反応式
[CH3:1][S:2][C:3]1[N:8]=[C:7](Cl)[C:6]([N+:10]([O-:12])=[O:11])=[C:5]([Cl:13])[N:4]=1.[CH3:14][N:15]([CH3:25])[C:16]([C:18]1[CH:19]=[C:20]([OH:24])[CH:21]=[CH:22][CH:23]=1)=[O:17].C(=O)([O-])[O-].[Cs+].[Cs+]>>[CH3:1][S:2][C:3]1[N:4]=[C:5]([Cl:13])[C:6]([N+:10]([O-:12])=[O:11])=[C:7]([O:24][C:20]2[CH:21]=[CH:22][CH:23]=[C:18]([C:16]([N:15]([CH3:25])[CH3:14])=[O:17])[CH:19]=2)[N:8]=1参加物
4
実験手順
In a similar manner, 2-methylthio-5-nitro-4,6-dichloropyrimidine was treated with 3-(dimethylaminocarbonyl)phenol in the presence of cesium carbonate to afford 2-methylthio-5-nitro-4-chloro-6-(3-dimethylaminocarbonylphenoxy)pyrimidine, a compound of formula (M).
出典と根拠
- ORDレコード
- ord-37f73696a95e4b3aae298dd2aa83f2de
- 出典データセット
- uspto-grants-1998_05
- 特許番号
- US05753635
関連ノート
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