Trifluoroacetic acid → HCID 131717449, compound
Reaction equation
[C:1]1([CH2:7][C:8]([NH:10][C@@H:11]2[C:41](=[O:42])[N:13]3[C:14]([C:29]([O:31]CC4C=CC(OC)=CC=4)=[O:30])=[C:15](/[CH:18]=[CH:19]/[CH2:20][N+:21]([CH2:25][C:26](=[O:28])[NH2:27])([CH2:23][CH3:24])[CH3:22])[CH2:16][S:17][C@H:12]23)=[O:9])[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1.[I-].[F:44][C:45]([F:50])([F:49])[C:46]([OH:48])=[O:47]>C1(OC)C=CC=CC=1>[F:44][C:45]([F:50])([F:49])[C:46]([O-:48])=[O:47].[C:1]1([CH2:7][C:8]([NH:10][C@@H:11]2[C:41](=[O:42])[N:13]3[C:14]([C:29]([OH:31])=[O:30])=[C:15](/[CH:18]=[CH:19]/[CH2:20][N+:21]([CH2:25][C:26](=[O:28])[NH2:27])([CH2:23][CH3:24])[CH3:22])[CH2:16][S:17][C@H:12]23)=[O:9])[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
In a manner similar to Example 5, the compound (23 g) of Example 11 was suspended in anisole (130 ml), followed by an addition of trifluoroacetic acid (140 ml) to obtain the target product (15.9 g).
Sources & evidence
- ORD record
- ord-697aa86e8e234b7099fc4b17af6b71fa
- Source dataset
- uspto-grants-1992_07
- Patent number
- US05128465
Reaction notes
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