JP2013528610A5

JP2013528610A5 -

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Publication number: JP2013528610A5
Authority: JP; Japan
Prior art keywords: alkyl; alkoxy; halo; imidazo; amino
Prior art date: 2011-05-27
Legal status : Granted

Application number

JP2013512850A

Other languages

English (en)

Japanese (ja)

Other versions

JP2013528610A (ja

JP5824040B2 (ja

Filing date

2011-05-27

Publication date

2014-07-10

2011-05-27 Application filed filed Critical

2011-05-27 Priority claimed from PCT/EP2011/058713 external-priority patent/WO2011151259A1/en

2013-07-11 Publication of JP2013528610A publication Critical patent/JP2013528610A/ja

2014-07-10 Publication of JP2013528610A5 publication Critical patent/JP2013528610A5/ja

2015-11-25 Application granted granted Critical

2015-11-25 Publication of JP5824040B2 publication Critical patent/JP5824040B2/ja

Status Expired - Fee Related legal-status Critical Current

2031-05-27 Anticipated expiration legal-status Critical

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-1 cyano - Chemical class 0.000 claims description 95
150000001875 compounds Chemical class 0.000 claims description 50
125000001072 heteroaryl group Chemical group 0.000 claims description 50
125000003118 aryl group Chemical group 0.000 claims description 47
229910052799 carbon Inorganic materials 0.000 claims description 38
150000003839 salts Chemical class 0.000 claims description 21
239000000203 mixture Substances 0.000 claims description 18
UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 16
206010028980 Neoplasm Diseases 0.000 claims description 16
239000001257 hydrogen Substances 0.000 claims description 16
229910052739 hydrogen Inorganic materials 0.000 claims description 16
208000037265 diseases, disorders, signs and symptoms Diseases 0.000 claims description 14
DNIAPMSPPWPWGF-UHFFFAOYSA-N Propylene glycol Chemical compound CC(O)CO DNIAPMSPPWPWGF-UHFFFAOYSA-N 0.000 claims description 11
239000002253 acid Substances 0.000 claims description 11
238000000034 method Methods 0.000 claims description 10
201000010099 disease Diseases 0.000 claims description 8
239000003795 chemical substances by application Substances 0.000 claims description 7
230000024932 T cell mediated immunity Effects 0.000 claims description 6
239000003814 drug Substances 0.000 claims description 6
230000004083 survival effect Effects 0.000 claims description 6
238000011282 treatment Methods 0.000 claims description 6
