U.S. patent application number 13/412946 was filed with the patent office on 2012-10-11 for 2-heteroaryl carboxamides.
This patent application is currently assigned to Bayer Schering Pharma AG. Invention is credited to Frank-Gerhard Boss, Christina Erb, Timo Flessner, Frank-Thorsten Hafner, Joachim Luithle, Katrin Schnizler, Franz-Josef Van Der Staay, Marja Van Kampen.
Application Number | 20120258964 13/412946 |
Document ID | / |
Family ID | 29740887 |
Filed Date | 2012-10-11 |
United States Patent
Application |
20120258964 |
Kind Code |
A1 |
Luithle; Joachim ; et
al. |
October 11, 2012 |
2-HETEROARYL CARBOXAMIDES
Abstract
The invention relates to novel 2-heteroaryl carboxamides and to
the use thereof for producing medicaments for the treatment and/or
prophylaxis of diseases and for improving perception,
concentration, learning and/or memory.
Inventors: |
Luithle; Joachim; (Wulfrath,
DE) ; Boss; Frank-Gerhard; (Berkshire, GB) ;
Erb; Christina; (Kriftel, DE) ; Hafner;
Frank-Thorsten; (Wuppertal, DE) ; Schnizler;
Katrin; (Rodenbach, DE) ; Flessner; Timo;
(Wuppertal, DE) ; Van Kampen; Marja; (Dusseldorf,
DE) ; Van Der Staay; Franz-Josef; (Dronten,
NL) |
Assignee: |
Bayer Schering Pharma AG
Berlin
DE
|
Family ID: |
29740887 |
Appl. No.: |
13/412946 |
Filed: |
March 6, 2012 |
Related U.S. Patent Documents
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Application
Number |
Filing Date |
Patent Number |
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13179957 |
Jul 11, 2011 |
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13412946 |
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10516777 |
Jan 13, 2006 |
7977485 |
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PCT/EP03/05735 |
Jun 2, 2003 |
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13179957 |
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Current U.S.
Class: |
514/230.8 ;
514/233.2; 514/253.04; 514/256; 514/305; 544/127; 544/333; 544/362;
546/133 |
Current CPC
Class: |
A61P 25/00 20180101;
A61P 25/28 20180101; C07D 453/02 20130101 |
Class at
Publication: |
514/230.8 ;
546/133; 514/305; 544/127; 514/233.2; 544/362; 514/253.04; 544/333;
514/256 |
International
Class: |
C07D 453/02 20060101
C07D453/02; A61K 31/5377 20060101 A61K031/5377; A61P 25/28 20060101
A61P025/28; A61K 31/506 20060101 A61K031/506; A61P 25/00 20060101
A61P025/00; A61K 31/439 20060101 A61K031/439; A61K 31/496 20060101
A61K031/496 |
Foreign Application Data
Date |
Code |
Application Number |
Jun 10, 2002 |
DE |
10225536.9 |
Dec 6, 2002 |
DE |
10257078.7 |
Dec 10, 2002 |
DE |
10257537.1 |
Feb 13, 2003 |
DE |
10305922.9 |
Claims
1. Compounds of the formula ##STR00242## in which R.sub.1 is
1-azabicyclo[2.2.2]oct-3-yl, which is optionally substituted via
the nitrogen atom by a radical selected from the group of
C.sub.1-C.sub.4-alkyl, benzyl and oxy, R.sup.2 is hydrogen or
C.sub.1-C.sub.6-alkyl, R.sup.3 is hydrogen, halogen or
C.sub.1-C.sub.6-alkyl, R.sup.4 is hydrogen, halogen, cyano, amino,
trifluoromethyl, trifluoromethoxy, C.sub.1-C.sub.6-alkyl,
C.sub.1-C.sub.6-alkylcarbonyl, C.sub.1-C.sub.6-alkylamino, formyl,
hydroxycarbonyl, C.sub.1-C.sub.6-alkoxy,
C.sub.1-C.sub.6-alkoxycarbonyl, C.sub.1-C.sub.6-alkylthio,
C.sub.1-C.sub.6-alkylcarbonylamino,
C.sub.1-C.sub.6-alkylaminocarbonyl,
C.sub.1-C.sub.4-alkylsulphonylamino,
C.sub.3-C.sub.8-cycloalkylcarbonylamino,
C.sub.3-C.sub.6-cycloalkylaminocarbonyl, pyrrolyl,
C.sub.1-C.sub.6-alkylaminocarbonylamino, heterocyclylcarbonyl,
heterocyclylcarbonylamino, heteroarylcarbonylamino, hydroxyl,
phenyl or heterocyclyl, where C.sub.1-C.sub.6-alkyl may optionally
be substituted by hydroxyl, cyano, amino,
C.sub.1-C.sub.6-alkylaminocarbonylamino,
C.sub.1-C.sub.6-alkylaminocarboxyl, heterocyclyl or aryl,
C.sub.1-C.sub.6-alkylaminocarbonyl may optionally be substituted by
C.sub.1-C.sub.6-alkoxy or C.sub.1-C.sub.6-alkylamino,
C.sub.1-C.sub.6-alkylcarbonylamino may optionally be substituted by
C.sub.1-C.sub.6-alkoxy, and heterocyclyl may optionally be
substituted by oxo, A is oxygen or sulphur, the ring B is benzo or
pyrido, each of which are optionally substituted by radicals from
the series halogen, cyano, formyl, trifluoromethyl,
trifluoromethoxy, nitro, amino, C.sub.1-C.sub.6-alkyl and
C.sub.1-C.sub.6-alkoxy, and E is C.ident.C, arylene and
heteroarylene, where arylene and heteroarylene may be substituted
by radicals from the series halogen, cyano, trifluoromethyl,
trifluoromethoxy, nitro, amino, C.sub.1-C.sub.6-alkoxy and
C.sub.1-C.sub.6-alkyl, and the solvates, salts or solvates of the
salts of these compounds.
2. Compounds according to claim 1, of the formula (I), in which
R.sup.1 is 1-azabicyclo[2.2.2]oct-3-yl, R.sup.2 is hydrogen or
C.sub.1-C.sub.4-alkyl, R.sup.3 is hydrogen, fluorine, chlorine,
bromine or C.sub.1-C.sub.4-alkyl, R.sup.4 is hydrogen, fluorine,
chlorine, bromine, cyano, amino, trifluoromethyl, trifluoromethoxy,
C.sub.1-C.sub.4-alkyl, C.sub.1-C.sub.4-alkylcarbonyl,
C.sub.1-C.sub.4-alkylamino, formyl, hydroxycarbonyl,
C.sub.1-C.sub.4-alkoxy, C.sub.1-C.sub.4-alkoxycarbonyl,
C.sub.1-C.sub.4-alkylcarbonylamino,
C.sub.1-C.sub.4-alkylaminocarbonyl,
C.sub.1-C.sub.4-alkylsulphonylamino,
C.sub.3-C.sub.6-cycloalkyl-carbonylamino,
C.sub.3-C.sub.6-cycloalkylaminocarbonyl, pyrrolyl,
C.sub.1-C.sub.4-alkylaminocarbonylamino, heterocyclylcarbonyl,
heterocyclylcarbonylamino, heteroarylcarbonylamino, hydroxyl,
phenyl or heterocyclyl, where C.sub.1-C.sub.4-alkyl may optionally
be substituted by hydroxyl, cyano, amino,
C.sub.1-C.sub.4-alkylaminocarbonylamino,
C.sub.1-C.sub.4-alkylaminocarboxyl, heterocyclyl or aryl,
C.sub.1-C.sub.4-alkylaminocarbonyl may optionally be substituted by
C.sub.1-C.sub.4-alkoxy or C.sub.1-C.sub.4-alkylamino,
C.sub.1-C.sub.4-alkylcarbonylamino may optionally be substituted by
C.sub.1-C.sub.4-alkoxy, and, heterocyclyl may optionally be
substituted by oxo, A is oxygen or sulphur; the ring B is benzo or
pyrido, each of which are optionally substituted by radicals from
the series halogen, cyano, trifluoromethyl, trifluoromethoxy and
C.sub.1-C.sub.4-alkyl, and E is C.ident.C, arylene and
heteroarylene, where arylene and heteroarylene may be substituted
by radicals from the series halogen, cyano, trifluoromethyl,
trifluoromethoxy, nitro, amino, C.sub.1-C.sub.4-alkoxy and
C.sub.1-C.sub.4-alkyl, and the solvates, salts or solvates of the
salts of these compounds.
3. Compounds according to claims 1 and 2, of the formula (I), in
which R.sup.1 is 1-azabicyclo[2.2.2]oct-3-yl, R.sup.2 and R.sup.3
are hydrogen, R.sup.4 is hydrogen, fluorine, chlorine, bromine,
cyano, amino, trifluoromethyl, trifluoromethoxy,
C.sub.1-C.sub.4-alkylcarbonyl, C.sub.1-C.sub.4-alkylamino, formyl,
hydroxycarbonyl, C.sub.1-C.sub.4-alkoxy,
C.sub.1-C.sub.4-alkoxycarbonyl, C.sub.1-C.sub.6-alkylthio,
C.sub.1-C.sub.4-alkylcarbonylamino,
C.sub.1-C.sub.4-alkylaminocarbonyl,
C.sub.1-C.sub.4-alkylsulphonylamino,
C.sub.3-C.sub.6-cycloalkyl-carbonylamino,
C.sub.3-C.sub.6-cycloalkylaminocarbonyl, pyrrolyl,
C.sub.1-C.sub.4-alkylaminocarbonylamino, heterocyclylcarbonyl,
heterocyclylcarbonylamino, heteroarylcarbonylamino, hydroxyl,
phenyl or heterocyclyl, where C.sub.1-C.sub.4-alkyl may optionally
be substituted by hydroxyl, cyano, amino,
C.sub.1-C.sub.4-alkylaminocarbonylamino,
C.sub.1-C.sub.4-alkylaminocarboxyl, heterocyclyl or aryl,
C.sub.1-C.sub.4-alkylaminocarbonyl may optionally be substituted by
C.sub.1-C.sub.4-alkoxy or C.sub.1-C.sub.4-alkylamino,
C.sub.1-C.sub.4-alkylcarbonylamino may optionally be substituted by
C.sub.1-C.sub.4-alkoxy, and heterocyclyl may optionally be
substituted by oxo, A is oxygen, the ring B is benzo or pyrido,
each of which are optionally substituted by radicals from the
series halogen, cyano, trifluoromethyl, trifluoromethoxy and
C.sub.1-C.sub.4-alkyl, and E is C.ident.C, arylene and
heteroarylene, where arylene and heteroarylene may be substituted
by radicals from the series halogen, cyano, trifluoromethyl,
trifluoromethoxy, nitro, amino, C.sub.1-C.sub.4-alkoxy and
C.sub.1-C.sub.4-alkyl, and the solvates, salts or solvates of the
salts of these compounds.
4. Compounds according to claims 1 to 3, of the formula (I), in
which R.sup.1 is 1-azabicyclo[2.2.2]oct-3-yl, R.sup.2 is hydrogen
or C.sub.1-C.sub.6-alkyl, R.sup.3 is hydrogen, halogen or
C.sub.1-C.sub.6-alkyl, R.sup.4 is hydrogen, halogen, cyano, amino,
trifluoromethyl, trifluoromethoxy, C.sub.1-C.sub.6-alkyl,
C.sub.1-C.sub.6-alkylcarbonyl, C.sub.1-C.sub.6-alkylamino, formyl,
hydroxycarbonyl, C.sub.1-C.sub.6-alkoxy,
C.sub.1-C.sub.6-alkoxycarbonyl, C.sub.1-C.sub.6-alkylthio,
C.sub.1-C.sub.6-alkylcarbonylamino,
C.sub.1-C.sub.4-alkylsulphonylamino,
C.sub.3-C.sub.8-cycloalkylcarbonylamino, pyrrolyl,
C.sub.1-C.sub.6-alkylaminocarbonylamino, heterocyclylcarbonyl,
phenyl or heterocyclyl, where C.sub.1-C.sub.6-alkyl may optionally
be substituted by hydroxyl, amino,
C.sub.1-C.sub.6-alkylaminocarbonylamino,
C.sub.1-C.sub.6-alkylaminocarboxyl, heterocyclyl or aryl,
C.sub.1-C.sub.6-alkylcarbonylamino may optionally be substituted by
C.sub.1-C.sub.6-alkoxy, and heterocyclyl may optionally be
substituted by oxo, A is oxygen or sulphur, the ring B is benzo or
pyrido, each of which are optionally substituted by radicals from
the series halogen, cyano, formyl, trifluoromethyl,
trifluoromethoxy, nitro, amino, C.sub.1-C.sub.6-alkyl and
C.sub.1-C.sub.6-alkoxy, and E is C.ident.C, arylene and
heteroarylene, where arylene and heteroarylene are optionally
substituted by radicals from the series halogen, cyano,
trifluoromethyl, trifluoromethoxy, nitro, amino,
C.sub.1-C.sub.6-alkoxy and C.sub.1-C.sub.6-alkyl, and the solvates,
salts or solvates of the salts of these compounds.
5. Compounds of the formula (I) according to claims 1 to 4, in
which R.sup.1 is 1'-azabicyclo[2.2.2]oct-3-yl, R.sup.2 is hydrogen
or C.sub.1-C.sub.6-alkyl, R.sup.3 is hydrogen, halogen or
C.sub.1-C.sub.6-alkyl, R.sup.4 is hydrogen, halogen, cyano,
trifluoromethyl, trifluoromethoxy, C.sub.1-C.sub.6-alkyl,
C.sub.1-C.sub.6-alkoxy or heterocyclyl, where alkyl is optionally
substituted by a hydroxyl radical, A is oxygen or sulphur, the ring
B is benzo or pyrido, each of which are optionally substituted by
radicals from the series halogen, cyano, trifluoromethyl,
trifluoromethoxy, nitro, amino, C.sub.1-C.sub.6-alkyl and
C.sub.1-C.sub.6-alkoxy, and E is C.ident.C, arylene or
heteroarylene, where arylene and heteroarylene are optionally
substituted by radicals from the series halogen, cyano,
trifluoromethyl, trifluoromethoxy, nitro, amino,
C.sub.1-C.sub.6-alkyl and C.sub.1-C.sub.6-alkoxy, and the solvates,
salts or solvates of the salts of these, compounds.
6. Compounds according to claims 1 to 5, of the formula
##STR00243## in which R.sup.1 is (3R)-1-azabicyclo[2.2.2]oct-3-yl,
R.sup.2 and R.sup.3 are, independently of one another, hydrogen or
methyl, R.sup.4 is hydrogen, halogen, cyano, trifluoromethyl,
trifluoromethoxy, C.sub.1-C.sub.6-alkyl, C.sub.1-C.sub.6-alkoxy or
heterocyclyl, where alkyl is optionally substituted by a hydroxyl
radical, and R.sup.B is hydrogen, halogen, cyano, trifluoromethyl,
trifluoromethoxy, nitro, amino, C.sub.1-C.sub.6-alkyl or
C.sub.1-C.sub.6-alkoxy, and the solvates, salts or solvates of the
salts of these compounds.
7. Compounds according to claims 1 to 6, of the formula
##STR00244## in which R.sup.1 is (3R)-1-azabicyclo[2.2.2]oct-3-yl,
R.sup.2 and R.sup.3 are, independently of one another, hydrogen or
methyl, R.sup.4 is hydrogen, halogen, cyano, trifluoromethyl,
trifluoromethoxy, C.sub.1-C.sub.6-alkyl, C.sub.1-C.sub.6-alkoxy or
heterocyclyl, where alkyl is optionally substituted by a hydroxyl
radical, and R.sup.B is hydrogen, halogen, cyano, trifluoromethyl,
trifluoromethoxy, nitro, amino, C.sub.1-C.sub.6-alkyl and
C.sub.1-C.sub.6-alkoxy, and the solvates, salts or solvates of the
salts of these compounds.
8. Compounds according to claims 1 to 7, where R.sup.1 is
(3R)-1-azabicyclo[2.2.2]oct-3-yl, R.sup.2 and R.sup.3 are hydrogen,
R.sup.4 is hydrogen, fluorine, chlorine, bromine, trifluoromethoxy,
hydroxymethyl, methoxy or 6-membered heterocyclyl and R.sup.B is
hydrogen, halogen, cyano, trifluoromethyl, trifluoromethoxy or
C.sub.1-C.sub.4-alkyl, and the solvates, salts or solvates of the
salts of these compounds.
9. Compounds according to claims 1 to 8, of the formula
##STR00245## in which E is phenylene, R.sup.4 is
C.sub.1-C.sub.6-alkoxy, aminomethyl, hydroxycarbonyl,
C.sub.3-C.sub.8-cycloalkyl-carbonylamino, a group of the formula
##STR00246## where R.sup.5 is C.sub.1-C.sub.6-alkyl, n is zero, 1,
2, 3 or 4, or 5- to 6-membered heterocyclyl which is optionally
substituted by oxo, A is sulphur or oxygen, and the solvates, salts
or solvates of the salts thereof.
10. Compounds according to claims 1 to 9, of the formula (Ic), in
which E is phenylene, R.sup.4 is C.sub.1-C.sub.4-alkoxy,
aminomethyl, hydroxycarbonyl,
C.sub.3-C.sub.6-cycloalkyl-carbonylamino, a group of the formula
##STR00247## where R.sup.5 is C.sub.1-C.sub.4-alkyl, n is zero, 1
or 2, or 5- to 6-membered heterocyclyl which is optionally
substituted by oxo, A is sulphur or oxygen, and the solvates, salts
or solvates of the salts thereof.
11. Compounds according to claims 1 to 10, of the following
formulae ##STR00248## ##STR00249## and the solvates, salts or
solvates of the salts of these compounds.
12. Process for the preparation of the compounds of the formula
(I), in which compounds of the formula X.sup.1-E-R.sup.4 (II), in
which R.sup.4 has the meanings indicated in claim 1, and X.sup.1 is
--B(OH).sub.2 or ##STR00250## in the case where E is arylene or
heteroarylene, and is hydrogen in the case where E is
--C.ident.C--, are reacted with a compound of the formula
##STR00251## in which R.sup.1, R.sup.2, R.sup.3, A and the ring B
have the meanings indicated in claim 1, and X.sup.2 is triflate or
halogen, preferably chlorine, bromine or iodine, and where
appropriate [A] the resulting compounds (I) are alkylated on the
quinuclidine nitrogen atom with appropriate alkylating reagents, or
[B] the resulting compounds (I) are oxidized on the quinuclidine
nitrogen atom with suitable oxidizing agents, and the resulting
compounds (I) are converted into their solvates, salts or solvates
of the salts where appropriate with the appropriate (i) solvents
and/or (ii) bases or acids.
13. Process for the preparation of the compounds of the invention,
in which compounds of the formula X.sup.1-E-R.sup.4 (II), in which
R.sup.4 has the meanings indicated in claim 1, and X.sup.1 is
--B(OH).sub.2 or ##STR00252## in the case where E is arylene or
heteroarylene, and is hydrogen in the case where E is
--C.ident.C--, are reacted with a compound of the formula
##STR00253## in which R.sup.1, R.sup.2, R.sup.3, A and the ring B
have the meanings indicated in claim 1, and X.sup.2 is triflate or
halogen, preferably chlorine, bromine or iodine, and the resulting
compounds (I) are converted into their solvates, salts or solvates
of the salts where appropriate with the appropriate (i) solvents
and/or (ii) bases or acids.
14. Compounds according to any of claims 1 to 11 for the treatment
and/or prophylaxis of diseases.
15. Medicament comprising at least one compound according to any of
claims 1 to 11 and at least one pharmaceutically acceptable,
essentially nontoxic carrier or excipient.
16. Use of compounds according to any of claims 1 to 11 for
producing a composition for improving perception, concentration,
learning and/or memory.
17. Use of compounds according to any of claims 1 to 11 for
producing a medicament for the treatment and/or prophylaxis of
impairments of perception, concentration, learning and/or
memory.
18. Medicament according to claim 15 for the treatment and/or
prophylaxis of impairments of perception, concentration, learning
and/or memory.
Description
[0001] The invention relates to novel 2-heteroaryl carboxamides,
processes for their preparation, and their use for producing
medicaments for the treatment and/or prophylaxis of diseases and
for improving perception, concentration, learning and/or
memory.
[0002] Nicotinic acetylcholine receptors (nAChR) form a large
family of ion channels which are activated by the messenger
acetylcholine which is produced in the body (Galzi et al.,
Neuropharmacol. 1995, 34, 563-582). A functional nAChR consists of
five subunits which may be different (certain combinations of
.alpha.1-9 and .beta.1-4,.gamma.,.delta.,.epsilon. subunits) or
identical (.alpha.7-9). This leads to the formation of a diversity
of subtypes which differ in the distribution in the muscles, the
nervous system and other organs (McGehee et al., Annu. Rev.
Physiol. 1995, 57, 521-546). Activation of nAChR leads to influx of
cations into the cell and to stimulation of nerve cells or muscle
cells. Selective activation of individual nAChR subtypes restricts
this stimulation to the cell types which have a corresponding
subtype and is thus able to avoid unwanted side effects such as,
for example, stimulation of nAChR in the muscles. Clinical
experiments with nicotine and experiments in various animal models
indicate that central nicotinic acetylchloline receptors are
involved in learning and memory processes (e.g. Rezvani et al.,
Biol. Psychiatry 2001, 49, 258-267). Nicotinic acetyl-choline
receptors of the alpha7 subtype (.alpha.7 nAChR) have a
particularly high concentration in regions of the brain which are
important for learning and memory, such as the hippocampus and the
cerebral cortex (Seguela et al., J. Neurosci. 1993, 13, 596-604).
The .alpha.7 nAChR has a particularly high permeability for calcium
ions, increases glutamatergic neurotransmission, influences the
growth of axons and, in this way, modulates neuronal plasticity
(Broide et al., Mol. Neurobiol. 1999, 20, 1-16).
[0003] Certain N-(1-azabicyclo[2.2.2]oct-3-yl)heteroaryl
carboxamides for the treatment of, inter alia, psychoses are
described in DE-A 37 24 059.
[0004] N-(Azabicycloalkyl)heteroaryl carboxamides, in particular
N-(1-azabicyclo-[2.2.2]oct-4-yl)benzothiophene-3-carboxamides, are
disclosed in WO 93/15073 and in EP-A 485 962 as intermediates for
the synthesis of pharmaceutically active compounds.
[0005] U.S. Pat. No. 4,605,652 and EP-A 372 335 disclose, for
example, N-(1-azabicyclo[2.2.2]oct-3-yl)thiophene-2-carboxamide and
its memory-improving effect.
[0006] JP-A 14 030 084 describes 1-azabicycloalkanes for the
treatment of, inter alia, dementia, attention deficit hyperactivity
disorder and impairments of learning and memory.
[0007] WO 02/44176, WO 02/085901, WO 01/60821, EP-A 1 231 212 and
EP-A 1 219 622 disclose further .alpha.7 nicotinic acetylcholine
receptor agonists for the treatment of central nervous system
diseases.
[0008] The present invention relates to compounds of the
formula
##STR00001##
in which [0009] R.sup.1 is 1-azabicyclo[2.2.2]oct-3-yl, which is
optionally substituted via the nitrogen atom by a radical selected
from the group of C.sub.1-C.sub.4-alkyl, benzyl and oxy, [0010]
R.sup.2 is hydrogen or C.sub.1-C.sub.6-alkyl, [0011] R.sup.3 is
hydrogen, halogen or C.sub.1-C.sub.6-alkyl, [0012] R.sup.4 is
hydrogen, halogen, cyano, amino, trifluoromethyl, trifluoromethoxy,
C.sub.1-C.sub.6-alkyl, C.sub.1-C.sub.6-alkylcarbonyl,
C.sub.1-C.sub.6-alkylamino; formyl, hydroxycarbonyl,
C.sub.1-C.sub.6-alkoxy, C.sub.1-C.sub.6-alkoxycarbonyl,
C.sub.1-C.sub.6-alkylthio, C.sub.1-C.sub.6-alkylcarbonylamino,
C.sub.1-C.sub.6-alkylaminocarbonyl,
C.sub.1-C.sub.4-alkylsulphonylamino,
C.sub.3-C.sub.8-cycloalkyl-carbonylamino,
C.sub.3-C.sub.6-cycloalkylaminocarbonyl, pyrrolyl,
C.sub.1-C.sub.6-alkylaminocarbonylamino, heterocyclylcarbonyl,
heterocyclylcarbonylamino, heteroarylcarbonylamino, hydroxyl,
phenyl or heterocyclyl, [0013] where [0014] C.sub.1-C.sub.6-alkyl
may optionally be substituted by hydroxyl, cyano, amino,
C.sub.1-C.sub.6-alkylaminocarbonylamino,
C.sub.1-C.sub.6-alkylaminocarbonyl, heterocyclyl or aryl, [0015]
C.sub.1-C.sub.6-alkylaminocarbonyl may optionally be substituted by
C.sub.1-C.sub.6-alkoxy or C.sub.1-C.sub.6-alkylamino, [0016]
C.sub.1-C.sub.6-alkylcarbonylamino may optionally be substituted by
C.sub.1-C.sub.6-alkoxy, and heterocyclyl may optionally be
substituted by oxo, [0017] A is oxygen or sulphur, [0018] the ring
B is benzo or pyrido, each of which are optionally substituted by
radicals from the series halogen, cyano, formyl, trifluoromethyl,
trifluoromethoxy, nitro, amino, C.sub.1-C.sub.6-alkyl and
C.sub.1-C.sub.6-alkoxy, [0019] and [0020] E is C.ident.C, arylene
and heteroarylene, where arylene and heteroarylene may be
substituted by radicals from the series halogen, cyano,
trifluoromethyl, trifluoromethoxy, nitro, amino,
C.sub.1-C.sub.6-alkoxy and C.sub.1-C.sub.6-alkyl, [0021] and the
solvates, salts or solvates of the salts of these compounds.
[0022] Solvates is the term used for the purposes of the invention
for those forms of the compounds which form a complex with solvent
molecules by coordination in the solid or liquid state. Hydrates
are a special form of solvates in which the coordination takes
place with water.
[0023] Salts which are preferred for the purposes of the invention
are physiologically acceptable salts of the compounds of the
invention.
[0024] Physiologically acceptable salts of the compounds (I) may be
acid addition salts of the compounds with mineral acids, carboxylic
acids or sulphonic acids. Particularly preferred examples are salts
with hydrochloric acid, hydrobromic acid, sulphuric acid,
phosphoric acid, methanesulphonic acid, ethanesulphonic acid,
toluenesulphonic acid, benzenesulphonic acid,
naphthalenedisulphonic acid, acetic acid, propionic acid, oxalic
acid, lactic acid, tartaric acid, citric acid, fumaric acid, maleic
acid or benzoic acid.
[0025] However, salts which may be mentioned are also salts with
conventional bases, such as, for example, alkali metal salts (e.g.
sodium or potassium salts), alkaline earth metal salts (e.g.
calcium or magnesium salts) or ammonium salts derived from ammonia
or organic amines such as, for example, monoethanolamine,
diethanolamine; triethanolamine, arginine, lysine,
dimethylaminoethanol, diethylamine, triethylamine,
ethyldiisopropylamine, procaine, dibenzylamine, N-methylmorpholine,
dihydroabietylamine, 1-ephenamine or methylpiperidine.
[0026] The compounds of the invention may exist in stereoisomeric
forms (enantiomers, diastereomers). The invention therefore relates
both to the enantiomers or diastereomers and to respective mixtures
thereof. These enantiomer and diastereomer mixtures can be
separated in a known manner into the stereoisomerically pure
constituents.
[0027] For the purposes of the present invention, the substituents
generally have the following meaning:
[0028] C.sub.1-C.sub.6- and C.sub.1-C.sub.4-alkoxy are a
straight-chain or branched alkoxy radical having 1 to 6, preferably
1 to 4, particularly preferably 1 to 3, carbon atoms. Nonlimiting
examples include methoxy, ethoxy, n-propoxy, isopropoxy,
tert-butoxy, n-pentoxy and n-hexoxy.
[0029] C.sub.1-C.sub.6- and C.sub.1-C.sub.4-alkyl are a
straight-chain or branched alkyl radical having 1 to 6, preferably
1 to 4, particularly preferably 1 to 3, carbon atoms. Nonlimiting
examples include methyl, ethyl, n-propyl, isopropyl, tert-butyl,
n-pentyl and n-hexyl.
[0030] C.sub.1-C.sub.6- and C.sub.1-C.sub.4-alkylamino is a
straight-chain or branched mono- or dialkylamino radical having 1
to 6, preferably having 1 to 4, carbon atoms per alkyl radical.
Nonlimiting examples include methylamino, dimethylamino,
ethylamino, diethylamino, n-propylamino, di-n-propylamino,
isopropylamino, diisopropylamino, tert-butylamino,
di-tert-butylamino, n-pentylamino, di-n-pentylamino, n-hexylamino,
di-n-hexylamino, ethylmethylamino, isopropylmethylamino,
n-butylethylamino, n-hexyl-1-pentylamino.
[0031] C.sub.1-C.sub.6- and C.sub.1-C.sub.4-alkylcarbonylamino is a
straight-chain or branched alkylcarbonylamino radical having 1 to
6, preferably having 1 to 4, and particularly preferably having 1
to 3, carbon atoms. Nonlimiting examples include
methylcarbonyl-amino, ethylcarbonylamino, n-propylcarbonylamino,
isopropylcarbonylamino, tert-butylcarbonylamino,
n-pentylcarbonylamino and n-hexylcarbonylamino.
[0032] C.sub.1-C.sub.6- and C.sub.1-C.sub.4-alkylaminocarboxyl is a
straight-chain or branched mono- or dialkylaminocarboxyl radical
having 1 to 6, preferably having 1 to 4, particularly preferably
having 1 to 3, carbon atoms per alkyl radical. Nonlimiting examples
include methylaminocarboxyl, dimethylaminocarboxyl,
ethylaminocarboxyl, diethylaminocarboxyl, n-propylaminocarboxyl,
di-n-propylaminocarboxyl, isopropyl-aminocarboxyl,
diisopropylaminocarboxyl, tert-butylaminocarboxyl,
di-tert-butyl-aminocarboxyl, n-pentylaminocarboxyl,
di-n-pentylaminocarboxyl, n-hexyl-aminocarboxyl,
di-n-hexylaminocarboxyl, ethylmethylaminocarboxyl,
isopropyl-methylaminocarboxyl, n-butylethylaminocarboxyl,
n-hexyl-1-pentylaminocarboxyl.
[0033] C.sub.1-C.sub.6- and C.sub.1-C.sub.4-alkylaminocarbonyl is a
straight-chain or branched mono- or dialkylaminocarbonyl radical
having 1 to 6, preferably having 1 to 4, particularly preferably
having 1 to 3, carbon atoms per alkyl radical. Nonlimiting examples
include methylaminocarbonyl, dimethylaminocarbonyl,
ethylaminocarbonyl, diethylaminocarbonyl, n-propylaminocarbonyl,
di-n-propylaminocarbonyl, isopropyl-aminocarbonyl,
diisopropylaminocarbonyl, tert-butylaminocarbonyl,
di-tert-butyl-aminocarbonyl, n-pentylaminocarbonyl,
di-n-pentylaminocarbonyl, n-hexylamino-carbonyl,
di-n-hexylaminocarbonyl, ethylmethylaminocarbonyl,
isopropylmethyl-aminocarbonyl, n-butylethylaminocarbonyl,
n-hexyl-1-pentylaminocarbonyl.
[0034] C.sub.1-C.sub.6- and C.sub.1-C.sub.4-alkylaminocarbonylamino
is a straight-chain or branched mono- or dialkylaminocarbonylamino
radical having 1 to 6, preferably having 1 to 4, particularly
preferably having 1 to 3, carbon atoms per alkyl radical.
Nonlimiting examples include methylaminocarbonylamino,
dimethylaminocarbonylamino, ethylaminocarbonyl-amino,
diethylaminocarbonylamino, n-propylaminocarbonylamino,
di-n-propylaminocarbonylamino, isopropylaminocarbonylamino,
diisopropylamino-carbonylamino, tert-butylaminocarbonylamino,
di-tert-butylaminocarbonylamino, n-pentylaminocarbonylamino,
di-n-pentylaminocarbonylamino, n-hexylamino-carbonylamino,
di-n-hexylaminocarbonylamino, ethylmethylaminocarbonylamino,
isopropylmethylaminocarbonylamino, n-butylethylaminocarbonylamino,
n-hexyl-1-pentylaminocarbonylamino.
[0035] C.sub.1-C.sub.6-Alkylcarbonyl is a straight-chain or
branched alkylcarbonyl radical having 1 to 6, preferably having 1
to 4, carbon atoms. Nonlimiting examples include: acetyl,
ethylcarbonyl, propylcarbonyl, isopropylcarbonyl, butylcarbonyl,
isobutylcarbonyl, tert-butylcarbonyl, pentylcarbonyl and
hexylcarbonyl.
[0036] C.sub.1-C.sub.4-Alkylsulphonylamino is a straight-chain or
branched alkylsulphonylamino radical having 1 to 4, preferably
having 1 to 3, carbon atoms. Mention may be made by way of example
and preferably of: methanesulphonylamino, ethanesulphonylamino,
n-propanesulphonylamino, isopropanesulphonylamino,
tert-butanesulphonylamino.
[0037] C.sub.1-C.sub.6- and C.sub.1-C.sub.4-alkoxycarbonyl is a
straight-chain or branched alkoxycarbonyl radical having 1 to 6,
preferably having 1 to 4 and particularly preferably having 1 to 3,
carbon atoms. Nonlimiting examples include methoxycarbonyl,
ethoxycarbonyl, n-propoxycarbonyl, isopropoxycarbonyl and
tert-butoxycarbonyl.
[0038] C.sub.1-C.sub.6- and C.sub.1-C.sub.4-alkoxycarbonylamino is
a straight-chain or branched alkoxycarbonylamino radical having 1
to 6, preferably having 1 to 4 and particularly preferably having 1
to 3, carbon atoms. Nonlimiting examples include
methoxycarbonylamino, ethoxycarbonylamino, n-propoxycarbonylamino,
isopropoxy-carbonylamino, tert-butoxycarbonylamino,
n-pentoxycarbonylamino and n-hexoxy-carbonylamino.
[0039] C.sub.3-C.sub.6-Cycloalkylaminocarbonyl is a 3- to
6-membered, preferably 5- to 6-membered cycloalkylaminocarbonyl
radical. Nonlimiting examples include cyclopropylaminocarbonyl,
cyclobutylaminocarbonyl, cyclopentylaminocarbonyl,
cyclohexylaminocarbonyl, cycloheptylaminocarbonyl and
cyclooctylaminocarbonyl.
[0040] C.sub.3-C.sub.8- and C.sub.5-C.sub.6-cycloalkylcarbonylamino
is a 3- to 8-membered, preferably 5- to 6-membered,
cycloalkylcarbonylamino radical. Nonlimiting examples include
cyclopropylcarbonylamino, cyclobutylcarbonylamino,
cyclopentylcarbonylamino, cyclohexylcarbonylamino,
cycloheptylcarbonylamino and cyclooctylcarboriylamino.
[0041] Heterocyclyl is a mono- or polycyclic, preferably mono- or
bicyclic, nonaromatic radical having, as a rule, 4 to 10,
preferably 5 to 8, ring atoms and up to 3, preferably 1.0 up to 2,
hetero ring members from the series N, O, S, SO, SO.sub.2. The
heterocyclyl radicals may be saturated or partially unsaturated.
Nonlimiting examples include 5- to 8-membered monocyclic saturated
heterocyclyl radicals having up to two hetero ring atoms from the
series O, N and S such as tetrahydrofuran-2-yl, piperazinyl,
N-methylpiperazinyl, pyrrolidin-2-yl, pyrrolidin-3-yl, pyrrolinyl,
piperidinyl, morpholinyl and perhydroazepinyl.
[0042] Heteroaryl is an aromatic, mono- or bicyclic radical having
5 to 10 ring atoms and up to 5 heteroatoms from the series S, O
and/or N. Preference is given to 5- to 6-membered heteroaryls
having up to 4 heteroatoms. The heteroaryl radical may be bonded
via a carbon atom or heteroatom. Nonlimiting examples include:
thienyl, furyl, pyrrolyl, thiazolyl, oxadiazolyl, oxazolyl,
isoxazolyl, imidazolyl, tetrazolyl, pyridyl, pyrimidinyl,
pyridazinyl, indolyl, indazolyl, benzofuranyl, benzothiophenyl,
quinolinyl, isoquinolinyl.
[0043] Heterocyclylcarbonylamino is a carbonylamino group which is
linked to a mono- or polycyclic, preferably mono- or bicyclic,
nonaromatic radical having; as a rule, 4 to 10, preferably 5 to 8,
ring atoms and up to 3, preferably up to 2, hetero ring members
from the series N, O, S, SO, SO.sub.2. The heterocyclyl radicals
may be saturated or partially unsaturated. Nonlimiting examples
include carbonylamino groups linked to 5- to 8-membered monocyclic
saturated heterocyclyl radicals having up to two hetero ring atoms
from the series O, N and S such as
tetrahydrofuran-2-ylcarbonylamino, piperazinylcarbonylamino,
N-methylpiperazinylcarbonylamino, pyrrolidin-2-ylcarb-onylamino,
pyrrolidin-3-ylcarbonylamino, pyrrolinylcarbonylamino,
piperidinyl-carbonylamino, morpholinylcarbonylamino and
perhydroazepinylcarbonylamino.
[0044] Heteroarylcarbonylamino is a carbonylamino group which is
linked to a mono- or bicyclic aromatic radical having 5 to 10 ring
atoms and up to 5 heteroatoms from the series S, O and/or N.
Preference is given to 5- to 6-membered heteroaryls having up to 4
heteroatoms. The heteroaryl radical may be bonded to the
carbonylamino group via a carbon atom or heteroatom. Nonlimiting
examples include: thienylcarbonylamino, furylcarbonylamino,
pyrrolylcarbonylamino, thiazolylcarbonylamino,
isoxazolylcarbonylamino, oxadiazolylcarbonylamino,
oxazolylcarbonylamino, imidazolylcarbonylamino,
tetrazolylcarbonylamino, pyridylcarbonylamino,
pyrimidinylcarbonylamino, pyridazinylcarbonylamino,
indolylcarbonylamino, indazolylcarbonylamino,
benzofuranylcarbonylamino, benzothiophenylcarbonylamino,
quinolinylcarbonylamino, isoquinolinylcarbonylamino.
[0045] Heterocyclylcarbonyl is a carbonyl group which is linked to
a mono- or polycyclic, preferably mono- or bicyclic, nonaromatic
radical having, as a rule, 4 to 10, preferably 5 to 8, ring atoms
and up to 3, preferably up to 2, hetero ring members from the
series N, O, S, SO, SO.sub.2. The heterocyclyl radicals may be
saturated or partially unsaturated. Nonlimiting examples include
carbonyl groups linked to 5- to 8-membered monocyclic saturated
heterocyclyl radicals having up to two hetero ring atoms from the
series O, N and S such as tetrahydrofuran-2-ylcarbonyl,
piperazinylcarbonyl, N-methylpiperazinylcarbonyl,
pyrrolidin-2-ylcarbonyl, pyrrolidin-3-ylcarbonyl,
pyrrolinylcarbonyl, piperidinylcarbonyl, morpholinyl-carbonyl and
perhydroazepinylcarbonyl.
[0046] Aryl is a mono- to tricyclic aromatic, carbocyclic radical
having, as a rule, 6 to 10 carbon ring atoms. Nonlimiting examples
include phenyl and naphthyl.
[0047] Halogen is fluorine, chlorine, bromine and iodine.
Preference is given to fluorine, chlorine and bromine, and
particular preference to fluorine and chlorine.
[0048] C.sub.1-C.sub.6- and C.sub.1-C.sub.4-alkylthio are a
straight-chain or branched alkylthio radical having 1 to 6,
preferably 1 to 4, particularly preferably 1 to 3, carbon atoms.
Nonlimiting examples include methylthio, ethylthio, n-propylthio,
isopropylthio, tert-butylthio, n-pentylthio and n-hexylthio.
[0049] When radicals in the compounds of the invention are
optionally substituted, unless indicated otherwise the radicals may
have one or more identical or different substituents.
[0050] Preference is given to compounds of the formula (I) in which
R.sup.1 is (3R)-1-aza-bicyclo[2.2.2]oct-3-yl, and R.sup.2, R.sup.3,
R.sup.4, A, E and the ring B have the meanings indicated above, and
the solvates, salts or solvates of the salts of these
compounds.
[0051] Preference is likewise given to compounds of the formula (I)
in which R.sup.2 is hydrogen or methyl, and R.sup.1, R.sup.3,
R.sup.4, A, E and the ring B have the meanings indicated above, and
the solvates, salts or solvates of the salts of these
compounds.
[0052] Particular preference is given to compounds of the formula
(I) in which R.sup.2 is hydrogen, and R.sup.1, R.sup.3, R.sup.4, A,
E and the ring B have the meanings indicated above, and the
solvates, salts or solvates of the salts of these compounds.
[0053] Preference is likewise given to compounds of the formula (I)
in which R.sup.3 is hydrogen or methyl, and R.sup.1, R.sup.2,
R.sup.4, A, E and the ring B have the meanings indicated above, and
the solvates, salts or solvates of the salts of these
compounds.
[0054] Particular preference is given to compounds of the formula
(I) in which R.sup.3 is hydrogen, and R.sup.1, R.sup.2, R.sup.4, A,
E and the ring B have the meanings indicated above, and the
solvates, salts or solvates of the salts of these compounds.
[0055] Preference is likewise given to compounds of the formula (I)
in which R.sup.4 is hydrogen, fluorine, chlorine, bromine,
trifluoromethoxy, hydroxymethyl, methoxy or 6-membered
heterocyclyl, and R.sup.1, R.sup.2, R.sup.3, A, E and the ring B
have the meanings indicated above, and the solvates, salts or
solvates of the salts of these compounds.
[0056] Preference is likewise given to compounds of the formula (I)
in which A is a sulphur atom, and R.sup.1, R.sup.2, R.sup.3,
R.sup.4, E and the ring B have the meanings indicated above, and
the solvates, salts or solvates of the salts of these
compounds.
[0057] Preference is likewise given to compounds of the formula (I)
in which A is an oxygen atom, and R.sup.1, R.sup.2, R.sup.3,
R.sup.4, E and the ring B have the meanings indicated above, and
the solvates, salts or solvates of the salts of these
compounds.
[0058] Preference is likewise given to compounds of the formula (I)
in which the ring B is benzo which is optionally substituted by 1
to 3 radicals from the series halogen, cyano, trifluoromethyl,
trifluoromethoxy and C.sub.1-C.sub.4-alkyl, and R.sup.1, R.sup.2,
R.sup.3, R.sup.4, A and E have the meanings indicated above, and
the solvates, salts or solvates of the salts of these
compounds.
[0059] Preference is likewise given to compounds of the formula (I)
in which E is phenylene which is optionally substituted by radicals
from the series fluorine, chlorine, bromine, cyano,
trifluoromethoxy, C.sub.1-C.sub.6-alkyl and C.sub.1-C.sub.6-alkoxy,
and R.sup.1, R.sup.2, R.sup.3, R.sup.4, A and the ring B have the
meanings indicated above, and the solvates, salts or solvates of
the salts of these compounds.
[0060] Preference is likewise given to compounds of the formula (I)
in which [0061] R.sup.1 is 1-azabicyclo[2.2.2]oct-3-yl, [0062]
R.sup.2 is hydrogen or C.sub.1-C.sub.4-alkyl, [0063] R.sup.3 is
hydrogen, fluorine, chlorine, bromine or C.sub.1-C.sub.4-alkyl,
[0064] R.sup.4 is hydrogen, fluorine, chlorine, bromine, cyano,
amino, trifluoromethyl, trifluoromethoxy, C.sub.1-C.sub.4-alkyl,
C.sub.1-C.sub.4-alkylcarbonyl, C.sub.1-C.sub.4-alkylamino, formyl,
hydroxycarbonyl, C.sub.1-C.sub.4-alkoxy,
C.sub.1-C.sub.4-alkoxycarbonyl, C.sub.1-C.sub.4-alkylthio,
C.sub.1-C.sub.4-alkylcarbonylamino,
C.sub.1-C.sub.4-alkylaminocarbonyl,
C.sub.1-C.sub.4-alkylsulphonylamino,
C.sub.3-C.sub.6-cycloalkylcarbonylamino,
C.sub.3-C.sub.6-cycloalkyl-aminocarbonyl, pyrrolyl,
C.sub.1-C.sub.4-alkylaminocarbonylamino, heterocyclyl-carbonyl,
heterocyclylcarbonylamino, heteroarylcarbonylamino, hydroxyl,
phenyl or heterocyclyl, [0065] where C.sub.1-C.sub.4-alkyl may
optionally be substituted by hydroxyl, cyano, amino,
C.sub.1-C.sub.4-alkylaminocarbonylamino,
C.sub.1-C.sub.4-alkylaminocarboxyl, heterocyclyl or aryl, [0066]
C.sub.1-C.sub.4-alkylaminocarbonyl may optionally be substituted by
C.sub.1-C.sub.4-alkoxy or C.sub.1-C.sub.4-alkylamino, [0067]
C.sub.1-C.sub.4-alkylcarbonylamino may optionally be substituted by
C.sub.1-C.sub.4-alkoxy, and heterocyclyl may optionally be
substituted by oxo, [0068] A is oxygen or sulphur, [0069] the ring
B is benzo or pyrido, each of which are optionally substituted by
radicals from the series halogen, cyano, trifluoromethyl,
trifluoromethoxy and C.sub.1-C.sub.4-alkyl, [0070] and [0071] E is
C.ident.C, arylene and heteroarylene, where arylene and
heteroarylene may be substituted by radicals from the series
halogen, cyano, trifluoromethyl, trifluoromethoxy, nitro, amino,
C.sub.1-C.sub.4-alkoxy and C.sub.1-C.sub.4-alkyl, [0072] and the
solvates, salts or solvates of the salts of these compounds.
