RU2450003C2 - Индазолы, бензотиазолы, бензоизотиазолы, бензоизоксазолы, пиразолопиридины, изотиазолопиридины, их получение и их применение - Google Patents
Индазолы, бензотиазолы, бензоизотиазолы, бензоизоксазолы, пиразолопиридины, изотиазолопиридины, их получение и их применение Download PDFInfo
- Publication number
- RU2450003C2 RU2450003C2 RU2008115268/04A RU2008115268A RU2450003C2 RU 2450003 C2 RU2450003 C2 RU 2450003C2 RU 2008115268/04 A RU2008115268/04 A RU 2008115268/04A RU 2008115268 A RU2008115268 A RU 2008115268A RU 2450003 C2 RU2450003 C2 RU 2450003C2
- Authority
- RU
- Russia
- Prior art keywords
- oct
- azabicyclo
- carboxamide
- benzisothiazole
- carbon atoms
- Prior art date
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- CSNIZNHTOVFARY-UHFFFAOYSA-N 1,2-benzothiazole Chemical class C1=CC=C2C=NSC2=C1 CSNIZNHTOVFARY-UHFFFAOYSA-N 0.000 title 1
- KTZQTRPPVKQPFO-UHFFFAOYSA-N 1,2-benzoxazole Chemical class C1=CC=C2C=NOC2=C1 KTZQTRPPVKQPFO-UHFFFAOYSA-N 0.000 title 1
- YJMPFOXUBAJFFA-UHFFFAOYSA-N [1,2]thiazolo[4,3-b]pyridine Chemical class C1=CC=NC2=CSN=C21 YJMPFOXUBAJFFA-UHFFFAOYSA-N 0.000 title 1
- IOJUPLGTWVMSFF-UHFFFAOYSA-N benzothiazole Chemical class C1=CC=C2SC=NC2=C1 IOJUPLGTWVMSFF-UHFFFAOYSA-N 0.000 title 1
- 150000002473 indoazoles Chemical class 0.000 title 1
- 150000005229 pyrazolopyridines Chemical class 0.000 title 1
- 125000004432 carbon atom Chemical group C* 0.000 claims abstract 170
- 150000001875 compounds Chemical class 0.000 claims abstract 116
- 125000000217 alkyl group Chemical group 0.000 claims abstract 71
- 150000003839 salts Chemical class 0.000 claims abstract 60
- 125000003545 alkoxy group Chemical group 0.000 claims abstract 36
- 239000012453 solvate Substances 0.000 claims abstract 30
- 150000001204 N-oxides Chemical class 0.000 claims abstract 24
- 239000000203 mixture Substances 0.000 claims abstract 24
- 125000001316 cycloalkyl alkyl group Chemical group 0.000 claims abstract 21
- 125000000753 cycloalkyl group Chemical group 0.000 claims abstract 20
- 239000003814 drug Substances 0.000 claims abstract 18
- 229920006395 saturated elastomer Polymers 0.000 claims abstract 16
- 125000004433 nitrogen atom Chemical group N* 0.000 claims abstract 13
- 125000000000 cycloalkoxy group Chemical group 0.000 claims abstract 12
- 229910052760 oxygen Inorganic materials 0.000 claims abstract 8
- 102000019315 Nicotinic acetylcholine receptors Human genes 0.000 claims abstract 7
- 108050006807 Nicotinic acetylcholine receptors Proteins 0.000 claims abstract 7
- 125000004430 oxygen atom Chemical group O* 0.000 claims abstract 7
- 125000004434 sulfur atom Chemical group 0.000 claims abstract 7
- 125000002947 alkylene group Chemical group 0.000 claims abstract 6
- 125000003118 aryl group Chemical group 0.000 claims abstract 6
- 125000000623 heterocyclic group Chemical group 0.000 claims abstract 6
- LLSRLLPHUVVLQJ-UHFFFAOYSA-N 1-cycloheptyldiazepane Chemical group C1CCCCCC1N1NCCCCC1 LLSRLLPHUVVLQJ-UHFFFAOYSA-N 0.000 claims abstract 5
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 claims abstract 5
- 230000004913 activation Effects 0.000 claims abstract 4
- 238000000034 method Methods 0.000 claims abstract 4
- 125000003226 pyrazolyl group Chemical group 0.000 claims abstract 4
- GGTBELZDHKHESR-UHFFFAOYSA-N 2-cycloheptyloxazepane Chemical group C1CCCCCC1N1OCCCCC1 GGTBELZDHKHESR-UHFFFAOYSA-N 0.000 claims abstract 3
- 230000000694 effects Effects 0.000 claims abstract 3
- 230000000638 stimulation Effects 0.000 claims abstract 3
- PPNCOQHHSGMKGI-UHFFFAOYSA-N 1-cyclononyldiazonane Chemical group C1CCCCCCCC1N1NCCCCCCC1 PPNCOQHHSGMKGI-UHFFFAOYSA-N 0.000 claims abstract 2
- NFDXQGNDWIPXQL-UHFFFAOYSA-N 1-cyclooctyldiazocane Chemical group C1CCCCCCC1N1NCCCCCC1 NFDXQGNDWIPXQL-UHFFFAOYSA-N 0.000 claims abstract 2
- 125000005047 dihydroimidazolyl group Chemical group N1(CNC=C1)* 0.000 claims abstract 2
- 229940079593 drug Drugs 0.000 claims abstract 2
- 239000008194 pharmaceutical composition Substances 0.000 claims abstract 2
- -1 hexahydropyrrolopyrazinyl Chemical group 0.000 claims 24
- 239000012458 free base Substances 0.000 claims 18
- 125000004429 atom Chemical group 0.000 claims 16
- 238000004519 manufacturing process Methods 0.000 claims 15
- 238000011282 treatment Methods 0.000 claims 15
- 239000002585 base Substances 0.000 claims 12
- HBAQYPYDRFILMT-UHFFFAOYSA-N 8-[3-(1-cyclopropylpyrazol-4-yl)-1H-pyrazolo[4,3-d]pyrimidin-5-yl]-3-methyl-3,8-diazabicyclo[3.2.1]octan-2-one Chemical class C1(CC1)N1N=CC(=C1)C1=NNC2=C1N=C(N=C2)N1C2C(N(CC1CC2)C)=O HBAQYPYDRFILMT-UHFFFAOYSA-N 0.000 claims 11
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 claims 9
- 125000005112 cycloalkylalkoxy group Chemical group 0.000 claims 7
- 206010012289 Dementia Diseases 0.000 claims 6
- 125000004183 alkoxy alkyl group Chemical group 0.000 claims 6
- 208000010877 cognitive disease Diseases 0.000 claims 6
- 125000004663 dialkyl amino group Chemical group 0.000 claims 6
- BDAGIHXWWSANSR-UHFFFAOYSA-M Formate Chemical compound [O-]C=O BDAGIHXWWSANSR-UHFFFAOYSA-M 0.000 claims 5
- 208000026139 Memory disease Diseases 0.000 claims 5
- 201000010099 disease Diseases 0.000 claims 5
- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 claims 5
- 206010027175 memory impairment Diseases 0.000 claims 5
- 208000000044 Amnesia Diseases 0.000 claims 4
- WQLZMRXMTRRRQR-IBGZPJMESA-N n-[(3r)-1-azabicyclo[2.2.2]octan-3-yl]-n-methyl-6-(oxan-4-yl)-1h-indazole-3-carboxamide Chemical compound CN([C@@H]1C2CCN(CC2)C1)C(=O)C(C1=CC=2)=NNC1=CC=2C1CCOCC1 WQLZMRXMTRRRQR-IBGZPJMESA-N 0.000 claims 4
- LJEXBQWZLZFSSN-OAHLLOKOSA-N n-[(3s)-1-azabicyclo[2.2.2]octan-3-yl]-1-ethyl-6-methoxyindazole-3-carboxamide Chemical compound C12=CC=C(OC)C=C2N(CC)N=C1C(=O)N[C@H]1C(CC2)CCN2C1 LJEXBQWZLZFSSN-OAHLLOKOSA-N 0.000 claims 4
- 238000011321 prophylaxis Methods 0.000 claims 4
- 125000001424 substituent group Chemical group 0.000 claims 4
- 208000024827 Alzheimer disease Diseases 0.000 claims 3
- 208000028698 Cognitive impairment Diseases 0.000 claims 3
