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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2301497Generated: November 1, 2026

N-benzyl-6-chloro-2-hydroxy-3-nitrobenzenesulfonamide → N-Benzyl-3-amino-6-chloro-2-hydroxybenzenesulfonamide

https://huagongshe.com/reaction/2301497

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-benzyl-6-chloro-2-hydroxy-3-nitrobenzenesulfonamideHCID 18373553—
CatalystPalladiumHCID 23938—
SolventEthyl AcetateHCID 8857—
ProductN-Benzyl-3-amino-6-chloro-2-hydroxybenzenesulfonamideHCID 1837345386.1%

Reaction Steps

To a solution of N-benzyl-6-chloro-2-hydroxy-3-nitrobenzenesulfonamide (180 mg, 0.52 mmol) in ethyl acetate, was added 10% Pd/C (70 mg). The mixture was flushed with argon, then stirred under a hydrogen atmosphere at balloon pressure for 1 hour at room temperature. The mixture was filtered through celite and the celite was washed with methanol. The solvent was evaporated to give the desired product (140 mg, 85%). 1H NMR (DMSO-d6): δ 8.73 (t, 1H), 7.24 (m, 5H), 6.78 (d, 1H), 4.09 (d, 2H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06500863B1
Source datasetuspto-grants-2002_12
ORD IDord-fbb9a8006a894737831e410b50ad26e0
Source noteuspto-grants-2002_12