[0073] Preference is likewise given to compounds of the formula (I)
in which [0074] R.sup.1 is 1-azabicyclo[2.2.2]oct-3-yl, [0075]
R.sup.2 and R.sup.3 are hydrogen, [0076] R.sup.4 is hydrogen,
fluorine, chlorine, bromine, cyano, amino, trifluoromethyl,
trifluoromethoxy, C.sub.1-C.sub.4-alkyl,
C.sub.1-C.sub.4-alkylcarbonyl, C.sub.1-C.sub.4-alkylamino, formyl,
hydroxycarbonyl, C.sub.1-C.sub.4-alkoxy,
C.sub.1-C.sub.4-alkoxycarbonyl, C.sub.1-C.sub.6-alkylthio,
C.sub.1-C.sub.4-alkylcarbonylamino,
C.sub.1-C.sub.4-alkylaminocarbonyl,
C.sub.1-C.sub.4-alkylsulphonylamino,
C.sub.3-C.sub.6-cycloalkylcarbonylamino,
C.sub.1-C.sub.6-cycloalkyl-aminocarbonyl, pyrrolyl,
C.sub.1-C.sub.4-alkylaminocarbonylamino, heterocyclyl-carbonyl,
heterocyclylcarbonylamino, heteroarylcarbonylamino, hydroxyl,
phenyl or heterocyclyl, [0077] where C.sub.1-C.sub.4-alkyl may
optionally be substituted by hydroxyl, cyano, amino,
C.sub.1-C.sub.4-alkylaminocarbonylamino,
C.sub.1-C.sub.4-alkylaminocarboxyl, heterocyclyl or aryl, [0078]
C.sub.1-C.sub.4-alkylaminocarbonyl may optionally be substituted by
C.sub.1-C.sub.4-alkoxy or C.sub.1-C.sub.4-alkylamino, [0079]
C.sub.1-C.sub.4-alkylcarbonylamino may optionally be substituted by
C.sub.1-C.sub.4-alkoxy, and heterocyclyl may optionally be
substituted by oxo, [0080] A is oxygen, [0081] the ring B is benzo
or pyrido, each of which are optionally substituted by radicals
from the series halogen, cyano, trifluoromethyl, trifluoromethoxy
and C.sub.1-C.sub.4-alkyl, [0082] and [0083] E is C.ident.C,
arylene and heteroarylene, where arylene and heteroarylene may be
substituted by radicals from the series halogen, cyano,
trifluoromethyl, trifluoromethoxy, nitro, amino,
C.sub.1-C.sub.4-alkoxy and C.sub.1-C.sub.4-alkyl, [0084] and the
solvates, salts or solvates of the salts of these compounds.
[0085] Preference is likewise given to compounds of the formula (I)
in which [0086] R.sup.1 is 1-azabicyclo[2.2.2]oct-3-yl, [0087]
R.sup.2 is hydrogen or C.sub.1-C.sub.6-alkyl, [0088] R.sup.3 is
hydrogen, halogen or C.sub.1-C.sub.6-alkyl, [0089] R.sup.4 is
hydrogen, halogen, cyano, amino, trifluoromethyl, trifluoromethoxy,
C.sub.1-C.sub.6-alkyl, C.sub.1-C.sub.6-alkylcarbonyl,
C.sub.1-C.sub.6-alkylamino, formyl, hydroxycarbonyl,
C.sub.1-C.sub.6-alkoxy, C.sub.1-C.sub.6-alkoxycarbonyl,
C.sub.1-C.sub.6-alkylthio, C.sub.1-C.sub.6-alkylcarbonylamino,
C.sub.1-C.sub.4-alkylsulphonylamino,
C.sub.3-C.sub.8-cycloalkylcarbonylamino, pyrrolyl,
C.sub.1-C.sub.6-alkylaminocarbonylamino, heterocyclylcarbonyl,
phenyl or heterocyclyl, [0090] where C.sub.1-C.sub.6-alkyl may
optionally be substituted by hydroxyl, amino,
C.sub.1-C.sub.6-alkylaminocarbonylamino,
C.sub.1-C.sub.6-alkylaminocarboxyl, heterocyclyl or aryl, [0091]
C.sub.1-C.sub.6-alkylcarbonylamino may optionally be substituted by
C.sub.1-C.sub.6-alkoxy, and [0092] heterocyclyl may optionally be
substituted by oxo, [0093] A is oxygen or sulphur, [0094] the ring
B is benzo or pyrido, each of which are optionally substituted by
radicals from the series halogen, cyano, formyl, trifluoromethyl,
trifluoromethoxy, nitro, amino, C.sub.1-C.sub.6-alkyl and
C.sub.1-C.sub.6-alkoxy, [0095] and [0096] E is C.ident.C, arylene
and heteroarylene, where arylene and heteroarylene may be
substituted by radicals from the series halogen, cyano,
trifluoromethyl, trifluoromethoxy, nitro, amino,
C.sub.1-C.sub.6-alkoxy and C.sub.1-C.sub.6-alkyl, [0097] and the
solvates, salts or solvates of the salts of these compounds.
[0098] Preference is likewise given to compounds of the formula (I)
in which [0099] R.sup.1 is 1-azabicyclo[2.2.2]oct-3-yl, [0100]
R.sup.2 is hydrogen or C.sub.1-C.sub.6-alkyl, [0101] R.sup.3 is
hydrogen, halogen or C.sub.1-C.sub.6-alkyl, [0102] R.sup.4 is
hydrogen, halogen, cyano, trifluoromethyl, trifluoromethoxy,
C.sub.1-C.sub.6-alkyl, C.sub.1-C.sub.6-alkoxy or heterocyclyl,
where alkyl is optionally substituted by a hydroxyl radical, [0103]
A is oxygen or sulphur, [0104] the ring B is benzo or pyrido, each
of which are optionally substituted by radicals from the series
halogen, cyano, trifluoromethyl, trifluoromethoxy, nitro; amino,
C.sub.1-C.sub.6-alkyl and C.sub.1-C.sub.6-alkoxy, [0105] and [0106]
E is C.ident.C, arylene or heteroarylene, where arylene and
heteroarylene may be substituted by radicals from the series
halogen, cyano, trifluoromethyl, trifluoromethoxy, nitro, amino,
C.sub.1-C.sub.6-alkyl and C.sub.1-C.sub.6-alkoxy, [0107] and the
solvates, salts or solvates of the salts of these compounds.
[0108] Preference is likewise given to compounds of the formula
##STR00002##
in which [0109] R.sup.1 is (3R)-1-azabicyclo[2.2.2]oct-3-yl, [0110]
R.sup.2 and R.sup.3 are, independently of one another, hydrogen or
methyl, [0111] R.sup.4 is hydrogen, halogen, cyano,
trifluoromethyl, trifluoromethoxy, C.sub.1-C.sub.6-alkyl,
C.sub.1-C.sub.6-alkoxy or heterocyclyl, where alkyl is optionally
substituted by a hydroxyl radical, [0112] and [0113] R.sup.B is
hydrogen, halogen, cyano, trifluoromethyl, trifluoromethoxy, nitro,
amino, C.sub.1-C.sub.6-alkyl or C.sub.1-C.sub.6-alkoxy, [0114] and
the solvates, salts or solvates of the salts of these
compounds.
[0115] Very particular preference is likewise given to compouds of
the formula (Ia) in which [0116] R.sup.1 is
(3R)-1-azabicyclo[2.2.2]oct-3-yl, [0117] R.sup.2 and R.sup.3 are
hydrogen, [0118] R.sup.4 is hydrogen, fluorine, chlorine, bromine,
trifluoromethoxy, hydroxymethyl, methoxy or 6-membered heterocyclyl
and [0119] R.sup.B is hydrogen, halogen, cyano, trifluoromethyl,
trifluoromethoxy or C.sub.1-C.sub.4-alkyl, [0120] and the solvates,
salts or solvates of the salts of these compounds.
[0121] Preference is likewise given to compounds of the formula
##STR00003##
in which [0122] R.sup.1 is (3R)-1-azabicyclo[2.2.2]oct-3-yl, [0123]
R.sup.2 and R.sup.3 are, independently of one another, hydrogen or
methyl, [0124] R.sup.4 is hydrogen, halogen, cyano,
trifluoromethyl, trifluoromethoxy, C.sub.1-C.sub.6-alkyl,
C.sub.1-C.sub.6-alkoxy or heterocyclyl, where alkyl is optionally
substituted by a hydroxyl radical, and [0125] R.sup.B is hydrogen,
halogen, cyano, trifluoromethyl, trifluoromethoxy, nitro, amino,
C.sub.1-C.sub.6-alkyl and C.sub.1-C.sub.6-alkoxy, [0126] and the
solvates, salts or solvates of the salts of these compounds.
[0127] Preference is likewise given to compounds of the formula
(Ib) in which [0128] R.sup.1 is (3R)-1-azabicyclo[2.2.2]oct-3-yl,
[0129] R.sup.2 and R.sup.3 are hydrogen, [0130] R.sup.4 is
hydrogen, fluorine, chlorine, bromine, trifluoromethoxy,
hydroxymethyl, methoxy or 6-membered heterocyclyl and [0131]
R.sup.B is hydrogen, halogen, cyano, trifluoromethyl,
trifluoromethoxy or C.sub.1-C.sub.4-alkyl, [0132] and the solvates,
salts or solvates of the salts of these compounds.
[0133] Preference is likewise given to compounds of the formula
##STR00004##
in which [0134] E is phenylene, [0135] R.sup.4 is
C.sub.1-C.sub.6-alkoxy, aminomethyl, hydroxycarbonyl,
C.sub.3-C.sub.8-cycloalkylcarbonyl-amino, a group of the
formula
[0135] ##STR00005## [0136] where [0137] R.sup.5 is
C.sub.1-C.sub.6-alkyl, [0138] n is zero, 1, 2, 3 or 4, [0139] or
[0140] 5- to 6-membered heterocyclyl which is optionally
substituted by oxo, [0141] A is sulphur or oxygen, [0142] and the
solvates, salts or solvates of the salts thereof.
[0143] The invention preferably relates to compounds of the formula
(I) in which [0144] E is phenylene, [0145] R.sup.4 is
C.sub.1-C.sub.4-alkoxy, aminomethyl, hydroxycarbonyl,
C.sub.3-C.sub.6-cycloalkylcarbonyl-amino, a group of the
formula
[0145] ##STR00006## [0146] where [0147] R.sup.5 is
C.sub.1-C.sub.4-alkyl, [0148] n is zero, 1 or 2, [0149] or [0150]
5- to 6-membered heterocyclyl which is optionally substituted by
oxo, [0151] A is sulphur or oxygen, [0152] and the solvates, salts
or solvates of the salts thereof.
[0153] The invention particularly preferably relates to compounds
of the following formulae
##STR00007## ##STR00008##
and the solvates, salts or solvates of the salts of these
compounds.
[0154] Very particular preference is given to combinations of two
or more of the preferred ranges mentioned above.
[0155] The invention further relates to processes for the
preparation of the compounds of the invention, in which compounds
of the formula
X.sup.1-E-R.sup.4 (II),
in which R.sup.4 has the abovementioned meanings, and
X.sup.1 is --B(OH).sub.2 or
[0156] ##STR00009## [0157] in the case where E is arylene or
heteroarylene, and is hydrogen in the case where E is
--C.ident.C--, are reacted with a compound of the formula
##STR00010##
[0157] in which R.sup.1, R.sup.2, R.sup.3, A and the ring B have
the abovementioned meanings, and X.sup.2 is triflate or halogen,
preferably chlorine, bromine or iodine, and where appropriate
[0158] [A] the resulting compounds (I) are alkylated on the
quinuclidine nitrogen atom using appropriate alkylating reagents,
or [0159] [B] the resulting compounds (I) are oxidized on the
quinuclidine nitrogen atom using suitable oxidizing agents, and the
resulting compounds (I) are converted into their solvates, salts or
solvates of the salts where appropriate with the appropriate (i)
solvents and/or (ii) bases or acids.
[0160] Reaction of the compounds (II) and (III) generally takes
place in an inert solvent in the presence of a transition metal
catalyst, in the presence of a base and, where appropriate, in the
presence of copper(I) iodide.
[0161] The process of the invention is preferably carried out in a
temperature range from 70.degree. C. to 110.degree. C. under
atmospheric pressure.
[0162] Examples of inert solvents are ethers such as dioxane,
tetrahydrofuran or 1,2-dimethoxyethane, hydrocarbons such as
benzene, xylene or toluene, nitroaromatic compounds such as
nitrobenzene, where appropriate N-alkylated carboxamides such as
dimethylformamide, dimethylacetamide, alkyl sulphoxides such as
dimethyl sulphoxide or cyclic lactams such as N-methylpyrrolidone.
Preference is given to solvents from the series dimethylformamide,
dimethylacetamide, dimethyl sulphoxide and 1,2-dimethoxyethane.
[0163] The transition metal catalysts preferably used are
palladium(0) or palladium(II) compounds, in particular
bis(diphenylphosphino)ferrocenepalladium(II) chloride,
dichlorobis(triphenylphosphine)palladium or
tetrakis(triphenylphosphine)-palladium(0).
[0164] Preferred bases are alkali metal hydroxides or salts such as
potassium acetate, sodium hydroxide, sodium bicarbonate or sodium
carbonate, where appropriate in the form of their aqueous
solutions.
[0165] Process steps [A] and [B] can be carried out in inert
solvents and at temperatures from -30 to 50.degree. C. and under
atmospheric pressure.
[0166] Bases which can be employed for process step [A] are alkali
metal hydrides such as potassium or sodium hydride, alkali metal
hydroxides such as sodium or potassium hydroxide or alkali metal
carbonates such as sodium or potassium carbonate.
[0167] Alkylating reagents which can be employed for process step
[A] are alkyl halides such as methyl iodide or benzyl halides such
as benzyl bromide.
[0168] An oxidizing agent particularly suitable for process step
[B] is hydrogen peroxide or metachloroperbenzoic acid.
[0169] The reactions metallized by transition metals can be carried
out in analogy to processes known from the literature, e.g.
reaction with alkynes: cf. N. Krause et al., J. Org. Chem. 1998,
63, 8551; with ketones, aromatic compounds and alkenes: cf. for
example, A. Suzuki, Acc. Chem. Res. 1982, 15, 178ff; Miyaura et al.
J. Am. Chem. Soc. 1989, 111, 314; J. K. Stille, Angew. Chem. 1986,
98, 504 and with substituted amines: cf. S. L. Buchwald et al., J.
Organomet. Chem. 1999, 576, 125ff. (see also J. Tsuji, Palladium
Reagents and Catalysts, Wiley, New York, 1995).
[0170] The compounds (II) are known or can be synthesized in
analogy to known processes from the appropriate precursors.
[0171] The compounds (III) can be prepared by reacting compounds of
the formula
R.sup.1R.sup.2NH (IV),
in which R' and R.sup.2 have the abovementioned meanings, with a
compound of the formula
##STR00011##
in which R.sup.3, X.sup.2, A and the ring B have the abovementioned
meanings, and X.sup.3 is hydroxyl or halogen, preferably bromine or
chlorine.
[0172] Reaction of the compounds (IV) and (V) takes place, if
X.sup.3 is halogen, generally in inert solvents, where appropriate
in the presence of a base, preferably in a temperature range from
0.degree. C. to 50.degree. C. under atmospheric pressure.
[0173] Examples of inert solvents are halohydrocarbons such as
methylene chloride, trichloromethane, tetrachloromethane,
trichloroethane, tetrachloroethane, 1,2-di-chloroethane or
trichloroethylene, ethers such as diethyl ether, methyl tert-butyl
ether, dioxane, tetrahydrofuran, glycol dimethyl ether or
diethylene glycol dimethyl ether, hydrocarbons such as benzene,
xylene, toluene, hexane, cyclohexane or petroleum fractions,
nitroaromatic compounds such as nitromethane, carboxylic esters
such as ethyl acetate, ketones such as acetone or 2-butanone,
optionally N-alkylated carboxamides such as dimethylformamide or
dimethylacetamide, alkyl sulphoxides such as dimethyl sulphoxide,
carbonitriles such as acetonitrile or heteroaromatic compounds such
as pyridine. Preference is given to dioxane, dimethylformamide or
methylene chloride.
[0174] Examples of bases are alkali metal hydroxides such as sodium
or potassium hydroxide, alkali metal carbonates and bicarbonates
such as cesium carbonate, sodium bicarbonate, sodium or potassium
carbonate, or amides such as lithium diisopropylamide, alkylamines
such as triethylamine or diisopropylethylamine, preferably
diisopropylethylamine or triethylamine, and other bases such as
DBU.
[0175] The reaction takes place, if X.sup.3 is hydroxyl, generally
in inert solvents in the presence of condensing agents, where
appropriate in the presence of a base, preferably in a temperature
range from 20 to 50.degree. C. under atmospheric pressure.
[0176] The term "inert solvents" includes for example
halohydrocarbons such as methylene chloride, trichloromethane,
tetrachloromethane, trichloroethane, tetrachloroethane,
1,2-dichloroethane or trichloroethylene, ethers such as diethyl
ether, methyl tert-butyl ether, dioxane, tetrahydrofuran, glycol
dimethyl ether or diethylene glycol dimethyl ether, hydrocarbons
such as benzene, xylene, toluene, hexane, cyclohexane or petroleum
fractions, nitroaromatic compounds such as nitromethane, carboxylic
esters such as ethyl acetate, ketones such as acetone, optionally
N-alkylated carboxamides such as dimethylformamide or
dimethylacetamide, alkyl sulphoxides such as dimethyl sulphoxide,
carbonitriles such as acetonitrile and heteroaromatic compounds
such as pyridine. Preference is given to tetrahydrofuran,
dimethylformamide, 1,2-dichloroethane or methylene chloride.
[0177] Condensing agents for the purposes of the invention are, for
example, carbodiimides such as, for example, N,N'-diethyl-,
N,N'-dipropyl-, N,N'-diisopropyl-, N,N'-dicyclo-hexylcarbodiimide,
N-(3-dimethylaminoisopropyl)-N'-ethylcarbodiimide hydro-chloride
(EDC), N-cyclohexylcarbodiimide-N-propyloxymethylpolystyrene
(PS-carbodiimide); carbonyl compounds such as carbonyldiimidazole;
1,2-oxazolium compounds such as
2-ethyl-5-phenyl-1,2-oxazolium-3-sulphate or
2-tert-butyl-5-methylisoxazolium perchlorate; acylamino compounds
such as 2-ethoxy-1-ethoxy-carbonyl-1,2-dihydroquinoline; in
addition propanephosphonic anhydride, isobutyl chloroformate,
bis(2-oxo-3-oxazolidinyl)phosphoryl chloride,
benzotriazolyloxy-tri(dimethylamino)phosphonium
hexafluorophosphate,
O-(benzotriazol-1-yl)-N,N,N',N'-tetramethyluronium
hexafluorophosphate (HBTU),
2-(2-oxo-1-(2H)-pyridyl)-1,1,3,3-tetramethyluronium
tetrafluoroborate (TPTU),
O-(7-azabenzotriazol-1-yl)-N,N,N',N'-tetramethyluronium
hexafluorophosphate (HATU),
benzotriazol-1-yloxytris(dimethylamino)phosphonium
hexafluorophosphate (BOP), and mixtures thereof.
[0178] It may be advantageous where appropriate to use the
condensing agent in the presence of an auxiliary nucleophile such
as, for example, 1-hydroxybenzotriazole (HOBt).
[0179] Examples of bases are alkali metal carbonates and
bicarbonates such as, for example, sodium or potassium carbonate or
bicarbonate, organic bases such as alkylamines, e.g. triethylamine,
or N-methylmorpholine, N-methylpiperidine, 4-dimethylamino-pyridine
or diisopropylethylamine.
[0180] Particular preference is given to the combination of
N-(3-dimethylaminoisopropyl)-M-ethylcarbodiimide hydrochloride
(EDC), 1-hydroxybenzotriazole (HOBt) and triethylamine in
dimethylformamide or of
O-(7-azabenzotriazol-1-yl)-N,N,N',N'-tetramethyluronium
hexafluorophosphate (HATU) and diisopropylethylamine in
dimethylformamide.
[0181] The compounds (IV) and (V) are known or can be synthesized
in analogy to known processes from the appropriate precursors (cf.,
for example, "Comprehensive Heterocyclic Chemistry", Katritzky et
al., editors; Elsevier, 1996).
[0182] Thus, for example, substituted benzothiophene-2-carboxylic
acids can be obtained from appropriately substituted
2-halobenzaldehydes by reaction with methyl mercaptoacetate (see,
for example, A. J. Bridges et al., Tetrahedron Lett 1992, 33, 7499)
and subsequent hydrolysis of the ester:
##STR00012##
[0183] The corresponding pyrido derivatives can be synthesized
starting from 2-halobenzonitriles by reaction with methyl
mercaptoacetate to give the 3-amino-benzothiophene-2-carboxylic
esters:
##STR00013##
[0184] The nitrogen atom shown in the ring may replace a CH group
at one of positions 1 to 4 in the aromatic system.
[0185] The amino function can be removed by diazotization. Finally,
the ester can be hydrolysed to give the target compound.
[0186] Substituted benzofuran-2-carboxylic acids can be obtained
for example as described by D. Bogdal et al., Tetrahedron 2000, 56,
8769.
[0187] The compounds of the invention are suitable for use as
medicaments for the treatment and/or prophylaxis of diseases in
humans and animals.
[0188] They act as .alpha.7 nAChR agonists and show a valuable
range of pharmacological effects which could not have been
predicted.
[0189] The compounds of the invention can, because of their
pharmacological properties, be employed alone or in combination
with other active ingredients for the treatment and/or prevention
of cognitive impairments, especially of Alzheimer's disease.
[0190] Because of their selective effect as .alpha.7 nAChR
agonists, they are particularly suitable for improving perception,
concentration, learning or memory, especially after cognitive
impairments like those occurring for example in mild cognitive
impairment, age-associated learning and memory impairments,
age-associated memory loss, vascular dementia, craniocerebral
trauma, stroke, dementia occurring after strokes (post-stroke
dementia), post-traumatic brain syndrome, general concentration
impairments, concentration impairments in children with learning
and memory problems, attention deficit hyperactivity disorder,
Alzheimer's disease, Lewy body dementia, dementia with degeneration
of the frontal lobes, including Pick's syndrome, Parkinson's
disease, progressive nuclear palsy, dementia with corticobasal
degeneration, amyotrophic lateral sclerosis (ALS), Huntington's
disease, multiple sclerosis, thalamic degeneration,
Creutzfeld-Jakob dementia, HIV dementia, schizophrenia,
schizophrenia with dementia or Korsakoffs psychosis.
[0191] The compounds of the invention can be employed alone or in
combination with other active ingredients for the prophylaxis and
treatment of acute and/or chronic pain (for a classification, see
"Classification of Chronic Pain, Descriptions of Chronic Pain
Syndromes and Definitions of Pain Terms", 2nd edition, Meskey and
Begduk, editors; IASP Press, Seattle, 1994), especially for the
treatment of cancer-induced pain and chronic neuropathic pain like,
for example, that associated with diabetic neuropathy, postherpetic
neuralgia, peripheral nerve damage, central pain (for example as a
consequence of cerebral ischaemia) and trigeminal neuralgia, and
other chronic pain such as, for example, lumbago, backache (low
back pain) or rheumatic pain. In addition, these active ingredients
are also suitable for the therapy of primary acute pain of any
origin and of secondary states of pain resulting therefrom, and for
the therapy of states of pain which were formerly acute and have
become chronic. The compounds of the invention can be employed
alone or in combination with other active ingredients for the
treatment of schizophrenia.
[0192] The in vitro effect of the compounds of the invention can be
shown in the following assays:
1. Determination of the Affinity of Test Substances for .alpha.7
nAChR by Inhibition of [.sup.3H]-Methyllycaconitine Binding to Rat
Brain Membranes
[0193] The [.sup.3H]-methyllycaconitine binding assay is a
modification of the method described by Davies et al. in
Neuropharmacol. 1999, 38, 679-690.
[0194] Rat brain tissue (hippocampus or whole brain) is homogenized
in homogenization buffer (10% w/v, 0.32 M sucrose, 1 mM EDTA, 0.1
mM phenylmethylsulphonyl fluoride (PMSF), 0.01% (w/v) NaN.sub.3, pH
7.4, 4.degree. C.) at 600 rpm in a glass homogenizer. The
homogenate is centrifuged (1000.times.g, 4.degree. C., 10 min) and
the supernatant is removed. The pellet is resuspended (20% w/v) and
the suspension is centrifuged (1000.times.g, 4.degree. C., 10 min).
The two supernatants are combined and centrifuged (15 000.times.g,
4.degree. C., 30 min). The pellet obtained in this way is referred
to as the P2 fraction.
[0195] The P2 pellet is suspended in, binding buffer (50 mM
Tris-HCl, 1 mM MgCl.sub.2, 120 mM NaCl, 5 mM KCl, 2 mM CaCl.sub.2,
pH 7.4), and the suspension is centrifuged (15 000.times.g,
4.degree. C., 30 min), twice.
[0196] The residue is resuspended in binding buffer and incubated
in a volume of 250 (amount of membrane protein 0.1-0.5 mg) in the
presence of 1-5 nM [.sup.3H]-methyl-lycaconitine 0.1% (w/v). BSA
(bovine serum albumin) and various concentrations of the test
substance at 21.degree. C. for 2.5 h. Incubation is then carried
out in the presence of 1 .mu.M .alpha.-bungarotoxin or 100 .mu.M
nicotine or 10 .mu.M MLA (methyllycaconitine).
[0197] The incubation is stopped by adding 4 ml PBS (20 mM
Na.sub.2HPO.sub.4, 5 mM KH.sub.2PO.sub.4, 150 mM NaCl, pH 7.4,
4.degree. C.) and filtering through type A/E glass fibre filters
(Gelman Sciences) which have previously been placed in 0.3% (v/v)
polyethyleneimine (PEI) for 3 h. The filters are washed twice with
4 ml of PBS (4.degree. C.), and the bound radioactivity is
determined by scintillation measurement. All the assays are carried
out in triplicate. The dissociation constant K.sub.i of the test
substance was determined from the IC.sub.50 of the compounds
(concentration of the test substance at which 50% of the ligand
bound to the receptor is displaced), the dissociation constant
K.sub.D and the concentration L of [.sup.3H]-methyllycaconitine
using the equation K.sub.i=IC.sub.50/(1+L/K.sub.D).
[0198] In place of [.sup.3H]-methyllycaconitine it is also possible
to employ other .alpha.7 nAChR-selective radioligands such as, for
example, [.sup.125I]-.alpha.-bungarotoxin or nonselective nAChR
radioligands together with inhibitors of other nAChRs.
[0199] Representative in vitro data for the effects of the
compounds of the invention are shown in Table A:
TABLE-US-00001 TABLE A Example No. K.sub.i (nM) 3 60 4 24 17 17 19
20 20 1.6 73 <1 75 <0.1 76 3.3 90 14 102 62 108 17 116 17 130
26 149 97 150 35 151 88 154 3 163 14 175 8.3 186 120
[0200] The suitability of the compounds of the invention for the
treatment of cognitive impairments can be shown in the following
animal models:
2. Object Recognition Test
[0201] The object recognition test is a memory test. It measures
the ability of rats (and mice) to distinguish between familiar and
unfamiliar objects.
[0202] The test is described by Blokland et al., NeuroReport 1998,
9, 4205-4208; A. Ennaceur et al., Behav. Brain Res. 1988, 31,
47-59; A. Ennaceur et al., Psychopharmacology 1992, 109, 321-330;
and Prickaerts et al., Eur. J. Pharmacol. 1997, 337, 125-136.
[0203] In a first run, a rat is confronted in an otherwise empty
observation arena of relatively large size by two identical
objects. The rat will investigate, i.e. sniff round and touch; both
objects extensively. In a second run, after an interval of 24
hours, the rat is put in the observation arena again. One of the
familiar objects has now been replaced by a new, unfamiliar object.
If a rat recognizes the familiar object, it will concentrate on
investigating the unfamiliar object. However, after 24 hours, a rat
has normally forgotten which object it investigated in the first
run, and it will therefore inspect both objects to the same extent.
Administration of a substance with a learning- and memory-improving
effect may lead to a rat recognizing the object seen in the first
run 24 hours previously as familiar. It will investigate the new,
unfamiliar object in more detail than the familiar one. This memory
ability is expressed in a discrimination index. A discrimination
index of zero means that the rat investigates both objects, the old
and the new, for equal times; that is to say it has not recognized
the old object and reacts to both objects as if they were new. A
discrimination index greater than zero means that the rat inspects
the new object longer than the old one; that is to say the rat has
recognized the old object.
3. Social Recognition Test:
[0204] The social recognition test is a test to examine the
learning- or memory-improving effect of test substances.
[0205] Adult rats housed in groups are placed singly in test cages
30 minutes before the start of the test. Four minutes before the
start of the test, the test animal is put in an observation box.
After this adaptation time, a juvenile animal is put in with the
test animal and the time for which the adult animal investigates
the juvenile animal is measured for 2 minutes (trial 1). All
behaviours clearly directed at the young animal are measured, i.e.
anogenital inspection, pursuit and fur care, during which the old
animal is no further than 1 cm from the young animal. The juvenile
animal is then taken out, and the adult is left in its test cage
(for 24-hour retention, the animal is returned to its home cage).
The adult test animal is treated with test substance before or
after the first test. Depending on the timing of the treatment, the
learning or the storage of the information about the young animal
can be influenced by the substance. After a fixed period
(retention), the test is repeated (trial 2). A larger difference
between the investigation times measured in trials 1 and 2 means
that the adult animal has remembered the young animal better.
[0206] The compounds of the invention are suitable for use as
medicaments for humans and animals.
[0207] The present invention also includes pharmaceutical
preparations which, besides inert, nontoxic, pharmaceutically
suitable excipients and carriers, contain one or more compounds of
the invention, or which consist of one or more compounds of the
invention, and to processes for producing these preparations.
[0208] The compounds of the invention are to be present in these
preparations in a concentration of from 0.1 to 99.5% by weight,
preferably from 0.5 to 95% by weight, of the complete mixture.
[0209] Besides the compounds of the invention, the pharmaceutical
preparations may also contain other active pharmaceutical
ingredients.
[0210] The abovementioned pharmaceutical preparations can be
produced by known methods in a conventional way.
[0211] The novel active ingredients can be converted in a known
manner into conventional formulations such as tablets, coated
tablets, pills, granules, aerosols, syrups, emulsions, suspensions
and solutions, using inert, nontoxic, pharmaceutically suitable
excipients or solvents. In these cases, the therapeutically active
compound should in each case be present in a concentration of about
0.5 to 90% by weight of the formulation, i.e. in amounts which are
sufficient to reach the stated dose range.
[0212] The formulations are produced for example by extending the
active ingredients with solvents and/or excipients, where
appropriate with use of emulsifiers and/or dispersants, it being
possible for example when water is used as diluent where
appropriate to use organic solvents as auxiliary solvents.
[0213] Administration can take place in a conventional way,
preferably orally, transdermally or parenterally, especially
perlingually or intravenously. However, it can also take place by
inhalation through the mouth or nose, for example with the aid of a
spray, or topically via the skin.
[0214] It has generally proved advantageous to administer amounts
of about 0.001 to 10 mg/kg, on oral administration preferably about
0.005 to 3 mg/kg, of body weight to achieve effective results.
[0215] It may, nevertheless, be necessary where appropriate to
deviate from the stated amounts, in particular as a function of the
body weight or of the mode of administration, of the individual
behaviour towards the medicament, the nature of its formulation and
the time or interval over which administration takes place. Thus,
it may be sufficient in some cases to make do with less than the
aforementioned minimum amount, whereas in other cases the stated
upper limit must be exceeded. Where larger amounts are
administered, it may be advisable to divide these into a plurality
of single doses over the day.
[0216] Unless indicated otherwise, all quantitative data relate to
percentages by weight. Solvent ratios, dilution ratios and
concentration data of liquid/liquid solutions are based in each
case on volume. The statement "w/v" means "weight/volume". Thus,
for example, "10% w/v" means: 100 ml of solution or suspension
contain 10g of substance.
ABBREVIATIONS
[0217] conc. Concentrated [0218] DAD Diode array detector [0219]
DBU 1,5-Diazabicyclo[4.3.0]non-5-ene [0220] DCI Desorption chemical
ionization (in MS) [0221] DMAP 4-N,N-Dimethylaminopyridine [0222]
DMF N,N-Dimethylformamide [0223] DMSO Dimethyl sulphoxide [0224]
EDC N'-(3-Dimethylaminopropyl)-N-ethylcarbodiimide.times.HCl [0225]
eq. equivalent(s) [0226] ESI Electrospray ionization (in MS) [0227]
HATU O-(7-Azabenzotriazol-1-yl)-N,N,N',N'-tetramethyluronium
hexafluorophosphate [0228] HOBt
1-Hydroxy-1H-benzotriazole.times.H.sub.2O [0229] HPLC High
pressure/high performance liquid chromatography [0230] LC-MS Liquid
chromatography with coupled mass spectroscopy [0231] MS Mass
spectroscopy [0232] NMR Nuclear magnetic resonance spectroscopy
[0233] PBS Phosphate-buffered saline [0234] PdCl.sub.2(dppf)
Bis(diphenylphosphino)ferrocenepalladium(II) chloride [0235]
PdCl.sub.2(PPh.sub.3).sub.2
Dichlorobis(triphenylphosphine)palladium [0236] Pd(PPh.sub.3).sub.4
Tetrakis(triphenylphosphine)palladium(0) [0237] Ph Phenyl [0238] RT
Room temperature [0239] R.sub.t Retention time (in HPLC) [0240]
TBTU O-(Benzotriazol-1-yl)-N,N,N',N'-tetramethyluronium
tetrafluoroborate [0241] THF Tetrahydrofuran [0242] TRIS
Tris(hydroxymethyl)aminomethane
HPLC and LC-MS Methods:
Method 1 (HPLC):
[0243] Instrument: HP 1100 with DAD; column: Kromasil RP-18, 60
mm.times.2 mm, 3.5 .mu.m; eluent: A=5 ml HClO.sub.4/L H.sub.2O,
eluent B=acetonitrile; gradient: 0 min 2% B, 0.5 min 2% B, 4.5 min
90% B, 6.5 min 90% B; flow rate: 0.75 mL/min; temperature:
30.degree. C.; detection: UV 210 nm.
Method 2 (LC-MS):
[0244] MS apparatus type: Micromass ZQ; HPLC apparatus type: Waters
Alliance 2790; column: symmetry C 18, 50 mm.times.2.1 mm, 3.5
.mu.m; eluent B: acetonitrile+0.05% formic acid, eluent A:
water+0.05% formic acid; gradient: 0 min 5% B.fwdarw.4.5 min 90%
B.fwdarw.5.5 min 90% B; oven: 50.degree. C.; flow rate: 1.0 mL/min;
UV detection: 210 nm.
Method 3 (LC-MS):
[0245] Instrument: Micromass Platform LCZ, HP 1100; column:
symmetry C18, 50 mm.times.2.1 mm, 3.5 .mu.m; eluent A: water+0.05%
formic acid, eluent B: acetonitrile+0.05% formic acid; gradient: 0
min 90% A.fwdarw.4.0 min 10% A.fwdarw.6.0 min 10% A; oven:
40.degree. C.; flow rate: 0.5 mL/min; UV detection: 208-400 nm.
Method 4 (LC-MS):
[0246] MS apparatus type: Micromass ZQ; HPLC apparatus type: Waters
Alliance 2790; column: Grom-Sil 120 ODS-4 HE 50 mm.times.2 mm, 3.0
.mu.m; eluent B: acetonitrile+0.05% formic acid, eluent A:
water+0.05% formic acid; gradient: 0.0 min 5% B.fwdarw.2.0 min 40%
B.fwdarw.4.5 min 90% B.fwdarw.5.5 min 90% B; oven: 45.degree. C.;
flow rate: 0.0 min 0.75 mL/min.fwdarw.4.5 min 0.75
mL/min.fwdarw.5.5 min 1.25 mL/min; UV detection: 210 nm.
Method 5 (LC-MS):
[0247] MS instrument: Micromass TOF (LCT); HPLC instrument:
2-column switching, Waters 2690; column: YMC-ODS-AQ, 50
mm.times.4.6 mm, 3.0 .mu.m; eluent A: water+0.1% formic acid,
eluent B: acetonitrile+0.1% formic acid; gradient: 0.0 min 100%
A.fwdarw.0.2 min 95% A.fwdarw.1.8 min 25% A.fwdarw.1.9 min 10%
A.fwdarw.3.2 min 10% A; oven: 40.degree. C.; flow rate: 3.0 mL/min;
UV detection: 210 nm.
Method 6 (LC-MS):
[0248] Flow injection, instrument: Micromass Platform LCZ+Quattro
LCZ; eluent A: water+0.05% formic acid, eluent B:
acetonitrile+0.05% formic acid; gradient: 0.0 min 30% A.fwdarw.1.0
min 30% A; flow rate: 0.2-0.3 mL/min; HPLC: instrument HP 1100; UV
detection: DAD.
Method 7 (HPLC):
[0249] Instrument: HP 1100 with DAD; column: Kromasil RP-18, 60
mm.times.2 mm, 3.5 .mu.m; eluent A: 5 ml HClO.sub.4/L H.sub.2O,
eluent B: acetonitrile; gradient: 0 min 2% B.fwdarw.0.5 min 2%
B.fwdarw.4.5 min 90% B.fwdarw.9 min 90% B; flow rate: 0.75 mL/min;
temperature: 30.degree. C.; UV detection: 210 nm.
Starting Compounds:
General Method A
Synthesis of methyl 1-benzothiophene-2-carboxylates
##STR00014##
[0251] Under an argon atmosphere, 1.5 equivalents of sodium hydride
(60% in liquid paraffin) are introduced into absolute DMSO
(0.60-1.26 M suspension). At room temperature, 1.1 equivalents of
methyl mercaptoacetate are slowly added dropwise to the reaction
mixture, and it is left to stir at room temperature until evolution
of hydrogen ceases (about 15 min). 1.0 equivalent of the
appropriate benzaldehyde are dissolved in absolute DMSO (1.60-3.36
M solution) and added at room temperature to the reaction mixture.
The reaction mixture is stirred until the reaction is complete
(about 5-10 min) and then poured into ice-water. The resulting
precipitate is filtered off with suction, dried at 40.degree. C. in
vacuo overnight and reacted further as crude product.
General method B
Synthesis of 1-benzothiophene-2-carboxylic acids
##STR00015##
[0253] A mixture of equal parts of THF and 2 N aqueous potassium
hydroxide solution (0.28-0.47 M solution) is added to the
appropriate methyl 1-benzothiophene-2-carboxylate. The reaction
mixture is left to stir at room temperature overnight. The THF is
removed in vacuo, and the aqueous reaction mixture is acidified
with concentrated hydrochloric acid. The resulting precipitate is
filtered off with suction and dried in vacuo at 40.degree. C.
General Method C
Amide linkage between 3-quinuclidinamine and 2-benzothiophene- or
2-benzo-furancarboxylic acids
[0254] 1.0 eq. of the appropriate enantiomeric 3-quinuclidinamine
hydrochloride is introduced together with 1 eq. of the carboxylic
acid and 1.2 eq. of HATU into DMF at 0.degree. C. After addition of
1.2 eq. of N,N-diisopropylethylamine, the mixture is stirred at RT.
After 30 min., a further 2.4 eq. of N,N-diisopropylethylamine are
added and the mixture is stirred at RT overnight.
EXAMPLE 1A
6-Bromo-1-benzofuran-2-carboxylic acid
##STR00016##
[0256] 8.0 g (39.8 mmol) of 4-bromo-2-hydroxybenzaldehyde and 1.47
g (3.98 mmol) of tetra-n-butylammonium iodide are mixed with 22 g
(159.19 mmol) of anhydrous potassium carbonate. 9.07 g (83.57 mmol)
of methyl chloroacetate are added. The reaction mixture is heated
at 130.degree. C. for 4 h and then cooled to 0.degree. C. in an ice
bath. 100 ml of THF and a solution of 13.4 g (238.8 mmol) of
potassium hydroxide in 50 ml of water are added, and the mixture is
then stirred at RT overnight. The THF is removed under reduced
pressure. The remaining aqueous phase is diluted with water and
acidified with conc. hydrochloric acid. The precipitated product is
filtered off and dried under high vacuum. Silica gel 60 (Merck,
Darmstadt; eluent: toluene, toluene/acetic acid 50:1,
toluene/acetic acid/methyl acetate 35:1:5) is used for final
purification. The solvent is removed under reduced pressure.
Finally, the last residues of solvent are removed under high
vacuum. 3.8 g (40% of theory) of the title compound are
isolated.
[0257] .sup.1H-NMR (400 MHz, methanol-d.sub.4): .delta.=7.91 (m,
1H), 7.61-7.51 (m, 3H).
[0258] HPLC (method 1): R.sub.1=4.1 min:
[0259] MS (ESIpos): m/z=258 (M+NH.sub.4).sup.+.
EXAMPLE 2A
N-[(3R)-1-Azabicyclo[2.2.2]oct-3-yl]-6-bromo-1-benzofuran-2-carboxamide
##STR00017##
[0261] 3.8 g (15.77 mmol) of 6-bromobenzofuran-2-carboxylic acid
(Example 1A), 3.14 g (15.77 mmol) of (R)-3-aminoquinuclidine
dihydrochloride, 7.19 g (18.92 mmol) of HATU, 7.34 g (56.76 mmol)
of N,N-diisopropylethylamine and 50 ml of DMF are reacted by
general method C. The crude product is taken up in methanol and
shaken together with acidic ion exchanger (Dowex.RTM. WX2-200) for
about 20 min. The loaded ion exchanger is washed successively with
methanol, dichloromethane and again with methanol. The product is
eluted with methanol/triethylamine 90:10. The solvent is removed in
a rotary evaporator under reduced pressure. Finally, the last
residues of solvent are removed under high vacuum. 5.14 g (85% of
theory) of the title compound are isolated. For analysis, a small
amount is converted into the hydrochloride with 4 N hydrogen
chloride in dioxane.
[0262] .sup.1H-NMR (200 MHz, DMSO-d.sub.6): .delta.=10.55 (br. s,
1H), 9.22 (d, 1H), 8.05 (s, 1H), 7.75-7.55 (m; 3H), 4.43-4.29 (m,
1H), 3.70-3.55 (m, 1H), 3.45-3.10 (m, 5H), 2.25-2.00 (m, 2H),
1.98-1.82 (m, 2H), 1.80-1.60 (m, 1H).
[0263] HPLC (method 1): R.sub.t=3.9 min.
[0264] MS (ESIpos): m/z=349 (M+H).sup.+.
[0265] LC-MS (method 2): R.sub.t=1.49 min.
[0266] MS (ESIpos): m/z=349 (M+H).sup.+.
EXAMPLE 3A
N-[(3R)-1-Azabicyclo[2.2.2]oct-3-yl]-5-bromo-1-benzofuran-2-carboxamide
hydrochloride
##STR00018##
[0268] 240 mg (0.98 mmol) of 5-bromobenzofuran-2-carboxylic acid,
200 mg (0.98 mmol) of (R)-3-aminoquinuclidine dihydrochloride, 450
mg (1.18 mmol) of HATU, 460 mg (3.54 mmol) of
N,N-diisopropylethylamine and 2.0 ml of DMF are reacted by general
method C. The reaction mixture is purified by preparative HPLC.
Finally, an excess of 1N hydrochloric acid is added to the product.
The solvent is removed under reduced pressure. 202 mg (53% of
theory) of the title compound are isolated.
[0269] .sup.1H-NMR (200 MHz, DMSO-d.sub.6): .delta.=9.38 (br. s,
1H), 8.88 (d, 1H), 7.60 (s, 1H), 7.38-7.20 (m, 2H), 7.09 (dd, 1H),
4.43-4.29 (m, 1H), 3.70-3.55 (m, 1H), 3.45-3.10 (m, 5H), 2.25-2.00
(m, 2H), 1.98-1.82 (m, 2H), 1.80-1.60 (m, 1H).
[0270] MS (ESIpos): m/z=349 (M+H).sup.+ (free base).
[0271] LC-MS (method 3): R.sub.t=2.71 min.
[0272] MS (ESIpos): m/z=349 (M+H).sup.+ (free base).
EXAMPLE 4A
7-Bromo-5-fluoro-1-benzofuran-2-carboxylic acid
##STR00019##
[0274] 1.0 g (5.24 mmol) of 2-bromo-4-fluorophenol is introduced
into 4.0 ml of trifluoroacetic acid. 1.47 g (10.47 mmol) of
hexamethylenetetramine are added in portions over the course of 20
min. The mixture is then boiled under reflux for 28 h. At RT, 6 ml
of water and 3 ml of 50% strength sulphuric acid are added. After 2
h, the mixture is extracted twice with a total of 60 ml of ethyl
acetate. The combined organic phases are washed four times with 1N
hydrochloric acid and once with water. Drying over magnesium
sulphate is followed by removal of the solvent under reduced
pressure. Finally, the last residues of solvent are removed under
high vacuum. The crude product (without further purification) and
0.19 g (0.52 mmol) of tetra-n-butylammonium iodide are mixed with
2.9 g (20.96 mmol) of anhydrous potassium carbonate. 1.19 g (11.0
mmol) of methyl chloroacetate are added. The reaction mixture is
heated at 130.degree. C. for 4 h and then cooled to 0.degree. C. in
an ice bath. 18 ml of THF and a solution of 1.76 g (31.44 mmol) of
potassium hydroxide in 18 ml of water are added. The mixture is
stirred at RT overnight. The solvent is removed under reduced
pressure. Dilution with water is followed by acidification with
concentrated hydrochloric acid. The mixture is extracted twice with
ethyl acetate. The combined organic phases are dried over magnesium
sulphate, and the solvent is removed in a rotary evaporator under
reduced pressure. Silicagel 60 (Merck, Darmstadt; eluent:
toluene/acetic acid 40:1) is used for purification. The solvent is
removed under reduced pressure. Finally, the last residues of
solvent are removed under high vacuum. 257 mg (19% of theory over
the two stages) of the title compound are isolated.
[0275] .sup.1H-NMR (400 MHz, methanol-d.sub.4): .delta.=7.60 (m,
1H), 7.48-7.35 (m, H).
[0276] HPLC (method 1): R.sub.t=4.1 min.
[0277] MS (ESIpos): m/z=276 (M+NH.sub.4).sup.+.
EXAMPLE 5A
N-[(3R)-1-Azabicyclo[2.2.2]oct-3-yl]-5-fluoro-7-bromo-1-benzofuran-2
##STR00020##
[0279] 143 mg (0.55 mmol) of
5-fluoro-7-bromo-1-benzofuran-2-carboxylic acid (Example 4A), 100
mg (0.50 mmol) of (R)-3-aminoquinuclidine dihydrochloride, 229.14
mg (0.6 mmol) of HATU, 234 mg (1.81 mmol) of
N,N-diisopropylethylamine and 2.0 ml of DMF are reacted by general
method C. DMF is removed under reduced pressure, and the crude
product is dissolved in 1N sodium hydroxide solution. The aqueous
phase is extracted with ethyl acetate, and the organic phase is
washed with saturated aqueous sodium chloride solution. The
combined organic phases are dried over magnesium sulphate, and the
solvent is removed in a rotary evaporator under reduced pressure.
