Substructure Search

719792

CC(=O)Nc1ccc(S(=O)(=O)N2CCCC2)cc1
Reaction #46106
N-[4-(pyrrolidine-1-sulfonyl)phenyl]acetamide
Yield 46.4%DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)Nc1ccc(S(=O)(=O)N(C)CCc2ccccn2)cc1
Reaction #46107
N-{4-[methyl-(2-pyridin-2-yl-ethyl)sulfamoyl]phenyl}acetamide
Yield 78.5%DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)Nc1ccc(S(=O)(=O)Nc2ccc(Cl)cc2C(=O)c2ccccc2)cc1Cl
Reaction #47155
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)Nc1ccc(S(=O)(=O)Nc2ccc(Cl)cc2C(=O)c2ccccc2)cc1
Reaction #47166
title compound
DOI: 10.6084/m9.figshare.5104873.v1
O=C1Nc2ccc(S(=O)(=O)Cl)cc2CC1CCOc1ccc(Cl)cc1Cl
Reaction #48532
product
Yield 47.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C1Cc2cc(S(=O)(=O)Cl)ccc2N1
Reaction #52587
5-chlorosulfonyl-2-oxindole
Yield 50.0%DOI: 10.6084/m9.figshare.5104873.v1
NS(=O)(=O)c1ccc2c(c1)CC(=O)N2
Reaction #52588
title compound
Yield 20.0%DOI: 10.6084/m9.figshare.5104873.v1
CNS(=O)(=O)c1ccc2c(c1)CC(=O)N2
Reaction #52589
5-methylaminosulfonyl-2-oxindole
Yield 88.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C1Cc2cc(S(=O)(=O)Nc3ccc(C(F)(F)F)cc3)ccc2N1
Reaction #52590
5-(4-trifluoromethylphenyl-aminosulfonyl)-2-oxindole
Yield 37.2%DOI: 10.6084/m9.figshare.5104873.v1
O=C1Cc2cc(S(=O)(=O)N3CCOCC3)ccc2N1
Reaction #52591
5-(morpholinosulfonyl)-2-oxindole
Yield 74.9%DOI: 10.6084/m9.figshare.5104873.v1
CNS(=O)(=O)c1ccc2c(c1)CC(=O)N2
Reaction #52757
5-methylaminosulfonyl-2-oxindole
Yield 88.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C1Cc2cc(S(=O)(=O)Cl)ccc2N1
Reaction #52799
5-chlorosulfonyl-2-oxindole
Yield 50.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)NS(=O)(=O)c1ccc2c(c1)CC(=O)N2
Reaction #52800
5-isopropylaminosulfonyl-2-oxindole
Yield 45.5%DOI: 10.6084/m9.figshare.5104873.v1
CC1=NN(c2ccc(S(=O)(=O)Cl)cc2)C(=O)C1N=Nc1ccccn1
Reaction #54396
orange solid
Yield 56.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)Nc1ccc(S(=O)O)cc1
Reaction #64072
4-Acetamido-benzenesulphinic acid
DOI: 10.6084/m9.figshare.5104873.v1
O=C1Nc2ccc(S(=O)(=O)Cl)cc2CC1CCOc1ccc(Cl)cc1Cl
Reaction #70659
product
Yield 47.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C1Cc2cc(S(=O)(=O)N3CCCC3)ccc2N1
Reaction #77387
5-(pyrrolidine-1-sulfonyl)-1,3-dihydro-indol-2-one
DOI: 10.6084/m9.figshare.5104873.v1
O=C1Cc2cc(S(=O)(=O)NCc3ccccc3)ccc2N1
Reaction #77388
2-oxo-2,3-dihydro-1H-indole-5-sulfonic acid benzylamide
Yield 66.1%DOI: 10.6084/m9.figshare.5104873.v1
O=C1Cc2cc(S(=O)(=O)NCc3ccc(F)cc3)ccc2N1
Reaction #77389
2-oxo-2,3-dihydro-1H-indole-5-sulfonic acid-4-fluoro-benzylamide
Yield 84.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C1Cc2cc(S(=O)(=O)Nc3cccc(Cl)c3)ccc2N1
Reaction #77390
2-oxo-2,3-dihydro-1H-indole-5-sulfonic acid (3-chloro-phenyl)-amide
Yield 74.0%DOI: 10.6084/m9.figshare.5104873.v1
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