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HRID 1988071作成日:2026年10月27日

Diethyl N-(4-aminobenzoyl)-L-glutamate → 2-[4-(Pyrimidin-2-ylamino)-benzoylamino]-pentanedioic acid diethyl ester

https://huagongshe.com/reaction/1988071

反応式

関与物質

役割名称HCID仕込み量
反応物Diethyl N-(4-aminobenzoyl)-L-glutamateHCID 73002—
反応物2-ChloropyrimidineHCID 74404—
溶媒DimethylformamideHCID 6228—
生成物2-[4-(Pyrimidin-2-ylamino)-benzoylamino]-pentanedioic acid diethyl esterHCID 6733420769.4%

反応条件

温度110 °C

反応手順

2-Chloropyrimidine (0.72 g, 6.3 mmol) and N-(4-aminobenzoyl)-L-glutamic acid diethyl ester (2.04 g, 6.3 mmol, 1 equiv.) were dissolved in DMF (4 mL) and the resulting mixture was heated to 110° C. for 3 hrs. Reaction was complete as determined by TLC. The mixture was cooled to room temperature and partitioned between ethyl acetate and water. The organic phase was washed with brine, dried over MgSO4, and concentrated by rotavap. The residue was purified by column chromatography (silica gel, 50% EtOAc/hexane) to afford 1.75 g of desired product 2-[4-(pyrimidin-2-ylamino)-benzoylamino]-pentanedioic acid diethyl ester in 69% yield. MS (ESI) m/z 399.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07553873B2
出典データセットuspto-grants-2009_06
ORD IDord-4842c3e460254e08a16f558392042157
出典メモuspto-grants-2009_06