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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 37815생성일: 2026년 10월 24일

Dimethylformamide → 3-(1,4,Diazabicyclo[3.2.2]non-4-ylcarbonyl)-1h-pyrazolo[3,4-c]pyridine

https://huagongshe.com/ko/reaction/37815

반응식

참여 물질

역할이름HCID투입량
반응물DimethylformamideHCID 6228—
반응물TriethylamineHCID 8471—
반응물1,4-Diazabicyclo(3.2.2)nonaneHCID 398407—
반응물HCID 178419486HCID 178419486—
촉매HCID 178479802HCID 178479802—
생성물3-(1,4,Diazabicyclo[3.2.2]non-4-ylcarbonyl)-1h-pyrazolo[3,4-c]pyridineHCID 68968013—

반응 조건

온도110 °C

반응 단계

1 g (5 mmol) of 3-bromo-1H-pyrazolo[3,4-c]-pyridine, 0.53 g (0.75 mmol) of bis(triphenylphosphino)dichloropalladium, 1.9 g (15.1 mmol) of 1,4-diazabicyclo[3.2.2]nonane and 3.5 ml (25 mmol) of triethylamine dissolved in 15 ml of N,N-dimethylformamide are successively introduced into a 50 ml reactor. The mixture is then purged with carbon monoxide and heated at 110° C. for 20 hours. The reaction medium is poured into 100 ml of water and the aqueous phase is extracted with chloroform. After drying the organic phases, they are dried, filtered and concentrated under reduced pressure. The residue is purified by chromatography on a column of silica gel, eluting with a mixture of chloroform, methanol and aqueous ammonia in 90/10/1 proportions.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08524706B2
출처 데이터셋uspto-grants-2013_09
ORD IDord-814e87e08ebe42e0a69e2333a633230c
출처 메모uspto-grants-2013_09