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HRID 82236作成日:2026年10月26日

Potassium Hydroxide → (5-((Diphenylmethylene)amino)pyridin-3-yl)(7H-pyrrolo[2,3-d]pyrimidin-5-yl)methanol

https://huagongshe.com/reaction/82236

反応式

関与物質

役割名称HCID仕込み量
反応物Potassium HydroxideHCID 14797—
反応物Ammonium ChlorideHCID 25517—
反応物7H-Pyrrolo(2,3-d)pyrimidineHCID 261591—
反応物5-((Diphenylmethylene)amino)nicotinaldehydeHCID 86672101—
溶媒MethanolHCID 887—
生成物(5-((Diphenylmethylene)amino)pyridin-3-yl)(7H-pyrrolo[2,3-d]pyrimidin-5-yl)methanolHCID 8667211062%

反応手順

A mixture of 7H-pyrrolo[2,3-d]pyrimidine (Preparation 202, 953 mg, 8.0 mmol), 5-[(diphenylmethylene)amino]nicotinaldehyde (Preparation 106, 3340 mg, 11.7 mmol) and KOH (1350 mg, 24 mmol) in MeOH (16 mL) was stirred for 16 hours at room temperature. The reaction was neutralized with saturated aqueous ammonium chloride solution and the mixture was extracted with EtOAc (3×200 mL). The combined organic layers were dried over sodium sulfate and concentrated in vacuo to obtain a crude residue. The crude material was purified by column chromatography on silica gel (EtOAc:MeOH=100:0 to 80:20,) to give the desired compound as a solid in 62% yield, 2003 mg.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08846698B2
出典データセットuspto-grants-2014_09
ORD IDord-c70979a564954ea4a279e7475fa73bef
出典メモuspto-grants-2014_09