RU2011121665A - Производные 7-гидроксибензимидазол-4-илметанона и содержащие их ингибиторы рвк - Google Patents
Производные 7-гидроксибензимидазол-4-илметанона и содержащие их ингибиторы рвк Download PDFInfo
- Publication number
- RU2011121665A RU2011121665A RU2011121665/13A RU2011121665A RU2011121665A RU 2011121665 A RU2011121665 A RU 2011121665A RU 2011121665/13 A RU2011121665/13 A RU 2011121665/13A RU 2011121665 A RU2011121665 A RU 2011121665A RU 2011121665 A RU2011121665 A RU 2011121665A
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- RU
- Russia
- Prior art keywords
- benzo
- hydroxy
- imidazole
- carboxamide
- piperidin
- Prior art date
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- 239000003112 inhibitor Substances 0.000 title claims 2
- 150000001875 compounds Chemical class 0.000 claims abstract 24
- -1 heptan-2-yl Chemical group 0.000 claims abstract 10
- 125000001424 substituent group Chemical group 0.000 claims abstract 6
- WVKPYYLOFMTDHB-UHFFFAOYSA-N 2-norbornyl radical Chemical group C1CC2[CH]CC1C2 WVKPYYLOFMTDHB-UHFFFAOYSA-N 0.000 claims abstract 4
- 125000000175 2-thienyl group Chemical group S1C([*])=C([H])C([H])=C1[H] 0.000 claims abstract 4
- 125000001511 cyclopentyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])(*)C1([H])[H] 0.000 claims abstract 4
- 125000001559 cyclopropyl group Chemical group [H]C1([H])C([H])([H])C1([H])* 0.000 claims abstract 4
- 125000000623 heterocyclic group Chemical group 0.000 claims abstract 4
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims abstract 4
- 125000004483 piperidin-3-yl group Chemical group N1CC(CCC1)* 0.000 claims abstract 3
- 125000002941 2-furyl group Chemical group O1C([*])=C([H])C([H])=C1[H] 0.000 claims abstract 2
- 125000004575 3-pyrrolidinyl group Chemical group [H]N1C([H])([H])C([H])([H])C([H])(*)C1([H])[H] 0.000 claims abstract 2
- 125000003806 alkyl carbonyl amino group Chemical group 0.000 claims abstract 2
- 150000001408 amides Chemical class 0.000 claims abstract 2
- 125000004397 aminosulfonyl group Chemical group NS(=O)(=O)* 0.000 claims abstract 2
- 125000004567 azetidin-3-yl group Chemical group N1CC(C1)* 0.000 claims abstract 2
- 125000002915 carbonyl group Chemical group [*:2]C([*:1])=O 0.000 claims abstract 2
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 claims abstract 2
- 125000006310 cycloalkyl amino group Chemical group 0.000 claims abstract 2
- 125000000113 cyclohexyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])(*)C([H])([H])C1([H])[H] 0.000 claims abstract 2
- 229910052736 halogen Inorganic materials 0.000 claims abstract 2
- 150000002367 halogens Chemical class 0.000 claims abstract 2
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims abstract 2
- 125000004043 oxo group Chemical group O=* 0.000 claims abstract 2
- LFGREXWGYUGZLY-UHFFFAOYSA-N phosphoryl Chemical group [P]=O LFGREXWGYUGZLY-UHFFFAOYSA-N 0.000 claims abstract 2
- 125000004194 piperazin-1-yl group Chemical group [H]N1C([H])([H])C([H])([H])N(*)C([H])([H])C1([H])[H] 0.000 claims abstract 2
