U.S. patent application number 12/815163 was filed with the patent office on 2011-03-17 for novel indoles are cannabinoid receptor ligands.
This patent application is currently assigned to Abbott Laboratories. Invention is credited to Michael J. Dart, Jennifer M. Frost, Michael D. Meyer, Karin Tietje.
Application Number | 20110065685 12/815163 |
Document ID | / |
Family ID | 36096265 |
Filed Date | 2011-03-17 |
United States Patent
Application |
20110065685 |
Kind Code |
A1 |
Frost; Jennifer M. ; et
al. |
March 17, 2011 |
NOVEL INDOLES ARE CANNABINOID RECEPTOR LIGANDS
Abstract
The present invention provides novel compounds of Formula (I)
##STR00001## which are CB.sub.2 selective ligands useful for the
treatment of pain.
Inventors: |
Frost; Jennifer M.;
(Grayslake, IL) ; Tietje; Karin; (Mundelein,
IL) ; Dart; Michael J.; (Highland Park, IL) ;
Meyer; Michael D.; (Lake Villa, IL) |
Assignee: |
Abbott Laboratories
Abbott Park
IL
|
Family ID: |
36096265 |
Appl. No.: |
12/815163 |
Filed: |
June 14, 2010 |
Related U.S. Patent Documents
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Application
Number |
Filing Date |
Patent Number |
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12370727 |
Feb 13, 2009 |
7750039 |
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12815163 |
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11315862 |
Dec 21, 2005 |
7560481 |
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12370727 |
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60637987 |
Dec 21, 2004 |
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Current U.S.
Class: |
514/217.08 ;
514/235.2; 514/323; 514/339; 514/365; 514/397; 514/414; 514/419;
540/602; 544/143; 546/201; 546/278.1; 548/181; 548/312.1; 548/465;
548/493 |
Current CPC
Class: |
A61P 11/08 20180101;
C07D 409/06 20130101; C07D 405/06 20130101; A61P 35/00 20180101;
A61P 29/00 20180101; A61P 11/00 20180101; A61P 21/04 20180101; A61P
9/00 20180101; C07D 417/06 20130101; A61P 37/00 20180101; A61P 1/12
20180101; A61P 1/16 20180101; A61P 37/02 20180101; C07D 403/06
20130101; A61P 17/06 20180101; A61P 25/04 20180101; C07D 401/06
20130101; A61P 3/10 20180101; A61P 19/02 20180101; C07D 209/12
20130101; A61P 11/02 20180101; A61P 11/06 20180101; A61P 17/00
20180101; C07D 413/06 20130101; A61P 25/00 20180101; A61P 37/08
20180101; A61P 31/18 20180101; A61P 37/06 20180101; A61P 43/00
20180101 |
Class at
Publication: |
514/217.08 ;
546/201; 544/143; 546/278.1; 548/312.1; 548/465; 548/493; 548/181;
540/602; 514/323; 514/235.2; 514/339; 514/397; 514/414; 514/419;
514/365 |
International
Class: |
A61K 31/404 20060101
A61K031/404; C07D 401/06 20060101 C07D401/06; C07D 413/06 20060101
C07D413/06; C07D 403/06 20060101 C07D403/06; C07D 405/06 20060101
C07D405/06; C07D 209/42 20060101 C07D209/42; C07D 417/06 20060101
C07D417/06; A61K 31/454 20060101 A61K031/454; A61K 31/5377 20060101
A61K031/5377; A61K 31/4439 20060101 A61K031/4439; A61K 31/4178
20060101 A61K031/4178; A61K 31/427 20060101 A61K031/427; A61K 31/55
20060101 A61K031/55; A61P 25/00 20060101 A61P025/00; A61P 29/00
20060101 A61P029/00; A61P 37/00 20060101 A61P037/00; A61P 35/00
20060101 A61P035/00; A61P 11/00 20060101 A61P011/00; A61P 9/00
20060101 A61P009/00 |
Claims
1. A compound of Formula (I) ##STR00005## or a pharmaceutically
acceptable salt or prodrug thereof, wherein R.sub.1 is selected
from the group consisting of alkoxyalkyl, alkylcarbonyl,
alkylcarbonylalkyl, alkylthioalkyl, arylalkyl, arylalkylcarbonyl,
azidoalkyl, cycloalkylalkyl, cycloalkylalkylcarbonyl, haloalkyl,
heteroarylalkyl, heteroarylalkylcarbonyl, heterocyclealkyl,
heterocyclealkylcarbonyl, hydroxyalkyl, mercaptoalkyl,
(NR.sub.AR.sub.B)carbonylalkyl, (NR.sub.AR.sub.B)sulfonylalkyl,
(NR.sub.CR.sub.D)alkyl, -LOR.sub.2, -LSR.sub.2, -LS(O)R.sub.2, and
-LS(O).sub.2R.sub.2; L is alkylene; R.sub.2 is selected from the
group consisting of alkyl, alkylcarbonyl, aryl, arylalkyl,
carboxyalkenylcarbonyl, carboxyalkyl, carboxyalkylcarbonyl,
cycloalkyl, cycloalkylalkyl, haloalkyl, heteroaryl,
heteroarylalkyl, heterocycle, heterocyclealkyl,
(NR.sub.AR.sub.B)carbonylalkenylcarbonyl,
(NR.sub.AR.sub.B)carbonylalkyl, and
(NR.sub.AR.sub.B)carbonylalkylcarbonyl; R.sub.3 is selected from
the group consisting of hydrogen, alkoxyalkyl, alkyl, and
haloalkyl; R.sub.4 is selected from the group consisting of
cyclopropyl, cyclobutyl, cyclopentyl, cycloheptyl, and cyclooctyl,
wherein the cyclopropyl, cyclobutyl, and cyclopentyl are
substituted with 1, 2, 3, 4, 5, or 6 substituents selected from the
group consisting of alkenyl, alkoxy, alkoxyalkyl, alkoxycarbonyl,
alkoxycarbonylalkyl, alkoxysulfonyl, alkyl, alkylcarbonyl,
alkylcarbonylalkyl, alkylcarbonyloxy, alkylthio, alkylthioalkyl,
alkynyl, carboxy, carboxyalkyl, cyano, cyanoalkyl, haloalkoxy,
haloalkyl, halogen, hydroxy, hydroxyalkyl, mercapto, mercaptoalkyl,
oxo, --NR.sub.ER.sub.F, (NR.sub.ER.sub.F)alkyl,
(NR.sub.GR.sub.H)carbonyl, (NR.sub.GR.sup.H)carbonylalkyl,
(NR.sub.GR.sup.H)sulfonyl, and (NR.sub.GR.sub.H)sulfonylalkyl,
wherein the cycloheptyl and cyclooctyl are optionally substituted
with 1, 2, 3, 4, 5, or 6 substituents selected from the group
consisting of alkenyl, alkoxy, alkoxyalkyl, alkoxycarbonyl,
alkoxycarbonylalkyl, alkoxysulfonyl, alkyl, alkylcarbonyl,
alkylcarbonylalkyl, alkylcarbonyloxy, alkylthio, alkylthioalkyl,
alkynyl, carboxy, carboxyalkyl, cyano, cyanoalkyl, haloalkoxy,
haloalkyl, halogen, hydroxy, hydroxyalkyl, mercapto, mercaptoalkyl,
oxo, --NR.sub.ER.sub.F, (NR.sub.ER.sub.F)alkyl,
(NR.sub.GR.sub.H)carbonyl, (NR.sub.GR.sub.H)carbonylalkyl,
(NR.sub.GR.sub.H)sulfonyl, and (NR.sub.GR.sub.H)sulfonylalkyl;
R.sub.5, R.sub.6, R.sub.7, and R.sub.8 are independently selected
from the group consisting of hydrogen, alkenyl, alkoxy,
alkoxyalkyl, alkoxycarbonyl, alkoxycarbonylalkoxy,
alkoxycarbonylalkyl, alkoxysulfonyl, alkyl, alkylcarbonyl,
alkylcarbonylalkyl, alkylcarbonyloxy, alkylsulfinyl,
alkylsulfinylalkyl, alkylsulfonyl, alkylsulfonylalkyl,
alkylsulfonyloxy, alkylthio, alkylthioalkyl, alkynyl, aryl,
arylalkoxy, arylalkyl, arylalkylthio, arylcarbonyl, aryloxy,
aryloxyalkyl, arylthio, arylthioalkyl, carboxy, carboxyalkenyl,
carboxyalkenylcarbonyl, carboxyalkenylcarbonyloxy, carboxy,
carboxyalkyl, carboxyalkylcarbonyl, carboxyalkylcarbonyloxy, cyano,
cyanoalkyl, cycloalkyl, cycloalkylalkoxy, cycloalkylalkyl,
cycloalkylcarbonyl, cycloalkyloxy, cycloalkyloxyalkyl, haloalkoxy,
haloalkyl, halogen, heteroaryl, heteroarylalkoxy, heteroarylalkyl,
heteroaryloxy, heteroaryloxyalkyl, heterocycle, heterocyclealkoxy,
heterocyclealkoxycarbonyl, heterocyclealkyl, heterocycleoxy,
heterocycleoxyalkyl, hydroxy, hydroxyalkoxy, hydroxyalkyl,
mercapto, mercaptoalkyl, nitro, --NR.sub.JR.sub.K,
(NR.sub.JR.sub.K)alkoxy, (NR.sub.JR.sub.K)alkyl,
(NR.sub.MR.sub.N)carbonyl, (NR.sub.MR.sub.N)carbonylalkyl,
(NR.sub.MR.sub.N)sulfonyl, and (NR.sub.MR.sub.N)sulfonylalkyl;
R.sub.A, R.sub.B, R.sub.G, R.sub.H, R.sub.M, and R.sub.N are
independently selected from the group consisting of hydrogen,
alkenyl, alkoxyalkyl, alkoxycarbonylalkyl, alkyl, alkynyl, aryl,
arylalkyl, cycloalkyl, cycloalkylalkyl, heteroaryl,
heteroarylalkyl, heterocycle, heterocyclealkyl, and hydroxyalkyl;
and R.sub.C, R.sub.D, R.sub.E, R.sub.E, R.sub.J, R.sub.K, are
independently selected from the group consisting of hydrogen,
alkenyl, alkoxyalkyl, alkoxycarbonyl, alkoxycarbonylalkyl, alkyl,
alkylcarbonyl, alkylsulfonyl, alkynyl, aryl, arylalkyl,
arylsulfonyl, arylalkylsulfonyl, cycloalkyl, cycloalkylalkyl,
cycloalkylsulfonyl, cycloalkylalkylsulfonyl, heteroaryl,
heteroarylalkyl, heteroarylsulfonyl, heteroarylalkylsulfonyl,
heterocycle, heterocyclealkyl, heterocyclesulfonyl, and
heterocyclealkylsulfonyl.
2. A compound according to claim 1 wherein R.sub.1 is selected from
the group consisting of alkoxyalkyl, alkylcarbonylalkyl,
alkylthioalkyl, arylalkyl, azidoalkyl, cycloalkylalkyl, haloalkyl,
heteroarylalkyl, heterocyclealkyl, heterocyclealkylcarbonyl,
hydroxyalkyl, mercaptoalkyl, (NR.sub.AR.sub.B)carbonylalkyl,
(NR.sub.AR.sub.B)sulfonylalkyl, (NR.sub.CR.sub.D)alkyl, and
-LOR.sub.2; L is alkylene; R.sub.2 is selected from the group
consisting of alkylcarbonyl, arylalkyl, and carboxyalkenylcarbonyl;
R.sub.3 is selected from the group consisting of hydrogen and alkyl
wherein the alkyl is methyl; R.sub.4 is selected from the group
consisting of cyclopropyl, cyclobutyl, cyclopentyl, and
cycloheptyl, wherein the cyclopropyl, cyclobutyl, and cyclopentyl
are substituted with 1, 2, 3, 4, 5, or 6 substituents selected from
the group consisting of alkyl and halogen; R.sub.5, R.sub.7, and
R.sub.8 are independently selected from the group consisting of
hydrogen, alkoxy, alkoxyalkyl, alkoxycarbonyl,
alkoxycarbonylalkoxy, alkyl, alkylsulfonyl, arylalkoxy, carboxy,
carboxyalkenylcarbonyloxy, carboxy, carboxyalkylcarbonyloxy, cyano,
haloalkoxy, haloalkyl, halogen, heterocyclealkoxycarbonyl, hydroxy,
hydroxyalkoxy, hydroxyalkyl, nitro, --NR.sub.JR.sub.K,
(NR.sub.JR.sub.K)alkoxy, (NR.sub.JR.sub.K)alkyl, and
(NR.sub.MR.sub.N)carbonyl; R.sub.A, R.sub.B, R.sub.M, and R.sub.N
are independently selected from the group consisting of hydrogen,
alkoxycarbonylalkyl, alkyl, and hydroxyalkyl; and R.sub.C, R.sub.D,
R.sub.J, R.sub.K, are independently selected from the group
consisting of hydrogen, alkoxycarbonyl, alkyl, and
alkylsulfonyl.
3. A compound according to claim 1 wherein R.sub.3 is selected from
the group consisting of hydrogen and alkyl wherein the alkyl is
methyl; and R.sub.4 is 2,2,3,3-tetramethylcyclopropyl.
4. A compound according to claim 1 wherein R.sub.1 is
heterocyclealkyl; R.sub.3 is selected from the group consisting of
hydrogen and alkyl wherein the alkyl is methyl; and R.sub.4 is
2,2,3,3-tetramethylcyclopropyl.
5. A compound according to claim 1 wherein R.sub.1 is
heteroarylalkyl; R.sub.3 is selected from the group consisting of
hydrogen and alkyl wherein the alkyl is methyl; and R.sub.4 is
2,2,3,3-tetramethylcyclopropyl.
6. A compound according to claim 1 wherein R.sub.1 is arylalkyl;
R.sub.3 is selected from the group consisting of hydrogen and alkyl
wherein the alkyl is methyl; and R.sub.4 is
2,2,3,3-tetramethylcyclopropyl.
7. A compound according to claim 1 wherein R.sub.1 is selected from
the group consisting of alkoxyalkyl, alkylcarbonylalkyl,
alkylthioalkyl, azidoalkyl, cycloalkylalkyl, haloalkyl,
heterocyclealkylcarbonyl, mercaptoalkyl,
(NR.sub.AR.sub.B)carbonylalkyl, (NR.sub.AR.sub.B)sulfonylalkyl,
(NR.sub.AR.sub.B)sulfonylalkyl, and (NR.sub.CR.sub.D)alkyl; R.sub.3
is selected from the group consisting of hydrogen and alkyl wherein
the alkyl is methyl; R.sub.4 is 2,2,3,3-tetramethylcyclopropyl;
R.sub.A and R.sub.B are independently selected from the group
consisting of hydrogen, alkoxycarbonylalkyl, alkyl, and
hydroxyalkyl; and R.sub.C and R.sub.D are independently selected
from the group consisting of hydrogen, alkoxycarbonyl, alkyl, and
alkylsulfonyl.
8. A compound according to claim 1 wherein R.sub.1 is -LOR.sub.2;
R.sub.2 is selected from the group consisting of alkylcarbonyl,
arylalkyl, and carboxyalkenylcarbonyl; R.sub.3 is selected from the
group consisting of hydrogen and alkyl wherein the alkyl is methyl;
R.sub.4 is 2,2,3,3-tetramethylcyclopropyl; and L is alkylene.
9. A compound according to claim 1 wherein R.sub.1 is hydroxyalkyl;
R.sub.3 is selected from the group consisting of hydrogen and alkyl
wherein the alkyl is methyl; and R.sub.4 is
2,2,3,3-tetramethylcyclopropyl.
10. A compound according to claim 1 wherein R.sub.1 is
alkylthioalkyl; R.sub.3 is selected from the group consisting of
hydrogen and alkyl wherein the alkyl is methyl; and R.sub.4 is
2,2,3,3-tetramethylcyclopropyl.
11. A compound according to claim 1 wherein R.sub.1 is
heterocyclealkyl; R.sub.3 is selected from the group consisting of
hydrogen and alkyl wherein the alkyl is methyl; and R.sub.4 is
2,2,3,3-tetrafluoro-1-methylcyclobutyl.
12. A compound according to claim 1 wherein R.sub.1 is
heterocyclealkyl; R.sub.3 is selected from the group consisting of
hydrogen and alkyl wherein the alkyl is methyl; and R.sub.4 is
cycloheptyl.
13. A compound selected from the group consisting of
{1-[(1-methylpiperidin-2-yl)methyl]-1H-indol-3-yl}(2,2,3,3-tetramethylcyc-
lopropyl)methanone;
[1-(2-morpholin-4-ylethyl)-1H-indol-3-yl](2,2,3,3-tetramethylcyclopropyl)-
methanone p-toluenesulfonic acid;
[1-(2-pyridin-2-ylethyl)-1H-indol-3-yl](2,2,3,3-tetramethylcyclopropyl)me-
thanone p-toluenesulfonic acid;
{1-[(1-methyl-1H-imidazol-2-yl)methyl]-1H-indol-3-yl}(2,2,3,3-tetramethyl-
cyclopropyl)methanone p-toluenesulfonic acid; tert-butyl
4-(2-{3-(2,2,3,3-tetramethylcyclopropyl)carbonyl]-1H-indol-1-yl}ethyl)pip-
eridine-1-carboxylate;
[1-(2-Piperidin-4-yl-ethyl)-1H-indol-3-yl]-(2,2,3,3-tetramethyl-cycloprop-
yl)-methanone p-toluenesulfonic acid;
{1-[2-(1-methylpiperidin-4-yl)ethyl]-1H-indol-3-yl}(2,2,3,3-tetramethylcy-
clopropyl)methanone p-toluenesulfonic acid;
[1-(2-tetrahydro-2H-pyran-4-ylethyl)-1H-indol-3-yl](2,2,3,3-tetramethylcy-
clopropyl)methanone;
[1-(2-pyrrolidin-1-ylethyl)-1H-indol-3-yl](2,2,3,3-tetramethylcyclopropyl-
)methanone p-toluenesulfonic acid;
(2,2,3,3-tetramethylcyclopropyl)[1-(2-thien-2-ylethyl)-1H-indol-3-yl]meth-
anone;
[1-(2-methoxyethyl)-1H-indol-3-yl](2,2,3,3-tetramethylcyclopropyl)m-
ethanone;
1-(2-{3-[(2,2,3,3-tetramethylcyclopropyl)carbonyl]-1H-indol-1-yl-
}ethyl)pyrrolidin-2-one;
1-(2-{3-[(2,2,3,3-tetramethylcyclopropyl)carbonyl]-1H-indol-1-yl}ethyl)py-
rrolidine-2,5-dione,
(1-[2-(4-methyl-1,3-thiazol-5-yl)ethyl]-1H-indol-3-yl)(2,2,3,3-tetramethy-
lcyclopropyl)methanone;
{1-[2-(dimethylamino)ethyl]-1H-indol-3-yl)(2,2,3,3-tetramethylcyclopropyl-
)methanone;
(2,2,3,3-tetramethylcyclopropyl)[1-(2-thien-3-ylethyl)-1H-indol-3-yl]meth-
anone;
{1-[2-(1-methylpyrrolidin-2-yl)ethyl]-1H-indol-3-yl}(2,2,3,3tetrame-
thylcyclopropyl)methanone p-toluenesulfonic acid;
[1-(tetrahydro-2H-pyran-4-ylmethyl)-1H-indol-3-yl](2,2,3,3-tetramethylcyc-
lopropyl)methanone;
[1-(2-pyridin-3-ylethyl)-1H-indol-3-yl](2,2,3,3-tetramethylcyclopropyl)me-
thanone;
{1-[2-(1H-pyrrol-1-yl)ethyl]-1H-indol-3-yl)(2,2,3,3-tetramethylcy-
clopropyl)methanone;
(1-{2-[4-(dimethylamino)phenyl]ethyl}-1H-indol-3-yl)(2,2,3,3-tetramethylc-
yclopropyl)methanone;
[1-(2-pyridin-4-ylethyl)-1H-indol-3-yl](2,2,3,3-tetramethylcyclopropyl)me-
thanone;
{1-[4-(benzyloxy)butyl]-1H-indol-3-yl}(2,2,3,3-tetramethylcyclopr-
opyl)methanone;
[1-(4-hydroxybutyl)-1H-indol-3-yl](2,2,3,3-tetramethylcyclopropyl)methano-
ne;
[1-(2-piperidin-1-ylethyl)-1H-indol-3-yl](2,2,3,3-tetramethylcycloprop-
yl)methanone;
{1-[4-(methylthio)butyl]-1H-indol-3-yl}(2,2,3,3-tetramethylcyclopropyl)me-
thanone;
[1-(3-morpholin-4-ylpropyl)-1H-indol-3-yl](2,2,3,3-tetramethylcyc-
lopropyl)methanone;
[1-(2-azepan-1-ylethyl)-1H-indol-3-yl](2,2,3,3-tetramethylcyclopropyl)met-
hanone;
[1-(2-piperazin-1-ylethyl)-1H-indol-3-yl](2,2,3,3-tetramethylcyclo-
propyl)methanone tris-trifluoroacetic acid;
{1-[2-(4-methylpiperazin-1-yl)ethyl]-1H-indol-3-yl}(2,2,3,3-tetramethylcy-
clopropyl)methanone;
3-(2-{3-(2,2,3,3-tetramethylcyclopropyl)carbonyl]-1H-indol-1-yl}ethyl)-1,-
3-oxazolidin-2-one;
[1-(tetrahydrofuran-3-ylmethyl)-1H-indol-3-yl](2,2,3,3-tetramethylcyclopr-
opyl)methanone;
(2,2,3,3-tetramethylcyclopropyl)[1-(4,4,4-trifluorobutyl)-1H-indol-3-yl]m-
ethanone;
(1-[2-(2,2-dimethyl-1,3-dioxolan-4-yl)ethyl]-1H-indol-3-yl}(2,2,-
3,3-tetramethylcyclopropyl)methanone;
[1-(3,4-dihydroxybutyl)-1H-indol-3-yl](2,2,3,3-tetramethylcyclopropyl)met-
hanone;
[1-(1,3-dioxolan-4-ylmethyl)-1H-indol-3-yl](2,2,3,3-tetramethylcyc-
lopropyl)methanone;
{1-[2-(benzyloxy)ethyl]-1H-indol-3-yl}(2,2,3,3-tetramethylcyclopropyl)met-
hanone;
[1-(2-hydroxyethyl)-1H-indol-3-yl](2,2,3,3-tetramethylcyclopropyl)-
methanone;
{1-[3-(benzyloxy)propyl]-1H-indol-3-yl}(2,2,3,3-tetramethylcycl-
opropyl)methanone;
[1-(3-hydroxypropyl)-1H-indol-3-yl](2,2,3,3-tetramethylcyclopropyl)methan-
one;
{1-[5-(benzyloxy)pentyl]-1H-indol-3-yl}(2,2,3,3-tetramethylcyclopropy-
l)methanone;
[1-(5-hydroxypentyl)-1H-indol-3-yl](2,2,3,3-tetramethylcyclopropyl)methan-
one;
[1-(3-methoxypropyl)-1H-indol-3-yl](2,2,3,3-tetramethylcyclopropyl)me-
thanone;
[1-(tetrahydro-2H-pyran-4-ylacetyl)-1H-indol-3-yl](2,2,3,3-tetram-
ethylcyclopropyl)methanone; methyl
4-({3-[(2,2,3,3-tetramethylcyclopropyl)carbonyl]-1H-indol-1-yl}methyl)cyc-
lohexanecarboxylate; 3-{3
[(2,2,3,3-tetramethylcyclopropyl)carbonyl]-1H-indol-1-yl)propanamide;
6-{3-[(2,2,3,3-tetramethylcyclopropyl)carbonyl]-1H-indol-1-yl}
hexan-2-one;
{1-[(2R)-2,3-dihydroxypropyl]-1H-indol-3-yl}(2,2,3,3-tetramethylcycloprop-
yl)methanone;
[2-methyl-1-(2-morpholin-4-ylethyl)-1H-indol-3-yl](2,2,3,3-tetramethylcyc-
lopropyl)methanone;
[1-(2-morpholin-4-ylethyl)-4-nitro-1H-indol-3-yl](2,2,3,3-tetramethylcycl-
opropyl)methanone;
[4-amino-1-(2-morpholin-4-ylethyl)-1H-indol-3-yl](2,2,3,3-tetramethylcycl-
opropyl)methanone;
cycloheptyl[1-(2-morpholin-4-ylethyl)-1H-indol-3-yl]methanone;
(2,2,3,3-tetrafluoro-1-methylcyclobutyl)[1-(tetrahydro-2H-pyran-4-ylmethy-
l)-1H-indol-3-yl]methanone;
4-{3-[(2,2,3,3-tetramethylcyclopropyl)carbonyl]-1H-indol-1-yl}butyl
acetate;
4-oxo-4-(4-{3-[(2,2,3,3-tetramethylcyclopropyl)carbonyl]-1H-indo-
l-1-yl}butoxy)but-2-enoic acid;
[6-chloro-1-(tetrahydro-2H-pyran-4-ylmethyl)-1H-indol-3-yl](2,2,3,3-tetra-
methylcyclopropyl)methanone;
4-({3-[(2,2,3,3-tetramethylcyclopropyl)carbonyl]-1H-indol-1-yl)methyl)phe-
nyl acetate;
[1-(4-hydroxybenzyl)-1H-indol-3-yl](2,2,3,3-tetramethylcyclopropyl)methan-
one,
[6-(benzyloxy)-1-(tetrahydro-2H-pyran-4-ylmethyl)-1H-indol-3-yl](2,2,-
3,3-tetramethylcyclopropyl)methanone;
[6-hydroxy-1-(tetrahydro-2H-pyran-4-ylmethyl)-1H-indol-3-yl](2,2,3,3-tetr-
amethylcyclopropyl)methanone;
4-oxo-4-({1-(tetrahydro-2H-pyran-4-ylmethyl)-3-[(2,2,3,3-tetramethylcyclo-
propyl)carbonyl]-1H-indol-6-yl}oxy)but-2-enoic acid;
[6-methoxy-1-(tetrahydro-2H-pyran-4-ylmethyl)-1H-indol-3-yl](2,2,3,3-tetr-
amethylcyclopropyl)methanone;
{1-[(2R)-tetrahydrofuran-2-ylmethyl]-1H-indol-3-yl}(2,2,3,3-tetramethylcy-
clopropyl)methanone;
[5-(benzyloxy)-1-(tetrahydro-2H-pyran-4-ylmethyl)-1H-indol-3-yl](2,2,3,3--
tetramethylcyclopropyl)methanone;
(1-benzyl-1H-indol-3-yl)(2,2,3,3-tetramethylcyclopropyl)methanone;
[7-(benzyloxy)-1-(tetrahydro-2H-pyran-4-ylmethyl)-1H-indol-3-yl](2,2,3,3--
tetramethylcyclopropyl)methanone;
[1-(4-methoxybenzyl)-1H-indol-3-yl](2,2,3,3-tetramethylcyclopropyl)methan-
one;
[1-(3-methoxybenzyl)-1H-indol-3-yl](2,2,3,3-tetramethylcyclopropyl)me-
thanone;
[5-hydroxy-1-(tetrahydro-2H-pyran-4-ylmethyl)-1H-indol-3-yl](2,2,-
3,3-tetramethylcyclopropyl)methanone;
[1-(1,3-benzodioxol-5-ylmethyl)-1H-indol-3-yl](2,2,3,3-tetramethylcyclopr-
opyl)methanone;
[7-hydroxy-1-(tetrahydro-2H-pyran-4-ylmethyl)-1H-indol-3-yl](2,2,3,3-tetr-
amethylcyclopropyl)methanone;
[1-(2,3-dihydro-1,4-benzodioxin-6-ylmethyl)-1H-indol-3-yl](2,2,3,3-tetram-
ethylcyclopropyl)methanone;
4-oxo-4-({1-(tetrahydro-2H-pyran-4-ylmethyl)-3-[(2,2,3,3-tetramethylcyclo-
propyl)carbonyl]-1H-indol-7-yl}oxy)but-2-enoic acid;
[7-methoxy-1-(tetrahydro-2H-pyran-4-ylmethyl)-1H-indol-3-yl](2,2,3,3-tetr-
amethylcyclopropyl)methanone; methyl
1-(tetrahydro-2H-pyran-4-ylmethyl)-3-[(2,2,3,3-tetramethylcyclopropyl)car-
bonyl]-1H-indole-6-carboxylate;
1-(tetrahydro-2H-pyran-4-ylmethyl)-3[{(2,2,3,3-tetramethylcyclopropyl)car-
bonyl]-1H-indole-6-carboxylic acid;
{1-[(5-chloro-1,2,4-thiadiazol-3-yl)methyl]-1H-indol-3-yl}(2,2,3,3-tetram-
ethylcyclopropyl)methanone;
4-oxo-4-({1-(tetrahydro-2H-pyran-4-ylmethyl)-3-[(2,2,3,3-tetramethylcyclo-
propyl)carbonyl]-1H-indol-5-yl}oxy)but-2-enoic acid;
[1-(1,3-benzothiazol-2-ylmethyl)-1H-indol-3-yl](2,2,3,3-tetramethylcyclop-
ropyl)methanone; ethyl
3-[({1-(tetrahydro-2H-pyran-4-ylmethyl)-3-[(2,2,3,3-tetramethylcyclopropy-
l)carbonyl]-1H-indol-6-yl}carbonyl)amino]propanoate;
[5-methoxy-1-(tetrahydro-2H-pyran-4-ylmethyl)-1H-indol-3-yl](2,2,3,3-tetr-
amethylcyclopropyl)methanone;
[4-(benzyloxy)-1-(tetrahydro-2H-pyran-4-ylmethyl)-1H-indol-3-yl](2,2,3,3--
tetramethylcyclopropyl)methanone;
1-(tetrahydro-2H-pyran-4-ylmethyl)-3-[(2,2,3,3-tetramethylcyclopropyl)car-
bonyl]-1H-indole-6-carboxamide,
1-(2-morpholin-4-ylethyl)-3-[(2,2,3,3-tetramethylcyclopropyl)carbonyl]-1H-
-indole-7-carboxylic acid; 2-morpholin-4-ylethyl
1-(2-morpholin-4-ylethyl)-3-[(2,2,3,3-tetramethylcyclopropyl)carbonyl]-1H-
-indole-7- carboxylate;
[4-hydroxy-1-(tetrahydro-2H-pyran-4-ylmethyl)-1H-indol-3-yl](2,2,3,3-tetr-
amethylcyclopropyl)methanone;
[4-methoxy-1-(tetrahydro-2H-pyran-4-ylmethyl)-1H-indol-3-yl](2,2,3,3-tetr-
amethylcyclopropyl)methanone;
[6-methyl-1-(tetrahydro-2H-pyran-4-ylmethyl)-1H-indol-3-yl](2,2,3,3-tetra-
methylcyclopropypmethanone;
[6-(benzyloxy)-1-(2-morpholin-4-ylethyl)-1H-indol-3-yl](2,2,3,3-tetrameth-
ylcyclopropyl)methanone;
[6-hydroxy-1-(2-morpholin-4-ylethyl)-1H-indol-3-yl](2,2,3,3-tetramethylcy-
clopropyl)methanone;
[6-methoxy-1-(2-morpholin-4-ylethyl)-1H-indol-3-yl](2,2,3,3-tetramethylcy-
clopropyl)methanone;
4-oxo-4-({1-(tetrahydro-2H-pyran-4-ylmethyl)-3-[(2,2,3,3-tetramethylcyclo-
propyl)carbonyl]-1H-indol-5-yl}oxy)butanoic acid;
(2,2-dichloro-1-methylcyclopropyl)[1-(tetrahydro-2H-pyran-4-ylmethyl)-1H--
indol-3-yl]methanone;
[1-(4-azidobutyl)-1H-indol-3-yl](2,2,3,3-tetramethylcyclopropyl)methanone-
;
[1-(2-azidoethyl)-1H-indol-3-yl](2,2,3,3-tetramethylcyclopropyl)methanon-
e;
N-(4-{3-[(2,2,3,3-tetramethylcyclopropyl)carbonyl]-1H-indol-1-yl}butyl)-
methanesulfonamide; ethyl
4-({1-(tetrahydro-2H-pyran-4-ylmethyl)-3-[(2,2,3,3-tetramethylcyclopropyl-
)carbonyl]-1H-indol-5-yl}oxy)butanoate;
[1-(3-azidopropyl)-1H-indol-3-yl](2,2,3,3-tetramethylcyclopropyl)methanon-
e;
{1-[(2S)-tetrahydrofuran-2-ylmethyl]-1H-indol-3-yl)(2,2,3,3-tetramethyl-
cyclopropyl)methanone;
[5-(4-hydroxybutoxy)-1-(tetrahydro-2H-pyran-4-ylmethyl)-1H-indol-3-yl](2,-
2,3,3-tetramethylcyclopropyl)methanone;
[5-(4-bromobutoxy)-1-(tetrahydro-2H-pyran-4-ylmethyl)-1H-indol-3-yl](2,2,-
3,3-tetramethylcyclopropyl)methanone;
[1-(5-azidopentyl)-1H-indol-3-yl](2,2,3,3-tetramethylcyclopropyl)methanon-
e;
N-(2-{3-[(2,2,3,3-tetramethylcyclopropyl)carbonyl]-1H-indol-1-yl}ethyl)-
methanesulfonamide; methyl
1-(tetrahydro-2H-pyran-4-ylmethyl)-3-[(2,2,3,3-tetramethylcyclopropyl)car-
bonyl]-1H-indole-5-carboxylate;
N-(3-{3-[(2,2,3,3-tetramethylcyclopropyl)carbonyl]-1H-indol-1-yl}
propyl)methanesulfonamide;
N-(5-{3-[(2,2,3,3-tetramethylcyclopropyl)carbonyl]-1H-indol-1-yl}pentyl)m-
ethanesulfonamide;
[5-(4-aminobutoxy)-1-(tetrahydro-2H-pyran-4-ylmethyl)-1H-indol-3-yl](2,2,-
3,3-tetramethylcyclopropyl)methanone;
[5-hydroxy-1-(2-morpholin-4-ylethyl)-1H-indol-3-yl](2,2,3,3-tetramethylcy-
clopropyl)methanone;
(2E)-4-({1-(2-morpholin-4-ylethyl)-3-[(2,2,3,3-tetramethylcyclopropyl)car-
bonyl]-1H-indol-5-yl}oxy)-4-oxobut-2-enoic acid;
[5-methoxy-1-(2-morpholin-4-ylethyl)-1H-indol-3-yl](2,2,3,3-tetramethylcy-
clopropyl)methanone;
N-[4-({1-(tetrahydro-2H-pyran-4-ylmethyl)-3-[(2,2,3,3-tetramethylcyclopro-
pyl)carbonyl]-1H-indol-5-yl}oxy)butyl]methanesulfonamide;
1-(tetrahydro-2H-pyran-4-ylmethyl)-3-[(2,2,3,3-tetramethylcyclopropyl)car-
bonyl]-1H-indole-5-carboxamide;
N-(2-hydroxyethyl)-1-(tetrahydro-2H-pyran-4-ylmethyl)-3-[(2,2,3,3-tetrame-
thylcyclopropyl)carbonyl]-1H-indole-5-carboxamide;
N-methyl-1-(tetrahydro-2H-pyran-4-ylmethyl)-3-[(2,2,3,3-tetramethylcyclop-
ropyl)carbonyl]-1H-indole-5-carboxamide;
1-(tetrahydro-2H-pyran-4-ylmethyl)-3-[(2,2,3,3-tetramethylcyclopropyl)car-
bonyl]1H-indole-5-carbonitrile;
[5-(benzyloxy)-6-methoxy-1-(tetrahydro-2H-pyran-4-ylmethyl)-1H-indol-3-yl-
](2,2,3,3-tetramethylcyclopropyl)methanone;
N,N-dimethyl-1-(tetrahydro-2H-pyran-4-ylmethyl)-3-[(2,2,3,3-tetramethylcy-
clopropyl)carbonyl]-1H-indole-5-carboxamide,
N-heptyl-1-(tetrahydro-2H-pyran-4-ylmethyl)-3-[(2,2,3,3-tetramethylcyclop-
ropyl)carbonyl]-1H-indole-5-carboxamide;
[5-hydroxy-6-methoxy-1-(tetrahydro-2H-pyran-4-ylmethyl)-1H-indol-3-yl](2,-
2,3,3-tetramethylcyclopropyl)methanone;
(2E)-4-({6-methoxy-1-(tetrahydro-2H-pyran-4-ylmethyl)-3-[(2,2,3,3-tetrame-
thylcyclopropyl)carbonyl]-1H-indol-5-yl}oxy)-4-oxobut-2-enoic acid;
(5-(benzyloxy)-1-[(2R)-tetrahydrofuran-2-ylmethyl]-1H-indol-3-yl}(2,2,3,3-
-tetramethylcyclopropyl)methanone;
[5-(aminomethyl)-1-(tetrahydro-2H-pyran-4-ylmethyl)-1H-indol-3-yl](2,2,3,-
3-tetramethylcyclopropyl)methanone;
{5-hydroxy-1-[(2R)-tetrahydrofuran-2-ylmethyl}-1H-indol-3-yl}(2,2,3,3-tet-
ramethylcyclopropyl)methanone;
N-({1-(tetrahydro-2H-pyran-4-ylmethyl)-3-[(2,2,3,3-tetramethylcyclopropyl-
)carbonyl]-1H-indol-5-yl}methyl)methanesulfonamide;
{5-(benzyloxy)-1[4-(benzyloxy)butyl]-1H-indol-3-yl}(2,2,3,3-tetramethylcy-
clopropyl)methanone;
[6-(methylsulfonyl)-1-(tetrahydro-2H-pyran-4-ylmethyl)-1H-indol-3-yl](2,2-
,3,3-tetramethylcyclopropyl)methanone;
[5-hydroxy-1-(4-hydroxybutyl)-1H-indol-3-yl](2,2,3,3-tetramethylcycloprop-
yl)methanone;
1-(tetrahydro-2H-pyran-4-ylmethyl)-3-[(2,2,3,3-tetramethylcyclopropyl)car-
bonyl]-1H-indole-6-carbonitrile;
[1-(tetrahydro-2H-pyran-4-ylmethyl)-6-(trifluoromethyl)-1H-indol-3-yl](2,-
2,3,3-tetramethylcyclopropyl)methanone;
[6-(aminomethyl)-1-(tetrahydro-2H-pyran-4-ylmethyl)-1H-indol-3-yl](2,2,3,-
3-tetramethylcyclopropyl)methanone;
N-({1-(tetrahydro-2H-pyran-4-ylmethyl)-3-[(2,2,3,3-tetramethylcyclopropyl-
)carbonyl]-1H-indol-6-yl}methyl)methanesulfonamide;
[5,6-dihydroxy-1-(tetrahydro-2H-pyran-4-ylmethyl)-1H-indol-3-yl](2,2,3,3--
tetramethylcyclopropyl)methanone; tetrahydro-2H-pyran-4-yl
{3-[(2,2,3,3-tetramethylcyclopropyl)carbonyl]-1H-indol-1-yl}acetic
acid; ethyl
tetrahydro-2H-pyran-4-yl{3-[(2,2,3,3-tetramethylcyclopropyl)carbony-
l]-1H-indol-1-yl}acetate; tert-butyl
1-(tetrahydro-2H-pyran-4-ylmethyl)-3-[(2,2,3,3-tetramethylcyclopropyl)car-
bonyl]-1H-indol-5-ylcarbamate;
[5-amino-1-(tetrahydro-2H-pyran-4-ylmethyl)-1H-indol-3-yl](2,2,3,3-tetram-
ethylcyclopropyl)methanonel;
[4,5,6,7-tetrafluoro-1-(tetrahydro-2H-pyran-4-ylmethyl)-1H-indol-3-yl](2,-
2,3,3-tetramethylcyclopropyl)methanone;
N-{1-(tetrahydro-2H-pyran-4-ylmethyl)-3-[(2,2,3,3-tetramethylcyclopropyl)-
carbonyl]-1H-indol-5-yl}methanesulfonamide;
[5-(hydroxymethyl)-1-(tetrahydro-2H-pyran-4-ylmethyl)-1H-indol-3-yl](2,2,-
3,3-tetramethylcyclopropyl)methanone;
[5-(methoxymethyl)-1-(tetrahydro-2H-pyran-4-ylmethyl)-1H-indol-3-yl](2,2,-
3,3-tetramethylcyclopropyl)methanone;
3-(2-{5-hydroxy-3-[(2,2,3,3-tetramethylcyclopropyl)carbonyl]-1H-indol-1-y-
l}ethyl)-1,3-oxazolidin-2-one;
3-(2-{5-(benzyloxy)-3-[(2,2,3,3-tetramethylcyclopropyl)carbonyl]-1H-indol-
-1-yl}ethyl)-1,3-oxazolidin-2-one;
N-methyl-1-(tetrahydro-2H-pyran-4-ylmethyl)-3-[(2,2,3,3-tetramethylcyclop-
ropyl)carbonyl]-1H-indole-6-carboxamide;
N,N-dimethyl-1-(tetrahydro-2H-pyran-4-ylmethyl)-3-[(2,2,3,3-tetramethylcy-
clopropyl)carbonyl]-1H-indole-6-carboxamide;
N-ethyl-1-(tetrahydro-2H-pyran-4-ylmethyl)-3-[(2,2,3,3-tetramethylcyclopr-
opyl)carbonyl]-1H-indole-6-carboxamide;
[1-(pyridin-3-ylmethyl)-1H-indol-3-yl](2,2,3,3-tetramethylcyclopropyl)met-
hanone;
[1-(pyridin-4-ylmethyl)-1H-indol-3-yl](2,2,3,3-tetramethylcyclopro-
pyl)methanone;
[5-bromo-1-(tetrahydro-2H-pyran-4-ylmethyl)-1H-indol-3-yl](2,2,3,3-tetram-
ethylcyclopropyl)methanone;
[5-(2-methoxyphenyl)-1-(tetrahydro-2H-pyran-4-ylmethyl)-1H-indol-3-yl](2,-
2,3,3-tetramethylcyclopropyl)methanone;
[5-phenyl-1-(tetrahydro-2H-pyran-4-ylmethyl)-1H-indol-3-yl](2,2,3,3-tetra-
methylcyclopropyl)methanone;
[5-(3-methoxyphenyl)-1-(tetrahydro-2H-pyran-4-ylmethyl)-1H-indol-3-yl](2,-
2,3,3-tetramethylcyclopropyl)methanone;
[5-chloro-1-(tetrahydro-2H-pyran-4-ylmethyl)-1H-indol-3-yl](2,2,3,3-tetra-
methylcyclopropyl)methanone;
[6-bromo-1-(tetrahydro-2H-pyran-4-ylmethyl)-1H-indol-3-yl](2,2,3,3-tetram-
ethylcyclopropyl)methanone;
[6-(2-methoxyphenyl)-1-(tetrahydro-2H-pyran-4-ylmethyl)-1H-indol-3-yl](2,-
2,3,3-tetramethylcyclopropyl)methanone;
[6-phenyl-1-(tetrahydro-2H-pyran-4-ylmethyl)-1H-indol-3-yl](2,2,3,3-tetra-
methylcyclopropyl)methanone;
[5-fluoro-1-(tetrahydro-2H-pyran-4-ylmethyl)-1H-indol-3-yl](2,2,3,3-tetra-
methylcyclopropyl)methanone; and
2-oxatricyclo[3.3.1.1.about.3,7.about.]dec-1-yl[1-(tetrahydro-2H-pyran-4--
ylmethyl)-1H-indol-3-yl]methanone.
14. (canceled)
15. A method of providing neuroprotection or treating pain,
nociceptive pain, or neuropathic pain, or a disorder selected from
the group consisting of inflammatory disorders, immune disorders,
neurological disorders, cancers of the immune system, respiratory
disorders, and cardiovascular disorders in a mammal in need of such
treatment comprising administering to the mammal a therapeutically
effective amount of a compound of Formula (I) of claim 1 or a
pharmaceutically acceptable salt thereof.
16.-19. (canceled)
20. A method of treating a disorder selected from the group
consisting of inflammatory disorders, immune disorders,
neurological disorders, cancers of the immune system, respiratory
disorders, and cardiovascular disorders in a mammal in need thereof
of such treatment comprising administering to the mammal a
therapeutically effective amount of a compound of Formula (I) of
claim 1 or a pharmaceutically acceptable sale thereof.
Description
[0001] This application claims priority from U.S. Provisional
Patent Application Ser. No. 60/637,987 filed Dec. 21, 2004,
incorporated herein by reference.
TECHNICAL FIELD
[0002] The present invention relates to indole derivatives,
compositions comprising such compounds, and methods of treating
conditions and disorders using such compounds and compositions.
BACKGROUND OF THE INVENTION
[0003] (-)-.DELTA..sup.9-Tetrahydrocannabinol (.DELTA..sup.9-THC),
the major psychoactive constituent of marijuana, exerts a broad
range of therapeutic effects through its interactions with two
cannabinoid (CB) receptor subtypes, CB.sub.1 and CB.sub.2. CB.sub.1
receptors are highly expressed in the central nervous system and to
a lesser degree in the periphery in a variety of tissues of the
cardiovascular and gastrointestinal systems. By contrast, CB.sub.2
receptors are most abundantly expressed in multiple lymphoid organs
and cells of the immune system, including spleen, thymus, tonsils,
bone marrow, pancreas and mast cells.
[0004] The psychotropic side effects caused by .DELTA..sup.9-THC
and other nonselective CB agonists are mediated by CB.sub.1
receptors. These CB.sub.1 receptor-mediated effects, such as
euphoria, sedation, hypothermia, catalepsy, and anxiety, have
limited the development and clinical utility of nonselective CB
agonists. Recent studies have demonstrated that CB.sub.2-selective
modulators are analgesic in preclinical models of nociceptive and
neuropathic pain without causing the adverse side effects
associated with CB.sub.1 receptor activation. Therefore, compounds
that selectively target CB.sub.2 receptors are an attractive
approach for the development of novel analgesics.
[0005] Pain is the most common symptom of disease and the most
frequent complaint with which patients present to physicians. Pain
is commonly segmented by duration (acute vs. chronic), intensity
(mild, moderate, and severe), and type (nociceptive vs.
neuropathic).
[0006] Nociceptive pain is the most well known type of pain, and is
caused by tissue injury detected by nociceptors at the site of
injury. After the injury, the site becomes a source of ongoing pain
and tenderness. This pain and tenderness are considered "acute"
nociceptive pain. This pain and tenderness gradually diminish as
healing progresses and disappear when healing is complete. Examples
of acute nociceptive pain include surgical procedures (post-op
pain) and bone fractures. Even though there may be no permanent
nerve damage, "chronic" nociceptive pain results from some
conditions when pain extends beyond six months. Examples of chronic
nociceptive pain include osteoarthritis, rheumatoid arthritis, and
musculoskeletal conditions (e.g., back pain), cancer pain, etc.
[0007] Neuropathic pain is defined as "pain initiated or caused by
a primary lesion or dysfunction in the nervous system" by the
International Association for the Study of Pain. Neuropathic pain
is not associated with nociceptive stimulation, although the
passage of nerve impulses that is ultimately perceived as pain by
the brain is the same in both nociceptive and neuropathic pain. The
term neuropathic pain encompasses a wide range of pain syndromes of
diverse etiologies. The three most commonly diagnosed pain types of
neuropathic nature are diabetic neuropathy, cancer neuropathy, and
HIV pain. In addition, neuropathic pain is diagnosed in patients
with a wide range of other disorders, including trigeminal
neuralgia, post-herpetic neuralgia, traumatic neuralgia, phantom
limb, as well as a number of other disorders of ill-defined or
unknown origin.
[0008] Managing the spectrum of pain etiologies remains a major
public health problem and both patients and clinicians are seeking
improved strategies to effectively manage pain. No currently
available therapies or drugs effectively treat all types of
nociceptive and neuropathic pain states. The compounds of the
present invention are novel CB.sub.2 receptor modulators that have
utility in treating pain, including nociceptive and neuropathic
pain.
[0009] The location of CB.sub.2 receptors on the surface of immune
cells suggests a role for these receptors in immunomodulation and
inflammation. Recent studies have demonstrated that CB.sub.2
receptor ligands have immunomodulatory and anti-inflammatory
properties. Therefore, compounds that selectively interact with
CB.sub.2 receptors offer a unique pharmacotherapy for the treatment
of immune and inflammatory disorders.
SUMMARY OF THE PRESENT INVENTION
[0010] In the principle embodiment, the present invention provides
compounds of Formula (I)
##STR00002##
[0011] or a pharmaceutically acceptable salt or prodrug thereof,
wherein
[0012] R.sub.1 is selected from the group consisting of
alkoxyalkyl, alkylcarbonyl, alkylcarbonylalkyl, alkylthioalkyl,
arylalkyl, arylalkylcarbonyl, azidoalkyl, cycloalkylalkyl,
cycloalkylalkylcarbonyl, haloalkyl, heteroarylalkyl,
heteroarylalkylcarbonyl, heterocyclealkyl,
heterocyclealkylcarbonyl, hydroxyalkyl, mercaptoalkyl,
(NR.sub.AR.sub.B)carbonylalkyl, (NR.sub.AR.sub.B)sulfonylalkyl,
(NR.sub.CR.sub.D)alkyl, -LOR.sub.2, -LSR.sub.2, -LS(O)R.sub.2, and
-LS(O).sub.2R.sub.2;
[0013] L is alkylene;
[0014] R.sub.2 is selected from the group consisting of alkyl,
alkylcarbonyl, aryl, arylalkyl, carboxyalkenylcarbonyl,
carboxyalkyl, carboxyalkylcarbonyl, cycloalkyl, cycloalkylalkyl,
haloalkyl, heteroaryl, heteroarylalkyl, heterocycle,
heterocyclealkyl, (NR.sub.AR.sub.B)carbonylalkenylcarbonyl,
(NR.sub.AR.sub.B)carbonylalkyl, and
(NR.sub.AR.sub.B)carbonylalkylcarbonyl;
[0015] R.sub.3 is selected from the group consisting of hydrogen,
alkoxyalkyl, alkyl, and haloalkyl;
[0016] R.sub.4 is selected from the group consisting of
cyclopropyl, cyclobutyl, cyclopentyl, cycloheptyl, and cyclooctyl,
wherein the cyclopropyl, cyclobutyl, and cyclopentyl are
substituted with 1, 2, 3, 4, 5, or 6 substituents selected from the
group consisting of alkenyl, alkoxy, alkoxyalkyl, alkoxycarbonyl,
alkoxycarbonylalkyl, alkoxysulfonyl, alkyl, alkylcarbonyl,
alkylcarbonylalkyl, alkylcarbonyloxy, alkylthio, alkylthioalkyl,
alkynyl, carboxy, carboxyalkyl, cyano, cyanoalkyl, haloalkoxy,
haloalkyl, halogen, hydroxy, hydroxyalkyl, mercapto, mercaptoalkyl,
oxo, --NR.sub.ER.sub.F, (NR.sub.ER.sub.F)alkyl,
(NR.sub.GR.sub.H)carbonyl, (NR.sub.GR.sub.H)carbonylalkyl,
(NR.sub.GR.sub.H)sulfonyl, and (NR.sub.GR.sub.H)sulfonylalkyl,
wherein the cycloheptyl and cyclooctyl are optionally substituted
with 1, 2, 3, 4, 5, or 6 substituents selected from the group
consisting of alkenyl, alkoxy, alkoxyalkyl, alkoxycarbonyl,
alkoxycarbonylalkyl, alkoxysulfonyl, alkyl, alkylcarbonyl,
alkylcarbonylalkyl, alkylcarbonyloxy, alkylthio, alkylthioalkyl,
alkynyl, carboxy, carboxyalkyl, cyano, cyanoalkyl, haloalkoxy,
haloalkyl, halogen, hydroxy, hydroxyalkyl, mercapto, mercaptoalkyl,
oxo, --NR.sub.ER.sub.F, (NR.sub.ER.sub.F)alkyl,
(NR.sub.GR.sub.H)carbonyl, (NR.sub.GR.sub.H)carbonylalkyl,
(NR.sub.GR.sub.H)sulfonyl, and (NR.sub.GR.sub.H)sulfonylalkyl;
[0017] R.sub.5, R.sub.6, R.sub.7, and R.sub.8 are independently
selected from the group consisting of hydrogen, alkenyl, alkoxy,
alkoxyalkyl, alkoxycarbonyl, alkoxycarbonylalkoxy,
alkoxycarbonylalkyl, alkoxysulfonyl, alkyl, alkylcarbonyl,
alkylcarbonylalkyl, alkylcarbonyloxy, alkylsulfinyl,
alkylsulfinylalkyl, alkylsulfonyl, alkylsulfonylalkyl,
alkylsulfonyloxy, alkylthio, alkylthioalkyl, alkynyl, aryl,
arylalkoxy, arylalkyl, arylalkylthio, arylcarbonyl, aryloxy,
aryloxyalkyl, arylthio, arylthioalkyl, carboxy, carboxyalkenyl,
carboxyalkenylcarbonyl, carboxyalkenylcarbonyloxy, carboxy,
carboxyalkyl, carboxyalkylcarbonyl, carboxyalkylcarbonyloxy, cyano,
cyanoalkyl, cycloalkyl, cycloalkylalkoxy, cycloalkylalkyl,
cycloalkylcarbonyl, cycloalkyloxy, cycloalkyloxyalkyl, haloalkoxy,
haloalkyl, halogen, heteroaryl, heteroarylalkoxy, heteroarylalkyl,
heteroaryloxy, heteroaryloxyalkyl, heterocycle, heterocyclealkoxy,
heterocyclealkoxycarbonyl, heterocyclealkyl, heterocycleoxy,
heterocycleoxyalkyl, hydroxy, hydroxyalkoxy, hydroxyalkyl,
mercapto, mercaptoalkyl, nitro, --NR.sub.JR.sub.K,
(NR.sub.JR.sub.K)alkoxy, (NR.sub.JR.sub.K)alkyl,
(NR.sub.MR.sub.N)carbonyl, (NR.sub.MR.sub.N)carbonylalkyl,
(NR.sub.MR.sub.N)sulfonyl, and (NR.sub.MR.sub.N)sulfonylalkyl;
[0018] R.sub.A, R.sub.B, R.sub.G, R.sub.H, R.sub.M, and R.sub.N are
independently selected from the group consisting of hydrogen,
alkenyl, alkoxyalkyl, alkoxycarbonylalkyl, alkyl, alkynyl, aryl,
arylalkyl, cycloalkyl, cycloalkylalkyl, heteroaryl,
heteroarylalkyl, heterocycle, heterocyclealkyl, and hydroxyalkyl;
and
[0019] R.sub.C, R.sub.D, R.sub.E, R.sub.F, R.sub.J, R.sub.K, are
independently selected from the group consisting of hydrogen,
alkenyl, alkoxyalkyl, alkoxycarbonyl, alkoxycarbonylalkyl, alkyl,
alkylcarbonyl, alkylsulfonyl, alkynyl, aryl, arylalkyl,
arylsulfonyl, arylalkylsulfonyl, cycloalkyl, cycloalkylalkyl,
cycloalkylsulfonyl, cycloalkylalkylsulfonyl, heteroaryl,
heteroarylalkyl, heteroarylsulfonyl, heteroarylalkylsulfonyl,
heterocycle, heterocyclealkyl, heterocyclesulfonyl, and
heterocyclealkylsulfonyl.
[0020] In another embodiment, the present invention provides a
pharmaceutical composition comprising a therapeutically effective
amount of a compound of Formula (I) or a pharmaceutically
acceptable salt thereof in combination with a pharmaceutically
acceptable carrier.
[0021] In another embodiment, the present invention provides a
method of treating pain in a mammal in need of such treatment
comprising administering to the mammal a therapeutically effective
amount of a compound of Formula (I) or a pharmaceutically
acceptable salt thereof.
[0022] In another embodiment, the present invention provides a
method of treating neuropathic pain in a mammal in need of such
treatment comprising administering to the mammal a therapeutically
effective amount of a compound of Formula (I) or a pharmaceutically
acceptable salt thereof.
[0023] In another embodiment, the present invention provides a
method of treating nociceptive pain in a mammal in need of such
treatment comprising administering to the mammal a therapeutically
effective amount of a compound of Formula (I) or a pharmaceutically
acceptable salt thereof.
[0024] In another embodiment, the present invention provides a
method of treating a disorder selected from the group consisting of
inflammatory disorders, immune disorders, neurological disorders,
cancers of the immune system, respiratory disorders, and
cardiovascular disorders in a mammal in need of such treatment
comprising administering to the mammal a therapeutically effective
amount of a compound of Formula (I) or a pharmaceutically
acceptable salt thereof.
[0025] In another embodiment, the present invention provides a
method of neuroprotection in a mammal in need of such treatment
comprising administering to the mammal a therapeutically effective
amount of a compound of Formula (I) or a pharmaceutically
acceptable salt thereof.
[0026] The present invention contemplates the use of a
therapeutically effective amount of a compound of Formula (I), or a
therapeutically acceptable salt thereof, to prepare a medicament
for treating nociceptive pain in a patient.
[0027] The present invention contemplates the use of a
therapeutically effective amount of a compound of Formula (I), or a
therapeutically acceptable salt thereof, to prepare a medicament
for treating neuropathic pain in a patient.
[0028] The present invention contemplates the use of a
therapeutically effective amount of a compound of Formula (I), or a
therapeutically acceptable salt thereof, to prepare a medicament
for treating inflammatory disorders, immune disorders, neurological
disorders, cancers of the immune system, respiratory disorders, or
cardiovascular disorders in a patient.
[0029] The present invention contemplates the use of a
therapeutically effective amount of a compound of Formula (I), or a
therapeutically acceptable salt thereof, to prepare a medicament
for providing neuroprotection in a patient.
DETAILED DESCRIPTION OF THE PRESENT INVENTION
##STR00003##
[0031] In one embodiment, the present invention provides compounds
of Formula (I) wherein R.sub.1 is selected from the group
consisting of alkoxyalkyl, alkylcarbonylalkyl, alkylthioalkyl,
arylalkyl, azidoalkyl, cycloalkylalkyl, haloalkyl, heteroarylalkyl,
heterocyclealkyl, heterocyclealkylcarbonyl, hydroxyalkyl,
mercaptoalkyl, (NR.sub.AR.sub.B)carbonylalkyl,
(NR.sub.AR.sub.B)sulfonylalkyl, (NR.sub.CR.sub.D)alkyl, and
-LOR.sub.2; L is alkylene; R.sub.2 is selected from the group
consisting of alkylcarbonyl, arylalkyl, and carboxyalkenylcarbonyl;
R.sub.3 is selected from the group consisting of hydrogen and alkyl
wherein the alkyl is methyl; R.sub.4 is selected from the group
consisting of cyclopropyl, cyclobutyl, cyclopentyl, and
cycloheptyl, wherein the cyclopropyl, cyclobutyl, and cyclopentyl
are substituted with 1, 2, 3, 4, 5, or 6 substituents selected from
the group consisting of alkyl and halogen; R.sub.5, R.sub.6,
R.sub.7, and R.sub.8 are independently selected from the group
consisting of hydrogen, alkoxy, alkoxyalkyl, alkoxycarbonyl,
alkoxycarbonylalkoxy, alkyl, alkylsulfonyl, arylalkoxy, carboxy,
carboxyalkenylcarbonyloxy, carboxy, carboxyalkylcarbonyloxy, cyano,
haloalkoxy, haloalkyl, halogen, heterocyclealkoxycarbonyl, hydroxy,
hydroxyalkoxy, hydroxyalkyl, nitro, --NR.sub.JR.sub.K,
(NR.sub.JR.sub.K)alkoxy, (NR.sub.JR.sub.K)alkyl, and
(NR.sub.MR.sub.N)carbonyl; R.sub.A, R.sub.B, R.sub.M, and R.sub.N
are independently selected from the group consisting of hydrogen,
alkoxycarbonylalkyl, alkyl, and hydroxyalkyl; and R.sub.C, R.sub.D,
R.sub.J, R.sub.K, are independently selected from the group
consisting of hydrogen, alkoxycarbonyl, alkyl, and
alkylsulfonyl.
[0032] In another embodiment, the present invention provides
compounds of Formula (I) wherein R.sub.3 is selected from the group
consisting of hydrogen and alkyl wherein the alkyl is methyl;
R.sub.4 is 2,2,3,3-tetramethylcyclopropyl and R.sub.1, R.sub.5,
R.sub.6, R.sub.7, and R.sub.8 are as defined in Formula (I).
