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HRID 47458作成日:2026年10月23日

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

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

反応式

関与物質

役割名称HCID仕込み量
反応物MethanolHCID 887—
反応物Acetic AnhydrideHCID 7918—
反応物Sodium AzideHCID 33557—
反応物3-Aminoisonicotinic acidHCID 459531—
生成物3-(5-methyl-1H-tetrazol-1-yl)pyridine-4-carboxylic acidHCID 22172664—

反応手順

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).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06699878B2
出典データセットuspto-grants-2004_03
ORD IDord-7a113dd9843c441590b768d08b556382
出典メモuspto-grants-2004_03