U.S. patent application number 15/610382 was filed with the patent office on 2018-03-15 for 5ht3 receptor antagonists.
The applicant listed for this patent is Takeda Pharmaceutical Company Limited. Invention is credited to Stephen Hitchcock, Maria Hopkins, Shota Kikuchi, Todd Macklin, Holger Monenschein, Holly Reichard, Huikai Sun.
Application Number | 20180072758 15/610382 |
Document ID | / |
Family ID | 48877569 |
Filed Date | 2018-03-15 |
United States Patent
Application |
20180072758 |
Kind Code |
A1 |
Hitchcock; Stephen ; et
al. |
March 15, 2018 |
5HT3 RECEPTOR ANTAGONISTS
Abstract
The present invention provides compounds of the formula:
##STR00001## that are 5-HT3 receptor antagonists and are therefore
useful for the treatment of diseases treatable by inhibition of
5-HT3 receptor such as emesis, pain, drug addiction,
neurodegenerative and psychiatric disorders, and GI disorders. Also
provided are pharmaceutical compositions containing such compounds
and processes for preparing such compounds.
Inventors: |
Hitchcock; Stephen; (San
Diego, CA) ; Monenschein; Holger; (San Diego, CA)
; Reichard; Holly; (San Diego, CA) ; Sun;
Huikai; (San Diego, CA) ; Kikuchi; Shota; (San
Diego, CA) ; Macklin; Todd; (San Diego, CA) ;
Hopkins; Maria; (San Diego, CA) |
|
Applicant: |
Name |
City |
State |
Country |
Type |
Takeda Pharmaceutical Company Limited |
Osaka |
|
JP |
|
|
Family ID: |
48877569 |
Appl. No.: |
15/610382 |
Filed: |
May 31, 2017 |
Related U.S. Patent Documents
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Application
Number |
Filing Date |
Patent Number |
|
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15064407 |
Mar 8, 2016 |
9695195 |
|
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15610382 |
|
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14415712 |
Jan 19, 2015 |
9303045 |
|
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PCT/US13/50762 |
Jul 16, 2013 |
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15064407 |
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61672709 |
Jul 17, 2012 |
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61708521 |
Oct 1, 2012 |
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Current U.S.
Class: |
1/1 |
Current CPC
Class: |
A61P 1/00 20180101; A61P
25/16 20180101; A61P 3/04 20180101; A61P 21/00 20180101; A61P 9/10
20180101; C07D 453/02 20130101; A61P 43/00 20180101; A61P 29/00
20180101; C07D 519/00 20130101; A61P 25/00 20180101; A61P 29/02
20180101; A61P 19/04 20180101; A61P 25/14 20180101; A61P 1/08
20180101; C07D 221/22 20130101; A61K 31/5386 20130101; A61P 25/18
20180101; A61K 31/19 20130101; C07D 498/08 20130101; A61P 25/06
20180101; C07D 471/04 20130101; C07D 471/08 20130101; A61P 25/24
20180101; A61P 1/04 20180101; C07C 53/40 20130101; C07D 451/12
20130101; A61P 37/02 20180101; A61P 25/04 20180101; A61P 25/22
20180101; A61P 25/30 20180101; A61P 39/02 20180101; A61P 1/14
20180101; C07C 53/18 20130101; A61P 39/00 20180101; A61P 25/28
20180101 |
International
Class: |
C07D 498/08 20060101
C07D498/08; C07D 471/08 20060101 C07D471/08; C07D 453/02 20060101
C07D453/02; C07C 53/40 20060101 C07C053/40; C07C 53/18 20060101
C07C053/18; A61K 31/19 20060101 A61K031/19; A61K 31/5386 20060101
A61K031/5386; C07D 519/00 20060101 C07D519/00; C07D 471/04 20060101
C07D471/04; C07D 451/12 20060101 C07D451/12; C07D 221/22 20060101
C07D221/22 |
Claims
1. A compound of Formula (I): ##STR00387## wherein: Z is O or
NR.sub.a; R.sub.a is hydrogen or C.sub.1-6 alkyl; R.sub.1 is a ring
of the formula (a)-(h) below: ##STR00388## wherein: R.sub.2 is
hydrogen, C.sub.1-6 alkyl, or C.sub.1-6 haloalkyl; each R.sub.3 is
independently hydrogen, C.sub.1-6 alkyl, C.sub.1-6 alkoxy,
C.sub.1-6 haloalkoxy, or halo and can be present on any carbon atom
in the rings; R.sub.4 is heteroaryl selected from the group
consisting of furanyl, thienyl, pyrrolyl, imidazolyl, oxazolyl,
isoxazolyl, oxadiazolyl, thiazolyl, isothiazolyl, thiadiazolyl,
triazolyl, tetrazolyl, pyrazinyl, pyridazinyl, pyrimidyl, azepinyl,
diazepinyl, quinolyl, isoquinolyl, quinolizidine, benzofuranyl,
benzothienyl, indolyl, isoindolyl, indazolyl, benzimidazolyl,
benzisothiazolyl, benzisoxazolyl, benzoxadiazolyl, benzoxazolyl,
benzothiazolyl, benzothiadiazolyl, benzotriazolyl, benzopyrazinyl,
benzopyrazidinyl, benzoazepinyl, benzodiazepinyl, imidazopyridyl,
pyrazolopyridyl, pyrrolopyridyl, quinazolyl, purinyl, furopyridyl,
and thienopyridyl, each R.sub.4 heteroaryl is optionally
substituted with one or two substituents independently selected
from C.sub.1-6 alkyl, C.sub.1-6 haloalkyl, C.sub.1-6 haloalkoxy,
C.sub.1-6 alkoxy, hydroxy, cyano, or halo; all of X.sub.1-X.sub.4
are CR.sub.5 or one of X.sub.1-X.sub.4 is N and the others are
CR.sub.5; each R.sub.5 is independently hydrogen, C.sub.1-6 alkyl,
halo, hydroxy, or cyano provided that at least one of R.sub.5 is
hydrogen; X.sub.5 is N or CR.sub.6 where R.sub.6 is hydrogen,
C.sub.1-6 alkyl, or halo; or a pharmaceutically acceptable salt
thereof or N-oxide thereof and provided that the compound of
Formula (I) is not:
N-(3)-1-azabicyclo[2.2.2]oct-3-yl-1-(3-thienyl)-1H-Indazole-3-carboxamide-
.
2. The compound or pharmaceutically acceptable salt of claim 1,
wherein R.sub.4 is selected from the group consisting of furanyl,
pyrrolyl, imidazolyl, oxazolyl, isoxazolyl, oxadiazolyl, thiazolyl,
isothiazolyl, thiadiazolyl, triazolyl, tetrazolyl, pyrazinyl,
pyridazinyl, each optionally substituted with one or two
substituents independently selected from C.sub.1-6 alkyl, C.sub.1-6
haloalkyl, C.sub.1-6 haloalkoxy, C.sub.1-6 alkoxy, hydroxy, cyano,
or halo.
3. The compound or pharmaceutically acceptable salt of claim 1,
wherein Z is O.
4. The compound or pharmaceutically acceptable salt of claim 1,
wherein Z is NH.
5. The compound or pharmaceutically acceptable salt of claim 1,
wherein R.sub.1 is a ring of formula (a), (d), (e), (f), or
(g).
6. The compound or pharmaceutically acceptable salt of claim 5,
wherein R.sub.1 is a ring of formula (a) or (d).
7. The compound or pharmaceutically acceptable salt of claim 5,
wherein R.sub.1 is a ring of formula (e), (f), or (g).
8. The compound or pharmaceutically acceptable salt of claim 5,
wherein R.sub.1 is a ring of formula (e).
9. The compound or pharmaceutically acceptable salt of claim 1,
wherein each R.sub.3 is hydrogen.
10. The compound or pharmaceutically acceptable salt of claim 1,
wherein R.sub.2 is methyl.
11. The compound or pharmaceutically acceptable salt of claim 1,
wherein is where all of X.sub.1-X.sub.4 are CR.sub.5 and each
R.sub.5 is hydrogen.
12. The compound or pharmaceutically acceptable salt of claim 11,
wherein X.sub.5 is N.
13. The compound or pharmaceutically acceptable salt of claim 11,
wherein X.sub.5 is CR.sub.6 and R.sub.6 is hydrogen.
14. A compound of claim 1 selected from:
(1R,3R,5S)-8-methyl-8-azabicyclo[3.2.1]octan-3-yl
5-fluoro-1-(2,2,2-trifluoroethyl)-1H-indole-3-carboxylate;
(1R,3R,5S)-8-methyl-8-azabicyclo[3.2.1]octan-3-yl
5-fluoro-1-((R)-tetrahydrofuran-3-yl)-1H-indole-3-carboxylate;
(1R,3R,5S)-8-methyl-8-azabicyclo[3.2.1]octan-3-yl
2-methyl-1-(methylsulfonyl)-1H-indole-3-carboxylate;
(1R,3R,5S)-9-methyl-9-azabicyclo[3.3.1]nonan-3-yl
1-(methylsulfonyl)-1H-indazole-3-carboxylate;
N-((1R,5S,7S)-9-methyl-3-oxa-9-azabicyclo[3.3.1]nonan-7-yl)-1-(2,2,2-trif-
luoroethyl)-1H-pyrrolo[2,3-b]pyridine-3-carboxamide;
N-((1R,5S,7S)-3-oxa-9-azabicyclo[3.3.1]nonan-7-yl)-5-fluoro-1-(2,2,2-trif-
luoroethyl)-1H-indole-3-carboxamide;
1-(2,2-difluoroethyl)-N-((1R,3R,5S)-9-methyl-9-azabicyclo[3.3.1]nonan-3-y-
l)-1H-indazole-3-carboxamide;
N-((1R,5S,7S)-9-methyl-3-oxa-9-azabicyclo[3.3.1]nonan-7-yl)-1-(2,2,2-trif-
luoroethyl)-1H-indole-3-carboxamide;
(1R,5S,7S)-3-oxa-9-azabicyclo[3.3.1]nonan-7-yl
1-(isopropylsulfonyl)-1H-indole-3-carboxylate;
1-(isopropylsulfonyl)-N-((1R,5S,7S)-9-methyl-3-oxa-9-azabicyclo[3.3.1]non-
an-7-yl)-1H-indole-3-carboxamide;
1-(2-fluoroethyl)-N-((1R,3R,5S)-9-methyl-9-azabicyclo[3.3.1]nonan-3-yl)-1-
H-indazole-3-carboxamide;
(1R,3R,5S)-8-methyl-8-azabicyclo[3.2.1]octan-3-yl
2-chloro-1-(methylsulfonyl)-1H-indole-3-carboxylate;
(1R,3R,5S)-8-azabicyclo[3.2.1]octan-3-yl
1-(2,2,2-trifluoroethyl)-1H-indole-3-carboxylate
(1R,3R,5S)-8-methyl-8-azabicyclo[3.2.1]octan-3-yl
1-(2-fluoroethyl)-2-methyl-1H-indole-3-carboxylate;
(1R,3R,5S)-9-methyl-9-azabicyclo[3.3.1]nonan-3-yl
1-(2-fluoroethyl)-1H-indazole-3-carboxylate;
(1R,3R,5S)-8-methyl-8-azabicyclo[3.2.1]octan-3-yl
1-(2,2,2-trifluoroethyl)-1H-indazole-3-carboxylate;
5-fluoro-N-((1R,3R,5S)-8-methyl-8-azabicyclo[3.2.1]octan-3-yl)-1-(methyls-
ulfonyl)-1H-indole-3-carboxamide;
(1R,5S,7S)-3-oxa-9-azabicyclo[3.3.1]nonan-7-yl
5-fluoro-1-(methylsulfonyl)-1H-indole-3-carboxylate;
1-(2,2-difluoroethyl)-N-((1R,5S,7S)-9-methyl-3-oxa-9-azabicyclo[3.3.1]non-
an-7-yl)-1H-indazole-3-carboxamide;
1-(2,2-difluoroethyl)-N-((1R,5S,7S)-9-methyl-3-oxa-9-azabicyclo[3.3.1]non-
an-7-yl)-1H-indole-3-carboxamide;
N-((1R,5S,7S)-9-methyl-3-oxa-9-azabicyclo[3.3.1]nonan-7-yl)-1-((S)-1,2,2,-
2-tetrafluoroethyl)-1H-pyrrolo[2,3-b]pyridine-3-carboxamide;
5-fluoro-1-(2,2,2-trifluoroethyl)-N-((1R,5S,7S)-9-(1,1,1-trideuteriomethy-
l)-3-oxa-9-azabicyclo[3.3.1]nonan-7-yl)-1H-pyrrolo[2,3-b]pyridine-3-carbox-
amide; (1R,5S,7S)-3-oxa-9-azabicyclo[3.3.1]nonan-7-yl
1-(pyrimidin-2-yl)-1H-indole-3-carboxylate;
(1R,3R,5S)-8-methyl-8-azabicyclo[3.2.1]octan-3-yl
1-(methylsulfonyl)-1H-indole-3-carboxylate;
(1R,3R,5S)-8-methyl-8-azabicyclo[3.2.1]octan-3-yl
1-(2,2-difluoroethyl)-5-fluoro-1H-indole-3-carboxylate;
(1R,3R,5S)-8-methyl-8-azabicyclo[3.2.1]octan-3-yl
2,3-dihydrooxazolo[3,2-a]indole-9-carboxylate;
(1R,3R,5S)-8-methyl-8-azabicyclo[3.2.1]octan-3-yl
5-fluoro-1-(tetrahydrofuran-3-yl)-1H-indole-3-carboxylate;
(1R,3R,5S)-9-methyl-9-azabicyclo[3.3.1]nonan-3-yl
2-chloro-1-(2-fluoroethyl)-1H-indole-3-carboxylate;
(1R,5S,7S)-3-oxa-9-azabicyclo[3.3.1]nonan-7-yl
1-(2,2-difluoroethyl)-5-fluoro-1H-indole-3-carboxylate;
(1R,5S,7S)-9-methyl-3-oxa-9-azabicyclo[3.3.1]nonan-7-yl
5-fluoro-1-(2,2,2-trifluoroethyl)-1H-indole-3-carboxylate;
(1R,5S,7S)-9-(2-fluoroethyl)-3-oxa-9-azabicyclo[3.3.1]nonan-7-yl
difluoroethyl)-5-fluoro-1H-indole-3-carboxylate;
(1R,3R,5S)-9-methyl-9-azabicyclo[3.3.1]nonan-3-yl
5-fluoro-1-(methylsulfonyl)-1H-indole-3-carboxylate;
5-fluoro-N-((1R,5S,7S)-9-methyl-3-oxa-9-azabicyclo[3.3.1]nonan-7-yl)-1-(2-
,2,2-trifluoroethyl)-1H-indole-3-carboxamide;
5-fluoro-N-((1R,5S,7S)-9-methyl-3-oxa-9-azabicyclo[3.3.1]nonan-7-yl)-1-(m-
ethylsulfonyl)-1H-indole-3-carboxamide; quinuclidin-4-yl
5-fluoro-1-(methylsulfonyl)-1H-indole-3-carboxylate;
N-((1R,5S,7S)-3-oxa-9-azabicyclo[3.3.1]nonan-7-yl)-1-(2,2,2-trifluoroethy-
l)-1H-pyrrolo[2,3-b]pyridine-3-carboxamide;
N-((1R,5S,7S)-3-oxa-9-azabicyclo[3.3.1]nonan-7-yl)-1-(2,2-difluoroethyl)--
5-fluoro-1H-pyrrolo[2,3-b]pyridine-3-carboxamide;
(1R,3R,5S)-8-methyl-8-azabicyclo[3.2.1]octan-3-yl
1-(2,2-difluoroethyl)-1H-indole-3-carboxylate;
(1R,3R,5S)-8-methyl-8-azabicyclo[3.2.1]octan-3-yl
1-(2,2,2-trifluoroethyl)-1H-pyrrolo[2,3-b]pyridine-3-carboxylate;
(1R,3R,5S)-8-methyl-8-azabicyclo[3.2.1]octan-3-yl
1-(tetrahydrofuran-3-yl)-1H-indole-3-carboxylate;
(1R,3R,5S)-8-methyl-8-azabicyclo[3.2.1]octan-3-yl
2-chloro-1-(2,2-difluoroethyl)-1H-indole-3-carboxylate;
(1R,3R,5S)-8-methyl-8-azabicyclo[3.2.1]octan-3-yl
2-chloro-1-(2,2,2-trifluoroethyl)-1H-indole-3-carboxylate;
(1R,3R,5S)-8-azabicyclo[3.2.1]octan-3-yl
1-(2,2-difluoroethyl)-1H-indole-3-carboxylate
N-((1R,3R,5S)-9-methyl-9-azabicyclo[3.3.1]nonan-3-yl)-1-(methylsulfonyl)--
1H-indazole-3-carboxamide;
(1R,5S,7S)-9-methyl-3-oxa-9-azabicyclo[3.3.1]nonan-7-yl
1-(methylsulfonyl)-1H-indole-3-carboxylate;
(1R,5S,7S)-9-methyl-3-oxa-9-azabicyclo[3.3.1]nonan-7-yl
1-(2,2-difluoroethyl)-1H-pyrrolo[2,3-b]pyridine-3-carboxylate;
(1R,5S,7S)-9-methyl-3-oxa-9-azabicyclo[3.3.1]nonan-7-yl
1-(2,2,2-trifluoroethyl)-1H-pyrrolo[2,3-b]pyridine-3-carboxylate;
(1R,5S,7S)-9-(2-fluoroethyl)-3-oxa-9-azabicyclo[3.3.1]nonan-7-yl
5-fluoro-1-(2,2,2-trifluoroethyl)-1H-indole-3-carboxylate;
(1R,5S,7S)-9-methyl-3-oxa-9-azabicyclo[3.3.1]nonan-7-yl
1-(2-fluoroethyl)-1H-indole-3-carboxylate;
5-fluoro-N-((1R,5S,7S)-9-methyl-3-oxa-9-azabicyclo[3.3.1]nonan-7-yl)-1-(2-
,2,2-trifluoroethyl)-1H-pyrrolo[2,3-b]pyridine-3-carboxamide;
5-fluoro-N-((1R,5S,7S)-9-methyl-3-oxa-9-azabicyclo[3.3.1]nonan-7-yl)-1-(1-
,1,2,2-tetrafluoroethyl)-1H-pyrrolo[2,3-b]pyridine-3-carboxamide;
(1R,5S,7S)-3-oxa-9-azabicyclo[3.3.1]nonan-7-yl
5-fluoro-1-(isopropylsulfonyl)-1H-indole-3-carboxylate;
(1R,3R,5S)-8-methyl-8-azabicyclo[3.2.1]octan-3-yl
2-chloro-1-(2-fluoroethyl)-1H-indole-3-carboxylate;
(1R,3R,5S)-8-methyl-8-azabicyclo[3.2.1]octan-3-yl
1-(2-fluoroethyl)-1H-indole-3-carboxylate;
(1R,3R,5S)-8-methyl-8-azabicyclo[3.2.1]octan-3-yl
1-(2-fluoroethyl)-1H-indazole-3-carboxylate;
(1R,5S,7S)-9-methyl-3-oxa-9-azabicyclo[3.3.1]nonan-7-yl
1-(2,2-difluoroethyl)-5-fluoro-1H-indole-3-carboxylate;
(1R,5S,7S)-3-oxa-9-azabicyclo[3.3.1]nonan-7-yl
5-fluoro-1-(2,2,2-trifluoroethyl)-1H-indole-3-carboxylate;
(1R,3R,5S)-9-methyl-9-azabicyclo[3.3.1]nonan-3-yl
1-(2,2-difluoroethyl)-5-fluoro-1H-indole-3-carboxylate;
(1R,3R,5S)-9-methyl-9-azabicyclo[3.3.1]nonan-3-yl
1-(2,2-difluoroethyl)-1H-pyrrolo[2,3-b]pyridine-3-carboxylate;
N-((1R,3R,5S)-8-methyl-8-azabicyclo[3.2.1]octan-3-yl)-1-(methylsulfonyl)--
1H-indazole-3-carboxamide;
1-(2,2-difluoroethyl)-5-fluoro-N-((1R,5S,7S)-9-methyl-3-oxa-9-azabicyclo[-
3.3.1]-nonan-7-yl)-1H-indole-3-carboxamide;
1-(2,2-difluoroethyl)-N-((1R,5S,7S)-9-methyl-3-oxa-9-azabicyclo[3.3.1]non-
an-7-yl)-1H-pyrrolo[2,3-b]pyridine-3-carboxamide;
N-((1R,5S,7S)-3-oxa-9-azabicyclo[3.3.1]nonan-7-yl)-1-(2,2-difluoroethyl)--
1H-indazole-3-carboxamide;
1-(2,2-difluoroethyl)-N-((1R,5S,7S)-9-methyl-3-oxa-9-azabicyclo[3.3.1]non-
an-7-yl)-1H-pyrazolo[3,4-b]pyridine-3-carboxamide;
(R)-1-(2,2-difluoroethyl)-N-(quinuclidin-3-yl)-1H-pyrrolo[2,3-b]pyridine--
3-carboxamide;
1-(2,2-difluoroethyl)-5-fluoro-N-((1R,5S,7S)-9-methyl-3-oxa-9-azabicyclo[-
3.3.1]-nonan-7-yl)-1H-pyrrolo[2,3-b]pyridine-3-carboxamide;
N-((1R,5S,7S)-9-methyl-3-oxa-9-azabicyclo[3.3.1]nonan-7-yl)-1-(1,1,1-trif-
luoro-2-methylpropan-2-yl)-1H-pyrrolo[2,3-b]pyridine-3-carboxamide;
N-((1R,5S,7S)-9-methyl-3-oxa-9-azabicyclo[3.3.1]nonan-7-yl)-1-((R)-1,2,2,-
2-tetrafluoroethyl)-1H-pyrrolo[2,3-b]pyridine-3-carboxamide;
(1R,3R,5S)-8-methyl-8-azabicyclo[3.2.1]octan-3-yl
1-(2,2-difluoroethyl)-1H-pyrrolo[2,3-b]pyridine-3-carboxylate;
(1R,3R,5S)-8-methyl-8-azabicyclo[3.2.1]octan-3-yl
1-(2,2-difluoroethyl)-2-methyl-1H-indole-3-carboxylate;
N-((1R,3R,5S)-8-methyl-8-azabicyclo[3.2.1]octan-3-yl)-1-(methylsulfonyl)--
1H-indole-3-carboxamide; 1-(2,2-difluoroethyl)-5-fluoro-N-((1R,3R,5
S)-8-methyl-8-azabicyclo[3.2.1]octan-3-yl)-1H-indole-3-carboxamide;
1-(2,2-difluoroethyl)-N-((1R,3R,5S)-8-methyl-8-azabicyclo[3.2.1]octan-3-y-
l)-1H-pyrrolo[2,3-b]pyridine-3-carboxamide;
1-(2,2-difluoroethyl)-N-((1R,3R,5S)-9-methyl-9-azabicyclo[3.3.1]nonan-3-y-
l)-1H-pyrrolo[2,3-b]pyridine-3-carboxamide;
N-((1R,5S,7S)-3-oxa-9-azabicyclo[3.3.1]nonan-7-yl)-5-fluoro-1-(methylsulf-
onyl)-1H-indole-3-carboxamide;
1-(2-fluoroethyl)-N-((1R,5S,7S)-9-methyl-3-oxa-9-azabicyclo[3.3.1]nonan-7-
-yl)-1H-indole-3-carboxamide;
N-((1R,5S,7S)-9-methyl-3-oxa-9-azabicyclo[3.3.1]nonan-7-yl)-1-(1,1,2,2-te-
trafluoroethyl)-1H-pyrrolo[2,3-b]pyridine-3-carboxamide;
N-((1R,5S,7S)-9-methyl-3-oxa-9-azabicyclo[3.3.1]nonan-7-yl)-1-(1,2,2,2-te-
trafluoroethyl)-1H-pyrrolo[2,3-b]pyridine-3-carboxamide;
N-((1R,5S,7S)-3-oxa-9-azabicyclo[3.3.1]nonan-7-yl)-1-(2,2-difluoroethyl)--
1H-pyrrolo[2,3-b]pyridine-3-carboxamide;
(1R,3R,5S)-8-methyl-8-azabicyclo[3.2.1]octan-3-yl
1-((S)-tetrahydrofuran-3-yl)-1H-indole-3-carboxylate;
(1R,3R,5S)-8-methyl-8-azabicyclo[3.2.1]octan-3-yl
2,3,4,5-tetrahydro-[1,3]oxazepino-[3,2-a]indole-11-carboxylate;
(1R,3R,5S)-8-methyl-8-azabicyclo[3.2.1]octan-3-yl
3,4-dihydro-2H-[1,3]oxazino[3,2-a]indole-10-carboxylate;
(1R,3R,5S)-8-methyl-8-azabicyclo[3.2.1]octan-3-yl
5-fluoro-1-(methylsulfonyl)-1H-indole-3-carboxylate;
(1R,3R,5S)-9-methyl-9-azabicyclo[3.3.1]nonan-3-yl
1-(2-fluoroethyl)-1H-indole-3-carboxylate;
(1R,3R,5S)-9-methyl-9-azabicyclo[3.3.1]nonan-3-yl
1-(2-fluoroethyl)-2-methyl-1H-indole-3-carboxylate;
(1R,3R,5S)-9-methyl-9-azabicyclo[3.3.1]nonan-3-yl
5-fluoro-1-(2,2,2-trifluoroethyl)-1H-indole-3-carboxylate;
1-(2,2-difluoroethyl)-N-((1R,3R,5S)-8-methyl-8-azabicyclo[3.2.1]octan-3-y-
l)-1H-indazole-3-carboxamide;
(1S,5R,6S)-4-oxa-1-azabicyclo[3.3.1]nonan-6-yl
1-(2,2-difluoroethyl)-5-fluoro-1H-indole-3-carboxylate;
5-fluoro-1-(isopropylsulfonyl)-N-((1R,5S,7S)-9-methyl-3-oxa-9-azabicyclo[-
3.3.1]-nonan-7-yl)-1H-indole-3-carboxamide;
(1R,3R,5S)-8-methyl-8-azabicyclo[3.2.1]octan-3-yl
1-((S)-tetrahydrofuran-3-yl)-1H-indole-3-carboxylate;
(1R,3R,5S)-8-methyl-8-azabicyclo[3.2.1]octan-3-yl
5-fluoro-1-((S)-tetrahydrofuran-3-yl)-1H-indole-3-carboxylate;
1-(2,2-difluoroethyl)-5-fluoro-N-((1R,3R,5S)-9-methyl-9-azabicyclo[3.3.1]-
nonan-3-yl)-1H-indole-3-carboxamide;
(1R,5S,7S)-9-methyl-3-oxa-9-azabicyclo[3.3.1]nonan-7-yl
5-fluoro-1-(methylsulfonyl)-1H-indole-3-carboxylate;
5-fluoro-N-((1R,3R,5S)-9-methyl-9-azabicyclo[3.3.1]nonan-3-yl)-1-(methyls-
ulfonyl)-1H-indole-3-carboxamide;
(1R,5S,7S)-3-oxa-9-azabicyclo[3.3.1]nonan-7-yl
1-(2,2-difluoroethyl)-1H-pyrrolo[2,3-b]pyridine-3-carboxylate;
N-((1R,3R,5S)-8-methyl-8-azabicyclo[3.2.1]octan-3-yl)-1-(2,2,2-trifluoroe-
thyl)-1H-pyrrolo[2,3-b]pyridine-3-carboxamide;
(1R,3R,5S)-9-methyl-9-azabicyclo[3.3.1]nonan-3-yl
1-(2,2,2-trifluoroethyl)-1H-pyrrolo[2,3-b]pyridine-3-carboxylate;
1-(2,2-difluoroethyl)-N-((1R,5S,7S)-9-(trifluoromethyl)-3-oxa-9-azabicycl-
o[3.3.1]-nonan-7-yl)-1H-pyrrolo[2,3-b]pyridine-3-carboxamide;
N-((1R,5S,7S)-3-oxa-9-azabicyclo[3.3.1]nonan-7-yl)-5-fluoro-1-(2,2,2-trif-
luoroethyl)-1H-pyrrolo[2,3-b]pyridine-3-carboxamide;
N-((1R,5S,7s)-9-methyl-3-oxa-9-azabicyclo[3.3.1]nonan-7-yl)-1-(pyrimidin--
2-yl)-1H-indole-3-carboxamide;
1-(2,2-difluoropropyl)-N-((1R,5S,7S)-9-methyl-3-oxa-9-azabicyclo[3.3.1]no-
nan-7-yl)-1H-pyrrolo[2,3-b]pyridine-3-carboxamide;
1-(2,2-difluoroethyl)-5-fluoro-N-((1R,5S,7S)-9-methyl-d.sub.3-3-oxa-9-aza-
bicyclo[3.3.1]nonan-7-yl)-1H-pyrrolo[2,3-b]pyridine-3-carboxamide;
N-((1R,5S,7S)-9-methyl-d.sub.3-3-oxa-9-azabicyclo[3.3.1]nonan-7-yl)-1-(me-
thylsulfonyl)-1H-indole-3-carboxamide;
N-((1R,5S,7S)-9-methyl-d.sub.3-3-oxa-9-azabicyclo[3.3.1]nonan-7-yl)-1-(is-
opropylsulfonyl)-1H-indole-3-carboxamide;
1-(2,2,2-trifluoroethyl)-5-fluoro-N-((1R,5S,7S)-9-methyl-d.sub.3-3-oxa-9--
azabicyclo-[3.3.1]nonan-7-yl)-1H-indole-3-carboxamide;
1-(2,2-difluoroethyl)-5-fluoro-N-((1R,5S,7S)-9-methyl-d.sub.3-3-oxa-9-aza-
bicyclo-[3.3.1]nonan-7-yl)-1H-indole-3-carboxamide;
(S)-1-(2,2-difluoroethyl)-N-(quinuclidin-3-yl)-1H-pyrrolo[2,3-b]pyridine--
3-carboxamide;
N-((1R,5S,7S)-9-methyl-3-oxa-9-azabicyclo[3.3.1]nonan-7-yl)-1-(pyridazin--
3-yl)-1H-indole-3-carboxamide;
N-((1R,5S,7S)-9-methyl-3-oxa-9-azabicyclo[3.3.1]nonan-7-yl)-1-(thiazol-2--
yl)-1H-indole-3-carboxamide;
N-((1R,5S,7S)-9-methyl-3-oxa-9-azabicyclo[3.3.1]nonan-7-yl)-1-(thiazol-5--
yl)-1H-indole-3-carboxamide;
N-((1R,5S,7S)-9-methyl-3-oxa-9-azabicyclo[3.3.1]nonan-7-yl)-1-(pyrimidin--
5-yl)-1H-indole-3-carboxamide;
N-((1R,5S,7S)-9-methyl-d.sub.3-3-oxa-9-azabicyclo[3.3.1]nonan-7-yl)-1-(py-
rimidin-2-yl)-1H-indole-3-carboxamide;
N-((1R,5S,7S)-9-methyl-d.sub.3-3-oxa-9-azabicyclo[3.3.1]nonan-7-yl)-1-(py-
ridazin-3-yl)-1H-indole-3-carboxamide;
(1R,5S,7S)-9-methyl-d.sub.3-3-oxa-9-azabicyclo[3.3.1]nonan-7-yl
1-(2,2,2-difluoroethyl)-1H-indole-3-carboxylate;
(1R,5S,7S)-9-methyl-d.sub.3-3-oxa-9-azabicyclo[3.3.1]nonan-7-yl
difluoroethyl)-1H-indole-3-carboxylate;
N-((1R,5S,7S)-9-methyl-d.sub.3-3-oxa-9-azabicyclo[3.3.1]nonan-7-yl)-1-(2,-
2,2-trifluoroethyl)-1H-indazole-3-carboxamide;
1-(2-fluoroethyl)-N-((1R,5S,7S)-9-methyl-d.sub.3-3-oxa-9-azabicyclo[3.3.1-
]nonan-7-yl)-1H-indole-3-carboxamide;
(1R,5S,7S)-3-oxa-9-azabicyclo[3.3.1]nonan-7-yl
1-(thiazol-2-yl)-1H-indole-3-carboxylate;
N-((1R,5S,7S)-9-methyl-3-oxa-9-azabicyclo[3.3.1]nonan-7-yl)-1-(pyrazin-2--
yl)-1H-indole-3-carboxamide;
N-((1R,5S,7S)-9-methyl-d.sub.3-3-oxa-9-azabicyclo[3.3.1]nonan-7-yl)-1-(py-
razin-2-yl)-1H-indole-3-carboxamide;
(1R,5S,7S)-3-oxa-9-azabicyclo[3.3.1]nonan-7-yl
1-(isopropylsulfonyl)-1H-indole-3-carboxylate;
(1R,5S,7S)-3-oxa-9-azabicyclo[3.3.1]nonan-7-yl
5-fluoro-1-(methylsulfonyl)-1H-indole-3-carboxylate;
(1R,5S,7S)-3-oxa-9-azabicyclo[3.3.1]nonan-7-yl
1-(ethylsulfonyl)-1H-indole-3-carboxylate;
(1R,5S,7S)-3-oxa-9-azabicyclo[3.3.1]nonan-7-yl
1-(cyclopropylsulfonyl)-1H-indole-3-carboxylate;
(1R,5S,7S)-3-oxa-9-azabicyclo[3.3.1]nonan-7-yl
1-(isobutylsulfonyl)-1H-indole-3-carboxylate;
(1R,5S,7s)-3-oxa-9-azabicyclo[3.3.1]nonan-7-yl
1-(pyridazin-3-yl)-1H-indole-3-carboxylate;
(1R,5S,7s)-9-methyl-3-oxa-9-azabicyclo[3.3.1]nonan-7-yl
1-(6-fluoropyridazin-3-yl)-1H-indole-3-carboxylate;
(1R,5S,7s)-3-oxa-9-azabicyclo[3.3.1]nonan-7-yl
1-(pyrazin-2-yl)-1H-indole-3-carboxylate;
(1R,5S,7s)-9-methyl-3-oxa-9-azabicyclo[3.3.1]nonan-7-yl
1-(cyanomethyl)-7-fluoro-1H-pyrrolo[2,3-c]pyridine-3-carboxylate;
(1R,5S,7s)-3-oxa-9-azabicyclo[3.3.1]nonan-7-yl
1-(isothiazol-4-yl)-1H-indole-3-carboxylate;
1-(isothiazol-4-yl)-N-((1R,5S,7s)-9-methyl-3-oxa-9-azabicyclo[3.3.1]nonan-
-7-yl)-1H-indole-3-carboxamide;
(1R,5S,7s)-3-oxa-9-azabicyclo[3.3.1]nonan-7-yl
1-(isothiazol-3-yl)-1H-indole-3-carboxylate;
N-((1R,5S,7s)-9-methyl-3-oxa-9-azabicyclo[3.3.1]nonan-7-yl)-1-(thiazol-2--
yl)-1H-pyrrolo[2,3-b]pyridine-3-carboxamide;
N-((1R,5S,7s)-9-methyl-3-oxa-9-azabicyclo[3.3.1]nonan-7-yl)-1-(thiazol-4--
yl)-1H-pyrrolo[2,3-b]pyridine-3-carboxamide;
N-((1R,5S,7s)-9-methyl-3-oxa-9-azabicyclo[3.3.1]nonan-7-yl)-1-(thiazol-5--
yl)-1H-pyrrolo[2,3-b]pyridine-3-carboxamide;
1-(isothiazol-3-yl)-N-((1R,5S,7s)-9-methyl-3-oxa-9-azabicyclo[3.3.1]nonan-
-7-yl)-1H-indole-3-carboxamide;
1-(1-methyl-1H-imidazol-5-yl)-N-((1R,5S,7s)-9-methyl-3-oxa-9-azabicyclo[3-
.3.1]nonan-7-yl)-1H-indole-3-carboxamide;
(1R,5S,7s)-3-oxa-9-azabicyclo[3.3.1]nonan-7-yl
1-(isothiazol-5-yl)-1H-indole-3-carboxylate;
1-(isothiazol-5-yl)-N-((1R,5S,7s)-9-methyl-3-oxa-9-azabicyclo[3.3.1]nonan-
-7-yl)-1H-indole-3-carboxamide;
1-(cyanomethyl)-N-((1R,5S,7s)-9-methyl-3-oxa-9-azabicyclo[3.3.1]nonan-7-y-
l)-1H-indole-3-carboxamide;
(1R,5S,7s)-9-methyl-3-oxa-9-azabicyclo[3.3.1]nonan-7-yl
5-cyano-1-(2-fluoroethyl)-1H-indole-3-carboxylate;
(1R,5S,7s)-9-methyl-3-oxa-9-azabicyclo[3.3.1]nonan-7-yl
5-cyano-1-(6-fluoropyridazin-3-yl)-1H-indole-3-carboxylate;
5-fluoro-N-((1R,5S,7s)-9-methyl-3-oxa-9-azabicyclo[3.3.1]nonan-7-yl)-1-(t-
hiazol-2-yl)-1H-pyrrolo[2,3-b]pyridine-3-carboxamide;
5-fluoro-N-((1R,5S,7s)-9-methyl-3-oxa-9-azabicyclo[3.3.1]nonan-7-yl)-1-(t-
hiazol-4-yl)-1H-pyrrolo[2,3-b]pyridine-3-carboxamide;
5-fluoro-N-((1R,5S,7s)-9-methyl-3-oxa-9-azabicyclo[3.3.1]nonan-7-yl)-1-(t-
hiazol-5-yl)-1H-pyrrolo[2,3-b]pyridine-3-carboxamide;
N-((1R,5S,7s)-9-methyl-3-oxa-9-azabicyclo[3.3.1]nonan-7-yl)-1-(thiazol-5--
yl)-1H-indazole-3-carboxamide;
(1R,5S,7s)-3-oxa-9-azabicyclo[3.3.1]nonan-7-yl
1-(1-methyl-2-oxo-1,2-dihydropyridin-4-yl)-1H-indole-3-carboxylate;
(1R,5S,7s)-9-methyl-3-oxa-9-azabicyclo[3.3.1]nonan-7-yl
1-(6-hydroxypyridazin-3-yl)-1H-indole-3-carboxylate;
(1R,5S,7s)-3-oxa-9-azabicyclo[3.3.1]nonan-7-yl
1-(2-cyanophenyl)-1H-indole-3-carboxylate;
(1R,5S,7s)-3-oxa-9-azabicyclo[3.3.1]nonan-7-yl
1-(3-cyanophenyl)-1H-indole-3-carboxylate;
N-((1R,5S,7s)-9-methyl-3-oxa-9-azabicyclo[3.3.1]nonan-7-yl)-1-phenyl-1H-i-
ndole-3-carboxamide; (1R,5S,7s)-3-oxa-9-azabicyclo[3.3.1]nonan-7-yl
1-(oxazol-2-yl)-1H-indole-3-carboxylate;
N-((1R,5S,7s)-9-methyl-3-oxa-9-azabicyclo[3.3.1]nonan-7-yl)-1-(oxazol-2-y-
l)-1H-indole-3-carboxamide;
(1R,5S,7s)-3-oxa-9-azabicyclo[3.3.1]nonan-7-yl
1-(4-cyanophenyl)-1H-indole-3-carboxylate;
(1R,5S,7S)-9-methyl-3-oxa-9-azabicyclo[3.3.1]nonan-7-yl
1-(pyrazin-2-yl)-1H-indole-3-carboxylate;
(1R,5S,7S)-9-methyl-3-oxa-9-azabicyclo[3.3.1]nonan-7-yl
1-(isothiazol-3-yl)-1H-indole-3-carboxylate;
(1R,5S,7S)-9-methyl-3-oxa-9-azabicyclo[3.3.1]nonan-7-yl
1-(thiazol-5-yl)-1H-indole-3-carboxylate;
(1R,5S,7S)-9-methyl-3-oxa-9-azabicyclo[3.3.1]nonan-7-yl
1-(5-fluoropyrazin-2-yl)-1H-indole-3-carboxylate;
N-((1R,5S,7S)-3-oxa-9-azabicyclo[3.3.1]nonan-7-yl)-1-(isothiazol-4-yl)-N--
methyl-1H-indole-3-carboxamide;
1-(isothiazol-4-yl)-N-methyl-N-((1R,5S,7S)-9-methyl-3-oxa-9-azabicyclo[3.-
3.1]nonan-7-yl)-1H-indole-3-carboxamide;
(1R,5S,7S)-3-oxa-9-azabicyclo[3.3.1]nonan-7-yl
1-(cyanomethyl)-1H-indole-3-carboxylate;
(1R,5S,7S)-9-methyl-3-oxa-9-azabicyclo[3.3.1]nonan-7-yl
1-(pyrimidin-2-yl)-1H-indole-3-carboxylate;
(1R,5S,7S)-9-methyl-3-oxa-9-azabicyclo[3.3.1]nonan-7-yl
1-(pyrimidin-5-yl)-1H-indole-3-carboxylate; and
N-((1R,5S,7S)-9-methyl-3-oxa-9-azabicyclo[3.3.1]nonan-7-yl)-1-(pyridazin--
4-yl)-1H-indole-3-carboxamide; or a pharmaceutically acceptable
salt of each above mentioned compound.
