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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2186143Generated: November 1, 2026

5-Bromothiophene-2-sulfonyl chloride → 4-(5-Bromo-2-thiophenesulfonyl)-1-[1-(tert-butoxycarbonyl)piperidin-4-ylmethyl]-2-piperazinone

https://huagongshe.com/reaction/2186143

Reaction equation

Participants

RoleNameHCIDCharge
Reactant5-Bromothiophene-2-sulfonyl chlorideHCID 2733924—
Reactant4-(2-Oxo-piperazin-1-ylmethyl)-piperidine-1-carboxylic acid tert-butyl esterHCID 23447514—
SolventEthyl AcetateHCID 8857—
SolventSodium BicarbonateHCID 516892—
Product4-(5-Bromo-2-thiophenesulfonyl)-1-[1-(tert-butoxycarbonyl)piperidin-4-ylmethyl]-2-piperazinoneHCID 2344757049%

Reaction Steps

To a solution of 1-[1-(tert-butoxycarbonyl)piperidin-4-ylmethyl]-2-piperazinone (500 mg) in ethyl acetate (15 ml) and sodium bicarbonate solution (10 ml) was added at 0° C. 5-bromo-2-thiophenesulfonyl chloride (440 mg), and the mixture was stirred at room temperature for 30 minutes. The organic layer was separated, washed with brine, dried and concentrated, and the residue was purified with silica gel column chromatography (hexane:ethyl acetate=2:3) to give colorless solid of the title compound (430 mg).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06403595B1
Source datasetuspto-grants-2002_06
ORD IDord-5e508e6953da49bb9d8b2f0c8cf82687
Source noteuspto-grants-2002_06