KR100847169B1 - 혈관형성 조절제로서의 피리미딘아민 - Google Patents

Info

Publication number

KR100847169B1

KR100847169B1 KR1020037008349A KR20037008349A KR100847169B1 KR 100847169 B1 KR100847169 B1 KR 100847169B1 KR 1020037008349 A KR1020037008349 A KR 1020037008349A KR 20037008349 A KR20037008349 A KR 20037008349A KR 100847169 B1 KR100847169 B1 KR 100847169B1

Authority

KR

South Korea

Prior art keywords

methyl

amino

indazol

delete delete

hydrogen

Prior art date

2000-12-21

Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)

Expired - Lifetime

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• 230000033115 angiogenesis Effects 0.000 title description 19
• LJXQPZWIHJMPQQ-UHFFFAOYSA-N pyrimidin-2-amine Chemical compound NC1=NC=CC=N1 LJXQPZWIHJMPQQ-UHFFFAOYSA-N 0.000 title 1
• 201000010099 disease Diseases 0.000 claims abstract description 35
• 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 claims abstract description 35
• 229910052739 hydrogen Inorganic materials 0.000 claims description 162
• 239000001257 hydrogen Substances 0.000 claims description 153
• 150000001875 compounds Chemical class 0.000 claims description 142
• 150000002431 hydrogen Chemical class 0.000 claims description 98
• -1 3-methyl-1 H -indazol-6-yl Chemical group 0.000 claims description 84
• 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 75
• KHBQMWCZKVMBLN-UHFFFAOYSA-N Benzenesulfonamide Chemical compound NS(=O)(=O)C1=CC=CC=C1 KHBQMWCZKVMBLN-UHFFFAOYSA-N 0.000 claims description 68
• 125000000217 alkyl group Chemical group 0.000 claims description 64
• 229910052736 halogen Inorganic materials 0.000 claims description 56
• 150000002367 halogens Chemical class 0.000 claims description 56
• 150000003839 salts Chemical class 0.000 claims description 56
• UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 55
• 239000012453 solvate Substances 0.000 claims description 45
• WEVYAHXRMPXWCK-UHFFFAOYSA-N Acetonitrile Chemical compound CC#N WEVYAHXRMPXWCK-UHFFFAOYSA-N 0.000 claims description 36
• 239000000460 chlorine Substances 0.000 claims description 35
• 239000008194 pharmaceutical composition Substances 0.000 claims description 25
• 206010028980 Neoplasm Diseases 0.000 claims description 24
