Trifluoroacetic acid → HCID 178454634, compound
Reaction equation
[F:1][C:2]([F:7])([F:6])[C:3]([OH:5])=[O:4].[NH2:8][N:9]=[CH:10][NH:11][C:12]1[CH:13]=[C:14]([C:18]([NH:20][C:21]2[CH:26]=[CH:25][C:24]([CH:27]([CH3:36])[CH2:28][C:29]([O:31]C(C)(C)C)=[O:30])=[CH:23][CH:22]=2)=[O:19])[CH:15]=[CH:16][CH:17]=1.C(O)(C(F)(F)F)=O>>[F:1][C:2]([F:7])([F:6])[C:3]([OH:5])=[O:4].[NH2:8][N:9]=[CH:10][NH:11][C:12]1[CH:13]=[C:14]([C:18]([NH:20][C:21]2[CH:26]=[CH:25][C:24]([CH:27]([CH3:36])[CH2:28][C:29]([OH:31])=[O:30])=[CH:23][CH:22]=2)=[O:19])[CH:15]=[CH:16][CH:17]=1Participants
3
Procedure
The compound of Example 30 was hydrolyzed with TFA under conditions similar to those described in Example 33.
Sources & evidence
- ORD record
- ord-c407e830d54f4794b85b4d9a12dd39f0
- Source dataset
- uspto-grants-1999_09
- Patent number
- US05952381
Reaction notes
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