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HRID 1704755作成日:2026年10月25日

1-ethyl-4-hydrazino-1H-pyrazolo[3,4-b]pyridine-5-carboxylic acid, ethyl ester → 8-Ethyl-4H-pyrazolo[4',3':5,6]pyrido[3,4-e][1,2,4]-triazolo[1,5-a]pyrimidin-5(8H)-one

https://huagongshe.com/reaction/1704755

反応式

関与物質

役割名称HCID仕込み量
反応物1-ethyl-4-hydrazino-1H-pyrazolo[3,4-b]pyridine-5-carboxylic acid, ethyl esterHCID 162357—
反応物Methanimidic acid, N-cyano-, ethyl esterHCID 9920370—
溶媒1,4-DioxaneHCID 31275—
生成物8-Ethyl-4H-pyrazolo[4',3':5,6]pyrido[3,4-e][1,2,4]-triazolo[1,5-a]pyrimidin-5(8H)-oneHCID 135593852—

反応手順

249 g. of 1-ethyl-4-hydrazino-1H-pyrazolo[3,4-b]-pyridine-5-carboxylic acid, ethyl ester (1 mol.) are refluxed in 1.5 liters of dry dioxane together with 98 g. of ethoxymethylene cyanamide for 12 hours. After cooling to room temperature, the precipitated 8-ethyl-4H-pyrazolo[4',3':5,6]pyrido[3,4-e][1,2,4]triazolo[1,5-a]-pyrimidin-5(8H)-one is filtered off and recrystallized from dimethylformanide, yield 135 g. (53%); m.p. 355°-356°.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04127655
出典データセットuspto-grants-1978_11
ORD IDord-c2f4d14374094373aec83390d6410216
出典メモuspto-grants-1978_11