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HRID 704238作成日:2026年10月26日

Acetone → 10-[1-(1-Pyrrolidinyl)-2-propyl]-2-phenothiazinecarboxylic acid hydrochloride

https://huagongshe.com/reaction/704238

反応式

関与物質

役割名称HCID仕込み量
反応物AcetoneHCID 180—
反応物Hydrochloric AcidHCID 313—
反応物Potassium HydroxideHCID 14797—
反応物10-[1-(1-Pyrrolidinyl)-2-propyl]-2-phenothiazinecarbonitrile hydrochlorideHCID 19020543—
溶媒Diethyl EtherHCID 3283—
生成物10-[1-(1-Pyrrolidinyl)-2-propyl]-2-phenothiazinecarboxylic acid hydrochlorideHCID 14536640—

反応手順

10-[(2RS)-1-(1-Pyrrolidinyl)-2-propyl]-2-phenothiazinecarbonitrile hydrochloride (3.72 g) is added to a solution of potassium hydroxide (1.7 g) in glycol (20 cc), and the mixture is stirred for 5 hours under reflux. After cooling, the yellow solution obtained is traeted with a 3N ethereal solution (10 cc) of hydrochloric acid, and diluted with acetone (100 cc) and ethyl ether (100 cc) and then filtered. The yellow filtrate, after priming, gives rise to the crystallization of a product, which is drained, washed with ethyl ether (2×10 cc) and dried under reduced pressure (5 mm Hg; 0.68 kPa) at 40° C. 10-[(2RS)-1-(1-Pyrrolidinyl)-2-propyl]-2-phenothiazinecarboxylic acid hydrochloride (3.5 g) is thereby obtained in the form of pale yellow crystals, m.p. 215°-217° C.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04985419
出典データセットuspto-grants-1991_01
ORD IDord-6e575cacd2934a42b2707d859b388d67
出典メモuspto-grants-1991_01