2,6-Dimethoxybenzoic Acid → HCID 67116899, compound

HRID 1525034Notes

Reaction equation

HRID 1525034 reaction equation
[CH2:1]1[CH:5]2[CH2:6][NH:7][CH2:8][CH:4]2[CH2:3][N:2]1[C:9]1[CH:18]=[N:17][C:16]2[C:11](=[CH:12][CH:13]=[CH:14][CH:15]=2)[N:10]=1.[CH3:19][O:20][C:21]1[CH:29]=[CH:28][CH:27]=[C:26]([O:30][CH3:31])[C:22]=1[C:23](O)=[O:24]>>[CH3:31][O:30][C:26]1[CH:27]=[CH:28][CH:29]=[C:21]([O:20][CH3:19])[C:22]=1[C:23]([N:7]1[CH2:6][CH:5]2[CH2:1][N:2]([C:9]3[CH:18]=[N:17][C:16]4[C:11](=[CH:12][CH:13]=[CH:14][CH:15]=4)[N:10]=3)[CH2:3][CH:4]2[CH2:8]1)=[O:24]

Participants

3

Reactant 2

HCID 151092,6-Dimethoxybenzoic AcidHCID 610372812-(Hexahydro-pyrrolo[3,4-c]pyrrol-2-yl)-quinoxaline

Product 1

HCID 67116899HCID 67116899, compound

Procedure

The title compound was prepared in a manner analogous to Example 15 utilizing Intermediate 35 and 2,6-dimethoxybenzoic acid. MS (ESI) mass calcd. for C23H24N4O3, 404.47; m/z found, 405.3 [M+H]+.

Sources & evidence

ORD record
ord-524a35dd744c4f8aac85946b00b65315
Source dataset
uspto-grants-2015_07
Patent number
US09079911B2

Reaction notes

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