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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 639346생성일: 2026년 10월 26일

Cyclopropanemethanol → 6-(4-Fluoro-phenyl)-5-cyclopropylmethoxy-pyrazine-2-carboxylic acid

https://huagongshe.com/reaction/639346

반응식

참여 물질

역할이름HCID투입량
반응물CyclopropanemethanolHCID 75644—
반응물Potassium tert-butoxideHCID 23665647—
반응물5-Bromo-6-(4-fluoro-phenyl)-pyrazine-2-carboxylic acid methyl esterHCID 86616957—
용매TetrahydrofuranHCID 8028—
생성물6-(4-Fluoro-phenyl)-5-cyclopropylmethoxy-pyrazine-2-carboxylic acidHCID 67504783—

반응 단계

Cyclopropyl-methanol (2.2 g, 30.6 mmol, 10.0 eq) was dissolved in dry tetrahydrofuran (10 ml, 20 vol) and potassium tert-butoxide (3.4 g, 30.6 mmol, 10.0 eq) added portion-wise. After stirring for 15 minutes at room temperature 5-bromo-6-(4-fluoro-phenyl)-pyrazine-2-carboxylic acid methyl ester (0.95 g, 3.06 mmol, 1.0 eq) was added drop-wise as a tetrahydrofuran (10 ml) solution. The reaction mixture was stirred overnight at room temperature or until deemed complete by HPLC-MS analysis. The solution was concentrated in vacuo and the residue re-dissolved in ethyl acetate (20 ml). The resulting solution was washed with water (5 ml) and the aqueous phase extracted with ethyl acetate (10 ml). The combined organic phases were dried over magnesium sulphate, filtered and concentrated in vacuo to afford 6-(4-fluoro-phenyl)-5-cyclopropylmethoxy-pyrazine-2-carboxylic acid. Yield=0.89 g (75%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07691863B2
출처 데이터셋uspto-grants-2010_04
ORD IDord-7d7136ad268a4ef39163d7a29ce897a4
출처 메모uspto-grants-2010_04