RU2458920C2 - Новые соединения - Google Patents
Новые соединения Download PDFInfo
- Publication number
- RU2458920C2 RU2458920C2 RU2009127644/04A RU2009127644A RU2458920C2 RU 2458920 C2 RU2458920 C2 RU 2458920C2 RU 2009127644/04 A RU2009127644/04 A RU 2009127644/04A RU 2009127644 A RU2009127644 A RU 2009127644A RU 2458920 C2 RU2458920 C2 RU 2458920C2
- Authority
- RU
- Russia
- Prior art keywords
- pyrazol
- dimethoxyphenyl
- ethyl
- carboxamide
- benzamide
- Prior art date
Links
- 150000001875 compounds Chemical class 0.000 title claims abstract 16
- 150000003839 salts Chemical class 0.000 claims abstract 7
- 230000000694 effects Effects 0.000 claims abstract 4
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims abstract 3
- 239000003814 drug Substances 0.000 claims abstract 3
- 229940125829 fibroblast growth factor receptor inhibitor Drugs 0.000 claims abstract 3
- 229910052739 hydrogen Inorganic materials 0.000 claims abstract 3
- 239000001257 hydrogen Substances 0.000 claims abstract 3
- 239000008194 pharmaceutical composition Substances 0.000 claims abstract 3
- -1 3,5-dimethoxyphenyl Chemical group 0.000 claims 45
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 claims 17
- 125000000956 methoxy group Chemical group [H]C([H])([H])O* 0.000 claims 10
- VRQMAABPASPXMW-HDICACEKSA-N AZD4547 Chemical compound COC1=CC(OC)=CC(CCC=2NN=C(NC(=O)C=3C=CC(=CC=3)N3C[C@@H](C)N[C@@H](C)C3)C=2)=C1 VRQMAABPASPXMW-HDICACEKSA-N 0.000 claims 2
- PFZTXTPVKAGHPW-UHFFFAOYSA-N n-[5-[2-(3,5-dimethoxyphenyl)ethyl]-1h-pyrazol-3-yl]-4-(3,4-dimethylpiperazin-1-yl)benzamide Chemical compound COC1=CC(OC)=CC(CCC=2NN=C(NC(=O)C=3C=CC(=CC=3)N3CC(C)N(C)CC3)C=2)=C1 PFZTXTPVKAGHPW-UHFFFAOYSA-N 0.000 claims 2
- QDXGKRWDQCEABB-UHFFFAOYSA-N pyrimidine-5-carboxamide Chemical compound NC(=O)C1=CN=CN=C1 QDXGKRWDQCEABB-UHFFFAOYSA-N 0.000 claims 2
- GSZMBOOFYZJXIE-UHFFFAOYSA-N 2-(4-cyclopropyl-1,4-diazepan-1-yl)-n-[5-[2-(3,5-dimethoxyphenyl)ethyl]-1h-pyrazol-3-yl]pyrimidine-5-carboxamide Chemical compound COC1=CC(OC)=CC(CCC2=NNC(NC(=O)C=3C=NC(=NC=3)N3CCN(CCC3)C3CC3)=C2)=C1 GSZMBOOFYZJXIE-UHFFFAOYSA-N 0.000 claims 1
- IDPLQWNTAFBGOW-UHFFFAOYSA-N 2-(4-cyclopropylpiperazin-1-yl)-n-[5-[2-(3,5-dimethoxyphenyl)ethyl]-1h-pyrazol-3-yl]pyrimidine-5-carboxamide Chemical compound COC1=CC(OC)=CC(CCC2=NNC(NC(=O)C=3C=NC(=NC=3)N3CCN(CC3)C3CC3)=C2)=C1 IDPLQWNTAFBGOW-UHFFFAOYSA-N 0.000 claims 1
- XUNYGASTGARZMD-UHFFFAOYSA-N 4-(1,3,4,6,7,8,9,9a-octahydropyrido[1,2-a]pyrazin-2-yl)-n-[5-[2-(3,5-dimethoxyphenyl)ethyl]-1h-pyrazol-3-yl]benzamide Chemical compound COC1=CC(OC)=CC(CCC2=NNC(NC(=O)C=3C=CC(=CC=3)N3CC4CCCCN4CC3)=C2)=C1 XUNYGASTGARZMD-UHFFFAOYSA-N 0.000 claims 1
- PLAXUYJGONDQAU-UHFFFAOYSA-N 4-(1,4-diazepan-1-yl)-n-[5-[2-(3,5-dimethoxyphenyl)ethyl]-1h-pyrazol-3-yl]benzamide Chemical compound COC1=CC(OC)=CC(CCC2=NNC(NC(=O)C=3C=CC(=CC=3)N3CCNCCC3)=C2)=C1 PLAXUYJGONDQAU-UHFFFAOYSA-N 0.000 claims 1
- VQZLJZIEDTZTQJ-UHFFFAOYSA-N 4-(1-cyclopropylpiperidin-4-yl)-n-[5-[2-(3,5-dimethoxyphenyl)ethyl]-1h-pyrazol-3-yl]benzamide Chemical compound COC1=CC(OC)=CC(CCC2=NNC(NC(=O)C=3C=CC(=CC=3)C3CCN(CC3)C3CC3)=C2)=C1 VQZLJZIEDTZTQJ-UHFFFAOYSA-N 0.000 claims 1
- AJRZAIWDKUDXTA-UHFFFAOYSA-N 4-(3,4,6,7,8,8a-hexahydro-1h-pyrrolo[1,2-a]pyrazin-2-yl)-n-[3-[(3,5-dimethoxyphenyl)methoxy]-1h-pyrazol-5-yl]benzamide Chemical compound COC1=CC(OC)=CC(COC2=NNC(NC(=O)C=3C=CC(=CC=3)N3CC4CCCN4CC3)=C2)=C1 AJRZAIWDKUDXTA-UHFFFAOYSA-N 0.000 claims 1
- FILOJIFKRJXQCS-UHFFFAOYSA-N 4-(3,4,6,7,8,8a-hexahydro-1h-pyrrolo[1,2-a]pyrazin-2-yl)-n-[5-[2-(3,5-dimethoxyphenyl)ethyl]-1h-pyrazol-3-yl]benzamide Chemical compound COC1=CC(OC)=CC(CCC2=NNC(NC(=O)C=3C=CC(=CC=3)N3CC4CCCN4CC3)=C2)=C1 FILOJIFKRJXQCS-UHFFFAOYSA-N 0.000 claims 1
