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HRID 27782作成日:2026年10月26日

2-Hydroxyquinoline → 5-(1-Hydroxy-2-isopropylaminobutyl)-8-p-methylbenzoyloxy-3,4-dihydrocarbostyril

https://huagongshe.com/reaction/27782

反応式

関与物質

役割名称HCID仕込み量
反応物2-HydroxyquinolineHCID 6038—
反応物Sodium MethoxideHCID 10942334—
反応物5-(1-Hydroxy-2-isopropylaminobutyl)-8-hydroxy-3,4-dihydrocarbostyril hydrochlorideHCID 23342111—
溶媒MethanolHCID 887—
生成物5-(1-Hydroxy-2-isopropylaminobutyl)-8-p-methylbenzoyloxy-3,4-dihydrocarbostyrilHCID 23342064—

反応手順

3.28 g of 5-(1-hydroxy-2-isopropylaminobutyl)-8-hydroxy-3,4-dihydrocarbostyril hydrochloride was dissolved in 50 ml of methanol, and a 20% methanolic solution of sodium methylate was added to the solution in an amount of 2 moles per mole of the starting carbostyril compound. The mixture was then concentrated to dryness, and the residue was dissolved in dimethylformamide. 1.7 g of p-toluylic acid chloride was added to the solution while cooling with ice-water and the mixture was stirred for 4 hours at room temperature. The reaction mixture was poured into ice-water and extracted with chloroform. A mixture of diethyl ether and petroleum benzene was added to the chloroform extract to obtain 1.94 g of crystalline 5-(1-hydroxy-2-isopropylaminobutyl)-8-p-methylbenzoyloxy-3,4-dihydrocarbostyril having a melting point of 151.5°-152.5° C. (after recrystallization from chloroform-n-hexane).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04223137
出典データセットuspto-grants-1980_09
ORD IDord-e1037e8dd75547f1aadf9b0d660bb31b
出典メモuspto-grants-1980_09