TWI692477B - 經取代嘧啶bmi-1抑制劑 - Google Patents
經取代嘧啶bmi-1抑制劑 Download PDFInfo
- Publication number
- TWI692477B TWI692477B TW102142556A TW102142556A TWI692477B TW I692477 B TWI692477 B TW I692477B TW 102142556 A TW102142556 A TW 102142556A TW 102142556 A TW102142556 A TW 102142556A TW I692477 B TWI692477 B TW I692477B
- Authority
- TW
- Taiwan
- Prior art keywords
- pyrimidine
- diamine
- benzimidazol
- alkyl
- phenyl
- Prior art date
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- 150000003230 pyrimidines Chemical class 0.000 title abstract description 8
- 229940123112 BMI1 inhibitor Drugs 0.000 title description 2
- 101100058550 Mus musculus Bmi1 gene Proteins 0.000 claims abstract description 196
- 206010028980 Neoplasm Diseases 0.000 claims abstract description 184
- 201000011510 cancer Diseases 0.000 claims abstract description 118
- 230000001404 mediated effect Effects 0.000 claims abstract description 56
- 150000001412 amines Chemical group 0.000 claims abstract description 28
- -1 1H-benzimidazolyl Chemical group 0.000 claims description 446
- 150000001875 compounds Chemical class 0.000 claims description 432
- 125000000217 alkyl group Chemical group 0.000 claims description 285
- 125000001072 heteroaryl group Chemical group 0.000 claims description 98
- 239000000203 mixture Substances 0.000 claims description 97
- 125000003282 alkyl amino group Chemical group 0.000 claims description 71
- 125000003545 alkoxy group Chemical group 0.000 claims description 59
- 239000003795 chemical substances by application Substances 0.000 claims description 51
- 125000005843 halogen group Chemical group 0.000 claims description 50
- 150000003839 salts Chemical class 0.000 claims description 43
- 125000003118 aryl group Chemical group 0.000 claims description 41
- 125000000623 heterocyclic group Chemical group 0.000 claims description 38
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims description 34
- 125000000753 cycloalkyl group Chemical group 0.000 claims description 31
- 239000002253 acid Substances 0.000 claims description 30
- 125000001424 substituent group Chemical group 0.000 claims description 29
- 125000004448 alkyl carbonyl group Chemical group 0.000 claims description 28
- 239000008194 pharmaceutical composition Substances 0.000 claims description 26
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims description 24
- 125000003342 alkenyl group Chemical group 0.000 claims description 22
- 125000004414 alkyl thio group Chemical group 0.000 claims description 22
- 125000004453 alkoxycarbonyl group Chemical group 0.000 claims description 21
- 125000004093 cyano group Chemical group *C#N 0.000 claims description 20