15. A pharmaceutical composition comprising a compound of claim 1,
or pharmaceutically acceptable salt thereof, and a pharmaceutically
acceptable excipient.
16. The use of a compound of claim 1, or pharmaceutically
acceptable salt thereof, as a medicament.
Description
CROSS REFERENCE TO RELATED APPLICATIONS
[0001] This application is a divisional of U.S. Ser. No. 15/064,407
filed Mar. 8, 2016, now issued as U.S. Pat. No. 9,695,195, which is
a divisional of U.S. Ser. No. 14/415,712 filed Jan. 19, 2015, now
issued as U.S. Pat. No. 9,303,045, which is a 35 U.S.C. .sctn. 371
U.S. National Stage Entry of International Application
PCT/US2013/050762 filed Jul. 16, 2013, which claims the benefit of
the priority date of provisional application U.S. 61/672,709 filed
Jul. 17, 2012 and provisional application U.S. 61/708,521 filed
Oct. 1, 2012; the contents of these applications are herein
incorporated by reference in their entireties.
FIELD OF INVENTION
[0002] The present invention provides compounds that are 5-HT3
receptor antagonists and are therefore useful for the treatment of
diseases treatable by inhibition of the 5-HT3 receptor such as
emesis, pain, drug addiction, neurodegenerative and psychiatric
disorders, and GI disorders. Also provided are pharmaceutical
compositions containing such compounds and processes for preparing
such compounds.
BACKGROUND
[0003] Serotonin type 3 (5-HT3) receptors are part of the
serotonergic system. Unlike other receptors of this system, which
are all G-protein coupled receptors, the 5-HT3 receptors are
ligand-gated ion channels and belongs to the superfamily of
Cys-loop receptors that include nicotinic acetylcholine,
.gamma.-aminobutyric acid (GABA)A and glycine receptors and a Zn+2
activated cation channel (see Davies et al., 2003, J. Biol. Chem.,
278, 712-717; Connolly et al., 2004, Biochem Soc Trans 32,
529-534). The 5-HT3 receptors are made up of 5 subunits arranged
around a central ion conducting pore, which is permeable to sodium,
potassium, and calcium ions (see Boess et al., 1995, J. Neurochem.
64, 1401-1405; Connolly et al., 2004, Biochem Soc Trans 32,
529-534). Binding of serotonin to the 5-HT3 receptors opens the
channel, which, in turn, leads to an excitatory response in
neurons. Functional data reported for 5-HT3 receptors refer to
5-HT3A or 5-HT3AB receptors since the properties of these receptor
subtypes have been most extensively studies to date.
[0004] 5-HT3 receptors are known to be expressed in the central
nervous system in regions involving vomiting reflex, processing of
pain, cognition and anxiety control and play a role in the
pathogenesis of diseases such as emesis, migraine, drug addiction,
and neurodegenerative and psychiatric disorders such as anxiety and
depression (see Hewlett et al., 2003 J. Clin. Psychiatry 64,
1025-1030; Kelley et al., 2003a, Eur J. Pharmacol., 461, 19-25;
Haus et al., 2000 Scand J Rheumatol Suppl 113, 55-58; and Faris et
al., 2006 J affect Disorder 92, 79-90), eating disorders (Hammer et
al., 1990 Am J Physiol 259, R627-R636, and Jiang & Gietzen 1994
Pharmacol Biochem Behav 47, 59-63), schizophrenia (see Hermann et
al. 1996 Biochem Biophys Res Commun 225, 957-960; Sirota et al.,
2000 Am J Psychiatry 157, 287-289; Adler et al., 2005 Am J
Psychiatry 162, 386-388; Koike et al., Levkovitz et al, 2005
Schizophr Res 76, 67-72), cognitive dysfunction associated with
schizophrenia (see Zhang et al., 2006 Schizophr Res 88, 102-110;
Akhondzadeh et al., 2009 Schizophr Res 107, 206-212), cognitive
dysfunction associated with Parkinson's disease, Huntington's
Chorea, presenile dementias and Alzheimer's disease (see Costall
and Naylor 2004 CNS Neurol Disord 3, 27-37) substance abuse and
addiction (see Johnson et al., 2002 Psycho-pharmacology (Berl) 160,
408-413; Johnson, 2004 CNS Drugs 18, 1105-1118; Dawes et al., 2005
Addict Behav 30, 1630-1637, Johnson 2006 Drug Alcohol Depend 84,
256-263), autish spectrum disorders (see Anderson et al
Neurogenetics 10, 209-216) and pain (see Kayser et al, 2007 Pain
130, 235; Glaum et al., 1998 Neurosci Lett 95, 313-317; Schworer
& Ramadori 1993 Clin Investig 71, 659; Thompson and Lummis 2007
Exp Opin Ther Targets, 11, 527-540). In addition, 5-HT3 receptors
are expressed in the GI tract and hence may play a role in GI
disorders such as dyspepsia, gastroesophagal reflux disease and
irritable bowel syndrome (see Graeff 1997 Psychiatr Clin North Am
20, 723; Thompson and Lummis 2007 Exp Opin Ther Targets, 11,
527-540; Barnes et al. 2009 Neuropharmacology 56, 273). Expression
of the 5-HT3A subunit has also been discovered extraneuronally in
immune cells such as monocyes, chondrocytes, T-cells, synovial
tissue and platelets (Fiebich et al., 2004 Scan J Rheumatol Suppl,
9-11, Stratz et al., 2008 Thromb Haemost 99, 784) and of 5-HT3A,
C-E within the lamina propia in the epithelium of the gut mucose
(Kapeller et al., J Comp Neuro., 2008; 509: 356-371) thus
suggesting they may be involved in immunological and inflammatory
diseases like atherosclerosis, tendomyopathies and
fibromyalgia.
[0005] The 5-HT3 antagonists currently on the market are approved
only for the treatment of emesis or irritable bowel syndrome. It is
desirable to discover 5-HT3 antagonists that can be used to treat
other diseases amenable to alleviation by 5-HT3 receptors such as
schizophrenia and cognitive disorder associated with schizophrenia.
The present invention can fulfill this and related needs. It is
desirable to discover 5-HT3 antagonists that have desirable
pharmacokinetic and pharmacodynamic properties, such as selectivity
over nicotinic-.alpha.7 receptors.
[0006] Certain antagonists the 5-HT3 receptor are described in U.S.
Pat. No. 4,789,763; U.S. Pat. No. 4,803,199; U.S. Pat. No.
4,886,808; U.S. Pat. No. 4,910,193; U.S. Pat. No. 5,334,831; EP 0
469 449; and EP 0 491 664. Certain inhibitors of TGF-.beta. are
described in EP 1 156 045 and certain treatment of nephritis is
described in EP1 243 268. Certain antagonists of 5-HT4 are
described in EP 0 708 105. Certain ligands of nicotinic-.alpha.7
receptors are described in WO 2007/038367. Certain P2X7 antagonists
are disclosed in WO 2009/023623.
SUMMARY
[0007] In a first aspect, this invention is directed to a compound
of Formula (IA):
##STR00002##
wherein:
Z is O or NR.sub.a;
[0008] R.sub.a is hydrogen or C.sub.1-6 alkyl; R.sub.1 is a ring of
the formula (a)-(h) below:
##STR00003##
wherein: R.sub.2 is hydrogen, C.sub.1-6 alkyl, or C.sub.1-6
haloalkyl; each R.sub.3 is independently hydrogen, C.sub.1-6 alkyl,
C.sub.1-6 alkoxy, C.sub.1-6 haloalkoxy, or halo and can be present
on any carbon atom in the rings; R.sub.4 is C.sub.1-6 haloalkyl;
C.sub.1-6 cyanoalkyl; C.sub.1-6 alkylsulfonyl; C.sub.3-8
cycloalkylsulfonyl; heteroaryl selected from the group consisting
of furanyl, thienyl, pyrrolyl, imidazolyl, oxazolyl, isoxazolyl,
oxadiazolyl, thiazolyl, isothiazolyl, thiadiazolyl, triazolyl,
tetrazolyl, pyrazinyl, pyridazinyl, pyrimidyl, azepinyl,
diazepinyl, quinolyl, isoquinolyl, quinolizidine, benzofuranyl,
benzothienyl, indolyl, isoindolyl, indazolyl, benzimidazolyl,
benzisothiazolyl, benzisoxazolyl, benzoxadiazolyl, benzoxazolyl,
benzothiazolyl, benzothiadiazolyl, benzotriazolyl, benzopyrazinyl,
benzopyrazidinyl, benzoazepinyl, benzodiazepinyl, imidazopyridyl,
pyrazolopyridyl, pyrrolopyridyl, quinazolyl, purinyl, furopyridyl,
and thienopyridyl, each R.sub.4 heteroaryl is optionally
substituted with one or two substituents independently selected
from C.sub.1-6 alkyl, C.sub.1-6 haloalkyl, C.sub.1-6 haloalkoxy,
C.sub.1-6 alkoxy, hydroxy, cyano, or halo; C.sub.3-6
heterocycloalkyl optionally substituted with one or two
substituents independently selected from C.sub.1-6 alkyl, C.sub.1-6
alkoxy, C.sub.1-6 haloalkoxy, C.sub.1-6 alkylsulfonyl, or halo;
C.sub.3-6 oxoheterocycloalkyl optionally substituted with one or
two substituents independently selected from C.sub.1-6 alkyl,
C.sub.1-6 alkoxy, C.sub.1-6 haloalkoxy, C.sub.1-6 alkylsulfonyl, or
halo; or phenyl optionally substituted with one, two, or three
substituents independently selected from C.sub.1-6 alkyl, C.sub.1-6
haloalkyl, C.sub.1-6 haloalkoxy, C.sub.1-6 alkoxy, hydroxyl, cyano,
or halo; all of X.sub.1-X.sub.4 are CR.sub.5 or one of
X.sub.1-X.sub.4 is N and the others are CR.sub.5; each R.sub.5 is
independently hydrogen, C.sub.1-6 alkyl, halo, hydroxy, or cyano
provided that at least one of R.sub.5 is hydrogen; X.sup.5 is N or
CR.sup.6 where R.sup.6 is hydrogen, C.sub.1-6 alkyl, or halo or
R.sup.6 together with R.sup.4 and atoms to which they are attached
form --O--(CH.sub.2).sub.2--, --O--(CH.sub.2).sub.3--, or
--O--(CH.sub.2).sub.4--; or a pharmaceutically acceptable salt
thereof or N-oxide thereof and provided that the compound of
Formula (IA) is not: [0009]
N-(3)-1-azabicyclo[2.2.2]oct-3-yl-6-bromo-1-(difluoromethyl)-1H-in-
dazole-3-carboxamide, [0010]
N-(3)-1-azabicyclo[2.2.2]oct-3-yl-1-(difluoromethyl)-6-methoxy-1H-indazol-
e-3-carboxamide, [0011]
N-(3)-1-azabicyclo[2.2.2]oct-3-yl-5-bromo-1-(2,2,2-trifluoroethyl)-1H-ind-
azole-3-carboxamide, [0012]
N-(3)-1-azabicyclo[2.2.2]oct-3-yl-5-methoxy-1-(2,2,2-trifluoroethyl)-1H-i-
ndazole-3-carboxamide, [0013] or
N-(3)-1-azabicyclo[2.2.2]oct-3-yl-1-(3-thienyl)-1H-indazole-3-carboxamide-
.
[0014] In one embodiment of the first aspect, the compounds have
Formula (I):
##STR00004##
wherein:
Z is O or NR.sub.a;
[0015] R.sub.a is hydrogen or C.sub.1-6 alkyl; R.sub.1 is a ring of
the formula (a)-(h) below:
##STR00005##
wherein: R.sub.2 is hydrogen, C.sub.1-6 alkyl, or C.sub.1-6
haloalkyl; each R.sub.3 is independently hydrogen, C.sub.1-6 alkyl,
C.sub.1-6 alkoxy, C.sub.1-6 haloalkoxy, or halo and can be present
on any carbon atom in the rings; R.sub.4 is heteroaryl selected
from the group consisting of furanyl, thienyl, pyrrolyl,
imidazolyl, oxazolyl, isoxazolyl, oxadiazolyl, thiazolyl,
isothiazolyl, thiadiazolyl, triazolyl, tetrazolyl, pyrazinyl,
pyridazinyl, pyrimidyl, azepinyl, diazepinyl, quinolyl,
isoquinolyl, quinolizidine, benzofuranyl, benzothienyl, indolyl,
isoindolyl, indazolyl, benzimidazolyl, benzisothiazolyl,
benzisoxazolyl, benzoxadiazolyl, benzoxazolyl, benzothiazolyl,
benzothiadiazolyl, benzotriazolyl, benzopyrazinyl,
benzopyrazidinyl, benzoazepinyl, benzodiazepinyl, imidazopyridyl,
pyrazolopyridyl, pyrrolopyridyl, quinazolyl, purinyl, furopyridyl,
and thienopyridyl; each R.sub.4 heteroaryl is optionally
substituted with one or two substituents independently selected
from C.sub.1-6 alkyl, C.sub.1-6 haloalkyl, C.sub.1-6 haloalkoxy,
C.sub.1-6 alkoxy, hydroxy, cyano, or halo; all of X.sub.1-X.sub.4
are CR.sub.5 or one of X.sub.1-X.sub.4 is N and the others are
CR.sub.5; each R.sub.5 is independently hydrogen, C.sub.1-6 alkyl,
halo, hydroxy, or cyano provided that at least one of R.sub.5 is
hydrogen; X.sup.5 is N or CR.sup.6 where R.sup.6 is hydrogen,
C.sub.1-6 alkyl, or halo or R.sup.6 together with R.sup.4 and atoms
to which they are attached form --O--(CH.sub.2).sub.2--,
--O--(CH.sub.2).sub.3--, or --O--(CH.sub.2).sub.4--; or a
pharmaceutically acceptable salt thereof or N-oxide thereof and
provided that the compound of Formula (I) is not:
N-(3)-1-azabicyclo[2.2.2]oct-3-yl-1-(3-thienyl)-1H-Indazole-3-carboxamide-
.
[0016] In a second aspect, this present invention is directed to a
pharmaceutical composition comprising a compound of Formula (IA) or
(I) (or any embodiments thereof disclosed herein) or a
pharmaceutically acceptable salt thereof and a pharmaceutically
acceptable excipient; provided the compound of Formula (IA) is not
N-(3)-1-azabicyclo[2.2.2]oct-3-yl-6-bromo-1-(difluoromethyl)-1H-Indazole--
3-carboxamide,
N-(3)-1-azabicyclo[2.2.2]oct-3-yl-1-(difluoromethyl)-6-methoxy-1H-Indazol-
e-3-carboxamide,
N-(3)-1-azabicyclo[2.2.2]oct-3-yl-5-bromo-1-(2,2,2-trifluoroethyl)-1H-Ind-
azole-3-carboxamide,
N-(3)-1-azabicyclo[2.2.2]oct-3-yl-5-methoxy-1-(2,2,2-trifluoroethyl)-1H-I-
ndazole-3-carboxamide, or
N-(3)-1-azabicyclo[2.2.2]oct-3-yl-1-(3-thienyl)-1H-Indazole-3-carboxamide
or the compound of Formula (I) is not
N-(3)-1-azabicyclo[2.2.2]oct-3-yl-1-(3-thienyl)-1H-Indazole-3-carboxamide-
; individual stereoisomers, or a pharmaceutically acceptable salt
thereof.
[0017] In a third aspect, this present invention is directed to a
method of treating a disease treatable by administration of a 5-HT3
receptor antagonist which method comprises administrating to the
patient a pharmaceutical composition comprising a compound of
Formula (IA) or (I) (or any embodiments thereof disclosed herein)
and/or a pharmaceutically acceptable salt and a pharmaceutically
acceptable excipient provided the compound of Formula (IA) is not
N-(3)-1-azabicyclo[2.2.2]oct-3-yl-6-bromo-1-(difluoromethyl)-1H-Indazole--
3-carboxamide,
N-(3)-1-azabicyclo[2.2.2]oct-3-yl-1-(difluoromethyl)-6-methoxy-1H-Indazol-
e-3-carboxamide,
N-(3)-1-azabicyclo[2.2.2]oct-3-yl-5-bromo-1-(2,2,2-trifluoroethyl)-1H-Ind-
azole-3-carboxamide,
N-(3)-1-azabicyclo[2.2.2]oct-3-yl-5-methoxy-1-(2,2,2-trifluoroethyl)-1H-I-
ndazole-3-carboxamide, or
N-(3)-1-azabicyclo[2.2.2]oct-3-yl-1-(3-thienyl)-1H-Indazole-3-carboxamide
or the compound of Formula (I) is not
N-(3)-1-azabicyclo[2.2.2]oct-3-yl-1-(3-thienyl)-1H-Indazole-3-carboxamide-
. That is, In a the present invention provides a method of treating
a disease treatable by administration of a 5-HT3 receptor
antagonist comprising: administrating to the patient in need
thereof an effective amount of a compound of Formula (IA) or (I)
(or any embodiments thereof disclosed herein) or a pharmaceutically
acceptable salt thereof provided the compound of Formula (IA) is
not
N-(3)-1-azabicyclo[2.2.2]oct-3-yl-6-bromo-1-(difluoromethyl)-1H-Indazole--
3-carboxamide,
N-(3)-1-azabicyclo[2.2.2]oct-3-yl-1-(difluoromethyl)-6-methoxy-1H-Indazol-
e-3-carboxamide,
N-(3)-1-azabicyclo[2.2.2]oct-3-yl-5-bromo-1-(2,2,2-trifluoroethyl)-1H-Ind-
azole-3-carboxamide,
N-(3)-1-azabicyclo[2.2.2]oct-3-yl-5-methoxy-1-(2,2,2-trifluoroethyl)-1H-I-
ndazole-3-carboxamide, or
N-(3)-1-azabicyclo[2.2.2]oct-3-yl-1-(3-thienyl)-1H-Indazole-3-carboxamide
or the compound of Formula (I) is not
N-(3)-1-azabicyclo[2.2.2]oct-3-yl-1-(3-thienyl)-1H-Indazole-3-carboxamide-
.
[0018] In one embodiment of the third aspect, the disease is
emesis, migraine, substance abuse and addiction, neurodegenerative
and psychiatric disorders such as anxiety and depression, eating
disorders, schizophrenia, cognitive dysfunction associated with
schizophrenia, Parkinson's disease, Huntington's Chorea, presenile
dementias and Alzheimer's disease, and pain; GI disorders such as
dyspepsia, gastroesophagal reflux disease, and irritable bowel
syndrome; and immunological disorders and inflammation such as
atherosclerosis, tendomyopathies and fibromyalgia. In another
embodiment of the third aspect the disease is schizophrenia or
cognitive dysfunction associated with schizophrenia.
[0019] In a fourth aspect, the compound of Formula (IA) or (I) (or
any embodiments thereof disclosed herein) or a pharmaceutically
acceptable salt thereof is administered in combination with an
antipsychotic drug provided the compound of Formula (IA) is not
N-(3)-1-azabicyclo[2.2.2]oct-3-yl-6-bromo-1-(difluoromethyl)-1H-Indazole--
3-carboxamide,
N-(3)-1-azabicyclo[2.2.2]oct-3-yl-1-(difluoromethyl)-6-methoxy-1H-Indazol-
e-3-carboxamide,
N-(3)-1-azabicyclo[2.2.2]oct-3-yl-5-bromo-1-(2,2,2-trifluoroethyl)-1H-Ind-
azole-3-carboxamide,
N-(3)-1-azabicyclo[2.2.2]oct-3-yl-5-methoxy-1-(2,2,2-trifluoroethyl)-1H-I-
ndazole-3-carboxamide, or
N-(3)-1-azabicyclo[2.2.2]oct-3-yl-1-(3-thienyl)-1H-Indazole-3-carboxamide
or the compound of Formula (I) is not
N-(3)-1-azabicyclo[2.2.2]oct-3-yl-1-(3-thienyl)-1H-Indazole-3-carboxamide-
. In one embodiment of the fourth aspect, the antipsychotic drug is
AMG 747, bitopertin (RG1678), RG1578, AMG579, GSK1018921,
aripiprazole, risperidone, olanzapine, quetiapine, ziprasidone, or
clozapine.
[0020] In a fifth aspect, the invention is directed to use of
compound of Formula (IA) or (I) (or any embodiments thereof
disclosed herein) or a pharmaceutically acceptable salt thereof as
a medicament; provided the compound of Formula (IA) is not
N-(3)-1-azabicyclo[2.2.2]oct-3-yl-6-bromo-1-(difluoromethyl)-1H-Indazole--
3-carboxamide,
N-(3)-1-azabicyclo[2.2.2]oct-3-yl-1-(difluoromethyl)-6-methoxy-1H-Indazol-
e-3-carboxamide,
N-(3)-1-azabicyclo[2.2.2]oct-3-yl-5-bromo-1-(2,2,2-trifluoroethyl)-1H-Ind-
azole-3-carboxamide,
N-(3)-1-azabicyclo[2.2.2]oct-3-yl-5-methoxy-1-(2,2,2-trifluoroethyl)-1H-I-
ndazole-3-carboxamide, or
N-(3)-1-azabicyclo[2.2.2]oct-3-yl-1-(3-thienyl)-1H-Indazole-3-carboxamide
or the compound of Formula (I) is not
N-(3)-1-azabicyclo[2.2.2]oct-3-yl-1-(3-thienyl)-1H-Indazole-3-carboxamide-
; individual stereoisomers, or a pharmaceutically acceptable salt
thereof.
[0021] In a sixth aspect, the invention is directed to a compound
of Formula (IA) or (I) (or any embodiments thereof disclosed
herein) or a pharmaceutically acceptable salt thereof for use as
medicament; provided the compound of Formula (IA) is not
N-(3)-1-azabicyclo[2.2.2]oct-3-yl-6-bromo-1-(difluoromethyl)-1H-Indazole--
3-carboxamide,
N-(3)-1-azabicyclo[2.2.2]oct-3-yl-1-(difluoromethyl)-6-methoxy-1H-Indazol-
e-3-carboxamide,
N-(3)-1-azabicyclo[2.2.2]oct-3-yl-5-bromo-1-(2,2,2-trifluoroethyl)-1H-Ind-
azole-3-carboxamide,
N-(3)-1-azabicyclo[2.2.2]oct-3-yl-5-methoxy-1-(2,2,2-trifluoroethyl)-1H-I-
ndazole-3-carboxamide, or
N-(3)-1-azabicyclo[2.2.2]oct-3-yl-1-(3-thienyl)-1H-Indazole-3-carboxamide
or the compound of Formula (I) is not
N-(3)-1-azabicyclo[2.2.2]oct-3-yl-1-(3-thienyl)-1H-Indazole-3-carboxamide-
; individual stereoisomers, or a pharmaceutically acceptable salt
thereof.
[0022] In one embodiment of the fifth and sixth aspects, the use is
for the treatment of emesis, migraine, substance abuse and
addiction, neurodegenerative and psychiatric disorders such as
anxiety and depression, eating disorders, schizophrenia, cognitive
dysfunction associated with schizophrenia, Parkinson's disease,
Huntington's Chorea, presenile dementias and Alzheimer's disease,
and pain; GI disorders such as dyspepsia, gastroesophagal reflux
disease, and irritable bowel syndrome; and immunological disorders
and inflammation such as atherosclerosis, tendomyopathies and
fibromyalgia. In another embodiment of the fifth and the sixth
aspects the use is for the treatment of schizophrenia or cognitive
dysfunction associated with schizophrenia also known as cognitive
impairment associated with schizophrenia. In yet another embodiment
of the fifth and the sixth aspects, and embodiments contained
therein, the compound of Formula (IA) or (I) is administered in
combination with an antipsychotic drug. In one embodiment, the
antipsychotic drug is AMG 747, bitopertin (RG1678), RG1578, AMG579,
GSK1018921, aripiprazole, risperidone, olanzapine, quetiapine, or
ziprasidone, clozapine.
DETAILED DESCRIPTION OF THE INVENTION
Definitions
[0023] Unless otherwise stated, the following terms used in the
specification and claims are defined for the purposes of this
Application and have the following meaning:
[0024] "C.sub.1-6 alkyl" means a linear saturated monovalent
hydrocarbon radical of one to six carbon atoms or a branched
saturated monovalent hydrocarbon radical of three to six carbon
atoms, e.g., methyl, ethyl, propyl, 2-propyl, butyl (including all
isomeric forms), pentyl (including all isomeric forms), and the
like.
[0025] "C.sub.1-6 alkoxy" means a --OR radical where R is C.sub.1-6
alkyl as defined above, e.g., methoxy, ethoxy, propoxy, or
2-propoxy, n-, iso-, or tert-butoxy, and the like.
[0026] "C.sub.1-6 alkylsulfonyl" means a --SO.sub.2R radical where
R is C.sub.1-6 alkyl as defined above, e.g., methylsulfonyl,
ethylsulfonyl, 2-propylsulfonyl, and the like.
[0027] "C.sub.3-8 cycloalkyl" means a 3 to 8 membered saturated
cyclic hydrocarbon radical e.g., cyclopropyl, cyclobutyl,
cyclopentyl, cyclohexyl, and the like.
[0028] "C.sub.3-8 cycloalkylsulfonyl" means a --SO.sub.2R radical
where R is C.sub.3-8 cycloalkyl as defined above, e.g.,
cyclopropylsulfonyl, and the like.
[0029] "C.sub.1-6 cyanoalkyl" means C.sub.1-6 alkyl radical as
defined above where one hydrogen atoms in the alkyl radical is
replaced by cyano, e.g., cyanoethyl, cyanopropyl, and the like.
[0030] "Halo" means fluoro, chloro, bromo, or iodo, preferably
fluoro or chloro.
[0031] "C.sub.1-6 haloalkyl" means C.sub.1-6 alkyl radical as
defined above, which is substituted with one or more halogen atoms,
preferably one to five halogen atoms, preferably fluorine or
chlorine, including those substituted with different halogens,
e.g., --CH.sub.2Cl, --CF.sub.3, --CHF.sub.2, --CH.sub.2CF.sub.3,
--CF.sub.2CF.sub.3, --CF(CH.sub.3).sub.2, and the like. When the
C.sub.1-6 alkyl is substituted with only fluoro, it can be referred
to in this Application as C.sub.1-6 fluoroalkyl.
