sulfamide

C[C@@H]1CN(Cc2ccc(F)cc2)[C@@H](C)CN1C(=O)COc1ccc(Cl)cc1CC(=O)NS(N)(=O)=O
Reaction #11751
title compound
المردود 12.7%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
O=S1(=O)N=C(c2ccccc2)C(c2ccccc2)=N1
Reaction #46987
product 14
المردود 84416.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
O=S1(=O)N=C(c2cccc(F)c2)C(c2cccc(F)c2)=N1
Reaction #46989
product 21
المردود 72.8%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
Cl.O=S1(=O)N=C(c2ccccc2)C(c2cccnc2)=N1
Reaction #47116
product 497
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
CCOC(=O)C1CCC(CNC(C)=O)CC1
Reaction #52024
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2005_02
NC1=NS(=O)(=O)Nc2ccccc21
Reaction #72638
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_09
Cc1cccc(NS(N)(=O)=O)c1C#N
Reaction #72640
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_09
Cc1nc2c(OCC3CCCCC3)cccn2c1C(=O)N[C@H]1CCCN(S(N)(=O)=O)C1.Cl
Reaction #92746
N-[(3S)-1-(aminosulfonyl)piperidin-3-yl]-8-(cyclohexylmethoxy)-2-methylimidazo[1,2-a]pyridine-3-carboxamide hydrochloride
المردود 68.9%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_09
NS(=O)(=O)NCCCNc1nonc1-c1noc(=O)n1-c1ccc(F)c(Br)c1
Reaction #156952
desired product
المردود 71.7%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
NS(=O)(=O)NCCCNc1nonc1-c1noc(=O)n1-c1cccc(C(F)(F)F)c1
Reaction #156978
N-{3-[(4-{5-oxo-4-[3-(trifluoromethyl)phenyl]-4,5-dihydro-1,2,4-oxadiazol-3-yl}-1,2,5-oxadiazol-3-yl)amino]propyl}sulfamide
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
N#Cc1cc(NC(=NO)c2nonc2NCCNS(N)(=O)=O)ccc1F
Reaction #156985
title compound
المردود 29.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
NS(=O)(=O)N1CCN(c2ccncc2)CC1
Reaction #177235
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CC(C)(C)OC(=O)Nc1ccc(C2CNS(=O)(=O)NC2)cc1
Reaction #180238
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
Cc1cnc(CN(CCCCNS(N)(=O)=O)Cc2ncccc2C(C)C)c(C)c1
Reaction #182518
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CC(C)N1Cc2ccccc2NS1(=O)=O
Reaction #185013
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CC1CN(S(N)(=O)=O)CC(C)N1
Reaction #188349
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
Cc1c([N+](=O)[O-])cc(C(N)=O)c2nc[nH]c12
Reaction #193545
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
O=S1(=O)NCc2ccccc2N1c1ccccc1F
Reaction #193789
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CC(c1c(Cl)ccc(F)c1Cl)c1c[nH]c2ncc(-c3cnn(C4CCN(S(N)(=O)=O)CC4)c3)cc12
Reaction #198231
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
O=[N+]([O-])c1ccc2c(c1)OS(=O)(=O)N2
Reaction #198534
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
الصفحة 1التالي