Water → HCID 53718133, compound

HRID 2351207Notes

Reaction equation

HRID 2351207 reaction equation
N1C=CC=CC=1.[CH3:7][O:8][N:9]=[C:10]([C:16]1[N:17]=[C:18]([NH2:21])[S:19][CH:20]=1)[C:11]([O:13][CH2:14][CH3:15])=[O:12].Cl[C:23]([O:25][CH2:26][CH3:27])=[O:24].O>C(OCC)(=O)C.CN(C)C=O>[CH3:7][O:8][N:9]=[C:10]([C:16]1[N:17]=[C:18]([NH:21][C:23]([O:25][CH2:26][CH3:27])=[O:24])[S:19][CH:20]=1)[C:11]([O:13][CH2:14][CH3:15])=[O:12]

Participants

7

Procedure

Pyridine (3 g.) was added to a solution of ethyl 2-methoxyimino-2-(2-amino-1,3-thiazol-4-yl)acetate (syn isomer) (6.5 g.) in a mixture of ethyl acetate (60 ml.) and dimethylformamide (20 ml.). To the solution was dropwise added with stirring at 4° C. ethyl chloroformate (8 g.). After adding water (50 ml.) to the reaction mixture, the organic layer was separated, washed with water and then with a saturated aqueous solution of sodium chloride and dried over magnesium sulfate. The solvent was distilled off under reduced pressure. The residue was subjected to column chromatography on silica gel (120 g.) using a mixture of ether and petroleum ether (5:2) as an eluent to give ethyl 2-methoxyimino-2-(2-ethoxycarbonylamino-1,3-thiazol-4-yl)acetate (syn isomer) (5.4 g.).

Workup

  1. additionTo the solution was dropwise added
  2. customthe organic layer was separated
  3. washwashed with water
  4. dry with materialwith a saturated aqueous solution of sodium chloride and dried over magnesium sulfate
  5. distillationThe solvent was distilled off under reduced pressure
  6. additiona mixture of ether and petroleum ether (5:2) as an eluent

Sources & evidence

ORD record
ord-0bcfe49a84c448179bc543b20984a724
Source dataset
uspto-grants-1989_10
Patent number
US04871860

Reaction notes

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