HCID 12428325, compound → HCID 131731526, compound

HRID 403920Notes

Reaction equation

HRID 403920 reaction equation
[NH2:1][C:2]1[CH:7]=[CH:6][C:5]([C:8]2[CH:9]=[C:10]3[C:14](=[CH:15][CH:16]=2)[C:13](=[O:17])[N:12]([C@@H:18]([CH:23]([CH3:25])[CH3:24])[C:19]([O:21][CH3:22])=[O:20])[CH2:11]3)=[CH:4][CH:3]=1.[CH3:26][O:27][C:28]1[CH:36]=[CH:35][C:31]([C:32](Br)=[O:33])=[CH:30][CH:29]=1>>[CH3:26][O:27][C:28]1[CH:36]=[CH:35][C:31]([C:32]([NH:1][C:2]2[CH:7]=[CH:6][C:5]([C:8]3[CH:9]=[C:10]4[C:14](=[CH:15][CH:16]=3)[C:13](=[O:17])[N:12]([C@@H:18]([CH:23]([CH3:25])[CH3:24])[C:19]([O:21][CH3:22])=[O:20])[CH2:11]4)=[CH:4][CH:3]=2)=[O:33])=[CH:30][CH:29]=1

Participants

3

Reactant 2

HCID 12428325HCID 12428325, compoundHCID 131731499(S)-Methyl 2-(5-(4-aminophenyl)-1-oxoisoindolin-2-yl)-3-methylbutanoate

Product 1

HCID 131731526HCID 131731526, compound

Procedure

The compound of example 310 was prepared analogous to compound of example 304 by reaction of compound of example 223 with 4-methoxy benzoyl bromide. The compound of example 310 was used directly without isolation, for the preparation of compound of example 311.

Sources & evidence

ORD record
ord-8f63466d3c9f4251b825a1575387d121
Source dataset
uspto-grants-2014_06
Patent number
US08748426B2

Reaction notes

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