or --C(O)--; [0007] W is
--C(O)--, --S(O).sub.2-- or --CR.sup.6R.sup.7--; [0008] R.sup.2 is
substituted phenyl, substituted pyridinyl or substituted
thiophenyl, wherein substituted phenyl, substituted pyridinyl and
substituted thiophenyl are substituted by R.sup.6, R.sup.7 and
R.sup.8; [0009] R.sup.3 is halogen, hydroxy, cyano,
C.sub.1-6-alkyl, C.sub.1-6-alkoxy,
C.sub.1-6-alkoxy-C.sub.1-6-alkyl, halo-C.sub.1-6-alkoxy,
halo-C.sub.1-6-alkyl, hydroxy-C.sub.1-6-alkyl,
C.sub.3-8-cycloalkyl, C.sub.3-8-cycloalkyl-C.sub.1-6-alkyl,
C.sub.3-8-cycloalkyl-C.sub.1-6-alkoxy, C.sub.3-8-cycloalkoxy,
C.sub.3-8-cycloalkoxy-C.sub.1-6-alkyl, C.sub.1-6-alkylamino,
C.sub.1-6-alkylcarbonylamino, C.sub.3-8-cycloalkylcarbonylamino,
C.sub.1-6-alkyltetrazolyl,
C.sub.1-6-alkyltetrazolyl-C.sub.1-6-alkyl or
heterocycloalkyl-C.sub.1-6-alkoxy; [0010] R.sup.4 and R.sup.5 are
independently selected from H, halogen, hydroxy, cyano,
C.sub.1-6-alkyl, C.sub.1-6-alkoxy,
C.sub.1-6-alkoxy-C.sub.1-6-alkyl, halo-C.sub.1-6-alkoxy,
halo-C.sub.1-6-alkyl, hydroxy-C.sub.1-6-alkyl,
C.sub.3-8-cycloalkyl, C.sub.3-8-cycloalkyl-C.sub.1-6-alkyl,
C.sub.3-8-cycloalkyl-C.sub.1-6-alkoxy, C.sub.3-8-cycloalkoxy,
C.sub.3-8-cycloalkoxy-C.sub.1-6-alkyl,
C.sub.1-6-alkylcarbonylamino, C.sub.3-8-cycloalkylcarbonylamino,
C.sub.1-6-alkyltetrazolyl,
C.sub.1-6-alkyltetrazolyl-C.sub.1-6-alkyl or
heterocycloalkyl-C.sub.1-6-alkoxy; [0011] R.sup.6 is aminosulfonyl;
[0012] R.sup.7 and R.sup.8 are independently selected from H,
halogen, hydroxy, cyano, C.sub.1-6-alkyl, C.sub.1-6-alkoxy,
C.sub.1-6-alkoxy-C.sub.1-6-alkyl, halo-C.sub.1-6-alkoxy,
halo-C.sub.1-6-alkyl, hydroxy-C.sub.1-6-alkyl,
C.sub.3-8-cycloalkyl, C.sub.3-8-cycloalkyl-C.sub.1-6-alkyl,
C.sub.3-8-cycloalkyl-C.sub.1-6-alkoxy, C.sub.3-8-cycloalkoxy and
C.sub.3-8-cycloalkoxy-C.sub.1-6-alkyl; [0013] m, n, p and q are
independently selected from 1 or 2; [0014] and pharmaceutically
acceptable salts.
[0015] Autotaxin (ATX) is a secreted enzyme also called
ectonucleotide pyrophosphatase/phosphodiesterase 2 or
lysophospholipase D that is important for converting
lysophosphatidyl choline (LPC) to the bioactive signaling molecule
lysophosphatidic acid (LPA). It has been shown that plasma LPA
levels are well correlated with ATX activity and hence ATX is
believed to be an important source of extracellular LPA. Early
experiments with a prototype ATX inhibitor have shown that such a
compound is able to inhibit the LPA synthesizing activity in mouse
plasma. Work conducted in the 1970s and early 1980s has
demonstrated that LPA can elicit a wide range of cellular
responses; including smooth muscle cell contraction, platelet
activation, cell proliferation, chemotaxis and others. LPA mediates
its effects via signaling to several G protein coupled receptors
(GPCRs); the first members were originally denoted Edg (endothelial
cell differentiation gene) receptors or ventricular zone gene-1
(vzg-1) but are now called LPA receptors. The prototypic group now
consists of LPA1/Edg-2/VZG-1, LPA2/Edg-4, and LPA3/Edg-7. Recently,
three additional LPA receptors LPA4/p2y9/GPR23, LPA5/GPR92 and
LPA6/p2Y5 have been described that are more closely related to
nucleotide-selective purinergic receptors than to the prototypic
LPA1-3 receptors. The ATX-LPA signaling axis is involved in a large
range of physiological and pathophysiological functions, including,
for example, nervous system function, vascular development,
cardiovascular physiology, reproduction, immune system function,
chronic inflammation, tumor metastasis and progression, organ
fibrosis as well as obesity and/or other metabolic diseases such as
diabetes mellitus. Therefore, increased activity of ATX and/or
increased levels of LPA, altered LPA receptor expression and
altered responses to LPA may contribute to the initiation,
progression and/or outcome of a number of different
pathophysiological conditions related to the ATX/LPA axis.
[0016] Carbonic anhydrases (CA) are a family of zinc-dependent
enzymes, which catalyze the equilibration between carbon dioxide
and water and hydrogencarbonate and a proton. The CA reaction is
involved in many physiological and pathological processes. Carbonic
anhydrase inhibition is useful for the treatment of ocular
conditions, conditions of reduced blood flow, cancer, edema and
inflammatory conditions including bacterial infections.
[0017] Dual acting ATX/CA inhibitors are expected to lower
intraocular pressure by facilitating two independent pathways, such
as inhibition of aqueous humor (AH) production through CA
inhibition at the ciliary body and facilitation of AH outflow by
ATX inhibition within the AH drainage system. In conditions of
vascular leakage in the eye such as diabetic retinopathy, age
related macular disease, or retinal vein occlusion, CA levels have
been shown or are expected to increase in the eye and facilitate an
increase in pH. This is expected to activate many hydrolytic
enzymes that can contribute to disease progression including ATX
suggesting additional ATX inhibition by shifting the pH
optimum.
[0018] In accordance with the invention, the compounds of formula
(I) or their pharmaceutically acceptable salts and esters can be
used for the treatment or prophylaxis of diseases, disorders or
conditions that are associated with the activity of autotaxin
and/or the biological activity of lysophosphatidic acid (LPA).
[0019] The compounds of formula (I) or their pharmaceutically
acceptable salts and esters herein inhibit autotaxin activity and
carbonic anhydrase activity therefore inhibit LPA production and
modulate LPA levels and associated signaling. Dual ATX/CA-II
inhibitors described herein are useful as agents for the treatment
or prevention of diseases or conditions in which ATX activity
and/or LPA signaling participates, is involved in the etiology or
pathology of the disease, or is otherwise associated with at least
one symptom of the disease. The ATX-LPA axis has been implicated
for example in angiogenesis, chronic inflammation, autoimmune
diseases, fibrotic diseases, cancer and tumor metastasis and
progression, ocular conditions, metabolic conditions such as
obesity and/or diabetes mellitus, conditions such as cholestatic or
other forms of chronic pruritus as well as acute and chronic organ
transplant rejection.
[0020] Objects of the present invention are the compounds of
formula (I) and their aforementioned salts and esters and their use
as therapeutically active substances, a process for the manufacture
of the said compounds, intermediates, pharmaceutical compositions,
medicaments containing the said compounds, their pharmaceutically
acceptable salts or esters, the use of the said compounds, salts or
esters for the treatment or prophylaxis of disorders or conditions
that are associated with the activity of ATX and/or the biological
activity of lysophosphatidic acid (LPA), particularly in the
treatment or prophylaxis of inflammatory conditions, conditions of
the nervous system, conditions of the respiratory system, vascular
and cardiovascular conditions, fibrotic diseases, cancer, ocular
conditions, metabolic conditions, cholestatic and other forms of
chronic pruritus and acute and -chronic organ transplant rejection,
and the use of the said compounds, salts or esters for the
production of medicaments for the treatment or prophylaxis of
inflammatory conditions, conditions of the nervous system,
conditions of the respiratory system, vascular and cardiovascular
conditions, fibrotic diseases, cancer, ocular conditions, metabolic
conditions, cholestatic and other forms of chronic pruritus and
acute and chronic organ transplant rejection. More particulary, the
compounds of formula (I) and their aforementioned salts and esters
and their use as therapeutically active substances, a process for
the manufacture of the said compounds, intermediates,
pharmaceutical compositions, medicaments containing the said
compounds, their pharmaceutically acceptable salts or esters, the
use of the said compounds, salts or esters for the treatment or
prophylaxis of ocular conditions, furthermore particularly
glaucoma.
[0021] The term "C.sub.1-6-alkoxy" denotes a group of the formula
--O--R', wherein R' is an C.sub.1-6-alkyl group. Examples of
C.sub.1-6-alkoxy group include methoxy, ethoxy, n-propoxy,
isopropoxy, n-butoxy, isobutoxy and tert-butoxy. Particular example
is methoxy.
[0022] The term "C.sub.2-6-alkenyl" denotes a monovalent linear or
branched hydrocarbon group of 2 to 6 carbon atoms with at least one
double bond. Particular example is ethylenyl.
[0023] The term "C.sub.1-6-alkoxy-C.sub.1-6-alkyl" denotes a
C.sub.1-6-alkyl group wherein at least one of the hydrogen atoms of
the C.sub.1-6-alkyl group is replaced by a C.sub.1-6-alkoxy group.
Particular examples are methoxymethyl, methoxyethyl, ethoxymethyl,
ethoxyethyl, iso-propoxymethyl and iso-propoxyethyl.
[0024] The term "C.sub.1-6-alkyl" denotes a monovalent linear or
branched saturated hydrocarbon group of 1 to 6 carbon atoms.
Examples of C.sub.1-6-alkyl include methyl, ethyl, propyl,
isopropyl, n-butyl, iso-butyl, sec-butyl, tert-butyl and pentyl.
Particular alkyl groups include methyl, ethyl, isopropyl, n-butyl
and sec-butyl.
[0025] The term "C.sub.1-6-alkylamino" a group of the formula
--NH--R', wherein R' is an C.sub.1-6-alkyl group. Particular
C.sub.1-6-alkylamino is a group of the formula --NH--R', wherein R'
is ter-butyl.
[0026] The term "C.sub.1-6-alkylcarbonylamino" denotes a group of
the formula --NH--C(O)--R', wherein R' is an C.sub.1-6-alkyl group.
Particular C.sub.1-6-alkylcarbonylamino is a group of the formula
--NH--C(O)--R', wherein R' is ter-butyl.
[0027] The term "C.sub.1-6-alkyltetrazolyl" denotes tetrazolyl
group substituted with one C.sub.1-6-alkyl group. Particular
C.sub.1-6-alkyltetrazolyl is methyltetrazolyl.
[0028] The term "C.sub.1-6-alkyltetrazolyl-C.sub.1-6-alkyl" denotes
C.sub.1-6-alkyl group wherein one of the hydrogen atoms of the
C.sub.1-6-alkyl group is replaced by a C.sub.1-6-alkyltetrazolyl
group. Particular example is methyltetrazolylmethyl.
[0029] The term "C.sub.2-6-alkynyl" denotes a monovalent linear or
branched hydrocarbon group of 2 to 6 carbon atoms with at least one
triple bond.
[0030] The term "amino" denotes the --NH.sub.2 group.
[0031] The term "aminosulfonyl" denotes --S(O).sub.2--NH.sub.2
group.
[0032] The term "cyano" denotes a --C.dbd.N group.
[0033] The term "C.sub.3-8-cycloalkoxy" denotes a group of the
formula --O--R', wherein R' is a C.sub.3-8-cycloalkyl.
[0034] The term "C.sub.3-8-cycloalkoxy-C.sub.1-6-alkyl" denotes a
C.sub.1-6-alkyl group wherein at least one of the hydrogen atoms of
the alkyl group is replaced by a C.sub.3-8-cycloalkoxy group.
[0035] The term "C.sub.3-8-cycloalkyl" denotes a monovalent
saturated monocyclic or bicyclic hydrocarbon group of 3 to 8 ring
carbon atoms. Bicyclic means a ring system consisting of two
saturated carbocycles having two carbon atoms in common. Examples
for monocyclic cycloalkyl are cyclopropyl, cyclobutanyl,
cyclopentyl, cyclohexyl or cycloheptyl. Examples for bicyclic
C.sub.3-s-cycloalkyl are bicyclo[2.2.1]heptanyl or
bicyclo[2.2.2]octanyl. Particular C.sub.3-8-cycloalkyl group is
cyclopropyl.
[0036] The term "C.sub.3-8-cycloalkyl-C.sub.1-6-alkoxy" denotes a
C.sub.1-6-alkoxy group wherein at least one of the hydrogen atoms
of the alkyl group is replaced by a C.sub.3-8-cycloalkyl group.
[0037] The term "C.sub.3-8-cycloalkyl-C.sub.1-6-alkyl" denotes a
C.sub.1-6-alkyl group wherein at least one of the hydrogen atoms of
the alkyl group is replaced by a C.sub.3-8-cycloalkyl group.
[0038] The term "C.sub.3-8-cycloalkylcarbonylamino" denotes a group
of the formula --NH--C(O)--R', wherein R' is a C.sub.3-8-cycloalkyl
group.
[0039] The term "halo-C.sub.1-6-alkoxy" denotes a C.sub.1-6-alkoxy
group wherein at least one of the hydrogen atoms of the alkoxy
group has been replaced by the same or different halogen atoms.
[0040] Particular examples are trifluoromethoxy.
[0041] The term "halogen" and "halo" are used interchangeably
herein and denote fluoro, chloro, bromo or iodo. Particular
halogens are chloro and fluoro.
[0042] The term "halo-C.sub.1-6-alkyl" denotes a C.sub.1-6-alkyl
group wherein at least one of the hydrogen atoms of the
C.sub.1-6-alkyl group has been replaced by the same or different
halogen atoms.
[0043] Particular examples are trifluoromethyl.
[0044] The term "heterocycloalkyl" denotes a monovalent saturated
or partly unsaturated mono- or bicyclic ring system of 4 to 9 ring
atoms, comprising 1, 2, or 3 ring heteroatoms selected from N, O
and S, the remaining ring atoms being carbon. Bicyclic means
consisting of two cycles having two ring atoms in common, i.e. the
bridge separating the two rings is either a single bond or a chain
of one or two ring atoms. Examples for monocyclic saturated
heterocycloalkyl are 4,5-dihydro-oxazolyl, oxetanyl, azetidinyl,
pyrrolidinyl, 2-oxo-pyrrolidin-3-yl, tetrahydrofuranyl,
tetrahydro-thienyl, pyrazolidinyl, imidazolidinyl, oxazolidinyl,
isoxazolidinyl, thiazolidinyl, piperidinyl, tetrahydropyranyl,
tetrahydrothiopyranyl, piperazinyl, morpholinyl, thiomorpholinyl,
1,1-dioxo-thiomorpholin-4-yl, azepanyl, diazepanyl,
homopiperazinyl, or oxazepanyl. Examples for bicyclic saturated
heterocycloalkyl are 8-aza-bicyclo[3.2.1]octyl, quinuclidinyl,
8-oxa-3-aza-bicyclo[3.2.1]octyl, 9-aza-bicyclo[3.3.1]nonyl,
3-oxa-9-aza-bicyclo[3.3.1]nonyl, or
3-thia-9-aza-bicyclo[3.3.1]nonyl. Examples for partly unsaturated
heterocycloalkyl are dihydrofuryl, imidazolinyl, dihydro-oxazolyl,
tetrahydro-pyridinyl, or dihydropyranyl. Particular example of
heterocycloalkyl group is tetrahydropyranyl.
[0045] The term "heterocycloalkyl-C.sub.1-6-alkoxy" denotes a
C.sub.1-6-alkoxy group wherein at least one of the hydrogen atoms
of the alkyl group is replaced by a heterocycloalkyl group.
Particular example of heterocycloalkyl-C.sub.1-6-alkoxy is
tetrahydropyranyl-C.sub.1-6-alkoxy, more particularly
tetrahydropyranylmethoxy.
[0046] The term "hydroxy" denotes a --OH group.
[0047] The term "hydroxy-C.sub.1-6-alkyl" denotes a C.sub.1-6-alkyl
group wherein one of the hydrogen atoms of the alkyl group is
replaced by a hydroxy group. Particular examples are hydroxymethyl
and hydroxyethyl.
[0048] The term "phenoxy" denotes a group of the formula --O--R',
wherein R' is a phenyl group.
[0049] The term "phenoxy-C.sub.1-6-alkyl" denotes a C.sub.1-6-alkyl
group wherein one of the hydrogen atoms of the alkyl group is
replaced by a phenoxy group.
[0050] The term "phenyl-C.sub.2-6-alkenyl" denotes a
C.sub.2-6-alkenyl group wherein one of the hydrogen atoms of the
alkyl group is replaced by a phenyl group. Particular example of
phenyl-C.sub.2-6-alkenyl is phenylethenyl.
[0051] The term "phenyl-C.sub.1-6-alkyl" denotes a C.sub.1-6-alkyl
group wherein one of the hydrogen atoms of the alkyl group is
replaced by a phenyl group. Particular examples of
phenyl-C.sub.1-6-alkyl are phenylmethyl and phenylethyl.
[0052] The term "phenyl-C.sub.2-6-alkynyl" denotes a
C.sub.2-6-alkynyl group wherein one of the hydrogen atoms of the
alkyl group is replaced by a phenyl group.
[0053] The term "pyridinyl-C.sub.2-6-alkenyl" denotes a
C.sub.2-6-alkenyl group wherein one of the hydrogen atoms of the
alkyl group is replaced by a pyridinyl group.
[0054] The term "pyridinyl-C.sub.1-6-alkyl" denotes a
C.sub.1-6-alkyl group wherein one of the hydrogen atoms of the
alkyl group is replaced by a pyridinyl group. Particular example of
pyridinyl-C.sub.1-6-alkyl is pyridinylmethyl, more particularly
2-pyridinylmethyl.
[0055] The term "pyridinyl-C.sub.2-6-alkynyl" denotes a
C.sub.2-6-alkynyl group wherein one of the hydrogen atoms of the
alkyl group is replaced by a pyridinyl group.
[0056] The term "thiophenyl-C.sub.2-6-alkenyl" denotes a
C.sub.2-6-alkenyl group wherein one of the hydrogen atoms of the
alkyl group is replaced by a thiophenyl group.
[0057] The term "thiophenyl-C.sub.1-6-alkyl" denotes a
C.sub.1-6-alkyl group wherein one of the hydrogen atoms of the
alkyl group is replaced by a thiophenyl group.
[0058] The term "thiophenyl-C.sub.2-6-alkynyl" denotes a
C.sub.2-6-alkynyl group wherein one of the hydrogen atoms of the
alkyl group is replaced by a thiophenyl group.
