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HRID 2232539作成日:2026年10月25日

Water → Ethyl 2-(3-methoxyphenyl)-4-quinazolinepropionate

https://huagongshe.com/reaction/2232539

反応式

関与物質

役割名称HCID仕込み量
反応物WaterHCID 962—
反応物TriethylamineHCID 8471—
反応物m-Anisoyl chlorideHCID 74374—
反応物Ethyl 4-(2-aminophenyl)-4-oxobutanoateHCID 21283602—
溶媒ChloroformHCID 6212—
生成物Ethyl 2-(3-methoxyphenyl)-4-quinazolinepropionateHCID 13769245—

反応手順

3-Methoxybenzoyl chloride (2.81 cc) is added at 5° C. to ethyl 3-(2-aminobenzoyl)propionate (2.21 g) and triethylamine (4.2 cc) in chloroform (25 cc). The mixture is left for 1 hour at room temperature (approximately 20° C.), water (25 cc) is added and the mixture decanted. The organic phase is evaporated under reduced pressure and the residue taken up with ammonium acetate (17 g). The mixture is brought to 100° C. for 7 hours and the acetic acid formed is then evaporated off under reduced pressure. The residue is poured into water (100 cc) and the aqueous phase extracted with ethyl acetate (3×50 cc). The aqueous phase is dried over magnesium sulphate, filtered and evaporated to dryness under reduced pressure. The residual product is chromatographed in silica gel with a cyclohexane/ethyl acetate (1:1 by volume) mixture as eluant. After recrystallization in ethanol, ethyl 2-(3-methoxyphenyl)-4-quinazolinepropionate (1.5 g), m.p. 70° C., is obtained.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04788204
出典データセットuspto-grants-1988_11
ORD IDord-718be82b29314e4eb59ec196f96c8a45
出典メモuspto-grants-1988_11