- 125000004574 piperidin-2-yl group Chemical group N1C(CCCC1)* 0.000 claims abstract 2
- 125000004482 piperidin-4-yl group Chemical group N1CCC(CC1)* 0.000 claims abstract 2
- 150000003839 salts Chemical class 0.000 claims abstract 2
- 239000012453 solvate Substances 0.000 claims abstract 2
- 125000002023 trifluoromethyl group Chemical group FC(F)(F)* 0.000 claims abstract 2
- 125000004169 (C1-C6) alkyl group Chemical group 0.000 claims 6
- 230000001419 dependent effect Effects 0.000 claims 4
- 201000010099 disease Diseases 0.000 claims 4
- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 claims 4
- 239000008194 pharmaceutical composition Substances 0.000 claims 4
- 125000004181 carboxyalkyl group Chemical group 0.000 claims 3
- 125000006376 (C3-C10) cycloalkyl group Chemical group 0.000 claims 2
- ZBNZAJFNDPPMDT-UHFFFAOYSA-N 1h-imidazole-5-carboxamide Chemical compound NC(=O)C1=CNC=N1 ZBNZAJFNDPPMDT-UHFFFAOYSA-N 0.000 claims 2
- 150000001409 amidines Chemical class 0.000 claims 2
- 150000001556 benzimidazoles Chemical class 0.000 claims 2
- 150000001732 carboxylic acid derivatives Chemical class 0.000 claims 2
- 238000000034 method Methods 0.000 claims 2
- FHHUOFULEQWBBV-UHFFFAOYSA-N (7-hydroxy-2-thiophen-2-yl-1h-benzimidazol-4-yl)-piperazin-1-ylmethanone Chemical compound C1=2N=C(C=3SC=CC=3)NC=2C(O)=CC=C1C(=O)N1CCNCC1 FHHUOFULEQWBBV-UHFFFAOYSA-N 0.000 claims 1
- 125000006727 (C1-C6) alkenyl group Chemical group 0.000 claims 1
- 125000004191 (C1-C6) alkoxy group Chemical group 0.000 claims 1
- 125000004454 (C1-C6) alkoxycarbonyl group Chemical group 0.000 claims 1
- 125000004890 (C1-C6) alkylamino group Chemical group 0.000 claims 1
- 125000004739 (C1-C6) alkylsulfonyl group Chemical group 0.000 claims 1
- 125000004845 (C1-C6) alkylsulfonylamino group Chemical group 0.000 claims 1
- 125000006728 (C1-C6) alkynyl group Chemical group 0.000 claims 1
- HYZJCKYKOHLVJF-UHFFFAOYSA-N 1H-benzimidazole Chemical compound C1=CC=C2NC=NC2=C1 HYZJCKYKOHLVJF-UHFFFAOYSA-N 0.000 claims 1
- PQOKBQCVPUXWDC-UHFFFAOYSA-N 2-(3-bicyclo[2.2.1]heptanyl)-7-hydroxy-n-(piperidin-3-ylmethyl)-1h-benzimidazole-4-carboxamide Chemical compound C1=2N=C(C3C4CCC(C4)C3)NC=2C(O)=CC=C1C(=O)NCC1CCCNC1 PQOKBQCVPUXWDC-UHFFFAOYSA-N 0.000 claims 1
- HTUPKTNEAWAZLK-WRSKWOSUSA-N 2-(3-bicyclo[2.2.1]heptanyl)-7-hydroxy-n-[(3s)-piperidin-3-yl]-1h-benzimidazole-4-carboxamide Chemical compound C1=2N=C(C3C4CCC(C4)C3)NC=2C(O)=CC=C1C(=O)N[C@H]1CCCNC1 HTUPKTNEAWAZLK-WRSKWOSUSA-N 0.000 claims 1
- MVEAHJYWRFCHHJ-VIFPVBQESA-N 2-(5-bromothiophen-2-yl)-7-hydroxy-n-[(3s)-piperidin-3-yl]-1h-benzimidazole-4-carboxamide Chemical compound C1=2N=C(C=3SC(Br)=CC=3)NC=2C(O)=CC=C1C(=O)N[C@H]1CCCNC1 MVEAHJYWRFCHHJ-VIFPVBQESA-N 0.000 claims 1
- VNAZLEQAHPPEOM-UHFFFAOYSA-N 2-cyclopentyl-7-hydroxy-n-(piperidin-2-ylmethyl)-1h-benzimidazole-4-carboxamide Chemical compound C1=2NC(C3CCCC3)=NC=2C(O)=CC=C1C(=O)NCC1CCCCN1 VNAZLEQAHPPEOM-UHFFFAOYSA-N 0.000 claims 1