The crude product is taken up in methanol and shaken together with
acidic ion exchanger (Dowex.RTM. WX2-200) for about 20 min. The
loaded ion exchanger is washed three times with 30 ml of methanol
each time, then with water, again with methanol, with
dichloromethane and finally again with methanol. The product is
eluted with methanol/triethylamine 95:5. The solvent is removed in
a rotary evaporator under reduced pressure. 181 mg (98% of theory)
of the title compound are isolated.
[0280] .sup.1H-NMR (400 MHz, methanol-d.sub.4): .delta.=7.59 (d,
1H), 7.53-7.46 (m, 2H), 4.24-4.18 (m, 1H), 3.34-3.29 (m, 1H),
3.07-2.97 (m, 1H), 2.93-2.77 (m, 4H), 2.13-2.05 (m, 1H), 1.98-1.86
(m, 1H), 1.84-1.75 (m, 2H), 1.63-1.53 (m, 1H).
[0281] MS (ESIpos): m/z=367 (M+H).sup.+.
[0282] LC-MS (method 3): R.sub.t=2.92 min.
[0283] MS (ESIpos): m/z=367 (M+H).sup.+.
EXAMPLE 6A
Methyl 7-bromo-1-benzothiophene-2-carboxylate
##STR00021##
[0285] Starting from 27.8 g (137.1 mmol) of
3-bromo-2-fluorobenzaldehyde, by general method A with 8.2 g (205.7
mmol) of sodium hydride (60% in liquid paraffin) and 16.0 g (150.9
mmol) of methyl mercaptoacetate, 20.57 g of a mixture of the title
compound and the corresponding acid (about 1:1) is obtained.
EXAMPLE 7A
7-Bromo-1-benzothiophene-2-carboxylic acid
##STR00022##
[0287] Starting from 10.0 g (36.9 mmol) of methyl
7-bromo-1-benzothiophene-2-carboxylate, by general method B 8.99 g
(91.0% of theory) of the desired product are obtained.
[0288] .sup.1H-NMR (200 MHz, DMSO-d.sub.6): .delta.=13.76 (br. s,
1H), 8.28 (s, 1H), 8.07 (d, 1H), 7.78 (d, 1H), 7.46 (dd, 1H).
[0289] HPLC (method 1): R.sub.t=4.4 min.
EXAMPLE 8A
N-(1-Azabicyclo[2.2.2]oct-3-yl)-7-bromo-1-benzothiophene-2-carboxamide
hydrochloride
##STR00023##
[0291] 903.8 mg (3.52 mmol) of
7-bromo-1-benzothiophene-2-carboxylic acid (Example 7A), 700 mg
(3.52 mmol) of (R)-3-aminoquinuclidine dihydrochloride, 1604.0 mg
(4.22 mmol) of HATU, 1635.7 mg (12.66 mmol) of
N,N-diisopropylethylamine and 7.0 ml of DMF are reacted by general
method C. The reaction mixture is purified by preparative HPLC. The
product is dissolved in a 1:1 mixture of 4 M hydrogen chloride in
dioxane and 1N hydrochloric acid and then concentrated and dried
under high vacuum. 1087 mg (77% of theory) of the title compound
are obtained.
[0292] .sup.1H-NMR (200 MHz, DMSO-d.sub.6): .delta.=10.01 (br. s,
1H), 9.15 (d, 1H), 8.47 (s, 1H), 8.02 (m, 1H), 7.74 (m, 1H), 7.43
(dd, 1H), 4.34 (m, 1H), 3.80-3.10 (m, 6H), 2.22 (m, 1H), 2.14 (m,
1H), 1.93 (m, 2H), 1.78 (m, 1H).
[0293] HPLC (method 1): R.sub.t=4.1 min.
[0294] MS (ESIpos): m/z=365 (M+H).sup.+ (free base).
EXAMPLE 9A
Methyl 6-bromo-1-benzothiophene-2-carboxylate
##STR00024##
[0296] Starting from 6.54 g (32.2 mmol) of
4-bromo-2-fluorobenzaldehyde, by general method A with 1.93 g (48.3
mmol) of sodium hydride (60% in liquid paraffin) and 3.76 g (35.5
mmol) of methyl mercaptoacetate, 4.06 g (46% of theory) of the
title compound are obtained.
[0297] .sup.1H-NMR (200 MHz, DMSO-d.sub.6): .delta.=8.42 (d, 1H),
8.22 (s, 1H), 7.98 (d, 1H), 7.65 (dd, 1H), 3.90 (s, 3H).
[0298] HPLC (method 1): R.sub.t=5.3 min.
[0299] MS (ESIpos): m/z=270 (M.sup.+).
EXAMPLE 10A
6-Bromo-1-benzothiophene-2-carboxylic acid
##STR00025##
[0301] Starting from 4.0 g (14.8 mmol) of methyl
6-bromo-1-benzothiophene-2-carboxylate (from Example 9A), by
general method B 3.55 g (94% of theory) of the desired product are
obtained.
[0302] .sup.1H-NMR (400 MHz, DMSO-d.sub.6): .delta.=13.48 (br. s,
1H), 8.38 (s, 1H), 8.22 (s, 1H), 7.96 (d, 1H), 7.63 (m, 1H).
[0303] HPLC (method 1): R.sub.t=4.5 min.
EXAMPLE 11A
N-[(3R)-1-Azabicyclo[2.2.2]oct-3-yl]-6-bromo-1-benzothiophene-2-carboxamid-
e hydrochloride
##STR00026##
[0305] 900.0 mg (3.50 mmol) of
6-bromo-1-benzothiophene-2-carboxylic acid (Example 10A), 697.0 mg
(3.50 mmol) of (R)-3-aminoquinuclidine dihydrochloride, 1597.1 mg
(4.20 mmol) of HATU, 1628.7 mg (12.60 mmol) of
N,N-diisopropylethylamine and 8.0 ml of DMF are reacted by general
method C. The reaction mixture is purified by preparative HPLC. The
product is dissolved in a 1:1 mixture of 4 M hydrogen chloride in
dioxane and 1N hydrochloric acid, and the solution is then
concentrated. Recrystallization from methanol/ethanol (1:10)
affords 594 mg (42% of theory) of the title compound in the form of
yellowish-brown crystals.
[0306] .sup.1H-NMR (300 MHz, DMSO-d.sub.6): .delta.=9.81 (br. s,
1H), 8.76 (m, 1H), 8.33 (s, 1H), 8.22 (s, 1H), 7.91 (d, 1H), 7.59
(dd, 1H), 4.15 (m, 1H), 3.51-2.93 (m, 6H), 2.12-1.92 (m, 2H), 1.79
(m, 2H), 1.58 (m, 1H).
[0307] HPLC (method 1): R.sub.r=4.1 min.
[0308] MS (ESIpos): m/z=364 (M.sup.+) (free base).
EXAMPLE 12A
Methyl 5-bromo-1-benzothiophene-2-carboxylate
##STR00027##
[0310] Starting from 2.99 g (14.7 mmol) of
5-bromo-2-fluorobenzaldehyde, by general method A with 0.88 g (22.1
mmol) of sodium hydride (60%) and 1.72 g (16.2 mmol) of methyl
mercaptoacetate, 2.76 g (69.1% of theory) of the title compound are
obtained.
[0311] .sup.1H-NMR (200 MHz, DMSO-d.sub.6): .delta.=8.29 (d, 1H),
8.18 (s, 1H), 8.08 (d, 1H), 7.69 (dd, 1H), 3.90 (s, 3H).
[0312] HPLC (method 1): R.sub.t=5.2 min.
[0313] MS (ESIpos): m/z=270 (M.sup.+).
EXAMPLE 13A
5-Bromo-1-benzothiophene-2-carboxylic acid
##STR00028##
[0315] Starting from 2.7 g (9.96 mmol) of methyl
5-bromo-1-benzothiophene-2-carboxylate (from Example 12A), by
general method B 2.41 g (94% of theory) of the desired product are
obtained.
[0316] .sup.1H-NMR (400 MHz, DMSO-d.sub.6): .delta.=13.67 (br. s,
1H), 8.27 (m, 1H), 8.10 (s, 1H), 8.05 (d, 1H), 7.66 (dd, 1H).
[0317] HPLC (method 1): R.sub.t=4.5 min.
EXAMPLE 14A
N-[(3R)-1-Azabicyclo[2.2.2]oct-3-yl]-5-bromo-1-benzothiophene-2-carboxamid-
e hydrochloride
##STR00029##
[0319] 133.7 mg (0.52 mmol) of
5-bromo-1-benzothiophene-2-carboxylic acid (Example 13A), 155.4 mg
(0.78 mmol) of (R)-3-aminoquinuclidine dihydrochloride, 296.7 mg
(0.78 mmol) of HATU, 369.8 mg (2.86 mmol) of
N,N-diisopropylethylamine and 1.5 ml of DMF are reacted by general
method C. The reaction mixture is purified by preparative HPLC. The
product is dissolved in acetonitrile, and an excess of 1N
hydrochloric acid is added. Finally, the solvent is removed. 175 mg
(84% of theory) of the title compound are isolated.
[0320] .sup.1H-NMR (200 MHz, DMSO-d.sub.6): .delta.=9.44 (br. s,
1H), 8.95 (d, 1H), 8.30-8.10 (m, 2H), 8.03 (d, 1H), 7.60 (m, 1H),
4.38-4.20 (m, 1H), 3.80-3.55 (m, 1H), 3.42-3.05 (m, 5H), 2.25-2.00
(m, 2H), 1.98-1.62 (m, 3H).
[0321] HPLC (method 1): R.sub.t=4.1 min.
[0322] MS (ESIpos): m/z=365 (M+H).sup.+ (free base).
EXAMPLE 15A
4-(4-Bromophenyl)morpholine
##STR00030##
[0324] A solution of 6.94 ml (134.8 mmol) of bromine in 25 ml of
acetic acid is slowly added dropwise over a period of 40 min to a
solution of 20 g (122.5 mmol) of N-phenylmorpholine in 170 ml of
acetic acid at room temperature. After stirring at room temperature
for 30 min, the reaction mixture is stirred into 750 ml of water
and adjusted to pH 11 with 45% strength sodium hydroxide solution.
The resulting precipitate is filtered off with suction, washed with
water and dried under high vacuum. Recrystallization from ethanol
results in 18.6 g (62.9% of theory) of the title compound.
[0325] .sup.1H-NMR (200 MHz, DMSO-d.sub.6): .delta.=7.37 (m, 2H),
6.89 (m, 2H), 3.73 (m, 4H), 3.08 (m, 4H).
[0326] HPLC (method 1): R.sub.t=3.9 min.
[0327] MS (ESIpos): m/z=242 (M+H).sup.+.
EXAMPLE 16A
4-(4-Bromophenyl)-3-morpholinone
##STR00031##
[0329] 1.41 g (6.20 mmol) of benzyltriethylammonium chloride and
0.98 g (6.20 mmol) of potassium permanganate are added to a
solution of 500 mg (2.07 mmol) of 4-(4-bromophenyl)morpholine
(Example 15A) in 10 ml of dichloromethane. After 5 h under reflux,
the contents of the flask are concentrated in vacuo, and the
residue is purified by preparative HPLC. The concentrated product
is dried under high vacuum. 217 mg (35.7% of theory) of the title
compound are obtained.
[0330] LC-MS (method 4): R.sub.t=2.9 min, m/z=255 (M.sup.+).
EXAMPLE 17A
3-(4-Morpholinyl)phenyl trifluoromethanesulphonate
##STR00032##
[0332] 2.18 ml (12.9 mmol) of trifluoromethanesulphonic anhydride
are slowly added dropwise to a solution, cooled to -10.degree. C.,
of 1.54 g (8.6 mmol) of 3-(4-morpholinyl)-phenol and 3.59 ml (25.8
mmol) of triethylamine in 10 ml of dichloromethane. The mixture is
stirred at -10.degree. C. for 30 min and then at 0.degree. C. for
30 min. It is washed successively with 10% strength sodium
bicarbonate solution, water and saturated sodium chloride solution,
dried over sodium sulphate and concentrated in vacuo, and the
residue is dried under high vacuum. 2.41 g (90.1% of theory) of the
title compound are obtained.
[0333] .sup.1H-NMR (200 MHz, CDCl.sub.3): .delta.=7.28 (m, 1H),
6.88 (m, 1H), 6.73 (m, 2H), 3.86 (m, 4H), 3.18 (m, 4H).
[0334] HPLC (method 1): R.sub.t=4.8 min.
[0335] MS (ESIpos): m/z=312 (M+H).sup.+.
EXAMPLE 18A
4-(4-Morpholinylcarbonyl)phenyl trifluoromethanesulphonate
##STR00033##
[0337] 1.23 ml (7.24 mmol) of trifluoromethanesulphonic anhydride
are slowly added dropwise to a solution, cooled to -10.degree. C.,
of 1.0 g (4.83 mmol) of 4-(4-morpholinyl-carbonyl)phenol and 2.02
ml (14.48 mmol) of triethylamine in 20 ml of dichloromethane. The
mixture is stirred at -10.degree. C. for 30 min and then at
0.degree. C. for 30 min. It is washed successively with 10%
strength sodium bicarbonate solution, water and saturated sodium
chloride solution, dried over sodium sulphate and concentrated in
vacuo, and the residue is dried under high vacuum. 1.71 g (94.6% of
theory) of the title compound are obtained.
[0338] .sup.1H-NMR (400 MHz, methanol-d.sub.4): .delta.=7.62 (m,
2H), 7.49 (m, 2H), 3.86-3.34 (m, 8H).
[0339] HPLC (method 1): R.sub.t=4.2 min.
[0340] MS (ESIpos): m/z=357 (M+NH.sub.4).sup.+.
EXAMPLE 19A
Methyl
7-[4-(4-morpholinyl)phenyl]-1-benzothiophene-2-carboxylate
##STR00034##
[0342] 3.42 ml of 2 M sodium carbonate solution and 83.5 mg (0.11
mmol) of PdCl.sub.2(dppf) are added to a solution of 619.1 mg (2.28
mmol) of methyl 7-bromo-1-benzothiophene-2-carboxylate (Example 6A)
and 520 mg (2.51 mmol) of 4-(4-morpholinyl)phenylboronic acid in 10
ml DMF. The mixture is heated at 80.degree. C. for 16h. Cooling is
followed by filtration through kieselguhr and purification by
preparative HPLC. The concentrated product is dried under high
vacuum. 146.7 mg (16.4% of theory) of the title compound are
obtained.
[0343] HPLC (method 1): R.sub.t4.6 min.
[0344] MS (ESIpos): m/z=354 (M+H).sup.+.
EXAMPLE 20A
7-[4-(4-Morpholinyl)phenyl]-1-benzothiophene-2-carboxylic acid
##STR00035##
[0346] A solution of 330 mg (0.77 mmol) of methyl
7-[4-(4-morpholinyl)phenyl]-1-benzo-thiophene-2-carboxylate
(Example 19A) in 6 ml of a 1:1 mixture of methanol and 2N potassium
hydroxide solution is stirred at room temperature for 2 h and at
50.degree. C. for 1 h. The reaction mixture is concentrated in
vacuo and, after addition of water, acidified with conc.
hydrochloric acid. The resulting precipitate is filtered off with
suction, washed twice with water and dried under high vacuum. 292
mg of crude product are obtained and reacted without further
purification.
EXAMPLE 21A
7-(2-Methoxyphenyl)-1-benzofuran-2-carboxylic acid
##STR00036##
[0348] 5.0 g (20.7 mmol) of 7-bromo-1-benzofuran-2-carboxylic acid
(Example 29A) and 3.78 g (24.9 mmol) of 2-methoxyphenylboronic acid
are introduced into 50 ml of DMF. Addition of 31.1 ml of 2 M sodium
carbonate solution and 1.2 g (1.04 mmol) of Pd(PPh.sub.3).sub.4 is
followed by heating to 90.degree. C. After 18 h, the solvent is
distilled out. The residue is partitioned between 1N hydrochloric
acid and ethyl acetate and extracted three times with 200 ml of
ethyl acetate each time. The organic phase is dried over sodium
sulphate and concentrated in vacuo. The residue is purified by
flash chromatography (silica gel, mobile phase:
dichloromethane/methanol/acetic acid 100:10:1). Concentration and
drying under high vacuum result in 2.97 g (53.2% of theory) of the
title compound.
[0349] .sup.1H-NMR (300 MHz, DMSO-d.sub.6): .delta.=13.46 (s, 1H),
7.73 (dd, 1H), 7.59 (s, 1H), 7.48-7.33 (m, 4H), 7.20 (d, 1H), 7.09
(m, 1H), 3.75 (s, 3H).
[0350] HPLC (method 1): R.sub.t=4.5 min.
[0351] MS (ESIpos): m/z=286 (M+NH.sub.4).sup.+.
EXAMPLE 22A
N-[(3S)-1-Azabicyclo[2.2.2]oct-3-yl]-7-bromo-1-benzothiophene-2-carboxamid-
e hydrochloride
##STR00037##
[0353] 3.58 g (18.7 mmol) of EDC, 2.52 g (18.7 mmol) of HOBt and
7.8 ml (56 mmol) of triethylamine are added to a solution, cooled
to 0.degree. C., of 4.0 g (15.6 mmol) of
7-bromo-1-benzothiophene-2-carboxylic acid (Example 7A) and 3.10 g
(15.6 mmol) of (S)-3-aminoquinuclidine dihydrochloride in 50 ml of
DMF. The mixture is stirred at room temperature for 18 h. The
reaction is stopped by adding 10% strength sodium bicarbonate
solution. The precipitate resulting after addition of ethyl acetate
is filtered off. The aqueous phase is extracted with ethyl acetate,
the combined organic phases are dried over sodium sulphate and
concentrated, and the residue is dried under high vacuum. 4.70 g
(68% of theory) of the title compound are obtained.
[0354] The spectroscopic data agree with those of the enantiomeric
compound (Example 8A).
EXAMPLE 23A
N-[(3R)-1-Azabicyclo[2.2.2]oct-3-yl]-6-(4-formylphenyl)-1-benzothiophene-2-
-carboxamide hydrochloride
##STR00038##
[0356] 200 mg (0.50 mmol) of
N-[(3R)-1-azabicyclo[2.2.2]oct-3-yl]-6-bromo-1-benzo-thiophene-2-carboxam-
ide hydrochloride (Example 11A) and 74.6 mg (0.50 mmol) of
4-formylphenylboronic acid are introduced into 2 ml of DMF.
Addition of 0.75 ml of 2 M sodium carbonate solution and 20.3 mg
(0.02 mmol) of PdCl.sub.2(dppf) is followed by heating to
80.degree. C. After 18 h, the reaction mixture is filtered through
kieselguhr and purified by preparative HPLC. The product fractions
are concentrated, mixed with a 5:1 mixture of methanol and 4 N
hydrogen chloride in dioxane and again concentrated. Drying under
high vacuum results in 163.8 mg (75.0% of theory) of the title
compound.
[0357] .sup.1H-NMR (200 MHz, DMSO-d.sub.6): .delta.=10.09 (s, 1H),
10.07 (br. s, 1H), 9.10 (d, 1H), 8.50 (m, 1H), 8.37 (s, 1H),
8.15-7.97 (m, 5H), 7.87 (dd, 1H), 4.33 (m, 1H), 3.68 (m, 1H),
3.45-3.12 (m, 5H), 2.23 (m, 1H), 2.16 (m, 1H), 1.91 (m, 2H), 1.76
(m, 1H).
[0358] HPLC (method 1): R.sub.t=4.1 min.
[0359] MS (ESIpos): m/z=391 (M+H).sup.+ (free base).
EXAMPLE 24A
Methyl 6-cyano-1-benzothiophene-2-carboxylate
##STR00039##
[0361] 4.08 g (23.2 mmol) of 4-cyano-2-nitrobenzaldehyde, 2.46 g
(23.2 mmol) of methyl mercaptoacetate and 6.46 ml (46.4 mmol) of
triethylamine are heated in 12.3 ml of DMSO at 80.degree. C. for
2.5 h. The reaction solution is added to 400 ml of ice-water. The
precipitate resulting after addition of 4 ml of acetic acid is
filtered off with suction, washed twice with water and dried in
vacuo at 50.degree. C. overnight. 4.19 g (83.2% of theory) of the
title compound are obtained.
[0362] .sup.1H-NMR (200 MHz, DMSO-d.sub.6): .delta.=8.73 (d, 1H),
8.32 (s, 1H), 8.21 (d, 1H), 7.85 (dd, 1H), 3.92 (s, 3H).
[0363] HPLC (method 1): R.sub.t=4.4 min.
[0364] MS (ESIpos): m/z=218 (M+H).sup.+.
EXAMPLE 25A
6-Cyano-1-benzothiophene-2-carboxylic acid
##STR00040##
[0366] In accordance with general method B, 0.49 g (61.6% of
theory) of the desired product is obtained starting from 0.6 g
(2.76 mmol) of methyl 6-cyano-1-benzothiophene-2-carboxylate
(Example 24A).
[0367] HPLC (method 1): R.sub.t=3.9 min.
[0368] MS (ESIpos): m/z=222 (M+H).sup.+.
EXAMPLE 26A
N-[(3R)-1-Azabicyclo[2.2.2]oct-3-yl]-6-cyano-1-benzothiophene-2-carboxamid-
e
##STR00041##
[0370] 320.8 mg (1.1 mmol) of 6-cyano-1-benzothiophene-2-carboxylic
acid (Example 25A), 200 mg (1.0 mmol) of (R)-3-aminoquinuclidine
dihydrochloride, 458.3 mg (1.21 mmol) of HATU, 467.3 mg (3.62 mmol)
of N,N-diisopropyl-ethylamine and 4.0 ml of DMF are reacted by
general method C. The reaction mixture is purified by preparative
HPLC. The product is dissolved in a mixture of methanol and 4 M
hydrogen chloride in dioxane and then concentrated and dried under
high vacuum. 222.1 mg (64% of theory) of the title compound are
obtained.
[0371] .sup.1H-NMR (300 MHz, DMSO-d.sub.6): .delta.=9.80 (m, 1H),
9.12 (d, 1H), 8.68 (s, 1H), 8.37 (s, 1H), 8.16 (d, 1H), 7.83 (dd,
1H), 4.33 (m, 1H), 3.76-3.05 (m, 6H), 2.23 (m, 1H), 2.13 (m, 1H),
1.92 (m, 2H), 1.76 (m, 1H).
[0372] HPLC (method 1): R.sub.t=3.6 min.
[0373] MS (ESIpos): m/z=312 (M+H).sup.+ (free base)
EXAMPLE 27A
6-[(Z)-Amino(hydroxyimino)methyl]-N-[(3R)-1-azabicyclo[2.2.2]oct-3-yl]-1-b-
enzothiophene-2-carboxamide dihydrochloride
##STR00042##
[0375] 800 mg (2.0 mmol) of
N-[(3R)-1-azabicyclo[2.2.2]oct-3-yl]-6-cyano-1-benzothiophene-2-carboxami-
de hydrochloride (Example 26A), 278.1 mg (4.0 mmol) of
hydroxylamine hydrochloride and 829.5 mg (6.0 mmol) of potassium
carbonate are heated in 8 ml of an 8:1 mixture of water and ethanol
at 80.degree. C. for 3 h. The mixture is purified by column
chromatography on silica gel (mobile phase:
dichloromethane/methanol/25% ammonia solution 100:20:4). The
product fractions are combined, concentrated, mixed with methanol
and 4 M hydrogen chloride in dioxane, then again concentrated and
dried under high vacuum. 447.3 mg (53.6% of theory) of the title
compound are obtained.
[0376] .sup.1H-NMR (200 MHz, DMSO-d.sub.6): .delta.=11.15 (m, 1H),
10.22 (m, 1H), 9.36 (d, 1H), 8.52 (s, 1H), 8.46 (m, 1H), 8.14 (d,
1H), 7.73 (dd, 1H), 4.33 (m, 1H), 3.93-3.10 (m, 6H), 2.32-2.05 (m,
2H), 1.93 (m, 2H), 1.75 (m, 1H).
[0377] HPLC (method 1): R.sub.t=2.9 min.
[0378] MS (ESIpos): =345 (M+H).sup.+ (free base).
EXAMPLE 28A
3-Bromo-2-hydroxybenzaldehyde
##STR00043##
[0380] 20.0 g (115.6 mmol) of 2-bromophenol are introduced into 500
ml of dry acetonitrile. 16.84 g (176.87 mmol) of dry magnesium
chloride, 23.4 g of paraformaldehyde granules and 41.9 ml (300.6
mmol) of triethylamine are added. The reaction mixture is heated
under reflux for 4 h and, after cooling to 0.degree. C., 300 ml of
2N hydrochloric acid are added. The aqueous phase is extracted
three times with 200 ml of diethyl ether each time. The organic
phase is dried over magnesium sulphate, and the solvent is removed
in vacuo. 24 g (64% of theory, 62% pure according to HPLC) of the
title compound are isolated and reacted further without further
purification.
[0381] HPLC (method 1): R.sub.t=4.25 min.
[0382] MS (ESIpos): m/z=202 (M+H).sup.+.
EXAMPLE 29A
7-Bromo-1-benzofuran-2-carboxylic acid
##STR00044##
[0384] 13.5 g (40.3 mmol) of 3-bromo-2-hydroxybenzaldehyde (Example
28A, 62% pure) are heated together with 9.18 g (84.62 mmol) of
methyl chloroacetate, 1.49 g (4.03 mmol) of tetra-n-butylammonium
iodide and 22.28 g (161.18 mmol) of potassium carbonate at
130.degree. C. for 6 h. After cooling to RT, 100 ml of water and
100 ml of THF, and 13.57 g (241.77 mmol) of potassium hydroxide are
added, and the mixture is stirred at RT overnight. The solvent is
removed under reduced pressure, and the residue is taken up in 400
ml of water and washed four times with a total of 400 ml of diethyl
ether. While cooling in ice, the pH is adjusted to 0 with
concentrated hydrochloric acid and five extractions with a total of
700 ml of ethyl acetate are carried out. The organic phase is
washed with 100 ml of saturated sodium chloride solution and then
dried over magnesium sulphate. The crude product is completely
freed of residual solvents under high vacuum and is stirred with 80
ml of diethyl ether. The product is filtered off and washed with a
little ice-cold diethyl ether. 4.8 g (47% of theory) of the title
compound are isolated.
[0385] .sup.1H-NMR (200 MHz, DMSO-d.sub.6): .delta.=13.5 (br. s,
1H), 7.86-7.72 (m, 2H), 7.79 (s, 1H), 7.31 (t, 1H).
[0386] MS (DCI/NH.sub.3): m/z=258 (M+NH.sub.4).sup.+.
EXAMPLE 30A
N-[(3R)-1-Azabicyclo[2.2.2]oct-3-yl]-7-bromo-1-benzofuran-2-carboxamide
##STR00045##
[0388] 5.20 g (21.57 mmol) of 7-bromobenzofuran-2-carboxylic acid
(Example 29A), 4.3 g (21.57 mmol) of (R)-3-aminoquimiclidine
dihydrochloride, 9.84 g (25.89 mmol) of HATU, 13.53 ml (74.68 mmol)
of N,N-diisopropylethylamine and 21 ml of DMF are reacted by
general method C. The solvent is removed under reduced pressure,
and the crude product is taken up in 100 ml of ethyl acetate and
washed 15 times with a total of 1.5 l of 1N sodium hydroxide
solution. The organic phase is dried over magnesium sulphate and
freed of solvent. 5.2 g (69% of theory) of the title compound are
isolated.
[0389] .sup.1H-NMR (300 MHz, DMSO-d.sub.6): .delta.=8.48 (d, 1H),
7.85-7.65 (m, 3H), 7.25 (t, 1H), 3.95 (m, 1H), 3.15 (m, 1H), 2.95
(m, 1H), 2.80-2.60 (m, 4H), 1.90 (m, 1H), 1.70 (m, 1H), 1.58 (m,
2H), 1.35 (m, 1H).
[0390] HPLC (method 1): R.sub.t=3.79 min.
[0391] MS (ESIpos): m/z=349 (M+H).sup.+
[0392] [.alpha.].sup.20.sub.D=26.9.degree. (c=0.50, methanol).
[0393] In some exemplary embodiments, the corresponding
hydrochloride is employed and is obtained by mixing the title
compound with a 5:1 mixture of methanol and 1N hydrochloric acid
and then concentrating and drying under high vacuum.
EXAMPLE 31A
N-[(3S)-1-Azabicyclo[2.2.2]oct-3-yl]-7-bromo-1-benzofuran-2-carboxamide
##STR00046##
[0395] 4.0 g (16.59 mmol) of 7-bromobenzofuran-2-carboxylic acid
(Example 29A), 3.3 g (16.59 mmol) of (S)-3-aminoquinuclidine
dihydrochloride, 7.57 g (19.91 mmol) of HATU, 10.41 ml (59.74 mmol)
of N,N-diisopropylethylamine and 21 ml of DMF are reacted by
general method C. The solvent is removed under reduced pressure,
and the crude product is taken up in 100 ml of ethyl acetate and
washed 15 times with a total of 1.5 l of 1N sodium hydroxide
solution. The organic phase is dried over magnesium sulphate and
freed of solvent. 5.0 g (85% of theory) of the title compound are
isolated.
[0396] The analytical data agree with those of Example 30A.
[0397] [.alpha.].sup.20.sub.D=-28.0.degree. (c=0.1, methanol).
EXAMPLE 32A
2-(4-Morpholinyl)phenyl trifluoromethanesulphonate
##STR00047##
[0399] 2.78 ml (16.4 mmol) of trifluoromethanesulphonic anhydride
are slowly added dropwise to a solution, cooled to -10.degree. C.,
of 2 g (10.9 mmol) of 2-(4-morpholinyl)-phenol and 4.57 ml (32.8
mmol) of triethylamine in 15 ml of dichloromethane. The mixture is
stirred at -10.degree. C. for 30 min and then at 0.degree. C. for
30 min. It is washed successively with 10% strength sodium
bicarbonate solution, water and saturated sodium chloride solution,
dried over sodium sulphate and concentrated in vacuo, and the
residue is dried under high vacuum. 3.48 g (87.6% of theory) of the
title compound are obtained.
[0400] HPLC (method 1): R.sub.t=4.9 min.
[0401] MS (ESIpos): ink=312 (M+H).sup.+.
EXAMPLE 33A
N-[(3R)-1-Azabicyclo[2.2.2]oct-3-yl]-6-(3-formylphenyl)-1-benzothiophene-2-
-carb-oxamide hydrochloride
##STR00048##
[0403] 200 mg (0.50 mmol) of
N-[(3R)-1-azabicyclo[2.2.2]oct-3-yl]-6-bromo-1-benzo-thiophene-2-carboxam-
ide hydrochloride (Example 11A) and 74.6 mg (0.50 mmol) of
3-formylphenylboronic acid are introduced into 1 ml of DMF.
Addition of 0.75 ml of 2 M sodium carbonate solution and 20.3 mg
(0.02 mmol) of PdCl.sub.2(dppf) is followed by heating to
80.degree. C. After 18 h, the reaction mixture is filtered through
kieselguhr and purified by preparative HPLC. The product fractions
are concentrated, mixed with a 5:1 mixture of methanol and 4N
hydrogen chloride in dioxane and again concentrated. Drying under
high vacuum results in 92.4 mg (39.5% of theory) of the title
compound.
[0404] HPLC (method 1): R.sub.t=4.11 min.
[0405] MS (ESIpos): m/z=391 (M+H).sup.+ (free base).
Exemplary Embodiments:
General Method D:
[0406] 1.5 eq. of bis(pinacolato)diboron, 3.25 eq. of dry potassium
acetate, 1.3 eq. of the substituted haloaromatic compound or of the
substituted aryl trifluoromethane-sulphonate are dissolved in DMF
(about 1 ml/mmol of haloaromatic compound or aryl
trifluoromethanesulphonate). Argon is passed through the reaction
mixture for 15 minutes and then 0.05 eq. of PdCl.sub.2(dppf) is
added and the mixture is heated at 90.degree. C. for 2 h. Then 1.0
eq. of the appropriate bromine-substituted
N-[(3R)-1-azabicyclo[2.2.2]oct-3-yl]benzothiophene-2-carboxamide or
N-[(3R)-1-azabicyclo-[2.2.2]oct-3-yl]benzofuran-2-carboxamide, 5
eq. of aqueous 2 M sodium carbonate solution and a further 0.05 eq.
of PdCl.sub.2(dppf) are added. The reaction mixture is heated at
90.degree. C. for 6-12 h. Purification takes place by preparative
HPLC. The resulting product (free base) is dissolved in methanol,
and an excess of 1N hydrochloric acid is added. The solvent is
removed under reduced pressure.
General method E: A solution of 50 mg (0.11 mmol) of
3-(2-{[(3R)-1-azabicyclo[2.2.2]oct-3-yl-amino]carbonyl}-1-benzothien-7-yl-
)benzoic acid hydrochloride (Example 75), 103 mg (0.27 mmol) of
HATU and 52.5 mg (0.41 mmol) of N,N-diisopropyl-ethylamine in 0.5
ml of DMF is added dropwise to a 2N solution of an amine (0.23
mmol) in DMF. After 16 h at room temperature, 0.1 ml of water is
added to the reaction mixture, which is then filtered and purified
by preparative HPLC. The product fractions are combined and, after
addition of 2 ml of 1N hydrochloric acid, concentrated in vacuo and
dried under high vacuum.
General Method F:
[0407] 0.24 mmol of acid chloride and 84 .mu.l (0.60 mmol) of
triethylamine are added to a solution of 50 mg (0.12 mmol) of
N-((3R)-quinuclidin-3-yl)-7-(3-amino-phenyl)benzo[b]thiophene-2-carboxami-
de hydrochloride (Example 21) in 0.5 ml of DMF. After one hour at
room temperature, 0.5 ml of 1N sodium hydroxide solution and 15 ml
of ethyl acetate are added to the reaction mixture, which is then
filtered. The concentrated organic phase is purified by preparative
HPLC. The product fractions are combined and, after addition of 1N
hydrochloric acid, again concentrated in vacuo and dried under high
vacuum.
EXAMPLE 1
N-[(3R)-1-Azabicyclo[2.2.2]oct-3-yl]-6-[2-(hydroxymethyl)phenyl]-1-benzofu-
ran-2-carboxamide
##STR00049##
[0409] A mixture of 130 mg (0.86 mmol) of
2-(hydroxymethyl)phenylboronic acid, 200 mg (0.57 mmol) of
N-[(3R)-1-azabicyclo[2.2.2]oct-3-yl]-6-bromo-1-benzofuran-2-carb-oxamide
(Example 2A), 1.72 ml (1.72 mmol) of 1N sodium hydroxide solution,
40 mg (0.06 mmol) of
1,1'-bis(diphenylphosphino)ferrocenepalladium(II) chloride and 2 ml
of DMF is heated at 80-85.degree. C. for 18 h. The solvent is
removed under reduced pressure. The crude product is purified on
silica gel 60 (Merck, Darmstadt; eluent: dichloromethane,
dichloromethane/methanol 20:1, dichloromethane/methanol/ammonia
80:20:2). The solvent is removed under reduced pressure. Finally,
the last residues of solvent are removed under high vacuum. 149 mg
(63% of theory) of the title compound are isolated.
[0410] .sup.1H-NMR (200 MHz, CDCl.sub.3): .delta.=7.71-7.28 (m,
8H), 6.77 (d, 1H), 4.62 (s, 2H), 4.28-4.12 (m, 1H), 3.56-3.38 (m,
1H), 3.04-2.78 (m, 4H), 2.75-2.59 (m, 1H), 2.16-2.02 (m, 1H),
1.93-1.66 (m, 3H), 1.66-1.45 (m, 1H).
[0411] HPLC (method 1): R.sub.t=3.6 min.
[0412] LC-MS (method 2): R.sub.t=1.49 min.
[0413] MS (ESIpos): m/z=377 (M+H).sup.+.
EXAMPLE 2
N-[(3R)-1-Azabicyclo[2.2.2]oct-3-yl]-6-[3-(hydroxymethyl)phenyl]-1-benzofu-
ran-2-carboxamide
##STR00050##
[0415] A mixture of 130 mg (0.86 mmol) of
3-(hydroxymethyl)phenylboronic acid, 200 mg (0.57 mmol) of
N-[(3R)-1-azabicyclo[2.2.2]oct-3-yl]-6-bromo-1-benzofuran-2-carb-oxamide
(Example 2A), 1.72 ml (1.72 mmol) of 1N sodium hydroxide solution,
40 mg (0.06 mmol) of
1,1'-bis(diphenylphosphino)ferrocenepalladium(II) chloride and 2 ml
of DMF is heated at 80-85.degree. C. for 18 h. The solvent is
removed under reduced pressure. The crude product is purified on
silica gel 60 (Merck, Darmstadt; eluent: dichloromethane,
dichloromethane/methanol 20:1, dichloromethane/methanol/ammonia
80:20:2). The solvent is removed under reduced pressure. Finally,
the last residues of solvent are removed under high vacuum. 127 mg
(54% of theory) of the title compound are isolated.
[0416] .sup.1H-NMR (200 MHz, CDCl.sub.3): .delta.=7.86 (d, 1H),
7.72-7.28 (m, 7H), 6.77 (d, 1H), 4.62 (s, 2H), 4.28-4.12 (m, 1H),
3.56-3.38 (m, 1H), 3.04-2.78 (m, 4H), 2.75-2.59 (m, 1H), 2.16-2.02
(m, 1H), 1.93-1.66 (m, 3H), 1.66-1.45 (m, 1H).
[0417] HPLC (method 1): R.sub.t=3.5 min.
[0418] LC-MS (method 2): R.sub.t=1.50 min.
[0419] MS (ESIpos): m/z=377 (M+H).sup.+.
EXAMPLE 3
N-[(3R)-1-Azabicyclo[2.2.2]oct-3-yl]-6-[4-(hydroxymethyl)phenyl]-1-benzofu-
ran-carboxamide
##STR00051##
[0421] A mixture of 130 mg (0.86 mmol) of
4-(hydroxymethyl)phenylboronic acid, 200 mg (0.57 mmol) of
N-[(3R)-1-azabicyclo[2.2.2]oct-3-yl]-6-bromo-1-benzofuran-2-carb-oxamide
(Example 2A), 1.72 ml (1.72 mmol) of 1N sodium hydroxide solution,
40 mg (0.06 mmol) of
1,1'-bis(diphenylphosphino)ferrocenepalladium(II) chloride and 2 ml
of DMF is heated at 80-85.degree. C. for 18 h. The solvent is
removed under reduced pressure. The crude product is purified on
silica gel 60 (Merck, Darmstadt; eluent: dichloromethane,
dichloromethane/methanol 20:1, dichloromethane/methanol/ammonia
80:20:2). The solvent is removed under reduced pressure. Finally,
the last residues of solvent are removed under high vacuum. 55 mg
(23% of theory) of the title compound are isolated.
[0422] .sup.1H-NMR (200 MHz, CDCl.sub.3): .delta.=7.83 (d, 1H),
7.69-7.28 (m, 7H), 6.77 (d, 1H), 4.62 (s, 2H), 4.28-4.12 (m, 1H),
3.56-3.38 (m, 1H), 3.04-2.78 (m, 4H), 2.75-2.59 (m, 1H), 2.16-2.02
(m, 1H), 1.93-1.66 (m, 3H), 1.66-1.45 (m, 1H).
[0423] HPLC (method 1): R.sub.t=3.5 min.
[0424] LC-MS (method 2): R.sub.t=1.46 min.
[0425] MS (ESIpos): m/z=377 (M+H).sup.+.
EXAMPLE 4
N-[(3R)-1-Azabicyclo[2.2.2]oct-3-yl]-6-[4-(4-morpholinyl)phenyl]-1-benzofu-
ran-2-carboxamide
##STR00052##
[0427] A mixture of 180 mg (0.86 mmol) of
4-(4-morpholinyl)phenylboronic acid, 200 mg (0.57 mmol) of
N-[(3R)-1-azabicyclo[2.2.2]oct-3-yl]-6-bromo-1-benzofuran-2-carb-oxamide
(Example 2A), 1.72 ml (1.72 mmol) of 1N sodium hydroxide solution,
40 mg (0.06 mmol) of
1,1'-bis(diphenylphosphino)ferrocenepalladium(II) chloride and 2 ml
of DMF is heated at 80-85.degree. C. for 18 h. The solvent is
removed under reduced pressure. The crude product is purified on
silica gel 60 (Merck, Darmstadt; eluent: dichloromethane,
dichloromethane/methanol 20:1, dichloromethane/methanol/ammonia
80:20:2). The solvent is removed under reduced pressure. Finally,
the last residues of solvent are removed under high vacuum. 79 mg
(32% of theory) of the title compound are isolated.
[0428] .sup.1H-NMR (200 MHz, CDCl.sub.3): .delta.=7.84-7.29 (m,
7H); 6.99 (d, 1H), 6.84-6.70 (m, 1H), 4.28-4.13 (m, 1H), 3.97-3.83
(m, 2H), 3.59-3.36 (m, 1H), 3.29-3.13 (m, 2H), 3.04-2.78 (m, 4H),
2.75-2.59 (m, 1H), 2.16-2.02 (m, 1H), 1.93-1.66 (m, 3H), 1.66-1.45
(m, 1H).
[0429] HPLC (method 1): R.sub.t=3.5 min.
[0430] LC-MS (method 2): R.sub.t=1.74 min.
[0431] MS (ESIpos): m/z=432 (m+H).sup.+.
EXAMPLE 5
N-[(3R)-1-Azabicyclo[2.2.2]oct-3-yl]-6-[4-(methoxy)phenyl]-1-benzofuran-2--
carboxamide
##STR00053##
[0433] A mixture of 130 mg (0.86 mmol) of 4-methoxyphenylboronic
acid, 200 mg (0.57 mmol) of
N-[(3R)-1-azabicyclo[2.2.2]oct-3-yl]-6-bromo-1-benzofuran-2-carb-oxamide
(Example 2A), 1.72 ml (1.72 mmol) of 1N sodium hydroxide solution,
40 mg (0.06 mmol) of
1,1'-bis(diphenylphosphino)ferrocenepalladium(II) chloride and 2 ml
of DMF is heated at 80-85.degree. C. for 18 h. The solvent is
removed under reduced pressure. The crude product is purified on
silica gel 60 (Merck, Darmstadt; eluent: dichloromethane,
dichloromethane/methanol 20:1, dichloromethane/methanol/ammonia
80:20:2). The solvent is removed under reduced pressure. Finally,
the last residues of solvent are removed under high, vacuum. 160 mg
(68% of theory) of the title compound are isolated.
[0434] .sup.1H-NMR (200 MHz, CDCl.sub.3): .delta.=7.84-7.75 (m,
1H), 7.62-7.45 (m, 5H), 6.99 (m, 2H), 6.84-6.70 (m, 1H), 4.28-4.13
(m, 1H), 3.87 (s, 3H), 3.59-3.36 (m, 1H), 3.04-2.78 (m, 4H),
2.75-2.59 (m, 1H), 2.16-2.02 (m, 1H), 1.93-1.66 (m, 3H), 1.66-1.45
(m, 1H).
[0435] HPLC (method 1): R.sub.t=4.0 min.
[0436] LC-MS (method 3): R.sub.t=3.2 min.
[0437] MS (ESIpos): m/z=377 (M+H).sup.+.
EXAMPLE 6
N-[(3R)-1-Azabicyclo[2.2.2]oct-3-yl]-6-[3-(methoxy)phenyl]-1-benzofuran-2--
carboxamide
##STR00054##
[0439] A mixture of 130 mg (0.86 mmol) of 3-methoxyphenylboronic
acid, 200 mg (0.57 mmol) of
N-[(3R)-1-azabicyclo[2.2.2]oct-3-yl]-6-bromo-1-benzofuran-2-carb-oxamide
(Example 2A), 1.72 ml (1.72 mmol) of 1N sodium hydroxide solution,
40 mg (0.06 mmol) of
1,1'-bis(diphenylphosphino)ferrocenepalladium(II) chloride and 2 ml
of DMF is heated at 80-85.degree. C. for 18 h. The solvent is
removed under reduced pressure. The crude product is purified on
silica gel 60 (Merck, Darmstadt; eluent: dichloromethane,
dichloromethane/methanol 20:1, dichloromethane/methanol/ammonia
80:20:2). The solvent is removed under reduced pressure. Finally,
the last residues of solvent are removed under high vacuum. 151 mg
(64% of theory) of the title compound are isolated.
[0440] .sup.1H-NMR (200 MHz, CDCl.sub.3): .delta.=7.90-7.80 (m,
1H), 7.72-7.08 (m, 5H), 6.95-6.85 (m, 1H), 6.84-6.70 (m, 1H),
4.28-4.13 (m, 1H), 3.87 (s, 3H), 3.59-3.36 (m, 1H), 3.04-2.78 (m,
4H), 2.75-2.59 (m, 1H), 2.16-2.02 (m, 1H), 1.93-1.66 (m, 3H),
1.66-1.45 (m, 1H).
[0441] HPLC (method 1): R.sub.t=4.0 min.
[0442] LC-MS (method 2): R.sub.t=1.87 min.
[0443] MS (ESIpos): m/z=377 (M+H).sup.+.
EXAMPLE 7
N-[(3R)-1-Azabicyclo[2.2.2]oct-3-yl]-6-(4-fluorophenyl)-1-benzofuran-2-car-
boxamide
##STR00055##
[0445] A mixture of 120 mg (0.86 mmol) of 4-fluorophenylboronic
acid, 200 mg (0.57 mmol) of
N-[(3R)-1-azabicyclo[2.2.2]oct-3-yl]-6-bromo-1-benzofuran-2-carb-oxamide
(Example 2A), 1.72 ml (1.72 mmol) of 1N sodium hydroxide solution,
40 mg (0.06 mmol) of
1,1'-bis(diphenylphosphino)ferrocenepalladium(II) chloride and 2 ml
of DMF is heated at 80-85.degree. C. for 18 h. The solvent is
removed under reduced pressure. The crude product is purified on
silica gel 60 (Merck, Darmstadt; eluent: dichloromethane,
dichloromethane/methanol 20:1, dichloromethane/methanol/ammonia
80:20:2). The solvent is removed under reduced pressure. Finally,
the last residues of solvent are removed under high vacuum. 155 mg
(68% of theory) of the title compound are isolated.
[0446] .sup.1H-NMR (200 MHz, CDCl.sub.3): .delta.=7.99 (s, 1H),
7.64-7.46 (m, 5H), 7.22-7.07 (m, 2H), 6.84-6.70 (m, 1H), 4.28-4.13
(m, 1H), 3.59-3.36 (m, 1H), 3.04-2.78 (m, 4H), 2.75-2.59 (m, 1H),
2.16-2.02 (m, 1H), 1.93-1.66 (m, 3H), 1.66-1.45 (m, 1H).
