Methyl 2-(1-oxo-5-(4-(3-(3-(trifluoromethyl)phenyl)ureido)phenyl)isoindolin-2-yl)acetate → 2-(1-Oxo-5-(4-(3-(3-(trifluoromethyl)phenyl)ureido)phenyl)isoindolin-2-yl)acetic acid
Reaction equation
CC(C)[C@@H:3]([N:7]1[CH2:15][C:14]2[C:9](=[CH:10][CH:11]=[C:12]([C:16]3[CH:21]=[CH:20][C:19]([NH:22][C:23]([NH:25][C:26]4[CH:31]=[CH:30][CH:29]=[C:28]([C:32]([F:35])([F:34])[F:33])[CH:27]=4)=[O:24])=[CH:18][CH:17]=3)[CH:13]=2)[C:8]1=[O:36])[C:4]([OH:6])=[O:5].O=C1C2C(=CC(C3C=CC(NC(NC4C=CC=C(C(F)(F)F)C=4)=O)=CC=3)=CC=2)CN1CC(OC)=O>>[O:36]=[C:8]1[C:9]2[C:14](=[CH:13][C:12]([C:16]3[CH:17]=[CH:18][C:19]([NH:22][C:23]([NH:25][C:26]4[CH:31]=[CH:30][CH:29]=[C:28]([C:32]([F:34])([F:33])[F:35])[CH:27]=4)=[O:24])=[CH:20][CH:21]=3)=[CH:11][CH:10]=2)[CH2:15][N:7]1[CH2:3][C:4]([OH:6])=[O:5]Participants
3
Reactant 2
Product 1
Procedure
The compound of example 364 was prepared analogous to the compound of example 361 by hydrolysis of the compound of example 363.
Sources & evidence
- ORD record
- ord-5e67916d53464f31865a2438abe35ca7
- Source dataset
- uspto-grants-2014_06
- Patent number
- US08748426B2
Reaction notes
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