반응식
Cl.Cl.[NH:3]([C:5]1[CH:6]=[N:7][CH:8]=[CH:9][CH:10]=1)[NH2:4].C(O[CH:14]=[CH:15][C:16]#[N:17])C.N(C1C=NC=CC=1)N>>[NH2:17][C:16]1[CH:15]=[CH:14][N:3]([C:5]2[CH:6]=[N:7][CH:8]=[CH:9][CH:10]=2)[N:4]=1참가 물질
4
실험 절차
In a typical reaction, 3-hydrazinopyridine.dihydrochloride and an anhydrous alcohol are introduced into a reaction vessel and the alkoxide base is gradually added. The mixture is stirred and the 3-ethoxyacrylonitrile is added. The mixture is stirred at about 80° C. until most of the 3-hydrazinopyridine has reacted. The mixture is allowed to cool and the excess base is neutralized with acid. The crude 3-(3-amino-1H-pyrazol-1-yl)pyridine (8a) is conveniently isolated and purified by standard techniques.
후처리
- customhas reacted
- temperatureto cool
출처 및 근거
- ORD 기록
- ord-ab7ed98085324deda24ca8a739700155
- 출처 데이터셋
- uspto-grants-2015_05
- 특허 번호
- US09029555B1
연결된 노트
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