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HRID 1463548作成日:2026年10月26日

Ethanol → N-Boc-4-cyanophenylalanine-N-methylamide

https://huagongshe.com/reaction/1463548

反応式

関与物質

役割名称HCID仕込み量
反応物EthanolHCID 702—
反応物4-MethylmorpholineHCID 7972—
反応物PentafluorophenolHCID 13041—
反応物N-(tert-Butoxycarbonyl)-4-cyano-L-phenylalanineHCID 7020841—
溶媒DichloromethaneHCID 6344—
生成物N-Boc-4-cyanophenylalanine-N-methylamideHCID 2285121092%

反応手順

A solution of N-Boc-4-cyanophenylalanine (1.92 g, 6.6 mmol) and pentafluorophenol (2.43 g, 13.2 mmol) in CH2Cl2 (30 ml) at 0° C. was treated with 4-methylmorpholine (0.74 g, 7.3 mmol). After stirring the reaction mixture for 3 hours, 8M methylazine in ethanol (15 ml, 19.8 mmol) was added and the reaction mixture left to stir at room temperature for 16 hours. The solvent was removed under pressure, the residue dissolved in CH2Cl2 (50 ml) and washed with saturated sodium bicarbonate (2×50 ml) , 1M citric acid (2×50 ml) and brine (50 ml). The CH2Cl2 layer was dried over MgSO4 and the solvent removed under pressure to yield the title compound as a white solid (1.84 g, 92%).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05300674
出典データセットuspto-grants-1994_04
ORD IDord-9949f6ba5f064ab3845911c82f62e8b6
出典メモuspto-grants-1994_04