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HRID 1979464作成日:2026年10月26日

3-Bromocyclohexene → (3R)-(-)-2-oxo-3-tert-butoxycarbonylamino-5-(2-cyclohexen-1-yl)-1,3,4,5-tetrahydro-2H-1,5-benzodiazepine

https://huagongshe.com/reaction/1979464

反応式

関与物質

役割名称HCID仕込み量
反応物3-BromocyclohexeneHCID 137057—
反応物Sodium BicarbonateHCID 516892—
反応物(R)-2-oxo-3-tert-butoxycarbonylamino-1,3,4,5-tetrahydro-2H-1,5-benzodiazepineHCID 12988641—
溶媒DimethylformamideHCID 6228—
生成物(3R)-(-)-2-oxo-3-tert-butoxycarbonylamino-5-(2-cyclohexen-1-yl)-1,3,4,5-tetrahydro-2H-1,5-benzodiazepineHCID 53946939100%

反応条件

温度50 °C

反応手順

3-Bromocyclohexene (7.06 g) and sodium bicarbonate (3.68 g) were added to a solution of (R)-(+)-2-oxo-3-tert-butoxycarbonylamino-1,3,4,5-tetrahydro-2H-1,5-benzodiazepine (6.08 g) in anhydrous N,N-dimethylformamide (50 ml), and the mixture was stirred at 50° C. for one hour. The reaction mixture was allowed to cool, ice-water was added, and extracted with ethyl acetate. The organic layer was washed with saturated brine, dried over anhydrous sodium sulfate. The solvent was evaporated under reduced pressure,the residue was purified by silica gel column chromatography(ethyl acetate:n-hexane=1:3), to thereby obtain 7.84 g of the titled compound.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06239131B1
出典データセットuspto-grants-2001_05
ORD IDord-c75f7bbd45844e82a5bc132c9d783059
出典メモuspto-grants-2001_05