JP5970537B2 - キナーゼ阻害薬として活性な置換ピリミジニル−ピロール - Google Patents

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Publication number

JP5970537B2

JP5970537B2 JP2014505570A JP2014505570A JP5970537B2 JP 5970537 B2 JP5970537 B2 JP 5970537B2 JP 2014505570 A JP2014505570 A JP 2014505570A JP 2014505570 A JP2014505570 A JP 2014505570A JP 5970537 B2 JP5970537 B2 JP 5970537B2

Authority

JP

Japan

Prior art keywords

pyrrole

carboxamide

chloro

aminopyrimidin

compound

Prior art date

2011-04-19

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 - Fee Related

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• BAJCRPRPWGNRKM-UHFFFAOYSA-N 2-(1h-pyrrol-2-yl)pyrimidine Chemical class C1=CNC(C=2N=CC=CN=2)=C1 BAJCRPRPWGNRKM-UHFFFAOYSA-N 0.000 title description 4
• 229940043355 kinase inhibitor Drugs 0.000 title 1
• 239000003757 phosphotransferase inhibitor Substances 0.000 title 1
• 150000001875 compounds Chemical class 0.000 claims description 208
• 238000000034 method Methods 0.000 claims description 62
• 238000006243 chemical reaction Methods 0.000 claims description 47
• -1 2-aminopyrimidin-4-yl Chemical group 0.000 claims description 45
• 150000003839 salts Chemical class 0.000 claims description 39
• ZMXDDKWLCZADIW-UHFFFAOYSA-N N,N-Dimethylformamide Chemical compound CN(C)C=O ZMXDDKWLCZADIW-UHFFFAOYSA-N 0.000 claims description 36
• 239000001257 hydrogen Substances 0.000 claims description 36
• 229910052739 hydrogen Inorganic materials 0.000 claims description 36
• 101000997832 Homo sapiens Tyrosine-protein kinase JAK2 Proteins 0.000 claims description 29
• 102100033444 Tyrosine-protein kinase JAK2 Human genes 0.000 claims description 29
• 125000004435 hydrogen atom Chemical group [H]* 0.000 claims description 27
• 238000002360 preparation method Methods 0.000 claims description 23
• 239000003814 drug Substances 0.000 claims description 18
• 125000000217 alkyl group Chemical group 0.000 claims description 14
• 230000000694 effects Effects 0.000 claims description 12
• 230000007062 hydrolysis Effects 0.000 claims description 11
• 238000006460 hydrolysis reaction Methods 0.000 claims description 11
• 239000008194 pharmaceutical composition Substances 0.000 claims description 11
• 101000934996 Homo sapiens Tyrosine-protein kinase JAK3 Proteins 0.000 claims description 10
• UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 9