[0032] "C.sub.1-6 haloalkoxy" means a --OR radical where R is
C.sub.1-6 haloalkyl as defined above e.g., --OCF.sub.3,
--OCHF.sub.2, and the like. When R is haloalkyl where the C.sub.1-6
alkyl is substituted with only fluoro, it can be referred to in
this Application as C.sub.1-6 fluoroalkoxy.
[0033] "C.sub.3-6 heterocycloalkyl" means a saturated or
unsaturated monovalent monocyclic group of 4 to 8 ring atoms in
which one or two ring atoms are heteroatom selected from N, O, or
S(O).sub.n, where n is an integer from 0 to 2, the remaining ring
atoms being C, unless stated otherwise. More specifically the term
heterocyclyl includes, but is not limited to, pyrrolyl,
piperidinyl, homopiperidinyl, morpholinyl, piperazinyl,
tetrahydrofuranyl, tetrahydropyranyl, thiomorpholinyl, and the
like. When the heterocyclyl ring is unsaturated it can contain one
or two ring double bonds provided that the ring is not
aromatic.
[0034] "C.sub.1-5 heteroaryl" means a monovalent monocyclic
aromatic radical of 5 or 6 ring atoms where one, two, or three,
ring atoms are heteroatom selected from N, O, or S, the remaining
ring atoms being carbon. Representative examples include, but are
not limited to, pyrrolyl, thienyl, thiazolyl, imidazolyl,
pyrazolyl, furanyl, oxazolyl, isoxazolyl, pyridinyl, pyrimidinyl,
pyrazinyl, pyridazinyl, triazolyl, and the like.
[0035] "C.sub.3-6 oxoheterocycloalkyl" means a saturated or
unsaturated monovalent monocyclic group of 4 to 8 ring atoms in
which one or two ring atoms are heteroatom selected from N, O, or
S(O).sub.n, where n is an integer from 0 to 2, and one or two rings
atoms are --C(O)--, the remaining ring atoms being C, unless stated
otherwise. More specifically the term heterocyclyl includes, but is
not limited to, 2-oxo-1,2-dihydropyridinyl, and the like. When the
heterocyclyl ring is unsaturated it can contain one or two ring
double bonds provided that the ring is not aromatic.
[0036] The present invention also includes the prodrugs of
compounds of Formula (IA) and (I). The term prodrug is intended to
represent covalently bonded carriers, which are capable of
releasing the active ingredient of Formula (IA) and (I)
respectively, when the prodrug is administered to a mammalian
subject. Release of the active ingredient occurs in vivo. Prodrugs
can be prepared by techniques known to one skilled in the art.
These techniques generally modify appropriate functional groups in
a given compound. These modified functional groups however
regenerate original functional groups in vivo or by routine
manipulation. Prodrugs of compounds of Formula (IA) and (I) include
compounds wherein a hydroxy, amino, carboxylic, or a similar group
is modified. Examples of prodrugs include, but are not limited to
esters (e.g., acetate, formate, and benzoate derivatives),
carbamates (e.g., N,N-dimethylaminocarbonyl) of hydroxy or amino
functional groups in compounds of Formula (IA) and (I)), amides
(e.g., trifluoroacetylamino, acetylamino, and the like), and the
like. Prodrugs of compounds of Formula (IA) and (I) are also within
the scope of this invention.
[0037] The present invention also includes protected derivatives of
compounds of Formula (IA) and (I). For example, when compounds of
Formula (IA) and (I) contain groups such as hydroxy, carboxy, thiol
or any group containing a nitrogen atom(s), these groups can be
protected with a suitable protecting groups. A comprehensive list
of suitable protective groups can be found in T. W. Greene,
Protective Groups in Organic Synthesis, John Wiley & Sons, Inc.
(1999), the disclosure of which is incorporated herein by reference
in its entirety. The protected derivatives of compounds of Formula
(IA) and (I) can be prepared by methods well known in the art.
[0038] A "pharmaceutically acceptable salt" of a compound means a
salt that is pharmaceutically acceptable and that possesses the
desired pharmacological activity of the parent compound. Such salts
include: acid addition salts, formed with inorganic acids such as
hydrochloric acid, hydrobromic acid, sulfuric acid, nitric acid,
phosphoric acid, and the like; or formed with organic acids such as
formic acid, acetic acid, propionic acid, hexanoic acid,
cyclopentanepropionic acid, glycolic acid, pyruvic acid, lactic
acid, malonic acid, succinic acid, malic acid, maleic acid, fumaric
acid, tartaric acid, citric acid, benzoic acid,
3-(4-hydroxybenzoyl)benzoic acid, cinnamic acid, mandelic acid,
methanesulfonic acid, ethanesulfonic acid, 1,2-ethanedisulfonic
acid, 2-hydroxyethanesulfonic acid, benzenesulfonic acid,
4-chlorobenzenesulfonic acid, 2-naphthalenesulfonic acid,
4-toluenesulfonic acid, camphorsulfonic acid, glucoheptonic acid,
4,4'-methylenebis-(3-hydroxy-2-ene-1-carboxylic acid),
3-phenylpropionic acid, trimethylacetic acid, tertiary butylacetic
acid, lauryl sulfuric acid, gluconic acid, glutamic acid,
hydroxynaphthoic acid, salicylic acid, stearic acid, muconic acid,
and the like; or salts formed when an acidic proton present in the
parent compound either is replaced by a metal ion, e.g., an alkali
metal ion, an alkaline earth ion, or an aluminum ion; or
coordinates with an organic base such as ethanolamine,
diethanolamine, triethanolamine, tromethamine, N-methylglucamine,
and the like. It is understood that the pharmaceutically acceptable
salts are non-toxic. Additional information on suitable
pharmaceutically acceptable salts can be found in Remington's
Pharmaceutical Sciences, 17th ed., Mack Publishing Company, Easton,
Pa., 1985, which is incorporated herein by reference.
[0039] The compounds of the present invention may have asymmetric
centers. Compounds of the present invention containing an
asymmetrically substituted atom may be isolated in optically active
or racemic forms. It is well known in the art how to prepare
optically active forms, such as by resolution of materials. All
chiral, diastereomeric, meso, racemic forms are within the scope of
this invention, unless the specific stereochemistry or isomeric
form is specifically indicated.
[0040] Additionally, as used herein the term C.sub.1-6 alkyl and
terms derived therefrom includes all the possible isomeric forms of
said C.sub.1-6 alkyl group. Furthermore, the cyclic groups such as
aryl, heteroaryl, C.sub.3-6 heterocycloalkyl include all the
positional isomers. Furthermore, all polymorphic forms and hydrates
of a compound of Formula (IA) and Formula (I) are within the scope
of this invention.
[0041] The terms "compound" and "a compound of the invention" and
"compound of the present invention" and the like, and their plural
expressions include the embodiment of Formula (IA) and Formula (I)
and the other more particular embodiments encompassed by Formula
(IA) and Formula (I) described herein and exemplified compounds
described herein and a pharmaceutically acceptable salt of each of
these embodiments. All references to compounds, include all
isotopes of the atoms contained therein, including
isotopically-labeled compounds.
[0042] The compounds of the present invention exist as tautomers.
All tautomeric forms the compounds of the invention are
contemplated to be within the scope of the present invention.
[0043] "Optional" or "optionally" means that the subsequently
described event or circumstance may but need not occur, and that
the description includes instances where the event or circumstance
occurs and instances in which it does not. For example, "C.sub.3-6
heterocycloalkyl group optionally substituted with an C.sub.1-6
alkyl group" means that the alkyl may but need not be present, and
the description includes situations where the heterocycloalkyl
group is substituted with an alkyl group and situations where the
heterocycloalkyl group is not substituted with alkyl.
[0044] A "pharmaceutically acceptable carrier or excipient" means a
carrier or an excipient that is useful in preparing a
pharmaceutical composition that is generally safe, non-toxic and
neither biologically nor otherwise undesirable, and includes a
carrier or an excipient that is acceptable for veterinary use as
well as human pharmaceutical use. "A pharmaceutically acceptable
carrier/excipient" as used in the specification and claims includes
both one and more than one such excipient. Pharmaceutically
acceptable excipients are well known in the art, such as those in
Remington's Pharmaceutical Sciences, 17th ed., Mack Publishing
Company, Easton, Pa., 1985.
[0045] The terms "condition," "disorder," and "disease" relate to
any unhealthy or abnormal state.
[0046] "Treat," "treating," or "treatment" of a disease
includes:
[0047] (1) preventing the disease, i.e. causing the clinical
symptoms of the disease not to develop in a mammal that may be
exposed to or predisposed to the disease but does not yet
experience or display symptoms of the disease;
[0048] (2) inhibiting the disease, i.e., arresting, controlling,
slowing, stopping, or reducing the development of the disease or
its clinical symptoms; or
[0049] (3) relieving the disease, i.e., causing regression of the
disease or its clinical symptoms or improvement of the disease or
its clinical symptoms
[0050] The terms "treat," "treating," and "treatment," do not
necessarily indicate a total elimination of any or all symptoms or
a cure of the disease.
[0051] As used herein the terms "patient" and "subject" includes
humans and non-human animals, for example, mammals, such as mice,
rats, guinea pigs, dogs, cats, rabbits, cows, horses, sheep, goats,
and pigs. The term also includes birds, fish, reptiles, amphibians,
and the like. It is understood that a more particular patient is a
human. Also, more particular patients and subjects are non-human
mammals, such as mice, rats, and dogs.
[0052] A "therapeutically effective amount" means the amount of a
compound of Formula (I) or Formula (IA) or a pharmaceutically
acceptable salt thereof that, when administered in single or
multiple doses, to a mammal for treating a disease, is sufficient
to effect such treatment for the disease. The "therapeutically
effective amount" will vary depending on the compound, the disease
and its severity and the age, weight, etc., of the mammal to be
treated, the degree of or involvement or the severity of the
condition, disorder, or disease, the response of the individual
patient; the particular compound administered; the mode of
administration; the bioavailability characteristics of the
preparation administered; the dose regimen selected; the use of
concomitant medication; and other relevant circumstances.
[0053] The term "disease treatable by administration of a 5-HT3
receptor antagonist" includes emesis, migraine, substance abuse and
addiction, neurodegenerative and psychiatric disorders such as
anxiety and depression, eating disorders, schizophrenia, cognitive
dysfunction associated with schizophrenia, Parkinson's disease,
Huntington's Chorea, presenile dementias and Alzheimer's disease,
and pain; GI disorders such as dyspepsia, gastroesophagal reflux
disease, and irritable bowel syndrome; and immunological disorders
and inflammation such as atherosclerosis, tendomyopathies and
fibromyalgia. In a particular embodiment the disease is cognitive
dysfunction associated with schizophrenia also known as cognitive
impairment associated with schizophrenia.
[0054] Representative compounds of the Invention are shown in Table
I below:
TABLE-US-00001 Cpd. No. ##STR00006## -Z-R.sup.1 Salt name MS Calcd.
MS Obs. (M + 1).sup.+ 1 ##STR00007## ##STR00008## TFA
(1R,3R,5S)-8-methyl-8- azabicyclo[3.2.1]octan-3-yl- 5-fluoro-1-
(2,2,2-trifluoroethyl)-1H-indole- 3-carboxylate; 2,2,2-
trifluoroacetate 384.3679 385.2 2 ##STR00009## ##STR00010## TFA
(1R,3R,5S)-8-methyl-8- azabicyclo[3.2.1]octan-3-yl 5-fluoro-1-
((R)-tetrahydrofuran- 3-yl)-1H-indole- 3-carboxylate; 2,2,2-
trifluoroacetate 372.4332 373.1 3 ##STR00011## ##STR00012## TFA
(1R,3R,5S)-8-methyl-8- azabicyclo[3.2.1]octan- 3-yl 2-methyl-
1-(methylsulfonyl)-1H-indole-3- carboxylate; 2,2,2-
trifluoroacetate 376.4698 377.25 4 ##STR00013## ##STR00014## TFA
(1R,3R,5S)-9-methyl-9- azabicyclo[3.3.1]nonan-3-yl 1-
(methylsulfonyl)-1H-indazole-3- carboxylate, 2,2,2-
trifluoroacetate 377.4579 378.2 5 ##STR00015## ##STR00016## TFA
N-((1R,5S,7S)-9-methyl-3-oxa-9- azabicyclo[3.3.1]nonan-7-yl)-
1-(2,2,2-trifluoroethyl)-1H- pyrrolo[2,3-b]pyridine-3- carboxamide,
2,2,2-trifluoroacetate 382.3802 383.3 6 ##STR00017## ##STR00018##
TFA N-((1R,5S,7S)-3-oxa-9- azabicyclo[3.3.1]nonan- 7-yl)-5-fluoro-
1-(2,2,2-trifluoroethyl)-1H- indole-3-carboxamide, 2,2,2-
trifluoroacetate 385.356 386.2 7 ##STR00019## ##STR00020## TFA
1-(2,2-difluoroethyl)-N- ((1R,3R,5S)-9-methyl-9-
azabicyclo[3.3.1]nonan-3-yl)-1H- indazole-3-carboxamide,
2,2,2-trifluoroacetate 362.4169 363.3 8 ##STR00021## ##STR00022##
N-((1R,5S,7S)-9-methyl-3-oxa-9- azabicyclo[3.3.1]nonan-7-yl)-
1-(2,2,2-trifluoroethyl)-1H- indole-3-carboxamide 381.3921 382.2 9
##STR00023## ##STR00024## TFA (1R,5S,7S)-3-oxa-9-
azabicyclo[3.3.1]nonan-7-yl)- (isopropylsulfonyl)-1H-indole-3-
carboxylate, 2,2,2- trifluoroacetate 392.4693 393.2 10 ##STR00025##
##STR00026## TFA 1-(isopropylsulfonyl)- N-((1R,5S,7S)-
9-methyl-3-oxa-9- azabicyclo[3.3.1]nonan-7-yl)- 1H-indole-
3-carboxamide, 2,2,2-trifluoroacetate 405.5111 406.2 12
##STR00027## ##STR00028## TFA 1-(2-fluoroethyl)-N-((1R,3R,5S)-9-
methyl-9-azabicyclo[3.3.1]- nonan-3-yl)-1H-indazole-3- carboxamide,
2,2,2-trifluoroacetate 344.4264 345.3 13 ##STR00029## ##STR00030##
TFA (1R,3R,5S)-8-methyl-8- azabicyclo[3.2.1]octan- 3-yl 2-chloro-1-
(methylsulfonyl)-1H-indole- 3-carboxylate, 2,2,2- trifluoroacetate
396.8883 397.2 14 ##STR00031## ##STR00032## TFA
(1R,3R,5S)-8-azabicyclo [3.2.1]octan-3-yl 1-(2,2,2-
trifluoroethyl)-1H-indole-3- carboxylate, 2,2,2-trifluoroacetate
352.3509 353.2 15 ##STR00033## ##STR00034## TFA
(1R,3R,5S)-8-methyl-8- azabicyclo[3.2.1]octan-3-yl 1-(2-
fluoroethyl)-2-methyl-1H-indole- 3-carboxylate, 2,2,2-
trifluoroacetate 344.4231 345.3 16 ##STR00035## ##STR00036## TFA
(1R,3R,5S)-9-methyl-9- azabicyclo[3.3.1]nonan-3-yl
1-(2-fluoroethyl)-1H- indazole-3-carboxylate,
2,2,2-trifluoroacetate; 2,2,2-trifluoroacetate 345.4112 346.2 17
##STR00037## ##STR00038## TFA (1R,3R,5S)-8-methyl-8-
azabicyclo[3.2.1]octan-3-yl 1-(2,2,2-
trifluoroethyl)-1H-indazole-3- carboxylate, 2,2,2- trifluoroacetate
367.3655 368.2 18 ##STR00039## ##STR00040## TFA
5-fluoro-N-((1R,3R,5S)- 8-methyl-8- azabicyclo[3.2.1]octan-3-
yl)-1-(methylsulfonyl)-1H-indole-3- carboxamide, 2,2,2-
trifluoroacetate 379.449 380.2 19 ##STR00041## ##STR00042## TFA
(1R,5S,7S)-3-oxa-9- azabicyclo[3.3.1]nonan- 7-yl 5-fluoro-1-
(methylsulfonyl)-1H-indole-3- carboxylate, 2,2,2- trifluoroacetate
382.4066 383.2 20 ##STR00043## ##STR00044## TFA
1-(2,2-difluoroethyl)-N- ((1R,5S,7S)-9-methyl-3-oxa-9-
azabicyclo[3.3.1]nonan-7-yl)- 1H-indazole-3- carboxamide,
2,2,2-trifluoroacetate 364.3897 365.3 21 ##STR00045## ##STR00046##
TFA 1-(2,2-difluoroethyl)-N- ((1R,5S,7S)-9-methyl-3-
oxa-9-azabicyclo[3.3.1]nonan-7-yl)- 1H-indole-3-carboxamide, 2,2,2-
trifluoroacetate 363.4016 364.2 22 ##STR00047## ##STR00048##
N-((1R,5S,7S)-9-methyl-3-oxa-9- azabicyclo[3.3.1]nonan-7-yl)-
1-((S)-1,2,2,2-tetrafluoroethyl)-1H- pyrrolo[2,3-b]pyridine-3-
carboxamide 400.3706 401 24 ##STR00049## ##STR00050## TFA
5-fluoro-1-(2,2,2-trifluoroethyl)-
N-((1R,5S,7S)-9-methyl-d.sub.3-3- oxa-9-azabicyclo[3.3.1]nonan-
7-yl)-1H-pyrrolo[2,3-b]pyridine- 3-carboxamide,
2,2,2-trifluoroacetate 403.3891 404.2 25 ##STR00051## ##STR00052##
TFA (1R,5S,7S)-3-oxa-9- azabicyclo[3.3.1]nonan- 7-yl 1-(pyrimidin-
2-yl)-1H-indole-3-carboxylate, 2,2,2-trifluoroacetate 364.3978
365.2 26 ##STR00053## ##STR00054## TFA (1R,3R,5S)-8-methyl-8-
azabicyclo[3.2.1]octan-3-yl 1- (methylsulfonyl)-1H-indole-3-
carboxylate, 2,2,2- trifluoroacetate 362.4433 363.2 27 ##STR00055##
##STR00056## TFA (1R,3R,5S)-8-methyl-8- azabicyclo[3.2.1]octan-3-yl
1-(2,2- difluoroethyl)-5-fluoro-1H- indole-3-carboxylate,
2,2,2-trifluoroacetate 366.3774 367 28 ##STR00057## ##STR00058##
TFA (1R,3R,5S)-8-methyl-8- azabicyclo[3.2.1]octan-3-yl 2,3-
dihydrooxazolo[3,2-a]indole- 9-carboxylate, 2,2,2- trifluoroacetate
326.3896 327.25 29 ##STR00059## ##STR00060## TFA
(1R,3R,5S)-8-methyl-8- azabicyclo[3.2.1]octan- 3-yl 5-fluoro-1-
(tetrahydrofuran-3-yl)-1H-indole-3- carboxylate, 2,2,2-
trifluoroacetate 372.4332 373.25 30 ##STR00061## ##STR00062## TFA
(1R,3R,5S)-9-methyl-9- azabicyclo[3.3.1]nonan- 3-yl 2-chloro-
1-(2-fluoroethyl)-1H-indole-3- carboxylate, 2,2,2- trifluoroacetate
378.8682 379.2 31 ##STR00063## ##STR00064## TFA (1R,5S,7S)-3-oxa-9-
azabicyclo[3.3.1]nonan- 7-yl 1-(2,2-difluoroethyl)-
5-fluoro-1H-indole-3- carboxylate, 2,2,2- trifluoroacetate 368.3503
369.2 32 ##STR00065## ##STR00066## TFA (1R,5S,7S)-9-methyl-3-oxa-9-
azabicyclo[3.3.1]nonan-7-yl 5- fluoro-1-(2,2,2-trifluoroethyl)-
1H-indole-3-carboxylate, 2,2,2- trifluoroacetate 400.3673 401.15 33
##STR00067## ##STR00068## TFA (1R,5S,7S)-9-(2-fluoroethyl)-3-
oxa-9-azabicyclo[3.3.1]nonan- 7-yl 1-(2,2-difluoroethyl)-5-
fluoro-1H-indole-3-carboxylate, 2,2,2-trifluoroacetate 414.3939
415.2 34 ##STR00069## ##STR00070## TFA (1R,3R,5S)-9-methyl-9-
azabicyclo[3.3.1]nonan- 3-yl 5-fluoro-1-
(methylsulfonyl)-1H-indole-3- carboxylate, 2,2,2- trifluoroacetate
394.4603 395.2 35 ##STR00071## ##STR00072## TFA
5-fluoro-N-((1R,5S,7S)-9- methyl-3-oxa-9-azabicyclo-
[3.3.1]nonan-7-yl)-1-(2,2,2- trifluoroethyl)-1H-indole-3-
carboxamide, 2,2,2- trifluoroacetate 399.3825 400.25 36
##STR00073## ##STR00074## TFA 5-fluoro-N-((1R,5S,7S)-9-methyl-
3-oxa-9-azabicyclo- [3.3.1]nonan-7-yl)-1-
(methylsulfonyl)-1H-indole-3- carboxamide, 2,2,2-trifluoroacetate
395.4484 396.2 37 ##STR00075## ##STR00076## TFA quinuclidin-4-yl
5-fluoro-1- (methylsulfonyl)-1H-indole-3- carboxylate,
2,2,2-trifluoroacetate 366.4072 367.2 38 ##STR00077## ##STR00078##
TFA N-((1R,5S,7S)-3-oxa-9- azabicyclo[3.3.1]nonan- 7-yl)-1-(2,2,2-
trifluoroethyl)-1H- pyrrolo[2,3-b]pyridine-3- carboxamide,
2,2,2-trifluoroacetate 368.3536 369.2 39 ##STR00079## ##STR00080##
TFA N-((1R,5S,7S)-3-oxa-9- azabicyclo[3.3.1]nonan- 7-yl)-1-(2,2-
difluoroethyl)-5-fluoro- 1H-pyrrolo[2,3-b]pyridine-3- carboxamide,
2,2,2-trifluoroacetate 368.3536 369.2 40 ##STR00081## ##STR00082##
TFA (1R,3R,5S)-8-methyl-8- azabicyclo[3.2.1]octan-3-yl 1-(2,2-
difluoroethyl)-1H-indole-3- carboxylate, 2,2,2-trifluoroacetate
348.387 349.3 41 ##STR00083## ##STR00084## TFA
(1R,3R,5S)-8-methyl-8- azabicyclo[3.2.1]octan- 3-yl 1-(2,2,2-
trifluoroethyl)-1H- pyrrolo[2,3-b]pyridine- 3-carboxylate, 2,2,2-
trifluoroacetate 367.3655 368.3 42 ##STR00085## ##STR00086## TFA
(1R,3R,5S)-8-methyl-8- azabicyclo[3.2.1]octan-3-yl 1-
(tetrahydrofuran-3-yl)-1H-indole-3- carboxylate, 2,2,2-
trifluoroacetate 354.4427 355.3 43 ##STR00087## ##STR00088## TFA
(1R,3R,5S)-8-methyl-8- azabicyclo[3.2.1]octan- 3-yl 2-chloro-1-
(2,2-difluoroethyl)-1H-indole-3- carboxylate, 2,2,2-
trifluoroacetate 382.832 383.2 44 ##STR00089## ##STR00090## TFA
(1R,3R,5S)-8-methyl-8- azabicyclo[3.2.1]octan- 3-yl 2-chloro-1-
(2,2,2-trifluoroethyl)-1H-indole-3- carboxylate, 2,2,2-
trifluoroacetate 400.8225 401.2 45 ##STR00091## ##STR00092## TFA
(1R,3R,5S)-8- azabicyclo[3.2.1]octan-3-yl 1-(2,2-difluoroethyl)-
1H-indole-3-carboxylate, 2,2,2-trifluoroacetate 334.3604 335.25 46
##STR00093## ##STR00094## TFA N-((1R,3R,5S)-9- methyl-9-azabicyclo
[3.3.1]nonan-3-yl)-1- (methylsulfonyl)-1H-indazole-3- carboxamide,
2,2,2- trifluoroacetate 376.4732 377.3 47 ##STR00095## ##STR00096##
TFA (1R,5S,7S)-9-methyl- 3-oxa-9- azabicyclo[3.3.1]nonan-7-yl 1-
(methylsulfonyl)-1H-indole-3- carboxylate, 2,2,2- trifluoroacetate
378.4427 379.15 48 ##STR00097## ##STR00098## (1R,5S,7S)-9-methyl-3-
oxa-9-azabicyclo [3.3.1]nonan-7-yl 1- (2,2-difluoroethyl)-
1H-pyrrolo[2,3-b]pyridine- 3-carboxylate 365.3745 366.2 49
##STR00099## ##STR00100## TFA (1R,5S,7S)-9-methyl-3-oxa-9-
azabicyclo[3.3.1]nonan-7-yl 1- (2,2,2-trifluoroethyl)-1H-
pyrrolo[2,3-b]pyridine- 3-carboxylate 2,2,2-trifluoroacetate
383.3649 384.2 50 ##STR00101## ##STR00102## TFA
(1R,5S,7S)-9-(2-fluoroethyl)-3- oxa-9-azabicyclo[3.3.1]nonan- 7-yl
5-fluoro-1-(2,2,2- trifluoroethyl)- 1H-indole-3-carboxylate
2,2,2-trifluoroacetate 432.3844 433.25 51 ##STR00103## ##STR00104##
TFA (1R,5S,7S)-9-methyl-3-oxa-9- azabicyclo[3.3.1]nonan-7-yl 1-
(2-fluoroethyl)-1H-indole-3- carboxylate, 2,2,2-trifluoroacetate
346.3959 347.3 52 ##STR00105## ##STR00106## TFA
5-fluoro-N-((1R,5S,7S)-9- methyl-3-oxa-9-azabicyclo[3.3.1]-
nonan-7-yl)-1-(2,2,-trifluoroethyl)- 1H-pyrrolo[2,3-b]pyridine-
3-carboxamide, 2,2,2- trifluoroacetate 400.3706 401.2 53
##STR00107## ##STR00108## TFA 5-fluoro-N-((1R,5S,7S)-9-
methyl-3-oxa-9-azabicyclo[3.3.1]- nonan-7-yl)-1-(1,1,2,2-
tetrafluoroethyl)-1H-pyrrolo[2,3- b]pyridine-3-carboxamide,
2,2,2-trifluoroacetate 418.3611 419.15 54 ##STR00109## ##STR00110##
TFA (1R,5S,7S)-3-oxa-9- azabicyclo[3.3.1]nonan- 7-yl 5-fluoro-1-
(isopropylsulfonyl)-1H-indole-3- carboxylate, 2,2,2-
trifluoroacetate 410.4597 411.15 55 ##STR00111## ##STR00112## TFA
(1R,3R,5S)-8-methyl-8- azabicyclo[3.2.1]octan- 3-yl 2-chloro-1-
(2-fluoroethyl)-1H-indole-3- carboxylate, 2,2,2-trifluoroacetate
364.8416 365.2 56 ##STR00113## ##STR00114## TFA
(1R,3R,5S)-8-methyl-8- azabicyclo[3.2.1]octan-3-yl 1-(2-
fluoroethyl)-1H-indole-3- carboxylate, 2,2,2-trifluoroacetate
330.3965 331.2 57 ##STR00115## ##STR00116## TFA
(1R,3R,5S)-8-methyl-8- azabicyclo[3.2.1]octan-3-yl 1-(2-
fluoroethyl)-1H-indazole-3- carboxylate, 2,2,2-trifluoroacetate
331.3846 332.3 58 ##STR00117## ##STR00118## TFA
(1R,5S,7S)-9-methyl-3- oxa-9-azabicyclo [3.3.1]nonan-7-yl 1-
(2,2-difluoroethyl)-5-fluoro- 1H-indole-3-carboxylate, 2,,2,2-
trifluoroacetate 382.3769 383.2 59 ##STR00119## ##STR00120## TFA
(1R,5S,7S)-3-oxa-9- azabicyclo[3.3.1]nonan- 7-yl 5-fluoro-1-
(2,2,2-trifluoroethyl)-1H- indole-3-carboxylate, 2,2,2-
trifluoroacetate 386.33407 387.2 60 ##STR00121## ##STR00122## TFA
(1R,3R,5S)-9-methyl-9- azabicyclo[3.3.1]nonan-3-yl 1-(2,2-
difluoroethyl)-5-fluoro- 1H-indole-3-carboxylate, 2,2,2-
trifluoroacetate 380.404 381.2
61 ##STR00123## ##STR00124## TFA (1R,3R,5S)-9-methyl-9-
azabicyclo[3.3.1]nonan-3-yl 1-(2,2- difluoroethyl)-1H-
pyrrolo[2,3-b]pyridine-3- carboxylate, 2,2,2- trifluoroacetate
363.4016 364.3 62 ##STR00125## ##STR00126## TFA
N-((1R,3R,5S)-8-methyl-8- azabicyclo[3.2.1]octan-3-yl)-1-
(methylsulfonyl)-1H-indazole- 3-carboxamide, 2,2,2-
trifluoroacetate 362.4466 363.2 63 ##STR00127## ##STR00128## TFA
1-(2,2-difluoroethyl)-5-fluoro- N-((1R,5S,7S)-9-methyl-3-oxa-
9-azabicyclo[3.3.1]nonan-7-yl)- 1H-indole-3-carboxamide,
2,2,2-trifluoroacetate 381.3921 382.25 64 ##STR00129## ##STR00130##
TFA 1-(2,2-difluoroethyl)-N- ((1R,5S,7S)-9-methyl-3-oxa-9-
azabicyclo[3.3.1]nonan-7-yl)- 1H-pyrrolo[2,3-b]pyridine-3-
carboxamide, 2,2,2-trifluoroacetate 364.3897 365.3 65 ##STR00131##
##STR00132## TFA N-((1R,5S,7S)-3-oxa-9- azabicyclo[3.3.1]nonan-
7-yl)-1-(2,2- difluoroethyl)-1H-indazole-3- carboxamide, 2,2,2-
trifluoroacetate 350.3631 351.2 66 ##STR00133## ##STR00134## TFA
1-(2,2-difluoroethyl)-N- ((1R,5S,7S)- 9-methyl-3-oxa-9-
azabicyclo[3.3.1]nonan-7-yl)- 1H-pyrazolo[3,4-b]pyridine-3-
carboxamide, 2,2,2-trifluoroacetate 365.3777 366.25 67 ##STR00135##
##STR00136## TFA (R)-1-(2,2-difluoroethyl)-
N-(quinuclidin-3-yl)-1H- pyrrolo[2,3- b]pyridine-3-carboxamide,
2,2,2-trifluoroacetate 334.3637 335.25 68 ##STR00137## ##STR00138##
TFA 1-(2,2-difluoroethyl)-5-fluoro- N-((1R,5S,7S)-9-methyl-3-oxa-
9-azabicyclo[3.3.1]nonan-7-yl)- 1H-pyrrolo[2,3-b]pyridine-3-
carboxamide, 2,2,2- trifluoroacetate 382.3802 383.25 69