- JLIHVNUIYBYZPX-LLVKDONJSA-N N-[(3S)-1-azabicyclo[2.2.2]octan-3-yl]-4-hydroxy-1H-indazole-3-carboxamide Chemical compound C1N(CC2)CCC2[C@@H]1NC(=O)C1=NNC2=C1C(O)=CC=C2 JLIHVNUIYBYZPX-LLVKDONJSA-N 0.000 claims 3
- ACFJWUDIYCFUQS-SNVBAGLBSA-N N-[(3S)-1-azabicyclo[2.2.2]octan-3-yl]-5,7-dibromo-4-hydroxy-2H-indazole-3-carboxamide Chemical compound C1N(CC2)CCC2[C@@H]1NC(=O)C1=NNC2=C1C(O)=C(Br)C=C2Br ACFJWUDIYCFUQS-SNVBAGLBSA-N 0.000 claims 3
- VVFPTCPKNDXWBF-LLVKDONJSA-N N-[(3S)-1-azabicyclo[2.2.2]octan-3-yl]-5-bromo-4-hydroxy-1H-indazole-3-carboxamide Chemical compound C1N(CC2)CCC2[C@@H]1NC(=O)C1=NNC2=C1C(O)=C(Br)C=C2 VVFPTCPKNDXWBF-LLVKDONJSA-N 0.000 claims 3
- GLTWIURZTPMBTA-GFCCVEGCSA-N N-[(3S)-1-azabicyclo[2.2.2]octan-3-yl]-6-hydroxy-1,2-benzothiazole-3-carboxamide Chemical compound C1N(CC2)CCC2[C@@H]1NC(=O)C1=NSC2=CC(O)=CC=C21 GLTWIURZTPMBTA-GFCCVEGCSA-N 0.000 claims 3
- 230000006984 memory degeneration Effects 0.000 claims 3
- 208000023060 memory loss Diseases 0.000 claims 3
- 208000027061 mild cognitive impairment Diseases 0.000 claims 3
- NBLLSKMFNOYWGA-AWEZNQCLSA-N n-[(3r)-1-azabicyclo[2.2.2]octan-3-yl]-5-(difluoromethoxy)-n-methyl-1h-indazole-3-carboxamide Chemical compound C1=C(OC(F)F)C=C2C(C(=O)N([C@@H]3C4CCN(CC4)C3)C)=NNC2=C1 NBLLSKMFNOYWGA-AWEZNQCLSA-N 0.000 claims 3
- CDIIRPQKBBSHHC-HNNXBMFYSA-N n-[(3r)-1-azabicyclo[2.2.2]octan-3-yl]-5-methoxy-n-methyl-1h-indazole-3-carboxamide Chemical compound C1N(CC2)CCC2[C@H]1N(C)C(=O)C1=NNC2=CC=C(OC)C=C21 CDIIRPQKBBSHHC-HNNXBMFYSA-N 0.000 claims 3
- DOUKNGQHWNTBGW-BJLQDIEVSA-N n-[(3r)-1-azabicyclo[2.2.2]octan-3-yl]-6-[(1s,4s)-5-cyclopropyl-2,5-diazabicyclo[2.2.1]heptan-2-yl]-1,2-benzothiazole-3-carboxamide Chemical compound C([C@]1(N(C=2C=C3SN=C(C3=CC=2)C(=O)N[C@@H]2C3CCN(CC3)C2)C[C@@]2(C1)[H])[H])N2C1CC1 DOUKNGQHWNTBGW-BJLQDIEVSA-N 0.000 claims 3
- NCJUWMDMIHBGSN-AWEZNQCLSA-N n-[(3r)-1-azabicyclo[2.2.2]octan-3-yl]-6-methoxy-n-methyl-1,2-benzothiazole-3-carboxamide Chemical compound C1N(CC2)CCC2[C@H]1N(C)C(=O)C1=NSC2=CC(OC)=CC=C21 NCJUWMDMIHBGSN-AWEZNQCLSA-N 0.000 claims 3
- YLWNWPRABKNCGA-CQSZACIVSA-N n-[(3s)-1-azabicyclo[2.2.2]octan-3-yl]-1-(difluoromethyl)-6-(1,3-thiazol-2-yl)indazole-3-carboxamide Chemical compound C1=C2N(C(F)F)N=C(C(=O)N[C@H]3C4CCN(CC4)C3)C2=CC=C1C1=NC=CS1 YLWNWPRABKNCGA-CQSZACIVSA-N 0.000 claims 3
- VQDFGMVDXFKJGX-CYBMUJFWSA-N n-[(3s)-1-azabicyclo[2.2.2]octan-3-yl]-1-(difluoromethyl)-6-methoxyindazole-3-carboxamide Chemical compound C1N(CC2)CCC2[C@@H]1NC(=O)C1=NN(C(F)F)C2=CC(OC)=CC=C21 VQDFGMVDXFKJGX-CYBMUJFWSA-N 0.000 claims 3
- OMIAFJAGVHVDCS-QGZVFWFLSA-N n-[(3s)-1-azabicyclo[2.2.2]octan-3-yl]-1-cyclopropyl-6-(1,3-thiazol-2-yl)indazole-3-carboxamide Chemical compound N([C@H]1C2CCN(CC2)C1)C(=O)C(C1=CC=C(C=C11)C=2SC=CN=2)=NN1C1CC1 OMIAFJAGVHVDCS-QGZVFWFLSA-N 0.000 claims 3
- MMPSJJWTNKNLSB-QGZVFWFLSA-N n-[(3s)-1-azabicyclo[2.2.2]octan-3-yl]-1-ethyl-6-(2-oxopyrrolidin-1-yl)indazole-3-carboxamide Chemical compound C1=C2N(CC)N=C(C(=O)N[C@H]3C4CCN(CC4)C3)C2=CC=C1N1CCCC1=O MMPSJJWTNKNLSB-QGZVFWFLSA-N 0.000 claims 3
- AVAQAIXJHLFBQM-MRXNPFEDSA-N n-[(3s)-1-azabicyclo[2.2.2]octan-3-yl]-1-methyl-6-(propylcarbamoylamino)indazole-3-carboxamide Chemical compound C1N(CC2)CCC2[C@@H]1NC(=O)C1=NN(C)C2=CC(NC(=O)NCCC)=CC=C21 AVAQAIXJHLFBQM-MRXNPFEDSA-N 0.000 claims 3
- IKXVBFQRYVFHDF-QGZVFWFLSA-N n-[(3s)-1-azabicyclo[2.2.2]octan-3-yl]-1-propan-2-yl-6-(1,3-thiazol-2-yl)indazole-3-carboxamide Chemical compound C1=C2N(C(C)C)N=C(C(=O)N[C@H]3C4CCN(CC4)C3)C2=CC=C1C1=NC=CS1 IKXVBFQRYVFHDF-QGZVFWFLSA-N 0.000 claims 3
- KALULFQIHKKFCX-CYBMUJFWSA-N n-[(3s)-1-azabicyclo[2.2.2]octan-3-yl]-5,6-dimethoxy-1h-indazole-3-carboxamide Chemical compound C1N(CC2)CCC2[C@@H]1NC(=O)C1=NNC2=C1C=C(OC)C(OC)=C2 KALULFQIHKKFCX-CYBMUJFWSA-N 0.000 claims 3
- NBLLSKMFNOYWGA-CQSZACIVSA-N n-[(3s)-1-azabicyclo[2.2.2]octan-3-yl]-5-(difluoromethoxy)-n-methyl-1h-indazole-3-carboxamide Chemical compound C1=C(OC(F)F)C=C2C(C(=O)N([C@H]3C4CCN(CC4)C3)C)=NNC2=C1 NBLLSKMFNOYWGA-CQSZACIVSA-N 0.000 claims 3
- JXJCOTSOYYIMTK-GFCCVEGCSA-N n-[(3s)-1-azabicyclo[2.2.2]octan-3-yl]-5-hydroxy-1,2-benzothiazole-3-carboxamide Chemical compound C1N(CC2)CCC2[C@@H]1NC(=O)C1=NSC2=CC=C(O)C=C21 JXJCOTSOYYIMTK-GFCCVEGCSA-N 0.000 claims 3
- CDIIRPQKBBSHHC-OAHLLOKOSA-N n-[(3s)-1-azabicyclo[2.2.2]octan-3-yl]-5-methoxy-n-methyl-1h-indazole-3-carboxamide Chemical compound C1N(CC2)CCC2[C@@H]1N(C)C(=O)C1=NNC2=CC=C(OC)C=C21 CDIIRPQKBBSHHC-OAHLLOKOSA-N 0.000 claims 3
- MRWSLRJLSYNXEP-QGZVFWFLSA-N n-[(3s)-1-azabicyclo[2.2.2]octan-3-yl]-6-(1,3-oxazol-2-yl)-1-propylindazole-3-carboxamide Chemical compound C1=C2N(CCC)N=C(C(=O)N[C@H]3C4CCN(CC4)C3)C2=CC=C1C1=NC=CO1 MRWSLRJLSYNXEP-QGZVFWFLSA-N 0.000 claims 3
- KJGZTJYVDPCJFK-KPMSDPLLSA-N n-[(3s)-1-azabicyclo[2.2.2]octan-3-yl]-6-(1-methylpyrrolidin-3-yl)oxy-1h-indazole-3-carboxamide Chemical compound C1N(C)CCC1OC1=CC=C(C(=NN2)C(=O)N[C@H]3C4CCN(CC4)C3)C2=C1 KJGZTJYVDPCJFK-KPMSDPLLSA-N 0.000 claims 3
- QANNTZCRFNSNGO-OMOCHNIRSA-N n-[(3s)-1-azabicyclo[2.2.2]octan-3-yl]-6-(3-methoxypyrrolidin-1-yl)-1,2-benzothiazole-3-carboxamide Chemical compound C1C(OC)CCN1C1=CC=C(C(=NS2)C(=O)N[C@H]3C4CCN(CC4)C3)C2=C1 QANNTZCRFNSNGO-OMOCHNIRSA-N 0.000 claims 3
- INXSFZUBPUKBAA-PKESZJFOSA-N n-[(3s)-1-azabicyclo[2.2.2]octan-3-yl]-6-(3-methoxypyrrolidin-1-yl)-1,2-benzothiazole-3-carboxamide;hydrochloride Chemical compound Cl.C1C(OC)CCN1C1=CC=C(C(=NS2)C(=O)N[C@H]3C4CCN(CC4)C3)C2=C1 INXSFZUBPUKBAA-PKESZJFOSA-N 0.000 claims 3
- IPCWFOOYKSCSLS-OAHLLOKOSA-N n-[(3s)-1-azabicyclo[2.2.2]octan-3-yl]-6-(cyclopropanecarbonylamino)-1-(difluoromethyl)indazole-3-carboxamide Chemical compound C1=C2N(C(F)F)N=C(C(=O)N[C@H]3C4CCN(CC4)C3)C2=CC=C1NC(=O)C1CC1 IPCWFOOYKSCSLS-OAHLLOKOSA-N 0.000 claims 3
- VNYHRDSBGYDAQL-GOSISDBHSA-N n-[(3s)-1-azabicyclo[2.2.2]octan-3-yl]-6-(cyclopropanecarbonylamino)-1-cyclopropylindazole-3-carboxamide Chemical compound C1CC1C(=O)NC(C=C12)=CC=C1C(C(=O)N[C@H]1C3CCN(CC3)C1)=NN2C1CC1 VNYHRDSBGYDAQL-GOSISDBHSA-N 0.000 claims 3
- FJAYSNIBBGLVJG-MRXNPFEDSA-N n-[(3s)-1-azabicyclo[2.2.2]octan-3-yl]-6-(cyclopropanecarbonylamino)-1-methylindazole-3-carboxamide Chemical compound C1=C2N(C)N=C(C(=O)N[C@H]3C4CCN(CC4)C3)C2=CC=C1NC(=O)C1CC1 FJAYSNIBBGLVJG-MRXNPFEDSA-N 0.000 claims 3