• 102100025387 Tyrosine-protein kinase JAK3 Human genes 0.000 claims description 9
• 125000004169 (C1-C6) alkyl group Chemical group 0.000 claims description 8
• 125000004093 cyano group Chemical group *C#N 0.000 claims description 8
• 108091000080 Phosphotransferase Proteins 0.000 claims description 7
• 238000005859 coupling reaction Methods 0.000 claims description 7
• 102000020233 phosphotransferase Human genes 0.000 claims description 7
• WETWJCDKMRHUPV-UHFFFAOYSA-N acetyl chloride Chemical compound CC(Cl)=O WETWJCDKMRHUPV-UHFFFAOYSA-N 0.000 claims description 6
• 239000012346 acetyl chloride Substances 0.000 claims description 6
• 230000002378 acidificating effect Effects 0.000 claims description 6
• 150000002148 esters Chemical class 0.000 claims description 6
• ZRALSGWEFCBTJO-UHFFFAOYSA-N anhydrous guanidine Natural products NC(N)=N ZRALSGWEFCBTJO-UHFFFAOYSA-N 0.000 claims description 5
• 229940127089 cytotoxic agent Drugs 0.000 claims description 5
• 239000003085 diluting agent Substances 0.000 claims description 5
• 239000003937 drug carrier Substances 0.000 claims description 5
• 230000008569 process Effects 0.000 claims description 5
• OVEPNDUIJPTNEM-UHFFFAOYSA-N 5-(2-aminopyrimidin-4-yl)-2-(2-chloro-5-cyanophenyl)-1h-pyrrole-3-carboxamide Chemical compound NC(=O)C=1C=C(C=2N=C(N)N=CC=2)NC=1C1=CC(C#N)=CC=C1Cl OVEPNDUIJPTNEM-UHFFFAOYSA-N 0.000 claims description 4
• CZUQYAXYBOEHCY-UHFFFAOYSA-N 5-(2-aminopyrimidin-4-yl)-2-[2-chloro-5-(trifluoromethyl)phenyl]-1h-pyrrole-3-carboxamide Chemical compound NC(=O)C=1C=C(C=2N=C(N)N=CC=2)NC=1C1=CC(C(F)(F)F)=CC=C1Cl CZUQYAXYBOEHCY-UHFFFAOYSA-N 0.000 claims description 4
• 101001043818 Mus musculus Interleukin-31 receptor subunit alpha Proteins 0.000 claims description 4
• CHJJGSNFBQVOTG-UHFFFAOYSA-N N-methyl-guanidine Natural products CNC(N)=N CHJJGSNFBQVOTG-UHFFFAOYSA-N 0.000 claims description 4
• KAESVJOAVNADME-UHFFFAOYSA-N Pyrrole Chemical compound C=1C=CNC=1 KAESVJOAVNADME-UHFFFAOYSA-N 0.000 claims description 4
• HCHKCACWOHOZIP-UHFFFAOYSA-N Zinc Chemical compound [Zn] HCHKCACWOHOZIP-UHFFFAOYSA-N 0.000 claims description 4
• 239000002253 acid Substances 0.000 claims description 4
• 230000009435 amidation Effects 0.000 claims description 4
• 238000007112 amidation reaction Methods 0.000 claims description 4
• 150000001732 carboxylic acid derivatives Chemical class 0.000 claims description 4
• 150000001733 carboxylic acid esters Chemical class 0.000 claims description 4
