Busqueda de Subestructura

Cc1ccc(S(=O)(=O)Cl)cc1

CCC(C)(C)c1ccc(S(=O)(=O)Nc2ncnc(OCCOc3ccc(Br)cn3)c2-c2ccc(C)cc2)cc1
Reaction #2367
4-tert-amyl-N-{6-[2-(5-bromopyridin-2-yloxy)ethoxy]-5-(4-methylphenyl)pyrimidin-4-yl}benzenesulfonamide
DOI: 10.6084/m9.figshare.5104873.v1
CSc1cnc(OCCOc2ncnc(NS(=O)(=O)c3ccc(C(C)(C)C)cc3)c2Br)nc1
Reaction #2412
N-{5-bromo-6-[2-(5-methylthiopyrimidin-2-yloxy)ethoxy]-pyrimidin-4-yl}-4-tert-butylbenzenesulfonamide
Rendimiento 85.5%DOI: 10.6084/m9.figshare.5104873.v1
COc1ccccc1NS(=O)(=O)c1ccc(C(=O)O)cc1
Reaction #2510
title compound
Rendimiento 95.7%DOI: 10.6084/m9.figshare.5104873.v1
—
Reaction #3010
glass
DOI: 10.6084/m9.figshare.5104873.v1
COc1cc(S(=O)(=O)N(C)C)ccc1-c1nc2c([nH]1)c(=O)n(C)c(=O)n2C
Reaction #3976
1,3-Dimethyl-8-(2-methoxy-4-dimethylaminosulfonyl-phenyl)-1H,3H-purin-2,6-dione
DOI: 10.6084/m9.figshare.5104873.v1
CNS(=O)(=O)c1ccc(-c2nc3c[nH][nH]c(=O)c-3n2)c(OC)c1
Reaction #3980
2-(2-Methoxy-4-methylaminosulfonyl-phenyl)-5H-imidazo[4,5-d]pyridazin-4-one
DOI: 10.6084/m9.figshare.5104873.v1
CC1(C)CCC(C)(C)c2cc(S(=O)(=O)Cl)ccc21
Reaction #6604
5,6,7,8-tetrahydro-5,5,8,8-tetramethylnaphthalene-2-sulfonyl chloride
DOI: 10.6084/m9.figshare.5104873.v1
O=C(N1CC2CC(C1)c1cc(S(=O)(=O)Cl)ccc12)C(F)(F)F
Reaction #10202
oil
Rendimiento 87.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)c1ccc(S(N)(=O)=O)cc1
Reaction #10728
4-acetyl-benzenesulfonamide
Rendimiento 93.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)c1ccc(S(=O)(=O)Nc2cnc3n(c2=O)[C@H](C(=O)NCc2ccc(C(=N)NC(=O)OC(C)(C)C)cc2)CC3)cc1
Reaction #11094
35a
Rendimiento 42.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)NS(=O)(=O)c1ccc(Cc2ccc3[nH]c(=O)cc(C(F)(F)F)c3c2)cc1
Reaction #11896
title compound
Rendimiento 45.0%DOI: 10.6084/m9.figshare.5104873.v1
CCCCNS(=O)(=O)c1ccc(Cc2ccc3[nH]c(=O)cc(C(F)(F)F)c3c2)cc1
Reaction #11897
title compound
Rendimiento 91.2%DOI: 10.6084/m9.figshare.5104873.v1
O=c1cc(C(F)(F)F)c2cc(Cc3ccc(S(=O)(=O)NCc4ccccc4)cc3)ccc2[nH]1
Reaction #11898
title compound
Rendimiento 61.9%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)c1ccc(S(=O)(=O)Cl)cc1
Reaction #43888
white solid
DOI: 10.6084/m9.figshare.5104873.v1
Cc1ccc(NS(=O)(=O)c2ccc(C(C)(C)C)cc2)cc1O
Reaction #44899
4-tert-butyl-N-(3-hydroxy-4-methyl-phenyl)-benzenesulfonamide
Rendimiento 78.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C(Nc1cccc(-c2ccc(S(=O)(=O)Cl)cc2)n1)C1(c2ccc3c(c2)OCO3)CC1
Reaction #46235
4-(6-(1-(Benzo[d][1,3]dioxol-5-yl)cyclopropane-carboxamido)pyridin-2-yl)benzene-1-sulfonyl chloride
DOI: 10.6084/m9.figshare.5104873.v1
CC1CCCN1S(=O)(=O)c1ccc(-c2cccc(NC(=O)C3(c4ccc5c(c4)OCO5)CC3)n2)cc1
Reaction #46236
1-(Benzo[d][1,3]dioxol-5-yl)-N-(6-(4-(2-methylpyrrolidin-1-ylsulfonyl)phenyl)pyridin-2-yl)cyclopropanecarboxamide
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)c1ccc(S(=O)(=O)Nc2ccc(Cl)cc2C(=O)c2ccccc2)cc1
Reaction #47147
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CCc1ccc(S(=O)(=O)Nc2ccc(Cl)cc2C(=O)c2ccccc2)cc1
Reaction #47151
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CCCCc1ccc(S(=O)(=O)Nc2ccc(Cl)cc2C(=O)c2ccccc2)cc1
Reaction #47152
title compound
DOI: 10.6084/m9.figshare.5104873.v1
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