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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1868153Generated: November 1, 2026

HCID 68552252, compound → HCID 57418374, compound

https://huagongshe.com/reaction/1868153

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 68552252HCID 68552252—
CatalystPalladiumHCID 23938—
SolventEthyl AcetateHCID 8857—
ProductHCID 57418374HCID 5741837462%

Reaction Steps

A solution of 4-(4-Fluoro-2-trifluoromethyl-phenyl)-2-methyl-1-(3-nitro-benzenesulfonyl)-piperazine (330 mg, 0.8 mmol) and a catalytic amount of 10% Pd/C in EtOAc (25 mL) was stirred under H2 (1 atm) at ambient temperature for two hours, after which the reduction was judged complete by TLC. The H2 removed under vacuum, and the reaction mixture was filtered through celite, and rinsed with EtOAc (3×25 mL), and the filtrate was concentrated in vacuo, affording 180 mg of the desired sulfonamide in >95% purity (62% yield). HRMS: calcd for C18H19F4N3O2S+H+, 418.12068. found ([M+H]+), 418.12119.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07632838B2
Source datasetuspto-grants-2009_12
ORD IDord-d69aedf4b3bc4a95a064e3ee98e5bf28
Source noteuspto-grants-2009_12