反応式
[NH2:1][C:2]1[N:7]=[C:6]([Cl:8])[CH:5]=[C:4]([NH2:9])[N:3]=1.[CH3:10][O:11][C:12](=[O:16])[CH2:13][N+:14]#[C-:15].[CH:17](=O)[C:18]1[O:22][CH:21]=[CH:20][CH:19]=1.[C:24](Cl)(=[O:26])[CH3:25]>Cl(O)(=O)(=O)=O>[Cl-:8].[C:24]([N+:1]1[C:17]([C:18]2[O:22][CH:21]=[CH:20][CH:19]=2)=[C:15]([NH:14][CH2:13][C:12]([O:11][CH3:10])=[O:16])[N:3]2[C:4]([NH2:9])=[CH:5][C:6]([Cl:8])=[N:7][C:2]=12)(=[O:26])[CH3:25]参加物
6
実験手順
Example 27 was carried out in accordance with the general directions for synthesis in process step a) from 1.0 ml (0.1 mmol) 2,6-diamino-4-chloro-pyrimidine (0.1 M, DCM), 0.575 ml (0.115 mmol) isocyanoacetic acid methyl ester solution (0.2 M, DCM), 0.500 ml (0.15 mmol) furfural 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.
出典と根拠
- ORDレコード
- ord-e09d80b009c94883976bbcd98164aff7
- 出典データセット
- uspto-grants-2006_08
- 特許番号
- US07087607B2
関連ノート
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