Water → 1-{4-[2-(3-Carboxypropionyloxy)ethylaminocarbonyl]butyl}-5-ethyl-5-phenyl-2,4,6(1H,3H,5H)-pyrimidinetrione
反応式
[CH2:1]([C:3]1([C:20]2[CH:25]=[CH:24][CH:23]=[CH:22][CH:21]=2)[C:8]([OH:9])=[N:7][C:6](=[O:10])[N:5]([CH2:11][CH2:12][CH2:13][CH2:14][C:15](OC)=[O:16])[C:4]1=[O:19])[CH3:2].[C:26]1(=[O:32])[O:31][C:29](=[O:30])[CH2:28][CH2:27]1.C[N:34]([C:36]1[CH:41]=CC=CN=1)C.[OH2:42]>C(Cl)(Cl)Cl.ClCCl>[C:29]([CH2:28][CH2:27][C:26]([O:31][CH2:41][CH2:36][NH:34][C:15]([CH2:14][CH2:13][CH2:12][CH2:11][N:5]1[C:4](=[O:19])[C:3]([CH2:1][CH3:2])([C:20]2[CH:21]=[CH:22][CH:23]=[CH:24][CH:25]=2)[C:8](=[O:9])[NH:7][C:6]1=[O:10])=[O:16])=[O:32])([OH:30])=[O:42]参加物
7
反応物 4
生成物 1
試薬・触媒・溶媒 2
実験手順
A mixture of the product from step 1 (2.9 g, 0.007 mole), succinic anhydride (0.7 g, 0.007 mole), and dimethylaminopyridine (0.9 g, 0.007 mole) in chloroform (100 mL) was heated with hot water (50°-60° C.) for 30 min and then stirred at room temperature for 3 days. Dichloromethane (300 mL) was added, and the mixture was washed with 10% hydrochloric acid solution (2×100 mL), washed with saturated sodium chloride solution (100 mL), dried over anhydrous magnesium sulfate, filtered, and solvent removed to give an oil which was used directly in the next step.
後処理
- washthe mixture was washed with 10% hydrochloric acid solution (2×100 mL)
- washwashed with saturated sodium chloride solution (100 mL)
- dry with materialdried over anhydrous magnesium sulfate
- filtrationfiltered
- customsolvent removed
- customto give an oil which
出典と根拠
- ORDレコード
- ord-a56e327f4959446e984c93cf72cc5e7f
- 出典データセット
- uspto-grants-1994_03
- 特許番号
- US05298403
反応ノート
読み込み中…