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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 238729생성일: 2026년 10월 25일

Triethylamine → HCID 23582278, 화합물

https://huagongshe.com/reaction/238729

반응식

참여 물질

역할이름HCID투입량
반응물TriethylamineHCID 8471—
반응물4-Fluoro-3-(trifluoromethyl)benzoyl ChlorideHCID 144253—
반응물(R)-1-(3-fluoro-5-(1,1,2,2-tetrafluoroethoxy)phenyl)-1-(4-fluorophenyl)-2-phenylethanamineHCID 59458485—
용매DichloromethaneHCID 6344—
생성물HCID 23582278HCID 2358227880%

반응 단계

To a solution of (R)-1-(3-fluoro-5-(1,1,2,2-tetrafluoroethoxy)phenyl)-1-(4-fluorophenyl)-2-phenylethanamine (30 mg, 0.079 mmol) in CH2Cl2 (0.2 mL) was added 4-fluoro-3-(trifluoromethyl)benzoyl chloride (0.048 mL, 0.158 mmol), followed by Et3N (0.04 mL, 0.158 mmol). The resulting mixture was stirred at room temperature for 5 h. The crude product was purified on a preparative HPLC column type using 30 to 100% CH3CN in H2O with 0.1% TFA for 10 minutes as mobile phase. The solvent was removed under reduced pressure to afford (R)-4-fluoro-N-(1-(3-fluoro-5-(1,1,2,2-tetrafluoroethoxy)phenyl)-1-(4-fluorophenyl)-2-phenylethyl)-3-(trifluoromethyl)benzamide (35 mg, 80% yield) as white powder. LC-MS (ESI) 568.30 (M+H), retention time=4.27 min (0-100% MeOH in H2O with 0.1% TFA in a 4-min run); Analytical HPLC: 3.95 min (0-100% CH3CN in H2O with 0.1% TFA in a 4-min run, purity 100%); 1H NMR (400 MHz, CD3OD) δ ppm 3.88-4.01 (m, 1H), 4.10 (d, J=13.18 Hz, 1H), 6.69 (d, J=7.47 Hz, 2H), 6.97-7.51 (m, 11H), 7.99 (d, J=5.71 Hz, 2H), 8.90 (s, 1H).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08642576B2
출처 데이터셋uspto-grants-2014_02
ORD IDord-3d6ac3bfa4484641999e6cb3208124de
출처 메모uspto-grants-2014_02