Sodium Hydroxide → 4-Methyl-1-oxo-1,2,3,4-tetrahydropyrazino[1,2-a]indole-7-carboxylic acid

HRID 1748245ノート

反応式

HRID 1748245 の反応式
[CH3:1][CH:2]1[N:7]2[C:8]3[CH:9]=[C:10]([C:15]([O:17]CC)=[O:16])[CH:11]=[CH:12][C:13]=3[CH:14]=[C:6]2[C:5](=[O:20])[NH:4][CH2:3]1.[OH-].[Na+]>C1COCC1.C(O)C>[CH3:1][CH:2]1[N:7]2[C:8]3[CH:9]=[C:10]([C:15]([OH:17])=[O:16])[CH:11]=[CH:12][C:13]=3[CH:14]=[C:6]2[C:5](=[O:20])[NH:4][CH2:3]1

参加物

4

反応条件

温度
75 °C

実験手順

To a suspension of ethyl 4-methyl-1-oxo-1,2,3,4-tetrahydropyrazino[1,2-a]indole-7-carboxylate (3.2 g, 11.8 mmol) in THF:ethanol (1:1, 50 mL) is added 1N NaOH solution (43 mL, 43 mmol). The reaction mixture is heated at 75° C. for 18 h. The solvents are removed and the residue is dissolved in water. The aqueous solution is washed with ether and acidified to pH 4 using 3N HCl solution. The resulting white solid is filtered and rinsed more ether to afford the title compound (2.2 g, 76%).

後処理

  1. customThe solvents are removed
  2. dissolutionthe residue is dissolved in water
  3. washThe aqueous solution is washed with ether
  4. filtrationThe resulting white solid is filtered
  5. washrinsed more ether

出典と根拠

ORDレコード
ord-a373eb7ff0054dc2a3579781626ad1c3
出典データセット
uspto-grants-2015_10
特許番号
US09150577B2

反応ノート

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