- DQLLQCMTQCCTEP-UHFFFAOYSA-N 2-cyclopentyl-7-hydroxy-n-(piperidin-3-ylmethyl)-1h-benzimidazole-4-carboxamide Chemical compound C1=2NC(C3CCCC3)=NC=2C(O)=CC=C1C(=O)NCC1CCCNC1 DQLLQCMTQCCTEP-UHFFFAOYSA-N 0.000 claims 1
- DMMFTUBCYQBWJG-LBPRGKRZSA-N 2-cyclopentyl-7-hydroxy-n-[(3s)-piperidin-3-yl]-1h-benzimidazole-4-carboxamide Chemical compound C1=2NC(C3CCCC3)=NC=2C(O)=CC=C1C(=O)N[C@H]1CCCNC1 DMMFTUBCYQBWJG-LBPRGKRZSA-N 0.000 claims 1
- NUIBNWKZKSUNBU-UHFFFAOYSA-N 2-cyclopropyl-7-hydroxy-n-(1-methylpiperidin-3-yl)-1h-benzimidazole-4-carboxamide Chemical compound C1N(C)CCCC1NC(=O)C1=CC=C(O)C2=C1NC(C1CC1)=N2 NUIBNWKZKSUNBU-UHFFFAOYSA-N 0.000 claims 1
- JQLOJXHUSKTZSN-UHFFFAOYSA-N 2-cyclopropyl-7-hydroxy-n-(piperidin-2-ylmethyl)-1h-benzimidazole-4-carboxamide Chemical compound C1=2NC(C3CC3)=NC=2C(O)=CC=C1C(=O)NCC1CCCCN1 JQLOJXHUSKTZSN-UHFFFAOYSA-N 0.000 claims 1
- VCFNQZLCDVKCQD-UHFFFAOYSA-N 2-cyclopropyl-7-hydroxy-n-(piperidin-3-ylmethyl)-1h-benzimidazole-4-carboxamide Chemical compound C1=2NC(C3CC3)=NC=2C(O)=CC=C1C(=O)NCC1CCCNC1 VCFNQZLCDVKCQD-UHFFFAOYSA-N 0.000 claims 1
- FOPKNXVYPWDCPH-UHFFFAOYSA-N 2-cyclopropyl-7-hydroxy-n-(piperidin-4-ylmethyl)-1h-benzimidazole-4-carboxamide Chemical compound C1=2NC(C3CC3)=NC=2C(O)=CC=C1C(=O)NCC1CCNCC1 FOPKNXVYPWDCPH-UHFFFAOYSA-N 0.000 claims 1
- VLDJPBYBKMFSBJ-JTQLQIEISA-N 2-cyclopropyl-7-hydroxy-n-[(3s)-piperidin-3-yl]-1h-benzimidazole-4-carboxamide Chemical compound C1=2NC(C3CC3)=NC=2C(O)=CC=C1C(=O)N[C@H]1CCCNC1 VLDJPBYBKMFSBJ-JTQLQIEISA-N 0.000 claims 1
- VLDJPBYBKMFSBJ-UHFFFAOYSA-N 2-cyclopropyl-7-hydroxy-n-piperidin-3-yl-1h-benzimidazole-4-carboxamide Chemical compound C1=2NC(C3CC3)=NC=2C(O)=CC=C1C(=O)NC1CCCNC1 VLDJPBYBKMFSBJ-UHFFFAOYSA-N 0.000 claims 1
- QWNYPKVETAWYSZ-UHFFFAOYSA-N 2-cyclopropyl-7-hydroxy-n-piperidin-4-yl-1h-benzimidazole-4-carboxamide Chemical compound C1=2NC(C3CC3)=NC=2C(O)=CC=C1C(=O)NC1CCNCC1 QWNYPKVETAWYSZ-UHFFFAOYSA-N 0.000 claims 1
- NEXCLKRXESRENY-UHFFFAOYSA-N 2-cyclopropyl-7-hydroxy-n-pyrrolidin-3-yl-1h-benzimidazole-4-carboxamide Chemical compound C1=2NC(C3CC3)=NC=2C(O)=CC=C1C(=O)NC1CCNC1 NEXCLKRXESRENY-UHFFFAOYSA-N 0.000 claims 1
- CWBZXCZNEOPRCN-ZDUSSCGKSA-N 7-hydroxy-2-(5-piperazin-1-ylthiophen-2-yl)-n-[(3s)-piperidin-3-yl]-1h-benzimidazole-4-carboxamide Chemical compound C1=2N=C(C=3SC(=CC=3)N3CCNCC3)NC=2C(O)=CC=C1C(=O)N[C@H]1CCCNC1 CWBZXCZNEOPRCN-ZDUSSCGKSA-N 0.000 claims 1
- HHWUJDYTPHLTIF-UHFFFAOYSA-N 7-hydroxy-2-phenyl-n-(piperidin-2-ylmethyl)-1h-benzimidazole-4-carboxamide Chemical compound C1=2NC(C=3C=CC=CC=3)=NC=2C(O)=CC=C1C(=O)NCC1CCCCN1 HHWUJDYTPHLTIF-UHFFFAOYSA-N 0.000 claims 1
- QUHAKLIRTFIRPF-UHFFFAOYSA-N 7-hydroxy-2-phenyl-n-(piperidin-3-ylmethyl)-1h-benzimidazole-4-carboxamide Chemical compound C1=2NC(C=3C=CC=CC=3)=NC=2C(O)=CC=C1C(=O)NCC1CCCNC1 QUHAKLIRTFIRPF-UHFFFAOYSA-N 0.000 claims 1
- HCOYOZKRGRMGIL-ZDUSSCGKSA-N 7-hydroxy-2-phenyl-n-[(3s)-piperidin-3-yl]-1h-benzimidazole-4-carboxamide Chemical compound C1=2NC(C=3C=CC=CC=3)=NC=2C(O)=CC=C1C(=O)N[C@H]1CCCNC1 HCOYOZKRGRMGIL-ZDUSSCGKSA-N 0.000 claims 1
