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HRID 1979394作成日:2026年10月25日

Hydrochloric Acid → 1-(2-toluoylmethyl)-2-oxo-3-tert-butoxycarbonylamino-5-(3-methyl-2-butenyl)-8-methyl-1,3,4,5-tetrahydro-2H-1,5-benzodiazepine

https://huagongshe.com/reaction/1979394

反応式

関与物質

役割名称HCID仕込み量
反応物Hydrochloric AcidHCID 313—
反応物Sodium HydroxideHCID 14798—
反応物2-Bromo-2'-methylacetophenoneHCID 12430676—
反応物2-oxo-3-tert-butoxycarbonylamino-5-(3-methyl-2-butenyl)-8-methyl-1,3,4,5-tetrahydro-2H-1,5-benzodiazepineHCID 21201744—
触媒Tetrabutylammonium BromideHCID 74236—
溶媒TolueneHCID 1140—
生成物1-(2-toluoylmethyl)-2-oxo-3-tert-butoxycarbonylamino-5-(3-methyl-2-butenyl)-8-methyl-1,3,4,5-tetrahydro-2H-1,5-benzodiazepineHCID 2120166759.3%

反応手順

2-Oxo-3-tert-butoxycarbonylamino-5-(3-methyl-2-butenyl)-8-methyl-1,3,4,5-tetrahydro-2H-1,5-benzodiazepine (965 mg) was suspended in toluene (14 ml), 2-bromo-2′-methylacetophenone (686 mg), 1N aqueous sodium hydroxide (7 ml) and tetran-butylammonium bromide (20 mg) were added, and the mixture was stirred overnight at room temperature. The reaction mixture was weakly acidified with 1N hydrochloric acid, extracted with methylene chloride. The organic layer was washed with saturated aqueous sodium bicarbonate, dried over anhydrous sodium sulfate, the solvent was evaporated under reduced pressure, and the residue was purified by silica gel column chromatography(chloroform:ethyl acetate=10:1), to thereby obtain 782 mg 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-0da8bf8cbca04f5fae723230506dd636
出典メモuspto-grants-2001_05