[0059] The term "pharmaceutically acceptable salts" refers to those
salts which retain the biological effectiveness and properties of
the free bases or free acids, which are not biologically or
otherwise undesirable. The salts are formed with inorganic acids
such as hydrochloric acid, hydrobromic acid, sulfuric acid, nitric
acid, phosphoric acid and the like, in particular hydrochloric
acid, and organic acids such as acetic acid, propionic acid,
glycolic acid, pyruvic acid, oxalic acid, maleic acid, malonic
acid, succinic acid, fumaric acid, tartaric acid, citric acid,
benzoic acid, cinnamic acid, mandelic acid, methanesulfonic acid,
ethanesulfonic acid, p-toluenesulfonic acid, salicylic acid,
N-acetylcystein and the like. In addition, these salts may be
prepared by addition of an inorganic base or an organic base to the
free acid. Salts derived from an inorganic base include, but are
not limited to, the sodium, potassium, lithium, ammonium, calcium,
magnesium salts and the like. Salts derived from organic bases
include, but are not limited to salts of primary, secondary, and
tertiary amines, substituted amines including naturally occurring
substituted amines, cyclic amines and basic ion exchange resins,
such as isopropylamine, trimethylamine, diethylamine,
triethylamine, tripropylamine, ethanolamine, lysine, arginine,
N-ethylpiperidine, piperidine, polyimine resins and the like.
Particular pharmaceutically acceptable salts of compounds of
formula (I) are the hydrochloride salts, methanesulfonic acid salts
and citric acid salts.
[0060] "Pharmaceutically acceptable esters" means that compounds of
general formula (I) may be derivatised at functional groups to
provide derivatives which are capable of conversion back to the
parent compounds in vivo. Examples of such compounds include
physiologically acceptable and metabolically labile ester
derivatives, such as methoxymethyl esters, methylthiomethyl esters
and pivaloyloxymethyl esters. Additionally, any physiologically
acceptable equivalents of the compounds of general formula (I),
similar to the metabolically labile esters, which are capable of
producing the parent compounds of general formula (I) in vivo, are
within the scope of this invention.
[0061] The term "protecting group" (PG) denotes a group which
selectively blocks a reactive site in a multifunctional compound
such that a chemical reaction can be carried out selectively at
another unprotected reactive site in the meaning conventionally
associated with it in synthetic chemistry. Protecting groups can be
removed at the appropriate point. Exemplary protecting groups are
amino-protecting groups, carboxy-protecting groups or
hydroxy-protecting groups. Particular protecting groups are the
tert-butoxycarbonyl (Boc), benzyloxycarbonyl (Cbz),
fluorenylmethoxycarbonyl (Fmoc) and benzyl (Bn) groups. Further
particular protecting groups are the tert-butoxycarbonyl (Boc) and
the fluorenylmethoxycarbonyl (Fmoc) groups. More particular
protecting group is the tert-butoxycarbonyl (Boc) group.
[0062] The abbreviation uM means microMolar and is equivalent to
the symbol .mu.M.
[0063] The abbreviation uL means microliter and is equivalent to
the symbol .mu.L.
[0064] The abbreviation ug means microgram and is equivalent to the
symbol .mu.g.
[0065] The compounds of formula (I) can contain several asymmetric
centers and can be present in the form of optically pure
enantiomers, mixtures of enantiomers such as, for example,
racemates, optically pure diastereoisomers, mixtures of
diastereoisomers, diastereoisomeric racemates or mixtures of
diastereoisomeric racemates.
[0066] According to the Cahn-Ingold-Prelog Convention the
asymmetric carbon atom can be of the "R" or "S" configuration.
[0067] Also an embodiment of the present invention are compounds
according to formula (I) as described herein and pharmaceutically
acceptable salts or esters thereof, in particular compounds
according to formula (I) as described herein and pharmaceutically
acceptable salts thereof, more particularly compounds according to
formula (I) as described herein.
[0068] Another embodiment of the present invention are compounds
according to formula (I) as described herein, wherein [0069]
R.sup.1 is substituted phenyl, substituted phenyl-C.sub.1-6-alkyl,
substituted phenoxy-C.sub.1-6-alkyl, substituted
phenyl-C.sub.2-6-alkenyl, substituted phenyl-C.sub.2-6-alkynyl,
substituted pyridinyl, substituted pyridinyl-C.sub.1-6-alkyl,
substituted pyridinyl-C.sub.2-6-alkenyl, substituted
pyridinyl-C.sub.2-6-alkynyl, substituted thiophenyl, substituted
thiophenyl-C.sub.1-6-alkyl, substituted
thiophenyl-C.sub.2-6-alkenyl or substituted
thiophenyl-C.sub.2-6-alkynyl, wherein substituted phenyl,
substituted phenyl-C.sub.1-6-alkyl, substituted
phenoxy-C.sub.1-6-alkyl, substituted phenyl-C.sub.2-6-alkenyl,
substituted phenyl-C.sub.2-6-alkynyl, substituted pyridinyl,
substituted pyridinyl-C.sub.1-6-alkyl, substituted
pyridinyl-C.sub.2-6-alkenyl, substituted
pyridinyl-C.sub.2-6-alkynyl, substituted thiophenyl, substituted
thiophenyl-C.sub.1-6-alkyl, substituted
thiophenyl-C.sub.2-6-alkenyl and substituted
thiophenyl-C.sub.2-6-alkynyl are substituted by R.sup.3, R.sup.4
and R.sup.5; [0070] Y is a --OC(O)-- or --C(O)--; [0071] W is
--C(O)--, --S(O).sub.2-- or --CR.sup.6R.sup.7--; [0072] R.sup.2 is
substituted phenyl, substituted pyridinyl or substituted
thiophenyl, wherein substituted phenyl, substituted pyridinyl and
substituted thiophenyl are substituted by R.sup.6, R.sup.7 and
R.sup.8; [0073] R.sup.3 is halogen, hydroxy, cyano,
C.sub.1-6-alkyl, C.sub.1-6-alkoxy,
C.sub.1-6-alkoxy-C.sub.1-6-alkyl, halo-C.sub.1-6-alkoxy,
halo-C.sub.1-6-alkyl, hydroxy-C.sub.1-6-alkyl,
C.sub.3-8-cycloalkyl, C.sub.3-8-cycloalkyl-C.sub.1-6-alkyl,
C.sub.3-8-cycloalkyl-C.sub.1-6-alkoxy, C.sub.3-8-cycloalkoxy,
C.sub.3-8-cycloalkoxy-C.sub.1-6-alkyl, C.sub.1-6-alkylamino,
C.sub.1-6-alkylcarbonylamino, C.sub.3-8-cycloalkylcarbonylamino,
C.sub.1-6-alkyltetrazolyl,
C.sub.1-6-alkyltetrazolyl-C.sub.1-6-alkyl or
heterocycloalkyl-C.sub.1-6-alkoxy; [0074] R.sup.4 and R.sup.5 are
independently selected from H, halogen, hydroxy, cyano,
C.sub.1-6-alkyl, C.sub.1-6-alkoxy,
C.sub.1-6-alkoxy-C.sub.1-6-alkyl, halo-C.sub.1-6-alkoxy,
halo-C.sub.1-6-alkyl, hydroxy-C.sub.1-6-alkyl,
C.sub.3-8-cycloalkyl, C.sub.3-8-cycloalkyl-C.sub.1-6-alkyl,
C.sub.3-8-cycloalkyl-C.sub.1-6-alkoxy, C.sub.3-8-cycloalkoxy,
C.sub.3-8-cycloalkoxy-C.sub.1-6-alkyl,
C.sub.1-6-alkylcarbonylamino, C.sub.3-8-cycloalkylcarbonylamino,
C.sub.1-6-alkyltetrazolyl,
C.sub.1-6-alkyltetrazolyl-C.sub.1-6-alkyl or
heterocycloalkyl-C.sub.1-6-alkoxy; [0075] R.sup.6 is aminosulfonyl;
[0076] R.sup.7 and R.sup.8 are independently selected from H,
halogen, hydroxy, cyano, C.sub.1-6-alkyl, C.sub.1-6-alkoxy,
C.sub.1-6-alkoxy-C.sub.1-6-alkyl, halo-C.sub.1-6-alkoxy,
halo-C.sub.1-6-alkyl, hydroxy-C.sub.1-6-alkyl,
C.sub.3-8-cycloalkyl, C.sub.3-8-cycloalkyl-C.sub.1-6-alkyl,
C.sub.3-8-cycloalkyl-C.sub.1-6-alkoxy, C.sub.3-8-cycloalkoxy and
C.sub.3-8-cycloalkoxy-C.sub.1-6-alkyl; [0077] m, n, p and q are
independently selected from 1 or 2; [0078] and pharmaceutically
acceptable salts.
[0079] Another embodiment of the present invention are compounds
according to formula (I) as described herein, wherein [0080]
R.sup.1 is substituted phenyl-C.sub.1-6-alkyl, substituted
phenoxy-C.sub.1-6-alkyl, substituted phenyl-C.sub.2-6-alkenyl,
substituted pyridinyl or substituted pyridinyl-C.sub.1-6-alkyl,
wherein substituted phenyl-C.sub.1-6-alkyl, substituted
phenoxy-C.sub.1-6-alkyl, substituted phenyl-C.sub.2-6-alkenyl,
substituted pyridinyl and substituted pyridinyl-C.sub.1-6-alkyl are
substituted by R.sup.3, R.sup.4 and R.sup.5; [0081] Y is a
--OC(O)-- or --C(O)--; [0082] W is --C(O)--; [0083] R.sup.2 is
substituted phenyl or substituted pyridinyl, wherein substituted
phenyl and substituted pyridinyl are substituted by R.sup.6,
R.sup.7 and R.sup.8; [0084] R.sup.3 is halo-C.sub.1-6-alkoxy,
C.sub.1-6-alkylamino, C.sub.1-6-alkylcarbonylamino,
C.sub.1-6-alkyltetrazolyl-C.sub.1-6-alkyl or
tetrahydropyranyl-C.sub.1-6-alkoxy; [0085] R.sup.4 is H, cyano,
halogen, C.sub.1-6-alkyl, halo-C.sub.1-6-alkyl or
C.sub.3-8-cycloalkyl; [0086] R.sup.5 is H; [0087] R.sup.6 is
aminosulfonyl; [0088] R.sup.7 and R.sup.8 are independently
selected from H or halogen; [0089] m and q are 1; [0090] n and p
are independently selected from 1 or 2; [0091] and pharmaceutically
acceptable salts.
[0092] A particular embodiment of the present invention are
compounds according to formula (I) as described herein, wherein
R.sup.1 is substituted phenyl-C.sub.1-6-alkyl, substituted
phenoxy-C.sub.1-6-alkyl, substituted phenyl-C.sub.2-6-alkenyl,
substituted quinolinyl-C.sub.1-6-alkyl, substituted pyridinyl or
substituted pyridinyl-C.sub.1-6-alkyl, wherein substituted
phenyl-C.sub.1-6-alkyl, substituted phenoxy-C.sub.1-6-alkyl,
substituted phenyl-C.sub.2-6-alkenyl, substituted
quinolinyl-C.sub.1-6-alkyl, substituted pyridinyl and substituted
pyridinyl-C.sub.1-6-alkyl are substituted by R.sup.3, R.sup.4 and
R.sup.5.
[0093] A particular embodiment of the present invention are
compounds according to formula (I) as described herein, wherein
R.sup.1 is substituted phenyl-C.sub.1-6-alkyl, substituted
phenoxy-C.sub.1-6-alkyl, substituted phenyl-C.sub.2-6-alkenyl,
substituted pyridinyl or substituted pyridinyl-C.sub.1-6-alkyl,
wherein substituted phenyl-C.sub.1-6-alkyl, substituted
phenoxy-C.sub.1-6-alkyl, substituted phenyl-C.sub.2-6-alkenyl,
substituted pyridinyl and substituted pyridinyl-C.sub.1-6-alkyl are
substituted by R.sup.3, R.sup.4 and R.sup.5.
[0094] A further particular embodiment of the present invention are
compounds according to formula (I) as described herein, wherein
R.sup.1 is pyridinyl-C.sub.1-6-alkyl substituted by R.sup.3,
R.sup.4 and R.sup.5.
[0095] A particular embodiment of the present invention are
compounds according to formula (I) as described herein, wherein Y
is --OC(O)--.
[0096] A particular embodiment of the present invention are
compounds according to formula (I) as described herein, wherein
R.sup.2 is substituted phenyl or substituted pyridinyl, wherein
substituted phenyl and substituted pyridinyl are substituted by
R.sup.6, R.sup.7 and R.sup.8.
[0097] A further particular embodiment of the present invention are
compounds according to formula (I) as described herein, wherein
R.sup.2 is phenyl substituted by R.sup.6, R.sup.7 and R.sup.8.
[0098] A particular embodiment of the present invention are
compounds according to formula (I) as described herein, wherein
R.sup.3 is halo-C.sub.1-6-alkoxy, C.sub.1-6-alkylcarbonylamino,
C.sub.1-6-alkyltetrazolyl-C.sub.1-6-alkyl,
C.sub.1-6-alkylpiperidinyl-C.sub.1-6-alkoxy or
tetrahydropyranyl-C.sub.1-6-alkoxy.
[0099] A particular embodiment of the present invention are
compounds according to formula (I) as described herein, wherein
R.sup.3 is halo-C.sub.1-6-alkoxy, C.sub.1-6-alkylcarbonylamino,
C.sub.1-6-alkyltetrazolyl-C.sub.1-6-alkyl or
tetrahydropyranyl-C.sub.1-6-alkoxy.
[0100] A further particular embodiment of the present invention are
compounds according to formula (I) as described herein, wherein
R.sup.3 is C.sub.1-6-alkylcarbonylamino.
[0101] A particular embodiment of the present invention are
compounds according to formula (I) as described herein, wherein
R.sup.4 is H, cyano, halogen, C.sub.1-6-alkyl, halo-C.sub.1-6-alkyl
or C.sub.3-8-cycloalkyl.
[0102] A further particular embodiment of the present invention are
compounds according to formula (I) as described herein, wherein
R.sup.4 is halo-C.sub.1-6-alkyl.
[0103] A particular embodiment of the present invention are
compounds according to formula (I) as described herein, wherein
R.sup.5 is H.
[0104] A particular embodiment of the present invention are
compounds according to formula (I) as described herein, wherein
R.sup.7 and R.sup.8 are independently selected from H or
halogen.
[0105] A further particular embodiment of the present invention are
compounds according to formula (I) as described herein, wherein
R.sup.7 is halogen.
[0106] A further particular embodiment of the present invention are
compounds according to formula (I) as described herein, wherein
R.sup.8 is H.
[0107] A particular embodiment of the present invention are
compounds according to formula (I) as described herein, wherein m
and q are 1 and n and p are independently selected from 1 or 2
[0108] A further particular embodiment of the present invention are
compounds according to formula (I) as described herein, wherein m,
n, p and q are 1.
[0109] A more particular embodiment of the present invention are
compounds according to formula (I) as described herein, wherein
[0110] R.sup.1 is pyridinyl-C.sub.1-6-alkyl substituted by R.sup.3,
R.sup.4 and R.sup.5; [0111] Y is --OC(O)--; [0112] W is --C(O)--;
[0113] R.sup.2 is phenyl substituted by R.sup.6, R.sup.7 and
R.sup.8; [0114] R.sup.3 is C.sub.1-6-alkylcarbonylamino; [0115]
R.sup.4 is halo-C.sub.1-6-alkyl; [0116] R.sup.5 is H; [0117]
R.sup.7 is halogen; [0118] R.sup.8 is H; [0119] m, n, p and q are 1
and pharmaceutically acceptable salts.
[0120] A particular embodiment of the present invention are
compounds according to formula I(a) as described herein,
##STR00003## [0121] wherein [0122] R.sup.1 is substituted
phenyl-C.sub.1-6-alkyl, substituted phenoxy-C.sub.1-6-alkyl,
substituted phenyl-C.sub.2-6-alkenyl, substituted pyridinyl or
substituted pyridinyl-C.sub.1-6-alkyl, wherein substituted
phenyl-C.sub.1-6-alkyl, substituted phenoxy-C.sub.1-6-alkyl,
substituted phenyl-C.sub.2-6-alkenyl, substituted pyridinyl and
substituted pyridinyl-C.sub.1-6-alkyl are substituted by R.sup.3,
R.sup.4 and R.sup.5; [0123] Y is a --OC(O)-- or --C(O)--; [0124] W
is --C(O)--; [0125] R.sup.3 is halo-C.sub.1-6-alkoxy,
C.sub.1-6-alkylcarbonylamino,
C.sub.1-6-alkyltetrazolyl-C.sub.1-6-alkyl or
tetrahydropyranyl-C.sub.1-6-alkoxy; [0126] R.sup.4 is H, cyano,
halogen, C.sub.1-6-alkyl, halo-C.sub.1-6-alkyl or
C.sub.3-8-cycloalkyl; [0127] R.sup.5 is H; [0128] R.sup.7 and
R.sup.8 are independently selected from H or halogen; [0129] m and
q are 1; [0130] n and p are independently selected from 1 or 2;
[0131] and pharmaceutically acceptable salts.
[0132] A further particular embodiment of the present invention are
compounds according to formula I(b) as described herein,
##STR00004## [0133] wherein [0134] R.sup.1 is
pyridinyl-C.sub.1-6-alkyl substituted by R.sup.3, R.sup.4 and
R.sup.5; [0135] Y is --OC(O)--; [0136] W is --C(O)--; [0137]
R.sup.3 is C.sub.1-6-alkylcarbonylamino; [0138] R.sup.4 is
halo-C.sub.1-6-alkyl; [0139] R.sup.5 is H; [0140] R.sup.7 is
halogen; [0141] R.sup.8 is H; [0142] m, n, p and q are 1 [0143] and
pharmaceutically acceptable salts.