- CPYWICDXAPUQNJ-UHFFFAOYSA-N 4-(4-cyclobutylpiperazin-1-yl)-n-[3-[(3,5-dimethoxyphenyl)methoxy]-1h-pyrazol-5-yl]benzamide Chemical compound COC1=CC(OC)=CC(COC2=NNC(NC(=O)C=3C=CC(=CC=3)N3CCN(CC3)C3CCC3)=C2)=C1 CPYWICDXAPUQNJ-UHFFFAOYSA-N 0.000 claims 1
- LHCIFVUABPXLJF-UHFFFAOYSA-N 4-(4-cyclobutylpiperazin-1-yl)-n-[5-[2-(3,5-dimethoxyphenyl)ethyl]-1h-pyrazol-3-yl]benzamide Chemical compound COC1=CC(OC)=CC(CCC=2NN=C(NC(=O)C=3C=CC(=CC=3)N3CCN(CC3)C3CCC3)C=2)=C1 LHCIFVUABPXLJF-UHFFFAOYSA-N 0.000 claims 1
- REPFWMXEYOBBGF-UHFFFAOYSA-N 4-(4-cyclopropyl-1,4-diazepan-1-yl)-n-[5-[2-(3,5-dimethoxyphenyl)ethyl]-1h-pyrazol-3-yl]benzamide Chemical compound COC1=CC(OC)=CC(CCC2=NNC(NC(=O)C=3C=CC(=CC=3)N3CCN(CCC3)C3CC3)=C2)=C1 REPFWMXEYOBBGF-UHFFFAOYSA-N 0.000 claims 1
- FICSDJQCXTVTCL-UHFFFAOYSA-N 4-(4-cyclopropylpiperazin-1-yl)-n-[3-[(3,5-dimethoxyphenyl)methoxy]-1h-pyrazol-5-yl]benzamide Chemical compound COC1=CC(OC)=CC(COC2=NNC(NC(=O)C=3C=CC(=CC=3)N3CCN(CC3)C3CC3)=C2)=C1 FICSDJQCXTVTCL-UHFFFAOYSA-N 0.000 claims 1
- AAKMLYNRXVOJET-UHFFFAOYSA-N 4-(4-cyclopropylpiperazin-1-yl)-n-[5-[2-(3,5-dimethoxyphenyl)ethyl]-1h-pyrazol-3-yl]benzamide Chemical compound COC1=CC(OC)=CC(CCC=2NN=C(NC(=O)C=3C=CC(=CC=3)N3CCN(CC3)C3CC3)C=2)=C1 AAKMLYNRXVOJET-UHFFFAOYSA-N 0.000 claims 1
- PKXJQHUMHSTQSA-CALCHBBNSA-N 5-[(3s,5r)-4-(cyanomethyl)-3,5-dimethylpiperazin-1-yl]-n-[3-[(3,5-dimethoxyphenyl)methoxy]-1h-pyrazol-5-yl]pyrazine-2-carboxamide Chemical compound COC1=CC(OC)=CC(COC2=NNC(NC(=O)C=3N=CC(=NC=3)N3C[C@@H](C)N(CC#N)[C@@H](C)C3)=C2)=C1 PKXJQHUMHSTQSA-CALCHBBNSA-N 0.000 claims 1
- CEIPMDRYPQMWNG-UHFFFAOYSA-N 5-[3-(diethylamino)pyrrolidin-1-yl]-n-[5-[2-(3,5-dimethoxyphenyl)ethyl]-1h-pyrazol-3-yl]pyrazine-2-carboxamide Chemical compound C1C(N(CC)CC)CCN1C1=CN=C(C(=O)NC=2NN=C(CCC=3C=C(OC)C=C(OC)C=3)C=2)C=N1 CEIPMDRYPQMWNG-UHFFFAOYSA-N 0.000 claims 1
- 108091008794 FGF receptors Proteins 0.000 claims 1
- 239000002671 adjuvant Substances 0.000 claims 1
- 239000003085 diluting agent Substances 0.000 claims 1
- 102000052178 fibroblast growth factor receptor activity proteins Human genes 0.000 claims 1
- 230000002401 inhibitory effect Effects 0.000 claims 1
- 238000004519 manufacturing process Methods 0.000 claims 1
- ADJDDCLUGPVSCT-UHFFFAOYSA-N n-(1-ethylpiperidin-4-yl)benzamide Chemical compound C1CN(CC)CCC1NC(=O)C1=CC=CC=C1 ADJDDCLUGPVSCT-UHFFFAOYSA-N 0.000 claims 1
- KABBUICSDDSZHY-UHFFFAOYSA-N n-[3-[(3,5-dimethoxyphenyl)methoxy]-1h-pyrazol-5-yl]-2-(4-methylpiperazin-1-yl)pyrimidine-5-carboxamide Chemical compound COC1=CC(OC)=CC(COC=2NN=C(NC(=O)C=3C=NC(=NC=3)N3CCN(C)CC3)C=2)=C1 KABBUICSDDSZHY-UHFFFAOYSA-N 0.000 claims 1
- APPRGXHIUOWFLJ-UHFFFAOYSA-N n-[3-[(3,5-dimethoxyphenyl)methoxy]-1h-pyrazol-5-yl]-4-(1-methylpiperidin-4-yl)benzamide Chemical compound COC1=CC(OC)=CC(COC2=NNC(NC(=O)C=3C=CC(=CC=3)C3CCN(C)CC3)=C2)=C1 APPRGXHIUOWFLJ-UHFFFAOYSA-N 0.000 claims 1
- KZTLOKUXUKISRM-UHFFFAOYSA-N n-[3-[(3,5-dimethoxyphenyl)methoxy]-1h-pyrazol-5-yl]-4-(3,3-dimethylpiperazin-1-yl)benzamide Chemical compound COC1=CC(OC)=CC(COC2=NNC(NC(=O)C=3C=CC(=CC=3)N3CC(C)(C)NCC3)=C2)=C1 KZTLOKUXUKISRM-UHFFFAOYSA-N 0.000 claims 1
- DFDRSTKZIRHZJZ-UHFFFAOYSA-N n-[3-[(3,5-dimethoxyphenyl)methoxy]-1h-pyrazol-5-yl]-4-(3,4-dimethylpiperazin-1-yl)benzamide Chemical compound COC1=CC(OC)=CC(COC2=NNC(NC(=O)C=3C=CC(=CC=3)N3CC(C)N(C)CC3)=C2)=C1 DFDRSTKZIRHZJZ-UHFFFAOYSA-N 0.000 claims 1
