反応式
[NH2:1][C:2]1[C:3](=[O:14])[N:4]([CH2:12][CH3:13])[C:5](=[O:11])[N:6]([CH2:9][CH3:10])[C:7]=1[NH2:8].[CH3:15][C:16]1[CH:26]=[CH:25][C:24]([CH3:27])=[CH:23][C:17]=1[CH:18]=[CH:19][C:20](O)=O>>[CH3:15][C:16]1[CH:26]=[CH:25][C:24]([CH3:27])=[CH:23][C:17]=1/[CH:18]=[CH:19]/[C:20]1[NH:1][C:2]2[C:3](=[O:14])[N:4]([CH2:12][CH3:13])[C:5](=[O:11])[N:6]([CH2:9][CH3:10])[C:7]=2[N:8]=1参加物
3
実験手順
Substantially the same procedure as in Example 7 was repeated using 3.00 g (15.1 mmol) of 5,6-diamino-1,3-diethyluracil and 3.20 g (18.2 mmol) of 2,5-dimethylcinnamic acid. Then, the resultant crude crystals were recrystallized from ethanol/toluene to give 2.56 g (yield of Compound 96 as white needles.
後処理
- customThen, the resultant crude crystals were recrystallized from ethanol/toluene
出典と根拠
- ORDレコード
- ord-ce62b3c419a34e52809337915a75aada
- 出典データセット
- uspto-grants-1996_01
- 特許番号
- US05484920
関連ノート
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