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HRID 395724作成日:2026年10月25日

Pyridine → N1-(4-methoxybenzoyl)-N2-(4-propylbenzoyl)-4-(tert-butyldimethylsilyloxy)-1,2-benzenediamine

https://huagongshe.com/reaction/395724

反応式

関与物質

役割名称HCID仕込み量
反応物PyridineHCID 1049—
反応物4-Propylbenzoyl chlorideHCID 104293—
反応物N1-(4-methoxybenzoyl)-4-(tert-butyldimethylsilyloxy)-1,2-benzenediamineHCID 54024338—
溶媒DichloromethaneHCID 6344—
生成物N1-(4-methoxybenzoyl)-N2-(4-propylbenzoyl)-4-(tert-butyldimethylsilyloxy)-1,2-benzenediamineHCID 54350608—

反応手順

To a solution of N1-(4-methoxybenzoyl)-4-(tert-butyldimethylsilyloxy)-1,2-benzenediamine (300 mg, 0.81 mmol) in methylene chloride (20 mL) was added pyridine (0.13 mL, 1.6 mmol) followed by 4-propylbenzoyl chloride (0.15 mL, 0.89 mmol). The reaction mixture was stirred for 4 h, diluted with methylene chloride, washed with saturated aqueous cupric sulfate solution, dried (magnesium sulfate), filtered, and concentrated in vacuo. The residue was chromatographed (silica gel, methylene chloride to 20% ethyl acetate/80% methylene chloride) to give 400 mg (95%) of the the title compound as a solid.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06605626B2
出典データセットuspto-grants-2003_08
ORD IDord-da33919a10a548e380113f33dfea8aa2
出典メモuspto-grants-2003_08