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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 128634생성일: 2026년 10월 26일

Aluminum(III) Chloride → 6-Hydroxy-4-(4-methoxyanilino)-7-methyl-1,8-naphthyridine-3-carboxylic acid hemihydrate

https://huagongshe.com/reaction/128634

반응식

참여 물질

역할이름HCID투입량
반응물Aluminum(III) ChlorideHCID 6451240—
반응물Ethyl 6-ethoxy-4-(4-methoxyanilino)-7-methyl-1,8-naphthyridine-3-carboxylateHCID 9907935—
용매DichloromethaneHCID 6344—
생성물6-Hydroxy-4-(4-methoxyanilino)-7-methyl-1,8-naphthyridine-3-carboxylic acid hemihydrateHCID 67624807—

반응 단계

A mixture of ethyl 4-(4-methoxyanilino)-6-ethoxy-7-methyl-1,8-naphthyridine-3-carboxylate (2.9 g) in dichloromethane (45 ml) was added rapidly to a suspension of powdered anhydrous aluminium chloride (12.8 g) in dichloromethane (115 ml) with stirring. The mixture was stirred for 24 hours at ambient temperature and then poured into ice/water. The mixture was stirred for 30 minutes then filtered. The residue was basified and partitioned between dichloromethane and water. The aqueous layer was evaporated to dryness. The residue was dissolved in propan-2-ol (150 ml) and then purified by column chromatography to give 6-hydroxy-4-(4-methoxyanilino)-7-methyl-1,8-naphthyridine-3-carboxylic acid hemihydrate, m.p. 267°-268° C. (with decomposition).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05464781
출처 데이터셋uspto-grants-1995_11
ORD IDord-e25a5979be754341adcd7bb4818aa142
출처 메모uspto-grants-1995_11