반응식
[NH2:1][C:2]1[N:7]=[CH:6][CH:5]=[CH:4][N:3]=1.[C:8]([N+:12]#[C-:13])([CH3:11])([CH3:10])[CH3:9].[CH:14](=O)[C:15]1[CH:20]=[CH:19][CH:18]=[CH:17][CH:16]=1.[C:22]([Cl:25])(=[O:24])[CH3:23]>Cl(O)(=O)(=O)=O>[Cl-:25].[C:22]([N+:1]1[C:14]([C:15]2[CH:20]=[CH:19][CH:18]=[CH:17][CH:16]=2)=[C:13]([NH:12][C:8]([CH3:11])([CH3:10])[CH3:9])[N:3]2[CH:4]=[CH:5][CH:6]=[N:7][C:2]=12)(=[O:24])[CH3:23]참가 물질
6
실험 절차
Example 3 was carried out in accordance with the general directions for synthesis in process step a) from 1.0 ml (0.1 mmol) 2-amino-pyrimidine (0.1 M, DCM), 0.575 ml (0.115 mmol) tert.-butylisonitrile solution (0.2 M, DCM), 0.500 ml (0.15 mmol) benzaldehyde solution (0.3 M, DCM) and 10 μl perchloric acid (w=20%) and in process step c) and d) by reacting the resultant reaction product with 0.4 mmol acetylchloride.
출처 및 근거
- ORD 기록
- ord-5ebe5abfa2ca49b9841445d97976bc23
- 출처 데이터셋
- uspto-grants-2006_08
- 특허 번호
- US07087607B2
연결된 노트
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