[0447] HPLC (method 1): R.sub.t=4.1 min.
[0448] LC-MS (method 2): R.sub.t=1.92 min.
[0449] MS (ESIpos): m/z=365 (M+H).sup.+.
EXAMPLE 8
N-[(3R)-1-Azabicyclo[2.2.2]oct-3-yl]-6-(4-trifluoromethoxyphenyl)-1-benzof-
uran-2-carboxamide
##STR00056##
[0451] A mixture of 180 mg (0.86 mmol) of
4-(trifluoromethoxy)phenylboronic acid, 200 mg (0.57 mmol) of
N-[(3R)-1-azabicyclo[2.2.2]oct-3-yl]-6-bromo-1-benzofuran-2-carboxamide
(Example 2A), 1.72 ml (1.72 mmol) of 1N sodium hydroxide solution,
40 mg (0.06 mmol) of
1,1'-bis(diphenylphosphino)ferrocenepalladium(II) chloride and 2 ml
of DMF is heated at 80-85.degree. C. for 18 h. The solvent is
removed under reduced pressure. The crude product is purified on
silica gel 60 (Merck, Darmstadt; eluent: dichloromethane,
dichloromethane/methanol 20:1, dichloromethane/methanol/ammonia
80:20:2). The solvent is removed under reduced pressure. Finally,
the last residues of solvent are removed under high vacuum. 155 mg
(68% of theory) of the title compound are isolated.
[0452] .sup.1H-NMR (200 MHz; CDCl.sub.3): .delta.=7.82 (s, 1H),
7.72-7.45 (m, 5H), 7.36-7.27 (m, 2H), 6.84-6.70 (m, 1H), 4.28-4.13
(m, 1H), 3.59-3.36 (m, 1H), 3.04-2.78 (m, 4H), 2.75-2.59 (m, 1H),
2.16-2.02 (m, 1H), 1.93-1.66 (m, 3H), 1.66-1.45 (m, 1H).
[0453] HPLC (method 1): R.sub.t=4.4 min.
[0454] LC-MS (method 2): R.sub.t=2.22 min.
[0455] MS (ESIpos): m/z=431 (M+H).sup.+.
EXAMPLE 9
N-[(3R)-1-Azabicyclo[2.2.2]oct-3-yl]-6-(3-hydroxy-1-propynyl)-1-benzofuran-
-2-carboxamide
##STR00057##
[0457] A mixture of 289 mg (5.15 mmol) of propargyl alcohol, 150 mg
(0.43 mmol) of
N-[(3R)-1-azabicyclo[2.2.2]oct-3-yl]-6-bromo-1-benzofuran-2-carb-
oxamide (Example 2A), 1.6 mg (0.01 mmol) of copper(I) iodide, 15 mg
(0.02 mmol) of bis(triphenylphosphine)palladium(II) chloride, 61 mg
(0.86 mmol) of pyrrolidine and 1 ml of THF is heated under reflux
overnight. The crude product is mixed with 10 ml of 1N sodium
hydroxide solution and extracted three times with a total of 100 ml
of ethyl acetate. The combined organic phases are dried over
magnesium sulphate, and the solvent is removed under reduced
pressure. The crude product is purified on silica gel 60 (Merck,
Darmstadt; eluent: dichloromethane/triethylamine 100:1, then
dichloromethane/methanol/triethylamine 100:1:1 to
dichloromethane/methanol/triethylamine 100:10:1). The solvent is
removed under reduced pressure. Finally, the last residues of
solvent are removed under high vacuum. 40 mg (27% of theory) of the
title compound are isolated.
[0458] HPLC (method 1): R.sub.t=3.3 min.
[0459] LC-MS (method 3): R.sub.t=2.6 min.
[0460] MS (ESIpos): m/z=325 (M+H).sup.+.
EXAMPLE 10
N-[(3R)-1-Azabicyclo[2.2.2]oct-3-yl]-5-fluoro-7-(4-fluorophenyl)-1-benzofu-
ran-2-carboxamide
##STR00058##
[0462] A mixture of 40 mg (0.29 mmol) of 4-fluorophenylboronic
acid, 70 mg (0.19 mmol) of
N-[(3R)-1-azabicyclo[2.2.2]oct-3-yl]-5-fluoro-7-bromo-1-benzofuran-2-carb-
oxamide (Example 5A), 0.57 ml (0.57 mmol) of 1N sodium hydroxide
solution, 14 mg (0.02 mmol) of
1,1'-bis(diphenylphosphino)ferrocenepalladium(II) chloride and 2 ml
of DMF is heated at 85.degree. C. overnight. The solvent is removed
under reduced pressure. The crude product is mixed with 1N sodium
hydroxide solution and extracted three times with a total of 100 ml
of ethyl acetate. The combined organic phases are dried over
magnesium sulphate, and the solvent is removed under reduced
pressure. The crude product is taken up in methanol and shaken
together with acidic ion exchanger (Dowex.RTM. WX2-200) for about
20 min. The loaded ion exchanger is washed three times with 30 ml
of methanol each time, then with water, again with methanol, with
dichloromethane, again with methanol, with THF and finally once
more with methanol. The product is eluted with
methanol/triethylamine 95:5. The solvent is removed in a rotary
evaporator under reduced pressure. Silica gel 60 (Merck, Darmstadt;
eluent: dichloromethane/triethylamine 100:1, then
dichloromethane/methanol/triethylamine 100:1:1 to
dichloromethane/methanol/triethylamine 100:10:1) is used for final
purification. The solvent is removed under reduced pressure.
Finally, the last residues of solvent are removed under high
vacuum. 51 mg (70% of theory) of the title compound are
isolated.
[0463] .sup.1H-NMR (400 MHz, methanol-d.sub.4): .delta.=7.99-7.90
(m, 2H), 7.59 (s, 1H), 7.45-7.35 (m, 2H), 7.30-7.22 (m, 2H),
4.24-4.18 (m, 1H), 3.34-3.29 (m, 1H), 3.07-2.97 (m, 1H), 2.93-2.77
(m, 4H), 2.13-2.05 (m, 1H), 1.98-1.86 (m, 1H), 1.84-1.75 (m, 2H),
1.63-1.53 (m, 1H).
[0464] HPLC (method 1): R.sub.t=43 min.
[0465] LC-MS (method 3): R.sub.t=3.08 min.
[0466] MS (ESIpos): m/z=383 (M+H).sup.+.
EXAMPLE 11
N-[(3R)-1-Azabicyclo[2.2.2]oct-3-yl]-5-fluoro-7-(4-trifluoromethoxyphenyl)-
-1-benzofuran-2-carboxamide
##STR00059##
[0468] A mixture of 40 mg (0.29 mmol) of
4-(trifluoromethoxy)phenylboronic acid, 70 mg (0.19 mmol) of
N-[(3R)-1-azabicyclo[2.2.2]oct-3-yl]-5-fluoro-7-bromo-1-benzofuran-2-carb-
oxamide (Example 5A), 0.57 ml (0.57 mmol) of 1N sodium hydroxide
solution, 14 mg (0.02 mmol) of
1,1'-bis(diphenyl-phosphino)ferrocenepalladium(II) chloride and 2
ml of DMF is heated at 85.degree. C. overnight. The solvent is
removed under reduced pressure. The crude product is mixed with 1N
sodium hydroxide solution and extracted three times with a total of
100 ml of ethyl acetate. The combined organic phases are dried over
magnesium sulphate, and the solvent is removed under reduced
pressure. The crude product is taken up in methanol and shaken
together with acidic ion exchanger (Dowex.RTM. WX2-200) for about
20 min. The loaded ion exchanger is washed three times with 30 ml
of methanol each time, then with water, again with methanol, with
dichloromethane, again with methanol, with THF and finally once
more with methanol. The product is eluted with
methanol/triethylamine 95:5. The solvent is removed in a rotary
evaporator under reduced pressure. Silica gel 60 (Merck, Darmstadt;
eluent: dichloromethane/triethylamine 100:1, then
dichloromethane/methanol/triethylamine 100:1:1 to
dichloromethane/methanol/triethylamine 100:10:1) is used for final
purification. The solvent is removed under reduced pressure.
Finally, the last residues of solvent are removed under high
vacuum. 52 mg (61% of theory) of the title compound are
isolated.
[0469] .sup.1H-NMR (400 MHz, methanol-d.sub.4): .delta.=8.08-8.00
(m, 2H), 7.59 (s, 1H), 7.49-741 (m, 4H), 4.24-4.18 (m, 1H),
3.34-3.29 (m, 1H), 3.07-2.97 (m, 1H), 2.93-2.77 (m, 4H), 2.13-2.05
(m, 1H), 1.98-1.86 (m, 1H), 1.84-1.75 (m, 2H), 1.63-1.53 (m,
1H).
[0470] HPLC (method 1): R.sub.t=4.6 min.
[0471] LC-MS (method 3): R.sub.t=3.37 min.
[0472] MS (ESIpos): m/z=449 (M+H).sup.+.
EXAMPLE 12
N-[(3R)-1-Azabicyclo[2.2.2]oct-3-yl]-5-phenyl-1-benzothiophene-2-carboxami-
de hydrochloride
##STR00060##
[0474] 0.15 ml of 2 M aqueous sodium carbonate solution and 4.1 mg
(0.005 mmol) of PdCl.sub.2(dppf) are added to a mixture of 40 mg
(0.10 mmol) of
N-[(3R)-1-azabicyclo[2.2.2]oct-3-yl]-5-bromo-1-benzothiophene-2-carboxami-
de hydrochloride (Example 14A) and 12.1 mg (0.10 mmol) of
phenylboronic acid in 1 ml of DMF. The reaction mixture is heated
at 80.degree. C. for 14 h, filtered through kieselguhr and
evaporated to dryness. Purification of the crude product by
preparative HPLC, subsequent addition of 1N hydrochloric acid and
drying under high vacuum result in 7.3 mg (18% of theory) of the
title compound.
[0475] HPLC (method 1): R.sub.t=4.2 min.
[0476] MS (ESIpos): m/z=363 (M+H).sup.+ (free base).
EXAMPLE 13
N-[(3R)-1-Azabicyclo[2.2.2]oct-3-yl]-6-phenyl-1-benzothiophene-2-carboxami-
de hydrochloride
##STR00061##
[0478] 0.15 ml of 2 M aqueous sodium carbonate solution and 4.1 mg
(0.005 mmol) of PdCl.sub.2(dppf) are added to a mixture of 40 mg
(0.10 mmol) of
N-[(3R)-1-azabicyclo[2.2.2]oct-3-yl]-6-bromo-1-benzothiophene-2-carboxami-
de hydrochloride (Example 11A) and 12.1 mg (0.10 mmol) of
phenylboronic acid in 1 ml of DMF. The reaction mixture is heated
at 80.degree. C. for 14 h, filtered through kieselguhr and
evaporated to dryness. Purification of the crude product by
preparative HPLC, subsequent addition of 1N hydrochloric acid and
drying under high vacuum result in 14.5 mg (37% of theory) of the
title compound.
[0479] .sup.1H-NMR (200 MHz, DMSO-d.sub.6): .delta.=9.91 (m, 1H),
9.02 (d, 1H), 8.38 (m, 1H), 8.32 (m, 1H), 8.06 (d, 1H), 7.78 (m,
3H), 7.58-7.37 (m, 3H), 4.32 (m, 1H), 3.78-3.03 (m, 6H), 2.28-2.05
(m, 2H), 1.93 (m, 2H), 1.78 (m, 1H).
[0480] HPLC (method 1): R.sub.t=4.2 min.
[0481] MS (ESIpos): m/z=363 (M+H).sup.+ (free base).
EXAMPLE 14
N-[(3R)-1-Azabicyclo[2.2.2]oct-3-yl]-6-(3-methoxyphenyl)-1-benzothiophene--
2-carboxamide hydrochloride
##STR00062##
[0483] 0.3 ml of 2 M aqueous sodium carbonate solution and 4.1 mg
(0.005 mmol) of PdCl.sub.2(dppf) are added to a mixture of 40 mg
(0.10 mmol) of
N-[(3R)-1-azabicyclo[2.2.2]oct-3-yl]-6-bromo-1-benzothiophene-2-carboxami-
de hydrochloride (Example 11A) and 15.1 mg (0.10 mmol) of
3-methoxyphenylboronic acid in 1 ml of DMF. The reaction mixture is
heated at 80.degree. C. for 14 h, filtered through kieselguhr and
evaporated to dryness. Purification of the crude product by
preparative HPLC, subsequent addition of 1N hydrochloric acid and
drying under high vacuum result in 25.5 mg (57% of theory) of the
title compound.
[0484] .sup.1H-NMR (200 MHz, DMSO-d.sub.6): .delta.=9.70 (s, 1H),
8.97 (d, 1H), 8.38 (m, 1H), 8.28 (m, 1H), 7.99 (m, 1H), 7.78 (m,
1H), 7.37 (m, 3H), 6.98 (m, 1H), 4.33 (m, 1H), 3.86 (s, 3H),
3.79-3.12 (m, 6H), 2.28-2.00 (m, 2H), 1.99-1.68 (m, 3H).
[0485] HPLC (method 1): R.sub.t=4.2 min.
[0486] MS (ESIpos): m/z=393 (M+H).sup.+ (free base).
EXAMPLE 15
N-[(3R)-1-Azabicyclo[2.2.2]oct-3-yl]-6-(3-hydroxy-1-propynyl)-1-benzothiop-
hene-2-carboxamide
##STR00063##
[0488] 120 mg (0.30 mmol) of
N-[(3R)-1-azabicyclo[2.2.2]oct-3-yl]-6-bromo-1-benzothiophene-2-carboxami-
de hydrochloride (Example 11A), 10.5 mg (0.01 mmol) of
PdCl.sub.2(PPh.sub.3).sub.2 and 4.6 mg (0.02 mmol) of copper(I)
iodide are dissolved in 1.5 ml of triethylamine/DMF (2:1) under
argon and stirred at 60.degree. C. for 1 h. Addition of 25.1 mg
(0.45 mmol) of propargyl alcohol is followed by heating at
70.degree. C. for a further 16 h. Cooling is followed by filtration
through kieselguhr and purification by preparative HPLC,
concentration and drying of the product under high vacuum. 12 mg
(11% of theory) of the title compound are obtained.
[0489] .sup.1H-NMR (200 MHz, DMSO-d.sub.6): .delta.=8.73 (d, 1H),
8.20 (m, 2H), 7.96 (d, 1H), 7.46 (dd, 1H), 4.34 (s, 2H), 4.09 (m,
1H), 3.32 (m, 1H), 3.16-2.77 (m, 5H), 1.99 (m, 1H), 1.91 (m, 1H),
1.70 (m, 2H), 1.49 (m, 1H).
[0490] HPLC (method 1): R.sub.t=3.4 min.
[0491] MS (ESIpos): m/z=341 (M+H).sup.+.
EXAMPLE 16
N-[(3R)-1-Azabicyclo[2.2.2]oct-3-yl]-7-phenyl-1-benzothiophene-2-carboxami-
de hydrochloride
##STR00064##
[0493] 0.14 ml of 2 M aqueous sodium carbonate solution and 5.7 mg
(0.007 mmol) of PdCl.sub.2(dppf) are added to a mixture of 56 mg
(0.14 mmol) of
N-[(3R)-1-azabicyclo[2.2.2]oct-3-yl]-7-bromo-1-benzothiophene-2-carboxami-
de hydrochloride (Example 8A) and 18.7 mg (0.15 mmol) of
phenylboronic acid in 1 ml of DMF. The reaction mixture is heated
to 80.degree. C. After 3 h at this temperature, a further 5.7 mg
(0.007 mmol) of PdCl.sub.2(dppf) are added, and the mixture is
stirred at 80.degree. C. for a further 12 h. The reaction mixture
is filtered through kieselguhr and evaporated to dryness.
Purification of the crude product by preparative HPLC, subsequent
addition of 1N hydrochloric acid and drying under high vacuum
result in 10.6 mg (18% of theory) of the title compound.
[0494] HPLC (method 1): R.sub.t=4.2 min.
[0495] MS (ESIpos): m/z=363 (M+H).sup.+ (free base).
EXAMPLE 17
N-[(3R)-1-Azabicyclo[2.2.2]oct-3-yl]-7-(3-methoxyphenyl)-1-benzothiophene--
2-carboxamide hydrochloride
##STR00065##
[0497] 0.16 ml of 2 M aqueous sodium carbonate solution and 4.2 mg
(0.005 mmol) of PdCl.sub.2(dppf) are added to a mixture of 49 mg
(0.10 mmol) of
N-[(3R)-1-azabicyclo[2.2.2]oct-3-yl]-7-bromo-1-benzothiophene-2-carboxami-
de hydrochloride (Example 8A) and 15.8 mg (0.10 mmol) of
3-methoxyphenylboronic acid in 1 ml of DMF. The reaction mixture is
heated at 80.degree. C. for 14 h, then filtered through kieselguhr
and evaporated to dryness. Purification of the crude product by
preparative HPLC, subsequent addition of 1N hydrochloric acid and
drying under high vacuum result in 8.0 mg (18% of theory) of the
title compound.
[0498] HPLC (method 1): R.sub.t=4.2 min.
[0499] MS (ESIpos): m/z=393 (M+H).sup.+ (free base).
EXAMPLE 18
N-[(3R)-1-Azabicyclo[2.2.2]oct-3-yl]-7-(2-methoxyphenyl)-1-benzothiophene--
2-carboxamide hydrochloride
##STR00066##
[0501] 0.22 ml of 2 M aqueous sodium, carbonate solution and 6.1 mg
(0.007 mmol) of PdCl.sub.2(dppf) are added to a mixture of 60 mg
(0.15 mmol) of
N-[(3R)-1-azabicyclo[2.2.2]oct-3-yl]-7-bromo-1-benzothiophene-2-carboxami-
de hydrochloride (Example 8A) and 22.7 mg (0.15 mmol) of
2-methoxyphenylboronic acid in 1 ml of DMF. The reaction mixture is
heated at 80.degree. C. for 14 h, then filtered through kieselguhr
and evaporated to dryness. Purification of the crude product by
preparative HPLC, subsequent addition of 1N hydrochloric acid and
drying under high vacuum result in 12.8 mg (18% of theory) of the
title compound.
[0502] HPLC (method 1): R.sub.t=4.2 min.
[0503] MS (ESIpos): m/z=393 (M+H).sup.+ (free base).
EXAMPLE 19
N-[(3R)-1-Azabicyclo[2.2.2]oct-3-yl]-7-[4-(4-morpholinyl)phenyl]-1-benzoth-
iophene-2-carboxamide hydrochloride
##STR00067##
[0505] 0.22 ml of 2 M aqueous sodium carbonate solution and 6.1 mg
(0.007 mmol) of PdCl.sub.2(dppf) are added to a mixture of 60 mg
(0.15 mmol) of
N-[(3R)-1-azabicyclo[2.2.2]oct-3-yl]-7-bromo-1-benzothiophene-2-carboxami-
de hydrochloride (Example 8A) and 30.9 mg (0.15 mmol) of
4-(4-morpholinyl)phenylboronic acid in 1 ml of DMF. The reaction
mixture is heated to 80.degree. C. After 4.5 h, a further 6.1 mg
(0.007 mmol) of PdCl.sub.2(dppf) are added. After a further 12 h,
the reaction mixture is filtered through kieselguhr and evaporated
to dryness. The crude product is purified by preparative HPLC. The
product is dissolved in methanol, and an excess of 4N hydrogen
chloride in dioxane is added. Drying under high vacuum results in
20.6 mg (25% of theory) of the title compound.
[0506] .sup.1H-NMR (300 MHz, methanol-d.sub.4): .delta.=8.21 (s,
1H), 7.97 (m, 2H), 7.93 (s, 1H), 7.83 (m, 2H), 7.57 (dd, 1H), 7.52
(m, 1H), 4.46 (m, 1H), 4.13 (m, 4H), 3.83 (m, 1H), 3.78 (m, 4H),
3.49 (m, 1H), 3.43-3.17 (m, 4H), 2.38 (m, 1H), 2.28 (m, 1H), 2.10
(m, 2H), 1.96 (m, 1H).
[0507] HPLC (method 1): R.sub.t=4.3 min.
[0508] MS (ESIpos): m/z=448 (M+H).sup.+ (free base).
EXAMPLE 20
N-[(3R)-1-Azabicyclo[2.2.2]oct-3-yl]-7-[4-(hydroxymethyl)phenyl]-1-benzo-t-
hiophene-2-carboxamide hydrochloride
##STR00068##
[0510] 60 mg (0.15 mmol) of
N-[(3R)-1-azabicyclo[2.2.2]oct-3-yl]-7-bromo-1-benzothiophene-2-carboxami-
de hydrochloride (Example 8A) and 22.7 mg (0.15 mmol) of
4-(hydroxymethyl)phenylboronic acid are introduced into 1 ml of
DMF. Addition of 0.22 ml of 2 M aqueous sodium carbonate solution
and 6.1 mg (0.01 mmol) of PdCl.sub.2(dppf) is followed by heating
to 80.degree. C. After 14 h, the reaction mixture is filtered
through kieselguhr and evaporated to dryness. The crude product is
purified by preparative HPLC. The product is dissolved in methanol
and an excess of 4N hydrogen chloride in dioxane is added. Drying
under high vacuum results in 9 mg (9% of theory) of the title
compound.
[0511] HPLC (method 1): R.sub.t=3.8 min.
[0512] MS (ESIpos): m/z=393 (M+H).sup.+ (free base).
[0513] The compounds listed in the following table are obtained in
an analogous manner:
TABLE-US-00002 TABLE 2 ##STR00069## MS (ESIpos): Example R.sub.1
[min.] m/z [M + H].sup.+ No. R (method 5) (free base) 21
##STR00070## 1.27 378 22 ##STR00071## 1.51 393 23 ##STR00072## 1.46
405 24 ##STR00073## 1.44 391 25 ##STR00074## 1.51 420 26
##STR00075## 1.45 391 27 ##STR00076## 1.53 420 28 ##STR00077## 1.46
405 29 ##STR00078## 1.59 410 30 ##STR00079## 1.48 369 31
##STR00080## 1.61 431 32 ##STR00081## 1.52 381 33 ##STR00082## 1.6
453 34 ##STR00083## 1.48 388 35 ##STR00084## 1.45 388 36
##STR00085## 1.53 399 37 ##STR00086## 1.52 399 38 ##STR00087## 1.54
410 39 ##STR00088## 1.51 381 40 ##STR00089## 1.6 410 41
##STR00090## 1.43 353 42 ##STR00091## 1.58 408 43 ##STR00092## 1.52
424 44 ##STR00093## 1.42 405 45 ##STR00094## 1.48 424 46
##STR00095## 1.53 411 47 ##STR00096## 1.56 408 48 ##STR00097## 1.58
395 49 ##STR00098## 1.43 391 50 ##STR00099## 1.38 397
EXAMPLE 51
7-[3-(Acetylamino)phenyl]-N-[(3R)-1-azabicyclo[2.2.2]oct-3-yl]-1-benzothio-
phene-2-carboxamide hydrochloride
##STR00100##
[0515] 0.75 ml of 2 M aqueous sodium carbonate solution and 20.3 mg
(0.02 mmol) of PdCl.sub.2(dppf) are added to a mixture of 200 mg
(0.50 mmol) of
N-[(3R)-1-bicyclo[2.2.2]oct-3-yl]-7-bromo-1-benzothiophene-2-carboxamide
hydrochloride (Example 8A) and 89.1 mg (0.50 mmol) of
3-(acetamido)phenylboronic acid in 2 ml of DMF. The reaction
mixture is heated at 80.degree. C. for 17 h. A further 89.1 mg
(0.50 mmol) of 3-(acetamido)phenylboronic acid, 1.5 ml of 1N sodium
hydroxide solution and 81.3 mg (0.1 mmol) of PdCl.sub.2(dppf) are
added, and the mixture is heated at 80.degree. C. for a further 18
h. After cooling, it is filtered through kieselguhr and purified by
preparative HPLC. The resulting crude product is further purified
by flash chromatography on silica gel (mobile phase:
dichloromethane/methanol/ammonia 100:10:2). The product fractions
are concentrated, taken up in a 5:1 mixture of methanol and 1N
hydrochloric acid and again concentrated. Drying under high vacuum
results in 243.2 mg (86.6% of theory) of the title compound.
[0516] .sup.1H-NMR (300 MHz, DMSO-d.sub.6): .delta.=10.16 (s, 1H),
10.10 (br. s, 1H), 9.03 (d, 1H), 8.38 (s, 1H), 8.06 (m, 1H), 7.98
(dd, 1H), 7.65 (m, 1H), 7.59 (dd, 1H), 7.51 (m, 1H), 7.48 (m, 1H),
7.37 (m, 1H), 4.33 (m, 1H), 3.66 (m, 1H), 3.45-3.13 (m, 5H), 2.22
(m, 1H), 2.14 (m, 1H), 2.08 (s, 3H), 1.91 (m, 2H), 1.75 (m,
1H).
[0517] HPLC (method 1): R.sub.t=3.9 min.
[0518] MS (ESIpos): m/z=420 (M+H).sup.+ (free base).
EXAMPLE 52
N-[(3R)-1-Azabicyclo[2.2.2]oct-3-yl]-6-[4-(4-morpholinyl)phenyl]-1-benzoth-
iophene-2-carboxamide hydrochloride
##STR00101##
[0520] 100 mg (0.25 mmol) of
N-[(3R)-1-azabicyclo[2.2.2]oct-3-yl]-6-bromo-1-benzo-thiophene-2-carboxam-
ide hydrochloride (Example 11A) and 51.5 mg (0.25 mmol) of
4-morpholinophenylboronic acid are introduced into 1 ml of DMF.
Addition of 0.37 ml of 2 M sodium carbonate solution and 10.2 mg
(0.01 mmol) of PdCl.sub.2(dppf) is followed by heating to
80.degree. C. After 16 h, a further 51.5 mg (0.25 mmol) of
4-morpholinophenylboronic acid, 0.37 ml of 2 M sodium carbonate
solution and 10.2 mg (0.01 mmol) of PdCl.sub.2(dppf) are added. The
mixture is heated at 80.degree. C. for a further 4 h. After
cooling, the reaction mixture is filtered through kieselguhr and
purified by preparative HPLC. The product fractions are
concentrated and, after addition of a 5:1 mixture of methanol and 4
M hydrogen chloride in dioxane, again concentrated. Drying under
high vacuum results in 83 mg (69% of theory) of the title
compound.
[0521] .sup.1H-NMR (200 MHz, DMSO-d.sub.6): .delta.=10.20 (br. s,
1H), 9.07 (d, 1H), 8.33 (s, 1H), 8.27 (s, 1H), 7.97 (d, 1H), 7.71
(m, 3H), 7.10 (m, 2H), 4.33 (m, 1H), 3.78 (m, 4H), 3.73-3.07 (m,
10H), 2.22 (m, 1H), 2.17 (m, 1H), 1.93 (m, 2H), 1.75 (m, 1H).
[0522] HPLC (method 1): R.sub.t=3.8 min.
[0523] MS (ESIpos): m/z=448 (M+H).sup.+ (free base).
EXAMPLE 53
N-[(3R)-1-Azabicyclo[2.2.2]oct-3-yl]-6-(5-methyl-1,2,4-oxadiazol-3-yl)-1-b-
enzo-thiophene-2-carboxamide hydrochloride
##STR00102##
[0525] 154 mg (0.37 mmol) of
6-[amino(hydroxyimino)methyl]-N-[(3R)-1-azabicyclo[2.2.2]-oct-3-yl]-1-ben-
zothiophene-2-carboxamide dihydrochloride (Example 27A) are
dissolved in 2 ml of DMF and 0.75 ml of THF. 250 mg of 4 .ANG.
molecular sieves are added, and the mixture is stirred at room
temperature for 30 min. Addition of 44.4 mg (1.11 mmol) of sodium
hydride (60% suspension in mineral oil) is followed by heating at
60.degree. C. for 20 min and then cooling to room temperature. A
solution of 90 .mu.l (1.11 mmol) of methyl acetate in 1 ml of THF
is then added to the reaction mixture, after which it is heated at
80.degree. C. for 14 h. Addition of a further 29.6 mg (0.74 mmol)
of sodium hydride (60% suspension in mineral oil) and 0.88 ml (11.1
mmol) of methyl acetate in 1 ml of THF is followed by heating at
70.degree. C. for a further 24 h. The reaction is stopped by adding
water. Purification takes place by preparative HPLC. The product
fractions are concentrated and, after addition of a 5:1 mixture of
methanol and 4N hydrogen chloride in dioxane, again concentrated.
Drying under high vacuum results in 41.9 mg (23.6% of theory) of
the title compound.
[0526] .sup.1H-NMR (300 MHz, DMSO-d.sub.6): .delta.=10.15 (br. s,
1H), 9.14 (d, 1H), 8.70 (m, 1H), 8.41 (s, 1H), 8.13 (d, 1H), 8.05
(m, 1H), 4.34 (m, 1H), 3.75-3.13 (m, 6H), 2.70 (s, 3H), 2.23 (m,
1H), 2.15 (m, 1H), 1.92 (m, 2H), 1.77 (m, 1H).
[0527] HPLC (method 1): R.sub.t=3.8 min.
[0528] MS (ESIpos): m/z=369 (M+H).sup.+ (free base)
EXAMPLE 54
N-[(3R)-1-Azabicyclo[2.2.2]oct-3-yl]-6-[2-(hydroxymethyl)phenyl]-1-benzo-t-
hiophene-2-carboxamide hydrochloride
##STR00103##
[0530] 100 mg (0.25 mmol) of
N-[(3R)-1-azabicyclo[2.2.2]oct-3-yl]-6-bromo-1-benzothiophene-2-carboxami-
de hydrochloride (Example 11A) and 37.8 mg (0.25 mmol) of
2-(hydroxymethyl)phenylboronic acid are introduced into 1 ml of
DMF. Addition of 0.37 ml of 2 M sodium carbonate solution and 10.2
mg (0.01 mmol) of PdCl.sub.2(dppf) is followed by heating to
80.degree. C. After 14 h, the reaction mixture is filtered through
kieselguhr and purified by separation twice by preparative HPLC.
The product fractions are concentrated and, after addition of a 5:1
mixture of methanol and 4N hydrogen chloride in dioxane, again
concentrated. Drying under high vacuum results in 27 mg (24.4% of
theory) of the title compound.
[0531] .sup.1H-NMR (200 MHz, DMSO-d.sub.6): .delta.=10.10 (br. s,
1H), 9.06 (d, 1H), 8.36 (s, 1H), 8.02 (m, 2H), 7.61 (m, 1H),
7.54-7.36 (m, 4H), 4.43 (s, 2H), 4.33 (m, 1H), 3.67 (m, 1H),
3.55-3.12 (m, 5H), 2.23 (m, 1H), 2.16 (m, 1H), 1.92 (m, 2H), 1.77
(m, 1H).
[0532] HPLC (method 1): R.sub.t=3.9 min.
[0533] MS (ESIpos): m/z=393 (M+H).sup.+ (free base)
EXAMPLE 55
N-[(3R)-1-Azabicyclo[2.2.2]oct-3-yl]-6-(5-phenyl-1,2,4-oxadiazol-3-yl)-1-b-
enzo-thiophene-2-carboxamide hydrochloride
##STR00104##
[0535] 110 mg (0.26 mmol) of
6-[amino(hydroxyimino)methyl]-N-[(3R)-1-azabicyclo-[2.2.2]oct-3-yl]-1-ben-
zothiophene-2-carboxamide dihydrochloride (Example 27A) are
dissolved in 2 ml of DMF and 0.75 ml of THF. 250 mg of 4 .ANG.
molecular sieves are added and the mixture is stirred at room
temperature for 30 min. Addition of 31.2 mg (0.79 mmol) of sodium
hydride (60% suspension in mineral oil) is followed by heating at
60.degree. C. for 20 min and then cooling to room temperature. A
solution of 100 .mu.l (0.79 mmol) of methyl benzoate in 1 ml of THF
is added to the reaction mixture, and it is heated at 80.degree. C.
for 14 h. A further 20.8 mg (0.52 mmol) of sodium hydride (60%
suspension in mineral oil) and 0.99 ml (7.91 mmol) of methyl
benzoate in 1 ml of THF are added, and the mixture is heated at
70.degree. C. for a further 24 h. The reaction is stopped by adding
water. Purification takes place by preparative HPLC. The product
fractions are concentrated and, after addition of a 5:1 mixture of
methanol and 4N hydrogen chloride in dioxane, again concentrated.
Drying under high vacuum results in 45.7 mg (32% of theory) of the
title compound.
[0536] 1.0 HPLC (method 1): R.sub.t=4.5 min.
[0537] MS (ESIpos): m/z=431 (M+H).sup.+ (free base).
EXAMPLE 56
N-[(3R)-1-Azabicyclo[2.2.2]oct-3-yl]-6-(5-benzyl-1,2,4-oxadiazol-3-yl)-1-b-
enzo-thiophene-2-carboxamide hydrochloride
##STR00105##
[0539] 110 mg (0.26 mmol) of
6-[amino(hydroxyimino)methyl]-N-[(3R)-1-azabicyclo[2.2.2]oct-3-yl]-1-benz-
othiophene-2-carboxamide dihydrochloride (Example 27A) are
dissolved in 2 ml of DMF and 0.75 ml of THF. 250 mg of 4 .ANG.
molecular sieves are added, and the mixture is stirred at room
temperature for 30 min. Addition of 31.2 mg (0.79 mmol) of sodium
hydride (60% suspension in mineral oil) is followed by heating at
60.degree. C. for 20 min and then cooling to room temperature. A
solution of 110 .mu.l (0.79 mmol) of methyl phenylacetate in 1 ml
of THF is added, and the mixture is heated at 80.degree. C. for 14
h. Addition of a further 20.8 mg (0.52 mmol) of sodium hydride (60%
suspension in mineral oil) and 1.14 ml (7.91 mmol) of methyl
phenylacetate in 1 ml of THF is followed by heating at 70.degree.
C. for a further 24 h. The reaction is stopped by adding water.
Purification takes place by preparative HPLC. The product fractions
are concentrated and, after addition of a 5:1 mixture of methanol
and 4N hydrogen chloride in dioxane, again concentrated. Drying
under high vacuum results in 4.1 mg (3% of theory) of the title
compound.
[0540] .sup.1H-NMR (300 MHz, methanol-d.sub.4): .delta.=8.63 (s,
1H), 8.11 (m, 2H), 8.04 (d, 1H), 7.43-7.27 (m, 5H), 4.47 (m, 1H),
4.38 (s, 2H), 3.87 (m, 1H), 3.52-3.20 (m, 5H); 2.40 (m, 1H), 2.28
(m, 1H), 2.11 (m, 2H), 1.97 (m, 1H).
[0541] HPLC (method 1): R.sub.t=4.4 min.
[0542] MS (ESIpos): m/z=445 (M+H).sup.+ (free base).
EXAMPLE 57
N-[(3R)-1-Azabicyclo[2.2.2]oct-3-yl]-6-[4-(4-morpholinylmethyl)phenyl]-1-b-
enzo-thiophene-2-carboxamide dihydrochloride
##STR00106##
[0544] 330 mg (3.75 mmol) of morpholine and 40 mg (0.56 mmol) of
sodium cyanoborohydride are successively added to a solution of 80
mg (0.19 mmol) of
N-[(3R)-1-azabicyclo[2.2.2]oct-3-yl]-6-(4-formylphenyl)-1-benzot-
hiophene-2-carboxamide hydrochloride (Example 23A) in 1.5 ml of a
6:1 mixture of methanol and acetic acid. 2 h at room temperature
and 6 h at 80.degree. C. are followed by purification by
preparative HPLC. The product fractions are concentrated and, after
addition of a 5:1 mixture of methanol and 1N hydrochloric acid,
again concentrated. Drying under high vacuum results in 87.7 mg
(88% of theory) of the title compound.
[0545] .sup.1H-NMR (400 MHz, DMSO-d.sub.6): .delta.=11.26 (br. s,
1H), 10.29 (br. s, 1H), 9.18 (d, 1H), 8.41 (m, 2H), 8.06 (d, 1H),
7.89 (m, 2H), 7.81 (d, 1H), 7.74 (m, 2H), 4.39 (m, 2H), 4.34 (m,
1H), 4.05-3.03 (m, 6H), 2.23 (m, 1H), 2.16 (m, 1H), 1.92 (m, 2H),
1.76 (m, 1H).
[0546] HPLC (method 1): R.sub.t=3.5 min.
[0547] MS (ESIpos): m/z=462 (M+H).sup.+ (free base).
EXAMPLE 58
N-[(3R)-1-Azabicyclo[2.2.2]oct-3-yl]-7-[4-(dimethylamino)phenyl]-1-benzo-t-
hiophene-2-carboxamide hydrochloride
##STR00107##
[0549] 0.33 ml of 2 M sodium carbonate solution and 9.1 mg (0.01
mmol) of PdCl.sub.2(dppf) are added to a mixture of 100 mg (0.22
mmol) of
N-[(3R)-1-azabicyclo[2.2.2]oct-3-yl]-7-bromo-1-benzothiophene-2-carboxami-
de hydrochloride (Example 8A) and 36.8 mg (0.22 mmol) of
4-(dimethylamino)phenylboronic acid in 1 ml of DMF. The reaction
mixture is heated at 80.degree. C. for 16 h. A further 36.8 mg
(0.22 mmol) of 4-(dimethylamino)phenylboronic acid, 36.5 mg (0.04
mmol) of PdCl.sub.2(dppf) and 0.67 ml of 1N sodium hydroxide
solution are added, and the mixture is heated at 80.degree. C. for
a further 3 h. Cooling is followed by filtration through kieselguhr
and purification by preparative HPLC. The product fractions are
concentrated, taken up in a 5:1 mixture of methanol and 1N
hydrochloric acid and again concentrated. Drying under high vacuum
results in 50.6 mg (47% of theory) of the title compound.
[0550] .sup.1H-NMR (300 MHz, methanol-d.sub.4): .delta.=8.26 (s,
1H), 7.95 (m, 3H), 7.80 (m, 2H), 7.58 (dd, 1H), 7.53 (m, 1H), 4.46
(m, 1H), 3.82 (m, 1H), 3.51 (m, 1H), 3.45-3.16 (m, 10H), 2.37 (m,
1H), 2.29 (m, 1H), 2.10 (m, 2H), 1.95 (m, 1H).
[0551] HPLC (method 1): R.sub.t=3.6 min.
[0552] MS (ESIpos): m/z=406 (M+H).sup.+ (free base).
EXAMPLE 59
N-[(3R)-1-Azabicyclo[2.2.2]oct-3-yl]-7-(2-thienyl)-1-benzothiophene-2-carb-
oxamide formate
##STR00108##
[0554] 100 mg (0.25 mmol) of
N-[(3R)-1-azabicyclo[2.2.2]oct-3-yl]-7-bromo-1-benzothio-phene-2-carboxam-
ide hydrochloride (Example 8A) and 31.9 mg (0.25 mmol) of
2-thiopheneboronic acid are introduced into 1.5 ml of DMF. Addition
of 0.37 ml of 2 M sodium carbonate solution and 9.11 mg (0.01 mmol)
of PdCl.sub.2(dppf) is followed by heating to 85.degree. C. After
14 h, the reaction mixture is filtered through kieselguhr and
purified by preparative HPLC (eluent A: acetonitrile, eluent B:
water+0.1% formic acid; gradient: 10% A.fwdarw.95% A). The product
fractions are concentrated and dried under high vacuum. 30 mg (28%
of theory) of the title compound are obtained.
[0555] .sup.1H-NMR (200 MHz, DMSO-d.sub.6): .delta.=8.80 (d, 1H),
8.33 (s, 1H), 8.23 (s, 1H), 7.97 (m, 1H), 7.72 (m, 3H), 7.55 (dd,
1H), 7.28 (dd, 1H), 4.12 (m, 1H), 3.36 (m, 1H), 3.18-2.80 (m, 5H),
2.03 (m, 1H), 1.95 (m, 1H), 1.74 (m, 2H), 1.52 (m, 1H).
[0556] HPLC (method 1): R.sub.t=4.2 min.
[0557] MS (ESIpos): m/z=369 (M+H).sup.+ (free base).
EXAMPLE 60
7-(5-Acetyl-2-thienyl)-N-[(3R)-1-azabicyclo[2.2.2]oct-3-yl]-1-benzothiophe-
ne-2-carboxamide hydrochloride
##STR00109##
[0559] 100 mg (0.25 mmol) of
N-[(3R)-1-azabicyclo[2.2.2]oct-3-yl]-7-bromo-1-benzothiophene-2-carboxami-
de hydrochloride (Example 8A) and 42.3 mg (0.25 mmol) of
5-acetyl-2-thienylboronic acid are introduced into 1.5 ml of DMF.
Addition of 0.37 ml of 2 M sodium carbonate solution and 9.11 mg
(0.01 mmol) of PdCl.sub.2(dppf) is followed by heating to
85.degree. C. After 14 h, the reaction mixture is filtered through
kieselguhr and purified by preparative HPLC. The product fractions
are concentrated, taken up in a 5:1 mixture of methanol and 1N
hydrochloric acid, again concentrated and dried under high vacuum.
52 mg (46% of theory) of the title compound are obtained.
[0560] .sup.1H-NMR (200 MHz, DMSO-d.sub.6): .delta.=10.25 (br. s,
1H), 9.23 (d, 1H), 8.49 (s, 1H), 8.08 (d, 1H), 8.06 (m, 1H), 7.89
(m, 1H), 7.82 (d, 1H), 7.61 (dd, 1H), 4.36 (m, 1H), 3.73-113 (m,
5H), 2.60 (s, 3H), 2.23 (m, 1H), 2.15 (m, 1H), 1.93 (m, 2H), 1.76
(m, 1H).
[0561] HPLC (method 1): R.sub.t=4.1 min.
[0562] MS (ESIpos): m/z=411 (M+H).sup.+ (free base).
EXAMPLE 61
N-[(3R)-1-Azabicyclo[2.2.2]oct-3-yl]-7-[4-(6-oxo-2-piperidinyl)phenyl]-1-b-
enzothiophene-2-carboxamide hydrochloride
##STR00110##
[0564] 123.4 mg (0.49 mmol) of 6-(4-bromophenyl)-2-piperidinone,
142.2 mg (0.56 mmol) of bis(pinacolato)diboron, 146.6 mg (1.49
mmol) of potassium acetate, 13.7 mg (0.02 mmol) of
PdCl.sub.2(dppf), 150 mg (0.37 mmol) of
N-[(3R)-1-azabicyclo[2.2.2]oct-3-yl]-7-bromo-1-benzothiophene-2-carboxami-
de hydrochloride (Example 8A), 0.93 ml of 2 M sodium carbonate
solution and a further 13.7 mg (0.02 mmol) of PdCl.sub.2(dppf) in 2
ml of DMF are reacted by general method D. Drying under high vacuum
results in 7.3 mg (4% of theory) of the title compound.
[0565] HPLC (method 1): R.sub.t=3.9 min.
[0566] MS (ESIpos): m/z=460 (M+H).sup.+ (free base).
EXAMPLE 62
N-[(3R)-1-Azabicyclo[2.2.2]oct-3-yl]-7-[3-(hydroxymethyl)phenyl]-1-benzoth-
iophene-2-carboxamide hydrochloride
##STR00111##
[0568] 200 mg (0.45 mmol) of
N-[(3R)-1-azabicyclo[2.2.2]oct-3-yl]-7-bromo-1-benzo-thiophene-2-carboxam-
ide hydrochloride (Example 8A) and 74.6 mg (0.49 mmol) of
3-(hydroxymethyl)phenylboronic acid are introduced into 3 ml of
DMF. Addition of 0.67 ml of 2 M sodium carbonate solution and 1.8.2
mg (0.02 mmol) of PdCl.sub.2(dppf) is followed by heating to
80.degree. C. After 14 h, the reaction mixture is filtered through
kieselguhr and purified by separation by preparative HPLC. The
product fractions are concentrated and, after addition of a 5:1
mixture of methanol and 4N hydrogen chloride in dioxane, again
concentrated. Drying under high vacuum results in 40 mg (19% of
theory) of the title compound.
[0569] .sup.1H-NMR (300 MHz, DMSO-d.sub.6): .delta.=10.47 (br. s,
1H), 9.17 (d, 1H), 8.47 (s, 1H), 7.96 (d, 1H), 7.67 (s, 1H),
7.63-7.47 (m, 4H), 7.43 (d, 1H), 4.61 (s, 2H), 4.33 (m, 1H), 3.62
(m, 1H), 3.39 (m, 2H), 3.20 (m, 3H), 2.11 (m, 1H), 2.15 (m, 1H),
1.91 (m, 2H), 1.75 (m, 1H).
[0570] HPLC (method 1): R.sub.t=3.9 min.
[0571] MS (ESIpos): m/z=393 (M+H).sup.+ (free base).
EXAMPLE 63
N-[(3R)-1-Azabicyclo[2.2.2]oct-3-yl]-7-[2-(4-morpholinyl)phenyl]-1-benzoth-
iophene-2-carboxamide hydrochloride
##STR00112##
[0573] 100 mg (0.41 mmol) of 4-(2-bromophenyl)morpholine, 121.0 mg
(0.48 mmol) of bis(pinacolato)diboron, 101.3 mg (1.03 mmol) of
potassium acetate, 11.6 mg (0.02 mmol) of PdCl.sub.2(dppf), 127.6
mg (0.32 mmol) of
N-[(3R)-1-azabicyclo[2.2.2]oct-3-yl]-7-bromo-1-benzothiophene-2-carboxami-
de hydrochloride (Example 8A), 0.79 ml of 2 M sodium carbonate
solution and a further 11.6 mg (0.02 mmol) of PdCl.sub.2(dppf) in 2
ml of DMF are reacted by general method D. Drying under high vacuum
results in 38.9 mg (48% of theory) of the title compound.
[0574] .sup.1H-NMR (200 MHz, DMSO-d.sub.6): .delta.=10.20 (br. s,
1H), 9.04 (d, 1H), 8.36 (s, 1H), 7.93 (dd, 1H), 7.55 (m, 2H), 7.45
(d, 1H), 7.37 (dd, 1H), 7.17 (m, 2H), 4.32 (m, 1H), 3.62 (m, 1H),
3.48-3.10 (m, 9H), 2.69 (m, 4H), 2.19 (m, 1H), 2.10 (m, 11-1), 1.90
(m, 2H), 1.73 (m, 1H).
[0575] HPLC (method 1): R.sub.t=4.3 min.
[0576] MS (ESIpos): m/z=448 (M+H).sup.+ (free base).
