بحث البنية الفرعية

159868

C=C(OCCCC)c1cc(C(=O)NCc2ccc(S(C)(=O)=O)cc2)c(=O)n(-c2cccc(C(F)(F)F)c2)c1C
Reaction #197546
DOI: 10.1039/C8SC04228D
Cc1c(-c2ccoc2)cc(C(=O)NCc2ccc(S(C)(=O)=O)cc2)c(=O)n1-c1cccc(C(F)(F)F)c1
Reaction #238535
DOI: 10.1039/C8SC04228D
Cc1c(-c2ccccc2)cc(C(=O)NCc2ccc(S(C)(=O)=O)cc2)c(=O)n1-c1cccc(C(F)(F)F)c1
Reaction #290273
DOI: 10.1039/C8SC04228D
Cc1cc(-c2cc(C(=O)NCc3ccc(S(C)(=O)=O)cc3)c(=O)n(-c3cccc(C(F)(F)F)c3)c2C)on1
Reaction #401055
DOI: 10.1039/C8SC04228D
Cc1nocc1-c1cc(C(=O)NCc2ccc(S(C)(=O)=O)cc2)c(=O)n(-c2cccc(C(F)(F)F)c2)c1C
Reaction #402548
DOI: 10.1039/C8SC04228D
Cc1c(I)cc(C(=O)NCc2ccc(S(C)(=O)=O)cc2)c(=O)n1-c1cccc(C(F)(F)F)c1
Reaction #646970
title compound
المردود 78.8%DOI: 10.6084/m9.figshare.5104873.v1
Cc1c(-c2ccccc2)cc(C(=O)NCc2ccc(S(C)(=O)=O)cc2)c(=O)n1-c1cccc(C(F)(F)F)c1
Reaction #646971
title compound
المردود 76.2%DOI: 10.6084/m9.figshare.5104873.v1
Cc1c(-c2ccoc2)cc(C(=O)NCc2ccc(S(C)(=O)=O)cc2)c(=O)n1-c1cccc(C(F)(F)F)c1
Reaction #646972
title compound
المردود 62.0%DOI: 10.6084/m9.figshare.5104873.v1
Cc1c(-c2cnccn2)cc(C(=O)NCc2ccc(S(C)(=O)=O)cc2)c(=O)n1-c1cccc(C(F)(F)F)c1
Reaction #646976
6-Methyl-N-[4-(methylsulfonyl)benzyl]-2-oxo-5-(pyrazin-2-yl)-1-[3-(trifluoro-methyl)phenyl]-1,2-dihydropyridine-3-carboxamide
DOI: 10.6084/m9.figshare.5104873.v1
Cc1c(-c2nccn2C)cc(C(=O)NCc2ccc(S(C)(=O)=O)cc2)c(=O)n1-c1cccc(C(F)(F)F)c1
Reaction #646977
title compound
المردود 10.0%DOI: 10.6084/m9.figshare.5104873.v1
Cc1c(-c2ncccn2)cc(C(=O)NCc2ccc(S(C)(=O)=O)cc2)c(=O)n1-c1cccc(C(F)(F)F)c1
Reaction #646978
title compound
المردود 27.1%DOI: 10.6084/m9.figshare.5104873.v1
Cc1nocc1-c1cc(C(=O)NCc2ccc(S(C)(=O)=O)cc2)c(=O)n(-c2cccc(C(F)(F)F)c2)c1C
Reaction #646979
6-Methyl-5-(3-methylisoxazol-4-yl)-N-[4-(methylsulfonyl)benzyl]-2-oxo-1-[3-(trifluoromethyl)phenyl]-1,2-dihydropyridine-3-carboxamide
DOI: 10.6084/m9.figshare.5104873.v1
Cc1cc(-c2cc(C(=O)NCc3ccc(S(C)(=O)=O)cc3)c(=O)n(-c3cccc(C(F)(F)F)c3)c2C)on1
Reaction #646980
title compound
DOI: 10.6084/m9.figshare.5104873.v1
C=C(OCCCC)c1cc(C(=O)NCc2ccc(S(C)(=O)=O)cc2)c(=O)n(-c2cccc(C(F)(F)F)c2)c1C
Reaction #646982
title compound
المردود 28.5%DOI: 10.6084/m9.figshare.5104873.v1
CCC(=O)c1cc(C(=O)NCc2ccc(S(C)(=O)=O)cc2)c(=O)n(-c2cccc(C(F)(F)F)c2)c1C
Reaction #646988
title compound
المردود 99.9%DOI: 10.6084/m9.figshare.5104873.v1
Cc1c(C#N)cc(C(=O)NCc2ccc(S(C)(=O)=O)cc2)c(=O)n1-c1cccc(C(F)(F)F)c1
Reaction #646993
title compound
المردود 24.0%DOI: 10.6084/m9.figshare.5104873.v1
Cc1c(-c2nccn2C)cc(C(=O)NCc2ccc(S(C)(=O)=O)cc2)c(=O)n1-c1cccc(C(F)(F)F)c1
Reaction #893742
DOI: 10.1039/C8SC04228D
Cc1nocc1-c1cc(C(=O)NCc2ccc(S(C)(=O)=O)cc2)c(=O)n(-c2cccc(C(F)(F)F)c2)c1C
Reaction #901335
DOI: 10.1039/C8SC04228D
Cc1c(-c2cnccn2)cc(C(=O)NCc2ccc(S(C)(=O)=O)cc2)c(=O)n1-c1cccc(C(F)(F)F)c1
Reaction #920987
DOI: 10.1039/C8SC04228D
Cc1c(-c2ncco2)cc(C(=O)NCc2ccc(S(C)(=O)=O)cc2)c(=O)n1-c1cccc(C(F)(F)F)c1
Reaction #1231852
DOI: 10.1039/C8SC04228D
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