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SCl

CNS(=O)(=O)c1cc(-c2nc3nc(OC)ncc3[nH]2)c(OC)cc1Cl
Reaction #3975
2-Methoxy-8-(2-methoxy-4-chloro-5-methylaminosulfonyl-phenyl)-purine
DOI: 10.6084/m9.figshare.5104873.v1
O=S(=O)(Cl)c1c(Cl)sc(Cl)c1Cl
Reaction #8728
solid
Выход 991.6%DOI: 10.6084/m9.figshare.5104873.v1
O=C(c1ccccc1)c1cc(Cl)ccc1NS(=O)(=O)c1ccc(Cl)cc1Cl
Reaction #47149
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)n1c(-c2ccc(OS(=O)(=O)c3c(Cl)cccc3Cl)c3c2C(=O)NC3)cc2cc(CN3CCCCC3)ccc21
Reaction #49424
4-(2,6-dichlorobenzenesulfonyloxy)-7-[1-(tert-butoxycarbonyl)-5-(piperidinomethyl)indol-2-yl]isoindolinone
Выход 37.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)n1c(-c2ccc(OS(=O)(=O)c3ccc(F)cc3Cl)c3c2C(=O)NC3)cc2cc(CN3CCCCC3)ccc21
Reaction #49428
4-(2-chloro-4-fluorobenzenesulfonyloxy)-7-[1-(tert-butoxycarbonyl)-5-(piperidinomethyl)indol-2-yl]isoindolinone
Выход 34.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)n1c(-c2ccc(OS(=O)(=O)Cc3ccccc3Cl)c3c2C(=O)NC3)cc2cc(CN3CCCCC3)ccc21
Reaction #49448
4-[(2-chlorophenyl)methanesulfonyloxy]-7-[1-(tert-butoxycarbonyl)-5-(piperidinomethyl)indol-2-yl]isoindolinone
Выход 37.7%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)n1c(-c2ccc(OS(=O)(=O)c3ccc(Cl)cc3Cl)c3c2C(=O)NC3)cc2cc(CN3CCCCC3)ccc21
Reaction #49455
4-(2,4-dichlorobenzenesulfonyloxy)-7-[1-(tert-butoxycarbonyl)-5-(piperidinomethyl)indol-2-yl]isoindolinone
Выход 55.0%DOI: 10.6084/m9.figshare.5104873.v1
CN(C)CCOc1cc(NS(=O)(=O)c2ccc(Oc3cccc(Cl)c3C#N)cc2)ccc1Cl
Reaction #51041
title compound
Выход 43.0%DOI: 10.6084/m9.figshare.5104873.v1
CN(C)CCOc1cc(NS(=O)(=O)c2ccc(Oc3cccc(Cl)c3C#N)cc2)ccc1C(F)(F)F
Reaction #51043
title compound
DOI: 10.6084/m9.figshare.5104873.v1
NCCCNS(=O)(=O)c1ccc(Oc2ccc(F)cc2)cc1
Reaction #51457
N-(3-aminopropyl)-4-(4-fluorophenoxy)benzenesulfonamide
DOI: 10.6084/m9.figshare.5104873.v1
COCCNS(=O)(=O)c1ccc(Cl)cc1Cl
Reaction #52202
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CCCNS(=O)(=O)c1ccc(Cl)cc1Cl
Reaction #52203
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)CNS(=O)(=O)c1ccc2cc(Cl)ccc2c1
Reaction #53315
title compound
Выход 101.4%DOI: 10.6084/m9.figshare.5104873.v1
Nc1n[nH]c2ccc(NS(=O)(=O)c3c(Cl)cccc3Cl)cc12
Reaction #53679
N-(3-amino-1H-indazol-5-yl)-2,6-dichlorobenzenesulfonamide
Выход 18.6%DOI: 10.6084/m9.figshare.5104873.v1
CC1=NN(c2ccc(S(=O)(=O)Cl)cc2)C(=O)C1N=Nc1ccccn1
Reaction #54396
orange solid
Выход 56.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C(N[C@@H](Cc1ccccc1)[C@H](O)CN(OC1CCCCC1)S(=O)(=O)c1ccc2c(c1)OCCO2)O[C@H]1CO[C@H]2OCC[C@H]21
Reaction #57483
(3R,3aS,6aR)hexahydrofuro[2,3-b]furan-3-yl (1S,2R)-1-benzyl-3-[(cyclohexyloxy)(2,3-dihydro-1,4-benzodioxin-6-ylsulfonyl)amino]-2-hydroxypropylcarbamate
Выход 86.0%DOI: 10.6084/m9.figshare.5104873.v1
CC1(c2ccc(S(=O)(=O)Cl)cc2)CCOCC1
Reaction #57802
4-(4-Methyl-tetrahydro-pyran-4-yl)-benzenesulfonyl Chloride
DOI: 10.6084/m9.figshare.5104873.v1
CC1(c2ccc(S(=O)(=O)Nc3ccc(Cl)cc3C(=O)c3ccncc3)cc2)CCOCC1
Reaction #57901
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CC1(c2ccc(S(=O)(=O)Nc3ccc(Cl)cc3C(=O)c3cccnc3)cc2)CCOCC1
Reaction #57902
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CC1(c2ccc(S(=O)(=O)Nc3ccc(Cl)cc3C(=O)c3ccccn3)cc2)CCOCC1
Reaction #57903
title compound
DOI: 10.6084/m9.figshare.5104873.v1
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