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HRID 1084828作成日:2026年10月25日

Pyridine → (3-Methoxyphenyl)hydrazine

https://huagongshe.com/reaction/1084828

反応式

関与物質

役割名称HCID仕込み量
反応物PyridineHCID 1049—
反応物1-(3-hydroxyphenyl)-3-phenyl-1H-pyrazolo[3,4-b]pyridineHCID 14796252—
生成物(3-Methoxyphenyl)hydrazineHCID 423605—

反応手順

Therein, among the starting compounds, for example, 1-(3-hydroxyphenyl)-3-phenyl-1H-pyrazolo[3,4-b]pyridine can be obtained by heating under reflux 2-chloro-3-benzoylpyridine and 3-methoxyphenylhydrazine in pyridine to obtain the corresponding hydrazone, and subjecting to ring-closure reaction the obtained hydrazone by heating under reflux in isopentyl alcohol with the use of potassium carbonate as a deacidifying agent to obtain 1-(3-methoxyphenyl)-3-phenyl-1H-pyrazolo[3,4-b]pyridine, followed by the elimination of the methoxy group thereof with the use of a butylmercaptanaluminium chloride system.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05006520
出典データセットuspto-grants-1991_04
ORD IDord-aa31c830ac6f4fd2b5b672117b4e011e
出典メモuspto-grants-1991_04