돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 240525생성일: 2026년 10월 26일

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

https://huagongshe.com/reaction/240525

반응식

참여 물질

역할이름HCID투입량
반응물TriethylamineHCID 8471—
반응물Oxalyl chlorideHCID 65578—
반응물5-Bromonicotinic acidHCID 88707—
반응물3,5-DifluoroanilineHCID 96595—
용매Acetic AcidHCID 176—
용매DimethylformamideHCID 6228—
용매DichloromethaneHCID 6344—
생성물5-bromo-N-(3,5-difluorophenyl)nicotinamideHCID 4160114993%

반응 단계

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)+.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08648084B2
출처 데이터셋uspto-grants-2014_02
ORD IDord-43a336d3036a41efac28a8d6ccaa9a9b
출처 메모uspto-grants-2014_02