##STR00139## ##STR00140## TFA N-((1R,5S,7S)-9-methyl-3-oxa-
9-azabicyclo[3.3.1]nonan-7-yl)- 1-(1,1,1-trifluoro-2-methylpropan-
2-yl)-1H-pyrrolo[2,3- b]pyridine-3-carboxamide,
2,2,2-trifluoroacetate 410.4333 411.3 70 ##STR00141## ##STR00142##
N-((1R,5S,7S)-9-methyl-3-oxa-9- azabicyclo[3.3.1]nonan-7-yl)-
1-((R)-1,2,2,2-tetrafluoroethyl)- 1H-pyrrolo[2,3-b]pyridine-3-
carboxamide 400.3706 401.1 72 ##STR00143## ##STR00144## TFA
(1R,3R,5S)-8-methyl-8- azabicyclo[3.2.1]octan-3-yl 1-(2,2-
difluoroethyl)-1H- pyrrolo[2,3-b]pyridine- 3-carboxylate, 2,2,2-
trifluoroacetate 349.3751 350.2 73 ##STR00145## ##STR00146## TFA
(1R,3R,5S)-8-methyl-8- azabicyclo[3.2.1]octan-3-yl 1-(2,2-
difluoroethyl)-2-methyl- 1H-indole- 3-carboxylate, 2,2,2-
trifluoroacetate 362.4136 363.25 74 ##STR00147## ##STR00148## TFA
N-((1R,3R,5S)-8-methyl-8- azabicyclo[3.2.1]octan-3-yl)-1-
(methylsulfonyl)-1H-indole- 3-carboxamide, 2,2,2- trifluoroacetate
361.4585 362.2 75 ##STR00149## ##STR00150## TFA
1-(2,2-difluoroethyl)-5-fluoro- N-((1R,3R,5S)-8-methyl-8-
azabicyclo[3.2.1]octan-3-yl)-1H- indole-3-carboxamide, 2,2,2-
trifluoroacetate 365.3927 366.2 76 ##STR00151## ##STR00152## TFA
1-(2,2-difluoroethyl)- N-((1R,3R,5S)-8-methyl- 8-azabicyclo-
[3.2.1]octan-3-yl)-1H- pyrrolo[2,3-b]pyridine-3- carboxamide,
2,2,2-trifluoroacetate 348.3903 349.25 77 ##STR00153## ##STR00154##
TFA 1-(2,2-difluoroethyl)- N-((1R,3R,5S)-9-methyl- 9-azabicyclo-
[3.3.1]nonan-3-yl)-1H- pyrrolo[2,3-b]pyridine- 3-carboxamide,
2,2,2-trifluoroacetate 362.4169 363.3 78 ##STR00155## ##STR00156##
TFA N-((1R,5S,7S)-3-oxa-9- azabicyclo[3.3.1]nonan- 7-yl)-5-fluoro-
1-(methylsulfonyl)-1H- indole-3-carboxamide, 2,2,2-
trifluoroacetate 381.4218 382.2 79 ##STR00157## ##STR00158## TFA
1-(2-fluoroethyl)-N- ((1R,5S,7S)-9-methyl- 3-oxa-9-azabicyclo-
[3.3.1]nonan-7-yl)-1H-indole-3- carboxamide, 2,2,2-
trifluoroacetate 345.4112 346.3 80 ##STR00159## ##STR00160## TFA
N-((1R,5S,7S)-9-methyl-3- oxa-9-azabicyclo[3.3.1] nonan-7-yl)-
1-(1,1,2,2-tetrafluoroethyl)- 1H-pyrrolo[2,3-b]pyridine-3-
carboxamide, 2,2,2- trifluoroacetate 400.3706 401.2 81 ##STR00161##
##STR00162## TFA N-((1R,5S,7S)-9-methyl-3- oxa-9-azabicyclo[3.3.1]
nonan-7-yl)- 1-(1,2,2,2-tetrafluoroethyl)-
1H-pyrrolo[2,3-b]pyridine-3- carboxamide, 2,2,2- trifluoroacetate
400.3706 401.2 82 ##STR00163## ##STR00164## TFA
N-((1R,5S,7S)-3-oxa-9- azabicyclo[3.3.1]nonan- 7-yl)-1-(2,2-
difluoroethyl)-1H- pyrrolo[2,3-b]pyridine-3- carboxamide,
2,2,2-trifluoroacetate 350.3631 351.2 83 ##STR00165## ##STR00166##
TFA (1R,3R,5S)-8-methyl-8- azabicyclo[3.2.1]octan- 3-yl 1-((R)-
tetrahydrofuran-3-yl)- 1H-indole-3-carboxylate, 2,2,2-
trifluoroacetate 354.4427 354.9 84 ##STR00167## ##STR00168## TFA
(1R,3R,5S)-8-methyl-8- azabicyclo[3.2.1]octan- 3-yl 2,3,4,5-
tetrahydro-[1,3]oxazepino [3,2-a]indole- 11-carboxylate, 2,2,2-
trifluoroacetate 354.4427 355.25 85 ##STR00169## ##STR00170## TFA
(1R,3R,5S)-8-methyl-8- azabicyclo[3.2.1]octan-3-yl 3,4-
dihydro-2H-[1,3]oxazino [3,2-a]indole- 10-carboxylate, 2,2,2-
trifluoroacetate 340.4162 341.3 86 ##STR00171## ##STR00172## TFA
(1R,3R,5S)-8-methyl-8- azabicyclo[3.2.1]octan-3-yl 5-fluoro-1-
(methylsulfonyl)-1H-indole-3- carboxylate, 2,2,2- trifluoroacetate
380.4337 381.2 87 ##STR00173## ##STR00174## TFA
(1R,3R,5S)-9-methyl-9- azabicyclo[3.3.1]nonan-3-yl 1-(2-
fluoroethyl)-1H-indole-3- carboxylate, 2,2,2-trifluoroacetate
344.4231 345.3 88 ##STR00175## ##STR00176## TFA
(1R,3R,5S)-9-methyl-9- azabicyclo[3.3.1]nonan-3-yl 1-(2-
fluoroethyl)-2-methyl- 1H-indole-3- carboxylate, 2,2,2-
trifluoroacetate 358.4497 359.3 89 ##STR00177## ##STR00178## TFA
(1R,3R,5S)-9-methyl-9- azabicyclo[3.3.1]nonan-3-yl 5- fluoro-1-
(2,2,2-trifluoroethyl)-1H- indole-3-carboxylate, 2,2,2-
trifluoroacetate 398.3945 399.2 90 ##STR00179## ##STR00180## TFA
1-(2,2-difluroethyl)-N- ((1R,3R,5S)- 8-methyl-8-azabicyclo-
[3.2.1]octan-3-yl)-1H- indazole-3- carboxamide, 2,2,2-
trifluoroacetate 348.3903 349.25 91 ##STR00181## ##STR00182## TFA
(1S,5R,6S)-4-oxa-1- azabicyclo[3.3.1]nonan- 6-yl 1-(2,2-
difluoroethyl)-5-fluoro- 1H-indole- 3-carboxylate, 2,2,2-
trifluoroacetate 368.3503 369.25 93 ##STR00183## ##STR00184## TFA
5-fluoro-1-(isopropylsulfonyl)- N-((1R,5S,7S)-9-methyl-3-oxa-
9-azabicyclo[3.3.1]nonan- 7-yl)-1H- indole-3-carboxamide,
2,2,2-trifluoroacetate 423.5016 424.2 95 ##STR00185## ##STR00186##
TFA (1R,3R,5S)-8-methyl-8- azabicyclo[3.2.1]ocatn-3-yl 1-(2,2,2-
trifluoroethyl)-1H-indole- 3-carboxylate, 2,2,2-trifluoroacetate
366.3774 367.2 96 ##STR00187## ##STR00188## TFA
(1R,3R,5S)-8-methyl-8- azabicyclo[3.2.1]octan- 3-yl 1-((S)-
tetrahydrofuran-3-yl)-1H-indole- 3-carboxylate, 2,2,2-
trifluoroacetate 354.4427 354.9 97 ##STR00189## ##STR00190##
(1R,3R,5S)-8-methyl-8- azabicyclo[3.2.1]octan-3-yl 5-fluoro-1-
((S)-tetrahydrofuran-3-yl)- 1H-indole-3-carboxylate 372.4332 373.1
98 ##STR00191## ##STR00192## TFA 1-(2,2-difluoroethyl)-5-
fluoro-N-((1R,3R,5S)-9-methyl-9- azabicyclo[3.3.1]nonan-3-yl)-
1H-indole-3-carboxamide, 2,2,2- trifluoroacetate 379.4193 380.2 99
##STR00193## ##STR00194## TFA (1R,5S,7S)-9-methyl-3-oxa-
9-azabicyclo[3.3.1]nonan-7-yl 5- fluoro-1-(methylsulfonyl)-
1H-indole-3- carboxylate, 2,2,2- trifluoroacetate 396.4331 397.15
100 ##STR00195## ##STR00196## TFA 5-fluoro-N-((1R,3R,5S)-9-methyl-
9-azabicyclo[3.3.1]nonan-3- yl)-1-(methylsulfonyl)-1H-
indole-3-carboxamide, 2,2,2- trifluoroacetate 393.4756 394.2 101
##STR00197## ##STR00198## TFA (1R,5S,7S)-3-oxa-9-
azabicyclo[3.3.1]nonan-7-yl 1-(2,2-difluoroethyl)-1H-
pyrrolo[2,3-b]pyridine- 3-carboxylate, 2,2,2- trifluoroacetate
351.3479 352.2 102 ##STR00199## ##STR00200## TFA
N-((1R,3R,5S)-8-methyl-8- azabicyclo[3.2.1]octan-3-yl)-1-
(2,2,2-trifluoroethyl)-1H- pyrrolo[2,3-b]pyridine-3- carboxamide,
2,2,2- trifluoroacetate 366.3807 367.2 103 ##STR00201##
##STR00202## TFA (1R,3R,5S)-9-methyl-9- azabicyclo[3.3.1]nonan-
3-yl 1-(2,2,2- trifluoroethyl)-1H- pyrrolo[2,3-b]pyridine-
3-carboxylate, 2,2,2- trifluoroacetate 381.3921 382.2 104
##STR00203## ##STR00204## TFA 1-(2,2-difluoroethyl)- N-((1R,5S,7S)-
9-(trifluoromethyl)-3-oxa- 9-azabicyclo[3.3.1]nonan-
7-yl)-1H-pyrrolo [2,3-b]pyridine-3- carboxamide, 2,2,2-
trifluoroacetate 418.3611 491.2 105 ##STR00205## ##STR00206## TFA
N-((1R,5S,7S)-3-oxa-9- azabicyclo[3.3.1]nonan- 7-yl)-5-fluoro-
1-(2,2,2-trifluoroethyl)- 1H-pyrrolo[2,3-b]pyridine-3- carboxamide,
2,2,2- trifluoroacetate 386.344 387.2 107 ##STR00207## ##STR00208##
TFA N-((1R,5S,7S)-9-methyl-3-oxa- 9-azabicyclo[3.3.1]nonan-7-yl)-
1-(pyrimidin-2-yl)-1H-indole- 3-carboxamide, 2,2,2-
trifluoroacetate 377.4396 378.2 108 ##STR00209## ##STR00210## TFA
1-(2,2-difluoropropyl)- N-((1R,5S,7S)- 9-methyl-3-oxa-9-
azabicyclo[3.3.1]nonan-7-yl)- 1H-pyrrolo[2,3-b]pyridine-3-
carboxamide, 2,2,2- trifluoroacetate 378.4163 379.2 109
##STR00211## ##STR00212## 1-(2,2-difluoroethyl)-5-fluoro-
N-((1R,5S,7S)-9-methyl-d.sub.3-3- oxa-9-azabicyclo[3.3.1]nonan-
7-yl)- 1H-pyrrolo[2,3-b]pyridine- 3-carboxamide 385.3986 386.3 110
##STR00213## ##STR00214## TFA N-((1R,5S,7S)-9-methyl-d.sub.3-
3-oxa-9-azabicyclo[3.3.1] nonan-7-yl)-1-
(methylsulfonyl)-1H-indole- 3-carboxamide, 2,2,2- trifluoroacetate
380.48 381.25 111 ##STR00215## ##STR00216## TFA
N-((1R,5S,7S)-9-methyl-d.sub.3-3- oxa-9-azabicyclo[3.3.1]nonan-7-
yl)-1-(isopropylsulfonyl)-1H- indole-3-carboxamide, 2,2,2-
trifluoroacetate 408.53 409.3 112 ##STR00217## ##STR00218## TFA
1-(2,2,2-trifluoroethyl)-5-fluoro-
N-((1R,5S,7S)-9-methyl-d.sub.3-3- oxa-9-azabicyclo[3.3.1]
nonan-7-yl)- 1H-indole-3-carboxamide, 2,2,2-trifluoroacetate 384.41
385.2 113 ##STR00219## ##STR00220## TFA
1-(2,2-difluoroethyl)-5-fluoro- N-((1R,5S,7S)-9-methyl-d.sub.3-3-
oxa-9-azabicyclo[3.3.1] nonan-7-yl)- 1H-indole-3-carboxamide,
2,2,2-trifluoroacetate 366.42 367.3 116 ##STR00221## ##STR00222##
TFA (S)-1-(2,2-difluoroethyl)-N- (quinuclidin-3-yl)-1H-pyrrolo[2,3-
b]pyridine-3-carboxamide, 2,2,2-trifluoroacetate 334.36 335.20 117
##STR00223## ##STR00224## TFA N-((1R,5S,7S)-9-methyl-3-
oxa-9-azabicyclo[3.3.1] nonan-7-yl)-
1-(pyridazin-3-yl)-1H-indole-3- carboxamide, 2,2,2-
trifluoroacetate 377.44 378.25 118 ##STR00225## ##STR00226## TFA
N-((1R,5S,7S)-9-methyl-3-oxa-9- azabicyclo[3.3.1]nonan-7-yl)-
1-(thiazol-2-yl)-1H-indole-3- carboxamide, 2,2,2- trifluoroacetate
382.48 383.2 119 ##STR00227## ##STR00228## TFA
N-((1R,5S,7S)-9-methyl-3- oxa-9-azabicyclo[3.3.1] nonan-7-yl)-
1-(thiazol-5-yl)-1H-indole-3- carboxamide, 2,2,2- trifluoroacetate
382.48 383.2 120 ##STR00229## ##STR00230## TFA
N-((1R,5S,7S)-9-methyl-3- oxa-9-azabicyclo[3.3.1] nonan-7-yl)-
1-(pyrimidin-5-yl)-1H-indole- 3-carboxamide, 2,2,2-
trifluoroacetate 377.44 378.25 122 ##STR00231## ##STR00232## TFA
N-((1R,5S,7S)-9-methyl-d.sub.3-3- oxa-9-azabicyclo[3.3.1]nonan-7-
yl)-1-(pyrimidin-2-yl)-1H-indole- 3-carboxamide, 2,2,2-
trifluoroacetate 380.46 381.25 123 ##STR00233## ##STR00234## TFA
N-((1R,5S,7S)-9-methyl-d.sub.3-3- oxa-9-azabicyclo[3.3.1]nonan-7-
yl)-1-(pyridazin-3-yl)-1H-indole- 3-carboxamide, 2,2,2-
trifluoroacetate 380.46 381.3 126 ##STR00235## ##STR00236## TFA
N-((1R,5S,7S)-9-methyl- d.sub.3-3-oxa-9- azabicyclo[3.3.1]nonan-7-
yl)-1-(2,2,2-trifluoroethyl)- 1H-indazole- 3-carboxamide, 2,2,2-
trifluoroacetate 385.4 386.25 127 ##STR00237## ##STR00238## TFA
1-(2-fluoroethyl)-N-((1R,5S,7S)- 9-methyl-d.sub.3-3-oxa-9-
azabicyclo[3.3.1]nonan-7-yl)-1H- indole-3-carboxamide, 2,2,2-
trifluoroacetate 348.43 349.3 128 ##STR00239## ##STR00240## TFA
(1R,5S,7S)-3-oxa-9- azabicyclo[3.3.1]nonan- 7-yl 1-(thiazol-2-
yl)-1H-indole-3-carboxyalate,
2,2,2-trifluoroacetate 369.44 370.2 129 ##STR00241## ##STR00242##
2TFA N-((1R,5S,7S)-9-methyl-3-oxa-9- azabicyclo[3.3.1]nonan-7-yl)-
1-(pyrazin-2-yl)-1H-indole-3- carboxamide, di-2,2,2-
trifluoroacetate 377.44 378.3 130 ##STR00243## ##STR00244##
N-((1R,5S,7S)-9-methyl-d.sub.3-3-oxa- 9-azabicyclo[3.3.1]nonan-7-
yl)-1-(pyrazin-2-yl)-1H- indole-3-carboxamide 380.46 381.3 131
##STR00245## ##STR00246## TFA (1R,5S,7S)-3-oxa-9-
azabicyclo[3.3.1]nonan-7-yl) 1- (isopropylsulfonyl)-1H-indole-3-
carboxylate, 2,2,2- trifluoroacetate 392.4693 393.2 132
##STR00247## ##STR00248## TFA (1R,5S,7S)-3-oxa-9-
azabicyclo[3.3.1]nonan- 7-yl 5-fluoro-1- (methyslulfonyl)-1H-
indole-3-carboxylate, 2,2,2- trifluoroacetate 364.42 365.2 133
##STR00249## ##STR00250## TFA (1R,5S,7S)-3-oxa-9-
azabicyclo[3.3.1]nonan-7-yl 1- (ethylsulfonyl)-1H-indole-3-
carboxylate, 2,2,2-trifluoroacetate 378.44 379.2 134 ##STR00251##
##STR00252## TFA (1R,5S,7S)-3-oxa-9- azabicyclo[3.3.1]nonan-7-yl 1-
(cyclopropylsulfonyl)-1H-indole-3- carboxylate, 2,2,2-
trifluoroacetate 390.45 391.2 135 ##STR00253## ##STR00254## TFA
(1R,5S,7S)-3-oxa-9- azabicyclo[3.3.1]nonan-7-yl 1-
(isobutylsulfonyl)-1H-indole-3- carboxylate, 2,2,2-
trifluoroacetate 406.5 407.2 136 ##STR00255## ##STR00256## TFA
(1R,5S,7s)-3-oxa-9- azabicyclo[3.3.1]nonan- 7-yl 1-(pyridazin-
3-yl)-1H-indole-3- carboxylate, 2,2,2- trifluoroacetic acid salt
364.398 365.20 137 ##STR00257## ##STR00258## TFA
(1R,5S,7s)-9-methyl-3-oxa- 9-azabicyclo[3.3.1]nonan-7-yl 1-
(6-fluoropyridazin-3-yl)- 1H-indole-3-carboxylate 396.415 397.20
141 ##STR00259## ##STR00260## TFA (1R,5S,7s)-3-oxa-9-
azabicyclo[3.3.1]nonan- 7-yl 1-(pyrazin-2-
yl)-1H-indole-3-carboxylate, 2,2,2-trifluoroacetic acid salt
364.398 365.20 142 ##STR00261## ##STR00262## TFA
(1R,5S,7s)-9-methyl-3-oxa- 9-azabicyclo[3.3.1]nonan-7-yl 1-
(cyanomethyl)-7-fluoro- 1H-pyrrolo[2,3-c]pyridine-3- carboxylate,
2,2,2- trifluoroacetic acid salt 358.367 359.15 143 ##STR00263##
##STR00264## TFA (1R,5S,7s)-3-oxa-9- azabicyclo[3.3.1]nonan- 7-yl
1-(isothiazol- 4-yl)-1H-indole-3-carboxylate, 2,2,2-trifluoroacetic
acid salt 369.437 370.15 144 ##STR00265## ##STR00266## TFA
1-(isothiazol-4-yl)-N-((1R,5S,7s)- 9-methyl-3-oxa-9-
azabicyclo[3.3.1]nonan-7-yl)- 1H-indole-3-carboxamide, 2,2,2-
trifluoroacetic acid salt 382.479 383.20 145 ##STR00267##
##STR00268## TFA (1R,5S,7s)-3-oxa-9- azabicyclo[3.3.1]nonan- 7-yl
1-(isothiazol- 3-yl)-1H-indole-3-carboxylate, 2,2,2-trifluoroacetic
acid salt 369.437 370.20 146 ##STR00269## ##STR00270## TFA
N-((1R,5S,7s)-9-methyl-3- oxa-9-azabicyclo[3.3.1] nonan-7-yl)-
1-(thiazol-2-yl)-1H- pyrrolo[2,3-b]pyridine- 3-carboxamide,
2,2,2-trifluoroacetic acid salt 383.467 384.20 147 ##STR00271##
##STR00272## TFA N-((1R,5S,7s)-9-methyl-3- oxa-9-azabicyclo[3.3.1]
nonan-7-yl)- 1-(thiazol-4-yl)-1H-pyrrolo[2,3-b]
pyridine-3-carboxamide, 2,2,2-trifluoroacetic acid salt 383.467
384.25 148 ##STR00273## ##STR00274## TFA N-((1R,5S,7s)-9-methyl-3-
oxa-9-azabicyclo[3.3.1] nonan-7-yl)-
1-(thiazol-5-yl)-1H-pyrrolo[2,3-b] pyridine-3-carboxamide,
2,2,2-trifluoroacetic acid salt 383.467 384.20 153 ##STR00275##
##STR00276## TFA 1-(siothiazol-3-yl)-N-((1R,5S,7s)-
9-methyl-3-oxa-9- azabicyclo[3.3.1]nonan-7-yl)-1H-
indole-3-carboxamide, 2,2,2- trifluoroacetic acid salt 382.479
383.20 154 ##STR00277## ##STR00278## TFA
1-(1-methyl-1H-imidazol-5-yl)- N-((1R,5S,7s)-9-methyl-3-oxo-
9-azabicyclo[3.3.1]nonan- 7-yl)-1H-indole-3-carboxamide 379.456
380.20 155 ##STR00279## ##STR00280## TFA (1R,5S,7s)-3-oxa-9-
azabicyclo[3.3.1]nonan- 7-yl 1-(isothiazol- 5-yl)-1H-indole-3-
carboxylate, 2,2,2- trifluoroacetic acid salt 369.497 370.10 158
##STR00281## ##STR00282## TFA 1-(isothiazol-5-yl)-N-((1R,5S,7s)-
9-methyl-3-oxa-9- azabicyclo[3.3.1]nonan- 7-yl)-1H-indole-3-
carboxamide, 2,2,2- trifluoroacetic acid salt 382.479 383.20 159
##STR00283## ##STR00284## TFA 1-(cyanomethyl)-N-((1R,5S,7s)-
9-methyl-3-oxa-9- azabicyclo[3.3.1]nonan-7-yl)-1H-
indole-3-carboxamide, 2,2,2- trifluoroacetic acid salt 338.404
339.20 160 ##STR00285## ##STR00286## TFA
(1R,5S,7s)-9-methyl-3-oxa-9- azabicyclo[3.3.1]nonan-7-yl 5-
cyano-1-(2-fluoroethyl)-1H-indole- 3-carboxylate, 2,2,2-
trifluoroacetic acid salt 371.405 372.30 161 ##STR00287##
##STR00288## TFA 1R,5S,7S)-9-methyl-3-oxa-9-
azabicyclo[3.3.1]nonan-7-yl 5- cyano-1-(6-
fluoropyridazin-3-yl)-1H- indole-3-carboxylate 421.424 423.25 162
##STR00289## ##STR00290## TFA 5-fluoro-N-((1R,5S,7s)-
9-methyl-3-oxa-9- azabicyclo[3.3.1]nonan-7-yl)-1-
(thiazol-2-yl)-1H-pyrrolo[2,3- b]pyridine-3-carboxamide,
2,2,2-trifluoroacetic acid salt 401.458 402.20 163 ##STR00291##
##STR00292## TFA 5-fluoro-N-((1R,5S,7s)-9- methyl-3-oxa-9-
azabicyclo[3.3.1]nonan-7-yl)-1- (thiazol-4-yl)-1H-pyrrolo[2,3-
b]pyridine-3-carboxamide, 2,2,2- trifluoroacetic acid salt 401.458
402.15 164 ##STR00293## ##STR00294## TFA 5-fluoro-N-((1R,5S,7s)-9-
methyl-3-oxa-9- azabicyclo[3.3.1]nonan-7-yl)-1-
(thiazol-5-yl)-1H-pyrrolo[2,3- b]pyridine-3-carboxamide, 2,2,2-
trifluoroacetic acid salt 401.458 402.20 165 ##STR00295##
##STR00296## TFA N-((1R,5S,7s)-9-methyl-3-oxa-
9-azabicyclo[3.3.1]nonan-7-yl)- 1-(thiazol-5-yl)-1H-indazole-3-
carboxamide, 2,2,2- trifluoroacetic acid salt 383.467 384.20 168
##STR00297## ##STR00298## TFA 1R,5S,7s)-3-oxa-9-
azabicyclo[3.3.1]nonan- 7-yl 1-(1-methyl-2-
oxo-1,2-dihydropyridin-4-yl)- 1H-indole-3-carboxylate, 2,2,2-
trifluoroacetic acid salt 393.436 374.25 169 ##STR00299##
##STR00300## TFA (1R,5S,7s)-9-methyl-3-oxa-
9-azabicyclo[3.3.1]nonan-7-yl 1- (6-hydroxypyridazin-3-yl)-
1H-indole-3-carboxylate, 2,2,2- trifluoroacetic acid salt 394.424
395.20 171 ##STR00301## ##STR00302## TFA (1R,5S,7s)-3-oxa-9-
azabicyclo[3.3.1]nonan-7-yl 1-(2- cyanophenyl)-1H-indole-3-
carboxylate, 2,2,2-triflurooacetic acid salt 387.431 388.20 172
##STR00303## ##STR00304## TFA (1R,5S,7s)-3-oxa-9-
azabicyclo[3.3.1]nonan-7-yl 1-(3- cyanophenyl)-1H-indole-3-
carboxylate, 2,2,2-trifluoroacetic acid salt 387.431 388.20 174
##STR00305## ##STR00306## TFA N-((1R,5S,7s)-9-methyl-3-oxa-9-
azabicyclo[3.3.1]nonan-7-yl)- 1-phenyl-1H-indole- 3-carboxamide,
2,2,2-trifluoroacetic acid salt 375.464 376.25 177 ##STR00307##
##STR00308## TFA (1R,5S,7s)-3-oxa-9- azabicyclo[3.3.1]nonan- 7-yl
1-(oxazol-2- yl)-1H-indole-3-carboxylate, 2,2,2-trifluoroacetic
acid salt 353.372 354.20 178 ##STR00309## ##STR00310## TFA
N-((1R,5S,7s)-9-methyl-3- oxa-9-azabicyclo[3.3.1] nonan-7-yl)-
1-(oxazol-2-yl)-1H-indole-3- carboxamide, 2,2,2-trifluoroacetic
acid salt 366.414 367.30 180 ##STR00311## ##STR00312## TFA
(1R,5S,7s)-3-oxa-9- azabicyclo[3.3.1]nonan-7-yl 1-(4-
cyanophenyl)-1H-indole-3- carboxylate, 2,2,2-trifluoroacetic acid
salt 387.431 388.20 181 ##STR00313## ##STR00314## TFA
(1R,5S,7S)-9-methyl-3-oxa- 9-azabicyclo[3.3.1]nonan-7-yl
1-(pyrazin-2-yl)-1H- indole-3-carboxylate 378.42 379.30 182
##STR00315## ##STR00316## TFA (1R,5S,7S)-9-methyl-3-oxa-
9-azabicyclo[3.3.1]nonan-7-yl 1-(isothiazol-3-yl)-1H-
indole-3-carboxylate 383.46 384.3 183 ##STR00317## ##STR00318## TFA
(1R,5S,7S)-9-methyl-3-oxa-9- azabicyclo[3.3.1]nonan-7-yl
1-(thiazol-5-yl)-1H- indole-3-carboxylate 383.46 384.25 184
##STR00319## ##STR00320## TFA (1R,5S,7S)-9-methyl-3-oxa-9-
azabicyclo[3.3.1]nonan-7-yl 1-(5-fluoropyrazin-2-yl)-
1H-indole-3-carboxylate 396.42 397.20 185 ##STR00321## ##STR00322##
TFA N-((1R,5S,7S)-3-oxa-9- azabicyclo[3.3.1]nonan-7-yl)-1-
(isothiazol-4-yl)-N-methyl-1H- indole-3-carboxamide 382.48 383.30
186 ##STR00323## ##STR00324## TFA 1-(isothiazol-4-yl)-N-methyl-
N-((1R,5S,7S)-9-methyl-3- oxa-9-azabicyclo[3.3.1]nonan-
7-yl)-1H-indole-3- carboxamide 396.51 397.30 187 ##STR00325##
##STR00326## TFA (1R,5S,7S)-3-oxa-9- azabicyclo[3.3.1]nonan-7-yl 1-
(cyanomethyl)-1H-indole-3- carboxylate 325.36 326.20 188
##STR00327## ##STR00328## TFA (1R,5S,7S)-9-methyl-3-oxa-9-
azabicyclo[3.3.1]nonan-7-yl 1-(pyrimidin-2-yl)-1H-
indole-3-carboxylate 378.42 379.30 189 ##STR00329## ##STR00330##
TFA (1R,5S,7S)-9-methyl-3-oxa-9- azabicyclo[3.3.1]nonan-7-yl
1-(pyrimidin-5-yl)-1H- indole-3-carboxylate 378.42 379.30 190
##STR00331## ##STR00332## TFA N-((1R,5S,7S)-9-methyl-3-oxa-
9-azabicyclo[3.3.1]nonan- 7-yl)-1-(pyridazin-4-yl)-1H-
indole-3-carboxamide 377.44 378.40
EMBODIMENTS
[0055] Compounds of Formula (I):
Embodiment (A)
[0056] In one embodiment, the compound of Formula (I) or a
pharmaceutically acceptable salt thereof, as defined in the Summary
is where R.sub.4 is heteroaryl selected from the group consisting
of furanyl, pyrrolyl, imidazolyl, oxazolyl, isoxazolyl,
oxadiazolyl, thiazolyl, isothiazolyl, thiadiazolyl, triazolyl,
tetrazolyl, pyrazinyl, pyridazinyl, pyrimidyl, azepinyl,
diazepinyl, quinolyl, isoquinolyl, quinolizidine, benzofuranyl,
benzothienyl, indolyl, isoindolyl, indazolyl, benzimidazolyl,
benzisothiazolyl, benzisoxazolyl, benzoxadiazolyl, benzoxazolyl,
benzothiazolyl, benzothiadiazolyl, benzotriazolyl, benzopyrazinyl,
benzopyrazidinyl, benzoazepinyl, benzodiazepinyl, imidazopyridyl,
pyrazolopyridyl, pyrrolopyridyl, quinazolyl, purinyl, furopyridyl,
and thienopyridyl; each optionally substituted with one or two
substituents independently selected from C.sub.1-6 alkyl, C.sub.1-6
haloalkyl, C.sub.1-6 haloalkoxy, C.sub.1-6 alkoxy, hydroxy, cyano,
or halo.
Embodiment (B)
[0057] In another embodiment, the compound of Formula (I) or a
pharmaceutically acceptable salt thereof as defined in the Summary
is where R.sub.4 is heteroaryl selected from the group consisting
of furanyl, pyrrolyl, imidazolyl, oxazolyl, isoxazolyl,
oxadiazolyl, thiazolyl, isothiazolyl, thiadiazolyl, triazolyl,
tetrazolyl, pyrazinyl, pyridazinyl, and pyrimidyl; each optionally
substituted with one or two substituents independently selected
from C.sub.1-6 alkyl, C.sub.1-6 haloalkyl, C.sub.1-6 haloalkoxy,
C.sub.1-6 alkoxy, hydroxy, cyano, or halo.
Embodiment (C)
[0058] In another embodiment, the compound of Formula (I) or a
pharmaceutically acceptable salt thereof as defined in the Summary
is where R.sub.4 is heteroaryl selected from the group consisting
of quinolyl, isoquinolyl, quinolizidine, benzofuranyl,
benzothienyl, indolyl, isoindolyl, indazolyl, benzimidazolyl,
benzisothiazolyl, benzisoxazolyl, benzoxadiazolyl, benzoxazolyl,
benzothiazolyl, benzothiadiazolyl, benzotriazolyl, benzopyrazinyl,
benzopyrazidinyl, benzoazepinyl, benzodiazepinyl, imidazopyridyl,
pyrazolopyridyl, pyrrolopyridyl, quinazolyl, purinyl, furopyridyl,
and thienopyridyl; each optionally substituted with one or two
substituents independently selected from C.sub.1-6 alkyl, C.sub.1-6
haloalkyl, C.sub.1-6 haloalkoxy, C.sub.1-6 alkoxy, hydroxy, cyano,
or halo.
Embodiment (D)
[0059] In another embodiment, the compound of Formula (I) or a
pharmaceutically acceptable salt thereof as defined in the Summary
is where R.sub.4 is pyrimidinyl, pyridazinyl, isothiazolyl,
thiazolyl, oxazolyl, isoxazolyl, or furanyl; each optionally
substituted with one or two substituents independently selected
from C.sub.1-6 alkyl, C.sub.1-6 haloalkyl, C.sub.1-6 haloalkoxy,
C.sub.1-6 alkoxy, or halo.
[0060] Within this embodiment, in another group of compounds,
R.sub.4 is heteroaryl oxazolyl optionally substituted with one or
two substituents independently selected from C.sub.1-6 alkyl,
C.sub.1-6 haloalkyl, C.sub.1-6 haloalkoxy, C.sub.1-6 alkoxy,
hydroxy, cyano, or halo.
[0061] Within this embodiment, in another group of compounds
R.sub.4 is pyrimidinyl optionally substituted with one or two
substituents independently selected from C.sub.1-6 alkyl, C.sub.1-6
haloalkyl, C.sub.1-6 haloalkoxy, cyano, C.sub.1-6 alkoxy, or
halo.
[0062] Within this embodiment, in another group of compounds
R.sub.4 is pyridazinyl optionally substituted with one or two
substituent(s), preferably one substituent, independently selected
from methyl, ethyl, isopropyl, difluoromethyl, 2-fluoroethyl,
trifluoromethyl, cyano, or fluoro.
[0063] Within this embodiment, in another group of compounds
R.sub.4 thiazolyl optionally substituted with one or two
substituents independently selected from C.sub.1-6 alkyl, C.sub.1-6
haloalkyl, C.sub.1-6 haloalkoxy, cyano, C.sub.1-6 alkoxy, or
halo.
[0064] Within this embodiment, in another group of compounds
R.sub.4 is pyrimidin-2-yl, pyridazin-3-yl, 6-fluoropyridazine-3-yl,
pyrazin-2-yl, thiazol-2-yl, thiazol-5-yl, isothiazol-3-yl,
isothiazol-4-yl, 1-methyl-1H-imidazol-5-yl, oxazol-2-yl, or
pyrimidin-5-yl.
Embodiment (E)
[0065] In one embodiment, the compound of Formula (I) or a
pharmaceutically acceptable salt thereof as defined in the Summary
and embodiments (A), (B), (C), and (D) above and embodiments
contained therein, is where Z is O.
Embodiment (F)
[0066] In one embodiment, the compound of Formula (I) or a
pharmaceutically acceptable salt thereof as defined in the Summary
and embodiments (A), (B), (C), and (D) above and embodiments
contained therein, is where Z is NR.sub.a. Within this embodiment,
in another group of compounds R.sub.a is hydrogen. Within this
embodiment, in another group of compounds R.sub.a is methyl.
Embodiment (G)
[0067] In one embodiment within embodiment G, the compound of
Formula (I) or a pharmaceutically acceptable salt thereof as
defined in the Summary and embodiments (A), (B), (C), (D), (E), and
(F) above and embodiments contained therein, is where R.sub.1 is a
ring of formula
##STR00333##
[0068] (a) Within groups in embodiment (G), in one group of
compounds R.sub.1 is a ring of formula (a) or (d). Within (a), in
one embodiment, R.sub.1 is a ring of formula
##STR00334##
[0069] (b) Within groups in embodiment (G), in another group of
compounds R.sub.1 is a ring of formula (e), (f) or (g). Within (b),
in one group of compounds R.sub.1 is a ring of formula (e). Within
(b), in one group of compounds R.sub.1 is a ring of formula (f) or
(g). Within (b), in one group of compounds R.sub.1 is a ring of
formula
##STR00335##
[0070] (i) Within groups in embodiment (G) and embodiments
contained therein i.e., (a) and (b) and groups contained therein,
in one group of compounds each R.sub.3 is independently hydrogen or
methyl. Within these groups of compounds in one group of compounds
each R.sub.3 is hydrogen.