- MKPGOIZSZGGKGK-CQSZACIVSA-N n-[(3s)-1-azabicyclo[2.2.2]octan-3-yl]-6-(difluoromethoxy)-n-methyl-1h-indazole-3-carboxamide Chemical compound FC(F)OC1=CC=C2C(C(=O)N([C@H]3C4CCN(CC4)C3)C)=NNC2=C1 MKPGOIZSZGGKGK-CQSZACIVSA-N 0.000 claims 3
- LJRMDUSLDCDSLB-QGZVFWFLSA-N n-[(3s)-1-azabicyclo[2.2.2]octan-3-yl]-6-(furan-3-ylmethoxy)-1,2-benzothiazole-3-carboxamide Chemical compound N([C@H]1C2CCN(CC2)C1)C(=O)C(C1=CC=2)=NSC1=CC=2OCC=1C=COC=1 LJRMDUSLDCDSLB-QGZVFWFLSA-N 0.000 claims 3
- MVRLDKKOIUWTMJ-GOSISDBHSA-N n-[(3s)-1-azabicyclo[2.2.2]octan-3-yl]-6-(oxan-4-yloxy)-1h-indazole-3-carboxamide Chemical compound N([C@H]1C2CCN(CC2)C1)C(=O)C(C1=CC=2)=NNC1=CC=2OC1CCOCC1 MVRLDKKOIUWTMJ-GOSISDBHSA-N 0.000 claims 3
- RTYNUJYXOCMKNQ-FBMWCMRBSA-N n-[(3s)-1-azabicyclo[2.2.2]octan-3-yl]-6-(oxolan-3-yloxy)-1h-indazole-3-carboxamide Chemical compound N([C@H]1C2CCN(CC2)C1)C(=O)C(C1=CC=2)=NNC1=CC=2OC1CCOC1 RTYNUJYXOCMKNQ-FBMWCMRBSA-N 0.000 claims 3
- QANNTZCRFNSNGO-NVXWUHKLSA-N n-[(3s)-1-azabicyclo[2.2.2]octan-3-yl]-6-[(3r)-3-methoxypyrrolidin-1-yl]-1,2-benzothiazole-3-carboxamide Chemical compound C1[C@H](OC)CCN1C1=CC=C(C(=NS2)C(=O)N[C@H]3C4CCN(CC4)C3)C2=C1 QANNTZCRFNSNGO-NVXWUHKLSA-N 0.000 claims 3
- QKJMBWFYXTZCSM-BZSJEYESSA-N n-[(3s)-1-azabicyclo[2.2.2]octan-3-yl]-6-[3-(difluoromethoxy)pyrrolidin-1-yl]-1,2-benzothiazole-3-carboxamide Chemical compound C1C(OC(F)F)CCN1C1=CC=C(C(=NS2)C(=O)N[C@H]3C4CCN(CC4)C3)C2=C1 QKJMBWFYXTZCSM-BZSJEYESSA-N 0.000 claims 3
- KNZGHBOYNALEPF-LLVKDONJSA-N n-[(3s)-1-azabicyclo[2.2.2]octan-3-yl]-7-hydroxy-2h-indazole-3-carboxamide Chemical compound C1N(CC2)CCC2[C@@H]1NC(=O)C1=NNC2=C1C=CC=C2O KNZGHBOYNALEPF-LLVKDONJSA-N 0.000 claims 3
- RDSODELYJDFMBF-LJQANCHMSA-N n-[(3s)-1-azabicyclo[2.2.2]octan-3-yl]-n-methyl-5-(oxan-4-yl)-1h-indazole-3-carboxamide Chemical compound CN([C@H]1C2CCN(CC2)C1)C(=O)C(C1=C2)=NNC1=CC=C2C1CCOCC1 RDSODELYJDFMBF-LJQANCHMSA-N 0.000 claims 3
- VHMKMIXTXOLLSO-MRXNPFEDSA-N n-[(3s)-1-azabicyclo[2.2.2]octan-3-yl]-n-methyl-6-(1,3-oxazol-2-yl)-1h-indazole-3-carboxamide Chemical compound CN([C@H]1C2CCN(CC2)C1)C(=O)C(C1=CC=2)=NNC1=CC=2C1=NC=CO1 VHMKMIXTXOLLSO-MRXNPFEDSA-N 0.000 claims 3
- WQLZMRXMTRRRQR-LJQANCHMSA-N n-[(3s)-1-azabicyclo[2.2.2]octan-3-yl]-n-methyl-6-(oxan-4-yl)-1h-indazole-3-carboxamide Chemical compound CN([C@H]1C2CCN(CC2)C1)C(=O)C(C1=CC=2)=NNC1=CC=2C1CCOCC1 WQLZMRXMTRRRQR-LJQANCHMSA-N 0.000 claims 3
- DKHMQEOYLYWADD-XSHJRRMESA-N (e)-[[(3s)-1-(chloromethyl)-1-azoniabicyclo[2.2.2]octan-3-yl]amino]-indazol-3-ylidenemethanolate;hydrochloride Chemical compound [Cl-].C1=CC=C2C(C(=O)N[C@H]3C4CC[N+](CC4)(C3)CCl)=NNC2=C1 DKHMQEOYLYWADD-XSHJRRMESA-N 0.000 claims 2
- LXABWBMNYBJOLI-UHFFFAOYSA-N 1H-indazole-3-carbonyl isocyanate Chemical compound C(=O)=NC(=O)C1=NNC2=CC=CC=C12 LXABWBMNYBJOLI-UHFFFAOYSA-N 0.000 claims 2
- WHGCUWGMCOHGCK-BTQNPOSSSA-N 3-[[(3s)-1-azabicyclo[2.2.2]octan-3-yl]carbamoyl]-1h-indazole-6-carboxylic acid;hydrochloride Chemical compound Cl.C1N(CC2)CCC2[C@@H]1NC(=O)C1=NNC2=CC(C(=O)O)=CC=C21 WHGCUWGMCOHGCK-BTQNPOSSSA-N 0.000 claims 2
- DNAZCSLXJXKFSN-VJIKYCBLSA-N 5-hydroxy-n-[(3s)-1-methyl-1-azoniabicyclo[2.2.2]octan-3-yl]-1,2-benzothiazole-3-carboxamide;iodide Chemical compound [I-].C1=C(O)C=C2C(C(=O)N[C@H]3C4CC[N+](CC4)(C3)C)=NSC2=C1 DNAZCSLXJXKFSN-VJIKYCBLSA-N 0.000 claims 2
- LKQIDYAVNNJMBQ-PPSBMQLTSA-N 6-(1,2,3,4,4a,5,7,7a-octahydropyrrolo[3,4-b]pyridin-6-yl)-n-[(3r)-1-azabicyclo[2.2.2]octan-3-yl]-1,2-benzothiazole-3-carboxamide Chemical compound C1C2CCCNC2CN1C1=CC=C2C(C(N[C@@H]3C4CCN(CC4)C3)=O)=NSC2=C1 LKQIDYAVNNJMBQ-PPSBMQLTSA-N 0.000 claims 2
- LKQIDYAVNNJMBQ-XUJQIHCRSA-N 6-(1,2,3,4,4a,5,7,7a-octahydropyrrolo[3,4-b]pyridin-6-yl)-n-[(3s)-1-azabicyclo[2.2.2]octan-3-yl]-1,2-benzothiazole-3-carboxamide Chemical compound C1C2CCCNC2CN1C1=CC=C2C(C(N[C@H]3C4CCN(CC4)C3)=O)=NSC2=C1 LKQIDYAVNNJMBQ-XUJQIHCRSA-N 0.000 claims 2
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- 229910052799 carbon Inorganic materials 0.000 claims 2
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- 125000004186 cyclopropylmethyl group Chemical group [H]C([H])(*)C1([H])C([H])([H])C1([H])[H] 0.000 claims 2
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- UPQISKWJVFVKIC-PKHIMPSTSA-N n-[(3r)-1-azabicyclo[2.2.2]octan-3-yl]-6-(3-methoxypyrrolidin-1-yl)-1h-indazole-3-carboxamide Chemical compound C1C(OC)CCN1C1=CC=C(C(=NN2)C(=O)N[C@@H]3C4CCN(CC4)C3)C2=C1 UPQISKWJVFVKIC-PKHIMPSTSA-N 0.000 claims 2
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- IYXVKOKQRMOGQC-KRWDZBQOSA-N n-[(3r)-1-azabicyclo[2.2.2]octan-3-yl]-6-(4-methylpiperazin-1-yl)-1,2-benzothiazole-3-carboxamide Chemical compound C1CN(C)CCN1C1=CC=C(C(=NS2)C(=O)N[C@@H]3C4CCN(CC4)C3)C2=C1 IYXVKOKQRMOGQC-KRWDZBQOSA-N 0.000 claims 2
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- IVYWDRAWLTUMFE-TVPLGVNVSA-N n-[(3r)-1-azabicyclo[2.2.2]octan-3-yl]-6-(8-methyl-3,8-diazabicyclo[3.2.1]octan-3-yl)-1,2-benzothiazole-3-carboxamide Chemical compound C1N(CC2)CCC2[C@H]1NC(=O)C1=NSC2=CC(N3CC4CCC(C3)N4C)=CC=C21 IVYWDRAWLTUMFE-TVPLGVNVSA-N 0.000 claims 2
- YASULIPENFCLRY-BJLQDIEVSA-N n-[(3r)-1-azabicyclo[2.2.2]octan-3-yl]-6-[(1s,4s)-2-(cyclopropanecarbonyl)-2,5-diazabicyclo[2.2.1]heptan-5-yl]-1,2-benzothiazole-3-carboxamide Chemical compound C([C@]1(N(C=2C=C3SN=C(C3=CC=2)C(=O)N[C@@H]2C3CCN(CC3)C2)C[C@@]2(C1)[H])[H])N2C(=O)C1CC1 YASULIPENFCLRY-BJLQDIEVSA-N 0.000 claims 2
- SDZSKCLXASPEBT-BQFCYCMXSA-N n-[(3r)-1-azabicyclo[2.2.2]octan-3-yl]-6-[(1s,4s)-5-(2,2,2-trifluoroethyl)-2,5-diazabicyclo[2.2.1]heptan-2-yl]-1,2-benzothiazole-3-carboxamide Chemical compound C1N(CC2)CCC2[C@H]1NC(=O)C1=NSC2=CC(N3C[C@]4(N(C[C@]3([H])C4)CC(F)(F)F)[H])=CC=C21 SDZSKCLXASPEBT-BQFCYCMXSA-N 0.000 claims 2
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- CHHKUKIZVHLZHF-AEFFLSMTSA-N n-[(3r)-1-azabicyclo[2.2.2]octan-3-yl]-6-[(3r)-3-(dimethylamino)pyrrolidin-1-yl]-1,2-benzothiazole-3-carboxamide Chemical compound C1[C@H](N(C)C)CCN1C1=CC=C(C(=NS2)C(=O)N[C@@H]3C4CCN(CC4)C3)C2=C1 CHHKUKIZVHLZHF-AEFFLSMTSA-N 0.000 claims 2
- MQHHLXJJSOOTSK-ZBFHGGJFSA-N n-[(3r)-1-azabicyclo[2.2.2]octan-3-yl]-6-[(3r)-3-hydroxypyrrolidin-1-yl]-1,2-benzothiazole-3-carboxamide Chemical compound C1[C@H](O)CCN1C1=CC=C(C(=NS2)C(=O)N[C@@H]3C4CCN(CC4)C3)C2=C1 MQHHLXJJSOOTSK-ZBFHGGJFSA-N 0.000 claims 2