• SWSQBOPZIKWTGO-UHFFFAOYSA-N dimethylaminoamidine Natural products CN(C)C(N)=N SWSQBOPZIKWTGO-UHFFFAOYSA-N 0.000 claims description 4
• 230000002401 inhibitory effect Effects 0.000 claims description 4
• 108090000623 proteins and genes Proteins 0.000 claims description 4
• 229910052725 zinc Inorganic materials 0.000 claims description 4
• 239000011701 zinc Substances 0.000 claims description 4
• YPBDHHDMOYAYHZ-UHFFFAOYSA-N 2-(5-chloro-2-methylphenyl)-5-(2-methylpyrimidin-4-yl)-1h-pyrrole-3-carboxamide Chemical compound CC1=NC=CC(C=2NC(=C(C(N)=O)C=2)C=2C(=CC=C(Cl)C=2)C)=N1 YPBDHHDMOYAYHZ-UHFFFAOYSA-N 0.000 claims description 3
• AOUBZGNTXINLBC-UHFFFAOYSA-N 2-(5-chloro-2-methylphenyl)-5-pyrimidin-4-yl-1h-pyrrole-3-carboxamide Chemical compound CC1=CC=C(Cl)C=C1C1=C(C(N)=O)C=C(C=2N=CN=CC=2)N1 AOUBZGNTXINLBC-UHFFFAOYSA-N 0.000 claims description 3
• WYZSMYOLNHLHHE-UHFFFAOYSA-N 5-(2-aminopyrimidin-4-yl)-2-(5-bromo-2-fluorophenyl)-1h-pyrrole-3-carboxamide Chemical compound NC(=O)C=1C=C(C=2N=C(N)N=CC=2)NC=1C1=CC(Br)=CC=C1F WYZSMYOLNHLHHE-UHFFFAOYSA-N 0.000 claims description 3
• GJWYRBQDZYWGDV-UHFFFAOYSA-N 5-(2-aminopyrimidin-4-yl)-2-(5-chloro-2-ethylphenyl)-1h-pyrrole-3-carboxamide Chemical compound CCC1=CC=C(Cl)C=C1C1=C(C(N)=O)C=C(C=2N=C(N)N=CC=2)N1 GJWYRBQDZYWGDV-UHFFFAOYSA-N 0.000 claims description 3
• GJXWIZZAJFWIMF-UHFFFAOYSA-N 5-(2-aminopyrimidin-4-yl)-2-(5-chloro-2-ethylphenyl)-n-(2-hydroxyethyl)-1h-pyrrole-3-carboxamide Chemical compound CCC1=CC=C(Cl)C=C1C1=C(C(=O)NCCO)C=C(C=2N=C(N)N=CC=2)N1 GJXWIZZAJFWIMF-UHFFFAOYSA-N 0.000 claims description 3
• XOLXUIBKIXHODU-UHFFFAOYSA-N 5-(2-aminopyrimidin-4-yl)-2-(5-chloro-2-hydroxyphenyl)-1H-pyrrole-3-carboxamide Chemical compound NC(=O)C=1C=C(C=2N=C(N)N=CC=2)NC=1C1=CC(Cl)=CC=C1O XOLXUIBKIXHODU-UHFFFAOYSA-N 0.000 claims description 3
• ABUHZFPSYFNGPG-UHFFFAOYSA-N 5-(2-aminopyrimidin-4-yl)-2-(5-chloro-2-methoxyphenyl)-1h-pyrrole-3-carboxamide Chemical compound COC1=CC=C(Cl)C=C1C1=C(C(N)=O)C=C(C=2N=C(N)N=CC=2)N1 ABUHZFPSYFNGPG-UHFFFAOYSA-N 0.000 claims description 3
• VUTRRZOGGHDIPB-UHFFFAOYSA-N 5-(2-aminopyrimidin-4-yl)-2-(5-chloro-2-methylphenyl)-1-(2,2,2-trifluoroethyl)pyrrole-3-carboxamide Chemical compound CC1=CC=C(Cl)C=C1C(N1CC(F)(F)F)=C(C(N)=O)C=C1C1=CC=NC(N)=N1 VUTRRZOGGHDIPB-UHFFFAOYSA-N 0.000 claims description 3
