o-(trifluoromethyl)benzenesulfonyl chloride

CC(C)(C)OC(=O)n1c(-c2ccc(OS(=O)(=O)c3ccccc3C(F)(F)F)c3c2C(=O)NC3)cc2cc(CN3CCCCC3)ccc21
Reaction #49422
4-(2-trifluoromethylbenzenesulfonyloxy)-7-[1-(tert-butoxycarbonyl)-5-(piperidinomethyl)indol-2-yl]isoindolinone
Ausbeute 41.3%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
CCOP(C)(=O)COS(=O)(=O)c1ccccc1C(F)(F)F
Reaction #184669
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CN(CCC#N)S(=O)(=O)c1ccccc1C(F)(F)F
Reaction #229064
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
O=C1C(Cl)=C(N2CCN(S(=O)(=O)c3ccccc3C(F)(F)F)CC2)C(=O)c2ccccc21
Reaction #243320
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
O=S(=O)(NCc1ccc(Br)s1)c1ccccc1C(F)(F)F
Reaction #247156
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
CCOC(=O)c1cc2cccc(NS(=O)(=O)c3ccccc3C(F)(F)F)c2[nH]1
Reaction #250434
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
CC(C)OP(=O)(COS(=O)(=O)c1ccccc1C(F)(F)F)OC(C)C
Reaction #275408
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
COC(C)CCOS(=O)(=O)c1ccccc1C(F)(F)F
Reaction #289173
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
COc1ccc(C2=NN(C3CCN(S(=O)(=O)c4ccccc4C(F)(F)F)CC3)C(=O)C2(C)C)cc1OC
Reaction #289634
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
O=S(=O)(c1ccccc1C(F)(F)F)N1CCN2C[C@H](Oc3cnc(C4CC4)cn3)C[C@H]2C1
Reaction #327610
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_02
COC(C)(C)CCOS(=O)(=O)c1ccccc1C(F)(F)F
Reaction #375899
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (8/10)
CCOP(=O)(COS(=O)(=O)c1ccccc1C(F)(F)F)OCC
Reaction #414185
desired product
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1993_12
CC(C)OP(=O)(COS(=O)(=O)c1ccccc1C(F)(F)F)OC(C)C
Reaction #414187
desired product
Ausbeute 64.2%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1993_12
CCOP(C)(=O)COS(=O)(=O)c1ccccc1C(F)(F)F
Reaction #414192
desired product
Ausbeute 14.5%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1993_12
CN(c1ccccc1)S(=O)(=O)c1ccccc1C(F)(F)F
Reaction #467739
2-trifluoromethyl-N-methylbenzene-sulfonanilide
Ausbeute 96.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2001_10
Cc1cc(O)cc(OS(=O)(=O)c2ccccc2C(F)(F)F)c1
Reaction #530076
title compound
Ausbeute 55.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1999_04
Cc1cc(NS(=O)(=O)c2ccccc2C(F)(F)F)cc(OCc2ccccc2)c1
Reaction #530086
title compound
Ausbeute 83.1%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1999_04
CCOC(=O)c1cc2cccc(NS(=O)(=O)c3ccccc3C(F)(F)F)c2[nH]1
Reaction #591915
title compound
Ausbeute 88.2%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_08
O=S(=O)(c1ccccc1C(F)(F)F)n1nc(Br)c2ccccc21
Reaction #595375
3-bromo-1-(2-(trifluoromethyl)phenylsulfonyl)-1H-indazole
Ausbeute 86.9%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2015_08
COc1ccc(C2=NN(C3CCN(S(=O)(=O)c4ccccc4C(F)(F)F)CC3)C(=O)C2(C)C)cc1OC
Reaction #611333
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_05
Seite 1Weiter