Recherche de Sous-structure

207322

CNC(=O)c1c(-c2ccccc2)noc1C
Reaction #8403
5-Methyl-3-phenyl-isoxazole-4-carboxylic acid methylamide
DOI: 10.6084/m9.figshare.5104873.v1
CNC(=O)c1c(C)noc1-c1ccccc1
Reaction #8405
3-Methyl-5-phenyl-isoxazole-4-carboxylic acid methylamide
DOI: 10.6084/m9.figshare.5104873.v1
C=CCOc1ccc(-c2noc(C)c2C(=O)OCC)cc1
Reaction #42680
crude product
Rendement 119.6%DOI: 10.6084/m9.figshare.5104873.v1
C=CCOc1ccc(-c2noc(C)c2C(=O)O)cc1
Reaction #42681
product
Rendement 100.7%DOI: 10.6084/m9.figshare.5104873.v1
Cc1ccc2c(N3CCN(CCc4cccc(NC(=O)c5c(C)noc5C)c4)CC3)cccc2n1
Reaction #44083
title compound
Rendement 56.0%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)c1c(C)noc1-c1ccc(Br)cc1
Reaction #73869
title compound
DOI: 10.6084/m9.figshare.5104873.v1
Cc1noc(-c2ccc(Br)cc2)c1C(=O)O
Reaction #73870
title compound
DOI: 10.6084/m9.figshare.5104873.v1
Cc1noc(-c2ccc(Br)cc2)c1NC(=O)OC(C)(C)C
Reaction #73871
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CCCCc1nc2c(N)nc3cccnc3c2n1CCNC(=O)c1c(C)noc1C
Reaction #75789
N-[2-(4-amino-2-butyl-1H-imidazo[4,5-c][1,5]naphthyridin-1-yl)ethyl]-3,5-dimethyl-4-isoxazolecarboxamide
Rendement 33.2%DOI: 10.6084/m9.figshare.5104873.v1
Cc1noc(-c2ccncc2)c1C(=O)O
Reaction #88851
title compound
Rendement 57.5%DOI: 10.6084/m9.figshare.5104873.v1
Cc1noc(-c2ccncc2)c1C(=O)N1CCC(O)(Cc2ccccc2)CC1
Reaction #88852
title compound
Rendement 62.8%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)c1c(-c2ccc([N+](=O)[O-])cc2)noc1-c1ccccc1
Reaction #162953
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)c1c(-c2ccc(N)cc2)noc1-c1ccccc1
Reaction #162954
title compound
DOI: 10.6084/m9.figshare.5104873.v1
O=C(O)c1c(-c2ccc(Nc3nc4ccc(F)cc4s3)cc2)noc1-c1ccccc1
Reaction #162955
title compound
Rendement 78.2%DOI: 10.6084/m9.figshare.5104873.v1
COC[C@H](NC(=O)c1c(-c2ccc(Nc3nc4ccc(F)cc4s3)cc2)noc1-c1ccccc1)C(=O)OC
Reaction #162956
title compound
Rendement 69.0%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)c1c(-c2cccc(F)c2)noc1C
Reaction #170384
title compound
Rendement 39.5%DOI: 10.6084/m9.figshare.5104873.v1
Cc1onc(-c2cccc(F)c2)c1CO
Reaction #170385
title compound
Rendement 75.3%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)c1c(-c2cccc(Cl)c2)noc1C
Reaction #170398
title compound
Rendement 40.0%DOI: 10.6084/m9.figshare.5104873.v1
Cc1onc(-c2cccc(Cl)c2)c1C(=O)O
Reaction #170399
title compound
Rendement 97.0%DOI: 10.6084/m9.figshare.5104873.v1
Cc1onc(-c2cccc(Cl)c2)c1CO
Reaction #170400
title compound
Rendement 78.0%DOI: 10.6084/m9.figshare.5104873.v1
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