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HRID 15124作成日:2026年10月26日

Formaldehyde → Methyl 2-[3-chloro-6-(methoxy)-1,5-naphthyridin-4-yl]-2-propenoate

https://huagongshe.com/reaction/15124

反応式

関与物質

役割名称HCID仕込み量
反応物FormaldehydeHCID 712—
反応物Ethyl AcetateHCID 8857—
反応物Potassium CarbonateHCID 11430—
反応物Methyl [3-chloro-6-(methyloxy)-[1,5]naphthyridin-4-yl]acetateHCID 57707490—
触媒Benzyl triethylammonium chlorideHCID 66133—
溶媒WaterHCID 962—
溶媒CyclohexaneHCID 8078—
生成物Methyl 2-[3-chloro-6-(methoxy)-1,5-naphthyridin-4-yl]-2-propenoateHCID 5748686889%

反応条件

温度80 °C

反応手順

To a solution of methyl [3-chloro-6-(methyloxy)-1,5-naphthyridin-4-yl]acetate (43 g, 162 mmol) in cyclohexane (1060 ml) was added benzyltriethylammonium chloride (71.2 g, 313 mmol), potassium carbonate (42 g, 304 mmol) and paraformaldehyde (42 g). The reaction mixture was then heated at 80° C. for 24 hours, cooled and treated with ethyl acetate and water. The aqueous was extracted with ethyl acetate. The combined organic phases were dried and the solvent was removed under reduced pressure. The residue was subjected to column chromatography on silica gel using a hexane and ethyl acetate gradient to provide the desired compound (40 g, 89%).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07732460B2
出典データセットuspto-grants-2010_06
ORD IDord-6b4e56ec1d8f4d4cac9a4ee473daecdc
出典メモuspto-grants-2010_06