p-(trifluoromethyl)benzenesulfonyl chloride

—
Reaction #3010
glass
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CC(C)(C)OC(=O)n1c(-c2ccc(OS(=O)(=O)c3ccc(C(F)(F)F)cc3)c3c2C(=O)NC3)cc2cc(CN3CCCCC3)ccc21
Reaction #49420
4-(4-trifluoromethylbenzenesulfonyloxy)-7-[1-(tert-butoxycarbonyl)-5-(piperidinomethyl)indol-2-yl]isoindolinone
수율 27.1%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
CN([C@H]1CC[C@H](O)CC1)S(=O)(=O)c1ccc(C(F)(F)F)cc1
Reaction #53825
trans-N-(4-Hydroxy-cyclohexyl)-N-methyl-4-trifluoromethyl-benzenesulfonamide
수율 77.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2005_02
O=S(=O)(N[C@H]1CC[C@H](O)CC1)c1ccc(C(F)(F)F)cc1
Reaction #53836
trans-N-(4-Hydroxy-cyclohexyl)-4-trifluoromethyl-benzenesulfonamide
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2005_02
C=CCN(C)CCCCC[C@H]1CC[C@H](N(C)S(=O)(=O)c2ccc(C(F)(F)F)cc2)CC1
Reaction #53881
trans-N-{4-[5-(Allyl-methyl-amino)-pentyl]-cyclohexyl}-N-methyl-4-trifluoromethyl-benzenesulfonamide
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2005_02
CCN(CCO)CCCCC[C@H]1CC[C@H](N(C)S(=O)(=O)c2ccc(C(F)(F)F)cc2)CC1
Reaction #53882
trans-N-(4-{5-[Ethyl-(2-hydroxy-ethyl)-amino]-pentyl}-cyclohexyl)-N-methyl-4-trifluoromethyl-benzenesulfonamide
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2005_02
CCN(CC)CCCCC[C@H]1CC[C@H](N(C)S(=O)(=O)c2ccc(C(F)(F)F)cc2)CC1
Reaction #53891
trans N-[4-(5-Diethylamino-pentyl)-cyclohexyl]-N-methyl-4-trifluoromethyl-benzenesulfonamide
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2005_02
CN([C@H]1CC[C@H](CCCCCN(CCO)CCO)CC1)S(=O)(=O)c1ccc(C(F)(F)F)cc1
Reaction #53892
trans-N-(4-{5-[Bis-(2-hydroxy-ethyl)-amino]-pentyl}-cyclohexyl)-N-methyl-4-trifluoromethyl-benzenesulfonamide
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2005_02
C=CCN(C)CCCC[C@H]1CC[C@H](N(C)S(=O)(=O)c2ccc(C(F)(F)F)cc2)CC1
Reaction #53904
trans-N-{4-[4-(Allyl-methyl-amino)-butyl]-cyclohexyl}-N-methyl-4-trifluoromethyl-benzenesulfonamide
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2005_02
CCN(CCO)CCCC[C@H]1CC[C@H](N(C)S(=O)(=O)c2ccc(C(F)(F)F)cc2)CC1
Reaction #53905
trans-N-(4-{4-[Ethyl-(2-hydroxy-ethyl)-amino]-butyl}-cyclohexyl)-N-methyl-4-trifluoromethyl-benzenesulfonamide
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2005_02
CN([C@H]1CC[C@H](CCCCN2CCCCC2)CC1)S(=O)(=O)c1ccc(C(F)(F)F)cc1
Reaction #53906
trans-N-Methyl-N-[4-(4-piperidin-1-yl-butyl)-cyclohexyl]-4-trifluoromethyl-benzenesulfonamide
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2005_02
CN(C)CCCC[C@H]1CC[C@H](N(C)S(=O)(=O)c2ccc(C(F)(F)F)cc2)CC1
Reaction #53907
trans-N-[4-(4-Dimethylamino-butyl)-cyclohexyl]-N-methyl-4-trifluoromethyl-benzenesulfonamide
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2005_02
CCCN(C)CCCC[C@H]1CC[C@H](N(C)S(=O)(=O)c2ccc(C(F)(F)F)cc2)CC1
Reaction #53908
trans-N-Methyl-N-{4-[4-(methyl-propyl-amino)-butyl]-cyclohexyl}-4-trifluoromethyl-benzenesulfonamide
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2005_02
CN([C@H]1CC[C@H](CCCCN(CCO)CCO)CC1)S(=O)(=O)c1ccc(C(F)(F)F)cc1
Reaction #53909
trans N-(4-{4-[Bis-(2-hydroxy-ethyl)-amino]-butyl}-cyclohexyl)-N-methyl-4-trifluoromethyl-benzenesulfonamide
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2005_02
O=S(=O)(N[C@H]1CC[C@H](CCCCCBr)CC1)c1ccc(C(F)(F)F)cc1
Reaction #53929
trans-N-[4-(5-Bromo-pentyl)-cyclohexyl]-4-trifluoromethyl-benzenesulfonamide
수율 91.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2005_02
CCN(CC)C(=O)CCCC[C@H]1CC[C@H](N(C)S(=O)(=O)c2ccc(C(F)(F)F)cc2)CC1
Reaction #53942
trans-5-{4-[Methyl-(4-trifluoromethyl-benzenesulfonyl)-amino]-cyclohexyl}-pentanoic acid diethylamide
수율 85.5%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2005_02
O=C(c1ccncc1)c1cc(Cl)ccc1NS(=O)(=O)c1ccc(C(F)(F)F)cc1
Reaction #57839
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_09
CC(C)(C)OC(=O)N1CCN(S(=O)(=O)c2ccc(C(F)(F)F)cc2)CC1
Reaction #69568
1,1-dimethylethyl 4-{[4-(trifluoromethyl)phenyl]sulfonyl}-1-piperazinecarboxylate
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_09
C[C@H]1CN(S(=O)(=O)c2ccc(C(F)(F)F)cc2)CCN1
Reaction #69570
title compound
수율 64.9%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_09
C[C@@H]1CN(C(=O)OC(C)(C)C)CCN1S(=O)(=O)c1ccc(C(F)(F)F)cc1
Reaction #69574
title compound
수율 110.8%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_09
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