• JOEGVALMDOEYRU-UHFFFAOYSA-N 5-(2-aminopyrimidin-4-yl)-2-(5-chloro-2-methylphenyl)-1-(2-hydroxyethyl)pyrrole-3-carboxamide Chemical compound CC1=CC=C(Cl)C=C1C(N1CCO)=C(C(N)=O)C=C1C1=CC=NC(N)=N1 JOEGVALMDOEYRU-UHFFFAOYSA-N 0.000 claims description 3
• QMGFZXHYEOADBG-UHFFFAOYSA-N 5-(2-aminopyrimidin-4-yl)-2-(5-chloro-2-methylphenyl)-1-methylpyrrole-3-carboxamide Chemical compound CC1=CC=C(Cl)C=C1C(N1C)=C(C(N)=O)C=C1C1=CC=NC(N)=N1 QMGFZXHYEOADBG-UHFFFAOYSA-N 0.000 claims description 3
• WNZGPMKWLNIIEW-UHFFFAOYSA-N 5-(2-aminopyrimidin-4-yl)-2-(5-chloro-2-methylphenyl)-n-(1-methylpiperidin-4-yl)-1h-pyrrole-3-carboxamide Chemical compound C1CN(C)CCC1NC(=O)C1=C(C=2C(=CC=C(Cl)C=2)C)NC(C=2N=C(N)N=CC=2)=C1 WNZGPMKWLNIIEW-UHFFFAOYSA-N 0.000 claims description 3
• ZFZZFNFVBXBXJG-UHFFFAOYSA-N 5-(2-aminopyrimidin-4-yl)-2-(5-chloro-2-methylphenyl)-n-(2,2-dimethylpropyl)-1h-pyrrole-3-carboxamide Chemical compound CC1=CC=C(Cl)C=C1C1=C(C(=O)NCC(C)(C)C)C=C(C=2N=C(N)N=CC=2)N1 ZFZZFNFVBXBXJG-UHFFFAOYSA-N 0.000 claims description 3
• PNYZVAIGFZQRDS-UHFFFAOYSA-N 5-(2-aminopyrimidin-4-yl)-2-(5-chloro-2-methylphenyl)-n-(2-fluoroethyl)-1h-pyrrole-3-carboxamide Chemical compound CC1=CC=C(Cl)C=C1C1=C(C(=O)NCCF)C=C(C=2N=C(N)N=CC=2)N1 PNYZVAIGFZQRDS-UHFFFAOYSA-N 0.000 claims description 3
• ZXKPOMXJHLXQKX-UHFFFAOYSA-N 5-(2-aminopyrimidin-4-yl)-2-(5-chloro-2-methylphenyl)-n-(2-hydroxyethyl)-1h-pyrrole-3-carboxamide Chemical compound CC1=CC=C(Cl)C=C1C1=C(C(=O)NCCO)C=C(C=2N=C(N)N=CC=2)N1 ZXKPOMXJHLXQKX-UHFFFAOYSA-N 0.000 claims description 3
• OSTUOGNGBFCXNG-UHFFFAOYSA-N 5-(2-aminopyrimidin-4-yl)-2-(5-chloro-2-methylphenyl)-n-(2-methoxyethyl)-1h-pyrrole-3-carboxamide Chemical compound COCCNC(=O)C=1C=C(C=2N=C(N)N=CC=2)NC=1C1=CC(Cl)=CC=C1C OSTUOGNGBFCXNG-UHFFFAOYSA-N 0.000 claims description 3
• JCPLJMMYNOZMBU-UHFFFAOYSA-N 5-(2-aminopyrimidin-4-yl)-2-(5-chloro-2-methylphenyl)-n-(2-methylpropyl)-1h-pyrrole-3-carboxamide Chemical compound CC(C)CNC(=O)C=1C=C(C=2N=C(N)N=CC=2)NC=1C1=CC(Cl)=CC=C1C JCPLJMMYNOZMBU-UHFFFAOYSA-N 0.000 claims description 3
• IKOXHEDMAJQABQ-UHFFFAOYSA-N 5-(2-aminopyrimidin-4-yl)-2-(5-chloro-2-methylphenyl)-n-(2-piperidin-1-ylethyl)-1h-pyrrole-3-carboxamide Chemical compound CC1=CC=C(Cl)C=C1C1=C(C(=O)NCCN2CCCCC2)C=C(C=2N=C(N)N=CC=2)N1 IKOXHEDMAJQABQ-UHFFFAOYSA-N 0.000 claims description 3
• JXROIQYBLXITAR-UHFFFAOYSA-N 5-(2-aminopyrimidin-4-yl)-2-(5-chloro-2-methylphenyl)-n-(3-hydroxypropyl)-1h-pyrrole-3-carboxamide Chemical compound CC1=CC=C(Cl)C=C1C1=C(C(=O)NCCCO)C=C(C=2N=C(N)N=CC=2)N1 JXROIQYBLXITAR-UHFFFAOYSA-N 0.000 claims description 3
