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HRID 1979470作成日:2026年10月26日

Sodium Bicarbonate → (3R)-2-oxo-3-tert-butoxycarbonylamino-5-[(1S)-2-pinen-10-yl]-1,3,4,5-tetrahydro-2H-1,5-benzodiazepine

https://huagongshe.com/reaction/1979470

反応式

関与物質

役割名称HCID仕込み量
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—
反応物(1s)-10-Chloro-2-pineneHCID 57140078—
溶媒MethanolHCID 887—
生成物(3R)-2-oxo-3-tert-butoxycarbonylamino-5-[(1S)-2-pinen-10-yl]-1,3,4,5-tetrahydro-2H-1,5-benzodiazepineHCID 7023961861.6%

反応手順

Sodium bicarbonate (2.02 g) and (1s)-10-chloro-2-pinene (4.1 g) were added to a solution of (R)-2-oxo-3-tert-butoxycarbonylamino-1,3,4,5-tetrahydro-2H-1,5-benzodiazepine (2.22 g) in anhydrous methanol (40 ml), and the mixture was refluxed overnight. The reaction mixture was concentrated under reduced pressure, water (200 ml) was added, and extracted with ethyl acetate (200 ml) twice. 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(n-hexane:ethyl acetate=4:1), to thereby obtain 2.03 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-847d882c8ab7426e9a72ca5617f6ae22
出典メモuspto-grants-2001_05