230000028709 inflammatory response Effects 0.000 claims description 5
208000032839 leukemia Diseases 0.000 claims description 5
229960001592 paclitaxel Drugs 0.000 claims description 5
230000035755 proliferation Effects 0.000 claims description 5
235000013772 propylene glycol Nutrition 0.000 claims description 5
125000001424 substituent group Chemical group 0.000 claims description 5
RCINICONZNJXQF-MZXODVADSA-N taxol Chemical compound O([C@@H]1[C@@]2(C[C@@H](C(C)=C(C2(C)C)[C@H](C([C@]2(C)[C@@H](O)C[C@H]3OC[C@]3([C@H]21)OC(C)=O)=O)OC(=O)C)OC(=O)[C@H](O)[C@@H](NC(=O)C=1C=CC=CC=1)C=1C=CC=CC=1)O)C(=O)C1=CC=CC=C1 RCINICONZNJXQF-MZXODVADSA-N 0.000 claims description 5
230000004222 uncontrolled growth Effects 0.000 claims description 5
UHDGCWIWMRVCDJ-CCXZUQQUSA-N Cytarabine Chemical compound O=C1N=C(N)C=CN1[C@H]1[C@@H](O)[C@H](O)[C@@H](CO)O1 UHDGCWIWMRVCDJ-CCXZUQQUSA-N 0.000 claims description 4
GHASVSINZRGABV-UHFFFAOYSA-N Fluorouracil Chemical compound FC1=CNC(=O)NC1=O GHASVSINZRGABV-UHFFFAOYSA-N 0.000 claims description 4
229930012538 Paclitaxel Natural products 0.000 claims description 4
230000001413 cellular effect Effects 0.000 claims description 4
229960002949 fluorouracil Drugs 0.000 claims description 4
230000008569 process Effects 0.000 claims description 4
229960004063 propylene glycol Drugs 0.000 claims description 4
229960004641 rituximab Drugs 0.000 claims description 4
WYWHKKSPHMUBEB-UHFFFAOYSA-N 6-Mercaptoguanine Natural products N1C(N)=NC(=S)C2=C1N=CN2 WYWHKKSPHMUBEB-UHFFFAOYSA-N 0.000 claims description 3
208000003174 Brain Neoplasms Diseases 0.000 claims description 3
CMSMOCZEIVJLDB-UHFFFAOYSA-N Cyclophosphamide Chemical compound ClCCN(CCCl)P1(=O)NCCCO1 CMSMOCZEIVJLDB-UHFFFAOYSA-N 0.000 claims description 3
206010027476 Metastases Diseases 0.000 claims description 3
ZDZOTLJHXYCWBA-VCVYQWHSSA-N N-debenzoyl-N-(tert-butoxycarbonyl)-10-deacetyltaxol Chemical compound O([C@H]1[C@H]2[C@@](C([C@H](O)C3=C(C)[C@@H](OC(=O)[C@H](O)[C@@H](NC(=O)OC(C)(C)C)C=4C=CC=CC=4)C[C@]1(O)C3(C)C)=O)(C)[C@@H](O)C[C@H]1OC[C@]12OC(=O)C)C(=O)C1=CC=CC=C1 ZDZOTLJHXYCWBA-VCVYQWHSSA-N 0.000 claims description 3
JXLYSJRDGCGARV-WWYNWVTFSA-N Vinblastine Natural products O=C(O[C@H]1[C@](O)(C(=O)OC)[C@@H]2N(C)c3c(cc(c(OC)c3)[C@]3(C(=O)OC)c4[nH]c5c(c4CCN4C[C@](O)(CC)C[C@H](C3)C4)cccc5)[C@@]32[C@H]2[C@@]1(CC)C=CCN2CC3)C JXLYSJRDGCGARV-WWYNWVTFSA-N 0.000 claims description 3
VSRXQHXAPYXROS-UHFFFAOYSA-N azanide;cyclobutane-1,1-dicarboxylic acid;platinum(2+) Chemical compound [NH2-].[NH2-].[Pt+2].OC(=O)C1(C(O)=O)CCC1 VSRXQHXAPYXROS-UHFFFAOYSA-N 0.000 claims description 3