[0071] (ii) Within groups in embodiment (G) and embodiments
contained therein i.e., (a) and (b) and groups contained therein,
in one group of compounds each R.sub.3 is independently hydrogen or
methyl and R.sub.2 is hydrogen. Within these groups of compounds in
one group of compounds R.sub.2 is hydrogen and each R.sub.3 is
hydrogen.
[0072] (iii) Within groups in embodiment (G) and embodiments
contained therein i.e., (a) and (b) and groups contained therein,
in one group of compounds each R.sub.3 is independently hydrogen or
methyl and R.sub.2 is C.sub.1-6 alkyl. Within these groups of
compounds in one group of compounds R.sub.2 is methyl, ethyl, or
propyl and each R.sub.3 is hydrogen. Within these groups of
compounds in one group of compounds R.sub.2 is methyl and each
R.sub.3 is hydrogen.
[0073] (iv) Within groups in embodiment (G) and embodiments
contained therein i.e., (a) and (b) and groups contained therein,
in one group of compounds each R.sub.3 is independently hydrogen or
methyl and R.sub.2 is C.sub.1-6 haloalkyl. Within these groups of
compounds in one group of compounds each R.sub.2 is
trifluoromethyl, 2-fluoroethyl, or 2,2,2-trifluoroethyl and each
R.sub.3 is hydrogen. Within these groups of compounds in one group
of compounds R.sub.2 is trifluoromethyl and each R.sub.3 is
hydrogen.
[0074] (v) Within groups in embodiment (G) and embodiments
contained therein i.e., (a) and (b) and groups contained therein,
in one group of compounds each R.sub.3 is independently hydrogen or
methyl.
Embodiment (H)
[0075] In another embodiment, the compound of Formula (I) or a
pharmaceutically acceptable salt thereof as defined in the Summary
and embodiments (A), (B), (C), (D), (E), and (F) above and
embodiments contained therein, is where R.sub.1 is a ring of
formula
##STR00336##
[0076] (a1) Within groups in embodiment (H), in one group of
compounds R.sub.1 is a ring of formula (c) or (h). Within this
embodiment, in one group of compounds the stereochemistry at the
chiral carbon is (R) or (S).
[0077] (b1) Within groups in embodiment (H), in one group of
compounds R.sup.1 is a ring of formula (b).
[0078] (vi) Within groups in embodiment (H) and embodiments
contained therein i.e., (a1) and (b1) and groups contained therein,
in one group of compounds each R.sub.3 is independently hydrogen or
methyl. Within these groups of compounds in one group of compounds
each R.sub.3 is hydrogen.
Embodiment I
[0079] In another embodiment, the compound of Formula (I) or a
pharmaceutically acceptable salt thereof as defined in the Summary
and embodiments (A), (B), (C), (D), (E), (F), (G), and (H) above
and groups contained therein, in one group of compounds, each of
X.sub.1, X.sub.2, X.sub.3, and X.sub.4 is CR.sub.5 and X.sub.5 is N
or CR.sub.6. Within this embodiment, in another group of compounds
each R.sub.5 is hydrogen.
[0080] (c1) Within the groups in embodiment I, in one group of
compounds, X.sub.5 is N.
[0081] (d1) Within the groups in embodiment I, in another group of
compounds X.sub.5 is CR.sub.6. Within these groups of compounds, in
one group of compounds X.sub.5 is CR.sub.6 and R.sub.6 is
hydrogen
[0082] Within the groups in embodiment I, in another group of
compounds one of R.sub.5 is fluoro, or cyano. Within this group of
compounds, in another group the R.sub.5 cyano is located at C-5
position, the nitrogen atom substituted with R.sub.4 being position
1. Within this group of compounds, in another group of compounds in
another group the R.sub.5 fluoro is located at C-5 position, the
nitrogen atom substituted with R.sup.4 being position 1.
Embodiment J
[0083] In another embodiment, the compound of Formula (I) or a
pharmaceutically acceptable salt thereof as defined in the Summary
and embodiments (A), (B), (C), (D), (E), (F), and (G), and (H)
above and groups is where one of X.sub.1, X.sub.2, X.sub.3, or
X.sub.4 is N and X.sub.5 is N or CR.sub.6. Within these groups of
compounds in one group of compounds X.sub.1 is N.
[0084] (e1) Within the groups in embodiment J, in one group of
compounds X.sub.5 is N.
[0085] (f1) Within the groups in embodiment J, in another group of
compounds X.sub.5 is CR.sub.6 and R.sub.6 is hydrogen.
[0086] Within the groups in embodiment J, in one group of compounds
each R.sub.5 is hydrogen.
[0087] Within the groups in embodiment J, (e1) and (f1), in another
group of compounds one of R.sub.5 is fluoro, or cyano. Within this
group of compounds, in another group the R.sub.5 cyano is located
at C-5 position, the nitrogen atom substituted with R.sub.4 being
position 1. Within this group of compounds, in another group of
compounds in another group the R.sub.5 fluoro is located at C-5
position, the nitrogen atom substituted with R.sub.4 being position
1.
Embodiment K
[0088] In another embodiment, the compound of Formula (I) or a
pharmaceutically acceptable salt thereof as defined in the Summary
and embodiments (E), (F), (G), and (H) above and groups contained
therein, in one group of compounds each of X.sub.1-X.sub.4 is
CR.sub.5 or one of X.sub.1-X.sub.4 is N and X.sub.5 is CR.sub.6
where R.sub.6 together with R.sub.4 forms --O--(CH.sub.2).sub.2--
or --O--(CH.sub.2).sub.3--.
[0089] (g1) Within the groups in embodiment K, in one group of
compounds each X.sub.1-X.sub.4 is CR.sub.5.
[0090] (h1) Within the groups in embodiment I, in another group of
compounds one of X.sub.1-X.sub.4 is N. Within the groups in
embodiment K, (g1) and (h1), in one group of compounds each R.sub.5
is hydrogen.
[0091] Within these groups of compounds, in one group of compounds
X.sub.1 is N.
[0092] Within the groups in embodiment K, (g1) and (h1), in another
group of compounds one of R.sub.5 is fluoro, or cyano. Within this
group of compounds, in another group the R.sub.5 cyano is located
at C-5 position, the nitrogen atom substituted with R.sub.4 being
position 1. Within this group of compounds, in another group of
compounds in another group the R.sub.5 fluoro is located at C-5
position, the nitrogen atom substituted with R.sub.4 being position
1.
[0093] Compounds of Formula (IA):
Embodiment (A1)
[0094] In one embodiment, the compound of Formula (IA) or a
pharmaceutically acceptable salt thereof, as defined in the Summary
is where R.sub.4 is C.sub.1-6 haloalkyl. Within this embodiment, in
another group of compounds R.sub.4 is 2,2,2-trifluoroethyl,
2,2-difluoroethyl, 2-fluoroethyl, 1,2,2,2-tetrafluoroethyl,
1,1,2,2,-tetrafluoroethyl, 1,1,1-trifluoro-2-methylpropan-2-yl,
(R)-1,2,2,2-tetrafluoroethyl, (S)-1,2,2,2-tetrafluoroethyl, or
2,2-difluoropropyl. Within this embodiment, in another group of
compounds R.sub.4 is 2,2-difluoroethyl. Within this embodiment, in
another group of compounds R.sub.4 is 2,2,2-trifluoroethyl.
Embodiment (B1)
[0095] In another embodiment, the compound of Formula (IA) or a
pharmaceutically acceptable salt thereof as defined in the Summary
is where R.sub.4 is C.sub.1-6 alkylsulfonyl or C.sub.3-8
cycloalkylsulfonyl. Within this embodiment, in one group of
compounds R.sub.4 is C.sub.1-6 alkylsulfonyl, preferably
methylsulfonyl, ethylsulfonyl, or isopropylsulfonyl. Within this
embodiment, in another group of compounds R.sub.4 is
methylsulfonyl. Within this embodiment, in another group of
compounds R.sub.4 is isopropylsulfonyl. Within this embodiment, in
another group of compounds R.sub.4 is C.sub.3-8
cycloalkylsulfonyl.
Embodiment (C1)
[0096] In another embodiment, the compound of Formula (IA) or a
pharmaceutically acceptable salt thereof as defined in the Summary
is where R.sub.4 is C.sub.3-6 heterocycloalkyl optionally
substituted with one or two substituents independently selected
from C.sub.1-6 alkyl, C.sub.1-6 alkoxy, C.sub.1-6 haloalkoxy,
C.sub.1-6 alkylsulfonyl, or halo. Within this embodiment, in one
group of compounds R.sub.4 is tetrahydrofuranyl, pyrrolidinyl,
azetidinyl, or piperidinyl. Within this embodiment, in one group of
compounds R.sub.4 is RS, R, or S tetrahydrofuran-3-yl.
Embodiment (D1)
[0097] In another embodiment, the compound of Formula (IA) or a
pharmaceutically acceptable salt thereof as defined in the Summary
is where R.sub.4 is C.sub.3-6 oxoheterocycloalkyl optionally
substituted with one or two substituents independently selected
from C.sub.1-6 alkyl, C.sub.1-6 alkoxy, C.sub.1-6 haloalkoxy,
C.sub.1-6 alkylsulfonyl, or halo.
Embodiment (E1)
[0098] In another embodiment, the compound of Formula (IA) or a
pharmaceutically acceptable salt thereof as defined in the Summary
is where R.sub.4 is C.sub.1-6 cyanoalkyl. Within this embodiment,
in one group of compounds R.sub.4 is cyanomethyl or
2-cyanoethyl.
Embodiment (F1)
[0099] In another embodiment, the compound of Formula (IA) or a
pharmaceutically acceptable salt thereof as defined in the Summary
is where R.sub.4 is C.sub.3-6 oxoheterocycloalkyl optionally
substituted with one or two substituents independently selected
from C.sub.1-6 alkyl, C.sub.1-6 alkoxy, C.sub.1-6 haloalkoxy,
C.sub.1-6 alkylsulfonyl, or halo.
[0100] Within this embodiment, in one group of compounds R.sub.4 is
1-methyl-2-oxo-1,2-dihydropyridin-4-yl,
1-methyl-2-oxo-1,2-dihydropyridin-5-yl, or
1-methyl-2-oxo-1,2-dihydropyridin-6-yl.
Embodiment (G1)
[0101] In another embodiment, the compound of Formula (IA) or a
pharmaceutically acceptable salt thereof as defined in the Summary
is where R.sub.4 is phenyl optionally substituted with one, two, or
three substituents independently selected from C.sub.1-6 alkyl,
C.sub.1-6 haloalkyl, C.sub.1-6 haloalkoxy, C.sub.1-6 alkoxy,
hydroxyl, cyano, or halo. Within this embodiment, in one group of
compounds R.sup.4 is phenyl optionally substituted with one, two,
or three substituents independently selected from methyl, cyano,
fluoro, chloro, hydroxyl, trifluoromethoxy or cyano.
Embodiment (H1)
[0102] In one embodiment, the compound of Formula (IA) or a
pharmaceutically acceptable salt thereof as defined in the Summary
and embodiments (A1), (B1), (C1), (D1), (E1), (F1), and (G1) above
and embodiments contained therein, is where Z is O.
Embodiment (I1)
[0103] In one embodiment, the compound of Formula (IA) or a
pharmaceutically acceptable salt thereof as defined in the Summary
and embodiments (A1), (B1), (C1), (D1), (E1), (F1), and (G1) above
and embodiments contained therein, is where Z is NR.sub.a. Within
this embodiment, in another group of compounds R.sub.a is hydrogen.
Within this embodiment, in another group of compounds R.sub.a is
methyl.
Embodiment (J1)
[0104] In one embodiment within embodiment J1, the compound of
Formula (IA) or a pharmaceutically acceptable salt thereof as
defined in the Summary and embodiments (A1), (B1), (C1), (D1),
(E1), (F1), (G1), and (H1) above and embodiments contained therein,
is where R.sup.1 is as disclosed in Embodiment G and groups (a),
(b), and (i)-(v) above.
Embodiment (K1)
[0105] In one embodiment within embodiment K1, the compound of
Formula (IA) or a pharmaceutically acceptable salt thereof as
defined in the Summary and embodiments (A1), (B1), (C1), (D1),
(E1), (F1), (G1), and (H1)) above and embodiments contained
therein, is where R.sub.1 is as disclosed in Embodiment H and
groups (a1), (b1), and (vi) above, including groups contained
therein.
Embodiment (L1)
[0106] In one embodiment within embodiment J1, the compound of
Formula (IA) or a pharmaceutically acceptable salt thereof as
defined in the Summary and embodiments (A1), (B1), (C1), (D1),
(E1), (F1), (G1) (H1), (I1), (J1), and (K1) above and embodiments
contained therein, X.sub.1-X.sub.4 and X5 are as disclosed in
Embodiment I and groups (c1), (d1) and groups contained therein
above, including groups contained therein.
Embodiment (M1)
[0107] In one embodiment within embodiment M1, the compound of
Formula (IA) or a pharmaceutically acceptable salt thereof as
defined in the Summary and embodiments (A1), (B1), (C1), (D1),
(E1), (F1), (G1) (H1), (I1), (J1) and (K1) above and embodiments
contained therein, X.sub.1-X.sub.4 and X5 are as in Embodiment J
and groups (e1), (f1) including groups contained therein above.
Embodiment (N1)
[0108] In one embodiment within embodiment M1, the compound of
Formula (IA) or a pharmaceutically acceptable salt thereof as
defined in the Summary and embodiments (A1), (B1), (C1), (D1),
(E1), (F1), (G1) (H1), (I1), (J1) and (K1) above and embodiments
contained therein, X.sub.1-X.sub.4 and X5 are as disclosed in
Embodiment K and groups (f1), (h1) including groups contained
therein above.
[0109] General Synthetic Scheme
[0110] Compounds of this invention can be made by the methods
depicted in the reaction schemes shown below and other methods
known in the art.
[0111] The starting materials and reagents used in preparing these
compounds are either available from commercial suppliers such as
Aldrich Chemical Co., (Milwaukee, Wis.), Bachem (Torrance, Calif.),
or Sigma (St. Louis, Mo.) or are prepared by methods known to those
skilled in the art following procedures set forth in references
such as Fieser and Fieser's Reagents for Organic Synthesis, Volumes
1-17 (John Wiley and Sons, 1991); Rodd's Chemistry of Carbon
Compounds, Volumes 1-5 and Supplementals (Elsevier Science
Publishers, 1989); Organic Reactions, Volumes 1-40 (John Wiley and
Sons, 1991), March's Advanced Organic Chemistry, (John Wiley and
Sons, 4th Edition) and Larock's Comprehensive Organic
Transformations (VCH Publishers Inc., 1989). These schemes are
merely illustrative of some methods by which the compounds of this
invention can be synthesized, and various modifications to these
schemes can be made and will be suggested to one skilled in the art
having referred to this disclosure. The starting materials and the
intermediates, and the final products of the reaction may be
isolated and purified if desired using conventional techniques,
including but not limited to filtration, distillation,
crystallization, chromatography and the like. Such materials may be
characterized using conventional means, including physical
constants and spectral data.
[0112] Unless specified to the contrary, the reactions described
herein take place at atmospheric pressure over a temperature range
from about -78.degree. C. to about 150.degree. C., more preferably
from about 0.degree. C. to about 12.degree. C. and most preferably
at about room (or ambient) temperature, e.g., about 20.degree.
C.
[0113] Compounds of Formula (I) can be prepared as illustrated and
described in Scheme A below.
##STR00337##
[0114] Step 1 involves formation of the C--N bond between R.sub.4
and N-1 nitrogen of the compound of formula 1 where R is an acid
protecting group such as C.sub.1-6 alkyl. The reaction conditions
utilized is based on the nature of the R.sub.4 group. When R.sub.4
is C.sub.1-6 haloalkyl the reaction is carried out by heating
compound 1 with an C.sub.1-6 alkyl halide respectively or C.sub.1-6
alkyl mesylate under standard alkylation reaction conditions e.g.,
in the presence of a base such as potassium carbonate, cesium
carbonate, and the like, in a suitable organic solvent such as DMF,
and the like. When R.sub.4 is C.sub.1-6 alkylsulfonyl or C.sub.3-8
cycloalkylsulfonyl, the reaction is carried out by reacting
compound 1 with C.sub.1-6 alkylsulfonyl halide or C.sub.3-8
cycloalkylsulfonyl halide in the presence of a suitable based such
as triethylamine, pyridine, and the like, in a suitable organic
solvent such as THF, DMF, and the like. When R.sub.4 is heteroaryl,
the C--N bond can either be formed by reacting heteroaryl halide
with a compound of formula 1 by displacement of halide or by
reacting heteroarylboronic acid with compound 1 under Chan-Lam
coupling conditions. Compounds of formula 1, R.sub.4LG, wherein LG
is a leaving group such as sulfonate or halo, and
R.sub.4B(OH).sub.2, or ester thereof, are either commercially
available or they can be prepared by methods well known in the art.
For example 5-fluoro-2-methylindole-3-carboxylic acid ethyl ester,
4,5-difluoro-2-methylindole-3-carboxylic acid ethyl ester,
1H-indole-3-carboxylic acid, 5-methoxy-, methyl ester,
5-fluoro-1H-indole-3-carboxylic acid methyl ester, ethyl
5-methyl-1H-indole-3-carboxylate,
4,5-difluoro-2-methylindole-3-carboxylic acid ethyl ester,
5-cyano-2-methyl-1H-indole-3-carboxylic acid methyl ester,
1H-indazole-3-carboxylic acid, 5-cyano-6-fluoro-, methyl ester,
1H-indazole-3-carboxylic acid, 5-cyano-, methyl ester,
1H-indazole-3-carboxylic acid, 5-methoxy-, ethyl ester,
1H-indazole-3-carboxylic acid, 5-methyl-, ethyl ester,
1H-indazole-3-carboxylic acid, 5-fluoro-, ethyl ester,
1H-pyrazolo[3,4-b]pyridine-3-carboxylic acid, 5-fluoro-, methyl
ester, 1H-pyrrolo[2,3-b]pyridine-3-carboxylic acid, 5-methyl-,
methyl ester, 1H-pyrrolo[2,3-b]pyridine-3-carboxylic acid,
5-fluoro-, methyl ester, CH.sub.3I, methylsulfonyl chloride,
ethylsulfonyl chloride, isopropylsulfonyl chloride,
cyclopropylsulfonyl chloride, 2-bromo-2,2,2-trifluoroethane, and
2-bromo-2,2-difluoroethane are commercially available.
[0115] Hydrolysis of the ester group under basic aqueous conditions
provides the corresponding compound of formula 2. Compound 2 is
then converted to a compound of Formula (I) where Z is NR.sub.a or
O or nitrogen protected derivative thereof, by forming an activated
acid derivative of compound 2, followed by reaction with
R.sub.1R.sub.aNH or R.sub.1OH where R.sub.1 is as defined in the
Summary or nitrogen protected derivative thereof. For example, the
activated acid derivative can be mixed anhydride such as with a
mixture of TFAA and TFA in toluene or CDI or Boc.sub.2O; or acid
halide such as with oxalyl chloride, thionyl chloride; or under
standard using standard peptide coupling reagents such as HATU in
the presence of a base such as N,N-diisopropylethylamine, and a
solvent, such as DMF and the like. When nitrogen protected
derivative of R.sub.1R.sub.aNH or R.sub.1OH are used, removal of
the protecting group provides the compound of Formula (I). Amines
and alcohols of formula R.sub.1R.sub.aNH or R.sub.1OH or nitrogen
protected derivative thereof are either commercially available or
they can be prepared by methods known in the art e.g
(1S,5R,6S)-4-oxa-1-azabicyclo[3.3.1]nonan-6-ol can be prepared as
described in Journal of Medicinal Chemistry, 1993, 36, 683-689.
[0116] Alternatively, compound of Formula I can be synthesized by
first coupling the acid derivative of compound 1 (R is H) with
R.sub.1R.sub.aNH or R.sub.1OH as described above, followed by
formation of N--C bond as described in Step 1 of Scheme A
above.
[0117] Detailed descriptions of synthesis of compounds of Formula
(I) via above procedures are provided in Working Examples
below.
[0118] Utility
[0119] 5-HT3 receptors are known to be expressed in the central
nervous system in regions involving vomiting reflex, processing of
pain, cognition and anxiety control and play a role in the
pathogenesis of diseases such as emesis, migraine, drug addiction,
and neurodegenerative and psychiatric disorders such as anxiety and
depression (see Hewlett et al., 2003 J Clin. Psychiatry 64,
1025-1030; Kelley et al., 2003a, Eur J. Pharmacol., 461, 19-25;
Haus et al., 2000 Scand J Rheumatol Suppl 113, 55-58; and Faris et
al., 2006 J affect Disorder 92, 79-90), eating disorders (Hammer et
al., 1990 Am J Physiol 259, R627-R636, and Jiang & Gietzen 1994
Pharmacol Biochem Behav 47, 59-63), schizophrenia (see Hermann et
al. 1996 Biochem Biophys Res Commun 225, 957-960; Sirota et al.,
2000 Am J Psychiatry 157, 287-289; Adler et al., 2005 Am J
Psychiatry 162, 386-388; Koike et al., Levkovitz et al,
2005Schizophr Res 76, 67-72), cognitive dysfunction associated with
schizophrenia (see Zhang et al., 2006 Schizophr Res 88, 102-110;
Akhondzadeh et al., 2009 Schizophr Res 107, 206-212), cognitive
dysfunction associated with Parkinson's disease, Huntington's
Chorea, presenile dementias and Alzheimer's disease (see Costall
and Naylor 2004 CNS Neurol Disord 3, 27-37) substance abuse and
addiction (see Johnson et al., 2002 Psycho-pharmacology (Berl) 160,
408-413; Johnson, 2004 CNS Drugs 18, 1105-1118; Dawes et al., 2005
Addict Behav 30, 1630-1637, Johnson 2006 Drug Alcohol Depend 84,
256-263), and pain (see Kayser et al, 2007 Pain 130, 235; Glaum et
al., 1998 Neurosci Lett 95, 313-317; Schworer & Ramadori 1993
Clin Investig 71, 659; Thompson and Lummis 2007 Exp Opin Ther
Targets, 11, 527-540). In addition, 5-HT3 receptors are expressed
in the GI tract and hence may play a role in GI disorders such as
dyspepsia, gastroesophagal reflux disease and irritable bowel
syndrome (see Graeff 1997 Psychiatr Clin North Am 20, 723; Thompson
and Lummis 2007 Exp Opin Ther Targets, 11, 527-540; Barnes et al.
2009 Neuropharmacology 56, 273). Expression of the 5-HT3A subunit
has also been discovered extraneuronally in immune cells such as
monocyes, chondrocytes, T-cells, synovial tissue and platelets
(Fiebich et al., 2004 Scan J Rheumatol Suppl, 9-11, Stratz et al.,
2008 Thromb Haemost 99, 784) and of 5-HT3A, C-E within the lamina
propia in the epithelium of the gut mucose (Kapeller et al., J Comp
Neuro., 2008; 509: 356-371) thus suggesting they may be involved in
immunological and inflammatory diseases like atherosclerosis,
tendomyopathies and fibromyalgia.
[0120] Testing
[0121] The 5-HT3 inhibitory activity of the compounds of the
present invention can be tested using the in vitro assay and in
vivo assay described in Biological Example 1 and 2 below.
[0122] Administration and Pharmaceutical Composition
[0123] In general, the compounds of this invention will be
administered in a therapeutically effective amount by any of the
accepted modes of administration for agents that serve similar
utilities. Therapeutically effective amounts of compounds of
Formula (I) may range from about 0.01 to about 75 mg per kg patient
body weight per day, which can be administered in single or
multiple doses. Preferably, the dosage level will be about 0.01 to
about 10 mg/kg per day; more preferably about 0.5 to about 5 mg/kg
per day or 0.1-2 mg/kg/day. For oral administration, the
compositions are preferably provided in the form of tablets
containing about 0.5 to about 200 milligrams of the active
ingredient, from about 0.5, 1.0, 5.0, 10, 15, 20, 25, 50, 75, 100,
150, or 200 milligrams of the active ingredient. The actual amount
of the compound of this invention, i.e., the active ingredient,
will depend upon numerous factors such as the severity of the
disease to be treated, the age and relative health of the subject,
the potency of the compound utilized, the route and form of
administration, and other factors. Although these dosages are based
on an average human subject having a mass of about 60 kg to about
70 kg, the physician will be able to determine the appropriate dose
for a patient (e.g., an infant) whose mass falls outside of this
weight range.
[0124] In general, compounds of this invention will be administered
as pharmaceutical compositions by any one of the following routes:
oral, systemic (e.g., transdermal, intranasal or by suppository),
or parenteral (e.g., intramuscular, intravenous or subcutaneous)
administration. The preferred manner of administration is oral
using a convenient daily dosage regimen, which can be adjusted
according to the degree of affliction. Compositions can take the
form of tablets, pills, capsules, semisolids, powders, sustained
release formulations, solutions, suspensions, elixirs, aerosols, or
any other appropriate compositions.
[0125] The choice of formulation depends on various factors such as
the mode of drug administration (e.g., for oral administration,
formulations in the form of tablets, pills or capsules are
preferred) and the bioavailability of the drug substance. Recently,
pharmaceutical formulations have been developed especially for
drugs that show poor bioavailability based upon the principle that
bioavailability can be increased by increasing the surface area
i.e., decreasing particle size. For example, U.S. Pat. No.
4,107,288 describes a pharmaceutical formulation having particles
in the size range from 10 to 1,000 nm in which the active material
is supported on a crosslinked matrix of macromolecules. U.S. Pat.
No. 5,145,684 describes the production of a pharmaceutical
formulation in which the drug substance is pulverized to
nanoparticles (average particle size of 400 nm) in the presence of
a surface modifier and then dispersed in a liquid medium to give a
pharmaceutical formulation that exhibits remarkably high
bioavailability.
[0126] The compositions are comprised of in general, a compound of
formula (I) in combination with at least one pharmaceutically
acceptable excipient. Acceptable excipients are non-toxic in the
amount used, aid administration, and do not adversely affect the
therapeutic benefit of the compound of formula (I). Such excipient
may be any solid, liquid, semi-solid or, in the case of an aerosol
composition, gaseous excipient that is generally available to one
of skill in the art.
[0127] Solid pharmaceutical excipients include starch, cellulose,
talc, glucose, lactose, sucrose, gelatin, malt, rice, flour, chalk,
silica gel, magnesium stearate, sodium stearate, glycerol
monostearate, sodium chloride, dried skim milk and the like. Liquid
and semisolid excipients may be selected from glycerol, propylene
glycol, water, ethanol and various oils, including those of
petroleum, animal, vegetable or synthetic origin, e.g., peanut oil,
soybean oil, mineral oil, sesame oil, etc. Preferred liquid
carriers, particularly for injectable solutions, include water,
saline, aqueous dextrose, and glycols.
[0128] Compressed gases may be used to disperse a compound of this
invention in aerosol form. Inert gases suitable for this purpose
are nitrogen, carbon dioxide, etc.
[0129] Other suitable pharmaceutical excipients and their
formulations are described in Remington's Pharmaceutical Sciences,
edited by E. W. Martin (Mack Publishing Company, 18th ed.,
1990).
[0130] The level of the compound in a formulation can vary within
the full range employed by those skilled in the art. Typically, the
formulation will contain, on a weight percent (wt %) basis, from
about 0.01-99.99 wt % of a compound of formula (I) based on the
total formulation, with the balance being one or more suitable
pharmaceutical excipients. Preferably, the compound is present at a
level of about 1-80 wt %.
[0131] The compounds of the present invention may be used in
combination with one or more other drugs in the treatment of
diseases or conditions for which compounds of the present invention
or the other drugs may have utility, where the combination of the
drugs together are safer or more effective than either drug alone.
Such other drug(s) may be administered, by a route and in an amount
commonly used therefore, contemporaneously or sequentially with a
compound of the present invention. When a compound of the present
invention is used contemporaneously with one or more other drugs, a
pharmaceutical composition in unit dosage form containing such
other drugs and the compound of the present invention can be used.
However, the combination therapy may also include therapies in
which the compound of the present invention and one or more other
drugs are administered on different overlapping schedules. It is
also contemplated that when used in combination with one or more
other active ingredients, the compounds of the present invention
and the other active ingredients may be used in lower doses than
when each is used singly.
[0132] Accordingly, the pharmaceutical compositions of the present
invention also include those that contain one or more other active
ingredients, in addition to a compound of the present
invention.
[0133] The above combinations include combinations of a compound of
the present invention not only with one other active compound, but
also with two or more other active compounds. Likewise, compounds
of the present invention may be used in combination with other
drugs that are used in the prevention, treatment, control,
amelioration, or reduction of risk of the diseases or conditions
for which compounds of the present invention are useful. Such other
drugs may be administered, by a route and in an amount commonly
used therefore, contemporaneously or sequentially with a compound
of the present invention. Accordingly, the pharmaceutical
compositions of the present invention also include those that also
contain one or more other active ingredients, in addition to a
compound of the present invention. The weight ratio of the compound
of the present invention to the second active ingredient may be
varied and will depend upon the effective dose of each ingredient.
Generally, an effective dose of each will be used.
[0134] In one embodiment, the compound of the present invention may
be administered in combination with anti-Alzheimer's agents,
beta-secretase inhibitors, gamma-secretase inhibitors, HMG-CoA
reductase inhibitors, NSAID's including ibuprofen, vitamin E, and
anti-amyloid antibodies. In another embodiment, the compound of the
present invention may be administered in combination with
sedatives, hypnotics, anxiolytics, antipsychotics, antianxiety
agents, cyclopyrrolones, imidazopyridines, pyrazolopyrimidines,
minor tranquilizers, melatonin agonists and antagonists,
melatonergic agents, benzodiazepines, barbiturates, mGlu2/3
agonists, 5HT-2 antagonists, PDE10 antagonists, GlyT1 inhibitors,
and the like, such as: adinazolam, allobarbital, alonimid,
alprazolam, amisulpride, amitriptyline, amobarbital, amoxapine,
aripiprazole, bentazepam, benzoctamine, brotizolam, bupropion,
busprione, butabarbital, butalbital, capuride, carbocloral, chloral
betaine, chloral hydrate, clomipramine, clonazepam, cloperidone,
clorazepate, chlordiazepoxide, clorethate, chlorpromazine,
clozapine, cyprazepam, desipramine, dexclamol, diazepam,
dichloralphenazone, divalproex, diphenhydramine, doxepin,
estazolam, ethchlorvynol, etomidate, fenobam, flunitrazepam,
flupentixol, fluphenazine, flurazepam, fluvoxamine, fluoxetine,
fosazepam, glutethimide, halazepam, haloperidol, hydroxyzine,
imipramine, lithium, lorazepam, lormetazepam, maprotiline,
mecloqualone, melatonin, mephobarbital, meprobamate, methaqualone,
midaflur, midazolam, nefazodone, nisobamate, nitrazepam,
nortriptyline, olanzapine, oxazepam, paraldehyde, paroxetine,
pentobarbital, perlapine, perphenazine, phenelzine, phenobarbital,
prazepam, promethazine, propofol, protriptyline, quazepam,
quetiapine, reclazepam, risperidone, roletamide, secobarbital,
sertraline, suproclone, temazopam, thioridazine, thiothixene,
tracazolate, kanylcypromaine, trazodone, triazolam, trepipam,
tricetamide, triclofos, trifluoperazine, trimetozine, trimipramine,
uldazepam, venlafaxine, zaleplon, ziprasidone, zolazepam, zolpidem,
[4-(3-fluoro-5-trifluoromethylpyridin-2-yl)piperazin-1-yl][5-me-
thanesulfonyl-2-((S)-2,2,2-trifluoro-1-methylethoxy)phenyl]methanone
(RG1678), glyt1 inhibitors disclosed in U.S. Pat. No. 7,538,114,
Table 1 in column 14, and salts thereof, and combinations
thereof.
[0135] In another embodiment, the compound of the present invention
may be administered in combination with levodopa (with or without a
selective extracerebral decarboxylase inhibitor such as carbidopa
or benserazide), anticholinergics such as biperiden (optionally as
its hydrochloride or lactate salt) and trihexyphenidyl (benzhexol)
hydrochloride, COMT inhibitors such as entacapone, MOA-B
inhibitors, antioxidants, A2a adenosine receptor antagonists,
cholinergic agonists, NMDA receptor antagonists, serotonin receptor
antagonists and dopamine receptor agonists such as alentemol,
bromocriptine, fenoldopam, lisuride, naxagolide, pergolide and
prarnipexole. It will be appreciated that the dopamine agonist may
be in the form of a pharmaceutically acceptable salt, for example,
alentemol hydrobromide, bromocriptine mesylate, fenoldopam
mesylate, naxagolide hydrochloride and pergolide mesylate. Lisuride
and pramipexol are commonly used in a non-salt form.
