An 203 Reaktionen beteiligt

18415

Cc1cc(C)c(S(=O)(=O)n2ccc3c(N4CCNCC4)cccc32)c(C)c1.Cl
Reaction #8413
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
Cc1cc(C)c(S(=O)(=O)NCCCCNS(=O)(=O)c2c(C)cc(C)cc2C)c(C)c1
Reaction #10569
( 1 )
Ausbeute 90.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
Cc1cc(C)c(S(=O)(=O)OCCC2CCN(S(=O)(=O)c3c(C)cc(C)cc3C)CC2)c(C)c1
Reaction #10570
N,O-Bis(2,4,6-trimethylbenzenesulfonyl)-4-piperidineethanol
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
Cc1cc(C)c(S(=O)(=O)NC(Cc2c[nH]c3ccccc23)C(F)(F)F)c(C)c1
Reaction #46779
title compounds
Ausbeute 67.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
Cc1cc(C)c(S(=O)(=O)NCCc2ccc(C(=CCCCC(=O)O)c3cccnc3)cc2)c(C)c1
Reaction #50409
crude product
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1995_06
CC1=C(c2ccccc2NS(=O)(=O)c2c(C)cc(C)cc2C)C(=O)CC1
Reaction #180496
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
Cc1cc(C)c(S(=O)(=O)n2nc(C(=O)O)c3ccccc32)c(C)c1
Reaction #203347
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
Cc1cc(C)c(S(=O)(=O)n2ncc3ccc(I)cc32)c(C)c1
Reaction #212882
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
Cc1cc(C)c(S(=O)(=O)[O-])c(C)c1.N[n+]1ccncc1NC(=O)C1CC1
Reaction #220256
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_06
CC(C)=NOS(=O)(=O)c1c(C)cc(C)cc1C
Reaction #247657
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
Cc1cc(C)c(S(=O)(=O)On2nnc3ccccc32)c(C)c1
Reaction #247747
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
Cc1cc(C)c(S(=O)(=O)[O-])c(C)c1
Reaction #266212
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
Cc1cc(C)c(S(=O)(=O)NCCCCC(NC(=O)OCC2c3ccccc3-c3ccccc32)C(=O)O)c(C)c1
Reaction #269976
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
Cc1cc(C)c(S(=O)(=O)NCC(O)(Cn2cncn2)c2ccc(Cl)cc2Cl)c(C)c1
Reaction #273572
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
COCCNC(=O)Nc1nc2cc(OS(=O)(=O)c3c(C)cc(C)cc3C)ccc2[nH]1
Reaction #302458
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
—
Reaction #317667
purple solid
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2009_07
Cc1cc(C)c(S(=O)(=O)Nc2ccc(N3CCCNCC3)cc2NS(=O)(=O)c2ccccc2)c(C)c1.Cl
Reaction #317704
N-{4-(1,4-diazepan-1-yl)-2-[(phenylsulfonyl)amino]phenyl}-2,4,6-trimethylbenzenesulfonamide hydrochloride
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2009_07
COC(=O)c1cc(F)c(OS(=O)(=O)c2c(C)cc(C)cc2C)nc1Nc1ccc(F)cc1F
Reaction #319633
methyl 2-(2,4-difluorophenylamino)-5-fluoro-6-(2,4,6-trimethylbenzenesulfonyloxy)nicotinate
Ausbeute 81.9%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1989_07
CCOC(=O)CC(=O)c1cc(F)c(OS(=O)(=O)c2c(C)cc(C)cc2C)nc1Nc1ccc(F)cc1F
Reaction #319646
ethyl 2-[2-(2,4-difluorophenylamino)-5-fluoro-6-(2,4,6-trimethylbenzenesulfonyloxy)nicotinoyl]acetate
Ausbeute 85.8%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1989_07
COC(=O)c1cc(F)c(OS(=O)(=O)c2c(C)cc(C)cc2C)nc1Nc1ccc(F)cc1F
Reaction #334111
methyl 2-(2,4-difluorophenylamino)-5-fluoro-6-(2,4,6-trimethylbenzenesulfonyloxy)nicotinate
Ausbeute 81.9%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1987_11
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