[0033] In another embodiment, the present invention provides
compounds of Formula (I) wherein R.sub.1 is heterocyclealkyl;
R.sub.3 is selected from the group consisting of hydrogen and alkyl
wherein the alkyl is methyl; R.sub.4 is
2,2,3,3-tetramethylcyclopropyl; and R.sub.5, R.sub.6, R.sub.7, and
R.sub.8 are as defined in Formula (I).
[0034] In another embodiment, the present invention provides
compounds of Formula (I) wherein R.sub.1 is heterocyclealkyl
wherein the heterocyclealkyl is selected from the group consisting
of 2-(azepan-1-yl)ethyl, 2-(2,2,-dimethyl-1,3-dioxolan-4-yl)ethyl,
(1,3-dioxolan-4-yl)methyl, (tetrahydrofuran-3-yl)methyl,
(2R)-(tetrahydrofuran-2-yl)methyl,
(2S)-(tetrahydrofuran-2-yl)methyl, 2-(morpholin-4-yl)ethyl,
3-(morpholin-4-yl)propyl, 2-(2-oxo-1,3-oxazolidin-3-yl)ethyl,
(1-methylpiperidin-2-yl)methyl, (piperidin-2-yl)methyl,
2-(piperidin-1-yl)ethyl, 2-(pyrrolidin-1-yl)ethyl,
2-(2-oxopyrrolidin-1-yl)ethyl, 2-(2,5-dioxopyrrolidin-1-yl)ethyl,
2-(tetrahydro-2H-pyran-4-yl)ethyl,
(tetrahydro-2H-pyran-4-yl)methyl, (tetrahydro-2H-pyran-4-yl)methyl,
carboxy(tetrahydro-2H-pyran-4-yl)methyl,
2-ethoxy-2-oxo-1-tetrahydro-2H-pyran-4-ylethyl,
2-piperazin-1-ylethyl, and 4-methyl-2-piperazin-1-ylethyl; R.sub.3
is selected from the group consisting of hydrogen and alkyl wherein
the alkyl is methyl; R.sub.4 is 2,2,3,3-tetramethylcyclopropyl;
R.sub.5, R.sub.6, R.sub.7, and R.sub.8 are independently selected
from the group consisting of hydrogen, alkoxy, alkoxyalkyl,
alkoxycarbonyl, alkoxycarbonylalkoxy, alkylsulfonyl, arylalkoxy,
carboxy, carboxyalkenylcarbonyloxy, carboxyalkylcarbonyloxy, cyano,
haloalkoxy, haloalkyl, halogen, heterocyclealkoxycarbonyl, hydroxy,
hydroxyalkoxy, hydroxyalkyl, nitro, --NR.sub.JR.sub.K,
(NR.sub.JR.sub.K)alkoxy, (NR.sub.JR.sub.K)alkyl, and
(NR.sub.MR.sub.N)carbonyl; R.sub.J and R.sub.K are independently
selected from the group consisting of hydrogen, alkoxycarbonyl,
alkyl, and alkylsulfonyl; and R.sub.M and R.sub.N are independently
selected from the group consisting of hydrogen,
alkoxycarbonylalkyl, alkyl, and hydroxyalkyl.
[0035] In another embodiment, the present invention provides
compounds of Formula (I) wherein R.sub.1 is heterocyclealkyl
wherein the heterocyclealkyl is selected from the group consisting
of 2-(azepan-1-yl)ethyl, 2-(2,2,-dimethyl-1,3-dioxolan-4-yl)ethyl,
(1,3-dioxolan-4-yl) methyl, (tetrahydrofuran-3-yl) methyl,
(2R)-(tetrahydrofuran-2-yl)methyl,
(2S)-(tetrahydrofuran-2-yl)methyl, 2-(morpholin-4-yl)ethyl,
3-(morpholin-4-yl)propyl, 2-(2-oxo-1,3-oxazolidin-3-yl)ethyl,
(1-methylpiperidin-2-yl)methyl, (piperidin-2-yl)methyl,
2-(piperidin-1-yl)ethyl, 2-(pyrrolidin-1-yl)ethyl,
2-(2-oxopyrrolidin-1-yl)ethyl, 2-(2,5-dioxopyrrolidin-1-yl)ethyl,
2-(tetrahydro-2H-pyran-4-yl)ethyl,
(tetrahydro-2H-pyran-4-yl)methyl, (tetrahydro-2H-pyran-4-yl)methyl,
carboxy(tetrahydro-2H-pyran-4-yl)methyl,
2-ethoxy-2-oxo-1-tetrahydro-2H-pyran-4-ylethyl,
2-piperazin-1-ylethyl, and 4-methyl-2-piperazin-1-ylethyl; R.sub.3
is selected from the group consisting of hydrogen and alkyl wherein
the alkyl is methyl; R.sub.4 is 2,2,3,3-tetramethylcyclopropyl; and
R.sub.5, R.sub.6, R.sub.7, and R.sub.8 are each hydrogen.
[0036] In another embodiment, the present invention provides
compounds of Formula (I) wherein R.sub.1 is heteroarylalkyl;
R.sub.3 is selected from the group consisting of hydrogen and alkyl
wherein the alkyl is methyl; R.sub.4 is
2,2,3,3-tetramethylcyclopropyl; R.sub.5, R.sub.6, R.sub.7, and
R.sub.8 are as defined in Formula (I).
[0037] In another embodiment, the present invention provides
compounds of Formula (I) wherein R.sub.1 is heteroarylalkyl wherein
the heteroarylalkyl is selected from the group consisting of
(1,3-benzothiazol-2-yl)methyl, (1H-imidazolyl-2-yl)methyl,
(1-methyl-1H-imidazolyl-2-yl)methyl, 2-pyridin-2-ylethyl,
2-pyridin-3-ylethyl, 2-pyridin-4-ylethyl, 2-(1H-pyrrol-1-yl)ethyl,
(5-chloro-1,2,4-thiadiazol-3-yl)methyl,
(1,2,4-thiadiazol-3-yl)methyl, 2-(4-methyl-1,3-thiazol-5-yl)ethyl,
2-(1,3-thiazol-5-yl)ethyl, 2-thien-2-ylethyl, and
2-thien-3-ylethyl; R.sub.3 is selected from the group consisting of
hydrogen and alkyl wherein the alkyl is methyl; R.sub.4 is
2,2,3,3-tetramethylcyclopropyl; R.sub.5, R.sub.6, R.sub.7, and
R.sub.8 are independently selected from the group consisting of
hydrogen, alkoxy, alkoxyalkyl, alkoxycarbonyl,
alkoxycarbonylalkoxy, alkylsulfonyl, arylalkoxy, carboxy,
carboxyalkenylcarbonyloxy, carboxyalkylcarbonyloxy, cyano,
haloalkoxy, haloalkyl, halogen, heterocyclealkoxycarbonyl, hydroxy,
hydroxyalkoxy, hydroxyalkyl, nitro, --NR.sub.JR.sub.K,
(NR.sub.JR.sub.K)alkoxy, (NR.sub.JR.sub.K)alkyl, and
(NR.sub.MR.sub.N)carbonyl; R.sub.J and R.sub.K are independently
selected from the group consisting of hydrogen, alkoxycarbonyl,
alkyl, and alkylsulfonyl; and R.sub.M and R.sub.N are independently
selected from the group consisting of hydrogen,
alkoxycarbonylalkyl, alkyl, and hydroxyalkyl.
[0038] In another embodiment, the present invention provides
compounds of Formula (I) wherein R.sub.1 is heteroarylalkyl wherein
the heteroarylalkyl is selected from the group consisting of
(1,3-benzothiazol-2-yl)methyl, (1H-imidazolyl-2-yl)methyl,
(1-methyl-1H-imidazolyl-2-yl)methyl, 2-pyridin-2-ylethyl,
2-pyridin-3-ylethyl, 2-pyridin-4-ylethyl, 2-(1H-pyrrol-1-yl)ethyl,
(5-chloro-1,2,4-thiadiazol-3-yl)methyl,
(1,2,4-thiadiazol-3-yl)methyl, 2-(4-methyl-1,3-thiazol-5-yl)ethyl,
2-(1,3-thiazol-5-yl)ethyl, 2-thien-2-ylethyl, and
2-thien-3-ylethyl; R.sub.3 is selected from the group consisting of
hydrogen and alkyl wherein the alkyl is methyl; R.sub.4 is
2,2,3,3-tetramethylcyclopropyl; and R.sub.5, R.sub.6, R.sub.7, and
R.sub.8 are each hydrogen.
[0039] In another embodiment, the present invention provides
compounds of Formula (I) wherein R.sub.1 is arylalkyl; R.sub.3 is
selected from the group consisting of hydrogen and alkyl wherein
the alkyl is methyl; R.sub.4 is 2,2,3,3-tetramethylcyclopropyl; and
R.sub.5, R.sub.6, R.sub.7, and R.sub.8 are as defined in Formula
(I).
[0040] In another embodiment, the present invention provides
compounds of Formula (I) wherein R.sub.1 is arylalkyl wherein the
arylalkyl is selected from the group consisting of
(1,3-benzodioxol-5-yl)methyl,
(2,3-dihydro-1,4-benzodioxin-6-yl)methyl, 4-(acetyloxy)benzyl,
benzyl, 2-phenylethyl, 3-phenylpropyl, 3-methoxybenzyl,
4-methoxybenzyl, and 4-hydroxybenzyl; R.sub.3 is selected from the
group consisting of hydrogen and alkyl wherein the alkyl is methyl;
R.sub.4 is 2,2,3,3-tetramethylcyclopropyl; R.sub.5, R.sub.6,
R.sub.7, and R.sub.8 are independently selected from the group
consisting of hydrogen, alkoxy, alkoxyalkyl, alkoxycarbonyl,
alkoxycarbonylalkoxy, alkylsulfonyl, arylalkoxy, carboxy,
carboxyalkenylcarbonyloxy, carboxyalkylcarbonyloxy, cyano,
haloalkoxy, haloalkyl, halogen, heterocyclealkoxycarbonyl, hydroxy,
hydroxyalkoxy, hydroxyalkyl, nitro, --NR.sub.JR.sub.K,
(NR.sub.JR.sub.K)alkoxy, (NR.sub.JR.sub.K)alkyl, and
(NR.sub.MR.sub.N)carbonyl; R.sub.J and R.sub.K are independently
selected from the group consisting of hydrogen, alkoxycarbonyl,
alkyl, and alkylsulfonyl; and R.sub.M and R.sub.N are independently
selected from the group consisting of hydrogen,
alkoxycarbonylalkyl, alkyl, and hydroxyalkyl.
[0041] In another embodiment, the present invention provides
compounds of Formula (I) wherein R.sub.1 is arylalkyl wherein the
arylalkyl is selected from the group consisting of
(1,3-benzodioxol-5-yl)methyl,
(2,3-dihydro-1,4-benzodioxin-6-yl)methyl, 4-(acetyloxy)benzyl,
benzyl, 2-phenylethyl, 3-phenylpropyl, 3-methoxybenzyl,
4-methoxybenzyl, and 4-hydroxybenzyl; R.sub.3 is selected from the
group consisting of hydrogen and alkyl wherein the alkyl is methyl;
R.sub.4 is 2,2,3,3-tetramethylcyclopropyl; and R.sub.5, R.sub.6,
R.sub.7, and R.sub.8 are each hydrogen.
[0042] In another embodiment, the present invention provides
compounds of Formula (I) wherein R.sub.1 is selected from the group
consisting of alkoxyalkyl, alkylcarbonylalkyl, alkylthioalkyl,
azidoalkyl, cycloalkylalkyl, haloalkyl, heterocyclealkylcarbonyl,
mercaptoalkyl, (NR.sub.AR.sub.B)carbonylalkyl,
(NR.sub.AR.sub.B)sulfonylalkyl, (NR.sub.AR.sub.B)sulfonylalkyl, and
(NR.sub.CR.sub.D)alkyl; R.sub.3 is selected from the group
consisting of hydrogen and alkyl wherein the alkyl is methyl;
R.sub.4 is 2,2,3,3-tetramethylcyclopropyl; R.sub.A and R.sub.B are
independently selected from the group consisting of hydrogen,
alkoxycarbonylalkyl, alkyl, and hydroxyalkyl; R.sub.C and R.sub.D
are independently selected from the group consisting of hydrogen,
alkoxycarbonyl, alkyl, and alkylsulfonyl; and R.sub.5, R.sub.6,
R.sub.7, and R.sub.8 are as defined in Formula (I).
[0043] In another embodiment, the present invention provides
compounds of Formula (I) wherein R.sub.1 is selected from the group
consisting of alkoxyalkyl, alkylcarbonylalkyl, alkylthioalkyl,
azidoalkyl, cycloalkylalkyl, haloalkyl, heterocyclealkylcarbonyl,
mercaptoalkyl, (NR.sub.AR.sub.B)carbonylalkyl,
(NR.sub.AR.sub.B)sulfonylalkyl, (NR.sub.AR.sub.B)sulfonylalkyl, and
(NR.sub.CR.sub.D)alkyl; R.sub.3 is selected from the group
consisting of hydrogen and alkyl wherein the alkyl is methyl;
R.sub.4 is 2,2,3,3-tetramethylcyclopropyl; R.sub.A and R.sub.B are
independently selected from the group consisting of hydrogen,
alkoxycarbonylalkyl, alkyl, and hydroxyalkyl; R.sub.CC and R.sub.D
are independently selected from the group consisting of hydrogen,
alkoxycarbonyl, alkyl, and alkylsulfonyl; R.sub.5, R.sub.6,
R.sub.7, and R.sub.8 are independently selected from the group
consisting of hydrogen, alkoxy, alkoxyalkyl, alkoxycarbonyl,
alkoxycarbonylalkoxy, alkylsulfonyl, arylalkoxy, carboxy,
carboxyalkenylcarbonyloxy, carboxyalkylcarbonyloxy, cyano,
haloalkoxy, haloalkyl, halogen, heterocyclealkoxycarbonyl, hydroxy,
hydroxyalkoxy, hydroxyalkyl, nitro, --NR.sub.JR.sub.K,
(NR.sub.JR.sub.K)alkoxy, (NR.sub.JR.sub.K)alkyl, and
(NR.sub.MR.sub.N)carbonyl; R.sub.J and R.sub.K are independently
selected from the group consisting of hydrogen, alkoxycarbonyl,
alkyl, and alkylsulfonyl; and R.sub.M and R.sub.N are independently
selected from the group consisting of hydrogen,
alkoxycarbonylalkyl, alkyl, and hydroxyalkyl.
[0044] In another embodiment, the present invention provides
compounds of Formula (I) wherein R.sub.1 is selected from the group
consisting of alkoxyalkyl, alkylcarbonylalkyl, alkylthioalkyl,
azidoalkyl, cycloalkylalkyl, haloalkyl, heterocyclealkylcarbonyl,
mercaptoalkyl, (NR.sub.AR.sub.B)carbonylalkyl,
(NR.sub.AR.sub.B)sulfonylalkyl, (NR.sub.AR.sub.B)sulfonylalkyl, and
(NR.sub.CR.sub.D)alkyl; R.sub.3 is selected from the group
consisting of hydrogen and alkyl wherein the alkyl is methyl;
R.sub.4 is 2,2,3,3-tetramethylcyclopropyl; R.sub.A and R.sub.B are
independently selected from the group consisting of hydrogen,
alkoxycarbonylalkyl, alkyl, and hydroxyalkyl; and R.sub.C and
R.sub.D are independently selected from the group consisting of
hydrogen, alkoxycarbonyl, alkyl, and alkylsulfonyl.
[0045] In another embodiment, the present invention provides
compounds of Formula (I) wherein R.sub.1 is -LOR.sub.2; L is
alkylene; R.sub.2 is selected from the group consisting of
alkylcarbonyl, arylalkyl, and carboxyalkenylcarbonyl; R.sub.3 is
selected from the group consisting of hydrogen and alkyl wherein
the alkyl is methyl; R.sub.4 is 2,2,3,3-tetramethylcyclopropyl; and
R.sub.5, R.sub.6, R.sub.7, and R.sub.8 are as defined in Formula
(I).
[0046] In another embodiment, the present invention provides
compounds of Formula (I) wherein R.sub.1 is -LOR.sub.2; L is
alkylene; R.sub.2 is selected from the group consisting of
alkylcarbonyl, arylalkyl, and carboxyalkenylcarbonyl; R.sub.3 is
selected from the group consisting of hydrogen and alkyl wherein
the alkyl is methyl; R.sub.4 is 2,2,3,3-tetramethylcyclopropyl;
R.sub.5, R.sub.6, R.sub.7, and R.sub.8 are independently selected
from the group consisting of hydrogen, alkoxy, alkoxyalkyl,
alkoxycarbonyl, alkoxycarbonylalkoxy, alkylsulfonyl, arylalkoxy,
carboxy, carboxyalkenylcarbonyloxy, carboxyalkylcarbonyloxy, cyano,
haloalkoxy, haloalkyl, halogen, heterocyclealkoxycarbonyl, hydroxy,
hydroxyalkoxy, hydroxyalkyl, nitro, --NR.sub.JR.sub.K,
(NR.sub.JR.sub.K)alkoxy, (NR.sub.JR.sub.K)alkyl, and
(NR.sub.MR.sub.N)carbonyl; R.sub.J and R.sub.K are independently
selected from the group consisting of hydrogen, alkoxycarbonyl,
alkyl, and alkylsulfonyl; and R.sub.M and R.sub.N are independently
selected from the group consisting of hydrogen,
alkoxycarbonylalkyl, alkyl, and hydroxyalkyl.
[0047] In another embodiment, the present invention provides
compounds of Formula (I) wherein R.sub.1 is -LOR.sub.2; L is
alkylene; R.sub.2 is selected from the group consisting of
alkylcarbonyl, arylalkyl, and carboxyalkenylcarbonyl; R.sub.3 is
selected from the group consisting of hydrogen and alkyl wherein
the alkyl is methyl; R.sub.4 is 2,2,3,3-tetramethylcyclopropyl; and
R.sub.5, R.sub.6, R.sub.7, and R.sub.8 are each hydrogen.
[0048] In another embodiment, the present invention provides
compounds of Formula (I) wherein R.sub.1 is hydroxyalkyl; R.sub.3
is selected from the group consisting of hydrogen and alkyl wherein
the alkyl is methyl; R.sub.4 is 2,2,3,3-tetramethylcyclopropyl; and
R.sub.5, R.sub.6, R.sub.7, and R.sub.8 are as defined in Formula
(I).
[0049] In another embodiment, the present invention provides
compounds of Formula (I) wherein R.sub.1 is hydroxyalkyl; R.sub.3
is selected from the group consisting of hydrogen and alkyl wherein
the alkyl is methyl; R.sub.4 is 2,2,3,3-tetramethylcyclopropyl;
R.sub.5, R.sub.6, R.sub.7, and R.sub.8 are independently selected
from the group consisting of hydrogen, alkoxy, alkoxyalkyl,
alkoxycarbonyl, alkoxycarbonylalkoxy, alkylsulfonyl, arylalkoxy,
carboxy, carboxyalkenylcarbonyloxy, carboxyalkylcarbonyloxy, cyano,
haloalkoxy, haloalkyl, halogen, heterocyclealkoxycarbonyl, hydroxy,
hydroxyalkoxy, hydroxyalkyl, nitro, --NR.sub.JR.sub.K,
(NR.sub.JR.sub.K)alkoxy, (NR.sub.JR.sub.K)alkyl, and
(NR.sub.MR.sub.N)carbonyl; R.sub.J and R.sub.K are independently
selected from the group consisting of hydrogen, alkoxycarbonyl,
alkyl, and alkylsulfonyl; and R.sub.M and R.sub.N are independently
selected from the group consisting of hydrogen,
alkoxycarbonylalkyl, alkyl, and hydroxyalkyl.
[0050] In another embodiment, the present invention provides
compounds of Formula (I) wherein R.sub.1 is hydroxyalkyl; R.sub.3
is selected from the group consisting of hydrogen and alkyl wherein
the alkyl is methyl; R.sub.4 is 2,2,3,3-tetramethylcyclopropyl; and
R.sub.5, R.sub.6, R.sub.7, and R.sub.8 are each hydrogen.
[0051] In another embodiment, the present invention provides
compounds of Formula (I) wherein R.sub.1 is alkylthioalkyl; R.sub.3
is selected from the group consisting of hydrogen and alkyl wherein
the alkyl is methyl; R.sub.4 is 2,2,3,3-tetramethylcyclopropyl; and
R.sub.5, R.sub.6, R.sub.7, and R.sub.8 are as defined in Formula
(I).
[0052] In another embodiment, the present invention provides
compounds of Formula (I) wherein R.sub.1 is alkylthioalkyl; R.sub.3
is selected from the group consisting of hydrogen and alkyl wherein
the alkyl is methyl; R.sub.4 is 2,2,3,3-tetramethylcyclopropyl;
R.sub.5, R.sub.6, R.sub.7, and R.sub.8 are independently selected
from the group consisting of hydrogen, alkoxy, alkoxyalkyl,
alkoxycarbonyl, alkoxycarbonylalkoxy, alkylsulfonyl, arylalkoxy,
carboxy, carboxyalkenylcarbonyloxy, carboxyalkylcarbonyloxy, cyano,
haloalkoxy, haloalkyl, halogen, heterocyclealkoxycarbonyl, hydroxy,
hydroxyalkoxy, hydroxyalkyl, nitro, --NR.sub.JR.sub.K,
(NR.sub.JR.sub.K)alkoxy, (NR.sub.JR.sub.K)alkyl, and
(NR.sub.MR.sub.N)carbonyl; R.sub.J and R.sub.K are independently
selected from the group consisting of hydrogen, alkoxycarbonyl,
alkyl, and alkylsulfonyl; and R.sub.M and R.sub.N are independently
selected from the group consisting of hydrogen,
alkoxycarbonylalkyl, alkyl, and hydroxyalkyl.
[0053] In another embodiment, the present invention provides
compounds of Formula (I) wherein R.sub.1 is alkylthioalkyl; R.sub.3
is selected from the group consisting of hydrogen and alkyl wherein
the alkyl is methyl; R.sub.4 is 2,2,3,3-tetramethylcyclopropyl; and
R.sub.5, R.sub.6, R.sub.7, and R.sub.8 are each hydrogen.
[0054] In another embodiment, the present invention provides
compounds of Formula (I) wherein R.sub.1 is heterocyclealkyl;
R.sub.3 is selected from the group consisting of hydrogen and alkyl
wherein the alkyl is methyl; R.sub.4 is
2,2,3,3-tetrafluoro-1-methylcyclobutyl; and R.sub.5, R.sub.6,
R.sub.7, and R.sub.8 are as defined in Formula (I).
[0055] In another embodiment, the present invention provides
compounds of Formula (I) wherein R.sub.1 is heterocyclealkyl
wherein the heterocyclealkyl is selected from the group consisting
of 2-(azepan-1-yl)ethyl, 2-(2,2,-dimethyl-1,3-dioxolan-4-yl)ethyl,
(1,3-dioxolan-4-yl)methyl, (tetrahydrofuran-3-yl)methyl,
(2R)-(tetrahydrofuran-2-yl)methyl,
(2S)-(tetrahydrofuran-2-yl)methyl, 2-(morpholin-4-yl)ethyl,
3-(morpholin-4-yl)propyl, 2-(2-oxo-1,3-oxazolidin-3-yl)ethyl,
(1-methylpiperidin-2-yl)methyl, (piperidin-2-yl)methyl,
2-(piperidin-1-yl)ethyl, 2-(pyrrolidin-1-yl)ethyl,
2-(2-oxopyrrolidin-1-yl)ethyl, 2-(2,5-dioxopyrrolidin-1-yl)ethyl,
2-(tetrahydro-2H-pyran-4-yl)ethyl,
(tetrahydro-2H-pyran-4-yl)methyl, (tetrahydro-2H-pyran-4-yl)methyl,
carboxy(tetrahydro-2H-pyran-4-yl)methyl,
2-ethoxy-2-oxo-1-tetrahydro-2H-pyran-4-ylethyl,
2-piperazin-1-ylethyl, and 4-methyl-2-piperazin-1-ylethyl; R.sub.3
is selected from the group consisting of hydrogen and alkyl wherein
the alkyl is methyl; R.sub.4 is
2,2,3,3-tetrafluoro-1-methylcyclobutyl; R.sub.5, R.sub.6, R.sub.7,
and R.sub.8 are independently selected from the group consisting of
hydrogen, alkoxy, alkoxyalkyl, alkoxycarbonyl,
alkoxycarbonylalkoxy, alkylsulfonyl, arylalkoxy, carboxy,
carboxyalkenylcarbonyloxy, carboxyalkylcarbonyloxy, cyano,
haloalkoxy, haloalkyl, halogen, heterocyclealkoxycarbonyl, hydroxy,
hydroxyalkoxy, hydroxyalkyl, nitro, --NR.sub.JR.sub.K,
(NR.sub.JR.sub.K)alkoxy, (NR.sub.JR.sub.K)alkyl, and
(NR.sub.MR.sub.N)carbonyl; R.sub.J and R.sub.K are independently
selected from the group consisting of hydrogen, alkoxycarbonyl,
alkyl, and alkylsulfonyl; and R.sub.M and R.sub.N are independently
selected from the group consisting of hydrogen,
alkoxycarbonylalkyl, alkyl, and hydroxyalkyl.
[0056] In another embodiment, the present invention provides
compounds of Formula (I) wherein R.sub.1 is heterocyclealkyl
wherein the heterocyclealkyl is selected from the group consisting
of 2-(azepan-1-yl)ethyl, 2-(2,2,-dimethyl-1,3-dioxolan-4-yl)ethyl,
(1,3-dioxolan-4-yl)methyl, (tetrahydrofuran-3-yl)methyl,
(2R)-(tetrahydrofuran-2-yl)methyl,
(2S)-(tetrahydrofuran-2-yl)methyl, 2-(morpholin-4-yl)ethyl,
3-(morpholin-4-yl)propyl, 2-(2-oxo-1,3-oxazolidin-3-yl)ethyl,
(1-methylpiperidin-2-yl)methyl, (piperidin-2-yl)methyl,
2-(piperidin-1-yl)ethyl, 2-(pyrrolidin-1-yl)ethyl,
2-(2-oxopyrrolidin-1-yl)ethyl, 2-(2,5-dioxopyrrolidin-1-yl)ethyl,
2-(tetrahydro-2H-pyran-4-yl)ethyl,
(tetrahydro-2H-pyran-4-yl)methyl, (tetrahydro-2H-pyran-4-yl)methyl,
carboxy(tetrahydro-2H-pyran-4-yl)methyl,
2-ethoxy-2-oxo-1-tetrahydro-2H-pyran-4-ylethyl,
2-piperazin-1-ylethyl, and 4-methyl-2-piperazin-1-ylethyl; R.sub.3
is selected from the group consisting of hydrogen and alkyl wherein
the alkyl is methyl; R.sub.4 is
2,2,3,3-tetrafluoro-1-methylcyclobutyl; and R.sub.5, R.sub.6,
R.sub.7, and R.sub.8 are each hydrogen.
[0057] In another embodiment, the present invention provides
compounds of Formula (I) wherein R.sub.1 is heterocyclealkyl;
R.sub.3 is selected from the group consisting of hydrogen and alkyl
wherein the alkyl is methyl; R.sub.4 is cycloheptyl; and R.sub.5,
R.sub.6, R.sub.7, and R.sub.8 are as defined in Formula (I).
[0058] In another embodiment, the present invention provides
compounds of Formula (I) wherein R.sub.1 is heterocyclealkyl
wherein the heterocyclealkyl is selected from the group consisting
of 2-(azepan-1-yl)ethyl, 2-(2,2,-dimethyl-1,3-dioxolan-4-yl)ethyl,
(1,3-dioxolan-4-yl)methyl, (tetrahydrofuran-3-yl)methyl,
(2R)-(tetrahydrofuran-2-yl)methyl,
(2S)-(tetrahydrofuran-2-yl)methyl, 2-(morpholin-4-yl)ethyl,
3-(morpholin-4-yl)propyl, 2-(2-oxo-1,3-oxazolidin-3-yl)ethyl,
(1-methylpiperidin-2-yl)methyl, (piperidin-2-yl)methyl,
2-(piperidin-1-yl)ethyl, 2-(pyrrolidin-1-yl)ethyl,
2-(2-oxopyrrolidin-1-yl)ethyl, 2-(2,5-dioxopyrrolidin-1-yl)ethyl,
2-(tetrahydro-2H-pyran-4-yl)ethyl,
(tetrahydro-2H-pyran-4-yl)methyl, (tetrahydro-2H-pyran-4-yl)methyl,
carboxy(tetrahydro-2H-pyran-4-yl)methyl,
2-ethoxy-2-oxo-1-tetrahydro-2H-pyran-4-ylethyl,
2-piperazin-1-ylethyl, and 4-methyl-2-piperazin-1-ylethyl; R.sub.3
is selected from the group consisting of hydrogen and alkyl wherein
the alkyl is methyl; R.sub.4 is cycloheptyl; R.sub.5, R.sub.6,
R.sub.7, and R.sub.8 are independently selected from the group
consisting of hydrogen, alkoxy, alkoxyalkyl, alkoxycarbonyl,
alkoxycarbonylalkoxy, alkylsulfonyl, arylalkoxy, carboxy,
carboxyalkenylcarbonyloxy, carboxyalkylcarbonyloxy, cyano,
haloalkoxy, haloalkyl, halogen, heterocyclealkoxycarbonyl, hydroxy,
hydroxyalkoxy, hydroxyalkyl, nitro, --NR.sub.JR.sub.K,
(NR.sub.JR.sub.K)alkoxy, (NR.sub.JR.sub.K)alkyl, and
(NR.sub.MR.sub.N)carbonyl; R.sub.J and R.sub.K are independently
selected from the group consisting of hydrogen, alkoxycarbonyl,
alkyl, and alkylsulfonyl; and R.sub.M and R.sub.N are independently
selected from the group consisting of hydrogen,
alkoxycarbonylalkyl, alkyl, and hydroxyalkyl.
[0059] In another embodiment, the present invention provides
compounds of Formula (I) wherein R.sub.1 is heterocyclealkyl
wherein the heterocyclealkyl is selected from the group consisting
of 2-(azepan-1-yl)ethyl, 2-(2,2,-dimethyl-1,3-dioxolan-4-yl)ethyl,
(1,3-dioxolan-4-yl)methyl, (tetrahydrofuran-3-yl)methyl,
(2R)-(tetrahydrofuran-2-yl)methyl,
(2S)-(tetrahydrofuran-2-yl)methyl, 2-(morpholin-4-yl)ethyl,
3-(morpholin-4-yl)propyl, 2-(2-oxo-1,3-oxazolidin-3-yl)ethyl,
(1-methylpiperidin-2-yl)methyl, (piperidin-2-yl)methyl,
2-(piperidin-1-yl)ethyl, 2-(pyrrolidin-1-yl)ethyl,
2-(2-oxopyrrolidin-1-yl)ethyl, 2-(2,5-dioxopyrrolidin-1-yl)ethyl,
2-(tetrahydro-2H-pyran-4-yl)ethyl,
(tetrahydro-2H-pyran-4-yl)methyl, (tetrahydro-2H-pyran-4-yl)methyl,
carboxy(tetrahydro-2H-pyran-4-yl)methyl,
2-ethoxy-2-oxo-1-tetrahydro-2H-pyran-4-ylethyl,
2-piperazin-1-ylethyl, and 4-methyl-2-piperazin-1-ylethyl; R.sub.3
is selected from the group consisting of hydrogen and alkyl wherein
the alkyl is methyl; R.sub.4 is cycloheptyl; and R.sub.5, R.sub.6,
R.sub.7, and R.sub.8 are each hydrogen.
Definition of Terms
[0060] All patents, patent applications, and literature references
cited in the specification are herein incorporated by reference in
their entirety. In the case of inconsistencies, the present
disclosure, including definitions, will prevail.
[0061] As used throughout this specification and the appended
claims, the following terms have the following meanings:
[0062] The term "alkenyl" as used herein, means a straight or
branched chain hydrocarbon containing from 2 to 10 carbons and
containing at least one carbon-carbon double bond formed by the
removal of two hydrogens. Representative examples of alkenyl
include, but are not limited to, ethenyl, 2-propenyl,
2-methyl-2-propenyl, 3-butenyl, 4-pentenyl, 5-hexenyl, 2-heptenyl,
2-methyl-1-heptenyl, and 3-decenyl.
[0063] The term "alkoxy" as used herein, means an alkyl group, as
defined herein, appended to the parent molecular moiety through an
oxygen atom. Representative examples of alkoxy include, but are not
limited to, methoxy, ethoxy, propoxy, 2-propoxy, butoxy,
tert-butoxy, pentyloxy, and hexyloxy.
[0064] The term "alkoxyalkoxy" as used herein, means an alkoxy
group, as defined herein, appended to the parent molecular moiety
through another alkoxy group, as defined herein. Representative
examples of alkoxyalkoxy include, but are not limited to,
tert-butoxymethoxy, 2-ethoxyethoxy, 2-methoxyethoxy, and
methoxymethoxy.
[0065] The term "alkoxyalkyl" as used herein, means an alkoxy
group, as defined herein, appended to the parent molecular moiety
through an alkyl group, as defined herein except for R.sub.1 in
Formula (I) wherein the alkoxy group is at least two carbons from
the indole nitrogen. Representative examples of alkoxyalkyl
include, but are not limited to, tert-butoxymethyl, 2-ethoxyethyl,
2-methoxyethyl, methoxymethyl, 3-methoxypropyl, 4-methoxybutyl, and
5-methoxypentyl.
[0066] The term "alkoxycarbonyl" as used herein, means an alkoxy
group, as defined herein, appended to the parent molecular moiety
through a carbonyl group, as defined herein. Representative
examples of alkoxycarbonyl include, but are not limited to,
methoxycarbonyl, ethoxycarbonyl, and tert-butoxycarbonyl.
[0067] The term "alkoxycarbonylalkoxy" as used herein, means an
alkoxycarbonyl group, as defined herein, appended to the parent
molecular moiety through an alkoxy group, as defined herein.
Representative examples of alkoxycarbonylalkoxy include, but are
not limited to, 3-ethoxy-3-oxopropoxy, 3-methoxy-3-oxopropoxy,
4-ethoxy-4-oxobutoxy, 5-methoxy-5-oxopentyloxy,
5-ethoxy-5-oxopentyloxy, 6-ethoxy-6-oxohexyloxy.
[0068] The term "alkoxycarbonylalkyl" as used herein, means an
alkoxycarbonyl group, as defined herein, appended to the parent
molecular moiety through an alkyl group, as defined herein.
Representative examples of alkoxycarbonylalkyl include, but are not
limited to, 3-ethoxy-3-oxopropyl, 3-methoxy-3-oxopropyl,
4-ethoxy-4-oxobutyl, 5-methoxy-5-oxopentyl, 5-ethoxy-5-oxopentyl,
6-ethoxy-6-oxohexyl.
[0069] The term "alkoxysulfonyl" as used herein, means an alkoxy
group, as defined herein, appended to the parent molecular moiety
through a sulfonyl group, as defined herein. Representative
examples of alkoxysulfonyl include, but are not limited to,
methoxysulfonyl, ethoxysulfonyl, and propoxysulfonyl.
[0070] The term "alkyl" as used herein, means a straight or
branched chain hydrocarbon containing from 1 to 10 carbon atoms.
Representative examples of alkyl include, but are not limited to,
methyl, ethyl, n-propyl, iso-propyl, n-butyl, sec-butyl, iso-butyl,
tert-butyl, n-pentyl, isopentyl, neopentyl, n-hexyl, 3-methylhexyl,
2,2-dimethylpentyl, 2,3-dimethylpentyl, n-heptyl, n-octyl, n-nonyl,
and n-decyl.
[0071] The term "alkylcarbonyl" as used herein, means an alkyl
group, as defined herein, appended to the parent molecular moiety
through a carbonyl group, as defined herein. Representative
examples of alkylcarbonyl include, but are not limited to, acetyl,
1-oxopropyl, 2,2-dimethyl-1-oxopropyl, 1-oxobutyl, and
1-oxopentyl.
[0072] The term "alkylcarbonylalkyl" as used herein, means an
alkylcarbonyl group, as defined herein, appended to the parent
molecular moiety through an alkyl group, as defined herein.
Representative examples of alkylcarbonylalkyl include, but are not
limited to, 2-oxopropyl, 3,3-dimethyl-2-oxopropyl, 3-oxobutyl,
3-oxopentyl, and 5-oxohexyl.
[0073] The term "alkylcarbonyloxy" as used herein, means an
alkylcarbonyl group, as defined herein, appended to the parent
molecular moiety through an oxygen atom. Representative examples of
alkylcarbonyloxy include, but are not limited to, acetyloxy,
ethylcarbonyloxy, and tert-butylcarbonyloxy.
[0074] The term "alkylene" means a divalent alkyl group derived
from a straight or branched chain hydrocarbon of from 2 to 10
carbon atoms. Representative examples of alkylene include, but are
not limited to, --CH.sub.2CH.sub.2--, --CH.sub.2CH.sub.2CH.sub.2--,
--CH.sub.2CH(-)CH.sub.3, --CH.sub.2CH.sub.2CH.sub.2CH.sub.2--,
--CH.sub.2CH(CH.sub.3)CH.sub.2--,
--CH.sub.2C(CH.sub.3).sub.2CH.sub.2--,
--CH.sub.2CH.sub.2CH.sub.2CH.sub.2CH.sub.2--,
--CH.sub.2CH.sub.2CH(-)CH.sub.2CH.sub.3,
--CH.sub.2CH.sub.2CH.sub.2CH.sub.2CH.sub.2CH.sub.2--,
--CH.sub.2CH.sub.2CH.sub.2CH.sub.2CH.sub.2CH.sub.2CH.sub.2--,
--CH.sub.2CH.sub.2CH.sub.2CH(-)CH.sub.2CH.sub.2CH.sub.3--,
--CH.sub.2CH(CH.sub.2CH.sub.3)CH.sub.2--, and
--CH.sub.2CH(CH.sub.2CH.sub.2--)CH.sub.3.
[0075] The term "alkylsulfinyl" as used herein, means an alkyl
group, as defined herein, appended to the parent molecular moiety
through a sulfinyl group, as defined herein. Representative
examples of alkylsulfinyl include, but are not limited to,
methylsulfinyl and ethylsulfinyl.
[0076] The term "alkylsulfinylalkyl" as used herein, means an
alkylsulfinyl group, as defined herein, appended to the parent
molecular moiety through an alkyl group, as defined herein.
Representative examples of alkylsulfinylalkyl include, but are not
limited to, methylsulfinylmethyl and ethylsulfinylmethyl.
[0077] The term "alkylsulfonyl" as used herein, means an alkyl
group, as defined herein, appended to the parent molecular moiety
through a sulfonyl group, as defined herein. Representative
examples of alkylsulfonyl include, but are not limited to,
methylsulfonyl and ethylsulfonyl.
[0078] The term "alkylsulfonylalkyl" as used herein, means an
alkylsulfonyl group, as defined herein, appended to the parent
molecular moiety through an alkyl group, as defined herein.
Representative examples of alkylsulfonylalkyl include, but are not
limited to, methylsulfonylmethyl and ethylsulfonylmethyl.
[0079] The term "alkylsulfonyloxy" as used herein, means an
alkylsulfonyl group, as defined herein, appended to the parent
molecular moiety through an oxygen atom, as defined herein.
[0080] The term "alkylthio" as used herein, means an alkyl group,
as defined herein, appended to the parent molecular moiety through
a sulfur atom. Representative examples of alkylthio include, but
are not limited, methylthio, ethylthio, tert-butylthio, and
hexylthio.
[0081] The term "alkylthioalkyl" as used herein, means an alkylthio
group, as defined herein, appended to the parent molecular moiety
through an alkyl group, as defined herein except for R.sub.1 in
Formula (I) wherein the alkylthio group is at least two carbons
from the indole nitrogen. Representative examples of alkylthioalkyl
include, but are not limited, methylthiomethyl, 2-(ethylthio)ethyl,
and 4-(methylthio)butyl.
[0082] The term "alkynyl" as used herein, means a straight or
branched chain hydrocarbon group containing from 2 to 10 carbon
atoms and containing at least one carbon-carbon triple bond.
Representative examples of alkynyl include, but are not limited, to
acetylenyl, 1-propynyl, 2-propynyl, 3-butynyl, 2-pentynyl, and
1-butynyl.
[0083] The term "aryl," as used herein, means a phenyl group or a
naphthyl group.
[0084] The aryl groups of the present invention can be optionally
substituted with one, two, three, four, or five substituents
independently selected from the group consisting of alkenyl,
alkoxy, alkoxyalkoxy, alkoxyalkyl, alkoxycarbonyl,
alkoxycarbonylalkyl, alkoxysulfonyl, alkyl, alkylcarbonyl,
alkylcarbonylalkyl, alkylcarbonyloxy, alkylthio, alkylthioalkyl,
alkynyl, carboxy, carboxyalkyl, cyano, cyanoalkyl, ethylenedioxy,
formyl, haloalkoxy, haloalkyl, halogen, hydroxy, hydroxyalkyl,
mercapto, methylenedioxy, nitro, --NZ.sub.1Z.sub.2,
(NZ.sub.1Z.sub.2)alkyl, (NZ.sub.1Z.sub.2)carbonyl, and
(NZ.sub.1Z.sub.2)sulfonyl. Representative examples of substituted
aryl include, but are not limited to, 3-(acetyloxy)phenyl,
4-(acetyloxy)phenyl, 3-(dimethylamino)phenyl,
4-(dimethylamino)phenyl, 3-hydroxyphenyl, 4-hydroxyphenyl,
3-methoxyphenyl, and 4-methoxyphenyl.
[0085] The term "arylalkoxy" as used herein, means an aryl group,
as defined herein, appended to the parent molecular moiety through
an alkoxy group, as defined herein. Representative examples of
arylalkoxy include, but are not limited to, benzyloxy,
2-phenylethoxy, and 3-phenylpropoxy.
[0086] The term "arylalkoxyalkyl" as used herein, means an
arylalkoxy group, as defined herein, appended to the parent
molecular moiety through an alkyl group, as defined herein.
Representative examples of arylalkoxyalkyl include, but are not
limited to, 4-(benzyloxy)butyl, 3-(benzyloxy)propyl,
2-(benzyloxy)ethyl, and 5-(benzyloxy)pentyl.
[0087] The term "arylalkyl" as used herein, means an aryl group, as
defined herein, appended to the parent molecular moiety through an
alkyl group, as defined herein. Representative examples of
arylalkyl include, but are not limited to,
(1,3-benzodioxol-5-yl)methyl,
(2,3-dihydro-1,4-benzodioxin-6-yl)methyl, 4-(acetyloxy)benzyl,
benzyl, 2-phenylethyl, 3-phenylpropyl,
2-(4-dimethylaminophenyl)ethyl, 2-naphth-2-ylethyl,
3-methoxybenzyl, 4-methoxybenzyl, and 4-hydroxybenzyl.
[0088] The term "arylalkylcarbonyl" as used herein, means an
arylalkyl group, as defined herein, appended to the parent
molecular moiety through a carbonyl group, as defined herein.
Representative examples of arylalkyl include, but are not limited
to, 2-phenylacetyl and 3-phenylpropanoyl.
[0089] The term "arylalkylsulfonyl" as used herein, means an
arylalkyl group, as defined herein, appended to the parent
molecular moiety through a sulfonyl group, as defined herein.
Representative examples of "arylalkylsulfonyl" include, but are not
limited to, benzylsulfonyl and 2-phenylethylsulfonyl.
[0090] The term "arylalkylthio" as used herein, means an arylalkyl
group, as defined herein, appended to the parent molecular moiety
through a sulfur atom. Representative examples of arylalkylthio
include, but are not limited to, 2-phenylethylthio,
3-naphth-2-ylpropylthio, and 5-phenylpentylthio.
[0091] The term "arylcarbonyl" as used herein, means an aryl group,
as defined herein, appended to the parent molecular moiety through
a carbonyl group, as defined herein. Representative examples of
arylcarbonyl include, but are not limited to, benzoyl and
naphthoyl.
[0092] The term "aryloxy" as used herein, means an aryl group, as
defined herein, appended to the parent molecular moiety through an
oxygen atom. Representative examples of aryloxy include, but are
not limited to, phenoxy, naphthyloxy, 3-bromophenoxy,
4-chlorophenoxy, 4-methylphenoxy, and 3,5-dimethoxyphenoxy.
[0093] The term "aryloxyalkyl" as used herein, means an aryloxy
group, as defined herein, appended to the parent molecular moiety
through an alkyl group, as defined herein. Representative examples
of aryloxyalkyl include, but are not limited to, 2-phenoxyethyl,
3-naphth-2-yloxypropyl and 3-bromophenoxymethyl.
[0094] The term "arylsulfonyl" as used herein, means an aryl group,
as defined herein, appended to the parent molecular moiety through
a sulfonyl group, as defined herein.
[0095] The term "arylthio" as used herein, means an aryl group, as
defined herein, appended to the parent molecular moiety through a
sulfur atom. Representative examples of arylthio include, but are
not limited to, phenylthio and 2-naphthylthio.
[0096] The term "arylthioalkyl" as used herein, means an arylthio
group, as defined herein, appended to the parent molecular moiety
through an alkyl group, as defined herein. Representative examples
of arylthioalkyl include, but are not limited to, phenylthiomethyl,
2-naphth-2-ylthioethyl, and 2-(phenylthio)ethyl.
[0097] The term "azide" as used herein, means a --N.sub.3
group.
[0098] The term "azidoalkyl" as used herein, means an azide group,
as defined herein, appended to the parent molecular moiety through
an alkyl group, as defined herein except for R.sub.1 in Formula (I)
wherein the azide group is at least two carbons from the indole
nitrogen. Representative examples of azidoalkyl include, but are
not limited to, 2-azidoethyl, 3-azidopropyl, and 4-azidobutyl.
[0099] The term "carbonyl" as used herein, means a --C(O)--
group.
[0100] The term "carboxy" as used herein, means a --CO.sub.2H
group.
[0101] The term "carboxyalkenyl" as used herein, means a carboxy
group, as defined herein, appended to the parent molecular moiety
through an alkenyl group, as defined herein. Representative
examples of carboxyalkenyl include, but are not limited to,
3-ethoxy-3-oxoprop-1-enyl.
[0102] The term "carboxyalkenylcarbonyl" as used herein, means a
carboxyalkenyl group, as defined herein, appended to the parent
molecular moiety through a carbonyl group, as defined herein.
Representative examples of carboxyalkenylcarbonyl include, but are
not limited to, 4-ethoxy-4-oxobut-2-enoyl.
[0103] The term "carboxyalkenylcarbonyloxy" as used herein, means a
carboxyalkenylcarbonyl group, as defined herein, appended to the
parent molecular moiety through an oxygen atom, as defined herein.
Representative examples of carboxyalkenylcarbonyloxy include, but
are not limited to, (3-carboxyprop-2-enoyl)oxy.
[0104] The term "carboxyalkyl" as used herein, means a carboxy
group, as defined herein, appended to the parent molecular moiety
through an alkyl group, as defined herein. Representative examples
of carboxyalkyl include, but are not limited to, carboxymethyl,
2-carboxyethyl, 3-carboxypropyl, 4-carboxybutyl, 5-carboxypentyl,
and 6-carboxyhexyl.
[0105] The term "carboxyalkylcarbonyl" as used herein, means a
carboxyalkyl group, as defined herein, appended to the parent
molecular moiety through a carbonyl group, as defined herein.
Representative examples of carboxyalkylcarbonyl include, but are
not limited to, 3-carboxypropanoyl and 4-carboxybutanoyl.
[0106] The term "carboxyalkylcarbonyloxy" as used herein, means a
carboxyalkylcarbonyl group, as defined herein, appended to the
parent molecular moiety through a oxygen atom, as defined herein.
Representative examples of carboxyalkylcarbonyloxy include, but are
not limited to, (3-carboxypropanoyl)oxy and
(4-carboxybutanoyl)oxy.
[0107] The term "cyano" as used herein, means a --CN group.
[0108] The term "cyanoalkyl" as used herein, means a cyano group,
as defined herein, appended to the parent molecular moiety through
an alkyl group, as defined herein. Representative examples of
cyanoalkyl include, but are not limited to, cyanomethyl,
2-cyanoethyl, and 3-cyanopropyl.
[0109] The term "cycloalkenyl" as used herein, means a cyclic
hydrocarbon containing from 3 to 8 carbons and containing at least
one carbon-carbon double bond formed by the removal of two
hydrogens. Representative examples of cycloalkenyl include, but are
not limited to, 2-cyclohexen-1-yl, 3-cyclohexen-1-yl,
2,4-cyclohexadien-1-yl and 3-cyclopenten-1-yl.
[0110] The term "cycloalkyl" as used herein, means a saturated
cyclic hydrocarbon group containing from 3 to 8 carbons, examples
of cycloalkyl include cyclopropyl, cyclobutyl, cyclopentyl,
cyclohexyl, cycloheptyl, and cyclooctyl.
[0111] The cycloalkyl groups of the present invention are
optionally substituted with 1, 2, 3, 4, 5, or 6 substituents
selected from the group consisting of alkenyl, alkoxy, alkoxyalkyl,
alkoxycarbonyl, alkoxycarbonylalkyl, alkoxysulfonyl, alkyl,
alkylcarbonyl, alkylcarbonylalkyl, alkylcarbonyloxy, alkylthio,
alkylthioalkyl, alkynyl, carboxy, carboxyalkyl, cyano, cyanoalkyl,
haloalkoxy, haloalkyl, halogen, hydroxy, hydroxyalkyl, mercapto,
mercaptoalkyl, oxo, --NZ.sub.1Z.sub.2, (NZ.sub.1Z.sub.2)alkyl,
(NZ.sub.1Z.sub.2)carbonyl, and (NZ.sub.1Z.sub.2)sulfonyl.
[0112] The term "cycloalkylalkoxy" as used herein, means a
cycloalkyl group, as defined herein, appended to the parent
molecular moiety through an alkoxy group, as defined herein.
Representative examples of cycloalkylalkoxy include, but are not
limited to, cyclopropylmethoxy, 2-cyclobutylethoxy,
cyclopentylmethoxy, cyclohexylmethoxy, and 4-cycloheptylbutoxy.
[0113] The term "cycloalkylalkyl" as used herein, means a
cycloalkyl group, as defined herein, appended to the parent
molecular moiety through an alkyl group, as defined herein.
Representative examples of cycloalkylalkyl include, but are not
limited to, cyclopropylmethyl, 2-cyclobutylethyl,
cyclopentylmethyl, cyclohexylmethyl, 4-cycloheptylbutyl, and
(4-methoxycarbonylcyclohexyl)methyl.
[0114] The term "cycloalkylalkylcarbonyl" as used herein, means a
cycloalkylalkyl group, as defined herein, appended to the parent
molecular moiety through a carbonyl group, as defined herein.
Representative examples of cycloalkylalkylcarbonyl include, but are
not limited to, 4-cyclopentylbutanoyl and
3-cyclopentylpropanoyl.
[0115] The term "cycloalkylalkylsulfonyl" as used herein, means a
cycloalkylalkyl group, as defined herein, appended to the parent
molecular moiety through a sulfonyl group, as defined herein.
Representative examples of cycloalkylalkylsulfonyl include, but are
not limited to, (2-cyclopentylethyl)sulfonyl and
(2-cyclopropylethyl)sulfonyl.
[0116] The term "cycloalkylcarbonyl" as used herein, means
cycloalkyl group, as defined herein, appended to the parent
molecular moiety through a carbonyl group, as defined herein.
Representative examples of cycloalkylcarbonyl include, but are not
limited to, cyclopropylcarbonyl, 2-cyclobutylcarbonyl, and
cyclohexylcarbonyl.
[0117] The term "cycloalkyloxy" as used herein, means cycloalkyl
group, as defined herein, appended to the parent molecular moiety
through an oxygen atom, as defined herein. Representative examples
of cycloalkyloxy include, but are not limited to, cyclopropyloxy,
cyclobutyloxy, cyclopentyloxy, cyclohexyloxy, cycloheptyloxy, and
cyclooctyloxy.
[0118] The term "cycloalkyloxyalkyl" as used herein, means
cycloalkyloxy group, as defined herein, appended to the parent
molecular moiety through an alkyl group, as defined herein.
Representative examples of cycloalkyloxyalkyl include, but are not
limited to, 2-(cyclopropyloxy)ethyl, 4-(cyclobutyloxy)pentyl,
cyclopentyloxymethyl, 3-(cyclohexyloxy)propyl,
cycloheptyloxymethyl, and 2-(cyclooctyloxy)ethyl.
[0119] The term "cycloalkylsulfonyl" as used herein, means a
cycloalkyl group, as defined herein, appended to the parent
molecular moiety through a sulfonyl group, as defined herein.
Representative examples of cyclalkylsulfonyl include, but are not
limited to, cyclopentylsulfonyl and cyclopropylsulfonyl.
[0120] The term "ethylenedioxy" as used herein, means a
--O(CH.sub.2).sub.2O-- group wherein the oxygen atoms of the
ethylenedioxy group are attached to the parent molecular moiety
through two adjacent carbon atoms forming a six membered ring.
[0121] The term "formyl" as used herein, means a --C(O)H group.
[0122] The term "halo" or "halogen" as used herein, means --Cl,
--Br, --I or --F.
[0123] The term "haloalkoxy" as used herein, means at least one
halogen, as defined herein, appended to the parent molecular moiety
through an alkoxy group, as defined herein. Representative examples
of haloalkoxy include, but are not limited to, chloromethoxy,
2-fluoroethoxy, trifluoromethoxy, and pentafluoroethoxy.
[0124] The term "haloalkyl" as used herein, means at least one
halogen, as defined herein, appended to the parent molecular moiety
through an alkyl group, as defined herein. Representative examples
of haloalkyl include, but are not limited to, chloromethyl,
2-fluoroethyl, trifluoromethyl, pentafluoroethyl,
2-chloro-3-fluoropentyl, and 4,4,4,-trifluorobutyl.
[0125] The term "heteroaryl," as used herein, means a monocyclic
heteroaryl ring or a bicyclic heteroaryl ring. The monocyclic
heteroaryl ring is a 5 or 6 membered ring. The 5 membered ring has
two double bonds and contains one, two, three or four heteroatoms
independently selected from the group consisting of N, O, and S.
The 6 membered ring has three double bonds and contains one, two,
three or four heteroatoms independently selected from the group
consisting of N, O, and S. The bicyclic heteroaryl ring consists of
the 5 or 6 membered heteroaryl ring fused to a phenyl group or the
5 or 6 membered heteroaryl ring fused to another 5 or 6 membered
heteroaryl ring. Nitrogen heteroatoms contained within the
heteroaryl may be optionally oxidized to the N-oxide or optionally
protected with a nitrogen protecting group known to those of skill
in the art. The heteroaryl is connected to the parent molecular
moiety through any carbon atom contained within the heteroaryl.
Representative examples of heteroaryl include, but are not limited
to, benzothiazolyl, benzothienyl, benzoxadiazolyl, cinnolinyl,
furopyridinyl, furyl, imidazolyl, indazolyl, indolyl, isoxazolyl,
isoquinolinyl, isothiazolyl, naphthyridinyl, oxadiazolyl, oxazolyl,
pyridinyl, pyridazinyl, pyrimidinyl, pyrazinyl, pyrazolyl,
pyrrolyl, pyridinium N-oxide, quinolinyl, tetrazolyl, thiadiazolyl,
thiazolyl, thienopyridinyl, thienyl, triazolyl, and triazinyl.
[0126] The heteroaryl groups of the present invention are
optionally substituted with 1, 2, 3, or 4 substituents
independently selected from the group consisting of alkenyl,
alkoxy, alkoxyalkoxy, alkoxyalkyl, alkoxycarbonyl,
alkoxycarbonylalkyl, alkoxysulfonyl, alkyl, alkylcarbonyl,
alkylcarbonylalkyl, alkylcarbonyloxy, alkylthio, alkylthioalkyl,
alkynyl, carboxy, carboxyalkyl, cyano, cyanoalkyl, formyl,
haloalkoxy, haloalkyl, halogen, hydroxy, hydroxyalkyl, mercapto,
nitro, --NZ.sub.1Z.sub.2, (NZ.sub.1Z.sub.2)alkyl,
(NZ.sub.1Z.sub.2)carbonyl, and (NZ.sub.1Z.sub.2)sulfonyl.
Representative examples of substituted heteroaryls include, but are
not limited to, 1-methyl-1H-imidazolyl,
5-chloro-1,2,4-thiadiazolyl, and 4-methyl-1,3-thiazolyl. Heteroaryl
groups of the present invention that are substituted may be present
as tautomers. The present invention encompasses all tautomers
including non-aromatic tautomers.
[0127] The term "heteroarylalkoxy" as used herein, means a
heteroaryl group, as defined herein, appended to the parent
molecular moiety through an alkoxy group, as defined herein.
Representative examples of heteroarylalkoxy include, but are not
limited to, fur-3-ylmethoxy, 1H-imidazol-2-ylmethoxy,
1H-imidazol-4-ylmethoxy, 1-(pyridin-4-yl)ethoxy,
pyridin-3-ylmethoxy, 6-chloropyridin-3-ylmethoxy,
pyridin-4-ylmethoxy, (6-(trifluoromethyl)pyridin-3-yl)methoxy,
(6-(cyano)pyridin-3-yl)methoxy, (2-(cyano)pyridin-4-yl)methoxy,
(5-(cyano)pyridin-2-yl)methoxy, (2-(chloro)pyridin-4-yl)methoxy,
pyrimidin-5-ylmethoxy, 2-(pyrimidin-2-yl)propoxy,
thien-2-ylmethoxy, and thien-3-ylmethoxy.
[0128] The term "heteroarylalkyl" as used herein, means a
heteroaryl, as defined herein, appended to the parent molecular
moiety through an alkyl group, as defined herein. Representative
examples of heteroarylalkyl include, but are not limited to,
(1H-imidazolyl-2-yl)methyl, (1-methyl-1H-imidazolyl-2-yl)methyl,
2-pyridin-2-ylethyl, 2-pyridin-3-ylethyl, 2-pyridin-4-ylethyl,
2-(1H-pyrrol-1-yl)ethyl, (5-chloro-1,2,4-thiadiazol-3-yl)methyl,
(1,2,4-thiadiazol-3-yl)methyl, 2-(4-methyl-1,3-thiazol-5-yl)ethyl,
2-(1,3-thiazol-5-yl)ethyl, 2-thien-2-ylethyl, and
2-thien-3-ylethyl.
[0129] The term "heteroarylalkylcarbonyl" as used herein, means a
heteroarylalkyl, as defined herein, appended to the parent
molecular moiety through a carbonyl group, as defined herein.
Representative example of heteroarylalkylcarbonyl include, but are
not limited to, (3-pyridin-3-ylpropyl)carbonyl and
(2-pyrimidin-5-ylethyl)carbonyl.
[0130] The term "heteroaryloxy" as used herein, means a heteroaryl
group, as defined herein, appended to the parent molecular moiety
through an oxygen atom. Representative examples of heteroaryloxy
include, but are not limited to, pyrimidinyloxy and
pyridinyloxy.
[0131] The term "heteroaryloxyalkyl" as used herein, means a
heteroaryloxy group, as defined herein, appended to the parent
molecular moiety through an alkyl group, as defined herein.
Representative examples of heteroaryloxyalkyl include, but are not
limited to, pyridinyloxymethyl and 2-quinolinyloxyethyl.
[0132] The term "heteroarylalkylsulfonyl" as used herein, means a
heteroarylalkyl, as defined herein, appended to the parent
molecular moiety through a sulfonyl group, as defined herein.
[0133] The term "heteroarylsulfonyl" as used herein, means a
heteroaryl, as defined herein, appended to the parent molecular
moiety through a sulfonyl group, as defined herein.
[0134] The term "heterocycle" or "heterocyclic" as used herein,
means a monocyclic or a bicyclic heterocyclic ring. The monocyclic
heterocyclic ring consists of a 3, 4, 5, 6 or 7 membered ring
containing at least one heteroatom independently selected from O, N
and S. The 3 or 4 membered ring contains 1 heteroatom selected from
the group consisting of O, N and S. The 5 membered ring contains
zero or one double bond and one, two or three heteroatoms selected
from the group consisting of O, N and S. The 6 or 7 membered ring
contains zero, one or two double bonds and one, two or three
heteroatoms selected from the group consisting of O, N and S.
