(S)-2-(6-(4-Benzamidophenyl)-1-oxoisoindolin-2-yl)-3-methylbutanoic acid → 2-Methyl-2-(1-oxo-6-(4-(4-(trifluoromethoxy)benzamido)phenyl)isoindolin-2-yl)propanoic acid

HRID 404040Notes

Reaction equation

HRID 404040 reaction equation
C(NC1C=CC(C2C=C3C(CN([C@@H](C(C)C)C(O)=O)C3=O)=CC=2)=CC=1)(=O)C1C=CC=CC=1.[CH3:33][C:34]([N:40]1[CH2:48][C:47]2[C:42](=[CH:43][C:44]([C:49]3[CH:54]=[CH:53][C:52]([NH:55][C:56](=[O:68])[C:57]4[CH:62]=[CH:61][C:60]([O:63][C:64]([F:67])([F:66])[F:65])=[CH:59][CH:58]=4)=[CH:51][CH:50]=3)=[CH:45][CH:46]=2)[C:41]1=[O:69])([CH3:39])[C:35]([O:37]C)=[O:36]>>[CH3:39][C:34]([N:40]1[CH2:48][C:47]2[C:42](=[CH:43][C:44]([C:49]3[CH:50]=[CH:51][C:52]([NH:55][C:56](=[O:68])[C:57]4[CH:62]=[CH:61][C:60]([O:63][C:64]([F:67])([F:65])[F:66])=[CH:59][CH:58]=4)=[CH:53][CH:54]=3)=[CH:45][CH:46]=2)[C:41]1=[O:69])([CH3:33])[C:35]([OH:37])=[O:36]

Participants

3

Reactant 2

HCID 53303631(S)-2-(6-(4-Benzamidophenyl)-1-oxoisoindolin-2-yl)-3-methylbutanoic acidHCID 67307203Methyl 2-methyl-2-(1-oxo-6-(4-(4-(trifluoromethoxy)benzamido)phenyl)iso indolin-2-yl)propanoate

Product 1

HCID 673066522-Methyl-2-(1-oxo-6-(4-(4-(trifluoromethoxy)benzamido)phenyl)isoindolin-2-yl)propanoic acidYield 71%

Procedure

The compound of example 523 was prepared analogous to compound of example 98 by hydrolysis of compound of example 522.

Sources & evidence

ORD record
ord-388d437ca7024b849fc4bd28b2fbc827
Source dataset
uspto-grants-2014_06
Patent number
US08748426B2

Reaction notes

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