Trifluoroacetic acid → HCID 22708164, compound
Reaction equation
[CH3:1][O:2][C:3]1[C:8]([CH3:9])=[CH:7][C:6]([NH:10][C:11]([CH:13]([NH:16][CH2:17][C:18]2[CH:34]=[CH:33][C:21]([O:22][C:23]([CH3:32])([CH3:31])[C:24]([O:26]C(C)(C)C)=[O:25])=[CH:20][CH:19]=2)[CH2:14][CH3:15])=[O:12])=[C:5]([CH3:35])[CH:4]=1.FC(F)(F)C(O)=O>ClCCl>[CH3:1][O:2][C:3]1[C:8]([CH3:9])=[CH:7][C:6]([NH:10][C:11]([CH:13]([NH:16][CH2:17][C:18]2[CH:19]=[CH:20][C:21]([O:22][C:23]([CH3:32])([CH3:31])[C:24]([OH:26])=[O:25])=[CH:33][CH:34]=2)[CH2:14][CH3:15])=[O:12])=[C:5]([CH3:35])[CH:4]=1Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
Similarly to the procedure of Example 1-9, 115 mg (0.237 mmol) of tert-butyl 2-(4-{[(1-{[(4-methoxy-2,5-dimethylphenyl)amino]carbonyl}propyl)amino]methyl}phenoxy)-2-methylpropionate (Example 1-8) are reacted with 0.46 ml (5.93 mmol) of trifluoroacetic acid in 3 ml of dichloromethane to give 100 mg (93%) of 2-(4-{[(1-{[(4-methoxy-2,5-dimethylphenyl)amino]carbonyl}propyl)amino]methyl}phenoxy)-2-methylpropionic acid.
Sources & evidence
- ORD record
- ord-17c8ffaa05fc47be8b276de95de322ea
- Source dataset
- uspto-grants-2004_06
- Patent number
- US06750236B2
Reaction notes
Loading…