• 125000003710 aryl alkyl group Chemical group 0.000 claims description 24
• 229910052801 chlorine Inorganic materials 0.000 claims description 22
• 125000000753 cycloalkyl group Chemical group 0.000 claims description 22
• 201000011510 cancer Diseases 0.000 claims description 21
• ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 claims description 20
• 125000003545 alkoxy group Chemical group 0.000 claims description 19
• 125000003118 aryl group Chemical group 0.000 claims description 17
• 125000004093 cyano group Chemical group *C#N 0.000 claims description 16
• 229910052757 nitrogen Inorganic materials 0.000 claims description 16
• 125000004966 cyanoalkyl group Chemical group 0.000 claims description 13
• KXDAEFPNCMNJSK-UHFFFAOYSA-N Benzamide Chemical compound NC(=O)C1=CC=CC=C1 KXDAEFPNCMNJSK-UHFFFAOYSA-N 0.000 claims description 12
• 125000001188 haloalkyl group Chemical group 0.000 claims description 12
• 125000002853 C1-C4 hydroxyalkyl group Chemical group 0.000 claims description 10
• 125000004438 haloalkoxy group Chemical group 0.000 claims description 10
• 125000000956 methoxy group Chemical group [H]C([H])([H])O* 0.000 claims description 10
• 125000006125 ethylsulfonyl group Chemical group 0.000 claims description 9
• 125000002924 primary amino group Chemical group [H]N([H])* 0.000 claims description 9
• 150000001408 amides Chemical class 0.000 claims description 8
• 239000003085 diluting agent Substances 0.000 claims description 7
• 239000003937 drug carrier Substances 0.000 claims description 7
• 239000000546 pharmaceutical excipient Substances 0.000 claims description 7
• JUJWROOIHBZHMG-UHFFFAOYSA-N Pyridine Chemical compound C1=CC=NC=C1 JUJWROOIHBZHMG-UHFFFAOYSA-N 0.000 claims description 5
• QDVXRMFTKAQZOJ-UHFFFAOYSA-N 4-n-(1,3-dimethylindazol-6-yl)-4-n-methyl-2-n-[3-(methylsulfonylmethyl)phenyl]pyrimidine-2,4-diamine Chemical compound C=1C=C2C(C)=NN(C)C2=CC=1N(C)C(N=1)=CC=NC=1NC1=CC=CC(CS(C)(=O)=O)=C1 QDVXRMFTKAQZOJ-UHFFFAOYSA-N 0.000 claims description 4
• OKMPHEGFRRVGRS-UHFFFAOYSA-N 4-n-(2,3-dimethylindazol-6-yl)-4-n-methyl-2-n-[3-(methylsulfonylmethyl)phenyl]pyrimidine-2,4-diamine Chemical compound C1=CC2=C(C)N(C)N=C2C=C1N(C)C(N=1)=CC=NC=1NC1=CC=CC(CS(C)(=O)=O)=C1 OKMPHEGFRRVGRS-UHFFFAOYSA-N 0.000 claims description 4