Representative examples of the monocyclic heterocyclic ring
include, but are not limited to, azetidinyl, azepanyl, aziridinyl,
diazepanyl, 1,3-dioxanyl, 1,3-dioxolanyl, 1,3-dithiolanyl,
1,3-dithianyl, imidazolinyl, imidazolidinyl, isothiazolinyl,
isothiazolidinyl, isoxazolinyl, isoxazolidinyl, morpholinyl,
oxadiazolinyl, oxadiazolidinyl, oxazolinyl, oxazolidinyl,
piperazinyl, piperidinyl, pyranyl, pyrazolinyl, pyrazolidinyl,
pyrrolinyl, pyrrolidinyl, tetrahydrofuranyl, tetrahydrothienyl,
thiadiazolinyl, thiadiazolidinyl, thiazolinyl, thiazolidinyl,
thiomorpholinyl, 1,1-dioxidothiomorpholinyl (thiomorpholine
sulfone), thiopyranyl, and trithianyl. The bicyclic heterocyclic
ring consists of the monocyclic heterocyclic ring fused to a
cycloalkyl group or the monocyclic heterocyclic ring fused to a
cycloalkenyl group or the monocyclic heterocyclic ring fused to
another monocyclic heterocyclic ring or the monocyclic heterocyclic
ring fused to an aryl group wherein the aryl group is an optionally
substituted phenyl group. The bicyclic heterocyclic ring can be
appended to the parent molecular moiety via any carbon or nitrogen
atom within the bicyclic heterocyclic ring while maintaining the
proper valence. Representative examples of the bicyclic
heterocyclic ring include, but are not limited to,
1,3-benzodioxolyl, 2,3-dihydro-1,4-benzodioxinyl,
1,2,3,4-tetrahydroquinoxalinyl, decahydroquinoxalinyl, and
octahydro-1,4-benzodioxinyl.
[0135] The heterocycles of this invention are optionally
substituted with 1, 2, 3, or 4 substituents independently selected
from the group consisting of alkenyl, alkoxy, alkoxyalkoxy,
alkoxyalkyl, alkoxycarbonyl, alkoxycarbonylalkyl, alkoxysulfonyl,
alkyl, alkylcarbonyl, alkylcarbonylalkyl, alkylcarbonyloxy,
alkylthio, alkylthioalkyl, alkynyl, carboxy, carboxyalkyl, cyano,
cyanoalkyl, formyl, haloalkoxy, haloalkyl, halogen, hydroxy,
hydroxyalkyl, mercapto, nitro, oxo, --NZ.sub.1Z.sub.2,
(NZ.sub.1Z.sub.2)alkyl, (NZ.sub.1Z.sub.2)carbonyl,
(NZ.sub.1Z.sub.2)sulfonyl. Representative examples of substituted
heterocycle include, but not limited to,
2,2-dimethyl-1,3-dioxolanyl, 4-methylpiperazinyl,
1-methylpiperidinyl, 1-methylpyrrolidinyl, 2,5-dioxopyrrolidinyl,
2-oxopyrrolidinyl, 2-oxo-1,3-oxazolidinyl, and
1-(tert-butoxycarbonyl)piperidinyl.
[0136] The term "heterocyclealkoxy" as used herein, means a
heterocycle group, as defined herein, appended to the parent
molecular moiety through an alkoxy group, as defined herein.
Representative examples of heterocyclealkoxy include, but are not
limited to, 2-morpholin-1-ylethoxy and 2-piperidin-1-ylethoxy.
[0137] The term "heterocyclealkoxycarbonyl" as used herein, means a
heterocyclealkoxy group, as defined herein, appended to the parent
molecular moiety through a carbonyl group. Representative examples
of heterocyclealkoxycarbonyl include, but are not limited to,
(2-morpholin-4-ylethoxy)carbonyl.
[0138] The term "heterocyclealkyl" as used herein, means a
heterocycle, as defined herein, appended to the parent molecular
moiety through an alkyl group, as defined herein, wherein the alkyl
group of the heterocyclealkyl at R.sub.1 of Formula (I) may be
optionally substituted with 1 substituent selected from the group
consisting of alkoxycarbonyl and carboxy. Representative examples
of heterocyclealkyl include, but are not limited to,
2-(azepan-1-yl)ethyl, 2-(2,2,-dimethyl-1,3-dioxolan-4-yl)ethyl,
(1,3-dioxolan-4-yl)methyl, (tetrahydrofuran-3-yl)methyl,
(2R)-(tetrahydrofuran-2-yl)methyl,
(2S)-(tetrahydrofuran-2-yl)methyl, 2-(morpholin-4-yl)ethyl,
3-(morpholin-4-yl)propyl, 2-(2-oxo-1,3-oxazolidin-3-yl)ethyl,
2-(piperazin-1-yl)ethyl, 2-(4-methylpiperazin-1-yl)ethyl,
2-(1-methylpiperidin-4-yl)ethyl, (1-methylpiperidin-2-yl)methyl,
2-(piperidin-4-yl)ethyl,
2-(1-tert-butoxycarbonylpiperidin-4-yl)ethyl,
(piperidin-2-yl)methyl, 2-(piperidin-1-yl)ethyl,
2-(pyrrolidin-1-yl)ethyl, 2-(1-methylpyrrolidin-2-yl)ethyl,
2-(2-oxopyrrolidin-1-yl)ethyl, 2-(2,5-dioxopyrrolidin-1-yl)ethyl,
2-(tetrahydro-2H-pyran-4-yl)ethyl,
(tetrahydro-2H-pyran-4-yl)methyl, (tetrahydro-2H-pyran-4-yl)methyl,
carboxy(tetrahydro-2H-pyran-4-yl)methyl, and
2-ethoxy-2-oxo-1-tetrahydro-2H-pyran-4-ylethyl.
[0139] The term "heterocyclealkylcarbonyl" as used herein, means a
heterocyclealkyl, as defined herein, appended to the parent
molecular moiety through a carbonyl group, as defined herein.
Representative examples of heterocyclealkylcarbonyl include, but
are not limited to, tetrahydro-2H-pyran-4-ylacetyl.
[0140] The term "heterocyclealkylsulfonyl" as used herein, means a
heterocyclealkyl, as defined herein, appended to the parent
molecular moiety through a sulfonyl group, as defined herein.
Representative example of "heterocyclealkylsulfonyl" include, but
are not limited to, (3-pyrrolidin-3-ylpropyl)sulfonyl and
(3-piperidin-4-ylpropyl)sulfonyl.
[0141] The term "heterocyclealkylthio" as used herein, means a
heterocyclealkyl group, as defined herein, appended to the parent
molecular moiety through a sulfur atom. Representative examples of
heterocyclealkylthio include, but are not limited to,
(3-pyrrolidin-3-ylpropyl)thio and (3-piperidin-4-ylpropyl)thio.
[0142] The term "heterocycleoxy" as used herein, means a
heterocycle group, as defined herein, appended to the parent
molecular moiety through an oxygen atom. Representative examples of
heterocycleoxy include, but are not limited to, piperidin-4-yloxy
and pyrrolidin-3-yloxy.
[0143] The term "heterocycleoxyalkyl" as used herein, means a
heterocycleoxy group, as defined herein, appended to the parent
molecular moiety through an alkyl group, as defined herein.
Representative examples of heterocycleoxyalkyl include, but are not
limited to, 2-(piperidin-4-yloxy)ethyl and
3-(piperidin-4-yloxy)propyl.
[0144] The term "heterocyclesulfonyl" as used herein, means a
heterocycle, as defined herein, appended to the parent molecular
moiety through a sulfonyl group, as defined herein. Representative
examples of "heterocyclesulfonyl" include, but are not limited to,
piperidin-4-ylsulfonyl and pyrrolidin-3-ylsulfonyl.
[0145] The term "hydroxy" as used herein, means an --OH group.
[0146] The term "hydroxyalkoxy" as used herein, means at least one
hydroxy group, as defined herein, is appended to the parent
molecular moiety through an alkoxy group, as defined herein.
Representative examples of hydroxyalkoxy include, but are not
limited to, hydroxymethyl, 2-hydroxyethoxy, 3-hydroxypropoxy,
2,3-dihydroxypropoxy, (2S) 2,3-dihydroxypropoxy, (2R)
2,3-dihydroxypropoxy, 2,3-dihydroxypentyloxy, 4-hydroxybutoxy,
2-ethyl-4-hydroxyheptyloxy, 3,4-dihydroxybutoxy, and
5-hydroxypentyloxy.
[0147] The term "hydroxyalkyl" as used herein, means at least one
hydroxy group, as defined herein, is appended to the parent
molecular moiety through an alkyl group, as defined herein except
for R.sub.1 in Formula (I) wherein the hydroxy group is at least
two carbons from the indole nitrogen. Representative examples of
hydroxyalkyl include, but are not limited to, hydroxymethyl,
2-hydroxyethyl, 3-hydroxypropyl, 2,3-dihydroxypropyl, (2S)
2,3-dihydroxypropyl, (2R) 2,3-dihydroxypropyl, 2,3-dihydroxypentyl,
4-hydroxybutyl, 2-ethyl-4-hydroxyheptyl, 3,4-dihydroxybutyl, and
5-hydroxypentyl.
[0148] The term "mercapto" as used herein, means a --SH group.
[0149] The term "mercaptoalkyl" as used herein, means a mercapto
group, as defined herein, appended to the parent molecular moiety
through an alkyl group, as defined herein except for R.sub.1 in
Formula (I) wherein the mercapto group is at least two carbons from
the indole nitrogen. Representative examples of mercaptoalkyl
include, but are not limited to, 2-mercaptoethyl and
3-mercaptopropyl.
[0150] The term "methylenedioxy" as used herein, means a
--OCH.sub.2O-- group wherein the oxygen atoms of the methylenedioxy
are attached to the parent molecular moiety through two adjacent
carbon atoms.
[0151] The term "nitrogen protecting group" as used herein, means
those groups intended to protect an amino group against undesirable
reactions during synthetic procedures. Preferred nitrogen
protecting groups are acetyl, benzoyl, benzyl, benzyloxycarbonyl
(Cbz), formyl, phenylsulfonyl, tert-butoxycarbonyl (Boc),
tert-butylacetyl, trifluoroacetyl, and triphenylmethyl
(trityl).
[0152] The term "nitro" as used herein, means a --NO.sub.2
group.
[0153] The term "NR.sub.AR.sub.B" as used herein, means two groups,
R.sub.A and R.sub.B, which are appended to the parent molecular
moiety through a nitrogen atom. R.sub.A and R.sub.B are each
independently selected from the group consisting of hydrogen,
alkenyl, alkoxyalkyl, alkoxycarbonylalkyl, alkyl, alkynyl, aryl,
arylalkyl, cycloalkyl, cycloalkylalkyl, heteroaryl,
heteroarylalkyl, heterocycle, heterocyclealkyl, and
hydroxyalkyl.
[0154] The term "(NR.sub.AR.sub.B)carbonyl" as used herein, means a
NR.sub.AR.sub.B group, as defined herein, appended to the parent
molecular moiety through a carbonyl group, as defined herein.
Representative examples of (NR.sub.AR.sub.B)carbonyl include, but
are not limited to, aminocarbonyl, (methylamino)carbonyl,
(dimethylamino)carbonyl, and (ethylmethylamino)carbonyl.
[0155] The term "(NR.sub.AR.sub.B)carbonylalkenyl" as used herein,
means a (NR.sub.AR.sub.B)carbonyl group, as defined herein,
appended to the parent molecular moiety through an alkenyl group,
as defined herein. Representative examples of
"(NR.sub.AR.sub.B)carbonylalkenyl" includes, but is not limited to,
4-amino-4-oxobut-1-enyl and 4-dimethylamino-4-oxobut-1-enyl.
[0156] The term "(NR.sub.AR.sub.B)carbonylalkenylcarbonyl" as used
herein, means a (NR.sub.AR.sub.B)carbonylalkenyl group, as defined
herein, appended to the parent molecular moiety through a carbonyl
group, as defined herein. Representative examples
(NR.sub.AR.sub.B)carbonylalkenylcarbonyl includes, but is not
limited to 6-(dimethylamino)-6-oxohex-3-enoyl and
6-(amino)-6-oxohex-3-enoyl.
[0157] The term "(NR.sub.AR.sub.B)carbonylalkyl" as used herein,
means a (NR.sub.AR.sub.B)carbonyl group, as defined herein,
appended to the parent molecular moiety through an alkyl group, as
defined herein. Representative examples of
(NR.sub.AR.sub.B)carbonylalkyl include, but are not limited to,
2-amino-2-oxoethyl, 3-amino-3-oxopropyl, and
4-amino-4-oxobutyl.
[0158] The term "(NR.sub.AR.sub.B)carbonylalkylcarbonyl" as used
herein, means a (NR.sub.AR.sub.B)carbonylalkyl group, as defined
herein, appended to the parent molecular moiety through a carbonyl
group, as defined herein. Representative examples
(NR.sub.AR.sub.B)carbonylalkylcarbonyl includes, but is not limited
to, 6-(dimethylamino)-6-oxohexanoyl and 6-amino-6-oxohexanoyl.
[0159] The term "(NR.sub.AR.sub.B)sulfonyl" as used herein, means a
NR.sub.AR.sub.B group, as defined herein, appended to the parent
molecular moiety through a sulfonyl group, as defined herein.
[0160] The term "(NR.sub.AR.sub.B)sulfonylalkyl" as used herein,
means a (NR.sub.AR.sub.B)sulfonyl group, as defined herein,
appended to the parent molecular moiety through an alkyl group, as
defined herein except for R.sub.1 in Formula (I) wherein the
(NR.sub.AR.sub.B)sulfonyl group is at least two carbons from the
indole nitrogen.
[0161] The term "NR.sub.CR.sub.D" as used herein, means two groups,
R.sub.C and R.sub.D, which are appended to the parent molecular
moiety through a nitrogen atom. R.sub.C and R.sub.D are each
independently selected from the group consisting of hydrogen,
alkenyl, alkoxyalkyl, alkoxycarbonyl, alkoxycarbonylalkyl, alkyl,
alkylcarbonyl, alkylsulfonyl, alkynyl, aryl, arylalkyl,
arylsulfonyl, arylalkylsulfonyl, cycloalkyl, cycloalkylalkyl,
cycloalkylsulfonyl, cycloalkylalkylsulfonyl, heteroaryl,
heteroarylalkyl, heteroarylsulfonyl, heteroarylalkylsulfonyl,
heterocycle, heterocyclealkyl, heterocyclesulfonyl, and
heterocyclealkylsulfonyl.
[0162] The term "(NR.sub.CR.sub.D)alkyl" as used herein, means a
NR.sub.CR.sub.D group, as defined herein, appended to the parent
molecular moiety through an alkyl group, as defined herein except
for R.sub.1 in Formula (I) wherein the NR.sub.CR.sub.D group is at
least two carbons from the indole nitrogen.
[0163] The term "NR.sub.ER.sub.F" as used herein, means two groups,
R.sub.E and R.sub.F, which are appended to the parent molecular
moiety through a nitrogen atom. R.sub.E and R.sub.F are each
independently selected from the group consisting of hydrogen,
alkenyl, alkoxyalkyl, alkoxycarbonyl, alkoxycarbonylalkyl, alkyl,
alkylcarbonyl, alkylsulfonyl, alkynyl, aryl, arylalkyl,
arylsulfonyl, arylalkylsulfonyl, cycloalkyl, cycloalkylalkyl,
cycloalkylsulfonyl, cycloalkylalkylsulfonyl, heteroaryl,
heteroarylalkyl, heteroarylsulfonyl, heteroarylalkylsulfonyl,
heterocycle, heterocyclealkyl, heterocyclesulfonyl, and
heterocyclealkylsulfonyl.
[0164] The term "(NR.sub.ER.sub.F)alkyl" as used herein, means a
NR.sub.ER.sub.F group, as defined herein, appended to the parent
molecular moiety through an alkyl group, as defined herein.
[0165] The term "NR.sub.GR.sub.H" as used herein, means two groups,
R.sub.G and R.sub.H, which are appended to the parent molecular
moiety through a nitrogen atom. R.sub.G and R.sub.H are each
independently selected from the group consisting of hydrogen,
alkenyl, alkoxyalkyl, alkoxycarbonylalkyl, alkyl, alkynyl, aryl,
arylalkyl, cycloalkyl, cycloalkylalkyl, heteroaryl,
heteroarylalkyl, heterocycle, heterocyclealkyl, and
hydroxyalkyl.
[0166] The term "(NR.sub.GR.sub.H)carbonyl" as used herein, means a
NR.sub.GR.sub.H group, as defined herein, appended to the parent
molecular moiety through a carbonyl group, as defined herein.
[0167] The term "(NR.sub.GR.sub.H)carbonylalkyl" as used herein,
means a (NR.sub.GR.sub.H)carbonyl group, as defined herein,
appended to the parent molecular moiety through an alkyl group, as
defined herein.
[0168] The term "(NR.sub.GR.sub.H)sulfonyl" as used herein, means a
NR.sub.GR.sub.H group, as defined herein, appended to the parent
molecular moiety through a sulfonyl group, as defined herein.
[0169] The term "(NR.sub.GR.sub.H)sulfonylalkyl" as used herein,
means a (NR.sub.GR.sub.H)sulfonyl group, as defined herein,
appended to the parent molecular moiety through an alkyl group, as
defined herein.
[0170] The term "NR.sub.JR.sub.K" as used herein, means two groups,
R.sub.J and R.sub.K, which are appended to the parent molecular
moiety through a nitrogen atom. R.sub.J and R.sub.K are each
independently selected from the group consisting of hydrogen,
alkenyl, alkoxyalkyl, alkoxycarbonyl, alkoxycarbonylalkyl, alkyl,
alkylcarbonyl, alkylsulfonyl, alkynyl, aryl, arylalkyl,
arylsulfonyl, arylalkylsulfonyl, cycloalkyl, cycloalkylalkyl,
cycloalkylsulfonyl, cycloalkylalkylsulfonyl, heteroaryl,
heteroarylalkyl, heteroarylsulfonyl, heteroarylalkylsulfonyl,
heterocycle, heterocyclealkyl, heterocyclesulfonyl, and
heterocyclealkylsulfonyl.
[0171] The term "(NR.sub.JR.sub.K)alkoxy" as used herein, means a
NR.sub.JR.sub.K group, as defined herein, appended to the parent
molecular moiety through an alkoxy group, as defined herein.
[0172] The term "(NR.sub.JR.sub.K)alkyl" as used herein, means a
NR.sub.JR.sub.K group, as defined herein, appended to the parent
molecular moiety through an alkyl group, as defined herein.
[0173] The term "NR.sub.MR.sub.N" as used herein, means two groups,
R.sub.M and R.sub.N, which are appended to the parent molecular
moiety through a nitrogen atom. R.sub.M and R.sub.N are each
independently selected from the group consisting of hydrogen,
alkenyl, alkoxyalkyl, alkoxycarbonylalkyl, alkyl, alkynyl, aryl,
arylalkyl, cycloalkyl, cycloalkylalkyl, heteroaryl,
heteroarylalkyl, heterocycle, heterocyclealkyl, and
hydroxyalkyl.
[0174] The term "(NR.sub.MR.sub.N)carbonyl" as used herein, means a
NR.sub.MR.sub.N group, as defined herein, appended to the parent
molecular moiety through a carbonyl group, as defined herein.
[0175] The term "(NR.sub.MR.sub.N)carbonylalkyl" as used herein,
means a (NR.sub.MR.sub.N)carbonyl group, as defined herein,
appended to the parent molecular moiety through an alkyl group, as
defined herein.
[0176] The term "(NR.sub.MR.sub.N)sulfonyl" as used herein, means a
NR.sub.MR.sub.N group, as defined herein, appended to the parent
molecular moiety through a sulfonyl group, as defined herein.
[0177] The term "(NR.sub.MR.sub.N)sulfonylalkyl" as used herein,
means a (NR.sub.MR.sub.N)sulfonyl group, as defined herein,
appended to the parent molecular moiety through an alkyl group, as
defined herein.
[0178] The term "NZ.sub.1Z.sub.2" as used herein, means two groups,
Z.sub.1 and Z.sub.2, which are appended to the parent molecular
moiety through a nitrogen atom. Z.sub.1 and Z.sub.2 are each
independently selected from the group consisting of hydrogen,
alkenyl, alkyl, alkylcarbonyl, alkylsulfonyl, alkynyl, aryl,
arylalkyl, formyl, heteroaryl, heteroarylalkyl, heterocycle, and
heterocyclealkyl. Representative examples of NZ.sub.1Z.sub.2
include, but are not limited to, amino, methylamino, acetylamino,
and acetylmethylamino.
[0179] The term "(NZ.sub.1Z.sub.2)alkyl" as used herein, means a
NZ.sub.1Z.sub.2 group, as defined herein, appended to the parent
molecular moiety through an alkyl group, as defined herein.
Representative examples of (NZ.sub.1Z.sub.2)alkyl include, but are
not limited to, aminocarbonyl, (methylamino)carbonyl,
(dimethylamino)carbonyl, and (ethylmethylamino)carbonyl.
[0180] The term "(NZ.sub.1Z.sub.2)carbonyl" as used herein, means a
NZ.sub.1Z.sub.2 group, as defined herein, appended to the parent
molecular moiety through a carbonyl group, as defined herein.
Representative examples of (NZ.sub.1Z.sub.2)carbonyl include, but
are not limited to, aminocarbonyl, (methylamino)carbonyl,
(dimethylamino)carbonyl, and (ethylmethylamino)carbonyl.
[0181] The term "(NZ.sub.1Z.sub.2)sulfonyl" as used herein, means a
NZ.sub.1Z.sub.2 group, as defined herein, appended to the parent
molecular moiety through a sulfonyl group, as defined herein.
Representative examples of (NZ.sub.1Z.sub.2)sulfonyl include, but
are not limited to, aminosulfonyl, (methylamino)sulfonyl,
(dimethylamino)sulfonyl, and (ethylmethylamino)sulfonyl.
[0182] The term "oxo" as used herein, means a .dbd.O moiety.
[0183] The term "sulfinyl" as used herein, means a .dbd.S(O)--
group.
[0184] The term "sulfonyl" as used herein, means a --S(O).sub.2--
group.
[0185] Compounds of the present invention may exist as
stereoisomers wherein, asymmetric or chiral centers are present.
These stereoisomers are "R" or "S" depending on the configuration
of substituents around the chiral carbon atom. The terms "R" and
"S" used herein are configurations as defined in IUPAC 1974
Recommendations for Section E, Fundamental Stereochemistry, Pure
Appl. Chem., 1976, 45: 13-30. The present invention contemplates
various stereoisomers and mixtures thereof and are specifically
included within the scope of this invention. Stereoisomers include
enantiomers and diastereomers, and mixtures of enantiomers or
diastereomers. Individual stereoisomers of compounds of the present
invention may be prepared synthetically from commercially available
starting materials which contain asymmetric or chiral centers or by
preparation of racemic mixtures followed by resolution well-known
to those of ordinary skill in the art. These methods of resolution
are exemplified by (1) attachment of a mixture of enantiomers to a
chiral auxiliary, separation of the resulting mixture of
diastereomers by recrystallization or chromatography and liberation
of the optically pure product from the auxiliary or (2) direct
separation of the mixture of optical enantiomers on chiral
chromatographic columns.
[0186] Compounds of the present invention were named by
ACD/ChemSketch version 5.06 (developed by Advanced Chemistry
Development, Inc., Toronto, ON, Canada) or were given names which
appeared to be consistent with ACD nomenclature.
Abbreviations
[0187] Abbreviations which have been used in the descriptions of
the Schemes and the Examples that follow are: DMF for
N,N-dimethylformamide; DMSO for dimethylsulfoxide; Et for ethyl; Me
for methyl; Ms for CH.sub.3 S(O).sub.2O--; Ph for phenyl; THF for
tetrahydrofuran; Ts for p-CH.sub.3PhS(O).sub.2O--; and Tf for
CF.sub.3S(O).sub.2O--.
Preparation of Compounds of the Present Invention
[0188] The compounds and processes of the present invention will be
better understood in connection with the following synthetic
Schemes and Examples which illustrate a means by which the
compounds of the present invention can be prepared.
##STR00004##
[0189] Indoles of formula (5), wherein R.sub.1, R.sub.3, R.sub.4,
R.sub.5, R.sub.6, R.sub.7, and R.sub.8 are as defined in Formula
(I), can be prepared using the method described in Scheme 1 or by
methods known to those of skill in the art. Indoles of formula (1),
purchased or prepared using methodology known to those of skill in
the art, can be treated with acid chlorides of formula (2), a
grignard reagent such as ethylgrignard (EtMgBr), and ZnCl.sub.2 in
a solvent such as methylene chloride to provide indoles of formula
(3). Indoles of formula (3) can be treated with a compound of
formula (4) and a base such as sodium hydride in a solvent such as
N,N-dimethylformamide to provide indoles of formula (5).
[0190] It is to be understood that substituents at the R.sub.1,
R.sub.5, R.sub.6, R.sub.7, or R.sub.8 positions of formula (1) (3),
or (5), can be further subjected to methods known to those of skill
in the art to provide compounds of the present invention.
Example 1
{1-[(1-methylpiperidin-2-yl)methyl]-1H-indol-3-yl}(2,2,3,3-tetramethylcycl-
opropyl)methanone
Example 1A
2,2,3,3-tetramethylcyclopropanecarbonyl Chloride
[0191] To a flask containing 2,2,3,3-tetramethylcyclopropane
carboxylic acid (Aldrich, 13.5 g, 95 mmol) was added 30 mL of
thionyl chloride (410 mmol, excess). This solution was warmed to
reflux and stirred for 2 h. The mixture was then cooled to ambient
temperature and concentrated under reduced pressure. The residue
was azeotroped three times with 10 mL of benzene to remove any
remaining thionyl chloride, and used without further
purification.
Example 1B
1H-indol-3-yl(2,2,3,3-tetramethylcyclopropyl)methanone
[0192] To a solution of indole (Aldrich, 11 g, 95 mmol) in 30 mL
dichloromethane at ambient temperature was added 105 mL of a 1 M
solution of ethyl magnesium bromide in tetrahydrofuran (THF) (105
mmol) dropwise via syringe pump. After the addition was complete,
the solution was stirred for 15 min at which time ZnCl.sub.2 (14 g,
105 mmol) was added. The mixture stirred for an additional 30 min
then the product of Example 1A (95 mmol) in 50 mL dichloromethane
was added via cannula. The mixture was stirred for 6 h then was
quenched with 50 mL saturated aqueous NH.sub.4Cl and diluted with
50 mL dichloromethane. The layers were separated and the aqueous
layer was extracted with 3.times.30 mL dichloromethane. The
combined organics were washed with 1.times.20 mL H.sub.2O then were
dried over anhydrous Na.sub.2SO.sub.4, filtered and concentrated
under reduced pressure. The crude material was purified via column
chromatography (SiO.sub.2, 50% ethyl acetate:hexanes) to give 9.7 g
of the major regioisomer
1H-indol-3-yl(2,2,3,3-tetramethylcyclopropyl)methanone (40 mmol,
42% yield) and 6.1 g of the minor regioisomer of
1-[(2,2,3,3-tetramethylcyclopropyl)carbonyl]-1H-indole (25 mmol,
27% yield). MS (major and minor regioisomers) (DCI/NH.sub.3) m/z
242 (M+H).sup.+.
Example 1C
(1-methylpiperidin-2-yl)methyl methanesulfonate
[0193] To a solution of 1-methyl-2-piperidine-methanol (Aldrich,
0.27 mL, 2.1 mmol) in 10 mL tetrahydrofuran (THF) at 0.degree. C.
was added triethylamine (0.87 mL, 6.22 mmol) followed by
methanesulfonyl chloride (0.24 mL, 3.1 mmol). The mixture was
stirred at 0.degree. C. for 10 min then the ice-bath was removed
and the reaction mixture was stirred at 23.degree. C. for an
additional 1.5 h. The reaction mixture was filtered though Celite
with THF and concentrated under reduced pressure. This crude
material was used directly in the next reaction.
Example 1D
{1-[(1-methylpiperidin-2-yl)methyl]-1H-indol-3-yl}(2,2,3,3-tetramethylcycl-
opropyl)methanone
[0194] To a solution of the major product of Example 1B (0.25 g,
1.0 mmol) in 5 mL DMF at 0.degree. C. was added NaH (60% dispersal
in mineral oil, 0.10 g, 2.6 mmol). This mixture was stirred at
0.degree. C. for 10 min then was warmed to ambient temperature and
allowed to stir for 30 min. The solution was again cooled to
0.degree. C. and the product of Example 1C (2.1 mmol) in 5 mL DMF
was added via cannula. The ice-bath was removed after the addition
was complete and the reaction mixture was warmed to 50.degree. C.
at which temperature it was stirred for 2 h. The mixture was cooled
to ambient temperature, diluted with 10 mL ethyl acetate and
quenched with 10 mL saturated, aqueous NH.sub.4Cl and 5 mL
H.sub.2O. The layers were separated and the aqueous layer was
extracted with 3.times.5 mL ethyl acetate and the combined organics
were dried over anhydrous Na.sub.2SO.sub.4, filtered, concentrated
and purified via column chromatography (SiO.sub.2, 1% NH.sub.4OH:
9% CH.sub.3OH: 90% dichloromethane) to give 0.18 g of the title
compound (0.51 mmol, 49% yield). MS (DCI/NH.sub.3) m/z 353
(M+H).sup.+.
Example 1E
{1-[(1-methylpiperidin-2-yl)methyl]-1H-indol-3-yl}(2,2,3,3-tetramethylcycl-
opropyl)methanone P-Toluenesulfonic Acid
[0195] To the product of Example 1D (0.18 g, 0.51 mmol) in 5 mL of
10% EtOH in ethyl acetate, was added p-toluenesulfonic acid
monohydrate (97 mg, 0.51 mmol). The resulting precipitate was
isolated via filtration resulting in 0.21 g of the title compound
(0.40 mmol, 78% yield). .sup.1H NMR (MeOH-d.sub.4, 300 MHz) .delta.
1.33 (s, 12H), 1.57 (m, 2H), 1.79 (m, 2H), 1.93 (m, 1H), 2.17 (s,
1H), 2.36 (s, 3H), 3.08 (s, 3H), 3.18 (m, 1H), 3.60 and 3.75 (m,
rotamers 1H), 4.37 and 4.95 (m, rotamers 1H), 7.23 (br d, J=7.8 Hz,
2H), 7.26 (m, 1H), 7.34 (ddd, J=7.1, 7.1, 1.4 Hz, 1H), 7.55 (m,
1H), 7.71 (br d, J=8.1 Hz, 2H) 8.12 (br s, 1H), 8.30 (d, J=7.8 Hz,
1H); MS (DCI/NH.sub.3) m/z 353 (M+H).sup.+; Anal. Calculated for
C.sub.23H.sub.32N.sub.2O.C.sub.7H.sub.8O.sub.3S.0.1H.sub.2O: C,
68.44; H, 7.70; N, 5.32. Found: C, 68.19; H, 7.61; N, 5.13.
Example 2
[1-(2-morpholin-4-ylethyl)-1H-indol-3-yl](2,2,3,3-tetramethylcyclopropyl)m-
ethanone P-Toluenesulfonic Acid
Example 2A
2-morpholin-4-ylethyl Methanesulfonate
[0196] A solution of 4-(2-hydroxylethyl)-morpholine (Aldrich, 5.1
mL, 42 mmol), triethylamine (17 mL, 124 mmol), and methanesulfonyl
chloride (4.8 mL, 62 mmol) in 100 mL THF were processed as
described in Example 1C to give the crude material which was used
directly in the next reaction.
Example 2B
[1-(2-morpholin-4-ylethyl)-1H-indol-3-yl](2,2,3,3-tetramethylcyclopropyl)m-
ethanone
[0197] The major product of Example 1B (5.0 g, 21 mmol), the
product of Example 2A (42 mmol) and NaH (60% dispersal in mineral
oil, 4.2 g, 104 mmol) in 40 mL dimethylformamide were processed as
in Example 1D. Purification via column chromatography (SiO.sub.2,
10% CH.sub.3OH: 90% EtOAc) gave 6.6 g of the title compound (18.6
mmol, 90% yield). MS (DCI/NH.sub.3) m/z 355 (M+H).sup.+.
Example 2C
[1-(2-morpholin-4-ylethyl)-1H-indol-3-yl](2,2,3,3-tetramethylcyclopropyl)m-
ethanone P-Toluenesulfonic Acid
[0198] p-Toluenesulfonic acid monohydrate (3.5 g, 19 mmol) and of
the product of Example 2B (6.6 g, 19 mmol) were processed as in
Example 1E. The crude material was concentrated under reduced
pressure and dried under reduced pressure to give 9.4 g of the
title compound (18 mmol, 96% yield). .sup.1H NMR (MeOH-d.sub.4, 300
MHz) .delta. 1.33 (s, 6H), 1.34 (s, 6H), 2.15 (s, 1H), 2.36 (s,
3H), 3.40 (m, 4H), 3.68 (dd, J=7.1, 7.1 Hz, 2H), 3.90 (m, 4H), 4.73
(dd, J=7.1, 7.1 Hz, 2H), 7.23 (br d, J=7.8 Hz, 2H), 7.26 (ddd,
J=8.1, 8.1, 1.4 Hz, 1H), 7.33 (ddd, J=7.1, 7.1, 1.0 Hz, 1H), 7.56
(br d, J=8.1 Hz, 1H), 7.72 (br d, J=8.5 Hz, 2H), 8.15 (s, 1H), 8.29
(dt, J=7.8, 1.0 Hz, 1H); MS (DCI/NH.sub.3) m/z 355 (M+H).sup.+;
Anal. Calculated for
C.sub.22H.sub.30N.sub.2O.sub.2.C.sub.7H.sub.8O.sub.3S: C, 66.13; H,
7.27; N, 5.32. Found: C, 66.24; H, 7.23; N, 5.19.
Example 3
[1-(2-pyridin-2-ylethyl)-1H-indol-3-yl](2,2,3,3-tetramethylcyclopropyl)met-
hanone P-Toluenesulfonic Acid
Example 3A
2-pyridin-2-ylethyl Methanesulfonate
[0199] A solution of 2-pyridin-2-yl-ethanol (Aldrich, 0.11 mL, 0.99
mmol), triethylamine (0.42 mL, 3.0 mmol), and methanesulfonyl
chloride (0.12 mL, 1.5 mmol) in 5 mL THF were processed as
described in Example 1C to give the crude title compound which was
used directly in the next reaction.
Example 3B
[1-(2-pyridin-2-ylethyl)-1H-indol-3-yl](2,2,3,3-tetramethylcyclopropyl)met-
hanone
[0200] The major product of Example 1B (0.12 g, 0.50 mmol), the
product of Example 3A (0.99 mmol), and NaH (60% dispersal in
mineral oil, 0.1 g, 2.5 mmol) in 10 mL dimethylformamide were
processed as in Example 1D. Purification via column chromatography
(SiO.sub.2, 50% hexanes: 50% EtOAc) provided 78 mg of the title
compound (0.23 mmol, 45% yield). MS (DCI/NH.sub.3) m/z 347
(M+H).sup.+.
Example 3C
[1-(2-pyridin-2-ylethyl)-1H-indol-3-yl](2,2,3,3-tetramethylcyclopropyl)met-
hanone P-Toluenesulfonic Acid
[0201] p-Toluenesulfonic acid monohydrate (44 mg, 0.23 mmol) and of
the product of Example 3B (78 mg, 0.23 mmol) were processed as in
Example 1E. Recrystallization with CH.sub.3OH and EtOAc gave 51 mg
of the title compound (0.10 mmol, 43% yield). .sup.1H NMR
(MeOH-d.sub.4, 300 MHz) .delta. 1.29 (s, 6H), 1.30 (s, 6H), 2.01
(s, 1H), 2.36 (s, 3H), 3.58 (t, J=6.8 Hz, 2H), 4.75 (t, J=6.5 Hz,
2H), 7.22 (m, 4H), 7.37 (m, 1H), 7.71 (br d, J=8.5 Hz, 2H), 7.76
(br d, J=7.8 Hz, 1H), 7.84 (m, 1H), 7.88 (s, 1H), 8.24 (m, 1H),
8.39 (ddd, J=7.8, 7.8, 1.7 Hz, 1H), 8.65 (br d, 5.1 Hz, 1H); MS
(DCI/NH.sub.3) m/z 347 (M+H).sup.+; Anal. Calculated for
C.sub.23H.sub.26N.sub.2O.C.sub.7H.sub.8O.sub.3S: C, 69.47; H, 6.61;
N, 5.40. Found: C, 69.13; H, 6.60; N, 5.28.
Example 4
{1-[(1-methyl-1H-imidazol-2-yl)methyl]-1H-indol-3-yl}(2,2,3,3-tetramethylc-
yclopropyl)methanone P-Toluenesulfonic Acid
Example 4A
(1-methyl-1H-imidazol-2-yl)methyl methanesulfonate
[0202] A solution of (1-methyl-1H-imidazol-2-yl)-methanol (Bionet
Research, 66 mg, 0.59 mmol), triethylamine (0.25 mL, 0.89 mmol),
and methanesulfonyl chloride (69 .mu.L, 0.89 mmol) in 5 mL THF were
processed as described in Example 1C to give the crude material
which was used directly in the next reaction.
Example 4B
{1-[(1-methyl-1H-imidazol-2-yl)methyl]-1H-indol-3-yl}(2,2,3,3-tetramethylc-
yclopropyl)methanone
[0203] The major product of Example 1B (0.10 g, 0.42 mmol), the
product of Example 4A (0.59 mmol) and NaH (60% dispersal in mineral
oil, 60 mg, 1.5 mmol) in 5 mL dimethylformamide were processed as
in Example 1D. Purification via column chromatography (SiO.sub.2,
100% EtOAc) afforded 25 mg of the title compound (0.075 mmol, 18%
yield). MS (DCI/NH.sub.3) m/z 336 (M+H).sup.+.
Example 4C
{1-[(1-methyl-1H-imidazol-2-yl)methyl]-1H-indol-3-yl}(2,2,3,3-tetramethylc-
yclopropyl)methanone P-Toluenesulfonic Acid
[0204] p-Toluenesulfonic acid monohydrate (14 mg, 0.075 mmol) and
the product of Example 4B (25 mg, 0.075 mmol) were processed as in
Example 1E. Recrystallization with CH.sub.3OH gave 16 mg of the
title compound (0.028 mmol, 37% yield). .sup.1H NMR (CDCl.sub.3,
300 MHz) .delta. 1.24 (s, 6H), 1.31 (s, 6H), 1.99 (s, 1H), 2.35 (s,
3H), 3.58 (s, 3H), 6.12 (br s, 2H), 6.96 (br s, 1H), 7.18 (br d,
J=8.1 Hz, 2H), 7.24 (m, 2H), 7.34 (m, 2H), 7.79 (br d, J=8.1 Hz,
2H), 8.09 (br s, 1H), 8.41 (dd, J=7.5, 1.4 Hz, 1H); MS
(DCI/NH.sub.3) m/z 336 (M+H).sup.+; Anal. Calculated for
C.sub.21H.sub.25N.sub.3O.C.sub.7H.sub.8O.sub.3S: C, 62.62; H, 6.53;
N, 7.28. Found: C, 62.37; H, 6.68; N, 7.26.
Example 5
tert-butyl
4-(2-{3-[(2,2,3,3-tetramethylcyclopropyl)carbonyl]-1H-indol-1-y-
l}ethyl)piperidine-1-carboxylate
Example 5A
tert-butyl
4-{[(methylsulfonyl)oxy]ethyl}piperidine-1-carboxylate
[0205] A solution of 4-(2-hydroxyethyl)-piperidine-1-carboxylic
acid tert-butyl ester (Aldrich, 0.50 g, 2.2 mmol), triethylamine
(0.91 mL, 6.5 mmol), and methanesulfonyl chloride (0.25 mL, 3.3
mmol) in 10 mL THF were processed as described in Example 1C to
give the crude title compound which was used directly in the next
reaction.
Example 5B
tert-butyl
4-(2-{3-[(2,2,3,3-tetramethylcyclopropyl)carbonyl]-1H-indol-1-y-
l}ethyl)piperidine-1-carboxylate
[0206] The major product of Example 1B (0.26 g, 1.1 mmol), the
product of Example 5A (2.2 mmol), and NaH (60% dispersal in mineral
oil, 0.22 g, 5.5 mmol) in 10 mL dimethylformamide were processed as
in Example 1D. Purification via column chromatography (SiO.sub.2,
1% NH.sub.4OH, 9% CH.sub.3OH: 90% CH.sub.2Cl.sub.2) provided 0.50 g
of the title compound (1.1 mmol, 98% yield). .sup.1H NMR
(CDCl.sub.3, 300 MHz) .delta. 1.24 (m, 3H), 1.31 (s, 6H), 1.35 (s,
6H), 1.46 (s, 9H), 1.72 (m, 2H), 1.86 (dd, J=14.9, 6.8 Hz, 2H),
1.93 (s, 1H), 2.67 (dd, J=14.9, 13.6 Hz, 2H), 4.11 (br d, J=12.9
Hz, 2H), 4.20 (dd, J=7.5, 7.5 Hz, 2H), 7.28 (m, 3H), 7.64 (s, 1H),
8.41 (ddd, J=7.5, 3.1, 2.0 Hz, 1H); MS (DCI/NH.sub.3) m/z 452
(M+H).sup.+; Anal. Calculated for
C.sub.28H.sub.40N.sub.2O.sub.3.0.5CH.sub.3OH: C, 73.04; H, 9.03; N,
5.98. Found: C, 73.00; H, 9.37; N, 6.06.
Example 6
[1-(2-Piperidin-4-yl-ethyl)-1H-indol-3-yl]-(2,2,3,3-tetramethyl-cyclopropy-
l)-methanone P-Toluenesulfonic Acid
Example 6A
[1-(2-piperidin-4-ylethyl)-1H-indol-3-yl](2,2,3,3-tetramethylcyclopropyl)m-
ethanone
[0207] To the product of Example 5B (0.42 g, 0.93 mmol) in 5 mL
dichloromethane at 0.degree. C. was added trifluoroacetic acid
(TFA, 3 mL, excess). The ice-bath was removed and the mixture
stirred at 23.degree. C. for 2 h then the mixture was concentrated
and purified via flash column chromatography (SiO.sub.2, 1%
NH.sub.4OH:9% CH.sub.3OH:90% dichloromethane) to give 0.30 g of the
title compound (0.85 mmol, 92% yield). MS (DCI/NH.sub.3) m/z 352
(M+H).sup.+.
Example 6B
[1-(2-piperidin-4-ylethyl)-1H-indol-3-yl](2,2,3,3-tetramethylcyclopropyl)m-
ethanone P-Toluenesulfonic Acid
[0208] p-Toluenesulfonic acid monohydrate (81 mg, 43 mmol) and the
product of Example 6A (0.15 g, 0.43 mmol) were processed as in
Example 1E. Recrystallization with CH.sub.3OH and EtOAc gave 0.16 g
of the title compound (0.28 mmol, 66% yield). .sup.1H NMR
(MeOH-d.sub.4, 300 MHz) .delta. 1.33 (s, 12H), 1.46 (m, 2H), 1.64
(m, 1H), 1.90 (dd, J=6.8, 6.8 Hz, 2H), 1.99 (br d, J=13.9 Hz, 2H),
2.15 (s, 1H), 2.35 (s, 3H), 2.93 (ddd, J=12.9, 12.9, 2.7 Hz, 2H),
3.36 (m, 2H), 4.33 (dd, J=7.1, 7.1 Hz, 2H), 7.20 (m, 1H), 7.23 (br
d, J=8.5 Hz, 2H), 7.26 (ddd, J=7.1, 7.1, 1.4 Hz, 1H), 7.48 (dt,
J=7.8, 1.0 Hz, 1H), 7.70 (br d, J=8.5 Hz, 2H), 8.08 (s, 1H), 8.25
(ddd, J=7.8, 1.4, 1.0 Hz, 1H); MS (DCI/NH.sub.3) m/z 353
(M+H).sup.+; Anal. Calculated for
C.sub.23H.sub.32N.sub.2O.1.25C.sub.7H.sub.8O.sub.3S: C, 66.64; H,
7.49; N, 4.90. Found: C, 66.53; H, 7.86; N, 4.77.
Example 7
{1-[2-(1-methylpiperidin-4-yl)ethyl]-1H-indol-3-yl}(2,2,3,3-tetramethylcyc-
lopropyl)methanone P-Toluenesulfonic Acid
Example 7A
{1-[2-(1-methylpiperidin-4-yl)ethyl]-1H-indol-3-yl}(2,2,3,3-tetramethylcyc-
lopropyl)methanone
[0209] To the product of Example 6A (0.15 g, 0.43 mmol) in 5 mL of
36% aqueous formaldehyde was added NaBH(OAc).sub.3 (0.17 g, 0.80
mmol). This mixture stirred at 23.degree. C. for 16 h then it was
diluted with 5 mL dichloromethane and was quenched with 3 mL
aqueous saturated NH.sub.4Cl and 3 mL H.sub.2O. The layers were
separated and the aqueous layer was extracted with 3.times.5 mL
dichloromethane. The combined organics were dried over
Na.sub.2SO.sub.4, filtered, concentrated and purified via column
chromatography (SiO.sub.2, 1% NH.sub.4OH: 9% CH.sub.3OH: 90%
dichloromethane) to give 0.15 g of the title compounds (0.41 mol,
95% yield). MS (DCI/NH.sub.3) m/z 367 (M+H).sup.+.
Example 7B
{1-[2-(1-methylpiperidin-4-yl)ethyl]-1H-indol-3-yl}(2,2,3,3-tetramethylcyc-
lopropyl)methanone P-Toluenesulfonic Acid
[0210] p-Toluenesulfonic acid monohydrate (78 mg, 0.41 mmol) and
the product of Example 7A (0.15 g, 0.41 mmol) were processed as in
Example 1E. Recrystallization with CH.sub.3OH and EtOAc provided 25
mg of the title compound (0.050 mmol, 12% yield). .sup.1H NMR
(MeOH-d.sub.4, 300 MHz) .delta. 1.33 (s, 12H), 1.54 (m, 3H), 1.91
(br q, J=7.1 Hz, 2H), 2.03 (m, 2H), 2.15 (s, 1H), 2.81 (s, 3H),
2.93 (m, 2H), 3.26 (m, 1H), 3.45 (m, 2H), 4.34 (t, J=7.1 Hz, 2H),
6.70 (s, 2H), 7.21 (dd, J=7.8, 1.0 Hz, 1H), 7.27 (dd, J=7.1, 1.4
Hz, 1H), 7.49 (br d, J=8.1 Hz, 1H), 8.09 (s, 1H), 8.25 (br d, J=7.1
Hz, 1H); MS (DCI/NH.sub.3) m/z 367 (M+H).sup.+; Anal. Calculated
for C.sub.24H.sub.34N.sub.2O.C.sub.4H.sub.4O.sub.4.0.5CH.sub.4O: C,
68.65; H, 8.09; N, 5.62. Found: C, 68.68; H, 8.49; N, 5.82.
Example 8
[1-(2-tetrahydro-2H-pyran-4-ylethyl)-1H-indol-3-yl](2,2,3,3-tetramethylcyc-
lopropyl)methanone
Example 8A
2-tetrahydro-2H-pyran-4-ylethanol
[0211] To 15 mL of tetrahydrofuran (THF) at 0.degree. C. was added
LiAlH.sub.4 (0.28 g, 7.3 mmol). This mixture was stirred for 10 min
then the ethyl tetrahydropyran-4-yl-acetate (Combi-Blocks Inc.,
0.50 g, 2.9 mmol) was added. The reaction was stirred for 5 min at
0.degree. C. then was allowed to warm to ambient temperature and
was stirred for 90 min. The reaction was quenched with excess
NaHSO.sub.4 10H.sub.2O and was stirred for 60 min. The mixture was
filtered through Celite. The filtrate was concentrated to give the
title compound which was carried on without further purification.
MS (DCI/NH.sub.3) m/z 131 (M+H).sup.+.
Example 8B
2-tetrahydro-2H-pyran-4-ylethyl Methanesulfonate
[0212] The product of Example 8A (2.9 mmol), triethylamine (1.2 mL,
8.7 mmol) and methanesulfonyl chloride (0.34 mL, 4.4 mmol) in 10 mL
tetrahydrofuran (THF) were reacted and the product isolated as in
Example 1C to give the title compound that was used directly in the
next reaction.
Example 8C
[1-(2-tetrahydro-2H-pyran-4-ylethyl)-1H-indol-3-yl](2,2,3,3-tetramethylcyc-
lopropyl)methanone
[0213] The major product of Example 1B (0.35 g, 1.5 mmol), the
product of Example 8B (2.9 mmol) and NaH (60% dispersal in mineral
oil, 0.29 g, 7.3 mmol) in 15 mL dimethylformamide (DMF) were
processed as in Example 1D. Purification via column chromatography
(SiO.sub.2, 50% hexanes: 50% EtOAc) gave 0.36 g of the title
compound in 70% three-step yield (1.0 mmol). .sup.1H NMR
(CDCl.sub.3, 300 MHz) .delta. 1.31 (s, 6H), 1.35 (s, 6H), 1.42 (dt,
J=12.4, 4.7 Hz, 2H), 1.60 (m, 2H), 1.69 (m, 1H), 1.86 (q, J=6.4 Hz,
2H), 1.94 (s, 1H), 3.37 (dt, J=11.5, 1.7 Hz, 2H), 3.98 (dd, J=11.5,
4.8 Hz, 2H), 4.20 (dd, J=7.5, 7.5 Hz, 2H), 7.29 (m, 3H), 7.65 (s,
1H), 8.40 (m, 1H); MS (DCI/NH.sub.3) m/z 354 (M+H).sup.+; Anal.
Calculated for C.sub.23H.sub.31NO.sub.2: C, 78.15; H, 8.84; N,
3.96. Found: C, 77.88; H, 8.89; N, 3.91.
Example 9
[1-(2-pyrrolidin-1-ylethyl)-1H-indol-3-yl](2,2,3,3-tetramethylcyclopropyl)-
methanone P-Toluenesulfonic Acid
Example 9A
2-pyrrolidin-1-ylethyl Methanesulfonate
[0214] The 1-(2-hydroxyethyl)-pyrrolidine (Aldrich, 0.14 g, 1.2
mmol), triethylamine (0.56 mL, 4.1 mmol), and methanesulfonyl
chloride (0.15 mL, 1.9 mmol) in 10 mL THF were processed as
described in Example 1C to give the title compound that was used
directly in the next reaction.
Example 9B
[1-(2-pyrrolidin-1-ylethyl)-1H-indol-3-yl](2,2,3,3-tetramethylcyclopropyl)-
methanone
[0215] The major product of Example 1B (0.15 g, 0.62 mmol), the
product of Example 9A (1.2 mmol) and NaH (60% dispersion in mineral
oil, 62 mg, 1.6 mmol) in 8 mL DMF were processed as in Example 1D.
Purification via column chromatography (SiO.sub.2, 2%
CH.sub.3OH:98% EtOAc) afforded 45 mg of the title compound (0.13
mmol, 21% yield. MS (DCI/NH.sub.3) m/z 338 (M+H).sup.+.
Example 9C
[1-(2-pyrrolidin-1-ylethyl)-1H-indol-3-yl](2,2,3,3-tetramethylcyclopropyl)-
methanone P-Toluenesulfonic Acid
[0216] p-Toluenesulfonic acid monohydrate (24 mg, 0.12 mmol) and
the product of Example 9B (41 mg, 0.12 mmol) were processed as in
Example 1E. Recrystallization with CH.sub.3OH, EtOAc and Et.sub.2O
provided 44 mg of the title compound (0.086 mmol, 14% yield).
.sup.1H NMR (MeOH-d.sub.4, 300 MHz) .delta. 1.33 (s, 6H), 1.34 (s,
6H), 2.06 (m, 4H), 2.17 (s, 1H), 2.36 (s, 3H), 3.16 (m, 2H), 3.59
(m, 2H), 3.75 (t, J=6.8 Hz, 2H), 4.67 (t, J=6.8 Hz, 2H), 7.23 (br
d, J=8.1 Hz, 2H), 7.30 (m, 2H), 7.56 (m, 1H), 7.71 (br d, J=8.1 Hz,
2H) 8.16 (s, 1H), 8.30 (m, 1H); MS (DCI/NH.sub.3) m/z 339
(M+H).sup.+; Anal. Calculated for
C.sub.22H.sub.30N.sub.2OO.C.sub.7H.sub.8O.sub.3S: C, 68.20; H,
7.50; N, 5.49. Found: C, 68.14; H, 7.51; N, 5.35.
Example 10
(2,2,3,3-tetramethylcyclopropyl)[1-(2-thien-2-ylethyl)-1H-indol-3-yl]metha-
none
Example 10A
2-thien-2-ylethyl Methanesulfonate
[0217] The 2-(2-thienyl)ethanol (Aldrich, 0.16 g, 1.2 mmol),
triethylamine (0.56 mL, 4.1 mmol), and methanesulfonyl chloride
(0.15 mL, 1.9 mmol) in 10 mL THF were processed as described in
Example 1C to give the title compound that was used directly in the
next reaction.
Example 10B
(2,2,3,3-tetramethylcyclopropyl)[1-(2-thien-2-ylethyl)-1H-indol-3-yl]metha-
none
[0218] The major product of Example 1B (0.15 g, 0.62 mmol), the
product of Example 10A (1.2 mmol) and NaH (60% dispersion in
mineral oil, 0.12 g, 3.1 mmol) in 8 mL DMF were processed as in
Example 1D. Purification via column chromatography (SiO.sub.2, 10%
EtOAc:90% hexanes) afforded 0.12 g of the title compound (0.33
mmol, 53% yield). .sup.1H NMR (CDCl.sub.3, 300 MHz) .delta. 1.26
(s, 6H), 1.31 (s, 6H), 1.81 (s, 1H), 3.37 (t, J=6.8 Hz, 2H), 4.42
(t, J=7.1 Hz, 2H), 6.66 (m, 1H), 6.91 (dd, J=5.1, 3.4 Hz, 1H), 7.19
(dd, J=5.1, 1.4 Hz, 1H), 7.29 (m, 2H), 7.33 (m, 1H), 7.43 (s, 1H),
8.42 (m, 1H); MS (DCI/NH.sub.3) m/z 352 (M+H).sup.+; Anal.
Calculated for C.sub.22H.sub.25NOS: C, 75.17; H, 7.17; N, 3.98.
Found: C, 74.99; H, 7.34; N, 3.91.
Example 11
[1-(2-methoxyethyl)-1H-indol-3-yl](2,2,3,3-tetramethylcyclopropyl)methanon-
e
Example 11A
2-methoxyethyl Methanesulfonate
[0219] The 2-methoxyethanol (Aldrich, 94 mg, 1.2 mmol),
triethylamine (0.56 mL, 4.1 mmol), and methanesulfonyl chloride
(0.15 mL, 1.9 mmol) in 10 mL THF were processed as described in
Example 1C to give the title compound that was used directly in the
next reaction.
Example 11B
[1-(2-methoxyethyl)-1H-indol-3-yl](2,2,3,3-tetramethylcyclopropyl)methanon-
e
[0220] The major product of Example 1B (0.15 g, 0.62 mmol), the
product of Example 11A (1.2 mmol) and NaH (60% dispersion in
mineral oil, 0.12 g, 3.1 mmol) in 8 mL DMF were processed as in
Example 1D. Purification via column chromatography (SiO.sub.2, 90%
hexanes 10% EtOAc) gave 0.122 g of the title compound (0.41 mmol,
66% yield). .sup.1H NMR (MeOH-d.sub.4, 300 MHz) .delta. 1.32 (s,
6H), 1.33 (s, 6H), 2.11 (s, 1H), 3.31 (s, 3H), 3.76 (dd, J=5.4, 5.4
Hz, 2H), 4.41 (dd, J=5.1, 5.1 Hz, 2H), 7.22 (m, 2H), 7.48 (m, 1H),
8.03 (s, 1H), 8.24 (m, 1H); MS (DCI/NH.sub.3) m/z 300 (M+H).sup.+;
Anal. Calculated for C.sub.19H.sub.25NO.sub.2: C, 76.22; H, 8.42;
N, 4.68. Found: C, 76.18; H, 8.73; N, 4.35.
Example 12
1-(2-{3-[(2,2,3,3-tetramethylcyclopropyl)carbonyl]-1H-indol-1-yl}ethyl)pyr-
rolidin-2-one
Example 12A
2-(2-oxopyrrolidin-1-yl)ethyl Methanesulfonate
[0221] The 1-(2-hydroxyethyl)-2-pyrrolidinone (Aldrich, 0.16 g, 1.2
mmol), triethylamine (0.56 mL, 4.1 mmol), and methanesulfonyl
chloride (0.15 mL, 1.9 mmol) in 10 mL THF were processed as
described in Example 1C to give the title compound that was used
directly in the next reaction.
Example 12B
1-(2-{3-[(2,2,3,3-tetramethylcyclopropyl)carbonyl]-1H-indol-1-yl}ethyl)pyr-
rolidin-2-one
[0222] The major product of Example 1B (0.15 g, 0.62 mmol), the
product of Example 12A (1.2 mmol) and NaH (60% dispersion in
mineral oil, 0.12 g, 3.1 mmol) in 8 mL DMF were processed as in
Example 1D. Purification via column chromatography (SiO.sub.2, 90%
hexanes:10% EtOAc) provided 0.12 g of the title compound (0.33
mmol, 53% yield). .sup.1H NMR (MeOH-d.sub.4, 300 MHz) .delta. 1.33
(s, 12H), 1.79 (m, 2H), 2.15 (s, 1H), 2.23 (dd, J=7.8, 7.8 Hz, 2H),
3.04 (dd, J=6.8, 6.8 Hz, 2H), 3.70 (dd, J=6.1, 6.1 Hz, 2H), 4.45
(dd, J=5.8, 5.8 Hz, 2H), 7.21 (td, J=8.1, 1.4 Hz, 1H), 7.28 (td,
J=7.1, 1.4 Hz, 1H), 7.50 (td, J=8.1, 1.0 Hz, 1H), 8.07 (s, 1H),
8.26 (ddd, J=7.8, 1.4, 0.7 Hz, 1H); MS (DCI/NH.sub.3) m/z 353
(M+H).sup.+; Anal. calculated for C.sub.22H.sub.28N.sub.2O.sub.2:
C, 74.97; H, 8.01; N, 7.95. Found: C, 74.62; H, 8.12; N, 7.88.
Example 13
1-(2-{3-[(2,2,3,3-tetramethylcyclopropyl)carbonyl]-1H-indol-1-yl}ethyl)pyr-
rolidine-2,5-dione
Example 13A
2-(2,5-dioxopyrrolidin-1-yl)ethyl Methanesulfonate
[0223] The N-(2-hydroxyethyl)succinimide (Aldrich, 0.19 g, 1.2
mmol), triethylamine (0.56 mL, 4.1 mmol), and methanesulfonyl
chloride (0.15 mL, 1.9 mmol) in 10 mL THF were processed as
described in Example 1C to give the title compound that was used
directly in the next reaction.
Example 13B
1-(2-{3-[(2,2,3,3-tetramethylcyclopropyl)carbonyl]-1H-indol-1-yl}ethyl)pyr-
rolidine-2,5-dione
[0224] The major product of Example 1B (0.15 g, 0.62 mmol), the
product of Example 13A (1.2 mmol) and NaH (60% dispersion in
mineral oil, 0.12 g, 3.1 mmol) in 8 mL DMF were processed as in
Example 1D. Purification via column chromatography (SiO.sub.2, 50%
hexanes 50% EtOAc) afforded 43 mg of the title compound (0.12 mmol,
18% yield). .sup.1H NMR (CDCl.sub.3, 300 MHz) .delta. 1.32 (s, 6H),
1.35 (s, 6H), 1.94 (s, 1H), 2.57 (s, 4H), 3.98 (t=7.1 Hz, 2H), 4.38
(t=7.2 Hz, 2H), 7.25 (td, J=7.1, 1.4 Hz, 1H), 7.29 (td, J=7.1, 1.7
Hz, 1H), 7.39 (m, 1H), 7.67 (s, 1H), 8.40 (m, 1H); MS
(DCI/NH.sub.3) m/z 366 (M+H).sup.+; Anal. Calculated for
C.sub.22H.sub.26N.sub.2O.sub.3.0.5H.sub.2O: C, 70.38; H, 7.25; N,
7.46. Found: C, 70.41; H, 6.94; N, 7.25.
Example 14
{1-[2-(4-methyl-1,3-thiazol-5-yl)ethyl]-1H-indol-3-yl}(2,2,3,3-tetramethyl-
cyclopropyl)methanone
Example 14A
2-(4-methyl-1,3-thiazol-5-yl)ethyl Methanesulfonate
[0225] The 4-methyl-5-thiazole ethanol (Aldrich, 0.18 g, 1.2 mmol),
triethylamine (0.56 mL, 4.1 mmol), and methanesulfonyl chloride
(0.15 mL, 1.9 mmol) in 10 mL THF were processed as described in
Example 1C to give the title compound that was used directly in the
next reaction.
