Teilstruktursuche

1429751

CC(C)(C)OC(=O)n1c(-c2ccc(OS(=O)(=O)c3cccc(C(F)(F)F)c3)c3c2C(=O)NC3)cc2cc(CN3CCCCC3)ccc21
Reaction #49445
4-(3-trifluoromethylbenzenesulfonyloxy)-7-[1-(tert-butoxycarbonyl)-5-(piperidinomethyl)indol-2-yl]isoindolinone
Ausbeute 58.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)NS(=O)(=O)c1cc(CN)cc(C(F)(F)F)c1
Reaction #70621
3-Aminomethyl-N-tert-butyl-5-trifluoromethyl-benzenesulfonamide
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)NS(=O)(=O)c1cc(CN)cc(C(F)(F)F)c1
Reaction #70641
3-Aminomethyl-N-tert-butyl-5-trifluoromethyl-benzenesulfonamide
DOI: 10.6084/m9.figshare.5104873.v1
C[C@H]1CN(S(=O)(=O)c2cc(C(F)(F)F)ccc2Br)CCN1C(=O)OC(C)(C)C
Reaction #71659
crude title compound
Ausbeute 103.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)N1CCN(S(=O)(=O)c2cc(C(F)(F)F)ccc2Br)CC1
Reaction #71661
1,1-dimethylethyl 4-{[2-bromo-5-(trifluoromethyl)phenyl]sulfonyl}-1-piperazinecarboxylate
DOI: 10.6084/m9.figshare.5104873.v1
CSc1ccc(Cl)cc1NS(=O)(=O)c1ccc(Cl)c(C(F)(F)F)c1
Reaction #157571
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)Sc1ccc(Cl)cc1NS(=O)(=O)c1ccc(Cl)c(C(F)(F)F)c1
Reaction #157572
title compound
DOI: 10.6084/m9.figshare.5104873.v1
O=S(=O)(Nc1cc(Cl)ccc1SCCO)c1ccc(Cl)c(C(F)(F)F)c1
Reaction #157573
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)NC(=O)CCSc1ccc(Cl)cc1NS(=O)(=O)c1ccc(Cl)c(C(F)(F)F)c1
Reaction #157588
title compound
DOI: 10.6084/m9.figshare.5104873.v1
O=S(=O)(Nc1cc(Cl)ccc1SCc1ncc[nH]1)c1ccc(Cl)c(C(F)(F)F)c1
Reaction #157599
title compound
DOI: 10.6084/m9.figshare.5104873.v1
O=S(=O)(Nc1cc(Cl)ccc1SCc1c[nH]cn1)c1ccc(Cl)c(C(F)(F)F)c1
Reaction #157600
title compound
DOI: 10.6084/m9.figshare.5104873.v1
O=S(=O)(Nc1cc(Cl)ccc1SCc1ccccc1)c1ccc(Cl)c(C(F)(F)F)c1
Reaction #157608
title compound
Ausbeute 80.3%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)c1ccc(CSc2ccc(Cl)cc2NS(=O)(=O)c2ccc(Cl)c(C(F)(F)F)c2)cc1
Reaction #157615
title compound
Ausbeute 66.0%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)c1cccc(CSc2ccc(Cl)cc2NS(=O)(=O)c2ccc(Cl)c(C(F)(F)F)c2)c1
Reaction #157620
title compound
Ausbeute 65.3%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)c1ccccc1CSc1ccc(Cl)cc1NS(=O)(=O)c1ccc(Cl)c(C(F)(F)F)c1
Reaction #157625
title compound
Ausbeute 37.3%DOI: 10.6084/m9.figshare.5104873.v1
CCN(CC)C(=O)CCSc1ccc(Cl)cc1NS(=O)(=O)c1ccc(Cl)c(C(F)(F)F)c1
Reaction #157631
title compound
Ausbeute 85.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C(CCSc1ccc(Cl)cc1NS(=O)(=O)c1ccc(Cl)c(C(F)(F)F)c1)N1CCCC1
Reaction #157633
title compound
Ausbeute 17.2%DOI: 10.6084/m9.figshare.5104873.v1
O=S(=O)(NC1CC1)c1cc(Br)cc(C(F)(F)F)c1
Reaction #168665
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)COc1c(F)c(Cl)cc2c1CCCC2NS(=O)(=O)c1cc(C(F)(F)F)cc(C(F)(F)F)c1
Reaction #172982
DOI: 10.1039/C8SC04228D
O=C(O)c1cc(C(F)(F)F)cc(S(=O)(=O)N2CCCC2)c1
Reaction #180881
DOI: 10.1039/C8SC04228D
Seite 1Weiter