229960004562 carboplatin Drugs 0.000 claims description 3
229960004316 cisplatin Drugs 0.000 claims description 3
DQLATGHUWYMOKM-UHFFFAOYSA-L cisplatin Chemical compound N[Pt](N)(Cl)Cl DQLATGHUWYMOKM-UHFFFAOYSA-L 0.000 claims description 3
229960004397 cyclophosphamide Drugs 0.000 claims description 3
229960000684 cytarabine Drugs 0.000 claims description 3
UREBDLICKHMUKA-CXSFZGCWSA-N dexamethasone Chemical compound C1CC2=CC(=O)C=C[C@]2(C)[C@]2(F)[C@@H]1[C@@H]1C[C@@H](C)[C@@](C(=O)CO)(O)[C@@]1(C)C[C@@H]2O UREBDLICKHMUKA-CXSFZGCWSA-N 0.000 claims description 3
239000003085 diluting agent Substances 0.000 claims description 3
229930013356 epothilone Natural products 0.000 claims description 3
229960005420 etoposide Drugs 0.000 claims description 3
VJJPUSNTGOMMGY-MRVIYFEKSA-N etoposide Chemical compound COC1=C(O)C(OC)=CC([C@@H]2C3=CC=4OCOC=4C=C3[C@@H](O[C@H]3[C@@H]([C@@H](O)[C@@H]4O[C@H](C)OC[C@H]4O3)O)[C@@H]3[C@@H]2C(OC3)=O)=C1 VJJPUSNTGOMMGY-MRVIYFEKSA-N 0.000 claims description 3
229960001101 ifosfamide Drugs 0.000 claims description 3
HOMGKSMUEGBAAB-UHFFFAOYSA-N ifosfamide Chemical compound ClCCNP1(=O)OCCCN1CCCl HOMGKSMUEGBAAB-UHFFFAOYSA-N 0.000 claims description 3
229960001156 mitoxantrone Drugs 0.000 claims description 3
KKZJGLLVHKMTCM-UHFFFAOYSA-N mitoxantrone Chemical compound O=C1C2=C(O)C=CC(O)=C2C(=O)C2=C1C(NCCNCCO)=CC=C2NCCNCCO KKZJGLLVHKMTCM-UHFFFAOYSA-N 0.000 claims description 3
CPTBDICYNRMXFX-UHFFFAOYSA-N procarbazine Chemical compound CNNCC1=CC=C(C(=O)NC(C)C)C=C1 CPTBDICYNRMXFX-UHFFFAOYSA-N 0.000 claims description 3
229960000624 procarbazine Drugs 0.000 claims description 3
229960003087 tioguanine Drugs 0.000 claims description 3
229960003048 vinblastine Drugs 0.000 claims description 3
JXLYSJRDGCGARV-XQKSVPLYSA-N vincaleukoblastine Chemical compound C([C@@H](C[C@]1(C(=O)OC)C=2C(=CC3=C([C@]45[C@H]([C@@]([C@H](OC(C)=O)[C@]6(CC)C=CCN([C@H]56)CC4)(O)C(=O)OC)N3C)C=2)OC)C[C@@](C2)(O)CC)N2CCC2=C1NC1=CC=CC=C21 JXLYSJRDGCGARV-XQKSVPLYSA-N 0.000 claims description 3
229960004528 vincristine Drugs 0.000 claims description 3
OGWKCGZFUXNPDA-UHFFFAOYSA-N vincristine Natural products C1C(CC)(O)CC(CC2(C(=O)OC)C=3C(=CC4=C(C56C(C(C(OC(C)=O)C7(CC)C=CCN(C67)CC5)(O)C(=O)OC)N4C=O)C=3)OC)CN1CCC1=C2NC2=CC=CC=C12 OGWKCGZFUXNPDA-UHFFFAOYSA-N 0.000 claims description 3
STQGQHZAVUOBTE-UHFFFAOYSA-N 7-Cyan-hept-2t-en-4,6-diinsaeure Natural products C1=2C(O)=C3C(=O)C=4C(OC)=CC=CC=4C(=O)C3=C(O)C=2CC(O)(C(C)=O)CC1OC1CC(N)C(O)C(C)O1 STQGQHZAVUOBTE-UHFFFAOYSA-N 0.000 claims description 2
