(S)-2-(6-(4-Benzamidophenyl)-1-oxoisoindolin-2-yl)-3-methylbutanoic acid → HCID 67306928, compound

HRID 403844Notes

Reaction equation

HRID 403844 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.[F:33][C:34]1[CH:66]=[CH:65][C:37]([C:38]([NH:40][C:41]2[CH:46]=[CH:45][C:44]([C:47]3[CH:55]=[C:54]4[C:50]([CH2:51][N:52]([C@@H:57]([CH:62]([CH3:64])[CH3:63])[C:58]([O:60]C)=[O:59])[C:53]4=[O:56])=[CH:49][CH:48]=3)=[CH:43][CH:42]=2)=[O:39])=[C:36]([C:67]([F:70])([F:69])[F:68])[CH:35]=1>>[F:33][C:34]1[CH:66]=[CH:65][C:37]([C:38]([NH:40][C:41]2[CH:46]=[CH:45][C:44]([C:47]3[CH:55]=[C:54]4[C:50]([CH2:51][N:52]([C@@H:57]([CH:62]([CH3:64])[CH3:63])[C:58]([OH:60])=[O:59])[C:53]4=[O:56])=[CH:49][CH:48]=3)=[CH:43][CH:42]=2)=[O:39])=[C:36]([C:67]([F:70])([F:68])[F:69])[CH:35]=1

Participants

3

Reactant 2

HCID 53303631(S)-2-(6-(4-Benzamidophenyl)-1-oxoisoindolin-2-yl)-3-methylbutanoic acidHCID 131731493HCID 131731493, compound

Product 1

HCID 67306928HCID 67306928, compoundYield 91%

Procedure

The compound of example 198 was prepared analogous to compound of example 98 by hydrolysis of compound of example 197.

Sources & evidence

ORD record
ord-2f9d35f6935741d0846f6615e87ae4ee
Source dataset
uspto-grants-2014_06
Patent number
US08748426B2

Reaction notes

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