戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 67483作成日:2026年10月23日

Sodium Carbonate Decahydrate → (S)-11,12,13,13a-tetrahydro-9-oxo-9H-imidazo[1,5-a]pyrrolo[2,1-c][1,4]benzodiazepine-1-carboxaldehyde-1-oxime

https://huagongshe.com/ja/reaction/67483

反応式

関与物質

役割名称HCID仕込み量
反応物Sodium Carbonate DecahydrateHCID 151402—
反応物Hydroxyamine hydrochlorideHCID 443297—
反応物(S)-11,12,13,13a-tetrahydro-9-oxo-9H-imidazo[1,5-a]pyrrolo[2,1-c][1,4]benzodiazepine-1-carboxaldehydeHCID 22822210—
溶媒WaterHCID 962—
生成物(S)-11,12,13,13a-tetrahydro-9-oxo-9H-imidazo[1,5-a]pyrrolo[2,1-c][1,4]benzodiazepine-1-carboxaldehyde-1-oximeHCID 86738267—

反応条件

温度70 °C

反応手順

A suspension of 2.67 g (10 mmol) of (S)-11,12,13,13a-tetrahydro-9-oxo-9H-imidazo[1,5-a]pyrrolo[2,1-c][1,4]benzodiazepine-1-carboxaldehyde and 0.85 g (12.5 mmol) of hydroxylamine hydrochloride in 60 ml of water is treated dropwise at room temperature with a solution of 3.57 g (12.5 mmol) of sodium carbonate decahydrate in 10 ml of water. The mixture is stirred at 70° C. for 4 hours. After cooling, the separated material is filtered off under suction, washed with water and recrystallised directly from 50 ml of dimethylformamide. There is obtained (S)-11,12,13,13a-tetrahydro-9-oxo-9H-imidazo[1,5-a]pyrrolo[2,1-c][1,4]benzodiazepine-1-carboxaldehyde-1-oxime of melting point 285° C.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04346034
出典データセットuspto-grants-1982_08
ORD IDord-bf09f41a8c194f0f87399c3ffd64e0e4
出典メモuspto-grants-1982_08