ethanesulfonyl chloride

CCn1ncc(C(=O)c2cc(C)c3c(c2C)C(C)(C)CCS3(=O)=O)c1OS(=O)(=O)CC
Reaction #1165
4,4,5,8-tetramethyl-6-(1-ethyl-5-ethanesulfonyloxypyrazol-4-yl)carbonylthiochroman-1,1-dioxide
Ausbeute 82.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CCS(=O)(=O)NCCSc1cccc2nccn12
Reaction #5536
desired product
Ausbeute 78.2%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1993_09
CCC1(c2c[nH]c3c(NS(=O)(=O)CC)cccc23)CCc2cc(F)ccc21
Reaction #41995
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
CCS(=O)(=O)Nc1cccc(-c2ccc3c(c2)CC(NS(=O)(=O)C(C)C)C3)c1
Reaction #46703
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
CCOC(=O)c1oc2cccc(NS(=O)(=O)CC)c2c1C
Reaction #57582
4-ethanesulfonylamino-3-methyl-benzofuran-2-carboxylic acid ethyl ester
Ausbeute 69.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_09
CCS(=O)(=O)N1CCC(Nc2ccc(C(=O)c3ccccc3F)c(N)n2)CC1
Reaction #58388
[2-Amino-6-(1-ethanesulfonyl-piperidin-4-ylamino)-pyridin-3-yl]-(2-fluoro-phenyl)-methanone
Ausbeute 60.8%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_09
CCS(=O)(=O)N1CCC(Nc2ccc(C(=O)c3cc(F)ccc3OC)c(N)n2)CC1
Reaction #58399
[2-amino-6-(1-ethanesulfonyl-piperidin-4-ylamino)-pyridin-3-yl]-(5-fluoro-2-methoxy-phenyl)-methanone
Ausbeute 63.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_09
CCS(=O)(=O)Nc1cccc(C#Cc2ccc(OC(F)F)cc2)c1
Reaction #58882
N-(3-{[4-(difluoromethoxy)phenyl]ethynyl}phenyl)ethanesulfonamide
Ausbeute 91.4%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_09
CCS(=O)(=O)Nc1ccc(F)c([N+](=O)[O-])c1
Reaction #65071
objective product
Ausbeute 93.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1995_05
CCS(=O)(=O)N1CCN(c2ccc(N3CCN(C(=O)OC(C)(C)C)c4ccccc43)nc2)CC1
Reaction #69986
4-[5-(4-(ethanesulphonyl)piperazin-1-yl)pyridin-2-yl]-3,4-dihydro-2H-quinoxaline-1-carboxylic acid tert-butyl ester
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_09
CCS(=O)(=O)Nc1cc(-c2ccc(F)cc2F)cc(-n2cnc3cc(-c4cn(C5CCOCC5)nn4)ccc32)c1
Reaction #92433
N-(2′,4′-difluoro-5-(5-(1-(tetrahydro-2H-pyran-4-yl)-1H-1,2,3-triazol-4-yl)-1H-benzo[d]imidazol-1-yl)-[1,1′-biphenyl]-3-yl)ethanesulfonamide
Ausbeute 42.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_09
CCS(=O)(=O)Nc1cc(-c2ccc(F)cc2F)cc(-n2cnc3cc(-c4c[nH]nn4)ccc32)c1
Reaction #92434
N-(5-(5-(1H-1,2,3-triazol-4-yl)-1H-benzo[d]imidazol-1-yl)-2′,4′-difluoro-[1,1′-biphenyl]-3-yl)ethanesulfonamide
Ausbeute 2.3%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_09
CCS(=O)(=O)Nc1cc(-c2ccc(F)cc2F)cc(-n2cnc3cc(-c4c[nH]nn4)cnc32)c1
Reaction #92439
N-(5-(6-(1H-1,2,3-triazol-4-yl)-3H-imidazo[4,5-b]pyridin-3-yl)-2′,4′-difluoro-[1,1′-biphenyl]-3-yl)ethanesulfonamide
Ausbeute 9.3%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_09
CCS(=O)(=O)Nc1cc(-c2ccc(F)cc2F)cc(-n2cnc3cc(-c4cn(C5CCOCC5)nn4)cnc32)c1
Reaction #92440
N-(2′,4′-difluoro-5-(6-(1-(tetrahydro-2H-pyran-4-yl)-1H-1,2,3-triazol-4-yl)-3H-imidazo[4,5-b]pyridin-3-yl)-[1,1′-biphenyl]-3-yl)ethanesulfonamide
Ausbeute 42.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_09
CCS(=O)(=O)Nc1cc(-c2ccc(F)cc2F)cc(-n2cnc3cc(-c4cn(CC5CC5)nn4)cnc32)c1
Reaction #92441
N-(5-(6-(1-(cyclopropylmethyl)-1H-1,2,3-triazol-4-yl)-3H-imidazo[4,5-b]-pyridin-3-yl)-2′,4′-difluoro-[1,1′-biphenyl]-3-yl)ethanesulfonamide
Ausbeute 33.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_09
CCS(=O)(=O)Nc1cc(-c2ccncc2F)cc(-n2cnc3cc(-c4cnn(C)c4)ccc32)c1
Reaction #92444
N-(3-(3-fluoropyridin-4-yl)-5-(5-(1-methyl-1H-pyrazol-4-yl)-1H-benzo[d]-imidazol-1-yl)phenyl)ethanesulfonamide
Ausbeute 15.1%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_09
CCS(=O)(=O)Nc1cc(-c2ccc(F)cc2F)cc(-n2cnc3cc(-c4cnn(CCC(C)(C)O)c4)ccc32)c1
Reaction #92447
N-(2′,4′-difluoro-5-(5-(1-(3-hydroxy-3-methylbutyl)-1H-pyrazol-4-yl)-1H-benzo[d]imidazol-1-yl)-[1,1′-biphenyl]-3-yl)ethanesulfonamide
Ausbeute 33.6%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_09
CCS(=O)(=O)Nc1cc(-c2ccc(F)cc2F)cc(-n2cnc3cc(Br)cnc32)c1
Reaction #92459
crude residue
Ausbeute 76.7%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_09
CCS(=O)(=O)Nc1cc(-c2cc(F)ccc2F)cc(-n2cnc3cc(-c4cnn(C)c4)ccc32)c1
Reaction #92466
N-(2′,5′-difluoro-5-(5-(1-methyl-1H-pyrazol-4-yl)-1H-benzo[d]imidazol-1-yl)-[1,1′-biphenyl]-3-yl)ethanesulfonamide
Ausbeute 16.2%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_09
CCS(=O)(=O)N1CC[C@H](Nc2nc(-c3c[nH]c4ncc(Cl)cc34)ncc2F)C1
Reaction #162069
399
Ausbeute 49.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
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