Example 14B
{1-[2-(4-methyl-1,3-thiazol-5-yl)ethyl]-1H-indol-3-yl}(2,2,3,3-tetramethyl-
cyclopropyl)methanone
[0226] The major product of Example 1B (0.15 g, 0.62 mmol), the
product of Example 14A (1.2 mmol) and NaH (60% dispersion in
mineral oil, 0.12 g, 3.1 mmol) in 8 mL DMF were processed as in
Example 1D. Purification via column chromatography (SiO.sub.2, 50%
hexanes 50% EtOAc) provided 73 mg of the title compound (0.20 mmol,
32% yield). .sup.1H NMR (CDCl.sub.3, 300 MHz) .delta. 1.26 (s, 6H),
1.32 (s, 6H), 1.81 (s, 1H), 2.15 (s, 3H), 3.33 (t, J=5.8 Hz, 2H),
4.39 (t, J=6.1 Hz, 2H), 7.28 (m, 2H), 7.29 (s, 1H), 7.39 (m, 1H),
8.41 (m, 1H), 8.64 (m, 1H); MS (DCI/NH.sub.3) m/z 366 (M+H).sup.+;
Anal. Calculated for C.sub.22H.sub.26N.sub.2OS.0.5H.sub.2O: C,
72.09; H, 7.15; N, 7.64. Found: C, 71.79; H, 7.29; N, 7.56.
Example 15
{1-[2-(dimethylamino)ethyl]-1H-indol-3-yl}(2,2,3,3-tetramethylcyclopropyl)-
methanone P-Toluenesulfonic Acid
Example 15A
2-(dimethylamino)ethyl Methanesulfonate
[0227] The N,N-dimethylethanolamine (Aldrich, 0.11 g, 1.2 mmol),
triethylamine (0.56 mL, 4.1 mmol), and methanesulfonyl chloride
(0.15 mL, 1.9 mmol) in 10 mL THF were processed as described in
Example 1C to give the title compound that was used directly in the
next reaction.
Example 15B
{1-[2-(dimethylamino)ethyl]-1H-indol-3-yl}(2,2,3,3-tetramethylcyclopropyl)-
methanone
[0228] The major product of Example 1B (0.15 g, 0.62 mmol), the
product of Example 15A (1.2 mmol) and NaH (60% dispersion in
mineral oil, 0.12 g, 3.1 mmol) in 8 mL DMF were processed as in
Example 1D. Purification via column chromatography (SiO.sub.2, 2%
CH.sub.3OH:98% EtOAc) afforded 0.12 g of the title compound (0.37
mmol, 60% yield). MS (DCI/NH.sub.3) m/z 313 (M+H).sup.+.
Example 15C
{1-[2-(dimethylamino)ethyl]-1H-indol-3-yl}(2,2,3,3-tetramethylcyclopropyl)-
methanone P-Toluenesulfonic Acid
[0229] p-Toluenesulfonic acid monohydrate (71 mg, 0.37 mmol) and
the product of Example 15B (0.12 g, 0.37 mmol) were processed as in
Example 1E. Recrystallization with CH.sub.3OH, EtOAc and Et.sub.2O
gave 0.12 g of the title compound (0.3 mmol, 81% yield). .sup.1H
NMR (MeOH-d.sub.4, 300 MHz) .delta. 1.33 (s, 6H), 1.34 (s, 6H),
2.16 (s, 1H), 2.36 (s, 3H), 2.98 (s, 6H), 3.68 (t, J=6.8 Hz, 2H),
4.70 (t, J=7.1 Hz, 2H), 7.22 (br d, J=8.1 Hz, 2H), 7.26 (m, 1H),
7.33 (ddd, J=8.1, 7.1, 1.4 Hz, 1H), 7.57 (br d, J=8.1 Hz, 1H), 7.70
(br d, J=8.1 Hz, 2H), 8.17 (s, 1H), 8.30 (ddd, J=7.8, 1.4, 0.7 Hz,
1H); MS (DCI/NH.sub.3) m/z 313 (M+H).sup.+; Anal. Calculated for
C.sub.20H.sub.28N.sub.2O.C.sub.7H.sub.8O.sub.3S: C, 66.91; H, 7.49;
N, 5.70. Found: C, 66.78; H, 7.39; N, 5.60.
Example 16
(2,2,3,3-tetramethylcyclopropyl)[1-(2-thien-3-ylethyl)-1H-indol-3-yl]metha-
none
Example 16A
2-thien-3-ylethyl Methanesulfonate
[0230] The 2-(3-thienyl)ethanol (Aldrich, 0.16 g, 1.2 mmol),
triethylamine (0.56 mL, 4.1 mmol), and methanesulfonyl chloride
(0.15 mL, 1.9 mmol) in 10 mL THF were processed as described in
Example 1C to give the title compound that was used directly in the
next reaction.
Example 16B
(2,2,3,3-tetramethylcyclopropyl)[1-(2-thien-3-ylethyl)-1H-indol-3-yl]metha-
none
[0231] The major product of Example 1B (0.15 g, 0.62 mmol), the
product of Example 16A (1.2 mmol) and NaH (60% dispersion in
mineral oil, 0.12 g, 3.1 mmol) in 8 mL DMF were processed as in
Example 1D. Purification via column chromatography (SiO.sub.2, 90%
hexanes 10% EtOAc) provided 0.15 g of the title compound (0.43
mmol, 69% yield). .sup.1H NMR (CDCl.sub.3, 300 MHz) .delta. 1.25
(s, 6H), 1.32 (s, 6H), 1.79 (s, 1H), 3.18 (t, J=6.8 Hz, 2H), 4.38
(t, J=6.8 Hz, 2H), 6.83 (m, 2H), 7.27 (m, 3H), 7.32 (m, 1H), 7.35
(s, 1H), 8.41 (m, 1H); MS (DCI/NH.sub.3) m/z 352 (M+H).sup.+; Anal.
calculated for C.sub.22H.sub.25NOS: C, 75.17; H, 7.17; N, 3.98.
Found: C, 75.24; H, 7.40; N, 3.86.
Example 17
{1-[2-(1-methylpyrrolidin-2-yl)ethyl]-1H-indol-3-yl}(2,2,3,3-tetramethylcy-
clopropyl)methanone P-Toluenesulfonic Acid
Example 17A
Methanesulfonic acid 2-(1-methyl-pyrrolidin-2-yl)-ethyl Ester
[0232] The 1-methyl-2-pyrrolidineethanol (Aldrich, 0.16 g, 1.2
mmol), triethylamine (0.56 mL, 4.1 mmol), and methanesulfonyl
chloride (0.15 mL, 1.9 mmol) in 10 mL THF were processed as
described in Example 1C to give the title compound that was used
directly in the next reaction.
Example 17B
{1-[2-(1-methylpyrrolidin-2-yl)ethyl]-1H-indol-3-yl}(2,2,3,3-tetramethylcy-
clopropyl)methanone
[0233] The major product of Example 1B (0.15 g, 0.62 mmol), the
product of Example 17A (1.2 mmol) and NaH (60% dispersion in
mineral oil, 0.12 g, 3.1 mmol) in 8 mL DMF were processed as in
Example 1D. Purification via column chromatography (SiO.sub.2, 10%
CH.sub.3OH:90% CH.sub.2Cl.sub.2) gave 85 mg of the title compound
(0.24 mmol, 39% yield). MS (DCI/NH.sub.3) m/z 353 (M+H).sup.+.
Example 17C
{1-[2-(1-methylpyrrolidin-2-yl)ethyl]-1H-indol-3-yl}(2,2,3,3-tetramethylcy-
clopropyl)methanone P-Toluenesulfonic Acid
[0234] p-Toluenesulfonic acid monohydrate (45 mg, 0.23 mmol) and
the product of Example 17B (80 mg, 0.23 mmol) were processed as in
Example 1E. Recrystallization with CH.sub.3OH, EtOAc and Et.sub.2O
provided 64 mg of the title compound (0.12 mmol, 54% yield).
.sup.1H NMR (MeOH-d.sub.4, 300 MHz) .delta. 1.33 (m, 12H), 1.79 (m,
1H), 2.09 (m, 3H), 2.16 (s, 1H), 2.33 (m, 1H), 2.35 (s, 3H), 2.57
(m, 1H), 2.88 (s, 3H), 3.12 (m, 1H), 3.32 (m, 1H), 3.64 (m, 1H),
4.41 (t, J=7.8 Hz, 2H), 7.22 (br d, J=8.8 Hz, 2H), 7.23 (m, 1H),
7.30 (td, J=7.1, 1.4 Hz, 1H), 7.53 (br d, J=7.8 Hz, 1H), 7.70 (br
d, J=8.1 Hz, 2H), 8.12 (s, 1H), 8.27 (br d, J=7.5 Hz, 1H); MS
(DCI/NH.sub.3) m/z 313 (M+H).sup.+; Anal. Calculated for
C.sub.23H.sub.32N.sub.2O.C.sub.7H.sub.8O.sub.3S.0.2H.sub.2O: C,
68.20; H, 7.71; N, 5.30. Found: C, 67.96; H, 7.83; N, 5.11.
Example 18
[1-(tetrahydro-2H-pyran-4-ylmethyl)-1H-indol-3-yl](2,2,3,3-tetramethylcycl-
opropyl)methanone
Example 18A
tetrahydro-2H-pyran-4-ylmethyl Methanesulfonate
[0235] The tetrahydropyran-4-methanol (Combi-Blocks, Inc., 0.15 g,
1.2 mmol), triethylamine (0.56 mL, 4.1 mmol), and methanesulfonyl
chloride (0.15 mL, 1.9 mmol) in 10 mL THF were processed as
described in Example 1C to give the title compound that was used
directly in the next reaction.
Example 18B
[1-(tetrahydro-2H-pyran-4-ylmethyl)-1H-indol-3-yl](2,2,3,3-tetramethylcycl-
opropyl)methanone
[0236] The major product of Example 1B (0.15 g, 0.62 mmol), the
product of Example 18A (1.2 mmol) and NaH (60% dispersion in
mineral oil, 0.12 g, 3.1 mmol) in 8 mL DMF were processed as in
Example 1D. Recrystallization with Et.sub.2O and hexanes afforded
0.19 g of the title compound (0.56 mmol, 90% yield). .sup.1H NMR
(CDCl.sub.3, 300 MHz) .delta. 1.31 (s, 6H), 1.35 (s, 6H), 1.46 (m,
4H), 1.94 (s, 1H), 2.16 (m, 1H), 3.33 (dt, J=11.5, 2.4 Hz, 2H),
3.98 (dd, J=10.5, 3.1 Hz, 2H), 4.04 (d, J=7.5 Hz, 2H), 7.27 (m,
2H), 7.33 (m, 1H), 7.61 (s, 1H), 8.40 (m, 1H); MS (DCI/NH.sub.3)
m/z 340 (M+H).sup.+; Anal. calculated for C.sub.22H.sub.29NO.sub.2:
C, 77.84; H, 8.61; N, 4.13. Found: C, 77.56; H, 8.84; N, 4.08.
Example 19
[1-(2-pyridin-3-ylethyl)-1H-indol-3-yl](2,2,3,3-tetramethylcyclopropyl)met-
hanone
Example 19A
2-pyridin-3-ylethyl Methanesulfonate
[0237] The 2-(3-pyridyl)ethan-1-ol (Maybridge, 0.15 g, 1.2 mmol),
triethylamine (0.56 mL, 4.1 mmol), and methanesulfonyl chloride
(0.15 mL, 1.9 mmol) in 10 mL THF were processed as described in
Example 1C to give the title compound that was used directly in the
next reaction.
Example 19B
[1-(2-pyridin-3-ylethyl)-1H-indol-3-yl](2,2,3,3-tetramethylcyclopropyl)met-
hanone
[0238] The major product of Example 1B (0.15 g, 0.62 mmol), the
product of Example 19A (1.2 mmol) and NaH (60% dispersion in
mineral oil, 0.12 g, 3.1 mmol) in 8 mL DMF were processed as in
Example 1D. Purification via column chromatography (SiO.sub.2, 50%
hexanes 50% EtOAc) gave 58 mg of the title compound (0.16 mmol, 25%
yield). .sup.1H NMR (CDCl.sub.3, 300 MHz) .delta. 1.25 (s, 6H),
1.32 (s, 6H), 1.79 (s, 1H), 3.23 (t, J=6.8 Hz, 2H), 4.44 (t, J=6.8
Hz, 2H), 7.23 (m, 2H), 7.28 (m, 3H), 7.36 (s, 1H), 8.42 (m, 1H),
8.54 (m, 2H); MS (DCI/NH.sub.3) m/z 347 (M+H).sup.+; Anal.
Calculated for
C.sub.23H.sub.26N.sub.2O.0.2C.sub.6H.sub.14.0.3H.sub.2O: C, 78.75;
H, 8.03; N, 7.59. Found: C, 78.76; H, 8.31; N, 7.87.
Example 20
{1-[2-(1H-pyrrol-1-yl)ethyl]-1H-indol-3-yl}(2,2,3,3-tetramethylcyclopropyl-
)methanone
Example 20A
2-(1H-pyrrol-1-yl)ethyl Methanesulfonate
[0239] The 1-(2-hydroxyethyl)pyrrole (TCI-US, 0.138 g, 1.2 mmol),
triethylamine (0.56 mL, 4.1 mmol), and methanesulfonyl chloride
(0.15 mL, 1.9 mmol) in 10 mL THF were processed as described in
Example 1C to give the title compound that was used directly in the
next reaction.
Example 20B
{1-[2-(1H-pyrrol-1-yl)ethyl]-1H-indol-3-yl}(2,2,3,3-tetramethylcyclopropyl-
)methanone
[0240] The major product of Example 1B (0.15 g, 0.62 mmol), the
product of Example 20A (1.2 mmol) and NaH (60% dispersion in
mineral oil, 0.12 g, 3.1 mmol) in 8 mL DMF were processed as in
Example 1D. Purification via column chromatography (SiO.sub.2, 80%
hexanes 20% EtOAc) gave 25 mg of the title compound (0.075 mmol,
12% yield). .sup.1H NMR (CDCl.sub.3, 300 MHz) .delta. 1.24 (s, 6H),
1.31 (s, 6H), 1.71 (s, 1H), 4.25 (m, 2H), 4.44 (m, 2H), 6.13 (t,
J=2.0 Hz, 2H), 6.41 (t, J=2.0 Hz, 2H), 6.92 (s, 1H), 7.28 (m, 3H),
8.42 (m, 1H); MS (DCI/NH.sub.3) m/z 335 (M+H).sup.+; Anal.
Calculated for
C.sub.22H.sub.26N.sub.2O.0.1C.sub.6H.sub.14.0.7H.sub.2O: C, 77.09;
H, 7.89; N, 7.62. Found: C, 76.94; H, 8.25; N, 7.91.
Example 21
(1-{2-[4-(dimethylamino)phenyl]ethyl}-1H-indol-3-yl)(2,2,3,3-tetramethylcy-
clopropyl)methanone
Example 21A
2-[4-(dimethylamino)phenyl]ethyl Methanesulfonate
[0241] The (4-dimethylamino)-phenethyl alcohol (Aldrich, 0.205 g,
1.2 mmol), triethylamine (0.56 mL, 4.1 mmol), and methanesulfonyl
chloride (0.15 mL, 1.9 mmol) in 10 mL THF were processed as
described in Example 1C to give the title compound that was used
directly in the next reaction.
Example 21B
(1-{2-[4-(dimethylamino)phenyl]ethyl}-1H-indol-3-yl)(2,2,3,3-tetramethylcy-
clopropyl)methanone
[0242] The major product of Example 1B (0.15 g, 0.62 mmol), the
product of Example 21A (1.2 mmol) and NaH (60% dispersion in
mineral oil, 0.12 g, 3.1 mmol) in 8 mL DMF were processed as in
Example 1D. Recrystallization with EtOAc and hexanes provided 0.15
g of the title compound (0.387 mmol, 62% yield). .sup.1H NMR
(CDCl.sub.3, 300 MHz) .delta. 1.21 (s, 6H), 1.24 (s, 6H), 1.85 (s,
1H), 2.86 (s, 6H), 3.01 (t, 2H), 4.44 (t, J=6.5 Hz, 2H), 6.65 (m,
2H), 6.83 (m, 2H), 7.19 (dt, J=7.8, 1.4 Hz, 1H), 7.26 (dt, J=7.1,
1.4 Hz, 1H), 7.48 (m, 1H), 7.49 (s, 1H), 8.22 (m, 1H); MS
(DCI/NH.sub.3) m/z 389 (M+H).sup.+; Anal. calculated for
C.sub.26H.sub.32N.sub.2O: C, 80.37; H, 8.30; N, 7.21. Found: C,
79.99; H, 8.58; N, 7.08.
Example 22
[1-(2-pyridin-4-ylethyl)-1H-indol-3-yl](2,2,3,3-tetramethylcyclopropyl)met-
hanone
Example 22A
2-pyridin-4-ylethyl Methanesulfonate
[0243] The 4-(2-hydroxyethyl)pyridine (Lancaster, 0.153 g, 1.2
mmol), triethylamine (0.56 mL, 4.1 mmol), and methanesulfonyl
chloride (0.15 mL, 1.9 mmol) in 10 mL THF were processed as
described in Example 1C to give the title compound that was used
directly in the next reaction.
Example 22B
[1-(2-pyridin-4-ylethyl)-1H-indol-3-yl](2,2,3,3-tetramethylcyclopropyl)met-
hanone
[0244] The major product of Example 1B (0.15 g, 0.62 mmol), the
product of Example 22A (1.2 mmol) and NaH (60% dispersion in
mineral oil, 0.12 g, 3.1 mmol) in 8 mL DMF were processed as in
Example 1D. Purification via column chromatography (SiO.sub.2, 50%
hexanes 50% EtOAc) afforded 42 mg of the title compound (0.12 mmol,
19% yield). .sup.1H NMR (CDCl.sub.3, 300 MHz) .delta. 1.25 (s, 6H),
1.31 (s, 6H), 1.78 (s, 1H), 3.20 (t, J=7.1 Hz, 2H), 4.44 (t, J=7.1
Hz, 2H), 7.03 (br d, J=5.4 Hz, 2H), 7.30 (m, 3H), 7.35 (s, 1H),
8.42 (m, 1H), 8.51 (br d, J=4.7 Hz, 2H); MS (DCI/NH.sub.3) m/z 347
(M+H).sup.+; Anal. Calculated for
C.sub.23H.sub.26N.sub.2O.0.3H.sub.2O: C, 78.51; H, 7.60; N, 7.96.
Found: C, 78.50; H, 7.31; N, 7.95.
Example 23
{1-[4-(benzyloxy)butyl]-1H-indol-3-yl}(2,2,3,3-tetramethylcyclopropyl)meth-
anone
Example 23A
4-(benzyloxy)butyl Methanesulfonate
[0245] The 1-benzyloxy-1-butanol (Aldrich, 0.22 g, 1.2 mmol),
triethylamine (0.56 mL, 4.1 mmol), and methanesulfonyl chloride
(0.15 mL, 1.9 mmol) in 10 mL THF were processed as described in
Example 1C to give the title compound that was used directly in the
next reaction.
Example 23B
{1-[4-(benzyloxy)butyl]-1H-indol-3-yl}(2,2,3,3-tetramethylcyclopropyl)meth-
anone
[0246] The major product of Example 1B (0.15 g, 0.62 mmol), the
product of Example 23A (1.2 mmol) and NaH (60% dispersion in
mineral oil, 0.12 g, 3.1 mmol) in 8 mL DMF were processed as in
Example 1D. Purification via column chromatography (SiO.sub.2, 80%
hexanes 20% EtOAc) gave 0.18 g of the title compound (0.45 mmol,
72% yield). .sup.1H NMR (CDCl.sub.3, 300 MHz) .delta. 1.29 (s, 6H),
1.34 (s, 6H), 1.66 (m, 2H), 1.93 (s, 1H), 2.01 (m, 2H), 3.50 (t,
J=6.1 Hz, 2H), 4.19 (t, J=7.1 Hz, 2H), 4.49 (s, 2H), 7.25 (m, 2H),
7.32 (m, 6H), 7.66 (s, 1H), 8.39 (m, 1H); MS (DCI/NH.sub.3) m/z 404
(M+H).sup.+; Anal. calculated for C.sub.27H.sub.33NO.sub.2: C,
80.36; H, 8.24; N, 3.47. Found: C, 79.99; H, 8.46; N, 3.30.
Example 24
[1-(4-hydroxybutyl)-1H-indol-3-yl](2,2,3,3-tetramethylcyclopropyl)methanon-
e
Example 24A
[1-(4-hydroxybutyl)-1H-indol-3-yl](2,2,3,3-tetramethylcyclopropyl)methanon-
e
[0247] To the product of Example 23B (0.18 g, 0.45 mmol) in 40 mL
ethanol (200 proof) was added 100 mg of Pd/C (10 wt % palladium on
activated carbon, Aldrich). This mixture was stirred under 1 atm of
H.sub.2 (balloon) for 18 hours after which time the mixture was
degassed three times with a N.sub.2 back-flush. The mixture was
then filtered, concentrated under reduced pressure and purified via
flash column chromatography (SiO.sub.2, 50% ethyl acetate:hexanes)
to give 85 mg of the title compound (0.27 mmol, 60% yield). .sup.1H
NMR (CDCl.sub.3, 300 MHz) .delta. 1.31 (s, 6H), 1.35 (s, 6H), 1.62
(m, 2H), 1.95 (s, 1H), 2.01 (m, 2H), 3.69 (t, J=6.1 Hz, 2H), 4.22
(t, J=7.1 Hz, 2H), 7.26 (m, 2H), 7.34 (m, 1H), 7.67 (s, 1H), 8.40
(m, 1H); MS (DCI/NH.sub.3) m/z 314 (M+H).sup.+; Anal. Calculated
for C.sub.20H.sub.27NO.sub.2.0.2H.sub.2O: C, 75.77; H, 8.71; N,
4.42. Found: C, 75.66; H, 8.60; N, 4.16.
Example 25
[1-(2-piperidin-1-ylethyl)-1H-indol-3-yl](2,2,3,3-tetramethylcyclopropyl)m-
ethanone
Example 25A
2-piperidin-1-ylethyl Methanesulfonate
[0248] The 1-piperidineethanol (Aldrich, 0.16 g, 1.2 mmol),
triethylamine (0.56 mL, 4.1 mmol), and methanesulfonyl chloride
(0.15 mL, 1.9 mmol) in 10 mL THF were processed as described in
Example 1C to give the title compound that was used directly in the
next reaction.
Example 25B
[1-(2-piperidin-1-ylethyl)-1H-indol-3-yl](2,2,3,3-tetramethylcyclopropyl)m-
ethanone
[0249] The major product of Example 1B (0.15 g, 0.62 mmol), the
product of Example 25A (1.2 mmol) and NaH (60% dispersion in
mineral oil, 0.12 g, 3.1 mmol) in 8 mL DMF were processed as in
Example 1D. Purification via column chromatography (SiO.sub.2, 50%
hexanes 50% EtOAc) afforded 0.21 g of the title compound (0.56
mmol, 91% yield). .sup.1H NMR (CDCl.sub.3, 300 MHz) .delta. 1.31
(s, 6H), 1.35 (s, 6H), 1.54 (m, 6H), 1.94 (s, 1H), 2.47 (m, 4H),
2.74 (m, 2H), 4.26 (m, 2H), 7.27 (m, 2H), 7.35 (m, 1H), 7.81 (br s,
1H), 8.41 (m, 1H); MS (DCI/NH.sub.3) m/z 353 (M+H).sup.+; Anal.
Calculated for
C.sub.23H.sub.26N.sub.2O.0.1C.sub.6H.sub.14.0.3H.sub.2O: C, 76.58;
H, 9.37; N, 7.57. Found: C, 76.48; H, 9.73; N, 7.82.
Example 26
{1-[4-(methylthio)butyl]-1H-indol-3-yl}(2,2,3,3-tetramethylcyclopropyl)met-
hanone
Example 26A
4-(methylthio)butyl Methanesulfonate
[0250] The 4-(methylthio)-1-butanol (Aldrich, 0.15 g, 1.2 mmol),
triethylamine (0.56 mL, 4.1 mmol), and methanesulfonyl chloride
(0.15 mL, 1.9 mmol) in 10 mL THF were processed as described in
Example 1C to give the title compound that was used directly in the
next reaction.
Example 26B
{1-[4-(methylthio)butyl]-1H-indol-3-yl}(2,2,3,3-tetramethylcyclopropyl)met-
hanone
[0251] The major product of Example 1B (0.15 g, 0.62 mmol), the
product of Example 26A (1.2 mmol) and NaH (60% dispersion in
mineral oil, 0.12 g, 3.1 mmol) in 8 mL DMF were processed as in
Example 1D. Purification via column chromatography (SiO.sub.2, 80%
hexanes 20% EtOAc) afforded 0.19 g of the title compound (0.55
mmol, 89% yield). .sup.1H NMR (CDCl.sub.3, 300 MHz) .delta. 1.31
(s, 6H), 1.35 (s, 6H), 1.66 (m, 2H), 1.95 (s, 1H), 2.03 (m, 2H),
2.06 (s, 3H), 2.53 (brt, J=6.8 Hz, 2H), 4.19 (t, J=7.1 Hz, 2H),
7.27 (m, 2H), 7.34 (m, 1H), 7.67 (s, 1H), 8.41 (m, 1H); MS
(DCI/NH.sub.3) m/z 344 (M+H).sup.+; Anal. calculated for
C.sub.23H.sub.26N.sub.2O: C, 73.42; H, 8.51; N, 4.08. Found: C,
73.36; H, 8.86; N, 4.00.
Example 27
[1-(3-morpholin-4-ylpropyl)-1H-indol-3-yl](2,2,3,3-tetramethylcyclopropyl)-
methanone
Example 27A
3-morpholin-4-ylpropyl Methanesulfonate
[0252] The 4-(3-hydroxypropyl)morpholine (Aldrich, 0.18 g, 1.2
mmol), triethylamine (0.56 mL, 4.1 mmol), and methanesulfonyl
chloride (0.15 mL, 1.9 mmol) in 10 mL THF were processed as
described in Example 1C to give the title compound that was used
directly in the next reaction.
Example 27B
[1-(3-morpholin-4-ylpropyl)-1H-indol-3-yl](2,2,3,3-tetramethylcyclopropyl)-
methanone
[0253] The major product of Example 1B (0.15 g, 0.62 mmol), the
product of Example 27A (1.2 mmol) and NaH (60% dispersion in
mineral oil, 0.12 g, 3.1 mmol) in 8 mL DMF were processed as in
Example 1D. Purification via column chromatography (SiO.sub.2, 20%
hexanes 80% EtOAc) yielded 0.15 g of the title compound (0.41 mmol,
66% yield). .sup.1H NMR (CDCl.sub.3, 300 MHz) .delta. 1.30 (s, 6H),
1.35 (s, 6H), 1.93 (s, 1H), 2.05 (m, 2H), 2.29 (m, 2H), 2.42 (m,
4H), 3.75 (m, 4H), 4.28 (t, J=6.5 Hz, 2H), 7.26 (m, 2H), 7.38 (m,
1H), 7.71 (s, 1H), 8.40 (m, 1H); MS (DCI/NH.sub.3) m/z 367
(M+H).sup.+; Anal. Calculated for C.sub.23H.sub.32N.sub.2O.sub.2:
C, 74.96; H, 8.75; N, 7.60. Found: C, 74.85; H, 8.91; N, 7.43.
Example 28
[1-(2-azepan-1-ylethyl)-1H-indol-3-yl](2,2,3,3-tetramethylcyclopropyl)meth-
anone
Example 28A
2-azepan-1-ylethyl Methanesulfonate
[0254] The N-(2-hydroxyethyl)hexamethyleneimine (Lancaster, 0.18 g,
1.2 mmol), triethylamine (0.56 mL, 4.1 mmol), and methanesulfonyl
chloride (0.15 mL, 1.9 mmol) in 10 mL THF were processed as
described in Example 1C to give the title compound that was used
directly in the next reaction.
Example 28B
[1-(2-azepan-1-ylethyl)-1H-indol-3-yl](2,2,3,3-tetramethylcyclopropyl)meth-
anone
[0255] The major product of Example 1B (0.15 g, 0.62 mmol), the
product of Example 28A (1.2 mmol) and NaH (60% dispersion in
mineral oil, 0.12 g, 3.1 mmol) in 8 mL DMF were processed as in
Example 1D. Purification via column chromatography (SiO.sub.2, 20%
hexanes 80% EtOAc) gave 0.19 g of the title compound (0.50 mmol,
81% yield). .sup.1H NMR (CDCl.sub.3, 300 MHz) .delta. 1.30 (s, 6H),
1.35 (s, 6H), 1.62 (m, 8H), 1.95 (s, 1H), 2.70 (m, 4H), 2.94 (m,
2H), 4.22 (m, 2H), 7.27 (m, 2H), 7.34 (m, 1H), 7.84 (s, 1H), 8.42
(m, 1H); MS (DCI/NH.sub.3) m/z 367 (M+H).sup.+; Anal. Calculated
for C.sub.23H.sub.32N.sub.2O.sub.2.0.2H.sub.2O: C, 77.50; H, 9.38;
N, 7.53. Found: C, 77.39; H, 9.68; N, 7.50.
Example 29
[1-(2-piperazin-1-ylethyl)-1H-indol-3-yl](2,2,3,3-tetramethylcyclopropyl)m-
ethanone Tris-Trifluoroacetic Acid
Example 29A
tert-butyl
4-{2-[(methylsulfonyl)oxy]ethyl}piperazine-1-carboxylate
[0256] A solution of
tert-butyl-4-(2-hydroxyethyl)-piperazine-1-carboxylate (Maybridge,
0.29 g, 1.2 mmol), triethylamine (0.56 mL, 4.1 mmol), and
methanesulfonyl chloride (0.15 mL, 1.9 mmol) in 10 mL THF were
processed as described in Example 1C to give the title compound
that was used directly in the next reaction.
Example 29B
tert-butyl
4-(2-{3-[(2,2,3,3-tetramethylcyclopropyl)carbonyl]-1H-indol-1-y-
l}ethyl)piperazine-1-carboxylate
[0257] The major product of Example 1B (0.15 g, 0.62 mmol), the
product of Example 29A (1.2 mmol) and NaH (60% dispersion in
mineral oil, 0.12 g, 3.1 mmol) in 8 mL DMF were processed as in
Example 1D. Purification via column chromatography (SiO.sub.2, 50%
hexanes 50% EtOAc) afforded 0.22 g of the title compound (0.48
mmol, 78% yield). MS (DCI/NH.sub.3) m/z 454 (M+H).sup.+.
Example 29C
[1-(2-piperazin-1-ylethyl)-1H-indol-3-yl](2,2,3,3-tetramethylcyclopropyl)m-
ethanone Tris-Trifluoroacetic Acid
[0258] To the product of Example 5B (0.42 g, 0.93 mmol) in 5 mL
dichloromethane at 0.degree. C. was added trifluoroacetic acid
(TFA, 3 mL, excess). The ice-bath was removed and the mixture
stirred at 23.degree. C. for 20 min then the mixture was
concentrated under reduced pressure. The residue was azeotroped
three times with 7 mL toluene to remove any remaining TFA. The
residue was then dissolved in ethyl acetate and concentrated under
reduced pressure. After sitting under vacuum for 16 hours, the
resulting solids were isolated to give 0.21 g of the title compound
(0.30 mmol, 63% yield). .sup.1H NMR (MeOH-d.sub.4, 300 MHz) .delta.
1.34 (s, 12H), 2.01 and 2.15 (s, 1H, rotamers), 2.73 and 2.78 (m,
4H, rotamers), 2.92 and 3.00 (t, J=6.1 Hz, 2H, rotamers), 3.14 and
3.18 (m, 4H, rotamers), 4.40 and 4.59 (t, J=6.4 Hz, 2H, rotamers),
7.21 (dt, J=7.1, 1.4 Hz, 1H), 7.28 (dt, J=7.1, 1.4 Hz, 1H), 7.51
(m, 1H), 8.09 (s, 1H), 8.24 (m, 1H); MS (DCI/NH.sub.3) m/z 354
(M+H).sup.+; Anal. Calculated for
C.sub.22H.sub.31N.sub.3O.3CF.sub.3CO.sub.2H.0.5H.sub.2O: C, 47.73;
H, 5.01; N, 5.96. Found: C, 47.65; H, 5.05; N, 5.83.
Example 30
{1-[2-(4-methylpiperazin-1-yl)ethyl]-1H-indol-3-yl}(2,2,3,3-tetramethylcyc-
lopropyl)methanone
[0259] The product of Example 29C (0.19 g, 0.27 mmol), formaldehyde
(36% aqueous solution, 10 mL), and NaBH(OAc).sub.3 (0.10 g, 0.47
mmol) were processed as in Example 7A. Purification via column
chromatography (SiO.sub.2, 1% NH.sub.4OH:5% CH.sub.3OH:94%
CH.sub.2Cl.sub.2) provided 65 mg of the title compound (0.17 mmol,
63% yield). .sup.1H NMR (MeOH-d.sub.4, 300 MHz) .delta. 1.33 (s,
12H), 2.13 (s, 1H), 2.27 (s, 3H), 2.51 (br m, 8H), 2.80 (t, J=6.4
Hz, 2H), 4.37 (t, J=6.4 Hz, 2H), 7.20 (m, 1H), 7.25 (m, 1H), 7.48
(m, 1H), 8.10 (s, 1H), 8.24 (m, 1H); MS (DCI/NH.sub.3) m/z 368
(M+H).sup.+; Anal. Calculated for
C.sub.23H.sub.33N.sub.3O.0.5CH.sub.3OH: C, 73.59; H, 9.20; N,
10.96. Found: C, 73.35; H, 9.56; N, 10.98.
Example 31
3-(2-{3-[(2,2,3,3-tetramethylcyclopropyl)carbonyl]-1H-indol-1-yl}ethyl)-1,-
3-oxazolidin-2-one
Example 31A
2-(2-oxo-1,3-oxazolidin-3-yl)ethyl Methanesulfonate
[0260] The 3-(2-hydroxyethyl)-2-oxazolidinone (Frinton
Laboratories, 0.16 g, 1.2 mmol), triethylamine (0.56 mL, 4.1 mmol),
and methanesulfonyl chloride (0.15 mL, 1.9 mmol) in 10 mL THF were
processed as described in Example 1C to give the title compound
which was used directly in the next reaction.
Example 31B
3-(2-{3-[(2,2,3,3-tetramethylcyclopropyl)carbonyl]-1H-indol-1-yl}ethyl)-1,-
3-oxazolidin-2-one
[0261] The major product of Example 1B (0.15 g, 0.62 mmol), the
product of Example 31A (1.2 mmol) and NaH (60% dispersion in
mineral oil, 0.12 g, 3.1 mmol) in 8 mL DMF were processed as in
Example 1D. Purification via column chromatography (SiO.sub.2, 20%
hexanes 80% EtOAc) gave 0.10 g of the title compound (0.27 mmol,
44% yield). .sup.1H NMR (MeOH-d.sub.4, 300 MHz) .delta. 1.33 (s,
12H), 2.14 (s, 1H), 3.24 (m, 2H), 3.70 (t, J=6.1 Hz, 2H), 4.12 (m,
2H), 4.48 (t, J=6.1 Hz, 2H), 7.22 (m, 1H), 7.29 (dt, J=7.1, 1.4 Hz,
1H), 7.54 (m, 1H), 8.10 (s, 1H), 8.27 (m, 1H); MS (DCI/NH.sub.3)
m/z 355 (M+H).sup.+; Anal. Calculated for
C.sub.21H.sub.26N.sub.2O.sub.3.0.9H.sub.2O: C, 68.05; H, 7.56; N,
7.56. Found: C, 68.23; H, 7.33; N, 7.47.
Example 32
[1-(tetrahydrofuran-3-ylmethyl)-1H-indol-3-yl](2,2,3,3-tetramethylcyclopro-
pyl)methanone
Example 32A
tetrahydrofuran-3-ylmethyl Methanesulfonate
[0262] The tetrahydro-3-furanmethanol (Aldrich, 0.13 g, 1.2 mmol),
triethylamine (0.56 mL, 4.1 mmol), and methanesulfonyl chloride
(0.15 mL, 1.9 mmol) in 10 mL THF were processed as described in
Example 1C to give the title compound that was used directly in the
next reaction.
Example 32B
[1-(tetrahydrofuran-3-ylmethyl)-1H-indol-3-yl](2,2,3,3-tetramethylcyclopro-
pyl)methanone
[0263] The major product of Example 1B (0.15 g, 0.62 mmol), the
product of Example 32A (1.2 mmol) and NaH (60% dispersion in
mineral oil, 0.12 g, 3.1 mmol) in 8 mL DMF were processed as in
Example 1D. Purification via column chromatography (SiO.sub.2, 70%
hexanes 30% EtOAc) afforded 0.16 g of the title compound (0.48
mmol, 77% yield). .sup.1H NMR (CDCl.sub.3, 300 MHz) .delta. 1.31
(s, 6H), 1.34 (s, 3H), 1.35 (s, 3H), 1.71 (m, 1H), 1.94 (s, 1H),
2.07 (m, 1H), 2.89 (m, 1H), 3.67 (m, 2H), 3.78 (m, 1H), 4.01 (m,
1H), 4.14 (d, J=7.8 Hz, 2H), 7.28 (m, 2H), 7.35 (m, 1H), 7.66 (s,
1H), 8.41 (m, 1H); MS (DCI/NH.sub.3) m/z 326 (M+H).sup.+; Anal.
Calculated for C.sub.21H.sub.27NO.sub.2: C, 77.50; H, 8.36; N,
4.30. Found: C, 77.33; H, 8.47; N, 4.26.
Example 33
(2,2,3,3-tetramethylcyclopropyl)[1-(4,4,4-trifluorobutyl)-1H-indol-3-yl]me-
thanone
Example 33A
4,4,4-trifluorobutyl Methanesulfonate
[0264] The 4,4,4-trifluoro-1-butanol (Lancaster, 0.16 g, 1.2 mmol),
triethylamine (0.56 mL, 4.1 mmol), and methanesulfonyl chloride
(0.15 mL, 1.9 mmol) in 10 mL THF were processed as described in
Example 1C to give the title compound that was used directly in the
next reaction.
Example 33B
(2,2,3,3-tetramethylcyclopropyl)[1-(4,4,4-trifluorobutyl)-1H-indol-3-yl]me-
thanone
[0265] The major product of Example 1B (0.15 g, 0.62 mmol), the
product of Example 33A (1.2 mmol) and NaH (60% dispersion in
mineral oil, 0.12 g, 3.1 mmol) in 8 mL DMF were processed as in
Example 1D. Purification via column chromatography (SiO.sub.2, 70%
hexanes 30% EtOAc) gave 0.19 g of the title compound (0.53 mmol,
86% yield). .sup.1H NMR (CDCl.sub.3, 300 MHz) .delta. 1.31 (s, 6H),
1.35 (s, 6H), 1.94 (s, 1H), 2.17 (m, 4H), 4.26 (br t, J=6.4 Hz,
2H), 7.30 (m, 3H), 7.64 (s, 1H), 8.41 (m, 1H); MS (DCI/NH.sub.3)
m/z 352 (M+H).sup.+; Anal. Calculated for
C.sub.20H.sub.24F.sub.3NO: C, 68.36; H, 6.88; N, 3.99. Found: C,
67.99; H, 7.18; N, 3.84.
Example 34
{1-[2-(2,2-dimethyl-1,3-dioxolan-4-yl)ethyl]-1H-indol-3-yl}(2,2,3,3-tetram-
ethylcyclopropyl)methanone
Example 34A
2-(2,2-dimethyl-1,3-dioxolan-4-yl)ethyl Methanesulfonate
[0266] The 4-(2-hydroxyethyl)-2,2-dimethyl-1,3-dioxolane (Aldrich,
0.19 g, 1.2 mmol), triethylamine (0.56 mL, 4.1 mmol), and
methanesulfonyl chloride (0.15 mL, 1.9 mmol) in 10 mL THF were
processed as described in Example 1C to give the title compound
that was used directly in the next reaction.
Example 34B
{1-[2-(2,2-dimethyl-1,3-dioxolan-4-yl)ethyl]-1H-indol-3-yl}(2,2,3,3-tetram-
ethylcyclopropyl)methanone
[0267] The major product of Example 1B (0.15 g, 0.62 mmol), the
product of Example 34A (1.2 mmol) and NaH (60% dispersion in
mineral oil, 0.12 g, 3.1 mmol) in 8 mL DMF were processed as in
Example 1D. Purification via column chromatography (SiO.sub.2, 80%
hexanes 20% EtOAc) afforded 0.12 g of the title compound (0.32
mmol, 52% yield). .sup.1H NMR (CDCl.sub.3, 300 MHz) .delta. 1.30
(s, 6H), 1.34 (s, 3H), 1.36 (s, 6H), 1.48 (s, 3H), 1.93 (s, 1H),
2.08 (m, 2H), 3.52 (m 1H), 3.99 (m, 2H), 4.36 (m, 2H), 7.27 (m,
2H), 7.38 (m, 1H), 7.71 (s, 1H), 8.41 (m, 1H); MS (DCI/NH.sub.3)
m/z 370 (M+H).sup.+; Anal. Calculated for C.sub.23H.sub.31NO.sub.3:
C, 74.76; H, 8.46; N, 3.79. Found: C, 74.43; H, 8.36; N, 3.70.
Example 35
[1-(3,4-dihydroxybutyl)-1H-indol-3-yl](2,2,3,3-tetramethylcyclopropyl)meth-
anone
[0268] To the product of Example 34B (0.11 g, 0.30 mmol) in 2 mL of
a 4:1 mixture of tetrahydropyran and water was added excess
p-toluenesulfonic acid (p-TSA, 0.1 g, 5.3 mmol). This mixture
stirred at ambient temperature for 24 h then was concentrated under
reduced pressure. The residue was purified via flash column
chromatography (SiO.sub.2, 100% ethyl acetate) to give 35 mg of the
title compound (0.10 mmol, 34% yield). .sup.1H NMR (CDCl.sub.3, 300
MHz) .delta. 1.31 (s, 6H), 1.35 (s, 6H), 1.67 (m, 2H), 1.95 (s,
1H), 1.97 (m, 2H), 3.46 (m, 1H), 3.63 (m, 2H), 4.39 (dd, J=8.1, 5.8
Hz, 2H), 7.27 (m, 2H), 7.39 (m, 1H), 7.72 (s, 1H), 8.39 (m, 1H); MS
(DCI/NH.sub.3) m/z 330 (M+H).sup.+; Anal. Calculated for
C.sub.20H.sub.27NO.sub.3.0.5H.sub.2O: C, 70.98; H, 8.34; N, 4.14.
Found: C, 70.68; H, 8.69; N, 3.86.
Example 36
[1-(1,3-dioxolan-4-ylmethyl)-1H-indol-3-yl](2,2,3,3-tetramethylcyclopropyl-
)methanone
Example 36A
1,3-dioxolan-4-ylmethyl Methanesulfonate
[0269] The glycerol formal (Aldrich, 0.26 g, 2.5 mmol),
triethylamine (1.1 mL, 8.3 mmol), and methanesulfonyl chloride
(0.30 mL, 3.7 mmol) in 20 mL THF were processed as described in
Example 1C to give the title compound that was used directly in the
next reaction.
Example 36B
[1-(1,3-dioxolan-4-ylmethyl)-1H-indol-3-yl](2,2,3,3-tetramethylcyclopropyl-
)methanone
[0270] The major product of Example 1B (0.30 g, 1.2 mmol), the
product of Example 36A (2.49 mmol) and NaH (60% dispersion in
mineral oil, 0.248 g, 6.22 mmol) in 16 mL DMF were processed as in
Example 1D. Purification via column chromatography (SiO.sub.2, 70%
hexanes:30% EtOAc) yielded 0.10 g of the title compound (0.305
mmol, 25% yield). .sup.1H NMR (CDCl.sub.3, 300 MHz) .delta. 1.31
(s, 6H), 1.34 (s, 3H), 1.35 (s, 3H), 1.95 (s, 1H), 3.71 (dd, J=8.5,
5.4 Hz, 1H), 3.99 (dd, J=8.8, 6.8 Hz, 1H), 4.28 (d, J=4.1 Hz, 1H),
4.30 (d, J=2.7 Hz, 1H), 4.46 (m, 1H), 4.89 (s, 1H), 5.09 (s, 1H),
7.28 (m, 2H), 7.34 (m, 1H), 7.74 (s, 1H), 8.42 (m, 1H); MS
(DCI/NH.sub.3) m/z 328 (M+H).sup.+; Anal. Calculated for
C.sub.20H.sub.25NO.sub.3: C, 73.37; H, 7.70; N, 4.28. Found: C,
72.94; H, 7.89; N, 4.13.
Example 37
{1-[2-(benzyloxy)ethyl]-1H-indol-3-yl}(2,2,3,3-tetramethylcyclopropyl)meth-
anone
Example 37A
2-(benzyloxy)ethyl Methanesulfonate
[0271] The 2-benzyloxyethanol (Aldrich, 0.25 g, 1.7 mmol),
triethylamine (0.67 mL, 5.0 mmol), and methanesulfonyl chloride
(0.19 mL, 2.5 mmol) in 20 mL THF were processed as described in
Example 1C to give the title compound that was used directly in the
next reaction.
Example 37B
{1-[2-(benzyloxy)ethyl]-1H-indol-3-yl}(2,2,3,3-tetramethylcyclopropyl)meth-
anone
[0272] The major product of Example 1B (0.20 g, 0.83 mmol), the
product of Example 37A (1.66 mmol) and NaH (60% dispersion in
mineral oil, 0.17 g, 4.1 mmol) in 10 mL DMF were processed as in
Example 1D. Purification via column chromatography (SiO.sub.2, 80%
hexanes 20% EtOAc) afforded 0.20 g of the title compound (0.54
mmol, 65% yield). .sup.1H NMR (CDCl.sub.3, 300 MHz) .delta. 1.27
(s, 6H), 1.34 (s, 6H), 1.92 (s, 1H), 3.84 (t, J=5.4 Hz, 2H), 4.36
(t, J=5.1 Hz, 2H), 4.47 (s, 2H), 7.23 (m, 4H), 7.29 (m, 4H), 7.77
(s, 1H), 8.43 (m, 1H); MS (DCI/NH.sub.3) m/z 376 (M+H).sup.+; Anal.
Calculated for C.sub.25H.sub.29NO.sub.2: C, 79.96; H, 7.78; N,
3.73. Found: C, 79.86; H, 7.63; N, 3.49.
Example 38
[1-(2-hydroxyethyl)-1H-indol-3-yl](2,2,3,3-tetramethylcyclopropyl)methanon-
e
[0273] To the product of Example 37B (0.19 g, 0.51 mmol) in 20 mL
ethanol (200 proof) was added Pd/C (0.10 g, 10 wt % palladium on
activated carbon, Aldrich). This mixture was stirred under 1 atm of
H.sub.2 (balloon) for 2 h after which time the reaction mixture was
degassed three times with a N.sub.2 back-flush. The mixture was
then filtered, concentrated under reduced pressure and purified via
flash column chromatography (SiO.sub.2, 30% ethyl acetate:hexanes)
to give 68 mg of the title compound (0.24 mmol, 47% yield). .sup.1H
NMR (CDCl.sub.3, 300 MHz) .delta. 1.30 (s, 6H), 1.35 (s, 6H), 1.95
(s, 1H), 4.03 (m, 2H), 4.33 (t, J=5.1 Hz, 2H), 7.28 (m, 2H), 7.36
(m, 1H), 7.76 (s, 1H), 8.43 (m, 1H); MS (DCI/NH.sub.3) m/z 286
(M+H).sup.+; Anal. calculated for C.sub.18H.sub.23NO.sub.2: C,
75.76; H, 8.12; N, 4.91. Found: C, 75.55; H, 7.82; N, 4.88.
Example 39
{1-[3-(benzyloxy)propyl]-1H-indol-3-yl}(2,2,3,3-tetramethylcyclopropyl)met-
hanone
Example 39A
3-(benzyloxy)propyl Methanesulfonate
[0274] The 3-benzyloxypropanol (Aldrich, 0.28 g, 1.7 mmol),
triethylamine (0.67 mL, 5.0 mmol), and methanesulfonyl chloride
(0.19 mL, 2.5 mmol) in 10 mL THF were processed as described in
Example 1C to give the title compound that was used directly in the
next reaction.
Example 39B
{1-[3-(benzyloxy)propyl]-1H-indol-3-yl}(2,2,3,3-tetramethylcyclopropyl)met-
hanone
[0275] The major product of Example 1B (0.20 g, 0.83 mmol), the
product of Example 39A (1.7 mmol) and NaH (60% dispersion in
mineral oil, 0.17 g, 4.1 mmol) in 10 mL DMF were processed as in
Example 1D. Purification via column chromatography (SiO.sub.2, 80%
hexanes 20% EtOAc) resulted in 0.27 g of the title compound (0.69
mmol, 84% yield). .sup.1H NMR (CDCl.sub.3, 300 MHz) .delta. 1.27
(s, 6H), 1.34 (s, 6H), 1.90 (s, 1H), 2.16 (m, 2H), 3.43 (t, J=5.4
Hz, 2H), 4.33 (t, J=6.8 Hz, 2H), 4.49 (s, 2H), 7.26 (m, 2H), 7.35
(m, 6H), 7.67 (s, 1H), 8.42 (m, 1H); MS (DCI/NH.sub.3) m/z 390
(M+H).sup.+; Anal. calculated for C.sub.26H.sub.31NO.sub.2: C,
80.17; H, 8.02; N, 3.60. Found: C, 79.91; H, 7.97; N, 3.36.
Example 40
[1-(3-hydroxypropyl)-1H-indol-3-yl](2,2,3,3-tetramethylcyclopropyl)methano-
ne
[0276] To the product of Example 39B (0.24 g, 0.62 mmol) in 40 mL
ethanol (200 proof) was added 200 mg of Pd/C (10 wt % palladium on
activated carbon, Aldrich). This mixture was stirred under 1 atm of
H.sub.2 (balloon) for 12 h after which time the reaction mixture
was degassed three times with a N.sub.2 back-flush. The mixture was
then filtered, concentrated under reduced pressure and purified via
flash column chromatography (SiO.sub.2, 30% ethyl acetate:hexanes)
to give 0.13 g of the title compound (0.43 mmol, 69% yield).
.sup.1H NMR (CDCl.sub.3, 300 MHz) .delta. 1.30 (s, 6H), 1.35 (s,
6H), 1.94 (s, 1H), 2.12 (m, 2H), 3.67 (t, J=5.8 Hz, 2H), 4.34 (t,
J=7.1 Hz, 2H), 7.26 (m, 2H), 7.38 (m, 1H), 7.71 (s, 1H), 8.41 (m,
1H); MS (DCI/NH.sub.3) m/z 300 (M+H).sup.+; Anal. Calculated for
C.sub.19H.sub.25NO.sub.2.0.2H.sub.2O: C, 75.31; H, 8.45; N, 4.62.
Found: C, 75.60; H, 8.11; N, 4.25.
Example 41
{1-[5-(benzyloxy)pentyl]-1H-indol-3-yl}(2,2,3,3-tetramethylcyclopropyl)met-
hanone
Example 41A
5-(benzyloxy)pentyl Methanesulfonate
[0277] The 5-benzyloxypentanol (Aldrich, 0.32 g, 1.7 mmol),
triethylamine (0.67 mL, 5.0 mmol), and methanesulfonyl chloride
(0.19 mL, 2.5 mmol) in 10 mL THF were processed as described in
Example 1C to give the title compound that was used directly in the
next reaction.
Example 41B
{1-[5-(benzyloxy)pentyl]-1H-indol-3-yl}(2,2,3,3-tetramethylcyclopropyl)met-
hanone
[0278] The major product of Example 1B (0.20 g, 0.83 mmol), the
product of Example 41A (1.7 mmol) and NaH (60% dispersion in
mineral oil, 0.17 g, 4.1 mmol) in 10 mL DMF were processed as in
Example 1D. Purification via column chromatography (SiO.sub.2, 80%
hexanes 20% EtOAc) gave 0.30 g of the title compound (0.71 mmol,
86% yield). .sup.1H NMR (CDCl.sub.3, 300 MHz) .delta. 1.30 (s, 6H),
1.34 (s, 6H), 1.46 (m, 2H), 1.67 (m, 2H), 1.91 (m, 2H), 1.94 (s,
1H), 3.46 (t, J=6.1 Hz, 2H), 4.15 (t, J=7.1 Hz, 2H), 4.48 (s, 2H),
7.26 (m, 2H), 7.31 (m, 6H), 7.65 (s, 1H), 8.40 (m, 1H); MS
(DCI/NH.sub.3) m/z 418 (M+H).sup.+; Anal. Calculated for
C.sub.28H.sub.35NO.sub.2: C, 80.54; H, 8.45; N, 3.35. Found: C,
80.22; H, 8.67; N, 3.30.
Example 42
[1-(5-hydroxypentyl)-1H-indol-3-yl](2,2,3,3-tetramethylcyclopropyl)methano-
ne
[0279] To the product of Example 41B (0.29 g, 0.69 mmol) in 40 mL
ethanol (200 proof) was added 200 mg of Pd/C (10 wt % palladium on
activated carbon, Aldrich). This mixture was stirred under 1 atm of
H.sub.2 (balloon) for 16 h after which time the reaction mixture
was degassed three times with a N.sub.2 back-flush. The mixture was
then filtered, concentrated under reduced pressure and purified via
flash column chromatography (SiO.sub.2, 50% ethyl acetate:hexanes)
to give 0.16 g of the title compound (0.47 mmol, 68% yield).
.sup.1H NMR (CDCl.sub.3, 300 MHz) .delta. 1.31 (s, 6H), 1.35 (s,
6H), 1.47 (m, 2H), 1.62 (m, 2H), 1.94 (m, 2H), 3.65 (t, J=6.4 Hz,
2H), 4.17 (t, J=7.1 Hz, 2H), 7.26 (m, 2H), 7.34 (m, 1H), 7.66 (s,
1H), 8.40 (m, 1H); MS (DCI/NH.sub.3) m/z 328 (M+H).sup.+; Anal.
Calculated for C.sub.21H.sub.29NO.sub.2.0.5H.sub.2O: C, 74.96; H,
8.99; N, 4.16. Found: C, 74.93; H, 9.06; N, 4.16.
Example 44
[1-(3-methoxypropyl)-1H-indol-3-yl](2,2,3,3-tetramethylcyclopropyl)methano-
ne
[0280] To a solution of the major product of Example 1B (0.15 g,
0.62 mmol) in 10 mL DMF at 0.degree. C. was added NaH (60%
dispersal in mineral oil, 0.10 g, 2.6 mmol). This mixture was
warmed to ambient temperature and allowed to stir for 1 h. The
solution was again cooled to 0.degree. C. and
1-bromo-3-methoxypropane (Matrix Scientific, 0.19 mg, 1.2 mmol) was
added. The reaction mixture was warmed to 45.degree. C. at which
temperature the reaction was allowed to stir for 4 h. The mixture
was cooled to ambient temperature, quenched with 10 mL saturated,
aqueous NH.sub.4Cl and ice. The layers were separated and the
aqueous layer was extracted with 3.times.10 mL ethyl acetate. The
combined organics were dried over anhydrous Na.sub.2SO.sub.4,
filtered, concentrated and purified via flash column chromatography
(SiO.sub.2, 30% ethyl acetate:hexanes) to give 0.12 g of the title
compound (0.38 mmol, 62% yield). .sup.1H NMR (CDCl.sub.3, 300 MHz)
.delta. 1.30 (s, 6H), 1.35 (s, 6H), 1.94 (s, 1H), 2.11 (m, 2H),
3.31 (t, J=5.8 Hz, 2H), 3.35 (s, 3H), 4.30 (t, J=6.8 Hz, 2H), 7.27
(m, 2H), 7.37 (m, 1H), 7.67 (s, 1H), 8.41 (m, 1H); MS
(DCI/NH.sub.3) m/z 314 (M+H).sup.+; Anal. Calculated for
C.sub.20H.sub.27NO.sub.2: C, 76.64; H, 8.68; N, 4.47. Found: C,
76.49; H, 8.57; N, 4.22.
Example 51
[1-(tetrahydro-2H-pyran-4-ylacetyl)-1H-indol-3-yl](2,2,3,3-tetramethylcycl-
opropyl)methanone
Example 51A
tetrahydro-2H-pyran-4-ylacetyl Chloride
[0281] A solution of tetrahydropyran-4-yl acetic acid
(Combi-Blocks, Inc., 0.18 g, 1.2 mmol) in thionyl chloride (7 mL,
96 mmol, excess) was refluxed for 1 h then was cooled to ambient
temperature and concentrated under reduced pressure. The residue
was azeotroped twice with 10 mL of benzene to remove any remaining
thionyl chloride. The resulting acid chloride was used without
further purification.
Example 51B
[1-(tetrahydro-2H-pyran-4-ylacetyl)-1H-indol-3-yl](2,2,3,3-tetramethylcycl-
opropyl)methanone
[0282] The major product of Example 1B (0.15 g, 0.62 mmol), the
product of Example 51A (1.2 mmol) and NaH (60% dispersion in
mineral oil, 75 mg, 3.1 mmol) in 5 mL DMF were processed as in
Example 1D. Recrystallization with EtOAc and hexanes resulted in
0.16 g of the title compound (0.44 mmol, 70% yield). .sup.1H NMR
(CDCl.sub.3, 300 MHz) .delta. 1.35 (s, 6H), 1.36 (s, 6H), 1.51 (m,
2H), 1.82 (m, 2H), 2.00 (m, 2H), 2.36 (m, 1H), 2.93 (m, 2H), 3.49
(dt, J=11.9, 2.0 Hz, 2H), 4.01 (dd, J=11.9, 4.1 Hz, 2H), 7.39 (m,
2H), 7.97 (s, 1H), 8.32 (m, 1H), 8.41 (m, 1H); MS (DCI/NH.sub.3)
m/z 368 (M+H).sup.+; Anal. Calculated for C.sub.23H.sub.29NO.sub.3:
C, 75.17; H, 7.95; N, 3.81. Found: C, 75.03; H, 8.06; N, 3.84.
Example 52
methyl
4-({3-[(2,2,3,3-tetramethylcyclopropyl)carbonyl]-1H-indol-1-yl}meth-
yl)cyclohexanecarboxylate
Example 52A
methyl 4-(hydroxymethyl)cyclohexanecarboxylate
[0283] To 4-hydroxymethylcyclohexanecarboxylic acid (TCI-JP, 0.50
g, 3.2 mmol) in 10 mL CH.sub.3OH was added 0.50 mL concentrated
H.sub.2SO.sub.4. This mixture was warmed to reflux and allowed to
stir for 2 h. The reaction mixture was then cooled and NH.sub.4OH
was added until the solution tested basic using pH paper. The
mixture was then extracted with 3.times.5 mL ethyl acetate. The
combined organic extracts were washed with saturated, aqueous NaCl
then were dried over anhydrous Na.sub.2SO.sub.4, filtered, and
concentrated under reduced pressure to give 0.45 g of the title
compound (0.26 mmol, 83% yield). MS (DCI/NH.sub.3) m/z 190
(M+NH.sub.4).sup.+.
Example 52B
methyl 4-{[(methylsulfonyl)oxy]methyl}cyclohexanecarboxylate
[0284] The product of Example 52A (0.214 g, 1.2 mmol),
triethylamine (0.52 mL, 3.73 mmol), and methanesulfonyl chloride
(0.144 mL, 1.9 mmol) in 10 mL THF were processed as described in
Example 1C to give the title compound that was used directly in the
next reaction.
Example 52C
methyl
4-({3-[(2,2,3,3-tetramethylcyclopropyl)carbonyl]-1H-indol-1-yl}meth-
yl)cyclohexanecarboxylate
[0285] The major product of Example 1B (0.15 g, 0.62 mmol), the
product of Example 52B (1.2 mmol) and NaH (60% dispersion in
mineral oil, 50 mg, 1.2 mmol) in 10 mL DMF were processed as in
Example 1D. Purification via column chromatography (SiO.sub.2, 80%
hexanes:20% EtOAc) gave 88 mg of the title compound (0.22 mmol, 36%
yield). .sup.1H NMR (CDCl.sub.3, 300 MHz) .delta. 1.31 (s, 6H),
1.32 (m, 2H), 1.34 (s, 6H), 1.55 (m, 4H), 1.93 (s, 1H), 2.07 (m,
3H), 2.62 (m, 1H), 3.72 (s, 3H), 4.02 (d, J=7.5 Hz, 2H), 7.25 (m,
2H), 7.32 (m, 1H), 7.60 (s, 1H), 8.40 (m, 1H); MS (DCI/NH.sub.3)
m/z 396 (M+H).sup.+; Anal. Calculated for C.sub.25H.sub.33NO.sub.3:
C, 75.91; H, 8.41; N, 3.54. Found: C, 75.63; H, 8.70; N, 3.33.
