Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 272303생성일: 2026년 10월 26일
Dimethylformamide → 3-(1,4,Diazabicyclo[3.2.2]non-4-ylcarbonyl)-1h-pyrazolo[3,4-c]pyridine
https://huagongshe.com/reaction/272303
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Dimethylformamide | HCID 6228 | — |
| 반응물 | Triethylamine | HCID 8471 | — |
| 반응물 | 1,4-Diazabicyclo(3.2.2)nonane | HCID 398407 | — |
| 반응물 | HCID 178419486 | HCID 178419486 | — |
| 촉매 | HCID 178479802 | HCID 178479802 | — |
| 생성물 | 3-(1,4,Diazabicyclo[3.2.2]non-4-ylcarbonyl)-1h-pyrazolo[3,4-c]pyridine | HCID 68968013 | — |
반응 단계
1 g (5 mmol) of 3-bromo-1H-pyrazolo[3,4-c]pyridine, 0.53 g (0.75 mmol) of bis(triphenyl-phosphino)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-dimethyl-formamide 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US07456171B2 |
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| 출처 데이터셋 | uspto-grants-2008_11 |
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| ORD ID | ord-3ad35ecf01b742cc9e1adcfb29e3e535 |
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| 출처 메모 | uspto-grants-2008_11 |
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