HCID 19605030, compound → HCID 21262374, compound
Reaction equation
C([O:4][CH2:5][C:6]1[S:10][C:9]2=[CH:11][N:12]=[CH:13][N:8]2[CH:7]=1)(=O)C>CO.C(=O)([O-])[O-].[K+].[K+]>[OH:4][CH2:5][C:6]1[S:10][C:9]2=[CH:11][N:12]=[CH:13][N:8]2[CH:7]=1Participants
4
Reactant 1
Product 1
Reagents, catalysts & solvents 2
Procedure
A 846 mg potion of 2-acetoxymethylimidazo[5,1-b]thiazole was dissolved in a mixed solution of 17 ml of methanol and 1 ml of an aqueous saturated potassium carbonate solution, followed by stirring at room temperature for 1.5 hours. Then, the reaction solution was filtered, and the filtrate was then concentrated under reduced pressure. The resulting residue was purified by a silica gel column chromatograph to obtain 550 mg of the title compound.
Workup
- filtrationThen, the reaction solution was filtered
- concentrationthe filtrate was then concentrated under reduced pressure
- customThe resulting residue was purified by a silica gel column chromatograph
Sources & evidence
- ORD record
- ord-25646c1fe70942cdaae2592f32695b16
- Source dataset
- uspto-grants-1999_11
- Patent number
- US05990101
Reaction notes
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