Potassium Carbonate → HCID 18707155, compound

HRID 1699563Notes

Reaction equation

HRID 1699563 reaction equation
[CH2:1]([O:3][C:4]1[CH:5]=[C:6]([C:13]2[S:14][CH:15]=[C:16]([C:18]3[CH:23]=[CH:22][C:21]([OH:24])=[C:20]([C:25]([O:27][CH3:28])=[O:26])[CH:19]=3)[N:17]=2)[CH:7]=[CH:8][C:9]=1[O:10][CH2:11][CH3:12])[CH3:2].C(=O)([O-])[O-].[K+].[K+].Br[CH2:36][C:37]([O:39][CH3:40])=[O:38]>CN(C)C=O>[CH2:1]([O:3][C:4]1[CH:5]=[C:6]([C:13]2[S:14][CH:15]=[C:16]([C:18]3[CH:23]=[CH:22][C:21]([O:24][CH2:36][C:37]([O:39][CH3:40])=[O:38])=[C:20]([C:25]([O:27][CH3:28])=[O:26])[CH:19]=3)[N:17]=2)[CH:7]=[CH:8][C:9]=1[O:10][CH2:11][CH3:12])[CH3:2]

Participants

5

Procedure

In 10 ml of dimethylformamide were suspended 1 g of 2- (3,4-diethoxyphenyl) 4-(4-hydroxy-3 methoxycarbonylphenyl)thiazole and 0.35 g of potassium carbonate. The suspension was stirred at room temperature for 30 minutes. Thereto was added 0.46 g of methyl bromoacetate. The mixture was stirred at the same temperature for 4 hours. The solvent was removed by distillation. The residue was extracted with 40 ml of dichloromethane. The extract was washed with 10 ml of water and 10 ml of a saturated aqueous sodium chloride solution, dried over magnesium sulfate. and subjected to distillation to remove the solvent, The residue was recrystallized from diisopropyl ether to obtain 1.1 g of 2-(3,4-diethoxyphenyl)-4-(4-methoxycarbonylmethoxy-3-methoxycarbonylphenyl) thiazole.

Workup

  1. stirringThe mixture was stirred at the same temperature for 4 hours
  2. customThe solvent was removed by distillation
  3. extractionThe residue was extracted with 40 ml of dichloromethane
  4. washThe extract was washed with 10 ml of water and 10 ml of a saturated aqueous sodium chloride solution
  5. dry with materialdried over magnesium sulfate
  6. distillationand subjected to distillation
  7. customto remove the solvent
  8. customThe residue was recrystallized from diisopropyl ether

Sources & evidence

ORD record
ord-69b0f21cc04947fdbcec89e5e3f3a5a1
Source dataset
uspto-grants-2002_02
Patent number
USRE037556E1

Reaction notes

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