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HRID 1685524Erstellt: 25. Oktober 2026

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

https://huagongshe.com/reaction/1685524

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktTriethylamineHCID 8471—
EduktOxalyl chlorideHCID 65578—
Edukt5-Bromonicotinic acidHCID 88707—
Edukt3,5-DifluoroanilineHCID 96595—
LösungsmittelAcetic AcidHCID 176—
LösungsmittelDimethylformamideHCID 6228—
LösungsmittelDichloromethaneHCID 6344—
Produkt5-bromo-N-(3,5-difluorophenyl)nicotinamideHCID 4160114993%

Reaktionsschritte

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)+.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08148408B2
Quelldatensatzuspto-grants-2012_04
ORD IDord-f52c81fc79e24d85b3f93f6952166dde
Quellennotizuspto-grants-2012_04