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HRID 47459作成日:2026年10月24日

Dimethylformamide diethylacetal → ethyl 3-(5-methyl-1H-tetrazol-1-yl)pyridine-4-carboxylate

https://huagongshe.com/ja/reaction/47459

反応式

関与物質

役割名称HCID仕込み量
反応物Dimethylformamide diethylacetalHCID 70913—
反応物3-(5-methyl-1H-tetrazol-1-yl)pyridine-4-carboxylic acidHCID 22172664—
溶媒DichloromethaneHCID 6344—
生成物ethyl 3-(5-methyl-1H-tetrazol-1-yl)pyridine-4-carboxylateHCID 22172739—

反応手順

Dimethylformamide diethyl acetal (46 mL) was added to a suspension of 3-(5-methyl-1H-tetrazol-1-yl)pyridine-4-carboxylic acid (36 g) in dichloromethane (800 mL). The reaction mixture was stirred at ambient temperature overnight then washed six times with water (500 mL), dried over magnesium sulfated, and concentrated under vacuum. The residue was recrystallized from ethyl acetate/hexanes to provide 40 g of ethyl 3-(5-methyl-1H-tetrazol-1-yl)pyridine-4-carboxylate as a solid.

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-e2660c48de33439390b2a581508cb241
出典メモuspto-grants-2004_03