Example 53
3-{3-[(2,2,3,3-tetramethylcyclopropyl)carbonyl]-1H-indol-1-yl}propanamide
[0286] The major product of Example 1B (0.20 g, 0.83 mmol),
3-chloropropionamide (Aldrich, 0.18 g, 1.7 mmol) and NaH (60%
dispersion in mineral oil, 0.10 g, 2.5 mmol) in 5 mL DMF were
processed as in Example 1D. Purification via column chromatography
(SiO.sub.2, 5% CH.sub.3OH: 95% EtOAc) afforded 26 mg of the title
compound (0.082 mmol, 10% yield). .sup.1H NMR (CDCl.sub.3, 300 MHz)
.delta. 1.30 (s, 6H), 1.33 (s, 6H), 1.92 (s, 1H), 2.75 (t, J=6.4
Hz, 2H), 4.55 (t, J=6.4 Hz, 2H), 5.27 (br s, 2H), 7.27 (m, 2H),
7.33 (m, 1H), 7.75 (s, 1H), 8.43 (m, 1H); MS (DCI/NH.sub.3) m/z 313
(M+H).sup.+; Anal. Calculated for
C.sub.19H.sub.24N.sub.2O.sub.2.0.25H.sub.2O: C, 72.01; H, 7.79; N,
8.84. Found: C, 71.86; H, 7.41; N, 8.68.
Example 54
6-{3-[(2,2,3,3-tetramethylcyclopropyl)carbonyl]-1H-indol-1-yl}hexan-2-one
[0287] The major product of Example 1B (0.20 g, 0.83 mmol),
2-chloro-2-hexanone (Aldrich, 0.22 g, 1.7 mmol) and NaH (60%
dispersion in mineral oil, 0.10 g, 2.5 mmol) in 5 mL DMF were
processed as in Example 1D. Purification via column chromatography
(SiO.sub.2, 50% hexanes:50% EtOAc) resulted in 43 mg of the title
compound (0.13 mmol, 15% yield). .sup.1H NMR (CDCl.sub.3, 300 MHz)
.delta. 1.31 (s, 6H), 1.35 (s, 6H), 1.65 (m, 4H), 1.89 (m, 2H),
1.95 (s, 1H), 2.11 (s, 3H), 2.46 (t, J=7.1 Hz, 2H), 4.17 (t, J=7.1
Hz, 2H), 7.27 (m, 2H), 7.33 (m, 1H), 7.67 (s, 1H), 8.40 (m, 1H); MS
(DCI/NH.sub.3) m/z 34 (M+H).sup.+; Anal. Calculated for
C.sub.22H.sub.29NO.sub.2: C, 77.84; H, 8.61; N, 4.13. Found: C,
77.57; H, 8.97; N, 3.84.
Example 55
{1-[(2R)-2,3-dihydroxypropyl]-1H-indol-3-yl}(2,2,3,3-tetramethylcyclopropy-
l)methanone
Example 55A
[(4S)-2,2-dimethyl-1,3-dioxolan-4-yl]methyl methanesulfonate
[0288] The (R)-(-)-2,2-dimethyl-1,3-dioxolane-4-methanol (Aldrich,
0.38 mL, 3.1 mmol), triethylamine (0.85 mL, 6.1 mmol), and
methanesulfonyl chloride (0.31 mL, 4.1 mmol) in 10 mL THF were
processed as described in Example 1C to give the title compound
that was used directly in the next reaction.
Example 55B
(1-{[(4R)-2,2-dimethyl-1,3-dioxolan-4-yl]methyl}-1H-indol-3-yl)(2,2,3,3-te-
tramethylcyclopropyl)methanone
[0289] The major product of Example 1B (0.49 g, 2.0 mmol), the
product of Example 55A (3.05 mmol) and NaH (60% dispersion in
mineral oil, 0.24 g, 6.1 mmol) in 15 mL DMF were processed as in
Example 1D to give 0.65 g of a 4.4:1 inseparable mixture of the
title compound and the major product of Example 1B. This mixture
was used without further purification. The mixture was isolated via
column chromatography (SiO.sub.2, 50% hexanes 50% EtOAc). Title
compound: MS (DCI/NH.sub.3) m/z 356 (M+H).sup.+; major product of
Example 1B: MS (DCI/NH.sub.3) m/z 242 (M+H).sup.+.
Example 55C
{1-[(2R)-2,3-dihydroxypropyl]-1H-indol-3-yl}(2,2,3,3-tetramethylcyclopropy-
l)methanone
[0290] To the mixture obtained from Example 55B in 10 mL THF was
added 5 mL H.sub.2O followed by 1.7 g of p-toluenesulfonic acid
monohydrate (9.1 mmol). This mixture was stirred at ambient
temperature for 16 hours then was concentrated under reduced
pressure. The residue was purified via column chromatography
(SiO.sub.2, 90% ethyl acetate:hexanes) to give 0.30 g of the title
compound (0.95 mmol, 47% two-step yield). .sup.1H NMR (CDCl.sub.3,
300 MHz) .delta. 1.30 (s, 6H), 1.34 (s, 3H), 1.35 (s, 3H), 1.93 (s,
1H), 3.59 (dd, J=11.2, 5.4 Hz, 1H), 3.77 (dd, J=11.2, 3.7 Hz, 1H),
4.24 (m, 3H), 7.27 (m, 2H), 7.38 (m, 1H), 7.75 (s, 1H), 8.41 (m,
1H); MS (DCI/NH.sub.3) m/z 316 (M+H).sup.+; Anal. Calculated for
C.sub.22H.sub.29NO.sub.2.0.1H.sub.2O: C, 71.94; H, 8.01; N, 4.42.
Found: C, 71.65; H, 8.03; N, 4.10.
Example 57
[2-methyl-1-(2-morpholin-4-ylethyl)-1H-indol-3-yl](2,2,3,3-tetramethylcycl-
opropyl)methanone Hydrochloride
Example 57A
(2-Methyl-1H-indol-3-yl)-(2,2,3,3-tetramethyl-cyclopropyl)-methanone
[0291] A mixture of 2-methylindole (0.75 g, 5.7 mmol),
ethylmagnesium bromide (1.0 M solution in THF, 6.6 mL, 6.6 mmol),
zinc chloride (1.0 M solution in Et.sub.2O, 6.6 mL, 6.6 mmol) and
the product of Example 1A (6.3 mmol) in 15 mL of dichloromethane
was processed as described in Example 1B to provide the title
compound (0.76 g, 3.0 mmol, 52% yield). MS (DCI/NH.sub.3) m/z 256
(M+H).sup.+.
Example 57B
[2-methyl-1-(2-morpholin-4-ylethyl)-1H-indol-3-yl](2,2,3,3-tetramethylcycl-
opropyl)methanone Hydrochloride
[0292] The product of Example 57A (0.22 g, 0.87 mmol), the product
of Example 2A (1.8 mmol), and NaH (60% dispersion in mineral oil,
0.18 g, 4.4 mmol) in 8 mL of DMF were processed as described in
Example 1D to provide the corresponding free base of the title
compound (0.25 g, 0.68 mmol, 78% yield), which was then treated
with 4 N HCl in dioxane (0.68 mmol, 0.17 mL) to afford the title
compound (0.15 g, 0.36 mmol, 53% yield). .sup.1H NMR (MeOH-d.sub.4,
300 MHz) .delta. ppm 1.36 (s, 6H), 1.38 (s, 6H), 2.22 (s, 1H), 2.72
(s, 3H), 3.14-3.37 (m, 2H), 3.44-3.53 (m, 3H), 3.53-3.64 (m, 1H),
3.80-3.96 (m, 2H), 4.01-4.15 (m, 2H), 4.63-4.71 (m, 2H), 7.23 (dt,
J=7.5, 1.4 Hz, 1H), 7.29 (dt, J=7.6, 1.4 Hz, 1H), 7.51-7.58 (m,
1H), 7.86-7.93 (m, 1H); MS (DCI/NH.sub.3) m/z 369 (M+H).sup.+;
Anal. Calculated for C.sub.22H.sub.29NO.sub.2.1.25HCl: C, 66.71; H,
8.09; N, 6.76. Found: C, 66.68; H, 8.20; N, 6.71.
Example 58
[4-amino-1-(2-morpholin-4-ylethyl)-1H-indol-3-yl](2,2,3,3-tetramethylcyclo-
propyl)methanone
Example 58A
(4-Nitro-1H-indol-3-yl)-(2,2,3,3-tetramethyl-cyclopropyl)-methanone
[0293] A mixture of 4-nitroindole (1.0 g, 6.2 mmol), ethylmagnesium
bromide (1.0 M in THF, 6.8 mL, 6.8 mmol), zinc chloride (1.0 M
solution in Et.sub.2O, 6.8 mL, 6.8 mmol) and the product of Example
1A (6.8 mmol) in 15 mL of dichloromethane was processed as
described in Example 1B to provide the title compound (0.15 g, 0.53
mmol, 8% yield). MS (DCI/NH.sub.3) m/z 287 (M+H).sup.+.
Example 58B
[1-(2-morpholin-4-ylethyl)-4-nitro-1H-indol-3-yl](2,2,3,3-tetramethylcyclo-
propyl)methanone
[0294] The product of Example 58A (0.15 g, 0.53 mmol), the product
of Example 2A (0.79 mmol) and NaH (60% dispersion in mineral oil,
63 mg, 1.6 mmol) in 10 mL of DMF 10 mL were processed as described
in Example 1D to provide the title compound (0.14 g, 0.35 mmol, 66%
yield). .sup.1H NMR (CDCl.sub.3, 300 MHz) .delta. ppm 1.28 (s, 6H),
1.35 (s, 6H), 1.79 (s, 1H), 2.44-2.55 (m, 4H), 2.78 (t, J=5.9 Hz,
2H), 3.63-3.77 (m, 4H), 4.29 (t, J=6.1 Hz, 2H), 7.33 (t, J=8.0 Hz,
1H), 7.56-7.64 (m, 1H), 7.73 (d, J=7.8 Hz, 1H), 7.77 (s, 1H); MS
(DCI/NH.sub.3) m/z 400 (M+H).sup.+; Anal. Calculated for
C.sub.22H.sub.29N.sub.3O.sub.4: C, 66.14; H, 7.32; N, 10.52. Found:
C, 65.80; H, 7.34; N, 10.49.
Example 59
[4-amino-1-(2-morpholin-4-ylethyl)-1H-indol-3-yl](2,2,3,3-tetramethylcyclo-
propyl)methanone
[0295] A mixture of the product of Example 58B (0.11 g, 0.28 mmol)
and 20 mg of Pd/C (10 weight % palladium on activated carbon) in 10
mL of EtOH was stirred under 1 atmosphere of H.sub.2 (balloon) for
4 hours. The system was purged with an inert nitrogen atmosphere.
The mixture was filtered, concentrated under reduced pressure and
purified via column chromatography (SiO.sub.2, 10% methanol in
dichloromethane containing 1% NH.sub.4OH) to afford a quantitative
yield of the title compound. .sup.1H NMR (CDCl.sub.3, 300 MHz)
.delta. ppm 11.30 (s, 12H), 1.93 (s, 1H), 2.49-2.66 (m, 4H),
2.75-2.95 (m, 2H), 3.69-3.83 (m, 4H), 4.17-4.40 (m, 2H), 6.40 (d,
J=7.1 Hz, 1H), 6.59 (d, J=7.8 Hz, 1H), 7.06 (t, J=8.0 Hz, 1H), 7.74
(s, 1H); MS (DCI/NH.sub.3) m/z 370 (M+H).sup.+; Anal. Calculated
for C.sub.22H.sub.31N.sub.3O.sub.2: C, 71.51; H, 8.46; N, 11.37.
Found: C, 71.49; H, 8.77;N, 11.14.
Example 60
cycloheptyl[1-(2-morpholin-4-ylethyl)-1H-indol-3-yl]methanone
Example 60A
cycloheptyl-(1H-indol-3-yl)-methanone
[0296] Cycloheptane carboxylic acid (1.5 g, 10 mmol) in 5 mL of
thionyl chloride was processed as described in Example 1A to
provide the corresponding acid chloride. The freshly prepared acid
chloride (10 mmol), indole (1.2 g, 10 mmol), ethylmagnesium bromide
(1.0 M solution in THF, 11 mL, 11 mmol), and zinc chloride (1.0 M
solution in Et.sub.2O, 11 mL, 11 mmol) in 20 mL of dichloromethane
were processed as described in Example 1B to provide the title
compound (0.36 g, 1.5 mmol, 15% yield). MS (DCI/NH.sub.3) m/z 242
(M+H).sup.+.
Example 60B
cycloheptyl[1-(2-morpholin-4-ylethyl)-1H-indol-3-yl]methanone
[0297] The product of Example 60A (0.10 g, 0.42 mmol), NaH (60%
dispersion in mineral oil, 50 mg, 1.2 mmol) and the product of
Example 2A (0.17 g, 0.83 mmol) in 8 mL of DMF were processed as
described in Example 1D to provide the title compound (78 mg, 0.22
mmol, 52% yield). .sup.1H NMR (CDCl.sub.3, 300 MHz) .delta. ppm
1.58-1.70 (m, 6H), 1.75-1.91 (m, 4H), 1.92-2.05 (m, 2H), 2.45-2.57
(m, 4H), 2.73-2.84 (m, 2H), 3.13-3.25 (m, 1H), 3.66-3.75 (m, 4H),
4.21-4.31 (m, 2H), 7.27-7.41 (m, 3H), 7.86 (s, 1H), 8.37-8.45 (m,
1H); MS (DCI/NH.sub.3) m/z 355 (M+H).sup.+; Anal. Calculated for
C.sub.22H.sub.30N.sub.2O.sub.2.0.2H.sub.2O: C, 73.79; H, 8.56; N,
7.82. Found: C, 73.76; H, 8.68; N, 7.77.
Example 61
(2,2,3,3-tetrafluoro-1-methylcyclobutyl)[1-(tetrahydro-2H-pyran-4-ylmethyl-
)-1H-indol-3-yl]methanone
Example 61A
(1H-Indol-3-yl)-(2,2,3,3-tetrafluoro-1-methylcyclobutyl)methanone
[0298] A mixture of
2,2,3,3-tetrafluoro-1-(methyl)-cyclobutanecarbonyl chloride (ABCR,
1.0 g, 4.9 mmol), indole (0.57 g, 4.9 mmol), ethylmagnesium bromide
(1.0 M solution in THF, 5.4 ml, 5.4 mmol) and zinc chloride (1.0 M
solution in Et.sub.2O, 5.4 mL, 5.4 mmol) in 50 mL of
dichloromethane was processed as described in Example 1B to provide
the title compound (0.40 g, 1.4 mmol, 29% yield). MS (DCI/NH.sub.3)
m/z 286 (M+H).sup.+.
Example 61B
(2,2,3,3-tetrafluoro-1-methylcyclobutyl)[1-(tetrahydro-2H-pyran-4-ylmethyl-
)-1H-indol-3-yl]methanone
[0299] The product of Example 61A (0.15 g, 0.53 mmol), the product
of Example 18A (1.1 mmol), and NaH (60% dispersion in mineral oil,
84 mg, 2.1 mmol) in 10 mL of DMF were processed as described in
Example 1D to provide the title compound (35 mg, 0.09 mmol, 17%
yield). .sup.1H NMR (CDCl.sub.3, 300 MHz) .delta. ppm 1.35-1.59 (m,
5H), 1.71 (s, 3H), 2.06-2.23 (m, 1H), 2.27-2.44 (m, 1H), 3.25-3.42
(m, 2H), 3.93-4.03 (m, 2H), 4.05-4.19 (m, 2H), 7.31-7.41 (m, 3H),
7.67 (d, J=1.7 Hz, 1H), 8.37-8.49 (m, 1H); MS (DCI/NH.sub.3) m/z
384 (M+H).sup.+; Anal. Calculated for C.sub.20H.sub.21FNO.sub.2: C,
62.66; H, 5.52; N, 3.65. Found: C, 63.00; H, 5.83; N, 3.66.
Example 62
cyclopentyl[1-(tetrahydro-2H-pyran-4-ylmethyl)-1H-indol-3-yl]methanone
Example 62A
cyclopentyl-(1H-indol-3-yl)-methanone
[0300] Cyclopentane carboxylic acid (1.1 g, 10 mmol) in 5 mL of
thionyl chloride was processed as described in Example 1A to
provide the corresponding acid chloride. The freshly prepared acid
chloride (10 mmol), indole (1.2 g, 10 mmol), ethylmagnesium bromide
(1.0 M solution in THF, 11 mL, 11 mmol), and zinc chloride (1.0 M
solution in Et.sub.2O, 11 mL, 11 mmol) in 30 mL of dichloromethane
were processed as described in Example 1B to provide the title
compound (0.51 g, 2.4 mmol, 24% yield). MS (DCI/NH.sub.3) m/z 214
(M+H).sup.+.
Example 62B
cyclopentyl[1-(tetrahydro-2H-pyran-4-ylmethyl)-1H-indol-3-yl]methanone
[0301] The product of Example 62A (0.10 g, 0.47 mmol), the product
of Example 18A (0.94 mmol), and NaH (60% dispersion in mineral oil,
57 mg, 1.4 mmol) in 10 mL of DMF were processed as described in
Example 1D to provide the title compound (45 mg, 0.14 mmol, 31%
yield). .sup.1H NMR (CDCl.sub.3, 300 MHz) .delta. ppm 1.34-1.48 (m,
2H), 1.48-1.53 (m, 2H), 1.62-1.72 (m, 2H), 1.73-1.85 (m, 2H),
1.87-2.07 (m, 4H), 2.08-2.22 (m, 1H), 3.33 (dt, J=11.6, 2.5 Hz,
2H), 3.45-3.61 (m, 1H), 3.92-4.03 (m, 2H), 4.05 (d, J=7.1 Hz, 2H),
7.27-7.39 (m, 3H), 7.72 (s, 1H), 8.40-8.47 (m, 1H); MS
(DCI/NH.sub.3) m/z 312 (M+H).sup.+; Anal. Calculated for
C.sub.20H.sub.25NO.sub.2.0.2H.sub.2O: C, 76.25; H, 8.13; N, 4.45.
Found: C, 76.29; H, 8.09; N, 4.56.
Example 63
cyclopentyl[1-(2-morpholin-4-ylethyl)-1H-indol-3-yl]methanone
[0302] The product of Example 62A (0.10 g, 0.47 mmol), NaH (60%
dispersion in mineral oil, 57 mg, 1.4 mmol) and the product of
Example 2A (0.94 mmol) in 10 mL of DMF were processed as described
in Example 1D to provide the title compound (15 mg, 0.04 mmol, 4%
yield). .sup.1H NMR (CDCl.sub.3, 300 MHz) .delta. ppm 1.61-1.72 (m,
2H), 1.72-1.84 (m, 2H), 1.86-2.08 (m, 4H), 2.41-2.57 (m, 4H),
2.73-2.85 (m, 2H), 3.45-3.61 (m, 1H), 3.62-3.79 (m, 4H), 4.18-4.36
(m, 2H), 7.27-7.43 (m, 3H), 8.02 (s, 1H), 8.38-8.49 (m, 1H); MS
(DCI/NH.sub.3) m/z 327 (M+H).sup.+; Anal. Calculated for
C.sub.20H.sub.26N.sub.2O.sub.2.0.2H.sub.2O: C, 72.78; H, 8.06; N,
8.49. Found: C, 72.78; H, 7.95; N, 8.54.
Example 64
4-{3-[(2,2,3,3-tetramethylcyclopropyl)carbonyl]-1H-indol-1-yl}butyl
Acetate
[0303] To a solution of the product of Example 24A (0.11 g, 0.35
mmol) in 2 mL of THF at ambient temperature was added pyridine (57
.mu.L, 0.70 mmol) followed by acetic anhydride (50 .mu.L, 0.53
mmol). The mixture was stirred at ambient temperature for 16 hours
then was quenched with 2 mL H.sub.2O. The mixture was diluted with
5 mL of EtOAc and the layers were separated. The aqueous layer was
extracted 3.times.3 mL of EtOAc and the combined organic extracts
were dried over anhydrous Na.sub.2SO.sub.4, filtered, concentrated
under reduced pressure and purified via column chromatography
(SiO.sub.2, 70% hexanes in EtOAc) to provide the title compound (85
mg, 0.24 mmol, 68% yield). .sup.1H NMR (CDCl.sub.3, 300 MHz)
.delta. ppm 1.31 (s, 6H), 1.35 (s, 6H), 1.62-1.76 (m, 2H),
1.92-2.01 (m, 2H), 1.95 (s, 1H), 2.04 (s, 3H), 4.10 (t, J=6.4 Hz,
2H), 4.20 (t, J=7.1 Hz, 2H), 7.24-7.37 (m, 3H), 7.66 (s, 1H),
8.37-8.43 (m, 1H); MS (DCI/NH.sub.3) m/z 356 (M+H).sup.+; Anal.
Calculated for
C.sub.22H.sub.29NO.sub.2.0.1C.sub.6H.sub.14.0.15C.sub.4H.sub.8O.sub.2:
C, 73.85; H, 8.44; N, 3.71. Found: C, 73.58; H, 8.70; N, 3.61.
Example 65
(2E)-4-oxo-4-(4-{3-[(2,2,3,3-tetramethylcyclopropyl)carbonyl]-1H-indol-1-y-
l}butoxy)but-2-enoic Acid
[0304] To a solution of the product of Example 24A (0.71 g, 2.3
mmol) in 140 mL Et.sub.2O at ambient temperature was added
triethylamine (0.32 mL, 2.3 mL) followed by fumaryl chloride (0.26
mL, 2.4 mmol). The mixture was stirred at ambient temperature for
30 minutes and then filtered. The filtrate was concentrated under
reduced pressure. The residue was dissolved in 10 mL of EtOAc and
washed 4.times.3 mL of H.sub.2O and 1.times.3 mL of brine and the
organic layer was dried over anhydrous Na.sub.2SO.sub.4, filtered,
concentrated under reduced pressure and purified via column
chromatography (9% CH.sub.3OH: 1% AcOH: 90% EtOAc) to provide the
title compound (0.42 g, 1.0 mmol, 44% yield). .sup.1H NMR
(CDCl.sub.3, 300 MHz) .delta. ppm 1.31 (s, 6H), 1.35 (s, 6H),
1.69-1.82 (m, 2H), 1.96 (s, 1H), 1.97-2.07 (m, 2H), 4.16-4.32 (m,
4H), 6.88 (d, J=6.4 Hz, 2H), 7.25-7.38 (m, 3H), 7.67 (s, 1H),
8.33-8.43 (m, 1H); MS (DCI/NH.sub.3) m/z 412 (M+H).sup.+; Anal.
Calculated for C.sub.24H.sub.29NO.sub.5: C, 70.05; H, 7.10; N,
3.40. Found: C, 69.80; H, 7.40; N, 3.25.
Example 66
[6-chloro-1-(tetrahydro-2H-pyran-4-ylmethyl)-1H-indol-3-yl](2,2,3,3-tetram-
ethylcyclopropyl)methanone
Example 66A
(6-chloro-1H-indol-3-yl)-(2,2,3,3-tetramethyl-cyclopropyl)-methanone
[0305] A mixture of 6-chloroindole (0.38 g, 2.5 mmol),
ethylmagnesium bromide (1.0 M solution in THF, 3.0 mL, 3.0 mmol),
zinc chloride (1.0 M solution in Et.sub.2O, 3.0 mL, 3.0 mmol) and
the product of Example 1A (3.0 mmol) in 10 mL of dichloromethane
was processed as described in Example 1B to provide the title
compound (0.23 g, 0.83 mmol, 34% yield). MS (DCI/NH.sub.3) m/z 276
(M+H).sup.+.
Example 66B
[6-chloro-1-(tetrahydro-2H-pyran-4-ylmethyl)-1H-indol-3-yl](2,2,3,3-tetram-
ethylcyclopropyl)methanone
[0306] The product of Example 66A (0.23 g, 0.83 mmol), the product
of Example 18A (1.4 mmol), and NaH (60% dispersion in mineral oil,
0.10 g, 2.5 mmol) in 10 mL of DMF were processed as described in
Example 1D to provide the title compound (85 mg, 0.22 mmol, 27%
yield). .sup.1H NMR (CDCl.sub.3, 300 MHz) .delta. ppm 1.30 (s, 6H),
1.34 (s, 6H), 1.38-1.61 (m, 4H), 1.89 (s, 1H), 2.06-2.22 (m, 1H),
3.35 (dt, J=11.6, 2.5 Hz, 2H), 3.94-4.03 (m, 4H), 7.22 (dd, J=8.6,
1.9 Hz, 1H), 7.31 (d, J=1.7 Hz, 1H), 7.58 (s, 1H), 8.33 (d, J=8.8
Hz, 1H); MS (DCI/NH.sub.3) m/z 374 (M+H).sup.+; Anal. Calculated
for C.sub.22H.sub.28ClNO.sub.2.0.2H.sub.2O0.2 C.sub.6H.sub.14: C,
70.59; H, 7.97; N, 3.55. Found: C, 70.48; H, 8.35; N, 3.79.
Example 67
4-({3-[(2,2,3,3-tetramethylcyclopropyl)carbonyl]-1H-indol-1-yl}methyl)phen-
yl Acetate
[0307] The major product of Example 1B (0.50 g, 2.1 mmol),
4-(chloromethyl)phenyl acetate (0.35 mL, 2.3 mmol) and NaH (60%
dispersion in mineral oil, 0.17 g, 4.1 mmol) in 10 mL of DMF were
processed as described in Example 1D to provide the title compound
(67 mg, 0.17 mmol, 8% yield) and the product of Example 68 (0.22 g,
0.60 mmol, 31% yield). .sup.1H NMR (CDCl.sub.3, 300 MHz) .delta.
ppm 1.28 (s, 6H), 1.35 (s, 6H), 1.93 (s, 1H), 2.29 (s, 3H), 5.36
(s, 2H), 7.02-7.10 (m, 2H), 7.11-7.19 (m, 2H), 7.22-7.33 (m, 3H),
7.68 (s, 1H), 8.39-8.47 (m, 1H); MS (DCI/NH.sub.3) m/z 390
(M+H).sup.+; Anal. Calculated for C.sub.25H.sub.27NO.sub.3: C,
77.09; H, 6.99; N, 3.60. Found: C, 76.87; H, 7.20; N, 3.35.
Example 68
[1-(4-hydroxybenzyl)-1H-indol-3-yl](2,2,3,3-tetramethylcyclopropyl)methano-
ne
[0308] The title compound was obtained by the method described in
Example 67. .sup.1H NMR (CDCl.sub.3, 300 MHz) .delta. ppm 1.27 (s,
6H), 1.34 (s, 6H), 1.92 (s, 1H), 5.27 (s, 2H), 6.75-6.84 (m, 2H),
7.01-7.10 (m, 2H), 7.18-7.33 (m, 3H), 7.66 (s, 1H), 8.36-8.45 (m,
1H); MS (DCI/NH.sub.3) m/z 348 (M+H).sup.+; Anal. Calculated for
C.sub.23H.sub.25NO.sub.2: C, 79.51; H, 7.25; N, 4.03.
[0309] Found: C, 79.43; H, 7.40; N, 3.81.
Example 69
[6-(benzyloxy)-1-(tetrahydro-2H-pyran-4-ylmethyl)-1H-indol-3-yl](2,2,3,3-t-
etramethylcyclopropyl)methanone
Example 69A
(6-Benzyloxy-1H-indol-3-yl)-(2,2,3,3-tetramethyl-cyclopropyl)-methanone
[0310] A mixture of 6-benzyloxyindole (Lancaster, 2.0 g, 9.0 mmol),
ethylmagnesium bromide (1.0 M solution in THF, 11 mL, 11 mmol),
zinc chloride (1.0 M solution in Et.sub.2O, 11 mL, 11 mmol) and the
product of Example 1A (13.4 mmol) in 30 mL of dichloromethane was
processed as described in Example 1B to provide the title compound
(2.0 g, 5.8 mmol, 64% yield). MS (DCI/NH.sub.3) m/z 348
(M+H).sup.+.
Example 69B
[6-(benzyloxy)-1-(tetrahydro-2H-pyran-4-ylmethyl)-1H-indol-3-yl](2,2,3,3-t-
etramethylcyclopropyl)methanone
[0311] The product of Example 69A (0.90 g, 2.6 mmol), the product
of Example 18A (4.4 mmol), and NaH (60% dispersion in mineral oil,
0.31 g, 7.8 mmol) in 15 mL of DMF were processed as described in
Example 1D to provide the title compound (0.87 g, 2.0 mmol, 75%
yield). .sup.1H NMR (CDCl.sub.3, 300 MHz) .delta. ppm 1.29 (s, 6H),
1.34 (s, 6H), 1.34-1.51 (m, 4H), 1.90 (s, 1H), 1.98-2.12 (m, 1H),
3.30 (dt, J=11.7, 2.4 Hz, 2H), 3.91-4.00 (m, 2H), 3.93 (d, J=7.1
Hz, 2H), 5.15 (s, 2H), 6.81 (d, J=2.4 Hz, 1H), 7.01 (dd, J=8.8, 2.0
Hz, 1H), 7.29-7.43 (m, 3H), 7.43-7.49 (m, 2H), 7.50 (s, 1H), 8.28
(d, J=8.8 Hz, 1H); MS (DCI/NH.sub.3) m/z 446 (M+H).sup.+; Anal.
Calculated for C.sub.29H.sub.35NO.sub.3: C, 78.17; H, 7.92; N,
3.14. Found: C, 78.03; H, 8.07; N, 3.16.
Example 70
[6-hydroxy-1-(tetrahydro-2H-pyran-4-ylmethyl)-1H-indol-3-yl](2,2,3,3-tetra-
methylcyclopropyl)methanone
[0312] The product of Example 69B (0.64 g, 1.4 mmol) and Pd/C (10
wt % palladium on activated carbon, 100 mg) in 20 mL of EtOH and 10
mL of EtOAc was stirred under 1 atmosphere of H.sub.2 (balloon) for
16 hours. The system was purged with an inert nitrogen atmosphere.
The mixture was filtered, concentrated under reduced pressure and
purified via column chromatography (SiO.sub.2, 50% hexanes in
EtOAc) to provide the title compound (0.48 g, 1.35 mmol, 94%
yield). .sup.1H NMR (CDCl.sub.3, 300 MHz) .delta. ppm 1.29 (s, 6H),
1.34 (s, 6H), 1.38-1.58 (m, 4H), 1.89 (s, 1H), 2.06-2.21 (m, 1H),
3.33 (dt, J=11.8, 2.2 Hz, 2H), 3.95 (d, J=7.1 Hz, 2H), 3.97-4.04
(m, 2H), 4.67 (s, 1H), 6.76-6.81 (m, 2H), 7.50 (s, 1H), 8.25 (d,
J=9.2 Hz, 1H); MS (DCI/NH.sub.3) m/z 356 (M+H).sup.+; Anal.
Calculated for C.sub.22H.sub.29NO.sub.3: C, 74.33; H, 8.22; N,
3.94. Found: C, 74.38; H, 7.96; N, 3.86.
Example 71
(2E)-4-oxo-4-({1-(tetrahydro-2H-pyran-4-ylmethyl)-3-[(2,2,3,3-tetramethylc-
yclopropyl)carbonyl]-1H-indol-6-yl}oxy)but-2-enoic Acid
[0313] The product of Example 70 (0.33 g, 0.93 mmol), furmaryl
chloride (0.11 mL, 0.98 mmol) and triethylamine (0.13 mL, 0.93
mmol) in 60 mL Et.sub.2O and 15 mL of THF were processed as
described in Example 65 to provide the title compound (0.36 g, 0.78
mmol, 84% yield). .sup.1H NMR (CDCl.sub.3, 300 MHz) .delta. ppm
1.31 (s, 6H), 1.34 (s, 6H), 1.37-1.60 (m, 4H), 1.92 (s, 1H),
2.08-2.22 (m, 1H), 3.35 (dt, J=11.6, 2.2 Hz, 2H), 3.94-4.05 (m,
2H), 4.01 (d, J=7.1 Hz, 2H), 7.02-7.08 (m, 1H), 7.12 (d, J=14.2 Hz,
2H), 7.17-7.20 (m, 1H), 7.63 (s, 1H), 8.42 (d, J=8.5 Hz, 1H); MS
(DCI/NH.sub.3) m/z 454 (M+H).sup.+; Anal. Calculated for
C.sub.26H.sub.31NO.sub.6: C, 68.86; H, 6.89; N, 3.09. Found: C,
68.70; H, 6.66; N, 3.33.
Example 72
[6-methoxy-1-(tetrahydro-2H-pyran-4-ylmethyl)-1H-indol-3-yl](2,2,3,3-tetra-
methylcyclopropyl)methanone
[0314] To a solution of the product of Example 70 (0.15 g, 0.42
mmol) in 10 mL of THF was added NaH (60% dispersion in mineral oil,
51 mg, 1.3 mmol) followed by CH.sub.3I (39 .mu.L, 0.63 mmol). The
mixture was stirred at ambient temperature for 18 hours then was
quenched with 3 mL of saturated aqueous NH.sub.4Cl. The mixture was
diluted with 10 mL of EtOAc, the layers were separated and the
aqueous layer was extracted with 3.times.3 mL of EtOAc. The
combined organic extracts were dried over anhydrous
Na.sub.2SO.sub.4, filtered, concentrated under reduced pressure and
purified via column chromatography (SiO.sub.2, 30% hexanes in
EtOAc) to provide the title compound (86 mg, 0.23 mmol, 55% yield).
.sup.1H NMR (CDCl.sub.3, 300 MHz) .delta. ppm 1.30 (s, 6H), 1.34
(s, 6H), 1.34-1.63 (m, 4H), 1.90 (s, 1H), 2.05-2.24 (m, 1H), 3.34
(dt, J=11.7, 2.4 Hz, 2H), 3.88 (s, 3H), 3.94-4.02 (m, 2H), 3.97 (d,
J=7.5 Hz, 2H), 6.77 (d, J=2.4 Hz, 1H), 6.92 (dd, J=8.8, 2.0 Hz,
1H), 7.51 (s, 1H), 8.28 (d, J=8.8 Hz, 1H); MS (DCI/NH.sub.3) m/z
370 (M+H).sup.+; Anal. Calculated for C.sub.23H.sub.31NO.sub.3: C,
74.76; H, 8.46; N, 3.79. Found: C, 74.53; H, 8.44; N, 3.49.
Example 73
{1-[(2R)-tetrahydrofuran-2-ylmethyl]-1H-indol-3-yl}(2,2,3,3-tetramethylcyc-
lopropyl)methanone
[0315] (R)-(-)-Tetrahydrofurfuryl alcohol (Lancaster, 0.33 mL, 3.4
mmol), methanesulfonyl chloride (0.35 mL, 4.5 mmol), and
triethylamine (0.78 mL, 5.6 mmol) in 10 mL of THF were processed as
described in Example 1C to provide the corresponding mesylate. The
major product of Example 1B (0.27 g, 1.1 mmol), the freshly
prepared mesylate (3.4 mmol) and NaH (60% dispersion in mineral
oil, 0.13 g, 3.4 mmol) in 10 mL of DMF were processed as described
in Example 1D to provide the title compound (0.28 g, 0.86 mmol, 77%
yield). .sup.1H NMR (CDCl.sub.3, 300 MHz) .delta. ppm 1.30 (s, 6H),
1.33 (s, 3H), 1.35 (s, 3H), 1.46-1.62 (m, 1H), 1.69-1.92 (m, 2H),
1.93-2.07 (m, 1H), 1.95 (s, 1H), 3.72-3.91 (m, 2H), 4.13-4.34 (m,
3H), 7.22-7.29 (m, 2H), 7.32-7.39 (m, 1H), 7.78 (s, 1H), 8.38-8.45
(m, 1H); MS (DCI/NH.sub.3) m/z 326 (M+H).sup.+; Anal. Calculated
for C.sub.21H.sub.27NO.sub.2.0.1H.sub.2O: C, 77.50; H, 8.36; N,
4.30. Found: C, 77.21; H, 8.34; N, 4.18.
Example 74
[5-(benzyloxy)-1-(tetrahydro-2H-pyran-4-ylmethyl)-1H-indol-3-yl](2,2,3,3-t-
etramethylcyclopropyl)methanone
Example 74A
(5-Benzyloxy-1H-indol-3-yl)-(2,2,3,3-tetramethyl-cyclopropyl)-methanone
[0316] A mixture of 5-benzyloxyindole (1.2 g, 5.6 mmol),
ethylmagnesium bromide (1.0 M solution in THF, 6.1 mL, 6.1 mmol),
zinc chloride (1.0 M solution in Et.sub.2O, 6.1 mL, 6.1 mmol) and
the product of Example 1A (5.6 mmol) in 25 mL of dichloromethane
was processed as described in Example 1B to provide the title
compound (0.53 g, 1.5 mmol, 27% yield). MS (DCI/NH.sub.3) m/z 348
(M+H).sup.+.
Example 74B
[5-(benzyloxy)-1-(tetrahydro-2H-pyran-4-ylmethyl)-1H-indol-3-yl](2,2,3,3-t-
etramethylcyclopropyl)methanone
[0317] The product of Example 74A (0.52 g, 1.5 mmol), the product
of Example 18A (2.6 mmol), and NaH (60% dispersion in mineral oil,
0.18 g, 4.5 mmol) in 12 mL of DMF were processed as described in
Example 1D to provide the title compound (0.45 g, 1.0 mmol, 67%
yield). .sup.1H NMR (MeOH-d.sub.4, 300 MHz) .delta. ppm 1.31-1.31
(m, 6H), 1.33 (s, 6H), 1.34-1.52 (m, 4H), 2.10 (s, 1H), 2.13-2.27
(m, 1H), 3.34-3.48 (m, 2H), 3.88-3.99 (m, 2H), 4.12 (d, J=7.5 Hz,
2H), 5.12 (s, 2H), 6.97 (dd, J=8.8, 2.4 Hz, 1H), 7.28-7.43 (m, 4H),
7.44-7.51 (m, 2H), 7.92 (d, J=2.4 Hz, 1H), 8.01 (s, 1H); MS
(DCI/NH.sub.3) m/z 446 (M+H).sup.+; Anal. Calculated for
C.sub.29H.sub.35NO.sub.3.0.8H.sub.2O: C, 75.72; H, 8.02; N, 3.04.
Found: C, 75.90; H, 7.78; N, 2.85.
Example 75
(1-benzyl-1H-indol-3-yl)(2,2,3,3-tetramethylcyclopropyl)methanone
[0318] The major product of Example 1B (0.15 g, 0.62 mmol), benzyl
bromide (0.15 mL, 1.2 mmol) and NaH (60% dispersion in mineral oil,
0.12 g, 3.1 mmol) in 12 mL of DMF were processed as described in
Example 1D to provide the title compound (0.19 g, 0.56 mmol, 90%
yield). .sup.1H NMR (MeOH-d.sub.4, 300 MHz) .delta. ppm 1.31 (s,
6H), 1.32 (s, 6H), 2.13 (s, 1H), 5.47 (s, 2H), 7.15-7.24 (m, 3H),
7.25-7.40 (m, 5H), 8.12 (s, 1H), 8.21-8.31 (m, 1H); MS
(DCI/NH.sub.3) m/z 332 (M+H).sup.+; Anal. Calculated for
C.sub.23H.sub.25NO: C, 83.34; H, 7.60; N, 4.23. Found: C, 83.22; H,
7.65; N, 4.02.
Example 76
[7-(benzyloxy)-1-(tetrahydro-2H-pyran-4-ylmethyl)-1H-indol-3-yl](2,2,3,3-t-
etramethylcyclopropyl)methanone
Example 76A
(7-Benzyloxy-1H-indol-3-yl)-(2,2,3,3-tetramethyl-cyclopropyl)-methanone
[0319] A mixture of 7-benzyloxyindole (Matrix Scientific, 2.0 g,
9.0 mmol), ethylmagnesium bromide (1.0 M solution in THF, 11 mL, 11
mmol), zinc chloride (1.0 M solution in Et.sub.2O, 11 mL, 11 mmol)
and the product of Example 1A (13.4 mmol) in 30 mL of
dichloromethane was processed as described in Example 1B to provide
the title compound (1.3 g, 3.6 mmol, 40% yield). MS (DCI/NH.sub.3)
m/z 348 (M+H).sup.+.
Example 76B
[7-(benzyloxy)-1-(tetrahydro-2H-pyran-4-ylmethyl)-1H-indol-3-yl](2,2,3,3-t-
etramethylcyclopropyl)methanone
[0320] The product of Example 76A (1.3 g, 3.6 mmol), the product of
Example 18A (6.1 mmol), and NaH (60% dispersion in mineral oil,
0.43 g, 11 mmol) in 20 mL of DMF were processed as described in
Example 1D to provide the title compound (1.2 g, 2.7 mmol, 75%
yield). .sup.1H NMR (CDCl.sub.3, 300 MHz) .delta. ppm 1.02-1.23 (m,
4H), 1.29 (s, 6H), 1.33 (s, 6H), 1.89 (s, 1H), 1.93-2.09 (m, 1H),
3.13 (dt, J=11.6, 2.5 Hz, 2H), 3.77-3.88 (m, 2H), 4.09 (d, J=7.1
Hz, 2H), 5.13 (s, 2H), 6.82 (d, J=7.8 Hz, 1H), 7.16 (t, J=7.8 Hz,
1H), 7.34-7.50 (m, 5H), 7.44 (s, 1H), 8.03 (dd, J=8.0, 0.8 Hz, 1H);
MS (DCI/NH.sub.3) m/z 446 (M+H).sup.+; Anal. Calculated for
C.sub.29H.sub.35NO.sub.3.0.2H.sub.2O: C, 77.54; H, 7.94; N, 3.12.
Found: C, 77.44; H, 7.81; N, 3.04.
Example 77
[1-(4-methoxybenzyl)-1H-indol-3-yl](2,2,3,3-tetramethylcyclopropyl)methano-
ne
[0321] The product of Example 68 (0.11 g, 0.32 mmol), NaH (60%
dispersion in mineral oil, 38 mg, 0.95 mmol) and iodomethane (50
.mu.L, 0.79 mmol) in 3 mL of THF were processed as described in
Example 72 to provide the title compound (70 mg, 0.19 mmol, 61%
yield). .sup.1H NMR (CDCl.sub.3, 300 MHz) .delta. ppm 1.27 (s, 6H),
1.34 (s, 6H), 1.92 (s, 1H), 3.79 (s, 3H), 5.29 (s, 2H), 6.81-6.92
(m, 2H), 7.07-7.15 (m, 2H), 7.18-7.33 (m, 3H), 7.66 (s, 1H),
8.37-8.45 (m, 1H); MS (DCI/NH.sub.3) m/z 362 (M+H).sup.+; Anal.
Calculated for C.sub.24H.sub.27NO.sub.2: C, 79.74; H, 7.53; N,
3.87. Found: C, 79.40; H, 7.27; N, 3.87.
Example 78
[1-(3-methoxybenzyl)-1H-indol-3-yl](2,2,3,3-tetramethylcyclopropyl)methano-
ne
[0322] The major product of Example 1B (0.15 g, 0.62 mmol),
1-chloromethyl-3-methoxybenzene (0.17 mL, 1.2 mmol) and NaH (60%
dispersion in mineral oil, 0.12 g, 3.1 mmol) in 10 mL of DMF were
processed as described in Example 1D to provide the title compound
(0.11 g, 0.30 mmol, 49% yield). .sup.1H NMR (MeOH-d.sub.4, 300 MHz)
.delta. ppm 1.31 (s, 6H), 1.32 (s, 6H), 2.13 (s, 1H), 3.72 (s, 3H),
5.44 (s, 2H), 6.72-6.79 (m, 2H), 6.80-6.87 (m, 1H), 7.16-7.28 (m,
3H), 7.32-7.42 (m, 1H), 8.12 (s, 1H), 8.21-8.30 (m, 1H); MS
(DCI/NH.sub.3) m/z 362 (M+H).sup.+; Anal. Calculated for
C.sub.24H.sub.27NO.sub.2: C, 79.74; H, 7.53; N, 3.87. Found: C,
80.02; H, 7.50; N, 3.70.
Example 79
[5-hydroxy-1-(tetrahydro-2H-pyran-4-ylmethyl)-1H-indol-3-yl](2,2,3,3-tetra-
methylcyclopropyl)methanone
[0323] A mixture of the product of Example 74B (0.38 g, 0.85 mmol)
and Pd/C (10 wt % palladium on activated carbon, 160 mg) in 30 mL
EtOH and 10 mL of EtOAc was processed as described in Example 70 to
provide the title compound (0.27 g, 0.75 mmol, 89% yield). .sup.1H
NMR (MeOH-d.sub.4, 300 MHz) .delta. ppm 1.31 (s, 12H), 1.33-1.54
(m, 4H), 2.08 (s, 1H), 2.10-2.25 (m, 1H), 3.37 (dt, J=11.5, 2.7 Hz,
2H), 3.88-3.98 (m, 2H), 4.09 (d, J=7.5 Hz, 2H), 6.79 (dd, J=8.8,
2.4 Hz, 1H), 7.31 (d, J=8.8 Hz, 1H), 7.66 (d, J=2.0 Hz, 1H), 7.95
(s, 1H); MS (DCI/NH.sub.3) m/z 356 (M+H).sup.+; Anal. Calculated
for C.sub.22H.sub.29NO.sub.3: C, 74.33; H, 8.22; N, 3.94. Found: C,
74.14; H, 8.21; N, 3.97.
Example 80
[1-(1,3-benzodioxol-5-ylmethyl)-1H-indol-3-yl](2,2,3,3-tetramethylcyclopro-
pyl)methanone
[0324] A mixture of piperonyl alcohol (0.16 g, 1.1 mmol),
methanesulfonyl chloride (0.11 mL, 1.4 mmol), and triethylamine
(0.29 mL, 2.1 mmol) in 10 mL of THF was processed as described in
Example 1C to provide the corresponding mesylate. The major product
of Example 1B (0.15 g, 0.62 mmol), the freshly prepared mesylate
(1.1 mmol) and NaH (60% dispersion in mineral oil, 75 mg, 1.9 mmol)
in 10 mL of DMF were processed as described in Example 1D to
provide the title compound (0.11 g, 0.30 mmol, 49% yield). .sup.1H
NMR (MeOH-d.sub.4, 300 MHz) .delta. ppm 1.31 (s, 6H), 1.32 (s, 6H),
2.13 (s, 1H), 5.36 (s, 2H), 5.91 (s, 2H), 6.69-6.79 (m, 3H),
7.15-7.22 (m, 2H), 7.36-7.43 (m, 1H), 8.11 (s, 1H), 8.21-8.29 (m,
1H); MS (DCI/NH.sub.3) m/z 376 (M+H).sup.+; Anal. Calculated for
C.sub.24H.sub.25NO.sub.3: C, 76.77; H, 6.71; N, 3.73. Found: C,
76.51; H, 6.70; N, 3.79.
Example 81
[7-hydroxy-1-(tetrahydro-2H-pyran-4-ylmethyl)-1H-indol-3-yl](2,2,3,3-tetra-
methylcyclopropyl)methanone
[0325] The product of Example 76B (1.1 g, 2.5 mmol) and Pd/C (10 wt
% palladium on activated carbon, 113 mg) in 50 mL of EtOH and 50 mL
of EtOAc were processed as described in Example 70 to provide the
title compound (0.79 g, 2.2 mmol, 87% yield). .sup.1H NMR
(CDCl.sub.3, 300 MHz) .delta. ppm 1.30 (s, 6H), 1.33 (s, 6H),
1.38-1.58 (m, 4H), 1.91 (s, 1H), 2.13-2.27 (m, 1H), 3.33 (dt,
J=11.4, 2.2 Hz, 2H), 3.92-4.03 (m, 2H), 4.31 (d, J=7.1 Hz, 2H),
6.63 (dd, J=7.8, 0.7 Hz, 1H), 7.04 (t, J=7.8 Hz, 1H), 7.51 (s, 1H),
7.95 (dd, J=8.1, 1.0 Hz, 1H); MS (DCI/NH.sub.3) m/z 356
(M+H).sup.+; Anal. Calculated for C.sub.22H.sub.29NO.sub.3: C,
74.33; H, 8.22; N, 3.94. Found: C, 74.43; H, 8.30; N, 3.98.
Example 82
[1-(2,3-dihydro-1,4-benzodioxin-6-ylmethyl)-1H-indol-3-yl](2,2,3,3-tetrame-
thylcyclopropyl)methanone
[0326] A mixture of 2,3-dihydro-1,4-benzodioxin-6-ylmethanol
(Acros, 0.18 g, 1.1 mmol), methanesulfonyl chloride (0.11 mL, 1.4
mmol), and triethylamine (0.29 mL, 2.1 mmol) in 10 mL of THF was
processed as described in Example 1C to provide the corresponding
mesylate.
[0327] The major product of Example 1B (0.15 g, 0.62 mmol), the
freshly prepared mesylate (1.1 mmol) and NaH (60% dispersion in
mineral oil, 75 mg, 1.9 mmol) in 10 mL of DMF were processed as
described in Example 1D to provide the title compound (0.14 g, 0.36
mmol, 58% yield). .sup.1H NMR (MeOH-d.sub.4, 300 MHz) .delta. ppm
1.31 (d, J=1.7 Hz, 6H), 1.32 (s, 6H), 2.12 (s, 1H), 4.19 (s, 4H),
5.33 (s, 2H), 6.68-6.75 (m, 2H), 6.75-6.81 (m, 1H), 7.15-7.24 (m,
2H), 7.35-7.41 (m, 1H), 8.09 (s, 1H), 8.21-8.29 (m, 1H); MS
(DCI/NH.sub.3) m/z 390 (M+H).sup.+; Anal. Calculated for
C.sub.25H.sub.27NO.sub.3: C, 77.09; H, 6.99; N, 3.60. Found: C,
76.87; H, 7.00; N, 3.61.
Example 83
(2E)-4-oxo-4-({1-(tetrahydro-2H-pyran-4-ylmethyl)-3-[(2,2,3,3-tetramethylc-
yclopropyl)carbonyl]-1H-indol-7-yl}oxy)but-2-enoic acid
[0328] The product of Example 81 (0.20 g, 0.56 mmol), furmaryl
chloride (68 .mu.L, 0.59 mmol) and triethylamine (78 .mu.L, 0.56
mmol) in 60 mL Et.sub.2O were processed as described in Example 65
to provide the title compound (0.11 g, 0.24 mmol, 42% yield).
.sup.1H NMR (CDCl.sub.3, 300 MHz) .delta. ppm 1.31 (s, 6H), 1.34
(s, 6H), 1.34-1.46 (m, 4H), 1.90 (s, 1H), 1.97-2.11 (m, 1H), 3.31
(dt, J=10.9, 4.1 Hz, 2H), 3.94-4.03 (m, 2H), 4.07 (d, J=7.5 Hz,
2H), 7.06 (d, J=7.1 Hz, 1H), 7.16 (d, J=3.7 Hz, 2H), 7.26 (t, J=7.8
Hz, 1H), 7.53 (s, 1H), 8.35 (d, J=8.8 Hz, 1H); MS (DCI/NH.sub.3)
m/z 454 (M+H).sup.+; Anal. Calculated for
C.sub.26H.sub.31NO.sub.6.0.2H.sub.2O: C, 68.31; H, 6.92; N, 3.06.
Found: C, 68.05; H, 6.83; N, 2.94.
Example 84
[7-methoxy-1-(tetrahydro-2H-pyran-4-ylmethyl)-1H-indol-3-yl](2,2,3,3-tetra-
methylcyclopropyl)methanone
[0329] The product of Example 81 (0.14 g, 0.39 mmol), NaH (60%
dispersion in mineral oil, 47 mg, 1.2 mmol) and iodomethane (61
.mu.L, 0.98 mmol) in 3 mL of THF were processed as described in
Example 72 to provide the title compound (88 mg, 0.24 mmol, 61%
yield). .sup.1H NMR (CDCl.sub.3, 300 MHz) .delta. ppm 1.30 (s, 6H),
1.33 (s, 6H), 1.34-1.52 (m, 4H), 1.90 (s, 1H), 2.04-2.20 (m, 1H),
3.32 (dt, J=11.4, 2.5 Hz, 2H), 3.94 (s, 3H), 3.95-4.02 (m, 2H),
4.28 (d, J=7.1 Hz, 2H), 6.71 (d, J=7.5 Hz, 1H), 7.15 (t, J=8.0 Hz,
1H), 7.48 (s, 1H), 8.00 (dd, J=8.0, 0.8 Hz, 1H); MS (DCI/NH.sub.3)
m/z 370 (M+H).sup.+; Anal. Calculated for
C.sub.23H.sub.31NO.sub.3.0.2H.sub.2O: C, 74.04; H, 8.48; N, 3.75.
Found: C, 74.10; H, 8.39; N, 3.72.
Example 85
methyl
1-(tetrahydro-2H-pyran-4-ylmethyl)-3-[(2,2,3,3-tetramethylcycloprop-
yl)carbonyl]-1H-indole-6-carboxylate
Example 85A
3-(2,2,3,3-Tetramethyl-cyclopropanecarbonyl)-1H-indole-6-carboxylic
Acid Methyl Ester
[0330] A mixture of methyl-indole-6-carboxylate (2.0 g, 11.4 mmol),
ethylmagnesium bromide (1.0 M solution in THF, 14 mL, 14 mmol),
zinc chloride (1.0 M solution in Et.sub.2O, 14 mL, 14 mmol) and the
product of Example 1A (17 mmol) in 30 mL of dichloromethane was
processed as described in Example 1B to provide the title compound
(1.35 g, 4.5 mmol, 40% yield). MS (DCI/NH.sub.3) m/z 300
(M+H).sup.+.
Example 85B
methyl
1-(tetrahydro-2H-pyran-4-ylmethyl)-3-[(2,2,3,3-tetramethylcycloprop-
yl)carbonyl]-1H-indole-6-carboxylate
[0331] The product of Example 85A (1.4 g, 4.5 mmol), the product of
Example 18A (9.0 mmol), and NaH (60% dispersion in mineral oil,
0.54 g, 14 mmol) in 30 mL of DMF were processed as described in
Example 1D to provide the title compounds (0.43 g, 1.1 mmol, 24%
yield) and the product of Example 86 (0.37 g, 0.97 mmol, 21%
yield). .sup.1H NMR (CDCl.sub.3, 300 MHz) .delta. ppm 1.32 (s, 6H),
1.35 (s, 6H), 1.40-1.54 (m, 4H), 1.93 (s, 1H), 2.10-2.24 (m, 1H),
3.34 (dt, J=11.4, 2.5 Hz, 2H), 3.96 (s, 3H), 3.97-4.03 (m, 2H),
4.10 (d, J=7.5 Hz, 2H), 7.73 (s, 1H), 7.94 (dd, J=8.5, 1.0 Hz, 1H),
8.09 (s, 1H), 8.44 (d, J=8.5 Hz, 1H); MS (DCI/NH.sub.3) m/z 398
(M+H).sup.+; Anal. Calculated for
C.sub.24H.sub.31NO.sub.4.0.1H.sub.2O: C, 72.19; H, 7.88; N, 3.51.
Found: C, 71.88; H, 7.79; N, 3.45.
Example 86
1-(tetrahydro-2H-pyran-4-ylmethyl)-3-[(2,2,3,3-tetramethylcyclopropyl)carb-
onyl]-1H-indole-6-carboxylic Acid
[0332] The title compound was obtained by the methods described in
Example 85: .sup.1H NMR (CDCl.sub.3, 300 MHz) .delta. ppm 1.32 (s,
6H), 1.35 (s, 6H), 1.41-1.61 (m, 4H), 1.93 (s, 1H), 2.14-2.24 (m,
1H), 3.35 (dt, J=11.6, 2.5 Hz, 2H), 3.95-4.04 (m, 2H), 4.12 (d,
J=7.5 Hz, 2H), 7.76 (s, 1H), 7.99 (dd, J=8.3, 1.5 Hz, 1H), 8.14 (s,
1H), 8.46 (d, J=7.8 Hz, 1H); MS (DCI/NH.sub.3) m/z 384 (M+H).sup.+;
Anal. Calculated for C.sub.23H.sub.29NO.sub.4.0.4H.sub.2O: C,
70.71; H, 7.69; N, 3.59. Found: C, 70.54; H, 7.54; N, 3.60.
Example 87
{1-[(5-chloro-1,2,4-thiadiazol-3-yl)methyl]-1H-indol-3-yl}(2,2,3,3-tetrame-
thylcyclopropyl)methanone
[0333] The major product of Example 1B (0.15 g, 0.62 mmol),
5-chloro-3-(chloromethyl)-1,2,4-thiadiazole (Maybridge, 0.21 g, 1.2
mmol) and NaH (60% dispersion in mineral oil, 0.12 g, 3.1 mmol) in
10 mL of DMF were processed as described in Example 1D to provide
the title compound (50 mg, 0.13 mmol, 22% yield). .sup.1H NMR
(CDCl.sub.3, 300 MHz) .delta. ppm 1.36 (s, 6H), 1.37 (s, 6H), 2.07
(s, 1H), 4.79 (s, 2H), 7.43 (dt, J=7.5, 1.2 Hz, 1H), 7.50 (dt,
J=7.7, 1.5 Hz, 1H), 7.85-7.92 (m, 1H), 8.34 (s, 1H), 8.47-8.54 (m,
1H); MS (DCI/NH.sub.3) m/z 374 (M+H).sup.+; Anal. Calculated for
C.sub.19H.sub.20ClN.sub.3OS.0.4H.sub.2O: C, 59.88; H, 5.50; N,
11.03. Found: C, 59.71; H, 5.07; N, 11.12.
Example 88
(2E)-4-oxo-4-({1-(tetrahydro-2H-pyran-4-ylmethyl)-3-[(2,2,3,3-tetramethylc-
yclopropyl)carbonyl]-1H-indol-5-yl}oxy)but-2-enoic acid
[0334] The product of Example 79 (77 mg, 0.22 mmol), furmaryl
chloride (25 .mu.L, 0.23 mmol) and triethylamine (30 .mu.L, 0.22
mmol) in 20 mL Et.sub.2O and 4 mL of THF were processed as
described in Example 65 to provide the title compound (51 mg, 0.11
mmol, 51% yield). .sup.1H NMR (MeOH-d.sub.4, 300 MHz) .delta. ppm
1.31 (s, 6H), 1.32 (s, 6H), 1.38-1.55 (m, 4H), 2.13 (s, 1H),
2.16-2.28 (m, 1H), 3.37 (dt, J=10.9, 2.4 Hz, 2H), 3.89-3.99 (m,
2H), 4.18 (d, J=7.5 Hz, 2H), 7.00 (d, J=1.7 Hz, 2H), 7.07 (dd,
J=8.8, 2.4 Hz, 1H), 7.55 (d, J=8.8 Hz, 1H), 8.03 (d, J=2.4 Hz, 1H),
8.14 (s, 1H); MS (DCI/NH.sub.3) m/z 454 (M+H).sup.+; Anal.
Calculated for C.sub.26H.sub.31NO.sub.6: C, 68.86; H, 6.89; N,
3.09. Found: C, 68.77; H, 6.72; N, 3.06.
Example 89
[1-(1,3-benzothiazol-2-ylmethyl)-1H-indol-3-yl](2,2,3,3-tetramethylcyclopr-
opyl)methanone
[0335] The 2-hydroxymethylbenzothiazole (Acros, 0.18 g, 1.1 mmol),
methanesulfonyl chloride (0.11 mL, 1.4 mmol), and triethylamine
(0.29 mL, 2.1 mmol) in 10 mL of THF were processed as described in
Example 1C to provide the corresponding mesylate. The major product
of Example 1B (0.15 g, 0.62 mmol), the freshly prepared mesylate
(1.1 mmol) and NaH (60% dispersion in mineral oil, 75 mg, 1.9 mmol)
in 10 mL of DMF were processed as described in Example 1D to
provide the title compound (55 mg, 0.14 mmol, 23% yield). .sup.1H
NMR (CDCl.sub.3, 300 MHz) .delta. ppm 1.31 (s, 6H), 1.36 (s, 6H),
1.97 (s, 1H), 5.76 (s, 2H), 7.26-7.32 (m, 2H), 7.35-7.45 (m, 2H),
7.51 (ddd, J=8.3, 7.3, 1.4 Hz, 1H), 7.76-7.82 (m, 1H), 7.84 (s,
1H), 8.05 (d, J=8.1 Hz, 1H), 8.39-8.49 (m, 1H); MS (DCI/NH.sub.3)
m/z 389 (M+H).sup.+; Anal. Calculated for
C.sub.24H.sub.24N.sub.2OS: C, 74.19; H, 6.23; N, 7.21. Found: C,
74.06; H, 6.25; N, 7.04.
