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HRID 73503作成日:2026年10月24日

3-Methylpyridine → (2S,5R)-6-benzyloxy-7-oxo-1,6-diaza-bicyclo[3.2.1]octane-2-carboxylic acid benzyl ester

https://huagongshe.com/ja/reaction/73503

反応式

関与物質

役割名称HCID仕込み量
反応物3-MethylpyridineHCID 7970—
反応物TriphosgeneHCID 94429—
反応物Sodium BicarbonateHCID 516892—
反応物Benzyl (2S,5R)-5-((benzyloxy)amino)piperidine-2-carboxylate oxalateHCID 70673933—
溶媒WaterHCID 962—
溶媒DichloromethaneHCID 6344—
生成物(2S,5R)-6-benzyloxy-7-oxo-1,6-diaza-bicyclo[3.2.1]octane-2-carboxylic acid benzyl esterHCID 57389438—

反応条件

温度0 °C

反応手順

3-picoline (45 ml, 464, 4 eq) was added to a slurry of benzyl (2S,5R)-5-[(benzyloxy)amino]piperidine-2-carboxylate ethanedioate (50 g, 116 mmol, 1 eq) in dichloromethane (1000 ml) at 0° C., followed by a solution of triphosgene (31.0 g, 104.4 mmol, 0.9 eq) in dichloromethane (200 ml). The mixture was stirred at 0° C. until the reaction was deemed to be complete. The reaction was quenched with a solution of sodium bicarbonate (24.4 g, 290 mmol, 2.5 eq) in water (300 ml), and the layers were separated. The aqueous layer was extracted with dichloromethane (100 ml) and the combined organic layers were washed with water. The organic layer was concentrated in vacuo to give (2S,5R)-6-benzyloxy-7-oxo-1,6-diaza-bicyclo[3.2.1]octane-2-carboxylic acid benzyl ester as a solution in dichloromethane.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08829191B2
出典データセットuspto-grants-2014_09
ORD IDord-338dc3c7bae043a6b4044df29382baec
出典メモuspto-grants-2014_09