戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 1606951作成日:2026年10月25日

Sodium amide → 3-[(Z)-2-chlorovinyl]-4,5-dihydro-5-methyl-6H-imidazo-[1,5-a][1,4]benzodiazepin-6-one

https://huagongshe.com/reaction/1606951

反応式

関与物質

役割名称HCID仕込み量
反応物Sodium amideHCID 24533—
反応物(Chloromethyl)triphenylphosphonium chlorideHCID 197823—
反応物5,6-dihydro-5-methyl-6-oxo-4H-imidazo[1,5-a][1,4]benzodiazepine-3-carboxaldehydeHCID 19833020—
溶媒TetrahydrofuranHCID 8028—
生成物3-[(Z)-2-chlorovinyl]-4,5-dihydro-5-methyl-6H-imidazo-[1,5-a][1,4]benzodiazepin-6-oneHCID 86743354—

反応手順

13.50 g of an equimolar mixture of chloromethyltriphenylphosphonium chloride and sodium amide were stirred for 15 minutes with 50 ml of tetrahydrofuran, whereby the temperature rose to 42°. 6.2 g (25.7 mmol) of 5,6-dihydro-5-methyl-6-oxo-4H-imidazo[1,5-a][1,4]benzodiazepine-3-carboxaldehyde were then added portionwise thereto, the mixture was stirred at room temperature for a further hour, filtered and the filtrate was evaporated. After chromatography of the residue on silica gel while eluting with cyclohexane/ether/isopropanol (3:3:1) there was obtained 3-[(Z)-2-chlorovinyl]-4,5-dihydro-5-methyl-6H-imidazo-[1,5-a][1,4]benzodiazepin-6-one of melting point 197°-199°.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04863920
出典データセットuspto-grants-1989_09
ORD IDord-5636b61a550c457f9c91d4045d745702
出典メモuspto-grants-1989_09