• 201000001320 Atherosclerosis Diseases 0.000 claims description 4
• OVTQMMYLOJBKOP-UHFFFAOYSA-N 1-[4-[[5-fluoro-4-[methyl-(3-methyl-2h-indazol-6-yl)amino]pyrimidin-2-yl]amino]phenyl]-n-methylmethanesulfonamide Chemical compound C1=CC(CS(=O)(=O)NC)=CC=C1NC1=NC=C(F)C(N(C)C=2C=C3NN=C(C)C3=CC=2)=N1 OVTQMMYLOJBKOP-UHFFFAOYSA-N 0.000 claims description 3
• BPGZHRULBGZUFP-UHFFFAOYSA-N 1-[4-methoxy-3-[[4-[(3-methyl-2h-indazol-6-yl)amino]pyrimidin-2-yl]amino]phenyl]propan-1-one Chemical compound CCC(=O)C1=CC=C(OC)C(NC=2N=C(NC=3C=C4NN=C(C)C4=CC=3)C=CN=2)=C1 BPGZHRULBGZUFP-UHFFFAOYSA-N 0.000 claims description 3
• MGSXZPZPZIPVHO-UHFFFAOYSA-N 2-[(3-methyl-2h-indazol-6-yl)-[2-[3-(methylsulfonylmethyl)anilino]pyrimidin-4-yl]amino]acetonitrile Chemical compound C=1C=C2C(C)=NNC2=CC=1N(CC#N)C(N=1)=CC=NC=1NC1=CC=CC(CS(C)(=O)=O)=C1 MGSXZPZPZIPVHO-UHFFFAOYSA-N 0.000 claims description 3
• MQYXDHFLBFNMAM-UHFFFAOYSA-N 2-[(3-methyl-2h-indazol-6-yl)-[2-[4-(methylsulfonylmethyl)anilino]pyrimidin-4-yl]amino]acetonitrile Chemical compound C=1C=C2C(C)=NNC2=CC=1N(CC#N)C(N=1)=CC=NC=1NC1=CC=C(CS(C)(=O)=O)C=C1 MQYXDHFLBFNMAM-UHFFFAOYSA-N 0.000 claims description 3
• YTTBOOLPGZCTSF-UHFFFAOYSA-N 3-[[4-[[2-[(3-chlorophenyl)methyl]-3-methylindazol-6-yl]-methylamino]pyrimidin-2-yl]amino]benzenesulfonamide Chemical compound C=1C=NC(NC=2C=C(C=CC=2)S(N)(=O)=O)=NC=1N(C)C(=CC1=N2)C=CC1=C(C)N2CC1=CC=CC(Cl)=C1 YTTBOOLPGZCTSF-UHFFFAOYSA-N 0.000 claims description 3
• CBNFOUWNKLWLNA-UHFFFAOYSA-N 3-[[5-fluoro-4-[methyl-(3-methyl-2h-indazol-6-yl)amino]pyrimidin-2-yl]amino]-4-methoxybenzamide Chemical compound COC1=CC=C(C(N)=O)C=C1NC1=NC=C(F)C(N(C)C=2C=C3NN=C(C)C3=CC=2)=N1 CBNFOUWNKLWLNA-UHFFFAOYSA-N 0.000 claims description 3
• ZUKWQTLSOWOKOR-UHFFFAOYSA-N 4-[[5-fluoro-4-[methyl-(3-methyl-2h-indazol-6-yl)amino]pyrimidin-2-yl]amino]-3-methoxybenzenesulfonamide Chemical compound COC1=CC(S(N)(=O)=O)=CC=C1NC1=NC=C(F)C(N(C)C=2C=C3NN=C(C)C3=CC=2)=N1 ZUKWQTLSOWOKOR-UHFFFAOYSA-N 0.000 claims description 3
• HQPNYDGAKWXWJL-UHFFFAOYSA-N 4-ethyl-2-N-(5-ethylsulfonyl-2-methoxyphenyl)-4-N-(3-methyl-2H-indazol-6-yl)-1H-pyrimidine-2,4-diamine Chemical compound C(C)C1(NC(=NC=C1)NC1=C(C=CC(=C1)S(=O)(=O)CC)OC)NC1=CC=C2C(=NNC2=C1)C HQPNYDGAKWXWJL-UHFFFAOYSA-N 0.000 claims description 3