[0136] In another embodiment, the compound of the present invention
may be administered in combination with a compound from the
phenothiazine, thioxanthene, heterocyclic dibenzazepine,
butyrophenone, diphenylbutylpiperidine and indolone classes of
neuroleptic agent. Suitable examples of phenothiazines include
chlorpromazine, mesoridazine, thioridazine, acetophenazine,
fluphenazine, perphenazine and trifluoperazine. Suitable examples
of thioxanthenes include chlorprothixene and thiothixene. An
example of a dibenzazepine is clozapine. An example of a
butyrophenone is haloperidol. An example of a
diphenylbutylpiperidine is pimozide. An example of an indolone is
molindolone. Other neuroleptic agents include loxapine, sulpiride
and risperidone. It will be appreciated that the neuroleptic agents
when used in combination with the subject compound may be in the
form of a pharmaceutically acceptable salt, for example,
chlorpromazine hydrochloride, mesoridazine besylate, thioridazine
hydrochloride, acetophenazine maleate, fluphenazine hydrochloride,
flurphenazine enathate, fluphenazine decanoate, trifluoperazine
hydrochloride, thiothixene hydrochloride, haloperidol decanoate,
loxapine succinate and molindone hydrochloride. Perphenazine,
chlorprothixene, clozapine, haloperidol, pimozide and risperidone
are commonly used in a non-salt form. Thus, the compound of the
present invention may be administered in combination with
acetophenazine, alentemol, aripiprazole, amisulpride, benzhexol,
bromocriptine, biperiden, chlorpromazine, chlorprothixene,
clozapine, diazepam, fenoldopam, fluphenazine, haloperidol,
levodopa, levodopa with benserazide, levodopa with carbidopa,
lisuride, loxapine, mesoridazine, molindolone, naxagolide,
olanzapine, pergolide, perphenazine, pimozide, pramipexole,
quetiapine, risperidone, sulpiride, tetrabenazine, trihexyphenidyl,
thioridazine, thiothixene, trifluoperazine or ziprasidone.
[0137] In another embodiment, the compound of the present invention
may be administered in combination with an anti-depressant or
anti-anxiety agent, including norepinephrine reuptake inhibitors
(including tertiary amine tricyclics and secondary amine
tricyclics), selective serotonin reuptake inhibitors (SSRIs),
monoamine oxidase inhibitors (MAOIs), reversible inhibitors of
monoamine oxidase (RIMAs), serotonin and noradrenaline reuptake
inhibitors (SNRIs), corticotropin releasing factor (CRF)
antagonists, adrenoreceptor antagonists, neurokinin-1 receptor
antagonists, atypical anti-depressants, benzodiazepines, 5-HTA
agonists or antagonists, especially 5-HTA partial agonists, and
corticotropin releasing factor (CRF) antagonists. Specific agents
include: amitriptyline, clomipramine, doxepin, imipramine and
trimipramine; amoxapine, desipramine, maprotiline, nortriptyline
and protriptyline; fluoxetine, fluvoxamine, paroxetine and
sertraline; isocarboxazid, phenelzine, tranylcypromine and
selegiline; moclobemide, venlafaxine; duloxetine; aprepitant;
bupropion, lithium, nefazodone, trazodone and viloxazine;
alprazolam, chlordiazepoxide, clonazepam, chlorazepate, diazepam,
halazepam, lorazepam, oxazepam and prazepam; buspirone, flesinoxan,
gepirone and ipsapirone, and pharmaceutically acceptable salts
thereof.
EXAMPLES
[0138] The following preparations of compounds of Formula (I) are
given to enable those skilled in the art to more clearly understand
and to practice the present invention. They should not be
considered as limiting the scope of the invention, but merely as
being illustrative and representative thereof.
Synthetic Procedures
Reference 1
Synthesis of (1R,5S,7S)-tert-butyl
7-hydroxy-3-oxa-9-azabicyclo[3.3.1]nonane-9-carboxylate
##STR00338##
[0140] Sodium borohydride (259 mg, 6.84 mmol) was added
portion-wise to a solution of (1R,5S)-tert-butyl
7-oxo-3-oxa-9-azabicyclo[3.3.1]nonane-9-carboxylate (550 mg, 2.279
mmol) in MeOH (4559 .mu.l) at 0.degree. C. After 5 min, the
reaction mixture was allowed to warm to RT then stirred for 30 min.
The mixture was concentrated under reduced pressure, dissolved in
EtOAc and washed with brine. The combined organic layers were dried
over anhydrous Na.sub.2SO.sub.4, filtered and concentrated under
reduced pressure to afford the title compound as a white solid,
which was used without further purification.
Reference 2
Synthesis of
(1R,5S,7S)-9-methyl-d3-oxa-9-azabicyclo[3.3.1]nonan-7-amine
##STR00339##
[0141] Step 1:
(1R,5S)-9-Methyl-d3-oxa-9-azabicyclo[3.3.1]nonan-7-one
[0142] To a solution of sodium dihydrogenphosphate hydrate (22.30
g, 162 mmol) and 2-hydroxypropane-1,2,3-tricarboxylic acid (4.90 g,
25.5 mmol) in water (Volume: 506 ml) was added in turn
methyl-d3-amine hydrogen chloride (5 g, 70.9 mmol) and
3-oxopentanedioic acid (11.91 g, 82 mmol). The pH was adjusted to
4.6 with a 10% aqueous solution of NaOH. A solution of
2,2'-oxydiacetaldehyde (3.62 g, 35.4 mmol) in 8 mL MeOH was added
at RT and the resulting mixture was stirred at RT for 3 days. 10%
aqueous NaOH was used to basify the reaction solution, and
extracted with DCM (100 mL). Purification with column
chromatography (SiO.sub.2; DCM/MeOH) gave the title compound as a
white solid.
Step 2:
(1R,5S)-9-methyl-d.sub.3-3-oxa-9-azabicyclo[3.3.1]nonan-7-one
oxime
[0143] A solution of
(1R,5S)-9-methy-d3-oxa-9-azabicyclo[3.3.1]nonan-7-one (1.65 g,
10.43 mmol), hydroxylamine hydrochloride (0.761 g, 10.95 mmol) and
pyridine (0.843 ml, 10.43 mmol) in EtOH (Volume: 52.1 ml) was
heated at 75.degree. C. for 3 h. After 0.2 mL of triethylamine was
added to the reaction solution, the solvent was removed.
Purification by column chromatography (SiO.sub.2; DCM/MeOH) gave
the title compound as a white solid.
Step 3:
(1R,5S,7S)-9-Methyl-d3-oxa-9-azabicyclo[3.3.1]nonan-7-amine
[0144] Sulfuric acid (1.108 ml, 20.78 mmol) was added dropwise over
15 min to a well-stirred solution of aluminum(III) lithium hydride
(1.0 M in THF, 41.6 ml, 41.6 mmol) in THF (Volume: 41.6 ml) at
0.degree. C. The mixture was stirred for another hour at 0.degree.
C. and then
(1R,5S)-9-methyl-d.sub.3-3-oxa-9-azabicyclo[3.3.1]nonan-7-one oxime
(1.8 g, 10.39 mmol) was added portionwise at 0.degree. C. The
reaction mixture was heated under reflux (80.degree. C.) for 1.5 h.
To the well-stirred reaction mixture, 1.58 mL of water, 2.37 mL of
10 M NaOH and 3.95 mL of water were subsequently added at 0.degree.
C. The resultant suspension was filtered through a pad of Celite
and washed with THF. The combined organic phase was concentrated
under reduced pressure to afford the title compound as a
pale-yellow oil, which was used without further purification.
Reference 3
Synthesis of
(1R,5S,7S)-9-(trifluoromethyl)-3-oxa-9-azabicyclo[3.3.1]nonan-7-amine
2,2,2-trifluoroacetate
##STR00340##
[0145] Step 1: Benzyl
(1R,5S,7S)-3-oxa-9-azabicyclo[3.3.1]nonan-7-ylcarbamate
[0146] Benzyl chloroformate (330 .mu.l, 2.319 mmol) was added to a
solution of (1R,5S,7S)-tert-butyl
7-amino-3-oxa-9-azabicyclo[3.3.1]nonane-9-carboxylate
2,2,2-trifluoroacetate (751.3 mg, 2.108 mmol) and triethylamine
(619 .mu.l, 4.43 mmol) in DCM (10 ml) at RT. After 14 h,
trifluoroacetic acid (2.4 mL, 31.6 mmol) was added to the reaction
mixture. After 15 min, the mixture was concentrated, dissolved with
DMF, filtered, and purified by HPLC followed by neutralization
(K.sub.2CO.sub.3) to afford the title compound as a colorless
oil.
Step 2: Benzyl
((1R,5S,7S)-9-(trifluoromethyl)-3-oxa-9-azabicyclo[3.3.1]nonan-7-yl)carba-
mate
[0147] A solution of benzyl
(1R,5S,7S)-3-oxa-9-azabicyclo[3.3.1]nonan-7-ylcarbamate (27 mg,
0.098 mmol) and dibromodifluoromethane (18.06 .mu.l, 0.195 mmol) in
DMSO (489 .mu.l) was treated with tetrakis(dimethylamino)ethylene
(50.1 .mu.l, 0.215 mmol), dropwise at 0.degree. C. The mixture
slowly warmed to RT overnight then was poured into a 1:1 mixture of
NaHCO.sub.3/Na.sub.2S.sub.2O.sub.3 and extracted twice with
Et.sub.2O. The combined extracts were concentrated and purified by
prep-TLC to give the title compound as a yellow oil.
Step 3:
(1R,5S,7S)-9-(Trifluoromethyl)-3-oxa-9-azabicyclo[3.3.1]nonan-7-am-
ine 2,2,2-trifluoroacetate
[0148] In a vial containing benzyl
((1R,5S,7S)-9-(trifluoromethyl)-3-oxa-9-azabicyclo[3.3.1]nonan-7-yl)carba-
mate (10 mg, 0.029 mmol), palladium on carbon (10 wt %, 1.020 mg,
9.58 .mu.mop, and TFA (4.47 .mu.l, 0.058 mmol) in MeOH (Volume: 145
.mu.l) was purged with hydrogen gas and left under 1 atm H2
atmosphere for 2 h. Filtration through a pad of Celite/MgSO.sub.4
(1:1) followed by concentration gave the title compound as a
colorless film, which was used without further purification.
Reference 4
Synthesis of (1S,5R,6S)-4-oxa-1-azabicyclo[3.3.1]nonan-6-ol;
(1R,5S,6R)-4-oxa-1-azabicyclo[3.3.1]nonan-6-ol
##STR00341##
[0149] Step 1: Ethyl
4-(3-ethoxy-3-oxopropyl)morpholine-2-carboxylate
[0150] A mixture of ethyl morpholine-2-carboxylate (3 g, 18.85
mmol) and ethyl acrylate (5 ml, 18.85 mmol) was heated at
100.degree. C. for 14 h. The reaction was cooled to RT then diluted
with Et.sub.2O and extracted with aqueous 3M HCl. The combined
aqueous layers were basified by solid K.sub.2CO.sub.3 and extracted
with DCM. The combined organic layers were dried over anhydrous
Na.sub.2SO.sub.4, filtered and concentrated under reduced pressure
to afford the title compound as a pale-yellow oil, which was used
without further purification.
Step 2: (1S,5R)-4-Oxa-1-azabicyclo[3.3.1]nonan-6-one
(1R,5S)-4-Oxa-1-azabicyclo[3.3.1]nonan-6-one
[0151] A solution of ethyl
4-(3-ethoxy-3-oxopropyl)morpholine-2-carboxylate (3.07 g, 11.84
mmol) in toluene (8 ml) was added to a suspension of potassium
2-methylpropan-2-olate (3.65 g, 32.6 mmol) in toluene (39.5 ml) at
120.degree. C. After being stirred at 120.degree. C. for 3 h, the
reaction mixture was cooled to RT and extracted with water (20 mL).
The aqueous layer was treated with conc. HCl (20 ml, 240 mmol) then
heated at 110.degree. C. for 14 h. The reaction mixture was cooled
to RT then concentrated under reduced pressure. The resulting solid
was taken up in saturated aq. K.sub.2CO.sub.3 and extracted with
DCM. The combined organic layers were dried over anhydrous
Na.sub.2SO.sub.4, filtered and concentrated under reduced pressure
to afford the title compounds as a brown oil, which was used
without further purification.
Step 3: (1S,5R,6S)-4-Oxa-1-azabicyclo[3.3.1]nonan-6-ol;
(1R,5S,6R)-4-Oxa-1-azabicyclo[3.3.1]nonan-6-ol
[0152] Sodium borohydride (53.6 mg, 1.417 mmol) was added to a
solution of (1S,5R)-4-oxa-1-azabicyclo[3.3.1]nonan-6-one and
(1R,5S)-4-oxa-1-azabicyclo[3.3.1]nonan-6-one (100 mg, 0.708 mmol)
in MeOH (3542 .mu.l) at 0.degree. C. The reaction mixture was
stirred at RT for 30 min, then concentrated under reduced pressure.
The residue was taken up in EtOAc and washed with brine. The
organic layer was dried over anhydrous Na.sub.2SO.sub.4, filtered
and concentrated under reduced pressure to afford the title
compounds as a yellow oil, which was used without further
purification
Reference 5
Synthesis of 1-(pyrimidin-5-yl)-1H-indole-3-carboxylic acid
##STR00342##
[0153] Step 1: Methyl
1-(pyrimidin-5-yl)-1H-indole-3-carboxylate
[0154] To a vial containing methyl 1H-indole-3-carboxylate (471 mg,
2.69 mmol), pyrimidin-5-ylboronic acid (1.0 g, 8.07 mmol), copper
(II) acetate (635 mg, 3.5 mmol), 4 {acute over (.ANG.)} molecular
sieves (4 g) and 1,10-phenanthroline (970 mg, 5.38 mmol) were added
DCM (10.7 ml) and triethylamine (0.375 ml, 2.69 mmol). The mixture
was stirred at RT for 7 days then filtered through a pad of Celite
(washed with MeOH). Evaporation and purification by HPLC (after
dilution with DMF and filtration) afforded the title compound as a
tan solid.
Step 2: 1-(pyrimidin-5-yl)-1H-indole-3-carboxylic acid
[0155] To a solution of methyl
1-(pyrimidin-5-yl)-1H-indole-3-carboxylate (16 mg, 0.063 mmol) in
water MeOH (316 .mu.l) was added 2M KOH (158 .mu.l, 0.316 mmol).
The mixture was heated at 80.degree. C. for 4 h then neutralized
with 1M HCl. The precipitate was collected by filtration to afford
the title compound as a white solid, which was used without further
purification.
[0156] Proceeding as described above
1-(pyrimidin-5-yl)-1H-indole-3-carboxylic acid was prepared.
Reference 6
Synthesis of 1-(pyrimidin-2-yl)-1H-indole-3-carboxylic acid
##STR00343##
[0157] Step 1: methyl
1-(pyrimidin-2-yl)-1H-indole-3-carboxylate
[0158] To a suspension of sodium hydride (46 mg, 1.142 mmol, 60%
dispersion in mineral oil) in DMF (1.1 mL) was added methyl
1H-indole-3-carboxylate (200 mg, 1.142 mmol) and 2-chloropyrimidine
(131 mg, 1.142 mmol) The resulting suspension was stirred at RT for
1 h. The reaction mixture was diluted with DMF, filtered, and
purified by HPLC to afford the title compound as a white-pink
solid.
Step 2: 1-(pyrimidin-2-yl)-1H-indole-3-carboxylic acid
[0159] The title compound was synthesized by utilizing similar
conditions as described in Reference 5, Step 2.
[0160] Proceeding as described above,
1-(pyrazin-2-yl)-1H-indole-3-carboxylic acid was synthesized.
Reference 7
Synthesis of 1-(thiazol-2-yl)-1H-indole-3-carboxylic acid
##STR00344##
[0161] Step 1: Methyl 1-(thiazol-2-yl)-1H-indole-3-carboxylate
[0162] To a solution of methyl 1H-indole-3-carboxylate (200 mg,
1.142 mmol) in NMP (Volume: 1142 .mu.l) were added 2-bromothiazole
(206 .mu.l, 2.283 mmol) and cesium carbonate (1116 mg, 3.42 mmol)
at RT. The mixture was heated at 110.degree. C. for 2 h, then
diluted with DMF, filtered and purified by HPLC to afford the title
compound as a brown solid.
Step 2: 1-(Thiazol-2-yl)-1H-indole-3-carboxylic acid
[0163] The title compound was synthesized by utilizing similar
conditions as described in Reference 5, Step 2.
[0164] Proceeding as described above,
1-(pyridazin-3-yl)-1H-indole-3-carboxylic acid; and
1-(thiazol-5-yl)-1H-indole-3-carboxylic acid was synthesized.
Reference 8
Synthesis of
1-(1,1,1-trifluoro-2-methylpropan-2-yl)-1H-pyrrolo[2,3-b]pyridine-3-carbo-
xylic acid
##STR00345##
[0165] Step 1:
2-(((1,1,1-Trifluoro-2-methylpropan-2-yl)amino)methylene)succinonitrile
[0166] A solution of ethyl formate (330 mg, 4.46 mmol) and
succinonitrile (300 mg, 3.75 mmol) in toluene (1561 .mu.l) was
added dropwise to a suspension of sodium methanolate (215 mg, 3.97
mmol) in toluene (1561 .mu.l) at 0.degree. C. After being stirred
at RT for 3 h, the reaction mixture was treated with
1,1,1-trifluoro-2-methylpropan-2-amine (486 mg, 3.82 mmol) and
acetic acid (255 .mu.l, 4.46 mmol) then heated at 120.degree. C.
for 3 h. After being cooled to RT, the reaction mixture was washed
with brine, then dried over anhydrous Na.sub.2SO.sub.4, filtered
and concentrated under reduced pressure to afford the title
compound as a brown oil, which was used without further
purification.
Step 2:
5-Amino-1-(1,1,1-trifluoro-2-methylpropan-2-yl)-1H-pyrrole-3-carbo-
nitrile
[0167] A solution of
2-(((1,1,1-trifluoro-2-methylpropan-2-yl)amino)methylene)succinonitrile
(187.2 mg, 0.862 mmol) in EtOH (539 .mu.l) was added to a solution
of KOH (87 mg, 1.551 mmol) in water (539 .mu.l) at RT. After being
stirred at RT for 4 h, the reaction mixture was concentrated under
reduced pressure. The residual brown solid was taken up in water
and sonicated. The resulting precipitate was collected by
filtration, dissolved in EtOAc, washed with brine, dried over
anhydrous Na.sub.2SO.sub.4, filtered and concentrated under reduced
pressure to afford the title compound as a brown solid, which was
used without further purification.
Step 3:
1-(1,1,1-Trifluoro-2-methylpropan-2-yl)-1H-pyrrolo[2,3-b]pyridine--
3-carbonitrile
[0168] 4-Methylbenzenesulfonic acid (10.57 mg, 0.061 mmol) was
added in one portion to a solution of
5-amino-1-(1,1,1-trifluoro-2-methylpropan-2-yl)-1H-pyrrole-3-carbonitrile
(133.3 mg, 0.614 mmol) and 1,1,3,3-tetramethoxypropane (111 .mu.l,
0.675 mmol) in toluene (1227 .mu.l) at RT. The mixture was heated
at 100.degree. C. for 1 h and purified directly by HPLC to afford
the title compound as a brown solid.
Step 4:
1-(1,1,1-Trifluoro-2-methylpropan-2-yl)-1H-pyrrolo[2,3-b]pyridine--
3-carboxylic acid
[0169] KOH (174 mg, 3.11 mmol) was added to a solution of
1-(1,1,1-trifluoro-2-methylpropan-2-yl)-1H-pyrrolo[2,3-b]pyridine-3-carbo-
nitrile (78.7 mg, 0.311 mmol) in 1:1:1 THF/MeOH/water (621 .mu.l)
at RT. After being stirred at 100.degree. C. for 4 h, the reaction
mixture was acidified (pH=2-3) by conc. HCl and the resulting
suspension was extracted with EtOAc. The combined organic layers
were concentrated to afford the title compound as a brown foam,
which was used without further purification.
Reference 9
Synthesis of 1-(methylsulfonyl)-1H-indazole-3-carboxylic acid
##STR00346##
[0171] Methanesulfonyl chloride (48.1 .mu.l, 0.617 mmol) was added
to a solution of 1H-indazole-3-carboxylic acid (100 mg, 0.617 mmol)
and triethylamine (86 .mu.l, 0.617 mmol) in THF (1542 .mu.l) and
the mixture was stirred for 1 h. The reaction was then poured into
water and extracted twice with EtOAc. The combined organic layers
were filtered through MgSO.sub.4 and concentrated to give the title
compound as a white solid, which was used without further
purification.
Reference 10
Synthesis of 5-fluoro-1-(methylsulfonyl)-1H-indole-3-carboxylic
acid
##STR00347##
[0172] Step 1: tert-Butyl
5-fluoro-1-(methylsulfonyl)-1H-indole-3-carboxylate
[0173] To a solution of tert-butyl 5-fluoro-1H-indole-3-carboxylate
(500 mg, 2.125 mmol) and triethylamine (1721 mg, 17.00 mmol) in THF
(5 ml) was added methanesulfonyl chloride (0.658 ml, 8.50 mmol).
The mixture was stirred at RT for 2 h. The reaction mixture was
then poured into water and extracted twice with Et.sub.2O. The
organic extracts were combined, filtered through MgSO.sub.4,
concentrated, and purified by column chromatography (SiO.sub.2,
EtOAc/hex) to afford the title compound as a white solid.
Step 2: 5-Fluoro-1-(methylsulfonyl)-1H-indole-3-carboxylic acid
[0174] A mixture of tert-butyl
5-fluoro-1-(methylsulfonyl)-1H-indole-3-carboxylate (150 mg, 0.479
mmol) and conc. HCl (0.2 ml, 2.394 mmol) in EtOAc (10 ml) was
stirred at RT for 2 h. The mixture was then partially concentrated,
and the resulting precipitate was collected by filtration, washed
with EtOAc and dried in vacuo to afford the title compound as a
white solid, which was used without further purification.
Reference 11
Synthesis of 5-fluoro-1-(isopropylsulfonyl)-1H-indole-3-carboxylic
acid
##STR00348##
[0175] Step 1: Methyl
1-(isopropylsulfonyl)-1H-indole-3-carboxylate
[0176] To a solution of methyl 1H-indole-3-carboxylate (0.234 g,
1.336 mmol) in THF (6.68 ml) was added sodium
bis(trimethylsilyl)amide (2.67 ml, 2.67 mmol) at RT. After 30 min,
propane-2-sulfonyl chloride (0.3 ml, 2.67 mmol) was added and the
mixture was stirred for 2 h. The reaction mixture was then poured
into brine and extracted twice with EtOAc. The combined extracts
were filtered through MgSO.sub.4 and concentrated to give the title
compound as a brown solid, which was used without further
purification.
Step 2: 5-Fluoro-1-(isopropylsulfonyl)-1H-indole-3-carboxylic
acid
[0177] The title compound was synthesized by utilizing similar
conditions as described in Reference 5, Step 2.
[0178] Proceeding as described above,
1-(isopropylsulfonyl)-1H-indole-3-carboxylic acid was
synthesized.
Reference 12
Synthesis of
(1R,5S,7s)-9-methyl-3-oxa-9-azabicyclo[3.3.1]nonan-7-yl
1H-indole-3-carboxylate
##STR00349##
[0180] To a solution of 1H-indole-3-carboxylic acid (250 mg, 1.551
mmol) in PhMe (5171 .mu.l) was added TFAA (219 .mu.l, 1.551 mmol)
then TFA (1293 .mu.l). The mixture was stirred for 30 min then
commercially available
(1R,5S,7s)-9-methyl-3-oxa-9-azabicyclo[3.3.1]nonan-7-ol (203 mg,
1.293 mmol) was added. The reaction mixture stirred at RT for 1 h
then was poured into aq NaHCO.sub.3 and stirred until pH=7 and
bubbling stopped. The reaction mixture was extracted with EtOAc and
dried over MgSO.sub.4. Purification by ISCO (0-20% MeOH/DCM)
yielded the title compound as a pink solid.
Reference 13
Synthesis of (1R,5S,7s)-tert-butyl
7-((1H-indole-3-carbonyl)oxy)-3-oxa-9-azabicyclo[3.3.1]nonane-9-carboxyla-
te
##STR00350##
[0181] Step 1:
(1R,5S,7s)-9-benzyl-3-oxa-9-azabicyclo[3.3.1]nonan-7-ol
[0182] Sodium borohydride (24.54 g, 649 mmol) was added portionwise
over 30 min to a suspension of
(1R,5S)-9-benzyl-3-oxa-9-azabicyclo[3.3.1]nonan-7-one (50 g, 216
mmol) in MeOH (540 ml) and THF (540 ml) at 0.degree. C. The mixture
was allowed to gradually warm to RT over 1 h. After an additional
hour at RT, the mixture was concentrated and the white residue was
partitioned between ethyl acetate and brine. The combined organic
layers were dried over Na.sub.2SO.sub.4, filtered and concentrated
under reduced pressure to afford the title compound as a white
solid, which was used without further purification.
Step 2: (1R,5S,7s)-9-benzyl-3-oxa-9-azabicyclo[3.3.1]nonan-7-ol
[0183] 2,2,2-Trifluoroacetic anhydride (34.5 ml, 244 mmol) and TFA
(123 ml) were subsequently added to a solution of
1H-indole-3-carboxylic acid (39.4 g, 244 mmol) in toluene (987 ml)
at RT. After 30 min,
(1R,5S,7s)-9-benzyl-3-oxa-9-azabicyclo[3.3.1]nonan-7-ol (51.8 g,
222 mmol) was added to the mixture in one portion at RT. After 2 h,
the mixture was concentrated under reduced pressure to the half of
the original volume. Then, 800 mL of 10% Na.sub.2CO.sub.3 (aq) was
added. The mixture was concentrated under reduced pressure until
most of the organic solvent was removed. The product was extracted
with ethyl acetate and the combined organic layers were washed with
brine, dried over Na.sub.2SO.sub.4, filtered and concentrated under
reduced pressure. The residual dark purple solid was triturated
with Et.sub.2O/EtOAc (4:1) to yield the title compound as a
white-pink solid.
Step 3: (1R,5S,7s)-3-oxa-9-azabicyclo[3.3.1]nonan-7-yl
1H-indole-3-carboxylate, hydrogen chloride salt
[0184] A suspension of
(1R,5S,7s)-9-benzyl-3-oxa-9-azabicyclo[3.3.1]nonan-7-yl
1H-indole-3-carboxylate (2 g, 5.31 mmol) and palladium on carbon
(200 mg, 1.879 mmol, 10 wt %) in EtOH (4.43 ml), THF (4.43 ml) and
3N HCl (4.43 ml) was stirred at RT under a hydrogen atmosphere
(balloon) for 14 h. Then, the mixture was filtered through a pad of
Celite and the filtrate was concentrated under reduced pressure to
afford the title compound as a pink solid, which was used without
further purification.
Step 4: (1R,5S,7s)-tert-butyl
7-((1H-indole-3-carbonyl)oxy)-3-oxa-9-azabicyclo[3.3.1]nonane-9-carboxyla-
te
[0185] Di-tert-butyl dicarbonate (1.275 g, 5.84 mmol) was added in
one portion to a suspension of
(1R,5S,7s)-3-oxa-9-azabicyclo[3.3.1]nonan-7-yl
1H-indole-3-carboxylate hydrochloride (1.714 g, 5.31 mmol) and
triethylamine (1.628 ml, 11.68 mmol) in THF (26.6 ml) at RT. After
1 h, the mixture was partitioned between sat. NH.sub.4Cl (aq) and
ethyl acetate. The aqueous layer was extracted with ethyl acetate
and combined organic layers were washed with brine, dried over
anhydrous Na.sub.2SO.sub.4, filtered and concentrated under reduced
pressure to afford the title compound as a pale-brown oil, which
was used without further purification.
Reference 14
Synthesis of 1-phenyl-1H-indole-3-carboxylic acid
##STR00351##
[0186] Step 1: methyl 1-phenyl-1H-indole-3-carboxylate
[0187] A 5 mL screwtop vial containing methyl
1H-indole-3-carboxylate (100 mg, 0.571 mmol) and potassium
phosphate (254 mg, 1.199 mmol) was degassed and purged with
nitrogen after the addition of each of the following in sequential
order: PhMe (1142 .mu.l), bromobenzene (59.7 .mu.l, 0.571 mmol),
(1R,2R)--N1,N2-dimethylcyclohexane-1,2-diamine (54.4 .mu.l, 0.342
mmol), and copper(I) iodide (32.6 mg, 0.171 mmol). The vial was
sealed, wrapped in aluminum foil, and heated to 110.degree. C. for
24 h. Concentration on silica gel and ISCO purification (20%
EtOAc/hexanes) gave the title compound as a white solid.
Step 2: 1-phenyl-1H-indole-3-carboxylic acid
[0188] To a solution of methyl 1-phenyl-1H-indole-3-carboxylate
(108 mg, 0.430 mmol) in MeOH (1433 .mu.l) was added aq KOH (1074
.mu.l, 2.149 mmol, 2 M). The mixture was heated at 90.degree. C.
for 1 h then the MeOH was removed under reduced pressure. The
residual aqueous layer was acidified with 1M HCl then extracted
with EtOAc. The combined organic layers were dried over anhydrous
MgSO.sub.4, filtered, and concentrated to afford the title compound
as a white solid, which was used without further purification.
[0189] The following carboxylic acids were prepared by a similar
procedure: 1-(isothiazol-4-yl)-1H-indole-3-carboxylic acid;
1-(isothiazol-3-yl)-1H-indole-3-carboxylic acid;
1-(isothiazol-5-yl)-1H-indole-3-carboxylic acid; and
1-(oxazol-2-yl)-1H-indole-3-carboxylic acid.
Reference 15
Synthesis of 1-(1-methyl-1H-imidazol-5-yl)-1H-indole-3-carboxylic
acid
##STR00352##
[0190] Step 1: methyl
1-(1-methyl-1H-imidazol-5-yl)-1H-indole-3-carboxylate
[0191] A solution of methyl 1H-indole-3-carboxylate (300 mg, 1.712
mmol) and 5-bromo-1-methyl-1H-imidazole (303 mg, 1.884 mmol) in
toluene (3425 .mu.l) was treated with
(1R,2R)--N1,N2-dimethylcyclohexane-1,2-diamine (82 .mu.l, 0.514
mmol), potassium phosphate (763 mg, 3.60 mmol) and copper(I) iodide
(98 mg, 0.514 mmol) and the resulting reaction mixture stirred at
110.degree. C. overnight. HPLC purification afforded the title
compound as a yellow solid.
Step 2: 1-(1-methyl-1H-imidazol-5-yl)-1H-indole-3-carboxylic
acid
[0192] A solution of methyl
1-(1-methyl-1H-imidazol-5-yl)-1H-indole-3-carboxylate (40 mg, 0.157
mmol) in THF (1567 .mu.l) was treated with potassium
trimethylsilanolate (223 mg, 1.567 mmol) in one portion at RT and
the resulting reaction mixture stirred overnight. ISCO purification
(10% MeOH/DCM) afforded the title compound as a white solid.
Reference 17
Synthesis of
1-(thiazol-2-yl)-1H-pyrrolo[2,3-b]pyridine-3-carboxylic acid
##STR00353##
[0193] Step 1: methyl
1-(thiazol-2-yl)-1H-pyrrolo[2,3-b]pyridine-3-carboxylate
[0194] A mixture of methyl 1H-pyrrolo[2,3-b]pyridine-3-carboxylate
(200 mg, 1.135 mmol), 2-bromothiazole (205 .mu.l, 2.271 mmol) and
cesium carbonate (1110 mg, 3.41 mmol) in NMP (1135 .mu.l) was
heated at 130.degree. C. for 2 h. The mixture was then purified by
HPLC to afford the title compound as a brownish-white solid.
Step 2: 1-(thiazol-2-yl)-1H-pyrrolo[2,3-b]pyridine-3-carboxylic
acid
[0195] Potassium hydroxide (38.5 mg, 0.687 mmol) was added to a
solution of methyl
1-(thiazol-2-yl)-1H-pyrrolo[2,3-b]pyridine-3-carboxylate (35.6 mg,
0.137 mmol) in MeOH (343 .mu.l) and water (343 .mu.l) at RT. The
mixture was heated at 100.degree. C. for 2 h. After cooling to RT,
the mixture was acidified with 2 N HCl and then concentrated under
reduced pressure. The crude mixture was used without further
purification.
[0196] The following carboxylic acids were prepared by a similar
procedure: 1-(thiazol-4-yl)-1H-pyrrolo[2,3-b]pyridine-3-carboxylic
acid; 1-(thiazol-5-yl)-1H-pyrrolo[2,3-b]pyridine-3-carboxylic acid;
5-fluoro-1-(thiazol-2-yl)-1H-pyrrolo[2,3-b]pyridine-3-carboxylic
acid;
5-fluoro-1-(thiazol-4-yl)-1H-pyrrolo[2,3-b]pyridine-3-carboxylic
acid;
5-fluoro-1-(thiazol-5-yl)-1H-pyrrolo[2,3-b]pyridine-3-carboxylic
acid and 1-(thiazol-5-yl)-1H-indazole-3-carboxylic acid.
Reference 18
tert-Butyl
(1R,5S,7S)-7-(methylamino)-3-oxa-9-azabicyclo[3.3.1]nonane-9-ca-
rboxylate
##STR00354##
[0198] In a vial containing (1R,5S,7S)-tert-butyl
7-amino-3-oxa-9-azabicyclo[3.3.1]nonane-9-carboxylate (108. mg,
0.446 mmol) and formaldehyde (39.8 .mu.l, 0.535 mmol) in DCE
(Volume: 1114 .mu.l) was added sodium triacetoxyborohydride (132
mg, 0.624 mmol) and stirred for 2 h. The mixture was poured into
10% NaOH, and extracted twice with DCM. The extracts were combined,
filtered through MgSO.sub.4, and concentrated to give the title
compound.
