16 件の反応に参加

172763

COc1cc(-c2cnc3c(c2)c(-c2cnn(Cc4cccc(F)c4)c2)cn3S(=O)(=O)c2ccc(C)cc2)cnc1NC(=O)OC(C)(C)C
Reaction #618797
titled compound
収率 93.2%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_05
Cc1ccc(S(=O)(=O)n2cc(-c3cnn(Cc4cccc(F)c4)c3)c3cc(-c4ccc(C5=CCN(C(=O)OC(C)(C)C)CC5)cc4)cnc32)cc1
Reaction #618799
tert-butyl 4-(4-(3-(1-(3-fluorobenzyl)-1H-pyrazol-4-yl)-1-tosyl-1H-pyrrolo[2,3-b]pyridin-5-yl)phenyl)-5,6-dihydropyridine-1(2H)-carboxylate
収率 88.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_05
Cc1ccc(S(=O)(=O)n2cc(-c3cnn(Cc4cccc(F)c4)c3)c3cc(-c4ccc(C5=CCN(C)CC5)cc4)cnc32)cc1
Reaction #618805
titled compound
収率 83.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_05
Cc1ccc(S(=O)(=O)n2cc(-c3cnn(Cc4cccc(F)c4)c3)c3cc(-c4ccc(C5CCN(C(=O)OC(C)(C)C)CC5)c(F)c4)cnc32)cc1
Reaction #618808
titled compound
収率 93.3%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_05
COc1cc(-c2cnc3c(c2)c(-c2cnn(Cc4cccc(F)c4)c2)cn3S(=O)(=O)c2ccc(C)cc2)ccc1C1CCN(C(=O)OC(C)(C)C)CC1
Reaction #618814
titled compound
収率 71.9%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_05
Cc1ccc(S(=O)(=O)n2cc(-c3cnn(Cc4cccc(F)c4)c3)c3cc(-c4cccc(CC5CCN(C(=O)OC(C)(C)C)CC5)c4)cnc32)cc1
Reaction #618851
titled compound
収率 63.1%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_05
Cc1ccc(S(=O)(=O)n2cc(-c3cnn(Cc4cccc(F)c4)c3)c3cc(-c4ccc(N5CCN(C(=O)OC(C)(C)C)CC5)c([N+](=O)[O-])c4)cnc32)cc1
Reaction #618860
tert-butyl 4-(4-(3-(1-(3-fluorobenzyl)-1H-pyrazol-4-yl)-1-tosyl-1H-pyrrolo[2,3-b]pyridin-5-yl)-2-nitrophenyl)piperazine-1-carboxylate
収率 33.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_05
CC(C)(C)OC(=O)N1CCN(c2ccc(-c3cnc4c(c3)c(-c3cnn(Cc5cccc(F)c5)c3)cn4C(=O)OC(C)(C)C)cc2NS(C)(=O)=O)CC1
Reaction #618864
titled compound
収率 18.7%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_05
COc1cc(N2CCN(C(=O)OC(C)(C)C)CC2)ccc1-c1cnc2c(c1)c(-c1cnn(Cc3cccc(F)c3)c1)cn2S(=O)(=O)c1ccc(C)cc1
Reaction #618890
titled compound
収率 686.4%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_05
COc1nc(N2CCN(C(=O)OC(C)(C)C)CC2)ccc1-c1cnc2c(c1)c(-c1cnn(Cc3cccc(F)c3)c1)cn2S(=O)(=O)c1ccc(C)cc1
Reaction #618960
titled compound
収率 85.3%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_05
Cc1ccc(S(=O)(=O)n2cc(-c3cnn(Cc4cccc(F)c4)c3)c3cc(-c4ccc(N5CCN(C(=O)OC(C)(C)C)CC5)cn4)cnc32)cc1
Reaction #618968
titled compound
収率 74.6%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_05
Cc1ccc(S(=O)(=O)n2cc(-c3cnn(Cc4cccc(F)c4)c3)c3cc(-c4cnc(N5CCN(C(=O)OC(C)(C)C)CC5)cn4)cnc32)cc1
Reaction #619008
titled compound
収率 82.6%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_05
Cc1ccc(S(=O)(=O)n2cc(-c3cnn(Cc4cccc(F)c4)c3)c3cc(-c4cnc(N5CCN(C(=O)OC(C)(C)C)CC5)c(F)c4)cnc32)cc1
Reaction #619038
titled compound
収率 88.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_05
COc1cc(-c2cnc3c(c2)c(-c2cnn(Cc4cccc(F)c4)c2)cn3S(=O)(=O)c2ccc(C)cc2)cnc1N1CCN(C(=O)OC(C)(C)C)CC1
Reaction #619040
titled compound
収率 70.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_05
Cc1ccc(S(=O)(=O)n2cc(-c3cnn(Cc4cccc(F)c4)c3)c3cc(-c4cnc(NC(=O)OC(C)(C)C)c(F)c4)cnc32)cc1
Reaction #619061
titled compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_05
C=CC(=O)Nc1cccc(Oc2ncnc(N)c2-c2cnn(Cc3cccc(F)c3)c2)c1
Reaction #1609341
N-(3-((6-amino-5-(1-(3-fluorobenzyl)-1H-pyrazol-4-yl)pyrimidin-4-yl)oxy)phenyl)acrylamide
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2015_07