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HRID 1046015作成日:2026年10月26日

Water → Methyl 1-(4-fluorophenyl)-2-oxo-1,2-dihydropyridine-3-carboxylate

https://huagongshe.com/reaction/1046015

反応式

関与物質

役割名称HCID仕込み量
反応物WaterHCID 962—
反応物4-FluoroanilineHCID 9731—
反応物Methyl 2-oxo-2H-pyran-3-carboxylateHCID 117704—
反応物1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochlorideHCID 2723939—
触媒4-(Dimethylamino)pyridineHCID 14284—
溶媒DimethylformamideHCID 6228—
生成物Methyl 1-(4-fluorophenyl)-2-oxo-1,2-dihydropyridine-3-carboxylateHCID 21081723—

反応手順

To a solution of 4-fluoroaniline (6.5 g, 58.4 mmol) in DMF (30 mL) at ice bath temperature was added methyl 2-oxo-2H-pyran-3-carboxylate (9.0 g, 58.4 mmol). The resulting mixture was stirred for 15 min cold and was then warmed to ambient temp for 3 hours. N-(3-Dimethylaminopropyl)-N′-ethylcarbodiimide hydrochloride (EDCI—HCl) (13.5 g, 70.0 mmol) and DMAP (1.43 g, 11.7 mmol) were added and the resulting mixture was stirred at ambient temp overnight. The reaction mixture was poured into water (300 mL), extracted with ethyl acetate (3×100 mL), washed with brine, dried over anhydrous Na2SO4 and concentrated in vacuo to obtain methyl 1-(4-fluorophenyl)-2-oxo-1,2-dihydropyridine-3-carboxylate. This crude product was used for the next step without further purification.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08569319B2
出典データセットuspto-grants-2013_10
ORD IDord-5b21c090da10449881c1e6e5cd981550
出典メモuspto-grants-2013_10