trifluoromethanesulfonyl chloride

O=S(=O)(OCC(F)(F)F)C(F)(F)F
Reaction #1798
2,2,2-trifluoroethyltriflate
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
O=S(=O)(OCC(F)(F)F)C(F)(F)F
Reaction #1799
2,2,2-trifluoroethyltriflate
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
O=S(=O)(OC(c1ccc(F)cc1)C(F)(F)F)C(F)(F)F
Reaction #45283
trifluoromethanesulfonic acid 2,2,2-trifluoro-1-(4-fluorophenyl)ethyl ester
수율 101.2%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
O=S(=O)(OC(c1ccc(F)cc1)C(F)(F)F)C(F)(F)F
Reaction #45289
trifluor-methanesulfonic acid 2,2,2-trifluoro-1(RS)-(4-fluorophenyl)ethyl ester
수율 74.9%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
CC(C)(C)OC(=O)n1c(-c2ccc(OS(=O)(=O)C(F)(F)F)c3c2C(=O)NC3)cc2cc(CN3CCCCC3)ccc21
Reaction #49463
4-trifluoromethanesulfonyloxy-7-[1-(tert-butoxycarbonyl)-5-(piperidinomethyl)indol-2-yl]isoindolinone
수율 93.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
CC(C)(C)OC(=O)n1c(-c2ccc(OS(=O)(=O)C(F)(F)F)c3c2C(=O)NC3)cc2cc(C=O)ccc21
Reaction #49471
4-trifluoromethanesulfonyloxy-7-[1-(tert-butoxycarbonyl)-5-formylindol-2-yl]isoindolinone
수율 62.1%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
CC(C)(C)OC(=O)n1c(-c2ccc(OS(=O)(=O)C(F)(F)F)c3c2C(=O)NC3)cc2cc(CN3CCN(CCO[Si](C)(C)C(C)(C)C)CC3)ccc21
Reaction #49498
4-trifluoromethanesulfonyloxy-7-{1-(tert-butoxycarbonyl)-5-[4-(2-tert-butyldimethylsilyloxyethyl)pyperazin-1-ylmethyl]indol-2-yl}isoindolinone
수율 77.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
CC(C)(C)OC(=O)n1c(-c2cc(OS(=O)(=O)C(F)(F)F)c(Cl)c3c2C(=O)NC3)cc2cc(CN3CCCCC3)ccc21
Reaction #49587
4-chloro-5-trifluoromethanesulfonyloxy-7-[1-(tert-butoxycarbonyl)-5-(piperidin-1-ylmethyl)indol-2-yl]isoindolinone
수율 71.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
O=C1CC(c2cccnc2)N1
Reaction #87990
pure product
수율 42.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_09
C[C@H](Nc1nc(Nc2cc(C3CC3)[nH]n2)c(F)cc1CNS(=O)(=O)C(F)(F)F)c1ccc(F)cc1
Reaction #163086
title compound
수율 15.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
CSc1ccc(OC(F)(F)C(OS(=O)(=O)C(F)(F)F)c2ccc(F)cc2)cc1
Reaction #174561
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CC1(C2CCCC2)Cc2cc(OS(=O)(=O)C(F)(F)F)c(Cl)c(Cl)c2C1=O
Reaction #175130
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
O=S(=O)(OCC(F)(F)C(F)(F)C(F)(F)C(F)(F)C(F)(F)C(F)(F)C(F)(F)F)C(F)(F)F
Reaction #199891
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CCCCC1(C2CCCC2)Cc2cc(OS(=O)(=O)C(F)(F)F)c(Cl)c(Cl)c2C1=O
Reaction #207113
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CCOC(=O)C=CC=CC(CC(C)N(C)C)(c1ccccc1)c1ccccc1
Reaction #224500
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
COc1cc2nccc(OS(=O)(=O)C(F)(F)F)c2cc1OC
Reaction #233858
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
COc1cc(OS(=O)(=O)C(F)(F)F)cc(Cl)c1CN1CCCCC1
Reaction #235057
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
O=C1OC(Cn2ccnn2)CN1c1ccc(C2=CCN(S(=O)(=O)C(F)(F)F)CC2)c(F)c1
Reaction #239823
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
COC(=O)c1c(-c2ccc(F)cc2)nc(OS(=O)(=O)C(F)(F)F)nc1C(C)C
Reaction #244295
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
O=C1NCCc2cc(OS(=O)(=O)C(F)(F)F)ccc21
Reaction #247619
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
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