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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 730003생성일: 2026년 10월 25일

Cesium carbonate → 5-[2-tert-Butyl-4-(4-fluorophenyl)oxazol-5-yl]-3-isobutyl-3H-imidazo[4,5-b]pyridin-2-ylamine

https://huagongshe.com/reaction/730003

반응식

참여 물질

역할이름HCID투입량
반응물Cesium carbonateHCID 10796—
반응물TriphenylphosphineHCID 11776—
반응물2-tert-Butyl-4-(4-fluorophenyl)oxazoleHCID 66869043—
반응물5-bromo-3-isobutyl-3H-imidazo[4,5-b]pyridin-2-ylamineHCID 86063644—
촉매palladium(II) acetateHCID 167845—
용매DimethylformamideHCID 6228—
생성물5-[2-tert-Butyl-4-(4-fluorophenyl)oxazol-5-yl]-3-isobutyl-3H-imidazo[4,5-b]pyridin-2-ylamineHCID 6887082834%

반응 단계

Bubble with nitrogen a suspension of 2-tert-butyl-4-(4-fluorophenyl)oxazole (0.145 g, 0.66 mmol), 5-bromo-3-isobutyl-3H-imidazo[4,5-b]pyridin-2-ylamine (0.355 g, 1.32 mmol), cesium carbonate (6.06 g, 18.6 mmol), palladium (II) acetate (0.201 g, 10%) and triphenylphosphine (0.14 g, 0.07 mmol) in DMF (1.5 mL). Heat the reaction at 100° C. overnight, cool to RT and partition between EtOAc and saturated aqueous NaCl. Wash the organic layer with saturated aqueous NaCl. Dry with Na2SO4, filter, concentrate, and purify (silica gel chromatography, eluting with 2% of 2M ammonia/MeOH in CH2Cl2 to give the title compound (0.07 g, 34%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07582652B2
출처 데이터셋uspto-grants-2009_09
ORD IDord-ebea77b7d7c54cd391eaca0d172e8e47
출처 메모uspto-grants-2009_09