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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1622360Generated: October 30, 2026

Chloroacetaldehyde → 2-(1-(3,5-Dichloropyridin-4-yl)piperidin-4-yl)thiazole

https://huagongshe.com/reaction/1622360

Reaction equation

Participants

RoleNameHCIDCharge
ReactantChloroacetaldehydeHCID 33—
Reactant1-(3,5-Dichloropyridin-4-yl)piperidine-4-carbothioamideHCID 58378279—
SolventEthanolHCID 702—
Product2-(1-(3,5-Dichloropyridin-4-yl)piperidin-4-yl)thiazoleHCID 45275352161.1%

Reaction Steps

To a solution of 1-(3,5-dichloropyridin-4-yl)piperidine-4-carbothioamide 24 (23 mg, 0.079 mmol) in ethanol (2 mL) was added chloroacetaldehyde (50% wt in H2O) (0.26 mL, 0.16 mmol) and the mixture was heated at reflux for 17 h. The mixture was concentrated and chloroform (10 mL) was added to the residue. The solution was washed with water (10 mL) and extracted with chloroform (10 mL). The combined organic extracts were washed with brine (10 mL), dried (MgSO4) and concentrated under reduced pressure to furnish a brown oil (40 mg). The crude product was purified by preparative tlc on silica gel (CH2Cl2, MeOH, 10:1, then hexane, EtOAc, 1:1) to furnish the title compound as a pale brown solid (5 mg, 20%), LC-MS (ESI) Rt 2.79 min, m/z 314 (100%, M+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08778925B2
Source datasetuspto-grants-2014_07
ORD IDord-b081def3bd90435bb67c34bd9a8b5571
Source noteuspto-grants-2014_07