EXAMPLE 64
2-(2-{[(3R)-1-Azabicyclo[2.2.2]oct-3-ylamino]carbonyl}-1-benzothien-7-yl)--
benzyl ethylcarbamate hydrochloride
##STR00113##
[0578] 32.5 .mu.l (0.23 mmol) of triethylamine and 16.6 mg (0.23
mmol) of ethyl isocyanate are added to a suspension of 50 mg (0.12
mmol) of
N-[(3R)-1-azabicyclo[2.2.2]oct-3-yl]-7-[2-(hydroxymethyl)phenyl]-1-benzot-
hiophene-2-carboxamide hydrochloride (Example 131) in 1 ml of a 5:1
mixture of THF and DMF. After 18 h at room temperature, a further
16.6 mg (0.23 mmol) of ethyl isocyanate and a catalytic amount of
4-N,N-dimethylaminopyridine are added. The mixture is stirred at
room temperature for a further 18 h. The reaction mixture is
concentrated in vacuo and purified by preparative HPLC. The product
fractions are concentrated and, after addition of a 5:1 mixture of
methanol and 1N hydrochloric acid, again concentrated. Drying under
high vacuum results in 28 mg (47% of theory) of the title
compound.
[0579] HPLC (method 1): R.sub.t=4.2 min.
[0580] MS (ESIpos): m/z=464 (M+H).sup.+ (free base).
EXAMPLE 65
2-(2-[(3R)-1-Azabicyclo[2.2.2]oct-3-ylamino
carbonyl]-1-benzothien-7-yl)benzyl methylcarbamate
hydrochloride
##STR00114##
[0582] 32.5 .mu.l (0.23 mmol) of triethylamine and 13.3 mg (0.23
mmol) of methyl isocyanate are added to a suspension of 50 mg (0.12
mmol) of
N-[(3R)-1-azabicyclo[2.2.2]oct-3-yl]-7-[2-(hydroxymethyl)phenyl]-1-benzot-
hiophene-2-carboxamide hydrochloride (Example 131) in 1 ml of a 5:1
mixture of THF and DMF. After 18 h at room temperature, a further
13.3 mg (0.23 mmol) of methyl isocyanate and a catalytic amount of
4-N,N-dimethylaminopyridine are added. The mixture is stirred at
room temperature for a further 18 h. The reaction mixture is
concentrated in vacuo and purified by preparative HPLC. The product
fractions are concentrated and, after addition of a 5:1 mixture of
methanol and 1N hydrochloric acid, again concentrated. Drying under
high vacuum results in 18 mg (30% of theory) of the title
compound.
[0583] .sup.1H-NMR (400 MHz, methanol-d.sub.4): .delta.=8.18 (s,
1H), 7.95 (m, 1H), 7.63-7.42 (m, 4H), 7.38 (m, 2H), 4.42 (m, 1H),
3.81 (m, 1H), 3.47 (m, 1H), 3.40-3.25 (m, 4H), 2.57 (m, 3H), 2.37
(m, 1H), 2.26 (m, 1H), 2.09 (m, 2H), 1.94 (m, 1H).
[0584] LC-MS (method 4): R.sub.t=2.7 min., m/z=464 (M+H).sup.+
(free base).
EXAMPLE 66
N-[(3R)-1-Azabicyclo[2.2.2]oct-3-yl]-7-[4-(2-oxo-1-pyrrolidinyl)phenyl]-1--
benzothiophene-2-carboxamide hydrochloride
##STR00115##
[0586] 116.5 mg (0.49 mmol) of 1-(4-bromophenyl)-2-pyrrolidinone,
142.2 mg (0.56 mmol) of bis(pinacolato)diboron, 119.1 mg (1.21
mmol) of potassium acetate, 13.7 mg (0.02 mmol) of
PdCl.sub.2(dppf), 150 mg (0.37 mmol) of
N-[(3R)-1-azabicyclo[2.2.2]oct-3-yl]-7-bromo-1-benzothiophene-2-carboxami-
de hydrochloride (Example 8A), 0.93 ml of 2 M sodium carbonate
solution and a further 13.7 mg (0.02 mmol) of PdCl.sub.2(dppf) in 2
ml of DMF are reacted by general method D. Drying under high vacuum
results in 71 mg (39% of theory) of the title compound.
[0587] .sup.1H-NMR (400 MHz, methanol-d.sub.4): .delta.=8.16 (s,
1H), 7.91 (d, 1H), 7.80 (m, 2H), 7.75 (m, 2H), 7.54 (dd, 1H), 7.51
(dd, 1H), 4.46 (m, 1H), 4.01 (m, 2H), 3.85 (m, 1H), 3.47 (m, 1H),
3.42-3.26 (m, 4H), 2.65 (m, 2H), 2.39 (m, 1H), 2.24 (m, 3H), 2.10
(m, 2H), 1.96 (m, 1H).
[0588] HPLC (method 1): R.sub.t=4.0 min.
[0589] MS (ESIpos): m/z=446 (M+H).sup.+ (free base).
EXAMPLE 67
N-[(3R)-1-Azabicyclo[2.2.2]oct-3-yl]-7-[4-(1-piperazinyl)phenyl]-1-benzoth-
iophene-2-carboxamide dihydrochloride
##STR00116##
[0591] 165.6 mg (0.49 mmol) of tert-butyl
4-(4-bromophenyl)-1-piperazinecarboxylate, 142.2 mg (0.56 mmol) of
bis(pinacolato)diboron, 119.1 mg (1.21 mmol) of potassium acetate,
13.7 mg (0.02 mmol) of PdCl.sub.2(dppf), 150 mg (0.37 mmol) of
N-[(3R)-1-azabicyclo[2.2.2]oct-3-yl]-7-bromo-1-benzothiophene-2-carboxami-
de hydrochloride (Example 8A), 0.93 ml of 2 M sodium carbonate
solution and a further 13.7 mg (0.02 mmol) of PdCl.sub.2(dppf) in 2
ml of DMF are reacted by general method D. The compound purified by
preparative HPLC is dissolved in 3 ml of methanol and, after
addition of 3 ml of 4 M hydrogen chloride in dioxane, stirred at
room temperature for 30 min. The contents of the flask are
concentrated in vacuo, and the residue is azeotropically distilled
with toluene twice. Drying under high vacuum results in 54 mg (28%
of theory) of the title compound.
[0592] .sup.1H-NMR (300 MHz, methanol-d.sub.4): .delta.=8.17 (s,
1H), 7.87 (dd, 1H), 7.66 (m, 2H), 7.52 (dd, 1H), 7.45 (dd, 1H),
7.18 (m, 2H), 4.45 (m, 1H), 3.83 (m, 1H), 3.75-3.13 (m, 13H), 2.38
(m, 1H), 2.28 (m, 1H), 2.10 (m, 2H), 1.95 (m, 1H).
[0593] HPLC (method 1): R.sub.t=3.7 min.
[0594] MS (ESIpos): m/z=447 (M+H).sup.+ (free base).
EXAMPLE 68
N-[(3R)-1-Azabicyclo[2.2.2]oct-3-yl]-7-[4-(3-oxo-4-morpholinyl)phenyl]-1-b-
enzothiophene-2-carboxamide hydrochloride
##STR00117##
[0596] 120 mg (0.39 mmol) of 4-(4-bromophenyl)-3-morpholinone,
115.3 mg (0.45 mmol) of bis(pinacolato)diboron, 96.6 mg (0.98 mmol)
of potassium acetate, 11.1 mg (0.02 mmol) of PdCl.sub.2(dppf),
121.6 mg (0.30 mmol) of
N-[(3R)-1-azabicyclo[2.2.2]oct-3-yl]-7-bromo-1-benzothiophene-2-carboxami-
de hydrochloride (Example 8A), 0.76 ml of 2 M sodium carbonate
solution and a further 11.1 mg (0.02 mmol) of PdCl.sub.2(dppf) in 2
ml of DMF are reacted by general method D. Drying under high vacuum
results in 24 mg (16% of theory) of the title compound.
[0597] .sup.1H-NMR (400 MHz, methanol-d.sub.4): .delta.=8.17 (s,
1H), 7.93 (d, 1H), 7.80 (m, 2H), 7.55 (m, 4H), 4.46 (m, 1H), 4.33
(s, 2H), 4.09 (m, 2H), 3.88 (m, 2H), 3.84 (m, 1H), 3.47 (m, 1H),
3.41-3.26 (m, 4H), 2.39 (m, 1H), 2.28 (m, 1H), 2.10 (m, 2H), 1.95
(m, 1H).
[0598] HPLC (method 1): R.sub.t=3.8 min.
[0599] MS (ESIpos): m/z=462 (M+H).sup.+ (free base).
EXAMPLE 69
N-[(3R)-1-Azabicyclo[2.2.2]oct-3-yl]-7-[3-(1-pyrrolidinyl)phenyl]-1-benzot-
hiophene-2-carboxamide hydrochloride
##STR00118##
[0601] 109.8 mg (0.49 mmol) of 1-(3-bromophenyl)pyrrolidine, 142.2
mg (0.56 mmol) of bis(pinacolato)diboron, 119.1 mg (1.21 mmol) of
potassium acetate, 13.7 mg (0.02 mmol) of PdCl.sub.2(dppf), 150.0
mg (0.37 mmol) of
N-[(3R)-1-azabicyclo[2.2.2]oct-3-yl]-7-bromo-1-benzothiophene-2-carboxami-
de hydrochloride (Example 8A), 0.93 ml of 2 M sodium carbonate
solution and a further 13.7 mg (0.02 mmol) of PdCl.sub.2(dppf) in 2
ml of DMF are reacted by general method D. Drying under high vacuum
results in 88.4 mg (51% of theory) of the title compound.
[0602] .sup.1H-NMR (200 MHz, DMSO-d.sub.6): .delta.=10.28 (br. s,
1H), 9.11 (d, 1H), 8.42 (s, 1H), 7.95 (dd, 1H), 7.55 (m, 2H), 7.36
(dd, 1H), 6.96 (d, 1H), 6.87 (s, 1H), 6.68 (m, 1H), 4.33 (m, 1H),
3.80-3.10 (m, 10H), 2.21 (m, 1H), 2.11 (m, 1H), 2.95 (m, 6H), 1.75
(m, 1H).
[0603] HPLC (method 1): R.sub.t=4.2 min.
[0604] MS (ESIpos): m/z=432 (M+H).sup.+ (free base).
EXAMPLE 70
N-[(3R)-1-Azabicyclo[2.2.2]oct-3-yl]-7-[3-(4-morpholinyl)phenyl]-1-benzoth-
iophene-2-carboxamide hydrochloride
##STR00119##
[0606] 151.1 mg (0.49 mmol) of 3-(4-morpholinyl)phenyl
trifluoromethanesulphonate (Example 17A), 142.2 mg (0.56 mmol) of
bis(pinacolato)diboron, 119.1 mg (1.21 mmol) of potassium acetate,
13.7 mg (0.02 mmol) of PdCl.sub.2(dppf), 150.0 mg (0.37 mmol) of
N-[(3R)-1-azabicyclo[2.2.2]oct-3-yl]-7-bromo-1-benzothiophene-2-carboxami-
de hydrochloride (Example 8A), 0.93 ml of 2 M sodium carbonate
solution and a further 13.7 mg (0.02 mmol) of PdCl.sub.2(dppf) in 2
ml of DMF are reacted by general method D. Drying under high vacuum
results in 125.3 mg (68% of theory) of the title compound.
[0607] .sup.1H-NMR (400 MHz, methanol-d.sub.4): .delta.=8.26 (s,
1H), 7.99 (m, 2H), 7.86 (d, 1H), 7.75 (m, 2H), 7.59 (m, 2H), 4.47
(m, 1H), 4.10 (m, 4H), 3.83 (m, 1H), 3.76 (m, 4H), 3.73 (m, 1H),
3.52 (m, 1H), 3.37 (m, 3H), 2.38 (m, 1H), 2.29 (m, 1H), 2.10 (m,
2H), 1.96 (m, 1H).
[0608] HPLC (method 1): R.sub.t=3.9 min.
[0609] MS (ESIpos): m/z=448 (M+H).sup.+ (free base).
EXAMPLE 71
N-[(3R)-1-Azabicyclo[2.2.2]oct-3-yl]-7-[4-(1-pyrrolidinyl)phenyl]-1-benzot-
hiophene-2-carboxamide dihydrochloride
##STR00120##
[0611] 109.8 mg (0.49 mmol) of 1-(4-bromophenyl)pyrrolidine, 142.2
mg (0.56 mmol) of bis(pinacolato)diboron, 119.1 mg (1.21 mmol) of
potassium acetate, 13.7 mg (0.02 mmol) of PdCl.sub.2(dppf), 150.0
mg (0.37 mmol) of
N-[(3R)-1-azabicyclo[2.2.2]oct-3-yl]-7-bromo-1-benzothiophene-2-carboxami-
de hydrochloride (Example 8A), 0.93 ml of 2 M sodium carbonate
solution and a further 13.7 mg (0.02 mmol) of PdCl.sub.2(dppf) in
2.5 ml of DMF are reacted by general method D. Drying under high
vacuum results in 24.8 mg (13% of theory) of the title
compound.
[0612] .sup.1H-NMR (400 MHz, methanol-d.sub.4): .delta.=8.26 (s,
1H), 7.98 (d, 1H), 7.92 (m, 2H); 7.75 (m, 2H), 7.58 (dd, 1H), 7.53
(d, 1H), 4.47 (m, 1H), 3.92-3.76 (m, 5H), 3.51 (m, 1H), 3.45-3.18
(m, 4H), 2.42-2.23 (m, 6H), 2.10 (m, 2H), 1.96 (m, 1H).
[0613] HPLC (method 1): R.sub.t=4.1 min.
[0614] MS (ESIpos): m/z=432 (M+H).sup.+ (free base).
EXAMPLE 72
N-[(3R)-1-Azabicyclo[2.2.2]oct-3-yl]-7-[4-(4-morpholinylcarbonyl)phenyl]-1-
-benzothiophene-2-carboxamide hydrochloride
##STR00121##
[0616] 164.7 mg (0.49 mmol) of 4-(4-morpholinylcarbonyl)phenyl
trifluoromethane-sulphonate (Example 18A), 142.2 mg (0.56 mmol) of
bis(pinacolato)diboron, 119.1 mg (1.21 mmol) of potassium acetate,
13.7 mg (0.02 mmol) of PdCl.sub.2(dppf), 150.0 mg (0.37 mmol) of
N-[(3R)-1-azabicyclo[2.2.2]oct-3-yl]-7-bromo-1-benzothiophene-2-carboxami-
de hydrochloride (Example 8A), 0.93 ml of 2 M sodium carbonate
solution and a further 13.7 mg (0.02 mmol) of PdCl.sub.2(dppf) in
2.5 ml of DMF are reacted by general method D. An initial
purification by preparative HPLC is followed by column
chromatography on silica gel (mobile phase:
dichloromethane/methanol/ammonia 90:9:1). Drying under high vacuum
results in 24.8 mg (13% of theory) of the title compound.
[0617] .sup.1H-NMR (400 MHz, methanol-d.sub.4): .delta.=8.22 (s,
1H), 7.97 (d, 1H), 7.83 (m, 2H), 7.62 (m, 2H), 7.55 (m, 2H), 4.47
(m, 1H), 3.90-3.26 (m, 14H), 2.38 (m, 1H), 2.28 (m, 1H), 2.10 (m,
2H), 1.96 (m, 1H).
[0618] HPLC (method 1): R.sub.t=3.8 min.
[0619] MS (ESIpos): m/z=476 (M+H).sup.+ (free base).
EXAMPLE 73
7-[2-(Aminomethyl)phenyl]-N-[(3R)-1-azabicyclo[2.2.2]oct-3-yl]-1-benzothio-
phene-2-carboxamide dihydrochloride
##STR00122##
[0621] 534.2 mg (1.87 mmol) of tert-butyl 2-bromobenzylcarbamate,
474.1 mg (1.87 mmol) of bis(pinacolato)diboron, 397.0 mg (4.04
mmol) of potassium acetate, 45.5 mg (0.06 mmol) of
PdCl.sub.2(dppf), 500 mg (1.24 mmol) of
N-[(3R)-1-azabicyclo[2.2.2]oct-3-yl]-7-bromo-1-benzothiophene-2-carboxami-
de hydrochloride (Example 8A), 3.11 ml of 2 M sodium carbonate
solution and a further 45.5 mg (0.06 mmol) of PdCl.sub.2(dppf) in
6.0 ml of DMF are reacted by general method D. Purification by
preparative HPLC is followed by concentration of the combined
product fractions, taking up in methanol, addition of 1N
hydrochloric acid, and stirring at room temperature for 30 min.
Concentration and drying under high vacuum result in 121 mg (20% of
theory) of the title compound.
[0622] HPLC (method 1): R.sub.t=3.6 min.
[0623] MS (ESIpos): m/z=392 (M+H).sup.+(free base).
EXAMPLE 74
N-[(3R)-1-Azabicyclo[2.2.2]oct-3-yl]-7-{3-[(2,2-dimethylpropanoyl)amino]ph-
enyl}-1-benzothiophene-2-carboxamide hydrochloride
##STR00123##
[0625] 143.5 mg (0.56 mmol) of
N-(3-bromophenyl)-2,2-dimethylpropanamide, 142.2 mg (0.56 mmol) of
bis(pinacolato)diboron, 119.1 mg (1.21 mmol) of potassium acetate,
13.7 mg (0.02 mmol) of PdCl.sub.2(dppf), 150.0 mg (0.37 mmol) of
N-[(3R)-1-azabicyclo[2.2.2]oct-3-yl]-7-bromo-1-benzothiophene-2-carboxami-
de hydrochloride (Example 8A), 0.93 ml of 2 M sodium carbonate
solution and a further 13.7 mg (0.02 mmol) of PdCl.sub.2(dppf) in
2.0 ml of DMF are reacted by general method D. An initial
purification by preparative HPLC is followed by column
chromatography on silica gel (mobile phase:
dichloromethane/methanol/ammonia 90:9:1). Drying under high vacuum
results in 32.4 mg (17% of theory) of the title compound.
[0626] .sup.1H-NMR (400 MHz, methanol-d.sub.4): .delta.=8.16 (s,
1H), 8.01 (m, 1H), 7.92 (m, 1H), 7.63-7.48 (m, 3H), 7.47 (m, 2H),
4.44 (m, 1H), 3.84 (m, 1H), 3.47 (m, 1H), 3.41-3.27 (m, 4H), 2.38
(m, 1H), 2.28 (m, 1H), 2.10 (m, 2H), 1.96 (m, 1H), 1.32 (s,
9H).
[0627] HPLC (method 1): R.sub.t=4.3 min.
[0628] MS (ESIpos): m/z=462 (M+H).sup.+ (free base).
EXAMPLE 75
3-(2-{[(3R)-1-Azabicyclo[2.2.2]oct-3-ylamino]carbonyl}-1-benzothien-7-yl)--
benzoic acid hydrochloride
##STR00124##
[0630] 200 mg (0.50 mmol) of
N-[(3R)-1-azabicyclo[2.2.2]oct-3-yl]-7-bromo-1-benzothiophene-2-carboxami-
de hydrochloride (Example 8A) and 82.6 mg (0.50 mmol) of
3-carboxyphenylboronic acid are introduced into 1.5 ml of DMF.
Addition of 0.78 ml of 2. M sodium carbonate solution and 20.3 mg
(0.02 mmol) of PdCl.sub.2(dppf) is followed by heating at
60.degree. C. After 18 h, a further 20.3 mg (0.02 mmol) of
PdCl.sub.2(dppf) are added, and the mixture is heated at 90.degree.
C. for a further 18 h. After cooling, the reaction mixture is
filtered through kieselguhr and purified by preparative HPLC. The
product fractions are concentrated and, after addition of a 3:1
mixture of acetonitrile and 1N hydrochloric acid, again
concentrated. Drying under high vacuum results in 103 mg (45% of
theory) of the title compound.
[0631] .sup.1H-NMR (300 MHz, DMSO-d.sub.6): .delta.=10.28 (br. s,
1H), 9.13 (d, 1H), 8.46 (s, 1H), 8.29 (m, 1H), 8.08-7.95 (m, 3H),
7.71 (dd, 1H), 7.60 (m, 2H), 4.33 (m, 1H), 3.85-3.12 (m, 6H), 2.22
(m, 1H), 2.15 (m, 1H), 1.91 (m, 2H), 1.75 (m, 1H).
[0632] HPLC (method 1): R.sub.1=3.9 min.
[0633] MS (ESIpos): m/z=407 (M+H).sup.+ (free base).
EXAMPLE 76
N-[(3R)-1-Azabicyclo[2.2.2]oct-3-yl]-7-[2-({[(methylamino)carbonyl]amino}--
methyl)phenyl]-1-benzothiophene-2-carboxamide hydrochloride
##STR00125##
[0635] 51.0 .mu.l (0.37 mmol) of triethylamine and 43.5 .mu.l (0.73
mmol) of methyl isocyanate are added to a suspension of 85 mg (0.18
mmol) of
7-[2-(aminomethyl)phenyl]-N-[(3R)-1-azabicyclo[2.2.2]oct-3-yl]-1-benzothi-
ophene-2-carboxamide dihydrochloride (Example 73) in 1 ml of a 5:1
mixture of THF and DMF. After 18 h at room temperature, the
reaction mixture is concentrated in vacuo and purified by
preparative HPLC. The product fractions are concentrated and, after
addition of a 5:1 mixture of methanol and 1N hydrochloric acid,
again concentrated. Drying under high vacuum results in 65.5 mg
(74% of theory) of the title compound.
[0636] .sup.1H-NMR (400 MHz, methanol-d.sub.4): .delta.=8.18 (s,
1H), 7.94 (d, 1H), 7.58-7.44 (m, 3H), 7.43-7.29 (m, 3H), 4.43 (m,
1H), 4.15 (m, 2H), 3.82 (m, 1H), 3.47 (m, 1H), 3.41-3.27 (m, 4H),
2.62 (s, 3H), 2.37 (m, 1H), 2.26 (m, 1H), 2.08 (m, 2H), 1.94 (m,
1H).
[0637] HPLC (method 1): R.sub.t=3.8 min.
[0638] LC-MS (method 4): R.sub.t=2.5 min.
[0639] MS (ESIpos): m/z=448 (M+H).sup.+ (free base).
EXAMPLE 77
N-[(3R)-1-Azabicyclo[2.2.2]oct-3-yl]-7-[3-(1H-pyrrol-1-yl)phenyl]-1-benzot-
hiophene-2-carboxamide hydrochloride
##STR00126##
[0641] 124.4 mg (0.56 mmol) of 1-(3-bromophenyl)-1H-pyrrole, 142.2
mg (0.56 mmol) of bis(pinacolato)diboron, 119.1 mg (1.21 mmol) of
potassium acetate, 13.7 mg (0.02 mmol) of PdCl.sub.2(dppf), 150.0
mg (0.37 mmol) of
N-[(3R)-1-azabicyclo[2.2.2]oct-3-yl]-7-bromo-1-benzothiophene-2-carboxami-
de hydrochloride (Example 8A), 0.93 ml of 2 M sodium carbonate
solution and a further 13.7 mg (0.02 mmol) of PdCl.sub.2(dppf) in
2.0 ml of DMF are reacted by general method D. Drying under high
vacuum results in 86.9 mg (48% of theory) of the title
compound.
[0642] .sup.1H-NMR (400 MHz; DMSO-d.sub.6): .delta.=9.92 (br. s,
1H), 9.03 (d, 1H), 8.39 (m, 1H), 8.02 (m, 1H), 7.88 (s, 1H),
7.77-7.57 (m, 5H), 7.49 (m, 2H), 6.31 (m, 2H), 4.32 (m, 1H), 3.67
(m, 1H), 3.57-3.13 (m, 5H), 2.21 (m, 1H), 2.13 (m, 1H), 1.90 (m,
2H), 1.75 (m, 1H).
[0643] HPLC (method 1): R.sub.t=4.5 min.
[0644] MS (ESIpos): m/z=428 (M+H).sup.+(free base).
EXAMPLE 78
N-[(3R)-1-Azabicyclo[2.2.2]oct-3-yl]-7-[3-(4-morpholinylcarbonyl)phenyl]-1-
-benzothiophene-2-carboxamide hydrochloride
##STR00127##
[0646] 103 mg (0.27 mmol) of HATU and 70.8 (0.41 mmol) of
N,N-diisopropylethyl-amine are added to a solution of 50 mg (0.11
mmol) of
3-(2-{[(3R)-1-azabicyclo[2.2.2]oct-3-ylamino]carbonyl}-1-benzothien-7--
yl)benzoic acid hydro-chloride (Example 75) and 19.7 .mu.l (0.23
mmol) of morpholine in 0.5 ml of DMF at 0.degree. C. The mixture is
stirred at room temperature for 18 h. After purification by
preparative HPLC, the product fractions are concentrated and, after
addition of a 3:1 mixture of acetonitrile and 1N hydrochloric acid,
again concentrated. Drying under high vacuum results in 43 mg (74%
of theory) of the title compound.
[0647] .sup.1H-NMR (200 MHz, DMSO-d.sub.6): .delta.=10.66 (br. s,
1H), 9.33 (d, 1H), 8.56 (s, 1H), 7.98 (dd, 1H), 7.87-7.45 (m, 6H),
4.34 (m, 1H), 3.87-3.06 (m, 14H), 2.18 (m, 2H), 1.90 (m, 2H), 1.74
(m, 1H).
[0648] HPLC (method 1): R.sub.t=3.8 min.
[0649] MS (ESIpos): m/z=476 (M+H).sup.+ (free base).
EXAMPLE 79
N-[(3S)-1-Azabicyclo[2.2.2]oct-3-yl]-7-[4-(4-morpholinyl)phenyl]-1-benzoth-
iophene-2-carboxamide hydrochloride
##STR00128##
[0651] 330.7 mg (0.87 mmol) of HATU and 112.4 mg (0.87 mmol) of
N,N-diisopropyl-ethylamine are added to a mixture of 144.3 mg (0.72
mmol) of S-3-amino-quinuclidine dihydrochloride and 300 mg (0.72
mmol) of 7-[4-(4-morpholinyl)-phenyl]-1-benzothiophene-2-carboxylic
acid (Example 20A) in 3 ml of DMF at 0.degree. C. After 30 min at
0.degree. C., a further 224.8 mg (1.74 mmol) of
N,N-diisopropylethylamine are added, and the mixture is stirred at
room temperature for 19 h. The reaction solution is mixed with a
little water and acetonitrile and purified by preparative HPLC. The
product fractions are concentrated and, after addition of a 3:1
mixture of methanol and 1N hydrochloric acid, again concentrated.
Drying under high vacuum results in 158 mg (45% of theory) of the
title compound.
[0652] The spectroscopic data agree with those of the enantiomeric
compound (Example 19).
EXAMPLE 80
N-[(3R)-1-Azabicyclo[2.2.2]oct-3-yl]-7-[3-(4-morpholinyl)phenyl]-1-benzofu-
ran-2-carboxamide hydrochloride
##STR00129##
[0654] 151.1 mg (0.49 mmol) of 3-(4-morpholinyl)phenyl
trifluoromethanesulphonate (Example 17A), 142.2 mg (0.56 mmol) of
bis(pinacolato)diboron, 119.1 mg (1.21 mmol) of potassium acetate,
13.7 mg (0.02 mmol) of PdCl.sub.2(dppf), 144 mg (0.37 mmol) of
N-[(3R)-1-azabicyclo[2.2.2]oct-3-yl]-7-bromo-1-benzofuran-2-carboxamide
hydrochloride (Example 30A), 0.93 ml of 2 M sodium carbonate
solution and a further 13.7 mg (0.02 mmol) of PdCl.sub.2(dppf) in 2
ml of DMF are reacted by general method D. Drying under high vacuum
results in 32 mg (18% of theory) of the title compound.
[0655] .sup.1H-NMR (300 MHz, DMSO-d.sub.6): .delta.=10.27 (br. s,
1H), 8.96 (d, 1H), 7.85 (s, 1H), 7.78 (m, 1H), 7.68 (m, 1H), 7.62
(m, 1H), 7.43 (m, 3H), 7.17 (m, 1H), 4.36 (m, 1H), 3.82 (m, 4H),
3.63 (m, 1H), 3.44-3.10 (m, 9H), 2.22 (m, 1H), 2.12 (m, 1H), 1.91
(m, 2H), 1.75 (m, 1H).
[0656] HPLC (method 1): R.sub.t=3.8 min.
[0657] MS (ESIpos): m/z=432 (M+H).sup.+ (free base)
EXAMPLE 81
7-(3-Aminophenyl)-N-[(3R)-1-azabicyclo[2.2.2]oct-3-yl]-1-benzothiophene-2--
carboxamide hydrochloride
##STR00130##
[0659] 200 mg (0.50 mmol) of
N-[(3R)-1-azabicyclo[2.2.2]oct-3-yl]-7-bromo-1-benzothiophene-2-carboxami-
de hydrochloride (Example 8A) and 68.2 mg (0.50 mmol) of
3-aminophenylboronic acid are introduced into 1.5 ml of DMF.
Addition of 0.78 ml of 2 M sodium carbonate solution and 20.3 mg
(0.02 mmol) of PdCl.sub.2(dppf) is followed by heating at
60.degree. C. for 18 h. After cooling, the reaction mixture is
filtered through kieselguhr and purified by separation by
preparative HPLC. The product fractions are concentrated and, after
addition of a 3:1 mixture of acetonitrile and 1N hydrochloric acid,
again concentrated. Drying under high vacuum results in 201 mg (98%
of theory) of the title compound.
[0660] .sup.1H-NMR (200 MHz, DMSO-d.sub.6): .delta.=10.63 (br. s,
1H), 9.33 (d, 1H), 8.57 (s, 1H), 8.00 (dd, 1H), 7.76-7.58 (m, 4H),
7.55 (m, 1H), 7.43 (m, 1H), 4.34 (m, 1H), 3.62 (m, 1H), 3.42 (m,
2H), 3.19 (m, 3H), 2.19 (m, 2H), 1.90 (m, 2H), 1.73 (m, 1H).
[0661] HPLC (method 1): R.sub.t=3.5 min.
[0662] MS (ESIpos): m/z=378 (M+H).sup.+ (free base).
EXAMPLE 82
N-[(3R)-1-Azabicyclo[2.2.2]oct-3-yl]-7-{3-[(methoxyacetyl)amino]phenyl}-1--
benzothiophene-2-carboxamide hydrochloride
##STR00131##
[0664] 96.4 mg (0.25 mmol) of HATU and 71.5 .mu.l (0.41 mmol) of
N,N-diisopropylethyl-amine are added to a solution of 50 mg (0.12
mmol) of
7-(3-aminophenyl)-N-[(3R)-1-azabicyclo[2.2.2]oct-3-yl]-1-benzothiophen-
e-2-carboxamide hydrochloride (Example 81) and 18.5 .mu.l (0.24
mmol) of methoxyacetic acid in 0.5 ml of DMF at 0.degree. C. The
mixture is stirred at room temperature for 3 h. Purification by
preparative HPLC is followed by concentration of the product
fractions and, after addition of a 3:1 mixture of acetonitrile and
1 N hydrochloric acid, concentration again. Drying under high
vacuum results in 7 mg (11% of theory) of the title compound.
[0665] .sup.1H-NMR (300 MHz, DMSO-d.sub.6): .delta.=10.13 (br. s,
1H), 9.97 (s, 1H), 9.04 (d, 1H), 8.39 (s, 1H), 8.13 (m, 1H), 7.98
(d, 1H), 7.76 (d, 1H), 7.58 (dd, 1H), 7.50 (m, 2H), 7.42 (m, 1H),
4.33 (m, 1H), 4.03 (s, 2H), 3.66 (m, 1H), 3.56-3.12 (m, 8H), 2.22
(m, 1H), 2.14 (m, 1H), 1.91 (m, 2H), 1.75 (m, 1H).
[0666] HPLC (method 1): R.sub.t=4.0 min.
[0667] MS (ESIpos): m/z=450 (M+H).sup.+ (free base).
EXAMPLE 83
N-[(3R)-1-Azabicyclo[2.2.2]oct-3-yl]-7-[4-(2-oxo-1-pyrrolidinyl)phenyl]-1--
benzo-furan-2-carboxamide hydrochloride
##STR00132##
[0669] 161.9 mg (0.67 mmol) of 1-(4-bromophenyl)-2-pyrrolidinone,
197.5 mg (0.78 mmol) of bis(pinacolato)diboron, 165.4 mg (1.69
mmol) of potassium acetate, 19.0 mg (0.03 mmol) of
PdCl.sub.2(dppf), 200 mg (0.52 mmol) of
N-[(3R)-1-azabicyclo[2.2.2]oct-3-yl]-7-bromo-1-benzofuran-2-carboxamide
hydrochloride (Example 30A), 1.30 ml of 2 M sodium carbonate
solution and a further 19.0 mg (0.03 mmol) of PdCl.sub.2(dppf) in
2.5 ml of DMF are reacted by general method D. Drying under high
vacuum results in 166.6 mg (65% of theory) of the title
compound.
[0670] .sup.1H-NMR (200 MHz, DMSO-d.sub.6): .delta.=10.06 (br. s,
1H), 8.96 (d, 1H), 7.97 (m, 1H), 7.94 (s, 1H), 7.83 (m, 3H), 7.78
(dd, 1H), 7.69 (dd, 1H), 7.43 (dd, 1H), 4.33 (m, 1H), 4.00-3.75 (m,
2H), 3.66 (m, 1H), 3.49-3.10 (m, 5H), 2.55 (m, 2H), 2.23 (m, 1H),
2.10 (m, 3H), 1.91 (m, 2H), 1.75 (m, 1H).
[0671] HPLC (method 1): R.sub.t=4.0 min.
[0672] MS (ESIpos): m/z=430.5 (M+H).sup.+ (free base).
EXAMPLE 84
7-[3-(Acetylamino)phenyl]-N-[(3S)-1-azabicyclo[2.2.2]oct-3-yl]-1-benzothio-
phene-2-carboxamide hydrochloride
##STR00133##
[0674] 0.67 ml of 2 M sodium carbonate solution and 18.3 mg (0.02
mmol) of PdCl.sub.2(dppf) are added to a mixture of 200 mg (0.45
mmol) of
N-[(3S)-1-azabicyclo[2.2.2]oct-3-yl]-7-bromo-1-benzothiophene-2-carboxami-
de hydrochloride (Example 22A) and 80.2 mg (0.45 mmol) of
3-(acetamido)phenylboronic acid in 2 ml of DMF. The reaction
mixture is heated at 80.degree. C. for 17 h. A further 40.1 mg
(0.22 mmol) of 3-(acetamido)phenylboronic acid, 1.34 ml of 1N
sodium hydroxide solution and 73.2 mg (0.09 mmol) of
PdCl.sub.2(dppf) are added, and the mixture is heated at 70.degree.
C. for a further 18 h. Cooling is followed by filtration through
kieselguhr and purification by preparative HPLC. The product
fractions are concentrated, taken up in a 5:1 mixture of methanol
and 1N hydrochloric acid and again concentrated. Drying under high
vacuum results in 124.5 mg (59% of theory) of the title
compound.
[0675] The spectroscopic data agree with those of the enantiomeric
compound (Example 51).
EXAMPLE 85
N-[(3S)-1-Azabicyclo[2.2.2]oct-3-yl]-7-(3-methoxyphenyl)-1-benzothiophene--
2-carboxamide hydrochloride
##STR00134##
[0677] 0.67 ml of 2 M aqueous sodium carbonate solution and 18.3 mg
(0.02 mmol) of PdCl.sub.2(dppf) are added to a mixture of 200 mg
(0.45 mmol) of
N-[(3S)-1-azabicyclo[2.2.2]oct-3-yl]-7-bromo-1-benzothiophene-2-carboxami-
de hydrochloride (Example 22A) and 68.1 mg (0.45 mmol) of
3-methoxyphenylboronic acid in 2 ml of DMF. The reaction mixture is
heated at 80.degree. C. for 17 h, filtered through kieselguhr and
evaporated to dryness. A purification by preparative HPLC is
followed by column chromatography on silica gel (mobile phase:
dichloromethane/methanol/ammonia 90:9:1). The product fractions are
concentrated, taken up in a 5:1 mixture of methanol and 1N
hydrochloric acid and again concentrated. Drying under high vacuum
results in 97.7 mg (48% of theory) of the title compound.
[0678] .sup.1H-NMR (200 MHz, DMSO-d.sub.6): .delta.=10.25 (br. s,
1H), 9.11 (d, 1H), 8.42 (s, 1H), 7.97 (dd, 1H), 7.56 (m, 2H), 7.47
(d, 1H), 7.30 (d, 1H), 7.24 (m, 1H), 7.06 (m, 1H), 4.32 (m, 1H),
3.83 (s, 3H), 3.63 (m, 1H), 3.49-3.10 (m, 5H), 2.20 (m, 1H), 2.13
(m, 1H), 1.90 (m, 2H), 1.74 (m, 1H).
[0679] The analytical data agree with those of the enantiomeric
compound (Example 17).
EXAMPLE 86
4-(2-{[(3R)-1-Azabicyclo[2.2.2]oct-3-ylamino]carbonyl}-1-benzofuran-7-yl)--
benzoic acid hydrochloride
##STR00135##
[0681] 150 mg (0.43 mmol) of
N-[(3R)-1-azabicyclo[2.2.2]oct-3-yl]-7-bromo-1-benzofuran-2-carboxamide
hydrochloride (Example 30A) and 71.3 mg (0.43 mmol) of
4-carboxyphenylboronic acid are introduced into 1.5 ml of DMF.
Addition of 0.64 ml of 2 M sodium carbonate solution and 17.5 mg
(0.02 mmol) of PdCl.sub.2(dppf) is followed by heating at
80.degree. C. for 18 h. After cooling, the reaction mixture is
filtered through kieselguhr, and the filtrate is concentrated and
partitioned between water and ethyl acetate. The aqueous phase is
washed with ethyl acetate and then concentrated. The crude product
is purified by preparative HPLC. The product fractions are combined
and concentrated and, after addition of a 3:1 mixture of
acetonitrile and 1N hydrochloric acid, again concentrated. The
crude product is stirred with acetonitrile. The precipitate is
filtered off with suction and dried under high vacuum to result in
37 mg (20% of theory) of the title compound.
[0682] .sup.1H-NMR (300 MHz, DMSO-d.sub.6): .delta.=10.37 (br. s,
1H), 9.15 (d, 1H), 8.08 (m, 4H), 7.93 (s, 1H), 7.85 (dd, 1H), 7.76
(dd, 1H), 7.47 (dd, 1H), 4.36 (m, 1H), 3.77-3.32 (m, 3H), 3.32 (m,
3H), 2.23 (m, 1H), 2.12 (m, 1H), 1.92 (m, 2H), 1.76 (m, 1H).
[0683] HPLC (method 1): R.sub.t=3.9 min.
[0684] MS (ESIpos): m/z=391 (M+H).sup.+ (free base).
EXAMPLE 87
N-[(3R)-1-Azabicyclo[2.2.2]oct-3-yl]-7-[3-(trifluoromethoxy)phenyl]-1-benz-
ofuran-2-carboxamide hydrochloride
##STR00136##
[0686] 200 mg (0.52 mmol) of
N-[(3R)-1-azabicyclo[2.2.2]oct-3-yl]-7-bromo-1-benzofuran-2-carboxamide
hydrochloride (Example 30A) and 106.8 mg (0.52 mmol) of
3-(trifluoromethoxy)phenylboronic acid are introduced into 2.0 ml
of DMF. Addition of 0.78 ml of 2 M sodium carbonate solution and
21.2 mg (0.03 mmol) of PdCl.sub.2(dppf) is followed by heating at
70.degree. C. for 17 h. After cooling, the reaction mixture is
filtered through kieselguhr and purified by preparative HPLC. The
product fractions are combined and concentrated and, after addition
of a 5:1 mixture of methanol and 1N hydrochloric acid, again
concentrated. Drying under high vacuum results in 48.8 mg (20% of
theory) of the title compound.
[0687] .sup.1H-NMR (200 MHz, DMSO-d.sub.6): .delta.=10.18 (br. s,
1H), 9.00 (d, 1H), 7.95 (m, 2H), 7.89 (s, 1H), 7.86 (m, 1H), 7.77
(m, 1H), 7.68 (m, 1H), 7.47 (m, 2H), 4.34 (m, 1H), 3.65 (m, 1H),
3.35 (m, 2H), 3.23 (m, 3H), 2.22 (m, 1H), 2.12 (m, 1H), 1.92 (m,
2H), 1.76 (m, 1H).
[0688] HPLC (method 1): R.sub.t=4.5 min.
[0689] MS (ESIpos): m/z=431 (M+H).sup.+ (free base).
EXAMPLE 88
N-[(3S)-1-Azabicyclo[2.2.2]oct-3-yl]-7-(2-methoxyphenyl)-1-benzothiophene--
2-carboxamide hydrochloride
##STR00137##
[0691] 0.67 ml of 2 M sodium carbonate solution and 18.3 mg (0.02
mmol) of PdCl.sub.2(dppf) are added to a mixture of 200 mg (0.45
mmol) of
N-[(3S)-1-azabicyclo[2.2.2]oct-3-yl]-7-bromo-1-benzothiophene-2-carboxami-
de hydrochloride (Example 22A) and 68.1 mg (0.45 mmol) of
2-methoxyphenylboronic acid in 2 ml of DMF. The reaction mixture is
heated at 70.degree. C. for 17 h and, after cooling, filtered
through kieselguhr and purified by preparative HPLC. The product
fractions are concentrated, taken up in a 5:1 mixture of methanol
and 1N hydrochloric acid and again concentrated. Drying under high
vacuum results in 112 mg (58% of theory) of the title compound.
[0692] .sup.1H-NMR (400 MHz, DMSO-d.sub.6): .delta.=10.38 (br. s,
1H), 9.07 (d, 1H), 8.38 (s, 1H), 7.95 (m, 1H), 7.50 (dd, 1H), 7.47
(m, 1H), 7.37 (m, 2H), 7.20 (d, 1H), 7.09 (dd, 1H), 4.31 (m, 1H),
3.73 (s, 3H), 3.62 (m, 1H), 3.35 (m, 2H), 3.19 (m, 3H), 2.19 (m,
1H), 2.13 (m, 1H), 1.90 (m, 2H), 1.73 (m, 1H).
[0693] The other analytical data agree with those of the
enantiomeric compound (Example 18).
EXAMPLE 89
N-[(3R)-1-Azabicyclo[2.2.2]oct-3-yl]-7-[3-(hydroxymethyl)phenyl]-1-benzofu-
ran-carboxamide hydrochloride
##STR00138##
[0695] 150 mg (0.43 mmol) of
N-[(3R)-1-azabicyclo[2.2.2]oct-3-yl]-7-bromo-1-benzofuran-2-carboxamide
hydrochloride (Example 30A) and 65.3 mg (0.43 mmol) of
3-(hydroxymethyl)phenylboronic acid are introduced into 1.5 ml of
DMF. Addition of 0.64 ml of 2 M sodium carbonate solution and 17.5
mg (0.02 mmol) of PdCl.sub.2(dppf) is followed by heating at
60.degree. C. for 18 h. A further 17.5 mg (0.02 mmol) of
PdCl.sub.2(dppf) are added and the mixture is stirred at 90.degree.
C. for a further 18 h. After cooling, the reaction mixture is
filtered through kieselguhr. A first purification by preparative
HPLC is followed by column chromatography on silica gel (mobile
phase: dichloromethane/methanol/ammonia 90:9:1). The product
fractions are combined and concentrated and, after addition of a
5:1 mixture of methanol and 4N hydrogen chloride in dioxane, again
concentrated. Drying under high vacuum results in 45 mg (24% of
theory) of the title compound.
[0696] .sup.1H-NMR (400 MHz, methanol-d.sub.4): .delta.=7.98 (m,
1H), 7.74 (m, 2H), 7.65 (m, 2H), 7.52 (dd, 1H), 7.42 (m, 2H), 4.72
(s, 2H), 4.51 (m, 1H), 3.87-3.26 (m, 6H), 2.39 (m, 1H), 2.23 (m,
1H), 2.10 (m, 2H), 1.95 (m, 1H).
[0697] HPLC (method 1): R.sub.t=3.9 min.
[0698] MS (ESIpos): m/z=377 (M+H).sup.+ (free base).
EXAMPLE 90
N-[(3R)-1-Azabicyclo[2.2.2]oct-3-yl]-7-[4-(3-oxo-4-morpholinyl)phenyl]-1-b-
enzo-furan-2-carboxamide hydrochloride
##STR00139##
[0700] 205.4 mg (0.70 mmol) of 4-(4-bromophenyl)-3-morpholinone
(Example 16A), 204.4 mg (0.81 mmol) of bis(pinacolato)diboron,
171.2 mg (1.74 mmol) of potassium acetate, 19.6 mg (0.03 mmol) of
PdCl.sub.2(dppf), 207 mg (0.54 mmol) of
N-[(3R)-1-azabicyclo[2.2.2]oct-3-yl]-7-bromo-1-benzofuran-2-carboxamide
hydro-chloride (Example 30A), 1.34 ml of 2 M sodium carbonate
solution and a further 19.6 mg (0.03 mmol) of PdCl.sub.2(dppf) in 2
ml of DMF are reacted by general method D. Drying under high vacuum
results in 233 mg (85% of theory) of the title compound.
[0701] .sup.1H-NMR (200 MHz, DMSO-d.sub.6): .delta.=10.32 (br. s,
1H), 9.07 (d, 1H), 7.95 (m, 3H), 7.80 (dd, 1H), 7.70 (dd, 1H), 7.59
(m, 2H), 7.44 (dd, 1H), 4.33 (m, 1H), 4.26 (s, 2H), 4.02 (m, 2H),
3.83 (m, 2H), 3.64 (m, 1H), 3.37 (m, 2H), 3.21 (m, 3H), 2.23 (m,
1H), 2.11 (m, 1H), 1.91 (m, 2H), 1.74 (m, 1H).
[0702] HPLC (method 1): R.sub.t=4.5 min.
[0703] MS (ESIpos): m/z=446 (M+H).sup.+ (free base).
EXAMPLE 91
[0704]
N-[(3R)-1-Azabicyclo[2.2.2]oct-3-yl]-7-[2-(4-morpholinyl)phenyl]-1--
benzofuran-2-carboxamide hydrochloride
##STR00140##
[0705] 225 mg (0.93 mmol) of 2-(4-morpholinyl)phenyl
trifluoromethanesulphonate (Example 32A), 272 mg (1.07 mmol) of
bis(pinacolato)diboron, 228 mg (2.33 mmol) of potassium acetate, 26
mg (0.04 mmol) of PdCl.sub.2(dppf), 250 mg (0.72 mmol) of
N-[(3R)-1-azabicyclo[2.2.2]oct-3-yl]-7-bromo-1-benzofuran-2-carboxamide
(Example 30A), 1.8 ml of 2 M sodium carbonate solution and a
further 26 mg (0.04 mmol) of PdCl.sub.2(dppf) in 2 ml of DMF are
reacted by general method D. Drying under high vacuum results in 82
mg (24% of theory) of the title compound.
