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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 15768생성일: 2026년 10월 24일

Cesium carbonate → Tert-butyl 4-(2-methylquinolin-5-yl)piperazine-1-carboxylate

https://huagongshe.com/ko/reaction/15768

반응식

참여 물질

역할이름HCID투입량
반응물Cesium carbonateHCID 10796—
반응물tert-Butyl piperazine-1-carboxylateHCID 143452—
반응물Binap, (A+-)-HCID 634876—
반응물2-Methylquinolin-5-yl trifluoromethanesulfonateHCID 49851899—
촉매palladium(II) acetateHCID 167845—
용매TolueneHCID 1140—
생성물Tert-butyl 4-(2-methylquinolin-5-yl)piperazine-1-carboxylateHCID 4985190062%

반응 단계

tert-Butyl 1-piperazine carboxylate (1.6 g; 1.2 eq), cesium carbonate (1.7 g; 1.5 eq), palladium acetate (0.33 g; 0.14 eq) and 2,2′-bis(diphenylphosphino)-1,1′-binaphthyl (0.97 mg; 0.15 eq) were added to a solution of 2-methyl-5-quinolinyl trifluoromethanesulfonate (D1) in toluene (20 mL) under an inert atmosphere. The reaction mixture was stirred at reflux under nitrogen for 8 hours. The reaction was quenched at room temperature using a saturated aqueous solution of ammonium chloride (15 mL) and extracted into ethyl acetate (3×20 mL). The organic layers were combined, dried over Na2SO4 and concentrated under reduced pressure. The crude was purified by flash chromatography, eluting with ethyl acetate/cyclohexane (3/7) affording the title compound in 62% yield (1.4 g).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07732600B2
출처 데이터셋uspto-grants-2010_06
ORD IDord-8a5315f9c363403ea8321f3dfc2a3dea
출처 메모uspto-grants-2010_06