[0144] Particular examples of compounds of formula (I) as described
herein are selected from [0145]
[3-(2,2-dimethylpropanoylamino)-5-(trifluoromethyl)pyridin-2-yl]methyl
2-(4-sulfamoylbenzoyl)-1,3,4,6-tetrahydropyrrolo[3,4-c]pyrrole-5-carboxyl-
ate; [0146]
[3-(2,2-dimethylpropanoylamino)-5-(trifluoromethyl)pyridin-2-yl]methyl
2-(2,5-difluoro-4-sulfamoylbenzoyl)-1,3,4,6-tetrahydropyrrolo[3,4-c]pyrro-
le-5-carboxylate; [0147]
[3-(2,2-dimethylpropanoylamino)-5-(trifluoromethyl)pyridin-2-yl]methyl
2-(3-chloro-4-sulfamoylbenzoyl)-1,3,4,6-tetrahydropyrrolo[3,4-c]pyrrole-5-
-carboxylate; [0148]
[3-(2,2-dimethylpropanoylamino)-5-(trifluoromethyl)pyridin-2-yl]methyl
2-(3-fluoro-4-sulfamoylbenzoyl)-1,3,4,6-tetrahydropyrrolo[3,4-c]pyrrole-5-
-carboxylate; [0149]
[3-(2,2-dimethylpropanoylamino)-5-(trifluoromethyl)pyridin-2-yl]methyl
2-(2-fluoro-4-sulfamoylbenzoyl)-1,3,4,6-tetrahydropyrrolo[3,4-c]pyrrole-5-
-carboxylate; [0150]
[3-(2,2-dimethylpropanoylamino)-5-(trifluoromethyl)pyridin-2-yl]methyl
2-(5-sulfamoylpyridine-2-carbonyl)-1,3,4,6-tetrahydropyrrolo[3,4-c]pyrrol-
e-5-carboxylate; [0151] 4-(trifluoromethoxy)benzyl
5-(4-sulfamoylbenzoyl)-3,4,5,6-tetrahydropyrrolo[3,4-c]pyrrole-2(1H)-carb-
oxylate; [0152]
6-[5-[2-cyclopropyl-6-(oxan-4-ylmethoxy)pyridine-4-carbonyl]-1,3,4,6-tetr-
ahydropyrrolo[3,4-c]pyrrole-2-carbonyl]pyridine-3-sulfonamide;
[0153]
4-[5-[2-cyclopropyl-6-(oxan-4-ylmethoxy)pyridine-4-carbonyl]-1,3,4,6-tetr-
ahydropyrrolo[3,4-c]pyrrole-2-carbonyl]-3-fluorobenzenesulfonamide;
[0154]
[3-(2,2-dimethylpropanoylamino)-5-(trifluoromethyl)pyridin-2-yl]methyl
2-(2,3-difluoro-4-sulfamoylbenzoyl)-1,3,4,6-tetrahydropyrrolo[3,4-c]pyrro-
le-5-carboxylate; [0155]
3-fluoro-4-(5-(3-(2-((5-methyl-2H-tetrazol-2-yl)methyl)-4-(trifluoromethy-
l)phenyl)propanoyl)-1,2,3,4,5,6-hexahydropyrrolo[3,4-c]pyrrole-2-carbonyl)-
benzenesulfonamide; [0156]
[3-(2,2-dimethylpropanoylamino)-5-(trifluoromethyl)pyridin-2-yl]methyl
2-(2,6-difluoro-4-sulfamoylbenzoyl)-1,3,4,6-tetrahydropyrrolo[3,4-c]pyrro-
le-5-carboxylate; [0157]
[5-chloro-3-(2,2-dimethylpropanoylamino)pyridin-2-yl]methyl
2-(2-fluoro-4-sulfamoylbenzoyl)-1,3,4,6-tetrahydropyrrolo[3,4-c]pyrrole-5-
-carboxylate; [0158]
[5-chloro-3-(2,2-dimethylpropanoylamino)pyridin-2-yl]methyl
2-(3-fluoro-4-sulfamoylbenzoyl)-1,3,4,6-tetrahydropyrrolo[3,4-c]pyrrole-5-
-carboxylate; [0159]
[5-chloro-3-(2,2-dimethylpropanoylamino)pyridin-2-yl]methyl
2-(2,3-difluoro-4-sulfamoylbenzoyl)-1,3,4,6-tetrahydropyrrolo[3,4-c]pyrro-
le-5-carboxylate; [0160]
[5-chloro-3-(2,2-dimethylpropanoylamino)pyridin-2-yl]methyl
2-(2,6-difluoro-4-sulfamoylbenzoyl)-1,3,4,6-tetrahydropyrrolo[3,4-c]pyrro-
le-5-carboxylate; [0161]
[5-chloro-3-(2,2-dimethylpropanoylamino)pyridin-2-yl]methyl
2-(2,5-difluoro-4-sulfamoylbenzoyl)-1,3,4,6-tetrahydropyrrolo[3,4-c]pyrro-
le-5-carboxylate; [0162]
[3-(2,2-dimethylpropanoylamino)-6-methylpyridin-2-yl]methyl
2-(2-fluoro-4-sulfamoylbenzoyl)-1,3,4,6-tetrahydropyrrolo[3,4-c]pyrrole-5-
-carboxylate; [0163]
[6-chloro-3-(2,2-dimethylpropanoylamino)pyridin-2-yl]methyl
2-(2-fluoro-4-sulfamoylbenzoyl)-1,3,4,6-tetrahydropyrrolo[3,4-c]pyrrole-5-
-carboxylate; [0164]
[3-(2,2-dimethylpropanoylamino)pyridin-2-yl]methyl
2-(2-fluoro-4-sulfamoylbenzoyl)-1,3,4,6-tetrahydropyrrolo[3,4-c]pyrrole-5-
-carboxylate; [0165]
[6-chloro-3-(2,2-dimethylpropanoylamino)pyridin-2-yl]methyl
2-(2,5-difluoro-4-sulfamoylbenzoyl)-1,3,4,6-tetrahydropyrrolo[3,4-c]pyrro-
le-5-carboxylate; [0166]
[6-chloro-3-(2,2-dimethylpropanoylamino)pyridin-2-yl]methyl
2-(3-fluoro-4-sulfamoylbenzoyl)-1,3,4,6-tetrahydropyrrolo[3,4-c]pyrrole-5-
-carboxylate; [0167]
[6-chloro-3-(2,2-dimethylpropanoylamino)pyridin-2-yl]methyl
2-(2,3-difluoro-4-sulfamoylbenzoyl)-1,3,4,6-tetrahydropyrrolo[3,4-c]pyrro-
le-5-carboxylate; [0168]
[6-chloro-3-(2,2-dimethylpropanoylamino)pyridin-2-yl]methyl
2-(2,6-difluoro-4-sulfamoylbenzoyl)-1,3,4,6-tetrahydropyrrolo[3,4-c]pyrro-
le-5-carboxylate; [0169]
[5-cyano-3-(2,2-dimethylpropanoylamino)pyridin-2-yl]methyl
2-(2-fluoro-4-sulfamoylbenzoyl)-1,3,4,6-tetrahydropyrrolo[3,4-c]pyrrole-5-
-carboxylate; [0170]
[5-cyano-3-(2,2-dimethylpropanoylamino)pyridin-2-yl]methyl
2-(2,6-difluoro-4-sulfamoylbenzoyl)-1,3,4,6-tetrahydropyrrolo[3,4-c]pyrro-
le-5-carboxylate; [0171]
[5-cyano-3-(2,2-dimethylpropanoylamino)pyridin-2-yl]methyl
2-(2,3-difluoro-4-sulfamoylbenzoyl)-1,3,4,6-tetrahydropyrrolo[3,4-c]pyrro-
le-5-carboxylate; [0172]
[5-cyano-3-(2,2-dimethylpropanoylamino)pyridin-2-yl]methyl
2-(2,5-difluoro-4-sulfamoylbenzoyl)-1,3,4,6-tetrahydropyrrolo[3,4-c]pyrro-
le-5-carboxylate; [0173]
[3-(2,2-dimethylpropanoylamino)-5-(trifluoromethyl)pyridin-2-yl]methyl
6-(2-fluoro-4-sulfamoylbenzoyl)-1,3,4,5,7,8-hexahydro-2,6-naphthyridine-2-
-carboxylate; [0174]
[5-chloro-4-cyano-2-(2,2-dimethylpropanoylamino)phenyl]methyl
2-(5-sulfamoylpyridine-2-carbonyl)-1,3,4,6-tetrahydropyrrolo[3,4-c]pyrrol-
e-5-carboxylate; [0175] [4-(trifluoromethoxy)phenyl]methyl
6-(2-fluoro-4-sulfamoylbenzoyl)-1,3,4,5,7,8-hexahydro-2,6-naphthyridine-2-
-carboxylate; [0176] [4-(trifluoromethoxy)phenyl]methyl
2-(5-sulfamoylpyridine-2-carbonyl)-1,3,4,6-tetrahydropyrrolo[3,4-c]pyrrol-
e-5-carboxylate; [0177] [4-(trifluoromethoxy)phenyl]methyl
2-(2-fluoro-4-sulfamoylbenzoyl)-1,3,4,6-tetrahydropyrrolo[3,4-c]pyrrole-5-
-carboxylate; [0178]
3-fluoro-4-[2-[(E)-3-[4-(trifluoromethoxy)phenyl]prop-2-enoyl]-1,3,4,6-te-
trahydropyrrolo[3,4-c]pyrrole-5-carbonyl]benzenesulfonamide; [0179]
6-[2-[3-[4-(trifluoromethoxy)phenyl]propanoyl]-1,3,4,6-tetrahydropyrrolo[-
3,4-c]pyrrole-5-carbonyl]pyridine-3-sulfonamide; [0180]
3-fluoro-4-[2-[3-[4-(trifluoromethoxy)phenyl]propanoyl]-1,3,4,6-tetrahydr-
opyrrolo[3,4-c]pyrrole-5-carbonyl]benzenesulfonamide; [0181]
6-[2-[(E)-3-[4-(trifluoromethoxy)phenyl]prop-2-enoyl]-1,3,4,6-tetrahydrop-
yrrolo[3,4-c]pyrrole-5-carbonyl]pyridine-3-sulfonamide; [0182]
6-[2-[2-[4-(trifluoromethoxy)phenoxy]acetyl]-1,3,4,6-tetrahydropyrrolo[3,-
4-c]pyrrole-5-carbonyl]pyridine-3-sulfonamide; [0183]
3-fluoro-4-[2-[2-[4-(trifluoromethoxy)phenoxy]acetyl]-1,3,4,6-tetrahydrop-
yrrolo[3,4-c]pyrrole-5-carbonyl]benzenesulfonamide; [0184]
4-[2-[3-[4-cyano-2-[(5-methyltetrazol-2-yl)methyl]phenyl]propanoyl]-1,3,4-
,6-tetrahydropyrrolo[3,4-c]pyrrole-5-carbonyl]-3-fluorobenzenesulfonamide;
[0185]
4-[2-[3-[4-chloro-2-[(5-methyltetrazol-2-yl)methyl]phenyl]propanoy-
l]-1,3,4,6-tetrahydropyrrolo[3,4-c]pyrrole-5-carbonyl]-3-fluorobenzenesulf-
onamide; [0186]
3-fluoro-4-[2-[3-[2-[(4-methyltriazol-2-yl)methyl]-4-(trifluoromethyl)phe-
nyl]propanoyl]-1,3,4,6-tetrahydropyrrolo[3,4-c]pyrrole-5-carbonyl]benzenes-
ulfonamide; [0187]
3-fluoro-4-[2-[3-[2-[(4-methyltriazol-1-yl)methyl]-4-(trifluoromethyl)phe-
nyl]propanoyl]-1,3,4,6-tetrahydropyrrolo[3,4-c]pyrrole-5-carbonyl]benzenes-
ulfonamide; [0188] and pharmaceutically acceptable salts
thereof.
[0189] Also particular examples of compounds of formula (I) as
described herein are selected from [0190]
[5,6-dichloro-3-(2,2-dimethylpropanoylamino)pyridin-2-yl]methyl
2-(2-fluoro-4-sulfamoylbenzoyl)-1,3,4,6-tetrahydropyrrolo[3,4-c]pyrrole-5-
-carboxylate; [0191]
[5,6-dichloro-3-(2,2-dimethylpropanoylamino)pyridin-2-yl]methyl
2-(2,3-difluoro-4-sulfamoylbenzoyl)-1,3,4,6-tetrahydropyrrolo[3,4-c]pyrro-
le-5-carboxylate; [0192]
[5,6-dichloro-3-(2,2-dimethylpropanoylamino)pyridin-2-yl]methyl
2-(2,6-difluoro-4-sulfamoylbenzoyl)-1,3,4,6-tetrahydropyrrolo[3,4-c]pyrro-
le-5-carboxylate; [0193]
[3-(2,2-dimethylpropanoylamino)-5-(trifluoromethyl)pyridin-2-yl]methyl
2-(3-fluoro-5-sulfamoylpyridine-2-carbonyl)-1,3,4,6-tetrahydropyrrolo[3,4-
-c]pyrrole-5-carboxylate; [0194]
4-[5-[2-cyclopropyl-6-(oxan-4-ylmethoxy)pyridine-4-carbonyl]-1,3,4,6-tetr-
ahydropyrrolo[3,4-c]pyrrole-2-carbonyl]-2,3-difluorobenzenesulfonamide;
[0195]
4-[5-[2-cyclopropyl-6-[(1-methylpiperidin-4-yl)methoxy]pyridine-4--
carbonyl]-1,3,4,6-tetrahydropyrrolo[3,4-c]pyrrole-2-carbonyl]-2,3-difluoro-
benzenesulfonamide; [0196]
[5-chloro-3-[(5-methyltetrazol-2-yl)methyl]pyridin-2-yl]methyl
2-(2-fluoro-4-sulfamoylbenzoyl)-1,3,4,6-tetrahydropyrrolo[3,4-c]pyrrole-5-
-carboxylate; [0197]
3-fluoro-4-[2-[3-[3-[(5-methyltetrazol-2-yl)methyl]-5-(trifluoromethyl)py-
ridin-2-yl]propanoyl]-1,3,4,6-tetrahydropyrrolo[3,4-c]pyrrole-5-carbonyl]b-
enzenesulfonamide; [0198]
5-fluoro-6-[2-[3-[2-[(5-methyltetrazol-2-yl)methyl]-4-(trifluoromethyl)ph-
enyl]propanoyl]-1,3,4,6-tetrahydropyrrolo[3,4-c]pyrrole-5-carbonyl]pyridin-
e-3-sulfonamide; [0199]
[3-(2,2-dimethylpropanoylamino)quinolin-2-yl]methyl
2-(2-fluoro-4-sulfamoylbenzoyl)-1,3,4,6-tetrahydropyrrolo[3,4-c]pyrrole-5-
-carboxylate; [0200]
[3-(2,2-dimethylpropanoylamino)-5-(trifluoromethyl)pyridin-2-yl]methyl
5-(2-fluoro-4-sulfamoylphenyl)sulfonyl-1,3,4,6-tetrahydropyrrolo[3,4-c]py-
rrole-2-carboxylate; and pharmaceutically acceptable salts thereof.
Further particular examples of compounds of formula (I) as
described herein are selected from [0201]
[3-(2,2-dimethylpropanoylamino)-5-(trifluoromethyl)pyridin-2-yl]methyl
2-(3-chloro-4-sulfamoylbenzoyl)-1,3,4,6-tetrahydropyrrolo[3,4-c]pyrrole-5-
-carboxylate; [0202]
[3-(2,2-dimethylpropanoylamino)-5-(trifluoromethyl)pyridin-2-yl]methyl
2-(3-fluoro-4-sulfamoylbenzoyl)-1,3,4,6-tetrahydropyrrolo[3,4-c]pyrrole-5-
-carboxylate; [0203]
[3-(2,2-dimethylpropanoylamino)-5-(trifluoromethyl)pyridin-2-yl]methyl
2-(2-fluoro-4-sulfamoylbenzoyl)-1,3,4,6-tetrahydropyrrolo[3,4-c]pyrrole-5-
-carboxylate; [0204]
[5-chloro-3-(2,2-dimethylpropanoylamino)pyridin-2-yl]methyl
2-(2,3-difluoro-4-sulfamoylbenzoyl)-1,3,4,6-tetrahydropyrrolo[3,4-c]pyrro-
le-5-carboxylate; and pharmaceutically acceptable salts
thereof.
[0205] Processes for the manufacture of compounds of formula (I) as
described herein are an object of the invention.
[0206] The preparation of compounds of formula (I) of the present
invention may be carried out in sequential or convergent synthetic
routes. Syntheses of the invention are shown in the following
general schemes. The skills required for carrying out the reactions
and purifications of the resulting products are known to those
persons skilled in the art. In case a mixture of enantiomers or
diastereoisomers is produced during a reaction, these enantiomers
or diastereoisomers can be separated by methods described herein or
known to the man skilled in the art such as e.g. (chiral)
chromatography or crystallization. The substituents and indices
used in the following description of the processes have the
significance given herein.
[0207] Compounds of general formula (I) can be synthesised from
amine precursor 1 and appropriate reagents, using methods well
known in the art.
##STR00005##
[0208] For instance, amine 1 is reacted with a suitable carboxylic
acid of formula R.sup.1--COOH (2) leading to a compound of formula
(I), wherein Y is --C(O)--. The reaction is performed in the
presence of a coupling agent such as 1,1'-carbonyldiimidazole,
N,N'-dicyclohexylcarbodiimide, 1-(3-dimethyl
aminopropyl)-3-ethyl-carbodiimide hydrochloride,
O-(benzotriazol-1-yl)-N,N,N',N'-tetramethyluronium
hexafluoro-phosphate,
O-(7-azabenzotriazol-1-yl)-N,N,N',N'-tetramethyluronium
hexafluoro-phosphate or bromo-tris-pyrrolidino-phosphonium
hexafluorophosphate, in aprotic solvents such as dichloromethane,
tetrahydrofuran, N,N-dimethylformamide, N-methylpyrrolidinone and
mixtures thereof at temperatures between -40.degree. C. and
80.degree. C. in the presence or absence of a base such as
triethylamine, diisopropylethylamine, 4-methylmorpholine and/or
4-(dimethylamino)pyridine.
[0209] Amine 1 can also be reacted with suitable acylating reagents
such as acyl chlorides of formula R.sup.1--COCl (3) to lead to
compounds of formula (I), wherein Y is --C(O)--. The reaction is
performed in a solvent such as dichloromethane, tetrahydrofuran, or
N,N-dimethylformamide, in the presence of a base such as
triethylamine or 4-methylmorpholine, at temperatures between
0.degree. C. and 80.degree. C.
[0210] Alternatively, amine 1 is reacted with a suitable
chloroformate ester of formula R.sup.1--O--C(O)--C.sub.1 (4), or
with an imidazole-1-carboxylate ester of formula (3), leading to a
compound of formula (I) wherein Y is --OC(O)--.
##STR00006##
[0211] The reaction is performed in a suitable solvent such as
dichloromethane, tetrahydrofuran, N,N-dimethylformamide,
acetonitrile, acetone, water, or mixtures thereof, in the presence
of a base, e. g., triethylamine, diisopropylethylamine, pyridine,
potassium hydrogencarbonate, potassium carbonate, at temperatures
between 0.degree. C. and the boiling point of the solvent or
solvent mixture.
[0212] Chloroformate esters 4 are commercially available or can be
synthesised from the corresponding alcohol of formula R.sup.1--OH,
by reaction with phosgene or a phosgene equivalent (e. g.,
diphosgene, triphosgene), as described in the literature.
[0213] Imidazole-1-carboxylate esters 5 are synthesised from the
corresponding alcohols of formula R.sup.1--OH, by reaction with
1,1'-carbonyldiimidazole. The reaction is performed at room
temperature, in a solvent such as dichloromethane, tetrahydrofuran
or acetonitrile. The imidazole-1-carboxylate esters 5 are typically
not isolated but directly reacted with amines 1 as described
above.
[0214] Alcohols of formula R.sup.1--OH are commercially available
or can be produced by methods described herein or known in the
art.
[0215] Carboxylic acids (2) and acyl halides (3) are commercially
available or can be prepared as described herein or in the
literature.
[0216] Amines of general formula 1 are synthesised from suitably
protected precursors 6.
##STR00007##
[0217] Suitable protective groups (PG) are tert-butoxycarbonyl or
benzyloxycarbonyl. The deprotection of intermediates 6 can be
performed using methods and reagents known in the art.
[0218] For instance, in the case where PG is benzyloxycarbonyl, the
deprotection may be performed by hydrogenation at pressures between
1 bar and 100 bar, in the presence of a suitable catalyst such as
palladium on activated charcoal, at temperatures between 20.degree.