- UHYZCMYXHGAMGC-UHFFFAOYSA-N 7-hydroxy-n-(1-methylpiperidin-3-yl)-2-thiophen-2-yl-1h-benzimidazole-4-carboxamide Chemical compound C1N(C)CCCC1NC(=O)C1=CC=C(O)C2=C1N=C(C=1SC=CC=1)N2 UHYZCMYXHGAMGC-UHFFFAOYSA-N 0.000 claims 1
- LRQSKLNGWMJWMJ-UHFFFAOYSA-N 7-hydroxy-n-(2-piperazin-1-ylethyl)-2-thiophen-2-yl-1h-benzimidazole-4-carboxamide Chemical compound C1=2N=C(C=3SC=CC=3)NC=2C(O)=CC=C1C(=O)NCCN1CCNCC1 LRQSKLNGWMJWMJ-UHFFFAOYSA-N 0.000 claims 1
- VYRHSZRZVBIDCD-UHFFFAOYSA-N 7-hydroxy-n-(piperidin-2-ylmethyl)-2-thiophen-2-yl-1h-benzimidazole-4-carboxamide Chemical compound C1=2N=C(C=3SC=CC=3)NC=2C(O)=CC=C1C(=O)NCC1CCCCN1 VYRHSZRZVBIDCD-UHFFFAOYSA-N 0.000 claims 1
- MTCFCASJWUBVGX-UHFFFAOYSA-N 7-hydroxy-n-(piperidin-3-ylmethyl)-2-thiophen-2-yl-1h-benzimidazole-4-carboxamide Chemical compound C1=2N=C(C=3SC=CC=3)NC=2C(O)=CC=C1C(=O)NCC1CCCNC1 MTCFCASJWUBVGX-UHFFFAOYSA-N 0.000 claims 1
- DLNUWZOWSGXCKJ-UHFFFAOYSA-N 7-hydroxy-n-(piperidin-4-ylmethyl)-2-thiophen-2-yl-1h-benzimidazole-4-carboxamide Chemical compound C1=2N=C(C=3SC=CC=3)NC=2C(O)=CC=C1C(=O)NCC1CCNCC1 DLNUWZOWSGXCKJ-UHFFFAOYSA-N 0.000 claims 1
- NJKUDKWJZPVSAI-UHFFFAOYSA-N 7-hydroxy-n-(pyrrolidin-3-ylmethyl)-2-thiophen-2-yl-1h-benzimidazole-4-carboxamide Chemical compound C1=2N=C(C=3SC=CC=3)NC=2C(O)=CC=C1C(=O)NCC1CCNC1 NJKUDKWJZPVSAI-UHFFFAOYSA-N 0.000 claims 1
- LJPSIRPRIUNDAT-SNVBAGLBSA-N 7-hydroxy-n-[(3r)-piperidin-3-yl]-2-thiophen-2-yl-1h-benzimidazole-4-carboxamide Chemical compound C1=2N=C(C=3SC=CC=3)NC=2C(O)=CC=C1C(=O)N[C@@H]1CCCNC1 LJPSIRPRIUNDAT-SNVBAGLBSA-N 0.000 claims 1
- FMCDOLBSRBSVDW-NSHDSACASA-N 7-hydroxy-n-[(3s)-piperidin-3-yl]-2-(thiophen-2-ylmethyl)-1h-benzimidazole-4-carboxamide Chemical compound C1=2N=C(CC=3SC=CC=3)NC=2C(O)=CC=C1C(=O)N[C@H]1CCCNC1 FMCDOLBSRBSVDW-NSHDSACASA-N 0.000 claims 1
- LJPSIRPRIUNDAT-JTQLQIEISA-N 7-hydroxy-n-[(3s)-piperidin-3-yl]-2-thiophen-2-yl-1h-benzimidazole-4-carboxamide Chemical compound C1=2N=C(C=3SC=CC=3)NC=2C(O)=CC=C1C(=O)N[C@H]1CCCNC1 LJPSIRPRIUNDAT-JTQLQIEISA-N 0.000 claims 1
- FQTGTVOVVRVTMG-GFCCVEGCSA-N 7-hydroxy-n-[[(3r)-piperidin-3-yl]methyl]-2-(thiophen-2-ylmethyl)-1h-benzimidazole-4-carboxamide Chemical compound C1=2N=C(CC=3SC=CC=3)NC=2C(O)=CC=C1C(=O)NC[C@@H]1CCCNC1 FQTGTVOVVRVTMG-GFCCVEGCSA-N 0.000 claims 1
- FQTGTVOVVRVTMG-LBPRGKRZSA-N 7-hydroxy-n-[[(3s)-piperidin-3-yl]methyl]-2-(thiophen-2-ylmethyl)-1h-benzimidazole-4-carboxamide Chemical compound C1=2N=C(CC=3SC=CC=3)NC=2C(O)=CC=C1C(=O)NC[C@H]1CCCNC1 FQTGTVOVVRVTMG-LBPRGKRZSA-N 0.000 claims 1
- LJPSIRPRIUNDAT-UHFFFAOYSA-N 7-hydroxy-n-piperidin-3-yl-2-thiophen-2-yl-1h-benzimidazole-4-carboxamide Chemical compound C1=2N=C(C=3SC=CC=3)NC=2C(O)=CC=C1C(=O)NC1CCCNC1 LJPSIRPRIUNDAT-UHFFFAOYSA-N 0.000 claims 1
- ITBAAQYBVUPCCT-UHFFFAOYSA-N 7-hydroxy-n-piperidin-4-yl-2-thiophen-2-yl-1h-benzimidazole-4-carboxamide Chemical compound C1=2N=C(C=3SC=CC=3)NC=2C(O)=CC=C1C(=O)NC1CCNCC1 ITBAAQYBVUPCCT-UHFFFAOYSA-N 0.000 claims 1
- WTHXQDHNQUSBSY-UHFFFAOYSA-N 7-hydroxy-n-pyrrolidin-3-yl-2-thiophen-2-yl-1h-benzimidazole-4-carboxamide Chemical compound C1=2N=C(C=3SC=CC=3)NC=2C(O)=CC=C1C(=O)NC1CCNC1 WTHXQDHNQUSBSY-UHFFFAOYSA-N 0.000 claims 1
