benzo[b]thiophene-2-sulfonyl chloride

N#Cc1cccc(CN2CC[C@H](NS(=O)(=O)c3cc4ccccc4s3)C2=O)c1
Reaction #2842
title compound
Yield 79.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
N#Cc1cc(CN2CC[C@H](NS(=O)(=O)c3cc4ccccc4s3)C2=O)ccc1N
Reaction #2866
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CC(C)(C)OC(=O)n1c(-c2ccc(OS(=O)(=O)c3cc4ccccc4s3)c3c2C(=O)NC3)cc2cc(CN3CCCCC3)ccc21
Reaction #49435
4-(benzothiophene-2-sulfonyloxy)-7-[1-(tert-butoxycarbonyl)-5-(piperidinomethyl)indol-2-yl]isoindolinone
Yield 33.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
O=[N+]([O-])c1c(S(=O)(=O)Cl)sc2ccccc12
Reaction #268807
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
O=C1C(NS(=O)(=O)c2cc3ccccc3s2)CCN1Cc1ccc2nccc(Cl)c2c1
Reaction #293220
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
Cc1noc(NS(=O)(=O)c2cc3ccccc3s2)c1C
Reaction #319934
light brown solid
Yield 60.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1997_01
Cc1noc(NS(=O)(=O)c2cc3ccccc3s2)c1C
Reaction #321504
light brown solid
Yield 60.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1997_01
O=[N+]([O-])c1c(S(=O)(=O)Cl)sc2ccccc12
Reaction #331470
product
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_02
CSc1nccc(-c2ccc(S(=O)(=O)NC3CCN(Cc4cccc(C#N)c4)C3=O)s2)n1
Reaction #390204
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (8/10)
O=[N+]([O-])c1c(S(=O)(=O)Cl)sc2ccccc12
Reaction #420746
product
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_11
O=[N+]([O-])c1c(S(=O)(=O)Cl)sc2ccccc12
Reaction #554603
product
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_01
O=[N+]([O-])c1c(S(=O)(=O)Cl)sc2ccccc12
Reaction #556332
product
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_01
O=[N+]([O-])c1c(S(=O)(=O)Cl)sc2ccccc12
Reaction #556334
product
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_01
O=[N+]([O-])c1c(S(=O)(=O)Cl)sc2ccccc12
Reaction #626621
product
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_10
O=Cc1cc(-c2ccccc2)n(S(=O)(=O)c2cc3ccccc3s2)c1
Reaction #641504
title compound
Yield 84.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2011_11
O=S(=O)(Nc1cccc(-c2nnn[nH]2)c1)c1cc2ccccc2s1
Reaction #676933
title compound
Yield 60.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_01
O=C(O)c1cccc(NS(=O)(=O)c2cc3ccccc3s2)c1
Reaction #676935
title compound
Yield 41.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_01
O=C1[C@@H](NS(=O)(=O)c2cc3ccccc3s2)CCN1Cc1ccc2ccc(Cl)nc2c1
Reaction #738794
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2001_08
O=C1[C@@H](NS(=O)(=O)c2cc3ccccc3s2)CCN1Cc1ccc2nccc(Cl)c2c1
Reaction #738823
title compound
Yield 60.5%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2001_08
Nc1ccccc1NS(=O)(=O)c1cc2ccccc2s1
Reaction #757456
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (3/10)
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