- QANNTZCRFNSNGO-WBVHZDCISA-N n-[(3r)-1-azabicyclo[2.2.2]octan-3-yl]-6-[(3r)-3-methoxypyrrolidin-1-yl]-1,2-benzothiazole-3-carboxamide Chemical compound C1[C@H](OC)CCN1C1=CC=C(C(=NS2)C(=O)N[C@@H]3C4CCN(CC4)C3)C2=C1 QANNTZCRFNSNGO-WBVHZDCISA-N 0.000 claims 2
- CHHKUKIZVHLZHF-WMZOPIPTSA-N n-[(3r)-1-azabicyclo[2.2.2]octan-3-yl]-6-[(3s)-3-(dimethylamino)pyrrolidin-1-yl]-1,2-benzothiazole-3-carboxamide Chemical compound C1[C@@H](N(C)C)CCN1C1=CC=C(C(=NS2)C(=O)N[C@@H]3C4CCN(CC4)C3)C2=C1 CHHKUKIZVHLZHF-WMZOPIPTSA-N 0.000 claims 2
- MQHHLXJJSOOTSK-HOCLYGCPSA-N n-[(3r)-1-azabicyclo[2.2.2]octan-3-yl]-6-[(3s)-3-hydroxypyrrolidin-1-yl]-1,2-benzothiazole-3-carboxamide Chemical compound C1[C@@H](O)CCN1C1=CC=C(C(=NS2)C(=O)N[C@@H]3C4CCN(CC4)C3)C2=C1 MQHHLXJJSOOTSK-HOCLYGCPSA-N 0.000 claims 2
- QANNTZCRFNSNGO-RDJZCZTQSA-N n-[(3r)-1-azabicyclo[2.2.2]octan-3-yl]-6-[(3s)-3-methoxypyrrolidin-1-yl]-1,2-benzothiazole-3-carboxamide Chemical compound C1[C@@H](OC)CCN1C1=CC=C(C(=NS2)C(=O)N[C@@H]3C4CCN(CC4)C3)C2=C1 QANNTZCRFNSNGO-RDJZCZTQSA-N 0.000 claims 2
- SALPMAXLHRQAPQ-QUENFVSXSA-N n-[(3r)-1-azabicyclo[2.2.2]octan-3-yl]-6-[1-(cyclopropanecarbonyl)-3,4,4a,5,7,7a-hexahydro-2h-pyrrolo[3,4-b]pyridin-6-yl]-1,2-benzothiazole-3-carboxamide Chemical compound N([C@@H]1C2CCN(CC2)C1)C(=O)C(C1=CC=2)=NSC1=CC=2N(CC12)CC1CCCN2C(=O)C1CC1 SALPMAXLHRQAPQ-QUENFVSXSA-N 0.000 claims 2
- OATHIWRWYYXFQI-ZYZRXSCRSA-N n-[(3r)-1-azabicyclo[2.2.2]octan-3-yl]-6-[3-(cyclopropylmethoxy)pyrrolidin-1-yl]-1h-indazole-3-carboxamide Chemical compound N([C@@H]1C2CCN(CC2)C1)C(=O)C(C1=CC=2)=NNC1=CC=2N(C1)CCC1OCC1CC1 OATHIWRWYYXFQI-ZYZRXSCRSA-N 0.000 claims 2
- SEZMMIPOBTXTEA-WMCAAGNKSA-N n-[(3r)-1-azabicyclo[2.2.2]octan-3-yl]-6-[3-(dimethylamino)pyrrolidin-1-yl]-2h-pyrazolo[3,4-b]pyridine-3-carboxamide Chemical compound C1C(N(C)C)CCN1C1=CC=C(C(=NN2)C(=O)N[C@@H]3C4CCN(CC4)C3)C2=N1 SEZMMIPOBTXTEA-WMCAAGNKSA-N 0.000 claims 2
- JRLOWLLNQWPBTN-IBYPIGCZSA-N n-[(3r)-1-azabicyclo[2.2.2]octan-3-yl]-6-[3-(methoxymethyl)pyrrolidin-1-yl]-1,2-benzothiazole-3-carboxamide Chemical compound C1C(COC)CCN1C1=CC=C(C(=NS2)C(=O)N[C@@H]3C4CCN(CC4)C3)C2=C1 JRLOWLLNQWPBTN-IBYPIGCZSA-N 0.000 claims 2
- OFFFQICGZLVGEA-JRZJBTRGSA-N n-[(3r)-1-azabicyclo[2.2.2]octan-3-yl]-6-[3-(methylamino)pyrrolidin-1-yl]-1,2-benzothiazole-3-carboxamide Chemical compound C1C(NC)CCN1C1=CC=C(C(=NS2)C(=O)N[C@@H]3C4CCN(CC4)C3)C2=C1 OFFFQICGZLVGEA-JRZJBTRGSA-N 0.000 claims 2
- YWHWECOSJZZXMH-IBGZPJMESA-N n-[(3r)-1-azabicyclo[2.2.2]octan-3-yl]-6-[4-(cyclopropanecarbonyl)piperazin-1-yl]-1,2-benzothiazole-3-carboxamide Chemical compound N([C@@H]1C2CCN(CC2)C1)C(=O)C(C1=CC=2)=NSC1=CC=2N(CC1)CCN1C(=O)C1CC1 YWHWECOSJZZXMH-IBGZPJMESA-N 0.000 claims 2
- HSNPCRQDMDXYQW-ZOWNYOTGSA-N n-[(3r)-1-azabicyclo[2.2.2]octan-3-yl]-6-methoxy-1,2-benzothiazole-3-carboxamide;hydrochloride Chemical compound Cl.C1N(CC2)CCC2[C@H]1NC(=O)C1=NSC2=CC(OC)=CC=C21 HSNPCRQDMDXYQW-ZOWNYOTGSA-N 0.000 claims 2
- GETRXZCCCNYYIV-HNNXBMFYSA-N n-[(3r)-1-azabicyclo[2.2.2]octan-3-yl]-6-methoxy-n-methyl-1h-indazole-3-carboxamide Chemical compound C1N(CC2)CCC2[C@H]1N(C)C(=O)C1=NNC2=CC(OC)=CC=C21 GETRXZCCCNYYIV-HNNXBMFYSA-N 0.000 claims 2
- OZIYFRRXGPXXDW-INIZCTEOSA-N n-[(3r)-1-azabicyclo[2.2.2]octan-3-yl]-6-piperazin-1-yl-1,2-benzothiazole-3-carboxamide Chemical compound N([C@@H]1C2CCN(CC2)C1)C(=O)C(C1=CC=2)=NSC1=CC=2N1CCNCC1 OZIYFRRXGPXXDW-INIZCTEOSA-N 0.000 claims 2
- NEHATUZWLDEXIQ-INIZCTEOSA-N n-[(3r)-1-azabicyclo[2.2.2]octan-3-yl]-6-pyrrolidin-1-yl-1,2-benzothiazole-3-carboxamide Chemical compound N([C@@H]1C2CCN(CC2)C1)C(=O)C(C1=CC=2)=NSC1=CC=2N1CCCC1 NEHATUZWLDEXIQ-INIZCTEOSA-N 0.000 claims 2
- PIDKUZOOEPTSPI-RDJZCZTQSA-N n-[(3r)-1-azabicyclo[2.2.2]octan-3-yl]-7-[(3s)-3-(dimethylamino)pyrrolidin-1-yl]-1,2-benzothiazole-3-carboxamide Chemical compound C1[C@@H](N(C)C)CCN1C1=CC=CC2=C1SN=C2C(=O)N[C@@H]1C(CC2)CCN2C1 PIDKUZOOEPTSPI-RDJZCZTQSA-N 0.000 claims 2
- OPNCHKXTZMMPLE-HOCLYGCPSA-N n-[(3r)-1-azabicyclo[2.2.2]octan-3-yl]-7-[(3s)-3-methoxypyrrolidin-1-yl]-1,2-benzothiazole-3-carboxamide Chemical compound C1[C@@H](OC)CCN1C1=CC=CC2=C1SN=C2C(=O)N[C@@H]1C(CC2)CCN2C1 OPNCHKXTZMMPLE-HOCLYGCPSA-N 0.000 claims 2
- JLEZTDHDKSJERM-NSHDSACASA-N n-[(3r)-1-azabicyclo[2.2.2]octan-3-yl]-[1,2]thiazolo[5,4-b]pyridine-3-carboxamide Chemical compound C1=CC=C2C(C(N[C@@H]3C4CCN(CC4)C3)=O)=NSC2=N1 JLEZTDHDKSJERM-NSHDSACASA-N 0.000 claims 2
- RDSODELYJDFMBF-IBGZPJMESA-N n-[(3r)-1-azabicyclo[2.2.2]octan-3-yl]-n-methyl-5-(oxan-4-yl)-1h-indazole-3-carboxamide Chemical compound CN([C@@H]1C2CCN(CC2)C1)C(=O)C(C1=C2)=NNC1=CC=C2C1CCOCC1 RDSODELYJDFMBF-IBGZPJMESA-N 0.000 claims 2
- YMWLIMACGUHANC-INIZCTEOSA-N n-[(3r)-1-azabicyclo[2.2.2]octan-3-yl]-n-methyl-6-(1,3-thiazol-2-yl)-1h-indazole-3-carboxamide Chemical compound CN([C@@H]1C2CCN(CC2)C1)C(=O)C(C1=CC=2)=NNC1=CC=2C1=NC=CS1 YMWLIMACGUHANC-INIZCTEOSA-N 0.000 claims 2
- PGEHQXWFCPTXLO-OAHLLOKOSA-N n-[(3s)-1-azabicyclo[2.2.2]octan-3-yl]-1-(difluoromethyl)-6-(propylcarbamoylamino)indazole-3-carboxamide Chemical compound C1N(CC2)CCC2[C@@H]1NC(=O)C1=NN(C(F)F)C2=CC(NC(=O)NCCC)=CC=C21 PGEHQXWFCPTXLO-OAHLLOKOSA-N 0.000 claims 2
- SMJVOFILIBVERT-GOSISDBHSA-N n-[(3s)-1-azabicyclo[2.2.2]octan-3-yl]-1-cyclopropyl-6-(propylcarbamoylamino)indazole-3-carboxamide Chemical compound C12=CC(NC(=O)NCCC)=CC=C2C(C(=O)N[C@H]2C3CCN(CC3)C2)=NN1C1CC1 SMJVOFILIBVERT-GOSISDBHSA-N 0.000 claims 2
- DLARADLKNHHUJE-MRXNPFEDSA-N n-[(3s)-1-azabicyclo[2.2.2]octan-3-yl]-1-ethyl-6-(1,3-oxazol-2-yl)indazole-3-carboxamide Chemical compound C1=C2N(CC)N=C(C(=O)N[C@H]3C4CCN(CC4)C3)C2=CC=C1C1=NC=CO1 DLARADLKNHHUJE-MRXNPFEDSA-N 0.000 claims 2
- KRLDSELWMMWNML-PKLMIRHRSA-N n-[(3s)-1-azabicyclo[2.2.2]octan-3-yl]-1-ethyl-6-(1,3-oxazol-2-yl)indazole-3-carboxamide;hydrochloride Chemical compound Cl.C1=C2N(CC)N=C(C(=O)N[C@H]3C4CCN(CC4)C3)C2=CC=C1C1=NC=CO1 KRLDSELWMMWNML-PKLMIRHRSA-N 0.000 claims 2
- AOPGWWFRFLXWRH-GOSISDBHSA-N n-[(3s)-1-azabicyclo[2.2.2]octan-3-yl]-1-ethyl-n-methyl-6-(1,3-oxazol-2-yl)indazole-3-carboxamide Chemical compound C1=C2N(CC)N=C(C(=O)N(C)[C@H]3C4CCN(CC4)C3)C2=CC=C1C1=NC=CO1 AOPGWWFRFLXWRH-GOSISDBHSA-N 0.000 claims 2