- 206010028980 Neoplasm Diseases 0.000 claims 1
- 239000002253 acid Substances 0.000 claims 1
- 150000001412 amines Chemical class 0.000 claims 1
- 125000002490 anilino group Chemical class [H]N(*)C1=C([H])C([H])=C([H])C([H])=C1[H] 0.000 claims 1
- 201000011510 cancer Diseases 0.000 claims 1
- 239000003937 drug carrier Substances 0.000 claims 1
- LPRBRUJYZCFLPE-UHFFFAOYSA-N n-(3-amino-1-adamantyl)-2-(3-bicyclo[2.2.1]heptanyl)-7-hydroxy-1h-benzimidazole-4-carboxamide Chemical compound C1C(N)(C2)CC(C3)CC1CC32NC(=O)C1=CC=C(O)C2=C1N=C(C1C3CCC(C3)C1)N2 LPRBRUJYZCFLPE-UHFFFAOYSA-N 0.000 claims 1
- YUVCSUSHDGIPKN-UHFFFAOYSA-N n-(3-amino-1-adamantyl)-7-hydroxy-2-thiophen-2-yl-1h-benzimidazole-4-carboxamide Chemical compound C1C(N)(C2)CC(C3)CC1CC32NC(=O)C(C=1N=2)=CC=C(O)C=1NC=2C1=CC=CS1 YUVCSUSHDGIPKN-UHFFFAOYSA-N 0.000 claims 1
- FLSNBMIFUBTWCA-UHFFFAOYSA-N n-(3-aminocyclohexyl)-2-(3-bicyclo[2.2.1]heptanyl)-7-hydroxy-1h-benzimidazole-4-carboxamide Chemical compound C1C(N)CCCC1NC(=O)C1=CC=C(O)C2=C1N=C(C1C3CCC(C3)C1)N2 FLSNBMIFUBTWCA-UHFFFAOYSA-N 0.000 claims 1
- KADSEBMOTREHLE-UHFFFAOYSA-N n-(4-aminocyclohexyl)-7-hydroxy-2-thiophen-2-yl-1h-benzimidazole-4-carboxamide Chemical compound C1CC(N)CCC1NC(=O)C1=CC=C(O)C2=C1N=C(C=1SC=CC=1)N2 KADSEBMOTREHLE-UHFFFAOYSA-N 0.000 claims 1
- LGKPKPRXQJVEDQ-UHFFFAOYSA-N n-(azetidin-3-ylmethyl)-2-cyclopropyl-7-hydroxy-1h-benzimidazole-4-carboxamide Chemical compound C1=2NC(C3CC3)=NC=2C(O)=CC=C1C(=O)NCC1CNC1 LGKPKPRXQJVEDQ-UHFFFAOYSA-N 0.000 claims 1
- QOQKTKZYZAUZTA-UHFFFAOYSA-N n-(azetidin-3-ylmethyl)-7-hydroxy-2-thiophen-2-yl-1h-benzimidazole-4-carboxamide Chemical compound C1=2N=C(C=3SC=CC=3)NC=2C(O)=CC=C1C(=O)NCC1CNC1 QOQKTKZYZAUZTA-UHFFFAOYSA-N 0.000 claims 1
- MRGFHHVXSDCNRD-UHFFFAOYSA-N n-[(4-aminocyclohexyl)methyl]-2-(3-bicyclo[2.2.1]heptanyl)-7-hydroxy-1h-benzimidazole-4-carboxamide Chemical compound C1CC(N)CCC1CNC(=O)C1=CC=C(O)C2=C1N=C(C1C3CCC(C3)C1)N2 MRGFHHVXSDCNRD-UHFFFAOYSA-N 0.000 claims 1
- 150000002825 nitriles Chemical class 0.000 claims 1
- 230000002265 prevention Effects 0.000 claims 1
- 238000007363 ring formation reaction Methods 0.000 claims 1
- 238000007127 saponification reaction Methods 0.000 claims 1
- OFVZXLPLXYMCFA-LBPRGKRZSA-N tert-butyl (3s)-3-[[2-(5-bromothiophen-2-yl)-7-hydroxy-1h-benzimidazole-4-carbonyl]amino]piperidine-1-carboxylate Chemical compound C1N(C(=O)OC(C)(C)C)CCC[C@@H]1NC(=O)C1=CC=C(O)C2=C1N=C(C=1SC(Br)=CC=1)N2 OFVZXLPLXYMCFA-LBPRGKRZSA-N 0.000 claims 1
- 125000000217 alkyl group Chemical group 0.000 abstract 6
- 125000000753 cycloalkyl group Chemical group 0.000 abstract 2
- 125000003342 alkenyl group Chemical group 0.000 abstract 1
- 125000003545 alkoxy group Chemical group 0.000 abstract 1
- 125000004453 alkoxycarbonyl group Chemical group 0.000 abstract 1
- 125000003282 alkyl amino group Chemical group 0.000 abstract 1
- 125000004390 alkyl sulfonyl group Chemical group 0.000 abstract 1
