Methanol → HCID 68707308, compound

HRID 1441715Notes

Reaction equation

HRID 1441715 reaction equation
[C:1]([O:4][C:5](=O)[CH3:6])(=[O:3])[CH3:2].[CH3:8][O:9][C:10]1[CH:11]=[C:12]([C:18]2[S:19][CH:20]=[C:21]([CH2:23][C:24](=[O:34])[CH2:25][C:26]3[CH:31]=CC(O)=[C:28]([OH:33])[CH:27]=3)[N:22]=2)[CH:13]=[CH:14][C:15]=1[O:16][CH3:17].C[OH:36].N1[CH:42]=[CH:41]C=CC=1>>[CH3:8][O:9][C:10]1[CH:11]=[C:12]([C:18]2[S:19][CH:20]=[C:21]([CH2:23][C:24](=[O:34])[CH2:25][C:26]3[CH:31]=[CH:6][C:5]([O:4][C:1](=[O:3])[CH3:2])=[C:28]([O:33][C:41](=[O:36])[CH3:42])[CH:27]=3)[N:22]=2)[CH:13]=[CH:14][C:15]=1[O:16][CH3:17]

Participants

5

Procedure

Acetic anhydride (2 ml, 20 mmol) was added dropwise at room temperature to a solution (4 ml) of 3-[2-(3,4-dimethoxyphenyl)thiazole-4-yl]-1-(3,4-dihydroxyphenyl)propanone (320 mg, 0.78 mmol) in pyridine at room temperature, followed by stirring at the same temperature for 1 hour. Methanol (10 ml) was added to the reaction mixture, stirring was carried out at room temperature for 1 hour, and the solvent was distilled off under reduced pressure. Subsequently, water was added, and extraction with ethyl acetate was performed. The residue was purified by silica gel column chromatography (eluent: ethyl acetate). The solvent was distilled off under reduced pressure, and the residue was recrystallized from an ethyl acetate/n-hexane mixed solvent, to thereby obtain 195 mg (yield: 54%) of 3-[2-(3,4-dimethoxyphenyl)thiazole-4-yl]-1-(3,4-diacetoxyphenyl)propanone as colorless needles.

Workup

  1. stirringstirring
  2. waitwas carried out at room temperature for 1 hour
  3. distillationthe solvent was distilled off under reduced pressure
  4. additionSubsequently, water was added
  5. extractionextraction with ethyl acetate
  6. customThe residue was purified by silica gel column chromatography (eluent: ethyl acetate)
  7. distillationThe solvent was distilled off under reduced pressure
  8. customthe residue was recrystallized from an ethyl acetate/n-hexane mixed solvent

Sources & evidence

ORD record
ord-bb82e7206cd34758a1bdcc3be0b63e3e
Source dataset
uspto-grants-2010_02
Patent number
US07655680B2

Reaction notes

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