- 239000002585 base Substances 0.000 claims description 19
- GOJUJUVQIVIZAV-UHFFFAOYSA-N 2-amino-4,6-dichloropyrimidine-5-carbaldehyde Chemical group NC1=NC(Cl)=C(C=O)C(Cl)=N1 GOJUJUVQIVIZAV-UHFFFAOYSA-N 0.000 claims description 18
- 125000000304 alkynyl group Chemical group 0.000 claims description 18
- 239000000546 pharmaceutical excipient Substances 0.000 claims description 17
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 claims description 16
- 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 claims description 16
- 125000004390 alkyl sulfonyl group Chemical group 0.000 claims description 15
- 229910052739 hydrogen Inorganic materials 0.000 claims description 15
- 239000001257 hydrogen Substances 0.000 claims description 15
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N EtOH Substances CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 claims description 13
- 125000004457 alkyl amino carbonyl group Chemical group 0.000 claims description 12
- 239000003814 drug Substances 0.000 claims description 12
- 125000004466 alkoxycarbonylamino group Chemical group 0.000 claims description 11
- 125000003806 alkyl carbonyl amino group Chemical group 0.000 claims description 11
- 230000002401 inhibitory effect Effects 0.000 claims description 11
- 125000002943 quinolinyl group Chemical group N1=C(C=CC2=CC=CC=C12)* 0.000 claims description 11
- 125000001769 aryl amino group Chemical group 0.000 claims description 10
- 125000004471 alkyl aminosulfonyl group Chemical group 0.000 claims description 9
- 125000002619 bicyclic group Chemical group 0.000 claims description 9
- 125000004435 hydrogen atom Chemical class [H]* 0.000 claims description 9
- 125000001041 indolyl group Chemical group 0.000 claims description 9
- 125000003349 3-pyridyl group Chemical group N1=C([H])C([*])=C([H])C([H])=C1[H] 0.000 claims description 8
- 125000003277 amino group Chemical group 0.000 claims description 8
- 239000012458 free base Substances 0.000 claims description 8
- 125000005842 heteroatom Chemical group 0.000 claims description 8
- 229910052757 nitrogen Inorganic materials 0.000 claims description 8
- 125000004430 oxygen atom Chemical group O* 0.000 claims description 8
- 125000005196 alkyl carbonyloxy group Chemical group 0.000 claims description 7
- 238000004519 manufacturing process Methods 0.000 claims description 7
- 125000004433 nitrogen atom Chemical group N* 0.000 claims description 7
- 150000001204 N-oxides Chemical class 0.000 claims description 6
- 125000006598 aminocarbonylamino group Chemical group 0.000 claims description 6
- 125000004209 (C1-C8) alkyl group Chemical group 0.000 claims description 5
