戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 893682作成日:2026年10月26日

Hydrochloric Acid → 6-(2-chloroethyl)-7-methyl-5H-(1,3)thiazolo(3,2-a)pyrimidin-5-one

https://huagongshe.com/reaction/893682

反応式

関与物質

役割名称HCID仕込み量
反応物Hydrochloric AcidHCID 313—
反応物2-AminothiazoleHCID 2155—
反応物2-AcetylbutyrolactoneHCID 10601—
反応物Phosphorus oxychlorideHCID 24813—
溶媒WaterHCID 962—
溶媒TolueneHCID 1140—
生成物6-(2-chloroethyl)-7-methyl-5H-(1,3)thiazolo(3,2-a)pyrimidin-5-oneHCID 817872—

反応手順

A mixture of 50 parts of 2-thiazolamine, 76 parts of 3-acetyl-4,5-dihydro-2(3H)-furanone, 1.2 parts of concentrated hydrochloric acid and 270 parts of methylbenzene was stirred and refluxed for 2 hours using a water-separator. The reaction mixture is cooled and 340 parts of phosphoryl chloride were added at a temperature between 20° and 30° c. The whole was heated slowly to 100°-110° C. and stirring was continued for 2 hours at this temperature. The reaction mixture was evaporated and the residue was poured onto a mixture of crushed ice and ammonium hydroxide. The product was extracted with trichloromethane. The extract was dried, filtered and evaporated. The residue was purified by column chromatography over silica gel using a mixture of trichloromethane and methanol (95:5 by volume) as eluent. The pure fractions were collected and the eluent was evaporated. The residue was crystallized from a mixture of 2-propanol and 1,1'-oxybisethane, yielding 36 parts of 6-(2-chloroethyl)-7-methyl-5H-thiazolo[3,2-a]pyrimidin-5-one (intermediate 172).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05126339
出典データセットuspto-grants-1992_06
ORD IDord-4e87cf8d775e4199b275e6f618d73dcf
出典メモuspto-grants-1992_06