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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1852968생성일: 2026년 10월 25일

Trifluoroacetic acid → 7-chloro-5-(1H-pyrazol-4-yl)imidazo[1,2-c]pyrimidine

https://huagongshe.com/reaction/1852968

반응식

참여 물질

역할이름HCID투입량
반응물Trifluoroacetic acidHCID 6422—
반응물7-chloro-5-(1-((2-(trimethylsilyl)ethoxy)methyl)-1H-pyrazol-4-yl)imidazo[1,2-c]pyrimidineHCID 86685295—
용매TolueneHCID 1140—
용매DichloromethaneHCID 6344—
생성물7-chloro-5-(1H-pyrazol-4-yl)imidazo[1,2-c]pyrimidineHCID 8668530265.5%

반응 단계

To a solution of 7-chloro-5-(1-((2-(trimethylsilyl)ethoxy)methyl)-1H-pyrazol-4-yl)imidazo[1,2-c]pyrimidine (Preparation G; 0.250 g, 0.715 mmol) in 3.5 mL of DCM was added 2,2,2,-trifluoroacetic acid (2.2 mL, 28.6 mmol) and allowed to stir at ambient temperature for 1 hour before the reaction mixture was diluted with 5 mL of toluene and then concentrated under reduced pressure. The resulting residue was dissolved in 2 mL of 7M ammonia in methanol and stirred at ambient temperature for 30 minutes. The reaction mixture was concentrated under reduced pressure and the resulting residue was purified by silica gel chromatography eluting with a gradient of 2-5% methanol in DCM with 1% ammonium hydroxide to afford 7-chloro-5-(1H-pyrazol-4-yl)imidazo[1,2-c]pyrimidine (0.107 g, 0.468 mmol, 65.5% yield). MS (apci) m/z=220.1 (M+H).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08962596B2
출처 데이터셋uspto-grants-2015_02
ORD IDord-d75c1c52ff91492baf82ac112123ec04
출처 메모uspto-grants-2015_02