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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 73733생성일: 2026년 10월 23일

Thionyl Chloride → 5-bromo-6-chloro-N-(4-(trifluoromethoxy)phenyl)nicotinamide

https://huagongshe.com/ko/reaction/73733

반응식

참여 물질

역할이름HCID투입량
반응물Thionyl ChlorideHCID 24386—
반응물DiisopropylethylamineHCID 81531—
반응물5-Bromo-6-chloropyridine-3-carboxylic acidHCID 285433—
반응물4-(Trifluoromethoxy)anilineHCID 600848—
용매TolueneHCID 1140—
용매DimethylformamideHCID 6228—
용매TetrahydrofuranHCID 8028—
생성물5-bromo-6-chloro-N-(4-(trifluoromethoxy)phenyl)nicotinamideHCID 86702595—

반응 조건

온도85 °C

반응 단계

A stirred solution of 5-bromo-6-chloro-nicotinic acid (375 g, 1.586 mol) and DMF (37 mL) in toluene (3.1 L) was treated dropwise with SOCl2 (347 mL, 4.758 mol) at RT and then stirred at 85° C. for 2.5 h. The solvent was evaporated off under reduced pressure and the residue was dissolved in THF (3.1 L), cooled to −25° C., treated firstly with DIPEA (543 mL, 3.172 mol) and then by the dropwise addition of a solution of 4-(trifluoromethoxy)aniline (295 g, 1.665 mol) in THF (3.1 L), After 30 min at 10° C. the solvent was evaporated off under reduced pressure and the residue was dissolved in TBME (4 L), washed with 1N HCl (2×1 L), a sat. solution of NaHCO3 (1 L) and brine (2×200 mL) and dried over Na2SO4. The solvent was evaporated off under reduced pressure and the product was crystallized from EtOAc/n-heptane to give the title compound as a beige crystalline solid. UPLC-MS (Condition 3) tR=1.25 min, m/z=393/395/397 [M−H]−; 1H-NMR (400 MHz, DMSO-d6) δ ppm 7.40 (d, J=8.60 Hz, 2H) 7.86 (d, J=8.60 Hz, 2H) 8.73 (d, J=2.20 Hz, 1H) 8.92 (d, J=2.20 Hz, 1H) 10.69 (s, 1H).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08829195B2
출처 데이터셋uspto-grants-2014_09
ORD IDord-9479971ea90d4884b669062ec6730206
출처 메모uspto-grants-2014_09