[0706] .sup.1H-NMR (400 MHz, DMSO-d.sub.6): .delta.=9.76 (s, 1H),
8.82 (d, 1H), 7.79 (s, 1H), 7.77 (d, 1H), 7.55 (d, 1H), 7.46-7.37
(m, 3H), 7.23-7.14 (m, 2H), 4.33 (m, 1H), 3.83-3.04 (m, 6H), 3.55
(s, 4H), 2.68 (s, 4H), 2.16 (m, 1H), 2.04 (m, 1H), 1.95-1.84 (m,
2H), 1.79-1.67 (m, 1H).
[0707] HPLC (method 1): R.sub.t=4.1 min.
[0708] MS (ESIpos): m/z=432 (M+H).sup.+ (free base).
EXAMPLE 92
[0709]
N-[(3R)-1-Azabicyclo[2.2.2]oct-3-yl]-7-[4-(4-morpholinyl)phenyl]-1--
benzofuran-2-carboxamide hydrochloride
##STR00141##
[0710] 444 mg (2.15 mmol) of 4-(4-morpholinyl)phenylboronic acid
and 4.3 ml of 1N sodium hydroxide solution are added to a mixture
of 500 mg (0.143 mmol) of
N-[(3R)-1-azabicyclo[2.2.2]oct-3-yl]-7-bromo-1-benzofuran-2-carboxamide
hydro-chloride (Example 30A) and 105 mg (0.14 mmol) of
PdCl.sub.2(dppf) in 5 ml of DMF. The reaction mixture is heated at
100.degree. C. overnight. The solvent is removed under reduced
pressure, and the crude product is taken up in methanol and
filtered through kieselguhr. Purification takes place by
preparative HPLC. The product fractions are concentrated and
dissolved in methanol, and an excess of 1N hydrochloric acid is
added. The solvent is removed under reduced pressure. Drying under
high vacuum results in 393 mg (59% of theory) of the title
compound.
[0711] .sup.1H-NMR (200 MHz, DMSO-d.sub.6): .delta.=10.45 (s, 1H),
9.10 (d, 1H), 7.91 (s, 1H), 7.87 (d, 1H), 7.75-7.55 (m, 2H), 7.40
(t, 1H), 7.18 (d, 2H), 4.40 (m, 1H), 3.80 (m, 4H), 3.75-3.00 (m,
6H), 3.20 (m, 4H), 2.30-2.02 (m, 2H), 2.00-1.62 (m, 3H).
[0712] HPLC (method 1): R.sub.t=3.79 min.
[0713] MS (ESIpos): m/z=432 (M+H).sup.+ (free base).
EXAMPLE 93
N-[(3R)-1-Azabicyclo[2.2.2]oct-3-yl]-5-[4-(4-morpholinyl)phenyl]-1-benzofu-
ran-2-carboxamide hydrochloride
##STR00142##
[0715] 177 mg (0.86 mmol) of 4-(4-morpholinyl)phenylboronic acid
and 2.15 ml of 1N sodium hydroxide solution are added to a mixture
of 250 mg (0.72 mmol) of
N-[(3R)-1-azabicyclo[2.2.2]oct-3-yl]-5-bromo-1-benzofuran-2-carb-
oxamide (Example 3A) and 52 mg (0.07 mmol) of PdCl.sub.2(dppf) in 3
ml of DMF. The reaction mixture is heated at 90.degree. C.
overnight. The solvent is removed under reduced pressure, and the
crude product is taken up in methanol and filtered through
kieselguhr. Purification takes place by preparative HPLC. The
product fractions are concentrated and dissolved in
acetonitrile/water, and an excess of 1N hydrochloric acid is added.
The solvent is removed under reduced pressure. Drying under high
vacuum results in 23 mg (7% of theory) of the title compound.
[0716] .sup.1H-NMR (200 MHz, DMSO-d.sub.6): .delta.=10.40 (s, 1H),
9.15 (d, 1H), 7.98 (s, 1H), 7.76-7.68 (m, 2H), 7.67-7.58 (m, 2H),
7.20-7.10 (d, 2H), 4.45 (m, 1H), 3.80 (m, 4H), 3.75-3.30 (m, 6H),
3.20 (m, 4H), 2.30-2.02 (m, 2H), 2.00-1.62 (m, 3H).
[0717] HPLC (method 1): R.sub.t=3.52 min.
[0718] MS (ESIpos): m/z=432 (M+H).sup.+ (free base).
EXAMPLE 94
N-[(3R)-1-Azabicyclo[2.2.2]oct-3-yl]-5-[4-(hydroxymethyl)phenyl]-1-benzofu-
ran-2-carboxamide
##STR00143##
[0720] 110 mg (0.73 mmol) of 4-(hydroxymethyl)phenylboronic acid
and 1.46 ml of 1N sodium hydroxide solution are added to a mixture
of 170 mg (0.49 mmol) of
N-[(3R)-1-azabicyclo[2.2.2]oct-3-yl]-5-bromo-1-benzofuran-2-carb-
oxamide (Example 3A) and 35 mg (0.05 mmol) of PdCl.sub.2(dppf) in 2
ml of DMF. The reaction mixture is heated at 85.degree. C.
overnight. The solvent is removed under reduced pressure. Addition
of a mixture of 1N sodium hydroxide solution and ethyl acetate to
the residue is followed by extraction of the aqueous phase once
more with ethyl acetate. The combined organic phases are washed
twice with each of 1N sodium hydroxide solution and saturated
sodium chloride solution, dried over magnesium sulphate and
concentrated in a rotary evaporator under reduced pressure. The
crude product is taken up in methanol and shaken together with
acidic ion exchanger (Dowex.RTM. WX2-200) for about 20 min. The
loaded ion exchanger is washed three times with 30 ml of methanol
each time, then with DMF, again with methanol, with
dichloromethane, again with methanol, with water and finally with
methanol again. The product is eluted with methanol/triethylamine
95:5. The solvent is removed in a rotary evaporator under reduced
pressure. 148 mg (80% of theory) of the title compound are
isolated.
[0721] .sup.1H-NMR (200 MHz, CDCl.sub.3): .delta.=7.85 (s, 1H),
7.70-7.35 (m, 7H), 6.77 (d, 1H), 4.62 (s, 2H), 4.28-4.12 (m, 1H),
156-3.38 (m, 1H), 3.04-2.78 (m, 4H), 2.75-2.59 (m, 1H), 2.16-2.02
(m, 1H), 1.93-1.66 (m, 3H), 1.66-1.50 (m, 1H).
[0722] HPLC (method 1): R.sub.t=3.65 min.
[0723] MS (ESIpos): m/z=377 (M+H).sup.+.
EXAMPLE 95
N-[(3R)-1-Azabicyclo[2.2.2]oct-3-yl]-5-[2-(hydroxymethyl)phenyl]-1-benzofu-
ran-2-carboxamide
##STR00144##
[0725] 110 mg (0.73 mmol) of 2-(hydroxymethyl)phenylboronic acid
and 1.46 ml of 1N sodium hydroxide solution are added to a mixture
of 170 mg (0.49 mmol) of
N-[(3R)-1-azabicyclo[2.2.2]oct-3-yl]-5-bromo-1-benzofuran-2-carb-
oxamide (Example 3A) and 35 mg (0.05 mmol) of PdCl.sub.2(dppf) in 2
ml of DMF. The reaction mixture is heated at 85.degree. C.
overnight. The solvent is removed under reduced pressure. Addition
of a mixture of 1N sodium hydroxide solution and ethyl acetate to
the residue is followed by extraction of the aqueous phase once
more with ethyl acetate. The combined organic phases are washed
twice with each of 1N sodium hydroxide solution and saturated
sodium chloride solution, dried over magnesium sulphate and
concentrated in a rotary evaporator under reduced pressure. The
crude product is taken up in methanol and shaken together with
acidic ion exchanger (Dowex.RTM. WX2-200) for about 20 min. The
loaded ion exchanger is washed three times with 30 ml of methanol
each time, then with DMF, again with methanol, with
dichloromethane, again with methanol, with water and finally with
methanol again. The product is eluted with methanol/triethylamine
95:5. The solvent is removed in a rotary evaporator under reduced
pressure. 140 mg (76% of theory) of the title compound are
isolated.
[0726] .sup.1H-NMR (300 MHz, CDCl.sub.3): .delta.=7.70-7.25 (m,
8H), 6.75 (d, 1H), 4.62 (s, 2H), 4.28-4.12 (m, 1H), 3.56-3.38 (m,
1H), 3.04-2.78 (m, 4H), 2.75-2.59 (m, 1H), 2.16-2.02 (m, 1H),
1.93-1.66 (m, 3H), 1.66-1.50 (m, 1H).
[0727] HPLC (method 1): R.sub.t=3.76 min.
[0728] MS (ESIpos): m/z=377 (M+H).sup.+.
EXAMPLE 96
N-[(3R)-1-Azabicyclo[2.2.2]oct-3-yl]-5-[4-(dimethylamino)phenyl]-1-benzofu-
ran-2-carboxamide
##STR00145##
[0730] 0.120 mg (0.73 mmol) of 4-(dimethylamino)phenylboronic acid
and 1.46 ml of 1N sodium hydroxide solution are added to a mixture
of 170 mg (0.49 mmol) of
N-[(3R)-1-azabicyclo[2.2.2]oct-3-yl]-5-bromo-1-benzofuran-2-carboxamide
(Example 3A) and 35 mg (0.05 mmol) of PdCl.sub.2(dppf) in 2 ml of
DMF. The reaction mixture is heated at 85.degree. C. overnight. The
solvent is removed under reduced pressure. Addition of a mixture of
1N sodium hydroxide solution and ethyl acetate to the residue is
followed by extraction of the aqueous phase once more with ethyl
acetate. The combined organic phases are washed twice with each of
1N sodium hydroxide solution and saturated sodium chloride
solution, dried over magnesium sulphate and concentrated in a
rotary evaporator under reduced pressure. The crude product is
taken up in methanol and shaken together with acidic ion exchanger
(Dowex.RTM. WX2-200) for about 20 min. The loaded ion exchanger is
washed three times with 30 ml of methanol each time, then with DMF,
again with methanol, with dichloromethane, again with methanol,
with water and finally with methanol again. The product is eluted
with methanol/triethylamine 95:5. The solvent is removed in a
rotary evaporator under reduced pressure. 138 mg (73% of theory) of
the title compound are isolated.
[0731] .sup.1H-NMR (200 MHz, CDCl.sub.3): .delta.=7.78 (d, 1H)
7.70-7.39 (m, 4H), 6.88-6.75 (m, 3H), 4.28-4.12 (m, 1H), 3.56-3.38
(m, 1H), 3.04-2.78 (m, 4H), 3.00 (s, 6H), 2.75-2.59 (m, 1H),
2.16-2.02 (m, 1H), 1.93-1.66 (m, 3H), 1.66-1.50 (m, 1H).
[0732] HPLC (method 1): R.sub.t=3.36 min.
[0733] MS (ESIpos): m/z=390 (M+H).sup.+.
EXAMPLE 97
N-[(3R)-1-Azabicyclo[2.2.2]oct-3-yl]-5-[4-(methoxy)phenyl]-1-benzofuran-2--
carboxamide hydrochloride
##STR00146##
[0735] 130 mg (0.86 mmol) of 4-(methoxy)phenylboronic acid and 2.15
ml of 1N sodium hydroxide solution are added to a mixture of 250 mg
(0.72 mmol) of
N-[(3R)-1-azabicyclo[2.2.2]oct-3-yl]-5-bromo-1-benzofuran-2-carboxamid-
e (Example 3A) and 52 mg (0.07 mmol) of PdCl.sub.2(dppf) in 3 ml of
DMF. The reaction mixture is heated at 90.degree. C. overnight. The
solvent is removed under reduced pressure, and the crude product is
taken up in methanol and filtered through kieselguhr. Purification
takes place by preparative HPLC. The product fractions are mixed
with an excess of 1N hydrochloric acid. The solvent is removed
under reduced pressure. Drying under high vacuum results in 127 mg
(39% of theory) of the title compound.
[0736] .sup.1H-NMR (200 MHz, DMSO-d.sub.6): .delta.=9.90 (s, 1H),
9.10 (d, 1H), 7.95 (m, 2H), 7.75-7.60 (m, 4H), 7.10-7.02 (m, 2H),
4.40 (m, 1H), 3.85 (m, 3H), 3.75-3.00 (m, 6H), 320 (m, 4H),
2.30-2.02 (m, 2H), 2.00-1.62 (m, 3H).
[0737] HPLC (method 1): R.sub.t=4.15 min.
[0738] MS (ESIpos): m/z=377 (M+H).sup.+ (free base).
EXAMPLE 98
N-[(3R)-1-Azabicyclo[2.2.2]oct-3-yl]-5-[3-(methoxy)phenyl]-1-benzofuran-ca-
rboxamide hydrochloride
##STR00147##
[0740] 130 mg (0.86 mmol) of 3-(methoxy)phenylboronic acid and 2.15
ml of 1N sodium hydroxide solution are added to a mixture of 250 mg
(0.72 mmol) of
N-[(3R)-1-azabicyclo[2.2.2]oct-3-yl]-5-bromo-1-benzofuran-2-carboxamid-
e (Example 3A) and 52 mg (0.07 mmol) of PdCl.sub.2(dppf) in 3 ml of
DMF. The reaction mixture is heated at 90.degree. C. overnight. The
solvent is removed under reduced pressure, and the crude product is
taken up in methanol and filtered through kieselguhr. Purification
takes place by preparative HPLC. The product fractions are mixed
with an excess of 1N hydrochloric acid. The solvent is removed
under reduced pressure. Drying under high vacuum results in 208 mg
(63% of theory) of the title compound.
[0741] .sup.1H-NMR (300 MHz, DMSO-d.sub.6): .delta.=10.0 (s, 1H),
9.10 (d, 1H), 8.05 (s, 1H), 7.80-7.65 (m, 3H), 7.42-7.18 (m, 3H),
6.93 (m, 1H), 4.35 (m, 1H), 3.85 (s, 3H), 3.75-3.00 (m, 6H), 3.20
(m, 4H), 2.30-2.02 (m, 2H), 2.00-1.62 (m, 3H).
[0742] HPLC (method 1): R.sub.t=4.19 min.
[0743] MS (ESIpos): m/z=377 (M+H).sup.+ (free base).
EXAMPLE 99
N-[(3R)-1-Azabicyclo[2.2.2]oct-3-yl]-7-[4-(methoxy)phenyl]-1-benzofuran-ca-
rboxamide hydrochloride
##STR00148##
[0745] 130 mg (0.86 mmol) of 4-(methoxy)phenylboronic acid and 2.58
ml of 1N sodium hydroxide solution are added to a mixture of 300 mg
(0.86 mmol) of
N-[(3R)-1-azabicyclo[2.2.2]oct-3-yl]-7-bromo-1-benzofuran-2-carboxamid-
e (Example 30A) and 63 mg (0.09 mmol) of PdCl.sub.2(dppf) in 4 ml
of DMF. The reaction mixture is heated at 95.degree. C. overnight.
The solvent is removed under reduced pressure, and the crude
product is taken up in methanol and filtered through kieselguhr.
Purification takes place by preparative HPLC. The product fractions
are mixed with an excess of 1N hydrochloric acid. The solvent is
removed under reduced pressure. Drying under high vacuum results in
165 mg (47% of theory) of the title compound.
[0746] .sup.1H-NMR (300 MHz, DMSO-d.sub.6): .delta.=10.4 (s, 1H),
9.00 (d, 1H), 8.05 (s, 1H), 7.90-7.82 (m, 3H), 7.75 (d, 1H), 7.62
(d, 1H), 7.40 (t, 1H), 7.15-7.05 (m, 2H), 4.35 (m, 1H), 3.85 (s,
3H), 3.65 (m, 1H), 3.48-3.30 (m, 2H), 3.25-3.10 (m, 3H), 2.25 (m,
1H), 2.18-2.05 (m, 1H), 1.98-1.88 (m, 2H), 1.80-1.63 (m, 1H).
[0747] HPLC (method 1): R.sub.t=4.18 min.
[0748] MS (ESIpos): m/z=377 (M+H).sup.+ (free base).
EXAMPLE 100
N-[(3S)-1-Azabicyclo[2.2.2]oct-3-yl]-7-(2-methoxyphenyl)-1-benzofuran-2-ca-
rboxamide hydrochloride
##STR00149##
[0750] 3.4 g (8.95 mmol) of HATU and 2.34 ml (13.42 mmol) of
N,N-diisopropylethyl-amine are added to a mixture of 890 mg (4.47
mmol) of S-3-aminoquinuclidine dihydrochloride and 1000 mg (3.73
mmol) of 7-(2-methoxyphenyl)-1-benzofuran-2-carboxylic acid
(Example 21A) in. 10 ml of DMF at 0.degree. C. After stirring at
room temperature for 18 h, the reaction solution is purified by
preparative HPLC. The product fractions are concentrated and, after
addition of 5 ml of 1N hydrochloric acid, again concentrated.
Drying under high vacuum results in 209 mg (13.6% of theory) of the
title compound.
[0751] The analytical data agree with those of the enantiomeric
compound (Example 102).
EXAMPLE 101
N-[(3R)-1-Azabicyclo[2.2.2]oct-3-yl]-7-[3-(methoxy)phenyl]-1-benzofuran-2--
carboxamide hydrochloride
##STR00150##
[0753] 98 mg (0.64 mmol) of 3-(methoxy)phenylboronic acid and 1.29
ml of 1N sodium hydroxide solution are added to a mixture of 150 mg
(0.43 mmol) of
N-[(3R)-1-azabicyclo[2.2.2]oct-3-yl]-7-bromo-1-benzofuran-2-carboxamid-
e (Example 30A) and 31 mg (0.04 mmol) of PdCl.sub.2(dppf) in 2 ml
of DMF. The reaction mixture is heated at 90.degree. C. overnight.
The solvent is removed under reduced pressure, and the crude
product is taken up in methanol and filtered through kieselguhr.
Purification takes place by preparative HPLC. The product is
dissolved in methanol and mixed with an excess of 1N hydrochloric
acid. The solvent is removed under reduced pressure, and the
residue is recrystallized from a little isopropanol. Drying under
high vacuum results in 159 mg (85% of theory) of the title
compound.
[0754] .sup.1H-NMR (400 MHz, DMSO-d.sub.6): .delta.=10.05 (s, 1H),
8.95 (d, 1H), 7.85 (s, 1H), 7.80 (d, 1H), 7.70 (d, 1H), 7.50-7.40
(m, 4H), 7.00 (m, 1H), 4.35 (m, 1H), 3.85 (s, 3H), 3.65 (m, 1H),
3.48-3.30 (m, 2H), 3.25-3.15 (m, 3H), 2.25 (m, 1H), 2.18-2.05 (m,
1H), 1.98-1.88 (m, 2H), 1.80-1.63 (m, 1H).
[0755] HPLC (method 1): R.sub.t=4.21 min.
[0756] MS (ESIpos): m/z=377 (M+H).sup.+ (free base).
EXAMPLE 102
N-[(3R)-1-Azabicyclo[2.2.2]oct-3-yl]-7-[2-(methoxy)phenyl]-1-benzofuran-2--
carboxamide hydrochloride
##STR00151##
[0757] Method a):
[0758] 98 mg (0.64 mmol) of 2-(methoxy)phenylboronic acid and 1.29
ml of 1N sodium hydroxide solution are added to a mixture of 150 mg
(0.43 mmol) of
N-[(3R)-1-azabicyclo[2.2.2]oct-3-yl]-7-bromo-1-benzofuran-2-carboxamid-
e (Example 30A) and 31 mg (0.04 mmol) of PdCl.sub.2(dppf) in 2 ml
of DMF. The reaction mixture is heated at 85.degree. C. overnight.
The solvent is removed under reduced pressure, and the crude
product is taken up in methanol and filtered through kieselguhr.
Further purification takes place by preparative HPLC. The product
is dissolved in methanol and mixed with an excess of 1N
hydrochloric acid. The solvent is removed under reduced pressure,
and the residue is recrystallized from a little isopropanol. Drying
under high vacuum results in 100 mg (62% of theory) of the title
compound.
[0759] .sup.1H-NMR (400 MHz, DMSO-d.sub.6): .delta.=10.08 (s, 1H),
8.91 (d, 1H), 7.87 (s, 1H), 7.84-7.74 (m, 2H), 7.53-7.33 (m, 3H),
7.25-7.00 (m, 2H), 4.35 (m, 1H), 3.75 (s, 3H), 3.65 (m, 1H),
3.48-3.30 (m, 2H), 3.25-3.15 (m, 3H), 2.25 (m, 1H), 2.18-2.05 (m,
1H), 1.98-1.88 (m, 2H), 1.80-1.63 (m, 1H).
[0760] HPLC (method 1): R.sub.t=4.16 min.
[0761] MS (ESIpos): m/z=377 (M+H).sup.+ (free base).
Method b):
[0762] 2.51 g (13.1 mmol) of EDC, 1.77 g (13.1 mmol) of HOBt and
5.47 ml (39.2 mmol) of triethylamine are added to a solution of
2.92 g (10.9 mmol) of 7-(2-methoxyphenyl)-1-benzofuran-2-carboxylic
acid (Example 21A) and 2.17 g (10.9 mmol) of
(R)-3-aminoquinuclidine dihydrochloride in 35 ml of DMF at
0.degree. C. After stirring at room temperature for 18 hours, a
further 434 mg (2.2 mmol) of (R)-3-aminoquinuclidine
dihydrochloride and 418 mg (2.2 mmol) of EDC are added. After 2 h
at 55.degree. C., the reaction solution is concentrated and the
residue is partitioned between 200 ml each of ethyl acetate and 2N
sodium hydroxide solution. The organic phase is washed. 15 times
with 100 ml of 2N sodium hydroxide solution each time. The combined
aqueous phases are back-extracted with 250 ml of ethyl acetate. The
combined organic phases are dried over sodium sulphate and
concentrated and, after addition of a 5:1 mixture of methanol and
1N hydrochloric acid to the residue, again concentrated and dried
under high vacuum. Recrystallization of the residue from 10 ml of a
10:1 mixture of isopropanol and ethanol results in 2.73 g (60.5% of
theory) of the title compound.
EXAMPLE 103
N-[(3R)-1-Azabicyclo[2.2.2]oct-3-yl]-7-[4-(methoxy)-3-pyridinyl]-1-benzofu-
ran-2-carboxamide hydrochloride
##STR00152##
[0764] 98 mg (0.64 mmol) of 4-methoxy-3-pyridinylboronic acid and
0.86 ml of 1N sodium hydroxide solution are added to a mixture of
100 mg (0.29 mmol) of
N-[(3R)-1-azabicyclo[2.2.2]oct-3-yl]-7-bromo-1-benzofuran-2-carb-
oxamide (Example 30A) and 21 mg (0.03 mmol) of PdCl.sub.2(dppf) in
2 ml of DMF. The reaction mixture is heated at 85.degree. C.
overnight. The solvent is removed under reduced pressure, and the
crude product is taken up in methanol and filtered through
kieselguhr. Purification takes place by preparative HPLC. The
product fractions are mixed with an excess of 1N hydrochloric acid.
The solvent is removed under reduced pressure. Drying under high
vacuum results in 58 mg (49% of theory) of the title compound.
[0765] .sup.1H-NMR (400 MHz, DMSO-d.sub.6): .delta.=10.55 (s, 1H),
9.20 (d, 1H), 9.05 (s, 1H), 8.95 (d, 1H), 7.96-7.89 (m, 2H), 7.82
(d, 1H), 7.65 (d, 1H), 7.50 (t, 1H), 4.35 (m, 1H), 4.10 (s, 3H),
3.65-3.15 (m, 6H), 2.20 (m, 1H), 2.18-2.05 (m, 1H), 1.98-1.88 (m,
2H), 1.80-1.63 (m, 1H).
[0766] HPLC (method 1): R.sub.t=3.35 min.
[0767] MS (ESIpos): m/z=378 (M+H).sup.+ (free base).
EXAMPLE 104
N-[(3R)-1-Azabicyclo[2.2.2]oct-3-yl]-7-[4-(4-morpholinylcarbonyl)phenyl]-1-
-benzo-furan-2-carboxamide hydrochloride
##STR00153##
[0769] 631 mg (1.43 mmol) of 4-(4-morpholinylcarbonyl)phenyl
trifluoromethane-sulphonate (Example 18A), 545 mg (2.15 mmol) of
bis(pinacolato)diboron, 456 mg (4.65 mmol) of potassium acetate, 52
mg (0.07 mmol) of PdCl.sub.2(dppf), 500 mg (1.43 mmol) of
N-[(3R)-1-azabicyclo[2.2.2]oct-3-yl]-7-bromo-1-benzofuran-2-carboxamide
(Example 30A), 3.6 ml of 2 M sodium carbonate solution and a
further 52 mg (0.07 mmol) of PdCl.sub.2(dppf) in 8 ml of DMF are
reacted by general method D. Drying under high vacuum results in
455 mg (61% of theory) of the title compound.
[0770] .sup.1H-NMR (400 MHz, DMSO-d.sub.6): .delta.=10.45 (s, 1H),
9.10 (d, 1H), 8.02-7.92 (m, 3H), 7.78 (d, 1H), 7.71 (d, 1H), 7.60
(d, 2H), 7.45 (t, 1H), 4.35 (m, 1H), 3.75-3.35 (m, 11H), 3.25-3.15
(m, 3H), 2.25 (m, 1H), 2.18-2.05 (m, 1H), 1.98-1.88 (m, 2H),
1.80-1.63 (m, 1H).
[0771] HPLC (method 1): R.sub.t=3.79 min.
[0772] MS (ESIpos): m/z=460 (M+H).sup.+ (free base).
EXAMPLE 105
N-[(3R)-1-Azabicyclo[2.2.2]oct-3-yl]-7-[3-(1-piperidinyl)phenyl]-1-benzofu-
ran-2-carboxamide dihydrochloride
##STR00154##
[0774] 311 mg (1.29 mmol) of 3-(1-piperidinyl)phenylboronic acid
and 3.44 ml of 1N sodium hydroxide solution are added to a mixture
of 300 mg (0.86 mmol) of
N-[(3R)-1-azabicyclo[2.2.2]oct-3-yl]-7-bromo-1-benzofuran-2-carb-
oxamide (Example 30A) and 63 mg (0.09 mmol) of PdCl.sub.2(dppf) in
4 ml of DMF. The reaction mixture is heated at 95.degree. C.
overnight. The solvent is removed under reduced pressure, and the
crude product is taken up in methanol and filtered through
kieselguhr. Purification takes place by preparative HPLC. The
product is dissolved in methanol, and an excess of 1N hydrochloric
acid is added. The solvent is removed under reduced pressure.
Drying under high vacuum results in 164 mg (41% of theory) of the
title compound.
[0775] .sup.1H-NMR (200 MHz, DMSO-d.sub.6): .delta.=10.55 (s, 1H),
9.10 (d, 1H), 8.75 (s, 1H), 7.95-7.63 (m, 7H), 7.45 (t, 1H), 4.35
(m, 1H), 4.13-3.40 (m, 7H), 3.35-3.10 (m, 3H), 2.15-1.50 (m,
11H).
[0776] HPLC (method 1): R.sub.t=3.72 min.
[0777] MS (ESIpos): m/z=430 (M+H).sup.+ (free base).
EXAMPLE 106
N-[(3R)-1-Azabicyclo[2.2.2]oct-3-yl]-7-(3-pyridinyl)-1-benzofuran-2-carbox-
amide dihydrochloride
##STR00155##
[0779] 70 mg (0.57 mmol) of 3-pyridineboronic acid and 0.86 ml of
1N sodium hydroxide solution are added to a mixture of 100 mg (0.86
mmol) of
N-[(3R)-1-azabicyclo[2.2.2]oct-3-yl]-7-bromo-1-benzofuran-2-carboxamide
(Example 30A) and 63 mg (0.09 mmol) of PdCl.sub.2(dppf) in 4 ml of
DMF. The reaction mixture is heated at 95.degree. C. overnight. The
solvent is removed under reduced pressure, and the crude product is
taken up in methanol and filtered through kieselguhr. Purification
takes place by preparative HPLC. The product is dissolved in
methanol, and an excess of 1N hydrochloric acid is added. The
solvent is removed under reduced pressure. Drying under high vacuum
results in 49 mg (45% of theory) of the title compound.
[0780] .sup.1H-NMR (300 MHz, DMSO-d.sub.6): .delta.=10.55 (s, 1H),
9.51 (s, 1H), 9.30 (d, 1H), 9.20 (s, 1H), 8.94-8.80 (m, 2H),
8.07-7.80 (m, 4H), 7.55 (t, 1H), 4.35 (m, 1H), 3.65-3.15 (m, 6H),
2.20 (m, 1H), 2.18-2.05 (m, 1H), 1.98-1.88 (m, 2H), 1.80-1.63 (m,
1H).
[0781] HPLC (method 1): R.sub.t=3.27 min.
[0782] MS (ESIpos): m/z=348 (M+H).sup.+ (free base).
EXAMPLE 107
N-[(3R)-1-Azabicyclo[2.2.2]oct-3-yl]-7-(3-{[(methylamino)carbonyl]amino}ph-
enyl)-1-benzofuran-2-carboxamide hydrochloride
##STR00156##
[0784] 63 mg (0.18 mmol) of
7-(3-aminophenyl)-N-[(3R)-1-azabicyclo[2.2.2]oct-3-yl]-1-benzofuran-2-car-
boxamide (Example 114), 40 mg (0.70 mmol) of methyl isocyanate and
0.12 ml (0.88 mmol) of triethylamine are heated in 3 ml of THF/DMF
(1:1) at 40.degree. C. overnight. A further 40 mg (0.70 mmol) of
methyl isocyanate and a catalytic amount of DMAP are added, and the
mixture is heated at 50.degree. C. overnight. Cooling is followed
by addition of water, filtration and removal of the solvent under
reduced pressure. Purification takes place by preparative HPLC. The
product is dissolved in methanol, and an excess of 1N hydrochloric
acid is added. The solvent is removed under reduced pressure.
Drying under high vacuum results in 18 mg (23% of theory) of the
title compound.
[0785] .sup.1H-NMR (400 MHz, DMSO-d.sub.6): .delta.=9.98 (s, 1H),
8.85 (s, 1H), 8.63 (d, 1H), 8.15 (s, 1H), 7.80 (m, 2H), 7.65 (d,
1H), 7.45 (t, 1H), 7.38 (s, 2H), 6.20 (m, 1H), 4.35 (m, 1H),
3.75-3.63 (m, 1H), 3.60-3.15 (m, 5H), 2.65 (s, 3H), 2.30 (m, 1H),
2.18-2.05 (m, 1H), 1.98-1.88 (m, 2H), 1.80-1.63 (m, 1H).
[0786] HPLC (method 1): R.sub.t=3.89 min.
[0787] MS (ESIpos): m/z=419 (M+H).sup.+ (free base).
EXAMPLE 108
N-[(3R)-1-Azabicyclo[2.2.2]oct-3-yl]-7-(3-{[(ethylamino)carbonyl]amino}phe-
nyl)-1-benzofuran-2-carboxamide hydrochloride
##STR00157##
[0789] 63 mg (0.18 mmol) of
7-(3-aminophenyl)-N-[(3R)-1-azabicyclo[2.2.2]oct-3-yl]-1-benzofuran-2-car-
boxamide (Example 114), 50 mg (0.70 mmol) of ethyl isocyanate and
0.12 ml (0.88 mmol) of triethylamine are heated in 3 ml of THF/DMF
(1:1) at. 40.degree. C. overnight. A further 50 mg (0.70 mmol) of
ethyl isocyanate and a catalytic amount of DMAP are added, and the
mixture is heated at 50.degree. C. overnight. Cooling is followed
by addition of water, filtration and removal of the solvent under
reduced pressure. Purification takes place by preparative HPLC. The
product is dissolved in methanol, and an excess of 1N hydrochloric
acid is added. The solvent is removed under reduced pressure.
Drying under high vacuum results in 15 mg (18% of theory) of the
title compound.
[0790] .sup.1H-NMR (400 MHz, DMSO-d.sub.6): .delta.=9.80 (s, 1H),
8.74 (s, 1H), 8.63 (d, 1H), 8.10 (s, 1H), 7.80 (m, 2H), 7.60 (d,
1H), 7.45 (t, 1H), 7.38 (s, 2H), 6.20 (m, 1H), 4.35 (m, 1H),
3.75-3.63 (m, 1H), 3.60-3.15 (m, 5H), 3.10 (m, 2H), 2.65 (s, 3H),
2.30 (m, 1H), 2.18-2.05 (m, 1H), 1.98-1.88 (m, 2H), 1.80-1.63 (m,
1H), 1.05 (t, 3H).
[0791] HPLC (method 1): R.sub.t=4.01 min.
[0792] MS (ESIpos): m/z=433 (M+H).sup.+ (free base).
EXAMPLE 109
N-[(3R)-1-Azabicyclo[2.2.2]oct-3-yl]-7-[3-({[(1-methylethyl)amino]carbonyl-
}-amino)phenyl]-1-benzofuran-2-carboxamide hydrochloride
##STR00158##
[0794] 50 mg (0.14 mmol) of
7-(3-aminophenyl)-N-[(3R)-1-azabicyclo[2.2.2]oct-3-yl]-1-benzofuran-2-car-
boxamide (Example 114), 47 mg (0.55 mmol) of isopropyl isocyanate
and 0.12 ml (0.88 mmol) of triethylamine are heated in 3 ml of
THF/DMF (1:1) at 40.degree. C. overnight. A further 47 mg (0.55
mmol) of isopropyl isocyanate and a catalytic amount of DMAP are
added, and the mixture is heated at 50.degree. C. overnight.
Cooling is followed by addition of water, filtration and removal of
the solvent under reduced pressure. Purification takes place by
preparative HPLC. The product is dissolved in methanol, and an
excess of 1N hydrochloric acid is added. The solvent is removed
under reduced pressure. Drying under high vacuum results in 13 mg
(18% of theory) of the title compound.
[0795] .sup.1H-NMR (400 MHz, DMSO-d.sub.6): .delta.=9.80 (s, 1H),
8.70 (d, 1H), 8.65 (s, 1H), 8.05 (s, 1H), 7.80 (m, 2H), 7.60 (d,
1H), 7.45 (t, 1H), 7.38 (s, 2H), 6.20 (m, 1H), 4.35 (m, 1H),
3.80-332 (m, 1H), 3.70-3.63 (m, 1H), 3.50-3.05 (m, 5H), 2.30 (m,
1H), 2.18-2.05 (m, 1H), 1.98-1.88 (m, 2H), 1.80-1.63 (m, 1H), 1.10
(d, 6H).
[0796] HPLC (method 1): R.sub.t=4.12 min.
[0797] MS (ESIpos): m/z=447 (M+H).sup.+ (free base).
EXAMPLE 110
N-[(3R)-1-Azabicyclo[2.2.2]oct-3-yl]-7-[3-({[(1,1-dimethylethyl)amino]carb-
onyl}-amino)phenyl]-1-benzofuran-2-carboxamide hydrochloride
##STR00159##
[0799] 63 mg (0.14 mmol) of
7-(3-aminophenyl)-N-[(3R)-1-azabicyclo[2.2.2]oct-3-yl]-1-benzofuran-2-car-
boxamide (Example 114), 69 mg (0.70 mmol) of tert-butyl isocyanate
and 0.12 ml (0.88 mmol) of triethylamine are heated in 3 ml of
THF/DMF (1:1) at 40.degree. C. overnight. A further 69 mg (0.70
mmol) of tert-butyl isocyanate and a catalytic amount of DMAP are
added, and the mixture is heated at 50.degree. C. overnight.
Cooling is followed by addition of water, filtration and removal of
the solvent under reduced pressure. Purification takes place by
preparative HPLC. The product is dissolved in methanol, and an
excess of 1N hydrochloric acid is added. The solvent is removed
under reduced pressure. Drying under high vacuum results in 8 mg
(9% of theory) of the title compound.
[0800] .sup.1H-NMR (400 MHz, DMSO-d.sub.6): .delta.=9.70 (s, 1H),
8.80 (d, 1H), 8.55 (s, 1H), 7.85 (s, 1H), 7.80 (m, 2H), 7.60 (d,
1H), 7.45 (t, 1H), 7.38 (s, 2H), 6.10 (m, 1H), 4.35 (m, 1H),
3.70-3.63 (m, 1H), 3.50-105 (m, 5H), 2.30 (m, 1H), 2.18-2.05 (m,
1H), 1.98-1.88 (m, 2H), 1.80-1.63 (m, 1H), 1.30 (s, 9H).
[0801] HPLC (method 1): R.sub.t=4.27 min.
[0802] MS (ESIpos): m/z=461 (M+H).sup.+ (free base).
EXAMPLE 111
N-[(3R)-1-Azabicyclo[2.2.2]oct-3-yl]-7-{3-[(methylsulphonyl)amino]phenyl}--
1-benzofuran-2-carboxamide hydrochloride
##STR00160##
[0804] 73 mg (0.20 mmol) of
7-(3-aminophenyl)-N-[(3R)-1-azabicyclo[2.2.2]oct-3-yl]-1-benzofuran-2-car-
boxamide (Example 114), 69 mg (0.61 mmol) of methansulphonyl
chloride and 0.14 ml (1.01 mmol) of triethylamine are heated in 3
ml of THF/DMF (1:1) at 50.degree. C. overnight Cooling is followed
by addition of water, filtration and removal of the solvent under
reduced pressure. Purification takes place by preparative HPLC. The
product is dissolved in methanol, and an excess of 1N hydrochloric
acid is added. The solvent is removed under reduced pressure.
Drying under high vacuum results in 16 mg (14% of theory) of the
title compound.
[0805] .sup.1H-NMR (300 MHz, DMSO-d.sub.6): .delta.=10.15 (s, 1H),
9.90 (s, 1H), 8.76 (d, 1H), 7.90 (s, 1H), 7.85-7.75 (m, 2H),
7.66-7:60 (m, 2H), 7.55-7.53 (m, 2H), 7.25 (m, 1H), 4.37 (m, 1H),
3.70-3.63 (m, 1H), 3.45-3.05 (m, 5H), 3.10 (s, 3H), 2.30 (m, 1H),
2.18-2.05 (m, 1H), 1.98-1.88 (m, 2H), 1.80-1.63 (m, 1H).
[0806] HPLC (method 1): R.sub.t=3.97 min.
[0807] MS (ESIpos): m/z=440 (M+H).sup.+ (free base).
EXAMPLE 112
N-[(3R)-1-Azabicyclo[2.2.2]oct-3-yl]-7-{2-[(cyclobutylcarbonyl)amino]pheny-
l}-1-benzofuran-2-carboxamide hydrochloride
##STR00161##
[0809] 60 mg (0.15 mmol) of
7-(2-aminophenyl)-N-[(3R)-1-azabicyclo[2.2.2]oct-3-yl]-1-benzofuran-2-car-
boxamide (Example 132), 26 mg (0.22 mmol) of cyclobutane-carbonyl
chloride and 0.06 ml (0.44 mmol) of triethylamine are shaken in 2
ml of THF/DMF (1:1) at RT overnight. The solvent is removed under
reduced pressure. Purification takes place by preparative HPLC. The
product is dissolved in methanol, and an excess of 1N hydrochloric
acid is added. The solvent is removed under reduced pressure.
Drying under high vacuum results in 39 mg (56% of theory) of the
title compound.
[0810] .sup.1H-NMR (300 MHz, DMSO-d.sub.6): .delta.=10.15 (s, 1H),
9.05 (s, 1H), 8.40 (d, 1H), 7.95 (s, 1H), 7.80-7.70 (m, 2H),
7.55-7.30 (m, 6H), 4.32 (m, 1H), 3.70-3.63 (m, 1H), 3.45-3.05 (m,
5H), 2.98-2.88 (m, 1H), 2.30 (m, 1H), 2.18-2.05 (m, 1H), 1.98-1.55
(m, 9H).
[0811] HPLC (method 1): R.sub.t=3.95 min.
[0812] MS (ESIpos): m/z=444 (M+H).sup.+ (free base).
EXAMPLE 113
N-[(3R)-1-Azabicyclo[2.2.2]oct-3-yl]-5-(5-pyrimidinyl)-1-benzofuran-2-carb-
oxamide hydrochloride
##STR00162##
[0814] 177 mg (0.86 mmol) of
5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyrimidine and 2.15
ml of 1N sodium hydroxide solution are added to a mixture of 250 mg
(0.72 mmol) of
N-[(3R)-1-azabicyclo[2.2.2]oct-3-yl]-5-bromo-1-benzofuran-2-carboxamid-
e (Example 3A) and 52 mg (0.07 mmol) of PdCl.sub.2(dppf) in 3 ml of
DMF.
[0815] The reaction mixture is heated at 90.degree. C. overnight.
The solvent is removed under reduced pressure, and the crude
product is taken up in methanol and filtered through kieselguhr.
Purification takes place by preparative HPLC. The product is
dissolved in methanol, and an excess of 1N hydrochloric acid is
added. The solvent is removed under reduced pressure.
Recrystallization of the residue from isopropanol and drying under
high vacuum results in 28 mg (10% of theory) of the title
compound.
[0816] .sup.1H-NMR (300 MHz, DMSO-d.sub.6): .delta.=10.30 (s, 1H),
9.22-9.13 (m, 4H), 8.24 (m, 1H), 7.93-7.81 (m, 3H), 4.39 (m, 1H),
3.68-3.48 (m, 1H), 3.45-3.13 (m, 5H), 2.28-2.20 (m, 1H), 2.18-2.07
(m, 1H), 1.97-1.88 (m, 2H), 1.80-1.57 (m, 1H).
[0817] HPLC (method 1): R.sub.t=3.26 min.
[0818] MS (ESIpos): m/z=349 (MH).sup.+ (free base).
EXAMPLE 114
7-(3-Aminophenyl)-N-[(3R)-1-azabicyclo[2.2.2]oct-3-yl]-1-benzofuran-2-carb-
oxamide.
##STR00163##
[0819] Method a):
[0820] 622 mg (1.68 mmol) of 3-aminophenylboronic acid hemisulphate
and 11.2 ml of 1N sodium hydroxide solution are added to a mixture
of 978 mg (2.80 mmol) of
N-[(3R)-1-azabicyclo[2.2.2]oct-3-yl]-7-bromo-1-benzofuran-2-carboxamide
(Example 30A) and 205 mg (0.28 mmol) of PdCl.sub.2(dppf) in 15 ml
of DMF. The reaction mixture is heated at 95.degree. C. overnight.
The crude product is filtered through kieselguhr, washed with DMF
and freed of solvent under reduced pressure. The residue is mixed
with 200 ml of 1N sodium hydroxide solution and 200 ml of ethyl
acetate. After separation of the phases, the organic phase is
washed twice more with 100 ml of 1N sodium hydroxide solution each
time and then once more with 100 ml of a saturated sodium chloride
solution. Drying over magnesium sulphate is followed by
purification of the crude product by preparative HPLC. After
removal of the solvent in a rotary evaporator it is possible to
obtain-875 mg (73% of theory) of the title compound in the form of
a white foam by twice adding dichloromethane and concentrating
again.
[0821] .sup.1H-NMR (300 MHz, DMSO-d.sub.6): .delta.=8.48 (d, 1H),
8.21 (s, 1H), 7.76-7.69 (m, 1H), 7.54 (d, 1H), 7.45-7.37 (m, 1H),
7.20-7.00 (m, 3H); 6.67-6.61 (m, 1H), 4.13-4.06 (m, 1H), 3.48-3.26
(m, 1H), 3.10-3.01 (m, 1H), 2.93-2.79 (m, 4H), 2.03 (m, 1H),
2.00-1.88 (m, 1H), 1.79-1.67 (m, 2H), 1.58-1.42 (m, 1H).
[0822] HPLC (method 1): R.sub.t=3.46 min.
[0823] MS (ESIpos): m/z=362 (M+H).sup.+.
Method b):
[0824] 419 mg (1.13 mmol) of
bis[3-(dihydroxyboranyl)anilinium]sulphate and 7.56 ml of 1N sodium
hydroxide solution are added to a mixture of 660 mg (1.89 mmol) of
N-[(3R)-1-azabicyclo[2.2.2]oct-3-yl]-7-bromo-1-benzofuran-2-carboxamide
(Example 30A) and 138 mg (0.19 mmol) of PdCl.sub.2(dppf) in 8 ml of
DMF. The reaction mixture is heated at 95.degree. C. overnight. The
solvent is removed under reduced pressure, and the crude product is
taken up in methanol and filtered through kieselguhr. Further
purification takes place by preparative HPLC. The solvent is
removed from the product fractions under reduced pressure. Drying
under high vacuum results in 485 mg (71% of theory) of the title
compound.
[0825] .sup.1H-NMR (300 MHz, DMSO-d.sub.6): .delta.=8.48 (d, 1H),
8.21 (s, 1H), 7.70 (s, 1H), 7.55 (m, 1H), 7.40 (t, 1H), 7.18 (t,
1H), 7.10-7.00 (m, 2H), 6.66 (m, 1H), 4.20 (br. s, 2H), 4.05 (m,
1H), 3.25 (m, 1H), 3.05 (m, 1H), 2.90-2.70 (m, 4H), 2.05 (m, 1H),
1.70 (m, 1H), 1.65 (m, 2H), 1.45 (m, 1H).
[0826] HPLC (method 1): R.sub.t=3.50 min.
[0827] MS (ESIpos): m/z=362 (M+H).sup.+.
EXAMPLE 115
7-[3-(Acetylamino)phenyl]-N-[(3R)-1-azabicyclo[2.2.2]oct-3-yl]-1-benzofura-
n-2-carboxamide hydrochloride
##STR00164##
[0829] 75 mg (0.16 mmol) of
7-(3-aminophenyl)-N-[(3R)-1-azabicyclo[2.2.2]oct-3-yl]-1-benzofuran-2-car-
boxamide (Example 114), 18 .mu.l (0.24 mmol) of acetyl chloride and
68 .mu.l (0.49 mmol) of triethylamine are stirred in 2 ml of THF at
RT overnight. The solvent is removed under reduced pressure.
Purification takes place by preparative HPLC. The product is
dissolved in methanol, and an excess of 1N hydrochloric acid is
added. Removal of the solvent under reduced pressure and drying
under high vacuum results in 51 mg (72% of theory) of the title
compound.
