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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 2383953생성일: 2026년 10월 26일

Methanol → 1-[3-Fluoro-4-(2,2,2-trifluoroacetyl)-phenyl]-3-(4-methyl-pyridin-3-yl)-imidazolidin-2-one

https://huagongshe.com/reaction/2383953

반응식

참여 물질

역할이름HCID투입량
반응물MethanolHCID 887—
반응물1-[3-Fluoro-4-(2,2,2-trifluoro-1-hydroxy-ethyl)-phenyl]-3-(4-methyl-pyridin-3-yl)-imidazolidin-2-oneHCID 59636227—
촉매Manganese dioxideHCID 14801—
용매DichloromethaneHCID 6344—
생성물1-[3-Fluoro-4-(2,2,2-trifluoroacetyl)-phenyl]-3-(4-methyl-pyridin-3-yl)-imidazolidin-2-oneHCID 5963619474.53%

반응 조건

온도50 °C

반응 단계

MnO2 (536 mg, 6.165 mmol) was added to 1-[3-fluoro-4-(2,2,2-trifluoro-1-hydroxy-ethyl)-phenyl]-3-(4-methyl-pyridin-3-yl)-imidazolidin-2-one (I-197a: 325 mg, 0.880 mmol) in DCM (20 mL) under nitrogen atmosphere. The resulting suspension was stirred at 50° C. overnight. The reaction was monitored by TLC (5% MeOH in DCM). The reaction mixture was cooled to room temperature and filtered through celite pad. The filtrate was washed with CHCl3, dried over Na2SO4 and concentrated. The concentrate was washed with hexane and dried to afford 240 mg of the product (74.53% yield).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08263635B2
출처 데이터셋uspto-grants-2012_09
ORD IDord-ee4cf1edb9684516b09950ee39a97b67
출처 메모uspto-grants-2012_09