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HRID 67346作成日:2026年10月23日

Water → 8-fluoro-4,5-dihydro-3-(hydroxymethyl)-5-methyl-6H-imidazo [1,5-a][1,4]benzodiazepin-6-one

https://huagongshe.com/ja/reaction/67346

反応式

関与物質

役割名称HCID仕込み量
反応物WaterHCID 962—
反応物FlumazenilHCID 3373—
反応物Lithium borohydrideHCID 4148881—
反応物Hydrate;hydrochlorideHCID 21885828—
溶媒TetrahydrofuranHCID 8028—
生成物8-fluoro-4,5-dihydro-3-(hydroxymethyl)-5-methyl-6H-imidazo [1,5-a][1,4]benzodiazepin-6-oneHCID 20515340—

反応条件

温度40 °C

反応手順

15.0 g (49.5 mmol) of ethyl 8-fluoro-5,6-dihydro-5-methyl-6-oxo-4H-imidazo[1,5-a][1,4]benzodiazepine-3-carboxylate are dissolved under argon in 450 ml of boiling absolute tetrahydrofuran (filtered over Alox) and added dropwise at 50° C. to a solution of 1.1 g (49.5 mmol) of lithium borohydride in 50 ml of absolute tetrahydrofuran. The mixture is stirred at 40° C. for 4 hours and at the boiling point for 2.5 hours. Subsequently, the mixture is decomposed at 40° C. with 20 ml of water and 20 ml of concentrated hydrochloric acid/water (1:1) and stirred at room temperature overnight. After removal of the tetrahydrofuran in vacuo, the residue is treated with 14 ml of concentrated ammonia. The mixture is left to crystallise in the cold and separated material is filtered off under suction and washed with water. After recrystallisation from ethanol, there is obtained 8-fluoro-4,5-dihydro-3-(hydroxymethyl)-5-methyl-6H-imidazo[ 1,5-a][1,4]benzodiazepin-6-one of melting point 221°-223° C.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04346031
出典データセットuspto-grants-1982_08
ORD IDord-01f48751b0e04f1c933bb4f701c04f98
出典メモuspto-grants-1982_08