- ZLKFERQDWYHBGK-UHFFFAOYSA-N FC=1C=CC2=C(N(C(=N2)C)C2=CC(=NC(=N2)NC2=CC=C(C=C2)C(F)(F)F)N)C1 Chemical compound FC=1C=CC2=C(N(C(=N2)C)C2=CC(=NC(=N2)NC2=CC=C(C=C2)C(F)(F)F)N)C1 ZLKFERQDWYHBGK-UHFFFAOYSA-N 0.000 claims description 5
- 125000004949 alkyl amino carbonyl amino group Chemical group 0.000 claims description 5
- 125000004432 carbon atom Chemical group C* 0.000 claims description 5
- 125000002349 hydroxyamino group Chemical group [H]ON([H])[*] 0.000 claims description 5
- CNPURSDMOWDNOQ-UHFFFAOYSA-N 4-methoxy-7h-pyrrolo[2,3-d]pyrimidin-2-amine Chemical group COC1=NC(N)=NC2=C1C=CN2 CNPURSDMOWDNOQ-UHFFFAOYSA-N 0.000 claims description 4
- ODGIMMLDVSWADK-UHFFFAOYSA-N 4-trifluoromethylaniline Chemical compound NC1=CC=C(C(F)(F)F)C=C1 ODGIMMLDVSWADK-UHFFFAOYSA-N 0.000 claims description 3
- AVXURJPOCDRRFD-UHFFFAOYSA-N Hydroxylamine Chemical group ON AVXURJPOCDRRFD-UHFFFAOYSA-N 0.000 claims description 3
- 125000003917 carbamoyl group Chemical group [H]N([H])C(*)=O 0.000 claims description 3
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 3
- RYIZSNJRUYFDTF-UHFFFAOYSA-N C(C)C1=NC2=C(N1C1=CC(=NC(=N1)NC1=CC=C(C=C1)C(F)(F)F)N)C=C(C=C2)F Chemical compound C(C)C1=NC2=C(N1C1=CC(=NC(=N1)NC1=CC=C(C=C1)C(F)(F)F)N)C=C(C=C2)F RYIZSNJRUYFDTF-UHFFFAOYSA-N 0.000 claims description 2
- LKXBUDLEPFZVQB-UHFFFAOYSA-N C1(CC1)C1=NC2=C(N1C1=CC(=NC(=N1)NC1=CC=C(C=C1)C(F)(F)F)N)C=C(C=C2)F Chemical compound C1(CC1)C1=NC2=C(N1C1=CC(=NC(=N1)NC1=CC=C(C=C1)C(F)(F)F)N)C=C(C=C2)F LKXBUDLEPFZVQB-UHFFFAOYSA-N 0.000 claims description 2
- CSPGXXIOHYEDNJ-UHFFFAOYSA-N FC1=CC2=C(N(C(=N2)C)C2=CC(=NC(=N2)NC2=CC=C(C=C2)C(F)(F)F)C#N)C=C1F Chemical compound FC1=CC2=C(N(C(=N2)C)C2=CC(=NC(=N2)NC2=CC=C(C=C2)C(F)(F)F)C#N)C=C1F CSPGXXIOHYEDNJ-UHFFFAOYSA-N 0.000 claims description 2
- 125000002971 oxazolyl group Chemical group 0.000 claims description 2
- YAAWASYJIRZXSZ-UHFFFAOYSA-N pyrimidine-2,4-diamine Chemical compound NC1=CC=NC(N)=N1 YAAWASYJIRZXSZ-UHFFFAOYSA-N 0.000 claims 30
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 claims 4
- GUODUMAXCIICRA-UHFFFAOYSA-N 2-[4-(trifluoromethyl)phenyl]-1H-pyrimidine-2,4-diamine Chemical compound FC(C1=CC=C(C=C1)C1(NC=CC(=N1)N)N)(F)F GUODUMAXCIICRA-UHFFFAOYSA-N 0.000 claims 3
- JFDZBHWFFUWGJE-UHFFFAOYSA-N benzonitrile Chemical compound N#CC1=CC=CC=C1 JFDZBHWFFUWGJE-UHFFFAOYSA-N 0.000 claims 3
- ZPZKNOPSVUNRBE-UHFFFAOYSA-N 2-(3-chloro-4-methoxyphenyl)-6-(2,5,6-trimethylbenzimidazol-1-yl)-1H-pyrimidine-2,4-diamine Chemical compound ClC=1C=C(C=CC=1OC)C1(NC(=CC(=N1)N)N1C(=NC2=C1C=C(C(=C2)C)C)C)N ZPZKNOPSVUNRBE-UHFFFAOYSA-N 0.000 claims 1
- SMTKNISUYHIXHB-UHFFFAOYSA-N 2-(4-methylphenyl)-6-(2,5,6-trimethylbenzimidazol-1-yl)-1H-pyrimidine-2,4-diamine Chemical compound CC1=CC=C(C=C1)C1(NC(=CC(=N1)N)N1C(=NC2=C1C=C(C(=C2)C)C)C)N SMTKNISUYHIXHB-UHFFFAOYSA-N 0.000 claims 1