- XHLPSFUPKCQDKE-QGZVFWFLSA-N n-[(3s)-1-azabicyclo[2.2.2]octan-3-yl]-1-propyl-6-(1,3-thiazol-2-yl)indazole-3-carboxamide Chemical compound C1=C2N(CCC)N=C(C(=O)N[C@H]3C4CCN(CC4)C3)C2=CC=C1C1=NC=CS1 XHLPSFUPKCQDKE-QGZVFWFLSA-N 0.000 claims 2
- ZGGYIVUEFFUZRX-GFCCVEGCSA-N n-[(3s)-1-azabicyclo[2.2.2]octan-3-yl]-1h-pyrazolo[3,4-c]pyridine-3-carboxamide Chemical compound N1=CC=C2C(C(N[C@H]3C4CCN(CC4)C3)=O)=NNC2=C1 ZGGYIVUEFFUZRX-GFCCVEGCSA-N 0.000 claims 2
- FADBLXHAAIWCTG-GFCCVEGCSA-N n-[(3s)-1-azabicyclo[2.2.2]octan-3-yl]-1h-pyrazolo[4,3-c]pyridine-3-carboxamide Chemical compound C1=NC=C2C(C(N[C@H]3C4CCN(CC4)C3)=O)=NNC2=C1 FADBLXHAAIWCTG-GFCCVEGCSA-N 0.000 claims 2
- HVKLEJMKAONLIB-GOSISDBHSA-N n-[(3s)-1-azabicyclo[2.2.2]octan-3-yl]-5-(4-methyl-1,4-diazepan-1-yl)-1,2-benzothiazole-3-carboxamide Chemical compound C1CN(C)CCCN1C1=CC=C(SN=C2C(=O)N[C@H]3C4CCN(CC4)C3)C2=C1 HVKLEJMKAONLIB-GOSISDBHSA-N 0.000 claims 2
- PPNSPIJCCHPEIW-NVXWUHKLSA-N n-[(3s)-1-azabicyclo[2.2.2]octan-3-yl]-5-[(3r)-3-methoxypyrrolidin-1-yl]-1,2-benzothiazole-3-carboxamide Chemical compound C1[C@H](OC)CCN1C1=CC=C(SN=C2C(=O)N[C@H]3C4CCN(CC4)C3)C2=C1 PPNSPIJCCHPEIW-NVXWUHKLSA-N 0.000 claims 2
- SJYNXACLXWOQGW-MAUKXSAKSA-N n-[(3s)-1-azabicyclo[2.2.2]octan-3-yl]-5-[(3s)-3-methoxypyrrolidin-1-yl]-1h-indazole-3-carboxamide Chemical compound C1[C@@H](OC)CCN1C1=CC=C(NN=C2C(=O)N[C@H]3C4CCN(CC4)C3)C2=C1 SJYNXACLXWOQGW-MAUKXSAKSA-N 0.000 claims 2
- UFVCXVYNCMTGHK-MRXNPFEDSA-N n-[(3s)-1-azabicyclo[2.2.2]octan-3-yl]-6-(1-methyl-4,5-dihydroimidazol-2-yl)-1h-indazole-3-carboxamide Chemical compound CN1CCN=C1C1=CC=C(C(=NN2)C(=O)N[C@H]3C4CCN(CC4)C3)C2=C1 UFVCXVYNCMTGHK-MRXNPFEDSA-N 0.000 claims 2
- ZZERMSWBCKXSJZ-OMOCHNIRSA-N n-[(3s)-1-azabicyclo[2.2.2]octan-3-yl]-6-(1-methylpyrrolidin-3-yl)oxy-1,2-benzothiazole-3-carboxamide Chemical compound C1N(C)CCC1OC1=CC=C(C(=NS2)C(=O)N[C@H]3C4CCN(CC4)C3)C2=C1 ZZERMSWBCKXSJZ-OMOCHNIRSA-N 0.000 claims 2
- GRUNLFXWKKKXLJ-GOSISDBHSA-N n-[(3s)-1-azabicyclo[2.2.2]octan-3-yl]-6-(2-oxo-3-propylimidazolidin-1-yl)-1h-indazole-3-carboxamide Chemical compound O=C1N(CCC)CCN1C1=CC=C(C(=NN2)C(=O)N[C@H]3C4CCN(CC4)C3)C2=C1 GRUNLFXWKKKXLJ-GOSISDBHSA-N 0.000 claims 2
- DOFXBGFMCIIQDS-BZSJEYESSA-N n-[(3s)-1-azabicyclo[2.2.2]octan-3-yl]-6-(3-ethoxypyrrolidin-1-yl)-7-fluoro-1,2-benzothiazole-3-carboxamide Chemical compound C1C(OCC)CCN1C1=CC=C(C(=NS2)C(=O)N[C@H]3C4CCN(CC4)C3)C2=C1F DOFXBGFMCIIQDS-BZSJEYESSA-N 0.000 claims 2
- WGFXFRVKAYTEOV-MRXNPFEDSA-N n-[(3s)-1-azabicyclo[2.2.2]octan-3-yl]-6-(3-ethyl-2-oxoimidazolidin-1-yl)-1,2-benzothiazole-3-carboxamide Chemical compound O=C1N(CC)CCN1C1=CC=C(C(=NS2)C(=O)N[C@H]3C4CCN(CC4)C3)C2=C1 WGFXFRVKAYTEOV-MRXNPFEDSA-N 0.000 claims 2
- MQHHLXJJSOOTSK-BZSJEYESSA-N n-[(3s)-1-azabicyclo[2.2.2]octan-3-yl]-6-(3-hydroxypyrrolidin-1-yl)-1,2-benzothiazole-3-carboxamide Chemical compound C1C(O)CCN1C1=CC=C(C(=NS2)C(=O)N[C@H]3C4CCN(CC4)C3)C2=C1 MQHHLXJJSOOTSK-BZSJEYESSA-N 0.000 claims 2
- VJGNOXVGSIIBKG-OMOCHNIRSA-N n-[(3s)-1-azabicyclo[2.2.2]octan-3-yl]-6-(3-methoxypyrrolidin-1-yl)-1,2-benzoxazole-3-carboxamide Chemical compound C1C(OC)CCN1C1=CC=C(C(=NO2)C(=O)N[C@H]3C4CCN(CC4)C3)C2=C1 VJGNOXVGSIIBKG-OMOCHNIRSA-N 0.000 claims 2
- BIBPBHIZDKQIOZ-PVQCJRHBSA-N n-[(3s)-1-azabicyclo[2.2.2]octan-3-yl]-6-(3-methyl-2-oxopyrrolidin-1-yl)-1,2-benzothiazole-3-carboxamide Chemical compound O=C1C(C)CCN1C1=CC=C(C(=NS2)C(=O)N[C@H]3C4CCN(CC4)C3)C2=C1 BIBPBHIZDKQIOZ-PVQCJRHBSA-N 0.000 claims 2
- JCBHEXJAZCRMNJ-MRXNPFEDSA-N n-[(3s)-1-azabicyclo[2.2.2]octan-3-yl]-6-(3-methylpyrazol-1-yl)-1,2-benzothiazole-3-carboxamide Chemical compound N1=C(C)C=CN1C1=CC=C(C(=NS2)C(=O)N[C@H]3C4CCN(CC4)C3)C2=C1 JCBHEXJAZCRMNJ-MRXNPFEDSA-N 0.000 claims 2
- AIEYPFNAZAQGDT-GOSISDBHSA-N n-[(3s)-1-azabicyclo[2.2.2]octan-3-yl]-6-(4-methyl-1,4-diazepan-1-yl)-1,2-benzothiazole-3-carboxamide Chemical compound C1CN(C)CCCN1C1=CC=C(C(=NS2)C(=O)N[C@H]3C4CCN(CC4)C3)C2=C1 AIEYPFNAZAQGDT-GOSISDBHSA-N 0.000 claims 2
- IYXVKOKQRMOGQC-QGZVFWFLSA-N n-[(3s)-1-azabicyclo[2.2.2]octan-3-yl]-6-(4-methylpiperazin-1-yl)-1,2-benzothiazole-3-carboxamide Chemical compound C1CN(C)CCN1C1=CC=C(C(=NS2)C(=O)N[C@H]3C4CCN(CC4)C3)C2=C1 IYXVKOKQRMOGQC-QGZVFWFLSA-N 0.000 claims 2
- XXXHTSQDIORPMB-GOSISDBHSA-N n-[(3s)-1-azabicyclo[2.2.2]octan-3-yl]-6-(4-methylpiperazine-1-carbonyl)-1h-indazole-3-carboxamide Chemical compound C1CN(C)CCN1C(=O)C1=CC=C(C(=NN2)C(=O)N[C@H]3C4CCN(CC4)C3)C2=C1 XXXHTSQDIORPMB-GOSISDBHSA-N 0.000 claims 2
- GPWNPAULGBLLEA-FAFZWHIHSA-N n-[(3s)-1-azabicyclo[2.2.2]octan-3-yl]-6-(5-methyl-2,5-diazabicyclo[2.2.2]octan-2-yl)-1,2-benzothiazole-3-carboxamide Chemical compound C1N(CC2)CCC2[C@@H]1NC(=O)C1=NSC2=CC(N3CC4CCC3CN4C)=CC=C21 GPWNPAULGBLLEA-FAFZWHIHSA-N 0.000 claims 2
- ZYXWSPGDIGRWLF-MRXNPFEDSA-N n-[(3s)-1-azabicyclo[2.2.2]octan-3-yl]-6-(5-methylpyrazol-1-yl)-1,2-benzothiazole-3-carboxamide Chemical compound CC1=CC=NN1C1=CC=C(C(=NS2)C(=O)N[C@H]3C4CCN(CC4)C3)C2=C1 ZYXWSPGDIGRWLF-MRXNPFEDSA-N 0.000 claims 2
- IVYWDRAWLTUMFE-FAFZWHIHSA-N n-[(3s)-1-azabicyclo[2.2.2]octan-3-yl]-6-(8-methyl-3,8-diazabicyclo[3.2.1]octan-3-yl)-1,2-benzothiazole-3-carboxamide Chemical compound C1N(CC2)CCC2[C@@H]1NC(=O)C1=NSC2=CC(N3CC4CCC(C3)N4C)=CC=C21 IVYWDRAWLTUMFE-FAFZWHIHSA-N 0.000 claims 2
- YIPLPZONCABMSW-JLJPHGGASA-N n-[(3s)-1-azabicyclo[2.2.2]octan-3-yl]-6-[(1s,4s)-2,5-diazabicyclo[2.2.1]heptan-2-yl]-1,2-benzothiazole-3-carboxamide Chemical compound C1N(CC2)CCC2[C@@H]1NC(=O)C1=NSC2=CC(N3C[C@]4(NC[C@]3([H])C4)[H])=CC=C21 YIPLPZONCABMSW-JLJPHGGASA-N 0.000 claims 2
- QWSOZFFRWVKTNH-YQQAZPJKSA-N n-[(3s)-1-azabicyclo[2.2.2]octan-3-yl]-6-[(1s,4s)-2-oxa-5-azabicyclo[2.2.1]heptan-5-yl]-1,2-benzothiazole-3-carboxamide Chemical compound C1N(CC2)CCC2[C@@H]1NC(=O)C1=NSC2=CC(N3C[C@]4(OC[C@]3([H])C4)[H])=CC=C21 QWSOZFFRWVKTNH-YQQAZPJKSA-N 0.000 claims 2
- FJXJLRUWWLSMTO-IRFCIJBXSA-N n-[(3s)-1-azabicyclo[2.2.2]octan-3-yl]-6-[(1s,4s)-5-(cyclopropylmethyl)-2,5-diazabicyclo[2.2.1]heptan-2-yl]-1,2-benzothiazole-3-carboxamide Chemical compound C([C@]1(N(C=2C=C3SN=C(C3=CC=2)C(=O)N[C@H]2C3CCN(CC3)C2)C[C@@]2(C1)[H])[H])N2CC1CC1 FJXJLRUWWLSMTO-IRFCIJBXSA-N 0.000 claims 2
