Water → ethyl 2-[2-(N-methyl-N-tert-pentyloxycarbonylamino)-1,3-thiazol-4-yl]glyoxylate

HRID 1659393Notes

Reaction equation

HRID 1659393 reaction equation
[Se](=O)=O.[OH2:4].[CH3:5][N:6]([C:15]1[S:16][CH:17]=[C:18]([CH2:20][C:21]([O:23][CH2:24][CH3:25])=[O:22])[N:19]=1)[C:7]([O:9][C:10]([CH2:13][CH3:14])([CH3:12])[CH3:11])=[O:8]>O1CCOCC1>[CH3:5][N:6]([C:15]1[S:16][CH:17]=[C:18]([C:20](=[O:4])[C:21]([O:23][CH2:24][CH3:25])=[O:22])[N:19]=1)[C:7]([O:9][C:10]([CH2:13][CH3:14])([CH3:11])[CH3:12])=[O:8]

Participants

5

Conditions

Temperature
110 °C

Procedure

A mixture of selenium dioxide (0.452 g.), dioxane (9 ml.) and water (0.36 ml.) was refluxed in bath at 110° C., and to the solution was added a solution of ethyl 2-[2-(N-methyl-N-tert-pentyloxycarbonylamino)-1,3-thiazol-4-yl]acetate (1.07 g.) and dioxane (9 ml.), and the mixture was stirred for 4.5 hours at the same temperature. After the reaction, the reaction mixture was filtered, and dioxane was distilled off from the filtrate under reduced pressure. To the residue were added water and ethyl acetate with stirring, and then ethyl acetate layer was separated. The ethyl acetate layer was dried over magnesium sulfate and then concentrated to give oil of ethyl 2-[2-(N-methyl-N-tert-pentyloxycarbonylamino)-1,3-thiazol-4-yl]glyoxylate (0.45 g.).

Workup

  1. customAfter the reaction
  2. filtrationthe reaction mixture was filtered
  3. distillationdioxane was distilled off from the filtrate under reduced pressure
  4. additionTo the residue were added water and ethyl acetate
  5. stirringwith stirring
  6. customethyl acetate layer was separated
  7. dry with materialThe ethyl acetate layer was dried over magnesium sulfate
  8. concentrationconcentrated

Sources & evidence

ORD record
ord-c120e6473ebc4fed8decf8ad008ca7b2
Source dataset
uspto-grants-1981_12
Patent number
US04303655

Reaction notes

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