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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1894368Generated: November 1, 2026

4-[3-(Benzhydryl-sulfamoyl)-propyl]-piperazine-1-carboxylic acid tert-butyl ester → Tert-butyl 4-(3-sulfamoylpropyl)piperazine-1-carboxylate

https://huagongshe.com/reaction/1894368

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-[3-(Benzhydryl-sulfamoyl)-propyl]-piperazine-1-carboxylic acid tert-butyl esterHCID 67205349—
CatalystPalladium hydroxideHCID 9942167—
SolventMethanolHCID 887—
ProductTert-butyl 4-(3-sulfamoylpropyl)piperazine-1-carboxylateHCID 6720527979.3%

Reaction Steps

A suspension of 4-[3-(benzhydryl-sulfamoyl)-propyl]-piperazine-1-carboxylic acid tert-butyl ester (650 mg, 1.37 mmol) and palladium hydroxide (1.154 g, 1.64 mmol, 20% w from Aldrich) in methanol (10 mL) was hydrogenated at room temperature overnight using a Parr apparatus (50 psi). The reaction mixture was filtered through a Celite cake, and the filtrate was concentrated. Purification of the crude residue by flash column chromatography (40 g of silica gel, eluting with methanol and ethyl acetate) gave 4-(3-sulfamoyl-propyl)-piperazine-1-carboxylic acid tert-butyl ester as an off-white solid (334 mg).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08513239B2
Source datasetuspto-grants-2013_08
ORD IDord-4a75503c7a394b4191d51d95743348e6
Source noteuspto-grants-2013_08