- ADTZRSTUJXIHGE-HDICACEKSA-N n-[3-[(3,5-dimethoxyphenyl)methoxy]-1h-pyrazol-5-yl]-4-[(3r,5s)-3,4,5-trimethylpiperazin-1-yl]benzamide Chemical compound COC1=CC(OC)=CC(COC2=NNC(NC(=O)C=3C=CC(=CC=3)N3C[C@@H](C)N(C)[C@@H](C)C3)=C2)=C1 ADTZRSTUJXIHGE-HDICACEKSA-N 0.000 claims 1
- AKOUAKDGWAGIOY-CALCHBBNSA-N n-[3-[(3,5-dimethoxyphenyl)methoxy]-1h-pyrazol-5-yl]-4-[(3r,5s)-3,5-dimethylpiperazin-1-yl]benzamide Chemical compound COC1=CC(OC)=CC(COC2=NNC(NC(=O)C=3C=CC(=CC=3)N3C[C@@H](C)N[C@@H](C)C3)=C2)=C1 AKOUAKDGWAGIOY-CALCHBBNSA-N 0.000 claims 1
- RCMFWEPHBXSEJD-UHFFFAOYSA-N n-[3-[(3,5-dimethoxyphenyl)methoxy]-1h-pyrazol-5-yl]-4-methoxybenzamide Chemical compound C1=CC(OC)=CC=C1C(=O)NC1=CC(OCC=2C=C(OC)C=C(OC)C=2)=NN1 RCMFWEPHBXSEJD-UHFFFAOYSA-N 0.000 claims 1
- VGRSGFKGDIBBDY-UHFFFAOYSA-N n-[3-[(3,5-dimethoxyphenyl)methoxy]-1h-pyrazol-5-yl]-5-(3,3-dimethylpiperazin-1-yl)thiophene-2-carboxamide Chemical compound COC1=CC(OC)=CC(COC2=NNC(NC(=O)C=3SC(=CC=3)N3CC(C)(C)NCC3)=C2)=C1 VGRSGFKGDIBBDY-UHFFFAOYSA-N 0.000 claims 1
- PQOAVCZIWSDZRF-UHFFFAOYSA-N n-[3-[(3,5-dimethoxyphenyl)methoxy]-1h-pyrazol-5-yl]-5-(4-methylpiperazin-1-yl)thiophene-2-carboxamide Chemical compound COC1=CC(OC)=CC(COC2=NNC(NC(=O)C=3SC(=CC=3)N3CCN(C)CC3)=C2)=C1 PQOAVCZIWSDZRF-UHFFFAOYSA-N 0.000 claims 1
- ZXQKDGVRECCNPW-GASCZTMLSA-N n-[3-[(3,5-dimethoxyphenyl)methoxy]-1h-pyrazol-5-yl]-5-[(3r,5s)-3,5-dimethylpiperazin-1-yl]thiophene-2-carboxamide Chemical compound COC1=CC(OC)=CC(COC2=NNC(NC(=O)C=3SC(=CC=3)N3C[C@@H](C)N[C@@H](C)C3)=C2)=C1 ZXQKDGVRECCNPW-GASCZTMLSA-N 0.000 claims 1
- XQOCOFYGTCSAOM-UHFFFAOYSA-N n-[5-[2-(3,5-dimethoxyphenyl)ethyl]-1h-pyrazol-3-yl]-2-(1-methylpiperidin-4-yl)pyrimidine-5-carboxamide Chemical compound COC1=CC(OC)=CC(CCC2=NNC(NC(=O)C=3C=NC(=NC=3)C3CCN(C)CC3)=C2)=C1 XQOCOFYGTCSAOM-UHFFFAOYSA-N 0.000 claims 1
- FVNRGESZWOWIOE-UHFFFAOYSA-N n-[5-[2-(3,5-dimethoxyphenyl)ethyl]-1h-pyrazol-3-yl]-2-(3,4-dimethylpiperazin-1-yl)pyrimidine-5-carboxamide Chemical compound COC1=CC(OC)=CC(CCC2=NNC(NC(=O)C=3C=NC(=NC=3)N3CC(C)N(C)CC3)=C2)=C1 FVNRGESZWOWIOE-UHFFFAOYSA-N 0.000 claims 1
- CZXNOIODNKWIMD-UHFFFAOYSA-N n-[5-[2-(3,5-dimethoxyphenyl)ethyl]-1h-pyrazol-3-yl]-2-(4-ethyl-1,4-diazepan-1-yl)pyrimidine-5-carboxamide Chemical compound C1CN(CC)CCCN1C1=NC=C(C(=O)NC=2NN=C(CCC=3C=C(OC)C=C(OC)C=3)C=2)C=N1 CZXNOIODNKWIMD-UHFFFAOYSA-N 0.000 claims 1
- FAHBNVACFBFOJF-UHFFFAOYSA-N n-[5-[2-(3,5-dimethoxyphenyl)ethyl]-1h-pyrazol-3-yl]-2-(4-ethyl-3-methylpiperazin-1-yl)pyrimidine-5-carboxamide Chemical compound C1C(C)N(CC)CCN1C1=NC=C(C(=O)NC=2NN=C(CCC=3C=C(OC)C=C(OC)C=3)C=2)C=N1 FAHBNVACFBFOJF-UHFFFAOYSA-N 0.000 claims 1
- MXXLFRNLGXFBFX-UHFFFAOYSA-N n-[5-[2-(3,5-dimethoxyphenyl)ethyl]-1h-pyrazol-3-yl]-2-(4-methyl-1,4-diazepan-1-yl)pyrimidine-5-carboxamide Chemical compound COC1=CC(OC)=CC(CCC2=NNC(NC(=O)C=3C=NC(=NC=3)N3CCN(C)CCC3)=C2)=C1 MXXLFRNLGXFBFX-UHFFFAOYSA-N 0.000 claims 1
- SBOMLRJHYLXHOT-UHFFFAOYSA-N n-[5-[2-(3,5-dimethoxyphenyl)ethyl]-1h-pyrazol-3-yl]-2-(4-methylpiperazin-1-yl)pyrimidine-5-carboxamide Chemical compound COC1=CC(OC)=CC(CCC2=NNC(NC(=O)C=3C=NC(=NC=3)N3CCN(C)CC3)=C2)=C1 SBOMLRJHYLXHOT-UHFFFAOYSA-N 0.000 claims 1
- BLSDFZNQLNQDHA-UHFFFAOYSA-N n-[5-[2-(3,5-dimethoxyphenyl)ethyl]-1h-pyrazol-3-yl]-2-(4-prop-2-enyl-1,4-diazepan-1-yl)pyrimidine-5-carboxamide Chemical compound COC1=CC(OC)=CC(CCC2=NNC(NC(=O)C=3C=NC(=NC=3)N3CCN(CC=C)CCC3)=C2)=C1 BLSDFZNQLNQDHA-UHFFFAOYSA-N 0.000 claims 1
- DVALSWWLWJAYFA-UHFFFAOYSA-N n-[5-[2-(3,5-dimethoxyphenyl)ethyl]-1h-pyrazol-3-yl]-2-(4-propan-2-yl-1,4-diazepan-1-yl)pyrimidine-5-carboxamide Chemical compound COC1=CC(OC)=CC(CCC2=NNC(NC(=O)C=3C=NC(=NC=3)N3CCN(CCC3)C(C)C)=C2)=C1 DVALSWWLWJAYFA-UHFFFAOYSA-N 0.000 claims 1
