Hydrogen chloride-ethyl acetate → HCID 54398599, compound

HRID 1424908Notes

Reaction equation

HRID 1424908 reaction equation
[Cl:1][C:2]1[N:3]=[C:4]([C:16]([O:18][CH2:19][CH3:20])=[O:17])[N:5](COCC[Si](C)(C)C)[C:6]=1[Cl:7].Cl.C(OCC)(=O)C>C(O)C>[Cl:7][C:6]1[N:5]=[C:4]([C:16]([O:18][CH2:19][CH3:20])=[O:17])[NH:3][C:2]=1[Cl:1]

Participants

4

Procedure

Ethyl 4,5-dichloro-1-{[2-(trimethylsilyl)ethoxy]methyl}-1H-imidazole-2-carboxylate obtained in Example (7b) (0.61 g, 1.79 mmol) was dissolved in ethanol (3 mL). A 4 N hydrochloric acid/ethyl acetate solution (15 mL) was added, and the mixture was heated under reflux for one hour. The reaction solution was concentrated under reduced pressure, diluted with ethyl acetate, washed with brine and dried over anhydrous sodium sulfate. Following concentration under reduced pressure, the residue was purified by silica gel column chromatography (elution solvent: hexane/ethyl acetate=10/1, 1/1) to obtain 0.24 g of the title compound as a pale yellow oily substance (65%).

Workup

  1. temperaturethe mixture was heated
  2. temperatureunder reflux for one hour
  3. concentrationThe reaction solution was concentrated under reduced pressure
  4. additiondiluted with ethyl acetate
  5. washwashed with brine
  6. dry with materialdried over anhydrous sodium sulfate
  7. concentrationconcentration under reduced pressure
  8. customthe residue was purified by silica gel column chromatography (elution solvent: hexane/ethyl acetate=10/1, 1/1)

Sources & evidence

ORD record
ord-de30e37fc586416d9ef85744b405806e
Source dataset
uspto-grants-2015_01
Patent number
US08927588B2

Reaction notes

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