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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1966752생성일: 2026년 10월 24일

Cesium carbonate → 5-{1-tert-Butyl-2-[2-(2,4-dimethyl-oxazol-5-yl)-phenyl]-1H-benzimidazol-5-yl}-pyrimidin-2-ylamine

https://huagongshe.com/ko/reaction/1966752

반응식

참여 물질

역할이름HCID투입량
반응물Cesium carbonateHCID 10796—
반응물TriphenylphosphineHCID 11776—
반응물2,4-DimethyloxazoleHCID 138961—
반응물5-[1-tert-butyl-2-(2-iodo-phenyl)-1H-benzimidazol-5-yl]-pyrimidin-2-ylamineHCID 58542069—
촉매palladium(II) acetateHCID 167845—
용매DimethylformamideHCID 6228—
용매Water ethylacetateHCID 22728543—
생성물5-{1-tert-Butyl-2-[2-(2,4-dimethyl-oxazol-5-yl)-phenyl]-1H-benzimidazol-5-yl}-pyrimidin-2-ylamineHCID 5854193041%

반응 조건

온도140 °C

반응 단계

To a vial are added 5-[1-tert-butyl-2-(2-iodo-phenyl)-1H-benzimidazol-5-yl]-pyrimidin-2-ylamine (50 mg, 0.107 mmol), 2,4-dimethyl-oxazole (21 mg, 0.216 mol), palladium(II) acetate (5 mg, 0.022 mmol), PPh3 (6 mg, 0.023 mmol) and Cs2CO3 (70 mg, 0.215 mmol) in DMF (1.5 mL). The reaction mixture is stirred at 140° C. for 18 hours. The reaction mixture is diluted with EtOAc/water. The organic layer is separated, washed with brine, dried under anhydrous Na2SO4, filtered and concentrated. The residue is purified by silica gel flash column chromatography with 0-5% MeOH/CH2Cl2 as the eluent. The product fractions are collected and concentrated to afford the title compound (19 mg, 41%) as an off-white solid. LCMS (ESMS): m/z 439.86 (M++1)

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08420655B2
출처 데이터셋uspto-grants-2013_04
ORD IDord-c897844a27c649219e060d5138cf8e00
출처 메모uspto-grants-2013_04