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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2413896Generated: November 1, 2026

Triethylamine → HCID 20154303, compound

https://huagongshe.com/reaction/2413896

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantAcetoxyacetyl chlorideHCID 26297—
ReactantHCID 20154278HCID 20154278—
SolventChloroformHCID 6212—
ProductHCID 20154303HCID 20154303—

Reaction Steps

To a suspension of 2-amino-4-(5-aminomethyl-2-thienyl) thiazole in 150 ml of chloroform is added 10 ml of triethylamine, and 3.1 g of acetoxyacetylchloride is added dropwise with stirring at room temperature (10°-35° C.). The whole mixture is stirred at room temperature for an hour, and then washed with water. The organic layer is separated, dried over anhydrous magnesium sulfate and concentrated under reduced pressure. The residue is recrystallized from ethanol to give 2-amino-4-(5-acetoxyacetylaminomethyl-2-thienyl) thiazole, melting at 149°-150° C. The corresponding maleate melts at 153°-154° C. with decomposition.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04720493
Source datasetuspto-grants-1988_01
ORD IDord-69ef727b6cb54d4abd86a08b82df35de
Source noteuspto-grants-1988_01