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HRID 1606992作成日:2026年10月25日

Iodine → 7-chloro-4,5-dihydro-3-(2-iodoethynyl)-5-methyl-6H-imidazo[1,5-a][1,4]benzodiazepin-6-one

https://huagongshe.com/reaction/1606992

反応式

関与物質

役割名称HCID仕込み量
反応物IodineHCID 807—
反応物Sodium HydroxideHCID 14798—
反応物7-chloro-3-ethynyl-4,5-dihydro-5-methyl-6H-imidazo[1,5-a][1,4]benzodiazepin-6-oneHCID 19851533—
溶媒MethanolHCID 887—
溶媒WaterHCID 962—
生成物7-chloro-4,5-dihydro-3-(2-iodoethynyl)-5-methyl-6H-imidazo[1,5-a][1,4]benzodiazepin-6-oneHCID 19851516—

反応手順

2.72 g (10 mmol) of 7-chloro-3-ethynyl-4,5-dihydro-5-methyl-6H-imidazo[1,5-a][1,4]benzodiazepin-6-one was suspended in 30 ml of methanol and cooled to 10°. There were then added simultaneously thereto in portions within about 10 minutes 5 ml of 28% sodium hydroxide solution and 3 g of iodine. After stirring at room temperature for 1 hour the suspension was diluted with about 30 ml of water, suction filtered and the suction filter cake was dried. By two recrystallizations from methylene chloride and ethyl acetate and from dioxane there was obtained 7-chloro-4,5-dihydro-3-(2-iodoethynyl)-5-methyl-6H-imidazo[1,5-a][1,4]benzodiazepin-6-one of melting point 215°-216°.

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-7c5d21ccf5ea48d69ca4307184a1ac4d
出典メモuspto-grants-1989_09