• VVCSHJRAAVFYAE-UHFFFAOYSA-N 5-(2-aminopyrimidin-4-yl)-2-(5-chloro-2-methylphenyl)-n-(furan-2-ylmethyl)-1h-pyrrole-3-carboxamide Chemical compound CC1=CC=C(Cl)C=C1C1=C(C(=O)NCC=2OC=CC=2)C=C(C=2N=C(N)N=CC=2)N1 VVCSHJRAAVFYAE-UHFFFAOYSA-N 0.000 claims description 3
• NKTCWCPLTZQABU-UHFFFAOYSA-N 5-(2-aminopyrimidin-4-yl)-2-(5-chloro-2-methylphenyl)-n-[2-(methylamino)ethyl]-1h-pyrrole-3-carboxamide Chemical compound CNCCNC(=O)C=1C=C(C=2N=C(N)N=CC=2)NC=1C1=CC(Cl)=CC=C1C NKTCWCPLTZQABU-UHFFFAOYSA-N 0.000 claims description 3
• KMWLMMWKLAILOY-UHFFFAOYSA-N 5-(2-aminopyrimidin-4-yl)-2-(5-chloro-2-propan-2-ylphenyl)-1h-pyrrole-3-carboxamide Chemical compound CC(C)C1=CC=C(Cl)C=C1C1=C(C(N)=O)C=C(C=2N=C(N)N=CC=2)N1 KMWLMMWKLAILOY-UHFFFAOYSA-N 0.000 claims description 3
• MOMYBDKTKLWNMV-UHFFFAOYSA-N 5-(2-aminopyrimidin-4-yl)-2-[2,5-bis(trifluoromethyl)phenyl]-1h-pyrrole-3-carboxamide Chemical compound NC(=O)C=1C=C(C=2N=C(N)N=CC=2)NC=1C1=CC(C(F)(F)F)=CC=C1C(F)(F)F MOMYBDKTKLWNMV-UHFFFAOYSA-N 0.000 claims description 3
• BRIIWIAIUSRCEY-UHFFFAOYSA-N 5-(2-aminopyrimidin-4-yl)-2-[2-chloro-5-(trifluoromethyl)phenyl]-n-methyl-1h-pyrrole-3-carboxamide Chemical compound CNC(=O)C=1C=C(C=2N=C(N)N=CC=2)NC=1C1=CC(C(F)(F)F)=CC=C1Cl BRIIWIAIUSRCEY-UHFFFAOYSA-N 0.000 claims description 3
• BOOUSDCCWQVKID-UHFFFAOYSA-N 5-(2-aminopyrimidin-4-yl)-2-[2-methyl-5-(trifluoromethyl)phenyl]-1h-pyrrole-3-carboxamide Chemical compound CC1=CC=C(C(F)(F)F)C=C1C1=C(C(N)=O)C=C(C=2N=C(N)N=CC=2)N1 BOOUSDCCWQVKID-UHFFFAOYSA-N 0.000 claims description 3
• FWVOSTMZZQGURQ-UHFFFAOYSA-N 5-(2-aminopyrimidin-4-yl)-2-[5-chloro-2-(trifluoromethyl)phenyl]-1h-pyrrole-3-carboxamide Chemical compound NC(=O)C=1C=C(C=2N=C(N)N=CC=2)NC=1C1=CC(Cl)=CC=C1C(F)(F)F FWVOSTMZZQGURQ-UHFFFAOYSA-N 0.000 claims description 3
• STEACKYPSKNGJJ-UHFFFAOYSA-N 5-(2-aminopyrimidin-4-yl)-n-benzyl-2-(5-chloro-2-methylphenyl)-1h-pyrrole-3-carboxamide Chemical compound CC1=CC=C(Cl)C=C1C1=C(C(=O)NCC=2C=CC=CC=2)C=C(C=2N=C(N)N=CC=2)N1 STEACKYPSKNGJJ-UHFFFAOYSA-N 0.000 claims description 3
• ZDACAYMVFNLNGY-UHFFFAOYSA-N 5-(2-aminopyrimidin-4-yl)-n-methyl-2-[2-methyl-5-(trifluoromethyl)phenyl]-1h-pyrrole-3-carboxamide Chemical compound CNC(=O)C=1C=C(C=2N=C(N)N=CC=2)NC=1C1=CC(C(F)(F)F)=CC=C1C ZDACAYMVFNLNGY-UHFFFAOYSA-N 0.000 claims description 3
