HCID 13060107, compound → HCID 13060126, compound
Reaction equation
[CH2:1]([C:3]1[S:7][C:6]2=[N:8][C:9]([C:11]([O:13]C)=[O:12])=[CH:10][N:5]2[C:4]=1[CH3:15])[CH3:2]>[OH-].[Na+]>[CH2:1]([C:3]1[S:7][C:6]2=[N:8][C:9]([C:11]([OH:13])=[O:12])=[CH:10][N:5]2[C:4]=1[CH3:15])[CH3:2]Participants
3
Reactant 1
Product 1
Reagents, catalysts & solvents 1
Procedure
1.5 g of 2-ethyl-3-methyl-6-carbomethoxy-imidazo-(2,1-b)thiazole(obtained as described in Example 45) are refluxed for 2 hours in 5 ml of 10% NaOH. The solution obtained is treated in the same manner as described in Example 49 to yield 1.2 g of 2-ethyl-3-methyl-imidazo-(2,1-b)thiazole-6-carboxylic acid m.p. 243°-245° C.
Workup
- customThe solution obtained
- additionis treated in the same manner
Sources & evidence
- ORD record
- ord-a623ba4f77794089bfb776c9df1da61a
- Source dataset
- uspto-grants-1981_05
- Patent number
- US04267339
Reaction notes
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