Recherche de Sous-structure

755413

CC(C)(C)OC(=O)N1CCC(c2ccc(Cl)cn2)CC1
Reaction #60667
tert-butyl 4-(5-chloropyridin-2-yl)piperidine-1-carboxylate
Rendement 16.0%DOI: 10.6084/m9.figshare.5104873.v1
Cc1ccc(Nc2cnc(-c3ccccc3)c(Cl)c2)c(C(=O)OC(C)(C)C)c1
Reaction #70337
tert-Butyl 2-(5-chloro-6-phenylpyridin-3-ylamino)-5-methylbenzoate
DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)c1ccc(Cl)cn1
Reaction #82788
compound
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)NCC(=O)c1ncc(Cl)cc1Cl
Reaction #84294
desired product
Rendement 59.6%DOI: 10.6084/m9.figshare.5104873.v1
C[C@H](NC(=O)OC(C)(C)C)C(=O)c1ncc(Cl)cc1Cl
Reaction #84301
desired product
Rendement 65.5%DOI: 10.6084/m9.figshare.5104873.v1
O=C(NCC(=O)c1ncc(Cl)cc1Cl)c1ccccc1C(F)(F)F
Reaction #84312
desired product
Rendement 23.1%DOI: 10.6084/m9.figshare.5104873.v1
CCc1cncc(-c2cc3c(cn2)cnn3-c2ccc(Cl)c(F)n2)c1
Reaction #86107
1-(5-chloro-6-fluoro-2-pyridyl)-6-(5-ethyl-3-pyridyl)pyrazolo[4,3-c]pyridine
Rendement 59.0%DOI: 10.6084/m9.figshare.5104873.v1
Cc1cncc(-c2cc3c(cn2)cnn3-c2ccc(Cl)c(F)n2)n1
Reaction #86163
1-(5-chloro-6-fluoro-2-pyridyl)-6-(6-methylpyrazin-2-yl)pyrazolo[4,3-c]pyridine
Rendement 48.1%DOI: 10.6084/m9.figshare.5104873.v1
Cc1ccc(-c2cnn(C)c2)c(C(=O)N2CCC[C@@H](C)[C@H]2CNc2ncc(Cl)cc2F)c1
Reaction #89300
title compound
DOI: 10.6084/m9.figshare.5104873.v1
Cc1ccc(-c2ccccn2)c(C(=O)N2CCC[C@@H](C)[C@H]2CNc2ccc(Cl)cn2)c1
Reaction #89319
title compound
DOI: 10.6084/m9.figshare.5104873.v1
Cc1ccc(-n2ccc(C)n2)c(C(=O)N2CCC[C@@H](C)[C@H]2CNc2ccc(Cl)cn2)c1
Reaction #89323
title compound
DOI: 10.6084/m9.figshare.5104873.v1
Cc1ccc(-n2ncc(C)n2)c(C(=O)N2CCC[C@@H](C)[C@H]2CNc2ccc(Cl)cn2)c1
Reaction #89324
title compound
DOI: 10.6084/m9.figshare.5104873.v1
Cc1ccc(-c2ncccn2)c(C(=O)N2CCC[C@@H](C)[C@H]2CNc2ccc(Cl)cn2)c1
Reaction #89340
title compound
DOI: 10.6084/m9.figshare.5104873.v1
Cc1ccc(-c2ccc(C(F)(F)F)cn2)c(C(=O)N2CCC[C@@H](C)[C@H]2CNc2ccc(Cl)cn2)c1
Reaction #89358
title compound
DOI: 10.6084/m9.figshare.5104873.v1
Cc1ccc(-c2ccc(F)cn2)c(C(=O)N2CCC[C@@H](C)[C@H]2CNc2ccc(Cl)cn2)c1
Reaction #89360
title compound
DOI: 10.6084/m9.figshare.5104873.v1
Cc1ccc(-n2cccn2)c(C(=O)N2CCC[C@@H](C)[C@H]2CNc2ccc(Cl)cn2)n1
Reaction #89375
title compound
DOI: 10.6084/m9.figshare.5104873.v1
Cc1ccc(-c2ccccn2)c(C(=O)N2CCC[C@@H](C)[C@H]2CNc2ccc(Cl)cn2)n1
Reaction #89376
title compound
DOI: 10.6084/m9.figshare.5104873.v1
Cc1ccc(-n2nccn2)c(C(=O)N2CCC[C@@H](C)[C@H]2CNc2ccc(Cl)cn2)n1
Reaction #89385
title compound
DOI: 10.6084/m9.figshare.5104873.v1
Cc1ccc(-c2ncccn2)c(C(=O)N2CCC[C@@H](C)[C@H]2CNc2ncc(Cl)cc2F)c1
Reaction #89387
title compound
DOI: 10.6084/m9.figshare.5104873.v1
Cc1ccc(-c2ncccn2)c(C(=O)N2CCC[C@@H](C)[C@H]2CNc2ccc(Cl)cn2)n1
Reaction #89395
title compound
DOI: 10.6084/m9.figshare.5104873.v1
Page 1Suivant