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1429753

O=C(c1ccc(NS(=O)(=O)c2cc(Cl)ccc2Cl)cc1)N1Cc2cccn2Cc2ccccc21
Reaction #3679
solid
Ausbeute 177.6%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)C[C@H]1C[C@@H](COS(=O)(=O)c2cc(Cl)ccc2Cl)OC(C)(C)O1
Reaction #6552
product
Ausbeute 137.9%DOI: 10.6084/m9.figshare.5104873.v1
Cl.O=S(=O)(c1cc(Cl)ccc1Cl)n1ccc2c(N3CCNCC3)cccc21
Reaction #8420
title compound
DOI: 10.6084/m9.figshare.5104873.v1
Cc1oc(-c2ccc(C(F)(F)F)cc2)cc1CSc1ccc(OCC(=O)O)c(Cl)c1
Reaction #9789
title compound
DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc(Cl)cc1S(N)(=O)=O
Reaction #11757
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CCNC(=NS(=O)(=O)c1cccc(Cl)c1)N1CC(C)(C)C=N1
Reaction #40792
brown oil
DOI: 10.6084/m9.figshare.5104873.v1
O=C(c1ccccc1)c1cc(Cl)ccc1NS(=O)(=O)c1ccc(Cl)c(Cl)c1
Reaction #47150
title compound
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
CN(C)S(=O)(=O)c1ccc(F)c(Cl)c1
Reaction #48823
title compound
Ausbeute 94.0%DOI: 10.6084/m9.figshare.5104873.v1
Cc1c(Cl)cccc1S(=O)(=O)Oc1ccc(-c2cc3cc(CN4CCCCC4)ccc3n2C(=O)OC(C)(C)C)c2c1CNC2=O
Reaction #49415
4-(2-methyl-3-chlorobenzenesulfonyloxy)-7-[1-(tert-butoxycarbonyl)-5-(piperidinomethyl)indol-2-yl]isoindolinone
Ausbeute 50.0%DOI: 10.6084/m9.figshare.5104873.v1
Cc1ccc(S(=O)(=O)Oc2ccc(-c3cc4cc(CN5CCCCC5)ccc4n3C(=O)OC(C)(C)C)c3c2CNC3=O)cc1Cl
Reaction #49416
4-(4-methyl-3-chlorobenzenesulfonyloxy)-7-[1-(tert-butoxycarbonyl)-5-(piperidinomethyl)indol-2-yl]isoindolinone
Ausbeute 47.3%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)n1c(-c2ccc(OS(=O)(=O)c3ccc(F)c(Cl)c3)c3c2C(=O)NC3)cc2cc(CN3CCCCC3)ccc21
Reaction #49417
4-(3-chloro-4-fluorobenzenesulfonyloxy)-7-[1-(tert-butoxycarbonyl)-5-(piperidinomethyl)indol-2-yl]isoindolinone
Ausbeute 17.4%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)n1c(-c2ccc(OS(=O)(=O)c3ccc(Cl)c(Cl)c3)c3c2C(=O)NC3)cc2cc(CN3CCCCC3)ccc21
Reaction #49419
4-(3,4-dichlorobenzenesulfonyloxy)-7-[1-(tert-butoxycarbonyl)-5-(piperidinomethyl)indol-2-yl]isoindolinone
Ausbeute 28.2%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)n1c(-c2ccc(OS(=O)(=O)c3cccc(Cl)c3)c3c2C(=O)NC3)cc2cc(CN3CCCCC3)ccc21
Reaction #49423
4-(3-chlorobenzenesulfonyloxy)-7-[1-(tert-butoxycarbonyl)-5-(piperidinomethyl)indol-2-yl]isoindolinone
Ausbeute 40.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)n1c(-c2ccc(OS(=O)(=O)c3cccc(Cl)c3Cl)c3c2C(=O)NC3)cc2cc(CN3CCCCC3)ccc21
Reaction #49425
4-(2,3-dichlorobenzenesulfonyloxy)-7-[1-(tert-butoxycarbonyl)-5-(piperidinomethyl)indol-2-yl]isoindolinone
Ausbeute 45.7%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)n1c(-c2ccc(OS(=O)(=O)c3cc(Cl)c(F)cc3F)c3c2C(=O)NC3)cc2cc(CN3CCCCC3)ccc21
Reaction #49429
4-(2,4-difluoro-5-chlorobenzenesulfonyloxy)-7-[1-(tert-butoxycarbonyl)-5-(piperidinomethyl)indol-2-yl]isoindolinone
Ausbeute 28.4%DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc(Cl)cc1S(=O)(=O)Oc1ccc(-c2cc3cc(CN4CCCCC4)ccc3n2C(=O)OC(C)(C)C)c2c1CNC2=O
Reaction #49431
4-(2-methoxy-5-chlorobenzenesulfonyloxy)-7-[1-(tert-butoxycarbonyl)-5-(piperidinomethyl)indol-2-yl]isoindolinone
Ausbeute 42.7%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)n1c(-c2ccc(OS(=O)(=O)c3cc(Cl)cc(Cl)c3)c3c2C(=O)NC3)cc2cc(CN3CCCCC3)ccc21
Reaction #49441
4-(3,5-dichlorobenzenesulfonyloxy)-7-[1-(tert-butoxycarbonyl)-5-(piperidinomethyl)indol-2-yl]isoindolinone
Ausbeute 44.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C(O)C1C2CCCCC2CN1S(=O)(=O)c1cc(Cl)cc(Cl)c1
Reaction #52155
N-(3,5-dichlorobenzenesulfonyl)-octahydro-isoindole-1-carboxylic acid
Ausbeute 192.7%DOI: 10.6084/m9.figshare.5104873.v1
O=S(=O)(Nc1ccc2[nH]nc(Cl)c2c1)c1ccc(Cl)c(Cl)c1
Reaction #53635
N-(3-chloro-1H-indazol-5-yl)-3,4-dichlorobenzenesulfonamide
Ausbeute 4.7%DOI: 10.6084/m9.figshare.5104873.v1
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