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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 241434생성일: 2026년 10월 27일

2-Aminopyrimidine → 2-Methyl-3-[4-(trifluoromethyl)phenyl]imidazo[1,2-a]pyrimidine

https://huagongshe.com/reaction/241434

반응식

참여 물질

역할이름HCID투입량
반응물2-AminopyrimidineHCID 7978—
반응물Sodium BicarbonateHCID 516892—
반응물2-Bromo-1-(4-(trifluoromethyl)phenyl)propan-1-oneHCID 10423819—
용매TolueneHCID 1140—
생성물2-Methyl-3-[4-(trifluoromethyl)phenyl]imidazo[1,2-a]pyrimidineHCID 7105977535.9%

반응 조건

온도95 °C

반응 단계

Add 2-bromo-1-(4-(trifluoromethyl)phenyl)propan-1-one (100 g, 0.356 mol), 2-aminopyrimidine (33.85 g, 0.356 mol), and sodium bicarbonate (59.8 g, 0.811 mol) to toluene (500 mL) at 25 to 30° C. Heat the mixture to 90 to 100° C. and stir for 24 hours. Thereafter cool the mixture to 40 to 45° C., and distill the title compound under reduced pressure. Cool the distillate to 25 to 30° C.; add water (1 L); and stir the mixture 4 hours. Filter the mixture collecting the solid, and then wash the solid with a 10% solution of MTBE (200 mL) in hexane. Dry the solid under vacuum at 45 to 50° C. for 12 hours to give the title compound (35.4 g, 35% yield). 1H NMR (300 MHz, CDCl3) δ 8.58 (q, 1H), 8.24-8.26 (d, J=6.6 Hz, 1H), 8.00-8.02 (d, J=8.1 Hz, 2H), 7.72-7.75 (d, J=8.4 Hz, 2H), 6.92-6.96 dd, J=3.9 Hz and 4.2 Hz, 1H), 2.69 (s, 3H).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08648200B2
출처 데이터셋uspto-grants-2014_02
ORD IDord-04cb4cf8fb1041d0b7d4eae0d9b417b2
출처 메모uspto-grants-2014_02