- VQVOAEBGMSWENC-UHFFFAOYSA-N 2-N-[4-(difluoromethoxy)-3-fluorophenyl]-6-(2-methylbenzimidazol-1-yl)pyrimidine-2,4-diamine 2-[3-fluoro-4-(trifluoromethyl)phenyl]-6-(2-methylbenzimidazol-1-yl)-1H-pyrimidine-2,4-diamine Chemical compound FC(OC1=C(C=C(C=C1)NC1=NC(=CC(=N1)N)N1C(=NC2=C1C=CC=C2)C)F)F.FC=2C=C(C=CC2C(F)(F)F)C2(NC(=CC(=N2)N)N2C(=NC1=C2C=CC=C1)C)N VQVOAEBGMSWENC-UHFFFAOYSA-N 0.000 claims 1
- GEFKLPJLQJIZIK-UHFFFAOYSA-N 2-[4-(difluoromethoxy)-3-fluorophenyl]-6-(2-ethyl-6-fluorobenzimidazol-1-yl)-1H-pyrimidine-2,4-diamine Chemical compound FC(OC1=C(C=C(C=C1)C1(NC(=CC(=N1)N)N1C(=NC2=C1C=C(C=C2)F)CC)N)F)F GEFKLPJLQJIZIK-UHFFFAOYSA-N 0.000 claims 1
- ULAPUNCOGWESBX-UHFFFAOYSA-N 2-[4-(difluoromethoxy)-3-fluorophenyl]-6-(5-fluoro-2-methylbenzimidazol-1-yl)-1H-pyrimidine-2,4-diamine Chemical compound FC(OC1=C(C=C(C=C1)C1(NC(=CC(=N1)N)N1C(=NC2=C1C=CC(=C2)F)C)N)F)F ULAPUNCOGWESBX-UHFFFAOYSA-N 0.000 claims 1
- JVBZMYGXBPXIRT-UHFFFAOYSA-N 2-[4-(difluoromethoxy)-3-fluorophenyl]-6-(6-fluoro-2-methylbenzimidazol-1-yl)-1H-pyrimidine-2,4-diamine Chemical compound FC(OC1=C(C=C(C=C1)C1(NC(=CC(=N1)N)N1C(=NC2=C1C=C(C=C2)F)C)N)F)F JVBZMYGXBPXIRT-UHFFFAOYSA-N 0.000 claims 1
- SMDMRLHUXRRRKI-UHFFFAOYSA-N 2-[4-(difluoromethoxy)phenyl]-6-(2-methylbenzimidazol-1-yl)-1H-pyrimidine-2,4-diamine Chemical compound FC(OC1=CC=C(C=C1)C1(NC(=CC(=N1)N)N1C(=NC2=C1C=CC=C2)C)N)F SMDMRLHUXRRRKI-UHFFFAOYSA-N 0.000 claims 1
- XQUSLGVVYKQHCP-UHFFFAOYSA-N 2-[4-(difluoromethoxy)phenyl]-6-(5,6-difluoro-2-methylbenzimidazol-1-yl)-1H-pyrimidine-2,4-diamine Chemical compound FC(OC1=CC=C(C=C1)C1(NC(=CC(=N1)N)N1C(=NC2=C1C=C(C(=C2)F)F)C)N)F XQUSLGVVYKQHCP-UHFFFAOYSA-N 0.000 claims 1
- ZOEZVBZFTKJNEE-UHFFFAOYSA-N 2-[4-(difluoromethoxy)phenyl]-6-(6-fluoro-2-propan-2-ylbenzimidazol-1-yl)-1H-pyrimidine-2,4-diamine Chemical compound FC(OC1=CC=C(C=C1)C1(NC(=CC(=N1)N)N1C(=NC2=C1C=C(C=C2)F)C(C)C)N)F ZOEZVBZFTKJNEE-UHFFFAOYSA-N 0.000 claims 1
- VVVGUDDIVWGFNM-UHFFFAOYSA-N 2-[4-(difluoromethoxy)phenyl]-6-[2-(difluoromethyl)-6-fluorobenzimidazol-1-yl]-1H-pyrimidine-2,4-diamine Chemical compound FC(OC1=CC=C(C=C1)C1(NC(=CC(=N1)N)N1C(=NC2=C1C=C(C=C2)F)C(F)F)N)F VVVGUDDIVWGFNM-UHFFFAOYSA-N 0.000 claims 1
- JBUUKDJZTHOULF-UHFFFAOYSA-N 2-[4-(difluoromethoxy)phenyl]-6-[6-fluoro-2-(methoxymethyl)benzimidazol-1-yl]-1H-pyrimidine-2,4-diamine Chemical compound FC(OC1=CC=C(C=C1)C1(NC(=CC(=N1)N)N1C(=NC2=C1C=C(C=C2)F)COC)N)F JBUUKDJZTHOULF-UHFFFAOYSA-N 0.000 claims 1
- DBPDDZUBZUBDMQ-UHFFFAOYSA-N 2-[6-(trifluoromethyl)pyridin-3-yl]-1H-pyrimidine-2,4-diamine Chemical compound FC(C1=CC=C(C=N1)C1(NC=CC(=N1)N)N)(F)F DBPDDZUBZUBDMQ-UHFFFAOYSA-N 0.000 claims 1