C. and 150.degree. C. in solvents such as methanol or ethanol.
[0219] Alternatively, in the case where PG is tert-butoxycarbonyl,
the deprotection may be performed in the presence of a suitable
acid, e. g, hydrochloric acid or trifluoroacetic acid, in a solvent
such as water, 2-propanol, dichloromethane, or 1,4-dioxane at
temperatures between 0.degree. C. and 30.degree. C.
[0220] Intermediates 6 can be produced from amine precursors of
general formula 7 by reaction with appropriate reagents, using
methods known in the art.
##STR00008##
[0221] For instance, 7 is reacted with alkylating agents of general
formula X--CR.sup.6R.sup.7--R.sup.2 (8) where X is a leaving group
such as C.sub.1, Br, I, or OSO.sub.2CH.sub.3, leading to 6, wherein
W is --CR.sup.6R.sup.7--. This reaction is performed in a solvent
such as tetrahydrofuran or N,N-dimethylformamide, in the presence
of a base, e. g. triethylamine or potassium carbonate, at
temperatures between 0.degree. C. and 100.degree. C.
[0222] Alternatively, for compounds of formula 6, wherein W is
--CR.sup.6R.sup.7--, R.sup.6 is hydrogen, alkyl or cycloalkyl, and
R.sup.7 is H, amine 7 is reacted with aldehydes or ketones of
general formula R.sup.6--C(O)--R.sup.2 (9) in a reductive amination
reaction, leading to 6. This reaction is performed in the presence
of a suitable reducing agent, e. g., sodium borohydride or sodium
triacetoxyborohydride, in a solvent such as methanol, acetic acid,
tetrahydrofuran, 1,2-dichloroethane or mixtures thereof, at
temperatures between 0.degree. C. and 50.degree. C.
[0223] Alternatively, amine 7 is reacted with a suitable carboxylic
acid of formula R.sup.2--COOH (10), leading to compounds of formula
6, wherein W is --C(O)--. The reaction is performed in the presence
of a coupling agent such as 1,1'-carbonyldiimidazole,
N,N'-dicyclohexylcarbodiimide,
1-(3-dimethylaminopropyl)-3-ethyl-carbodiimide hydrochloride,
0-(benzotriazol-1-yl)-N,N,N',N'-tetramethyluronium
hexafluoro-phosphate,
0-(7-azabenzotriazol-1-yl)-N,N,N',N'-tetramethyluronium
hexafluoro-phosphate or bromo-tris-pyrrolidino-phosphonium
hexafluorophosphate, in aprotic solvents such as dichloromethane,
tetrahydrofuran, N,N-dimethylformamide, N-methylpyrrolidinone and
mixtures thereof at temperatures between -40.degree. C. and
80.degree. C. in the presence or absence of a base such as
triethylamine, diisopropylethylamine, 4-methylmorpholine and/or
4-(dimethylamino)pyridine.
[0224] Alternatively, amine 7 is reacted with a suitable sulfonyl
chloride of formula R.sup.2--SO.sub.2C.sub.1 (11), leading to
compounds of formula 6, wherein W is --S(O.sub.2)--. The reaction
is performed in a suitable solvent such as dichloromethane,
tetrahydrofuran, N,N-dimethylformamide, acetonitrile, acetone,
water, or mixtures thereof, in the presence of a base, e. g.
triethylamine, diisopropylethylamine, pyridine, potassium
hydrogencarbonate, potassium carbonate, at temperatures between
0.degree. C. and the boiling point of the solvent or solvent
mixture. Amines 7, alkylating agents 8, aldehydes/ketones 9,
carboxylic acids 10, and sulfonyl chlorides 11 are commercially
available or can be synthesised as described herein or in the
literature.
[0225] Compounds of formula (I), can be produced from amine
precursors of general formula 12 by reaction with appropriate
reagents, using methods known in the art.
##STR00009##
[0226] For instance, an amine of formula 12 is reacted with
alkylating agents of general formula X--CR.sup.6R.sup.7--R.sup.2
(8) where X is a leaving group such as C.sub.1, Br, I, or
OSO.sub.2CH.sub.3, leading to compounds of formula (I), wherein W
is --CR.sup.6R.sup.7--. This reaction is performed in a solvent
such as tetrahydrofuran or N,N-dimethylformamide, in the presence
of a base, e. g., triethylamine or potassium carbonate, at
temperatures between 0.degree. C. and 100.degree. C.
[0227] Alternatively, an amine of formula 12 is reacted with
aldehydes or ketones of general formula R.sup.6--C(O)--R.sup.2 (9)
in a reductive amination reaction, leading to compounds of formula
(I) wherein W is --CR.sup.6R.sup.7--, R.sup.6 is hydrogen, alkyl or
cycloalkyl, and R.sup.7 is H. This reaction is performed in the
presence of a suitable reducing agent, e. g. sodium borohydride or
sodium triacetoxyborohydride, in a solvent such as methanol, acetic
acid, tetrahydrofuran, 1,2-dichloroethane or mixtures thereof, at
temperatures between 0.degree. C. and 50.degree. C.
[0228] Alternatively, amine 12 is reacted with a suitable
carboxylic acid of formula R.sup.2--COOH (10), leading to compounds
of formula (I) wherein W is --C(O)--. The reaction is performed in
the presence of a coupling agent such as 1,1'-carbonyldiimidazole,
N,N'-dicyclohexylcarbodiimide,
1-(3-dimethylaminopropyl)-3-ethyl-carbodiimide hydrochloride,
0-(benzotriazol-1-yl)-N,N,N',N'-tetramethyluronium
hexafluoro-phosphate,
O-(7-azabenzotriazol-1-yl)-N,N,N',N'-tetramethyluronium
hexafluoro-phosphate or bromo-tris-pyrrolidino-phosphonium
hexafluorophosphate, in aprotic solvents such as dichloromethane,
tetrahydrofuran, N,N-dimethylformamide, N-methylpyrrolidinone and
mixtures thereof at temperatures between
-40.degree. C. and 80.degree. C. in the presence or absence of a
base such as triethylamine, diisopropylethylamine,
4-methylmorpholine and/or 4-(dimethylamino)pyridine.
[0229] Alternatively, amine 12 is reacted with a suitable sulfonyl
chloride of formula R.sup.2--SO.sub.2C.sub.1 (11), leading to (I)
wherein W is --S(O.sub.2)--. The reaction is performed in a
suitable solvent such as dichloromethane, tetrahydrofuran,
N,N-dimethylformamide, acetonitrile, acetone, water, or mixtures
thereof, in the presence of a base, e. g. triethylamine,
diisopropylethylamine, pyridine, potassium hydrogencarbonate,
potassium carbonate, at temperatures between 0.degree. C. and the
boiling point of the solvent or solvent mixture.
[0230] Amines 12 can be synthesised from their tert-butyl carbamate
derivatives of formula 13 by carbamate deprotection. The
deprotection may be performed in the presence of a suitable acid,
e. g., hydrochloric acid or trifluoroacetic acid, in a solvent such
as water, 2-propanol, dichloromethane, or 1,4-dioxane, at
temperatures between 0.degree. C. and 30.degree. C.
##STR00010##
[0231] tert-Butyl carbamates 13 can be synthesised from amine
precursors of formula 14 and appropriate reagents, using methods
well known in the art.
##STR00011##
[0232] For instance, amine 14 is reacted with a suitable carboxylic
acid of formula R.sup.1--COOH (2) leading to compounds of formula
13, wherein Y is --C(O)--. The reaction is performed in the
presence of a coupling agent such as 1,1'-carbonyldiimidazole,
N,N'-dicyclohexylcarbodiimide,
1-(3-dimethylaminopropyl)-3-ethyl-carbodiimide hydrochloride,
O-(benzotriazol-1-yl)-N,N,N',N'-tetramethyluronium
hexafluoro-phosphate,
O-(7-azabenzotriazol-1-yl)-N,N,N',N'-tetramethyluronium
hexafluoro-phosphate or bromo-tris-pyrrolidino-phosphonium
hexafluorophosphate, in aprotic solvents such as dichloromethane,
tetrahydrofuran, N,N-dimethylformamide, N-methylpyrrolidinone and
mixtures thereof at temperatures between -40.degree. C. and
80.degree. C. in the presence or absence of a base such as
triethylamine, diisopropylethylamine, 4-methylmorpholine and/or
4-(dimethylamino)pyridine.
[0233] Amine 14 can also be reacted with suitable acylating
reagents, such as acyl chlorides of formula R.sup.1--COCl (3) to
provide compounds of formula 13, wherein Y is --C(O)--. The
reaction is performed in a solvent such as dichloromethane,
tetrahydrofuran, or N,N-dimethylformamide, in the presence of a
base such as triethylamine or 4-methylmorpholine, at temperatures
between 0.degree. C. and 80.degree. C.
[0234] Alternatively, amine 14 is reacted with a suitable
chloroformate ester of formula R.sup.1--O--C(O)--C.sub.1 (4), or
with an imidazole-1-carboxylate ester of formula 5, leading to a
compound of formula 13, wherein Y is --OC(O)--. The reaction is
performed in a suitable solvent such as dichloromethane,
tetrahydrofuran, N,N-dimethylformamide, acetonitrile, acetone,
water, or mixtures thereof, in the presence of a base, e. g.,
triethylamine, diisopropylethylamine, pyridine, potassium
hydrogencarbonate, potassium carbonate, at temperatures between
0.degree. C. and the boiling point of the solvent or solvent
mixture.
[0235] Alternatively, amine 14 can be reacted with a phosgene or a
phosgene equivalent (e. g., triphosgene) to the corresponding
N-chlorocarbonylamine 14A, in the presence of a base (e. g.,
pyridine) in a suitable solvent, e. g., dichloromethane, at
temperatures between -78.degree. C. and +20.degree. C.
N-Chlorocarbonylamine 14A is then reacted with alcohol of formula
R.sup.1--OH, leading to a compound of formula 13, wherein Y is
--OC(O)--. This reaction is performed in a suitable solvent (e. g.,
acetonitrile of dichloromethane) in the presence of a suitable base
(e. g., sodium hydride, pyridine or polystyrene-bound
2-tert-butylimino-2-diethylamino-1,3-dimethylperhydro-1,3,2-diazaphosphor-
ine), at temperatures between 20.degree. C. and the boiling point
of the solvent.
##STR00012##
[0236] Amines of formula 14 are commercially available or can be
produced as described herein or in the literature.
[0237] Also an embodiment of the present invention is a process to
prepare a compound of formula (I) as defined above comprising the
reaction of a compound of formula (II) in the presence of a
compound of formula (III);
##STR00013##
[0238] wherein R.sup.1, R.sup.2, m, n, p and q are as defined above
and W is --C(O)--.
[0239] In particular, in the presence of a coupling agent such as
1,1'-carbonyldiimidazole, N,N'-dicyclohexylcarbodiimide,
1-(3-dimethylaminopropyl)-3-ethyl-carbodiimide hydrochloride,
0-(benzotriazol-1-yl)-N,N,N',N'-tetramethyluronium
hexafluoro-phosphate,
O-(7-azabenzotriazol-1-yl)-N,N,N',N'-tetramethyluronium
hexafluoro-phosphate or bromo-tris-pyrrolidino-phosphonium
hexafluorophosphate, particularly
O-(7-azabenzotriazol-1-yl)-N,N,N',N'-tetramethyluronium
hexafluoro-phosphate, in an aprotic solvent such as
dichloromethane, tetrahydrofuran, N,N-dimethylformamide,
N-methylpyrrolidinone and mixtures thereof, particularly
N,N-dimethylformamide, in the presence or absence of a base such as
triethylamine, diisopropylethylamine, 4-methylmorpholine and/or
4-(dimethylamino)pyridine, particularly in the presence of
4-methylmorpholine and at a temperature comprised between
-78.degree. C. and reflux, particularly between -10.degree. C. and
room temperature.
[0240] Also an object of the present invention is a compound
according to formula (I) as described herein for use as a
therapeutically active substance.
[0241] Likewise an object of the present invention is a
pharmaceutical composition comprising a compound according to
formula (I) as described herein and a therapeutically inert
carrier.
[0242] A particular embodiment of the present invention is a
compound according to formula (I) as described herein for the
treatment or prophylaxis of ocular conditions, particularly
glaucoma.
[0243] The present invention also relates to the use of a compound
according to formula (I) as described herein for the preparation of
a medicament for the treatment or prophylaxis of ocular conditions,
particularly glaucoma.
[0244] Also an object of the invention is a method for the
treatment or prophylaxis of ocular conditions, particularly
glaucoma, which method comprises administering an effective amount
of a compound according to formula (I) as described herein.
[0245] Inflammatory conditions include, but are not limited to,
arthritis, osteoarthritis, multiple sclerosis, systemic lupus
erythematodes, inflammatory bowel disease, abnormal evacuation
disorder and the like as well as inflammatory airways diseases such
as idiopathic pulmonary fibrosis (IPF), chronic obstructive
pulmonary disease (COPD) or chronic asthma bronchiale.
[0246] Further conditions of the respiratory system include, but
are not limited to, other diffuse parenchymal lung diseases of
different etiologies including iatrogenic drug-induced fibrosis,
occupational and/or environmental induced fibrosis, systemic
diseases and vasculitides, granulomatous diseases (sarcoidosis,
hypersensitivity pneumonia), collagen vascular disease, alveolar
proteinosis, Langerhans cell granulomatosis,
lymphangioleiomyomatosis, inherited diseases (Hermansky-Pudlak
Syndrome, tuberous sclerosis, neurofibromatosis, metabolic storage
disorders, familial interstitial lung disease), radiation induced
fibrosis, silicosis, asbestos induced pulmonary fibrosis or acute
respiratory distress syndrome (ARDS).
[0247] Conditions of the nervous system include, but are not
limited to, neuropathic pain, schizophrenia, neuro-inflammation
(e.g. astrogliosis), peripheral and/or autonomic (diabetic)
neuropathies and the like.
[0248] Vascular conditions include, but are not limited to,
atherosclerosis, thrombotic vascular disease as well as thrombotic
microangiopathies, proliferative arteriopathy (such as swollen
myointimal cells surrounded by mucinous extracellular matrix and
nodular thickening), atherosclerosis, decreased vascular compliance
(such as stiffness, reduced ventricular compliance and reduced
vascular compliance), endothelial dysfunction and the like.
[0249] Cardiovascular conditions include, but are not limited to,
acute coronary syndrome, coronary heart disease, myocardial
infarction, arterial and pulmonary hypertension, cardiac arrhythmia
such as atrial fibrillation, stroke and other vascular damage.
[0250] Fibrotic diseases include, but are not limited to myocardial
and vascular fibrosis, pulmonary fibrosis, skin fibrosis,
scleroderma and encapsulating peritonitis.
[0251] Cancer and cancer metastasis include, but are not limited
to, breast cancer, ovarian cancer, lung cancer, prostate cancer,
mesothelioma, glioma, gastrointestinal cancers and progression and
metastatic aggressiveness thereof.
[0252] Ocular conditions include, but are not limited to,
proliferative and non-proliferative (diabetic) retinopathy, dry and
wet age-related macular degeneration (AMD), macular edema, central
arterial/venous occlusion, traumatic injury, glaucoma and the like.
Particularly, the ocular condition is glaucoma.
[0253] Metabolic conditions include, but are not limited to,
obesity and diabetes.
[0254] Also an embodiment of the present invention are compounds of
formula (I) as described herein, when manufactured according to any
one of the described processes.
Assay Procedures
[0255] Production of Human Full Length ATX, with and without His
Tag
[0256] Autotaxin (ATX-ENPP2) Cloning:
[0257] cDNA was prepared from commercial human hematopoietic cells
total RNA and used as template in overlapping PCR to generate a
full length human ENPP2 ORF with or without a 3'-6.times.His tag.
These full length inserts were cloned into the pcDNA3.1V5-His TOPO
(Invitrogen) vector. The DNA sequences of several single clones
were verified. The DNA from a correct full length clone was used to
transfect Hek293 cells for verification of protein expression. The
sequence of the encoded ENPP2 conforms to Swissprot entry Q13822,
with or without the additional C-terminal 6.times.His tag.
[0258] ATX Fermentation:
[0259] Recombinant protein was produced by large-scale transient
transfection in 20 L controlled stirred tank bioreactors
(Sartorius). During cell growth and transfection, temperature,
stirrer speed, pH and dissolved oxygen concentration were
maintained at 37.degree. C., 120 rpm, 7.1 and 30% DO, respectively.
FreeStyle 293-F cells (Invitrogen) were cultivated in suspension in
FreeStyle 293 medium (Invitrogen) and transfected at ca.
1-1.5.times.10E6 cells/mL with above plasmid DNAs using X-tremeGENE
Ro-1539 (commercial product, Roche Diagnostics) as complexing
agent. Cells were fed a concentrated nutrient solution (J Immunol
Methods 194 (1996), 19, 1-199 (page 193)) and induced by sodium
butyrate (2 mM) at 72 h post-transfection and harvested at 96 h
post-transfection. Expression was analyzed by Western Blot,
enzymatic assay and/or analytical IMAC chromatography. After
cooling the cell suspension to 4.degree. C. in a flow-through heat
exchanger, cell separation and sterile filtration of supernatant
was performed by filtration through Zeta Plus 60M02 E16 (Cuno) and
Sartopore 2 XLG (Sartorius) filter units. The supernatant was
stored at 4.degree. C. prior to purification.
[0260] ATX Purification:
[0261] 20 liter of culture supernatant were conditioned for
ultrafiltration by adding Brij 35 to a final concentration of 0.02%
and by adjusting the pH to 7.0 using 1 M HCl. Then the supernatant
was first microfiltred through a 0.2 Dm Ultran-Pilot Open Channel
PES filter (Whatman) and afterwards concentrated to 1 liter through
an Ultran-Pilot Screen Channel PES filter with 30 kDa MWCO
(Whatman). Prior to IMAC chromatography, NiSO.sub.4 was added to a
final concentration of 1 mM. The cleared supernatant was then
applied to a HisTrap column (GE Healthcare) previously equilibrated
in 50 mM Na.sub.2HPO.sub.4 pH 7.0, 0.5 M NaCl, 10% glycerol, 0.3%
CHAPS, 0.02% NaN.sub.3. The column was washed stepwise with the
same buffer containing 20 mM, 40 mM and 50 mM imidazole,
respectively. The protein was subsequently eluted using a linear
gradient to 0.5 M imidazole in 15 column volumes. ATX containing
fractions were pooled and concentrated using an Amicon cell
equipped with a 30 kDa PES filter membrane. The protein was further
purified by size exclusion chromatography on Superdex S-200 prep
grade (XK 26/100) (GE Healthcare) in 20 mM BICINE pH 8.5, 0.15 M
NaCl, 10% glycerol, 0.3% CHAPS, 0.02% NaN.sub.3. Final yield of
protein after purification was 5-10 mg ATX per liter of culture
supernatant. The protein was stored at -80.degree. C.
Human ATX Enzyme Inhibition Assay
[0262] ATX inhibition was measured by a fluorescence quenching
assay using a specifically labeled substrate analogue (MR121
substrate). To obtain this MR121 substrate, BOC and TBS protected
6-amino-hexanoic acid
(R)-3-({2-[3-(2-{2-[2-(2-amino-ethoxy)-ethoxy]-ethoxy}-ethoxy)-propionyla-
mino]-ethoxy}-hydroxy-phosphoryloxy)-2-hydroxy-propyl ester
(Ferguson et al., Org Lett 2006, 8 (10), 2023) was labeled with
MR121 fluorophore (CAS
185308-24-1,1-(3-carboxypropyl)-11-ethyl-1,2,3,4,8,9,10,11-octahydro-dipy-
rido[3,2-b:2',3'-i]phenoxazin-13-ium) on the free amine of the
ethanolamine side and then, after deprotection, subsequently with
tryptophan on the side of the aminohexanoic acid.