- MQHHLXJJSOOTSK-GDBMZVCRSA-N n-[(3s)-1-azabicyclo[2.2.2]octan-3-yl]-6-[(3r)-3-hydroxypyrrolidin-1-yl]-1,2-benzothiazole-3-carboxamide Chemical compound C1[C@H](O)CCN1C1=CC=C(C(=NS2)C(=O)N[C@H]3C4CCN(CC4)C3)C2=C1 MQHHLXJJSOOTSK-GDBMZVCRSA-N 0.000 claims 2
- VJGNOXVGSIIBKG-NVXWUHKLSA-N n-[(3s)-1-azabicyclo[2.2.2]octan-3-yl]-6-[(3r)-3-methoxypyrrolidin-1-yl]-1,2-benzoxazole-3-carboxamide Chemical compound C1[C@H](OC)CCN1C1=CC=C(C(=NO2)C(=O)N[C@H]3C4CCN(CC4)C3)C2=C1 VJGNOXVGSIIBKG-NVXWUHKLSA-N 0.000 claims 2
- CHHKUKIZVHLZHF-FUHWJXTLSA-N n-[(3s)-1-azabicyclo[2.2.2]octan-3-yl]-6-[(3s)-3-(dimethylamino)pyrrolidin-1-yl]-1,2-benzothiazole-3-carboxamide Chemical compound C1[C@@H](N(C)C)CCN1C1=CC=C(C(=NS2)C(=O)N[C@H]3C4CCN(CC4)C3)C2=C1 CHHKUKIZVHLZHF-FUHWJXTLSA-N 0.000 claims 2
- MQHHLXJJSOOTSK-GOEBONIOSA-N n-[(3s)-1-azabicyclo[2.2.2]octan-3-yl]-6-[(3s)-3-hydroxypyrrolidin-1-yl]-1,2-benzothiazole-3-carboxamide Chemical compound C1[C@@H](O)CCN1C1=CC=C(C(=NS2)C(=O)N[C@H]3C4CCN(CC4)C3)C2=C1 MQHHLXJJSOOTSK-GOEBONIOSA-N 0.000 claims 2
- AFFLFHWMOOWDQB-ROPPNANJSA-N n-[(3s)-1-azabicyclo[2.2.2]octan-3-yl]-6-[3-(cyclopropylmethoxy)pyrrolidin-1-yl]-1,2-benzothiazole-3-carboxamide Chemical compound N([C@H]1C2CCN(CC2)C1)C(=O)C(C1=CC=2)=NSC1=CC=2N(C1)CCC1OCC1CC1 AFFLFHWMOOWDQB-ROPPNANJSA-N 0.000 claims 2
- OATHIWRWYYXFQI-BDPMCISCSA-N n-[(3s)-1-azabicyclo[2.2.2]octan-3-yl]-6-[3-(cyclopropylmethoxy)pyrrolidin-1-yl]-1h-indazole-3-carboxamide Chemical compound N([C@H]1C2CCN(CC2)C1)C(=O)C(C1=CC=2)=NNC1=CC=2N(C1)CCC1OCC1CC1 OATHIWRWYYXFQI-BDPMCISCSA-N 0.000 claims 2
- JRLOWLLNQWPBTN-XPKAQORNSA-N n-[(3s)-1-azabicyclo[2.2.2]octan-3-yl]-6-[3-(methoxymethyl)pyrrolidin-1-yl]-1,2-benzothiazole-3-carboxamide Chemical compound C1C(COC)CCN1C1=CC=C(C(=NS2)C(=O)N[C@H]3C4CCN(CC4)C3)C2=C1 JRLOWLLNQWPBTN-XPKAQORNSA-N 0.000 claims 2
- OFFFQICGZLVGEA-FBMWCMRBSA-N n-[(3s)-1-azabicyclo[2.2.2]octan-3-yl]-6-[3-(methylamino)pyrrolidin-1-yl]-1,2-benzothiazole-3-carboxamide Chemical compound C1C(NC)CCN1C1=CC=C(C(=NS2)C(=O)N[C@H]3C4CCN(CC4)C3)C2=C1 OFFFQICGZLVGEA-FBMWCMRBSA-N 0.000 claims 2
- GOZVSIAXGOLHQP-LJQANCHMSA-N n-[(3s)-1-azabicyclo[2.2.2]octan-3-yl]-6-[4-(dimethylamino)piperidin-1-yl]-1,2-benzothiazole-3-carboxamide Chemical compound C1CC(N(C)C)CCN1C1=CC=C(C(=NS2)C(=O)N[C@H]3C4CCN(CC4)C3)C2=C1 GOZVSIAXGOLHQP-LJQANCHMSA-N 0.000 claims 2
- QAGHJHKGEQIEOP-SNVBAGLBSA-N n-[(3s)-1-azabicyclo[2.2.2]octan-3-yl]-6-chloro-[1,2]thiazolo[5,4-b]pyridine-3-carboxamide Chemical compound C1N(CC2)CCC2[C@@H]1NC(=O)C1=NSC2=NC(Cl)=CC=C21 QAGHJHKGEQIEOP-SNVBAGLBSA-N 0.000 claims 2
- XIYQUORHPQHVQN-CQSZACIVSA-N n-[(3s)-1-azabicyclo[2.2.2]octan-3-yl]-6-cyano-1h-indazole-3-carboxamide Chemical compound N#CC1=CC=C2C(C(N[C@H]3C4CCN(CC4)C3)=O)=NNC2=C1 XIYQUORHPQHVQN-CQSZACIVSA-N 0.000 claims 2
- HVNVCUMJPZIHBY-SNVBAGLBSA-N n-[(3s)-1-azabicyclo[2.2.2]octan-3-yl]-6-fluoro-2h-pyrazolo[3,4-b]pyridine-3-carboxamide Chemical compound C1N(CC2)CCC2[C@@H]1NC(=O)C1=NNC2=NC(F)=CC=C21 HVNVCUMJPZIHBY-SNVBAGLBSA-N 0.000 claims 2
- CHOAZMBKIMGLCK-OAHLLOKOSA-N n-[(3s)-1-azabicyclo[2.2.2]octan-3-yl]-6-imidazol-1-yl-1,2-benzothiazole-3-carboxamide Chemical compound N([C@H]1C2CCN(CC2)C1)C(=O)C(C1=CC=2)=NSC1=CC=2N1C=CN=C1 CHOAZMBKIMGLCK-OAHLLOKOSA-N 0.000 claims 2
- HSNPCRQDMDXYQW-BTQNPOSSSA-N n-[(3s)-1-azabicyclo[2.2.2]octan-3-yl]-6-methoxy-1,2-benzothiazole-3-carboxamide;hydrochloride Chemical compound Cl.C1N(CC2)CCC2[C@@H]1NC(=O)C1=NSC2=CC(OC)=CC=C21 HSNPCRQDMDXYQW-BTQNPOSSSA-N 0.000 claims 2
- LSJTZJHCZCUIPE-BTQNPOSSSA-N n-[(3s)-1-azabicyclo[2.2.2]octan-3-yl]-6-methoxy-1,2-benzoxazole-3-carboxamide;hydrochloride Chemical compound Cl.C1N(CC2)CCC2[C@@H]1NC(=O)C1=NOC2=CC(OC)=CC=C21 LSJTZJHCZCUIPE-BTQNPOSSSA-N 0.000 claims 2
- RAYAZVOIVKZYFJ-LLVKDONJSA-N n-[(3s)-1-azabicyclo[2.2.2]octan-3-yl]-6-methoxy-[1,2]thiazolo[5,4-b]pyridine-3-carboxamide Chemical compound C1N(CC2)CCC2[C@@H]1NC(=O)C1=NSC2=NC(OC)=CC=C21 RAYAZVOIVKZYFJ-LLVKDONJSA-N 0.000 claims 2
- ACWVOGYINHFSIT-QGZVFWFLSA-N n-[(3s)-1-azabicyclo[2.2.2]octan-3-yl]-6-phenyl-2h-pyrazolo[3,4-b]pyridine-3-carboxamide Chemical compound N([C@H]1C2CCN(CC2)C1)C(=O)C(C1=CC=2)=NNC1=NC=2C1=CC=CC=C1 ACWVOGYINHFSIT-QGZVFWFLSA-N 0.000 claims 2
- OZIYFRRXGPXXDW-MRXNPFEDSA-N n-[(3s)-1-azabicyclo[2.2.2]octan-3-yl]-6-piperazin-1-yl-1,2-benzothiazole-3-carboxamide Chemical compound N([C@H]1C2CCN(CC2)C1)C(=O)C(C1=CC=2)=NSC1=CC=2N1CCNCC1 OZIYFRRXGPXXDW-MRXNPFEDSA-N 0.000 claims 2
- QVXODGVLNJLYCN-OAHLLOKOSA-N n-[(3s)-1-azabicyclo[2.2.2]octan-3-yl]-6-pyrazol-1-yl-1,2-benzothiazole-3-carboxamide Chemical compound N([C@H]1C2CCN(CC2)C1)C(=O)C(C1=CC=2)=NSC1=CC=2N1C=CC=N1 QVXODGVLNJLYCN-OAHLLOKOSA-N 0.000 claims 2
- ZCZQEVPJJXRPAQ-MRXNPFEDSA-N n-[(3s)-1-azabicyclo[2.2.2]octan-3-yl]-6-pyrrol-1-yl-1,2-benzothiazole-3-carboxamide Chemical compound N([C@H]1C2CCN(CC2)C1)C(=O)C(C1=CC=2)=NSC1=CC=2N1C=CC=C1 ZCZQEVPJJXRPAQ-MRXNPFEDSA-N 0.000 claims 2
- NEHATUZWLDEXIQ-MRXNPFEDSA-N n-[(3s)-1-azabicyclo[2.2.2]octan-3-yl]-6-pyrrolidin-1-yl-1,2-benzothiazole-3-carboxamide Chemical compound N([C@H]1C2CCN(CC2)C1)C(=O)C(C1=CC=2)=NSC1=CC=2N1CCCC1 NEHATUZWLDEXIQ-MRXNPFEDSA-N 0.000 claims 2
- OPNCHKXTZMMPLE-BZSJEYESSA-N n-[(3s)-1-azabicyclo[2.2.2]octan-3-yl]-7-(3-methoxypyrrolidin-1-yl)-1,2-benzothiazole-3-carboxamide Chemical compound C1C(OC)CCN1C1=CC=CC2=C1SN=C2C(=O)N[C@H]1C(CC2)CCN2C1 OPNCHKXTZMMPLE-BZSJEYESSA-N 0.000 claims 2
- JVYMJXLBAWTLFZ-OFQRWUPVSA-N n-[(3s)-1-azabicyclo[2.2.2]octan-3-yl]-7-[(1s,4s)-2-oxa-5-azabicyclo[2.2.1]heptan-5-yl]-1,2-benzothiazole-3-carboxamide Chemical compound C1N(CC2)CCC2[C@@H]1NC(=O)C1=NSC2=C1C=CC=C2N1C[C@@]2([H])OC[C@]1([H])C2 JVYMJXLBAWTLFZ-OFQRWUPVSA-N 0.000 claims 2
- GLTJKJAUUMPZNP-UKRRQHHQSA-N n-[(3s)-1-azabicyclo[2.2.2]octan-3-yl]-7-[(3r)-3-hydroxypyrrolidin-1-yl]-1,2-benzothiazole-3-carboxamide Chemical compound C1[C@H](O)CCN1C1=CC=CC2=C1SN=C2C(=O)N[C@H]1C(CC2)CCN2C1 GLTJKJAUUMPZNP-UKRRQHHQSA-N 0.000 claims 2
- OPNCHKXTZMMPLE-GDBMZVCRSA-N n-[(3s)-1-azabicyclo[2.2.2]octan-3-yl]-7-[(3r)-3-methoxypyrrolidin-1-yl]-1,2-benzothiazole-3-carboxamide Chemical compound C1[C@H](OC)CCN1C1=CC=CC2=C1SN=C2C(=O)N[C@H]1C(CC2)CCN2C1 OPNCHKXTZMMPLE-GDBMZVCRSA-N 0.000 claims 2
