Lithium Hydroxide → HCID 68701098, compound
Reaction equation
C([O:3][C:4]([C:6]1[N:7]=[CH:8][S:9][C:10]=1[NH:11][CH:12]1[CH2:14][CH2:13]1)=[O:5])C.[Li+:15].[OH-]>C1COCC1.CO>[CH:12]1([NH:11][C:10]2[S:9][CH:8]=[N:7][C:6]=2[C:4]([O-:5])=[O:3])[CH2:13][CH2:14]1.[Li+:15]Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
198 mg of 5-cyclopropylamino-thiazole-4-carboxylic acid ethyl ester (0.93 mmol) were dissolved in a 3:1 mixture of THF/methanol (2 ml) and 1.4 ml of a 1N LiOH-solution were added. The reaction mixture was stirred at RT for 3 days, then concentrated in vacuo and the remaining residue was dried. This gave 191 mg of a yellow solid containing the crude title compound (contaminated with excess of lithium hydroxide) that was used in the following step without further purification. MS (ISP) 182.9 (M−H)−.
Workup
- additionwere added
- concentrationconcentrated in vacuo
- customthe remaining residue was dried
- additionThis gave 191 mg of a yellow solid containing the crude title compound (contaminated with excess of lithium hydroxide) that
- customwas used in the following step without further purification
Sources & evidence
- ORD record
- ord-3410eabc3dcc4a9f89efd6d824c807a7
- Source dataset
- uspto-grants-2010_03
- Patent number
- US07678818B2
Reaction notes
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