- 125000004656 alkyl sulfonylamino group Chemical group 0.000 abstract 1
- 125000000304 alkynyl group Chemical group 0.000 abstract 1
- 125000002619 bicyclic group Chemical group 0.000 abstract 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D235/00—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, condensed with other rings
- C07D235/02—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, condensed with other rings condensed with carbocyclic rings or ring systems
- C07D235/04—Benzimidazoles; Hydrogenated benzimidazoles
- C07D235/06—Benzimidazoles; Hydrogenated benzimidazoles with only hydrogen atoms, hydrocarbon or substituted hydrocarbon radicals, directly attached in position 2
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D235/00—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, condensed with other rings
- C07D235/02—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, condensed with other rings condensed with carbocyclic rings or ring systems
- C07D235/04—Benzimidazoles; Hydrogenated benzimidazoles
- C07D235/06—Benzimidazoles; Hydrogenated benzimidazoles with only hydrogen atoms, hydrocarbon or substituted hydrocarbon radicals, directly attached in position 2
- C07D235/08—Radicals containing only hydrogen and carbon atoms
-
- 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
- A61K31/41—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with two or more ring hetero atoms, at least one of which being nitrogen, e.g. tetrazole
- A61K31/4164—1,3-Diazoles
- A61K31/4184—1,3-Diazoles condensed with carbocyclic rings, e.g. benzimidazoles
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P35/00—Antineoplastic agents
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P43/00—Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D235/00—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, condensed with other rings
- C07D235/02—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, condensed with other rings condensed with carbocyclic rings or ring systems
- C07D235/04—Benzimidazoles; Hydrogenated benzimidazoles
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D401/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom
- C07D401/02—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings
- C07D401/12—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings linked by a chain containing hetero atoms as chain links
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D409/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms
- C07D409/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms containing two hetero rings
- C07D409/04—Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms containing two hetero rings directly linked by a ring-member-to-ring-member bond
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D409/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms
- C07D409/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms containing two hetero rings
- C07D409/06—Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms containing two hetero rings linked by a carbon chain containing only aliphatic carbon atoms
