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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 128632생성일: 2026년 10월 26일

Water → 5-(4-Methoxyanilino)-1,8-naphthyridin-2-ylmethanol

https://huagongshe.com/reaction/128632

반응식

참여 물질

역할이름HCID투입량
반응물WaterHCID 962—
반응물Methyl 5-(4-methoxyanilino)-1,8-naphthyridine-2-carboxylateHCID 19374293—
반응물LithiumtriethylborohydrideHCID 23664628—
용매TetrahydrofuranHCID 8028—
생성물5-(4-Methoxyanilino)-1,8-naphthyridin-2-ylmethanolHCID 19374262—

반응 조건

온도0 °C

반응 단계

A mixture of methyl 5-(4-methoxyanilino)-1,8-naphthyridine-2-carboxylate (1.0 g) and dry THF (100 ml) was stirred at 0° C. while lithium triethylborohydride (a 1M solution in THF, 6.5 ml) was added over 10 minutes. After stirring at 0° C. for 1 hour further lithium triethylborohydride solution (3 ml) was added. The mixture was stirred for a further 1.5 hours at 0° C. Water (100 ml) was added cautiously and the mixture was extracted with ethyl acetate. The ethyl acetate extract was extracted with 0.5M hydrochloric acid. The acid extract was washed with ethyl acetate, basified with sodium bicarbonate and extracted with dichloromethane:methanol (3:1) (2×200 ml) to give a residue which was triturated with methanol and filtered. The solid obtained was triturated with ethyl acetate and filtered to give 5-(4-methoxyanilino)-1,8-naphthyridin-2-ylmethanol, m.p. 275°-281° C.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05464781
출처 데이터셋uspto-grants-1995_11
ORD IDord-849c8c1917134b6f811ca33b593a73ef
출처 메모uspto-grants-1995_11