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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 15124생성일: 2026년 10월 25일

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

https://huagongshe.com/reaction/15124

반응식

참여 물질

역할이름HCID투입량
반응물FormaldehydeHCID 712—
반응물Ethyl AcetateHCID 8857—
반응물Potassium CarbonateHCID 11430—
반응물Methyl [3-chloro-6-(methyloxy)-[1,5]naphthyridin-4-yl]acetateHCID 57707490—
촉매Benzyl triethylammonium chlorideHCID 66133—
용매WaterHCID 962—
용매CyclohexaneHCID 8078—
생성물Methyl 2-[3-chloro-6-(methoxy)-1,5-naphthyridin-4-yl]-2-propenoateHCID 5748686889%

반응 조건

온도80 °C

반응 단계

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%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07732460B2
출처 데이터셋uspto-grants-2010_06
ORD IDord-6b4e56ec1d8f4d4cac9a4ee473daecdc
출처 메모uspto-grants-2010_06