• JRMPYMHBRVUPFL-UHFFFAOYSA-N 4-ethynyl-4-N-(3-methyl-2H-indazol-6-yl)-2-N-[3-(methylsulfonylmethyl)phenyl]-1H-pyrimidine-2,4-diamine Chemical compound C(#C)C1(NC(=NC=C1)NC1=CC(=CC=C1)CS(=O)(=O)C)NC1=CC=C2C(=NNC2=C1)C JRMPYMHBRVUPFL-UHFFFAOYSA-N 0.000 claims description 3
• PNOUUBLTWLHHGL-UHFFFAOYSA-N 4-methyl-4-N-(3-methyl-2H-indazol-6-yl)-2-N-(3-methylsulfonylphenyl)-1H-pyrimidine-2,4-diamine Chemical compound CC1(NC(=NC=C1)NC1=CC(=CC=C1)S(=O)(=O)C)NC1=CC=C2C(=NNC2=C1)C PNOUUBLTWLHHGL-UHFFFAOYSA-N 0.000 claims description 3
• CCAVHDVJKVYFCH-UHFFFAOYSA-N 5-fluoro-2-n-(2-methoxy-5-propan-2-ylsulfonylphenyl)-4-n-methyl-4-n-(3-methyl-2h-indazol-6-yl)pyrimidine-2,4-diamine Chemical compound COC1=CC=C(S(=O)(=O)C(C)C)C=C1NC1=NC=C(F)C(N(C)C=2C=C3NN=C(C)C3=CC=2)=N1 CCAVHDVJKVYFCH-UHFFFAOYSA-N 0.000 claims description 3
• ANCNAKDZYQJJFB-UHFFFAOYSA-N 5-fluoro-4-n-methyl-4-n-(3-methyl-2h-indazol-6-yl)-2-n-(4-methylsulfonylphenyl)pyrimidine-2,4-diamine Chemical compound C=1C=C2C(C)=NNC2=CC=1N(C)C(C(=CN=1)F)=NC=1NC1=CC=C(S(C)(=O)=O)C=C1 ANCNAKDZYQJJFB-UHFFFAOYSA-N 0.000 claims description 3
• IJIKZGCUKZGSHO-UHFFFAOYSA-N 5-fluoro-4-n-methyl-4-n-(3-methyl-2h-indazol-6-yl)-2-n-[3-(methylsulfonylmethyl)phenyl]pyrimidine-2,4-diamine Chemical compound C=1C=C2C(C)=NNC2=CC=1N(C)C(C(=CN=1)F)=NC=1NC1=CC=CC(CS(C)(=O)=O)=C1 IJIKZGCUKZGSHO-UHFFFAOYSA-N 0.000 claims description 3
• PEPCTCTXEHWCJZ-UHFFFAOYSA-N C(C(C)C)S(=O)(=O)C=1C=CC(=C(C=1)C1(NC=CC(=N1)NC1=CC=C2C(=NNC2=C1)C)N)OC Chemical compound C(C(C)C)S(=O)(=O)C=1C=CC(=C(C=1)C1(NC=CC(=N1)NC1=CC=C2C(=NNC2=C1)C)N)OC PEPCTCTXEHWCJZ-UHFFFAOYSA-N 0.000 claims description 3
• GLVWCBDZFXYOPH-UHFFFAOYSA-N C(C)(C)S(=O)(=O)CC1=CC=C(C=C1)C1(NC=CC(=N1)N(C1=CC=C2C(=NNC2=C1)C)C)N Chemical compound C(C)(C)S(=O)(=O)CC1=CC=C(C=C1)C1(NC=CC(=N1)N(C1=CC=C2C(=NNC2=C1)C)C)N GLVWCBDZFXYOPH-UHFFFAOYSA-N 0.000 claims description 3
• SOFVXWOEBIPQLP-UHFFFAOYSA-N C(C)(C)S(=O)(=O)CC=1C=C(C=CC=1)C1(NC=CC(=N1)N(C1=CC=C2C(=NNC2=C1)C)C)N Chemical compound C(C)(C)S(=O)(=O)CC=1C=C(C=CC=1)C1(NC=CC(=N1)N(C1=CC=C2C(=NNC2=C1)C)C)N SOFVXWOEBIPQLP-UHFFFAOYSA-N 0.000 claims description 3
