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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 47458생성일: 2026년 10월 23일

Methanol → 3-(5-methyl-1H-tetrazol-1-yl)pyridine-4-carboxylic acid

https://huagongshe.com/ko/reaction/47458

반응식

참여 물질

역할이름HCID투입량
반응물MethanolHCID 887—
반응물Acetic AnhydrideHCID 7918—
반응물Sodium AzideHCID 33557—
반응물3-Aminoisonicotinic acidHCID 459531—
생성물3-(5-methyl-1H-tetrazol-1-yl)pyridine-4-carboxylic acidHCID 22172664—

반응 단계

3-Aminopyridine-4-carboxylic acid (50.0 g, 0.36 mol) was suspended in acetic anhydride (250 mL) then heated at reflux for 2 hours. The reaction mixture was concentrated under vacuum. The solid residue was slurried with heptane then concentrated under vacuum. The resulting solid was covered with acetic acid (300 mL), then sodium azide (23.5 g, 0.36 mol) was added. The reaction exothermed to 50° C. The reaction mixture was allowed to stir at ambient temperature overnight. The precipitate was isolated by filtration then slurried with methanol and filtered. The solid was dissolved in 10% sodium hydroxide. The solution was heated on a steam bath for 30 minutes, allowed to cool to ambient temperature then neutralized with 6N hydrochloric acid. The resulting precipitate was isolated by filtration, washed with water and dried to provide 64.5 g of 3-(5-methyl-1H-tetrazol-1-yl)pyridine-4-carboxylic acid as an off white solid, m.p. 214-215° C. (decomposition).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06699878B2
출처 데이터셋uspto-grants-2004_03
ORD IDord-7a113dd9843c441590b768d08b556382
출처 메모uspto-grants-2004_03