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HRID 338827作成日:2026年10月27日

Pyridine → (S)-benzyl 3-carbamoyl-3-methylpyrrolidine-1-carboxylate

https://huagongshe.com/reaction/338827

反応式

関与物質

役割名称HCID仕込み量
反応物PyridineHCID 1049—
反応物Di-tert-butyl dicarbonateHCID 90495—
反応物(S)-1-((benzyloxy)carbonyl)-3-methylpyrrolidine-3-carboxylic acidHCID 76853756—
反応物Water ammonium hydroxideHCID 86589665—
溶媒WaterHCID 962—
溶媒Ethyl AcetateHCID 8857—
生成物(S)-benzyl 3-carbamoyl-3-methylpyrrolidine-1-carboxylateHCID 8670739895.6%

反応手順

To a mixture of (S)-1-(benzyloxycarbonyl)-3-methylpyrrolidine-3-carboxylic acid (32.87 g, 124.8 mmol), Boc2O (29.97 g, 137.3 mmol) in ethyl acetate (200 mL) was added pyridine (12.62 mL, 156.1 mmol) and the reaction mixture was stirred at ambient temperature for 3 hours. A solution of 28-30% w/w NH4OH/water (21.79 mL, 162.3 mmol) was added. The reaction was stirred at ambient temperature for 5 hours. Water (50 mL) was added. The organic layer was separated, washed with 1N HCl (50 mL) and brine, dried and concentrated under reduced pressure to give (S)-benzyl 3-carbamoyl-3-methylpyrrolidine-1-carboxylate (31.30 g, 119.3 mmol, 95.6% yield) as an oil.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08889704B2
出典データセットuspto-grants-2014_11
ORD IDord-a151995ce2644fc89a3d897ae133fc4c
出典メモuspto-grants-2014_11