Water → 1-{4-[2-(3-Carboxypropionyloxy)ethylaminocarbonyl]butyl}-5-ethyl-5-phenyl-2,4,6(1H,3H,5H)-pyrimidinetrione

HRID 1450144ノート

反応式

HRID 1450144 の反応式
[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

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

  1. washthe mixture was washed with 10% hydrochloric acid solution (2×100 mL)
  2. washwashed with saturated sodium chloride solution (100 mL)
  3. dry with materialdried over anhydrous magnesium sulfate
  4. filtrationfiltered
  5. customsolvent removed
  6. customto give an oil which

出典と根拠

ORDレコード
ord-89e4b88de961493f8a97aac142ab3884
出典データセット
uspto-grants-1997_02
特許番号
US05601994

反応ノート

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