[0830] .sup.1H-NMR (300 MHz, DMSO-d.sub.6): .delta.=10.37 (s, 1H),
10.30 (br. s, 1H), 8.67-8.59 (m, 2H), 7.82-7.68 (m, 3H), 7.58-7.41
(m, 4H), 4.40 (m, 1H), 3.73-3.60 (m, 1H), 3.48-3.37 (m, 1H),
3.78-3.15 (m, 4H), 2.29 (m, 1H), 2.19-2.09 (m, 1H), 2.13 (s, 3H),
1.98-1.90 (m, 2H), 1.81-1.69 (m, 1H).
[0831] HPLC (method 1): R.sub.t=4.04 min.
[0832] MS (ESIpos): m/z=404 (M+H).sup.+ (free base).
EXAMPLE 116
N-[(3R)-1-Azabicyclo[2.2.2]oct-3-yl]-7-{3-[(cyclopropylcarbonyl)amino]phen-
yl}-benzofuran-2-carboxamide hydrochloride
##STR00165##
[0834] 75 mg (0.21 mmol) of
7-(3-aminophenyl)-N-[(3R)-1-azabicyclo[2.2.2]oct-3-yl]-1-benzofuran-2-car-
boxamide (Example 114), 28 .mu.l (0.31 mmol) of
cyclopropyl-carbonyl chloride and 87 .mu.l (0.62 mmol) of
triethylamine are stirred in 2 ml of THF at RT overnight. After
addition of water, the solvent is removed under reduced pressure.
Purification takes place by preparative HPLC. The product is
dissolved in methanol, and an excess of 1N hydrochloric acid is
added. Removal of the solvent under reduced pressure and drying
under high vacuum result in 55 mg (57% of theory) of the title
compound.
[0835] .sup.1H-NMR (300 MHz, DMSO-d.sub.6): .delta.=10.53 (s, 1H),
10.08 (br. s, 1H), 8.83 (m, 1H), 8.28 (s, 1H), 7.82-7.75 (m, 2H),
7.71 (d, 1H), 7.62 (d, 1H), 7.58-7.50 (m, 1H), 7.48-7.41 (m, 2H),
4.38 (m, 1H), 3.71-3.60 (m, 1H), 150-3.15 (m, 5H), 2.27 (m, 1H),
2.21-2.11 (m, 1H), 1.99-1.82 (m, 3H), 1.80-1.71 (m, 1H), 0.88-0.77
(m, 4H).
HPLC (method 1): R.sub.t=4.07 min.
[0836] MS (ESIpos): m/z=430 (M+H).sup.+ (free base).
EXAMPLE 117
N-[(3R)-1-Azabicyclo[2.2.2]oct-3-yl]-7-(3-{[(methoxy)acetyl]amino}phenyl)--
1-benzofuran-2-carboxamide hydrochloride
##STR00166##
[0838] 75 mg (0.21 mmol) of
7-(3-aminophenyl)-N-[(3R)-1-azabicyclo[2.2.2]oct-3-yl]-1-benzofuran-2-car-
boxamide (Example 114), 21 .mu.l (0.31 mmol) of methoxyacetyl
chloride and 87 .mu.l (0.62 mmol) of triethylamine are stirred in 2
ml of THF at RT overnight. After addition of water, the solvent is
removed under reduced pressure. Purification takes place by
preparative HPLC. The product is dissolved in methanol, and an
excess of 1N hydrochloric acid is added. Removal of the solvent
under reduced pressure and drying under high vacuum result in 56 mg
(55% of theory) of the title compound.
[0839] .sup.1H-NMR (300 MHz, DMSO-d.sub.6): .delta.=10.17 (br. s,
1H), 10.10 (s, 1H), 8.63-8.55 (m, 2H), 7.82-7.68 (m, 3H), 7.64-7.57
(m, 2H), 7.52-7.41 (m, 2H), 4.39 (m, 1H), 4.10 (s, 2H), 3.71-3.61
(m, 1H), 3.49-3.14 (m, 5H), 3.41 (s, 3H), 2.29 (m, 1H), 2.19-2.05
(m, 1H), 1.99-1.89 (m, 2H), 1.80-1.69 (m, 1H).
[0840] HPLC (method 1): R.sub.t=4.07 min.
[0841] MS (ESIpos): m/z=434 (M+H).sup.+ (free base).
EXAMPLE 118
N-[(3R)-1-Azabicyclo[2.2.2]oct-3-yl]-7-{3-[(cyclobutylcarbonyl)amino]pheny-
l}-1-benzofuran-2-carboxamide hydrochloride
##STR00167##
[0843] 75 mg (0.21 mmol) of
7-(3-aminophenyl)-N-[(3R)-1-azabicyclo[2.2.2]oct-3-yl]-1-benzofuran-2-car-
boxamide (Example 114), 37 mg (0.31 mmol) of cyclobutanecarbonyl
chloride and 87 .mu.l (0.62 mmol) of triethylamine are stirred in 2
ml of THF at RT overnight. After addition of water, the solvent is
removed under reduced pressure. Purification takes place by
preparative HPLC. The product is dissolved in methanol, and an
excess of 1N hydrochloric acid is added. Removal of the solvent
under reduced pressure and drying under high vacuum result in 57 mg
(57% of theory) of the title compound.
[0844] .sup.1H-NMR (300 MHz, DMSO-d.sub.6): .delta.=10.14 (br. s,
1H), 10.07 (s, 1H), 8.82 (d, 1H), 8.35 (s, 1H), 7.80-7.78 (m, 2H),
7.74-7.61 (m, 2H), 7.57-7.41 (m, 3H), 4.36 (m, 1H), 3.70-3.61 (m,
1H), 3.45-3.13 (m, 5H), 2.30-1.67 (m, 12H).
[0845] HPLC (method 1): R.sub.t=4.22 min.
[0846] MS (ESIpos): m/z=444 (M+H).sup.+ (free base).
EXAMPLE 119
N-[(3R)-1-Azabicyclo[2.2.2]oct-3-yl]-7-{2-[(cyclopropylcarbonyl)amino]phen-
yl}-1-benzofuran-2-carboxamide hydrochloride
##STR00168##
[0848] 60 mg (0.15 mmol) of
7-(2-aminophenyl)-N-[(3R)-1-azabicyclo[2.2.2]oct-3-yl]-1-benzofuran-2-car-
boxamide (Example 132), 20 .mu.l (0.31 mmol) of
cyclopropyl-carbonyl chloride and 87 .mu.l (0.62 mmol) of
triethylamine are stirred in. 2 ml of THF/DMF (1:1) at RT
overnight. After addition of water, the solvent is removed under
reduced pressure. Purification takes place by preparative HPLC. The
product is dissolved in methanol, and an excess of 1N hydrochloric
acid is added. Removal of the solvent under reduced pressure and
drying under high vacuum result in 27 mg (40% of theory) of the
title compound.
[0849] .sup.1H-NMR (300 MHz, DMSO-d.sub.6): .delta.=10.07 (br. s,
1H), 9.48 (s, 1H), 8.84 (d, 1H), 7.83-7.77 (m, 1H), 7.72 (m, 1H),
7.54-7.31 (m, 6H); 4.30 (m, 1H), 3.70-3.61 (m, 1H), 3.37-3.03 (m,
5H), 2.23 (m, 1H), 2.14-2.03 (m, 1H), 1.95-1.83 (m, 2H), 1.79-1.68
(m, 1H), 1.53 (m, 1H), 1.31-1.15 (m, 4H).
[0850] HPLC (method 1): R.sub.t=3.85 min.
[0851] MS (ESIpos): m/z=430 (M+H).sup.+ (free base).
EXAMPLE 120
N-[(3R)-1-Azabicyclo[2.2.2]oct-3-yl]-7-(2-{[(methoxy)acetyl]amino}phenyl)--
1-benzofuran-2-carboxamide hydrochloride
##STR00169##
[0853] 60 mg (0.15 mmol) of
7-(2-aminophenyl)-N-[(3R)-1-azabicyclo[2.2.2]oct-3-yl]-1-benzofuran-2-car-
boxamide (Example 132), 20 .mu.l (0.22 mmol) of methoxyacetyl
chloride and 61 .mu.l (0.44 mmol) of triethylamine are stirred in 2
ml of THF/DMF (1:1) at RT overnight. After addition of water, the
solvent is removed under reduced pressure. Purification takes place
by preparative HPLC. The product is dissolved in methanol, and an
excess of 1N hydrochloric acid is added. Removal of the solvent
under reduced pressure and drying under high vacuum result in 29 mg
(40% of theory) of the title compound.
[0854] .sup.1H-NMR (300 MHz, DMSO-d.sub.6): .delta.=10.15 (br. s,
1H), 9.05 (s, 1H), 8.53 (d, 1H), 7.88-7.73 (m, 3H), 7.52-7.34 (m,
5H), 4.33 (m, 1H), 3.77 (s, 2H), 3.69-3.59 (m, 1H), 3.44-3.14 (m,
5H), 3.04 (s, 3H), 2.22 (m, 1H), 2.18-2.05 (m, 1H), 1.96-1.84 (m,
2H), 1.80-1.67 (m, 1H).
[0855] HPLC (method 1): R.sub.t=3.84 min.
[0856] MS (ESIpos): m/z=434 (M+H).sup.+ (free base).
EXAMPLE 121
N-[(3S)-1-Azabicyclo[2.2.2]oct-3-yl]-7-[4-(4-morpholinyl)phenyl]-1-benzofu-
ran-2-carboxamide hydrochloride
##STR00170##
[0858] 107 mg (0.52 mmol) of 4-morpholinophenylboronic acid and
1.72 ml of 1N sodium hydroxide solution are added to a mixture of
150 mg (0.43 mmol) of
N-[(3S)-1-azabicyclo[2.2.2]oct-3-yl]-7-bromo-1-benzofuran-2-carboxamid-
e (Example 31A) and 35 mg (0.04 mmol) of PdCl.sub.2(dppf) in 4 ml
of DMF. The reaction mixture is heated at. 95.degree. C. overnight.
The crude product is filtered through kieselguhr, and, after
washing with DMF, the solvent is removed under reduced pressure. To
remove the last residues of catalyst, a further filtration through
silica gel is carried out, washing with dichloromethane and
methanol. The crude product is purified by preparative HPLC. The
product is dissolved in methanol, and an excess of 1N hydrochloric
acid is added. Removal of the solvent under reduced pressure and
drying under high vacuum result in 84 mg (42% of theory) of the
title compound.
[0859] .sup.1H-NMR (300 MHz, DMSO-d.sub.6): .delta.=10.48 (br. s,
1H), 9.05 (d, 1H), 7.90-7.82 (m, 3H), 7.70 (d, 1H), 7.63 (d, 1H),
7.42-7.35 (m, 1H), 7.20-7.12 (m, 2H), 4.40-4.31 (m, 1H), 3.84-3.77
(m, 4H), 3.69-3.57 (m, 1H), 3.48-3.12 (m, 9H), 2.22 (m, 1H),
2.19-2.08 (m, 1H), 1.96-1.85 (m, 2H), 1.80-1.71 (m, 1H).
[0860] HPLC (method 1): R.sub.t=3.82 min.
[0861] MS (ESIpos): m/z=432 (M+H).sup.+.
EXAMPLE 122
N-[(3S)-1-Azabicyclo[2.2.2]oct-3-yl]-7-[2-(hydroxymethyl)phenyl]-1-benzofu-
ran-2-carboxamide hydrochloride
##STR00171##
[0863] 78 mg (0.52 mmol) of 2-(hydroxymethyl)phenylboronic acid and
1.72 ml of 1N sodium hydroxide solution are added to a mixture of
150 mg (0.43 mmol) of
N-[(3S)-1-azabicyclo[2.2.2]oct-3-yl]-7-bromo-1-benzofuran-2-carb-
oxamide (Example 31A) and 35 mg (0.04 mmol) of PdCl.sub.2(dppf) in
3 ml of DMF. The reaction mixture is heated at 95.degree. C.
overnight. The crude product is filtered through kieselguhr, and,
after washing with DMF, the solvent is removed under reduced
pressure. To remove the last residues of catalyst, a further
filtration through silica gel is carried out, washing with
dichloromethane and methanol. The crude product is purified by
preparative HPLC. The product is dissolved in methanol, and an
excess of 1N hydrochloric acid is added. Removal of the solvent
under reduced pressure and drying under high vacuum result in 81 mg
(46% of theory) of the title compound.
[0864] .sup.1H-NMR (300 MHz, DMSO-d.sub.6): .delta.=10.12 (br. s,
1H), 8.94 (d, 1H), 7.91-7.79 (m, 3H), 7.69 (d, 1H), 7.53-7.32 (m,
5H), 4.33-4.22 (m, 3H), 3.68-3.57 (m, 1H), 3.48-3.12 (m, 5H), 2.19
(m, 1H), 2.15-2.04 (m, 1H), 1.94-1.83 (m, 2H), 1.79-1.67 (m,
1H).
[0865] HPLC (method 1): R.sub.t=3.87 min.
[0866] MS (ESIpos): m/z=377 (M+H).sup.+.
EXAMPLE 123
N-[(3S)-1-Azabicyclo[2.2.2]oct-3-yl]-7-(3-pyridinyl)-1-benzofuran-2-carbox-
amide hydrochloride
##STR00172##
[0868] 63 mg (0.57 mmol) of 3-pyridineboronic acid, and 1.72 ml of
1N sodium hydroxide solution are added to a mixture of 150 mg (0.43
mmol) of
N-[(3S)-1-azabicyclo[2.2.2]oct-3-yl]-7-bromo-1-benzofuran-2-carboxamide
(Example 31A) and 35 mg (0.04 mmol) of PdCl.sub.2(dppf) in 4 ml of
DMF. The reaction mixture is heated at 95.degree. C. overnight. The
solvent is removed under reduced pressure and the crude product is
taken up in methanol and filtered through kieselguhr. To remove the
last residues of catalyst, a further filtration through silica gel
is carried out, washing with dichloromethane and methanol.
Purification takes place by preparative HPLC. The product is
dissolved in methanol, and an excess of 1N hydrochloric acid is
added. The solvent is removed under reduced pressure. Drying under
high vacuum results in 76 mg (42% of theory) of the title
compound.
[0869] .sup.1H-NMR (300 MHz, DMSO-d.sub.6): .delta.=10.49 (s, 1H),
9.51 (s, 1H), 9.30 (d, 1H), 8.94-8.80 (m, 2H), 8.07-7.80 (m, 4H),
7.55 (t, 1H), 4.35 (m, 1H), 3.65-3.15 (m, 6H), 2.20 (m, 1H),
2.18-2.05 (m, 1H), 1.98-1.88 (m, 2H), 1.80-1.63 (m, 1H).
HPLC (method 1): R.sub.t=3.30 min.
[0870] MS (ESIpos): m/z=348 (M+H).sup.+ (free base).
EXAMPLE 124
N-[(3S)-1-Azabicyclo[2.2.2]oct-3-yl]-7-[4-(methoxy)phenyl]-1-benzofuran-2--
carboxamide hydrochloride
##STR00173##
[0872] 78 mg (0.52 mmol) of 4-(methoxy)phenylboronic acid and 1.72
ml of 1N sodium hydroxide solution are added to a mixture of 150 mg
(0.43 mmol) of
N-[(3S)-1-azabicyclo[2.2.2]oct-3-yl]-7-bromo-1-benzofuran-2-carboxamid-
e (Example 31A) and 35 mg (0.04 mmol) of PdCl.sub.2(dppf) in 4 ml
of DMF. The reaction mixture is heated at 95.degree. C. overnight.
The solvent is removed under reduced pressure and the crude product
is taken up in methanol and filtered through kieselguhr. To remove
the last residues of catalyst, a further filtration through silica
gel is carried out, washing with dichloromethane and methanol.
Purification takes place by preparative HPLC. An excess of 1N
hydrochloric acid is added to the product fractions. The solvent is
removed under reduced pressure. Drying under high vacuum results in
27 mg (15% of theory) of the title compound.
[0873] The analytical data agree with those of the enantiomeric
compound (Example 99).
EXAMPLE 125
N-[(3S)-1-Azabicyclo[2.2.2]oct-3-yl]-7-[3-(methoxy)phenyl]-1-benzofuran-2--
carboxamide hydrochloride
##STR00174##
[0875] 78 mg (0.52 mmol) of 3-(methoxy)phenylboronic acid and 1.72
ml of 1N sodium hydroxide solution are added to a mixture of 150 mg
(0.43 mmol) of
N-[(3S)-1-azabicyclo[2.2.2]oct-3-yl]-7-bromo-1-benzofuran-2-carboxamid-
e (Example 31A) and 35 mg (0.04 mmol) of PdCl.sub.2(dppf) in 3 ml
of DMF. The reaction mixture is heated at 95.degree. C. overnight.
The solvent is removed under reduced pressure and the crude product
is taken up in methanol and filtered through kieselguhr. To remove
the last residues of catalyst, a further filtration through silica
gel is carried out, washing with dichloromethane and methanol.
Purification takes place by preparative HPLC. The product is
dissolved in methanol, and an excess of 1N hydrochloric acid is
added. The solvent is removed under reduced pressure. Drying under
high vacuum results in 23 mg (13% of theory) of the title
compound.
[0876] The analytical data agree with those of the enantiomeric
compound (Example 101).
EXAMPLE 126
N-[(3R)-1-Azabicyclo[2.2.2]oct-3-yl]-7-[2-({[(1-methylethyl)amino]carbonyl-
}-amino)phenyl]-1-benzofuran-2-carboxamide hydrochloride
##STR00175##
[0878] 75 mg (0.16 mmol) of
7-(2-aminophenyl)-N-[(3R)-1-azabicyclo[2.2.2]oct-3-yl]-1-benzofuran-2-car-
boxamide (Example 132), 65 .mu.l (0.66 mmol) of isopropyl
isocyanate and 114 .mu.l (0.82 mmol) of triethylamine are heated in
3 ml of THF/DMF (1:1) at 50.degree. C. for 48 h. Cooling is
followed by addition of water, filtration and removal of the
solvent under reduced pressure. Purification takes place by
preparative HPLC. The product is dissolved in methanol, and an
excess of 1N hydrochloric acid is added. The solvent is removed
under reduced pressure. Drying under high vacuum results in 21 mg
(26% of theory) of the title compound.
[0879] .sup.1H-NMR (300 MHz, DMSO-d.sub.6): .delta.=10.09 (br. s,
1H), 8.60 (d, 1H), 7.88-7.77 (m, 3H), 7.46-7.33 (m, 3H), 7.29 (dd,
1H), 7.19-7.10 (m, 1H), 6.22 (br. s, 1H), 4.29 (m, 1H), 3.75-3.54
(m, 2H), 3.39-3.13 (m, 5H), 2.22 (m, 1H), 2.15-2.02 (m, 1H),
1.96-1.86 (m, 2H), 1.80-1.69 (m, 1H), 0.96 (d, 6H).
[0880] HPLC (method 1): R.sub.t=3.92 min.
[0881] MS (ESIpos): m/z=447 (M+H).sup.+ (free base).
EXAMPLE 127
N-[(3R)-1-Azabicyclo[2.2.2]oct-3-yl]-7-(2-{[(ethylamino)carbonyl]amino}phe-
nyl)-1-benzofuran-2-carboxamide hydrochloride
##STR00176##
[0883] 75 mg (0.16 mmol) of
7-(2-aminophenyl)-N-[(3R)-1-azabicyclo[2.2.2]oct-3-yl]-1-benzofuran-2-car-
boxamide (Example 132), 50 .mu.l (0.66 mmol) of ethyl isocyanate
and 110 .mu.l (0.82 mmol) of triethylamine are heated together with
a catalytic amount of DMAP in 3 ml of THF/DMF (1:1) at 50.degree.
C. for 48 h. Cooling is followed by addition of water, filtration
and removal of the solvent under reduced pressure. Purification
takes place by preparative HPLC. The product is dissolved in
methanol, and an excess of 1N hydrochloric acid is added. The
solvent is removed under reduced pressure. Drying under high vacuum
results in 10 mg (12% of theory) of the title compound.
[0884] .sup.1H-NMR (300 MHz, DMSO-d.sub.6): .delta.=10.41 (br. s,
1H), 9.30 (d, 1H), 8.69 (d, 1H), 7.96-7.78 (m, 3H), 7.59-7.11 (m,
4H), 4.30 (m, 1H), 3.69-3.54 (m, 1H), 3.40-3.13 (m, 5H), 2.99 (q,
2H), 2.24-2.19 (m, 1H), 2.17-2.04 (m, 1H), 1.96-1.84 (m, 2H),
1.80-1.64 (m, 1H), 0.92 (t, 3H).
[0885] HPLC (method 1): R.sub.t=3.86 min.
[0886] MS (ESIpos): m/z=433 (M+H).sup.+ (free base).
EXAMPLE 128
N-[(3R)-1-Azabicyclo[2.2.2]oct-3-yl]-7-(2-{[(methylamino)carbonyl]amino}ph-
enyl)-1-benzofuran-2-carboxamide hydrochloride
##STR00177##
[0888] 75 mg (0.16 mmol) of
7-(2-aminophenyl)-N-[(3R)-1-azabicyclo[2.2.2]oct-3-yl]-1-benzofuran-2-car-
boxamide (Example 132), 37 mg (0.66 mmol) of methyl isocyanate and
110 .mu.l (0.82 mmol) of triethylamine are heated together with a
catalytic amount of DMAP in 3 ml of THF/DMF (1:1) at 50.degree. C.
overnight. Cooling is followed by addition of water, filtration and
removal of the solvent under reduced pressure. Purification takes
place by preparative HPLC. The product is dissolved in methanol,
and an excess of 1N hydrochloric acid is added. The solvent is
removed under reduced pressure. Drying under high vacuum results in
29 mg (35% of theory) of the title compound.
[0889] .sup.1H-NMR (300 MHz, DMSO-d.sub.6): .delta.=10.22 (br. s,
1H), 8.60 (d, 1H), 8.69 (d, 1H), 7.86-7.74 (m, 3H), 7.51-7.28 (m,
5H), 7.18-7.11 (m, 1H), 6.21 (br. s, 1H), 4.29 (m, 1H), 3.69-3.58
(m, 1H), 3.38-3.13 (m, 5H), 2.51 (s, 3H), 2.28-2.22 (m, 1H),
2.18-2.04 (m, 1H), 1.99-1.87 (m, 2H), 1.82-1.68 (m, 1H).
[0890] HPLC (method 1): R.sub.t=3.72 min.
[0891] MS (ESIpos): m/z=419 (M+H).sup.+ (free base).
EXAMPLE 129
N-[(3R)-1-Azabicyclo[2.2.2]oct-3-yl]-7-[2-({[(1,1-dimethylethyl)amino]carb-
onyl}-amino)phenyl]-1-benzofuran-2-carboxamide hydrochloride
##STR00178##
[0893] 75 mg (0.16 mmol) of
7-(2-aminophenyl)-N-[(3R)-1-azabicyclo[2.2.2]oct-3-yl]-1-benzofuran-2-car-
boxamide (Example 132), 65 mg (0.66 mmol) of 1,1-dimethylethyl
isocyanate and 110 .mu.l (0.82 mmol) of triethylamine are heated
together with a catalytic amount of DMAP in 3 ml of THF/DMF (1:1)
at 50.degree. C. overnight. Cooling is followed by addition of
water, filtration and removal of the solvent under reduced
pressure. Purification takes place by preparative HPLC. The product
is dissolved in methanol, and an excess of 1N hydrochloric acid is
added. The solvent is removed under reduced pressure. Drying under
high vacuum results in 10 mg (12% of theory) of the title
compound.
[0894] HPLC (method 1): R.sub.t=4.06 min.
[0895] MS (ESIpos): m/z=461 (M+H).sup.+ (free base).
EXAMPLE 130
N-[(3R)-1-Azabicyclo[2.2.2]oct-3-yl]-7-[2-(methoxy)phenyl]-1-benzofuran-2--
carboxamide
##STR00179##
[0897] 600 mg (1.45 mmol) of
N-[(3R)-1-azabicyclo[2.2.2]oct-3-yl]-7-[2-(methoxy)phenyl]-1-benzofuran-2-
-carboxamide hydrochloride (Example 102) are dissolved in 15 ml of
ethyl acetate and extracted three times with 1N sodium hydroxide
solution. The organic phase is dried over sodium sulphate and then
concentrated. Drying under high vacuum results in 534 mg (97.6% of
theory) of the title compound.
[0898] .sup.1H-NMR (200 MHz, DMSO-d.sub.6): .delta.=8.34 (d, 1H),
7.72 (dd, 1H), 7.70 (s, 1H), 7.50-7.30 (m, 4H), 7.20 (m, 1H), 7.08
(m, 1H), 3.93 (m, 1H), 3.76 (s, 3H), 3.11 (m, 1H), 2.86 (m, 1H),
2.69 (m, 4H), 1.86 (m, 1H), 1.75 (m, 1H), 1.58 (m, 2H), 1.32 (m,
1H).
[0899] HPLC (method 1): R.sub.t=4.1 min.
[0900] MS (ESIpos): m/z=377 (M+H).sup.+.
EXAMPLE 131
N-[(3R)-1-Azabicyclo[2.2.2]oct-3-yl]-7-[2-(hydroxymethyl)phenyl]-1-benzoth-
iophene-2-carboxamide hydrochloride
##STR00180##
[0902] 200 mg (0.45 mmol) of
N-[(3R)-1-azabicyclo[2.2.2]oct-3-yl]-7-bromo-1-benzothiophene-2-carboxami-
de hydrochloride (Example 8A) and 67.9 mg (0.45 mmol) of
2-(hydroxymethyl)phenylboronic acid are introduced into 2 ml of
DMF. Addition of 0.67 ml of 2 M sodium carbonate solution and 18.2
mg (0.02 mmol) of PdCl.sub.2(dppf) is followed by heating at
80.degree. C. After 18 h, the reaction mixture is filtered through
kieselguhr and purified by separation by preparative HPLC. The
product fractions are concentrated and, after addition of a 5:1
mixture of methanol and 4N hydrogen chloride in dioxane, again
concentrated. Drying under high vacuum results in 148 mg (72% of
theory) of the title compound.
[0903] .sup.1H-NMR (300 MHz, DMSO-d.sub.6): .delta.=10.30 (br. s,
1H), 9.10 (d, 1H), 8.47 (s, 1H), 8.07 (d, 1H), 7.78 (d, 1H),
7.68-7.54 (m, 2H), 7.52-7.39 (m, 3H), 4.40 (m, 1H), 4.36 (s, 2H);
3.72 (m, 1H), 3.53-3.20 (m, 5H), 2.29 (m, 1H), 2.21 (m, 1H), 2.00
(m, 2H), 1.82 (m, 1H).
[0904] HPLC (method 1): R.sub.t=3.9 min.
[0905] MS (ESIpos): m/z=393 (M+H).sup.+ (free base).
EXAMPLE 132
7-(2-Aminophenyl)-N-[(3R)-1-azabicyclo[2.2.2]oct-3-yl]-1-benzofuran-2-carb-
oxamide
##STR00181##
[0907] 752 mg (3.44 mmol) of
2-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenylamine and
11.45 ml of 1N sodium hydroxide solution are added to a mixture of
1.0 g (2.86 mmol) of
N-[(3R)-1-azabicyclo[2.2.2]oct-3-yl]-7-bromo-1-benzofuran-2-carb-
oxamide (Example 30A) 234 mg (0.29 mmol) of PdCl.sub.2(dppf) in 15
ml of DMF. The reaction mixture is heated at 95.degree. C.
overnight and then filtered through kieselguhr. The solvent is then
removed under reduced pressure, and the residue is taken up in 100
ml of ethyl acetate and 100 ml of 1N sodium hydroxide solution. The
organic phase is washed twice with 1N sodium hydroxide solution and
once with saturated sodium chloride solution. The combined organic
phases are dried over magnesium sulphate, and the solvent is
removed in a rotary evaporator under reduced pressure. The crude
product is taken up in methanol and shaken together with acidic ion
exchanger (Dowex.RTM. WX2-200) for about 30 min. The loaded ion
exchanger is washed three times with 30 ml of methanol each time
and then with DMF. It is washed successively with methanol,
dichloromethane, methanol, water, methanol, dichloromethane,
methanol, THF and finally once again with methanol. The product is
eluted with methanol/triethylamine 95:5. The solvent is removed in
a rotary evaporator under reduced pressure. Drying under high
vacuum results in 601 mg (48% of theory) of the title compound in
sufficient purity for further reactions.
[0908] HPLC (method 1): R.sub.t=3.51 min.
[0909] MS (ESIpos): m/z=362 (M+H).sup.+.
EXAMPLE 133
N-[(3S)-1-Azabicyclo[2.2.2]oct-3-yl]-7-[4-(4-morpholinylcarbonyl)phenyl]-1-
-benzothiophene-2-carboxamide hydrochloride
##STR00182##
[0911] 244.0 mg (0.65 mmol) of 4-(4-morpholinylcarbonyl)phenyl
trifluoromethane-sulphonate (Example 18A), 189.6 mg (0.75 mmol) of
bis(pinacolato)diboron, 158.8 mg (1.62 mmol) of potassium acetate,
18.2 mg (0.02 mmol) of PdCl.sub.2 (dppf), 200.0 mg (0.50 mmol) of
N-[(3S)-1-azabicyclo[2.2.2]oct-3-yl]-7-bromo-1-benzothiophene-2-carboxami-
de hydrochloride (Example 22A), 1.24 ml of 2 M sodium carbonate
solution and a further 18.2 mg (0.02 mmol) of PdCl.sub.2(dppf) in
2.5 ml of DMF are reacted by general method D. Drying under high
vacuum results in 76.8 mg (30.1% of theory) of the title
compound.
[0912] The spectroscopic data agree with those of the enantiomeric
compound (Example 72).
EXAMPLE 134
N-[(3S)-1-Azabicyclo[2.2.2]oct-3-yl]-7-[3-(4-morpholinyl)phenyl]-1-benzoth-
iophene-2-carboxamide hydrochloride
##STR00183##
[0914] 143.3 mg (0.49 mmol) of 3-(4-morpholinyl)phenyl
trifluoromethanesulphonate (Example 17A), 142.2 mg (0.56 mmol) of
bis(pinacolato)diboron, 119.1 mg (1.21 mmol) of potassium acetate,
13.7 mg (0.02 mmol) of PdCl.sub.2(dppf), 150 mg (0.37 mmol) of
N-[(3S)-1-azabicyclo[2.2.2]oct-3-yl]-7-bromo-1-benzothiophene-2-carboxami-
de hydrochloride (Example 22A), 0.93 ml of 2 M sodium carbonate
solution and a further 13.7 mg (0.02 mmol) of PdCl.sub.2(dppf) in
2.0 ml of DMF are reacted by general method D. Drying under high
vacuum results in 67 mg (37.1% of theory) of the title
compound.
[0915] The spectroscopic data agree with those of the enantiomeric
compound (Example 70).
EXAMPLE 135
N-[(3R)-1-Azabicyclo[2.2.2]oct-{3-yl]-7-(3-[(cyclopropylamino)carbonyl]phe-
nyl}-1-benzothiophene-2-carboxamide hydrochloride
##STR00184##
[0917] 50 mg (0.11 mmol) of
3-(2-{[(3R)-1-azabicyclo[2.2.2]oct-3-ylamino]carbonyl}-1-benzothien-7-yl)-
benzoic acid hydrochloride (Example 75) and 12.9 mg (0.23 mmol) of
cyclopropylamine are reacted together by general method E. 17.6 mg
(31.1% of theory) of the title compound are obtained.
[0918] .sup.1H-NMR (400 MHz, methanol-d.sub.4): .delta.=8.18 (s,
1H), 8.15 (s, 1H), 7.93 (d, 1H), 7.88 (m, 2H), 7.62 (dd, 1H), 7.56
(m, 2H), 4.45 (m, 1H), 3.84 (m, 1H), 3.48 (m, 1H), 3.42-3.27 (m,
4H), 2.89 (m, 1H), 2.38 (m, 1H), 2.28 (m, 1H), 2.10 (m, 2H), 1.96
(m, 1H), 0.82 (m, 2H), 0.67 (m, 2H).
[0919] HPLC (method 1): R.sub.t=3.95 min.
[0920] LC-MS (method 6): R.sub.t=3.36 min.; m/z=445 (M+H).sup.+
(free base)
EXAMPLE 136
[0921]
N-[(3R)-1-Azabicyclo[2.2.2]oct-3-yl]-7-(3-{[ethyl(methyl)amino]carb-
onyl}phenyl)-1-benzothiophene-2-carboxamide hydrochloride
##STR00185##
[0922] 50 mg (0.11 mmol) of
3-(2-{[(3R)-1-azabicyclo[2.2.2]oct-3-ylamino]carbonyl}-1-benzothien-7-yl)-
benzoic acid hydrochloride (Example 75) and 13.3 mg (0.23 mmol) of
ethylmethylamine are reacted together by general method E. 20.1 mg
(36.8% of theory) of the title compound are obtained.
[0923] .sup.1H-NMR (400 MHz, methanol-d.sub.4): .delta.=8.19 (s,
1H), 7.95 (d, 1H), 7.82 (d, 1H), 7.73 (m, 1H), 7.64 (dd, 1H),
7.60-7.46 (m, 3H), 4.45 (m, 1H), 3.83 (m, 1H), 3.61 (m, 1H),
3.51-3.28 (m, 6H), 3.10 (m, 3H), 2.39 (m, 1H), 2.28 (m, 1H), 2.10
(m, 2H), 1.96 (m, 1H), 1.23 (m, 3H).
[0924] HPLC (method 1): R.sub.t=4.00 min.
[0925] LC-MS (method 6): R.sub.t=3.40 min.; m/z=447 (M+H).sup.+
(free base).
EXAMPLE 137
N-[(3R)-1-Azabicyclo[2.2.2]oct-3-yl]-7-[3-(2,5-dihydro-1H-pyrrol-1-ylcarbo-
nyl)-phenyl]-1-benzothiophene-2-carboxamide hydrochloride
##STR00186##
[0927] 50 mg (0.11 mmol) of
3-(2-{[(3R)-1-azabicyclo[2.2.2]oct-3-ylamino]carbonyl}-1-benzothien-7-yl)-
benzoic acid hydrochloride (Example 75) and 15.6 mg (0:23 mmol) of
3-pyrroline are reacted together by general method E. 20 mg (35.9%
of theory) of the title compound are obtained.
[0928] HPLC (method 1): R=4.00 min.
[0929] LC-MS (method 6): R.sub.t=3.40 min.; m/z=457 (M+H).sup.+
(free base)
EXAMPLE 138
N-[(3R)-1-Azabicyclo[2.2.2]oct-3-yl]-7-(3-{[(3-methoxypropyl)amino]carbony-
l}-phenyl)-1-benzothiophene-2-carboxamide hydrochloride
##STR00187##
[0931] 50 mg (0.11 mmol) of
3-(2-{[(3R)-1-azabicyclo[2.2.2]oct-3-ylamino]carbonyl}-1-benzothien-7-yl)-
benzoic acid hydrochloride (Example 75) and 20.1 mg (0.23 mmol) of
3-methoxypropylamine are reacted together by general method E. 29.2
mg (49.8% of theory) of the title compound are obtained.
[0932] HPLC (method 1): R.sub.t=3.94 min.
[0933] LC-MS (method 6): R.sub.t=3.37 min.; m/z=477 (M+H).sup.+
(free base).
EXAMPLE 139
N-[(3R)-1-Azabicyclo[2.2.2]oct-3-yl]-7-(3-{[(2-methoxyethyl)(methyl)amino]-
-carbonyl}phenyl)-1-benzothiophene-2-carboxamide hydrochloride
##STR00188##
[0935] 50 mg (0.11 mmol) of
3-(2-{[(3R)-1-azabicyclo[2.2.2]oct-3-ylamino]carbonyl}-1-benzothien-7-yl)-
benzoic acid hydrochloride (Example 75) and 20.1 mg (0.23 mmol) of
(2-methoxyethyl)methylamine are reacted together by general method
E. 20.5 mg (31.8% of theory) of the title compound are
obtained.
[0936] HPLC (method 1): R.sub.t=3.93 min.
[0937] LC-MS (method 6): R.sub.t=3.35 min.; m/z=477 (M+H).sup.+
(free base)
EXAMPLE 140
N-[(3R)-1-Azabicyclo[2.2.2]oct-3-yl]-7-(3-{[(3-ethoxypropyl)amino]carbonyl-
}-phenyl)-1-benzothiophene-2-carboxamide hydrochloride
##STR00189##
[0939] 50 mg (0.11 mmol) of
3-(2-{[(3R)-1-azabicyclo[2.2.2]oct-3-ylamino]carbonyl}-1-benzothien-7-yOb-
enzoic acid hydrochloride (Example 75) and 20.1 mg (0.23 mmol) of
3-ethoxypropylamine are reacted together by general method E. 23.4
mg (37.1% of theory) of the title compound are obtained.
[0940] .sup.1H-NMR (400 MHz, methanol-d.sub.4): .delta.=8.18 (s,
1H), 8.15 (s, 1H), 7.94 (d, 1H), 7.89 (m, 2H), 7.64 (dd, 1H), 7.56
(m, 2H), 4.45 (m, 1H), 3.84 (m, 1H), 3.55 (m, 2H), 3.53-3.25 (m,
9H), 2.39 (m, 1H), 2.28 (m, 1H), 2.10 (m, 2H), 1.96 (m, 1H), 1.91
(m, 2H), 1.17 (m, 3H).
[0941] HPLC (method 1): R.sub.t=4.07 min.
[0942] LC-MS (method 6): R.sub.t=3.46 min.; m/z=491 (M+H).sup.+
(free base).
EXAMPLE 141
N-[(3R)-1-Azabicyclo[2.2.2]oct-3-yl]-7-{3-[(4-methyl-1-piperazinyl)carbony-
l]-phenyl}-1-benzothiophene-2-carboxamide dihydrochloride
##STR00190##
[0944] 50 mg (0.11 mmol) of
3-(2-{[(3R)-1-azabicyclo[2.2.2]oct-3-ylamino]carbonyl}-1-benzothien-7-yOb-
enzoic acid hydrochloride (Example 75) and 22.6 mg (0.23 mmol) of
N-methylpiperazine are reacted together by general method E. 4.2 mg
(6.6% of theory) of the title compound are obtained.
[0945] .sup.1H-NMR (400 MHz, methanol-d.sub.4): .delta.=8.23 (s,
1H), 7.97 (dd, 1H), 7.88 (m, 2H), 7.69 (m, 1H), 7.57 (m, 3H), 4.46
(m, 1H), 3.84 (m, 1H), 3.50 (m, 1H), 3.46-3.25 (m, 12H), 2.97 (s,
3H), 2.39 (m, 1H), 2.29 (m, 1H), 2.10 (m, 2H), 1.96 (m, 1H).
[0946] HPLC (method 1): R.sub.t=3.62 min.
[0947] LC-MS (method 6): R.sub.t=2.94 min.; m/z=488 (M+H).sup.+
(free base).
EXAMPLE 142
N-[(3R)-1-Azabicyclo[2.2.2]oct-3-yl]-7-{3-[(cyclobutylcarbonyl)amino]pheny-
l}-1-benzothiophene-2-carboxamide hydrochloride
##STR00191##
[0949] 50 mg (0.12 mmol) of
7-(3-aminophenyl)-N-[(3R)-1-azabicyclo[2.2.2]oct-3-yl]-1-benzothiophene-2-
-carboxamide hydrochloride (Example 21) and 28.6 mg (0.24 mmol) of
cyclobutanecarbonyl chloride are reacted together by general method
F. 38 mg (61.3% of theory) of the title compound are obtained.
[0950] HPLC (method 1): R.sub.t=4.22 min.
[0951] MS (ESIpos): m/z=460 (M+H).sup.+ (free base).
EXAMPLE 143
N-[3-(2-{[(3R)-1-Azabicyclo[2.2.2]oct-3-ylamino]carbonyl}-1-benzothien-7-y-
l)-phenyl]-5-isoxazolecarboxamide hydrochloride
##STR00192##
[0953] 50 mg (0.12 mmol) of
7-(3-aminophenyl)-N-[(3R)-1-azabicyclo[2.2.2]oct-3-yl]-1-benzothiophene-2-
-carboxamide hydrochloride (Example 21) and 31.8 mg (0.24 mmol) of
isoxazole-5-carbonyl chloride are reacted together by general
method F. 44.4 mg (72.6% of theory) of the title compound are
obtained.
[0954] .sup.1H-NMR (400 MHz, methanol-d.sub.4): .delta.=8.58 (d,
1H), 8.18 (s, 2H), 7.93 (dd, 1H), 7.79 (m, 1H), 7.55 (m, 4H), 7.13
(m, 1H), 4.45 (m, 1H), 3.83 (m, 1H), 3.48 (m, 1H), 3.42-3.27 (m,
4H), 2.39 (m, 1H), 2.28 (m, 1H), 2.10 (m, 2H), 1.96 (m, 1H).
[0955] HPLC (method 1): R.sub.t=4.12 min.
[0956] MS (ESIpos): m/z=473 (M+H).sup.+ (free base)
EXAMPLE 144
N-[(3R)-1-Azabicyclo[2.2.2]oct-3-yl]-7-{3-[(cyclopentylcarbonyl)amino]phen-
yl}-1-benzothiophene-2-carboxamide hydrochloride
##STR00193##
[0958] 50 mg (0.12 mmol) of
7-(3-aminophenyl)-N-[(3R)-1-azabicyclo[2.2.2]oct-3-yl]-1-benzothiophene-2-
-carboxamide hydrochloride (Example 21) and 32 mg (0.24 mmol) of
cyclopentylcarbonyl chloride are reacted together by general method
F. 30.5 mg (52.8% of theory) of the title compound are
obtained.
[0959] .sup.1H-NMR (400 MHz, methanol-d.sub.4): .delta.=8.17 (s,
1H), 8.03 (m, 1H), 7.91 (dd, 1H), 7.60 (m, 1H), 7.57-7.38 (m, 4H),
4.45 (m, 1H), 3.83 (m, 1H), 3.48 (m, 1H), 3.42-3.27 (m, 4H), 2.86
(m, 1H), 2.38 (m, 1H), 2.28 (m, 1H), 2.10 (m, 2H), 1.96 (m, 3H),
1.90-1.72 (m, 4H), 1.66 (m, 2H).
[0960] HPLC (method 1): R.sub.t=4.40 min.
[0961] MS (ESIpos): m/z=474 (M+H).sup.+ (free base).
EXAMPLE 145
N-[(3R)-1-Azabicyclo[2.2.2]oct-3-yl]-7-{3-[(cyclohexylcarbonyl)amino]pheny-
l}-1-benzothiophene-2-carboxamide hydrochloride
##STR00194##
[0963] 50 mg (0.12 mmol) of
7-(3-aminophenyl)-N-[(3R)-1-azabicyclo[2.2.2]oct-3-yl]-1-benzothiophene-2-
-carboxamide hydrochloride (Example 21) and 35.4 mg (0.24 mmol) of
cyclohexylcarbonyl chloride are reacted together by general method
F. 9.8 mg (16.2% of theory) of the title compound are obtained.
[0964] HPLC (method 1): R.sub.t=4.51 min.
[0965] MS (ESIpos): m/z=488 (M+H).sup.+ (free base).
EXAMPLE 146
N-[(3R)-1-Azabicyclo[2.2.2]oct-3-yl]-7-{3-[(tetrahydro-2-furanylcarbonyl)a-
mino]-phenyl}-1-benzothiophene-2-carboxamide hydrochloride
##STR00195##
[0967] 50 mg (0.12 mmol) of
7-(3-aminophenyl)-N-[(3R)-1-azabicyclo[2.2.2]oct-3-yl]-1-benzothiophene-2-
-carboxamide hydrochloride (Example 21) and 32.5 mg (0.24 mmol) of
tetrahydrofuran-2-carbonyl chloride are reacted together by general
method F. 40.9 mg (68.1% of theory) of the title compound are
obtained.
[0968] .sup.1H-NMR (400 MHz, methanol-d.sub.4): .delta.=8.17 (s,
1H), 8.04 (s, 1H), 7.91 (d, 1H), 7.61 (m, 1H), 7.58-7.40 (m, 4H),
4.46 (m, 1H), 4.04 (dd, 1H), 3.92 (m, 2H), 3.83 (m, 2H), 3.48 (m,
1H), 3.42-3.27 (m, 4H), 3.23 (m, 1H), 2.38 (m, 1H), 2.28 (m, 1H),
2.22 (m, 2H), 2.10 (m, 2H), 1.96 (m, 1H).
[0969] HPLC (method 1): R.sub.t=3.99 min.
[0970] MS (ESIpos): m/z=476 (M+H).sup.+ (free base).
EXAMPLE 147
N-[(3R)-1-Azabicyclo[2.2.2]oct-3-yl]-7-[3-(isobutyrylamino)phenyl]-1-benzo-
thiophene-2-carboxamide hydrochloride
##STR00196##
[0972] 50 mg (0.12 mmol) of
7-(3-aminophenyl)-N-[(3R)-1-azabicyclo[2.2.2]oct-3-yl]-1-benzothiophene-2-
-carboxamide hydrochloride (Example 21) and 25.7 mg (0.24 mmol) of
isobutyryl chloride are reacted together by general method F. 35.1
mg (64.9% of theory) of the title compound are obtained.
[0973] .sup.1H-NMR (400 MHz, methanol-d.sub.4): .delta.=8.17 (s,
1H), 8.03 (s, 1H), 7.90 (d, 1H), 7.61 (m, 1H), 7.57-7.40 (m, 4H),
4.45 (m, 1H), 3.83 (m, 1H), 3.48 (m, 1H), 3.42-3.27 (m, 4H), 2.68
(m, 1H), 2.38 (m, 1H), 2.28 (m, 1H), 2.10 (m, 2H), 1.96 (m, 1H),
1.21 (d, 6H).
[0974] HPLC (method 1): R.sub.t=4.19 Min.
[0975] MS (ESIpos): m/z=448 (M+H).sup.+ (free base).
EXAMPLE 148
N-[(3R)-1-Azabicyclo[2.2.2]oct-3-yl]-7-[3-(2-furoylamino)phenyl]-1-benzoth-
iophene-2-carboxamide hydrochloride
##STR00197##
[0977] 50 mg (0.12 mmol) of
7-(3-aminophenyl)-N-[(3R)-1-azabicyclo[2.2.2]oct-3-yl]-1-benzothiophene-2-
-carboxamide hydrochloride (Example 21) and 31.5 mg (0.24 mmol) of
furan-2-carbonyl chloride are reacted together by general method F.
29.1 mg (51.1% of theory) of the title compound are obtained.
