反応式
[Cl-:1].[NH2:2][C:3]([NH:5][N:6]=[CH:7][C:8]1[C:13]([C:14](=[O:18])[N:15]([CH3:17])[CH3:16])=[C:12]([OH:19])[CH:11]=[C:10](C)[N+:9]=1[CH3:21])=[O:4].OC1C(C=O)=NC=CC=1.OC1C(C=O)=NC(C)=CC=1.[Cl-].NC(NN=CC1C(O)=CC(C(=O)N(C)C)=C[N+]=1C)=O.C(C1C=CC(O)=CN=1)=O>>[Cl-:1].[NH2:2][C:3]([NH:5][N:6]=[CH:7][C:8]1[C:13]([C:14](=[O:18])[N:15]([CH3:16])[CH3:17])=[C:12]([OH:19])[CH:11]=[CH:10][N+:9]=1[CH3:21])=[O:4]参加物
6
反応物 5
生成物 1
実験手順
2-[[(Aminocarbonyl)hydrazono]methyl]-3-(N,N-dimethylcarbamoyl)hydroxy-1,6-dimethyl pyridinium chloride can be made by the same procedure replacing 3-hydroxy-2-pyridine aldehyde in the above example with 3-hydroxy-6-methyl-2-pyridine aldehyde. 2-[[(Aminocarbonyl)hydrazono]methyl]-5-(N,N-dimethylcarbamoyl)hydroxy-1-methyl pyridinium chloride can be made by the same procedure replacing 3-hydroxy-2-pyridine aldehyde in the above example with 2-formyl-5-hydroxy pyridine.
出典と根拠
- ORDレコード
- ord-8f25c4e53a2b48edb40ff9e5f6eae184
- 出典データセット
- uspto-grants-1998_02
- 特許番号
- US05714615
関連ノート
読み込み中…