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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 507288Generated: October 25, 2026

Ethyl bromopyruvate → 2-Piperidine-4-yl-thiazole-4-carboxylic acid ethyl ester

https://huagongshe.com/reaction/507288

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl bromopyruvateHCID 66144—
Reactanttert-Butyl 4-carbamothioylpiperidine-1-carboxylateHCID 2735648—
SolventEthanolHCID 702—
Product2-Piperidine-4-yl-thiazole-4-carboxylic acid ethyl esterHCID 57935959—

Reaction Conditions

Temperature70 °C

Reaction Steps

A mixture of 10 g (41 mmol) 4-thiocarbamoyl-piperidine-1-carboxylic acid tert-butyl ester (commercially available) and 7.98 g (41 mmol) ethyl bromopyruvate (commercially available) in 120 ml ethanol was stirred at 70° C. for 90 min. The mixture was evaporated to dryness, Na2CO3 aq. was added and the residue was extracted with ethyl acetate. The organic phases were washed with NaCl aq., dried with MgSO4 and evaporated to dryness. The residue was purified on silica eluting with DCM/MeOH/25% NH3 in water 100/20/1 to yield after evaporation of the product fractions 7.28 g (74%) of the title compound as light brown solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07786143B2
Source datasetuspto-grants-2010_08
ORD IDord-0d3c725b12274cf9a1c6d1826071b2fb
Source noteuspto-grants-2010_08