بحث البنية الفرعية

1347194

CC(c1ccc(-c2ncc(C(=O)NC3CC3)s2)cc1)N1CCC(CC(C)(C)C#N)(c2ccccc2)OC1=O
Reaction #193631
DOI: 10.1039/C8SC04228D
CC(C)Nc1nnc(-c2ccc3[nH]cc(-c4ncc(C(=O)NC5CC5)s4)c3c2)o1
Reaction #721472
desired product
DOI: 10.6084/m9.figshare.5104873.v1
Cc1ccc(S(=O)(=O)n2cc(-c3ncc(C(=O)NC4CC4)s3)c3cc(-c4nnc(NC(C)C)o4)ccc32)cc1
Reaction #721473
N-cyclopropyl-2-(5-(5-(isopropylamino)-1,3,4-oxadiazol-2-yl)-1-tosyl-1H-indol-3-yl)thiazole-5-carb oxamide
المردود 75.0%DOI: 10.6084/m9.figshare.5104873.v1
C[C@@H](c1ccc(-c2ncc(C(=O)NC3CC3)s2)cc1)N1CC[C@](CC(C)(C)O)(c2ccccc2)OC1=O
Reaction #1133266
title compound
DOI: 10.6084/m9.figshare.5104873.v1
C[C@@H](c1ccc(-c2ncc(C(=O)NC3CC3)s2)cc1)N1CC[C@](CC(C)(C)C#N)(c2ccccc2)OC1=O
Reaction #1133267
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CC(c1ccc(-c2ncc(C(=O)NC3CC3)s2)cc1)N1CCC(CC(C)(C)O)(c2ccccc2)OC1=O
Reaction #2228535
DOI: 10.1039/C8SC04228D