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HRID 1698769作成日:2026年10月25日

Potassium Carbonate → (R)-2-((tert-Butoxycarbonyl)amino)-3-((2-nitrophenyl)amino)propanoic acid

https://huagongshe.com/reaction/1698769

反応式

関与物質

役割名称HCID仕込み量
反応物Potassium CarbonateHCID 11430—
反応物1-Fluoro-2-nitrobenzeneHCID 73895—
反応物3-Amino-N-(tert-butoxycarbonyl)-D-alanineHCID 7020984—
溶媒DimethylformamideHCID 6228—
生成物(R)-2-((tert-Butoxycarbonyl)amino)-3-((2-nitrophenyl)amino)propanoic acidHCID 5451259899%

反応条件

温度70 °C

反応手順

To a solution of 2-fluoronitrobenzene (3.45 g) in N,N-dimethylformamide (60 mL), (R)-(−)-2-tert-butoxycarbonylamino-3-amino-propionic acid (5 g) and potassium carbonate (6.77 g) were added, followed by stirring overnight at 70° C. The reaction mixture was allowed to cool down, poured into ice water, and then extracted with ethyl acetate. After 1 N hydrochloric acid was added to the aqueous layer to adjust pH to 3, the aqueous layer was extracted with ethyl acetate. The organic layer was washed with brine and dried over anhydrous sodium sulfate. The solvent was then evaporated under reduced pressure. n-Hexane was added to the residue to for crystallization. The resultant crystals were collected by filtration, whereby the title compound (7.9 g) was obtained. Yield: 99%.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06344452B1
出典データセットuspto-grants-2002_02
ORD IDord-19f5d793898a4c83b763ac3eed7429f5
出典メモuspto-grants-2002_02