Example 90
ethyl
N-({1-(tetrahydro-2H-pyran-4-ylmethyl)-3-[(2,2,3,3-tetramethylcyclop-
ropyl)carbonyl]-1H-indol-6-yl}carbonyl)-beta-alaninate
[0336] To a solution of the product of Example 86 (0.26 g, 0.68
mmol) in 5 mL of EtOAc was added 1,1'-carbonyldiimidazole (0.13 g,
0.81 mmol). The mixture was stirred at ambient temperature for 3
hours then .beta.-alanine ethyl ester hydrochloride (0.13 g, 0.81
mmol) in 1 mL H.sub.2O was added. The reaction mixture was stirred
at ambient temperature for 1 hour then warmed to reflux and allowed
to stir for 16 h. The mixture was cooled to ambient temperature,
quenched with 5 mL of saturated aqueous NaHCO.sub.3 and the layers
were separated. The aqueous layer was extracted 3.times.3 mL of
EtOAc and the combined organic extracts were dried over anhydrous
Na.sub.2SO.sub.4, filtered, concentrated under reduced pressure and
purified via column chromatography (50% hexanes in EtOAc) to
provide the title compound (55 mg, 0.11 mmol, 17% yield). .sup.1H
NMR (CDCl.sub.3, 300 MHz) .delta. ppm 1.28 (t, J=7.1 Hz, 3H), 1.32
(s, 6H), 1.35 (s, 6H), 1.39-1.55 (m, 4H), 1.92 (s, 1H), 2.13-2.23
(m, 1H), 2.68 (dd, J=5.8 Hz, 2H), 3.33 (dt, J=11.6, 2.5 Hz, 2H),
3.78 (q, J=6.0 Hz, 2H), 3.92-4.02 (m, 2H), 4.10 (d, J=7.5 Hz, 2H),
4.19 (q, J=7.1 Hz, 2H), 6.90-6.98 (m, 1H), 7.49 (dd, J=8.5, 1.7 Hz,
1H), 7.70 (s, 1H), 8.01 (d, J=0.7 Hz, 1H), 8.42 (d, J=8.5 Hz, 1H);
MS (DCI/NH.sub.3) m/z 483 (M+H).sup.+; Anal. Calculated for
C.sub.28H.sub.38N.sub.2O.sub.5: C, 69.68; H, 7.94; N, 5.80. Found:
C, 69.00; H, 7.71; N, 5.79.
Example 91
[5-methoxy-1-(tetrahydro-2H-pyran-4-ylmethyl)-1H-indol-3-yl](2,2,3,3-tetra-
methylcyclopropyl)methanone
[0337] The product of Example 79 (0.11 g, 0.30 mmol), NaH (60%
dispersion in mineral oil, 48 mg, 1.2 mmol) and iodomethane (76
.mu.L, 0.90 mmol) in 10 mL of THF were processed as described in
Example 72 to provide the title compound (59 mg, 0.16 mmol, 53%
yield). .sup.1H NMR (CDCl.sub.3, 300 MHz) .delta. ppm 1.30 (s, 6H),
1.35 (s, 6H), 1.37-1.53 (m, 4H), 1.89 (s, 1H), 2.04-2.21 (m, 1H),
3.33 (dt, J=11.6, 2.5 Hz, 2H), 3.89 (s, 3H), 3.94-4.00 (m, 2H),
4.00 (d, J=7.5 Hz, 2H), 6.92 (dd, J=9.0, 2.5 Hz, 1H), 7.21 (d,
J=9.2 Hz, 1H), 7.56 (s, 1H), 7.92 (d, J=2.7 Hz, 1H); MS
(DCI/NH.sub.3) m/z 370 (M+H).sup.+; Anal. Calculated for
C.sub.23H.sub.31NO.sub.3.0.2H.sub.2O: C, 74.04; H, 8.48; N, 3.75.
Found: C, 73.92; H, 8.31; N, 3.66.
Example 92
[4-(benzyloxy)-1-(tetrahydro-2H-pyran-4-ylmethyl)-1H-indol-3-yl](2,2,3,3-t-
etramethylcyclopropyl)methanone
Example 92A
(4-Benzyloxy-1H-indol-3-yl)-(2,2,3,3-tetramethyl-cyclopropyl)-methanone
[0338] A mixture of 4-benzyloxyindole (1.1 g, 4.8 mmol),
ethylmagnesium bromide (1.0 M solution in THF, 5.2 mL, 5.2 mmol),
zinc chloride (1.0 M solution in Et.sub.2O, 5.2 mL, 5.2 mmol) and
the product of Example 1A (4.8 mmol) in 25 mL of dichloromethane
was processed as described in Example 1B to provide the title
compound (0.56 g, 1.6 mmol, 34% yield). MS (DCI/NH.sub.3) m/z 348
(M+H).sup.+.
Example 92B
[4-(benzyloxy)-1-(tetrahydro-2H-pyran-4-ylmethyl)-1H-indol-3-yl](2,2,3,3-t-
etramethylcyclopropyl)methanone
[0339] The product of Example 92A (0.56 g, 1.6 mmol), the product
of Example 18A (2.7 mmol), and NaH (60% dispersion in mineral oil,
0.19 g, 4.8 mmol) in 12 mL of DMF were processed as described in
Example 1D to provide the title compound (0.49 g, 1.1 mmol, 68%
yield). .sup.1H NMR (CDCl.sub.3, 300 MHz) .delta. ppm 1.14 (s, 6H),
1.31 (s, 6H), 1.34-1.53 (m, 4H), 2.05 (s, 1H), 2.06-2.20 (m, 1H),
3.32 (dt, J=11.6, 2.2 Hz, 2H), 3.92-3.98 (m, 2H), 3.97 (d, J=7.1
Hz, 2H), 5.29 (s, 2H), 6.66 (d, J=8.1 Hz, 1H), 6.95 (d, J=7.8 Hz,
1H), 7.13 (t, J=8.0 Hz, 1H), 7.27-7.39 (m, 3H), 7.44-7.54 (m, 3H);
MS (DCI/NH.sub.3) m/z 446 (M+H).sup.+; Anal. Calculated for
C.sub.29H.sub.35NO.sub.3: C, 78.17; H, 7.92; N, 3.14. Found: C,
78.25; H, 7.79; N, 3.18.
Example 93
1-(tetrahydro-2H-pyran-4-ylmethyl)-3-[(2,2,3,3-tetramethylcyclopropyl)carb-
onyl]-1H-indole-6-carboxamide
[0340] To a solution of the product of Example 86 (0.10 g, 0.27
mmol) in 5 mL of EtOAc was added 1,1'-carbonyldiimidazole (57 mg,
0.35 mmol). The mixture was stirred at ambient temperature for 3
hour then 1 mL of concentrated aqueous ammonium hydroxide was added
(15 mmol). The reaction mixture was stirred at 35.degree. C. for 16
hours then was cooled to ambient temperature, quenched with 5 mL of
saturated aqueous NaHCO.sub.3 and the layers were separated. The
aqueous layer was extracted 3.times.3 mL of EtOAc and the combined
organic extracts were dried over anhydrous Na.sub.2SO.sub.4,
filtered, concentrated under reduced pressure and purified via
column chromatography (10% CH.sub.3OH in EtOAc) to provide the
title compound (52 mg, 0.14 mmol, 50% yield). .sup.1H NMR
(MeOH-d.sub.4, 300 MHz) .delta. ppm 1.33 (s, 6H), 1.33 (s, 6H),
1.40-1.54 (m, 4H), 2.16 (s, 1H), 2.20-2.31 (m, 1H), 3.38 (dt,
J=11.2, 3.1 Hz, 2H), 3.89-3.98 (m, 2H), 4.22 (d, J=7.5 Hz, 2H),
7.74 (dd, J=8.5, 1.7 Hz, 1H), 8.10 (d, J=1.0 Hz, 1H), 8.22 (s, 1H),
8.30-8.35 (m, 1H); MS (DCI/NH.sub.3) m/z 383 (M+H).sup.+; Anal.
Calculated for C.sub.23H.sub.30N.sub.2O.sub.3.0.5
C.sub.2H.sub.4O.sub.2 (acetic acid): C, 69.88; H, 7.82; N, 6.79.
Found: C, 69.70; H, 7.42; N, 6.79.
Example 94
1-(2-morpholin-4-ylethyl)-3-[(2,2,3,3-tetramethylcyclopropyl)carbonyl]-1H--
indole-7-carboxylic acid
[0341] The title compound was obtained by the methods described in
Example 95. .sup.1H NMR (CDCl.sub.3, 300 MHz) .delta. ppm 1.32 (s,
6H), 1.36 (s, 6H), 1.98 (s, 1H), 2.56-2.75 (m, 4H), 2.78-2.91 (m,
2H), 3.76-3.91 (m, 4H), 4.48-4.62 (m, 2H), 7.32 (t, J=7.6 Hz, 1H),
7.85 (s, 1 H), 7.95 (d, J=7.5 Hz, 1H), 8.69 (d, J=7.8 Hz, 1H); MS
(DCI/NH.sub.3) m/z 399 (M+H).sup.+; Anal. Calculated for
C.sub.23H.sub.30N.sub.2O.sub.4: C, 68.32; H, 7.59; N, 7.03. Found:
C, 68.92; H, 7.57; N, 6.93.
Example 95
2-morpholin-4-ylethyl
1-(2-morpholin-4-ylethyl)-3-[(2,2,3,3-tetramethylcyclopropyl)carbonyl]-1H-
-indole-7-carboxylate Dihydrochloride
Example 95A
3-(2,2,3,3-Tetramethyl-cyclopropanecarbonyl)-1H-indole-7-carboxylic
Acid Methyl Ester
[0342] A mixture of methyl-indole-7-carboxylate (Maybridge, 1.0 g,
5.7 mmol), ethylmagnesium bromide (1.0 M solution in THF, 6.9 mL,
6.9 mmol), zinc chloride (1.0 M solution in Et.sub.2O, 6.9 mL, 6.9
mmol) and the product of Example 1A (7.4 mmol) in 25 mL of
dichloromethane was processed as described in Example 1B to provide
the title compound (1.1 g, 3.6 mmol, 63% yield). MS (DCI/NH.sub.3)
m/z 300 (M+H).sup.+.
Example 95B
2-morpholin-4-ylethyl
1-(2-morpholin-4-ylethyl)-3-[(2,2,3,3-tetramethylcyclopropyl)carbonyl]-1H-
-indole-7-carboxylate Dihydrochloride
[0343] The product of Example 95A (0.47 g, 2.1 mmol), the product
of Example 2A (3.1 mmol) and NaH (60% dispersion in mineral oil,
0.16 g, 4.1 mmol) in 10 mL of DMF were processed as described in
Example 1D to provide the title compound of Example 94 (0.13 g,
0.33 mmol, 16% yield) and the free base of the morpholinylethyl
ester (30 mg, 0.06 mmol, 2% yield), which was treated with 4 N HCl
in dioxane (0.12 mmol, 60 .mu.L) to provide the title compound (25
mg, 0.04 mmol, 67% yield). .sup.1H NMR (MeOH-d.sub.4, 300 MHz)
.delta. ppm 1.34 (s, 6H), 1.35 (s, 6H), 2.19 (s, 1H), 3.12-3.29 (m,
4H), 3.32-3.47 (m, 4H), 3.70-3.78 (m, 4H), 3.86-4.09 (m, 8H),
4.80-4.84 (m, 2H), 4.88-4.97 (m, 2H), 7.33 (t, J=7.8 Hz, 1H), 8.00
(dd, J=7.5, 0.7 Hz, 1H), 8.28 (s, 1H), 8.69 (dd, J=8.1, 1.4 Hz,
1H); MS (DCI/NH.sub.3) m/z 512 (M+H).sup.+; Anal. Calculated for
C.sub.22H.sub.29NO.sub.2-2HCl: C, 59.58; H, 7.41; N, 7.19. Found:
C, 59.71; H, 7.45;N, 7.11.
Example 96
[4-hydroxy-1-(tetrahydro-2H-pyran-4-ylmethyl)-1H-indol-3-yl](2,2,3,3-tetra-
methylcyclopropyl)methanone
[0344] The product of Example 92B (0.44 g, 0.98 mmol) and Pd/C (10
wt % palladium on activated carbon, 200 mg) in 60 mL EtOH were
processed as described in Example 70 to provide the title compound
(0.23 g, 0.65 mmol, 67% yield). .sup.1H NMR (CDCl.sub.3, 300 MHz)
.delta. ppm 1.31 (s, 6H), 1.33 (s, 6H), 1.38-1.58 (m, 4H), 1.90 (s,
1H), 2.08-2.25 (m, 1H), 3.34 (dt, J=11.7, 2.4 Hz, 2H), 3.95-4.03
(m, 2H), 3.99 (d, J=7.5 Hz, 2H), 6.69 (d, J=7.8 Hz, 1H), 6.75 (d,
J=8.1 Hz, 1H), 7.18 (t, J=8.0 Hz, 1H), 7.53 (s, 1H), 12.04 (s, 1H);
MS (DCI/NH.sub.3) m/z 356 (M+H).sup.+; Anal. Calculated for
C.sub.22H.sub.29NO.sub.3: 74.33; H, 8.22; N, 3.94. Found: C, 74.08;
H, 8.16; N, 3.86.
Example 97
[4-methoxy-1-(tetrahydro-2H-pyran-4-ylmethyl)-1H-indol-3-yl](2,2,3,3-tetra-
methylcyclopropyl)methanone
[0345] The product of Example 96 (63 mg, 0.18 mmol), NaH (60%
dispersion in mineral oil, 28 mg, 0.71 mmol) and iodomethane (45
.mu.L, 0.53 mmol) in 5 mL of THF were processed as described in
Example 72 to provide the title compound (53 mg, 0.14 mmol, 81%
yield). .sup.1H NMR (CDCl.sub.3, 300 MHz) .delta. ppm 1.28 (s, 6H),
1.35 (s, 6H), 1.37-1.52 (m, 4H), 2.02-2.17 (m, 1H), 2.53 (s, 1H),
3.31 (dt, J=11.6, 2.2 Hz, 2H), 3.93-4.00 (m, 4H), 3.95 (s, 3H),
6.67 (d, J=7.8 Hz, 1H), 6.95 (d, J=7.8 Hz, 1H), 7.20 (t, J=8.0 Hz,
1H), 7.47 (s, 1H); MS (DCI/NH.sub.3) m/z 370 (M+H).sup.+; Anal.
Calculated for C.sub.23H.sub.31NO.sub.3: C, 74.76; H, 8.46; N,
3.79. Found: C, 74.76; H, 8.63; N, 3.79.
Example 98
[6-methyl-1-(tetrahydro-2H-pyran-4-ylmethyl)-1H-indol-3-yl](2,2,3,3-tetram-
ethylcyclopropyl)methanone
Example 98A
(6-Methyl-1H-indol-3-yl)-(2,2,3,3-tetramethylcyclopropyl)methanone
[0346] A mixture of 6-methylindole (1.0 g, 7.6 mmol),
ethylmagnesium bromide (1.0 M solution in THF, 9.1 mL, 9.1 mmol),
zinc chloride (1.0 M solution in Et.sub.2O, 9.1 mL, 9.1 mmol) and
the product of Example 1A (11 mmol) in 25 mL of dichloromethane was
processed as described in Example 1B to provide the title compound
(1.3 g, 5.0 mmol, 65% yield). MS (DCI/NH.sub.3) m/z 256
(M+H).sup.+.
Example 98B
[6-methyl-1-(tetrahydro-2H-pyran-4-ylmethyl)-1H-indol-3-yl](2,2,3,3-tetram-
ethylcyclopropyl)methanone
[0347] The product of Example 98A (0.38 g, 1.5 mmol), the product
of Example 18A (3.0 mmol), and NaH (60% dispersion in mineral oil,
0.18 g, 4.5 mmol) in 10 mL of DMF were processed as described in
Example 1D to provide the title compound (0.17 g, 0.48 mmol, 32%
yield). .sup.1H NMR (CDCl.sub.3, 300 MHz) .delta. ppm 1.30 (s, 6H),
1.34 (s, 6H), 1.38-1.63 (m, 4H), 1.93 (s, 1H), 2.07-2.23 (m, 1H),
2.49 (s, 3H), 3.34 (dt, J=11.7, 2.4 Hz, 2H), 3.93-4.04 (m, 2H),
4.00 (d, J=7.1 Hz, 2H), 7.06-7.13 (m, 1H), 7.11 (s, 1H), 7.55 (s,
1H), 8.25 (d, J=8.8 Hz, 1H); MS (DCI/NH.sub.3) m/z 354 (M+H).sup.+;
Anal. Calculated for C.sub.23H.sub.31NO.sub.2: C, 78.15; H, 8.84;
N, 3.96. Found: C, 78.03; H, 8.64; N, 3.92.
Example 99
[6-(benzyloxy)-1-(2-morpholin-4-ylethyl)-1H-indol-3-yl](2,2,3,3-tetramethy-
lcyclopropyl)methanone
[0348] The product of Example 69A (0.96 g, 2.8 mmol), the product
of Example 2A (4.1 mmol), and NaH (60% dispersion in mineral oil,
0.33 g, 8.3 mmol) in 20 mL of DMF were processed as described in
Example 1D to provide the title compound (1.2 g, 2.7 mmol, 96%
yield). .sup.1H NMR (CDCl.sub.3, 300 MHz) .delta. ppm 1.30 (s, 6H),
1.34 (s, 6H), 1.90 (s, 1H), 2.42-2.54 (m, 4H), 2.73 (t, J=6.6 Hz,
2H), 3.65-3.77 (m, 4H), 4.17 (t, J=6.3 Hz, 2H), 5.14 (s, 2H), 6.86
(s, 1H), 7.00 (dd, J=8.6, 2.2 Hz, 1H), 7.31-7.44 (m, 3H), 7.43-7.50
(m, 2H), 7.65 (s, 1H), 8.29 (d, J=8.8 Hz, 1H); MS (DCI/NH.sub.3)
m/z 461 (M+H).sup.+; Anal. Calculated for C.sub.23H.sub.31NO.sub.2:
C, 75.62; H, 7.88; N, 6.08. Found: C, 75.31; H, 7.81; N, 6.04.
Example 100
[6-hydroxy-1-(2-morpholin-4-ylethyl)-1H-indol-3-yl](2,2,3,3-tetramethylcyc-
lopropyl)methanone
[0349] The product of Example 99 (1.0 g, 2.2 mmol) and Pd/C (10 wt
% palladium on activated carbon, 100 mg) in 20 mL EtOH and 10 mL of
EtOAc were processed as described in Example 70 to provide the
title compound (0.75 g, 2.0 mmol, 90% yield). .sup.1H NMR
(CDCl.sub.3, 300 MHz) .delta. ppm 1.30 (s, 6H), 1.34 (s, 6H), 1.89
(s, 1H), 2.45-2.64 (m, 4H), 2.74-2.89 (m, 2H), 3.67-3.80 (m, 4H),
4.14-4.30 (m, 2H), 6.79 (dd, J=8.5, 2.4 Hz, 1H), 6.81-6.85 (m, 1H),
7.65 (s, 1H), 8.24 (d, J=8.5 Hz, 1H); MS (DCI/NH.sub.3) m/z 371
(M+H).sup.+; Anal. Calculated for C.sub.22H.sub.30N.sub.2O.sub.3:
C, 71.32; H, 8.16; N, 7.56. Found: C, 71.18; H, 8.33; N, 7.52.
Example 101
[6-methoxy-1-(2-morpholin-4-ylethyl)-1H-indol-3-yl](2,2,3,3-tetramethylcyc-
lopropyl)methanone
[0350] The product of Example 100 (0.20 g, 0.54 mmol), NaH (60%
dispersion in mineral oil, 65 mg, 1.6 mmol) and iodomethane (84
.mu.L, 1.4 mmol) in 5 mL of THF were processed as described in
Example 72 to provide the title compound (70 mg, 0.18 mmol, 34%
yield). .sup.1H NMR (CDCl.sub.3, 300 MHz) .delta. ppm 1.30 (s, 6H),
1.34 (s, 6H), 1.90 (s, 1H), 2.51 (t, 4H), 2.78 (t, J=6.4 Hz, 2H),
3.66-3.75 (m, 4H), 3.84-3.92 (m, 3H), 4.20 (t, J=6.6 Hz, 2H), 6.80
(s, 1H), 6.91 (dd, J=8.8, 2.0 Hz, 1H), 7.66 (s, 1H), 8.28 (d, J=8.8
Hz, 1H); MS (DCI/NH.sub.3) m/z 385 (M+H).sup.+; Anal. Calculated
for C.sub.23H.sub.32N.sub.2O.sub.2: C, 71.84; H, 8.39; N, 7.29.
Found: C, 71.73; H, 8.42; N, 7.12.
Example 102
4-oxo-4-({1-(tetrahydro-2H-pyran-4-ylmethyl)-3-[(2,2,3,3-tetramethylcyclop-
ropyl)carbonyl]-1H-indol-5-yl}oxy)butanoic Acid
[0351] The product of Example 79 (0.13 g, 0.37 mmol) and succinic
anhydride (0.11 g, 1.1 mmol) were combined in 5 mL pyridine. This
mixture was warmed to reflux and allowed to stir for 18 h. The
mixture was cooled to ambient temperature and poured into .about.10
mL of ice and water. This mixture was extracted with 3.times.5 mL
of EtOAc. The combined organic extracts were dried over anhydrous
Na.sub.2SO.sub.4, filtered, concentrated under reduced pressure and
purified via column chromatography (SiO.sub.2, 9:1:0.1
EtOAc:CH.sub.3OH:AcOH) to provide the title compound (90 mg, 0.20
mmol, 54% yield). .sup.1H NMR (MeOH-d.sub.4,300 MHz) .delta. ppm
1.31 (s, 6H), 1.32 (s, 6H), 1.37-1.54 (m, 4H), 2.12 (s, 1H),
2.13-2.27 (m, 1H), 2.71 (t, J=6.4 Hz, 2H), 2.85-2.92 (m, 2H),
3.32-3.43 (m, 2H), 3.89-3.99 (m, 2H), 4.16 (d, J=7.5 Hz, 2H), 7.01
(dd, J=8.8, 2.4 Hz, 1H), 7.51 (d, J=8.8 Hz, 1H), 7.97 (d, J=2.0 Hz,
1H), 8.10 (s, 1H); MS (DCI/NH.sub.3) m/z 456 (M+H).sup.+; Anal.
Calculated for C.sub.26H.sub.33NO.sub.6: C, 68.55; H, 7.30; N,
3.07. Found: C, 68.15; H, 7.40; N, 2.99.
Example 103
(2,2-dichloro-1-methylcyclopropyl)[1-(tetrahydro-2H-pyran-4-ylmethyl)-1H-i-
ndol-3-yl]methanone
Example 103A
(2,2-Dichloro-1-methyl-cyclopropyl)-(1H-indol-3-yl)methanone
[0352] A mixture of 2,2-dichloro-1-methylcyclopropane carboxylic
acid (1.0 g, 5.9 mmol) in 5 mL of thionyl chloride was processed as
described in Example 1A to provide the corresponding acid chloride.
The freshly prepared acid chloride (5.9 mmol), indole (0.69 g, 5.9
mmol), ethylmagnesium bromide (1.0 M solution in THF, 6.5 mL, 6.5
mmol), and zinc chloride (1.0 M solution in Et.sub.2O, 6.5 mL, 6.5
mmol) in 30 mL of dichloromethane were processed as described in
Example 1B to provide the title compound (0.36 g, 1.3 mmol, 23%
yield). MS (DCI/NH.sub.3) m/z 268 (M+H).sup.+.
Example 103B
(2,2-dichloro-1-methylcyclopropyl)[1-(tetrahydro-2H-pyran-4-ylmethyl)-1H-i-
ndol-3-yl]methanone
[0353] The product of Example 103A (0.18 g, 0.68 mmol), the product
of Example 18A (1.2 mmol), and NaH (60% dispersion in mineral oil,
82 mg, 2.0 mmol) in 10 mL of DMF were processed as described in
Example 1D to provide the title compound (80 mg, 0.22 mmol, 32%
yield). .sup.1H NMR (CDCl.sub.3,300 MHz) .delta. ppm 1.40-1.62 (m,
5H), 1.76 (s, 3H), 2.09-2.22 (m, 1H), 2.25 (d, J=7.5 Hz, 1H), 3.34
(dq, J=11.6, 6.2, 2.5 Hz, 2H), 3.93-4.04 (m, 2H), 4.03-4.22 (m,
2H), 7.30-7.43 (m, 3H), 7.73 (s, 1H), 8.31-8.40 (m, 1H); MS
(DCI/NH.sub.3) m/z 366 (M+H).sup.+; Anal. Calculated for
C.sub.19H.sub.21Cl.sub.2NO.sub.2.0.1 C.sub.6H.sub.14: C, 62.79; H,
6.02; N, 3.74. Found: C, 63.09; H, 5.77; N, 3.40.
Example 104
[1-(4-azidobutyl)-1H-indol-3-yl](2,2,3,3-tetramethylcyclopropyl)methanone
[0354] To a solution of the product of Example 24A (0.29 g, 0.93
mmol) in 10 mL of THF at 0.degree. C. was added triethylamine (0.39
mL, 2.8 mmol) followed by methanesulfonyl chloride (0.14 mL, 1.9
mmol). The ice bath was removed and the mixture was stirred at
ambient temperature for 2 h. The mixture was filtered and the
filtrate was concentrated under reduced pressure to afford the
corresponding mesylate. To a solution of the freshly prepared
mesylate (0.93 mmol) in 5 mL of DMF was added sodium azide (0.18 g,
2.8 mmol). The mixture was warmed to 80.degree. C. and was stirred
for 4 h. The mixture was then cooled to ambient temperature,
diluted with 5 mL of dichloromethane, and quenched with 3 mL of
saturated aqueous NaHCO.sub.3. The layers were separated and the
aqueous layer was extracted with 3.times.5 mL of dichloromethane.
The combined organic extracts were dried over anhydrous
Na.sub.2SO.sub.4, filtered, concentrated under reduced pressure and
purified via column chromatography (SiO.sub.2, 50% hexanes in
EtOAc) to provide the title compound (0.30 g, 0.89 mmol, 95%
yield). .sup.1H NMR (CDCl.sub.3, 300 MHz) .delta. ppm 1.31 (s, 6H),
1.35 (s, 6H), 1.59-1.72 (m, 2H), 1.95 (s, 1H), 1.96-2.06 (m, 2H),
3.33 (t, J=6.6 Hz, 2H), 4.21 (t, J=7.1 Hz, 2H), 7.26-7.38 (m, 3H),
7.65 (s, 1H), 8.37-8.44 (m, 1H); MS (DCI/NH.sub.3) m/z 339
(M+H).sup.+; Anal. Calculated for C.sub.20H.sub.26N.sub.4O: C,
70.98; H, 7.74; N, 16.55. Found: C, 70.67; H, 7.89; N, 14.14.
Example 105
[1-(2-azidoethyl)-1H-indol-3-yl](2,2,3,3-tetramethylcyclopropyl)methanone
[0355] The product of Example 38 (0.46 g, 1.6 mmol),
methanesulfonyl chloride (0.27 mL, 3.6 mmol), triethylamine (0.74
mL, 5.3 mmol) and NaN.sub.3 (0.31 g, 4.8 mmol) were processed as
described in Example 104 to provide the title compound (0.32 g,
0.10 mmol, 65% yield). .sup.1H NMR (CDCl.sub.3, 300 MHz) .delta.
ppm 1.31 (s, 6H), 1.35 (s, 6H), 1.95 (s, 1H), 3.74 (t, J=5.8 Hz,
2H), 4.32 (t, J=5.9 Hz, 2H), 7.28-7.35 (m, 3H), 7.70 (s, 1H),
8.39-8.47 (m, 1H); MS (DCI/NH.sub.3) m/z 311 (M+H).sup.+; Anal.
Calculated for C.sub.18H.sub.22N.sub.4O: C, 69.65; H, 7.14; N,
18.05. Found: C, 69.30; H, 7.03; N, 17.83.
Example 106
N-(4-{3-[(2,2,3,3-tetramethylcyclopropyl)carbonyl]-1H-indol-1-yl}butyl)met-
hanesulfonamide
Example 106A
[1-(4-Amino-butyl)-1H-indol-3-yl]-(2,2,3,3-tetramethyl-cyclopropyl)-methan-
one
[0356] To a solution of the product of Example 104 (0.28 g, 0.82
mmol) in 7 mL of THF and 3.5 mL H.sub.2O was added
triphenylphosphine (0.24 g, 0.91 mmol). The mixture was stirred at
ambient temperature for 72 hours then diluted with 5 mL of EtOAc.
The layers were separated and the aqueous layer was extracted with
3.times.3 mL of EtOAc. The combined organic extracts were dried
over anhydrous Na.sub.2SO.sub.4, filtered, concentrated under
reduced pressure and purified via column chromatography (SiO.sub.2,
9:1:0.1 CH.sub.2Cl.sub.2:CH.sub.3O H:NH.sub.4OH) to provide the
title compound (0.23 g, 0.73 mmol, 89% yield). MS (DCI/NH.sub.3)
m/z 313 (M+H).sup.+.
Example 106B
N-(4-{3-[(2,2,3,3-tetramethylcyclopropyl)carbonyl]-1H-indol-1-yl}butyl)met-
hanesulfonamide
[0357] To a solution of the product of Example 106A (0.21 g, 0.67
mmol) in 5 mL of THF at 0.degree. C. was added triethylamine (0.19
mL, 1.3 mmol) followed by methanesulfonyl chloride (57 .mu.L, 0.74
mmol). The ice bath was removed and the mixture was stirred at
ambient temperature for 6 h. The mixture was filtered and the
filtrate was concentrated under reduced pressure. The residue was
purified via column chromatography (SiO.sub.2, 20% hexanes in
EtOAc) to provide the title compound (0.19 g, 0.49 mmol, 73%
yield). .sup.1H NMR (CDCl.sub.3, 300 MHz) .delta. ppm 1.32 (s, 6H),
1.35 (s, 6H), 1.57-1.67 (m, 2H), 1.94-2.06 (m, 2H), 1.96 (s, 1H),
2.91 (s, 3H), 3.08-3.20 (m, 2H), 4.09-4.18 (m, 1H), 4.22 (t, J=6.8
Hz, 2H), 7.26-7.36 (m, 3H), 7.67 (s, 1H), 8.38-8.45 (m, 1H); MS
(DCI/NH.sub.3) m/z 391 (M+H).sup.+; Anal. Calculated for
C.sub.21H.sub.30N.sub.2O.sub.3S: C, 64.58; H, 7.74; N, 7.17. Found:
C, 64.35; H, 7.69; N, 7.00.
Example 107
ethyl
4-({1-(tetrahydro-2H-pyran-4-ylmethyl)-3-[(2,2,3,3-tetramethylcyclop-
ropyl)carbonyl]-1H-indol-5-yl}oxy)butanoate
[0358] To a solution of the product of Example 79 (0.21 g, 0.59
mmol) in 5 mL of DMF was added Cs.sub.2CO.sub.3 (0.58 g, 1.8 mmol)
followed by ethyl 4-bromobutyrate (0.13 mL, 0.89 mmol). This
mixture was warmed to 90.degree. C. and was stirred for 90 minutes.
The mixture was then cooled to ambient temperature, quenched with 3
mL of saturated aqueous NH.sub.4Cl and diluted with 5 mL of EtOAc.
The layers were separated, the aqueous layer was extracted
3.times.3 mL of EtOAc and the combined organic extracts were dried
over anhydrous Na.sub.2SO.sub.4, filtered, concentrated under
reduced pressure and purified via column chromatography (SiO.sub.2,
50% hexanes in EtOAc) to provide the title compound (0.26 g, 0.55
mmol, 94% yield). .sup.1H NMR (CDCl.sub.3, 300 MHz) .delta. ppm
1.26 (t, J=7.3 Hz, 3H), 1.30 (s, 6H), 1.34 (s, 6H), 1.37-1.60 (m,
4H), 1.88 (s, 1H), 2.07-2.18 (m, 2H), 2.52 (t, J=7.3 Hz, 2H), 3.33
(dt, J=11.7, 2.4 Hz, 2H), 3.93-4.02 (m, 2H), 3.99 (d, J=7.1 Hz,
2H), 4.05-4.20 (m, 5H), 6.91 (dd, J=8.8, 2.4 Hz, 1H), 7.20 (d,
J=8.8 Hz, 1H), 7.55 (s, 1H), 7.90 (d, J=2.4 Hz, 1H); MS
(DCI/NH.sub.3) m/z 470 (M+H).sup.+; Anal. Calculated for
C.sub.28H.sub.32NO.sub.5: C, 71.61; H, 8.37; N, 2.98. Found: C,
71.64; H, 8.49; N, 2.92.
Example 108
[1-(3-azidopropyl)-1H-indol-3-yl](2,2,3,3-tetramethylcyclopropyl)methanone
[0359] The product of Example 40 (0.41 g, 1.4 mmol),
methanesulfonyl chloride (0.23 mL, 3.0 mmol), triethylamine (0.63
mL, 4.5 mmol) and sodium azide (0.27 g, 4.1 mmol) were processed
according to the methods described in Example 104 to afford the
title compound (0.31 g, 0.95 mmol, 70% yield). .sup.1H NMR
(CDCl.sub.3, 300 MHz) .delta. ppm 1.31 (s, 6H), 1.35 (s, 6 H), 1.94
(s, 1H), 2.07-2.20 (m, 2H), 3.32 (t, J=6.1 Hz, 2H), 4.30 (t, J=6.6
Hz, 2H), 7.27-7.38 (m, 3H), 7.66 (s, 1H), 8.37-8.45 (m, 1H); MS
(DCI/NH.sub.3) m/z 325 (M+H).sup.+; Anal. Calculated for
C.sub.19H.sub.24N.sub.4O.0.1H.sub.2O: C, 69.95; H, 7.48; N, 17.17.
Found: C, 69.87; H, 7.39; N, 17.13.
Example 109
{1-[(2S)-tetrahydrofuran-2-ylmethyl]-1H-indol-3-yl}(2,2,3,3-tetramethylcyc-
lopropyl)methanone
Example 109A
(S)-(tetrahydro-furan-2-yl)methanol
[0360] To a flask containing 60 mL of THF at 0.degree. C. was added
lithium aluminum hydride (0.98 g, 26 mmol). The mixture was stirred
at 0.degree. C. for 5 minutes then (s)-(-)-tetrahydro-2-furoic acid
(1.0 g, 8.6 mmol) in 5 mL of THF was added dropwise via syringe.
This mixture was warmed to reflux and was allowed to stir for 18 h.
The mixture was then cooled to 0.degree. C. and quenched by the
slow addition of Na.sub.2SO.sub.4 10H.sub.2O (excess). The mixture
was filtered and the filtrate was concentrated under reduced
pressure to afford the title compound. MS (DCI/NH.sub.3) m/z 103
(M+H).sup.+.
Example 109B
{1-[(2S)-tetrahydrofuran-2-ylmethyl]-1H-indol-3-yl}(2,2,3,3-tetramethylcyc-
lopropyl)methanone
[0361] The product of Example 109A (0.38 g, 3.7 mmol),
methanesulfonyl chloride (0.34 mL, 4.4 mmol), and triethylamine
(0.70 mL, 5.0 mmol) in 15 mL of THF were processed as described in
Example 1C to provide the corresponding mesylate. The major product
of Example 1B (0.30 g, 1.2 mmol), the freshly prepared mesylate
(3.7 mmol) and NaH (60% dispersion in mineral oil, 0.15 g, 3.7
mmol) in 12 mL of DMF were processed as described in Example 1D to
provide the title compound (0.23 g, 0.70 mmol, 56% yield). .sup.1H
NMR (CDCl.sub.3, 300 MHz) .delta. ppm 1.30 (s, 6H), 1.34 (s, 3H),
1.35 (s, 3H), 1.50-1.64 (m, 1H), 1.70-1.92 (m, 2H), 1.95 (s, 1H),
1.96-2.08 (m, 1H), 3.72-3.92 (m, 2H), 4.10-4.36 (m, 3H), 7.24-7.29
(m, 2H), 7.32-7.39 (m, 1H), 7.79 (s, 1H), 8.38-8.45 (m, 1H); MS
(DCI/NH.sub.3) m/z 326 (M+H).sup.+; Anal. Calculated for
C.sub.21H.sub.27NO.sub.2: C, 77.50; H, 8.36; N, 4.30. Found: C,
77.25; H, 8.68; N, 4.33.
Example 110
[5-(4-hydroxybutoxy)-1-(tetrahydro-2H-pyran-4-ylmethyl)-1H-indol-3-yl](2,2-
,3,3-tetramethylcyclopropyl)methanone
[0362] The product of Example 79 (0.57 g, 1.6 mmol),
4-bromo-1-butanol (TCI-America, 0.37 g, 2.4 mmol) and
Cs.sub.2CO.sub.3 (1.6 g, 4.8 mmol) in 10 mL of DMF were processed
as described in Example 107 to provide the title compound (75 mg,
0.18 mmol, 11% yield) and the product of Example 111 (0.24 g, 0.50
mmol, 31% yield). .sup.1H NMR (CDCl.sub.3, 300 MHz) .delta. ppm
1.30 (s, 6H), 1.34 (s, 6H), 1.38-1.59 (m, 4H), 1.74-1.82 (m, 3H),
1.85-1.95 (m, 2H), 1.88 (s, 1H), 2.08-2.20 (m, 1H), 3.33 (dt,
J=11.5, 2.4 Hz, 2H), 3.74 (t, J=6.3 Hz, 2H), 3.93-4.03 (m, 2H),
4.00 (d, J=7.1 Hz, 2H), 4.11 (t, J=7.0 Hz, 2H), 6.92 (dd, J=9.0,
2.5 Hz, 1H), 7.21 (d, J=8.8 Hz, 1H), 7.56 (s, 1H), 7.93 (d, J=2.4
Hz, 1H); MS (DCI/NH.sub.3) m/z 428 (M+H).sup.+; Anal. Calculated
for C.sub.26H.sub.37NO.sub.4: C, 73.03; H, 8.72; N, 3.28. Found: C,
72.68; H, 8.43; N, 3.12.
Example 111
[5-(4-bromobutoxy)-1-(tetrahydro-2H-pyran-4-ylmethyl)-1H-indol-3-yl](2,2,3-
,3-tetramethylcyclopropyl)methanone
[0363] The title compound was obtained using the method described
in Example 110: .sup.1H NMR (CDCl.sub.3, 300 MHz) .delta. ppm 1.30
(s, 6H), 1.34 (s, 6H), 1.39-1.70 (m, 5H), 1.88 (s, 1H), 1.92-2.00
(m, 2H), 2.06-2.15 (m, 2H), 3.33 (dt, J=11.6, 2.2 Hz, 2H),
3.41-3.46 (m, 1H), 3.50 (t, J=6.6 Hz, 2H), 3.94-4.02 (m, 2H), 4.00
(d, J=7.1 Hz, 2H), 4.09 (t, J=5.8 Hz, 2H), 6.91 (dd, J=8.8, 2.4 Hz,
1H), 7.21 (d, J=8.8 Hz, 1H), 7.56 (s, 1H), 7.92 (d, J=2.4 Hz, 1H);
MS (DCI/NH.sub.3) m/z 490, 492 (M+H).sup.+; Anal. Calculated for
C.sub.26H.sub.36BrNO.sub.3: C, 63.67; H, 7.40; N, 2.86. Found: C,
64.04; H, 7.60; N, 2.67.
Example 112
[1-(6-azidohexyl)-1H-indol-3-yl](2,2,3,3-tetramethylcyclopropyl)methanone
[0364] The product of Example 42 (0.54 g, 1.7 mmol),
methanesulfonyl chloride (0.28 mL, 3.6 mmol), triethylamine (0.76
mL, 5.5 mmol) and sodium azide (0.32 g, 5.0 mmol) were processed as
in Example 104 to afford the title compound (0.37 g, 1.0 mmol, 63%
yield). .sup.1H NMR (CDCl.sub.3, 300 MHz) .delta. ppm 1.31 (s, 6H),
1.35 (s, 6H), 1.40-1.51 (m, 2H), 1.58-1.69 (m, 2H), 1.87-1.99 (m,
2H), 1.95 (s, 1H), 3.28 (t, J=6.8 Hz, 2H), 4.18 (t, J=7.1 Hz, 2H),
7.26-7.36 (m, 3H), 7.65 (s, 1H), 8.37-8.44 (m, 1H); MS
(DCI/NH.sub.3) m/z 353 (M+H).sup.+; Anal. Calculated for
C.sub.21H.sub.28N.sub.4O 0.1H.sub.2O: C, 71.20; H, 8.02; N, 15.81.
Found: C, 70.95; H, 7.97; N, 15.70.
Example 113
N-(2-{3-[(2,2,3,3-tetramethylcyclopropyl)carbonyl]-1H-indol-1-yl}ethyl)met-
hanesulfonamide
Example 113A
[1-(2-Amino-ethyl)-1H-indol-3-yl]-(2,2,3,3-tetramethyl-cyclopropyl)-methan-
one
[0365] The product of Example 105 (0.28 g, 0.90 mmol) and
triphenylphospine (0.26 g, 0.99 mmol) in 9.5 mL of THF and 0.5 mL
H.sub.2O were processed as described in Example 106A to provide the
title compound (0.17 g, 0.60 mmol, 66% yield). MS (DCI/NH.sub.3)
m/z 285 (M+H).sup.+.
Example 113B
N-(2-{3-[(2,2,3,3-tetramethylcyclopropyl)carbonyl]-1H-indol-1-yl}ethyl)met-
hanesulfonamide
[0366] The product of Example 113A (0.16 g, 0.55 mmol),
methanesulfonyl chloride (64 .mu.L, 0.83 mmol) and triethylamine
(0.23 mL, 1.7 mmol) in 10 mL of THF were processed as described in
Example 106B to provide the title compound (0.16 g, 0.44 mmol, 80%
yield). .sup.1H NMR (CDCl.sub.3, 300 MHz) .delta. ppm 1.31 (s, 6H),
1.35 (s, 6H), 1.94 (s, 1H), 2.83 (s, 3H), 3.57 (q, J=6.1 Hz, 2H),
4.39 (t, J=5.8 Hz, 2H), 4.40-4.47 (m, 1H), 7.26-7.41 (m, 3H), 7.73
(s, 1H), 8.38-8.46 (m, 1H); MS (DCI/NH.sub.3) m/z 363 (M+H).sup.+;
Anal. Calculated for C.sub.19H.sub.26N.sub.2O.sub.3S.0.2H.sub.2O:
C, 62.34; H, 7.27; N, 7.65. Found: C, 62.58; H, 7.10; N, 7.32.
Example 114
methyl
1-(tetrahydro-2H-pyran-4-ylmethyl)-3-[(2,2,3,3-tetramethylcycloprop-
yl)carbonyl]-1H-indole-5-carboxylate
Example 114A
3-(2,2,3,3-Tetramethyl-cyclopropanecarbonyl)-1H-indole-5-carboxylic
Acid Methyl Ester
[0367] Methyl-indole-5-carboxylate (Lancaster, 3.0 g, 17 mmol),
ethylmagnesium bromide (1.0 M solution in THF, 21 mL, 21 mmol),
zinc chloride (1.0 M solution in Et.sub.2O, 21 mL, 21 mmol) and the
product of Example 1A (26 mmol) in 50 mL of dichloromethane were
processed as described in Example 1B to provide the title compound
(3.4 g, 11 mmol, 66% yield). MS (DCI/NH.sub.3) m/z 300
(M+H).sup.+.
Example 114B
methyl
1-(tetrahydro-2H-pyran-4-ylmethyl)-3-[(2,2,3,3-tetramethylcycloprop-
yl)carbonyl]-1H-indole-5-carboxylate
[0368] The product of Example 114A (1.5 g, 5.1 mmol), the product
of Example 18A (10 mmol), and NaH (60% dispersion in mineral oil,
0.61 g, 15 mmol) in 40 mL of DMF were processed as described in
Example 1D to provide the title compound (0.89 g, 2.2 mmol, 44%
yield) and
1-(tetrahydro-2H-pyran-4-ylmethyl)-3-[(2,2,3,3-tetramethylcyclopropyl)car-
bonyl]-1H-indole-5-carboxylic acid as a minor product (0.21 g, 0.55
mmol, 11% yield, MS (DCI/NH.sub.3) m/z 384 (M+H).sup.+ for the
carboxylic acid). Data for Example 114B (major product): .sup.1H
NMR (CDCl.sub.3, 300 MHz) .delta. ppm 1.33 (s, 6H), 1.36 (s, 6H),
1.40-1.58 (m, 4H), 1.95 (s, 1H), 2.06-2.24 (m, 1H), 3.34 (dt,
J=11.6, 2.5 Hz, 2H), 3.92 (s, 3H), 3.94-4.01 (m, 2H), 4.06 (d,
J=7.1 Hz, 2H), 7.36 (d, J=8.8 Hz, 1H), 7.66 (s, 1H), 8.00 (dd,
J=8.5, 1.7 Hz, 1H), 9.12 (dd, J=1.7, 0.7 Hz, 1H); MS (DCI/NH.sub.3)
m/z 398 (M+H).sup.+; Anal. Calculated for C.sub.24H.sub.31NO.sub.4:
C, 72.52; H, 7.86; N, 3.52. Found: C, 72.53; H, 7.90; N, 3.48.
Example 115
N-(3-{3-[(2,2,3,3-tetramethylcyclopropyl)carbonyl]-1H-indol-1-yl}propyl)me-
thanesulfonamide
Example 115A
[1-(3-Amino-propyl)-1H-indol-3-yl]-(2,2,3,3-tetramethyl-cyclopropyl)-metha-
none
[0369] The product of Example 108 (0.28 g, 0.88 mmol) and
triphenylphospine (0.25 g, 0.96 mmol) in 9.5 mL of THF and 0.5 mL
of H.sub.2O were processed as described in Example 106A to provide
the title compound (0.20 g, 0.66 mmol, 76% yield). MS
(DCI/NH.sub.3) m/z 299 (M+H).sup.+.
Example 115B
N-(3-{3-[(2,2,3,3-tetramethylcyclopropyl)carbonyl]-1H-indol-1-yl}propyl)me-
thanesulfonamide
[0370] The product of Example 115A (0.19 g, 0.64 mmol),
methanesulfonyl chloride (74 .mu.L, 0.96 mmol) and triethylamine
(0.27 mL, 1.9 mmol) in 10 mL of THF were processed as described in
Example 106B to provide the title compound (60 mg, 0.16 mmol, 25%
yield). .sup.1H NMR (CDCl.sub.3, 300 MHz) .delta. ppm 1.31 (s, 6H),
1.35 (s, 6H), 1.99 (s, 1H), 2.09-2.23 (m, 2H), 2.94 (s, 3H),
3.09-3.21 (m, 2H), 4.28-4.32 (m, 1H), 4.33 (t, J=6.6 Hz, 2H),
7.28-7.37 (m, 3H), 7.78 (s, 1H), 8.38-8.45 (m, 1H); MS
(DCI/NH.sub.3) m/z 377 (M+H).sup.+; Anal. Calculated for
C.sub.20H.sub.28N.sub.2O.sub.3S: C, 63.80; H, 7.50; N, 7.44. Found:
C, 63.44; H, 7.29; N, 7.67.
Example 116
N-(5-{3-[(2,2,3,3-tetramethylcyclopropyl)carbonyl]-1H-indol-1-yl}pentyl)me-
thanesulfonamide
Example 116A
[1-(5-Amino-pentyl)-1H-indol-3-yl]-(2,2,3,3-tetramethyl-cyclopropyl)-metha-
none
[0371] The product of Example 112 (0.33 g, 0.95 mmol) and
triphenylphospine (0.27 g, 1.0 mmol) in 9.5 mL of THF and 0.5 mL of
H.sub.2O were processed as described in Example 106A to provide the
title compound (0.27 g, 0.82 mmol, 87% yield). MS (DCI/NH.sub.3)
m/z 327 (M+H).sup.+.
Example 116B
N-(5-{3-[(2,2,3,3-tetramethylcyclopropyl)carbonyl]-1H-indol-1-yl}pentyl)me-
thanesulfonamide
[0372] The product of Example 116A (0.26 g, 0.80 mmol),
methanesulfonyl chloride (93 .mu.L, 1.2 mmol) and triethylamine
(0.34 mL, 2.4 mmol) in 15 mL of THF were processed as described in
Example 106B to provide the title compound (24 g, 0.59 mmol, 74%
yield). .sup.1H NMR (CDCl.sub.3, 300 MHz) .delta. ppm 1.31 (s, 6H),
1.35 (s, 6H), 1.36-1.49 (m, 2H), 1.55-1.65 (m, 2H), 1.86-1.99 (m,
2H), 1.96 (s, 1H), 2.91 (s, 3H), 3.11 (q, J=6.8 Hz, 2H), 4.12-4.19
(m, 1H), 4.18 (t, J=7.0 Hz, 2H), 7.26-7.38 (m, 3H), 7.66 (s, 1H),
8.36-8.45 (m, 1H); MS (DCI/NH.sub.3) m/z 405 (M+H).sup.+; Anal.
Calculated for C.sub.22H.sub.32N.sub.2O.sub.3S.0.3H.sub.2O: C,
64.45; H, 8.01; N, 6.83. Found: C, 64.14; H, 7.66; N, 6.78.
Example 117
[5-(4-aminobutoxy)-1-(tetrahydro-2H-pyran-4-ylmethyl)-1H-indol-3-yl](2,2,3-
,3-tetramethylcyclopropyl)methanone
Example 117A
[5-(4-Azido-butoxy)-1-(tetrahydro-pyran-4-ylmethyl)-1H-indol-3-yl]-(2,2,3,-
3-tetramethyl-cyclopropyl)-methanone
[0373] A mixture of the product of Example 111 (0.20 g, 0.42 mmol)
and sodium azide (81 mg, 1.2 mmol) in 5 mL of DMF was warmed to
80.degree. C. and stirred for 2 h. The mixture was cooled to
ambient temperature, quenched with 3 mL of H.sub.2O and diluted
with 5 mL of EtOAc. The layers were separated, the aqueous layer
was extracted 3.times.3 mL of EtOAc and the combined organic
extracts were dried over anhydrous Na.sub.2SO.sub.4, filtered, and
concentrated under reduced pressure to provide the title compound
(0.19 g, 0.42 mmol, 100% yield). MS (DCI/NH.sub.3) m/z 453
(M+H).sup.+.
Example 117B
[5-(4-aminobutoxy)-1-(tetrahydro-2H-pyran-4-ylmethyl)-1H-indol-3-yl](2,2,3-
,3-tetramethylcyclopropyl)methanone
[0374] The product of Example 117A (0.19 g, 0.42 mmol) and
triphenylphosphine (0.12 g, 0.46 mmol) in 4 mL of THF and 2 mL of
H.sub.2O were processed as described in Example 106A to provide the
title compound (0.17 g, 0.40 mmol, 95% yield). .sup.1H NMR
(CDCl.sub.3, 300 MHz) .delta. ppm 1.28 (s, 6H), 1.33 (s, 6H),
1.39-1.60 (m, 4H), 1.59-1.78 (m, 2H), 1.80-2.02 (m, 4H), 1.89 (s,
1H), 2.05-2.22 (m, 1H), 3.10 (t, J=6.8 Hz, 2H), 3.22-3.37 (m, 2H),
3.86-4.11 (m, 4H), 6.92 (dd, J=9.0, 2.2 Hz, 1H), 7.20 (d, J=9.2 Hz,
1H), 7.59 (s, 1H), 7.87 (d, J=2.4 Hz, 1H); MS (DCI/NH.sub.3) m/z
427 (M+H).sup.+; Anal. Calculated for
C.sub.26H.sub.38N.sub.2O.sub.3.1H.sub.2O: C, 70.24; H, 9.07; N,
6.30. Found: C, 69.94; H, 9.05; N, 6.21.
Example 118
[5-hydroxy-1-(2-morpholin-4-ylethyl)-1H-indol-3-yl](2,2,3,3-tetramethylcyc-
lopropyl)methanone
Example 118A
[5-Benzyloxy-1-(2-morpholin-4-yl-ethyl)-1H-indol-3-yl]-(2,2,3,3-tetramethy-
l-cyclopropyl)-methanone
[0375] The product of Example 74A (1.1 g, 3.0 mmol), the product of
Example 2A (5.1 mmol), and NaH (60% dispersion in mineral oil, 0.36
g, 9.1 mmol) in 25 mL of DMF were processed as described in Example
1D to provide the title compound (1.2 g, 2.6 mmol, 86% yield). MS
(DCI/NH.sub.3) m/z 461 (M+H).sup.+.
Example 118B
[5-hydroxy-1-(2-morpholin-4-ylethyl)-1H-indol-3-yl](2,2,3,3-tetramethylcyc-
lopropyl)methanone
[0376] The product of Example 118A (1.2 g, 2.5 mmol) and Pd/C (10
wt % palladium on activated carbon, 120 mg) in 50 mL of EtOH were
processed as described in Example 70 to provide the title compound
(0.85 g, 2.3 mmol, 92% yield). .sup.1H NMR (CDCl.sub.3, 300 MHz)
.delta. ppm 1.30 (s, 6H), 1.34 (s, 6H), 1.87 (s, 1H), 2.41-2.58 (m,
4H), 2.70-2.84 (m, 2H), 3.66-3.81 (m, 4H), 4.16-4.28 (m, 2H),
4.84-4.98 (m, 1H), 6.87 (dd, J=8.8, 2.4 Hz, 1H), 7.21 (d, J=8.8 Hz,
1H), 7.73 (s, 1H), 7.88 (d, J=2.7 Hz, 1H); MS (DCI/NH.sub.3) m/z
371 (M+H).sup.+; Anal. Calculated for
C.sub.22H.sub.30N.sub.2O.sub.3: C, 71.32; H, 8.16; N, 7.56. Found:
C, 71.08; H, 7.94; N, 7.36.
Example 119
(2E)-4-({1-(2-morpholin-4-ylethyl)-3-[(2,2,3,3-tetramethylcyclopropyl)carb-
onyl]-1H-indol-5-yl}oxy)-4-oxobut-2-enoic Acid
[0377] The product of Example 118B (0.15 g, 0.41 mmol), furmaryl
chloride (46 .mu.L, 0.43 mmol) and triethylamine (57 .mu.L, 0.41
mmol) in 40 mL of Et.sub.2O and 20 mL of THF were processed as
described in Example 65 to provide the title compound (60 mg, 0.13
mmol, 32% yield). .sup.1H NMR (MeOH-d.sub.4, 300 MHz) .delta. ppm
1.32 (s, 6H), 1.33 (s, 6H), 2.01 (s, 1H), 2.56-2.63 (m, 4H), 2.88
(t, J=6.4 Hz, 2H), 3.66-3.72 (m, 4H), 4.42 (t, J=6.4 Hz, 2H), 7.00
(s, 2H), 7.08 (dd, J=8.8, 2.4 Hz, 1H), 7.55 (d, J=8.8 Hz, 1H), 8.03
(d, J=2.4 Hz, 1H), 8.19 (s, 1H); MS (DCI/NH.sub.3) m/z 469
(M+H).sup.+; Anal. Calculated for C.sub.26H.sub.32N.sub.2O.sub.6:
C, 65.64; H, 6.35; N, 5.89. Found: C, 65.45; H, 6.63; N, 5.64.
Example 120
[5-methoxy-1-(2-morpholin-4-ylethyl)-1H-indol-3-yl](2,2,3,3-tetramethylcyc-
lopropyl)methanone
[0378] The product of Example 118B (0.15 g, 0.41 mmol),
Cs.sub.2CO.sub.3 (0.4 g, 1.2 mmol) and CH.sub.3I (51 .mu.L, 0.61
mmol) in 5 mL of DMF combined and stirred at ambient temperature
for 72 h. The mixture was quenched with 3 mL NH.sub.4Cl and diluted
with 5 mL of EtOAc. The layers were separated and the aqueous layer
was extracted 3.times.3 mL of EtOAc. The combined organic extracts
were washed with 1.times.5 mL of saturated aqueous NaCl, dried over
anhydrous Na.sub.2SO.sub.4, filtered, concentrated under reduced
pressure and recrystallized with 4:1 hexanes:EtOAc to provide the
title compound (75 mg, 0.20 mmol, 48% yield). .sup.1H NMR
(MeOH-d.sub.4, 300 MHz) .delta. ppm 1.33 (s, 12H), 2.10 (s, 1H),
2.47-2.53 (m, 4H), 2.77 (t, J=6.4 Hz, 2H), 3.63-3.69 (m, 4H), 3.84
(s, 3H), 4.33 (t, J=6.4 Hz, 2H), 6.89 (dd, J=8.8, 2.7 Hz, 1H), 7.38
(d, J=8.8 Hz, 1H), 7.81 (d, J=2.4 Hz, 1H), 8.06 (s, 1H); MS
(DCI/NH.sub.3) m/z 385 (M+H).sup.+; Anal. Calculated for
C.sub.23H.sub.32N.sub.2O.sub.3: C, 71.84; H, 8.39; N, 7.29. Found:
C, 71.65; H, 8.46; N, 7.08.
Example 121
N-[4-({1-(tetrahydro-2H-pyran-4-ylmethyl)-3-[(2,2,3,3-tetramethylcycloprop-
yl)carbonyl]-1H-indol-5-yl}oxy)butyl]methanesulfonamide
[0379] The product of Example 117B (75 mg, 0.18 mmol),
methanesulfonyl chloride (20 .mu.L, 0.26 mmol) and triethylamine
(74 .mu.L, 0.53 mmol) in 2 mL of THF were processed as described in
Example 106B to provide the title compound (60 mg, 0.12 mmol, 66%
yield). .sup.1H NMR (CDCl.sub.3, 300 MHz) .delta. ppm 1.30 (s, 6H),
1.34 (s, 6H), 1.36-1.63 (m, 4H), 1.88 (s, 4H), 1.88 (s, 1H),
2.06-2.20 (m, 1H), 2.97 (s, 3H), 3.21-3.28 (m, 2H), 3.33 (dt,
J=11.7, 2.4 Hz, 2H), 3.41-3.54 (m, 1H), 3.93-4.03 (m, 2H), 4.00 (d,
J=7.1 Hz, 2H), 4.05-4.15 (m, 2H), 6.92 (dd, J=8.8, 2.7 Hz, 1H),
7.22 (d, J=8.8 Hz, 1H), 7.57 (s, 1H), 7.92 (d, J=2.4 Hz, 1H); MS
(DCI/NH.sub.3) m/z 505 (M+H).sup.+; Anal. Calculated for
C.sub.27H.sub.40N.sub.2O.sub.5S: C, 64.26; H, 7.99; N, 5.55. Found:
C, 64.22; H, 7.93; N, 5.43.
Example 122
1-(tetrahydro-2H-pyran-4-ylmethyl)-3-[(2,2,3,3-tetramethylcyclopropyl)carb-
onyl]-1H-indole-5-carboxamide
[0380] A mixture
1-(tetrahydro-2H-pyran-4-ylmethyl)-3-[(2,2,3,3-tetramethylcyclopropyl)car-
bonyl]-1H-indole-5-carboxylic acid (0.10 g, 0.26 mmol, the minor
product of Example 114 B), 1,1'-carbonyldimidazole (55 mg, 0.34
mmol) and concentrated aqueous NH.sub.4OH (2 mL) in 5 mL of EtOAc
and 3 mL of THF was processed as described in Example 93 to provide
the title compound (20 mg, 0.052 mmol, 20% yield). .sup.1H NMR
(CDCl.sub.3, 300 MHz) .delta. ppm 1.32 (s, 6H), 1.36 (s, 6H),
1.39-1.58 (m, 4H), 1.92 (s, 1H), 2.08-2.23 (m, 1H), 3.34 (dt,
J=11.4, 2.5 Hz, 2H), 3.94-4.04 (m, 2H), 4.08 (d, J=7.1 Hz, 2H),
7.41 (d, J=8.5 Hz, 1H), 7.67 (s, 1H), 7.98 (dd, J=8.5, 1.4 Hz, 1H),
8.84 (d, J=1.0 Hz, 1H); MS (DCI/NH.sub.3) m/z 383 (M+H).sup.+;
Anal. Calculated for C.sub.23H.sub.30N.sub.2O.sub.3.0.4H.sub.2O: C,
70.89; H, 7.97; N, 7.19. Found: C, 70.77; H, 7.91; N, 7.32.
