반응식
[CH2:1]([NH:3][CH2:4][C:5]1[CH:10]=[C:9]([Cl:11])[CH:8]=[CH:7][C:6]=1[O:12][CH2:13][C:14]([CH3:16])=[CH2:15])[CH3:2].Cl[C:18]1[N:23]=[N:22][C:21]([C:24]([NH2:26])=[O:25])=[CH:20][CH:19]=1.C(N(C(C)C)CC)(C)C>CN(C=O)C.O>[Cl:11][C:9]1[CH:8]=[CH:7][C:6]([O:12][CH2:13][C:14]([CH3:16])=[CH2:15])=[C:5]([CH:10]=1)[CH2:4][N:3]([C:18]1[N:23]=[N:22][C:21]([C:24]([NH2:26])=[O:25])=[CH:20][CH:19]=1)[CH2:1][CH3:2]참가 물질
반응물 3
생성물 1
시약·촉매·용매 2
실험 절차
A mixture of N-ethyl-5-chloro-2-(2-methylprop-2-en-1-yloxy)benzylamine (reference example 16) (13.8 g, 50 mM), 6-chloropyridazine-3-carboxamide (7.9 g, 50 mM) and di-isopropylethylamine (20.0 ml, 115 mM) in DMF (50 ml) was stirred at reflux for 16 hours. The mixture was cooled and diluted with water (200 ml) giving an oil which was allowed to settle out (1 hour). The supernatant liquor was decanted and the residual brown gum dissolved in dichloromethane (250 ml) and washed with 2N hydrochloric acid (100 ml). The product was obtained by eluting the organic layer through silica, adjusting the solvent to dichloromethane/isopropanol (19:1) and collecting relevant fractions, which were combined and evaporated to give the title compound as a gum (10.5 g, 58%).
후처리
- temperatureat reflux for 16 hours
- temperatureThe mixture was cooled
- customgiving an oil which
- custom(1 hour)
- customThe supernatant liquor was decanted
- dissolutionthe residual brown gum dissolved in dichloromethane (250 ml)
- washwashed with 2N hydrochloric acid (100 ml)
- customThe product was obtained
- washby eluting the organic layer through silica
- customcollecting relevant fractions, which
- customevaporated
출처 및 근거
- ORD 기록
- ord-a8bc73af172c49169e86b91fd96c8325
- 출처 데이터셋
- uspto-grants-2000_08
- 특허 번호
- US06100258
연결된 노트
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