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HRID 128632作成日:2026年10月26日

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

https://huagongshe.com/reaction/128632

反応式

関与物質

役割名称HCID仕込み量
反応物WaterHCID 962—
反応物Methyl 5-(4-methoxyanilino)-1,8-naphthyridine-2-carboxylateHCID 19374293—
反応物LithiumtriethylborohydrideHCID 23664628—
溶媒TetrahydrofuranHCID 8028—
生成物5-(4-Methoxyanilino)-1,8-naphthyridin-2-ylmethanolHCID 19374262—

反応条件

温度0 °C

反応手順

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.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05464781
出典データセットuspto-grants-1995_11
ORD IDord-849c8c1917134b6f811ca33b593a73ef
出典メモuspto-grants-1995_11