N-tert-butyl-5-amino-2-methoxycarbonylbenzenesulfonamide

COC(=O)c1ccc(NC=O)cc1S(=O)(=O)NC(C)(C)C
Reaction #1094
N-tert-Butyl-5-formylamino-2-methoxycarbonylbenzenesulfonamide
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
COC(=O)c1ccc(NN)cc1S(=O)(=O)NC(C)(C)C
Reaction #287884
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
COC(=O)c1ccc(NC=O)cc1S(=O)(=O)NC(C)(C)C
Reaction #297847
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
COC(=O)c1ccc(NN)cc1S(=O)(=O)NC(C)(C)C
Reaction #668838
methyl 2-(N-tert-butylsulfamoyl)-4-hydrazinobenzoate
Выход 70.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1999_07
COC(=O)c1ccc(NN)cc1S(=O)(=O)NC(C)(C)C
Reaction #1544702
methyl 2-(N-tert-butylsulfamoyl)-4-hydrazinobenzoate
Выход 70.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_12
CCOC(=O)N(N=C[N+](=O)[O-])c1ccc(C(=O)OC)c(S(=O)(=O)NC(C)(C)C)c1
Reaction #2357320
methyl 2-(N-tert-butylsulfamoyl)-4-(ethoxycarbonylnitromethylenehydrazino)benzoate
Выход 60.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2001_12
COC(=O)c1ccc(NC=O)cc1S(=O)(=O)NC(C)(C)C
Reaction #2486768
N-tert-Butyl-5-formylamino-2-methoxycarbonylbenzenesulfonamide
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1995_09