[0263] Assay working solutions were made as follows:
Assay buffer (50 mM Tris-HCl, 140 mM NaCl, 5 mM KCl, 1 mM
CaCl.sub.2, 1 mM MgCl.sub.2, 0.01% Triton-X-100, pH 8.0; ATX
solution: ATX (human His-tagged) stock solution (1.08 mg/mL in 20
mM bicine, pH 8.5, 0.15 M NaCl, 10% glycerol, 0.3% CHAPS, 0.02%
NaN.sub.3), diluted to 1.4-2.5.times. final concentration in assay
buffer; MR121 substrate solution: MR121 substrate stock solution
(800 .mu.M MR121 substrate in DMSO), diluted to 2-5.times. final
concentration in assay buffer.
[0264] Test compounds (10 mM stock in DMSO, 8 .mu.L) were obtained
in 384 well sample plates (Corning Costar #3655) and diluted with 8
.mu.L DMSO. Row-wise serial dilutions were made by transferring 8
.mu.L cpd solution to the next row up to row O. The compound and
control solutions were mixed five times and 2 .mu.L were
transferred to 384 well assay plates (Corning Costar #3702). Then,
15 .mu.L of 41.7 nM ATX solution was added (30 nM final
concentration), mixed five times and then incubated for 15 minutes
at 30.degree. C. 10 .mu.L of MR121 substrate solution was added (1
.mu.M final concentration), mixed 30 times and then incubated for
15 minutes at 30.degree. C. Fluorescence was then measured every 2
minutes for 1 hour (Perkin Elmer plate: vision multimode reader);
light intensity: 2.5%; exp. time: 1.4 sec, Filter: Fluo_630/690 nm)
and IC.sub.50 values were calculated from these readouts.
Human Carbonic Anhydrase-II Inhibition Assay
[0265] Human carbonic anhydrase II (hCA-II) inhibition was measured
by an absorbance method using 4-nitrophenyl acetate (4-NPA) as its
substrate. 4-NPA can be catalyzed by active hCA II via a
zinc-hydroxide mechanism. The nitrophenolate in the products can be
ionized to generate a bright yellow anion with high absorbance at
348 to 400 nm, as reported in the literature (Armstrong et al., J.
Biol. Chem. 1966, 241, 5137-5149). OD340 nm was chosen for
detecting hCA II substrate conversion.
Assay working solutions were made as follows: Assay buffer: 50 mM
MOPS, 33 mM Na.sub.2SO.sub.4, 1 mM EDTA, 0.5 mg/ml BSA, pH 7.5;
Enzyme solution: hCA-II (human, full length) stock solution (1.0
mg/mL in 20 mM HEPES, 50 mM NaCl, pH 7.4), diluted to 2133.times.
final concentration in assay buffer; 4-NPA substrate solution:
4-NPA substrate stock solution (250 mM in DMSO, stored at
-20.degree. C.), diluted to 50.times. final concentration in
deionized water.
[0266] Test compounds (10 mM stock in DMSO, 100 .mu.L) were
obtained in 96-well sample plates (Corning Costar #3655) and
diluted to 0.5 mM. Column-wise serial dilutions were made by
transferring 20 .mu.L compound solutions to the next column, from
column 3 up to 22. After this, 1.2 .mu.L were transferred to 384
well assay plates (Corning Costar #3701). Then 30 .mu.L of 16 nM
hCA II solution was added (8 nM final concentration), mixed five
times. 30 .mu.L of 4-NPA substrate solution was added (2.5 mM final
concentration), mixed five times. Absorbance at 340 nm was then
measured immediately as time zero. The assay plates were incubated
at room temperature for 1 hour and then measured as time 1 hour
(Perkin Elmer EnVision 2103; Filter: Photometric 340; Light
intensity 60%; Number of flashes: 10). IC.sub.50 values and K.sub.i
values were calculated from these readouts.
TABLE-US-00001 Ex ATX IC50 (.mu.M) CA-II IC50 (.mu.M) 1.00 0.006
0.014 1.01 0.01 0.007 1.02 0.005 0.010 1.03 0.005 0.009 1.04 0.004
0.005 1.05 0.007 0.011 1.06 0.005 0.010 1.07 0.012 0.018 1.08 0.008
0.006 1.09 0.027 0.010 1.10 0.008 0.019 1.11 0.009 0.027 1.12 0.006
0.0129 1.13 0.002 0.0206 1.14 0.015 0.0166 1.15 0.008 0.0129 1.16
0.009 0.0102 1.17 0.011 0.004 1.18 0.002 0.001 1.19 0.01 0.004 1.20
0.015 0.002 1.21 0.012 0.003 1.22 0.006 0.002 1.23 0.01 0.001 1.24
0.003 0.007 1.25 0.003 0.008 1.26 0.003 0.003 1.27 0.008 0.018 1.28
0.001 2.00 0.001 0.024 2.01 0.014 0.018 2.02 0.003 0.008 2.03 0.002
0.006 3.00 0.005 0.009 3.01 0.005 0.012 3.02 0.006 0.005 3.06 0.002
0.016 3.03 0.004 0.017 3.07 0.004 0.005 3.04 0.007 0.017 3.08 0.001
0.006 3.05 0.004 0.009 3.09 0.001 0.011 1.29 0.011 0.0012 1.30 0.01
0.0042 1.31 0.01 0.0115 1.32 0.005 0.0025 1.33 0.001 0.0023 1.34
0.012 0.001 2.04 0.012 0.0019 3.10 0.002 0.005 4.00 0.01 0.0038
4.01 0.003 0.0036 5.00 0.007 0.0176
[0267] Compounds of formula (I) and their pharmaceutically
acceptable salts or esters thereof as described herein have
IC.sub.50 values between 0.00001 .mu.M and 1000 .mu.M, particular
compounds have IC.sub.50 values between 0.0005 .mu.M and 500 .mu.M,
further particular compounds have IC.sub.50 values between 0.0005
.mu.M and 50 .mu.M, more particular compounds have IC.sub.50 values
between 0.0005 .mu.M and 5 .mu.M. These results have been obtained
by using the enzymatic assay described above.
[0268] The compounds of formula (I) and their pharmaceutically
acceptable salts can be used as medicaments (e.g. in the form of
pharmaceutical preparations). The pharmaceutical preparations can
be administered internally, such as orally (e.g. in the form of
tablets, coated tablets, dragees, hard and soft gelatin capsules,
solutions, emulsions or suspensions), nasally (e.g. in the form of
nasal sprays), rectally (e.g. in the form of suppositories) or
topical ocularly (e.g. in the form of solutions, ointments, gels or
water soluble polymeric inserts). However, the administration can
also be effected parenterally, such as intramuscularly,
intravenously, or intraocularly (e.g. in the form of sterile
injection solutions).
[0269] The compounds of formula (I) and their pharmaceutically
acceptable salts can be processed with pharmaceutically inert,
inorganic or organic adjuvants for the production of tablets,
coated tablets, dragees, hard gelatin capsules, injection solutions
or topical formulations Lactose, corn starch or derivatives
thereof, talc, stearic acid or its salts etc. can be used, for
example, as such adjuvants for tablets, dragees and hard gelatin
capsules.
[0270] Suitable adjuvants for soft gelatin capsules, are, for
example, vegetable oils, waxes, fats, semi-solid substances and
liquid polyols, etc.
[0271] Suitable adjuvants for the production of solutions and
syrups are, for example, water, polyols, saccharose, invert sugar,
glucose, etc.
[0272] Suitable adjuvants for injection solutions are, for example,
water, alcohols, polyols, glycerol, vegetable oils, etc.
[0273] Suitable adjuvants for suppositories are, for example,
natural or hardened oils, waxes, fats, semi-solid or liquid
polyols, etc.
[0274] Suitable adjuvants for topical ocular formulations are, for
example, cyclodextrins, mannitol or many other carriers and
excipients known in the art.
[0275] Moreover, the pharmaceutical preparations can contain
preservatives, solubilizers, viscosity-increasing substances,
stabilizers, wetting agents, emulsifiers, sweeteners, colorants,
flavorants, salts for varying the osmotic pressure, buffers,
masking agents or antioxidants. They can also contain still other
therapeutically valuable substances.
[0276] The dosage can vary in wide limits and will, of course, be
fitted to the individual requirements in each particular case. In
general, in the case of oral administration a daily dosage of about
0.1 mg to 20 mg per kg body weight, preferably about 0.5 mg to 4 mg
per kg body weight (e.g. about 300 mg per person), divided into
preferably 1-3 individual doses, which can consist, for example, of
the same amounts, should it be appropriate. In the case of topical
administration, the formulation can contain 0.001% to 15% by weight
of medicament and the required dose, which can be between 0.1 and
25 mg in can be administered either by single dose per day or per
week, or by multiple doses (2 to 4) per day, or by multiple doses
per week It will, however, be clear that the upper or lower limit
given herein can be exceeded when this is shown to be
indicated.
[0277] The invention is illustrated hereinafter by Examples, which
have no limiting character.
[0278] In case the preparative examples are obtained as a mixture
of enantiomers, the pure enantiomers can be obtained by methods
described herein or by methods known to those skilled in the art,
such as e.g. chiral chromatography or crystallization.
EXAMPLES
[0279] All examples and intermediates were prepared under nitrogen
atmosphere if not specified otherwise.
[0280] Abbreviations: aq.=aqueous; CAS-RN=Chemical Abstracts
Service Registry Number; HPLC=high performance liquid
chromatography; MS=mass spectrum; sat.=saturated
Example 1
[3-(2,2-Dimethylpropanoylamino)-5-(trifluoromethyl)pyridin-2-yl]methyl
2-(4-sulfamoylbenzoyl)-1,3,4,6-tetrahydropyrrolo[3,4-c]pyrrole-5-carboxyl-
ate
##STR00014##
[0282] To a solution of
(3-pivalamido-5-(trifluoromethyl)pyridin-2-yl)methyl
3,4,5,6-tetrahydropyrrolo[3,4-c]pyrrole-2(1H)-carboxylate
dihydrochloride (intermediate 4; 50 mg, 92.7 .mu.mol),
4-methylmorpholine (46.9 mg, 464 .mu.mol) and 4-sulfamoylbenzoic
acid (CAS-RN 138-41-0; 19.4 mg, 92.7 .mu.mol) in
N,N-dimethylformamide (3 mL) was added
O-(7-azabenzotriazol-1-yl)-N,N,N',N'-tetramethyluronium
hexafluoro-phosphate (35.3 mg, 92.7 .mu.mol). The clear dark brown
solution was stirred at room temperature for 18 h, then partitioned
between sat. aq. sodium hydrogen carbonate solution and ethyl
acetate/2-methyltetrahydrofuran 4:1. The organic layer was washed
with sat. aq. ammonium chloride solution and brine, dried over
magnesium sulfate, filtered and evaporated. Chromatography (silica
gel; gradient dichloromethane to dichloromethane/methanol/25% aq.
ammonia solution 90:10:0.25) afforded the title compound (41 mg,
74%). Light yellow foam, MS: 596.2 (M+H).sup.+.
[0283] The following examples were produced in analogy to example
1, replacing (3-pivalamido-5-(trifluoromethyl)pyridin-2-yl)methyl
3,4,5,6-tetrahydropyrrolo[3,4-c]pyrrole-2(1H)-carboxylate
dihydrochloride (intermediate 4) by the appropriate amine and and
4-sulfamoylbenzoic acid by the appropriate carboxylic acid.
TABLE-US-00002 Ex. Systematic Name Amine/Carboxylic acid MS, m/e
1.01 ##STR00015## (3-pivalamido-5-
(trifluoromethyl)pyridin-2-yl)methyl 3,4,5,6-tetrahydropyrrolo[3,4-
c]pyrrole-2(1H)-carboxylate hydrochloride (intermediate
4)/2,5-difluoro-4- sulfamoylbenzoic acid (intermediate 7) 632.2 (M
+ H).sup.+ 1.02 ##STR00016## (3-pivalamido-5-
(trifluoromethyl)pyridin-2-yl)methyl 3,4,5,6-tetrahydropyrrolo[3,4-
c]pyrrole-2(1H)-carboxylate dihydrochloride (intermediate 4)/3-
chloro-4-sulfamoylbenzoic acid (CAS-RN 62971-72-6) 630.1 (M +
H).sup.+ 1.03 ##STR00017## (3-pivalmido-5-
(trifluoromethyl)pyridin-2-yl)methyl 3,4,5,6-tetrahydropyrrolo[3,4-
c]pyrrole-2(1H)-carboxylate dihydrochloride (intermediate 4)/3-
fluoro-4-sulfamoylbenzoic acid (CAS-RN 244606-37-9) 614.2 (M +
H).sup.+ 1.04 ##STR00018## (3-pivalamido-5-
(trifluoromethyl)pyridin-2-yl)methyl 3,4,5,6-tetrahydropyrrolo[3,4-
c]pyrrole-2(1H)-carboxylate dihydrochloride (intermediate 4)/2-
fluoro-4-sulfamoylbenzoic acid (CAS-RN 714968-42-0) 614.2 (M +
H).sup.+ 1.05 ##STR00019## (3-pivalamido-5-
(trifluoromethyl)pyridin-2-yl)methyl 3,4,5,6-tetrahydropyrrolo[3,4-
c]pyrrole-2(1H)-carboxylate dihydrochloride (intermediate 4)/5-
sulfamoylpicolinic acid (CAS-RN 1308677-67-9) 597.2 (M + H).sup.+
1.06 ##STR00020## 4-(trifluoromethoxy)benzyl 3,4,5,6-
tetrahydropyrrolo[3,4-c]pyrrole- 2(1H)-carboxylate hydrochloride
(intermediate 1)/4-sulfamoylbenzoic acid (CAS-RN 138-41-0) 510.2 (M
- H).sup.- 1.07 ##STR00021## [2-cyclopropyl-6-(oxan-4-
ylmethoxy)pyridin-4-yl]-(2,3,4,6-
tetrahydro-1H-pyrrolo[3,4-c]pyrrol-5- yl)methanone (intermediate
2)/5- sulfamoylpicolinic acid (CAS-RN 1308677-67-9) 552.3 (M -
H).sup.- 1.08 ##STR00022## [2-cyclopropyl-6-(oxan-4-
ylmethoxy)pyridin-4-yl]-(2,3,4,6-
tetrahydro-1H-pyrrolo[3,4-c]pyrrol-5- yl)methanone (intermediate
2)/2- fluoro-4-sulfamoylbenzoic acid (CAS-RN 714968-42-0) 569.3 (M
- H).sup.- 1.09 ##STR00023## (3-pivalamido-5-
(trifluoromethyl)pyridin-2-yl)methyl 3,4,5,6-tetrahydropyrrolo[3,4-
c]pyrrole-2(1H)-carboxylate hydrochloride (intermediate 4)/2,3-
difluoro-4-sulfamoylbenzoic acid (intermediate 7.01) 632.2 (M +
H).sup.+ 1.10 ##STR00024## 3-[2-[(5-methyltetrazol-2-yl)methyl]-
4-(trifluoromethyl)phenyl]-1-(2,3,4,6-
tetrahydro-1H-pyrrolo[3,4-c]pyrrol-5- yl)propan-1-one (intermediate
3)/2- fluoro-4-sulfamoylbenzoic acid (CAS-RN 714968-42-0) 608.2 (M
+ H).sup.+ 1.11 ##STR00025## (3-pivalamido-5-
(trifluoromethyl)pyridin-2-yl)methyl 3,4,5,6-tetrahydropyrrolo[3,4-
c]pyrrole-2(1H)-carboxylate hydrochloride (intermediate 4)/2,6-
difluoro-4-sulfamoylbenzoic acid (intermediate 7.02) 632.2 (M +
H).sup.+ 1.12 ##STR00026## (5-chloro-3-pivalamidopyridin-2-
yl)methyl 3,4,5,6- tetrahydropyrrolo[3,4-c]pyrrole-
2(1H)-carboxylate dihydrochloride (intermediate 4.02/
2-fluoro-4-sulfamoylbenzoic acid (CAS-RN 714968-42-0) 580.2 (M +
H).sup.+ 1.13 ##STR00027## (5-chloro-3-pivalamidopyridin-2-
yl)methyl 3,4,5,6- tetrahydropyrrolo[3,4-c]pyrrole-
2(1H)-carboxylate dihydrochloride (intermediate 4.02)/3-fluoro-4-
sulfamoylbenzoic acid (CAS-RN 244606-37-9) 580.2 (M + H).sup.+ 1.14
##STR00028## (5-chloro-3-pivalamidopyridin-2- yl)methyl 3,4,5,6-
tetrahydropyrrolo[3,4-c]pyrrole- 2(1H)-carboxylate dihydrochloride
(intermediate 4.02)/2,3-difluoro-4- sulfamoylbenzoic acid
(intermediate 7.01) 598.3 (M + H).sup.+ 1.15 ##STR00029##
(5-chloro-3-pivalamidopyridin-2- yl)methyl 3,4,5,6-
tetrahydropyrrolo[3,4-c]pyrrole- 2(1H)-carboxylate dihydrochloride
(intermediate 4.02)/2,6-difluoro-4- sulfamoylbenzoic acid
(intermediate 7.02) 598.3 (M + H).sup.+ 1.16 ##STR00030##
(5-chloro-3-pivalamidopyridin-2- yl)methyl 3,4,5,6-
tetrahydropyrrolo[3,4-c]pyrrole- 2(1H)-carboxylate dihydrochloride
