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HRID 358472作成日:2026年10月25日

Ethanol → Ethyl 2-((dimethylamino)methyl)thiazole-4-carboxylate

https://huagongshe.com/reaction/358472

反応式

関与物質

役割名称HCID仕込み量
反応物EthanolHCID 702—
反応物Ethyl bromopyruvateHCID 66144—
反応物N,N-Dimethylaminothioacetamide hydrochlorideHCID 13121932—
溶媒WaterHCID 962—
溶媒Diethyl EtherHCID 3283—
生成物Ethyl 2-((dimethylamino)methyl)thiazole-4-carboxylateHCID 2039211—

反応手順

A reaction mixture was prepared containing 15.5 g. of dimethylaminothioacetamide hydrochloride, 20.5 g. of ethyl bromopyruvate and 100 ml. of ethanol. The reaction mixture was heated to refluxing temperature for about four hours after which time the solvent was removed in vacuo in a rotary evaporator. The residue, containing ethyl 2-dimethylaminomethyl-4-thiazolecarboxylate formed in the above reaction, was dissolved in a mixture of ether and water. The aqueous layer was separated. The ether layer was extracted with an equal volume of water and then discarded. The two aqueous layers were combined and washed with ether. The ether layer was again discarded and the aqueous layer cooled to a temperature in the range of 0°-5° C. Solid potassium carbonate was added until the aqueous layer gave a basic reaction to litmus. An oil separated comprising ethyl 2-dimethylaminomethyl-4-thiazolecarboxylate free base. The oily layer was extracted with ether and the ether extract separated and dried. The ether was removed by evaporation in vacuo. The resulting residue was purified by gradient high pressure liquid chromatography (silica ethyl acetate). Ethyl 2-dimethylaminomethyl-4-thiazolecarboxylate thus obtained had the following physical characteristics:

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04468399
出典データセットuspto-grants-1984_08
ORD IDord-d7cc5060a35a465399a53624fafdc06a
出典メモuspto-grants-1984_08