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HRID 844895作成日:2026年10月26日

Water → N-[(2,6-difluorophenyl)carbonyl]-4-(1,3,6-trimethyl-2,4-dioxo-5-pyrimidinyl)-L-phenylalanine 1-(acetoxy)ethyl ester

https://huagongshe.com/reaction/844895

反応式

関与物質

役割名称HCID仕込み量
反応物WaterHCID 962—
反応物Sodium BicarbonateHCID 516892—
反応物1-Chloroethyl acetateHCID 521865—
反応物CH9Z955RV6HCID 69337579—
溶媒DimethylformamideHCID 6228—
生成物N-[(2,6-difluorophenyl)carbonyl]-4-(1,3,6-trimethyl-2,4-dioxo-5-pyrimidinyl)-L-phenylalanine 1-(acetoxy)ethyl esterHCID 1023070966%

反応手順

To a suspension of N-[(2,6-difluorophenyl)carbonyl]-4-(1,3,6-trimethyl-2,4-dioxo-5-pyrimidinyl)-L-phenylalanine (0.743 mmol, 340 mg) and sodium bicarbonate (5.94 mmol, 499 mg) in DMF (3.0 mL) was added 1-chloroethyl acetate (5.94 mmol, 0.73 g) at room temperature. The mixture was stirred for 48 h at room temperature. Then, the reaction mixture was poured into water (50 mL) and was extracted with ethyl acetate (3×25 mL). The combined extracts were washed with brine solution (80 mL) and were dried over anhydrous sodium sulfate. Filtration of the drying agent and concentration of the filtrate gave the crude product which was purified by silica gel chromatography using a Biotage (40m) column to obtain 265 mg (66% yield) of N-[(2,6-difluorophenyl)carbonyl]-4-(1,3,6-trimethyl-2,4-dioxo-5-pyrimidinyl)-L-phenylalanine 1-(acetoxy)ethyl ester as an amorphous white solid. ES-HRMS m/e calcd for C27H27F2N3O7 (M+Na) 566.1709, found 566.1710.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06380387B1
出典データセットuspto-grants-2002_04
ORD IDord-ea99ccc1f846449f9a73b24a70d27196
出典メモuspto-grants-2002_04