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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 543781Generated: October 28, 2026

Methyl 7-chloro-6-oxoheptanoate → HCID 20202828, compound

https://huagongshe.com/reaction/543781

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl 7-chloro-6-oxoheptanoateHCID 15576276—
ReactantHCID 178512206HCID 178512206—
SolventEthanolHCID 702—
ProductHCID 20202828HCID 20202828—

Reaction Steps

To a solution of methyl 7-chloro-6-oxoheptanoate (2.0 g.) in hot EtOH (20 ml.) was added a solution of 2,2,2-trifluoroethylamidinothiourea (2.1 g.) in hot EtOH (20 ml.). The resulting mixture was heated under reflux for 1 hour. The mixture was then evaporated to dryness and the residue partitioned between ether (20 ml.) and water (60 ml.). The aqueous layer was separated and basified with sodium bicarbonate and extracted with EtOAc. The EtOAc solution was evaporated to dryness and the residue crystallised from EtOAc/ether containing a small amount of acetone to give methyl 5-[2-(2-[2,2,2-trifluoroethyl]guanidino)thiazol-4-yl]valerate which was used without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04447441
Source datasetuspto-grants-1984_05
ORD IDord-f4f84448db5c48d2889f6ef096580f2c
Source noteuspto-grants-1984_05