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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 461998Generated: October 29, 2026

Triethylamine → HCID 21391851, compound

https://huagongshe.com/reaction/461998

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantEthyl chloroformateHCID 10928—
Reactant2-Ethylthio-5-carboxythiazoleHCID 21391910—
ReactantHCID 21391941HCID 21391941—
SolventTetrahydrofuranHCID 8028—
ProductHCID 21391851HCID 21391851—

Reaction Conditions

Temperature-30 °C

Reaction Steps

In this preparation 0.1 mole of 2-ethylthio-5-carboxythiazole is dissolved in 300 ml. of anhydrous tetrahydrofuran, under nitrogen, and 0.1 moles of triethylamine is added and the resulting mixture cooled to -30° C. 0.1 Mole of ethylchloroformate is then added dropwise with stirring and the resulting mixture allowed to warm to 0° C. The mixture is then stirred for ten minutes, then cooled to -30° C and 0.11 moles of 2-(bicyclo[2.2.1]hept-7-yl)ethylamine in 50 ml. of tetrahydrofuran added dropwise. The mixture is allowed to warm to room temperature (about 20° C), poured in 500 ml. of ethyl acetate, washed with water, then washed with saturated aqueous sodium chloride solution, and dried over anhydrous magnesium sulfate. The mixture is then filtered and the resulting filtrate evaporated under vacuum yielding 2-ethylthio-5-[2-(bicyclo[2.2.1]hept-7-yl)ethylaminocarbonyl]-thiazole as a solid, which is then further purified by recrystallization from ethyl acetate.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04064258
Source datasetuspto-grants-1977_12
ORD IDord-24e4c78a942d4cc49e3096ba2807cd27
Source noteuspto-grants-1977_12