4-Aminophenol → 4-(3-Aminophenoxy)-N-methylpyridine-2-carboxamide

HRID 658468Notes

Reaction equation

HRID 658468 reaction equation
[CH3:1][NH:2][C:3]([C:5]1[CH:10]=[C:9]([O:11][C:12]2[CH:17]=[CH:16][C:15](N)=[CH:14][CH:13]=2)[CH:8]=[CH:7][N:6]=1)=[O:4].[NH2:19]C1C=CC(O)=CC=1>>[CH3:1][NH:2][C:3]([C:5]1[CH:10]=[C:9]([O:11][C:12]2[CH:17]=[CH:16][CH:15]=[C:14]([NH2:19])[CH:13]=2)[CH:8]=[CH:7][N:6]=1)=[O:4]

Participants

3

Reactant 2

HCID 4034-AminophenolHCID 166551294-(4-Aminophenoxy)-N-methylpicolinamide

Product 1

HCID 236145574-(3-Aminophenoxy)-N-methylpyridine-2-carboxamide

Procedure

The title compound was prepared in the same manner described for 4-(4-aminophenoxy)pyridine-2-carboxylic acid methylamide, substituting 3-aminophenol for 4-aminophenol. 1H-NMR (DMSO-d6) δ 8.75 (br q, J=4.8 Hz, 1H), 8.48 (d, J=6.3 Hz, 1H), 7.39 (d, J=2.1 Hz, 1H), 7.15 to 7.07 (m, 2H), 5.51 to 6.47 (m, 1H), 6.31 to 6.24 (m, 2H), 5.40 (s, 2H), 2.77 (d, J=5.1 Hz, 3H).

Sources & evidence

ORD record
ord-bb768feed75a43988383ea67838c1a15
Source dataset
uspto-grants-2011_12
Patent number
US08076488B2

Reaction notes

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