Trifluoroacetic acid → HCID 67127028, compound
Reaction equation
[NH:1]1[C:5]2=[N:6][CH:7]=[C:8]([O:10][C:11]3[CH:45]=[C:44]([N:46]4[CH2:51][CH2:50][N:49]([CH2:52][C:53]5[CH2:58][CH2:57][C:56]([CH3:60])([CH3:59])[CH2:55][C:54]=5[C:61]5[CH:66]=[CH:65][C:64]([Cl:67])=[CH:63][CH:62]=5)[CH2:48][CH2:47]4)[CH:43]=[CH:42][C:12]=3[C:13]([NH:15][S:16]([C:19]3[CH:24]=[CH:23][C:22]([NH:25][CH:26]4[CH2:31][CH2:30][N:29](C(OC(C)(C)C)=O)[CH2:28][CH2:27]4)=[C:21]([N+:39]([O-:41])=[O:40])[CH:20]=3)(=[O:18])=[O:17])=[O:14])[CH:9]=[C:4]2[CH:3]=[CH:2]1.FC(F)(F)C(O)=O>ClCCl>[NH:1]1[C:5]2=[N:6][CH:7]=[C:8]([O:10][C:11]3[CH:45]=[C:44]([N:46]4[CH2:47][CH2:48][N:49]([CH2:52][C:53]5[CH2:58][CH2:57][C:56]([CH3:60])([CH3:59])[CH2:55][C:54]=5[C:61]5[CH:62]=[CH:63][C:64]([Cl:67])=[CH:65][CH:66]=5)[CH2:50][CH2:51]4)[CH:43]=[CH:42][C:12]=3[C:13]([NH:15][S:16]([C:19]3[CH:24]=[CH:23][C:22]([NH:25][CH:26]4[CH2:31][CH2:30][NH:29][CH2:28][CH2:27]4)=[C:21]([N+:39]([O-:41])=[O:40])[CH:20]=3)(=[O:18])=[O:17])=[O:14])[CH:9]=[C:4]2[CH:3]=[CH:2]1Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
To a cooled (0° C.) solution of EXAMPLE 139A (960 mg) in dichloromethane (10 mL) was added dropwise trifluoroacetic acid (5 mL). The mixture was stirred at the temperature for 3 hours. Then, the mixture was concentrated under vacuum and the residue was dissolved in dichloromethane (200 mL) and washed with aqueous NaHCO3 and brine. After drying over Na2SO4, the mixture was filtered, and evaporation of the solvent from the filtrate gave the title compound.
Workup
- concentrationThen, the mixture was concentrated under vacuum
- dissolutionthe residue was dissolved in dichloromethane (200 mL)
- washwashed with aqueous NaHCO3 and brine
- dry with materialAfter drying over Na2SO4
- filtrationthe mixture was filtered
- customevaporation of the solvent from the filtrate
Sources & evidence
- ORD record
- ord-14b5cb1229784dd2b38c99ce117e95d0
- Source dataset
- uspto-grants-2013_10
- Patent number
- US08546399B2
Reaction notes
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