• 239000002841 Lewis acid Substances 0.000 claims description 3
• DHKHKXVYLBGOIT-UHFFFAOYSA-N acetaldehyde Diethyl Acetal Natural products CCOC(C)OCC DHKHKXVYLBGOIT-UHFFFAOYSA-N 0.000 claims description 3
• 150000001409 amidines Chemical class 0.000 claims description 3
• 239000002246 antineoplastic agent Substances 0.000 claims description 3
• 150000002357 guanidines Chemical class 0.000 claims description 3
• 150000007517 lewis acids Chemical class 0.000 claims description 3
• 238000004519 manufacturing process Methods 0.000 claims description 3
• RCEHZMJNOKHNLP-UHFFFAOYSA-N n-(2-aminoethyl)-5-(2-aminopyrimidin-4-yl)-2-(5-chloro-2-methylphenyl)-1h-pyrrole-3-carboxamide Chemical compound CC1=CC=C(Cl)C=C1C1=C(C(=O)NCCN)C=C(C=2N=C(N)N=CC=2)N1 RCEHZMJNOKHNLP-UHFFFAOYSA-N 0.000 claims description 3
• 239000000546 pharmaceutical excipient Substances 0.000 claims description 3
• 102000004169 proteins and genes Human genes 0.000 claims description 3
• MIEONHFLSVAHFB-UHFFFAOYSA-N 5-(2-aminopyrimidin-4-yl)-2-(2,5-dichlorophenyl)-1h-pyrrole-3-carboxamide Chemical compound NC(=O)C=1C=C(C=2N=C(N)N=CC=2)NC=1C1=CC(Cl)=CC=C1Cl MIEONHFLSVAHFB-UHFFFAOYSA-N 0.000 claims description 2
• WIVPUMFEYLUDQN-UHFFFAOYSA-N 5-(2-aminopyrimidin-4-yl)-2-(2-chloro-5-ethylphenyl)-1h-pyrrole-3-carboxamide Chemical compound CCC1=CC=C(Cl)C(C2=C(C=C(N2)C=2N=C(N)N=CC=2)C(N)=O)=C1 WIVPUMFEYLUDQN-UHFFFAOYSA-N 0.000 claims description 2
• MEUXPZAVSXUFCT-UHFFFAOYSA-N 5-(2-aminopyrimidin-4-yl)-2-(2-chloro-5-methoxyphenyl)-1h-pyrrole-3-carboxamide Chemical compound COC1=CC=C(Cl)C(C2=C(C=C(N2)C=2N=C(N)N=CC=2)C(N)=O)=C1 MEUXPZAVSXUFCT-UHFFFAOYSA-N 0.000 claims description 2
• MDONDWLCISBSBA-UHFFFAOYSA-N 5-(2-aminopyrimidin-4-yl)-2-(2-chloro-5-methylphenyl)-1h-pyrrole-3-carboxamide Chemical compound CC1=CC=C(Cl)C(C2=C(C=C(N2)C=2N=C(N)N=CC=2)C(N)=O)=C1 MDONDWLCISBSBA-UHFFFAOYSA-N 0.000 claims description 2
• ZTRQFNINWJXNEQ-UHFFFAOYSA-N 5-(2-aminopyrimidin-4-yl)-2-(5-bromo-2-methoxyphenyl)-1h-pyrrole-3-carboxamide Chemical compound COC1=CC=C(Br)C=C1C1=C(C(N)=O)C=C(C=2N=C(N)N=CC=2)N1 ZTRQFNINWJXNEQ-UHFFFAOYSA-N 0.000 claims description 2
• WQFWOIDYTKRNCW-UHFFFAOYSA-N 5-(2-aminopyrimidin-4-yl)-2-(5-chloro-2-ethylphenyl)-1-methylpyrrole-3-carboxamide Chemical compound CCC1=CC=C(Cl)C=C1C(N1C)=C(C(N)=O)C=C1C1=CC=NC(N)=N1 WQFWOIDYTKRNCW-UHFFFAOYSA-N 0.000 claims description 2