- VHGCPAWEEVYUGT-UHFFFAOYSA-N 6-(2-ethylbenzimidazol-1-yl)-5-fluoro-2-N-[4-(trifluoromethyl)phenyl]pyrimidine-2,4-diamine Chemical compound CCc1nc2ccccc2n1-c1nc(Nc2ccc(cc2)C(F)(F)F)nc(N)c1F VHGCPAWEEVYUGT-UHFFFAOYSA-N 0.000 claims 1
- NJXICRJXDBDCMY-UHFFFAOYSA-N 6-[2-(methoxymethyl)benzimidazol-1-yl]-2-N-[4-(trifluoromethyl)phenyl]pyrimidine-2,4-diamine Chemical compound COCc1nc2ccccc2n1-c1cc(N)nc(Nc2ccc(cc2)C(F)(F)F)n1 NJXICRJXDBDCMY-UHFFFAOYSA-N 0.000 claims 1
- UFSZGTGHGMGGSH-UHFFFAOYSA-N BrC1=CC=C(C=C1)NC1=NC(=CC(=N1)N)N1C(=NC2=C1C=CC=C2)C.O2COC1=C2C=CC(=C1)C1(NC(=CC(=N1)N)N1C(=NC2=C1C=CC=C2)C)N Chemical compound BrC1=CC=C(C=C1)NC1=NC(=CC(=N1)N)N1C(=NC2=C1C=CC=C2)C.O2COC1=C2C=CC(=C1)C1(NC(=CC(=N1)N)N1C(=NC2=C1C=CC=C2)C)N UFSZGTGHGMGGSH-UHFFFAOYSA-N 0.000 claims 1
- GPVJKNAZBWNDCK-UHFFFAOYSA-N C(C)C1=NC2=C(N1C1=C(C(=NC(=N1)NC1=CC=C(C=C1)C(F)(F)F)N)F)C=C(C=C2)F Chemical compound C(C)C1=NC2=C(N1C1=C(C(=NC(=N1)NC1=CC=C(C=C1)C(F)(F)F)N)F)C=C(C=C2)F GPVJKNAZBWNDCK-UHFFFAOYSA-N 0.000 claims 1
- IMLHOFPXDKRHGG-UHFFFAOYSA-N C(C)C1=NC2=C(N1C1=CC(=NC(=N1)NC1=CC(=CC=C1)C)N)C=C(C=C2)F.C(C)C2=NC1=C(N2C2=CC(=NC(=N2)NC2=CC(=CC=C2)OC)N)C=C(C=C1)F Chemical compound C(C)C1=NC2=C(N1C1=CC(=NC(=N1)NC1=CC(=CC=C1)C)N)C=C(C=C2)F.C(C)C2=NC1=C(N2C2=CC(=NC(=N2)NC2=CC(=CC=C2)OC)N)C=C(C=C1)F IMLHOFPXDKRHGG-UHFFFAOYSA-N 0.000 claims 1
- MZHJHEKYPPCEFN-UHFFFAOYSA-N C(C)C1=NC2=C(N1C1=CC(=NC(=N1)NC1=CC=C(C=C1)C(F)(F)F)N)C=C(C=C2)F.C(C)C2=NC1=C(N2C2=CC(=[N+](C(=N2)NC2=CC=C(C=C2)C(F)(F)F)[O-])N)C=CC=C1 Chemical compound C(C)C1=NC2=C(N1C1=CC(=NC(=N1)NC1=CC=C(C=C1)C(F)(F)F)N)C=C(C=C2)F.C(C)C2=NC1=C(N2C2=CC(=[N+](C(=N2)NC2=CC=C(C=C2)C(F)(F)F)[O-])N)C=CC=C1 MZHJHEKYPPCEFN-UHFFFAOYSA-N 0.000 claims 1
- PFTWICZZYOGGCM-UHFFFAOYSA-N C1(CC1)C1=NC2=C(N1C1=CC(=NC(=N1)NC1=CC(=C(C=C1)OC(F)F)F)N)C=C(C=C2)F Chemical compound C1(CC1)C1=NC2=C(N1C1=CC(=NC(=N1)NC1=CC(=C(C=C1)OC(F)F)F)N)C=C(C=C2)F PFTWICZZYOGGCM-UHFFFAOYSA-N 0.000 claims 1
- DQUCIBDXZZUKHO-UHFFFAOYSA-N C1(CC1)C1=NC2=C(N1C1=CC(=NC(=N1)NC1=CC=C(C=C1)C(F)(F)F)N)C=CC(=C2)F Chemical compound C1(CC1)C1=NC2=C(N1C1=CC(=NC(=N1)NC1=CC=C(C=C1)C(F)(F)F)N)C=CC(=C2)F DQUCIBDXZZUKHO-UHFFFAOYSA-N 0.000 claims 1
- ULKOCOFOEXRHRA-UHFFFAOYSA-N C1(CC1)C1=NC2=C(N1C1=CC(=NC(=N1)NC1=CC=C(C=C1)OC(F)F)N)C=CC(=C2)F Chemical compound C1(CC1)C1=NC2=C(N1C1=CC(=NC(=N1)NC1=CC=C(C=C1)OC(F)F)N)C=CC(=C2)F ULKOCOFOEXRHRA-UHFFFAOYSA-N 0.000 claims 1
- YRFJLNMAMIMQSD-UHFFFAOYSA-N C1(CC1)C1=NN2C(C=C(C=C2)OC)=C1C1=CC(=NC(=N1)NC1=CC=C(C=C1)C(F)(F)F)N Chemical compound C1(CC1)C1=NN2C(C=C(C=C2)OC)=C1C1=CC(=NC(=N1)NC1=CC=C(C=C1)C(F)(F)F)N YRFJLNMAMIMQSD-UHFFFAOYSA-N 0.000 claims 1