Example 1
Synthesis of
(1R,3R,5S)-8-methyl-8-azabicyclo[3.2.1]octan-3-yl1-(2,2-difluoroethyl)-1H-
-pyrrolo[2,3-b]pyridine-3-carboxylate 2,2,2-trifluoroacetate
##STR00355##
[0199] Step 1: (1R,3R,5S)-8-methyl-8-azabicyclo[3.2.1]octan-3-yl
1H-pyrrolo[2,3-b]pyridine-3-carboxylate 2,2,2-trifluoroacetate
[0200] Oxalyl dichloride (318 .mu.l, 3.70 mmol) was added to a
solution of 1H-pyrrolo[2,3-b]pyridine-3-carboxylic acid (500 mg,
3.08 mmol) and a drop of DMF in DMC (Volume: 10.0 ml) at 0.degree.
C. After 1 h, the mixture was allowed to warm to RT and
concentrated under reduced pressure. The residue was redissolved in
DCM (Volume: 10.0 ml).
(1R,3R,5S)-8-methyl-8-azabicyclo[3.2.1]octan-3-ol (653 mg, 4.63
mmol) and N,N-diisopropylethylamine (1343 .mu.l, 7.71 mmol) were
added to the suspension. After being stirred at RT for 14 h, the
mixture was diluted with DMF, filtered and purified by HPLC to
afford the title compound as a colorless oil.
Step 2: Synthesis of
(1R,3R,5S)-8-methyl-8-azabicyclo[3.2.1]octan-3-yl
difluoroethyl)-1H-pyrrolo[2,3-b]pyridine-3-carboxylate
2,2,2-trifluoroacetate
[0201] 2-Bromo-1,1-difluoroethane (54.4 mg, 0.376 mmol) was added
in one portion to a suspension of
(1R,3R,5S)-8-methyl-8-azabicyclo[3.2.1]octan-3-yl
1H-pyrrolo[2,3-b]pyridine-3-carboxylate 2,2,2-trifluoroacetate (50
mg, 0.125 mmol) and K.sub.2CO.sub.3 (87 mg, 0.626 mmol) in DMF
(Volume: 626 .mu.l) at RT. The mixture was heated at 70.degree. C.
for 14 h, cooled to RT, diluted with DMF, filtered, and purified by
HPLC to afford the title compound as a colorless oil. MS (ESI, pos.
ion) m/z: 350.2 (M+1).
Example 2
Synthesis of
N-((1R,3R,5S)-9-methyl-9-azabicyclo[3.3.1]nonan-3-yl)-1-(methylsulfonyl)--
1H-indazole-3-carboxamide 2,2,2-trifluoroacetic acid
##STR00356##
[0203] A mixture of 1-(methylsulfonyl)-1H-indazole-3-carboxylic
acid (60 mg, 0.250 mmol; see Reference 9 for the synthesis),
di-tert-butyl dicarbonate (75 .mu.l, 0.325 mmol),
(1R,3R,5S)-9-methyl-9-azabicyclo[3.3.1]nonan-3-ol (38.8 mg, 0.250
mmol), and DMAP (3.05 mg, 0.025 mmol) in THF (1249 .mu.l) was
heated to 80.degree. C. overnight. Concentration and HPLC
purification (after dilution with DMF and filtration) gave the
title compound as a clear oil. MS (ESI, pos. ion) m/z: 378.2
(M+1).
Example 3
Synthesis of quinuclidin-4-yl
5-fluoro-1-(methylsulfonyl)-1H-indole-3-carboxylate
2,2,2-trifluoroacetic acid
##STR00357##
[0205] In a vial containing
5-fluoro-1-(methylsulfonyl)-1H-indole-3-carboxylic acid (20 mg,
0.078 mmol; see Reference 10 for the synthesis) and trifluoroacetic
anhydride (10.98 .mu.l, 0.078 mmol) in toluene (259 .mu.l) was
added TFA (64.8 .mu.l). After 30 min, quinuclidin-4-ol (8.24 mg,
0.065 mmol) was added and the mixture was stirred at RT overnight.
Direct HPLC purification (after dilution with DMF and filtration)
gave the title compound as a clear film. MS (ESI, pos. ion) m/z:
367.2 (M+1).
[0206] Compound 181 in Table 1 was synthesized as described in
Example 3 above.
Example 4
Synthesis of (1R,3R,5S)-8-methyl-8-azabicyclo[3.2.1]octan-3-yl
2-chloro-1-(2,2-difluoroethyl)-1H-indole-3-carboxylate
2,2,2-trifluoroacetate
##STR00358##
[0207] Step 1: (1R,3R,5S)-8-methyl-8-azabicyclo[3.2.1]octan-3-yl
2-chloro-1H-indole-3-carboxylate 2,2,2-trifluoroacetate
[0208] The title compound was synthesized by utilizing similar
conditions as described in Example 3 above.
Step 2: (1R,3R,5S)-8-methyl-8-azabicyclo[3.2.1]octan-3-yl
2-chloro-1-(2,2-difluoroethyl)-1H-indole-3-carboxylate
2,2,2-trifluoroacetate
[0209] A solution of
(1R,3R,5S)-8-methyl-8-azabicyclo[3.2.1]octan-3-yl
2-chloro-1H-indole-3-carboxylate 2,2,2-trifluoroacetate (23 mg,
0.053 mmol), 2-bromo-1,1-difluoroethane (23.11 mg, 0.159 mmol) and
K.sub.2CO.sub.3 (36.7 mg, 0.266 mmol) in DMF (266 .mu.l) was heated
at 80.degree. C. for 14 h. After cooling to RT, the mixture was
diluted with DMF, filtered and purified by HPLC to afford the title
compound as a white solid. MS (ESI, pos. ion) m/z: 383.2 (M+1)
[0210] Compounds in Table 1 above 1, 2, 15, 27, 40, 56, 83, 88, 95,
96, and 97 were synthesized as described in Example 4 above. Step 1
of compound 41 was carried out as in Example 1, followed by Step 2
of Example 4.
Example 5
Synthesis of (1R,3R,5S)-8-azabicyclo[3.2.1]octan-3-yl
1-(2,2,2-trifluoroethyl)-1H-indole-3-carboxylate
2,2,2-trifluoroacetate
##STR00359##
[0211] Steps 1 and 2:
(1R,3R,5S)-8-((Benzyloxy)carbonyl)-8-azabicyclo[3.2.1]octan-3-yl
1-(2,2,2-trifluoroethyl)-1H-indole-3-carboxylate
[0212]
(1R,3R,5S)-8-((Benzyloxy)carbonyl)-8-azabicyclo[3.2.1]octan-3-yl
1-(2,2,2-trifluoroethyl)-1H-indole-3-carboxylate (prepared as
described in Example 1 above) was covered to the title compound by
utilizing a similar procedure as described in Example 4 above.
Step 3: (1R,3R,5S)-8-Azabicyclo[3.2.1]octan-3-yl
1-(2,2,2-trifluoroethyl)-1H-indole-3-carboxylate
2,2,2-trifluoroacetate
[0213] A suspension of
(1R,3R,5S)-8-((benzyloxy)carbonyl)-8-azabicyclo[3.2.1]octan-3-yl
1-(2,2,2-trifluoroethyl)-1H-indole-3-carboxylate (47.7 mg, 0.098
mmol) and palladium on carbon (10 wt %, 5 mg, 4.70 .mu.mol) was
stirred under 1 atm H2 atmosphere in EtOH/EtOAc (1:1, Volume: 980
.mu.l) at RT. After 2 h, the mixture was filtered through a pad of
Celite and the filtrate was concentrated, diluted with DMF and
purified by HPLC to afford the title compound as a colorless oil.
MS (ESI, pos. ion) m/z: 353.2 (M+1)
[0214] Utilizing a similar procedure as described above compound 45
in Table 1 above was prepared.
Example 6
Synthesis of
(1R,3R,5S)-8-methyl-8-azabicyclo[3.2.1]octan-3-yl2-chloro-1-(methylsulfon-
yl)-1H-indole-3-carboxylate 2,2,2-trifluoroacetate
##STR00360##
[0215] Step 1: (1R,3R,5S)-8-Methyl-8-azabicyclo[3.2.1]octan-3-yl
2-chloro-1H-indole-3-carboxylate 2,2,2-trifluoroacetate
[0216] The title compound was synthesized by similar conditions as
described in Example 3 above.
Step 2: (1R,3R,5S)-8-Methyl-8-azabicyclo[3.2.1]octan-3-yl
2-chloro-1-(methylsulfonyl)-1H-indole-3-carboxylate
2,2,2-trifluoroacetate
[0217] Sodium bis(trimethylsilyl)amide (1.0 M THF, 150 .mu.l, 0.150
mmol) was added to a solution of
(1R,3R,5S)-8-methyl-8-azabicyclo[3.2.1]octan-3-yl
2-chloro-1H-indole-3-carboxylate 2,2,2-trifluoroacetate (28.3 mg,
0.065 mmol) in THF (327 .mu.l) at 0.degree. C. After 5 min,
methanesulfonyl chloride (6.58 .mu.l, 0.085 mmol) was added and the
mixture was stirred at RT for 1 h. The mixture was diluted with
DMF, filtered and purified by HPLC to afford the title compound as
a colorless film. MS (ESI, pos. ion) m/z: 397.2 (M+1).
[0218] Utilizing a similar procedure as described above, compounds
3, 26, 34, 86, and 99 in Table 1 above were prepared.
Example 7
N-((1R,5S,7S)-9-methyl-3-oxa-9-azabicyclo[3.3.1]nonan-7-yl)-1-(1,1,1-trifl-
uoro-2-methylpropan-2-yl)-1H-pyrrolo[2,3-b]pyridine-3-carboxamide
2,2,2-trifluoroacetate
##STR00361##
[0220] HATU (34.1 mg, 0.090 mmol) was added to a solution of
1-(1,1,1-trifluoro-2-methylpropan-2-yl)-1H-pyrrolo[2,3-b]pyridine-3-carbo-
xylic acid (24.4 mg, 0.090 mmol; See Reference 8 for the
synthesis),
(1R,5S,7S)-9-methyl-3-oxa-9-azabicyclo[3.3.1]nonan-7-amine (14.00
mg, 0.090 mmol) and N,N-diisopropylethylamine (46.8 .mu.l, 0.269
mmol) in DMF (Volume: 179 .mu.l) at RT. After 20 min, the mixture
was diluted with DMF, filtered and purified by HPLC to afford the
title compound as a yellow film. MS (ESI, pos. ion) m/z: 411.3
(M+1).
[0221] Compounds 10, 36, 46, 69, 71, 92, 93, 94, 107, 111, 114,
117-123 in Table 1 above were synthesized by utilizing a similar
procedure as described in Example 7 above using the carboxylic acid
intermediate prepared by procedures indicated below:
[0222] Compound 69 (Reference 8); 71 (Reference 5); 92 (Reference
6); 94 (Reference 5); 107 (Reference 6); 10 (Reference 11); 36
(Reference 10); 46 (Reference 9); 93 (Reference 11); 111 (Reference
2 for the amine synthesis and Reference 11 for the carboxylic acid
synthesis); 114 (Reference 2 for the amine synthesis and Reference
5 for the carboxylic acid synthesis); 117 (Reference 7); 118
(Reference 7); 119 (Reference 7); 120 (Reference 5); 121 (Reference
2 for the amine synthesis and Reference 6 for the carboxylic acid
synthesis); 122 (Reference 2 for the amine synthesis and Reference
6 for the carboxylic acid synthesis); 123 (Reference 2 for the
amine synthesis and Reference 7 for the carboxylic acid
synthesis)
Example 8
Synthesis of
1-(2,2-difluoroethyl)-N-((1R,3R,5S)-8-methyl-8-azabicyclo[3.2.1]octan-3-y-
l)-1H-indazole-3-carboxamide 2,2,2-trifluoroacetate
##STR00362##
[0223] Step 1:
N-((1R,3R,5S)-8-Methyl-8-azabicyclo[3.2.1]octan-3-yl)-1H-indazole-3-carbo-
xamide 2,2,2-trifluoroacetate
[0224] The title compound was synthesized by utilizing similar
conditions as described in Example 7.
Step 2:
1-(2,2-Difluoroethyl)-N-((1R,3R,5S)-8-methyl-8-azabicyclo[3.2.1]oc-
tan-3-yl)-1H-indazole-3-carboxamide 2,2,2-trifluoroacetate
[0225] Similar conditions as described in Example 4, Step 2 were
utilized to afford the title compound as a colorless film. MS (ESI,
pos. ion) m/z: 349.25 (M+1)
[0226] Following compounds in Table 1 above were synthesized by
utilizing a similar procedure as described in Example 8 above:
Compounds 7, 12, 20, 66, 75, and 98.
Example 9
Synthesis of
N-((1R,3R,5S)-8-methyl-8-azabicyclo[3.2.1]octan-3-yl)-1-(methylsulfonyl)--
1H-indazole-3-carboxamide 2,2,2-trifluoroacetate
##STR00363##
[0227] Step 1:
N-((1R,3R,5S)-8-Methyl-8-azabicyclo[3.2.1]octan-3-yl)-1H-indazole-3-carbo-
xamide 2,2,2-trifluoroacetate
[0228] The title compound was synthesized by utilizing similar
conditions as described in Example 7 above.
Step 2:
N-((1R,3R,5S)-8-Methyl-8-azabicyclo[3.2.1]octan-3-yl)-1-(methylsul-
fonyl)-1H-indazole-3-carboxamide 2,2,2-trifluoroacetate
[0229] Similar conditions as described in Example 6, Step 2 were
utilized to afford the title compound as a colorless film. MS (ESI,
pos. ion) m/z: 363.2 (M+1)
[0230] Following compounds in Table 1 above were synthesized by
utilizing a similar procedure as described in Example 9 above:
Compounds 18, 74, 101, and 110 (azabicyclic intermediate prepared
by Reference 2).
Example 10
Synthesis of (1R,3R,5S)-9-methyl-9-azabicyclo[3.3.1]nonan-3-yl
1-(2,2-difluoroethyl)-1H-pyrrolo[2,3-b]pyridine-3-carboxylate
2,2,2-trifluoroacetate
##STR00364##
[0231] Step 1: Methyl
1-(2,2-difluoroethyl)-1H-pyrrolo[2,3-b]pyridine-3-carboxylate
[0232] 2-Bromo-1,1-difluoroethane (677 .mu.l, 8.51 mmol) was added
to a suspension of methyl 1H-pyrrolo[2,3-b]pyridine-3-carboxylate
(500 mg, 2.84 mmol) and K.sub.2CO.sub.3 (1177 mg, 8.51 mmol) in DMF
(2838 .mu.l) at RT. The mixture was heated at 70.degree. C. for 14
h and purified by column chromatography (SiO.sub.2; DCM/MeOH) to
afford the title compound as a white solid.
Step 2:
1-(2,2-Difluoroethyl)-1H-pyrrolo[2,3-b]pyridine-3-carboxylic
acid
[0233] The title compound was synthesized by utilizing similar
conditions as described in Reference 5, Step 2.
Step 3:
(1R,3R,5S)-9-Methyl-9-azabicyclo[3.3.1]nonan-3-yl1-(2,2-difluoroet-
hyl)-1H-pyrrolo[2,3-b]pyridine-3-carboxylate
2,2,2-trifluoroacetate
[0234] CDI (14.34 mg, 0.088 mmol) was added to a solution of
1-(2,2-difluoroethyl)-1H-pyrrolo[2,3-b]pyridine-3-carboxylic acid
(20 mg, 0.088 mmol) in DMF (Volume: 442 .mu.l) at RT and the
resulting mixture was heated at 60.degree. C. for 1 h. In a
separate vial, sodium hydride (4.24 mg, 0.106 mmol) was added to a
solution of (1R,3R,5S)-9-methyl-9-azabicyclo[3.3.1]nonan-3-ol
(16.47 mg, 0.106 mmol) in DMF (Volume: 442 .mu.l) at RT and the
resulting mixture was heated at 60.degree. C. for 1 h. The
resulting alkoxide solution was added to the imidazolide solution
and the mixture was heated at 70.degree. C. for 2 h. The mixture
was diluted with DMF, filtered and purified by HPLC to afford the
title compound as a colorless film. MS (ESI, pos. ion) m/z: 364.3
(M+1).
[0235] Compounds 16, 57, 91, 103, 17, 60, 116 and 89 in Table 1
above were synthesized by utilizing a similar procedure as
described in Example 10 above unless indicated otherwise below:
Compound 16 (Similar conditions as described in Example 2 above
were utilized for Step 3); Compound 57 (Similar conditions as
described in Example 2 above were utilized for Step 3); Compound 91
(Similar conditions as described in Example 3 above were utilized
for Step 3); Compound 103 (Similar conditions as described in
Example 3 above were utilized for Step 3); Compound 17 (Similar
conditions as described in Example 2 above were utilized for Step
3); Compound 60 (Similar conditions as described in Example 3 above
were utilized for Step 3); and Compound 89 (Similar conditions as
described in Example 3 above were utilized for Step 3).
Example 11
Synthesis of
1-(2,2-difluoroethyl)-N-((1R,5S,7S)-9-methyl-3-oxa-9-azabicyclo[3.3.1]non-
an-7-yl)-1H-pyrrolo[2,3-b]pyridine-3-carboxamide
2,2,2-trifluoroacetate
##STR00365##
[0236] Step 1 and 2:
1-(2,2-Difluoroethyl)-1H-pyrrolo[2,3-b]pyridine-3-carboxylic
acid
[0237] The title compound was synthesized by utilizing similar
conditions as described in Example 10, Steps 1 and 2.
Step 3:
1-(2,2-Difluoroethyl)-N-((1R,5S,7S)-9-methyl-3-oxa-9-azabicyclo[3.-
3.1]nonan-7-yl)-1H-pyrrolo[2,3-b]pyridine-3-carboxamide
2,2,2-trifluoroacetate
[0238] Similar conditions as described in Example 7 were utilized
to afford the title compound as a colorless oil. MS (ESI, pos. ion)
m/z: 365.3 (M+1)
[0239] Following compounds in Table 1 above were synthesized by
utilizing a similar procedure as described in Example 11: Compounds
5, 9, 21, 22, 52, 53, 63, 67, 68, 70, 76, 77, 79, 80, 81, 102, 104
(Reference 3 for amine synthesis), 108, 109 (Reference 2 for amine
synthesis), 112, 113, 126 & 127 (Reference 2 for amine
synthesis).
Example 12
Synthesis of (1R,5S,7S)-3-oxa-9-azabicyclo[3.3.1]nonan-7-yl
1-(2,2-difluoroethyl)-1H-pyrrolo[2,3-b]pyridine-3-carboxylate
2,2,2-trifluoroacetate
##STR00366##
[0240] Step 1: (1R,5S,7S)-tert-Butyl
7-((1-(2,2-difluoroethyl)-1H-pyrrolo[2,3-b]pyridine-3-carbonyl)oxy)-3-oxa-
-9-azabicyclo[3.3.1]nonane-9-carboxylate
[0241] The title compound was synthesized by utilizing a similar
procedure as described in Example 10 above,
Step 2: (1R,5S,7S)-3-Oxa-9-azabicyclo[3.3.1]nonan-7-yl
1-(2,2-difluoroethyl)-1H-pyrrolo[2,3-b]pyridine-3-carboxylate
2,2,2-trifluoroacetate
[0242] TFA (325 .mu.l) was added to a solution of
(1R,5S,7S)-tert-butyl
7-((1-(2,2-difluoroethyl)-1H-pyrrolo[2,3-b]pyridine-3-carbonyl)oxy)-3-oxa-
-9-azabicyclo[3.3.1]nonane-9-carboxylate (58.6 mg, 0.130 mmol) in
DCM (325 .mu.l) at RT. After 10 min, the reaction mixture was
diluted with DMF, filtered and purified by HPLC to afford the title
compound as a white solid. MS (ESI, pos. ion) m/z: 352.2 (M+1)
Example 13
Synthesis of (1R,5S,7S)-3-Oxa-9-azabicyclo[3.3.1]nonan-7-yl
1-(2,2-difluoroethyl)-5-fluoro-1H-indole-3-carboxylate
2,2,2-trifluoroacetic acid
##STR00367##
[0243] Steps 1 and 2:
1-(2,2-Difluoroethyl)-5-fluoro-1H-indole-3-carboxylic acid
[0244] The title compound was synthesized by utilizing similar
conditions as described in Example 10, Step 1 and 2.
Step 3: (1R,5S,7S)-3-Oxa-9-azabicyclo[3.3.1]nonan-7-yl
1-(2,2-difluoroethyl)-5-fluoro-1H-indole-3-carboxylate
2,2,2-trifluoroacetic acid
[0245] In a vial containing
1-(2,2-difluoroethyl)-5-fluoro-1H-indole-3-carboxylic acid (100 mg,
0.411 mmol) and trifluoroacetic anhydride (58.1 .mu.l, 0.411 mmol)
in toluene (1371 .mu.l) was added TFA (343 .mu.l). The reaction
mixture was stirred at RT for 30 min then (1R,5S,7S)-tert-butyl
7-hydroxy-3-oxa-9-azabicyclo[3.3.1]nonane-9-carboxylate (83 mg,
0.343 mmol; see Reference 1 for the synthesis) was added and
stirring continued for 2 h. Direct HPLC purification (after
dilution with DMF and filtration) gave the title compound as a
white solid. MS (ESI, pos. ion) m/z: 369.2 (M+1).
[0246] Following compounds in Table 1 above were synthesized by
utilizing a similar procedure as described in Example 13 above
Compounds 11, 23, 25, 54, 59, and 128 using acid synthesized by the
procedure indicated below:
Example 54 (See Reference 11 for the carboxylic acid synthesis)
Example 11 (See Reference 5 for the carboxylic acid synthesis)
Example 23 (See Reference 6 for the carboxylic acid synthesis)
Example 25 (See Reference 6 for the carboxylic acid synthesis)
Example 128 (See Reference 7 for the carboxylic acid
synthesis).
Example 14
Synthesis of
(1R,5S,7S)-9-methyl-3-oxa-9-azabicyclo[3.3.1]nonan-7-yl
1-(2,2-difluoroethyl)-1H-pyrrolo[2,3-b]pyridine-3-carboxylate
2,2,2-trifluoroacetate
##STR00368##
[0247] Steps 1 and 2:
(1R,5S,7S)-3-Oxa-9-azabicyclo[3.3.1]nonan-7-yl
1-(2,2-difluoroethyl)-1H-pyrrolo[2,3-b]pyridine-3-carboxylate
[0248] The title compound was synthesized by utilizing similar
conditions as described in Example 12 above.
Step 3: (1R,5S,7S)-9-Methyl-3-oxa-9-azabicyclo[3.3.1]nonan-7-yl
1-(2,2-difluoroethyl)-1H-pyrrolo[2,3-b]pyridine-3-carboxylate
2,2,2-trifluoroacetate
[0249] Sodium triacetoxyborohydride (11.44 mg, 0.054 mmol) was
added to a solution of
(1R,5S,7S)-3-oxa-9-azabicyclo[3.3.1]nonan-7-yl
1-(2,2-difluoroethyl)-1H-pyrrolo[2,3-b]pyridine-3-carboxylate
(15.81 mg, 0.045 mmol) and formaldehyde (4.91 mg, 0.054 mmol) in
DCM (225 .mu.l) at RT. After 15 min, the reaction mixture was
diluted with DMF, filtered and purified by HPLC to afford the title
compound as a colorless film. MS (ESI, pos. ion) m/z: 366.2
(M+1).
[0250] Compounds 32, 49, and 58 in Table 1 above were synthesized
by utilizing a similar procedure as described in Example 14
above.
Example 15
Synthesis of
(1R,5S,7S)-9-(2-fluoroethyl)-3-oxa-9-azabicyclo[3.3.1]nonan-7-yl
1-(2,2-difluoroethyl)-5-fluoro-1H-indole-3-carboxylate,
2,2,2-trifluoroacetic acid
##STR00369##
[0251] Step 1: (1R,5S,7S)-3-Oxa-9-azabicyclo[3.3.1]nonan-7-yl
1-(2,2-difluoroethyl)-5-fluoro-1H-indole-3-carboxylate
2,2,2-trifluoroacetic acid
[0252] The title compound was synthesized by utilizing similar
procedure as described in Example 13 above.
Step 2:
(1R,5S,7S)-9-(2-Fluoroethyl)-3-oxa-9-azabicyclo[3.3.1]nonan-7-yl
1-(2,2-difluoroethyl)-5-fluoro-1H-indole-3-carboxylate,
2,2,2-trifluoroacetic acid
[0253] A solution of (1R,5S,7S)-3-oxa-9-azabicyclo[3.3.1]nonan-7-yl
1-(2,2-difluoroethyl)-5-fluoro-1H-indole-3-carboxylate
2,2,2-trifluoroacetate (20 mg, 0.041 mmol), triethylamine (28.9
.mu.l, 0.207 mmol), and 1-bromo-2-fluoroethane (9.29 .mu.l, 0.124
mmol) in MeCN (415 .mu.l) was heated to 100.degree. C. for 2 days.
HPLC purification (after dilution with DMF and filtration) gave the
title compound as a white solid. MS (ESI, pos. ion) m/z: 415.2
(M+1)
[0254] Compound 50 in Table 1 above was synthesized by utilizing a
similar procedure as described in Example 15 above.
Example 16
Synthesis of
N-((1R,5S,7S)-3-oxa-9-azabicyclo[3.3.1]nonan-7-yl)-5-fluoro-1-(2,2,2-trif-
luoroethyl)-1H-indole-3-carboxamide 2,2,2-trifluoroacetic acid
##STR00370##
[0255] Step 1: (1R,5S,7S)-tert-Butyl
7-(5-fluoro-1-(2,2,2-trifluoroethyl)-1H-indole-3-carboxamido)-3-oxa-9-aza-
bicyclo[3.3.1]nonane-9-carboxylate
[0256] The title compound was synthesized by a similar procedure as
described in Example 11 above.
Step 2:
N-((1R,5S,7S)-3-Oxa-9-azabicyclo[3.3.1]nonan-7-yl)-5-fluoro-1-(2,2-
,2-trifluoroethyl)-1H-indole-3-carboxamide, 2,2,2-trifluoroacetic
acid salt
[0257] Similar conditions as described in Example 12, Step 2 were
utilized to afford the title compound as a clear oil. MS (ESI, pos.
ion) m/z: 386.2 (M+1).
[0258] Following compounds in Table 1 above were synthesized by
utilizing a similar procedure as described in Example 16 above:
Compounds 39, 38, 65 (Step 1 used from Example 8 above), 78 (see
Reference 10 for carboxylic acid synthesis), 82, 105, and 185.
Example 17
Synthesis of
N-((1R,5S,7S)-3-oxa-9-azabicyclo[3.3.1]nonan-7-yl)-5-fluoro-1-(2,2,2-trif-
luoroethyl)-1H-indole-3-carboxamide 2,2,2-trifluoroacetate
##STR00371##
[0259] Step 1 and 2:
N-((1R,5S,7S)-3-Oxa-9-azabicyclo[3.3.1]nonan-7-yl)-5-fluoro-1-(2,2,2-trif-
luoroethyl)-1H-indole-3-carboxamide 2,2,2-trifluoroacetate
[0260] The title compound was synthesized by utilizing similar
conditions as described in Example 16 above.
Step 3:
N-((1R,5S,7S)-3-Oxa-9-azabicyclo[3.3.1]nonan-7-yl)-5-fluoro-1-(2,2-
,2-trifluoroethyl)-1H-indole-3-carboxamide
2,2,2-trifluoroacetate
[0261] Similar conditions as described in Example 14, Step 3 were
utilized to afford the title compound as a clear film. MS (ESI,
pos. ion) m/z: 400.25 (M+1)
[0262] Compounds 129 and 186 in Table 1 above was synthesized by
utilizing a similar procedure as described in Example 17 above.
Carboxylic acid was synthesized using method in Reference 6
above)
Example 18
Synthesis of
5-fluoro-N-((1R,5S,7S)-9-methyl-d.sub.3-3-oxa-9-azabicyclo[3.3.1]nonan-7--
yl)-1-(2,2,2-trifluoroethyl)-1H-pyrrolo[2,3-b]pyridine-3-carboxamide
2,2,2-trifluoroacetate
##STR00372##
[0263] Steps 1 and 2:
N-((1R,5S,7S)-3-Oxa-9-azabicyclo[3.3.1]nonan-7-yl)-5-fluoro-1-(2,2,2-trif-
luoroethyl)-1H-pyrrolo[2,3-b]pyridine-3-carboxamide
2,2,2-trifluoroacetate
[0264] The title compound was synthesized by utilizing similar
conditions as described in Example 16 above.
Step 3:
5-Fluoro-N-((1R,5S,7S)-9-methyl-d.sub.3-3-oxa-9-azabicyclo[3.3.1]n-
onan-7-yl)-1-(2,2,2-trifluoroethyl)-1H-pyrrolo[2,3-b]pyridine-3-carboxamid-
e 2,2,2-trifluoroacetate
[0265] A mixture of
N-((1R,5S,7S)-3-oxa-9-azabicyclo[3.3.1]nonan-7-yl)-5-fluoro-1-(2,2,2-trif-
luoroethyl)-1H-pyrrolo[2,3-b]pyridine-3-carboxamide
2,2,2-trifluoroacetate (16.2 mg, 0.032 mmol),
methyl-d.sub.3-4-methylbenzenesulfonate (12.25 mg, 0.065 mmol) and
K.sub.2CO.sub.3 (13.42 mg, 0.097 mmol) in MeCN (324 .mu.l) was
heated at 80.degree. C. for 10 min and purified by HPLC (after
dilution with DMF and filtration). Neutralization with
K.sub.2CO.sub.3 and prep-TLC (DCM/MeOH) afforded the title compound
as a colorless film. MS (ESI, pos. ion) m/z: 404.2 (M+1)
[0266] Compound 130 in Table 1 above were synthesized by utilizing
a similar procedure as described in Example 18 above.
Example 19
Synthesis of (1R,3R,5S)-8-methyl-8-azabicyclo[3.2.1]octan-3-yl
3,4-dihydro-2H-[1,3]oxazino[3,2-a]indole-10-carboxylate
2,2,2-trifluoroacetate
##STR00373##
[0267] Step 1: (1R,3R,5S)-8-Methyl-8-azabicyclo[3.2.1]octan-3-yl
2-(3-bromopropoxy)-1H-indole-3-carboxylate
[0268] NCS (35.2 mg, 0.264 mmol) was added to a suspension of
(1R,3R,5S)-8-methyl-8-azabicyclo[3.2.1]octan-3-yl
1H-indole-3-carboxylate (50 mg, 0.176 mmol) and 4 {acute over
(.ANG.)} MS (100 mg) in chloroform (879 .mu.l) at RT. After 30 min,
3-bromopropan-1-ol (48.9 mg, 0.352 mmol) was added to the solution.
After being stirred at RT for 14 h, the reaction mixture was
filtered through a pad of Celite. The filtrate was washed with
brine, dried over anhydrous Na.sub.2SO.sub.4, filtered and
concentrated under reduced pressure to afford the title compound,
which was used without further purification.
Step 2: (1R,3R,5S)-8-Methyl-8-azabicyclo[3.2.1]octan-3-yl
3,4-dihydro-2H-[1,3]oxazino[3,2-a]indole-10-carboxylate
2,2,2-trifluoroacetate
[0269] (1R,3R,5S)-8-Methyl-8-azabicyclo[3.2.1]octan-3-yl
2-(3-bromopropoxy)-1H-indole-3-carboxylate (74.2 mg, 0.176 mmol)
and K.sub.2CO.sub.3 (73.0 mg, 0.528 mmol) were suspended in acetone
(1760 .mu.l) at RT. After being stirred for 24 h, the reaction
mixture was diluted with DMF, filtered and purified by HPLC to
afford the title compound as colorless film. MS (ESI, pos. ion)
m/z: 341.3 (M+1)
[0270] Compounds 28 and 84 in Table 1 above were synthesized by
utilizing a similar procedure as described in Example 19 above.
Example 20
Synthesis of
(1R,5S,7S)-9-methyl-3-oxa-9-azabicyclo[3.3.1]nonan-7-yl
1-(2-fluoroethyl)-1H-indole-3-carboxylate 2,2,2-trifluoroacetic
acid
##STR00374##
[0271] Steps 1, 2 and 3:
(1R,5S,7S)-9-Methyl-3-oxa-9-azabicyclo[3.3.1]nonan-7-yl
1H-indole-3-carboxylate
[0272] The title compound was synthesized by utilizing a similar
procedure as described in Example 14 above. Similar conditions as
described in Example 1 above were utilized for Step 1.
Step 4: (1R,5S,7S)-9-Methyl-3-oxa-9-azabicyclo[3.3.1]nonan-7-yl
1-(2-fluoroethyl)-1H-indole-3-carboxylate 2,2,2-trifluoroacetic
acid
[0273] Sodium hydride (11.98 mg, 0.300 mmol, 60% dispersion in
mineral oil) was added to a solution of
(1R,5S,7S)-9-methyl-3-oxa-9-azabicyclo[3.3.1]nonan-7-yl
1H-indole-3-carboxylate (60 mg, 0.200 mmol) in DMF (600 .mu.l) at
RT. After 15 min, 1-bromo-2-fluoroethane (22.38 .mu.l, 0.300 mmol)
was added and the reaction was stirred for a further 1 h. Direct
HPLC purification (after dilution with DMF and filtration) gave the
title compound as a clear oil. MS (ESI, pos. ion) m/z: 347.3
(M+1).
Example 21
Synthesis of
(1R,5S,7S)-9-methyl-3-oxa-9-azabicyclo[3.3.1]nonan-7-yl
1-(methylsulfonyl)-1H-indole-3-carboxylate 2,2,2-trifluoroacetic
acid
##STR00375##
[0274] Steps 1, 2 and 3:
(1R,5S,7S)-9-Methyl-3-oxa-9-azabicyclo[3.3.1]nonan-7-yl
1H-indole-3-carboxylate 2,2,2-trifluoroacetate
[0275] The title compound was synthesized by utilizing a similar
procedure as described in Example 14 above. Similar conditions as
described in Example 1 above were utilized for Step 1.
