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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 461684Generated: October 30, 2026

Triethylamine → HCID 21391851, compound

https://huagongshe.com/reaction/461684

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 mole 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 mole 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 into 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 numberUS04064135
Source datasetuspto-grants-1977_12
ORD IDord-e7e045df007e409fa3d58290e1b96ffb
Source noteuspto-grants-1977_12