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HRID 2376726作成日:2026年10月26日

Pyrazol-3-ylamine → 4,6-Bis(4-fluorophenyl)-5-(4-pyridyl)-1H-pyrazolo[3,4-b]pyridine

https://huagongshe.com/reaction/2376726

反応式

関与物質

役割名称HCID仕込み量
反応物Pyrazol-3-ylamineHCID 74561—
反応物1-(4-Fluorophenyl)-2-(4-pyridyl)vinyl 4-fluorobenzoateHCID 68445862—
触媒Hydrochloric AcidHCID 313—
溶媒EthanolHCID 702—
溶媒MethanolHCID 887—
溶媒ChloroformHCID 6212—
生成物4,6-Bis(4-fluorophenyl)-5-(4-pyridyl)-1H-pyrazolo[3,4-b]pyridineHCID 1196137423%

反応手順

To a solution of 3-amino-2H-pyrazole (60 mg, 71.8 mmol) in EtOH (2 mL) and 1 drop of 37% HCl, 1-(4-fluorophenyl)-2-(4-pyridyl)vinyl 4-fluorobenzoate (0.22 g, 65.0 mmol, obtained in reference example 4) was added under argon atmosphere. This was heated to reflux for 3 days. The mixture was diluted with CHCl3 and MeOH. It was washed with saturated NaHCO3. The aqueous phase was extracted with CHCl3 (×2). The organic phase was dried over Na2SO4 and concentrated to dryness. The crude product obtained was purified by chromatography on silica gel using hexane-EtOAc mixtures of increasing polarity as eluent, to afford 58 mg of the desired product in a solid white form (yield: 23%).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07468376B2
出典データセットuspto-grants-2008_12
ORD IDord-a57c4f152ad846918e0ddb3c6980ccd6
出典メモuspto-grants-2008_12