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- JOXIMZWYDAKGHI-UHFFFAOYSA-N toluene-4-sulfonic acid Chemical group CC1=CC=C(S(O)(=O)=O)C=C1 JOXIMZWYDAKGHI-UHFFFAOYSA-N 0.000 claims 1
- ITMCEJHCFYSIIV-UHFFFAOYSA-M triflate Chemical group [O-]S(=O)(=O)C(F)(F)F ITMCEJHCFYSIIV-UHFFFAOYSA-M 0.000 claims 1
- 125000006413 ring segment Chemical group 0.000 abstract 2
- 125000005960 1,4-diazepanyl group Chemical group 0.000 abstract 1
- 230000004071 biological effect Effects 0.000 abstract 1
- 239000000126 substance Substances 0.000 abstract 1
- 0 *[C@@](C1C(CC2)CCN2C1)N(CC(*)=**=C(C=NN1*)C1=*)I Chemical compound *[C@@](C1C(CC2)CCN2C1)N(CC(*)=**=C(C=NN1*)C1=*)I 0.000 description 16
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D453/00—Heterocyclic compounds containing quinuclidine or iso-quinuclidine ring systems, e.g. quinine alkaloids
- C07D453/02—Heterocyclic compounds containing quinuclidine or iso-quinuclidine ring systems, e.g. quinine alkaloids containing not further condensed quinuclidine ring systems
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/435—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom
-
- A—HUMAN NECESSITIES
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- A61P25/04—Centrally acting analgesics, e.g. opioids
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- A61P25/14—Drugs for disorders of the nervous system for treating abnormal movements, e.g. chorea, dyskinesia
- A61P25/16—Anti-Parkinson drugs
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- A—HUMAN NECESSITIES
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- A—HUMAN NECESSITIES
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- A61P25/00—Drugs for disorders of the nervous system
- A61P25/28—Drugs for disorders of the nervous system for treating neurodegenerative disorders of the central nervous system, e.g. nootropic agents, cognition enhancers, drugs for treating Alzheimer's disease or other forms of dementia
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- A61P3/04—Anorexiants; Antiobesity agents
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- A—HUMAN NECESSITIES
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- A61P3/00—Drugs for disorders of the metabolism
- A61P3/08—Drugs for disorders of the metabolism for glucose homeostasis
- A61P3/10—Drugs for disorders of the metabolism for glucose homeostasis for hyperglycaemia, e.g. antidiabetics
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- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
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- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
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Landscapes
- Health & Medical Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- General Health & Medical Sciences (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Engineering & Computer Science (AREA)
- Veterinary Medicine (AREA)
- Medicinal Chemistry (AREA)
- Public Health (AREA)
- Pharmacology & Pharmacy (AREA)
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- General Chemical & Material Sciences (AREA)
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- Chemical Kinetics & Catalysis (AREA)
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- Rheumatology (AREA)
- Communicable Diseases (AREA)
- Hospice & Palliative Care (AREA)
- Epidemiology (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
- Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
- Nitrogen And Oxygen Or Sulfur-Condensed Heterocyclic Ring Systems (AREA)
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US71955205P | 2005-09-23 | 2005-09-23 | |
| US60/719,552 | 2005-09-23 |
Publications (2)
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| RU2008115268A RU2008115268A (ru) | 2009-10-27 |
| RU2450003C2 true RU2450003C2 (ru) | 2012-05-10 |
Family
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Family Applications (1)
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Country Status (12)
| Country | Link |
|---|---|
| EP (1) | EP1940833A1 (enExample) |
| JP (1) | JP2009509964A (enExample) |
| KR (1) | KR20080048550A (enExample) |
| CN (1) | CN101312968A (enExample) |
| AU (1) | AU2006295397A1 (enExample) |
| BR (1) | BRPI0617534A2 (enExample) |
| CA (1) | CA2622677A1 (enExample) |
| IL (1) | IL190358A0 (enExample) |
| RU (1) | RU2450003C2 (enExample) |
| SG (1) | SG165417A1 (enExample) |
| WO (1) | WO2007038367A1 (enExample) |
| ZA (1) | ZA200802342B (enExample) |
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| Publication number | Priority date | Publication date | Assignee | Title |
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| DE10164139A1 (de) | 2001-12-27 | 2003-07-10 | Bayer Ag | 2-Heteroarylcarbonsäureamide |
| KR101280333B1 (ko) | 2006-03-28 | 2013-07-02 | 하이 포인트 파마슈티칼스, 엘엘씨 | 히스타민 ｈ３ 수용체 활성을 갖는 벤조티아졸 |
| SA08290475B1 (ar) | 2007-08-02 | 2013-06-22 | Targacept Inc | (2s، 3r)-n-(2-((3-بيردينيل)ميثيل)-1-آزا بيسيكلو[2، 2، 2]أوكت-3-يل)بنزو فيوران-2-كربوكساميد، وصور أملاحه الجديدة وطرق استخدامه |
| MX2010005298A (es) * | 2007-11-16 | 2010-06-30 | Rigel Pharmaceuticals Inc | Compuestos de carboxamida, sulfonamida y amina para trastornos metabolicos. |
| BRPI0908807A2 (pt) * | 2008-02-15 | 2015-07-28 | Hoffmann La Roche | Derivados de 3-alquil-piperazina e usos dos mesmos |
| CA2740311C (en) * | 2008-10-13 | 2013-09-17 | F. Hoffmann-La Roche Ag | Diazonium-free method to make an indazole intermediate in the synthesis of bicyclic 5-(trifluormethoxy)-1h-3-indazolecarboxylic acid amides |
| SI2889033T1 (en) | 2008-11-19 | 2018-08-31 | Forum Pharmaceuticals Inc. | Treatment of negative symptoms of schizophrenia with (R) -7-chloro-N- (chonylidin-3-yl) benzo (B) thiophene-2-carboxamide and pharmaceutically acceptable salts thereof |
| TW201031664A (en) | 2009-01-26 | 2010-09-01 | Targacept Inc | Preparation and therapeutic applications of (2S,3R)-N-2-((3-pyridinyl)methyl)-1-azabicyclo[2.2.2]oct-3-yl)-3,5-difluorobenzamide |
| JO3250B1 (ar) | 2009-09-22 | 2018-09-16 | Novartis Ag | إستعمال منشطات مستقبل نيكوتينيك أسيتيل كولين ألفا 7 |