• YCSRKCLLXHHELU-UHFFFAOYSA-N C(C)S(=O)(=O)C1=CC=C(C=C1)C1(NC=CC(=N1)N(C1=CC=C2C(=NNC2=C1)C)C)N Chemical compound C(C)S(=O)(=O)C1=CC=C(C=C1)C1(NC=CC(=N1)N(C1=CC=C2C(=NNC2=C1)C)C)N YCSRKCLLXHHELU-UHFFFAOYSA-N 0.000 claims description 3
• IDELGVLOWFHGCY-UHFFFAOYSA-N C(C)S(=O)(=O)C=1C=CC(=C(C1)C1(NC=CC(=N1)N(C1=CC=C2C(=NNC2=C1)C)C)N)OC Chemical compound C(C)S(=O)(=O)C=1C=CC(=C(C1)C1(NC=CC(=N1)N(C1=CC=C2C(=NNC2=C1)C)C)N)OC IDELGVLOWFHGCY-UHFFFAOYSA-N 0.000 claims description 3
• XJJKEJHOYVBADS-UHFFFAOYSA-N C(C)S(=O)(=O)C=1C=CC(=C(C=1)C1(NC=C(C(=N1)N(C1=CC=C2C(=NNC2=C1)C)C)F)N)OC Chemical compound C(C)S(=O)(=O)C=1C=CC(=C(C=1)C1(NC=C(C(=N1)N(C1=CC=C2C(=NNC2=C1)C)C)F)N)OC XJJKEJHOYVBADS-UHFFFAOYSA-N 0.000 claims description 3
• FAXGGDSKPYJFOH-UHFFFAOYSA-N C(C)S(=O)(=O)C=1C=CC(=C(C=1)C1(NC=CC(=N1)NC1=CC=C2C(=NNC2=C1)C)N)OC Chemical compound C(C)S(=O)(=O)C=1C=CC(=C(C=1)C1(NC=CC(=N1)NC1=CC=C2C(=NNC2=C1)C)N)OC FAXGGDSKPYJFOH-UHFFFAOYSA-N 0.000 claims description 3
• PRDBESRYYRCCHH-UHFFFAOYSA-N COC1=C(C=C(C=C1)S(=O)(=O)C)C1(NC=CC(=N1)N(C1=CC=C2C(=NNC2=C1)C)C)N Chemical compound COC1=C(C=C(C=C1)S(=O)(=O)C)C1(NC=CC(=N1)N(C1=CC=C2C(=NNC2=C1)C)C)N PRDBESRYYRCCHH-UHFFFAOYSA-N 0.000 claims description 3
• UASUSCJYVCCVKA-UHFFFAOYSA-N COC1=C(C=C(C=C1)S(=O)(=O)CC1=NOC(=C1)C)C1(NC=CC(=N1)NC1=CC=C2C(=NNC2=C1)C)N Chemical compound COC1=C(C=C(C=C1)S(=O)(=O)CC1=NOC(=C1)C)C1(NC=CC(=N1)NC1=CC=C2C(=NNC2=C1)C)N UASUSCJYVCCVKA-UHFFFAOYSA-N 0.000 claims description 3
• QEWLKWPRUPEKSW-UHFFFAOYSA-N FC(C(=O)O)(F)F.CC1=NNC2=CC(=CC=C12)C1(NC=NC(=N1)NC1=CC(=CC=C1)CS(=O)(=O)C)N Chemical class FC(C(=O)O)(F)F.CC1=NNC2=CC(=CC=C12)C1(NC=NC(=N1)NC1=CC(=CC=C1)CS(=O)(=O)C)N QEWLKWPRUPEKSW-UHFFFAOYSA-N 0.000 claims description 3
• IWZSOGITOHUCSQ-UHFFFAOYSA-N FC1=C(C=C(C=C1)S(=O)(=O)C)C1(NC=CC(=N1)N(C1=CC=C2C(=NNC2=C1)C)C)N Chemical compound FC1=C(C=C(C=C1)S(=O)(=O)C)C1(NC=CC(=N1)N(C1=CC=C2C(=NNC2=C1)C)C)N IWZSOGITOHUCSQ-UHFFFAOYSA-N 0.000 claims description 3
• 206010038923 Retinopathy Diseases 0.000 claims description 3
• 208000037976 chronic inflammation Diseases 0.000 claims description 3
• 208000037893 chronic inflammatory disorder Diseases 0.000 claims description 3
• 208000028867 ischemia Diseases 0.000 claims description 3
