2-Amino-3-methoxypyridine → N-(3-Methoxypyridin-2-yl)-2-(4-(1-methylpropyl)phenoxy)nonanoic amide

HRID 2379608Notes

Reaction equation

HRID 2379608 reaction equation
[CH3:1][O:2][C:3]1[C:4]([NH2:9])=[N:5][CH:6]=[CH:7][CH:8]=1.[CH3:10][CH:11]([C:14]1[CH:31]=[CH:30][C:17]([O:18][CH:19]([CH2:23][CH2:24][CH2:25][CH2:26][CH2:27][CH2:28][CH3:29])[C:20](O)=[O:21])=[CH:16][CH:15]=1)[CH2:12][CH3:13]>>[CH3:1][O:2][C:3]1[C:4]([NH:9][C:20](=[O:21])[CH:19]([O:18][C:17]2[CH:30]=[CH:31][C:14]([CH:11]([CH3:10])[CH2:12][CH3:13])=[CH:15][CH:16]=2)[CH2:23][CH2:24][CH2:25][CH2:26][CH2:27][CH2:28][CH3:29])=[N:5][CH:6]=[CH:7][CH:8]=1

Participants

3

Procedure

3-Methoxy-2-aminopyridine, prepared by reduction of the corresponding nitro compound according to Example 31, was coupled with 2-(4-(1-methylpropyl)phenoxynonanoic acid according to Example 25 to give the title compound.

Sources & evidence

ORD record
ord-5daa41d3f1c34042b07dcf693ddefab3
Source dataset
uspto-grants-1994_11
Patent number
US05362878

Reaction notes

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