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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 648217Generated: October 30, 2026

Ethoxalyl chloride → HCID 20482445, compound

https://huagongshe.com/reaction/648217

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthoxalyl chlorideHCID 20884—
ReactantHCID 13386489HCID 13386489—
SolventPyridineHCID 1049—
SolventTetrahydrofuranHCID 8028—
ProductHCID 20482445HCID 2048244530.5%

Reaction Steps

To a solution of 2-amino-4-(4-benzhydrylpiperazin-1-ylmethyl)thiazole (1.8 g) in tetrahydrofuran (5 ml) and pyridine (10 ml) was added dropwise ethoxalyl chloride (1.1 g) under ice-cooling with stirring, and the stirring was continued at the same temperature for an hour. After concentration of the reaction mixture, the residue was extracted with ethyl acetate, washed with water, dried over anhydrous magnesium sulfate and then evaporated to dryness to give a residue, which was chromatographed on silica gel using ethyl acetate as an eluent. The eluates containing the desired compound were collected and evaporated, followed by recrystallization from a mixture of ethyl acetate and n-hexane to obtain pale yellow crystals (0.7 g) of 4-(4-benzhydrylpiperazin-1-ylmethyl)-2-ethoxalylaminothiazole, mp 125°-128° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04411900
Source datasetuspto-grants-1983_10
ORD IDord-c3ee0f6a8d5e43fa9e28d946bc532670
Source noteuspto-grants-1983_10