108010006654 Bleomycin Proteins 0.000 claims description 2
GAGWJHPBXLXJQN-UORFTKCHSA-N Capecitabine Chemical compound C1=C(F)C(NC(=O)OCCCCC)=NC(=O)N1[C@H]1[C@H](O)[C@H](O)[C@@H](C)O1 GAGWJHPBXLXJQN-UORFTKCHSA-N 0.000 claims description 2
GAGWJHPBXLXJQN-UHFFFAOYSA-N Capecitabine Natural products C1=C(F)C(NC(=O)OCCCCC)=NC(=O)N1C1C(O)C(O)C(C)O1 GAGWJHPBXLXJQN-UHFFFAOYSA-N 0.000 claims description 2
PTOAARAWEBMLNO-KVQBGUIXSA-N Cladribine Chemical compound C1=NC=2C(N)=NC(Cl)=NC=2N1[C@H]1C[C@H](O)[C@@H](CO)O1 PTOAARAWEBMLNO-KVQBGUIXSA-N 0.000 claims description 2
208000002699 Digestive System Neoplasms Diseases 0.000 claims description 2
208000001976 Endocrine Gland Neoplasms Diseases 0.000 claims description 2
208000009849 Female Genital Neoplasms Diseases 0.000 claims description 2
XDXDZDZNSLXDNA-TZNDIEGXSA-N Idarubicin Chemical compound C1[C@H](N)[C@H](O)[C@H](C)O[C@H]1O[C@@H]1C2=C(O)C(C(=O)C3=CC=CC=C3C3=O)=C3C(O)=C2C[C@@](O)(C(C)=O)C1 XDXDZDZNSLXDNA-TZNDIEGXSA-N 0.000 claims description 2
XDXDZDZNSLXDNA-UHFFFAOYSA-N Idarubicin Natural products C1C(N)C(O)C(C)OC1OC1C2=C(O)C(C(=O)C3=CC=CC=C3C3=O)=C3C(O)=C2CC(O)(C(C)=O)C1 XDXDZDZNSLXDNA-UHFFFAOYSA-N 0.000 claims description 2
206010061218 Inflammation Diseases 0.000 claims description 2
206010025323 Lymphomas Diseases 0.000 claims description 2
201000003793 Myelodysplastic syndrome Diseases 0.000 claims description 2
206010029098 Neoplasm skin Diseases 0.000 claims description 2
208000000453 Skin Neoplasms Diseases 0.000 claims description 2
229940123237 Taxane Drugs 0.000 claims description 2
235000018936 Vitellaria paradoxa Nutrition 0.000 claims description 2
229960001561 bleomycin Drugs 0.000 claims description 2
OYVAGSVQBOHSSS-UAPAGMARSA-O bleomycin A2 Chemical compound N([C@H](C(=O)N[C@H](C)[C@@H](O)[C@H](C)C(=O)N[C@@H]([C@H](O)C)C(=O)NCCC=1SC=C(N=1)C=1SC=C(N=1)C(=O)NCCC[S+](C)C)[C@@H](O[C@H]1[C@H]([C@@H](O)[C@H](O)[C@H](CO)O1)O[C@@H]1[C@H]([C@@H](OC(N)=O)[C@H](O)[C@@H](CO)O1)O)C=1N=CNC=1)C(=O)C1=NC([C@H](CC(N)=O)NC[C@H](N)C(N)=O)=NC(N)=C1C OYVAGSVQBOHSSS-UAPAGMARSA-O 0.000 claims description 2
229960001467 bortezomib Drugs 0.000 claims description 2
GXJABQQUPOEUTA-RDJZCZTQSA-N bortezomib Chemical compound C([C@@H](C(=O)N[C@@H](CC(C)C)B(O)O)NC(=O)C=1N=CC=NC=1)C1=CC=CC=C1 GXJABQQUPOEUTA-RDJZCZTQSA-N 0.000 claims description 2
229960004117 capecitabine Drugs 0.000 claims description 2
229960004630 chlorambucil Drugs 0.000 claims description 2