Example 123
N-(2-hydroxyethyl)-1-(tetrahydro-2H-pyran-4-ylmethyl)-3-[(2,2,3,3-tetramet-
hylcyclopropyl)carbonyl]-1H-indole-5-carboxamide
[0381] A mixture
1-(tetrahydro-2H-pyran-4-ylmethyl)-3-[(2,2,3,3-tetramethylcyclopropyl)car-
bonyl]-1H-indole-5-carboxylic acid (0.10 g, 0.26 mmol, the minor
product of Example 114 B), 1,1'-carbonyldimidazole (55 mg, 0.34
mmol) and ethanolamine (21 .mu.L, 0.34 mmol) in 4 mL of EtOAc and 3
mL of THF was processed as described in Example 93 to provide the
title compound (51 mg, 0.12 mmol, 46% yield). .sup.1H NMR
(DMSO-d.sub.6,300 MHz) .delta. ppm 1.27 (s, 12H), 1.30-1.45 (m,
4H), 2.05-2.19 (m, 1H), 2.23 (s, 1H), 3.22 (dt, J=11.1, 3.2 Hz,
2H), 3.31-3.39 (m, 2H), 3.52 (q, J=6.0 Hz, 2H), 3.83 (d, 2H), 4.17
(d, J=7.1 Hz, 2H), 4.70 (t, J=5.6 Hz, 1H), 7.66 (d, J=8.1 Hz, 1H),
7.74 (dd, J=8.5, 1.7 Hz, 1H), 8.35 (t, J=5.8 Hz, 1H), 8.38 (s, 1H),
8.74 (d, J=1.4 Hz, 1H); MS (DCI/NH.sub.3) m/z 427 (M+H).sup.+;
Anal. Calculated for C.sub.25H.sub.34N.sub.2O.sub.4.0.3H.sub.2O: C,
69.51; H, 8.07; N, 6.49. Found: C, 69.36; H, 7.88; N, 6.27.
Example 124
N-methyl-1-(tetrahydro-2H-pyran-4-ylmethyl)-3-[(2,2,3,3-tetramethylcyclopr-
opyl)carbonyl]-1H-indole-5-carboxamide
[0382] A mixture
1-(tetrahydro-2H-pyran-4-ylmethyl)-3-[(2,2,3,3-tetramethylcyclopropyl)car-
bonyl]-1H-indole-5-carboxylic acid (0.10 g, 0.26 mmol, the minor
product of Example 114 B), 1,1'-carbonyldimidazole (55 mg, 0.34
mmol) and methylamine (2 M solution in THF, 0.2 mL, 0.4 mmol) in 4
mL of EtOAc and 3 mL of THF was processed as described in Example
93 to provide the title compound (14 mg, 0.035 mmol, 14% yield).
.sup.1H NMR (DMSO-d.sub.6, 300 MHz) .delta. ppm 1.27 (s, 12H),
1.30-1.46 (m, 4H), 2.03-2.17 (m, 1H), 2.22 (s, 1H), 2.79 (d, J=4.7
Hz, 3H), 3.22 (dt, J=11.4, 3.1 Hz, 2H), 3.80-3.88 (m, 2H), 4.17 (d,
J=7.5 Hz, 2H), 7.63-7.77 (m, 2H), 8.32-8.37 (m, 1H), 8.38 (s, 1H),
8.74 (d, J=1.4 Hz, 1H); MS (DCI/NH.sub.3) m/z 397 (M+H).sup.+;
Anal. Calculated for C.sub.24H.sub.32N.sub.2O.sub.2.0.3H.sub.2O: C,
71.72; H, 8.18; N, 6.97. Found: C, 71.96; H, 8.19; N, 6.69.
Example 125
1-(tetrahydro-2H-pyran-4-ylmethyl)-3-[(2,2,3,3-tetramethylcyclopropyl)carb-
onyl]-1H-indole-5-carbonitrile
Example 125A
3-(2,2,3,3-Tetramethyl-cyclopropanecarbonyl)-1H-indole-5-carbonitrile
[0383] A mixture of 5-cyanoindole (1.42 g, 10 mmol), ethylmagnesium
bromide (1.0 M solution in THF, 11 mL, 11 mmol), zinc chloride (1.0
M solution in Et.sub.2O, 11 mL, 11 mmol) and the product of Example
1A (10 mmol) in 30 mL of dichloromethane was processed as described
in Example 1B to provide the title compound (0.45 g, 1.7 mmol, 17%
yield). MS (DCI/NH.sub.3) m/z 267 (M+H).sup.+.
Example 125B
1-(tetrahydro-2H-pyran-4-ylmethyl)-3-[(2,2,3,3-tetramethylcyclopropyl)carb-
onyl]-1H-indole-5-carbonitrile
[0384] The product of Example 125A (0.45 g, 1.7 mmol), the product
of Example 18A (2.9 mmol), and NaH (60% dispersion in mineral oil,
0.20 g, 5.1 mmol) in DMF (10 mL) were processed as described in
Example 1D to provide the title compound (0.41 g, 1.1 mmol, 66%
yield). .sup.1H NMR (CDCl.sub.3, 300 MHz) .delta. ppm 1.32 (s, 6H),
1.35 (s, 6H), 1.39-1.55 (m, 4H), 1.89 (s, 1H), 2.05-2.21 (m, 1H),
3.34 (dt, J=11.5, 2.7 Hz, 2H), 3.94-4.03 (m, 2H), 4.07 (d, J=7.5
Hz, 2H), 7.39 (d, J=8.5 Hz, 1H), 7.52 (dd, J=11.8, 1.7 Hz, 1H),
7.69 (s, 1H), 8.83 (d, J=1.7 Hz, 1H); MS (DCI/NH.sub.3) m/z 365
(M+H).sup.+; Anal. Calculated for C.sub.23H.sub.28N.sub.2O.sub.2:
C, 75.79; H, 7.74; N, 7.69. Found: C, 75.54; H, 7.85; N, 7.78.
Example 126
[5-(benzyloxy)-6-methoxy-1-(tetrahydro-2H-pyran-4-ylmethyl)-1H-indol-3-yl]-
(2,2,3,3-tetramethylcyclopropyl)methanone
Example 126A
(5-Benzyloxy-6-methoxy-1H-indol-3-yl)-(2,2,3,3-tetramethyl-cyclopropyl)-me-
thanone
[0385] A mixture of 5-benzyloxy-6-methoxyindole (Sigma, 2.0 g, 7.9
mmol), ethylmagnesium bromide (1.0 M solution in THF, 9.5 mL, 9.5
mmol), zinc chloride (1.0 M solution in Et.sub.2O, 9.5 mL, 9.5
mmol) and the product of Example 1A (12 mmol) was processed as
described in Example 1B to provide the title compound (2.0 g, 5.2
mmol, 66% yield). MS (DCI/NH.sub.3) m/z 378 (M+H).sup.+.
Example 126B
[5-(benzyloxy)-6-methoxy-1-(tetrahydro-2H-pyran-4-ylmethyl)-1H-indol-3-yl]-
(2,2,3,3-tetramethylcyclopropyl)methanone
[0386] The product of Example 126A (0.98 g, 2.6 mmol), the product
of Example 18A (4.4 mmol), and NaH (60% dispersion in mineral oil,
0.31 g, 7.8 mmol) in DMF (20 mL) were processed as described in
Example 1D to provide the title compound (1.2 g, 2.5 mmol, 96%
yield). .sup.1H NMR (CDCl.sub.3, 300 MHz) .delta. ppm 1.29 (s, 6H),
1.34 (s, 6H), 1.37-1.51 (m, 4H), 1.85-1.90 (m, 1H), 2.07-2.20 (m,
1H), 3.35 (dt, J=11.6, 2.2 Hz, 2H), 3.94 (s, 3H), 3.96-4.03 (m,
2H), 3.98 (d, J=7.5 Hz, 2H), 5.19 (s, 2H), 6.79 (s, 1H), 7.28-7.41
(m, 3H), 7.48 (s, 1H), 7.50-7.54 (m, 2H), 8.04 (s, 1H); MS
(DCI/NH.sub.3) m/z 476 (M+H).sup.+; Anal. Calculated for
C.sub.30H.sub.37NO.sub.4: C, 75.76; H, 7.84; N, 2.94. Found: C,
75.56; H, 7.92; N, 2.94.
Example 127
N,N-dimethyl-1-(tetrahydro-2H-pyran-4-ylmethyl)-3-[(2,2,3,3-tetramethylcyc-
lopropyl)carbonyl]-1H-indole-5-carboxamide
[0387] A mixture
1-(tetrahydro-2H-pyran-4-ylmethyl)-3-[(2,2,3,3-tetramethylcyclopropyl)car-
bonyl]-1H-indole-5-carboxylic acid (0.10 g, 0.26 mmol, the minor
product of Example 114 B), 1,1'-carbonyldimidazole (55 mg, 0.34
mmol) and dimethylamine (2 M solution in THF, 0.17 mL, 0.34 mmol)
in 4 mL of EtOAc and 3 mL of THF was processed as described in
Example 93 to provide the title compound (38 mg, 0.093 mmol, 35%
yield). .sup.1H NMR (DMSO-d.sub.6, 300 MHz) .delta. ppm 1.25 (s,
6H), 1.27 (s, 6H), 1.29-1.48 (m, 4H), 2.03-2.18 (m, 1H), 2.20 (s,
1H), 2.97 (s, 6H), 3.23 (dt, J=11.3, 2.9 Hz, 2H), 3.78-3.89 (m,
2H), 4.17 (d, J=7.1 Hz, 2H), 7.27 (dd, J=8.5, 1.7 Hz, 1H), 7.66 (d,
J=9.2 Hz, 1H), 8.27 (d, J=1.4 Hz, 1H), 8.37 (s, 1H); MS
(DCI/NH.sub.3) m/z 411 (M+H).sup.+; Anal. Calculated for
C.sub.25H.sub.34N.sub.2O.sub.3.0.2H.sub.2O: C, 72.50; H, 8.37; N,
6.76. Found: C, 72.51; H, 8.29; N, 6.66.
Example 128
N-heptyl-1-(tetrahydro-2H-pyran-4-ylmethyl)-3-[(2,2,3,3-tetramethylcyclopr-
opyl)carbonyl]-1H-indole-5-carboxamide
[0388] A mixture
1-(tetrahydro-2H-pyran-4-ylmethyl)-3-[(2,2,3,3-tetramethylcyclopropyl)car-
bonyl]-1H-indole-5-carboxylic acid (0.10 g, 0.26 mmol, the minor
product of Example 114 B), 1,1'-carbonyldimidazole (55 mg, 0.34
mmol) and heptylamine (50 .mu.L, 0.34 mmol) in 4 mL of EtOAc and 3
mL of THF was processed as described in Example 93 to provide the
title compound (25 mg, 0.052 mmol, 20% yield). .sup.1H NMR
(MeOH-d.sub.4, 300 MHz) .delta. ppm 0.87-0.95 (m, 3H), 1.34 (s,
12H), 1.37-1.43 (m, 7H), 1.43-1.51 (m, 6H), 1.58-1.71 (m, 2H),
2.13-2.27 (m, 1H), 2.18 (s, 1H), 3.32-3.37 (m, 2H), 3.40 (t, J=7.1
Hz, 2H), 3.87-3.97 (m, 2H), 4.19 (d, J=7.1 Hz, 2H), 7.58 (d, J=8.8
Hz, 1H), 7.75 (dd, J=8.6, 1.9 Hz, 1H), 8.16 (s, 1H), 8.77 (d, J=1.7
Hz, 1H); MS (DCI/NH.sub.3) m/z 481 (M+H).sup.+; Anal. Calculated
for C.sub.30H.sub.44N.sub.2O.sub.3.0.2H.sub.2O: C, 74.40; H, 9.24;
N, 5.78. Found: C, 74.43; H, 9.00; N, 5.81.
Example 129
[5-hydroxy-6-methoxy-1-(tetrahydro-2H-pyran-4-ylmethyl)-1H-indol-3-yl](2,2-
,3,3-tetramethylcyclopropyl)methanone
[0389] The product of Example 126B (1.0 g, 2.2 mmol) and Pd/C (10
wt % palladium on activated carbon, 100 mg) in 20 mL EtOH and 5 mL
of EtOAc were processed as described in Example 70 to provide the
title compound (0.86 g, 2.2 mmol, 100% yield). .sup.1H NMR
(MeOH-d.sub.4, 300 MHz) .delta. ppm 1.31 (s, 12H), 1.34-1.57 (m,
4H), 2.07 (s, 1H), 2.11-2.24 (m, 1H), 3.37 (dt, J=11.5, 2.7 Hz,
2H), 3.89-3.97 (m, 2H), 3.93 (s, 3H), 4.09 (d, J=7.1 Hz, 2H), 7.01
(s, 1H), 7.67 (s, 1H), 7.84 (s, 1H); MS (DCI/NH.sub.3) m/z 386
(M+H).sup.+; Anal. Calculated for
C.sub.23H.sub.31NO.sub.4.0.1H.sub.2O: C, 71.33; H, 8.12; N, 3.62.
Found: C, 71.15; H, 7.87; N, 3.53.
Example 130
(2E)-4-({6-methoxy-1-(tetrahydro-2H-pyran-4-ylmethyl)-3-[(2,2,3,3-tetramet-
hylcyclopropyl)carbonyl]-1H-indol-5-yl}oxy)-4-oxobut-2-enoic
acid
[0390] The product of Example 129 (0.23 g, 0.60 mmol), furmaryl
chloride (68 .mu.L, 0.63 mmol) and triethylamine (83 .mu.L, 0.60
mmol) in 60 mL Et.sub.2O and 5 mL of THF were processed as
described in Example 65 to provide the title compound (0.13 mg,
0.26 mmol, 44% yield). .sup.1H NMR (MeOH-d.sub.4,300 MHz) .delta.
ppm 1.31 (s, 6H), 1.31 (s, 6H), 1.40-1.56 (m, 4H), 2.11 (s, 1H),
2.14-2.25 (m, 1H), 3.38 (dt, J=11.5, 3.1 Hz, 2H), 3.89 (s, 3H),
3.90-3.98 (m, 2H), 4.16 (d, J=7.5 Hz, 2H), 6.99 (d, J=4.7 Hz, 2H),
7.17 (s, 1H), 7.94 (s, 1H), 8.00 (s, 1H); MS (DCI/NH.sub.3) m/z 484
(M+H).sup.+; Anal. Calculated for C.sub.27H.sub.33NO.sub.7: C,
67.06; H, 6.88; N, 2.90. Found: C, 66.91; H, 6.81; N, 2.80.
Example 131
{5-(benzyloxy)-1-[(2R)-tetrahydrofuran-2-ylmethyl]-1H-indol-3-yl}(2,2,3,3--
tetramethylcyclopropyl)methanone
[0391] The product of Example 74A (0.61 g, 1.8 mmol), the mesylate
of (R)-(-)-tetrahydrofurfuryl alcohol (Lancaster, 0.33 g, 3.1
mmol), and NaH (60% dispersion in mineral oil, 0.22 g, 5.5 mmol) in
10 mL of DMF were processed as described in Example 1D to provide
the title compound (0.70 g, 1.6 mmol, 88% yield). .sup.1H NMR
(CDCl.sub.3,300 MHz) .delta. ppm 1.30 (s, 6H), 1.34 (s, 3H), 1.36
(s, 3H), 1.51-1.63 (m, 1H), 1.70-1.89 (m, 2H), 1.91 (s, 1H),
1.93-2.07 (m, 1H), 3.73-3.89 (m, 2H), 4.11-4.32 (m, 3H), 5.14 (s,
2H), 6.99 (dd, J=9.0, 2.5 Hz, 1H), 7.26 (t, J=4.4 Hz, 1H),
7.30-7.43 (m, 3H), 7.45-7.51 (m, 2H), 7.74 (s, 1H), 8.07 (d, J=2.4
Hz, 1H); MS (DCI/NH.sub.3) m/z 432 (M+H).sup.+; Anal. Calculated
for C.sub.28H.sub.33NO.sub.3: C, 77.93; H, 7.71; N, 3.25. Found: C,
77.82; H, 7.72; N, 3.22.
Example 132
[5-(aminomethyl)-1-(tetrahydro-2H-pyran-4-ylmethyl)-1H-indol-3-yl](2,2,3,3-
-tetramethylcyclopropyl)methanone
[0392] The product of Example 125B (0.34 g, 0.93 mmol) and
Raney-Nickel (RaNi 2800 slurry in water, 100 mg) in 2 mL of a 20%
NH.sub.3 in MeOH were placed under 60 psi of hydrogen. The mixture
was shaken at ambient temperature for 16 hours and then filtered.
The resulting material was concentrated under reduced pressure and
purified via flash column chromatography (SiO.sub.2, 9:1:0.1
CH.sub.2Cl.sub.2: CH.sub.3OH:NH.sub.4OH) to provide the title
compound (0.17 g, 0.46 mmol, 50% yield). .sup.1H NMR (CDCl.sub.3,
300 MHz) .delta. ppm 1.29 (s, 6H), 1.32 (s, 6H), 1.35-1.55 (m, 4H),
1.91 (s, 1H), 2.05-2.19 (m, 1H), 3.32 (dt, J=11.5, 2.0 Hz, 2H),
3.92-4.06 (m, 4H), 7.29-7.41 (m, 2H), 7.61 (s, 1H), 8.34 (s, 1H);
MS (DCI/NH.sub.3) m/z 369 (M+H).sup.+; Anal. Calculated for
C.sub.23H.sub.32N.sub.2O.sub.2.0.4H.sub.2O: C, 73.53; H, 8.80; N,
7.46. Found: C, 73.41; H, 8.61; N, 7.44.
Example 133
{5-hydroxy-1-[(2R)-tetrahydrofuran-2-ylmethyl]-1H-indol-3-yl}(2,2,3,3-tetr-
amethylcyclopropyl)methanone
[0393] The product of Example 131 (0.70 g, 1.6 mmol) and Pd/C (10
wt % palladium on activated carbon, 350 mg) in 30 mL EtOH were
processed as described in Example 70 to provide the title compound
(0.35 g, 1.0 mmol, 64% yield). .sup.1H NMR (MeOH-d.sub.4, 300 MHz)
.delta. ppm 1.30 (s, 3H), 1.31 (s, 9H), 1.57-1.70 (m, 1H),
1.73-1.92 (m, 2H), 1.99-2.09 (m, 1H), 2.05 (s, 1H), 3.69-3.88 (m,
2H), 4.16-4.36 (m, 3H), 6.78 (dd, J=8.8, 2.7 Hz, 1H), 7.33 (dd,
J=8.8, 0.7 Hz, 1H), 7.65 (d, J=2.0 Hz, 1H), 7.96 (s, 1H); MS
(DCI/NH.sub.3) m/z 342 (M+H).sup.+; Anal. Calculated for
C.sub.21H.sub.27NO.sub.3.0.2H.sub.2O: C, 73.10; H, 8.00; N, 4.06.
Found: C, 73.32; H, 8.11; N, 4.01.
Example 134
N-({1-(tetrahydro-2H-pyran-4-ylmethyl)-3-[(2,2,3,3-tetramethylcyclopropyl)-
carbonyl]-1H-indol-5-yl}methyl)methanesulfonamide
[0394] The product of Example 132 (0.16 g, 0.45 mmol),
methanesulfonyl chloride (52 .mu.L, 0.67 mmol) and triethylamine
(0.19 mL, 1.3 mmol) in 10 mL of THF were processed as described in
Example 106B to provide the title compound (0.16 g, 0.35 mmol, 78%
yield). .sup.1H NMR (MeOH-d.sub.4, 300 MHz) .delta. ppm 1.33 (s,
12H), 1.36-1.55 (m, 4H), 2.14 (s, 1H), 2.15-2.26 (m, 1H), 2.83 (s,
3H), 3.32-3.40 (m, 2H), 3.88-3.97 (m, 2H), 4.15 (d, J=7.5 Hz, 2H),
4.35 (s, 2H), 7.32 (dd, J=8.5, 1.7 Hz, 1H), 7.51 (d, J=8.5 Hz, 1H),
8.07 (s, 1H), 8.28 (d, J=1.4 Hz, 1H); MS (DCI/NH.sub.3) m/z 447
(M+H).sup.+; Anal. Calculated for
C.sub.24H.sub.34N.sub.2O.sub.4S.0.1H.sub.2O: C, 64.29; H, 7.69; N,
6.25. Found: C, 64.12; H, 7.73; N, 6.19.
Example 135
{5-(benzyloxy)-1-[4-(benzyloxy)butyl]-1H-indol-3-yl}(2,2,3,3-tetramethylcy-
clopropyl)methanone
[0395] The product of Example 74A (0.71 g, 2.0 mmol), product of
Example 23A (3.5 mmol), and NaH (60% dispersion in mineral oil,
0.12 g, 3.1 mmol) in 12 mL of DMF were processed as described in
Example 1D to provide the title compound (0.37 g, 0.73 mmol, 36%
yield). .sup.1H NMR (CDCl.sub.3, 300 MHz) .delta. ppm 1.29 (s, 6H),
1.35 (s, 6H), 1.60-1.73 (m, 2H), 1.88 (s, 1H), 1.94-2.07 (m, 2H),
3.50 (t, J=6.1 Hz, 2H), 4.16 (t, J=7.1 Hz, 2H), 4.49 (s, 2H), 5.14
(s, 2H), 6.98 (dd, J=8.8, 2.7 Hz, 1H), 7.21 (d, J=8.8 Hz, 1H),
7.28-7.43 (m, 8H), 7.45-7.51 (m, 2H), 7.62 (s, 1H), 8.06 (d, J=2.4
Hz, 1H); MS (DCI/NH.sub.3) m/z 510 (M+H).sup.+; Anal. Calculated
for C.sub.34H.sub.39NO.sub.3: C, 80.12; H, 7.71; N, 2.75. Found: C,
79.77; H, 7.58; N, 2.70.
Example 136
[6-(methylsulfonyl)-1-(tetrahydro-2H-pyran-4-ylmethyl)-1H-indol-3-yl](2,2,-
3,3-tetramethylcyclopropyl)methanone
Example 136A
(6-Methanesulfonyl-1H-indol-3-yl)-(2,2,3,3-tetramethyl-cyclopropyl)-methan-
one
[0396] The 6-(methylsulfonyl)-1H-indole (Apollo Scientific, 1.0 g,
5.1 mmol), ethylmagnesium bromide (1.0 M solution in THF, 6.1 mL,
6.1 mmol), zinc chloride (1.0 M solution in Et.sub.2O, 6.1 mL, 6.1
mmol) and the product of Example 1A (7.7 mmol) were processed as
described in Example 1B to provide the title compound (0.21 g, 0.66
mmol, 13% yield). MS (DCI/NH.sub.3) m/z 378 (M+H).sup.+.
Example 136B
[6-(methylsulfonyl)-1-(tetrahydro-2H-pyran-4-ylmethyl)-1H-indol-3-yl](2,2,-
3,3-tetramethylcyclopropyl)methanone
[0397] The product of Example 136A (0.21 g, 0.66 mmol), the product
of Example 18A (1.3 mmol), and NaH (60% dispersion in mineral oil,
79 mg, 2.0 mmol) in DMF (10 mL) were processed as described in
Example 1D to provide the title compound (0.18 g, 0.43 mmol, 65%
yield). .sup.1H NMR (CDCl.sub.3, 300 MHz) .delta. ppm 1.32 (s, 6H),
1.35 (s, 6H), 1.37-1.55 (m, 4H), 1.92 (s, 1H), 2.09-2.27 (m, 1H),
3.11 (s, 3H), 3.35 (dt, J=11.5, 2.7 Hz, 2H), 3.93-4.04 (m, 2H),
4.12 (d, J=7.5 Hz, 2H), 7.77 (dd, J=8.5, 1.7 Hz, 1H), 7.79 (s, 1H),
7.99 (d, J=1.4 Hz, 1H), 8.61 (d, J=8.5 Hz, 1H); MS (DCI/NH.sub.3)
m/z 418 (M+H).sup.+; Anal. Calculated for
C.sub.23H.sub.31NO.sub.4S: C, 66.16; H, 7.48; N, 3.35. Found: C,
65.77; H, 7.23; N, 3.35.
Example 137
[5-hydroxy-1-(4-hydroxybutyl)-1H-indol-3-yl](2,2,3,3-tetramethylcyclopropy-
l)methanone
[0398] The product of Example 135 (0.36 g, 0.71 mmol) and Pd/C (10
wt % palladium on activated carbon, 360 mg) in 50 mL EtOH were
processed as described in Example 70 to provide the title compound
(0.16 g, 0.48 mmol, 68% yield). .sup.1H NMR (MeOH-d.sub.4, 300 MHz)
.delta. ppm 1.31 (s, 12H), 1.47-1.61 (m, 2H), 1.87-2.01 (m, 2H),
2.08 (s, 1H), 3.57 (t, J=6.4 Hz, 2H), 4.23 (t, J=7.1 Hz, 2H), 6.79
(dd, J=8.8, 2.7 Hz, 1H), 7.30 (d, J=8.8 Hz, 1H), 7.66 (d, J=2.4 Hz,
1H), 7.97 (s, 1H); MS (DCI/NH.sub.3) m/z 330 (M+H).sup.+; Anal.
Calculated for C.sub.20H.sub.27NO.sub.3: C, 72.92; H, 8.26; N,
4.25. Found: C, 72.76; H, 8.21; N, 4.19.
Example 138
1-(tetrahydro-2H-pyran-4-ylmethyl)-3-[(2,2,3,3-tetramethylcyclopropyl)carb-
onyl]-1H-indole-6-carbonitrile
Example 138A
3-(2,2,3,3-Tetramethyl-cyclopropanecarbonyl)-1H-indole-6-carbonitrile
[0399] A mixture of 6-cyanoindole (Lancaster, 1.0 g, 7.0 mmol),
ethylmagnesium bromide (1.0 M solution in THF, 8.4 mL, 8.4 mmol),
zinc chloride (1.0 M solution in Et.sub.2O, 8.4 mL, 8.4 mmol) and
the product of Example 1A (11 mmol) was processed as described in
Example 1B to provide the title compound (0.91 g, 3.4 mmol, 49%
yield). MS (DCI/NH.sub.3) m/z 267 (M+H).sup.+.
Example 138B
1-(tetrahydro-2H-pyran-4-ylmethyl)-3-[(2,2,3,3-tetramethylcyclopropyl)carb-
onyl]-1H-indole-6-carbonitrile
[0400] The product of Example 138A (0.91 g, 3.4 mmol), the product
of Example 18A (5.8 mmol), and NaH (60% dispersion in mineral oil,
0.37 g, 9.1 mmol) in DMF (20 mL) were processed as described in
Example 1D to provide the title compound (0.87 g, 2.4 mmol, 70%
yield). .sup.1H NMR (CDCl.sub.3, 300 MHz) .delta. ppm 1.32 (s, 6H),
1.34 (s, 6H), 1.39-1.57 (m, 4H), 1.90 (s, 1H), 2.06-2.22 (m, 1H),
3.36 (dt, J=11.5, 2.7 Hz, 2H), 3.96-4.04 (m, 2H), 4.07 (d, J=7.5
Hz, 2H), 7.49 (dd, J=8.5, 1.4 Hz, 1H), 7.67 (d, J=0.7 Hz, 1H), 7.75
(s, 1H), 8.51 (d, J=8.1 Hz, 1H); MS (DCI/NH.sub.3) m/z 365
(M+H).sup.+; Anal. Calculated for C.sub.23H.sub.28N.sub.2O.sub.2:
C, 75.79; H, 7.74; N, 7.69. Found: C, 75.64; H, 7.61; N, 7.36.
Example 139
[1-(tetrahydro-2H-pyran-4-ylmethyl)-6-(trifluoromethyl)-1H-indol-3-yl](2,2-
,3,3-tetramethylcyclopropyl)methanone
Example 139A
(2,2,3,3-Tetramethyl-cyclopropyl)-(6-trifluoromethyl-1H-indol-3-yl)methano-
ne
[0401] A mixture of 6-(trifluoromethyl)indole (Lancaster, 1.0 g,
5.4 mmol), ethylmagnesium bromide (1.0 M solution in THF, 6.6 mL,
6.6 mmol), zinc chloride (1.0 M solution in Et.sub.2O, 6.6 mL, 6.6
mmol) and the product of Example 1A (8.1 mmol) in 40 mL of
dichloromethane was processed as described in Example 1B to provide
the title compound (0.17 g, 0.53 mmol, 10% yield). MS
(DCI/NH.sub.3) m/z 310 (M+H).sup.+.
Example 139B
[1-(tetrahydro-2H-pyran-4-ylmethyl)-6-(trifluoromethyl)-1H-indol-3-yl](2,2-
,3,3-tetramethylcyclopropyl)methanone
[0402] The product of Example 139A (0.16 g, 0.52 mmol), the product
of Example 18A (0.89 mmol), and NaH (60% dispersion in mineral oil,
63 mg, 1.6 mmol) in DMF (10 mL) were processed as described in
Example 1D to provide the title compound (70 mg, 0.17 mmol, 33%
yield). .sup.1H NMR (CDCl.sub.3, 300 MHz) .delta. ppm 1.32 (s, 6H),
1.35 (s, 6H), 1.37-1.58 (m, 4H), 1.92 (s, 1H), 2.09-2.24 (m, 1H),
3.36 (dt, J=11.5, 2.7 Hz, 2H), 3.95-4.04 (m, 2H), 4.09 (d, J=7.1
Hz, 2H), 7.50 (dd, J=8.6, 1.2 Hz, 1H), 7.58 (d, J=0.7 Hz, 1H),
7.69-7.77 (m, 1H), 8.51 (d, J=8.5 Hz, 1H); MS (DCI/NH.sub.3) m/z
408 (M+H).sup.+; Anal. Calculated for
C.sub.23H.sub.28F.sub.3NO.sub.2.0.1H.sub.2O: C, 67.50; H, 6.94; N,
3.42. Found: C, 67.20; H, 6.88; N, 3.42.
Example 140
[6-(aminomethyl)-1-(tetrahydro-2H-pyran-4-ylmethyl)-1H-indol-3-yl](2,2,3,3-
-tetramethylcyclopropyl)methanone
[0403] The product of Example 138B (0.75 g, 2.1 mmol), Raney-Nickel
(RaNi 2800 slurry in water, 225 mg) and H.sub.2 (60 psi) in 4 mL of
a 20% NH.sub.3 in MeOH solution were processed as described in
Example 132 to provide the title compound (0.75 g, 2.0 mmol, 99%
yield). .sup.1H NMR (MeOH-d.sub.4, 300 MHz) .delta. ppm 1.32 (s,
12H), 1.37-1.55 (m, 4H), 2.13 (s, 1H), 2.16-2.31 (m, 1H), 3.37 (dt,
J=11.2, 3.1 Hz, 2H), 3.89-3.97 (m, 2H), 3.95 (s, 2H), 4.16 (d,
J=7.5 Hz, 2H), 7.20 (dd, J=8.1, 1.4 Hz, 1H), 7.50 (d, J=0.7 Hz,
1H), 8.04 (s, 1H), 8.22 (d, J=8.5 Hz, 1H); MS (DCI/NH.sub.3) m/z
369 (M+H).sup.+; Anal. Calculated for
C.sub.23H.sub.32N.sub.2O.sub.2.0.3H.sub.2O: C, 73.88; H, 8.79; N,
7.49. Found: C, 73.69; H, 8.52; N, 7.41.
Example 141
N-({1-(tetrahydro-2H-pyran-4-ylmethyl)-3-[(2,2,3,3-tetramethylcyclopropyl)-
carbonyl]-1H-indol-6-yl}methyl)methanesulfonamide
[0404] The product of Example 140 (0.73 g, 2.0 mmol),
methanesulfonyl chloride (0.24 mL, 3.1 mmol) and triethylamine
(0.86 mL, 6.2 mmol) in 30 mL of THF were processed as described in
Example 106B to provide the title compound (0.52 g, 1.2 mmol, 58%
yield). .sup.1H NMR (CDCl.sub.3, 300 MHz) .delta. ppm 1.31 (s, 6H),
1.35 (s, 6H), 1.39-1.59 (m, 4H), 1.92 (s, 1H), 2.07-2.22 (m, 1H),
2.85 (s, 3H), 3.35 (dt, J=11.6, 2.5 Hz, 2H), 3.94-4.02 (m, 2H),
4.05 (d, J=7.5 Hz, 2H), 4.45 (s, 2H), 4.63 (s, 1H), 7.21 (dd,
J=8.3, 1.5 Hz, 1H), 7.35 (s, 1H), 7.63 (s, 1H), 8.40 (d, J=8.5 Hz,
1H); MS (DCI/NH.sub.3) m/z 447 (M+H).sup.+; Anal. Calculated for
C.sub.24H.sub.34N.sub.2O.sub.4S: C, 64.54; H, 7.67; N, 6.27. Found:
C, 64.23; H, 7.64; N, 6.13.
Example 142
[5,6-dihydroxy-1-(tetrahydro-2H-pyran-4-ylmethyl)-1H-indol-3-yl](2,2,3,3-t-
etramethylcyclopropyl)methanone
Example 142A
(5,6-Bis-benzyloxy-1H-indol-3-yl)-(2,2,3,3-tetramethyl-cyclopropyl)-methan-
one
[0405] The 5,6-dibenzyloxyindole (Sigma, 0.60 g, 1.8 mmol),
ethylmagnesium bromide (1.0 M solution in THF, 2.2 mL, 2.2 mmol),
zinc chloride (1.0 M solution in Et.sub.2O, 2.2 mL, 2.2 mmol) and
the product of Example 1A (2.7 mmol) in 20 mL of dichloromethane
were processed as described in Example 1B to provide the title
compound (0.45 g, 0.99 mmol, 55% yield). MS (DCI/NH.sub.3) m/z 454
(M+H).sup.+.
Example 142B
[5,6-Bis-benzyloxy-1-(tetrahydro-pyran-4-ylmethyl)-1H-indol-3-yl]-(2,2,3,3-
-tetramethyl-cyclopropyl)-methanone
[0406] The product of Example 142A (0.45 g, 0.99 mmol), the product
of Example 18A (2.0 mmol), and NaH (60% dispersion in mineral oil,
0.12 g, 3.0 mmol) in DMF (15 mL) were processed as described in
Example 1D to provide the title compound (0.45 g, 0.82 mmol, 82%
yield). MS (DCI/NH.sub.3) m/z 552 (M+H).sup.+.
Example 142C
[5,6-dihydroxy-1-(tetrahydro-2H-pyran-4-ylmethyl)-1H-indol-3-yl](2,2,3,3-t-
etramethylcyclopropyl)methanone
[0407] The product of Example 142B (0.45 g, 0.82 mmol) and Pd/C (10
wt % palladium on activated carbon, 450 mg) in 8 mL EtOH were
processed as described in Example 70 to provide the title compound
(0.12 g, 0.32 mmol, 39% yield). .sup.1H NMR (CDCl.sub.3, 300 MHz)
.delta. ppm 1.29 (s, 6H), 1.32 (s, 6H), 1.36-1.57 (m, 4H), 1.86 (s,
1H), 2.07-2.17 (m, 1H), 3.33 (dt, J=11.6, 2.2 Hz, 2H), 3.93 (d,
J=7.5 Hz, 2H), 3.94-4.01 (m, 2H), 6.86 (s, 1H), 7.47 (s, 1H), 7.95
(s, 1H); MS (DCI/NH.sub.3) m/z 372 (M+H).sup.+; Anal. Calculated
for C.sub.22H.sub.29NO.sub.4.0.1H.sub.2O: C, 70.79; H, 7.88; N,
3.75. Found: C, 70.70; H, 7.86; N, 3.68.
Example 143
tetrahydro-2H-pyran-4-yl{3-[(2,2,3,3-tetramethylcyclopropyl)carbonyl]-1H-i-
ndol-1-yl}acetic Acid
Example 143A
(tetrahydro-pyran-4-ylidene)-acetic acid ethyl ester
[0408] To a solution of tetrahydro-4H-pyran-4-one (5.0 g, 50 mmol)
in 150 mL toluene at ambient temperature was added
carbethoxymethylenetriphenyl phosphorane (17.4 g, 50 mmol.). The
mixture was warmed to 50.degree. C. and allowed to stir for 16 h.
The mixture was cooled to ambient temperature, concentrated under
reduced pressure and purified by column chromatography (Si.sub.2O,
50% hexanes in EtOAc) to provide the title compound (2.2 g, 13
mmol, 26% yield). MS (DCI/NH.sub.3) m/z 171 (M+H).sup.+.
Example 143B
(tetrahydro-pyran-4-yl)-acetic acid ethyl ester
[0409] The product of Example 143A (2.2 g, 13 mmol) and Pd/C (10 wt
% palladium on activated carbon, 220 mg) in 30 mL EtOH were
processed as described in Example 70 to provide the title compound
(2.0 g, 12 mmol, 91% yield). MS (DCI/NH.sub.3) m/z 173
(M+H).sup.+.
Example 143C
bromo-(tetrahydro-pyran-4-yl)-acetic Acid Ethyl Ester
[0410] To a solution of lithium diisopropylamide (1.8 M in
THF/heptane/ethylbenzne, 3.6 mL, 6.4 mmol) in 10 mL of THF at
-78.degree. C. was added trimethylsilyl chloride (1.4 mL, 11 mmol)
dropwise via syringe pump. The product of Example 143B (1.0 g, 5.8
mmol) in 5 mL of THF was then added to the mixture dropwise via
syringe pump. The mixture was stirred at -78.degree. C. for 2 hours
then N-bromosuccinimide (NBS, 1.1 g, 6.0 mmol) in 10 mL of THF was
added dropwise via syringe pump. The reaction mixture was allowed
to warm slowly to ambient temperature and was stirred for 16 h. The
mixture was then concentrated under reduced pressure and the
residue was dissolved in 20 mL of EtOAc, washed 1.times.5 mL of
H.sub.2O. The aqueous layer was extracted 3.times.5 mL of EtOAc and
the combined organic extracts were dried over anhydrous
Na.sub.2SO.sub.4, filtered, concentrated under reduced pressure and
purified via column chromatography (SiO.sub.2, 70% hexanes in
EtOAc) to provide the title compound (0.70 g, 2.8 mmol, 48% yield).
MS (DCI/NH.sub.3) m/z 268 (M+NH.sub.4).sup.+.
Example 143D
tetrahydro-2H-pyran-4-yl{3-[(2,2,3,3-tetramethylcyclopropyl)carbonyl]-1H-i-
ndol-1-yl}acetic
[0411] The major product of Example 1B (0.56 g, 2.3 mmol), the
product of Example 143C (0.70 g, 2.8 mmol), and NaH (60% dispersion
in mineral oil, 0.28 g, 7.0 mmol) in DMF (10 mL) were processed as
described in Example 1D to provide the title compound (0.43 g, 1.0
mmol, 45% yield). .sup.1H NMR (MeOH-d.sub.4, 300 MHz) .delta. ppm
1.06-1.16 (m, 1H), 1.30 (s, 3H), 1.30-1.36 (m, 1H), 1.33 (s, 6H),
1.34 (s, 3H), 1.56 (ddd, J=24.8, 11.8, 4.7 Hz, 1H), 1.84-1.93 (m,
1H), 1.99 (s, 1H), 2.58-2.76 (m, 1H), 3.37 (dt, J=12.0, 2.5 Hz,
1H), 3.49 (dt, J=11.8, 2.2 Hz, 1H), 3.81-3.90 (m, 1H), 3.95-4.04
(m, 1H), 4.97 (d, J=10.2 Hz, 1H), 7.18-7.31 (m, 2H), 7.54-7.59 (m,
1H), 8.23 (s, 1H), 8.27 (ddd, J=7.5, 1.4, 0.7 Hz, 1H); MS
(DCI/NH.sub.3) m/z 384 (M+H).sup.+; Anal. Calculated for
C.sub.23H.sub.29NO.sub.4.0.1H.sub.2O: C, 71.70; H, 7.64; N, 3.64.
Found: C, 71.56; H, 7.56; N, 3.61
Example 144
ethyl
tetrahydro-2H-pyran-4-yl{3-[(2,2,3,3-tetramethylcyclopropyl)carbonyl-
]-1H-indol-1-yl}acetate
[0412] To a solution of the product of Example 143D (0.19 g, 0.50
mmol) in 10 mL EtOH at ambient temperature was added 0.5 mL
concentrated H.sub.2SO.sub.4 (8 mmol). This mixture was warmed to
reflux and stirred for 6 h. The mixture was cooled to ambient
temperature and then quenched with excess NaHCO.sub.3. This mixture
was concentrated under reduced pressure and the residue was diluted
with 20 mL of EtOAc and 20 mL H.sub.2O. The layers were separated
and the organic extracts was washed 1.times.5 mL H.sub.2O. The
combined aqueous layers were extracted 3.times.5 mL of EtOAc and
the combined organic extracts were dried over anhydrous
Na.sub.2SO.sub.4, filtered, concentrated under reduced pressure and
purified via column chromatography (SiO.sub.2, 50% hexanes in
EtOAc) to provide the title compound (40 mg, 0.097 mmol, 19%
yield). .sup.1H NMR (CDCl.sub.3, 300 MHz) .delta. ppm 1.09-1.19 (m,
1H), 1.27 (t, J=7.1 Hz, 3H), 1.32 (s, 3H), 1.32 (s, 6H), 1.35 (s,
3H), 1.50-1.64 (m, 2H), 1.68-1.79 (m, 1H), 1.97 (s, 1H), 2.46-2.62
(m, 1H), 3.33 (dt, J=11.8, 2.2 Hz, 1H), 3.46 (dt, J=11.7, 2.4 Hz,
1H), 3.83-3.92 (m, 1H), 3.99-4.09 (m, 1H), 4.13-4.31 (m, 2H), 4.74
(d, J=10.5 Hz, 1H), 7.25-7.34 (m, 2H), 7.37-7.43 (m, 1H), 7.96 (s,
1H), 8.38-8.43 (m, 1H); MS (DCI/NH.sub.3) m/z 412 (M+H).sup.+;
Anal. Calculated for C.sub.25H.sub.33NO.sub.4: C, 72.96; H, 8.08;
N, 3.40. Found: C, 72.89; H, 8.03; N, 3.36.
Example 145
tert-butyl
1-(tetrahydro-2H-pyran-4-ylmethyl)-3-[(2,2,3,3-tetramethylcyclo-
propyl)carbonyl]-1H-indol-5-ylcarbamate
Example 145A
(1H-indol-5-yl)-carbamic acid tert-butyl ester
[0413] To a solution 5-aminoindole (1.0 g, 7.6 mmol) in 100 mL of
EtOAc was added di-tert-butyldicarbonate (4.1 g. 19 mmol). The
mixture was stirred at ambient temperature for 24 hours and then
was quenched with 20 mL H.sub.2O. The layers were separated and the
aqueous layer was extracted 3.times.10 mL of EtOAc. The combined
organic extracts were dried over anhydrous Na.sub.2SO.sub.4,
filtered, concentrated under reduced pressure and purified via
flash column chromatography (SiO.sub.2, 50% hexanes in EtOAc) to
provide the title compound (1.8 g, 7.7 mmol, >100% yield). MS
(DCI/NH.sub.3) m/z 233 (M+H).sup.+.
Example 145B
[3-(2,2,3,3-Tetramethyl-cyclopropanecarbonyl)-1H-indol-5-yl]-carbamic
Acid Tert-Butyl Ester
[0414] The product of Example 145A (1.7 g. 7.3 mmol),
ethylmagnesium bromide (1.0 M solution in THF, 9.4 mL, 9.4 mmol),
zinc chloride (1.0 M solution in Et.sub.2O, 9.4 mL, 9.4 mmol) and
the product of Example 1A (12 mmol) in 30 mL of dichloromethane
were processed as described in Example 1B to provide the title
compound (1.6 g, 4.6 mmol, 60% yield). MS (DCI/NH.sub.3) m/z 357
(M+H).sup.+.
Example 145C
tert-butyl
1-(tetrahydro-2H-pyran-4-ylmethyl)-3-[(2,2,3,3-tetramethylcyclo-
propyl)carbonyl]-1H-indol-5-ylcarbamate
[0415] The product of Example 145B (1.6 g, 4.6 mmol), the product
of Example 18A (7.8 mmol), and NaH (60% dispersion in mineral oil,
0.55 g, 14 mmol) in DMF (25 mL) were processed as described in
Example 1D to provide the title compound (0.55 g, 1.2 mmol, 26%
yield). .sup.1H NMR (CDCl.sub.3, 300 MHz) .delta. ppm 1.30 (s, 6H),
1.33 (s, 6H), 1.37-1.50 (m, 4H), 1.52 (s, 9H), 1.89 (s, 1H),
2.06-2.22 (m, 1H), 3.32 (dt, J=11.6, 2.5 Hz, 2H), 3.92-3.98 (m,
2H), 4.01 (d, J=7.1 Hz, 2H), 6.50 (s, 1H), 7.22-7.30 (m, 1H), 7.57
(s, 1H), 7.60-7.67 (m, 1H), 8.11 (d, J=2.0 Hz, 1H); MS
(DCI/NH.sub.3) m/z 455 (M+H).sup.+; Anal. Calculated for
C.sub.27H.sub.38N.sub.2O.sub.4: C, 71.34; H, 8.43; N, 6.16. Found:
C, 71.27; H, 8.32; N, 6.04.
Example 146
[5-amino-1-(tetrahydro-2H-pyran-4-ylmethyl)-1H-indol-3-yl](2,2,3,3-tetrame-
thylcyclopropyl)methanone Trifluoroacetic Acid
[0416] To a solution of the product of Example 145C (0.50 g, 1.1
mmol) in 35 mL of dichloromethane was added 5 mL trifluoroacetic
acid (67 mmol). The mixture was stirred at ambient temperature for
1 hour then was concentrated under reduced pressure and 5 mL
toluene was added. The mixture was again concentrated under reduced
pressure and the addition of toluene followed by concentration was
repeated. The residue was stirred in 8 mL of EtOAc at ambient
temperature for 2 hours and the resulting solids were isolated via
filtration to provide the title compound (0.40 g, 0.85 mmol, 77%
yield). .sup.1H NMR (MeOH-d.sub.4, 300 MHz) .delta. ppm 1.33 (s,
12H), 1.38-1.51 (m, 4H), 2.12-2.29 (m, 1H), 2.17 (s, 1H), 3.32-3.41
(m, 2H), 3.88-3.98 (m, 2H), 4.21 (d, J=7.5 Hz, 2H), 7.25 (dd,
J=8.6, 2.2 Hz, 1H), 7.70 (dd, J=8.8, 0.7 Hz, 1H), 8.26 (s, 1H),
8.32-8.35 (m, 1H); MS (DCI/NH.sub.3) m/z 355 (M+H).sup.+; Anal.
Calculated for C.sub.22H.sub.30N.sub.2O.sub.2.
CF.sub.3CO.sub.2H.0.4H.sub.2O: C, 60.59; H, 6.74; N, 5.89. Found:
C, 60.38; H, 6.53; N, 6.17.
Example 147
[4,5,6,7-tetrafluoro-1-(tetrahydro-2H-pyran-4-ylmethyl)-1H-indol-3-yl](2,2-
,3,3-tetramethylcyclopropyl)methanone
Example 147A
(4,5,6,7-tetrafluoro-1H-indol-3-yl)-(2,2,3,3-tetramethyl-cyclopropyl)-meth-
anone
[0417] A mixture of 4,5,6,7-tetrafluoroindole (Matrix Scientific,
1.0 g. 5.3 mmol), ethylmagnesium bromide (1.0 M solution in THF,
6.4 mL, 6.4 mmol), zinc chloride (1.0 M solution in Et.sub.2O, 6.4
mL, 6.4 mmol) and the product of Example 1A (7.9 mmol) in 40 mL of
dichloromethane was processed as described in Example 1B to provide
the title compound (0.19 g, 0.61 mmol, 12% yield). MS
(DCI/NH.sub.3) m/z 314 (M+H).sup.+.
Example 147B
[4,5,6,7-tetrafluoro-1-(tetrahydro-2H-pyran-4-ylmethyl)-1H-indol-3-yl](2,2-
,3,3-tetramethylcyclopropyl)methanone
[0418] The product of Example 147A (91 mg, 0.29 mmol), the product
of Example 18A (0.49 mmol), and NaH (60% dispersion in mineral oil,
38 mg, 0.96 mmol) in DMF (6 mL) were processed as described in
Example 1D to provide the title compound (11 mg, 0.027 mmol, 9%
yield). .sup.1H NMR (MeOH-d.sub.4, 300 MHz) .delta. ppm 1.33 (s,
12H), 1.40-1.58 (m, 4H), 2.05-2.18 (m, 1H), 2.08 (s, 1H), 3.41 (dt,
J=11.2, 2.4 Hz, 2H), 3.95-4.04 (m, 2H), 4.22 (d, J=7.1 Hz, 2H),
7.78 (s, 1H); MS (DCI/NH.sub.3) m/z 412 (M+H).sup.+; Anal.
Calculated for C.sub.22H.sub.25F.sub.4NO.sub.2: C, 64.22; H, 6.12;
N, 3.40. Found: C, 63.88; H, 6.17; N, 3.41.
Example 148
N-{1-(tetrahydro-2H-pyran-4-ylmethyl)-3-[(2,2,3,3-tetramethylcyclopropyl)c-
arbonyl]-1H-indol-5-yl}methanesulfonamide
[0419] The product of Example 146 (0.20 g, 0.46 mmol),
methanesulfonyl chloride (50 .mu.L, 0.63 mmol) and triethylamine
(0.26 mL, 1.9 mmol) in 10 mL of THF were processed as described in
Example 106B to provide the title compound (0.12 g, 0.28 mmol, 60%
yield). .sup.1H NMR (CDCl.sub.3, 300 MHz) .delta. ppm 1.31 (s, 6H),
1.34 (s, 6H), 1.38-1.57 (m, 4H), 1.89 (s, 1H), 2.07-2.25 (m, 1H),
2.97 (s, 3H), 3.34 (dt, J=11.6, 2.5 Hz, 2H), 3.95-4.02 (m, 2H),
4.04 (d, J=7.5 Hz, 2H), 6.28 (s, 1H), 7.33 (d, J=8.8 Hz, 1H), 7.42
(dd, J=8.8, 2.0 Hz, 1H), 7.64 (s, 1H), 8.20 (d, J=2.0 Hz, 1H); MS
(DCI/NH.sub.3) m/z 433 (M+H).sup.+; Anal. Calculated for
C.sub.23H.sub.32N.sub.2C.sub.4S: C, 63.86; H, 7.46; N, 6.48. Found:
C, 63.48; H, 7.19; N, 6.23.
Example 149
[5-(hydroxymethyl)-1-(tetrahydro-2H-pyran-4-ylmethyl)-1H-indol-3-yl](2,2,3-
,3-tetramethylcyclopropyl)methanone
Example 149A
5-(tert-Butyl-dimethyl-silanyloxymethyl)-1H-indole
[0420] To a solution of indole-1-methanol (Combi-Blocks, 1.0 g, 6.8
mmol) in 50 mL of dichloromethane was added imidazole (0.56 g, 8.2
mmol) followed by tert-butyldimethylsilyl chloride (1.1 g, 7.0
mmol). The mixture was stirred at ambient temperature for 17 hours
then 10 mL H.sub.2O was added and the layers were separated. The
aqueous layer was extracted 3.times.5 mL of dichloromethane and the
combined organic extracts were dried over anhydrous
Na.sub.2SO.sub.4, filtered, concentrated under reduced pressure and
purified via flash column chromatography (SiO.sub.2, 80% hexanes in
EtOAc) to provide the title compound (1.6 g, 6.2 mmol, 91% yield).
MS (DCI/NH.sub.3) m/z 262 (M+H).sup.+.
Example 149B
[5-(tert-Butyl-dimethyl-silanyloxymethyl)-1H-indol-3-yl]-(2,2,3,3-tetramet-
hyl-cyclopropyl)-methanone
[0421] The product of Example 149A (1.6 g. 6.2 mmol),
ethylmagnesium bromide (1.0 M solution in THF, 7.5 mL, 7.5 mmol),
zinc chloride (1.0 M solution in Et.sub.2O, 7.5 mL, 7.5 mmol) and
the product of Example 1A (9.4 mmol) in 30 mL of dichloromethane
were processed as described in Example 1B to provide the title
compound (0.90 g, 2.3 mmol, 38% yield). MS (DCI/NH.sub.3) m/z 386
(M+H).sup.+.
Example 149C
[5-(hydroxymethyl)-1-(tetrahydro-2H-pyran-4-ylmethyl)-1H-indol-3-yl](2,2,3-
,3-tetramethylcyclopropyl)methanone
[0422] The product of Example 149B (0.88 g, 2.3 mmol), the product
of Example 18A (3.9 mmol), and NaH (60% dispersion in mineral oil,
0.28 g, 6.9 mmol) in DMF (12 mL) were processed as described in
Example 1D to provide the title compound (0.20 g, 0.54 mmol, 24%
yield, major product) as well as the corresponding
tert-butyldimethylsilyl ether (0.17 g, 0.35 mmol, 15% yield).
.sup.1H NMR (CDCl.sub.3, 300 MHz) .delta. ppm 1.31 (s, 6H), 1.35
(s, 6H), 1.38-1.62 (m, 4H), 1.92 (s, 1H), 2.09-2.22 (m, 1H),
2.55-2.74 (m, 1H), 3.25-3.46 (m, 2H), 3.93-4.02 (m, 2H), 4.04 (d,
J=7.5 Hz, 2H), 4.79 (s, 2H), 7.32-7.37 (m, 2H), 7.62 (s, 1H), 8.41
(s, 1H); MS (DCI/NH.sub.3) m/z 370 (M+H).sup.+; Anal. Calculated
for C.sub.23H.sub.31NO.sub.3.0.9H.sub.2O: C, 71.62; H, 8.57; N,
3.63. Found: C, 71.57; H, 8.29; N, 3.70.
Example 150
[5-(methoxymethyl)-1-(tetrahydro-2H-pyran-4-ylmethyl)-1H-indol-3-yl](2,2,3-
,3-tetramethylcyclopropyl)methanone
[0423] The major product of Example 149C (0.10 g, 0.28 mmol), NaH
(60% dispersion in mineral oil, 45 mg, 1.1 mmol) and CH.sub.3I (71
.mu.L, 0.84 mmol) in 10 mL of THF were processed as described in
Example 72 to provide the title compound (60 mg, 0.16 mmol, 56%
yield). .sup.1H NMR (CDCl.sub.3, 300 MHz) .delta. ppm 1.31 (s, 6H),
1.35 (s, 6H), 1.38-1.56 (m, 4H), 1.92 (s, 1H), 2.09-2.22 (m, 1H),
3.32 (dt, J=11.5, 2.7 Hz, 2H), 3.37 (s, 3H), 3.93-4.02 (m, 2H),
4.04 (d, J=7.5 Hz, 2H), 4.57 (s, 2H), 7.33 (d, J=1.4 Hz, 2H), 7.61
(s, 1H), 8.38 (s, 1H); MS (DCI/NH.sub.3) m/z 384 (M+H).sup.+; Anal.
Calculated for C.sub.24H.sub.33NO.sub.3.0.2H.sub.2O: C, 74.46; H,
8.70; N, 3.62. Found: C, 74.25; H, 8.20; N, 3.54.
Example 151
3-(2-{5-hydroxy-3-[(2,2,3,3-tetramethylcyclopropyl)carbonyl]-1H-indol-1-yl-
}ethyl)-1,3-oxazolidin-2-one
[0424] The product of Example 152 (0.50 g, 1.1 mmol) and Pd/C (10
wt % palladium on activated carbon, 110 mg) in 20 mL EtOH were
processed as described in Example 70 to provide the title compound
(0.26 g, 0.69 mmol, 64% yield). .sup.1H NMR (CDCl.sub.3, 300 MHz)
.delta. ppm 1.30 (s, 6H), 1.34 (s, 6H), 1.87 (s, 1H), 2.92 (dd,
J=8.1 Hz, 8.1 Hz, 2H), 3.66 (t, J=5.8 Hz, 2H), 4.08 (dd, J=7.5 Hz,
7.5 Hz, 2H), 4.39 (t, J=5.8 Hz, 2H), 6.90 (dd, J=8.8, 2.4 Hz, 1H),
7.25 (d, J=8.8 Hz, 1H), 7.64 (s, 1H), 7.90 (d, J=2.4 Hz, 1H); MS
(DCI/NH.sub.3) m/z 371 (M+H).sup.+; Anal. Calculated for
C.sub.21H.sub.26N.sub.2O.sub.4.0.1H.sub.2O: C, 67.94; H, 6.84; N,
7.55. Found: C, 67.84; H, 7.05; N, 7.35.
Example 152
3-(2-{5-(benzyloxy)-3-[(2,2,3,3-tetramethylcyclopropyl)carbonyl]-1H-indol--
1-yl}ethyl)-1,3-oxazolidin-2-one
[0425] The product of Example 74A (0.60 g, 1.7 mmol), the product
of Example 31A (3.5 mmol), and NaH (60% dispersion in mineral oil,
0.21 g, 5.2 mmol) in 20 mL of DMF were processed as described in
Example 1D to provide the title compound (0.55 g, 1.2 mmol, 70%
yield). .sup.1H NMR (CDCl.sub.3, 300 MHz) .delta. ppm 1.31 (s, 6H),
1.36 (s, 6H), 1.90 (s, 1H), 2.90-2.96 (m, 2H), 3.67 (t, J=5.8 Hz,
2H), 4.08 (dd, J=8.6, 7.3 Hz, 2H), 4.40 (t, J=5.9 Hz, 2H), 5.14 (s,
2H), 7.03 (dd, J=9.0, 2.5 Hz, 1H), 7.27-7.45 (m, 4H), 7.45-7.52 (m,
2H), 7.65 (s, 1H), 8.08 (d, J=2.7 Hz, 1H); MS (DCI/NH.sub.3) m/z
461 (M+H).sup.+; Anal. Calculated for
C.sub.28H.sub.32N.sub.2O.sub.4.0.2H.sub.2O: C, 72.45; H, 7.04; N,
6.04. Found: C, 72.43; H, 7.00; N, 6.13.
Example 153
N-methyl-1-(tetrahydro-2H-pyran-4-ylmethyl)-3-[(2,2,3,3-tetramethylcyclopr-
opyl)carbonyl]-1H-indole-6-carboxamide
[0426] To a solution of the product of Example 86 (0.24 g, 0.63
mmol), methylamine (2.0 M solution in THF, 0.38 mL, 0.75 mmol) and
diisopropylethyl amine (0.27 mL, 1.6 mmol) in 5 mL of THF was added
o-(7-azabenzotriazol-1-yl)-N,N,N',N'-tetramethyluronium
hexafluorophosphate (HATU, 0.25 g, 0.66 mmol). The mixture was
stirred at ambient temperature for 16 hours and then was quenched
with 5 mL H.sub.2O and diluted with 10 mL of EtOAc. The layers were
separated, the aqueous layer was extracted 2.times.5 mL of EtOAc
and the combined organic extracts were dried over Na.sub.2SO.sub.4,
filtered, concentrated under reduced pressure. The residue was
purified via column chromatography (SiO.sub.2, 10% CH.sub.3OH in
EtOAc) to provide the title compound (80 mg, 0.20 mmol, 32% yield).
.sup.1H NMR (MeOH-d.sub.4, 300 MHz) .delta. ppm 1.33 (d, J=1.4 Hz,
6H), 1.33 (s, 6H), 1.40-1.54 (m, 4H), 2.16 (s, 1H), 2.18-2.32 (m,
1H), 2.96 (s, 3H), 3.33-3.43 (m, 2H), 3.90-3.98 (m, 2H), 4.21 (d,
J=7.5 Hz, 2H), 7.67 (dd, J=8.3, 1.5 Hz, 1H), 8.02 (dd, J=1.4, 0.7
Hz, 1H), 8.21 (s, 1H), 8.31 (dd, J=8.5, 0.7 Hz, 1H); MS
(DCI/NH.sub.3) m/z 397 (M+H).sup.+; Anal. Calculated for
C.sub.24H.sub.32N.sub.2O.sub.3: C, 72.70; H, 8.13; N, 7.06. Found:
C, 72.52; H, 8.40; N, 7.05.