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D409/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms
- C07D409/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms containing two hetero rings
- C07D409/12—Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms containing two hetero rings linked by a chain containing hetero atoms as chain links
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- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- General Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Veterinary Medicine (AREA)
- Public Health (AREA)
- Medicinal Chemistry (AREA)
- Animal Behavior & Ethology (AREA)
- Pharmacology & Pharmacy (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- General Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Engineering & Computer Science (AREA)
- Epidemiology (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Plural Heterocyclic Compounds (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US10980108P | 2008-10-30 | 2008-10-30 | |
| US61/109,801 | 2008-10-30 | ||
| PCT/US2009/052228 WO2010051085A1 (en) | 2008-10-30 | 2009-07-30 | 7-hydroxy-benzoimidazole-4-yl-methanone derivatives and pbk inhibitors containing the same |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| RU2011121665A true RU2011121665A (ru) | 2012-12-10 |
Family
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Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| RU2011121665/13A RU2011121665A (ru) | 2008-10-30 | 2009-07-30 | Производные 7-гидроксибензимидазол-4-илметанона и содержащие их ингибиторы рвк |
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| US (1) | US20110263566A1 (enExample) |
| EP (1) | EP2364087A4 (enExample) |
| JP (1) | JP2012507525A (enExample) |
| KR (1) | KR20110079847A (enExample) |
| CN (1) | CN102271514A (enExample) |
| AU (1) | AU2009310310A1 (enExample) |
| BR (1) | BRPI0919977A2 (enExample) |
| CA (1) | CA2741988A1 (enExample) |
| CO (1) | CO6361855A2 (enExample) |
| IL (1) | IL212544A0 (enExample) |
| MX (1) | MX2011004414A (enExample) |
| RU (1) | RU2011121665A (enExample) |
| WO (1) | WO2010051085A1 (enExample) |
| ZA (1) | ZA201103964B (enExample) |
Families Citing this family (10)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| KR20090064378A (ko) | 2006-08-10 | 2009-06-18 | 온코세라피 사이언스 가부시키가이샤 | 유방암 관련 유전자 및 폴리펩티드 |
| RU2011107227A (ru) * | 2008-07-30 | 2012-09-10 | Онкотерапи Сайенс, Инк. (Jp) | Бензоимидазольные производные и ингибиторы гликоген-синтаза-киназы-3 бета, содержащие такие производные |
| EP2358365A4 (en) * | 2008-11-20 | 2012-05-30 | Oncotherapy Science Inc | GLYCOGEN SYNTHASE KINASE 3 BETA HEMMER WITH 7-HYDROXY BENZOIMIDAZOLE-4-YL METHANONE DERIVATIVES |
| CN101619058A (zh) * | 2009-01-08 | 2010-01-06 | 上海交通大学 | 一种苯并咪唑-4-酰胺型衍生物 |
| US9556117B2 (en) * | 2012-12-18 | 2017-01-31 | Actelion Pharmaceuticals Ltd. | Indole carboxamide derivatives as P2X7 receptor antagonists |
