sulfathiazole

O=C(O)CCC(=O)Nc1ccc(S(=O)(=O)Nc2nccs2)cc1
Reaction #44932
succinylsulfathiazole
المردود 67.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
CC(C)(C)[Si](O[C@H](CCO)C(=O)Nc1ccc(S(=O)(=O)Nc2nccs2)cc1)(c1ccccc1)c1ccccc1
Reaction #164465
amide
المردود 95.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
O=C1C=CC(=O)N1
Reaction #182351
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
O=C(Nc1ccc(S(=O)(=O)Nc2nccs2)cc1)c1cc2cc(Cl)cc(Cl)c2[nH]1
Reaction #306729
5,7-Dichloro-1H-indol-2-carboxylic acid [4-(thiazol-2-ylsulfamoyl)-phenyl]-amide
المردود 90.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2012_06
O=C(COc1ccnc2c(C(F)(F)F)cccc12)Nc1ccc(S(=O)(=O)Nc2nccs2)cc1
Reaction #306731
solid
المردود 69.5%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2012_06
O=C(Nc1ccc(S(=O)(=O)Nc2nccs2)cc1)C(Cl)c1ccccc1
Reaction #306734
2-Chloro-2-phenyl-N-[4-(thiazol-2-ylsulfamoyl)-phenyl]-acetamide
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2012_06
O=C(CCCl)Nc1ccc(S(=O)(=O)Nc2nccs2)cc1
Reaction #306735
3-Chloro-N-[4-(thiazol-2-ylsulfamoyl)-phenyl]-propionamide
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2012_06
CC(C)(C)[Si](O[C@H](CCO)C(=O)Nc1ccc(S(=O)(=O)Nc2nccs2)cc1)(c1ccccc1)c1ccccc1
Reaction #507968
amide
المردود 95.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2012_01
O=C(O)CCC(=O)Nc1ccc(S(=O)(=O)Nc2nccs2)cc1
Reaction #624844
succinylsulfathiazole
المردود 67.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_10
O=C(Nc1ccc(S(=O)(=O)Nc2nccs2)cc1)C(CCO)N1CCc2c(Cl)cccc21
Reaction #769478
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (3/10)
O=C1Nc2ccc3ncsc3c2C1=CNc1ccc(S(=O)(=O)Nc2nccs2)cc1
Reaction #928053
title compound
المردود 33.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2002_04
CC(C)(C)[Si](O[C@@H](CCO)C(=O)Nc1ccc(S(=O)(=O)Nc2nccs2)cc1)(c1ccccc1)c1ccccc1
Reaction #1185852
amide
المردود 99.8%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2012_03
O=C(O)CCC(=O)Nc1ccc(S(=O)(=O)Nc2nccs2)cc1
Reaction #1186778
succinylsulfathiazole
المردود 67.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2012_03
O=S(=O)(Cl)c1ccc(S(=O)(=O)Nc2nccs2)cc1
Reaction #1260294
4-chlorosulfonyl-N-(2-thiazolyl)benzenesulfonamide
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_11
O=S(=O)(Cl)c1ccc(S(=O)(=O)Nc2nccs2)cc1
Reaction #1321903
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (5/10)
O=C1Nc2ccc3ncsc3c2C1=CNc1ccc(S(=O)(=O)Nc2nccs2)cc1
Reaction #1351190
title compound
المردود 33.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2003_04
O=C(Nc1ccc(S(=O)(=O)Nc2nccs2)cc1)c1cc2cc(Cl)cc(Cl)c2[nH]1
Reaction #1521832
5,7-Dichloro-1H-indol-2-carboxylic acid [4-(thiazol-2-ylsulfamoyl)-phenyl]-amide
المردود 90.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2009_11
O=C(COc1ccnc2c(C(F)(F)F)cccc12)Nc1ccc(S(=O)(=O)Nc2nccs2)cc1
Reaction #1521834
solid
المردود 69.5%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2009_11
O=C(Nc1ccc(S(=O)(=O)Nc2nccs2)cc1)C(Cl)c1ccccc1
Reaction #1521837
2-Chloro-2-phenyl-N-[4-(thiazol-2-ylsulfamoyl)-phenyl]-acetamide
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2009_11
O=C(CCCl)Nc1ccc(S(=O)(=O)Nc2nccs2)cc1
Reaction #1521838
3-Chloro-N-[4-(thiazol-2-ylsulfamoyl)-phenyl]-propionamide
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2009_11
الصفحة 1التالي