Hydrochloric Acid → [[2-[(4-Acetyl-3-hydroxy-2-propylbenzyl)thio]-pyrimidin-4-yl]oxy]acetic acid

HRID 1381584ノート

反応式

HRID 1381584 の反応式
[C:1]([C:4]1[CH:24]=[CH:23][C:7]([CH2:8][S:9][C:10]2[N:15]=[C:14]([O:16][CH2:17][C:18]([O:20]CC)=[O:19])[CH:13]=[CH:12][N:11]=2)=[C:6]([CH2:25][CH2:26][CH3:27])[C:5]=1[OH:28])(=[O:3])[CH3:2].[OH-].[Na+].C(OCC)(=O)C.Cl>CO>[C:1]([C:4]1[CH:24]=[CH:23][C:7]([CH2:8][S:9][C:10]2[N:15]=[C:14]([O:16][CH2:17][C:18]([OH:20])=[O:19])[CH:13]=[CH:12][N:11]=2)=[C:6]([CH2:25][CH2:26][CH3:27])[C:5]=1[OH:28])(=[O:3])[CH3:2]

参加物

6

反応条件

温度
60 °C

実験手順

In 2 ml of 90% methanol was dissolved 0.06 g of ethyl [[2-[(4-acetyl-3-hydroxy-2-propylbenzyl)thio]-pyrimidin-4-yl]oxy]acetate obtained in Example 15 with heating at 60° C. Further 1 ml of a 1N aqueous sodium hydroxide solution was added to the solution followed by stirring at 60° C. for 15 minutes. An aqueous sodium hydroxide solution and ethyl acetate were added to the reaction mixture to fractionate. The aqueous phase was made acidic with 2N hydrochloric acid and extracted with ethyl acetate. The extract was washed with water and then dried over anhydrous magnesium sulfate. The solvent was then distilled off. The thus obtained solid was recrystallized from isopropyl alcohol to give 0.02 g of [[2-[(4-acetyl-3-hydroxy-2-propylbenzyl)thio]-pyrimidin-4-yl]oxy]acetic acid.

後処理

  1. extractionextracted with ethyl acetate
  2. washThe extract was washed with water
  3. dry with materialdried over anhydrous magnesium sulfate
  4. distillationThe solvent was then distilled off
  5. customThe thus obtained solid was recrystallized from isopropyl alcohol

出典と根拠

ORDレコード
ord-b5bc97e892ac4870b8e77302ffa53569
出典データセット
uspto-grants-1989_02
特許番号
US04803211

反応ノート

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