(intermediate 4.02)/2,5-difluoro-4- sulfamoylbenzoic acid
(intermeidate 7) 598.3 (M + H).sup.+ 1.17 ##STR00031##
(6-methyl-3-pivalamidopyridin-2- yl)methyl 3,4,5,6-
tetrahydropyrrolo[3,4-c]pyrrole- 2(1H)-carboxylate dihydrochloride
(intermediate 4.07)/2-fluoro-4- sulfamoylbenzoic acid (CAS-RN
714968-42-0) 560.4 (M + H).sup.+ 1.18 ##STR00032##
(6-chloro-3-pivalamidopyridin-2- yl)methyl 3,4,5,6-
tetrahydropyrrolo[3,4-c]pyrrole- 2(1H)-carboxylate hydrochloride
(intermediate 4.04)/2-fluoro-4- sulfamoylbenzoic acid (CAS-RN
714968-42-0) 580.3 (M + H).sup.+ 1.19 ##STR00033##
(3-pivalamidopyridin-2-yl)methyl 3,4,5,6-tetrahydropyrrolo[3,4-
c]pyrrole-2(1H)-carboxylate hydrochloride (intermediate 4.05)/2-
fluoro-4-sulfamoylbenzoic acid (CAS-RN 714968-42-0) 544.4 (M -
H).sup.- 1.20 ##STR00034## (6-chloro-3-pivalamidopyridin-2-
yl)methyl 3,4,5,6- tetrahydropyrrolo[3,4-c]pyrrole-
2(1H)-carboxylate hydrochloride (intermediate 4.04)/2,5-difluoro-4-
sulfamoylbenzoic acid/(intermediate 7) 598.3 (M + H).sup.+ 1.21
##STR00035## (6-chloro-3-pivalamidopyridin-2- yl)methyl 3,4,5,6-
tetrahydropyrrolo[3,4-c]pyrrole- 2(1H)-carboxylate hydrochloride
(intermediate 4.04)/3-fluoro-4- sulfamoylbenzoic acid (CAS-RN
244606-37-9) 580.3 (M + H).sup.+ 1.22 ##STR00036##
(6-chloro-3-pivalamidopyridin-2- yl)methyl 3,4,5,6-
tetrahydropyrrolo[3,4-c]pyrrole- 2(1H)-carboxylate hydrochloride
(intermediate 4.04)/2,3-difluoro-4- sulfamoylbenzoic acid
(intermediate 7.01) 598.3 (M + H).sup.+ 1.23 ##STR00037##
(6-chloro-3-pivalamidopyridin-2- yl)methyl 3,4,5,6-
tetrahydropyrrolo[3,4-c]pyrrole- 2(1H)-carboxylate hydrochloride
(intermediate 4.04)/2,6-difluoro-4- sulfamoylbenzoic acid
(intermediate 7.02) 598.3 (M + H).sup.+ 1.24 ##STR00038##
(5-cyano-3-pivalamidopyridin-2- yl)methyl 3,4,5,6-
tetrahydropyrrolo[3,4-c]pyrrole- 2(1H)-carboxylate dihydrochloride
(intermediate 4.06)/2-fluoro-4- sulfamoylbenzoic acid (CAS-RN
714968-42-0) 571.5 (M + H).sup.+ 1.25 ##STR00039##
(5-cyano-3-pivalamidopyridin-2- yl)methyl 3,4,5,6-
tetrahydropyrrolo[3,4-c]pyrrole- 2(1H)-carboxylate dihydrochloride
(intermediate 4.06)/2,6-difluoro-4- sulfamoylbenzoic acid
(intermediate 7.02) 589.3 (M + H).sup.+ 1.26 ##STR00040##
(5-cyano-3-pivalamidopyridin-2- yl)methyl 3,4,5,6-
tetrahydropyrrolo[3,4-c]pyrrole- 2(1H)-carboxylate dihydrochloride
(intermediate 4.06)/2,3-difluoro-4- sulfamoylbenzoic acid
(intermediate 7.01) 589.3 (M + H).sup.+ 1.27 ##STR00041##
(5-cyano-3-pivalamidopyridin-2- yl)methyl 3,4,5,6-
tetrahydropyrrolo[3,4-c]pyrrole- 2(1H)-carboxylate dihydrochloride
(intermeidate 4.06)/2,5-difluoro-4- sulfamoylbenzoic acid
(intermediate 7) 589.3 (M + H).sup.+ 1.28 ##STR00042##
(3-pivalamido-5- (trifluoromethyl)pyridin-2-yl)methyl
3,4,5,6,7,8-hexahydro-2,6- naphthyridine-2(1H)-carboxylate
hydrochloride (intermediate 4.01)/2- fluoro-4-sulfamoylbenzoic acid
(CAS-RN 714968-42-0) 642.3 (M + H).sup.+ 1.29 ##STR00043##
[5,6-dichloro-3-(2,2- dimethylpropanoylamino)pyridin-2- yl]methyl
2,3,4,6-tetrahydro-1H- pyrrolo[3,4-c]pyrrole-5-carboxylate
hydrochloride (intermediate 4.03)/2- fluoro-4-sulfamoylbenzoic acid
(CAS-RN 71468-42-0) 614.2 (M + H).sup.+ 1.30 ##STR00044##
[5,6-dichloro-3-(2,2- dimethylpropanoylamino)pyridin-2- yl]methyl
2,3,4,6-tetrahydro-1H- pyrrolo[3,4-c]pyrrole-5-carboxylate
hydrochloride (intermeidate 4.03)/ 2,3-difluoro-4-sulfamoylbenzoic
acid (intermeidate 7.01) 630.3 (M - H).sup.- 1.31 ##STR00045##
[5,6-dichloro-3-(2,2- dimethylpropanoylamino)pyridin-2- yl]methyl
2,3,4,6-tetrahydro-1H- pyrrolo[3,4-c]pyrrole-5-carboxylate
hydrochloride (intermediate 4.03)/ 2,6-difluoro-4-sulfamoylbenzoic
acid (intermediate 7.02) 632.2 (M + H).sup.+ 1.32 ##STR00046##
(3-pivalamido-5- (trifluoromethyl)pyridin-2-yl)methyl
3,4,5,6-tetrahydropyrrolo[3,4- c]pyrrole-2(1H)-carboxylate
hydrochloride (intermediate 4)/3- fluoro-5-sulfamoylpyridine-2-
carboxylic acid (intermediate 11) 615.2 (M + H).sup.+ 1.33
##STR00047## [2-Cyclopropyl-6-(oxan-4-
ylmethoxy)pyridin-4-yl]-(2,3,4,6-
tetrahydro-1H-pyrrolo[3,4-c]pyrrol-5- yl)methanone (intermediate
2)/2,3- difluoro-4-sulfamoylbenzoic acid (intermediate 7.01) 589.2
(M + H).sup.+ 1.34 ##STR00048##
[2-cyclopropyl-6-[(1-methylpiperidin-
4-yl)methoxy]pyridin-4-yl]-(2,3,4,6-
tetrahydro-1H-pyrrolo[3,4-c]pyrrol-5- yl)methanone (intermediate
2.01)/ 2,3-difluoro-4-sulfamoylbenzoic acid (intermediate 7.01)
602.3 (M + H).sup.+
Example 2
[5-Chloro-4-cyano-2-(2,2-dimethylpropanoylamino)phenyl]methyl
2-(5-sulfamoylpyridine-2-carbonyl)-1,3,4,6-tetrahydropyrrolo[3,4-c]pyrrol-
e-5-carboxylate
##STR00049##
[0285] To a clear colourless solution of
N-(4-chloro-5-cyano-2-(hydroxymethyl)phenyl)pivalamide
(intermediate 6; 35 mg, 131 .mu.mol) was added
1,1'-carbonyldiimidazole (21.3 mg, 131 .mu.mol) at room
temperature. After 90 min the reaction mixture was heated at
50.degree. C. for 30 min, then allowed to cool to room temperature,
then
6-(1,2,3,4,5,6-hexahydropyrrolo[3,4-c]pyrrole-2-carbonyl)pyridine-3-sulfo-
namide dihydrochloride (intermediate 5.01; 48.2 mg, 131 .mu.mol)
and triethylamine (66.4 mg, 656 .mu.mol) were added. The reaction
was heated at reflux for 18 h, then partitioned between ethyl
acetate and sat. aq. ammonium chloride solution. The organic layer
was washed with sat. aq. sodium hydrogen carbonate solution and
brine, dried over magnesium sulfate, filtered and evaporated. The
residue was triturated in dichloromethane and the precipitate
collected by filtration to afford the title compound (41 mg, 53%).
White solid, MS: 585.2 (M-H).sup.-.
[0286] The following examples were produced in analogy to example
2, replacing
6-(1,2,3,4,5,6-hexahydropyrrolo[3,4-c]pyrrole-2-carbonyl)pyridi-
ne-3-sulfonamide dihydrochloride (intermediate 5.01) by the
appropriate amine and and
N-(4-chloro-5-cyano-2-(hydroxymethyl)phenyl)pivalamide
(intermediate 6) by the appropriate alcohol.
TABLE-US-00003 Ex. Systematic Name Amine/Alcohol MS, m/e 2.01
##STR00050## 3-fluoro-4-(1,2,3,4,5,6,7,8-octahydro-
2,6-naphthyridine-2- carbonyl)benzenesulfonamide hydrochloride
(intermediate 5.02)/ (4- (trifluoromethoxy)phenyl)methanol (CAS-RN
1736-74-9) 556.3 (M - H).sup.- 2.02 ##STR00051##
6-(1,2,3,4,5,6-hexahydropyrrolo[3,4-
c]pyrrole-2-carbonyl)pyridine-3- sulfonamide dihydrochloride
(intermediate 5.01)/(4- (trifluoromethoxy)phenyl)methanol (CAS-RN
1736-74-9) 511.2 (M - H).sup.- 2.03 ##STR00052##
3-fluoro-4-(1,2,3,4,5,6- hexahydropyrrolo[3,4-c]pyrrole-2-
carbonyl)benzenesulfonamide dihydrochloride (intermediate 5)/(4-
(trifluoromethoxy)phenyl)methanol (CAS-RN 1736-74-9) 528.2 (M -
H).sup.- 2.04 ##STR00053## 3-fluoro-4-(1,2,3,4,5,6-
hexahydropyrrolo[3,4-c]pyrrole-2- carbonyl)benzenesulfonamide
dihydrochloride (intermediate 5)/[5- chloro-3-[(5-methyltetrazol-2-
yl)methyl]pyridin-2-yl]methanol (intermediate 10) 477.1 (M +
H).sup.+
Example 3
3-Fluoro-4-[2-[(E)-3-[4-(trifluoromethoxy)phenyl]prop-2-enoyl]-1,3,4,6-tet-
rahydropyrrolo[3,4-c]pyrrole-5-carbonyl]benzenesulfonamide
##STR00054##
[0288] To a clear brown solution of
3-fluoro-4-(1,2,3,4,5,6-hexahydropyrrolo[3,4-c]pyrrole-2-carbonyl)benzene-
sulfonamide dihydrochloride (intermediate 5; 51.9 mg, 135 .mu.mol),
(E)-3-(4-(trifluoromethoxy)phenyl)acrylic acid (CAS-RN 199679-35-1;
31.4 mg, 135 .mu.mol) and 4-methylmorpholine (68.3 mg, 675 .mu.mol)
in N,N-dimethylformamide (4 mL) was added
O-(7-azabenzotriazol-1-yl)-N,N,N',N'-tetramethyluronium
hexafluoro-phosphate (51.4 mg, 135 .mu.mol), then after 18 h the
reaction mixture was partitioned between sat. aq. sodium
hydrogencarbonate solution and ethyl
acetate/2-methyltetrahydrofuran 4:1. The organic layer was washed
with sat. aq. ammonium chloride solution and brine, dried over
magnesium sulfate, filtered and evaporated. The residue was
triturated with ethyl acetate/heptane and the precipitate collected
by filtration to afford the title compound (45 mg, 63%). White
solid, MS: 524.2 (M-H).sup.-.
[0289] The following examples were produced in analogy to example
3, replacing
3-fluoro-4-(1,2,3,4,5,6-hexahydropyrrolo[3,4-c]pyrrole-2-carbon-
yl)benzenesulfonamide dihydrochloride (intermediate 5) by the
appropriate amine and and (E)-3-(4-(trifluoromethoxy)phenyl)acrylic
acid (CAS-RN 199679-35-1) by the appropriate carboxylic acid.
TABLE-US-00004 Ex. Systematic Name Amine/Carboxylic acid MS, m/e
3.01 ##STR00055## 6-(1,2,3,4,5,6-hexahydropyrrolo[3,4-
c]pyrrole-2-carbonyl)pyridine-3- sulfonamide dihydrochloride
(intermediate 5.01)/3-(4- (trifluoromethoxy)phenyl)propanoic acid
(CAS-RN 886499-74-7) 509.2 (M - H).sup.- 3.02 ##STR00056##
3-fluoro-4-(1,2,3,4,5,6-hexahydro- pyrrolo[3,4-c]pyrrole-2-
carbonyl)benzenesulfonamide dihydrochloride (intermediate 5)/3- (4-
(trifluoromethoxy)phenyl)propanoic acid (CAS-RN 886499-74-7) 526.2
(M - H).sup.- 3.03 ##STR00057##
6-(1,2,3,4,5,6-hexahydropyrrolo[3,4-
c]pyrrole-2-carbonyl)pyridine-3- sulfonamide dihydrochloride
(intermediate 5.01)/(E)-3-(4- (trifluoromethoxy)phenyl)acrylic acid
(CAS-RN 199679-35-1) 507.2 (M - H).sup.- 3.04 ##STR00058##
6-(1,2,3,4,5,6-hexahydropyrrolo[3,4-
c]pyrrole-2-carbonyl)pyridine-3- sulfonamide dihydrochloride
(intermediate 5.01)/2-(4- (trifluoromethoxy)phenoxy)acetic acid
(CAS-RN 72220-50-9) 511.2 (M - H).sup.- 3.05 ##STR00059##
3-fluoro-4-(1,2,3,4,5,6- hexahydropyrrolo[3,4-c]pyrrole-2-
carbonyl)benzenesulfonamide dihydrochloride (intermediate 5)/2-
(4-(trifluoromethoxy)phenoxy)acetic acid (CAS-RN 72220-50-9) 528.2
(M - H).sup.- 3.06 ##STR00060## 3-fluoro-4-(1,2,3,4,5,6-
hexahydropyrrolo[3,4-c]pyrrole-2- carbonyl)benzenesulfonamide
dihydrochloride (intermediate 5)/3-
(4-cyano-2-((5-methyl-2H-tetrazol-2- yl)methyl)phenyl)propanoic
acid (intermediate 8.01) 565.3 (M + H).sup.+ 3.07 ##STR00061##
3-fluoro-4-(1,2,3,4,5,6- hexahydropyrrolo[3,4-c]pyrrole-2-
carbonyl)benzenesulfonamide dihydrochloride (intermediate 5)/3-
(4-chloro-2-((5-methyl-2H-tetrazol-2- yl)methyl)phenyl)propanoic
acid (intermediate 8.02) 574.3 (M + H).sup.+ 3.08 ##STR00062##
3-fluoro-4-(1,2,3,4,5,6,- hexahydropyrrolo[3,4-c]pyrrole-2-
carbonyl)benzenesulfonamide hydrochloride (intermediate 5)/3-(2-
((4-methyl-2H-1,2,3-triazol-2- yl)methyl)-4-
(trifluoromethyl)phenyl)propanoic acid (intermediate 8.03) 604.4 (M
- H).sup.- 3.09 ##STR00063## 3-fluoro-4-(1,2,3,4,5,6-
hexahydropyrrolo[3,4-c]pyrrole-2- carbonyl)benzenesulfonamide
hydrochloride (intermediate 5)/3-(2- ((4-methyl-1H-1,2,3-triazol-1-
yl)methyl)-4- (trifluoromethyl)phenyl)propanoic acid (intermediate
9) 605.5 (M - H).sup.- 3.10 ##STR00064## 3-fluoro-4-(1,2,3,4,5,6-
hexahydropyrrolo[3,4-c]pyrrole-2- carbonyl)benzenesulfonamide
hydrochloride (intermediate 5)/3-[3-
[(5-methyltetrazol-2-yl)methyl]-5- (trifluoromethyl)pyridin-2-
yl]propanoic acid (intermediate 8.04) 609.2 (M + H).sup.+
Example 4
5-fluoro-6-[2-[3-[2-[(5-methyltetrazol-2-yl)methyl]-4-(trifluoromethyl)phe-
nyl]propanoyl]-1,3,4,6-tetrahydropyrrolo[3,4-c]pyrrole-5-carbonyl]pyridine-
-3-sulfonamide
##STR00065##
[0291] Trifluoroacetic acid (199 mg, 1.75 mmol) was added to a
solution of tert-butyl
5-(3-fluoro-5-sulfamoylpicolinoyl)-3,4,5,6-tetrahydropyrrolo[3,4-c]pyrrol-
e-2(1H)-carboxylate (intermediate 12; 36 mg, 87.3 .mu.mol) in
dichloromethane (3 mL). The reaction mixture was stirred at
40.degree. C. for 2 h. Then the mixture was directly evaporated and
the residue was combined with N,N-dimethylformamide (3 mL) and
N-methylmorpholine (88.3 mg, 873 .mu.mol),
3-(2-((5-methyl-2H-tetrazol-2-yl)methyl)-4-(trifluoromethyl)phenyl)propan-
oic acid (intermediate 8; 27.4 mg, 87.3 .mu.mol) and finally
O-(7-azabenzotriazol-1-yl)-N,N,N',N'-tetramethyluronium
hexafluoro-phosphate (36.5 mg, 96 .mu.mol). The mixture was stirred
for 18 h at room temperature and then partitioned between sat. aq.
ammonium chloride solution and ethyl acetate. The organic layer was
washed with brine, dried over magnesium sulfate, filtered and
evaporated. Chromatography (silica gel; gradient dichloromethane to
dichloromethane/methanol/25% aq. ammonia solution 90:10:0.25)
afforded the title compound (34 mg, 64%). White solid, MS: 609.2
(M+H).sup.+.
[0292] The following example was produced in analogy to example 4,
replacing of tert-butyl
5-(3-fluoro-5-sulfamoylpicolinoyl)-3,4,5,6-tetrahydropyrrolo[3,4-c]pyrrol-
e-2(1H)-carboxylate (intermediate 12) by the appropriate carbamate
and
3-(2-((5-methyl-2H-tetrazol-2-yl)methyl)-4-(trifluoromethyl)phenyl)propan-
oic acid (intermediate 8) by the appropriate carboxylic acid.
TABLE-US-00005 Ex. Systematic Name Carbamate/carboxylic acid MS,
m/e 4.01 ##STR00066## 5-O-tert-butyl 2-O-[[3-(2,2-
dimethylpropanoylamino)quinolin-2- yl]methyl] 1,3,4,6-
tetrahydropyrrolo[3,4-c]pyrrole-2,5- dicarboxylate (intermediate
13)/2- fluoro-4-sulfamoylbenzoic acid (CAS-RN 714968-42-0) 596.3 (M
+ H).sup.+
Example 5
[3-(2,2-dimethylpropanoylamino)-5-(trifluoromethyl)pyridin-2-yl]methyl
5-(2-fluoro-4-sulfamoylphenyl)sulfonyl-1,3,4,6-tetrahydropyrrolo[3,4-c]py-
rrole-2-carboxylate
##STR00067##
[0294] To a solution of
(3-pivalamido-5-(trifluoromethyl)pyridin-2-yl)methyl
3,4,5,6-tetrahydropyrrolo[3,4-c]pyrrole-2(1H)-carboxylate
dihydrochloride (intermediate 4; 60 mg, 134 .mu.mol) and pyridine
(106 mg, 1.34 mmol) in tetrahydrofuran (2 mL) was added a solution
of 2-fluoro-4-sulfamoylbenzene-1-sulfonyl chloride (CAS-RN
52295-72-4; 72.3 mg, 240 .mu.mol) in tetrahydrofuran (2 mL). After
stirring at 50.degree. C. for 48 h the reaction mixture was
partitioned between sat. aq. ammonium chloride solution and ethyl
acetate. The organic layer was washed with brine, dried over
magnesium sulfate, filtered and evaporated. Chromatography (silica
gel; gradient ethyl acetate/heptane 1:1 to 4:1) afforded the title
compound (42 mg, 48%). White solid, MS: 650.2 (M+H).sup.+.