- VHIJSBLWIJRAQN-CALCHBBNSA-N n-[5-[2-(3,5-dimethoxyphenyl)ethyl]-1h-pyrazol-3-yl]-2-[(3r,5s)-3,4,5-trimethylpiperazin-1-yl]pyrimidine-5-carboxamide Chemical compound COC1=CC(OC)=CC(CCC2=NNC(NC(=O)C=3C=NC(=NC=3)N3C[C@@H](C)N(C)[C@@H](C)C3)=C2)=C1 VHIJSBLWIJRAQN-CALCHBBNSA-N 0.000 claims 1
- QEAUOXZTRVBQEI-UHFFFAOYSA-N n-[5-[2-(3,5-dimethoxyphenyl)ethyl]-1h-pyrazol-3-yl]-4-(1-methylpiperidin-4-yl)benzamide Chemical compound COC1=CC(OC)=CC(CCC=2NN=C(NC(=O)C=3C=CC(=CC=3)C3CCN(C)CC3)C=2)=C1 QEAUOXZTRVBQEI-UHFFFAOYSA-N 0.000 claims 1
- KJHGWDAUJWJTCZ-UHFFFAOYSA-N n-[5-[2-(3,5-dimethoxyphenyl)ethyl]-1h-pyrazol-3-yl]-4-(1-prop-2-enylpiperidin-4-yl)benzamide Chemical compound COC1=CC(OC)=CC(CCC2=NNC(NC(=O)C=3C=CC(=CC=3)C3CCN(CC=C)CC3)=C2)=C1 KJHGWDAUJWJTCZ-UHFFFAOYSA-N 0.000 claims 1
- LJZRBNAGMCJTIR-UHFFFAOYSA-N n-[5-[2-(3,5-dimethoxyphenyl)ethyl]-1h-pyrazol-3-yl]-4-(1-prop-2-ynylpiperidin-4-yl)benzamide Chemical compound COC1=CC(OC)=CC(CCC2=NNC(NC(=O)C=3C=CC(=CC=3)C3CCN(CC#C)CC3)=C2)=C1 LJZRBNAGMCJTIR-UHFFFAOYSA-N 0.000 claims 1
- DCXJUCGEYZYQKT-UHFFFAOYSA-N n-[5-[2-(3,5-dimethoxyphenyl)ethyl]-1h-pyrazol-3-yl]-4-(2-ethoxyethoxy)benzamide Chemical compound C1=CC(OCCOCC)=CC=C1C(=O)NC1=NNC(CCC=2C=C(OC)C=C(OC)C=2)=C1 DCXJUCGEYZYQKT-UHFFFAOYSA-N 0.000 claims 1
- OFPZHPFNAAUZHU-UHFFFAOYSA-N n-[5-[2-(3,5-dimethoxyphenyl)ethyl]-1h-pyrazol-3-yl]-4-(3,3-dimethylpiperazin-1-yl)benzamide Chemical compound COC1=CC(OC)=CC(CCC2=NNC(NC(=O)C=3C=CC(=CC=3)N3CC(C)(C)NCC3)=C2)=C1 OFPZHPFNAAUZHU-UHFFFAOYSA-N 0.000 claims 1
- WCSHYWQDZXNEEQ-UHFFFAOYSA-N n-[5-[2-(3,5-dimethoxyphenyl)ethyl]-1h-pyrazol-3-yl]-4-(3,4,5-trimethylpiperazin-1-yl)benzamide Chemical compound COC1=CC(OC)=CC(CCC=2NN=C(NC(=O)C=3C=CC(=CC=3)N3CC(C)N(C)C(C)C3)C=2)=C1 WCSHYWQDZXNEEQ-UHFFFAOYSA-N 0.000 claims 1
- VRQMAABPASPXMW-UHFFFAOYSA-N n-[5-[2-(3,5-dimethoxyphenyl)ethyl]-1h-pyrazol-3-yl]-4-(3,5-dimethylpiperazin-1-yl)benzamide Chemical compound COC1=CC(OC)=CC(CCC2=NNC(NC(=O)C=3C=CC(=CC=3)N3CC(C)NC(C)C3)=C2)=C1 VRQMAABPASPXMW-UHFFFAOYSA-N 0.000 claims 1
- UECZYORGLPLSJC-UHFFFAOYSA-N n-[5-[2-(3,5-dimethoxyphenyl)ethyl]-1h-pyrazol-3-yl]-4-(4-ethyl-1,4-diazepan-1-yl)benzamide Chemical compound C1CN(CC)CCCN1C1=CC=C(C(=O)NC=2NN=C(CCC=3C=C(OC)C=C(OC)C=3)C=2)C=C1 UECZYORGLPLSJC-UHFFFAOYSA-N 0.000 claims 1
- UJJSGJULFHMHMJ-UHFFFAOYSA-N n-[5-[2-(3,5-dimethoxyphenyl)ethyl]-1h-pyrazol-3-yl]-4-(4-ethylpiperazin-1-yl)benzamide Chemical compound C1CN(CC)CCN1C1=CC=C(C(=O)NC=2NN=C(CCC=3C=C(OC)C=C(OC)C=3)C=2)C=C1 UJJSGJULFHMHMJ-UHFFFAOYSA-N 0.000 claims 1
- WTLALQRLHBXTHM-UHFFFAOYSA-N n-[5-[2-(3,5-dimethoxyphenyl)ethyl]-1h-pyrazol-3-yl]-4-(4-methyl-1,4-diazepan-1-yl)benzamide Chemical compound COC1=CC(OC)=CC(CCC2=NNC(NC(=O)C=3C=CC(=CC=3)N3CCN(C)CCC3)=C2)=C1 WTLALQRLHBXTHM-UHFFFAOYSA-N 0.000 claims 1
- WVIFYEUDNSJDCL-UHFFFAOYSA-N n-[5-[2-(3,5-dimethoxyphenyl)ethyl]-1h-pyrazol-3-yl]-4-(4-prop-2-enyl-1,4-diazepan-1-yl)benzamide Chemical compound COC1=CC(OC)=CC(CCC2=NNC(NC(=O)C=3C=CC(=CC=3)N3CCN(CC=C)CCC3)=C2)=C1 WVIFYEUDNSJDCL-UHFFFAOYSA-N 0.000 claims 1
- KJPXHCOJCLZPHO-UHFFFAOYSA-N n-[5-[2-(3,5-dimethoxyphenyl)ethyl]-1h-pyrazol-3-yl]-4-(4-propan-2-yl-1,4-diazepan-1-yl)benzamide Chemical compound COC1=CC(OC)=CC(CCC2=NNC(NC(=O)C=3C=CC(=CC=3)N3CCN(CCC3)C(C)C)=C2)=C1 KJPXHCOJCLZPHO-UHFFFAOYSA-N 0.000 claims 1
- OLTKVTPQMIIGOU-UHFFFAOYSA-N n-[5-[2-(3,5-dimethoxyphenyl)ethyl]-1h-pyrazol-3-yl]-4-(4-propan-2-ylpiperazin-1-yl)benzamide Chemical compound COC1=CC(OC)=CC(CCC=2NN=C(NC(=O)C=3C=CC(=CC=3)N3CCN(CC3)C(C)C)C=2)=C1 OLTKVTPQMIIGOU-UHFFFAOYSA-N 0.000 claims 1
