Trifluoroacetic acid → Trifluoroacetic acid
Reaction equation
[C:1]([NH:4][C:5]1[C:10]([Cl:11])=[CH:9][C:8]([CH2:12][C:13](=[N:30]C(=O)OC(C)(C)C)[NH:14][C:15](=[O:29])[CH2:16][C:17](=[N:26][O:27][CH3:28])[C:18]2[CH:23]=[CH:22][C:21]([O:24][CH3:25])=[CH:20][CH:19]=2)=[CH:7][C:6]=1[Cl:38])(=[O:3])[CH3:2].[C:39]([OH:45])([C:41]([F:44])([F:43])[F:42])=[O:40]>ClCCl>[C:1]([NH:4][C:5]1[C:6]([Cl:38])=[CH:7][C:8]([CH2:12][C:13](=[N:14][C:15](=[O:29])[CH2:16][C:17](=[N:26][O:27][CH3:28])[C:18]2[CH:23]=[CH:22][C:21]([O:24][CH3:25])=[CH:20][CH:19]=2)[NH2:30])=[CH:9][C:10]=1[Cl:11])(=[O:3])[CH3:2].[C:39]([OH:45])([C:41]([F:44])([F:43])[F:42])=[O:40]Participants
5
Reactant 2
Product 2
Reagents, catalysts & solvents 1
Procedure
To a solution of tert-butyl 2-(4-acetamido-3,5-dichlorophenyl)-1-(3-(methoxyimino)-3-(4-methoxyphenyl)-propanamido)ethylidenecarbamate (12 mg) in dichloromethane (0.10 mL) was added TFA (0.10 mL), and the resulting mixture was stirred at room temperature for 12 h. The solvents were removed in vacuo to give the title compound as its TFA salt (10 mg). Retention time: 1.75 min (method A). MS (ESI) (M+H)+ 482.19.
Workup
- customThe solvents were removed in vacuo
Sources & evidence
- ORD record
- ord-ad41e7a820c846878685a87a3e3e3769
- Source dataset
- uspto-grants-2008_06
- Patent number
- US07390925B2
Reaction notes
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