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HRID 240525作成日:2026年10月27日

Triethylamine → 5-bromo-N-(3,5-difluorophenyl)nicotinamide

https://huagongshe.com/reaction/240525

反応式

関与物質

役割名称HCID仕込み量
反応物TriethylamineHCID 8471—
反応物Oxalyl chlorideHCID 65578—
反応物5-Bromonicotinic acidHCID 88707—
反応物3,5-DifluoroanilineHCID 96595—
溶媒Acetic AcidHCID 176—
溶媒DimethylformamideHCID 6228—
溶媒DichloromethaneHCID 6344—
生成物5-bromo-N-(3,5-difluorophenyl)nicotinamideHCID 4160114993%

反応手順

Oxalyl chloride (1.2 mL) and DMF (25 μL) were added to 5-bromonicotinic acid (1.0 g, 4.95 mmol) suspended in CH2Cl2 (30 mL). The resulting mixture was stirred at room temperature for 12 min. It was then concentrated to dryness and azeotroped with toluene. The residual was then dissolved in toluene (30 mL). 3,5-Difluoroaniline (1.0 g, 7.8 mmol) was added followed by triethylamine (1.1 mL, 7.5 mmol). The resulting suspension was stirred at room temperature for 10 min. The reaction mixture was taken in 5% acetic acid(aq) (300 mL) and extracted with ethyl acetate (2×200 mL). The combined organic extract was washed with 1.0 M Na2CO3(aq) (2×100 mL) and brine. The organic layers were combined, dried (Na2SO4) and concentrated to dryness to provide the title compound (1.4 g, 93%). MS (APCI) m/z 313, 315 (M+H)+.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08648084B2
出典データセットuspto-grants-2014_02
ORD IDord-43a336d3036a41efac28a8d6ccaa9a9b
出典メモuspto-grants-2014_02