[0978] .sup.1H-NMR (400 MHz, methanol-d.sub.4): .delta.=8.17 (s,
2H), 7.91 (d, 1H), 7.74 (m, 2H), 7.58-7.47 (m, 4H), 7.29 (d, 1H),
6.65 (m, 1H), 4.44 (m, 1H), 3.83 (m, 1H), 3.47 (m, 1H), 3.42-3.27
(m, 4H), 2.38 (m, 1H), 2.28 (m, 1H), 2.10 (m, 2H); 1.96 (m, 1H).
HPLC (method 1): R.sub.t=4.19 min.
[0979] MS (ESIpos): m/z=472 (M+H).sup.+ (free base).
EXAMPLE 149
3-(2-{[(3R)-1-Azabicyclo[2.2.2]oct-3-ylamino]carbonyl}-1-benzofuran-7-yl)--
benzoic acid hydrochloride
##STR00198##
[0981] 4.3 ml of 2 M aqueous sodium carbonate solution and 116.9 mg
(0.14 mmol) of PdCl.sub.2(dppf) are added to a mixture of 1104 mg
(2.86 mmol) of
N-[(3R)-1-azabicyclo[2.2.2]oct-3-yl]-7-bromo-1-benzofuran-2-carboxamid-
e hydrochloride (Example 30A) and 475 mg (2.86 mmol) of
3-carboxyphenylboronic acid in 10 ml of DMF. The reaction mixture
is heated at 90.degree. C. for 18 h and then filtered through
kieselguhr and evaporated to dryness. Purification of the crude
product by preparative HPLC, subsequent addition of a 3:1 mixture
of acetonitrile and 1N hydrochloric acid, concentrating and drying
under high vacuum result in 724 mg (59.2% of theory) of the title
compound.
[0982] .sup.1H-NMR (400 MHz, methanol-d.sub.4): .delta.=8.62 (s,
1H), 8.11 (d, 1H), 8.08 (d, 1H), 7.76 (d, 1H), 7.73-7.61 (m, 3H),
7.46 (dd, 1H), 4.49 (m, 1H), 3.83 (m, 1H), 3.48 (m, 1H), 3.43-3.27
(m, 4H), 2.40 (m, 1H), 2.28 (m, 1H), 2.10 (m, 2H), 1.96 (m,
1H).
[0983] HPLC (method 1): R.sub.t=3.89 min.
[0984] MS (ESIpos): m/z=391 (M+H).sup.+ (free base)
EXAMPLE 150
N-[(3R)-1-Azabicyclo[2.2.2]oct-3-yl]-7-[2-(hydroxymethyl)phenyl]-1-benzofu-
ran-carboxamide hydrochloride
##STR00199##
[0986] 0.64 ml of 2 M aqueous sodium carbonate solution and 17.5 mg
(0.02 mmol) of PdCl.sub.2(dppf) are added to a mixture of 150 mg
(0.43 mmol) of
N-[(3R)-1-azabicyclo[2.2.2]oct-3-yl]-7-bromo-1-benzofuran-2-carboxamide
hydrochloride (Example 30A) and 65.3 mg (0.43 mmol) of
2-(hydroxymethyl)phenylboronic acid in 1.5 ml of DMF. The reaction
mixture is heated at 90.degree. C. for 18 h and then filtered
through kieselguhr and evaporated to dryness. Purification of the
crude product by preparative HPLC, subsequent addition of a 3:1
mixture of acetonitrile and 1N hydrochloric acid, concentration and
drying under high vacuum result in 13 mg (7.1% of theory) of the
title compound.
[0987] HPLC (method 1): R.sub.t=3.87 min.
[0988] MS (ESIpos): m/z=377 (M+H).sup.+ (free base)
EXAMPLE 151
N-[(3R)-1-Azabicyclo[2.2.2]oct-3-yl]-7-(2,5-dimethoxyphenyl)-1-benzofuran--
2-carboxamide hydrochloride
##STR00200##
[0990] 0.78 ml of 2 M aqueous sodium carbonate solution and 21.2 mg
(0.03 mmol) of PdCl.sub.2(dppf) are added to a mixture of 200 mg
(0.52 mmol) of
N-[(3R)-1-azabicyclo[2.2.2]oct-3-yl]-7-bromo-1-benzofuran-2-carboxamide
hydrochloride (Example 30A) and 94.4 mg (0.52 mmol) of
2,5-dimethoxyphenylboronic acid in 2 ml of DMF. The reaction
mixture is heated at 70.degree. C. for 17 h and then filtered
through kieselguhr and evaporated to dryness. Purification of the
crude product by preparative HPLC, subsequent addition of a 3:1
mixture of methanol and 1N hydrochloric acid, concentration and
drying under high vacuum result in 75 mg (31.7% of theory) of the
title compound.
[0991] HPLC (method 1): R.sub.t=4.15 min.
[0992] MS (ESIpos): m/z=407 (M+H).sup.+ (free base).
EXAMPLE 152
7-[2-(Aminomethyl)phenyl]-N-[(3R)-1-azabicyclo[2.2.2]oct-3-yl]-1-benzofura-
n-2-carboxamide dihydrochloride
##STR00201##
[0994] 500 mg (1.75 mmol) of tert-butyl 2-bromoberizylcarbamate,
512 mg (2.02 mmol) of bis(pinacolato)diboron, 428.7 mg (4.37 mmol)
of potassium acetate, 49.2 mg (0.07 mmol) of PdCl.sub.2(dppf),
518.4 mg (1.34 mmol) of
N-[(3R)-1-azabicyclo[2.2.2]oct-3-yl]-7-bromo-1-benzofuran-2-carboxamide
hydrochloride (Example 30A), 3.36 ml of 2 M sodium carbonate
solution and a further 49.2 mg (0.07 mmol) of PdCl.sub.2(dppf) in 5
ml of DMF are reacted by general method D. The crude product which
has been dried under high vacuum is stirred in 8 ml of a 1:1
mixture of methanol and 4 M hydrogen chloride in dioxane at room
temperature for 2 h. The reaction solution is concentrated and the
resulting crude product is purified by preparative HPLC. The
product fractions are concentrated and, after addition of a 3:1
mixture of methanol and 1N hydrochloric acid, again concentrated
and dried under high vacuum. 245.5 mg (44.5% of theory) of the
title compound are obtained.
[0995] .sup.1H-NMR (300 MHz, DMSO-d.sub.6): .delta.=10.48 (br. s,
1H), 9.26 (d, 1H), 8.47 (br. s, 3H), 8.05 (s, 1H), 7.88 (dd, 1H),
7.80 (d, 1H), 7.62-7.40 (m, 5H), 4.31 (m, 1H), 3.86 (m, 2H), 3.48
(m, 1H), 3.51-3.10 (m, 5H), 2.18 (m, 1H), 2.11 (m, 1H), 1.90 (m,
2H), 1.71 (m, 1H).
[0996] HPLC (method 7): R.sub.t=3.55 min.
[0997] MS (ESIpos): m/z=376 (M+H).sup.+ (free base).
EXAMPLE 153
3-(2-{[(3S)-1-Azabicyclo[2.2.2]oct-3-ylamino]carbonyl}-1-benzofuran-7-yl)--
benzoic acid hydrochloride
##STR00202##
[0999] 3.89 ml of 2 M aqueous sodium carbonate solution and 105.9
mg (0.13 mmol) of PdCl.sub.2(dppf) are added to a mixture of 1000
mg (2.59 mmol) of
N-[(3S)-1-azabicyclo[2.2.2]oct-3-yl]-7-bromo-1-benzofuran-2-carboxamid-
e hydrochloride (free base: Example 31A) and 430.2 mg (2.59 mmol)
of 3-carboxyphenylboronic acid in. 8 ml of DMF. The reaction
mixture is heated at 70.degree. C. for 18 h and then filtered
through kieselguhr and evaporated to dryness. Purification of the
crude product by preparative HPLC, subsequent addition of a 3:1
mixture of methanol and 1N hydrochloric acid, concentration and
drying under high vacuum result in 142.5 mg 1.5 (12% of theory) and
a further 627.9 mg (of 80% purity) of the title compound.
[1000] The spectroscopic data agree with those of the enantiomeric
compound (Example 149).
EXAMPLE 154
N-[(3R)-1-Azabicyclo[2.2.2]oct-3-yl]-7-{3-[(cyclopropylamino)carbonyl]phen-
yl}-1-benzofuran-2-carboxamide hydrochloride
##STR00203##
[1002] 50 mg (0.12 mmol) of
3-(2-{[(3R)-1-azabicyclo[2.2.2]oct-3-ylamino]carbonyl}-1-benzofuran-7-yl)-
benzoic acid hydrochloride (Example 149) and 13.4 mg (0.23 mmol) of
cyclopropylamine are reacted together by general method E. 20 mg
(32.2% of theory) of the title compound are obtained.
[1003] HPLC (method 1): R.sub.t=3.93 min.
[1004] LC-MS (method 6): R.sub.t=3.33 min.; m/z=429 (M+H).sup.+
(free base).
EXAMPLE 155
N-[(3R)-1-Azabicyclo[2.2.2]oct-3-yl]-7-(3-{[ethyl(methyl)amino]carbonyl}ph-
enyl)-1-benzofuran-2-carboxamide hydrochloride
##STR00204##
[1006] 50 mg (0.12 mmol) of
3-(2-{[(3R)-1-azabicyclo[2.2.2]oct-3-ylamino]carbonyl}-1-benzofuran-7-yl)-
benzoic acid hydrochloride (Example 149) and 13.9 mg (0.23 mmol) of
methylethylamine are reacted together by general method E. 19.8 mg
(29.4% of theory) of the title compound are obtained.
[1007] HPLC (method 1): R.sub.t=4.03 min.
[1008] LC-MS (method 6): R.sub.t=3.38 min.; m/z=431 (M+H).sup.+
(free base).
EXAMPLE 156
N-[(3R)-1-Azabicyclo[2.2.2]oct-3-yl]-7-{3-[(butylamino)carbonyl]phenyl}-1--
benzo-furan-2-carboxamide hydrochloride
##STR00205##
[1010] 50 mg (0.12 mmol) of
3-(2-{[(3R)-1-azabicyclo[2.2.2]oct-3-ylamino]carbonyl}-1-benzofuran-7-yl)-
benzoic acid hydrochloride (Example 149) and 17.1 mg (0.23 mmol) of
n-butylamine are reacted together by general method E. 15.2 mg
(26.2% of theory) of the title compound are obtained.
[1011] HPLC (method 1): R.sub.t=4.21 min.
[1012] LC-MS (method 6): R.sub.t=3.49 min.; m/z=445 (M+H).sup.+
(free base).
EXAMPLE 157
N-[(3R)-1-Azabicyclo[2.2.2]oct-3-yl]-7-{3-[(isobutylamino)carbonyl]phenyl}-
-1-benzofuran-2-carboxamide hydrochloride
##STR00206##
[1014] 50 mg (0.12 mmol) of
3-(2-{[(3R)-1-azabicyclo[2.2.2]oct-3-ylamino]carbonyl}-1-benzofuran-7-yl)-
benzoic acid hydrochloride (Example 149) and 17.1 mg (0.23 mmol) of
iso-butylamine are reacted together by general method E. 15.2 mg
(26.9% of theory) of the title compound are obtained.
[1015] HPLC (method 1): R.sub.t=4.18 min.
[1016] LC-MS (method 6): R.sub.t=3.49 min.; m/z=445 (WH).sup.+
(free base).
EXAMPLE 158
N-[(3R)-1-Azabicyclo[2.2.2]oct-3-yl]-7-[3-(1-piperidinylcarbonyl)phenyl]-1-
-benzo-furan-2-carboxamide hydrochloride
##STR00207##
[1018] 50 mg (0.12 mmol) of
3-(2-{[(3R)-1-azabicyclo[2.2.2]oct-3-ylamino]carbonyl}-1-benzofuran-7-yl)-
benzoic acid hydrochloride (Example 149) and 20.0 mg (0.23 mmol) of
piperidine are reacted together by general method E. 16.4 mg (27.6%
of theory) of the title compound are obtained.
[1019] HPLC (method 1): R.sub.t=4.22 min.
[1020] LC-MS (method 6): R.sub.t=3.51 min.; m/z=457 (M+H).sup.+
(free base)
EXAMPLE 159
N-[(3R)-1-Azabicyclo[2.2.2]oct-3-yl]-7-[3-{[2-(dimethylamino)ethyl]amino}--
carbonyl)phenyl]-1-benzofuran-2-carboxamide hydrochloride
##STR00208##
[1022] 50 mg (0.12 mmol) of
3-(2-{[(3R)-1-azabicyclo[2.2.2]oct-3-ylamino]carbonyl}-1-benzofuran-7-yl)-
benzoic acid hydrochloride (Example 149) and 20.7 mg (0.23 mmol) of
N-(2-aminoethyl)-N,N-dimethylamine are reacted together by general
method E. 17.4 mg (24.8% of theory) of the title compound are
obtained.
[1023] HPLC (method 1): R.sub.t=3.64 min.
[1024] LC-MS (method 6): R.sub.t=2.93 min.; m/z=460 (M+H).sup.+
(free base).
EXAMPLE 160
N-[(3R)-1-Azabicyclo[2.2.2]oct-3-yl]-7-(3-{[(3-methoxypropyl)amino]carbony-
l}-phenyl)-1-benzofuran-2-carboxamide hydrochloride
##STR00209##
[1026] 50 mg (0.12 mmol) of
3-(2-{[(3R)-1-azabicyclo[2.2.2]oct-3-ylamino]carbonyl}-1-benzofuran-7-yl)-
benzoic acid hydrochloride (Example 149) and 20.9 mg (0.23 mmol) of
3-methoxypropylamine are reacted together by general method E. 22.7
mg (36.4% of theory) of the title compound are obtained.
[1027] HPLC (method 1): R.sub.t=3.93 min.
[1028] LC-MS (method 6): R.sub.t=3.36 min.; m/z=461 (M+H).sup.+
(free base)
EXAMPLE 161
N-[(3R)-1-Azabicyclo[2.2.2]oct-3-yl]-7-(3-{[(2-methoxyethyl)(methyl)amino]-
-carbonyl}phenyl)-1-benzofuran-2-carboxamide hydrochloride
##STR00210##
[1030] 50 mg (0.12 mmol) of
3-(2-{[(3R)-1-azabicyclo[2.2.2]oct-3-ylamino]carbonyl}-1-benzofuran-7-yl)-
benzoic acid hydrochloride (Example 149) and 20.9 mg (0.23 mmol) of
N-(2-methoxyethyl)-N-methylamine are reacted together by general
method E. 20.4 mg (31.3% of theory) of the title compound are
obtained.
[1031] HPLC (method 1): R.sub.t=3.96 min.
[1032] LC-MS (method 6): R.sub.t=3.34 min.; m/z=461 (M+H).sup.+
(free base)
EXAMPLE 162
N-[(3R)-1-Azabicyclo[2.2.2]oct-3-yl]-7-(3-{[(3-ethoxypropyl)amino]carbonyl-
}-phenyl)-1-benzofuran-2-carboxamide hydrochloride
##STR00211##
[1034] 50 mg (0.12 mmol) of
3-(2-{[(3R)-1-azabicyclo[2.2.2]oct-3-ylamino]carbonyl}-1-benzofuran-7-yl)-
benzoic acid hydrochloride (Example 149) and 24.2 mg (0.23 mmol) of
3-ethoxypropylamine are reacted together by general method E. 17.8
mg (28.9% of theory) of the title compound are obtained.
[1035] HPLC (method 1): R.sub.t=4.06 min.
[1036] LC-MS (method 6): R.sub.t=3.43 min.; m/z=475 (M+H).sup.+
(free base).
EXAMPLE 163
N-[(3R)-1-Azabicyclo[2.2.2]oct-3-yl]-7-{3-[(4-methyl-1-piperazinyl)carbony-
l]-phenyl}-1-benzofuran-2-carboxamide dihydrochloride
##STR00212##
[1038] 50 mg (0.12 mmol) of
3-(2-{[(3R)-1-azabicyclo[2.2.2]oct-3-ylamino]carbonyl}-1-benzofuran-7-yl)-
benzoic acid hydrochloride (Example 149) and 23.5 mg (0.23 mmol) of
N-methylpiperazine are reacted together by general method E. 29.6
mg (41.9% of theory) of the title compound are obtained.
[1039] HPLC (method 1): R.sub.t=3.60 min.
[1040] LC-MS (method 6): R.sub.t=2.91 min.; m/z=472 (M+H).sup.+
(free base).
EXAMPLE 164
N-[(3S)-1-Azabicyclo[2.2.2]oct-3-yl]-7-(3-{[ethyl(methyl)amino]carbonyl}ph-
enyl)-1-benzofuran-2-carboxamide hydrochloride
##STR00213##
[1042] 50 mg (0.12 mmol) of
3-(2-{[(3S)-1-azabicyclo[2.2.2]oct-3-ylamino]carbonyl}-1-benzofuran-7-yl)-
benzoic acid hydrochloride (Example 153) and 13.9 mg (0.23 mmol) of
methylethylamine are reacted together by general method E. 50.1 mg
(91.4% of theory) of the title compound are obtained.
[1043] The spectroscopic data agree with those of the enantiomeric
compound (Example 155).
EXAMPLE 165
N-[(3S)-1-Azabicyclo[2.2.2]oct-3-yl]-7-{3-[(butylamino)carbonyl]phenyl}-1--
benzo-furan-2-carboxamide hydrochloride
##STR00214##
[1045] 50 mg (0.12 mmol) of
3-(2-{[(3S)-1-azabicyclo[2.2.2]oct-3-ylamino]carbonyl}-1-benzofuran-7-yl)-
benzoic acid hydrochloride (Example 153) and 17.1 mg (0.23 mmol) of
n-butylamine are reacted together by general method E. 49.4 mg
(87.5% of theory) of the title compound are obtained.
[1046] The spectroscopic data agree with those of the enantiomeric
compound (Example 156).
EXAMPLE 166
N-[(3S)-1-Azabicyclo[2.2.2]oct-3-yl]-7-{3-[(isobutylamino)carbonyl]phenyl}-
-1-benzofuran-2-carboxamide hydrochloride
##STR00215##
[1048] 50 mg (0.12 mmol) of
3-(2-{[(3S)-1-azabicyclo[2.2.2]oct-3-ylamino]carbonyl}-1-benzofuran-7-yl)-
benzoic acid hydrochloride (Example 153) and 17.1 mg (0.23 mmol) of
iso-butylamine are reacted together by general method E. 40.3 mg
(71.4% of theory) of the title compound are obtained.
[1049] The spectroscopic data agree with those of the enantiomeric
compound (Example 157).
EXAMPLE 167
N-[(3S)-1-Azabicyclo[2.2.2]oct-3-yl]-7-[3-(1-piperidinylcarbonyl)phenyl]-1-
-benzo-furan-2-carboxamide hydrochloride
##STR00216##
[1051] 50 mg (0.12 mmol) of
3-(2-{[(3S)-1-azabicyclo[2.2.4]oct-3-ylamino]carbonyl}-1-benzofuran-7-yl)-
benzoic acid hydrochloride (Example 153) and 20.0 mg (0.23 mmol) of
piperidine are reacted together by general method E. 29.7 mg (49.9%
of theory) of the title compound are obtained.
[1052] The spectroscopic data agree with those of the enantiomeric
compound (Example 158).
EXAMPLE 168
N-[(3S)-1-Azabicyclo[2.2.2]oct-3-yl]-7-[3-({[2-(dimethylamino)ethyl]amino}-
-carbonyl)phenyl]-1-benzofuran-2-carboxamide hydrochloride
##STR00217##
[1054] 50 mg (0.12 mmol) of
3-(2-{[(3S)-1-azabicyclo[2.2.2]oct-3-ylamino]carbonyl}-1-benzofuran-7-yl)-
benzoic acid hydrochloride (Example 153) and 20.7 mg (0.23 mmol) of
N-(2-aminoethyl)-N,N-dimethylamine are reacted together by general
method E. 42.5 mg (64.5% of theory) of the title compound are
obtained.
[1055] The spectroscopic data agree with those of the enantiomeric
compound (Example 159).
EXAMPLE 169
N-[(3S)-1-Azabicyclo[2.2.2]oct-3-yl]-7-(3-{[(3-methoxypropyl)amino]carbony-
l}-phenyl)-1-benzofuran-2-carboxamide hydrochloride
##STR00218##
[1057] 50 mg (0.12 mmol) of
3-(2-{[(3S)-1-azabicyclo[2.2.2]oct-3-ylamino]carbonyl}-1-benzofuran-7-yl)-
benzoic acid hydrochloride (Example 153) and 20.9 mg (0.23 mmol) of
3-methoxypropylamine are reacted together by general method E. 29.8
mg (44.5% of theory) of the title compound are obtained.
[1058] The spectroscopic data agree with those of the enantiomeric
compound (Example 160).
EXAMPLE 170
N-[(3S)-1-Azabicyclo[2.2.2]oct-3-yl]-7-(3-{[(2-methoxyethyl)(methyl)amino]-
-carbonyl}phenyl)-1-benzofuran-2-carboxamide hydrochloride
##STR00219##
[1060] 50 mg (0.12 mmol) of
3-(2-{[(3S)-1-azabicyclo[2.2.2]oct-3-ylamino]carbonyl}-1-benzofuran-7-yl)-
benzoic acid hydrochloride (Example 153) and 20.9 mg (0.23 mmol) of
N-(2-methoxyethyl)-N-methylamine are reacted together by general
method E. 22.1 mg (35.1% of theory) of the title compound are
obtained.
[1061] The spectroscopic data agree with those of the enantiomeric
compound (Example 161).
EXAMPLE 171
N-[(3S)-1-Azabicyclo[2.2.2]oct-3-yl]-7-(3-{[(3-ethoxypropyl)amino]carbonyl-
}-phenyl)-1-benzofuran-2-carboxamide hydrochloride
##STR00220##
[1063] 50 mg (0.12 mmol) of
3-(2-{[(3S)-1-azabicyclo[2.2.2]oct-3-ylamino]carbonyl}-1-benzofuran-7-yl)-
benzoic acid hydrochloride (Example 153) and 24.2 mg (0.23 mmol) of
3-ethoxypropylamine are reacted together by general method E. 23.6
mg (36.9% of theory) of the title compound are obtained.
[1064] The spectroscopic data agree with those of the enantiomeric
compound (Example 162).
EXAMPLE 172
N-[(3S)-1-Azabicyclo[2.2.2]oct-3-yl]-7-{3-[(4-methyl-1-piperazinyl)carbony-
l]-phenyl}-1-benzofuran-2-carboxamide dihydrochloride
##STR00221##
[1066] 50 mg (0.12 mmol) of
3-(2-{[(3S)-1-azabicyclo[2.2.2]oct-3-ylamino]carbonyl}-1-benzofuran-7-yl)-
benzoic acid hydrochloride (Example 153) and 23.5 mg (0.23 mmol) of
N-methylpiperazine are reacted together by general method E. 9.2 mg
(15.4% of theory) of the title compound are obtained.
[1067] The spectroscopic data agree with those of the enantiomeric
compound (Example 163).
EXAMPLE 173
N-[(3R)-1-Azabicyclo[2.2.2]oct-3-yl]-7-[3-(1-pyrrolidinyl)phenyl]-1-benzof-
uran-2-carboxamide hydrochloride
##STR00222##
[1069] 114.3 mg (0.51 mmol) of 1-(3-bromophenyl)pyrrolidine, 148.1
mg (0.58 mmol) of bis(pinacolato)diboron, 124.1 mg (1.26 mmol) of
potassium acetate, 14.2 mg (0.02 mmol) of PdCl.sub.2(dppf), 150 mg
(0.39 mmol) of
N-[(3R)-1-azabicyclo[2.2.2]oct-3-yl]-7-bromo-1-benzofuran-2-carboxamide
hydrochloride (Example 30A), 0.97 ml of 2 M sodium carbonate
solution and a further 14.2 mg (0.02 mmol) of PdCl.sub.2(dppf) in
2.0 ml of DMF are reacted by general method D. Drying under high
vacuum results in 95.6 mg (54.4% of theory) of the title
compound.
[1070] HPLC (method 1): R.sub.t=3.85 min.
[1071] MS (ESIpos): m/z=416 (M+H).sup.+ (free base).
EXAMPLE 174
7-[2-(Aminomethyl)phenyl]-N-[(3S)-1-azabicyclo[2.2.2]oct-3-yl]-1-benzofura-
n-2-carboxamide dihydrochloride
##STR00223##
[1073] 500 mg (1.75 mmol) of tert-butyl 2-bromobenzylcarbamate, 512
mg (2.02 mmol) of bis(pinacolato)diboron, 428.7 mg (4.37 mmol) of
potassium acetate, 49.2 mg (0.07 mmol) of PdCl.sub.2(dppf), 518.4
mg (1.34 mmol) of
N-[(3S)-1-azabicyclo[2.2.2]oct-3-yl]-7-bromo-1-benzofuran-2-carboxamide
hydrochloride (free base: Example 31A), 3.36 ml of 2 M sodium
carbonate solution and a further 49.2 mg (0.07 mmol) of
PdCl.sub.2(dppf) in 5 ml of DMF are reacted by general method D.
The crude product which has been dried under high vacuum is stirred
in 4 ml of a 1:1 mixture of methanol and 4 M hydrogen chloride in
dioxane at room temperature for 2 h. The reaction solution is
concentrated, and the resulting crude product is purified by
preparative HPLC. The product fractions are concentrated and, after
addition of a 3:1 mixture of methanol and 1N hydrochloric acid,
again concentrated and dried under high vacuum. 121.6 mg (22.4% of
theory) of the title compound are obtained.
[1074] The spectroscopic data agree with those of the enantiomeric
compound (Example 152).
EXAMPLE 175
N-[(3R)-1-Azabicyclo[2.2.2]oct-3-yl]-7-(2-({[(methylamino)carbonyl]amino}--
methyl)phenyl]-1-benzofuran-2-carboxamide hydrochloride
##STR00224##
[1076] 62.2 .mu.l (0.45 mmol) of triethylamine and 53 .mu.l (0.89
mmol) of methyl isocyanate are added to a solution of 100 mg (0.22
mmol) of
7-[2-(aminomethyl)phenyl]-N-[(3R)-1-azabicyclo[2.2.2]oct-3-yl]-1-benzofur-
an-2-carboxamide dihydrochloride (Example 152) in 1 ml of a 5:1
mixture of THF and DMF. After 18 h at room temperature, the
reaction mixture is concentrated and purified by preparative HPLC.
The product fractions are concentrated and, after addition of a 3:1
mixture of methanol and 1N hydrochloric acid, again concentrated
and dried under high vacuum. 75 mg (66% of theory) of the title
compound are obtained.
[1077] .sup.1H-NMR (400 MHz, methanol-d.sub.4): .delta.=7.78 (m,
1H), 7.68 (s, 1H), 7.52-7.30 (m, 6H), 4.47 (m, 1H), 4.23 (m, 2H),
3.77 (m, 1H), 3.53-3.25 (m, 5H), 2.69 (s, 3H), 2.37 (m, 1H), 2.20
(m, 1H), 2.08 (m, 2H), 1.88 (m, 1H).
[1078] HPLC (method 1): R.sub.t=3.78 min.
[1079] MS (ESIpos): m/z=433 (M+H).sup.+ (free base)
EXAMPLE 176
[1080]
N-[(3S)-1-Azabicyclo[2.2.2]oct-3-yl]-7-[2-({[(methylamino)carbonyl]-
amino}-methyl)phenyl]-1-benzofuran-2-carboxamide hydrochloride
##STR00225##
[1081] 36 .mu.l (0.26 mmol) of triethylamine and 29.5 .mu.l (0.52
mmol) of methyl isocyanate are added to a solution of 57.9 mg (0.13
mmol) of
7-[2-(aminomethyl)phenyl]-N-[(3S)-1-azabicyclo[2.2.2]oct-3-yl]-1-benzofur-
an-2-carboxamide dihydrochloride (Example 174) in 0.7 ml of a 5:1
mixture of THF and DMF. After. 18 h at room temperature, the
reaction mixture is concentrated and purified by preparative HPLC.
The product fractions are concentrated and, after addition of a 3:1
mixture of methanol and 1N hydrochloric acid, again concentrated
and dried under high vacuum. 49.2 mg (81.2% of theory) of the title
compound are obtained.
[1082] The spectroscopic data agree with those of the enantiomeric
compound (Example 175).
EXAMPLE 177
N-[(3R)-1-Azabicyclo[2.2.2]oct-3-yl]-7-{3-[(2,2-dimethylpropanoyl)amino]ph-
enyl}-1-benzofuran-2-carboxamide hydrochloride
##STR00226##
[1084] 50 mg (0.14 mmol) of
7-(3-aminophenyl)-N-[(3R)-1-azabicyclo[2.2.2]oct-3-yl]-1-benzofuran-2-car-
boxamide (Example 114) and 33.4 mg (0.28 mmol) of pivaloyl chloride
are reacted together by general method F. 15.2 mg (20.7% of theory)
of the title compound are obtained.
[1085] HPLC (method 1): R.sub.t=4.30 min.
[1086] MS (ESIpos): m/z=446 (M+H).sup.+ (free base).
EXAMPLE 178
N-[3-(2-{[(3R)-1-Azabicyclo[2.2.2]oct-3-ylamino]carbonyl}-1-benzofuran-7-y-
l)-phenyl]-5-isoxazolecarboxamide hydrochloride
##STR00227##
[1088] 50 mg (0.14 mmol) of
7-(3-aminophenyl)-N-[(3R)-1-azabicyclo[2.2.2]oct-3-yl]-1-benzofuran-2-car-
boxamide (Example 114) and 36.4 mg (0.28 mmol) of
5-isoxazolecarbonyl chloride are reacted together by general method
F. 39.6 mg (53.3% of theory) of the title compound are
obtained.
[1089] HPLC (method 1): R.sub.t=4.18 min.
[1090] MS (ESIpos): m/z=457 (M+H).sup.+ (free base)
EXAMPLE 179
N-[(3R)-1-Azabicyclo[2.2.2]oct-3-yl]-7-{3-[(cyclopentylcarbonyl)amino]phen-
yl}-1-benzofuran-2-carboxamide hydrochloride
##STR00228##
[1092] 50 mg (0.14 mmol) of
7-(3-aminophenyl)-N-[(3R)-1-azabicyclo[2.2.2]oct-3-yl]-1-benzofuran-2-car-
boxamide (Example 114) and 36.7 mg (0.28 mmol) of
cyclopentanecarbonyl chloride are reacted together by general
method F. 33.2 mg (45.1% of theory) of the title compound are
obtained.
[1093] HPLC (method 1): R.sub.t=4.38 min.
[1094] MS (ESIpos): m/z=458 (M+H).sup.+ (free base).
EXAMPLE 180
N-[(3R)-1-Azabicyclo[2.2.2]oct-3-yl]-7-[3-(isobutyrylamino)phenyl]-1-benzo-
furan-2-carboxamide hydrochloride
##STR00229##
[1096] 50 mg (0.14 mmol) of
7-(3-aminophenyl)-N-[(3R)-1-azabicyclo[2.2.2]oct-3-yl]-1-benzofuran-2-car-
boxamide (Example 114) and 29.5 mg (0.28 mmol) of isobutyryl
chloride are reacted together by general method F. 12.8 mg (19.5%
of theory) of the title compound are obtained.
[1097] HPLC (method 1): R.sub.t=4.19 min.
[1098] MS (ESIpos): m/z=432 (M+H).sup.+ (free base).
EXAMPLE 181
N-[(3R)-1-Azabicyclo[2.2.2]oct-3-yl]-7-[3-(2-furoylamino)phenyl]-1-benzofu-
ran-carboxamide hydrochloride
##STR00230##
[1100] 50 mg (0.14 mmol) of
7-(3-aminophenyl)-N-[(3R)-1-azabicyclo[2.2.2]oct-3-yl]-1-benzofuran-2-car-
boxamide (Example 114) and 36.1 mg (0.28 mmol) of furan-2-carbonyl
chloride are reacted together by general method. F. 7.4 mg (10.6%
of theory) of the title compound are obtained.
[1101] HPLC (method 1): R.sub.t=4.27 min.
[1102] MS (ESIpos): m/z=456 (M+H).sup.+ (free base)
EXAMPLE 182
N-[(3R)-1-Azabicyclo[2.2.2]oct-3-yl]-7-(2-methoxyphenyl)-1-benzofuran-2-ca-
rboxamide acetate
##STR00231##
[1104] 95.9 mg (0.25 mmol) of
N-[(3R)-1-azabicyclo[2.2.2]oct-3-yl]-7-(2-methoxyphenyl)-1-benzofuran-2-c-
arboxamide (Example 130) are dissolved in 2 ml of methanol. After
addition of 15.3 mg (0.25 mmol) of acetic acid, the mixture is
concentrated and the residue is dried under high vacuum. 114.9 mg
(99.7% of theory) of the title compound are obtained.
[1105] .sup.1H-NMR (200 MHz, DMSO-d.sub.6): .delta.=8.37 (d, 1H),
7.74 (dd, 1H), 7.71 (s, 1H), 7.50-7.33 (m, 4H), 7.20 (d, 1H), 7.08
(m, 1H), 3.93 (m, 1H), 3.76 (s, 3H), 3.10 (m, 1H), 2.87 (m, 1H),
2.78-2.60 (m, 4H), 1.90 (s, 3H), 1.87 (m, 1H), 1.75 (m, 1H), 1.58
(m, 2H), 1.33 (m, 1H).
EXAMPLE 183
N-[(3R)-1-Azabicyclo[2.2.2]oct-3-yl]-7-(2-methoxyphenyl)-1-benzofuran-2-ca-
rboxamide tosylate
##STR00232##
[1107] 95.9 mg (0.25 mmol) of
N-[(3R)-1-azabicyclo[2.2.2]oct-3-yl]-7-(2-methoxyphenyl)-1-benzofuran-2-c-
arboxamide (Example 130) are dissolved in 2 ml of methanol. After
addition of 49.2 mg (0.25 mmol) of p-toluenesulphonic acid, the
mixture is concentrated and the residue is dried under high vacuum.
143 mg (99.4% of theory) of the title compound are obtained.
[1108] .sup.1H-NMR (200 MHz, DMSO-d.sub.6): .delta.=9.34 (br. s,
1H), 8.70 (d, 1H), 737 (dd, 1H), 7.72 (s, 1H), 7:52-7.35 (m, 6H),
7.21 (d, 1H), 7.15-7.04 (m, 3H), 4.30 (m, 1H), 3.76 (s, 3H), 3.68
(m, 1H), 3.33-3.11 (m, 5H), 2.29 (s, 3H), 2.19 (m, 1H), 2.07 (m,
1H), 1.91 (m, 2H), 1.74 (m, 1H).
EXAMPLE 184
N-[(3R)-1-Azabicyclo[2.2.2]oct-3-yl]-7-(2-methoxyphenyl)-1-benzofuran-2-ca-
rboxamide fumarate
##STR00233##
[1110] 95.9 mg (0.25 mmol) of
N-[(3R)-1-azabicyclo[2.2.2]oct-3-yl]-7-(2-methoxyphenyl)-1-benzofuran-2-c-
arboxamide (Example 130) are dissolved in 1.5 ml of acetone. After
addition of 29.6 mg (0.25 mmol) of fumaric acid in 1 ml of hot
isopropanol, the mixture is stirred at 50.degree. C. for 30 min and
then concentrated, and the residue is dried under high vacuum.
124.2 mg (99% of theory) of the title compound are obtained.
[1111] .sup.1H-NMR (200 MHz, DMSO-d.sub.6): .delta.=8.62 (d, 1H),
7.76 (dd, 1H), 7.72 (s, 1H), 7.49-7.33 (m, 4H), 7.21 (d, 1H), 7.09
(m, 1H), 6.50 (s, 2H), 4.16 (m, 1H), 3.76 (s, 3H), 3.38 (m, 1H),
3.11 (m, 1H), 3.06-2.85 (m, 4H), 2.03 (m, 1H), 1.92 (m, 1H), 1.76
(m, 2H), 1.56 (m, 1H).
EXAMPLE 185
N-[(3R)-1-Azabicyclo[2.2.2]oct-3-yl]-7-(2-methoxyphenyl)-1-benzofuran-2-ca-
rboxamide oxalate
##STR00234##
[1113] 95.9 mg (0.25 mmol) of
N-[(3R)-1-azabicyclo[2.2.2]oct-3-yl]-7-(2-methoxyphenyl)-1-benzofuran-2-c-
arboxamide (Example 130) are dissolved in 1.5 ml of acetone. After
addition of 22.9 mg (0.25 mmol) of oxalic acid in 1 ml of hot
isopropanol, the mixture is stirred at 50.degree. C. for 30 min and
then concentrated, and the residue is dried under high vacuum.
117.6 mg (99% of theory) of the title compound are obtained.
[1114] .sup.1H-NMR (200 MHz, DMSO-d.sub.6): .delta.=8.75 (d, 1H),
7.77 (dd, 1H), 7.72 (s, 1H), 7.50-7.33 (m, 4H), 7.20 (d, 1H), 7.09
(m, 1H), 4.28 (m, 1H), 3.75 (s, 3H), 3.62 (m, 1H), 3.32-3.08 (m,
5H), 2.17 (m, 1H), 2.04 (m, 1H), 1.89 (m, 2H), 1.71 (m, 1H).
EXAMPLE 186
N-[(3R)-1-Azabicyclo[2.2.2]oct-3-yl]-7-(2-hydroxyphenyl)-1-benzofuran-2-ca-
rboxamide
##STR00235##
[1116] 2.42 ml of a 1 M boron tribromide solution in
dichloromethane are added dropwise to a suspenion, cooled to
-20.degree. C., of 200 mg (0.48 mmol) of
N-[(3R)-1-azabicyclo[2.2.2]oct-3-yl]-7-(2-methoxyphenyl)-1-benzo-
furan-2-carboxamide hydro-chloride (Example 102) in 8 ml of
dichloromethane. After 2 h, the reaction is stopped by adding
diethyl ether. The mixture is stirred at room temperature for 30
min and, after addition of water, neutralized with 1N sodium
hydroxide solution. After extraction with ethyl acetate, the
organic phases are combined and dried over sodium sulphate.
Concentration and drying under high vacuum result in 125.9 mg
(71.7% of theory) of the title compound.
[1117] HPLC (method 1): R.sub.t=3.84 min.
[1118] MS (ESIpos): m/z=363 (M+H).sup.+.
EXAMPLE 187
(3R)-3-({[7-(2-Methoxyphenyl)-1-benzofuran-2-yl]carbonyl}amino)-1-methyl-1-
-azoniabicyclo[2.2.2]octane chloride
##STR00236##
[1120] 60.5 mg (1.51 mmol) of sodium hydride (60% suspension in
mineral oil) are added to a solution, cooled to -20.degree. C., of
250 mg (0.61 mmol) of
N-[(3R)-1-azabicyclo[2.2.2]oct-3-yl]-7-(2-methoxyphenyl)-1-benzo-
furan-2-carboxamide hydro-chloride (Example 102) in 2.5 ml of DMF.
After 30 min at room temperature and renewed cooling to -20.degree.
C., 33.9 .mu.l (0.54 mmol) of iodomethane are added. After 18 h at
room temperature, the reaction is stopped by adding water. The
reaction mixture is purified by preparative HPLC. The product
fractions are concentrated, codistilled with 1N hydrochloric acid,
again concentrated and dried under high vacuum. 206 mg (79.7% of
theory) of the title compound are obtained.
[1121] .sup.1H-NMR (200 MHz, DMSO-d.sub.6): .delta.=9.23 (d, 1H),
8.02 (s, 1H), 7.77 (d, 1H), 7.46 (dd, 1H), 7.39 (m, 3H), 7.20 (d,
1H), 7.09 (dd, 1H), 4.32 (m, 1H), 3.83 (m, 1H), 3.75 (s, 3H), 3.63
(m, 1H), 3.49-3.33 (m, 4H), 2.96 (s, 3H), 2.27 (m, 1H), 2.20 (m,
1H), 1.97 (m, 2H), 1.83 (m, 1H).
[1122] HPLC (method 1): R.sub.t=4.19 min.
[1123] MS (ESIpos): m/z=391 (M+H).sup.+.
EXAMPLE 188
(3R)-1-Benzyl-3-({[7-(2-methoxyphenyl)-1-benzofuran-2-yl]carbonyl}amino)-1-
-azoniabicyclo[2.2.2]octane bromide
##STR00237##
[1125] 288 .mu.l (2.42 mmol) of benzyl bromide and 502 mg (3.63
mmol) of potassium carbonate are added to a solution of 500 mg
(1.21 mmol) of
N-[(3R)-1-azabicyclo[2.2.2]oct-3-yl]-7-(2-methoxyphenyl)-1-benzofuran-2-c-
arboxamide hydrochloride (Example 102) in 12.5 ml of DMF. After 20
h at 50.degree. C., the reaction mixture is purified by preparative
HPLC. The product fractions are concentrated and, after addition of
50% strength hydrobromic acid, again concentrated and dried under
high vacuum. Recrystallization from cyclohexane/acetone affords 537
mg (77% of theory) of the title compound.
[1126] HPLC (method 1): R.sub.t=4.44 min.
[1127] MS (ESIpos): m/z=467 (M+H).sup.+.
EXAMPLE 189
(3R)-3-[{[7-(2-Methoxyphenyl)-1-benzofuran-2-yl]carbonyl}(methyl)amino]-1--
methyl-1-azoniabicyclo[2.2.2]octane chloride
##STR00238##
[1129] 84.8 mg (2.12 mmol) of sodium hydride (60% suspension in
mineral oil) are added to a solution, cooled to -20.degree. C., of
250 mg (0.61 mmol) of
N-[(3R)-1-azabicyclo[2.2.2]oct-3-yl]-7-(2-methoxyphenyl)-1-benzo-
furan-2-carboxamide hydro chloride (Example 102) in 2.5 ml of DMF.
After 30 min at room temperature and renewed cooling to -20.degree.
C., 94.2 .mu.l (1.51 mmol) of iodomethane are added. After 18 h at
room temperature, the reaction is stopped by adding water. The
reaction mixture is purified by preparative HPLC. The product
fractions are concentrated, codistilled with a 1:1 mixture of
methanol and 4 M hydrogen chloride in dioxane, again concentrated
and dried under high vacuum. 58 mg (21.7% of theory) of the title
compound are obtained.
[1130] HPLC (method 1): R.sub.t=4.17 min.
[1131] MS (ESIpos): m/z=405 (M+H).sup.+.
EXAMPLE 190
7-(2-Methoxyphenyl)-N-[(3R)-1-oxido-1-azabicyclo[2.2.2]oct-3-yl]-1-benzofu-
ran-2-carboxamide
##STR00239##
[1133] 35.8 .mu.l (0.35 mmol) of 30% strength hydrogen peroxide are
added to a solution, cooled to 0.degree. C., of 110 mg (0.29 mmol)
of
N-[(3R)-1-azabicyclo[2.2.2]oct-3-yl]-7-(2-methoxyphenyl)-1-benzofuran-2-c-
arboxamide (Example 130) in 2 ml of methanol. After 18 h at room
temperature, a further 35.8 .mu.l (0.35 mmol) of 30% strength
hydrogen peroxide are added. After a further 18 h at room
temperature, the reaction solution is concentrated, and the residue
is dried under high vacuum. 111.5 mg (97.2% of theory) of the title
compound are obtained.
[1134] .sup.1H-NMR (400 MHz, methanol-d.sub.4): .delta.=7.69 (d,
1H), 7.59 (s, 1H), 7.41 (m, 3H), 7.37 (dd, 1H), 7.16 (d, 1H), 7.08
(dd, 1H), 4.57 (m, 1H), 3.78 (s, 3H), 3.75 (m, 1H), 3.43-3.30 (m,
5H), 2.22 (m, 2H), 2.13 (m, 2H), 1.99 (m, 1H).
[1135] HPLC (method 1): R.sub.t=4.18 min.
[1136] MS (ESIpos): m/z=393 (M+H).sup.+.
EXAMPLE 191
[1137]
N-[(3R)-1-Azabicyclo[2.2.2]oct-3-yl]-6-[3-(4-morpholinylmethyl)phen-
yl]-1-benzo-thiophene-2-carboxamide dihydrochloride
##STR00240##
[1138] 290 mg (3.32 mmol) of morpholine and 31 mg (0.50 mmol) of
sodium cyanoborohydride are successively added to a solution of 80
mg (0.17 mmol) of
N-[(3R)-1-azabicyclo[2.2.2]oct-3-yl]-6-(3-formyl-phenyl)-1-benzo-
thiophene-2-carboxamide hydrochloride (Example 33A) in 1.0 ml of a
6:1 mixture of methanol and acetic acid. After 18 h at 80.degree.
C., purification is carried out by preparative HPLC. The product
fractions are concentrated and, after addition of a 5:1 mixture of
methanol and 1N hydrochloric acid, again concentrated: Drying under
high vacuum results in 47 mg (49.8% of theory) of the title
compound.
[1139] HPLC (method 1): R.sub.t=3.64 min.
[1140] MS (ESIpos): m/z=462 (M+H).sup.+ (free base)
EXAMPLE 192
7-(5-Acetyl-2-thienyl)-N-[(3R)-1-azabicyclo[2.2.2]oct-3-yl]-1-benzofuran-2-
-carboxamide hydrochloride
##STR00241##
[1142] 0.58 ml of 2 M aqueous sodium carbonate solution and 15.9 mg
(0.02 mmol) of PdCl.sub.2(dppf) are added to a mixture of 150 mg
(0.39 mmol) of
N-[(3R)-1-azabicyclo[2.2.2]oct-3-yl]-7-bromo-1-benzofuran-2-carboxamide
hydrochloride (Example 30A) and 66.1 mg (0.39 mmol) of
5-acetyl-2-thienylboronic acid in 2 ml of DMF. The reaction mixture
is heated at 70.degree. C. for 18 h and then filtered through
kieselguhr and evaporated to dryness. Purification of the crude
product by preparative HPLC, subsequent addition of a 1:1 mixture
of methanol and 1N hydrochloric acid, concentration and drying
under high vacuum result in 83.6 mg (49.9% of theory) of the title
compound.
[1143] .sup.1H-NMR (400 MHz, DMSO-d.sub.6): .delta.=10.29 (br. s,
1H), 9.10 (d, 1H), 8.07 (m, 2H), 7.95 (m, 1H), 7.93 (d, 1H), 7.87
(d, 1H), 7.46 (dd, 1H), 4.38 (m, 1H), 3.63 (m, 1H), 3.40 (m, 2H),
3.23 (m, 3H), 2.60 (s, 3H), 2.27 (m, 1H), 2.16 (m, 1H), 1.94 (m,
2H), 1.77 (m, 1H).
[1144] HPLC (method 1): R.sub.t=3.99 min.
[1145] MS (ESIpos): m/z=495 (M+H).sup.+ (free base)
* * * * *