3,5-Dimethoxybenzoyl chloride → HCID 131731488, compound

HRID 403834Notes

Reaction equation

HRID 403834 reaction equation
C(NC1C=CC(C2C=C3C(CN([C@@H](C(C)C)C(OC)=O)C3=O)=CC=2)=CC=1)(=O)C1C=CC=CC=1.[NH2:34][C:35]1[CH:40]=[CH:39][C:38]([C:41]2[CH:49]=[C:48]3[C:44]([CH2:45][N:46]([C@@H:51]([CH:56]([CH3:58])[CH3:57])[C:52]([O:54][CH3:55])=[O:53])[C:47]3=[O:50])=[CH:43][CH:42]=2)=[CH:37][CH:36]=1.[CH3:59][O:60][C:61]1[CH:62]=[C:63]([CH:67]=[C:68]([O:70][CH3:71])[CH:69]=1)[C:64](Cl)=[O:65]>>[CH3:71][O:70][C:68]1[CH:67]=[C:63]([CH:62]=[C:61]([O:60][CH3:59])[CH:69]=1)[C:64]([NH:34][C:35]1[CH:36]=[CH:37][C:38]([C:41]2[CH:49]=[C:48]3[C:44]([CH2:45][N:46]([C@@H:51]([CH:56]([CH3:58])[CH3:57])[C:52]([O:54][CH3:55])=[O:53])[C:47]3=[O:50])=[CH:43][CH:42]=2)=[CH:39][CH:40]=1)=[O:65]

Participants

4

Reactant 3

HCID 870033,5-Dimethoxybenzoyl chlorideHCID 123625862(S)-Methyl 2-(6-(4-benzamidophenyl)-1-oxoisoindolin-2-yl)-3-methylbutanoateHCID 131731441(S)-Methyl 2-(6-(4-aminophenyl)-1-oxoisoindolin-2-yl)-3-methylbutanoate

Product 1

HCID 131731488HCID 131731488, compound

Procedure

The compound of example 179 was prepared analogous to compound of example 97 by reaction of compound of example 6 with 3,5-dimethoxy benzoyl chloride. The compound of example 179 was used directly without isolation for the preparation of compound of example 180.

Sources & evidence

ORD record
ord-740a4f2597784734a25ca0c397b4c9fa
Source dataset
uspto-grants-2014_06
Patent number
US08748426B2

Reaction notes

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