Поиск подструктуры

118889

N#Cc1cnc(N)c(C#N)c1
Reaction #4542
2-Amino-3,5-dicyanopyridine
Выход 73.0%DOI: 10.6084/m9.figshare.5104873.v1
Cc1c(C#N)cnc(N)c1C#N
Reaction #4543
2-Amino-4-methyl-3,5-pyridinedicarbonitrile
Выход 86.0%DOI: 10.6084/m9.figshare.5104873.v1
Cc1ccc(N)nc1Cl
Reaction #46226
6-chloro-5-methyl-pyridin-2-ylamine
Выход 36.0%DOI: 10.6084/m9.figshare.5104873.v1
Nc1ccc(C(F)(F)F)c(Cl)n1
Reaction #46227
6-chloro-5-(trifluoromethyl)pyridin-2-amine
Выход 46.0%DOI: 10.6084/m9.figshare.5104873.v1
N#Cc1c(-c2ccccc2)cc(N2CCOCC2)nc1Cl
Reaction #56159
2-chloro-6-morpholino-4-phenyl-3-cyano-pyridine
Выход 86.1%DOI: 10.6084/m9.figshare.5104873.v1
Nc1n[nH]c2nc(N3CCOCC3)cc(-c3ccccc3)c12
Reaction #56160
3-amino-6-morpholino-4-phenyl-1H-pyrazolo[3,4-b]pyridine
DOI: 10.6084/m9.figshare.5104873.v1
Cc1ccc(NC(=O)C2(c3ccc4c(c3)OC(F)(F)O4)CC2)nc1Cl
Reaction #67737
N-(6-chloro-5-methylpyridin-2-yl)-1-(2,2-difluorobenzo[d][1,3]dioxol-5-yl)cyclopropanecarboxamide
DOI: 10.6084/m9.figshare.5104873.v1
Cc1ccc(NC(=O)C2(c3ccc4c(c3)OC(F)(F)O4)CC2)nc1NCc1ccccc1
Reaction #67738
N-(6-(benzylamino)-5-methylpyridin-2-yl)-1-(2,2-difluorobenzo[d][1,3]dioxol-5-yl)cyclopropanecarboxamide
DOI: 10.6084/m9.figshare.5104873.v1
Cc1cc(N(C)C)nc(Cl)c1C#N
Reaction #81818
title compound
DOI: 10.6084/m9.figshare.5104873.v1
Cc1c(Br)c(N(C)C)nc(Cl)c1C#N
Reaction #81819
title compound
Выход 98.9%DOI: 10.6084/m9.figshare.5104873.v1
Cc1c(Br)c(N(C)C)nc(Cl)c1C(N)=O
Reaction #81820
title compound
DOI: 10.6084/m9.figshare.5104873.v1
Cc1cc(-n2ccnc2)nc(Cl)c1C(N)=O
Reaction #81831
title compound
DOI: 10.6084/m9.figshare.5104873.v1
Cc1cncc(-c2cc3c(cn2)cnn3-c2ccc(C(F)(F)F)c(N3CCC[C@H](NC(=O)OC(C)(C)C)C3)n2)n1
Reaction #86200
tert-butyl N-[(3S)-1-[6-[6-(6-methylpyrazin-2-yl)pyrazolo[4,3-c]pyridin-1-yl]-3-(trifluoromethyl)-2-pyridyl]-3-piperidyl]carbamate
Выход 76.2%DOI: 10.6084/m9.figshare.5104873.v1
C[C@H](Nc1nc(Nc2cc(C3CC3)[nH]n2)c(F)cc1C#N)c1ccc(F)cc1
Reaction #163040
title compound
Выход 51.6%DOI: 10.6084/m9.figshare.5104873.v1
C[C@H](Nc1nc(Nc2cc(C3CC3)[nH]n2)c(Cl)cc1C#N)c1ccc(F)cn1
Reaction #163068
title compound
Выход 52.0%DOI: 10.6084/m9.figshare.5104873.v1
Cc1cc(Nc2nc(NC(C)c3ncc(F)cn3)c(C#N)cc2Cl)n[nH]1
Reaction #163098
title compound
Выход 18.2%DOI: 10.6084/m9.figshare.5104873.v1
C[C@H](Nc1nc(Nc2cc(C3CC3)[nH]n2)c(F)c(I)c1C#N)c1ccc(F)cc1
Reaction #163099
title compound
Выход 20.0%DOI: 10.6084/m9.figshare.5104873.v1
N#Cc1cc(F)c(Nc2cc(C3CC3)[nH]n2)nc1Cl
Reaction #163100
title compound
Выход 73.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)Oc1cc(Nc2nc(Cl)c(C#N)cc2F)n[nH]1
Reaction #163101
title compound
Выход 50.0%DOI: 10.6084/m9.figshare.5104873.v1
N#Cc1c(Cl)nc(Nc2cc(C3CC3)[nH]n2)c(F)c1I
Reaction #163120
title compound
Выход 29.5%DOI: 10.6084/m9.figshare.5104873.v1
Страница 1Далее