- GLVDAZNVZRUWAW-UHFFFAOYSA-N n-[5-[2-(3,5-dimethoxyphenyl)ethyl]-1h-pyrazol-3-yl]-4-(dimethylamino)benzamide Chemical compound COC1=CC(OC)=CC(CCC=2NN=C(NC(=O)C=3C=CC(=CC=3)N(C)C)C=2)=C1 GLVDAZNVZRUWAW-UHFFFAOYSA-N 0.000 claims 1
- WCSHYWQDZXNEEQ-KDURUIRLSA-N n-[5-[2-(3,5-dimethoxyphenyl)ethyl]-1h-pyrazol-3-yl]-4-[(3s,5r)-3,4,5-trimethylpiperazin-1-yl]benzamide Chemical compound COC1=CC(OC)=CC(CCC2=NNC(NC(=O)C=3C=CC(=CC=3)N3C[C@@H](C)N(C)[C@@H](C)C3)=C2)=C1 WCSHYWQDZXNEEQ-KDURUIRLSA-N 0.000 claims 1
- SRVZIPFKDSFEGJ-UHFFFAOYSA-N n-[5-[2-(3,5-dimethoxyphenyl)ethyl]-1h-pyrazol-3-yl]-4-[(dimethylamino)methyl]benzamide Chemical compound COC1=CC(OC)=CC(CCC=2NN=C(NC(=O)C=3C=CC(CN(C)C)=CC=3)C=2)=C1 SRVZIPFKDSFEGJ-UHFFFAOYSA-N 0.000 claims 1
- UTGYYSGHKXUZKG-UHFFFAOYSA-N n-[5-[2-(3,5-dimethoxyphenyl)ethyl]-1h-pyrazol-3-yl]-4-[1-(2-methoxyethyl)piperidin-4-yl]benzamide Chemical compound C1CN(CCOC)CCC1C1=CC=C(C(=O)NC=2NN=C(CCC=3C=C(OC)C=C(OC)C=3)C=2)C=C1 UTGYYSGHKXUZKG-UHFFFAOYSA-N 0.000 claims 1
- CCFZQBPNVWLORY-UHFFFAOYSA-N n-[5-[2-(3,5-dimethoxyphenyl)ethyl]-1h-pyrazol-3-yl]-4-[4-(1-hydroxypropan-2-yl)piperazin-1-yl]benzamide Chemical compound COC1=CC(OC)=CC(CCC2=NNC(NC(=O)C=3C=CC(=CC=3)N3CCN(CC3)C(C)CO)=C2)=C1 CCFZQBPNVWLORY-UHFFFAOYSA-N 0.000 claims 1
- YRUSWYQIJJOVDF-UHFFFAOYSA-N n-[5-[2-(3,5-dimethoxyphenyl)ethyl]-1h-pyrazol-3-yl]-4-[[methyl(oxolan-2-ylmethyl)amino]methyl]benzamide Chemical compound COC1=CC(OC)=CC(CCC=2NN=C(NC(=O)C=3C=CC(CN(C)CC4OCCC4)=CC=3)C=2)=C1 YRUSWYQIJJOVDF-UHFFFAOYSA-N 0.000 claims 1
- PWQTURYNFGJDOR-UHFFFAOYSA-N n-[5-[2-(3,5-dimethoxyphenyl)ethyl]-1h-pyrazol-3-yl]-4-methoxybenzamide Chemical compound C1=CC(OC)=CC=C1C(=O)NC1=CC(CCC=2C=C(OC)C=C(OC)C=2)=NN1 PWQTURYNFGJDOR-UHFFFAOYSA-N 0.000 claims 1
- PUTWNWIKRNTSFT-UHFFFAOYSA-N n-[5-[2-(3,5-dimethoxyphenyl)ethyl]-1h-pyrazol-3-yl]-4-morpholin-4-ylbenzamide Chemical compound COC1=CC(OC)=CC(CCC2=NNC(NC(=O)C=3C=CC(=CC=3)N3CCOCC3)=C2)=C1 PUTWNWIKRNTSFT-UHFFFAOYSA-N 0.000 claims 1
- LENFIJCVVDHYLK-UHFFFAOYSA-N n-[5-[2-(3,5-dimethoxyphenyl)ethyl]-1h-pyrazol-3-yl]-4-piperazin-1-ylbenzamide Chemical compound COC1=CC(OC)=CC(CCC=2NN=C(NC(=O)C=3C=CC(=CC=3)N3CCNCC3)C=2)=C1 LENFIJCVVDHYLK-UHFFFAOYSA-N 0.000 claims 1
- ZNGRBVZIZAFWNU-UHFFFAOYSA-N n-[5-[2-(3,5-dimethoxyphenyl)ethyl]-1h-pyrazol-3-yl]-5-(4-ethyl-1,4-diazepan-1-yl)pyrazine-2-carboxamide Chemical compound C1CN(CC)CCCN1C1=CN=C(C(=O)NC=2NN=C(CCC=3C=C(OC)C=C(OC)C=3)C=2)C=N1 ZNGRBVZIZAFWNU-UHFFFAOYSA-N 0.000 claims 1
- IYRCAAUUYKMAKQ-UHFFFAOYSA-N n-[5-[2-(3,5-dimethoxyphenyl)ethyl]-1h-pyrazol-3-yl]-5-(4-methyl-1,4-diazepan-1-yl)pyrazine-2-carboxamide Chemical compound COC1=CC(OC)=CC(CCC2=NNC(NC(=O)C=3N=CC(=NC=3)N3CCN(C)CCC3)=C2)=C1 IYRCAAUUYKMAKQ-UHFFFAOYSA-N 0.000 claims 1
- QNYYEKOVXHHXDJ-UHFFFAOYSA-N n-[5-[2-(3,5-dimethoxyphenyl)ethyl]-1h-pyrazol-3-yl]-5-(4-methyl-1,4-diazepan-1-yl)thiophene-2-carboxamide Chemical compound COC1=CC(OC)=CC(CCC2=NNC(NC(=O)C=3SC(=CC=3)N3CCN(C)CCC3)=C2)=C1 QNYYEKOVXHHXDJ-UHFFFAOYSA-N 0.000 claims 1
- OVNWQCURJHAVGY-UHFFFAOYSA-N n-[5-[2-(3,5-dimethoxyphenyl)ethyl]-1h-pyrazol-3-yl]-5-(4-methylpiperazin-1-yl)thiophene-2-carboxamide Chemical compound COC1=CC(OC)=CC(CCC2=NNC(NC(=O)C=3SC(=CC=3)N3CCN(C)CC3)=C2)=C1 OVNWQCURJHAVGY-UHFFFAOYSA-N 0.000 claims 1
- ZHEDYWJKMMIMFT-UHFFFAOYSA-N n-[5-[2-(3,5-dimethoxyphenyl)ethyl]-1h-pyrazol-3-yl]-5-(4-propan-2-yl-1,4-diazepan-1-yl)thiophene-2-carboxamide Chemical compound COC1=CC(OC)=CC(CCC2=NNC(NC(=O)C=3SC(=CC=3)N3CCN(CCC3)C(C)C)=C2)=C1 ZHEDYWJKMMIMFT-UHFFFAOYSA-N 0.000 claims 1