JCKYGMPEJWAADB-UHFFFAOYSA-N chlorambucil Chemical compound OC(=O)CCCC1=CC=C(N(CCCl)CCCl)C=C1 JCKYGMPEJWAADB-UHFFFAOYSA-N 0.000 claims description 2
STQGQHZAVUOBTE-VGBVRHCVSA-N daunorubicin Chemical compound O([C@H]1C[C@@](O)(CC=2C(O)=C3C(=O)C=4C=CC=C(C=4C(=O)C3=C(O)C=21)OC)C(C)=O)[C@H]1C[C@H](N)[C@H](O)[C@H](C)O1 STQGQHZAVUOBTE-VGBVRHCVSA-N 0.000 claims description 2
229960000975 daunorubicin Drugs 0.000 claims description 2
229960003668 docetaxel Drugs 0.000 claims description 2
201000011523 endocrine gland cancer Diseases 0.000 claims description 2
HESCAJZNRMSMJG-KKQRBIROSA-N epothilone A Chemical class C/C([C@@H]1C[C@@H]2O[C@@H]2CCC[C@@H]([C@@H]([C@@H](C)C(=O)C(C)(C)[C@@H](O)CC(=O)O1)O)C)=C\C1=CSC(C)=N1 HESCAJZNRMSMJG-KKQRBIROSA-N 0.000 claims description 2
229960000390 fludarabine Drugs 0.000 claims description 2
GIUYCYHIANZCFB-FJFJXFQQSA-N fludarabine phosphate Chemical compound C1=NC=2C(N)=NC(F)=NC=2N1[C@@H]1O[C@H](COP(O)(O)=O)[C@@H](O)[C@@H]1O GIUYCYHIANZCFB-FJFJXFQQSA-N 0.000 claims description 2
229960002074 flutamide Drugs 0.000 claims description 2
MKXKFYHWDHIYRV-UHFFFAOYSA-N flutamide Chemical compound CC(C)C(=O)NC1=CC=C([N+]([O-])=O)C(C(F)(F)F)=C1 MKXKFYHWDHIYRV-UHFFFAOYSA-N 0.000 claims description 2
125000000524 functional group Chemical group 0.000 claims description 2
208000014829 head and neck neoplasm Diseases 0.000 claims description 2
208000024200 hematopoietic and lymphoid system neoplasm Diseases 0.000 claims description 2
229960000908 idarubicin Drugs 0.000 claims description 2
230000004054 inflammatory process Effects 0.000 claims description 2
FABUFPQFXZVHFB-CFWQTKTJSA-N ixabepilone Chemical compound C/C([C@@H]1C[C@@H]2O[C@]2(C)CCC[C@@H]([C@@H]([C@H](C)C(=O)C(C)(C)[C@H](O)CC(=O)N1)O)C)=C\C1=CSC(C)=N1 FABUFPQFXZVHFB-CFWQTKTJSA-N 0.000 claims description 2
229960002014 ixabepilone Drugs 0.000 claims description 2
210000003734 kidney Anatomy 0.000 claims description 2
230000001404 mediated effect Effects 0.000 claims description 2
229960001924 melphalan Drugs 0.000 claims description 2
SGDBTWWWUNNDEQ-LBPRGKRZSA-N melphalan Chemical compound OC(=O)[C@@H](N)CC1=CC=C(N(CCCl)CCCl)C=C1 SGDBTWWWUNNDEQ-LBPRGKRZSA-N 0.000 claims description 2
230000002265 prevention Effects 0.000 claims description 2
208000023958 prostate neoplasm Diseases 0.000 claims description 2
201000004477 skin sarcoma Diseases 0.000 claims description 2
125000005843 halogen group Chemical group 0.000 claims 56
125000000592 heterocycloalkyl group Chemical group 0.000 claims 51
