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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1841919Generated: November 2, 2026

4-[4-(1-Oxo-but-2-ynylamino)-benzenesulfonyl]-piperazine-1-carboxylic acid tert-butyl ester → 4-(4-(Z)-But-2-enoylamino-benzenesulfonyl)-piperazine-1-carboxylic acid tert-butyl ester

https://huagongshe.com/reaction/1841919

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-[4-(1-Oxo-but-2-ynylamino)-benzenesulfonyl]-piperazine-1-carboxylic acid tert-butyl esterHCID 56954720—
CatalystLindlars catalystHCID 131709914—
SolventMethanolHCID 887—
Product4-(4-(Z)-But-2-enoylamino-benzenesulfonyl)-piperazine-1-carboxylic acid tert-butyl esterHCID 5695450244.4%

Reaction Steps

Lindlar's catalyst (0.005 g, 0.001 mmol) was added in one portion to a stirred solution of 4-[4-(1-oxo-but-2-ynylamino)-benzenesulfonyl]-piperazine-1-carboxylic acid tert-butyl ester (0.05 g, 0.11 mmol) in methanol (5 ml) at room temperature, the resulting mixture was then stirred at room temperature under a hydrogen atmosphere for 2 hours. After this time, the reaction mixture was filtered through celite and concentrated under vacuum to give the title compound (0.02 g, 40% yield) as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08946197B2
Source datasetuspto-grants-2015_02
ORD IDord-918e9c28892e4434b87a8eb2dbabd953
Source noteuspto-grants-2015_02