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HRID 1433746作成日:2026年10月27日

Pyridine → (1-Fluorocarbonyl-2-phenyl-propyl)-carbamic acid tert-butyl ester

https://huagongshe.com/reaction/1433746

反応式

関与物質

役割名称HCID仕込み量
反応物PyridineHCID 1049—
反応物Cyanuric fluorideHCID 12664—
反応物(2S,3S)-2-((tert-Butoxycarbonyl)amino)-3-phenylbutanoic acidHCID 7021178—
溶媒DichloromethaneHCID 6344—
生成物(1-Fluorocarbonyl-2-phenyl-propyl)-carbamic acid tert-butyl esterHCID 87517560—

反応手順

To a solution of (2S,3S)-2-tert-butoxycarbonylamino-3-phenyl-butyric acid (838 mg, 3.0 mmol) in dichloromethane (10 mL) at −35° C. was added dry pyridine (255 μL, 3.15 mmol) and cyanuric fluoride (375 μL, 4.5 mmol) under an atmosphere of dry argon. The mixture was stirred for 1.5 hours while maintaining the temperature between −35 and −25° C. A small amount of ice was added to the reaction mixture and the mixture stirred vigorously for 15 minutes. The organic layer was decanted away from the aqueous solution and the aqueous layer extracted with dichloromethane (2×10 mL). The combined organic layers were washed with ice cold water (15 mL), dried over sodium sulfate, filtered and concentrated in vacuo to give (1-fluorocarbonyl-2-phenyl-propyl)-carbamic acid tert-butyl ester which was used in the subsequent step without further purification.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07612212B2
出典データセットuspto-grants-2009_11
ORD IDord-0dfd7448cbba4e059c35e0105354547d
出典メモuspto-grants-2009_11