An 20 Reaktionen beteiligt

1040964

O=C(Cc1ccnc(Cl)n1)c1cccc(NS(=O)(=O)c2c(F)cccc2F)c1F
Reaction #211768
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
COC(=O)c1cccc(NS(=O)(=O)c2c(F)cccc2F)c1F
Reaction #252757
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
COC(=O)c1cccc(NS(=O)(=O)c2c(F)cccc2F)c1F
Reaction #326431
title compound
Ausbeute 87.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_02
O=C(Cc1ccnc(Cl)n1)c1cccc(NS(=O)(=O)c2c(F)cccc2F)c1F
Reaction #326432
title compound
Ausbeute 71.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_02
COC(=O)c1cccc(NS(=O)(=O)c2c(F)cccc2F)c1F
Reaction #326558
methyl 3-{[(2,6-difluorophenyl)sulfonyl]amino}-2-fluorobenzoate
Ausbeute 91.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_02
O=C(Cc1ccnc(Cl)n1)c1cccc(NS(=O)(=O)c2c(F)cccc2F)c1F
Reaction #326559
N-{3-[(2-chloro-4-pyrimidinyl)acetyl]-2-fluorophenyl}-2,6-difluorobenzenesulfonamide
Ausbeute 76.4%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_02
COC(=O)c1cccc(NS(=O)(=O)c2c(F)cccc2F)c1F
Reaction #677205
title compound
Ausbeute 87.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_01
O=C(Cc1ccnc(Cl)n1)c1cccc(NS(=O)(=O)c2c(F)cccc2F)c1F
Reaction #677206
title compound
Ausbeute 71.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_01
O=C(Cc1ccnc(Cl)n1)c1cccc(NS(=O)(=O)c2c(F)cccc2F)c1F
Reaction #677331
N-{3-[(2-chloro-4-pyrimidinyl)acetyl]-2-fluorophenyl}-2,6-difluorobenzenesulfonamide
Ausbeute 76.4%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_01
O=C(Cc1ccnc(Cl)n1)c1cccc(NS(=O)(=O)c2c(F)cccc2F)c1F
Reaction #894616
DOI: 10.1039/C8SC04228DTest data from https://doi.org/10.1039/C8SC04228D
O=C(Cc1ccnc(Cl)n1)c1cccc(NS(=O)(=O)c2c(F)cccc2F)c1F
Reaction #1289405
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (5/10)
COC(=O)c1cccc(NS(=O)(=O)c2c(F)cccc2F)c1F
Reaction #1758098
title compound
Ausbeute 87.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2011_08
O=C(Cc1ccnc(Cl)n1)c1cccc(NS(=O)(=O)c2c(F)cccc2F)c1F
Reaction #1758099
title compound
Ausbeute 71.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2011_08
O=C(Cc1ccnc(Cl)n1)c1cccc(NS(=O)(=O)c2c(F)cccc2F)c1F
Reaction #1758228
N-{3-[(2-chloro-4-pyrimidinyl)acetyl]-2-fluorophenyl}-2,6-difluorobenzenesulfonamide
Ausbeute 76.4%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2011_08
O=C(Cc1ccnc(Cl)n1)c1cccc(NS(=O)(=O)c2c(F)cccc2F)c1F
Reaction #1933250
N-{3-[(2-chloro-4-pyrimidinyl)acetyl]-2-fluorophenyl}-2,6-difluorobenzenesulfonamide
Ausbeute 76.4%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2015_02
O=C(Cc1ccnc(Cl)n1)c1cccc(NS(=O)(=O)c2c(F)cccc2F)c1F
Reaction #2030098
N-(3-(2-(2-chloropyrimidin-4-yl)acetyl)-2-fluorophenyl)-2,6-difluorobenzenesulfonamide
Ausbeute 33.3%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_03
COC(=O)c1cccc(NS(=O)(=O)c2c(F)cccc2F)c1F
Reaction #2048922
title compound
Ausbeute 87.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_04
O=C(Cc1ccnc(Cl)n1)c1cccc(NS(=O)(=O)c2c(F)cccc2F)c1F
Reaction #2048923
title compound
Ausbeute 71.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_04
O=C(Cc1ccnc(Cl)n1)c1cccc(NS(=O)(=O)c2c(F)cccc2F)c1F
Reaction #2049050
N-{3-[(2-chloro-4-pyrimidinyl)acetyl]-2-fluorophenyl}-2,6-difluorobenzenesulfonamide
Ausbeute 76.4%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_04
O=C(Cc1ccnc(Cl)n1)c1cccc(NS(=O)(=O)c2c(F)cccc2F)c1F
Reaction #2455640
N-{3-[(2-chloro-4-pyrimidinyl)acetyl]-2-fluorophenyl}-2,6-difluorobenzenesulfonamide
Ausbeute 76.4%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_04