benzo[b]thiophene-2-sulfonyl chloride

Cc1noc(NS(=O)(=O)c2cc3ccccc3s2)c1C
Reaction #785276
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (3/10)
Nc1ccccc1NS(=O)(=O)c1cc2ccccc2s1
Reaction #817386
benzo[b]thiophene-2-sulfonic acid (2-amino-phenyl)-amide
Yield 78.8%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2009_09
O=S(=O)(Nc1ccccc1NS(=O)(=O)c1cc2ccccc2s1)c1ccc(Cl)cc1
Reaction #817398
benzo[b]thiophene-2-sulfonic acid [2-(4-chlorobenzenesulfonylamino)phenyl]-amide
Yield 75.2%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2009_09
O=S(=O)(Nc1ccc(F)cc1NS(=O)(=O)c1cc2ccccc2s1)c1cc2ccccc2s1
Reaction #817422
N,N′-(4-fluoro-1,2-phenylene)bis(1-benzothiophene-2-sulfonamide)
Yield 37.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2009_09
N#Cc1ccc(NS(=O)(=O)c2cc3ccccc3s2)c(NS(=O)(=O)c2cc3ccccc3s2)c1
Reaction #817423
N,N′-(4-cyano-1,2-phenylene)bis(1-benzothiophene-2-sulfonamide)
Yield 35.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2009_09
O=S(=O)(Nc1ccc(Cl)cc1NS(=O)(=O)c1cc2ccccc2s1)c1cc2ccccc2s1
Reaction #817424
N,N′-(4-chloro-1,2-phenylene)bis(1-benzothiophene-2-sulfonamide)
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2009_09
O=S(=O)(Nc1ccc(Br)cc1NS(=O)(=O)c1cc2ccccc2s1)c1cc2ccccc2s1
Reaction #817425
N,N′-(4-bromo-1,2-phenylene)bis(1-benzothiophene-2-sulfonamide)
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2009_09
COc1ccc(NS(=O)(=O)c2cc3ccccc3s2)c(NS(=O)(=O)c2cc3ccccc3s2)c1
Reaction #817426
N,N′-(4-methoxy-1,2-phenylene)bis(1-benzothiophene-2-sulfonamide)
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2009_09
O=S(=O)(Nc1cc(Cl)c(Cl)cc1NS(=O)(=O)c1cc2ccccc2s1)c1cc2ccccc2s1
Reaction #817428
N,N′-(4,5-Dichloro-1,2-phenylene)bis(1-benzothiophene-2-sulfonamide)
Yield 63.8%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2009_09
O=S(=O)(Nc1ccc(C(F)(F)F)cc1NS(=O)(=O)c1cc2ccccc2s1)c1cc2ccccc2s1
Reaction #817429
N,N′-(4-Trifluoromethyl-1,2-phenylene)bis(1-benzothiophene-2-sulfonamide)
Yield 53.3%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2009_09
O=S(=O)(Nc1cc(F)c(Cl)cc1NS(=O)(=O)c1cc2ccccc2s1)c1cc2ccccc2s1
Reaction #817430
N,N′-(4-chloro-5-fluoro-1,2-phenylene)bis(1-benzothiophene-2-sulfonamide)
Yield 59.2%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2009_09
O=C1C(NS(=O)(=O)c2cc3ccccc3s2)CCN1Cc1ccc2ccc(Cl)nc2c1
Reaction #904151
DOI: 10.1039/C8SC04228DTest data from https://doi.org/10.1039/C8SC04228D
O=Cc1cc(-c2ccccc2)n(S(=O)(=O)c2cc3ccccc3s2)c1
Reaction #1024051
DOI: 10.1039/C8SC04228DValidation data from https://doi.org/10.1039/C8SC04228D
O=Cc1cn(S(=O)(=O)c2cc3ccccc3s2)c(-c2ccccc2)n1
Reaction #1221246
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (7/10)
Cc1noc(NS(=O)(=O)c2cc3ccccc3s2)c1C
Reaction #1254016
light brown solid
Yield 60.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2003_09
O=[N+]([O-])c1c(S(=O)(=O)Cl)sc2ccccc12
Reaction #1269817
product
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_03
Cc1noc(NS(=O)(=O)c2cc3ccccc3s2)c1C
Reaction #1338852
light brown solid
Yield 60.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2002_01
O=[N+]([O-])c1c(S(=O)(=O)Cl)sc2ccccc12
Reaction #1486653
product
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_12
—
Reaction #1723966
crude product
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2000_03
N#Cc1cc(CN2CC[C@H](NS(=O)(=O)c3cc4ccccc4s3)C2=O)ccc1N
Reaction #1723970
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2000_03
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