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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 10560생성일: 2026년 10월 25일

Water → 4-(4-Methoxy-5-isoquinolyl)amino-1-(tert-butoxycarbonyl)piperidine

https://huagongshe.com/reaction/10560

반응식

참여 물질

역할이름HCID투입량
반응물WaterHCID 962—
반응물Sodium MethoxideHCID 10942334—
반응물4-(4-Bromo-5-isoquinolyl)amino-1-(tert-butoxycarbonyl)piperidineHCID 21979972—
촉매Copper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
용매MethanolHCID 887—
용매PyridineHCID 1049—
생성물4-(4-Methoxy-5-isoquinolyl)amino-1-(tert-butoxycarbonyl)piperidineHCID 21979974—

반응 조건

온도65 °C

반응 단계

A suspension of Intermediate 71 (600 mg) and copper(I) iodide (141 mg, Kanto Chemicals) in methanol (5.5 ml) and pyridine (5.5 ml) was added with sodium methoxide (28% methanol solution, 1.7 ml, Wako Pure Chemical Industries) and stirred with heating at 65° C. for 24 hours. The reaction mixture was cooled to room temperature, then added with water (30 ml) and extracted three times with ethyl acetate (20 ml for each time). The combined organic layer was washed twice with saturated brine (30 ml for each time) and dried over anhydrous sodium sulfate. The solvent was evaporated under reduced pressure, and the residue was purified by silica gel column chromatography (n-hexane:ethyl acetate=1:2) to obtain the title compound (364 mg).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07094789B2
출처 데이터셋uspto-grants-2006_08
ORD IDord-e66b85a64f8c49938e94e99c298be080
출처 메모uspto-grants-2006_08