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HRID 30401作成日:2026年10月25日

Phenylhydrazine → HCID 178518862、化合物

https://huagongshe.com/reaction/30401

反応式

関与物質

役割名称HCID仕込み量
反応物PhenylhydrazineHCID 7516—
反応物HydrazineHCID 9321—
反応物Nicotinoyl chlorideHCID 82604—
反応物1H-pyrazolo(3,4-b)pyridineHCID 2755850—
反応物2-Chloronicotinoyl chlorideHCID 2774541—
溶媒DichloromethaneHCID 6344—
溶媒TriethylamineHCID 8471—
生成物HCID 178518862HCID 178518862—

反応手順

Scheme 4 depicts the synthesis of the 1H-pyrazolo[3,4-b]pyridine q. A nicotinoylchloride k (e.g., 2-chloronicotinoyl chloride) is reacted with a hydrazine m (e.g., phenylhydrazine) and a base such as triethylamine in a solvent such as anhydrous methylene chloride to give o (e.g., 1-phenyl-1H-pyrazolo[3,4-b]pyridin-3-ol). The compound o is then cyclized by heating at 175° C. to provide p. p is reacted as in the transformation of d to g in Scheme 1 to provide q.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07423054B2
出典データセットuspto-grants-2008_09
ORD IDord-92e1e1747f1e438698152e155671ed1e
出典メモuspto-grants-2008_09