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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 350210생성일: 2026년 10월 26일

Dimethylformamide → 3-[3-ethoxy-1-[4-(2-quinolylmethoxy)benzyl]-1H-pyrazol-4-yl]propionic acid

https://huagongshe.com/reaction/350210

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참여 물질

역할이름HCID투입량
반응물DimethylformamideHCID 6228—
반응물Potassium CarbonateHCID 11430—
반응물2-(Chloromethyl)quinoline hydrochlorideHCID 3083823—
반응물ethyl 3-[3-ethoxy-1-(4-hydroxybenzyl)-1H-pyrazol-4-yl]propionateHCID 23024904—
용매WaterHCID 962—
생성물3-[3-ethoxy-1-[4-(2-quinolylmethoxy)benzyl]-1H-pyrazol-4-yl]propionic acidHCID 6942282386.1%

반응 조건

온도80 °C

반응 단계

A mixture of ethyl 3-[3-ethoxy-1-(4-hydroxybenzyl)-1H-pyrazol-4-yl]propionate (360 mg), 2-chloromethylquinoline hydrochloride (270 mg), potassium carbonate (300 mg) and N,N-dimethylformamide (10 ml) was stirred at 80° C. for 5 hours. The reaction mixture was poured into water, and extracted with ethyl acetate. The ethyl acetate layer was washed with saturated aqueous sodium chloride solution, dried (MgSO4), and concentrated. The residue was subjected to silica gel column chromatography to obtain a colorless oily substance from the fraction eluted with ethyl acetate-hexane (1:1, volume ratio). After a mixture of the resulting oily substance, 1N aqueous sodium hydroxide solution (5 ml), tetrahydrofuran (5 ml) and ethanol (5 ml) was stirred at room temperature for 2 hours, 1N hydrochloric acid (5 ml) was added to the mixture, and then the mixture was extracted with ethyl acetate. The ethyl acetate layer was washed with saturated aqueous sodium chloride solution, dried (MgSO4) and concentrated. The resulting colorless crystals were collected by filtration to obtain 3-[3-ethoxy-1-[4-(2-quinolylmethoxy)benzyl]-1H-pyrazol-4-yl]propionic acid (420 mg, yield: 86%). This was recrystallized from acetone-hexane. Melting point: 140–141° C.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07179823B1
출처 데이터셋uspto-grants-2007_02
ORD IDord-9aa8e20c878242cb9ccad44b6e39fce8
출처 메모uspto-grants-2007_02