| US20110172428A1 (en) | 2010-01-12 | 2011-07-14 | Shan-Ming Kuang | Methods for the preparation of indazole-3-carboxylic acid and n-(s)-1-azabicyclo[2.2.2]oct-3-yl-1h-indazole-3-carboxamide hydrochloride salt |
| US8481555B2 (en) * | 2010-04-30 | 2013-07-09 | Bristol-Myers Squibb Company | Aza-bicyclic amine N-oxide compounds as alpha-7 nicotinic acetylcholine receptor ligand pro-drugs |
| CN103221411B (zh) | 2010-05-17 | 2016-05-11 | 富瑞姆制药公司 | (R)-7-氯-N-(奎宁环-3-基)苯并[b]噻吩-2-甲酰胺盐酸盐单水合物的晶型 |
| US8242276B2 (en) | 2010-06-30 | 2012-08-14 | Hoffmann-La Roche Inc. | Methods for the preparation of N-(S)-1-azabicyclo[2.2.2]oct-3-yl-1H-indazole-3-carboxamide hydrochloride salt |
| US20130225560A1 (en) | 2010-07-26 | 2013-08-29 | Envivo Pharmaceuticals, Inc. | Treatment of Cognitive Disorders with Certain Alpha-7 Nicotinic Acid Receptor Agonists in Combination with Acetylcholinesterase Inhibitors |
| AR086791A1 (es) * | 2011-07-01 | 2014-01-22 | Lundbeck & Co As H | Moduladores alostericos positivos del receptor de acetilcolina nicotinico |
| AU2013259871A1 (en) | 2012-05-08 | 2014-11-20 | Forum Pharmaceuticals Inc. | Methods of maintaining, treating or improving cognitive function |
| JOP20130213B1 (ar) | 2012-07-17 | 2021-08-17 | Takeda Pharmaceuticals Co | معارضات لمستقبلht3-5 |
| JOP20130273B1 (ar) * | 2012-09-11 | 2021-08-17 | Genzyme Corp | مثبطات انزيم (سينثاز) غلوكوسيل سيراميد |
| JP6249952B2 (ja) * | 2012-10-16 | 2017-12-20 | 武田薬品工業株式会社 | 複素環化合物 |
| JP2016526538A (ja) | 2013-06-20 | 2016-09-05 | バイエル・クロップサイエンス・アクチェンゲゼルシャフト | 殺ダニ剤及び殺虫剤としてのアリールスルフィド誘導体及びアリールスルホキシド誘導体 |
| WO2015018754A1 (en) * | 2013-08-08 | 2015-02-12 | Boehringer Ingelheim International Gmbh | Novel pyrazine amide compounds |
| CA2942687A1 (en) | 2014-03-20 | 2015-09-24 | Samumed, Llc | 5-substituted indazole-3-carboxamides and preparation and use thereof |
| KR101532211B1 (ko) * | 2014-04-30 | 2015-06-30 | 세종대학교산학협력단 | Ampk 억제기능에 기반한 뇌졸중 치료용 약학적 조성물 및 방법 |
| HUE055175T2 (hu) | 2014-09-29 | 2021-11-29 | Takeda Pharmaceuticals Co | Az 1-(1-metil-1H-pirazol-4-il)-N-((1R,5S,7S)-9-metil-3-oxa-9-azabiciklo[3.3.1] nonan-7-il)-1H-indol-3-karboxamid kristályos formája |
| JP2018516973A (ja) * | 2015-06-10 | 2018-06-28 | フォーラム・ファーマシューティカルズ・インコーポレイテッドＦｏｒｕｍ Ｐｈａｒｍａｃｅｕｔｉｃａｌｓ Ｉｎｃ． | α７−ニコチン性アセチルコリン受容体のアゴニストとしてのアミノベンゾイソオキサゾール化合物 |
| EP3334740A4 (en) * | 2015-08-12 | 2019-02-06 | Axovant Sciences GmbH | GEMINAL SUBSTITUTED AMINOBENZISOXAZOLE COMPOUNDS AS AGONISTS OF ALPHA 7-NICOTINIC ACETYLCHOLINE RECEPTORS |
| CA3251507A1 (en) * | 2015-10-16 | 2025-05-21 | Abbvie Inc | Use of a solid dosage form comprising (3s,4r)-3-ethyl-4-(3h-imidazo[1,2-a]pyrrolo[2,3-e]pyrazin-8-yl)-n-(2,2,2-trifluoroethyl)pyrrolidine-1-carboxamide for treating rheumatoid arthritis |
| US20200115353A1 (en) | 2017-04-06 | 2020-04-16 | Inventiva | New compounds inhibitors of the yap/taz-tead interaction and their use in the treatment of malignant mesothelioma |
| EP3632908A1 (en) | 2018-10-02 | 2020-04-08 | Inventiva | Inhibitors of the yap/taz-tead interaction and their use in the treatment of cancer |
| TW202142236A (zh) | 2020-02-03 | 2021-11-16 | 美商健臻公司 | 用於治療與溶體儲積症相關的神經症狀之方法 |
| US11618751B1 (en) | 2022-03-25 | 2023-04-04 | Ventus Therapeutics U.S., Inc. | Pyrido-[3,4-d]pyridazine amine derivatives useful as NLRP3 derivatives |
| AU2021311131A1 (en) | 2020-07-24 | 2023-03-23 | Genzyme Corporation | Pharmaceutical compositions comprising venglustat |
| US11319319B1 (en) | 2021-04-07 | 2022-05-03 | Ventus Therapeutics U.S., Inc. | Compounds for inhibiting NLRP3 and uses thereof |
| US12331048B2 (en) | 2022-10-31 | 2025-06-17 | Ventus Therapeutics U.S., Inc. | Pyrido-[3,4-d]pyridazine amine derivatives useful as NLRP3 inhibitors |
Citations (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| RU2067979C1 (ru) * | 1992-02-04 | 1996-10-20 | Эйсай Ко. Лтд. | Производное аминобензойной кислоты или его фармацевтически приемлемая соль |
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| AR036040A1 (es) * | 2001-06-12 | 2004-08-04 | Upjohn Co | Compuestos de heteroarilo multiciclicos sustituidos con quinuclidinas y composiciones farmaceuticas que los contienen |
| AR036041A1 (es) * | 2001-06-12 | 2004-08-04 | Upjohn Co | Compuestos aromaticos heterociclicos sustituidos con quinuclidina y composiciones farmaceuticas que los contienen |
| DE10162375A1 (de) * | 2001-12-19 | 2003-07-10 | Bayer Ag | Bicyclische N-Aryl-amide |
| PL375533A1 (en) * | 2002-08-14 | 2005-11-28 | Neurosearch A/S | Novel quinuclidine derivatives and their use |
| CA2499128C (en) * | 2002-09-25 | 2012-07-31 | Memory Pharmaceuticals Corporation | Indazoles, benzothiazoles, and benzoisothiazoles, and preparation and uses thereof |
| EP1587511A2 (en) * | 2003-01-22 | 2005-10-26 | Pharmacia & Upjohn Company LLC | Treatment of diseases with alpha-7 nach receptor full agonists |
| US7396833B2 (en) * | 2003-12-22 | 2008-07-08 | Memory Pharmaceuticals Corporation | Indoles, 1H-indazoles, 1,2-benzisoxazoles, and 1,2-benzisothiazoles, and preparation and uses thereof |
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- 2006-09-22 AU AU2006295397A patent/AU2006295397A1/en not_active Abandoned
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- 2006-09-22 EP EP06815264A patent/EP1940833A1/en not_active Withdrawn
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Patent Citations (1)
| Publication number | Priority date | Publication date | Assignee | Title |
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| RU2067979C1 (ru) * | 1992-02-04 | 1996-10-20 | Эйсай Ко. Лтд. | Производное аминобензойной кислоты или его фармацевтически приемлемая соль |
Also Published As
| Publication number | Publication date |
|---|---|
| BRPI0617534A2 (pt) | 2011-07-26 |
| CA2622677A1 (en) | 2007-04-05 |
| IL190358A0 (en) | 2009-09-22 |
| SG165417A1 (en) | 2010-10-28 |
| RU2008115268A (ru) | 2009-10-27 |
| CN101312968A (zh) | 2008-11-26 |
| AU2006295397A1 (en) | 2007-04-05 |
| EP1940833A1 (en) | 2008-07-09 |
| ZA200802342B (en) | 2009-03-25 |
| JP2009509964A (ja) | 2009-03-12 |
| KR20080048550A (ko) | 2008-06-02 |
| WO2007038367A1 (en) | 2007-04-05 |
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