(S)-2-(6-(4-Benzamidophenyl)-1-oxoisoindolin-2-yl)-3-methylbutanoic acid → HCID 67305530, compound

HRID 403850Notes

Reaction equation

HRID 403850 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]([CH3:65])[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:63])[C:57]4[CH:62]=[CH:61][CH:60]=[N:59][CH:58]=4)=[CH:51][CH:50]=3)=[CH:45][CH:46]=2)[C:41]1=[O:64])[C:36]([O:38]C)=[O:37]>>[CH3:33][CH:34]([CH3:65])[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:63])[C:57]4[CH:62]=[CH:61][CH:60]=[N:59][CH:58]=4)=[CH:51][CH:50]=3)=[CH:45][CH:46]=2)[C:41]1=[O:64])[C:36]([OH:38])=[O:37]

Participants

3

Reactant 2

HCID 53303631(S)-2-(6-(4-Benzamidophenyl)-1-oxoisoindolin-2-yl)-3-methylbutanoic acidHCID 53303943HCID 53303943, compound

Product 1

HCID 67305530HCID 67305530, compoundYield 51.63%

Procedure

The compound of example 207 was prepared analogous to compound of example 98 by hydrolysis of compound of example 206.

Sources & evidence

ORD record
ord-8381f15ab9144c52a96b284fe8bc1d81
Source dataset
uspto-grants-2014_06
Patent number
US08748426B2

Reaction notes

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