| CN105017221B (zh) * | 2014-04-30 | 2019-05-28 | 中国医学科学院药物研究所 | 苯并咪唑衍生物及其制法和药物组合物与用途 |
| ES2828961T3 (es) * | 2015-07-30 | 2021-05-28 | Daiichi Sankyo Co Ltd | Agente terapéutico y/o profiláctico para leucemia/linfoma de células T del adulto |
| WO2019124608A1 (ko) * | 2017-12-22 | 2019-06-27 | 경상대학교병원 | 4'-(p-톨루엔설포닐아미도)-4-하이드록시칼콘을 유효성분으로 함유하는 류마티스 관절염 예방 또는 치료용 약학 조성물 |
| CN109320461B (zh) * | 2018-12-12 | 2020-02-07 | 迪嘉药业集团有限公司 | 一种替米沙坦中间体的制备方法 |
| CA3134613A1 (en) | 2019-04-02 | 2020-10-08 | Aligos Therapeutics, Inc. | Compounds targeting prmt5 |
Family Cites Families (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US6288100B1 (en) * | 1995-06-06 | 2001-09-11 | American Home Products Corporation | Benzimidazole derivatives |
| US20040002524A1 (en) * | 2002-06-24 | 2004-01-01 | Richard Chesworth | Benzimidazole compounds and their use as estrogen agonists/antagonists |
| JP2006515013A (ja) * | 2003-01-23 | 2006-05-18 | クリスタルジェノミクス、インコーポレイテッド | グリコーゲン合成酵素キナーゼ３β活性抑制剤、組成物及びその製造方法 |
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2009
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- 2009-07-30 BR BRPI0919977-2A patent/BRPI0919977A2/pt not_active IP Right Cessation
- 2009-07-30 US US13/126,741 patent/US20110263566A1/en not_active Abandoned
- 2009-07-30 WO PCT/US2009/052228 patent/WO2010051085A1/en not_active Ceased
- 2009-07-30 EP EP09823973A patent/EP2364087A4/en not_active Withdrawn
- 2009-07-30 KR KR1020117011835A patent/KR20110079847A/ko not_active Withdrawn
- 2009-07-30 CN CN2009801533867A patent/CN102271514A/zh not_active Withdrawn
- 2009-07-30 RU RU2011121665/13A patent/RU2011121665A/ru not_active Application Discontinuation
- 2009-07-30 JP JP2011534550A patent/JP2012507525A/ja not_active Withdrawn
- 2009-07-30 MX MX2011004414A patent/MX2011004414A/es unknown
- 2009-07-30 CA CA2741988A patent/CA2741988A1/en not_active Abandoned
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2011
- 2011-04-28 IL IL212544A patent/IL212544A0/en unknown
- 2011-05-17 CO CO11060496A patent/CO6361855A2/es not_active Application Discontinuation
- 2011-05-30 ZA ZA2011/03964A patent/ZA201103964B/en unknown
Also Published As
| Publication number | Publication date |
|---|---|
| EP2364087A1 (en) | 2011-09-14 |
| IL212544A0 (en) | 2011-06-30 |
| MX2011004414A (es) | 2011-06-21 |
| US20110263566A1 (en) | 2011-10-27 |
| AU2009310310A2 (en) | 2011-10-06 |
| JP2012507525A (ja) | 2012-03-29 |
| CA2741988A1 (en) | 2010-05-06 |
| EP2364087A4 (en) | 2012-05-30 |
| ZA201103964B (en) | 2012-02-29 |
| KR20110079847A (ko) | 2011-07-08 |
| CN102271514A (zh) | 2011-12-07 |
| WO2010051085A1 (en) | 2010-05-06 |
| AU2009310310A1 (en) | 2010-05-06 |
| BRPI0919977A2 (pt) | 2015-08-25 |
| CO6361855A2 (es) | 2012-01-20 |
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Legal Events
| Date | Code | Title | Description |
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| FA93 | Acknowledgement of application withdrawn (no request for examination) |
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