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HRID 731985作成日:2026年10月25日

Ammonium Acetate → 3-[(3-fluoro-6-methylphenanthridin-5(6H)-yl)carbonyl]phenol

https://huagongshe.com/reaction/731985

反応式

関与物質

役割名称HCID仕込み量
反応物Ammonium AcetateHCID 517165—
反応物Sodium cyanoborohydrideHCID 5003444—
反応物1-(2',4'-Difluoro-1,1'-biphenyl-2-yl)ethanoneHCID 22482272—
反応物1-[2-(2,4-Difluorophenyl)phenyl]ethan-1-amineHCID 22482376—
溶媒MethanolHCID 887—
生成物3-[(3-fluoro-6-methylphenanthridin-5(6H)-yl)carbonyl]phenolHCID 11500912—

反応手順

1-(-2′,4′-difluoro-biphenyl-2-yl)-ethylamine—The title compound was prepared from 1-(2′,4′-difluoro-1,1′-biphenyl-2-yl)ethanone (3.67 g, 15.8 mmol), anhydrous methanol (200 mL), ammonium acetate (12.2 g, 158 mmol), and sodium cyanoborohydride (1.99 g, 31.6 mmol) according to the procedure and in the same manner as described in Example 24, step b resulting in the isolation of a clear oil that was used without further purification. MS [(ES+), m/z]: 217 [M-16]+, benzylic cation as a result of the loss of NH2.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07585871B2
出典データセットuspto-grants-2009_09
ORD IDord-1b36fa801b1d4d6c9ac0302aa85ce949
出典メモuspto-grants-2009_09