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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 6883Generated: October 26, 2026

N-cyclopropyl-4-fluoro-3-nitrobenzenesulfonamide → 3-amino-N-cyclopropyl-4-fluorobenzene-1-sulfonamide

https://huagongshe.com/reaction/6883

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-cyclopropyl-4-fluoro-3-nitrobenzenesulfonamideHCID 8469273—
CatalystPalladiumHCID 23938—
SolventEthanolHCID 702—
Product3-amino-N-cyclopropyl-4-fluorobenzene-1-sulfonamideHCID 2201912295.5%

Reaction Steps

The mixture of N-cyclopropyl-4-fluoro-3-nitrobenzenesulfonamide (520 mg, 2 mmol) and Pd/C (10%, 100 mg) in EtOH was hydrogenated (1 atm) overnight. The mixture was filtered through a short pad of celite and concentrated in vacuo to afford N-cyclopropyl-4-fluoro-3-aminobenzenesulfonamide (440 mg, 95%) as an ivory solid. LC/MS; (M+H)+=231.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07084160B2
Source datasetuspto-grants-2006_08
ORD IDord-742bd07a01d3417fa9f833046b9b7c41
Source noteuspto-grants-2006_08