Example 154
N,N-dimethyl-1-(tetrahydro-2H-pyran-4-ylmethyl)-3-[(2,2,3,3-tetramethylcyc-
lopropyl)carbonyl]-1H-indole-6-carboxamide
[0427] To a solution of the product of Example 86 (0.15 g, 0.39
mmol), dimethylamine (40 wt % in water, 19 .mu.L, 0.38 mmol),
i-Pr.sub.2NEt (0.20 mL, 1.2 mmol) and
o-(7-azabenzotriazol-1-yl)-N,N,N',N'-tetramethyluronium
hexafluorophosphate (HATU, 0.15 g, 0.40 mmol) in 10 mL of THF were
processed as described in Example 153 to provide the title compound
(50 mg, 0.12 mmol, 31% yield). .sup.1H NMR (AcOH-d.sub.4, 300 MHz)
.delta. ppm 1.30-1.32 (m, 6H), 1.33 (s, 6H), 1.44-1.59 (m, 4H),
2.12 (s, 1H), 2.17-2.29 (m, 1H), 3.08 (s, 3H), 3.16 (s, 3H), 3.40
(dt, J=11.6, 2.1 Hz, 2H), 4.01-4.08 (m, 2H), 4.16 (d, J=7.3 Hz,
2H), 7.33 (dd, J=8.4, 0.8 Hz, 1H), 7.75 (s, 1H), 8.05 (s, 1H), 8.36
(d, J=8.2 Hz, 1H); MS (DCI/NH.sub.3) m/z 411 (M+H).sup.+; Anal.
Calculated for C.sub.25H.sub.34N.sub.2O.sub.3: C, 73.14; H, 8.35;
N, 6.82. Found: C, 72.93; H, 8.18; N, 6.74.
Example 155
N-ethyl-1-(tetrahydro-2H-pyran-4-ylmethyl)-3-[(2,2,3,3-tetramethylcyclopro-
pyl)carbonyl]-1H-indole-6-carboxamide
[0428] To a solution of the product of Example 86 (0.15 g, 0.39
mmol), ethylamine (2.0 M solution in THF, 0.38 mL, 0.76 mmol),
i-Pr.sub.2NEt (0.20 mL, 1.2 mmol) and
o-(7-azabenzotriazol-1-yl)-N,N,N',N'-tetramethyluronium
hexafluorophosphate (HATU, 0.15 g, 0.40 mmol) in 10 mL of THF were
processed as described in Example 153 to provide the title compound
(60 mg, 0.15 mmol, 38% yield). .sup.1H NMR (CDCl.sub.3, 300 MHz)
.delta. ppm 1.29 (t, J=7.1 Hz, 3H), 1.32 (s, 6H), 1.35 (s, 6H),
1.39-1.57 (m, 4H), 1.92 (s, 1H), 2.12-2.26 (m, 1H), 3.33 (dt,
J=11.4, 2.2 Hz, 2H), 3.50-3.62 (m, 2H), 3.92-4.02 (m, 2H), 4.10 (d,
J=7.5 Hz, 2H), 6.20-6.29 (m, 1H), 7.47 (d, J=8.5 Hz, 1H), 7.70 (s,
1H), 8.04 (s, 1H), 8.43 (d, J=8.1 Hz, 1H); MS (DCI/NH.sub.3) m/z
411 (M+H).sup.+; Anal. Calculated for
C.sub.25H.sub.34N.sub.2O.sub.3.0.7H.sub.2O: C, 70.96; H, 8.43; N,
6.62. Found: C, 70.81; H, 8.12; N, 6.76.
Example 156
[1-(pyridin-3-ylmethyl)-1H-indol-3-yl](2,2,3,3-tetramethylcyclopropyl)meth-
anone
[0429] The 3-pyridylcarbinol (0.21 mL, 2.1 mmol), methanesulfonyl
chloride (0.33 mL, 4.2 mmol), and triethylamine (0.93 mL, 6.7 mmol)
in 20 mL of THF were processed as described in Example 1C to
provide the corresponding mesylate. The major product of Example 1B
(0.30 g, 1.2 mmol), the freshly prepared mesylate (2.1 mmol) and
NaH (60% dispersion in mineral oil, 0.23 g, 5.8 mmol) in 25 mL of
DMF were processed as described in Example 1D to provide the title
compound (0.31 g, 0.94 mmol, 79% yield). .sup.1H NMR (CDCl.sub.3,
300 MHz) .delta. ppm 1.29 (s, 6H), 1.35 (s, 6H), 1.94 (s, 1H), 5.44
(s, 2H), 7.18-7.31 (m, 3H), 7.33-7.41 (m, 1H), 7.45-7.53 (m, 1H),
7.71 (s, 1H), 8.39-8.47 (m, 1H), 8.53-8.68 (m, 2H); MS
(DCI/NH.sub.3) m/z 333 (M+H).sup.+; Anal. Calculated for
C.sub.22H.sub.24N.sub.2O.0.2H.sub.2O: C, 78.63; H, 7.32; N, 8.34.
Found: C, 78.48; H, 7.20; N, 8.17.
Example 157
[1-(pyridin-4-ylmethyl)-1H-indol-3-yl](2,2,3,3-tetramethylcyclopropyl)meth-
anone
[0430] The 4-pyridylcarbinol (0.24 g, 2.1 mmol), methanesulfonyl
chloride (0.33 mL, 4.2 mmol), and triethylamine (0.93 mL, 6.7 mmol)
in 20 mL of THF were processed as described in Example 1C to
provide the corresponding mesylate. The major product of Example 1B
(0.30 g, 1.2 mmol), the freshly prepared mesylate (2.1 mmol) and
NaH (60% dispersion in mineral oil, 0.23 g, 5.8 mmol) in 25 mL of
DMF were processed as described in Example 1D to provide the title
compound (0.31 g, 0.94 mmol, 79% yield). .sup.1H NMR (CDCl.sub.3,
300 MHz) .delta. ppm 1.30 (s, 6H), 1.36 (s, 6H), 1.95 (s, 1H), 5.43
(s, 2H), 7.04-7.09 (m, 2H), 7.11-7.16 (m, 1H), 7.20-7.34 (m, 2H),
7.71 (s, 1H), 8.42-8.49 (m, 1H), 8.53-8.65 (m, 2H); MS
(DCI/NH.sub.3) m/z 333 (M+H).sup.+; Anal. Calculated for
C.sub.22H.sub.24N.sub.2O: C, 79.48; H, 7.28; N, 8.43. Found: C,
79.42; H, 7.33; N, 8.43.
Example 158
[5-bromo-1-(tetrahydro-2H-pyran-4-ylmethyl)-1H-indol-3-yl](2,2,3,3-tetrame-
thylcyclopropyl)methanone
Example 158A
(5-Bromo-1H-indol-3-yl)-(2,2,3,3-tetramethyl-cyclopropyl)-methanone
[0431] A mixture of 5-bromoindole (5.0 g. 26 mmol), ethylmagnesium
bromide (1.0 M solution in THF, 31 mL, 31 mmol), zinc chloride (1.0
M solution in Et.sub.2O, 31 mL, 31 mmol) and the product of Example
1A (38 mmol) in 100 mL of dichloromethane was processed as
described in Example 1B to provide the title compound (3.1 g, 9.8
mmol, 38% yield). MS (DCI/NH.sub.3) m/z 321, 322 (M+H).sup.+.
Example 158B
[5-bromo-1-(tetrahydro-2H-pyran-4-ylmethyl)-1H-indol-3-yl](2,2,3,3-tetrame-
thylcyclopropyl)methanone
[0432] The product of Example 158A (3.1 g, 9.8 mmol), the product
of Example 18A (17 mmol), and NaH (60% dispersion in mineral oil,
1.8 g, 46 mmol) in DMF (30 mL) were processed as described in
Example 1D to provide the title compound (3.4 g, 8.2 mmol, 83%
yield). .sup.1H NMR (CDCl.sub.3, 300 MHz) .delta. ppm 1.31 (s, 6H),
1.34 (s, 6H), 1.37-1.56 (m, 4H), 1.88 (s, 1H), 2.05-2.21 (m, 1H),
3.33 (dt, J=11.6, 2.5 Hz, 2H), 3.93-4.00 (m, 2H), 4.01 (d, J=7.5
Hz, 2H), 7.20 (d, J=8.8 Hz, 1H), 7.37 (dd, J=8.6, 1.9 Hz, 1H), 7.59
(s, 1H), 8.61 (d, J=1.7 Hz, 1H); MS (DCI/NH.sub.3) m/z 418, 420
(M+H).sup.+; Anal. Calculated for C.sub.22H.sub.28BrNO.sub.2: C,
63.16; H, 6.75; N, 3.35. Found: C, 62.92; H, 6.79; N, 3.24.
Example 159
[5-(2-methoxyphenyl)-1-(tetrahydro-2H-pyran-4-ylmethyl)-1H-indol-3-yl](2,2-
,3,3-tetramethylcyclopropyl)methanone
[0433] The product of Example 158B (0.20 g, 0.48 mmol),
2-methoxyphenylboronic acid (0.15 g, 0.96 mmol),
tris(dibenzylideneacetone)dipalladium (0) (Pd.sub.2dba.sub.3,
Strem, 17 mg, 0.019 mmol),
1,3-bis(2,6-di-1-propylphenyl)imidazolium chloride (Strem, 20 mg,
0.048 mmol) and 3 mL of 2 N aqueous Na.sub.2CO.sub.3 were combined
in 20 mL toluene. The system was degassed under vacuum and the
flask refilled with N.sub.2. This was repeated three times then the
mixture was warmed to 85.degree. C. and stirred for 48 h. The
mixture was cooled to ambient temperature, the layers separated and
the organic layer was dried over anhydrous Na.sub.2SO.sub.4,
filtered, concentrated under reduced pressure and purified via
flash column chromatography (SiO.sub.2, 50% hexanes in EtOAc) to
provide the title compound (0.17 g, 0.37 mmol, 77% yield). .sup.1H
NMR (CDCl.sub.3, 300 MHz) .delta. ppm 1.30 (s, 6H), 1.33 (s, 6H),
1.37-1.53 (m, 4H), 1.97 (s, 1H), 2.11-2.26 (m, 1H), 3.35 (dt,
J=11.7, 2.4 Hz, 2H), 3.81 (s, 3H), 3.95-4.03 (m, 2H), 4.05 (d,
J=7.5 Hz, 2H), 6.95-7.07 (m, 2H), 7.26-7.33 (m, 1H), 7.35 (dd,
J=8.5, 0.7 Hz, 1H), 7.41 (dd, J=7.5, 1.7 Hz, 1H), 7.50 (dd, J=8.5,
1.7 Hz, 1H), 7.62 (s, 1H), 8.51 (d, J=1.7 Hz, 1H); MS
(DCI/NH.sub.3) m/z 446 (M+H).sup.+; Anal. Calculated for
C.sub.29H.sub.35NO.sub.3.0.1H.sub.2O: C, 77.85; H, 7.93; N, 3.13.
Found: C, 77.74; H, 7.92; N, 3.11.
Example 160
[5-phenyl-1-(tetrahydro-2H-pyran-4-ylmethyl)-1H-indol-3-yl](2,2,3,3-tetram-
ethylcyclopropyl)methanone
[0434] The product of Example 158B (0.20 g, 0.48 mmol),
phenylboronic acid (0.12 g, 0.96 mmol),
tris(dibenzylideneacetone)dipalladium (0) (Pd.sub.2 dba.sub.3,
Strem, 17 mg, 0.019 mmol),
1,3-bis(2,6-di-1-propylphenyl)imidazolium chloride (Strem, 20 mg,
0.048 mmol) and 3 mL of 2 N aqueous Na.sub.2CO.sub.3 in 20 mL
toluene were processed as described in Example 159 to provide the
title compound (47 mg, 0.11 mmol, 24% yield). .sup.1H NMR
(CDCl.sub.3, 300 MHz) .delta. ppm 1.32 (s, 6H), 1.36 (s, 6H),
1.40-1.57 (m, 4H), 1.95 (s, 1H), 2.11-2.27 (m, 1H), 3.35 (dt,
J=11.7, 2.4 Hz, 2H), 3.95-4.04 (m, 2H), 4.07 (d, J=7.5 Hz, 2H),
7.27-7.34 (m, 1H), 7.36-7.47 (m, 3H), 7.55 (dd, J=8.5, 1.7 Hz, 1H),
7.64 (s, 1H), 7.67-7.73 (m, 2H), 8.67 (d, J=1.7 Hz, 1H); MS
(DCI/NH.sub.3) m/z 416 (M+H).sup.+; Anal. Calculated for
C.sub.28H.sub.33NO.sub.2.0.1H.sub.2O: C, 80.58; H, 8.02; N, 3.36.
Found: C, 80.36; H, 7.90; N, 3.48.
Example 162
[5-(3-methoxyphenyl)-1-(tetrahydro-2H-pyran-4-ylmethyl)-1H-indol-3-yl](2,2-
,3,3-tetramethylcyclopropyl)methanone
[0435] The product of Example 158B (0.20 g, 0.48 mmol),
3-methoxyphenylboronic acid (0.15 g, 0.96 mmol),
tris(dibenzylideneacetone)dipalladium (0) (Pd.sub.2 dba.sub.3,
Strem, 17 mg, 0.019 mmol),
1,3-bis(2,6-di-1-propylphenyl)imidazolium chloride (Strem, 20 mg,
0.048 mmol) and 3 mL of 2 N aqueous Na.sub.2CO.sub.3 in 20 mL
toluene were processed as described in Example 159 to provide the
title compound (12 mg, 0.026 mmol, 5% yield). .sup.1H NMR
(CDCl.sub.3, 300 MHz) .delta. ppm 1.32 (s, 6H), 1.35 (s, 6H),
1.37-1.62 (m, 4H), 1.95 (s, 1H), 2.10-2.23 (m, 1H), 3.35 (dt,
J=11.6, 2.2 Hz, 2H), 3.87 (s, 3H), 3.94-4.03 (m, 2H), 4.06 (d,
J=7.1 Hz, 2H), 6.87 (ddd, J=7.9, 2.5, 1.2 Hz, 1H), 7.19-7.23 (m,
1H), 7.27-7.41 (m, 3H), 7.53 (dd, J=8.6, 1.9 Hz, 1H), 7.64 (s, 1H),
8.65 (d, J=1.4 Hz, 1H); MS (DCI/NH.sub.3) m/z 446 (M+H).sup.+;
Anal. Calculated for C.sub.29H.sub.35NO.sub.3.0.6H.sub.2O: C,
76.32; H, 7.99; N, 3.07. Found: C, 76.11; H, 7.60; N, 2.89.
Example 164
[5-chloro-1-(tetrahydro-2H-pyran-4-ylmethyl)-1H-indol-3-yl](2,2,3,3-tetram-
ethylcyclopropyl)methanone
Example 164A
(5-Chloro-1H-indol-3-yl)-(2,2,3,3-tetramethyl-cyclopropyl)-methanone
[0436] A mixture of 5-chloroindole (0.30 g. 2.0 mmol),
ethylmagnesium bromide (1.0 M solution in THF, 2.4 mL, 2.4 mmol),
zinc chloride (1.0 M solution in Et.sub.2O, 2.4 mL, 2.4 mmol) and
the product of Example 1A (3.0 mmol) in 15 mL of dichloromethane
was processed as described in Example 1B to provide the title
compound (0.23 g, 0.85 mmol, 43% yield). MS (DCI/NH.sub.3) m/z 276
(M+H).sup.+.
Example 164B
[5-chloro-1-(tetrahydro-2H-pyran-4-ylmethyl)-1H-indol-3-yl](2,2,3,3-tetram-
ethylcyclopropyl)methanone
[0437] The product of Example 164A (85 mg, 0.31 mmol), the product
of Example 18A (1.4 mmol), and NaH (60% dispersion in mineral oil,
58 mg, 1.5 mmol) in DMF (5 mL) were processed as described in
Example 1D to provide the title compound (56 mg, 0.15 mmol, 48%
yield). .sup.1H NMR (CDCl.sub.3, 300 MHz) .delta. ppm 1.31 (s, 6H),
1.34 (s, 6H), 1.37-1.55 (m, 4H), 1.88 (s, 1H), 2.07-2.20 (m, 1H),
3.33 (dt, J=11.6, 2.5 Hz, 2H), 3.94-4.00 (m, 2H), 4.02 (d, J=7.1
Hz, 2H), 7.23-7.27 (m, 2H), 7.61 (s, 1H), 8.44 (t, J=1.4 Hz, 1H);
MS (DCI/NH.sub.3) m/z 374 (M+H).sup.+; Anal. Calculated for
C.sub.22H.sub.28ClNO.sub.2.0.1H.sub.2O: C, 70.33; H, 7.57; N, 3.73.
Found: C, 70.25; H, 7.58; N, 3.71.
Example 165
[6-bromo-1-(tetrahydro-2H-pyran-4-ylmethyl)-1H-indol-3-yl](2,2,3,3-tetrame-
thylcyclopropyl)methanone
Example 165A
(6-Bromo-1H-indol-3-yl)-(2,2,3,3-tetramethyl-cyclopropyl)-methanone
[0438] A mixture of 6-bromoindole (2.0 g. 10 mmol), ethylmagnesium
bromide (1.0 M solution in THF, 12 mL, 12 mmol), zinc chloride (1.0
M solution in Et.sub.2O, 12 mL, 12 mmol) and the product of Example
1A (15 mmol) in 50 mL of dichloromethane was processed as described
in Example 1B to provide the title compound (1.4 g, 4.4 mmol, 44%
yield). MS (DCI/NH.sub.3) m/z 320, 322 (M+H).sup.+.
Example 165B
[6-bromo-1-(tetrahydro-2H-pyran-4-ylmethyl)-1H-indol-3-yl](2,2,3,3-tetrame-
thylcyclopropyl)methanone
[0439] The product of Example 165A (1.3 g, 4.0 mmol), the product
of Example 18A (6.8 mmol), and NaH (60% dispersion in mineral oil,
0.75 g, 19 mmol) in DMF (15 mL) were processed as described in
Example 1D to provide the title compound (0.64 g, 1.5 mmol, 39%
yield). .sup.1H NMR (CDCl.sub.3, 300 MHz) .delta. ppm 1.30 (s, 6H),
1.34 (s, 6H), 1.39-1.57 (m, 4H), 1.89 (s, 1H), 2.03-2.23 (m, 1H),
3.35 (dt, J=11.7, 2.4 Hz, 2H), 3.94-4.05 (m, 2H), 3.99 (d, J=7.5
Hz, 2H), 7.36 (dd, J=8.5, 1.7 Hz, 1H), 7.47 (d, J=1.7 Hz, 1H), 7.56
(s, 1H), 8.28 (d, J=8.5 Hz, 1H); MS (DCI/NH.sub.3) m/z 418, 420
(M+H).sup.+; Anal. Calculated for C.sub.22H.sub.28BrNO.sub.2: C,
63.16; H, 6.75; N, 3.35. Found: C, 63.02; H, 6.49; N, 3.31.
Example 166
[6-(2-methoxyphenyl)-1-(tetrahydro-2H-pyran-4-ylmethyl)-1H-indol-3-yl](2,2-
,3,3-tetramethylcyclopropyl)methanone
[0440] The product of Example 165B (0.15 g, 0.36 mmol),
2-methoxyphenylboronic acid (0.12 g, 0.72 mmol),
tris(dibenzylideneacetone)dipalladium (0) (Pd.sub.2 dba.sub.3,
Strem, 13 mg, 0.014 mmol),
1,3-bis(2,6-di-1-propylphenyl)imidazolium chloride (Strem, 15 mg,
0.036 mmol) and 3 mL of 2N aqueous Na.sub.2CO.sub.3 in 20 mL
toluene were processed as described in Example 159 to provide the
title compound (0.12 g, 0.27 mmol, 76% yield). .sup.1H NMR
(CDCl.sub.3, 300 MHz) .delta. ppm 1.32 (s, 6H), 1.35 (s, 6H),
1.37-1.60 (m, 4H), 1.97 (s, 1H), 2.09-2.28 (m, 1H), 3.32 (dt,
J=11.6, 2.2 Hz, 2H), 3.82 (s, 3H), 3.93-4.02 (m, 2H), 4.05 (d,
J=7.5 Hz, 2H), 6.98-7.10 (m, 2H), 7.30-7.53 (m, 4H), 7.63 (s, 1H),
8.38 (d, J=8.5 Hz, 1H); MS (DCI/NH.sub.3) m/z 446 (M+H).sup.+;
Anal. Calculated for C.sub.29H.sub.35NO.sub.3: C, 78.17; H, 7.92;
N, 3.14. Found: C, 77.83; H, 7.94; N, 2.97.
Example 167
[6-phenyl-1-(tetrahydro-2H-pyran-4-ylmethyl)-1H-indol-3-yl](2,2,3,3-tetram-
ethylcyclopropyl)methanone
[0441] The product of Example 165B (0.15 g, 0.36 mmol),
phenylboronic acid (88 mg, 0.72 mmol),
tris(dibenzylideneacetone)dipalladium (0) (Pd.sub.2 dba.sub.3,
Strem, 13 mg, 0.014 mmol),
1,3-bis(2,6-di-1-propylphenyl)imidazolium chloride (Strem, 15 mg,
0.036 mmol) and 3 mL of 2N aqueous Na.sub.2CO.sub.3 in 20 mL
toluene were processed as described in Example 159 to provide the
title compound (0.10 g, 0.25 mmol, 69% yield). .sup.1H NMR
(CDCl.sub.3, 300 MHz) .delta. ppm 1.32 (s, 6H), 1.36 (s, 6H),
1.40-1.52 (m, 4H), 1.96 (s, 1H), 2.10-2.26 (m, 1H), 3.34 (dt,
J=11.7, 2.4 Hz, 2H), 3.93-4.03 (m, 2H), 4.09 (d, J=7.1 Hz, 2H),
7.31-7.40 (m, 1H), 7.42-7.56 (m, 4H), 7.61-7.69 (m, 3H), 8.44 (d,
J=9.2 Hz, 1H); MS (DCI/NH.sub.3) m/z 416 (M+H).sup.+; Anal.
Calculated for C.sub.28H.sub.33NO.sub.2: C, 80.93; H, 8.00; N,
3.37. Found: C, 80.67; H, 8.04; N, 3.39.
Example 168
[5-fluoro-1-(tetrahydro-2H-pyran-4-ylmethyl)-1H-indol-3-yl](2,2,3,3-tetram-
ethylcyclopropyl)methanone
Example 168A
(5-fluoro-1H-indol-3-yl)-(2,2,3,3-tetramethyl-cyclopropyl)-methanone
[0442] A mixture of 5-fluoroindole (0.34 g. 2.5 mmol),
ethylmagnesium bromide (1.0 M solution in THF, 3.0 mL, 3.0 mmol),
zinc chloride (1.0 M solution in Et.sub.2O, 3.0 mL, 3.0 mmol) and
the product of Example 1A (3.7 mmol) in 25 mL of dichloromethane
was processed as described in Example 1B to provide the title
compound (0.26 g, 1.0 mmol, 40% yield). MS (DCI/NH.sub.3) m/z 260
(M+H).sup.+.
Example 168B
[5-fluoro-1-(tetrahydro-2H-pyran-4-ylmethyl)-1H-indol-3-yl](2,2,3,3-tetram-
ethylcyclopropyl)methanone
[0443] The product of Example 168A (0.26 g, 1.0 mmol), the product
of Example 18A (1.7 mmol), and NaH (60% dispersion in mineral oil,
0.19 g, 4.7 mmol) in DMF (10 mL) were processed as described in
Example 1D to provide the title compound (80 mg, 0.22 mmol, 22%
yield). .sup.1H NMR (CDCl.sub.3, 300 MHz) .delta. ppm 1.31 (s, 6H),
1.34 (s, 6H), 1.38-1.53 (m, 4H), 1.88 (s, 1H), 2.06-2.20 (m, 1H),
3.34 (dt, J=11.6, 2.5 Hz, 2H), 3.95-4.01 (m, 2H), 4.02 (d, J=7.1
Hz, 2H), 7.02 (dt, J=8.9, 2.5 Hz, 1H), 7.21-7.25 (m, 1H), 7.63 (s,
1H), 8.10 (dd, J=10.0, 2.5 Hz, 1H); MS (DCI/NH.sub.3) m/z 358
(M+H).sup.+; Anal. Calculated for C.sub.22H.sub.28FNO.sub.2: C,
73.92; H, 7.90; N, 3.92. Found: C, 73.87; H, 7.97; N, 3.93.
In Vitro Methods
Human CB.sub.2 Radioligand Binding Assays:
[0444] HEK293 cells stably expressing human CB.sub.2 receptors were
grown until a confluent monolayer was formed. Briefly, the cells
were harvested and homogenized in TE buffer (50 mM Tris-HCl, 1 mM
MgCl.sub.2, and 1 mM EDTA) using a polytron for 2.times.10 second
bursts in the presence of protease inhibitors, followed by
centrifugation at 45,000.times.g for 20 minutes. The final membrane
pellet was re-homogenized in storage buffer (50 mM Tris-HCl, 1 mM
MgCl.sub.2, and 1 mM EDTA and 10% sucrose) and frozen at
-78.degree. C. until used. Saturation binding reactions were
initiated by the addition of membrane preparation (protein
concentration of 5 .mu.g/well for human CB.sub.2) into wells of a
deep well plate containing ([.sup.3H]CP-55,940 (120 Ci/mmol, a
nonselective CB agonist commercially available from Tocris) in
assay buffer (50 mM Tris, 2.5 mM EDTA, 5 mM MgCl.sub.2, and 0.5
mg/mL fatty acid free BSA, pH 7.4). After 90 min incubation at
30.degree. C., binding reaction was terminated by the addition of
300 .mu.l/well of cold assay buffer followed by rapid vacuum
filtration through a UniFilter-96 GF/C filter plates (pre-soaked in
1 mg/mL BSA for 2 hours). The bound activity was counted in a
TopCount using Microscint-20. Saturation experiments were conducted
with twelve concentrations of [.sup.3H]CP-55,940 ranging from 0.01
to 8 nM. Competition experiments were conducted with 0.5 nM
[.sup.3H]CP-55,940 and five concentrations (1 nM to 10 .mu.M) of
displacing ligands. The addition of 10 .mu.M unlabeled CP-55,940
(Tocris, Ellisville, Mo.) was used to assess nonspecific
binding.
[0445] The compounds of the present invention bound (Ki) to
CB.sub.2 receptors less than about 10,000 nM. In a more preferred
embodiment, compounds of the present invention bound to CB.sub.2
receptors less than about 200 nM.
Human CB.sub.1 Radioligand Binding Assay:
[0446] HEK293 human CB.sub.1 membranes were purchased from Perkin
Elmer. Binding was initiated by the addition of membranes (8-12
.mu.g per well) into wells (Scienceware 96-well DeepWell plate,
VWR, West Chester, Pa.) containing [.sup.3H]CP-55,940 (120 Ci/mmol,
Perkin Elmer, Boston, Mass.) and a sufficient volume of assay
buffer (50 mM Tris, 2.5 mM EDTA, 5 mM MgCl.sub.2, and 0.5 mg/mL
fatty acid free BSA, pH 7.4) to bring the total volume to 250
.mu.L. After incubation (30.degree. C. for 90 minutes), binding was
terminated by the addition of 300 .mu.L per well of cold assay
buffer and rapid vacuum filtration (FilterMate Cell Harvester,
Perkin Elmer, Boston, Mass.) through a UniFilter-96 GF/C filter
plate (Perkin Elmer, Boston, Mass.) (pre-soaked in 0.3% PEI at
least 3 hours), followed by five washes with cold assay buffer. The
bound activity was counted in the TopCount using Microscint-20
(both from Perkin Elmer, Boston, Mass.). Competition experiments
were conducted with 1 nM [.sup.3H]CP-55,940 and five concentrations
(1 nM to 10 .mu.M) of displacing ligands. The addition of 10 .mu.M
unlabeled CP-55,940 (Tocris, Ellisville, Mo.) was used to assess
nonspecific binding.
[0447] The CB.sub.1 and CB.sub.2 radioligand binding assays
described herein can be utilized to ascertain the selectivity of
compounds of the present invention for binding to CB.sub.2 relative
to CB.sub.1 receptors.
In Vivo Methods:
Animals
[0448] Adult male Sprague-Dawley rats (250-300 g body weight,
Charles River Laboratories, Portage, Mich.) were used. Animal
handling and experimental protocols were approved by the
Institutional Animal Care and Use Committee (IACUC) at Abbott
Laboratories. For all surgical procedures, animals were maintained
under halothane anesthesia (4% to induce, 2% to maintain), and the
incision sites were sterilized using a 10% povidone-iodine solution
prior to and after surgeries.
Complete Freund's Adjuvant (CFA) Model of Inflammatory Pain
[0449] Chronic inflammatory thermal hyperalgesia was induced by
injection of 150 .mu.l of a 50% solution of CFA in phosphate
buffered saline (PBS) into the plantar surface of the right hind
paw in rats; control animals received only PBS treatment. Thermal
hyperalgesia was assessed 48 hours post CFA injection. Thermal
hyperalgesia was determined using a commercially available thermal
paw stimulator (University Anesthesiology Research and Development
Group (UARDG), University of California, San Diego, Calif.)
described by Hargreaves et al. (Hargreaves, et. al., 1988, Pain 32,
77). Rats were placed into individual plastic cubicles mounted on a
glass surface maintained at 30.degree. C., and allowed a 20 min
habituation period. A thermal stimulus, in the form of radiant heat
emitted from a focused projection bulb, was then applied to the
plantar surface of each hind paw. The stimulus current was
maintained at 4.50.+-.0.05 amp, and the maximum time of exposure
was set at 20.48 sec to limit possible tissue damage. The elapsed
time until a brisk withdrawal of the hind paw from the thermal
stimulus was recorded automatically using photodiode motion
sensors. The right and left hind paw of each rat was tested in
three sequential trials at approximately 5-minute intervals. Paw
withdrawal latency (PWL) was calculated as the mean of the two
shortest latencies.
[0450] Representative compounds of the present invention showed
efficacy at less than about 300 micromoles/kg in the Complete
Freund's Adjuvant (CFA) model of inflammatory pain. In a more
preferred embodiment, compounds of the present invention showed
efficacy at less than about 50 micromoles/kg in the Complete
Freund's Adjuvant (CFA) model of inflammatory pain.
Spinal Nerve Ligation Model of Neuropathic Pain
[0451] A model of spinal nerve ligation-induced (SNL model)
neuropathic pain was produced using the procedure originally
described by Kim and Chung (Kim, S. H. and J. M. Chung, 1992, An
experimental model for peripheral neuropathy produced by segmental
spinal nerve ligation in the rat, Pain 50, 355). The left L5 and L6
spinal nerves of the rat were isolated adjacent to the vertebral
column and tightly ligated with a 5-0 silk suture distal to the
DRG, and care was taken to avoid injury of the L4 spinal nerve.
Sham rats underwent the same procedure, but without nerve ligation.
All animals were allowed to recover for at least one week and not
more than three weeks prior to assessment of tactile allodynia.
[0452] Tactile allodynia was measured using calibrated von Frey
filaments (Stoelting, Wood Dale, Ill.) as previously described
(Chaplan, S. R., F. W. Bach, J. W. Pogrel, J. M. Chung and T. L.
Yaksh, 1994, Quantitative assessment of tactile allodynia in the
rat paw, J. Neurosci. Methods 53, 55). Rats were placed into
inverted individual plastic containers (20.times.12.5.times.20 cm)
on top of a suspended wire mesh grid, and acclimated to the test
chambers for 20 minutes. The von Frey filaments were presented
perpendicularly to the plantar surface of the selected hind paw,
and then held in this position for approximately 8 sec with enough
force to cause a slight bend in the filament. Positive responses
included an abrupt withdrawal of the hind paw from the stimulus, or
flinching behavior immediately following removal of the stimulus. A
50% withdrawal threshold was determined using an up-down procedure
(Dixon, W. J., 1980, Efficient analysis of experimental
observations, Ann. Rev. Pharmacol. Toxicol. 20, 441). Only rats
with a baseline threshold score of less that 4.25 g were used in
this study, and animals demonstrating motor deficit were excluded.
Tactile allodynia thresholds were also assessed in several control
groups, including naive, sham-operated, and saline infused animals
a well as in the contralateral paws of nerve-injured rats.
[0453] Representative compounds of the present invention showed
efficacy at less than about 300 micromoles/kg in the spinal nerve
ligation model of neuropathic pain. In a more preferred embodiment,
compounds of the present invention showed efficacy at less than
about 100 micromoles/kg in the spinal nerve ligation model of
neuropathic pain.
[0454] The data contained herein demonstrates that compounds of the
present invention bind to the CB.sub.2 receptor. Certain compounds
of the present invention were shown to have an analgesic effect in
two types of animal pain models relating to neuropathic and
nociceptive pain.
[0455] In addition to the data contained herein, several lines of
evidence support the assertion that CB.sub.2 receptors play a role
in analgesia. For example, Zimmer et al. have reported that the
nonselective cannabinoid agonist .DELTA..sup.9-THC retains some
analgesic efficacy in CB.sub.1 receptor knockout mice (Zimmer, A.,
et al., Proc. Nat. Acad. Sci., 1999, 96, 5780-5785). HU-308 is one
of the first highly selective CB.sub.2 agonists identified that
elicits an antinociceptive response in the rat formalin model of
persistent pain (Hanus, L., et al., Proc. Nat. Acad. Sci., 1999,
96, 14228-14233). The CB.sub.2-selective cannabiniod ligand AM-1241
exhibits robust analgesic efficacy in animal models of acute
thermal pain (Malan, T. P., et al., Pain, 2001, 93, 239-245;
Ibrahim, M. M., et al., Proc. Nat. Acad. Sci., 2005, 102(8),
3093-3098), persistent pain (Hohmann, A. G., et al., J. Pharmacol.
Exp. Ther., 2004, 308, 446-453), inflammatory pain (Nackley, A. G.,
et al., Neuroscience, 2003, 119, 747-757; Quartilho, A. et al.,
Anesthesiology, 2003, 99, 955-60), and neuropathic pain (Ibrahim,
M. M., et al., Proc. Nat. Acad. Sci., 2003, 100, 10529-10533). The
CB.sub.2-selective partial agonist GW405833, also known as L768242,
is efficacious in rodent models of neuropathic, incisional, and
both chronic and acute inflammatory pain (Valenzano, K. J., et al.,
Neuropharmacology, 2005, 48, 658-672 and Clayton, N., et al., Pain,
2002, 96, 253-260). The analgesic effects induced by these
CB.sub.2-selective ligands are blocked by CB.sub.2 and not by
CB.sub.1 receptor antagonists. Furthermore, at fully efficacious
doses, AM-1241 and GW405833 are devoid of typical CB.sub.1
receptor-mediated CNS side effects, providing evidence that
modulation of CB.sub.2 receptors can produce broad-spectrum pain
relief with reduced side-effect liability.
[0456] The potential exists for CB.sub.2 modulators to have opioid
sparing effects. A synergy between the analgesic effects of
morphine and the nonselective CB agonist .DELTA..sup.9-THC has been
documented (Cichewicz, D. L., Life Sci. 2004, 74, 1317-1324).
Therefore, CB.sub.2 ligands have additive or synergistic analgesic
effects when used in combination with lower doses of morphine or
other opioids, providing a strategy for reducing adverse opioid
events, such as tolerance, constipation, and respiratory
depression, without sacrificing analgesic efficacy.
[0457] CB.sub.2 receptors are present in tissues and cell types
associated with immune functions and CB.sub.2 receptor mRNA is
expressed by human B cells, natural killer cells, monocytes,
neutrophils, and T cells (Galiegue et al., Eur. J. Biochem., 1995,
232, 54-61). Studies with CB.sub.2 knockout mice have suggested a
role for CB.sub.2 receptors in modulating the immune system
(Buckley, N. E., et al., Eur. J. Pharmacol. 2000, 396, 141-149).
Although immune cell development and differentiation are similar in
knockout and wild type animals, the immunosuppressive effects of
.DELTA..sup.9-THC are absent in the CB.sub.2 receptor knockout
mice, providing evidence for the involvement of CB.sub.2 receptors
in immunomodulation. As such, selective CB.sub.2 modulators are
useful for the treatment of autoimmune diseases including but not
limited to multiple sclerosis, rheumatoid arthritis, systemic
lupus, myasthenia gravis, type I diabetes, irritable bowel
syndrome, psoriasis, psoriatic arthritis, and hepatitis; and immune
related disorders including but not limited to tissue rejection in
organ transplants, gluten-sensitive enteropathy (Celiac disease),
asthma, chronic obstructive pulmonary disease, emphysema,
bronchitis, acute respiratory distress syndrome, allergies,
allergic rhinitis, dermatitis, and Sjogren's syndrome.
[0458] Microglial cells are considered to be the immune cells of
the central nervous system (CNS) where they regulate the initiation
and progression of immune responses. They are quiescent and resting
having a ramified morphology as long as the CNS is healthy.
Microglia express a variety of receptors enabling them to survey
the CNS and respond to pathological events. Insult or injury to the
CNS leads to microglial cell activation, which is characterized by
various morphological changes allowing response to the lesion.
Ramifications are retracted and microglia are transformed into
amoeboid-like cells with phagocytic function. They can proliferate,
rapidly migrate to the site of injury, and produce and release
cytokines, chemokines and complement components (Watkins L. R., et
al., Trends in Neuroscience, 2001, 24(8), 450; Kreutzberg, G. W.,
Trends Neurosci., 1996, 19, 312-318). CB.sub.2 receptor expression
on microglia is dependent upon inflammatory state with higher
levels of CB.sub.2 found in primed, proliferating, and migrating
microglia relative to resting or fully activated microglial
(Carlisle, S. J., et al. Int. Immunopharmacol., 2002, 2, 69).
Neuroinflammation induces many changes in microglia cell morphology
and there is an upregulation of CB.sub.2 receptors and other
components of the endocannabinoid system. It is conceivable that
CB.sub.2 receptors may be more susceptible to pharmacological
effects during neuroinflammation (Walter, L., Stella, N., Br. J.
Pharmacol. 2004, 141, 775-785). Neuroinflammation occurs in several
neurodegenerative diseases, and induction of microglial CB.sub.2
receptors has been observed (Carrier, E. J., et al., Current Drug
Targets--CNS & Neurological Disorders, 2005, 4, 657-665). Thus,
CB.sub.2 ligands may be clinically useful for the treatment of
neuroinflammation.
[0459] CB.sub.2 receptor expression has been detected in
perivascular microglial cells within normal, healthy human
cerebellum (Nunez, E., et al., Synapse, 2004, 58, 208-213).
Perivascular cells are immunoregulatory cells located adjacent to
CNS blood vessels and, along with parenchymal microglia and
astrocytes, they play a pivotal role in maintaining CNS homeostasis
and blood-brain barrier functionality (Williams, K., et al., Glia,
2001, 36, 156-164). CB.sub.2 receptor expression has also been
detected on cerebromicrovascular endothelial cells, which represent
a main component of the blood-brain barrier (Golech, S. A., et al.,
Mol. Brain. Res., 2004, 132, 87-92). A recent report demonstrated
that CB.sub.2 receptor expression is up-regulated in the brains of
macaques with simian immunodeficiency virus-induced encephalitis
(Benito, C., et al., J. Neurosci. 2005, 25(10), 2530-2536). Thus,
compounds that affect CB.sub.2 signaling may protect the
blood-brain barrier and be clinically useful in the treatment of
neuroinflammation and a variety of neuroinflammatory disorders
including retroviral encephalitis, which occurs with human
immunodeficiency virus (HIV) infection in the CNS.
[0460] Multiple sclerosis is common immune-mediated disease of the
CNS in which the ability of neurons to conduct impulses becomes
impaired through demyelination and axonal damage. The demyelination
occurs as a consequence of chronic inflammation and ultimately
leads to a broad range of clinical symptoms that fluctuate
unpredictably and generally worsen with age. These include painful
muscle spasms, tremor, ataxia, motor weakness, sphincter
dysfunction, and difficulty speaking (Pertwee, R. G., Pharmacol.
Ther. 2002, 95, 165-174). The CB.sub.2 receptor is up-regulated on
activated microglial cells during experimental autoimmune
encephalomyelitis (EAE) (Maresz, K., et al., J. Neurochem. 2005,
95, 437-445). CB.sub.2 receptor activation prevents the recruitment
of inflammatory cells such as leukocytes into the CNS (Ni, X., et
al., Multiple Sclerosis, 2004, 10, 158-164) and plays a protective
role in experimental, progressive demyelination (Arevalo-Martin,
A.; et al., J. Neurosci., 2003, 23(7), 2511-2516), which are
critical features in the development of multiple sclerosis. Thus,
CB.sub.2 receptor modulators provide a unique treatment for
demyelinating pathologies.
[0461] Alzheimer's disease is a chronic neurodegenerative disorder
accounting for the most common form of elderly dementia. Recent
studies have revealed that CB.sub.2 receptor expression is
upregulated in neuritic plaque-associated microglia from brains of
Alzheimer's disease patients (Benito, C., et al., J. Neurosci.,
2003, 23(35), 11136-11141). In vitro, treatment with the CB.sub.2
agonist JWH-133 abrogated .beta.-amyloid-induced microglial
activation and neurotoxicity, effects that can be blocked by the
CB.sub.2 antagonist SR144528 (Ramirez, B. G., et al., J. Neurosci.
2005, 25(8), 1904-1913). CB.sub.2 modulators possess both
anti-inflammatory and neuroprotective actions and thus have
clinical utility in treating neuroinflammation and in providing
neuroprotection associated with the development of Alzheimer's
disease.
[0462] Increased levels of epithelial CB.sub.2 receptor expression
are observed in human inflammatory bowel disease tissue (Wright,
K., et al., Gastroenterology, 2005, 129, 437-453). Activation of
CB.sub.2 receptors re-established normal gastrointestinal transit
after endotoxic inflammation was induced in rats (Mathison, R., et
al., Br. J. Pharmacol. 2004, 142, 1247-1254). CB.sub.2 receptor
activation in a human colonic epithelial cell line inhibited
TNF-.alpha.-induced interleukin-8 (IL-8) release (Ihenetu, K. et
al., Eur. J. Pharmacol. 2003, 458, 207-215). Chemokines released
from the epithelium, such as the neutrophil chemoattractant IL-8,
are upregulated in inflammatory bowel disease (Warhurst, A. C., et
al., Gut, 1998, 42, 208-213). Thus, administration of CB.sub.2
receptor modulators represents a novel approach for the treatment
of inflammation and disorders of the gastrointestinal tract
including but not limited to inflammatory bowel disease, irritable
bowel syndrome, secretory diarrhea, ulcerative colitis, Crohn's
disease and gastroesophageal reflux disease (GERD).
[0463] Hepatic fibrosis occurs as a response to chronic liver
injury and ultimately leads to cirrhosis, which is a major
worldwide health issue due to the severe accompanying complications
of portal hypertension, liver failure, and hepatocellular carcinoma
(Lotersztajn, S., et al., Annu. Rev. Pharmacol. Toxicol., 2005, 45,
605-628). Although CB.sub.2 receptors were not detectable in normal
human liver, CB.sub.2 receptors were expressed liver biopsy
specimens from patients with cirrhosis. Activation of CB.sub.2
receptors in cultured hepatic myofibroblasts produced potent
antifibrogenic effects (Julien, B., et al., Gastroenterology, 2005,
128, 742-755). In addition, CB.sub.2 knockout mice developed
enhanced liver fibrosis after chronic administration of carbon
tetrachloride relative to wild-type mice. Administration of
CB.sub.2 receptor modulators represents a unique approach for the
treatment of liver fibrosis.
[0464] CB.sub.2 receptors are involved in the neuroprotective and
anti-inflammatory mechanisms induced by the interleukin-1 receptor
antagonist (IL-1ra) (Molina-Holgado, F., et al., J. Neurosci.,
2003, 23(16), 6470-6474). IL-1ra is an important anti-inflammatory
cytokine that protects against ischemic, excitotoxic, and traumatic
brain insults. CB.sub.2 receptors play a role in mediating these
neuroprotective effects indicating that CB.sub.2 ligands are useful
in the treatment of traumatic brain injury, stroke, and in
mitigating brain damage.
[0465] Cough is a dominant and persistent symptom of many
inflammatory lung diseases, including asthma, chronic obstructive
pulmonary disease, viral infections, and pulmonary fibrosis (Patel,
H. J., et al., Brit. J. Pharmacol., 2003, 140, 261-268). Recent
studies have provided evidence for the existence of neuronal
CB.sub.2 receptors in the airways, and have demonstrated a role for
CB.sub.2 receptor activation in cough suppression (Patel, H. J., et
al., Brit. J. Pharmacol., 2003, 140, 261-268 and Yoshihara, S., et
al., Am. J. Respir. Crit. Care Med., 2004, 170, 941-946). Both
exogenous and endogenous cannabinoid ligands inhibit the activation
of C-fibers via CB.sub.2 receptors and reduce neurogenic
inflammatory reactions in airway tissues (Yoshihara, S., et al., J.
Pharmacol. Sci. 2005, 98(1), 77-82; Yoshihara, S., et al., Allergy
and Immunology, 2005, 138, 80-87). Thus, CB.sub.2-selective
modulators have utility as antitussive agents for the treatment
pulmonary inflammation, chronic cough, and a variety of airway
inflammatory diseases including but not limited to asthma, chronic
obstructive pulmonary disease, and pulmonary fibrosis.
[0466] Osteoporosis is a disease characterized by reduced bone
mass, which leads to deterioration of bone microstructure and
increased susceptibility to fracture. Age is associated with bone
loss and it is estimated that 50% of all Caucasian women will have
osteoporosis by the age of 80 (Ralston, S. H., Curr. Opin.
Pharmacol., 2003, 3, 286-290). There is a substantial genetic
contribution to bone mass density and the CB.sub.2 receptor gene is
associated with human osteoporosis (Karsak, M., et al., Human
Molecular Genetics, 2005, 14(22), 3389-3396). Osteoclasts and
osteoblasts are largely responsible for maintaining bone structure
and function through a process called remodeling, which involves
resorption and synthesis of bone (Boyle, W. J., et al., Nature,
2003, 423, 337-342). CB.sub.2 receptor expression has been detected
on osteoclasts and osteoblastic precursor cells, and administration
of a CB.sub.2 agonist in mice caused a dose-dependent increase in
bone formation (Grotenhermen, F. and Muller-Vahl, K., Expert Opin.
Pharmacother., 2003, 4(12), 2367-2371). Cannabinoid inverse
agonists, including the CB.sub.2-selective inverse agonist
SR144528, have been shown to inhibit osteoclast activity and
reverse ovariectomy-induced bone loss in mice, which is a model for
post-menopausal osteoporosis (Ralston, S. H., et al., Nature
Medicine, 2005, 11, 774-779). Thus, CB.sub.2 modulators are useful
for the treatment and prevention of osteoporosis, osteoarthritis,
and bone disorders.
[0467] Artherosclerosis is a chronic inflammatory disease and is a
leading cause of heart disease and stroke. CB.sub.2 receptors have
been detected in both human and mouse atherosclerotic plaques.
Administration of low doses of THC in apolipoprotein E knockout
mice slowed the progression of atherosclerotic lesions, and these
effects were inhibited by the CB.sub.2-selective antagonist
SR144528 (Steffens, S., et al., Nature, 2005, 434, 782-786). Thus,
compounds with activity at the CB.sub.2 receptor are clinically
useful for the treatment of atheroscelorsis.
[0468] CB.sub.2 receptors are expressed on malignant cells of the
immune system and targeting CB.sub.2 receptors to induce apoptosis
may constitute a novel approach to treating malignancies of the
immune system. Selective CB.sub.2 agonists induce regression of
malignant gliomas (Sanchez, C., et al., Cancer Res., 2001, 61,
5784-5789), skin carcinomas (Casanova, M. L., et al., J. Clin.
Invest., 2003, 111, 43-50), and lymphomas (McKallip, R. J., et al.,
Blood, 2002, 15(2), 637-634). Thus, CB.sub.2 modulators have
utility as anticancer agents against tumors of immune origin.
[0469] Activation of CB.sub.2 receptors has been demonstrated to
protect the heart against the deleterious effects of ischemia and
reperfusion (Lepicier, P., et al., Brit. J. Pharm. 2003, 139,
805-815; Bouchard, J.-F., et al., Life Sci. 2003, 72, 1859-1870;
Filippo, C. D., et al., J. Leukoc. Biol. 2004, 75, 453-459). Thus,
CB.sub.2 modulators have utility for the treatment or prophylaxis
of cardiovascular disease and the development of myocardial
infarction.
[0470] The present invention also provides pharmaceutical
compositions that comprise compounds of the present invention. The
pharmaceutical compositions comprise compounds of the present
invention formulated together with one or more non-toxic
pharmaceutically acceptable carriers.
[0471] The pharmaceutical compositions of this invention can be
administered to humans and other mammals orally, rectally,
parenterally, intracistemally, intravaginally, topically (as by
powders, ointments or drops), bucally or as an oral or nasal spray.
The term "parenterally," as used herein, refers to modes of
administration that include intravenous, intramuscular,
intraperitoneal, intrasternal, subcutaneous and intraarticular
injection and infusion.
[0472] The term "pharmaceutically acceptable carrier," as used
herein, means a non-toxic, inert solid, semi-solid or liquid
filler, diluent, encapsulating material or formulation auxiliary of
any type. Some examples of materials which can serve as
pharmaceutically acceptable carriers are sugars such as, but not
limited to, lactose, glucose and sucrose; starches such as, but not
limited to, corn starch and potato starch; cellulose and its
derivatives such as, but not limited to, sodium carboxymethyl
cellulose, ethyl cellulose and cellulose acetate; powdered
tragacanth; malt; gelatin; talc; excipients such as, but not
limited to, cocoa butter and suppository waxes; oils such as, but
not limited to, peanut oil, cottonseed oil, safflower oil, sesame
oil, olive oil, corn oil and soybean oil; glycols; such as
propylene glycol; esters such as, but not limited to, ethyl oleate
and ethyl laurate; agar; buffering agents such as, but not limited
to, magnesium hydroxide and aluminum hydroxide; alginic acid;
pyrogen-free water; isotonic saline; Ringer's solution; ethyl
alcohol, and phosphate buffer solutions, as well as other non-toxic
compatible lubricants such as, but not limited to, sodium lauryl
sulfate and magnesium stearate, as well as coloring agents,
releasing agents, coating agents, sweetening, flavoring and
perfuming agents, preservatives and antioxidants can also be
present in the composition, according to the judgment of the
formulator.
[0473] Pharmaceutical compositions of this invention for parenteral
injection comprise pharmaceutically acceptable sterile aqueous or
nonaqueous solutions, dispersions, suspensions or emulsions as well
as sterile powders for reconstitution into sterile injectable
solutions or dispersions just prior to use. Examples of suitable
aqueous and nonaqueous carriers, diluents, solvents or vehicles
include water, ethanol, polyols (such as glycerol, propylene
glycol, polyethylene glycol and the like), vegetable oils (such as
olive oil), injectable organic esters (such as ethyl oleate) and
suitable mixtures thereof. Proper fluidity can be maintained, for
example, by the use of coating materials such as lecithin, by the
maintenance of the required particle size in the case of
dispersions and by the use of surfactants.
[0474] These compositions may also contain adjuvants such as
preservatives, wetting agents, emulsifying agents and dispersing
agents. Prevention of the action of microorganisms can be ensured
by the inclusion of various antibacterial and antifungal agents,
for example, paraben, chlorobutanol, phenol sorbic acid and the
like. It may also be desirable to include isotonic agents such as
sugars, sodium chloride and the like. Prolonged absorption of the
injectable pharmaceutical form can be brought about by the
inclusion of agents, which delay absorption such as aluminum
monostearate and gelatin.
[0475] In some cases, in order to prolong the effect of the drug,
it is desirable to slow the absorption of the drug from
subcutaneous or intramuscular injection. This can be accomplished
by the use of a liquid suspension of crystalline or amorphous
material with poor water solubility. The rate of absorption of the
drug then depends upon its rate of dissolution that, in turn, may
depend upon crystal size and crystalline form. Alternatively,
delayed absorption of a parenterally administered drug form is
accomplished by dissolving or suspending the drug in an oil
vehicle.
[0476] Injectable depot forms are made by forming microencapsule
matrices of the drug in biodegradable polymers such as
polylactide-polyglycolide. Depending upon the ratio of drug to
polymer and the nature of the particular polymer employed, the rate
of drug release can be controlled. Examples of other biodegradable
polymers include poly(orthoesters) and poly(anhydrides). Depot
injectable formulations are also prepared by entrapping the drug in
liposomes or microemulsions, which are compatible with body
tissues.
[0477] The injectable formulations can be sterilized, for example,
by filtration through a bacterial-retaining filter or by
incorporating sterilizing agents in the form of sterile solid
compositions which can be dissolved or dispersed in sterile water
or other sterile injectable medium just prior to use.
[0478] Solid dosage forms for oral administration include capsules,
tablets, pills, powders and granules. In such solid dosage forms,
the active compound may be mixed with at least one inert,
pharmaceutically acceptable carrier or excipient, such as sodium
citrate or dicalcium phosphate and/or a) fillers or extenders such
as starches, lactose, sucrose, glucose, mannitol and silicic acid;
b) binders such as carboxymethylcellulose, alginates, gelatin,
polyvinylpyrrolidone, sucrose and acacia; c) humectants such as
glycerol; d) disintegrating agents such as agar-agar, calcium
carbonate, potato or tapioca starch, alginic acid, certain
silicates and sodium carbonate; e) solution retarding agents such
as paraffin; f) absorption accelerators such as quaternary ammonium
compounds; g) wetting agents such as cetyl alcohol and glycerol
monostearate; h) absorbents such as kaolin and bentonite clay and
i) lubricants such as talc, calcium stearate, magnesium stearate,
solid polyethylene glycols, sodium lauryl sulfate and mixtures
thereof. In the case of capsules, tablets and pills, the dosage
form may also comprise buffering agents.
[0479] Solid compositions of a similar type may also be employed as
fillers in soft and hard-filled gelatin capsules using such
carriers as lactose or milk sugar as well as high molecular weight
polyethylene glycols and the like.
[0480] The solid dosage forms of tablets, dragees, capsules, pills
and granules can be prepared with coatings and shells such as
enteric coatings and other coatings well-known in the
pharmaceutical formulating art. They may optionally contain
opacifying agents and may also be of a composition such that they
release the active ingredient(s) only, or preferentially, in a
certain part of the intestinal tract, optionally, in a delayed
manner. Examples of embedding compositions that can be used include
polymeric substances and waxes.
[0481] The active compounds can also be in micro-encapsulated form,
if appropriate, with one or more of the above-mentioned
carriers.
[0482] Liquid dosage forms for oral administration include
pharmaceutically acceptable emulsions, solutions, suspensions,
syrups and elixirs. In addition to the active compounds, the liquid
dosage forms may contain inert diluents commonly used in the art
such as, for example, water or other solvents, solubilizing agents
and emulsifiers such as ethyl alcohol, isopropyl alcohol, ethyl
carbonate, ethyl acetate, benzyl alcohol, benzyl benzoate,
propylene glycol, 1,3-butylene glycol, dimethyl formamide, oils (in
particular, cottonseed, groundnut, corn, germ, olive, castor and
sesame oils), glycerol, tetrahydrofurfuryl alcohol, polyethylene
glycols and fatty acid esters of sorbitan and mixtures thereof.
[0483] Besides inert diluents, the oral compositions may also
include adjuvants such as wetting agents, emulsifying and
suspending agents, sweetening, flavoring and perfuming agents.
[0484] Suspensions, in addition to the active compounds, may
contain suspending agents as, for example, ethoxylated isostearyl
alcohols, polyoxyethylene sorbitol and sorbitan esters,
microcrystalline cellulose, aluminum metahydroxide, bentonite,
agar-agar, tragacanth and mixtures thereof.
[0485] Compositions for rectal or vaginal administration are
preferably suppositories which can be prepared by mixing the
compounds of this invention with suitable non-irritating carriers
or carriers such as cocoa butter, polyethylene glycol or a
suppository wax which are solid at room temperature but liquid at
body temperature and therefore melt in the rectum or vaginal cavity
and release the active compound.
[0486] Compounds of the present invention can also be administered
in the form of liposomes. As is known in the art, liposomes are
generally derived from phospholipids or other lipid substances.
Liposomes are formed by mono- or multi-lamellar hydrated liquid
crystals that are dispersed in an aqueous medium. Any non-toxic,
physiologically acceptable and metabolizable lipid capable of
forming liposomes can be used. The present compositions in liposome
form can contain, in addition to a compound of the present
invention, stabilizers, preservatives, excipients and the like. The
preferred lipids are natural and synthetic phospholipids and
phosphatidyl cholines (lecithins) used separately or together.
[0487] Methods to form liposomes are known in the art. See, for
example, Prescott, Ed., Methods in Cell Biology, Volume XIV,
Academic Press, New York, N.Y. (1976), p. 33 et seq.
[0488] Dosage forms for topical administration of a compound of
this invention include powders, sprays, ointments and inhalants.
The active compound may be mixed under sterile conditions with a
pharmaceutically acceptable carrier and any needed preservatives,
buffers or propellants, which may be required. Opthalmic
formulations, eye ointments, powders and solutions are also
contemplated as being within the scope of this invention.
[0489] Actual dosage levels of active ingredients in the
pharmaceutical compositions of this invention can be varied so as
to obtain an amount of the active compound(s) that is effective to
achieve the desired therapeutic response for a particular patient,
compositions and mode of administration. The selected dosage level
will depend upon the activity of the particular compound, the route
of administration, the severity of the condition being treated and
the condition and prior medical history of the patient being
treated.
[0490] When used in the above or other treatments, a
therapeutically effective amount of one of the compounds of the
present invention can be employed in pure form or, where such forms
exist, in pharmaceutically acceptable salt, ester or prodrug form.
The phrase "therapeutically effective amount" of the compound of
the invention means a sufficient amount of the compound to treat
disorders, at a reasonable benefit/risk ratio applicable to any
medical treatment. It will be understood, however, that the total
daily usage of the compounds and compositions of the present
invention will be decided by the attending physician within the
scope of sound medical judgement. The specific therapeutically
effective dose level for any particular patient will depend upon a
variety of factors including the disorder being treated and the
severity of the disorder; activity of the specific compound
employed; the specific composition employed; the age, body weight,
general health, sex and diet of the patient; the time of
administration, route of administration, and rate of excretion of
the specific compound employed; the duration of the treatment;
drugs used in combination or coincidental with the specific
compound employed; and like factors well known in the medical
arts.
[0491] The term "pharmaceutically acceptable salt," as used herein,
means salts derived from inorganic or organic acids. The salts can
be prepared in situ during the final isolation and purification of
compounds of Formula (J) or separately by reacting the free base of
a compound of Formula (I) with an inorganic or organic acid.
Representative acid addition salts include, but are not limited to,
acetate, adipate, alginate, citrate, aspartate, benzoate,
benzenesulfonate, bisulfate, butyrate, camphorate,
camphorsulfonate, digluconate, glycerophosphate, hemisulfate,
heptanoate, hexanoate, fumarate, hydrochloride, hydrobromide,
hydroiodide, 2-hydroxyethansulfonate (isethionate), lactate,
maleate, fumarate, methanesulfonate, nicotinate,
2-naphthalenesulfonate, oxalate, pamoate, pectinate, persulfate,
3-phenylpropionate, picrate, pivalate, propionate, succinate,
sulfate, (L) tartrate, (D) tartrate, (DL) tartrate, thiocyanate,
phosphate, glutamate, bicarbonate, p-toluenesulfonate, and
undecanoate.
[0492] The term "pharmaceutically acceptable prodrug" or "prodrug,"
as used herein, represents those prodrugs of the compounds of the
present invention which are, within the scope of sound medical
judgement, suitable for use in contact with the tissues of humans
and lower animals without undue toxicity, irritation, allergic
response, and the like. Prodrugs of the present invention may be
rapidly transformed in vivo to compounds of Formula (I), for
example, by hydrolysis in blood.
[0493] The present invention contemplates compounds of Formula (I)
formed by synthetic means or formed by in vivo
biotransformation.
[0494] The compounds of the invention can exist in unsolvated as
well as solvated forms, including hydrated forms, such as
hemi-hydrates. In general, the solvated forms, with
pharmaceutically acceptable solvents such as water and ethanol
among others, are equivalent to the unsolvated forms for the
purposes of the invention.
[0495] The total daily dose of the compounds of this invention
administered to a human or lower animal may range from about 0.003
to about 30 mg/kg/day. For purposes of oral administration, more
preferable doses can be in the range of from about 0.01 to about 10
mg/kg/day. If desired, the effective daily dose can be divided into
multiple doses for purposes of administration; consequently, single
dose compositions may contain such amounts or submultiples thereof
to make up the daily dose.
* * * * *