2-chlorobenzenesulfonyl chloride

O=C(c1ccc(NS(=O)(=O)c2ccccc2Cl)cc1)N1Cc2cccn2Cc2ccccc21
Reaction #3676
white crystals
المردود 20.9%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CC(C)(C)OC(=O)n1c(-c2ccc(OS(=O)(=O)c3ccccc3Cl)c3c2C(=O)NC3)cc2cc(CN3CCCCC3)ccc21
Reaction #49421
4-(2-chlorobenzenesulfonyloxy)-7-[1-(tert-butoxycarbonyl)-5-(piperidinomethyl)indol-2-yl]isoindolinone
المردود 75.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
O=S(=O)(N[C@@H]1Cc2ccc(Cn3cc(CO)c(C(F)(F)F)n3)cc2C1)c1ccccc1Cl
Reaction #71286
title compound
المردود 31.5%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_09
O=S(=O)(N[C@H]1Cc2ccc(Cn3cc(CO)c(C(F)(F)F)n3)cc2C1)c1ccccc1Cl
Reaction #71287
title compound
المردود 56.3%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_09
O=C(c1ccc(NS(=O)(=O)c2ccccc2Cl)cc1)N1Cc2cccn2Cc2ccccc21
Reaction #83497
white crystals
المردود 20.9%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1997_04
COc1ccc(C(=O)Nc2ccccc2)cc1NS(=O)(=O)c1ccccc1Cl
Reaction #173834
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CC(C)CN(Cc1cc(Br)cs1)S(=O)(=O)c1ccccc1Cl
Reaction #191291
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
COc1ccc(C2=NN(C3CCN(S(=O)(=O)c4ccccc4Cl)CC3)C(=O)C2(C)C)cc1OC
Reaction #193165
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
O=C1CC2(CCN(c3ccc(CC(F)(F)F)cc3)C2=O)CCN1S(=O)(=O)c1ccccc1Cl
Reaction #209142
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CN(c1ccccc1)S(=O)(=O)c1ccccc1Cl
Reaction #213804
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
Cc1cccnc1C1CCNCC1
Reaction #223385
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
O=C(O)C(CO)NS(=O)(=O)c1ccccc1Cl
Reaction #228485
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
COc1nc(Cl)cnc1NS(=O)(=O)c1ccccc1Cl
Reaction #235778
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
CCOC(=O)C1(N2CCN(S(=O)(=O)c3ccccc3Cl)CC2)CCC1
Reaction #242098
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
O=C1C2CC(NS(=O)(=O)c3ccccc3Cl)CC2CN1c1ccc(OC(F)(F)F)cc1
Reaction #243034
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
CC(C)n1cc(C(=O)c2cncc(NS(=O)(=O)c3ccccc3Cl)c2)c2c(N)ncnc21
Reaction #248633
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
O=S(=O)(c1ccccc1Cl)N1CCN(c2cccc(F)c2C(F)(F)F)CC1
Reaction #259390
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
O=S(=O)(NC1Cc2ccc(Cn3cc(CO)c(C(F)(F)F)n3)cc2C1)c1ccccc1Cl
Reaction #266375
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
O=S(=O)(c1ccccc1Cl)N1CCC(c2ncccc2C(F)(F)F)CC1
Reaction #273018
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
Cc1cc(C)c2ccc(NS(=O)(=O)c3ccccc3Cl)nc2n1
Reaction #275993
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
الصفحة 1التالي