Trifluoroacetic acid → HCID 131717452, compound
Reaction equation
[CH:1]([NH:3][C@@H:4]1[C:34](=[O:35])[N:6]2[C:7]([C:22]([O:24]CC3C=CC(OC)=CC=3)=[O:23])=[C:8](/[CH:11]=[CH:12]/[CH2:13][N+:14]([CH2:18][C:19](=[O:21])[NH2:20])([CH2:16][CH3:17])[CH3:15])[CH2:9][S:10][C@H:5]12)=[O:2].[I-].[F:37][C:38]([F:43])([F:42])[C:39]([OH:41])=[O:40]>C1(OC)C=CC=CC=1>[F:37][C:38]([F:43])([F:42])[C:39]([O-:41])=[O:40].[CH:1]([NH:3][C@@H:4]1[C:34](=[O:35])[N:6]2[C:7]([C:22]([OH:24])=[O:23])=[C:8](/[CH:11]=[CH:12]/[CH2:13][N+:14]([CH2:18][C:19](=[O:21])[NH2:20])([CH2:16][CH3:17])[CH3:15])[CH2:9][S:10][C@H:5]12)=[O:2]Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
In a similar manner as in Example 5, the compound (3.4 g) of Example 25 was suspended in anisole (20 ml), followed by an addition of trifluoroacetic acid (23 ml) to obtain the target compound (2.04 g).
Sources & evidence
- ORD record
- ord-64a4f8d9a38f49438c38acbacf0fa5a3
- Source dataset
- uspto-grants-1992_07
- Patent number
- US05128465
Reaction notes
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