2-Amino-3-Hydroxypyridine → HCID 24738341, compound

HRID 731614Notes

Reaction equation

HRID 731614 reaction equation
Br[CH2:2][C:3]([C:5]1[C:6]([C:11]2[CH:16]=[CH:15][CH:14]=[CH:13][CH:12]=2)=[N:7][O:8][C:9]=1[CH3:10])=[O:4].[NH2:17][C:18]1[C:23]([OH:24])=[CH:22][CH:21]=[CH:20][N:19]=1>>[CH3:10][C:9]1[O:8][N:7]=[C:6]([C:11]2[CH:16]=[CH:15][CH:14]=[CH:13][CH:12]=2)[C:5]=1[C:3](=[O:4])[CH2:2][O:24][C:23]1[C:18]2[N:19]([CH:2]=[C:3]([C:5]3[C:6]([C:11]4[CH:16]=[CH:15][CH:14]=[CH:13][CH:12]=4)=[N:7][O:8][C:9]=3[CH3:10])[N:17]=2)[CH:20]=[CH:21][CH:22]=1

Participants

3

Reactant 2

HCID 281142-Amino-3-HydroxypyridineHCID 27355314-(Bromoacetyl)-5-methyl-3-phenylisoxazole

Product 1

HCID 24738341HCID 24738341, compoundYield 7%

Procedure

As described for Example 2, 4-(bromoacetyl)-5-methyl-3-phenylisoxazole (commercially available) (140 mg, 0.5 mmol) was converted, using 2-amino-3-hydroxypyridine instead of 2-amino-3-methylpyridine, to the title compound (18 mg, 7%) which was obtained as a yellow foam. MS: m/e=491.3 [M+H]+.

Sources & evidence

ORD record
ord-91ac6ed0d1ae40ac8c444e7b272cf6d4
Source dataset
uspto-grants-2009_09
Patent number
US07585874B2

Reaction notes

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