INTERMEDIATES
Intermediate 1
4-(Trifluoromethoxy)benzyl
3,4,5,6-tetrahydropyrrolo[3,4-c]pyrrole-2(1H)-carboxylate
hydrochloride
Step 1: 2-tert-Butyl 5-(4-(trifluoromethoxy)benzyl)
4,6-dihydropyrrolo[3,4-c]pyrrole-2,5(1H,3H)-dicarboxylate
[0295] To a solution of [4-(trifluoromethoxy)phenyl]methanol
(CAS-RN 1736-74-9; 233 mg, 1.21 mmol) in acetonitrile (10 mL) was
added 1,1'-carbonyldiimidazole (197 mg, 1.21 mmol). The reaction
was heated at 50.degree. C. for 3 h, then triethylamine (736 mg,
7.28 mmol) and tert-butyl
3,4,5,6-tetrahydropyrrolo[3,4-c]pyrrole-2(1H)-carboxylate
hydrochloride (CAS-RN 1208929-16-1; 315 mg, 1.21 mmol) were added
and the reaction mixture was heated at reflux for another 15 h.
After cooling the reaction mixture was partitioned between ethyl
acetate and sat. aq. ammonium chloride solution. The organic layer
was washed with sat. aq. sodium hydrogen carbonate solution and
brine, dried over magnesium sulfate, filtered, and evaporated.
Chromatography (silica gel; gradient dichloromethane to
dichloromethane/methanol/25% aq. ammonia solution 95:5:0.25%
afforded the title compound (458 mg, 88%). Brown semisolid, MS:
446.1 (M+NH.sub.4).sup.+.
Step 2: 4-(Trifluoromethoxy)benzyl
3,4,5,6-tetrahydropyrrolo[3,4-c]pyrrole-2(1H)-carboxylate
hydrochloride
[0296] To a brown solution of 2-tert-butyl
5-(4-(trifluoromethoxy)benzyl)
4,6-dihydropyrrolo[3,4-c]pyrrole-2,5(1H,3H)-dicarboxylate (452 mg,
1.06 mmol) in 2-propanol (3 mL) was added hydrochloric acid
solution (5-6 M in 2-propanol, 5.91 mL, 29.5 mmol). The solution
was stirred for 16 h, then concentrated in vacuo. The residue was
triturated in tert-butyl methyl ether and the precipitate collected
by filtration to produce the title compound (350 mg, 91%). Light
brown solid, MS: 329.1 (M+H).sup.+.
Intermediate 2
[2-Cyclopropyl-6-(oxan-4-ylmethoxy)pyridin-4-yl]-(2,3,4,6-tetrahydro-H-pyr-
rolo[3,4-c]pyrrol-5-yl)methanone
Step 1: tert-butyl
5-(6-cyclopropyl-2-oxo-1,2-dihydropyridine-4-carbonyl)-3,4,5,6-tetrahydro-
pyrrolo[3,4-c]pyrrole-2(1H)-carboxylate
[0297] To a solution of and tert-butyl
3,4,5,6-tetrahydropyrrolo[3,4-c]pyrrole-2(1H)-carboxylate
hydrochloride (CAS-RN 1208929-16-1; 300 mg, 1.16 mmol) in
N,N-dimethylformamide (5 mL) were added 4-methylmorpholine (584 mg,
5.78 mmol), 6-cyclopropyl-2-oxo-1,2-dihydropyridine-4-carboxylic
acid (CAS-RN 150190-28-6; 218 mg, 1.16 mmol) and
O-(7-azabenzotriazol-1-yl)-N,N,N',N'-tetramethyluronium
hexafluoro-phosphate (483 mg, 1.27 mmol). The reaction mixture was
stirred for 18 h, then partitioned between sat. aq. ammonium
chloride solution and ethyl acetate. The organic layer was washed
with brine, dried over magnesium sulfate, filtered and evaporated.
Chromatography (silica gel, gradient dichloromethane to
dichloromethane/methanol/25% aq. ammonia solution 90:10:0.25
produced the title compound (390 mg, 86%). White foam, MS: 372.2
(M+H).sup.+.
Step 2: tert-Butyl
5-(2-cyclopropyl-6-((tetrahydro-2H-pyran-4-yl)methoxy)isonicotinoyl)-3,4,-
5,6-tetrahydropyrrolo[3,4-c]pyrrole-2(1H)-carboxylate
[0298] A mixture of tert-butyl
5-(6-cyclopropyl-2-oxo-1,2-dihydropyridine-4-carbonyl)-3,4,5,6-tetrahydro-
pyrrolo[3,4-c]pyrrole-2(1H)-carboxylate (385 mg, 985 .mu.mol),
potassium carbonate (272 mg, 1.97 mmol) and
4-(iodomethyl)tetrahydro-2H-pyran (459 mg, 1.97 mmol) in
acetonitrile (8 mL) was heated at 90.degree. C. for 48 h, then
partitioned between sat. aq. ammonium chloride solution and ethyl
acetate. The organic layer was washed with brine, dried over
magnesium sulfate, filtered and evaporated. The residue was
chromatographed (silica gel; gradient dichloromethane to
dichloromethane/methanol/25% aq. ammonia solution 95:5:0.25) to
produce the title compound (390 mg, 84%). White foam, MS: 470.3
(M+H).sup.+.
Step 3:
[2-Cyclopropyl-6-(oxan-4-ylmethoxy)pyridin-4-yl]-(2,3,4,6-tetrahyd-
ro-1H-pyrrolo[3,4-c]pyrrol-5-yl)methanone
[0299] Trifluoroacetic acid (1.41 g, 12.3 mmol) was added at room
temperature to a solution of tert-butyl
5-(2-cyclopropyl-6-((tetrahydro-2H-pyran-4-yl)methoxy)isonicotinoyl)-3,4,-
5,6-tetrahydropyrrolo[3,4-c]pyrrole-2(1H)-carboxylate (386 mg, 822
.mu.mol) in dichloromethane (8 mL), then after 5 h the solution was
concentrated and the residue partitioned between dichloromethane
and 2 M aq. sodium hydroxide solution. The organic phase was washed
with brine, dried over magnesium sulfate, filtered and evaporated
to produce the title compound (298 mg, 98%). Off-white foam, MS:
370.2 (M+H).sup.+.
Intermediate 2.01
[2-Cyclopropyl-6-[(1-methylpiperidin-4-yl)methoxy]pyridin-4-yl]-(2,3,4,6-t-
etrahydro-1H-pyrrolo[3,4-c]pyrrol-5-yl)methanone
[0300] The title compound was produced in analogy to intermediate
2, replacing 4-(iodomethyl)tetrahydro-2H-pyran with
4-(bromomethyl)-1-methylpiperidine hydrobromide (CAS-RN
98338-26-2). Yellow oil, MS: 383.3 (M+H).sup.+.
Intermediate 3
3-[2-[(5-Methyltetrazol-2-yl)methyl]-4-(trifluoromethyl)phenyl]-1-(2,3,4,6-
-tetrahydro-1H-pyrrolo[3,4-c]pyrrol-5-yl)propan-1-one
Step 1: tert-butyl
5-(3-(2-((5-methyl-2H-tetrazol-2-yl)methyl)-4-(trifluoromethyl)phenyl)pro-
panoyl)-3,4,5,6-tetrahydropyrrolo[3,4-c]pyrrole-2(1H)-carboxylate
[0301] The title compound was produced in analogy to intermediate
2, step 1, replacing
6-cyclopropyl-2-oxo-1,2-dihydropyridine-4-carboxylic acid by
3-(2-((5-methyl-2H-tetrazol-2-yl)methyl)-4-(trifluoromethyl)phenyl)propan-
oic acid (intermediate 8). Light yellow gum, MS: 505.4
(M-H).sup.-.
Step 2:
3-[2-[(5-Methyltetrazol-2-yl)methyl]-4-(trifluoromethyl)phenyl]-1--
(2,3,4,6-tetrahydro-1H-pyrrolo[3,4-c]pyrrol-5-yl)propan-1-one
[0302] Trifluoroacetic acid (1.84 g, 16.1 mmol) was added at room
temperature to a solution of tert-butyl
5-(3-(2-((5-methyl-2H-tetrazol-2-yl)methyl)-4-(trifluoromethyl)phenyl)pro-
panoyl)-3,4,5,6-tetrahydropyrrolo[3,4-c]pyrrole-2(1H)-carboxylate
(573 mg, 1.07 mmol) in dichloromethane (5 mL), then after 4 h the
reaction mixtrue was concentrated in vacuo. The residue was taken
up in dichloromethane, washed with 2 M aq. sodium hydroxide
solution, dried over magnesium sulfate, filtered and evaporated.
Chromatography (silica gel; gradient dichloromethane/methanol/25%
aq. ammonia solution 95:5:0.25 to 90:10:0.25 produced the title
compound (344 mg, 79%). Light yellow foam, MS: 407.2
(M+H).sup.+.
Intermediate 4
(3-Pivalamido-5-(trifluoromethyl)pyridin-2-yl)methyl
3,4,5,6-tetrahydropyrrolo[3,4-c]pyrrole-2(1H)-carboxylate
hydrochloride
Step 1: tert-Butyl
5-(chlorocarbonyl)-3,4,5,6-tetrahydropyrrolo[3,4-c]pyrrole-2(1H)-carboxyl-
ate
[0303] To a light brown mixture of tert-butyl
3,4,5,6-tetrahydropyrrolo[3,4-c]pyrrole-2(1H)-carboxylate
hydrochloride (CAS-RN 1208929-16-1; 800 mg, 3.08 mmol) and pyridine
(1.34 g, 16.9 mmol) in dichloromethane (12 mL) was added dropwise a
solution of triphosgene (411 mg, 1.39 mmol) in dichloromethane (7
mL) at 0.degree. C. After 30 min the ice-bath was removed, then
after 1 h the reaction mixture was partitioned between 1 M aq.
hydrochloric acid solution and dichloromethane. The organic layer
was washed with water and brine, dried over magnesium sulfate,
filtered and evaporated to afford the title compound (844 mg,
100%). Yellow solid, MS: 217.0 (M+H-isobutene).sup.+.
Step 2: 2-tert-Butyl
5-((3-pivalamido-5-(trifluoromethyl)pyridin-2-yl)methyl)
4,6-dihydropyrrolo[3,4-c]pyrrole-2,5(1H,3H)-dicarboxylate
[0304] To a solution of tert-butyl
5-(chlorocarbonyl)-3,4,5,6-tetrahydropyrrolo[3,4-c]pyrrole-2(1H)-carboxyl-
ate (834 mg, 3.06 mmol) in acetonitrile (60 mL) was added
N-(2-(hydroxymethyl)-5-(trifluoromethyl)pyridin-3-yl)pivalamide
(intermediate 14; 650 mg, 2.35 mmol) and PS-BEMP (CAS-RN
1446424-86-7; 2.58 g). The orange suspension was heated to reflux
and stirred for 68 h. The insoluble solid was filtered off and
washed with acetonitrile. PS-Trisamine (CAS-RN 1226492-10-9; 860
mg, 2.35 mmol) was added to the filtrate and the reaction mixture
was stirred at room temperature for 4 h, then insoluble material
was removed by filtration and the filtrate evaporated.
Chromatography (silica gel; gradient dichloromethane to
dichloromethane/methanol/25% aq. ammonia solution 95:5:0.25
afforded the title compound (935 mg, 78%). Light yellow foam, MS:
513.2 (M+H).sup.+.
Step 3: (3-Pivalamido-5-(trifluoromethyl)pyridin-2-yl)methyl
3,4,5,6-tetrahydropyrrolo[3,4-c]pyrrole-2(1H)-carboxylate
hydrochloride
[0305] To a light yellow solution of 2-tert-butyl
5-((3-pivalamido-5-(trifluoromethyl)pyridin-2-yl)methyl)
4,6-dihydropyrrolo[3,4-c]pyrrole-2,5(1H,3H)-dicarboxylate (925 mg,
1.80 mmol) in 2-propanol (5 mL) was added hydrochloric acid (5-6 M
in 2-propanol, 10.1 mL, 50.5 mmol) at room temperature, then after
14 h the solution was evaporated and the residue triturated in
tert-butyl methyl ether. The precipitate was collected by
filtration to afford the title compound (762 mg, 94%). Light brown
solid, MS: 411.3 (M-H).sup.-.
[0306] The following intermediates were produced in analogy to
intermediate 4 replacing tert-butyl
3,4,5,6-tetrahydropyrrolo[3,4-c]pyrrole-2(1H)-carboxylate
hydrochloride (CAS-RN 1208929-16-1) by the appropriate amine and
N-(2-(hydroxymethyl)-5-(trifluoromethyl)pyridin-3-yl)pivalamide
(intermediate 14) by the appropriate alcohol.
TABLE-US-00006 No. Systematic Name Amine/alcohol MS, m/e 4.01
(3-pivalamido-5- tert-butyl 3,4,5,6,7,8- 439.4
(trifluoromethyl)pyridin-2- hexahydro-2,6-naphthyridine- (M -
H).sup.- yl)methyl 3,4,5,6,7,8-hexahydro- 2(1H)-carboxylate (CAS-
2,6-naphthyridine-2(1H)- RN 1528909-20-7)/N-(2- carboxylate
hydrochloride (hydroxymethyl)-5- (trifluoromethyl)pyridin-3-
yl)pivalamide (intermediate 14) 4.02 (5-chloro-3- tert-butyl
3,4,5,6- 377.3 pivalamidopyridin-2-yl)methyl tetrahydropyrrolo[3,4-
(M - H).sup.- 3,4,5,6-tetrahydropyrrolo[3,4-
c]pyrrole-2(1H)-carboxylate c]pyrrole-2(1H)-carboxylate
hydrochloride CAS-RN dihydrochloride 1208929-16-1/N-(5-chloro-2-
(hydroxymethyl)pyridin-3- yl)pivalamide (intermediate 14.01) 4.03
[5,6-dichloro-3-(2,2- tert-butyl 3,4,5,6- 411.3
dimethylpropanoylamino)pyridin- tetrahydropyrrolo[3,4- (M -
H).sup.- 2-yl]methyl 2,3,4,6-tetrahydro-
c]pyrrole-2(1H)-carboxylate 1H-pyrrolo[3,4-c]pyrrole-5-
hydrochloride CAS-RN carboxylate hydrochloride 1208929-16-1/N-[5,6-
dichloro-2-(hydroxymethyl)- 3-pyridyl]-2,2-dimethyl- propenamide
14.02) 4.04 (6-chloro-3- tert-butyl 3,4,5,6- 379.1
pivalamidopyridin-2-yl)methyl tetrahydropyrrolo[3,4- (M + H).sup.+
3,4,5,6-tetrahydropyrrolo[3,4- c]pyrrole-2(1H)-carboxylate
c]pyrrole-2(1H)-carboxylate hydrochloride CAS-RN hydrochloride
1208929-16-1/N-[6-chloro-2- (hydroxymethyl)pyridin-3-
yl]-2,2-dimethylpropanamide (intermediate 14.03) 4.05
(3-pivalamidopyridin-2-yl)methyl tert-butyl 3,4,5,6- 345.2
3,4,5,6-tetrahydropyrrolo[3,4- tetrahydropyrrolo[3,4- (M + H).sup.+
c]pyrrole-2(1H)-carboxylate c]pyrrole-2(1H)-carboxylate
hydrochloride hydrochloride CAS-RN 1208929-16-1/N-[2-
(hydroxymethyl)-3-pyridyl]- 2,2-dimethyl-propanamide (intermediate
14.04) 4.06 (5-cyano-3-pivalamidopyridin- tert-butyl 3,4,5,6- 368.4
2-yl)methyl 3,4,5,6- tetrahydropyrrolo[3,4- (M - H).sup.-
tetrahydropyrrolo[3,4- c]pyrrole-2(1H)-carboxylate
c]pyrrole-2(1H)-carboxylate hydrochloride CAS-RN dihydrochloride
1208929-16-1/N-(5-cyano-2- (hydroxymethyl)pyridin- 3-yl)pivalamide
(intermediate 6.01) 4.07 (6-methyl-3-pivalamidopyridin- tert-butyl
3,4,5,6- 359.2 2-yl)methyl 3,4,5,6- tetrahydropyrrolo[3,4- (M +
H).sup.+ tetrahydropyrrolo[3,4- c]pyrrole-2(1H)-carboxylate
c]pyrrole-2(1H)-carboxylate hydrochloride CAS-RN dihydrochloride
1208929-16-1/N-[2- (hydroxymethyl)-6-methyl-3-
pyridyl]-2,2-dimethyl- propenamide (intermediate 14.05)
Intermediate 5
3-Fluoro-4-(1,2,3,4,5,6-hexahydropyrrolo[3,4-c]pyrrole-2-carbonyl)benzenes-
ulfonamide dihydrochloride
Step 1: tert-butyl
5-(2-fluoro-4-sulfamoylbenzoyl)-3,4,5,6-tetrahydropyrrolo[3,4-c]pyrrole-2-
(1H)-carboxylate
[0307] O-(7-Azabenzotriazol-1-yl)-N,N,N',N'-tetramethyluronium
hexafluoro-phosphate (623 mg, 1.64 mmol) was added at 0.degree. C.
to a solution of tert-butyl
3,4,5,6-tetrahydropyrrolo[3,4-c]pyrrole-2(1H)-carboxylate
hydrochloride (CAS-RN 1208929-16-1; 404 mg, 1.64 mmol),
2-fluoro-4-sulfamoylbenzoic acid (CAS-RN 714968-42-0; 359 mg, 1.64
mmol) and 4-methylmorpholine (828 mg, 8.19 mmol) in
N,N-dimethylformamide (10 mL) After 10 min the ice bath was
removed, then after 16 h the reaction mixture was partitioned
between sat aq. sodium hydrogencarbonate solution and ethyl
acetate/2-methyltetrahydrofuran 4:1. The organic layer was washed
with sat. aq. ammonium chloride solution and brine, dried over
magnesium sulfate filtered, and evaporated. Chromatography (silica
gel; gradient ethyl acetate to methanol) afforded the title
compound (555 mg; 82%). Light yellow solid. MS: 412.1
(M+H).sup.+.
Step 2:
3-Fluoro-4-(1,2,3,4,5,6-hexahydropyrrolo[3,4-c]pyrrole-2-carbonyl)-
benzenesulfonamide dihydrochloride
[0308] To a solution of tert-butyl
5-(2-fluoro-4-sulfamoylbenzoyl)-3,4,5,6-tetrahydropyrrolo[3,4-c]pyrrole-2-
(1H)-carboxylate (570 mg, 1.39 mmol) in 2-propanol (4 mL) was added
hydrochloric acid solution (5 M-6 M in 2-propanol, 6.1 mL, 30.5
mmol) at room temperature, then after 18 h the reaction mixture was
concentrated under vacuum to produce the title compound (448 mg,
84%). Light red solid, MS: 310.1 (M-H).sup.-.
[0309] The following intermediates were produced in analogy to
intermediate 5, replacing tert-butyl
3,4,5,6-tetrahydropyrrolo[3,4-c]pyrrole-2(1H)-carboxylate
hydrochloride by the appropriate amine and
2-fluoro-4-sulfamoylbenzoic acid by the appropriate carboxylic
acid.
