돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 57895생성일: 2026년 10월 25일

N,N'-Dimethylethylenediamine → tert-butyl N-[(3S)-1-[3-methoxy-6-[6-(6-methylpyrazin-2-yl)pyrazolo[4,3-c]pyridin-1-yl]-2-pyridyl]-3-piperidyl]carbamate

https://huagongshe.com/reaction/57895

반응식

참여 물질

역할이름HCID투입량
반응물N,N'-DimethylethylenediamineHCID 8070—
반응물Potassium CarbonateHCID 11430—
반응물6-(6-methylpyrazin-2-yl)-1H-pyrazolo[4,3-c]pyridineHCID 86707080—
반응물tert-butyl N-[(3S)-1-(6-bromo-3-methoxy-2-pyridyl)-3-piperidyl]carbamateHCID 86707086—
촉매Copper iodideHCID 83717—
용매1,4-DioxaneHCID 31275—
생성물tert-butyl N-[(3S)-1-[3-methoxy-6-[6-(6-methylpyrazin-2-yl)pyrazolo[4,3-c]pyridin-1-yl]-2-pyridyl]-3-piperidyl]carbamateHCID 8670708758.3%

반응 조건

온도100 °C

반응 단계

A mixture of 6-(6-methylpyrazin-2-yl)-1H-pyrazolo[4,3-c]pyridine (0.4734 mmol; 100.0 mg), tert-butyl N-[(3S)-1-(6-bromo-3-methoxy-2-pyridyl)-3-piperidyl]carbamate (0.5681 mmol, 219.5 mg), N,N′-Dimethylethylenediamine (0.4734 mmol; 41.73 mg; 0.0471 mL), copper iodide (0.4734 mmol; 91.08 mg), and potassium carbonate (0.5208 mmol; 72.70 mg) in 1,4-Dioxane (10 mL) was purged with Argon, then sealed and stirred at 100° C. overnight. The mixture was cooled to room temperature, and then filtered through Celite. The filtrate was concentrated; the residue was purified on silica eluted with 0 to 100% EtOAc in DCM to afford tert-butyl N-[(3S)-1-[3-methoxy-6-[6-(6-methylpyrazin-2-yl)pyrazolo[4,3-c]pyridin-1-yl]-2-pyridyl]-3-piperidyl]carbamate as a tan solid (142.5 mg, 58%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09434725B2
출처 데이터셋uspto-grants-2016_09
ORD IDord-5391cd1c9a1b47f2a558cb72146f6c8a
출처 메모uspto-grants-2016_09