- KEAJRGGTUHJFQR-UHFFFAOYSA-N CC1=NC2=C(N1C1=CC(=NC(=N1)NC1=CC=C(C=C1)C(F)(F)F)N)C=CC=C2.Cl.CC2=NC1=C(N2C2=CC(=NC(=N2)NC2=CC=C(C=C2)C(F)(F)F)N)C=CC=C1 Chemical compound CC1=NC2=C(N1C1=CC(=NC(=N1)NC1=CC=C(C=C1)C(F)(F)F)N)C=CC=C2.Cl.CC2=NC1=C(N2C2=CC(=NC(=N2)NC2=CC=C(C=C2)C(F)(F)F)N)C=CC=C1 KEAJRGGTUHJFQR-UHFFFAOYSA-N 0.000 claims 1
- GKSQFGOQBMXDTN-UHFFFAOYSA-N CC1=NC2=C(N1C1=CC(=NC(=N1)NC1=CC=C(C=C1)C)N)C=CC=C2.CC2=NC1=C(N2C2=CC(=NC(=N2)NC2=CC(=CC=C2)C)N)C=CC=C1 Chemical compound CC1=NC2=C(N1C1=CC(=NC(=N1)NC1=CC=C(C=C1)C)N)C=CC=C2.CC2=NC1=C(N2C2=CC(=NC(=N2)NC2=CC(=CC=C2)C)N)C=CC=C1 GKSQFGOQBMXDTN-UHFFFAOYSA-N 0.000 claims 1
- RMBHRHSCMXOAAK-UHFFFAOYSA-N CC1=NOC(=C1C1=CC(=NC(=N1)NC1=CC=C(C=C1)C)N)C.CC1=NOC(=C1C1=CC(=NC(=N1)NC1=CC=C(C=C1)OC)N)C Chemical compound CC1=NOC(=C1C1=CC(=NC(=N1)NC1=CC=C(C=C1)C)N)C.CC1=NOC(=C1C1=CC(=NC(=N1)NC1=CC=C(C=C1)OC)N)C RMBHRHSCMXOAAK-UHFFFAOYSA-N 0.000 claims 1
- VKXXZUHNZWXELK-UHFFFAOYSA-N CCc1nc2ccc(Cl)cc2n1-c1cc(N)nc(Nc2ccc(cc2)C(F)(F)F)n1 Chemical compound CCc1nc2ccc(Cl)cc2n1-c1cc(N)nc(Nc2ccc(cc2)C(F)(F)F)n1 VKXXZUHNZWXELK-UHFFFAOYSA-N 0.000 claims 1
- COXWZZJELSWXBH-UHFFFAOYSA-N CN(C1=CC=C(C=C1)NC1=NC(=CC(=N1)N)N1C(=NC2=C1C=C(C=C2)F)CC)C.C(C)C2=NC1=C(N2C2=CC(=NC(=N2)NC2=CC=C(C=C2)OC)N)C=C(C=C1)F Chemical compound CN(C1=CC=C(C=C1)NC1=NC(=CC(=N1)N)N1C(=NC2=C1C=C(C=C2)F)CC)C.C(C)C2=NC1=C(N2C2=CC(=NC(=N2)NC2=CC=C(C=C2)OC)N)C=C(C=C1)F COXWZZJELSWXBH-UHFFFAOYSA-N 0.000 claims 1
- APVNWTYMKFWTSV-UHFFFAOYSA-N COc1ccn2nc(C)c(-c3cc(Cl)nc(Nc4ccc(cc4)C(F)(F)F)n3)c2c1 Chemical compound COc1ccn2nc(C)c(-c3cc(Cl)nc(Nc4ccc(cc4)C(F)(F)F)n3)c2c1 APVNWTYMKFWTSV-UHFFFAOYSA-N 0.000 claims 1
- RBSDRIFVZMGRIX-UHFFFAOYSA-N CS(O)(=O)=O.Cc1nc2ccc(F)cc2n1-c1cc(N)nc(Nc2ccc(cc2)C(F)(F)F)n1 Chemical compound CS(O)(=O)=O.Cc1nc2ccc(F)cc2n1-c1cc(N)nc(Nc2ccc(cc2)C(F)(F)F)n1 RBSDRIFVZMGRIX-UHFFFAOYSA-N 0.000 claims 1
- ARZKGHFASKMVAO-UHFFFAOYSA-N Cc1nc2cc(F)c(F)cc2n1-c1cc(Cl)nc(Nc2ccc(c(F)c2)C(F)(F)F)n1 Chemical compound Cc1nc2cc(F)c(F)cc2n1-c1cc(Cl)nc(Nc2ccc(c(F)c2)C(F)(F)F)n1 ARZKGHFASKMVAO-UHFFFAOYSA-N 0.000 claims 1
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Classifications
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- 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
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D239/00—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings
- C07D239/02—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings
- C07D239/24—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings having three or more double bonds between ring members or between ring members and non-ring members
- C07D239/28—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings having three or more 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, directly attached to ring carbon atoms
