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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2296674Generated: October 31, 2026

HCID 53729896, compound → HCID 53732363, compound

https://huagongshe.com/reaction/2296674

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 53729896HCID 53729896—
SolventWaterHCID 962—
SolventTrifluoroacetic acidHCID 6422—
SolventAnisoleHCID 7519—
ProductHCID 53732363HCID 5373236374.8%

Reaction Steps

A mixture of (2R)-4-[2-(acetylamino)ethanesulfonyl]-N-tert-butoxy-1-[5-(4-fluorophenyl)thiophene-2-sulfonyl]-2-piperazinecarboxamide (130 mg) in anisole (1 ml), trifluoroacetic acid (1 ml) and H2O (0.02 ml) was stirred at ambient temperature overnight, and then at 50 ° C. for 5 hours. The mixture was concentrated in vacuo, and the residue was purified by SiO2 column chromatography, eluted with MeOH in CHCl3=2% then 5%. The fractions containing the desired product were combined and concentrated in vacuo. The residue was triturated with diisopropyl ether to give 88 mg of (2R)-4-[2-(acetylamino)ethanesulfonyl]-1-(5-(4-fluorophenyl)thiophene-2-sulfonyl]-N-hydroxy-2-piperazinecarboxamide.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06489324B2
Source datasetuspto-grants-2002_12
ORD IDord-324700230d154aa8a0772f316cd94d81
Source noteuspto-grants-2002_12