Trifluoroacetic acid → HCID 59540396, compound
Reaction equation
[CH3:1][O:2][CH2:3][C:4]([NH:6][C@@H:7]([C:15]([CH3:18])([CH3:17])[CH3:16])[C:8]([O:10]C(C)(C)C)=[O:9])=[O:5].FC(F)(F)C(O)=O>ClCCl>[CH3:1][O:2][CH2:3][C:4]([NH:6][C@@H:7]([C:15]([CH3:18])([CH3:17])[CH3:16])[C:8]([OH:10])=[O:9])=[O:5]Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Conditions
- Temperature
- 25 °C
Procedure
A solution of the product from Example 55A (0.012 g, 0.038 mmol) in dichloromethane (0.2 mL) was treated with trifluoroacetic acid (0.2 mL), stirred at 25° C. for 1 hour and concentrated. The residue was azeotroped with toluene to give the title compound, which was used without further purification.
Workup
- concentrationconcentrated
- customThe residue was azeotroped with toluene
Sources & evidence
- ORD record
- ord-50f423b07ee945839041fb86f430fa58
- Source dataset
- uspto-grants-2010_11
- Patent number
- US07834043B2
Reaction notes
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