Step 4: (1R,5S,7S)-9-Methyl-3-oxa-9-azabicyclo[3.3.1]nonan-7-yl
1-(methylsulfonyl)-1H-indole-3-carboxylate 2,2,2-trifluoroacetic
acid
[0276] Similar conditions as described in Example 6, Step 2 were
utilized to afford the title compound as a colorless oil. MS (ESI,
pos. ion) m/z: 379.15 (M+1).
Example 22
Synthesis of
(1R,5S,7S)-3-oxa-9-azabicyclo[3.3.1]nonan-7-yl1-(isopropylsulfonyl)-1H-in-
dole-3-carboxylate 2,2,2-trifluoroacetate
##STR00376##
[0277] Step 1: (1R,5S,7S)-3-Oxa-9-azabicyclo[3.3.1]nonan-7-yl
1H-indole-3-carboxylate 2,2,2-trifluoroacetate
[0278] The title compound was synthesized by utilizing similar
conditions as described in Example 13, Step 3.
Step 2: (1R,5S,7S)-tert-Butyl
7-((1H-indole-3-carbonyl)oxy)-3-oxa-9-azabicyclo[3.3.1]-nonane-9-carboxyl-
ate
[0279] Di-tert-butyl dicarbonate (168 .mu.l, 0.731 mmol) was added
to a solution of (1R,5S,7S)-3-oxa-9-azabicyclo[3.3.1]nonan-7-yl
1H-indole-3-carboxylate 2,2,2-trifluoroacetate (278.6 mg, 0.696
mmol) and N,N-diisopropylethylamine (182 .mu.l, 1.044 mmol) in THF
(Volume: 3479 .mu.l) at RT. After 30 min, the mixture was
concentrated under reduced pressure, taken up in EtOAc, washed with
saturated aqueous NH.sub.4Cl and brine. The combined organic layers
were dried over anhydrous Na.sub.2SO.sub.4, filtered and
concentrated under reduced pressure to afford the title compound as
a white foam.
Step 3: (1R,5S,7S)-3-Oxa-9-azabicyclo[3.3.1]nonan-7-yl
1-(isopropylsulfonyl)-1H-indole-3-carboxylate
2,2,2-trifluoroacetate
[0280] In a round-bottom flask containing (1R,5S,7S)-tert-butyl
7-((1H-indole-3-carbonyl)oxy)-3-oxa-9-azabicyclo[3.3.1]nonane-9-carboxyla-
te (304 mg, 0.787 mmol) in THF (Volume: 7867 .mu.l) in a water bath
was added sodium hydride (60% in mineral oil, 47.2 mg, 1.180 mmol)
and the white mixture was stirred for 20 min. Propane-2-sulfonyl
chloride (177 .mu.l, 1.573 mmol) was then added slowly and the
solution became clear. After 30 min, HCl (4.0 M in dioxane, 9833
.mu.l, 39.3 mmol) was then added and the mixture was heated to
50.degree. C. for 30 min. Concentration and HPLC purification
(after dilution with DMF and filtration) gave the title compound as
a clear oil. MS (ESI, pos. ion) m/z: 393.2 (M+1).
[0281] Compounds 19, 132, 133, 134, and 135 in Table 1 above were
synthesized by utilizing a similar procedure as described in
Example 22 above.
Example 24
Synthesis of (1R,5S,7s)-3-oxa-9-azabicyclo[3.3.1]nonan-7-yl
1-(pyridazin-3-yl)-1H-indole-3-carboxylate, 2,2,2-trifluoroacetic
acid salt
##STR00377##
[0283] To a solution of (1R,5S,7s)-tert-butyl
7-((1H-indole-3-carbonyl)oxy)-3-oxa-9-azabicyclo[3.3.1]nonane-9-carboxyla-
te (20 mg, 0.052 mmol) in NMP (104 .mu.l) was added cesium
carbonate (67.5 mg, 0.207 mmol) and 3-chloropyridazine (17.78 mg,
0.155 mmol). The mixture was heated at 110.degree. C. for 3 h.
Purification by HPLC gave the title compound as a tan solid. MS
(ESI, pos. ion) m/z: 365.20 (M+1).
Example 25
Synthesis of
(1R,5S,7s)-9-methyl-3-oxa-9-azabicyclo[3.3.1]nonan-7-yl
1-(6-fluoropyridazin-3-yl)-1H-indole-3-carboxylate
##STR00378##
[0285] To a solution of
(1R,5S,7s)-9-methyl-3-oxa-9-azabicyclo[3.3.1]nonan-7-yl
1H-indole-3-carboxylate (10 mg, 0.033 mmol) in THF (333 .mu.l) was
added NaH (1.332 mg, 0.033 mmol, 60% suspension in mineral oil) and
3,6-difluoropyridazine (5.80 mg, 0.050 mmol). The mixture was
stirred at RT for 1 h then purified by ISCO (0-20% MeOH/DCM) to
give the title compound as a white solid. MS (ESI, pos. ion) m/z:
397.20 (M+1).
Example 26
Synthesis of
N-((1R,5S,7s)-9-methyl-3-oxa-9-azabicyclo[3.3.1]nonan-7-yl)-1-phenyl-1H-i-
ndole-3-carboxamide, 2,2,2-trifluoroacetic acid salt
##STR00379##
[0287] A 5 mL screwtop vial containing
1-phenyl-1H-indole-3-carboxylic acid (20 mg, 0.084 mmol), HATU
(32.1 mg, 0.084 mmol), and N-ethyl-N-isopropylpropan-2-amine (58.9
IA, 0.337 mmol) in DMF (421 .mu.l) was stirred for 10 min then
(1R,5S,7s)-9-methyl-3-oxa-9-azabicyclo[3.3.1]nonan-7-amine
2,2,2-trifluoroacetate (22.78 mg, 0.084 mmol) was added and stirred
for 1 h. Direct HPLC purification afforded the title compound as a
white foam. MS (ESI, pos. ion) m/z: 376.25 (M+1).
[0288] The following compounds were prepared by a similar
procedure, either with commercially available carboxylic acids or
those synthesized according to reference compound procedures:
1-(1-methyl-1H-imidazol-5-yl)-N-((1R,5S,7s)-9-methyl-3-oxa-9-azabicyclo[3-
.3.1]nonan-7-yl)-1H-indole-3-carboxamide, 2,2,2-trifluoroacetic
acid salt;
1-(cyanomethyl)-N-((1R,5S,7s)-9-methyl-3-oxa-9-azabicyclo[3.3.1]nonan-7-y-
l)-1H-indole-3-carboxamide, 2,2,2-trifluoroacetic acid salt;
N-((1R,5S,7s)-9-methyl-3-oxa-9-azabicyclo[3.3.1]nonan-7-yl)-1-(thiazol-2--
yl)-1H-pyrrolo[2,3-b]pyridine-3-carboxamide, 2,2,2-trifluoroacetic
acid salt;
N-((1R,5S,7s)-9-methyl-3-oxa-9-azabicyclo[3.3.1]nonan-7-yl)-1-(thia-
zol-4-yl)-1H-pyrrolo[2,3-b]pyridine-3-carboxamide,
2,2,2-trifluoroacetic acid salt;
N-((1R,5S,7s)-9-methyl-3-oxa-9-azabicyclo[3.3.1]nonan-7-yl)-1-(thiazol-5--
yl)-1H-pyrrolo[2,3-b]pyridine-3-carboxamide, 2,2,2-trifluoroacetic
acid salt;
5-fluoro-N-((1R,5S,7s)-9-methyl-3-oxa-9-azabicyclo[3.3.1]nonan-7-yl-
)-1-(thiazol-2-yl)-1H-pyrrolo[2,3-b]pyridine-3-carboxamide,
2,2,2-trifluoroacetic acid salt;
5-fluoro-N-((1R,5S,7s)-9-methyl-3-oxa-9-azabicyclo[3.3.1]nonan-7-yl)-1-(t-
hiazol-4-yl)-1H-pyrrolo[2,3-b]pyridine-3-carboxamide,
2,2,2-trifluoroacetic acid salt;
5-fluoro-N-((1R,5S,7s)-9-methyl-3-oxa-9-azabicyclo[3.3.1]nonan-7-yl)-1-(t-
hiazol-5-yl)-1H-pyrrolo[2,3-b]pyridine-3-carboxamide,
2,2,2-trifluoroacetic acid salt;
N-((1R,5S,7s)-9-methyl-3-oxa-9-azabicyclo[3.3.1]nonan-7-yl)-1-(thiazol-5--
yl)-1H-indazole-3-carboxamide, 2,2,2-trifluoroacetic acid salt;
1-(isothiazol-4-yl)-N-((1R,5S,7s)-9-methyl-3-oxa-9-azabicyclo[3.3.1]nonan-
-7-yl)-1H-indole-3-carboxamide, 2,2,2-trifluoroacetic acid salt;
1-(isothiazol-3-yl)-N-((1R,5S,7s)-9-methyl-3-oxa-9-azabicyclo[3.3.1]nonan-
-7-yl)-1H-indole-3-carboxamide, 2,2,2-trifluoroacetic acid salt;
1-(isothiazol-5-yl)-N-((1R,5S,7s)-9-methyl-3-oxa-9-azabicyclo[3.3.1]nonan-
-7-yl)-1H-indole-3-carboxamide, 2,2,2-trifluoroacetic acid salt;
N-((1R,5S,7s)-9-methyl-3-oxa-9-azabicyclo[3.3.1]nonan-7-yl)-1-(oxazol-2-y-
l)-1H-indole-3-carboxamide, 2,2,2-trifluoroacetic acid salt;
N-((1R,5S,7S)-9-methyl-3-oxa-9-azabicyclo[3.3.1]nonan-7-yl)-1-(pyridazin--
4-yl)-1H-indole-3-carboxamide;
N-((1R,5S,7S)-9-methyl-3-oxa-9-azabicyclo[3.3.1]nonan-7-yl)-1-(pyridazin--
4-yl)-1H-indole-3-carboxamide; and
(1R,5S,7S)-9-methyl-3-oxa-9-azabicyclo[3.3.1]nonan-7-yl
1-(pyrimidin-2-yl)-1H-indole-3-carboxylate.
Example 27
Synthesis of (1R,5S,7s)-3-oxa-9-azabicyclo[3.3.1]nonan-7-yl
1-(pyrazin-2-yl)-1H-indole-3-carboxylate, 2,2,2-trifluoroacetic
acid salt
##STR00380##
[0289] Step 1: (1R,5S,7s)-tert-butyl
7-((1-(pyrazin-2-yl)-1H-indole-3-carbonyl)oxy)-3-oxa-9-azabicyclo[3.3.1]n-
onane-9-carboxylate
[0290] A solution of (1R,5S,7s)-tert-butyl
7-((1H-indole-3-carbonyl)oxy)-3-oxa-9-azabicyclo[3.3.1]nonane-9-carboxyla-
te (36 mg, 0.093 mmol) in DMF (466 .mu.l) was treated with sodium
hydride (4.10 mg, 0.102 mmol, 60% suspension in mineral oil) at RT
and the solution was stirred for 30 min. 2-fluoropyrazine (8.29
.mu.l, 0.102 mmol) was then added, the vial capped and the
resulting reaction mixture stirred at 90.degree. C. for 4 h. The
reaction mixture was quenched with a few drops of methanol,
followed by ISCO purification (20% EtOAc/hexanes) to afford the
title compound as a white solid.
Step 2:
(1R,5S,7s)-3-oxa-9-azabicyclo[3.3.1]nonan-7-yl1-(pyrazin-2-yl)-1H--
indole-3-carboxylate, 2,2,2-trifluoroacetic acid salt
[0291] A solution of (1R,5S,7s)-tert-butyl
7-((1-(pyrazin-2-yl)-1H-indole-3-carbonyl)oxy)-3-oxa-9-azabicyclo[3.3.1]n-
onane-9-carboxylate (30 mg, 0.065 mmol) in DCM (646 .mu.l) was
treated with TFA (74.6 .mu.l, 0.969 mmol) dropwise at RT and the
resulting reaction mixture was stirred for 3 h. ISCO purification
(5% MeOH/DCM) afforded the title compound as a white solid. MS
(ESI, pos. ion) m/z: 365.20 (M+1).
[0292] The following compound was prepared by a similar procedure:
(1R,5S,7S)-3-oxa-9-azabicyclo[3.3.1]nonan-7-yl
1-(cyanomethyl)-1H-indole-3-carboxylate.
Example 28
Synthesis of (1R,5S,7s)-3-oxa-9-azabicyclo[3.3.1]nonan-7-yl
1-(2-cyanophenyl)-1H-indole-3-carboxylate, 2,2,2-trifluoroacetic
acid salt
##STR00381##
[0293] Step 1: (1R,5S,7s)-tert-butyl
7-((1-(2-cyanophenyl)-1H-indole-3-carbonyl)oxy)-3-oxa-9-azabicyclo[3.3.1]-
nonane-9-carboxylate
[0294] A solution of (1R,5S,7s)-tert-butyl
7-((1H-indole-3-carbonyl)oxy)-3-oxa-9-azabicyclo[3.3.1]nonane-9-carboxyla-
te (30 mg, 0.078 mmol) and 2-bromobenzonitrile (15.54 mg, 0.085
mmol) in toluene (155 .mu.l) was treated with
(1R,2R)--N1,N2-dimethylcyclohexane-1,2-diamine (2.53 .mu.l, 0.016
mmol), potassium phosphate (36.3 mg, 0.171 mmol) and copper(I)
iodide (4.44 mg, 0.023 mmol) and the resulting reaction mixture
stirred at 110.degree. C. for 12 h. HPLC purification afforded the
title compound as an orange solid.
Step 2: (1R,5S,7s)-3-oxa-9-azabicyclo[3.3.1]nonan-7-yl
1-(2-cyanophenyl)-1H-indole-3-carboxylate, 2,2,2-trifluoroacetic
acid salt
[0295] A solution of (1R,5S,7s)-tert-butyl
7-((1-(2-cyanophenyl)-1H-indole-3-carbonyl)oxy)-3-oxa-9-azabicyclo[3.3.1]-
nonane-9-carboxylate 2,2,2-trifluoroacetate (14 mg, 0.023 mmol) in
DCM (233 .mu.l) was treated with TFA (17.93 .mu.l, 0.233 mmol) at
RT and the resulting reaction mixture stirred for 1 h. ISCO
purification (10% MeOH/DCM) afforded the title compound as a white
solid. MS (ESI, pos. ion) m/z: 388.20 (M+1).
[0296] The following compounds were prepared by a similar
procedure, where Boc group was removed either with TFA or HCl:
(1R,5S,7s)-3-oxa-9-azabicyclo[3.3.1]nonan-7-yl
1-(3-cyanophenyl)-1H-indole-3-carboxylate, 2,2,2-trifluoroacetic
acid salt; (1R,5S,7s)-3-oxa-9-azabicyclo[3.3.1]nonan-7-yl
1-(4-cyanophenyl)-1H-indole-3-carboxylate, 2,2,2-trifluoroacetic
acid salt; (1R,5S,7s)-3-oxa-9-azabicyclo[3.3.1]nonan-7-yl
1-(isothiazol-4-yl)-1H-indole-3-carboxylate, 2,2,2-trifluoroacetic
acid salt; (1R,5S,7s)-3-oxa-9-azabicyclo[3.3.1]nonan-7-yl
1-(isothiazol-3-yl)-1H-indole-3-carboxylate, 2,2,2-trifluoroacetic
acid salt; (1R,5S,7s)-3-oxa-9-azabicyclo[3.3.1]nonan-7-yl
1-(isothiazol-5-yl)-1H-indole-3-carboxylate, 2,2,2-trifluoroacetic
acid salt; (1R,5S,7s)-3-oxa-9-azabicyclo[3.3.1]nonan-7-yl;
(1R,5S,7s)-3-oxa-9-azabicyclo[3.3.1]nonan-7-yl
1-(1-methyl-2-oxo-1,2-dihydropyridin-4-yl)-1H-indole-3-carboxylate,
2,2,2-trifluoroacetic acid salt; and
(1R,5S,7s)-3-oxa-9-azabicyclo[3.3.1]nonan-7-yl
1-(oxazol-2-yl)-1H-indole-3-carboxylate, 2,2,2-trifluoroacetic acid
salt.
Example 29
Synthesis of
(1R,5S,7s)-9-methyl-3-oxa-9-azabicyclo[3.3.1]nonan-7-yl
1-(cyanomethyl)-7-fluoro-1H-pyrrolo[2,3-c]pyridine-3-carboxylate,
2,2,2-trifluoroacetic acid salt
##STR00382##
[0297] Step 1:
(1R,5S,7s)-9-methyl-3-oxa-9-azabicyclo[3.3.1]nonan-7-yl
7-fluoro-1H-pyrrolo[2,3-c]pyridine-3-carboxylate
[0298] Di(1H-imidazol-1-yl)methanone (113 mg, 0.696 mmol) was added
to a solution of 7-fluoro-1H-pyrrolo[2,3-c]pyridine-3-carboxylic
acid (104.5 mg, 0.580 mmol) in DMF (1160 .mu.l) at RT. After 1 h,
(1R,5S,7s)-9-methyl-3-oxa-9-azabicyclo[3.3.1]nonan-7-ol (182 mg,
1.160 mmol) was added to the mixture and the resulting brown
solution was heated at 100.degree. C. for 3 days. The reaction
mixture was then directly purified by HPLC, followed by
neutralization (with NaHCO.sub.3) and prep-TLC (DCM/MeOH) to afford
the title compound as a white solid.
Step 2: (1R,5S,7s)-9-methyl-3-oxa-9-azabicyclo[3.3.1]nonan-7-yl
1-(cyanomethyl)-7-fluoro-1H-pyrrolo[2,3-c]pyridine-3-carboxylate,
2,2,2-trifluoroacetic acid salt
[0299] Sodium hydride (20.19 mg, 0.505 mmol, 60% suspension in
mineral oil) was added to a solution of
(1R,5S,7s)-9-methyl-3-oxa-9-azabicyclo[3.3.1]nonan-7-yl
7-fluoro-1H-pyrrolo[2,3-c]pyridine-3-carboxylate
2,2,2-trifluoroacetate (109.4 mg, 0.252 mmol) in DMF (841 .mu.l) at
RT. After 10 min, 2-bromoacetonitrile (17.58 .mu.l, 0.252 mmol) was
added to the mixture at RT. After 30 min, the mixture was directly
purified by HPLC to afford the title compound as a white solid. MS
(ESI, pos. ion) m/z: 359.15 (M+1).
Example 30
Synthesis of
(1R,5S,7s)-9-methyl-3-oxa-9-azabicyclo[3.3.1]nonan-7-yl
5-cyano-1-(2-fluoroethyl)-1H-indole-3-carboxylate,
2,2,2-trifluoroacetic acid salt
##STR00383##
[0300] Step 1:
(1R,5S,7s)-9-methyl-3-oxa-9-azabicyclo[3.3.1]nonan-7-yl5-cyano-1H-indole--
3-carboxylate, 2,2,2-trifluoroacetic acid salt
[0301] 2,2,2-Trifluoroacetic anhydride (64.5 .mu.l, 0.457 mmol) was
added to a solution of 5-cyano-1H-indole-3-carboxylic acid (85 mg,
0.457 mmol) in toluene (1660 .mu.l) and TFA (415 .mu.l) at RT.
After 15 min,
(1R,5S,7s)-9-methyl-3-oxa-9-azabicyclo[3.3.1]nonan-7-ol (65.3 mg,
0.415 mmol) was added to the mixture. After 1 h, the mixture was
directly purified by HPLC to afford the title compound as a
colorless oil.
Step 2: (1R,5S,7s)-9-methyl-3-oxa-9-azabicyclo[3.3.1]nonan-7-yl
5-cyano-1-(2-fluoroethyl)-1H-indole-3-carboxylate,
2,2,2-trifluoroacetic acid salt
[0302] Sodium hydride (6.28 mg, 0.157 mmol, 60% suspension in
mineral oil) was added to a solution of
(1R,5S,7s)-9-methyl-3-oxa-9-azabicyclo[3.3.1]nonan-7-yl
5-cyano-1H-indole-3-carboxylate 2,2,2-trifluoroacetate (30 mg,
0.068 mmol) in DMF (341 .mu.l) at RT. After 10 min,
1-bromo-2-fluoroethane (11.27 mg, 0.089 mmol) was added to the
mixture at RT. After 30 min, the reaction mixture was directly
purified by HPLC to yield the title compound as a white solid. MS
(ESI, pos. ion) m/z: 359.15 (M+1).
[0303] The following compound was prepared by a similar procedure:
(1R,5S,7s)-9-methyl-3-oxa-9-azabicyclo[3.3.1]nonan-7-yl
5-cyano-1-(6-fluoropyridazin-3-yl)-1H-indole-3-carboxylate.
Example 32
Synthesis of
(1R,5S,7s)-9-methyl-3-oxa-9-azabicyclo[3.3.1]nonan-7-yl
1-(6-hydroxypyridazin-3-yl)-1H-indole-3-carboxylate,
2,2,2-trifluoroacetic acid salt
##STR00384##
[0305] Potassium trimethylsilanolate (5.83 mg, 0.045 mmol) was
added to a solution of
(1R,5S,7s)-9-methyl-3-oxa-9-azabicyclo[3.3.1]nonan-7-yl
1-(6-fluoropyridazin-3-yl)-1H-indole-3-carboxylate (18 mg, 0.045
mmol) in THF (227 .mu.l) at RT. After 1 h, 2M aq KOH (100 uL) was
added and the mixture was stirred at RT for 14 h. HPLC purification
yielded the title compound as a white solid. MS (ESI, pos. ion)
m/z: 395.20 (M+1).
Example 33
(1R,5S,7S)-9-methyl-3-oxa-9-azabicyclo[3.3.1]nonan-7-yl
1-(5-fluoropyrazin-2-yl)-1H-indole-3-carboxylate,
2,2,2-trifluoroacetic acid salt
##STR00385##
[0307] A solution of
(1R,5S,7S)-9-methyl-3-oxa-9-azabicyclo[3.3.1]nonan-7-yl
1-(5-chloropyrazin-2-yl)-1H-indole-3-carboxylate (10 mg, 0.024
mmol), 1,4,7,10,13,16-hexaoxacyclooctadecane (3.20 mg, 0.012 mmol)
and potassium fluoride (4.22 mg, 0.073 mmol) was heated at
120.degree. C. for 1 h. Direct HPLC purification gave the title
compound as a white solid. MS (ESI, pos. ion) m/z: 397.20
(M+1).
Example 34
Synthesis of
(1R,5S,7S)-9-methyl-3-oxa-9-azabicyclo[3.3.1]nonan-7-yl
1-(isothiazol-3-yl)-1H-indole-3-carboxylate, 2,2,2-trifluoroacetic
acid salt
##STR00386##
[0309] A solution of
(1R,5S,7S)-9-methyl-3-oxa-9-azabicyclo[3.3.1]nonan-7-yl
1H-indole-3-carboxylate (200 mg, 0.666 mmol) and 3-bromoisothiazole
(138 mg, 0.799 mmol) in toluene (Volume: 1332 .mu.l) was treated
with (1R,2R)--N1,N2-dimethylcyclohexane-1,2-diamine (32.6 .mu.l,
0.200 mmol), potassium phosphate (306 mg, 1.398 mmol) and copper(I)
iodide (38.0 mg, 0.200 mmol). The resulting reaction mixture was
stirred at 120.degree. C. overnight. HPLC purification afforded the
title compound as a tan solid. MS (ESI, pos. ion) m/z: 384.3
(M+1).
[0310] Compound 189 in Table 1 above was synthesized by utilizing a
similar procedure as described in Example 34 above.
BIOLOGICAL EXAMPLES
Biological Example 1
Inhibition of Ca Flux Activity of 5-HT3 In Vitro Assay
[0311] The 5-HT3 antagonist activity of the compounds of the
invention was determined by measuring the ability of the compounds
to inhibit the calcium flux activity of 3HT3a receptor expressed in
HEK-293T cells. HEK-293T cells were transfected with the 5-HT3a
expression construct using Xtreme Gene 9 (Roche) in 150 mm tissue
culture treated plates and incubated for 24 hours at 37.degree. C.
Cells were then split and plated at a density of 60K cells/well in
poly-lysine coated, black 96-well plates with clear bottoms (BD
BioSciences) and incubated overnight at 37.degree. C. Growth media
was removed and cells loaded with 200 uL calcium indicator dye in
HBSS containing 20 mM HEPES (Calcium 5 Assay kit, Molecular
Devices) and incubated at 37.degree. C. for 1 hour. While cells
were incubating, the 10.times. antagonist and agonist/antagonist
addition plates were made. For 10.times. antagonist plate: half log
serial dilutions (final concentrations range from 10.sup.-7 through
10.sup.-10 with the bottom well a negative, no ligand control) were
made from test compounds in DMSO at a 1000.times. concentration and
then diluted to 10.times. in HBSS/20 mM HEPES. For addition plate:
5HT was diluted to 100.times. in HBSS/20 mM HEPES (final
concentration in the assay--216 nM) and 15 uL was added to each
well of the addition plate, 15 uL of 10.times. compound was also
added to the addition plate, and finally 120 uL of HBSS/20 mM HEPES
(for a total of 150 uL). Cells were then removed from the incubator
and equilibrated to room temperature for 10 minutes, then 22.5 uL
of 10.times. test compounds were added in triplicate to the plates
and incubated at room temperature for 10 minutes (Tropisetron was
used as a positive control in every assay). Test plate and addition
plate were loaded into the FlexStation III (Molecular Devices), and
using the fluidics, 22.5 uL compound additions were made (at
t=.about.17 seconds), and fluorescence was measured for 90 seconds,
reading every 2.2 seconds. Data sets were analyzed as max minus min
using Software Max Pro (Molecular Devices). IC.sub.50 curves were
generated using non-linear regression in GraphPad Prism.
[0312] Approximate IC.sub.50 values of a representative number of
compounds of the invention this assay are provided in the Table 2
below.
TABLE-US-00002 TABLE 2 Cpd. No. Cpd. No. Cpd. No. from from from
Table I Table I Table I above IC50 [nM] above IC50 [nM] above IC50
[nM] 1 2.13 2 1.71 3 1.03 4 1.4 5 1.35 6 2.33 7 0.49 8 0.68 9 1.8
10 0.57 11 0.95 12 0.45 13 0.93 14 3.71 15 0.53 16 3.25 17 4.39 18
4.06 19 7.72 20 0.4 21 0.40 22 1.13 24 1.06 25 3.88 26 0.54 27 0.89
28 1.08 29 0.95 30 0.20 31 1.29 32 1.38 33 14.41 34 0.74 35 0.54 36
0.50 37 >1000 38 1.82 39 24.1 40 0.78 41 5.56 42 0.94 43 1.02 44
1.87 45 3.09 46 0.59 47 0.33 48 0.84 49 1.82 50 13.0 51 0.60 52
1.05 53 1.05 54 5.61 55 0.90 56 0.53 57 >1000 58 0.24 59 2.36 60
0.44 61 1.0 62 0.75 63 0.49 64 1.43 65 4.09 66 1.07 67 >1000 68
0.95 69 1.06 70 1.13 71 0.51 72 3.59 73 3.15 74 0.42 75 3.15 76
1.22 77 10.5 78 4.81 79 0.41 80 1.03 81 1.44 82 >1000 83 1.04 84
1.64 85 1.04 86 2.48 87 0.18 88 0.22 89 0.66 90 0.75 91 >1000 93
1.39 95 0.89 96 0.83 97 1.45 98 5.45 99 0.29 100 12.79 101 >1000
102 >1000 103 8.2 104 >1000 105 34.13 107 1.1 108 1.05 109
1.11 110 111 0.77 112 0.53 113 0.23 116 >1000 117 0.39 118 0.86
119 0.40 120 0.39 122 1.01 123 0.28 126 0.86 127 0.22 128 2.16 129
0.64 130 0.55 131 1.93 132 2.30 133 1.50 134 1.99 135 11.7 136
0.914 137 0.681 141 1.119 142 0.9457 143 0.4155 144 0.61 145 2.71
146 0.702 147 0.40 148 0.40 153 0.87 154 0.328 155 1.26 158 1.36
159 0.2985 160 0.746 161 >1000 162 1.81 163 1.81 164 1.1795 165
1.533 168 1.165 169 0.5975 170 1.5 171 1.1055 172 2.89 174 2.065
175 0.861 177 3.219 178 1.027 180 5.914 181 1.10 182 1.62 183 1.27
184 1.25 185 3.06 186 1.50 187 1.18 188 1.75 189 0.46 190 0.75
Biological Example 2
Rodent Novel Object Recognition (NOR) Assay in
Phencyclidine-Induced Cognitive Deficits Modeling Schizophrenia
[0313] The aim of this study was to investigate the ability of the
compounds of the invention to improve subchronic PCP-induced
impairment in cognition memory using the NOR task in the rat, a
paradigm of relevance to cognition in schizophrenia. Adult male
Sprague-Dawley rats (250-350 g; Harlan, USA) were used for the
experiments. Animal were acclimated to the facility for 7 days
prior to experimentation. Seven groups of 14 animals per group were
used for the experiment. One group of animals received vehicle
(0.9% saline twice daily) and the remaining six groups received PCP
(2.5 mg/kg, s.c. twice daily) for 7 days, followed by 5-days drug
free. On the test day, the animals were allowed to acclimate to the
testing room for 30 min prior to initiation of experiments.
Experiments were carried out in a white plexiglass chamber,
designated as experimental arena. The arena was placed in a dark
experimental room that was illuminated by a halogen lamp, providing
a dim light to the arena.
[0314] Animals were placed in the arena for a 5 minute period to
freely explore the test chamber in the absence of objects
(habituation). Animals were then returned to their home cage
immediately upon completion of habituation for a 120 min period.
(1R,3R,5S)-8-Methyl-8-azabicyclo[3.2.1]octan-3-yl
1-(2,2,2-trifluoroethyl)-1H-indole-3-carboxylate (0.1, 1, 10 mg/kg
s.c.), or vehicle (veh, saline) was administered 120 min prior to
T1 and galantamine (5 mg/kg, i.p.) was administered 30 min prior to
T1. Animals were returned to the arena which contained two
identical objects (plastic balls) placed at one end of the arena
(acquisition, T1), and allowed to explore for a 5 min period. The
time spent exploring the two objects was recorded. Animals were
once again returned to the home cage for a period of 120 min
(ITT).
[0315] ITI was followed by the retention phase (T2) where one of
the objects presented in the first trial was replaced by a novel
object and animals were allowed to explore for an additional 5 min
period. Again, the time spent exploring the two objects was
recorded.
[0316] For the retention phase, the differences between the time
spent exploring the familiar object and the novel object were
examined. All sessions were recorded and scored blindly for the
time exploring objects. Exploration is defined as touching the
object or directing nose towards object at a distance less that 2
cm. A minimal exploration criterion was used such that only animals
with exploration time of greater than 5 seconds per object were
included.
[0317] Comparisons of all treatment groups were conducted using a
one-way ANOVA followed by a Bonferroni's post hoc test for multiple
comparisons.
[0318] Results:
[0319] Vehicle/vehicle-treated animals displayed a statistically
significant discrimination between familiar (TF) and novel objects
(TN) [27.99.+-.2.77 (TN) versus 15.74.+-.2.118 (TF)] at a 2 h ITI,
indicative of good performance and/or lack or cognitive deficit. In
contrast, the vehicle/PCP-treated animals displayed a statistically
non-significant discrimination between familiar and novel objects
[23.31.+-.1.998 (TN) versus 17.13.+-.1.112 (TF)].
Galantamine-treated animals, the positive control group, displayed
a statistically significant discrimination between familiar and
novel objects [22.8.+-.2.2 (TN) versus 11.19.+-.1.376 (TF)] at a 2
h ITI, indicative of reversal of the PCP-induced cognitive
deficits. (1R,3R,5S)-8-methyl-8-azabicyclo[3.2.1]octan-3-yl
1-(2,2,2-trifluoroethyl)-1H-indole-3-carboxylate did not
demonstrate a statistically significant discrimination between
familiar and novel objects at 0.1 mg/kg [0.01 mg/kg 22.9.+-.3.65
(TN) versus 12.5.+-.2.152 (TF)] but demonstrated a statistically
significant discrimination between familiar and novel objects at 1
and 10 mg/kg, [0.1 mg/kg: 25.3.+-.2.51 (TN) versus 12.7.+-.1.027
(TF)], [10 mg/kg 22.8.+-.2.48 (TN) versus 9.831.+-.1.53 (TF)],
indicative of an attenuation of PCP-induced cognitive deficits.
Formulation Examples
[0320] The following are representative pharmaceutical formulations
containing a compound of Formula (I).
Tablet Formulation
[0321] The following ingredients are mixed intimately and pressed
into single scored tablets.
TABLE-US-00003 Capsule Formulation Ingredient Quantity per tablet
compound of this invention 0.5-150 mg cornstarch 50 mg
croscarmellose sodium 25 mg lactose 120 mg magnesium stearate 5
mg
[0322] The following ingredients are mixed intimately and loaded
into a hard-shell gelatin capsule.
TABLE-US-00004 Injectable Formulation Ingredient Quantity per
capsule compound of this invention 0.5-150 mg lactose spray dried
148 mg magnesium stearate 2 mg
[0323] Compound of the invention (e.g., compound 1) in 2% HPMC, 1%
Tween 80 in DI water, pH 2.2 with MSA, q.s. to at least 20
mg/mL.
* * * * *