- CDLCIPZEXTYNPH-UHFFFAOYSA-N n-[5-[2-(3,5-dimethoxyphenyl)ethyl]-1h-pyrazol-3-yl]-5-[3-(dimethylamino)pyrrolidin-1-yl]pyrazine-2-carboxamide Chemical compound COC1=CC(OC)=CC(CCC2=NNC(NC(=O)C=3N=CC(=NC=3)N3CC(CC3)N(C)C)=C2)=C1 CDLCIPZEXTYNPH-UHFFFAOYSA-N 0.000 claims 1
- NCZOJGDOHRHOQD-UHFFFAOYSA-N n-[5-[2-(3,5-dimethoxyphenyl)ethyl]-1h-pyrazol-3-yl]-5-[3-(methylamino)pyrrolidin-1-yl]pyrazine-2-carboxamide Chemical compound C1C(NC)CCN1C1=CN=C(C(=O)NC=2NN=C(CCC=3C=C(OC)C=C(OC)C=3)C=2)C=N1 NCZOJGDOHRHOQD-UHFFFAOYSA-N 0.000 claims 1
- XVRPCVLXVGHVAA-UHFFFAOYSA-N n-[5-[2-(3,5-dimethoxyphenyl)ethyl]-1h-pyrazol-3-yl]-5-piperazin-1-ylthiophene-2-carboxamide Chemical compound COC1=CC(OC)=CC(CCC=2NN=C(NC(=O)C=3SC(=CC=3)N3CCNCC3)C=2)=C1 XVRPCVLXVGHVAA-UHFFFAOYSA-N 0.000 claims 1
- YVHYCABINBWMSD-UHFFFAOYSA-N n-[5-[2-(3,5-dimethoxyphenyl)ethyl]-1h-pyrazol-3-yl]benzamide Chemical compound COC1=CC(OC)=CC(CCC2=NNC(NC(=O)C=3C=CC=CC=3)=C2)=C1 YVHYCABINBWMSD-UHFFFAOYSA-N 0.000 claims 1
- JNHJFIWNWXVPHO-UHFFFAOYSA-N n-[5-[2-(3-methoxyphenyl)ethyl]-1h-pyrazol-3-yl]-4-(4-methylsulfonylpiperazin-1-yl)benzamide Chemical compound COC1=CC=CC(CCC=2NN=C(NC(=O)C=3C=CC(=CC=3)N3CCN(CC3)S(C)(=O)=O)C=2)=C1 JNHJFIWNWXVPHO-UHFFFAOYSA-N 0.000 claims 1
- 125000004307 pyrazin-2-yl group Chemical group [H]C1=C([H])N=C(*)C([H])=N1 0.000 claims 1
- IPEHBUMCGVEMRF-UHFFFAOYSA-N pyrazinecarboxamide Chemical compound NC(=O)C1=CN=CC=N1 IPEHBUMCGVEMRF-UHFFFAOYSA-N 0.000 claims 1
- 239000003560 cancer drug Substances 0.000 abstract 1
- 230000001747 exhibiting effect Effects 0.000 abstract 1
- 239000000126 substance Substances 0.000 abstract 1
- GFRZOWRMOWGEDB-UHFFFAOYSA-N CC(C)N(CCC1)CCN1c1ccc(C)[s]1 Chemical compound CC(C)N(CCC1)CCN1c1ccc(C)[s]1 GFRZOWRMOWGEDB-UHFFFAOYSA-N 0.000 description 1
- HZGDKYAMWFSKTK-UHFFFAOYSA-N CCN(CCC1)CCN1c1ncc(C)nc1 Chemical compound CCN(CCC1)CCN1c1ncc(C)nc1 HZGDKYAMWFSKTK-UHFFFAOYSA-N 0.000 description 1
- PFEGDHSFEMEZHE-UHFFFAOYSA-N CN(CC1)CCN1c1nccnc1 Chemical compound CN(CC1)CCN1c1nccnc1 PFEGDHSFEMEZHE-UHFFFAOYSA-N 0.000 description 1
- NHYCCXDSMVULPF-BETUJISGSA-N C[C@H](C1)N(C)[C@@H](C)CN1c1ccc(C)cc1 Chemical compound C[C@H](C1)N(C)[C@@H](C)CN1c1ccc(C)cc1 NHYCCXDSMVULPF-BETUJISGSA-N 0.000 description 1
- LPLPRBVLOBOLMP-PHIMTYICSA-N C[C@H](C1)N(C)[C@@H](C)CN1c1ncc(C)nc1 Chemical compound C[C@H](C1)N(C)[C@@H](C)CN1c1ncc(C)nc1 LPLPRBVLOBOLMP-PHIMTYICSA-N 0.000 description 1
- DITPYHUUCLUERE-UHFFFAOYSA-N Cc1ccc(N2CCN(C)CCC2)[s]1 Chemical compound Cc1ccc(N2CCN(C)CCC2)[s]1 DITPYHUUCLUERE-UHFFFAOYSA-N 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D231/00—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings
- C07D231/02—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings
- C07D231/10—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members
- C07D231/14—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
- C07D231/38—Nitrogen atoms
- C07D231/40—Acylated on said nitrogen atom
-
- 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
- A61K31/415—1,2-Diazoles
-
- 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
- A61P35/00—Antineoplastic agents
- A61P35/02—Antineoplastic agents specific for leukemia
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- 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
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- 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
- C07D401/06—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 carbon chain containing only aliphatic carbon atoms
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- 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
