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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1844544Generated: October 29, 2026

Ethanol → HCID 71203610, compound

https://huagongshe.com/reaction/1844544

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthanolHCID 702—
ReactantPiperidineHCID 8082—
ReactantHCID 71185518HCID 71185518—
SolventEthyl AcetateHCID 8857—
ProductHCID 71203610HCID 7120361073%

Reaction Conditions

Temperature92.5 °C

Reaction Steps

Piperidine (1.84 g, 21.63 mmol) was added to a stirred solution of ethyl 5-(4-methoxyphenyl)-4-methylthiazole-2-carboxylate (prepared according to the procedure reported in WO 2006/089076, 0.6 g, 2.16 mmol) in a ethanol (10 ml) in a tube at 25° C. under nitrogen atmosphere. The tube was agitated for about 15 minutes under nitrogen and was sealed. The reaction mixture was heated at 90-95° C. for 15 hr with stirring. The progress of the reaction was monitored by TLC. The reaction mixture was then cooled to 25° C. and was concentrated under reduced pressure. The residue obtained was dissolved in ethyl acetate (50 ml). The mixture was washed with saturated sodium bicarbonate solution (20 ml). The separated organic layer was concentrated under reduced pressure to obtain a crude product, which was then purified by flash column chromatography using 40% ethyl acetate in hexanes as an eluent to obtain the title compound (0.50 g, 73.0%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08946432B2
Source datasetuspto-grants-2015_02
ORD IDord-fc6c47b3856f4a14aeba67c6f8eac176
Source noteuspto-grants-2015_02