1,1,3,3-Tetramethylguanidine → HCID 57036510、化合物
反応式
Cl([O-])(=O)(=O)=O.[CH3:6][C:7]1[N+:12]2[C:13]3[C:18]([C:19]([CH3:21])([CH3:20])[C:11]=2[CH:10]=[CH:9][CH:8]=1)=[CH:17][CH:16]=[CH:15][CH:14]=3.N([CH:29]=[C:30]1[C:35](=[O:36])[N:34]([CH2:37][CH3:38])[C:33](=[S:39])[N:32]([CH2:40][CH3:41])[C:31]1=[O:42])C1C=CC=CC=1.CN(C)C(=N)N(C)C>C(#N)C>[CH2:37]([N:34]1[C:35](=[O:36])[C:30](=[CH:29][CH:6]=[C:7]2[N:12]3[C:13]4[C:18]([C:19]([CH3:21])([CH3:20])[C:11]3=[CH:10][CH:9]=[CH:8]2)=[CH:17][CH:16]=[CH:15][CH:14]=4)[C:31](=[O:42])[N:32]([CH2:40][CH3:41])[C:33]1=[S:39])[CH3:38]参加物
5
実験手順
6,10,10-Trimethylpyrido[1,2-a]indolium perchlorate (0.62 g.) and 5-anilinomethylene-1,3-diethyl-2-thiobarbituric acid (0.6 g.) are dissolved in acetonitrile. Tetramethylguanidine (0.23 g.) is added and the reaction mixture is stirred at room temperature overnight. The precipitated dye is filtered off and recrystallized from acetonitrile. The λmax of the product in a mixture of pyridine and methyl alcohol is 513 nm.
後処理
- filtrationThe precipitated dye is filtered off
- customrecrystallized from acetonitrile
- additionThe λmax of the product in a mixture of pyridine and methyl alcohol
出典と根拠
- ORDレコード
- ord-51bfed45694d4ab889a9449f148d2acc
- 出典データセット
- uspto-grants-1977_01
- 特許番号
- US04003750
反応ノート
読み込み中…