TABLE-US-00007 No. Systematic Name Amine/alcohol MS, m/e 5.01
6-(1,2,3,4,5,6- tert-butyl 3,4,5,6- 293.1 hexahydropyrrolo[3,4-
tetrahydropyrrolo[3,4- (M - H).sup.- c]pyrrole-2-carbonyl)pyridine-
c]pyrrole-2(1H)- 3-sulfonamide dihydrochloride carboxylate
hydrochloride (CAS-RN 1208929-16-1)/5- sulfamoylpicolinic acid
(CAS-RN 1308677-67-9) 5.02 3-fluoro-4-(1,2,3,4,5,6,7,8- tert-butyl
3,4,5,6,7,8- 338.3 octahydro-2,6-naphthyridine-2- hexahydro-2,6- (M
- H).sup.- carbonyl)benzenesulfonamide naphthyridine-2(1H)-
hydrochloride carboxylate (CAS-RN 1528909-20-7)/2-fluoro-
4-sulfamoylbenzoic acid (CAS-RN 714968-42-0)
Intermediate 6
N-(4-Chloro-5-cyano-2-(hydroxymethyl)phenyl)pivalamide
Step 1: Methyl
4-bromo-5-chloro-2-(2,2-dimethylpropanoylamino)benzoate
[0310] To a brown solution of methyl
2-amino-4-bromo-5-chlorobenzoate (CAS-RN 1445322-56-4; 311 mg, 1.06
mmol) in pyridine (4 mL) was added pivaloyl chloride (215 mg, 1.74
mmol) at 0.degree. C. After 20 min the ice-bath was removed. Then
after additional stirring at 50.degree. C. for 3 h the reaction
mixture was partitioned between 1 M aq. hydrochloric acid solution
and ethyl acetate. The organic layer was washed with water and
brine, dried over magnesium sulfate, filtered and evaporated.
Chromatography (silica gel; gradient dichloromethane/heptane 3:7 to
1:1) afforded the title compound (279 mg, 76%). White solid, MS:
350.1 (M+H).sup.+.
Step 2: Methyl
5-chloro-4-cyano-2-(2,2-dimethylpropanoylamino)benzoate
[0311] A mixture of methyl
4-bromo-5-chloro-2-(2,2-dimethylpropanoylamino)benzoate (274 mg,
786 .mu.mol), tris(dibenzylideneacetone)dipalladium(0) (CAS-RN
51364-51-3; 7.2 mg, 7.86 .mu.mol),
1,1'-bis(diphenylphosphino)ferrocene (CAS-RN 12150-46-8; 13.1 mg,
23.6 .mu.mol), and zinc cyanide (50.8 mg, 432 .mu.mol), zinc powder
(2.06 mg, 31.4 .mu.mol) and zinc acetate (5.77 mg, 31.4 .mu.mol) in
N,N-dimethylformamide (8 mL) and water (50 .mu.L) was heated for 20
min at 130.degree. C. under microwave irradiation. After removal of
insoluble material under vacuum and concentration of the filtrate,
the residue was partitioned between 50% aq. sodium
hydrogencarbonate solution and ethyl acetate. The organic layer was
washed with brine, dried over magnesium sulfate, filtered and
evaporated. Chromatography (silica gel; gradient heptane to
dichloromethane) produced the title compound (213 mg, 92%). Light
yellow solid, 295.0 (M+H).sup.+.
Step 3: N-(4-Chloro-5-cyano-2-(hydroxymethyl)phenyl)pivalamide
[0312] To a solution of methyl
5-chloro-4-cyano-2-pivalamidobenzoate (204 mg, 692 .mu.mol) in
tetrahydrofuran (5 mL) was added a solution of calcium chloride
(154 mg, 1.38 mmol) in ethanol (5 mL), then sodium borohydride (105
mg, 2.77 mmol) was added in three portions over a period of 30 min.
The white suspension was stirred for 90 min at room temperature,
then partitioned between ethyl acetate and sat. aq. ammonium
chloride solution. The organic layer was washed with brine, dried
over magnesium sulfate, filtered, and evaporated. Chromatography
(silica gel; gradient heptane/ethyl acetate 4:1 to 1:1) afforded
the title compound (153 mg, 83%). White solid, MS: 267.2
(M+H).sup.+.
Intermediate 6.01
N-(5-Cyano-2-(hydroxymethyl)pyridin-3-yl)pivalamide
[0313] The title compound was produced in analogy to example 6,
replacing methyl 2-amino-4-bromo-5-chlorobenzoate (CAS-RN
1445322-56-4) by methyl 3-amino-5-bromopicolinate (CAS-RN
1072448-08-8). Light yellow solid, MS: 234.2 (M+H).sup.+.
Intermediate 7
2,5-Difluoro-4-sulfamoylbenzoic acid
[0314] To a stirring suspension of
2,5-difluoro-4-methylbenzenesulfonamide (CAS-RN 1204573-30-7; 500
mg, 2.29 mmol) in water (25 mL) at reflux was added portionwise
potassium permanganate (1.63 g, 10.3 mmol) over 2 h. The reaction
mixture was stirred at reflux for additional 30 min, then it was
allowed to cool and stirred at room temperature for further 24 h.
After removal of insoluble material through filtration the filtrate
was acidified to pH 1 with 37% aq. hydrochloric acid solution and
extracted several times with ethyl acetate. The combined organic
layers were dried over magnesium sulfate and evaporated to dryness
to afford the title compound (394 mg, 65%). White solid, MS: 236.0
(M-H).sup.-.
[0315] The following intermediates were produced in analogy to
intermediate 7, replacing 2,5-difluoro-4-methylbenzenesulfonamide
by the appropriate starting material.
TABLE-US-00008 No. Systematic name Starting material MS, m/e 7.01
2,3-difluoro-4- 2,3-difluoro-4-methyl- 236.0 sulfamoylbenzoic
benzene-sulfonamide (M - H).sup.- acid (CAS-RN 1204573-30-7) 7.02
2,6-difluoro-4- 3,5-difluoro-4-methyl- 236.0 sulfamoylbenzoic
benzene-sulfonamide (M - H)- acid (CAS-RN 1239964-24-9)
Intermediate 8
3-(2-((5-Methyl-2H-tetrazol-2-yl)methyl)-4-(trifluoromethyl)phenyl)propano-
ic acid
Step 1:
2-(2-Bromo-5-(trifluoromethyl)benzyl)-5-methyl-2H-tetrazole
[0316] A mixture of 5-methyl-2H-tetrazole (CAS-RN 4076-36-2; 1.50
g, 17.5 mmol), potassium carbonate (2.42 g, 17.5 mmol) and
1-bromo-2-(bromomethyl)-4-(trifluoromethyl)benzene (CAS-RN
886496-63-5; 5.73 g, 17.5 mmol) in acetone (75 mL) was heated at
reflux for 1 h. After cooling the reaction mixture was partitioned
between ice water and ethyl acetate. The organic layer was washed
with brine, dried over magnesium sulfate, filtered, and evaporated
in vacuo. Chromatography (silica gel; gradient heptane to ethyl
acetate) produced the title compound (2.62 g, 46%). Colourless oil,
MS: 321.0 (M+H).sup.+.
Step 2: (E)-Ethyl
3-(2-((5-methyl-2H-tetrazol-2-yl)methyl)-4-(trifluoromethyl)phenyl)acryla-
te
[0317] To a colourless solution of
2-(2-bromo-5-(trifluoromethyl)benzyl)-5-methyl-2H-tetrazole (2.62
g, 8.16 mmol) in N,N-dimethylformamide (32 mL) was added
triethylamine (2.48 g, 24.5 mmol), ethyl acrylate (990 mg, 9.79
mmol), palladium(II) acetate (36.6 mg, 163 .mu.mol) and
tri-o-tolylphosphine (CAS-RN 6163-58-2; 199 mg, 653 .mu.mol). The
light yellow reaction mixture was evacuated, and backfilled with
argon. After stirring at 120.degree. C. for 17 h the mixture was
partitioned between sat. aq. ammonium chloride solution and ethyl
acetate. The organic layer was washed with brine, dried over
magnesium sulfate, filtered, and evaporated. Chromatography (silica
gel; gradient heptane to ethyl acetate) produced the title compound
(2.48 g, 89%). White solid, MS: 341.1 (M+H).sup.+.
Step 3: Ethyl
3-(2-((5-methyl-2H-tetrazol-2-yl)methyl)-4-(trifluoromethyl)phenyl)propan-
oate
[0318] A solution of (E)-ethyl
3-(2-((5-methyl-2H-tetrazol-2-yl)methyl)-4-(trifluoromethyl)phenyl)-acryl-
ate (2.60 g, 7.64 mmol) in ethanol (32 mL) was stirred under a
hydrogen atmosphere (1 bar) in the presence of palladium (10% on
activated charcoal; 407 mg, 382 .mu.mol). After 18 h insoluble
material was removed by filtration through diatomaceous earth, and
the filtrate was evaporated to produce the title compound (2.30 g,
88%). Grey oil, MS: 343.1 (M+H).sup.+.
Step 4:
3-(2-((5-Methyl-2H-tetrazol-2-yl)methyl)-4-(trifluoromethyl)phenyl-
)propanoic acid
[0319] To a solution of ethyl
3-(2-((5-methyl-2H-tetrazol-2-yl)methyl)-4-(trifluoromethyl)phenyl)-propa-
noate (2.3 g, 6.72 mmol) in tetrahydrofuran (25 mL) and water (25
mL) was added lithium hydroxide monohydrate (564 mg, 13.4 mmol) and
the resulting mixture was stirred at room temperature for 18 h,
then partially evaporated in order to remove the tetrahydrofuran.
The aqueous phase was acidified with 1 M aq. hydrochloric acid
solution to pH 1 and extracted several times with ethyl acetate.
The combined organic layers were dried over magnesium sulfate,
filtered, and evaporated to produce the title compound (2.21 g,
quant.). Light yellow oil, MS: 313.2 (M-H).sup.-.
[0320] The following intermediates were produced in analogy to
intermediate 8, replacing
1-bromo-2-(bromomethyl)-4-(trifluoromethyl)benzene (CAS-RN
886496-63-5) and 5-methyl-2H-tetrazole by the appropriate halide
and azole, respectively.
TABLE-US-00009 No. Systematic name Halide/azole MS, m/e 8.01
3-(4-cyano-2-((5-methyl-2H- 4-bromo-3-(bromomethyl)- 270.3
tetrazol-2-yl)methyl)phenyl)- benzonitrile (CAS- (M - H).sup.-
propanoic acid RN 190197-86-5)/5-methyl- 2H-tetrazole 8.02
3-(4-chloro-2-((5-methyl-2H- 1-bromo-2-(bromomethyl)-4- 279.2
tetrazol-2-yl)methyl)phenyl)- chlorobenzene (CAS- (M - H).sup.-
propanoic acid RN 66192-24-3)/5-methyl- 2H-tetrazole 8.03
3-(2-((4-methyl-2H-1,2,3- 1-bromo-2-(bromomethyl)-4- 314.2
triazol-2-yl)methyl)-4- (trifluoromethyl)benzene (M + H).sup.+
(trifluoromethyl)phenyl)propanoic (CAS-RN 886496-63-5)/4- acid
methyl-1H-1,2,3-triazole 8.04 3-[3-[(5-methyltetrazol-
3-(bromomethyl)-2-chloro-5- 314.2 2-yl)methyl]-5-
(trifluoromethyl)pyridine (M - H).sup.- (trifluoromethyl)pyridin-
(CAS-RN 1227588-09-1)/5- 2-yl]propanoic acid
methyl-2H-tetrazole
Intermediate 9
3-[2-[(4-Methyltriazol-1-yl)methyl]-4-(trifluoromethyl)phenyl]propanoic
acid
Step 1: 2-(Azidomethyl)-1-bromo-4-(trifluoromethyl)benzene
[0321] To a clear colourless solution of
1-bromo-2-(bromomethyl)-4-(trifluoromethyl)benzene (CAS-RN
886496-63-5; 1.016 g, 3.20 mmol) in N,N-dimethylformamide (20 mL)
was added sodium azide (229 mg, 3.52 mmol). The reaction mixture
was stirred at 120.degree. C. for 24 h and then concentrated under
vacuum. The residue was partitioned between sat. aq. sodium
hydrogencarbonate solution and ethyl acetate. The organic layer was
washed with brine, dried over magnesium sulfate, filtered, and
evapoarted. Chromatography (silica gel; gradient heptane to
dichloromethane) afforded the title compound (520 mg; 58%).
Colourless liquid, MS: 281.0 (M+H).sup.+.
Step 2:
1-[[2-Bromo-5-(trifluoromethyl)phenyl]methyl]-4-methyltriazole
[0322] A mixture of
2-(azidomethyl)-1-bromo-4-(trifluoromethyl)benzene (591 mg, 2.11
mmol), 1-(trimethylsilyl)-1-propyne (222 mg, 295 .mu.l, 1.92 mmol),
copper(I) bromide (41.3 mg, 288 .mu.mol) and triethylamine (194 mg,
267 .mu.l, 1.92 mmol) in N,N-dimethylformamide (5 mL) was heated at
100.degree. C. for 30 min under microwave irradiation. After
cooling the reaction mixture was partitioned between sat. aq.
ammonium chloride solution and ethyl acetate. The organic layer was
washed with water and brine, dried over magnesium sulfate,
filtered, and evaporated. Chromatography (silica gel; gradient
dichloromethane/heptane 1:4 to dichloromethane and then to
dichloromethane/methanol/25% aq. ammonia solution 90:10:0.25)
produced the title compound (214 mg, 35%). Dark brown oil, MS:
322.1 (M+H).sup.+.
Step 3: Ethyl
(E)-3-[2-[(4-methyltriazol-1-yl)methyl]-4-(trifluoromethyl)phenyl]prop-2--
enoate
[0323] The title compound was produced in analogy to intermediate
8, step 2 from
1-(2-bromo-5-(trifluoromethyl)benzyl)-4-methyl-1H-1,2,3-triazole.
Dark brown solid, MS: 340.2 (M+H).sup.+.
Step 4: Ethyl
3-[2-[(4-methyltriazol-1-yl)methyl]-4-(trifluoromethyl)phenyl]propanoate
[0324] The title compound was produced in analogy to intermediate
8, step 3 from ethyl
(E)-3-[2-[(4-methyltriazol-1-yl)methyl]-4-(trifluoromethyl)phenyl]prop-2--
enoate using methanol. Brown oil, MS: 342.2 (M+H).sup.+.
Step 5:
3-[2-[(4-Methyltriazol-1-yl)methyl]-4-(trifluoromethyl)phenyl]prop-
anoic acid
[0325] The title compound was produced in analogy to intermediate
8, step 4 from ethyl
3-[2-[(4-methyltriazol-1-yl)methyl]-4-(trifluoromethyl)phenyl]propanoate.
White solid, MS: 314.2 (M+H).sup.+.
Intermediate 10
[5-Chloro-3-[(5-methyltetrazol-2-yl)methyl]pyridin-2-yl]methanol
Step 1: Methyl
5-chloro-3-[(5-methyltetrazol-2-yl)methyl]pyridine-2-carboxylate
[0326] The title compound was produced in analogy to intermediate
8, step 1 from methyl
3-(bromomethyl)-5-chloro-pyridine-2-carboxylate (CAS-RN
1260667-62-6). White solid, MS: 268.1 (M+H).sup.+.
Step 2:
[5-Chloro-3-[(5-methyltetrazol-2-yl)methyl]pyridin-2-yl]methanol
[0327] The title compound was produced in analogy to intermediate
6, step 3 from methyl
5-chloro-3-[(5-methyltetrazol-2-yl)methyl]pyridine-2-carboxylate.
Off-white semisolid, MS: 240.1 (M+H).sup.+.
Intermediate 11
3-Fluoro-5-sulfamoylpyridine-2-carboxylic acid
Step 1:
N'-[(6-Chloro-5-fluoro-3-pyridyl)sulfonyl]-N,N-dimethyl-formamidin-
e
[0328] A solution of 1,1-dimethoxy-N,N-dimethyl-methanamine (CAS-RN
4637-24-5; 332 mg, 2.71 mmol) in acetonitrile (1 mL) was added
dropwise to another stirring solution of
6-chloro-5-fluoro-pyridine-3-sulfonamide (CAS-RN 1803571-80-3; 500
mg, 2.26 mmol) and acetonitrile (4 mL). The mixture was stirred for
1 h at room temperature and then directly evaporated at high vacuum
to afford the title compound (600 mg, quant.). White solid, MS:
266.1 (M+H).sup.+.
Step 2: Ethyl
5-[(E)-dimethylaminomethyleneamino]sulfonyl-3-fluoro-pyridine-2-carboxyla-
te
[0329] A mixture of
N'-[(6-chloro-5-fluoro-3-pyridyl)sulfonyl]-N,N-dimethyl-formamidine
(150 mg, 565 .mu.mol),
1,1'-bis(diphenylphosphino)ferrocene-palladium(II)dichloride
dichloromethane complex (CAS-RN 95464-05-4; 55.3 mg, 67.7 .mu.mol),
triethylamine (143 mg, 1.41 mmol) and ethanol (3 mL) was stirred
under a carbon monoxide atmosphere (7 bar) at 100.degree. C., then
concentrated in vacuo. Chromatography (silica gel, gradient heptane
to heptane/ethyl acetate 1:2) afforded the title compound (118 mg,
62%). Light red solid, MS: 304.1 (M+H).sup.+.
Step 2: 3-Fluoro-5-sulfamoylpyridine-2-carboxylic acid
[0330] To a solution of ethyl
5-[(E)-dimethylaminomethyleneamino]sulfonyl-3-fluoro-pyridine-2-carboxyla-
te (114 mg, 338 .mu.mol) in methanol (2 mL) was added 2.5 M aq.
sodium hydroxide solution (2 mL, 5 mmol). The yellow solution was
stirred at room temperature for 3 h and then partitioned between 1
M hydrochloric acid solution and ethyl acetate. The organic layer
was washed with brine, dried over magnesium sulfate, filtered, and
evaporated to afford the title compound (65 mg, 70%). Light brown
solid, MS: 219.1 (M-H).sup.-.
Intermediate 12
tert-Butyl
2-(3-fluoro-5-sulfamoylpyridine-2-carbonyl)-1,3,4,6-tetrahydrop-
yrrolo[3,4-c]pyrrole-5-carboxylate
[0331] The title compound was produced in analogy to intermediate
5, step 1 replacing 2-fluoro-4-sulfamoylbenzoic acid (CAS-RN
714968-42-0) by 3-fluoro-5-sulfamoylpyridine-2-carboxylic acid
(Intermediate 11). White solid, MS: 413.2 (M+H).sup.+.
Intermediate 13
5-O-tert-Butyl
2-O-[[3-(2,2-dimethylpropanoylamino)quinolin-2-yl]methyl]
1,3,4,6-tetrahydropyrrolo[3,4-c]pyrrole-2,5-dicarboxylate
[0332] The title compound was produced in analogy to intermediate
4, step 1 and step 2 replacing
N-(2-(hydroxymethyl)-5-(trifluoromethyl)pyridin-3-yl)pivalamide
(intermediate 14) by
N-[2-(hydroxymethyl)-3-quinolyl]-2,2-dimethyl-propanamide
(Intermediate 14.06). Light yellow foam, MS: 495.3 (M+H).sup.+.
Intermediate 14
N-(2-(Hydroxymethyl)-5-(trifluoromethyl)pyridin-3-yl)pivalamide
Step 1: Methyl 3-pivalam