• FHCXJZSNEBTJKE-UHFFFAOYSA-N n-[2-methyl-5-[[4-[methyl-(3-methyl-2h-indazol-6-yl)amino]-1,3,5-triazin-2-yl]amino]phenyl]methanesulfonamide Chemical compound C=1C=C2C(C)=NNC2=CC=1N(C)C(N=1)=NC=NC=1NC1=CC=C(C)C(NS(C)(=O)=O)=C1 FHCXJZSNEBTJKE-UHFFFAOYSA-N 0.000 claims description 3
• YDHRSWAPJJCSGX-UHFFFAOYSA-N n-[3-[[4-[ethyl-(3-methyl-2h-indazol-6-yl)amino]pyrimidin-2-yl]amino]phenyl]acetamide Chemical compound C=1C=C2C(C)=NNC2=CC=1N(CC)C(N=1)=CC=NC=1NC1=CC=CC(NC(C)=O)=C1 YDHRSWAPJJCSGX-UHFFFAOYSA-N 0.000 claims description 3
• AXBKRLMNVZOBIH-UHFFFAOYSA-N n-[3-[[4-[methyl-(3-methyl-2h-indazol-6-yl)amino]pyrimidin-2-yl]amino]phenyl]acetamide Chemical compound C=1C=C2C(C)=NNC2=CC=1N(C)C(N=1)=CC=NC=1NC1=CC=CC(NC(C)=O)=C1 AXBKRLMNVZOBIH-UHFFFAOYSA-N 0.000 claims description 3
• RBENAORRCGKTLF-UHFFFAOYSA-N n-[3-[[4-[methyl-(3-methyl-2h-indazol-6-yl)amino]pyrimidin-2-yl]amino]phenyl]methanesulfonamide Chemical compound C=1C=C2C(C)=NNC2=CC=1N(C)C(N=1)=CC=NC=1NC1=CC=CC(NS(C)(=O)=O)=C1 RBENAORRCGKTLF-UHFFFAOYSA-N 0.000 claims description 3
• CCDZAMNZEXREEV-UHFFFAOYSA-N n-[[3-[[4-[methyl-(3-methyl-2h-indazol-6-yl)amino]pyrimidin-2-yl]amino]phenyl]methyl]methanesulfonamide Chemical compound C=1C=C2C(C)=NNC2=CC=1N(C)C(N=1)=CC=NC=1NC1=CC=CC(CNS(C)(=O)=O)=C1 CCDZAMNZEXREEV-UHFFFAOYSA-N 0.000 claims description 3
• WSOASQNARKHWJC-UHFFFAOYSA-N n-[[4-[[4-[methyl-(3-methyl-2h-indazol-6-yl)amino]pyrimidin-2-yl]amino]phenyl]methyl]ethanesulfonamide Chemical compound C1=CC(CNS(=O)(=O)CC)=CC=C1NC1=NC=CC(N(C)C=2C=C3NN=C(C)C3=CC=2)=N1 WSOASQNARKHWJC-UHFFFAOYSA-N 0.000 claims description 3
• CUIHSIWYWATEQL-UHFFFAOYSA-N pazopanib Chemical compound C1=CC2=C(C)N(C)N=C2C=C1N(C)C(N=1)=CC=NC=1NC1=CC=C(C)C(S(N)(=O)=O)=C1 CUIHSIWYWATEQL-UHFFFAOYSA-N 0.000 claims description 3
• DSWWZJMZQVRSAG-UHFFFAOYSA-N 3-[[5-fluoro-4-[methyl-(3-methyl-2h-indazol-6-yl)amino]pyrimidin-2-yl]amino]-n-propan-2-ylbenzenesulfonamide Chemical compound CC(C)NS(=O)(=O)C1=CC=CC(NC=2N=C(C(F)=CN=2)N(C)C=2C=C3NN=C(C)C3=CC=2)=C1 DSWWZJMZQVRSAG-UHFFFAOYSA-N 0.000 claims description 2
• NRAGRPIQSKNAQS-UHFFFAOYSA-N 4-(2,3-dimethylindazol-6-yl)-4-N-methyl-2-N-[4-(methylsulfonylmethyl)phenyl]-1H-pyrimidine-2,4-diamine Chemical compound CN1N=C2C=C(C=CC2=C1C)C1(NC(=NC=C1)NC1=CC=C(C=C1)CS(=O)(=O)C)NC NRAGRPIQSKNAQS-UHFFFAOYSA-N 0.000 claims description 2
