Поиск подструктуры

770251

Cc1cc(C#N)cc(C(=O)NC2(C3CC3)CC2)c1NC(=O)c1cc(C(F)(F)F)nn1-c1ncccc1Cl
Reaction #279468
DOI: 10.1039/C8SC04228D
N#Cc1cc2cn[nH]c2c(C(=O)NC2(C3CC3)CC2)c1NC(=O)c1cc(C(F)(F)F)nn1-c1ncccc1Cl
Reaction #332795
product
DOI: 10.6084/m9.figshare.5104873.v1
COc1cc(C(=O)Nc2c(C)cc3cn[nH]c3c2C(=O)NC2(C3CC3)CC2)n(-c2ncccc2Cl)n1
Reaction #332798
6-{[2-(3-chloro-pyridin-2-yl)-5-methoxy-2H-pyrazole-3-carbonyl]-amino}-5-methyl-1H-indazole-7-carboxylic acid bicyclopropyl-1-ylamide
DOI: 10.6084/m9.figshare.5104873.v1
C#Cc1cc2cn[nH]c2c(C(=O)NC2(C3CC3)CC2)c1NC(=O)c1cc(C(F)(F)F)nn1-c1ncccc1Cl
Reaction #332809
product
DOI: 10.6084/m9.figshare.5104873.v1
O=C(NC1(C2CC2)CC1)c1c(NC(=O)c2cc(Cl)nn2-c2ncccc2Cl)c(Cl)cc2cn[nH]c12
Reaction #332812
product
Выход 91.8%DOI: 10.6084/m9.figshare.5104873.v1
COc1cc(C(=O)Nc2c(Cl)cc3c(Br)n[nH]c3c2C(=O)NC2(C3CC3)CC2)n(-c2ncccc2Cl)n1
Reaction #332818
solid
Выход 56.0%DOI: 10.6084/m9.figshare.5104873.v1
Cc1n[nH]c2c(C(=O)NC3(C4CC4)CC3)c(NC(=O)c3cc(C(F)(F)F)nn3-c3ncccc3Cl)c(Cl)cc12
Reaction #332822
solid
Выход 48.4%DOI: 10.6084/m9.figshare.5104873.v1
COCCCc1cc(O)cc(CN(C(=O)C(CNC(=O)OC(C)(C)C)Cc2ccc(OCCOc3c(Cl)cc(C)cc3Cl)cc2)C2(C3CC3)CC2)c1
Reaction #649052
title compound
DOI: 10.6084/m9.figshare.5104873.v1
COCCCc1cc(O)cc(CN(C(=O)C(CN)Cc2ccc(OCCOc3c(Cl)cc(C)cc3Cl)cc2)C2CC2)c1
Reaction #649053
title compound
DOI: 10.6084/m9.figshare.5104873.v1
COCCCc1cc(CN(C(=O)C(CNC(=O)OC(C)(C)C)Cc2ccc(OCCOc3c(Cl)cc(C)cc3Cl)cc2)C2CC2)cc(OCCCSC)c1
Reaction #649056
title compound
DOI: 10.6084/m9.figshare.5104873.v1
COCCCc1cc(CN(C(=O)C(CNC(=O)OC(C)(C)C)Cc2ccc(OCCOc3c(Cl)cc(C)cc3Cl)cc2)C2CC2)cc(OCCc2ccccn2)c1
Reaction #649059
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CCNC(=O)Oc1cc(CCCOC)cc(CN(C(=O)C(CNC(=O)OC(C)(C)C)Cc2ccc(OCCOc3c(Cl)cc(C)cc3Cl)cc2)C2CC2)c1
Reaction #649069
title compound
DOI: 10.6084/m9.figshare.5104873.v1
COCCCc1cc(CN(C(=O)C(CNC(=O)OC(C)(C)C)Cc2ccc(OCCOc3c(Cl)cc(C)cc3Cl)cc2)C2CC2)cc(OC(=O)NCC(C)(C)C(N)=O)c1
Reaction #649071
title compound
DOI: 10.6084/m9.figshare.5104873.v1
Cc1cc(C#N)cc(C(=O)NC2(C3CC3)CC2)c1NC(=O)c1cc(C(F)(F)F)nn1-c1ncccc1Cl
Reaction #1906456
title compound
Выход 57.4%DOI: 10.6084/m9.figshare.5104873.v1
Cc1cc(C#N)cc(C(=O)NC2(C3CC3)CC2)c1NC(=O)c1cc(C(F)(F)F)nn1-c1ncccc1Cl
Reaction #1906457
title compound
Выход 101.2%DOI: 10.6084/m9.figshare.5104873.v1
Cc1cc(I)cc(C(=O)NC2(C3CC3)CC2)c1NC(=O)c1cc(C(F)(F)F)nn1-c1ncccc1Cl
Reaction #1906458
title compound
DOI: 10.6084/m9.figshare.5104873.v1
Cc1cc(C#N)cc(C(=O)NC2(C3CC3)CC2)c1N
Reaction #1906460
2-Amino-N-bicyclopropyl-1-yl-5-cyano-3-methyl-benzamide
DOI: 10.6084/m9.figshare.5104873.v1