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HRID 1662025作成日:2026年10月26日

Ammonium Chloride → Ethyl 1-(4-fluorophenyl)-4-methyl-2-oxo-1,2-dihydropyridine-3-carboxylate

https://huagongshe.com/reaction/1662025

反応式

関与物質

役割名称HCID仕込み量
反応物Ammonium ChlorideHCID 25517—
反応物Dimethylformamide dimethyl acetalHCID 78373—
反応物Ethyl 2-(4-fluorophenylcarbamoyl)-3-methylbut-2-enoateHCID 66767015—
溶媒Ethyl AcetateHCID 8857—
生成物Ethyl 1-(4-fluorophenyl)-4-methyl-2-oxo-1,2-dihydropyridine-3-carboxylateHCID 6676714362.5%

反応条件

温度90 °C

反応手順

A mixture of ethyl 2-(4-fluorophenylcarbamoyl)-3-methylbut-2-enoate (1.85 g, 6.97 mmol) and N,N-dimethylformamide dimethyl acetal (5 mL, 37.45 mmol) is stirred at 90° C. for 90 min. After the reaction is cooled, EtOAc (30 mL) and saturated NH4Cl solution (20 mL) are added. The organic phase is separated, dried and concentrated. The residue is purified by silica gel column chromatography eluting with DCM:MeOH (10:1). The fractions containing product are concentrated, and the residue is mixed with ether to give 1.2 g of yellow solid which is filtered and discarded. The filtrate is concentrated and purified again by silica gel column chromatography eluting with DCM:MeOH (20:1) to give the product (500 mg, 26% yield). MS (m/z): 276.1 (M+H).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08030302B2
出典データセットuspto-grants-2011_10
ORD IDord-b4bec93afae042889ba97f088d11eea0
出典メモuspto-grants-2011_10