- 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
- C07D401/14—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 three or more hetero rings
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D403/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00
- C07D403/02—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings
- C07D403/12—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings linked by a chain containing hetero atoms as chain links
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D405/00—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom
- C07D405/02—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing two hetero rings
- C07D405/06—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing two hetero rings linked by a carbon chain containing only aliphatic carbon atoms
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D405/00—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom
- C07D405/02—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing two hetero rings
- C07D405/12—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero 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
- C07D409/12—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
-
- 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
- C07D409/14—Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms containing three or more hetero rings
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D413/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms
- C07D413/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing two hetero rings
- C07D413/12—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing two hetero rings linked by a chain containing hetero atoms as chain links
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D471/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00
- C07D471/02—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00 in which the condensed system contains two hetero rings
- C07D471/04—Ortho-condensed systems
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D487/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00
- C07D487/02—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00 in which the condensed system contains two hetero rings
- C07D487/04—Ortho-condensed systems
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- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- General Health & Medical Sciences (AREA)
- Veterinary Medicine (AREA)
- Public Health (AREA)
- Medicinal Chemistry (AREA)
- Pharmacology & Pharmacy (AREA)
- Life Sciences & Earth Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- General Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Epidemiology (AREA)
- Engineering & Computer Science (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Hematology (AREA)
- Oncology (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Plural Heterocyclic Compounds (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
- Steroid Compounds (AREA)
Applications Claiming Priority (4)
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| US87119006P | 2006-12-21 | 2006-12-21 | |
| US60/871,190 | 2006-12-21 | ||
| US98554207P | 2007-11-05 | 2007-11-05 | |
| US60/985,542 | 2007-11-05 |
Publications (2)
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| RU2009127644A RU2009127644A (ru) | 2011-01-27 |
| RU2458920C2 true RU2458920C2 (ru) | 2012-08-20 |
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| RU2009127644/04A RU2458920C2 (ru) | 2006-12-21 | 2007-12-20 | Новые соединения |