- C07D239/46—Two or more oxygen, sulphur or nitrogen atoms
- C07D239/48—Two nitrogen atoms
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- 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
- A61K31/4353—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 ortho- or peri-condensed with heterocyclic ring systems
- A61K31/437—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 ortho- or peri-condensed with heterocyclic ring systems the heterocyclic ring system containing a five-membered ring having nitrogen as a ring hetero atom, e.g. indolizine, beta-carboline
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- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/495—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with two or more nitrogen atoms as the only ring heteroatoms, e.g. piperazine or tetrazines
- A61K31/505—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim
- A61K31/506—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim not condensed and containing further heterocyclic rings
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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
- C07D401/04—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 directly linked by a ring-member-to-ring-member bond
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- 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
- C07D403/04—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 directly linked by a ring-member-to-ring-member bond
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- A—HUMAN NECESSITIES
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- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K2300/00—Mixtures or combinations of active ingredients, wherein at least one active ingredient is fully defined in groups A61K31/00 - A61K41/00
Landscapes
- Chemical & Material Sciences (AREA)
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- Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Pharmacology & Pharmacy (AREA)
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- General Health & Medical Sciences (AREA)
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- Bioinformatics & Cheminformatics (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
- Plural Heterocyclic Compounds (AREA)
- Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
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| TWI692477B (zh) * | 2013-08-30 | 2020-05-01 | 美商Ptc治療公司 | 經取代嘧啶bmi-1抑制劑 |
| GB201321736D0 (en) * | 2013-12-09 | 2014-01-22 | Ucb Pharma Sa | Therapeutic agents |
| IL291017B2 (en) | 2015-10-21 | 2023-11-01 | Otsuka Pharma Co Ltd | Benzolactam compounds as protein kinase inhibitors |
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