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HRID 895927作成日:2026年10月25日

Water → N-[(2,6-dichlorophenyl)carbonyl]-4-[1,6-dimethyl-4-(trifluoromethyl)-2-oxo-3-pyridinyl]-L-phenylalanine ethyl ester

https://huagongshe.com/reaction/895927

反応式

関与物質

役割名称HCID仕込み量
反応物WaterHCID 962—
反応物IodoethaneHCID 6340—
反応物Sodium BicarbonateHCID 516892—
反応物RO-0505376HCID 9806910—
溶媒DimethylformamideHCID 6228—
生成物N-[(2,6-dichlorophenyl)carbonyl]-4-[1,6-dimethyl-4-(trifluoromethyl)-2-oxo-3-pyridinyl]-L-phenylalanine ethyl esterHCID 1020960185%

反応手順

To a suspension of N-[(2,6-dichlorophenyl)carbonyl]-4-[1,6-dimethyl-4-(trifluoromethyl)-2-oxo-3-pyridinyl]-L-phenylalanine (145 mg, 0.275 mmol) and sodium bicarbonate (185 mg, 2.2 mmol) in DMF (2 mL) was added iodoethane (343 mg, 2.2 mmol) at room temperature. The mixture was stirred for 72 h at room temperature. Then, the reaction mixture was poured into water (30 mL) and was extracted with ethyl acetate (3×20 mL). The combined organic extracts were washed with brine solution (60 mL) and were dried over anhydrous magnesium sulfate. Filtration of the drying agent and concentration of the filtrate gave 129 mg (85% yield) of N-[(2,6-dichlorophenyl)carbonyl]-4-[1,6-dimethyl-4-(trifluoromethyl)-2-oxo-3-pyridinyl]-L-phenylalanine ethyl ester as a crystalline white solid: mp 86-91° C. ES-HRMS m/e calcd for C26H23Cl2F3N2O4 (M+Na) 577.0876. found 577.0887.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06916933B2
出典データセットuspto-grants-2005_07
ORD IDord-d3364df3e22d41a78f7b65f355bbe18d
出典メモuspto-grants-2005_07