• MKQLDHOHEOAOHJ-UHFFFAOYSA-N 4-(3-ethyl-2H-indazol-6-yl)-5-fluoro-4-N-methyl-2-N-[3-(methylsulfonylmethyl)phenyl]-1H-pyrimidine-2,4-diamine Chemical compound C(C)C1=NNC2=CC(=CC=C12)C1(NC(=NC=C1F)NC1=CC(=CC=C1)CS(=O)(=O)C)NC MKQLDHOHEOAOHJ-UHFFFAOYSA-N 0.000 claims description 2
• IQNXIJSPNSRSLK-UHFFFAOYSA-N 4-methyl-4-N-(3-methyl-2H-indazol-6-yl)-2-N-(3-methylsulfinylphenyl)-1H-pyrimidine-2,4-diamine Chemical compound CC1(NC(=NC=C1)NC1=CC(=CC=C1)S(=O)C)NC1=CC=C2C(=NNC2=C1)C IQNXIJSPNSRSLK-UHFFFAOYSA-N 0.000 claims description 2
• GPVSHRYDJMVNJP-UHFFFAOYSA-N 4-methyl-4-N-(3-methyl-2H-indazol-6-yl)-2-N-(3-methylsulfonylphenyl)-1H-1,3,5-triazine-2,4-diamine Chemical compound CC1(NC=NC(=N1)NC1=CC(=CC=C1)S(=O)(=O)C)NC1=CC=C2C(=NNC2=C1)C GPVSHRYDJMVNJP-UHFFFAOYSA-N 0.000 claims description 2
• AJJWFOBQWWYSKG-UHFFFAOYSA-N 4-n-methyl-4-n-(3-methyl-2h-indazol-6-yl)-2-n-[3-(methylsulfonylmethyl)phenyl]pyrimidine-2,4-diamine Chemical compound C=1C=C2C(C)=NNC2=CC=1N(C)C(N=1)=CC=NC=1NC1=CC=CC(CS(C)(=O)=O)=C1 AJJWFOBQWWYSKG-UHFFFAOYSA-N 0.000 claims description 2
• IDXNGTHGCYPLSM-UHFFFAOYSA-N 5-[[4-[(2,3-dimethylindazol-6-yl)-methylamino]-1,3,5-triazin-2-yl]amino]-2-methylbenzenesulfonamide Chemical class C1=CC2=C(C)N(C)N=C2C=C1N(C)C(N=1)=NC=NC=1NC1=CC=C(C)C(S(N)(=O)=O)=C1 IDXNGTHGCYPLSM-UHFFFAOYSA-N 0.000 claims description 2
• AQRABUUXKQANHS-UHFFFAOYSA-N 5-fluoro-4-n-methyl-4-n-(3-methyl-2h-indazol-6-yl)-2-n-[3-(propan-2-ylsulfonylmethyl)phenyl]pyrimidine-2,4-diamine Chemical compound CC(C)S(=O)(=O)CC1=CC=CC(NC=2N=C(C(F)=CN=2)N(C)C=2C=C3NN=C(C)C3=CC=2)=C1 AQRABUUXKQANHS-UHFFFAOYSA-N 0.000 claims description 2
• AYHVTCLZDJHJSE-UHFFFAOYSA-N n-[4-[[4-[methyl-(3-methyl-2h-indazol-6-yl)amino]-1,3,5-triazin-2-yl]amino]phenyl]acetamide Chemical compound C=1C=C2C(C)=NNC2=CC=1N(C)C(N=1)=NC=NC=1NC1=CC=C(NC(C)=O)C=C1 AYHVTCLZDJHJSE-UHFFFAOYSA-N 0.000 claims description 2
• ARZWRWBLDKOLFV-UHFFFAOYSA-N n-[5-[[5-fluoro-4-[methyl-(3-methyl-2h-indazol-6-yl)amino]pyrimidin-2-yl]amino]-2-methylphenyl]methanesulfonamide Chemical compound C=1C=C2C(C)=NNC2=CC=1N(C)C(C(=CN=1)F)=NC=1NC1=CC=C(C)C(NS(C)(=O)=O)=C1 ARZWRWBLDKOLFV-UHFFFAOYSA-N 0.000 claims description 2
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