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Cited By (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| RU2719428C2 (ru) * | 2014-08-19 | 2020-04-17 | Шанхай Хайхэ Фармасьютикал Ко., Лтд. | Индазольные соединения в качестве ингибиторов киназы fgfr, их получение и применение |
| RU2797889C2 (ru) * | 2019-01-31 | 2023-06-09 | Пфайзер Инк. | 3-карбониламино-5-циклопентил-1h-пиразольные соединения, обладающие активностью ингибиторов cdk2 |
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| US7737149B2 (en) * | 2006-12-21 | 2010-06-15 | Astrazeneca Ab | N-[5-[2-(3,5-dimethoxyphenyl)ethyl]-2H-pyrazol-3-yl]-4-(3,5-dimethylpiperazin-1-yl)benzamide and salts thereof |
| MX2009006706A (es) | 2006-12-22 | 2009-07-02 | Astex Therapeutics Ltd | Compuestos heterociclicos biciclicos como inhibidores del receptor del factor de crecimiento de fibroblastos. |
| US8131527B1 (en) | 2006-12-22 | 2012-03-06 | Astex Therapeutics Ltd. | FGFR pharmacophore compounds |
| JP5442449B2 (ja) | 2006-12-22 | 2014-03-12 | アステックス、セラピューティックス、リミテッド | 新規化合物 |
| DE102007026341A1 (de) | 2007-06-06 | 2008-12-11 | Merck Patent Gmbh | Benzoxazolonderivate |
| DE102007032507A1 (de) | 2007-07-12 | 2009-04-02 | Merck Patent Gmbh | Pyridazinonderivate |
| HRP20140047T1 (en) | 2007-08-22 | 2014-02-14 | Astrazeneca Ab | Cycloptopyl amide derivatives |
| GB0720041D0 (en) | 2007-10-12 | 2007-11-21 | Astex Therapeutics Ltd | New Compounds |
| GB0720038D0 (en) | 2007-10-12 | 2007-11-21 | Astex Therapeutics Ltd | New compounds |
| DE102007061963A1 (de) | 2007-12-21 | 2009-06-25 | Merck Patent Gmbh | Pyridazinonderivate |
| DE102008019907A1 (de) | 2008-04-21 | 2009-10-22 | Merck Patent Gmbh | Pyridazinonderivate |
| GB0810902D0 (en) | 2008-06-13 | 2008-07-23 | Astex Therapeutics Ltd | New compounds |
| DE102008028905A1 (de) | 2008-06-18 | 2009-12-24 | Merck Patent Gmbh | 3-(3-Pyrimidin-2-yl-benzyl)-[1,2,4]triazolo[4,3-b]pyridazinderivate |
| PE20110062A1 (es) * | 2008-06-19 | 2011-03-09 | Astrazeneca Ab | N-(3-(3,5-dimetoxifenetil)-1h-pirazol-5-il)-4-(3,4-dimetilpiperazin-1-il)benzamida y sales del mismo |
| HRP20130993T1 (hr) | 2008-12-22 | 2013-11-22 | Merck Patent Gmbh | Novi polimorfni oblici 6-(1-metil-1h-pirazol-4-il)-2-{3-[5-(2-morfolin-4-il-etoksi)-pirimidin-2-il]-benzil}-2h-piridazin-3-on dihidrogenfosfata i postupak njihove proizvodnje |
| TW201039825A (en) | 2009-02-20 | 2010-11-16 | Astrazeneca Ab | Cyclopropyl amide derivatives 983 |
| GB0906472D0 (en) | 2009-04-15 | 2009-05-20 | Astex Therapeutics Ltd | New compounds |
| GB0906470D0 (en) | 2009-04-15 | 2009-05-20 | Astex Therapeutics Ltd | New compounds |
| AR078411A1 (es) * | 2009-05-07 | 2011-11-09 | Lilly Co Eli | Compuesto de vinil imidazolilo y composicion farmaceutica que lo comprende |
| CA2790040A1 (en) * | 2010-02-18 | 2011-08-25 | Astrazeneca Ab | Processes for making cyclopropyl amide derivatives and intermediates associated therewith |
| SG186885A1 (en) | 2010-06-04 | 2013-02-28 | Albany Molecular Res Inc | Glycine transporter-1 inhibitors, methods of making them, and uses thereof |
| US8754114B2 (en) | 2010-12-22 | 2014-06-17 | Incyte Corporation | Substituted imidazopyridazines and benzimidazoles as inhibitors of FGFR3 |
| US9255072B2 (en) | 2011-03-04 | 2016-02-09 | National Health Rsearch Institutes | Pyrazole compounds and thiazole compounds as protein kinases inhibitors |
| EP2821402B1 (en) | 2012-02-28 | 2019-08-21 | Astellas Pharma Inc. | Nitrogen-containing aromatic heterocyclic compound |
| HK1205528A1 (en) | 2012-03-08 | 2015-12-18 | Astellas Pharma Inc. | Novel fgfr3 fusion product |
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