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HRID 1649235作成日:2026年10月27日

Vesnarinone → 1-Benzyl-6-[4-(3,4-dimethoxybenzoyl)-1-piperazinyl]-3,4-dihydrocarbostyril hemihydrate

https://huagongshe.com/reaction/1649235

反応式

関与物質

役割名称HCID仕込み量
反応物VesnarinoneHCID 5663—
反応物DimethylformamideHCID 6228—
反応物Benzyl ChlorideHCID 7503—
反応物Sodium hydrideHCID 24758—
溶媒WaterHCID 962—
生成物1-Benzyl-6-[4-(3,4-dimethoxybenzoyl)-1-piperazinyl]-3,4-dihydrocarbostyril hemihydrateHCID 88739270—

反応手順

6-[4-(3,4-Dimethoxybenzoyl)-1-piperazinyl]-3,4-dihydrocarbostyril (500 mg) and 70 mg of 60% oily sodium hydride were mixed with 5 ml of DMF and stirred at room temperature for 1 hour. Then, to the mixture was added dropwise 3 ml of DMF solution containing 0.17 ml of benzylchloride. After stirring for 4 hours at room temperature, the reaction mixture was poured into a large amount of water and organic substances were extracted with chloroform. The chloroform layer was washed with water and dehydrated. Chloroform was distilled off and the residue was recrystallized from ethanol to give 150 mg of 1-benzyl-6-[4-(3,4-dimethoxybenzoyl)-1-piperazinyl]-3,4-dihydrocarbostyril hemihydrate, m.p. 131.5°-132.5° C., yellow powders. Elemental Analysis for

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04415572
出典データセットuspto-grants-1983_11
ORD IDord-9f8f5f37da7c44aab41dab4ec74ca058
出典メモuspto-grants-1983_11