Trifluoroacetic acid → HCID 61144904, compound
Reaction equation
[CH3:1][C:2]([CH3:23])([CH3:22])[C@H:3]([NH:11][C:12](=[O:21])[CH2:13][O:14][C:15]1[CH:20]=[CH:19][CH:18]=[CH:17][CH:16]=1)[C:4]([O:6]C(C)(C)C)=[O:5].FC(F)(F)C(O)=O>ClCCl>[CH3:1][C:2]([CH3:23])([CH3:22])[C@H:3]([NH:11][C:12](=[O:21])[CH2:13][O:14][C:15]1[CH:20]=[CH:19][CH:18]=[CH:17][CH:16]=1)[C:4]([OH:6])=[O:5]Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Conditions
- Temperature
- 25 °C
Procedure
A solution of the product from Example 54A (0.012 g, 0.038 mmol) in dichloromethane (0.2 mL) was treated with trifluoroacetic acid (0.2 mL) and the reaction was stirred at 25° C. for 1 hour and concentrated. The concentrate was azeotroped with toluene to give the title compound, which was used without further purification.
Workup
- concentrationconcentrated
- customThe concentrate was azeotroped with toluene
Sources & evidence
- ORD record
- ord-ab1bff6e309244ef987fa468acafc51e
- Source dataset
- uspto-grants-2010_11
- Patent number
- US07834043B2
Reaction notes
Loading…