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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 2090322생성일: 2026년 10월 26일

4-Cyanopiperidine → 1-{2-[2-Amino-6-(4-methylpiperazin-1-yl)pyrimidin-4-yl]-1,2,3,4-tetrahydroisoquinolin-7-yl}piperidine-4-carbonitrile

https://huagongshe.com/reaction/2090322

반응식

참여 물질

역할이름HCID투입량
반응물4-CyanopiperidineHCID 138223—
반응물Sodium t-butoxideHCID 23676156—
반응물4-(7-bromo-3,4-dihydroisoquinolin-2(1H)-yl)-6-(4-methylpiperazin-1-yl)pyrimidin-2-amineHCID 46701048—
촉매2-(2'-Di-tert-butylphosphine)biphenylpalladium(II) acetateHCID 11982262—
생성물1-{2-[2-Amino-6-(4-methylpiperazin-1-yl)pyrimidin-4-yl]-1,2,3,4-tetrahydroisoquinolin-7-yl}piperidine-4-carbonitrileHCID 46701462—

반응 조건

온도120 °C

반응 단계

A mixture of 4-(7-bromo-3,4-dihydroisoquinolin-2(1H)-yl)-6-(4-methylpiperazin-1-yl)pyrimidin-2-amine (40 mg, 0.1 mmol), piperidine-4-carbonitrile (22 mg, 0.20 mmol, Oakwood, Cat. No. 024547), sodium tert-butoxide (23 mg, 0.24 mmol), 2-(2′-di-tert-butylphosphine)biphenyl palladium(II) acetate (2.8 mg, 0.0060 mmol, Aldrich, Cat. No. 655414) in 1,4-dioxane (1 mL) was degassed with nitrogen and then heated at 120° C. overnight. The reaction mixture was cooled to r.t. and concentrated under reduced pressure. The residue was dissolved in MeOH and purified by RP-HPLC (pH=10) to afford the desired compound. LCMS (M+H)+: m/z=433.3.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08436008B2
출처 데이터셋uspto-grants-2013_05
ORD IDord-7d41bb556b24467fb5db54ab3a41d640
출처 메모uspto-grants-2013_05