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558352

CCn1c(-c2ccccc2)c(C(c2ccccc2C)N2CCCC2)c2ccccc21
Reaction #9098
1-Ethyl-2-phenyl-3-(pyrrolidin-1-yl-o-tolylmethyl)-1H-indole
DOI: 10.6084/m9.figshare.5104873.v1
CCn1c(-c2ccccc2)c(C(c2ccccc2)N2CCCC2)c2ccccc21
Reaction #9102
1-Ethyl-2-phenyl-3-(phenylpyrrolidin-1-yl-methyl)-1H-indole
DOI: 10.6084/m9.figshare.5104873.v1
CCn1c(-c2ccccc2)c(C(c2ccccc2OC)N2CCCC2)c2ccccc21
Reaction #9103
1-Ethyl-3-[(2-methoxyphenyl)-pyrrolidin-1-yl-methyl]-2-phenyl-1H-indole
DOI: 10.6084/m9.figshare.5104873.v1
Cc1c(C(=O)NCc2ccc(F)c(F)c2)c2cc(N)ccc2n1Cc1ccccc1
Reaction #44908
5-amino-1-benzyl-2-methyl-1H-indole-3-carboxylic acid, 3,4-difluorobenzylamide
Rendement 104.3%DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)Nc1ccc2c(c1)c(C(=O)NCc1ccc(F)c(F)c1)c(C)n2Cc1ccccc1
Reaction #44909
5-acetamido-1-benzyl-2-methyl-1H-indole-3-carboxylic acid, 3,4-difluorobenzylamide
Rendement 68.9%DOI: 10.6084/m9.figshare.5104873.v1
CN(C)CCn1cc(CN(C)C(=O)/C=C/c2cnc3c(c2)CCC(=O)N3)c2ccccc21
Reaction #46598
title compound
Rendement 17.2%DOI: 10.6084/m9.figshare.5104873.v1
CN(C)C(=O)c1cn(CC#N)c2cc(Br)ccc12
Reaction #51693
6-Bromo-1-cyanomethyl-1H-indole-3-carboxylic acid dimethylamide
Rendement 63.0%DOI: 10.6084/m9.figshare.5104873.v1
CN(C)C(=O)c1cn(CC#N)c2cc(Br)ccc12
Reaction #51694
6-Bromo-1-cyanomethyl-1H-indole-3-carboxylic acid dimethylamide
DOI: 10.6084/m9.figshare.5104873.v1
CN(C)C(=O)c1cn(CC#N)c2cc(Cl)ccc12
Reaction #51695
6-chloro-1-cyanomethyl-1H-indole-3-carboxylic acid dimethylamide
Rendement 46.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)c1c(C(=O)NCc2ccc(F)c(F)c2)c2ccc(OC3CCOC3)cc2n1Cc1ccccc1
Reaction #68324
title compound
Rendement 86.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)c1c(C(=O)NCc2ccc(F)c(F)c2)c2ccc(OC3CCCO3)cc2n1Cc1ccccc1
Reaction #68332
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)c1c(C(=O)NCc2ccc(F)c(F)c2)c2ccc(-c3nnco3)cc2n1Cc1ccccc1
Reaction #68374
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)Oc1ccc2c(C(=O)NCc3ccc(F)c(F)c3)c(C3=NCCO3)n(Cc3ccccn3)c2c1
Reaction #68383
title compound
DOI: 10.6084/m9.figshare.5104873.v1
C/C(=N\O)c1c(C(=O)NCc2ccc(F)c(F)c2)c2ccc(OC(C)C)cc2n1Cc1ccccn1
Reaction #68387
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CO/N=C(\C)c1c(C(=O)NCc2ccc(F)c(F)c2)c2ccc(OC(C)C)cc2n1Cc1ccccn1
Reaction #68388
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)c1c(C(=O)NCc2ccc(F)c(F)c2)c2ccc(N3CCCC3=O)cc2n1Cc1ccccc1
Reaction #68403
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)c1c(C(=O)NCc2ccc(F)c(F)c2)c2ccc(OCc3ncco3)cc2n1Cc1ccccc1
Reaction #68405
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)c1c(C(=O)NCc2ccc(F)c(F)c2)c2ccc(Oc3nccs3)cc2n1Cc1ccccc1
Reaction #68406
title compound
DOI: 10.6084/m9.figshare.5104873.v1
Cc1noc(C)c1-c1ccc2c(C(=O)NCc3ccc(F)c(F)c3)c(C(C)C)n(Cc3ccccn3)c2c1
Reaction #68437
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CCCOc1ccc2c(C(=O)NCc3ccc(F)c(F)c3)c(C(C)C)n(Cc3ncco3)c2c1
Reaction #68440
title compound
DOI: 10.6084/m9.figshare.5104873.v1
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