Recherche de Sous-structure

Fc1ccc(S)cc1

CC(=O)N1CCCC1c1cc2[nH]c(-c3ccccn3)nc2cc1Sc1ccc(F)cc1
Reaction #41635
compound
DOI: 10.6084/m9.figshare.5104873.v1
CCCc1nc2cc(NS(=O)(=O)c3ccc(F)cc3)ccc2n1CC(=O)OC(C)(C)C
Reaction #43805
crude sub-title compound
DOI: 10.6084/m9.figshare.5104873.v1
CCCc1nc2cc(NS(=O)(=O)c3ccc(F)cc3)ccc2n1CC(=O)OC(C)(C)C
Reaction #43819
crude sub-titled compound
DOI: 10.6084/m9.figshare.5104873.v1
CC[C@@H]1Cc2[nH]ncc2[C@H](CC)N1S(=O)(=O)c1ccc(F)cc1
Reaction #44045
cis-4,6-Diethyl-5-(4-fluorophenylsulfonyl)-4,5,6,7-tetrahydro-1H-pyrazolo[4,3-c]pyridine
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)N1CC[C@H](S(=O)(=O)c2ccc(N3CCN4CCC[C@H]4C3)cc2Cl)C1
Reaction #66325
oil
Rendement 96.0%DOI: 10.6084/m9.figshare.5104873.v1
O=S(=O)(Nc1ccc(F)cn1)c1cc(Cl)c(Oc2ccc(C(F)(F)F)cc2C2CCNCC2)cc1F
Reaction #74527
title compound
DOI: 10.6084/m9.figshare.5104873.v1
Nc1cc(-c2cc(Cl)ccc2Oc2cc(F)c(S(=O)(=O)Nc3ccncn3)cc2Cl)ccn1
Reaction #74535
title compound
DOI: 10.6084/m9.figshare.5104873.v1
Cn1nccc1-c1cc(Cl)ccc1Oc1cc(F)c(S(=O)(=O)Nc2ccncn2)cc1Cl
Reaction #74536
desired product
Rendement 27.0%DOI: 10.6084/m9.figshare.5104873.v1
COCN(c1ccc(F)cn1)S(=O)(=O)c1cc(Cl)c(F)cc1F
Reaction #74612
title compound
DOI: 10.6084/m9.figshare.5104873.v1
—
Reaction #74680
colorless oil
DOI: 10.6084/m9.figshare.5104873.v1
CC(O)(CS(=O)(=O)c1ccc(F)cc1)c1cc2cc(Cl)c(C(F)(F)F)cc2[nH]1
Reaction #84221
title product
DOI: 10.6084/m9.figshare.5104873.v1
CC(O)(CSc1ccc(F)cc1)c1cc2cc(Cl)c(C(F)(F)F)cc2[nH]1
Reaction #84239
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CCN(CC)C/C=C\c1cc(F)ccc1S(=O)(=O)Cc1ccc2c(c1C(=O)O)OC[C@@H]1C[C@H]21
Reaction #87943
cis-(1aRS,7bSR)-5-[2-((Z)-3-diethylaminoprop-1-enyl)-4-fluorobenzenesulfonylmethyl]-1,1a,2,7b-tetrahydrocyclopropa[c]chromene-4-carboxylic acid
Rendement 17.9%DOI: 10.6084/m9.figshare.5104873.v1
CCN(CC)C/C=C\c1cc(F)ccc1S(=O)(=O)Cc1ccc2c(c1C(=O)OC)OC[C@@H]1C[C@H]21
Reaction #87944
methyl cis-(1aRS,7bSR)-5-[2-((Z)-3-diethylaminoprop-1-enyl)-4-fluorobenzenesulfonylmethyl]-1,1a,2,7b-tetrahydrocyclopropa[c]chromene-4-carboxylate
Rendement 101.9%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)COc1ccc(CNS(=O)(=O)c2ccc(F)cc2)cc1Br
Reaction #155772
t-butyl 2-(2-bromo-4-((4-fluorophenylsulfonamido)methyl)phenoxy)acetate
Rendement 48.2%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)COc1ccc(CNS(=O)(=O)c2ccc(F)cc2)cc1-c1cccc(C#N)c1
Reaction #155773
t-butyl 2-(2-(3-cyanophenyl)-4-((4-fluorophenylsulfonamido)methyl)phenoxy)acetate
Rendement 76.1%DOI: 10.6084/m9.figshare.5104873.v1
Nc1cccc(CSc2ccc(F)cc2NS(=O)(=O)c2cc3ccccc3o2)c1
Reaction #157561
title product
Rendement 59.0%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)c1cccc(CSc2ccc(F)cc2NS(=O)(=O)c2cc3ccccc3o2)c1
Reaction #157638
title compound
Rendement 50.0%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)c1ccc(CSc2ccc(F)cc2NS(=O)(=O)c2cc3ccccc3o2)cc1
Reaction #157640
title compound
Rendement 66.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)c1nc(-c2ccc(F)c(NS(=O)(=O)c3ccc(F)cc3F)c2)c(-c2ccnc(NCCS(C)(=O)=O)n2)s1
Reaction #175002
DOI: 10.1039/C8SC04228D
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