125000005913 (C3-C6) cycloalkyl group Chemical group 0.000 claims 47
125000000882 C2-C6 alkenyl group Chemical group 0.000 claims 34
125000002924 primary amino group Chemical group [H]N([H])* 0.000 claims 33
125000004435 hydrogen atom Chemical group [H]* 0.000 claims 29
125000003601 C2-C6 alkynyl group Chemical group 0.000 claims 21
125000004093 cyano group Chemical group *C#N 0.000 claims 21
125000000959 isobutyl group Chemical group [H]C([H])([H])C([H])(C([H])([H])[H])C([H])([H])* 0.000 claims 14
125000004944 pyrazin-3-yl group Chemical group [H]C1=C([H])N=C(*)C([H])=N1 0.000 claims 14
125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims 12
150000001204 N-oxides Chemical class 0.000 claims 10
239000012453 solvate Substances 0.000 claims 10
KXDAEFPNCMNJSK-UHFFFAOYSA-N benzene carboxamide Natural products NC(=O)C1=CC=CC=C1 KXDAEFPNCMNJSK-UHFFFAOYSA-N 0.000 claims 9
125000005418 aryl aryl group Chemical group 0.000 claims 5
QOXOZONBQWIKDA-UHFFFAOYSA-N 3-hydroxypropyl Chemical group [CH2]CCO QOXOZONBQWIKDA-UHFFFAOYSA-N 0.000 claims 2
AOJJSUZBOXZQNB-TZSSRYMLSA-N Doxorubicin Chemical compound O([C@H]1C[C@@](O)(CC=2C(O)=C3C(=O)C=4C=CC=C(C=4C(=O)C3=C(O)C=21)OC)C(=O)CO)[C@H]1C[C@H](N)[C@H](O)[C@H](C)O1 AOJJSUZBOXZQNB-TZSSRYMLSA-N 0.000 claims 2
LRHPLDYGYMQRHN-UHFFFAOYSA-N N-Butanol Chemical compound CCCCO LRHPLDYGYMQRHN-UHFFFAOYSA-N 0.000 claims 2
125000002877 alkyl aryl group Chemical group 0.000 claims 2
150000004677 hydrates Chemical class 0.000 claims 2
230000036571 hydration Effects 0.000 claims 2
238000006703 hydration reaction Methods 0.000 claims 2
125000006316 iso-butyl amino group Chemical group [H]N(*)C([H])([H])C([H])(C([H])([H])[H])C([H])([H])[H] 0.000 claims 2
206010061289 metastatic neoplasm Diseases 0.000 claims 2
125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims 2
WGYKZJWCGVVSQN-UHFFFAOYSA-N propylamine Chemical group CCCN WGYKZJWCGVVSQN-UHFFFAOYSA-N 0.000 claims 2
125000005505 thiomorpholino group Chemical group 0.000 claims 2
125000004778 2,2-difluoroethyl group Chemical group [H]C([H])(*)C([H])(F)F 0.000 claims 1
WSHPFVZKPKNXLP-UHFFFAOYSA-N 2-(1-methylcyclopropyl)benzamide Chemical compound C=1C=CC=C(C(N)=O)C=1C1(C)CC1 WSHPFVZKPKNXLP-UHFFFAOYSA-N 0.000 claims 1
VOXBZHOHGGBLCQ-UHFFFAOYSA-N 2-amino-3,7-dihydropurine-6-thione;hydrate Chemical compound O.N1C(N)=NC(=S)C2=C1N=CN2.N1C(N)=NC(=S)C2=C1N=CN2 VOXBZHOHGGBLCQ-UHFFFAOYSA-N 0.000 claims 1
125000006325 2-propenyl amino group Chemical group [H]C([H])=C([H])C([H])([H])N([H])* 0.000 claims 1
