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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 57871생성일: 2026년 10월 25일

Sodium Carbonate → Tert-butyl 4-[6-[6-(1-ethylpyrazol-4-yl)pyrazolo[4,3-c]pyridin-1-yl]pyrazin-2-yl]-1,4-diazepane-1-carboxylate

https://huagongshe.com/reaction/57871

반응식

참여 물질

역할이름HCID투입량
반응물Sodium CarbonateHCID 10340—
반응물Potassium AcetateHCID 517044—
반응물1-Ethyl-1H-pyrazole-4-boronic acid, pinacol esterHCID 11379045—
반응물Tert-butyl 4-[6-(6-chloropyrazolo[4,3-c]pyridin-1-yl)pyrazin-2-yl]-1,4-diazepane-1-carboxylateHCID 86707066—
촉매HCID 178418807HCID 178418807—
용매AcetonitrileHCID 6342—
생성물Tert-butyl 4-[6-[6-(1-ethylpyrazol-4-yl)pyrazolo[4,3-c]pyridin-1-yl]pyrazin-2-yl]-1,4-diazepane-1-carboxylateHCID 86707067102.7%

반응 조건

온도150 °C

반응 단계

A mixture of tert-butyl 4-[6-(6-chloropyrazolo[4,3-c]pyridin-1-yl)pyrazin-2-yl]-1,4-diazepane-1-carboxylate (0.2526 mmol; 108.6 mg), 1-ethyl-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyrazole (0.3789 mmol; 84.16 mg), [1,1′-bis(diphenylphosphino)ferrocene]dichloropalladium(II) dichloromethane adduct (0.02526 mmol; 21.1 mg), potassium acetate (0.3789 mmol; 0.38 mL) and sodium carbonate (0.3789 mmol; 0.38 mL) in Acetonitrile (10 mL) in a pressure tube was heated under microwave at 150° C. for 15 min. The mixture was cooled to room temperature. The layers were separated. The aqueous layer was extracted with EtOAc. The combined organic layers were concentrated. The residue was purified on silica eluted with 0 to 5% MeOH in DCM with 1% NH4OH to afford tert-butyl 4-[6-[6-(1-ethylpyrazol-4-yl)pyrazolo[4,3-c]pyridin-1-yl]pyrazin-2-yl]-1,4-diazepane-1-carboxylate (127 mg, ˜100%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09434725B2
출처 데이터셋uspto-grants-2016_09
ORD IDord-cfa5379407e3408fa8d3e1534644b6ac
출처 메모uspto-grants-2016_09