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HRID 1906148作成日:2026年10月25日

Ammonia → 2-(4-Chlorophenyl)-3-(2-oxo-1-pyrrolidinylmethyl)-6-methylimidazo[1,2-a]pyridine

https://huagongshe.com/reaction/1906148

反応式

関与物質

役割名称HCID仕込み量
反応物AmmoniaHCID 222—
反応物Sulfuric AcidHCID 1118—
反応物2-Pyrrolidinone, 1-(hydroxymethyl)-HCID 84911—
反応物2-(4-Chlorophenyl)-6-methylimidazo[1,2-a]pyridineHCID 735911—
溶媒WaterHCID 962—
生成物2-(4-Chlorophenyl)-3-(2-oxo-1-pyrrolidinylmethyl)-6-methylimidazo[1,2-a]pyridineHCID 13589601—

反応手順

An intimate mixture is prepared of 4.8 g (0.02 mol) of 2-(4-chlorophenyl)-6-methylimidazo[1,2-a]pyridine and 2.53 g (0.022 mol) of N-hydroxymethyl-2-pyrrolidinone, and this is then introduced into 20 ml of concentrated sulphuric acid. The solution is stirred for one day at room temperature, then poured into 800 ml of water, and 55 ml of ammonia solution are added. The lactam is extracted with methylene chloride, the organic phase is washed, dried and evaporated, and the residue is purified by chromatography, eluting with a 70:30 ethyl acetate, toluene mixture. The white solid obtained melts at 186°-187.5° C.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04650796
出典データセットuspto-grants-1987_03
ORD IDord-d734378739904929b8c1d367de515346
出典メモuspto-grants-1987_03