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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1931408Generated: November 3, 2026

Piperidine → HCID 68537123, compound

https://huagongshe.com/reaction/1931408

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPiperidineHCID 8082—
ReactantSodium hydrideHCID 24758—
ReactantHCID 68537700HCID 68537700—
SolventDimethylformamideHCID 6228—
ProductHCID 68537123HCID 68537123—

Reaction Steps

27.5 mg (0.63 mmol) of sodium hydride (55% in mineral oil) were added to 53.6 mg (0.63 mmol) of piperidine in 2 ml of DMF. After stirring at room temperature for 30 min, 150 mg (0.42 mmol) of 3-methyl-3-[2-(4-trifluoromethyl-phenyl)-thiazol-4-yl]-butyric acid ethyl ester in 2 ml of DMF were added, and the reaction mixture was stirred at room temperature for 2 h. After evaporation, water and dichloromethane were added, the organic phase was separated, washed with water, dried, and evaporated. The product was purified by RP18 chromatography. Yield: 6.3 mg.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08188291B2
Source datasetuspto-grants-2012_05
ORD IDord-1906d63586d14b4c88ae3b122a0329d3
Source noteuspto-grants-2012_05