GMMFTXWDTNSPRY-UHFFFAOYSA-N 3-[3-[4-(2-cyclopropyl-1h-imidazol-5-yl)phenyl]-8-(2-methylprop-2-enylamino)imidazo[1,2-a]pyrazin-6-yl]prop-2-yn-1-ol Chemical compound C=1N=C2C(NCC(=C)C)=NC(C#CCO)=CN2C=1C(C=C1)=CC=C1C(N1)=CN=C1C1CC1 GMMFTXWDTNSPRY-UHFFFAOYSA-N 0.000 claims 1
SLIXJNVGBFXHJA-UHFFFAOYSA-N 3-[3-[4-(2-cyclopropyl-1h-imidazol-5-yl)phenyl]-8-(4,4,4-trifluorobutylamino)imidazo[1,2-a]pyrazin-6-yl]prop-2-yn-1-ol Chemical compound C=1N=C2C(NCCCC(F)(F)F)=NC(C#CCO)=CN2C=1C(C=C1)=CC=C1C(N1)=CN=C1C1CC1 SLIXJNVGBFXHJA-UHFFFAOYSA-N 0.000 claims 1
YQPHGJXCHXNTMG-UHFFFAOYSA-N 3-[8-(cyclobutylmethylamino)-3-[4-(2-cyclopropyl-1h-imidazol-5-yl)phenyl]imidazo[1,2-a]pyrazin-6-yl]prop-2-yn-1-ol Chemical compound N=1C(C#CCO)=CN2C(C=3C=CC(=CC=3)C=3NC(=NC=3)C3CC3)=CN=C2C=1NCC1CCC1 YQPHGJXCHXNTMG-UHFFFAOYSA-N 0.000 claims 1
LOPVAUAMTOQZMH-UHFFFAOYSA-N 4-[2-[3-[4-(cyclopropylcarbamoyl)phenyl]-8-(2-methylpropylamino)imidazo[1,2-a]pyrazin-6-yl]ethynyl]benzamide Chemical compound C=1N=C2C(NCC(C)C)=NC(C#CC=3C=CC(=CC=3)C(N)=O)=CN2C=1C(C=C1)=CC=C1C(=O)NC1CC1 LOPVAUAMTOQZMH-UHFFFAOYSA-N 0.000 claims 1
NECFVPYNODMISP-UHFFFAOYSA-N 4-[6-(2-cyclohexylethynyl)-8-(2-methylpropylamino)imidazo[1,2-a]pyrazin-3-yl]-n-cyclopropylbenzamide Chemical compound C=1N=C2C(NCC(C)C)=NC(C#CC3CCCCC3)=CN2C=1C(C=C1)=CC=C1C(=O)NC1CC1 NECFVPYNODMISP-UHFFFAOYSA-N 0.000 claims 1
PNNPELOXIAYGKY-UHFFFAOYSA-N 4-[6-(2-cyclopentylethynyl)-8-(2-methylpropylamino)imidazo[1,2-a]pyrazin-3-yl]-n-cyclopropylbenzamide Chemical compound C=1N=C2C(NCC(C)C)=NC(C#CC3CCCC3)=CN2C=1C(C=C1)=CC=C1C(=O)NC1CC1 PNNPELOXIAYGKY-UHFFFAOYSA-N 0.000 claims 1
VHQGSJZKTKAZKM-UHFFFAOYSA-N 4-[6-(3-aminoprop-1-ynyl)-8-(2-methylpropylamino)imidazo[1,2-a]pyrazin-3-yl]-n-cyclopropylbenzamide Chemical compound C=1N=C2C(NCC(C)C)=NC(C#CCN)=CN2C=1C(C=C1)=CC=C1C(=O)NC1CC1 VHQGSJZKTKAZKM-UHFFFAOYSA-N 0.000 claims 1
NZRVNQXILCXBFD-UHFFFAOYSA-N 4-[6-(5-cyanopent-1-ynyl)-8-(2-methylpropylamino)imidazo[1,2-a]pyrazin-3-yl]-n-cyclopropylbenzamide Chemical compound C=1N=C2C(NCC(C)C)=NC(C#CCCCC#N)=CN2C=1C(C=C1)=CC=C1C(=O)NC1CC1 NZRVNQXILCXBFD-UHFFFAOYSA-N 0.000 claims 1
DNAPUPZAPABKLH-UHFFFAOYSA-N 4-[6-[3-(carbamoylamino)prop-1-ynyl]-8-(2-methylpropylamino)imidazo[1,2-a]pyrazin-3-yl]-n-cyclopropylbenzamide Chemical compound C=1N=C2C(NCC(C)C)=NC(C#CCNC(N)=O)=CN2C=1C(C=C1)=CC=C1C(=O)NC1CC1 DNAPUPZAPABKLH-UHFFFAOYSA-N 0.000 claims 1
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JP2013512850A 2010-06-01 2011-05-27 置換イミダゾピラジン Expired - Fee Related JP5824040B2 (ja)