• CUQICKMLWKMIKB-UHFFFAOYSA-N 5-(2-aminopyrimidin-4-yl)-2-(5-chloro-2-ethylphenyl)-n,n-dimethyl-1h-pyrrole-3-carboxamide Chemical compound CCC1=CC=C(Cl)C=C1C1=C(C(=O)N(C)C)C=C(C=2N=C(N)N=CC=2)N1 CUQICKMLWKMIKB-UHFFFAOYSA-N 0.000 claims description 2
• VKIAXIXFWORXFB-UHFFFAOYSA-N 5-(2-aminopyrimidin-4-yl)-2-(5-chloro-2-ethylphenyl)-n-methyl-1h-pyrrole-3-carboxamide Chemical compound CCC1=CC=C(Cl)C=C1C1=C(C(=O)NC)C=C(C=2N=C(N)N=CC=2)N1 VKIAXIXFWORXFB-UHFFFAOYSA-N 0.000 claims description 2
• GPSCMUMAFNLGBT-UHFFFAOYSA-N 5-(2-aminopyrimidin-4-yl)-2-(5-chloro-2-methylphenyl)-1-ethylpyrrole-3-carboxamide Chemical compound CCN1C(C=2N=C(N)N=CC=2)=CC(C(N)=O)=C1C1=CC(Cl)=CC=C1C GPSCMUMAFNLGBT-UHFFFAOYSA-N 0.000 claims description 2
• DQDASFFHMDSYAZ-UHFFFAOYSA-N 5-(2-aminopyrimidin-4-yl)-2-(5-chloro-2-methylphenyl)-1h-pyrrole-3-carboxamide Chemical compound CC1=CC=C(Cl)C=C1C1=C(C(N)=O)C=C(C=2N=C(N)N=CC=2)N1 DQDASFFHMDSYAZ-UHFFFAOYSA-N 0.000 claims description 2
• QIHLJTBBSVIFSD-UHFFFAOYSA-N 5-(2-aminopyrimidin-4-yl)-2-(5-chloro-2-methylphenyl)-n,n-dimethyl-1h-pyrrole-3-carboxamide Chemical compound CN(C)C(=O)C=1C=C(C=2N=C(N)N=CC=2)NC=1C1=CC(Cl)=CC=C1C QIHLJTBBSVIFSD-UHFFFAOYSA-N 0.000 claims description 2
• RMCUEMSKMGVKOG-UHFFFAOYSA-N 5-(2-aminopyrimidin-4-yl)-2-(5-chloro-2-methylphenyl)-n-ethyl-1h-pyrrole-3-carboxamide Chemical compound CCNC(=O)C=1C=C(C=2N=C(N)N=CC=2)NC=1C1=CC(Cl)=CC=C1C RMCUEMSKMGVKOG-UHFFFAOYSA-N 0.000 claims description 2
• BFOWVKRAGHVYJA-UHFFFAOYSA-N 5-(2-aminopyrimidin-4-yl)-2-(5-chloro-2-methylphenyl)-n-methyl-1h-pyrrole-3-carboxamide Chemical compound CNC(=O)C=1C=C(C=2N=C(N)N=CC=2)NC=1C1=CC(Cl)=CC=C1C BFOWVKRAGHVYJA-UHFFFAOYSA-N 0.000 claims description 2
• AOBREUVPEFZVPG-UHFFFAOYSA-N 5-(2-aminopyrimidin-4-yl)-2-(5-chloro-2-methylphenyl)-n-phenyl-1h-pyrrole-3-carboxamide Chemical compound CC1=CC=C(Cl)C=C1C1=C(C(=O)NC=2C=CC=CC=2)C=C(C=2N=C(N)N=CC=2)N1 AOBREUVPEFZVPG-UHFFFAOYSA-N 0.000 claims description 2
• LIJKTJFYXDIILH-UHFFFAOYSA-N 5-(2-aminopyrimidin-4-yl)-2-(5-cyano-2-methylphenyl)-1h-pyrrole-3-carboxamide Chemical compound CC1=CC=C(C#N)C=C1C1=C(C(N)=O)C=C(C=2N=C(N)N=CC=2)N1 LIJKTJFYXDIILH-UHFFFAOYSA-N 0.000 claims description 2
• LNLCSFSRFGZNPP-UHFFFAOYSA-N 5-(2-aminopyrimidin-4-yl)-2-[2-chloro-5-(hydroxymethyl)phenyl]-1h-pyrrole-3-carboxamide Chemical compound NC(=O)C=1C=C(C=2N=C(N)N=CC=2)NC=1C1=CC(CO)=CC=C1Cl LNLCSFSRFGZNPP-UHFFFAOYSA-N 0.000 claims description 2
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