(S)-2-(6-(4-Benzamidophenyl)-1-oxoisoindolin-2-yl)-3-methylbutanoic acid → HCID 70975403, compound

HRID 403806Notes

Reaction equation

HRID 403806 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][CH:34]([CH3:71])[C@H:35]([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:69])[C:57]4[CH:62]=[C:61]([O:63][CH3:64])[C:60]([O:65][CH3:66])=[C:59]([O:67][CH3:68])[CH:58]=4)=[CH:51][CH:50]=3)=[CH:45][CH:46]=2)[C:41]1=[O:70])[C:36]([O:38]C)=[O:37]>>[CH3:33][CH:34]([CH3:71])[C@H:35]([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:69])[C:57]4[CH:58]=[C:59]([O:67][CH3:68])[C:60]([O:65][CH3:66])=[C:61]([O:63][CH3:64])[CH:62]=4)=[CH:53][CH:54]=3)=[CH:45][CH:46]=2)[C:41]1=[O:70])[C:36]([OH:38])=[O:37]

Participants

3

Reactant 2

HCID 53303631(S)-2-(6-(4-Benzamidophenyl)-1-oxoisoindolin-2-yl)-3-methylbutanoic acidHCID 53303741HCID 53303741, compound

Product 1

HCID 70975403HCID 70975403, compoundYield 83%

Procedure

The compound of example 144 was prepared analogous to compound of example 98 by hydrolysis of compound of example 143.

Sources & evidence

ORD record
ord-e7b78c2fea6e46c48ff6aa4f96a18e46
Source dataset
uspto-grants-2014_06
Patent number
US08748426B2

Reaction notes

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