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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 997Generated: October 23, 2026

methyl 2-(N-tert-butylsulfamoyl)-4-nitrobenzoate → methyl 4-amino-2-(N-tert-butylsulfamoyl)benzoate

https://huagongshe.com/en/reaction/997

Reaction equation

Participants

RoleNameHCIDCharge
Reactantmethyl 2-(N-tert-butylsulfamoyl)-4-nitrobenzoateHCID 15240542—
ReactantHCID 178418361HCID 178418361—
SolventMethanolHCID 887—
Productmethyl 4-amino-2-(N-tert-butylsulfamoyl)benzoateHCID 10946074—

Reaction Steps

25.08 g (0.079 mol) of N-tert-butyl-2-methoxycarbonyl-5-nitrobenzenesulfonamide are dissolved in 1000 ml of MeOH. 0.50 g of Pd--C (10%) is added and the mixture is shaken under a hydrogen atmosphere (1 atm) until the uptake of hydrogen has finished. The catalyst is separated off and the solvent is removed by distillation. The residue is induced to crystallize by stirring with a little ethyl acetate. The resulting N-tert-butyl-5-amino-2-methoxycarbonylbenzenesulfonamide (18.3 g; 80.9% of theory) melts at 193° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05723409
Source datasetuspto-grants-1998_03
ORD IDord-5441fae977e64216866214e130a2476a
Source noteuspto-grants-1998_03