Water → HCID 18707160, compound

HRID 263595Notes

Reaction equation

HRID 263595 reaction equation
FC(F)(F)S([O:6][S:7]([C:10]([F:13])([F:12])[F:11])(=[O:9])=[O:8])(=O)=O.[CH2:16]([O:18][C:19]1[CH:20]=[C:21]([C:28]2[S:29][CH:30]=[C:31]([C:33]3[CH:38]=[CH:37][C:36](O)=[C:35]([C:40]([O:42][CH3:43])=[O:41])[CH:34]=3)[N:32]=2)[CH:22]=[CH:23][C:24]=1[O:25][CH2:26][CH3:27])[CH3:17].C(N(CC)CC)C.O>ClCCl>[CH2:16]([O:18][C:19]1[CH:20]=[C:21]([C:28]2[S:29][CH:30]=[C:31]([C:33]3[CH:38]=[CH:37][C:36]([O:6][S:7]([C:10]([F:11])([F:12])[F:13])(=[O:8])=[O:9])=[C:35]([C:40]([O:42][CH3:43])=[O:41])[CH:34]=3)[N:32]=2)[CH:22]=[CH:23][C:24]=1[O:25][CH2:26][CH3:27])[CH3:17]

Participants

6

Procedure

8.5 g of trifluoromethanesulfonic acid anhydride was added to a solution of 10 g of 2-(3,4-diethoxyphenyl)-4-(3-methoxycarbonyl-4-hydroxyphenyl)-thiazole dissolved in 100 ml of dichloromethane. Thereto was dropwise added 6 ml of triethylamine with stirring under ice-cooling. The reaction mixture was stirred at room temperature for 2 hours. Thereto was added 40 ml of water for phase separation. The organic layer was dried and subjected to distillation to remove the solvent. The residue was recrystallized from ethanol to obtain 12.7 g of 2-(3,4-diethoxyphenyl)-4-(3-methoxycarbonyl-4-trifluoromethanesulfonyloxyphenyl)thiazole as a white powder.

Workup

  1. temperaturecooling
  2. stirringThe reaction mixture was stirred at room temperature for 2 hours
  3. customfor phase separation
  4. customThe organic layer was dried
  5. distillationsubjected to distillation
  6. customto remove the solvent
  7. customThe residue was recrystallized from ethanol

Sources & evidence

ORD record
ord-576b84f8ed64449d938db96866f49713
Source dataset
uspto-grants-1997_07
Patent number
US05643932

Reaction notes

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