Methanol → HCID 44159846, compound
Reaction equation
[OH:1][CH2:2][C:3]1[CH:7]=[C:6]([C:8]2[C:9]([NH:14]C(=O)C(C)(C)C)=[N:10][CH:11]=[CH:12][CH:13]=2)[O:5][N:4]=1.CO.[OH-].[Na+]>C(O)(=O)C>[NH2:14][C:9]1[C:8]([C:6]2[O:5][N:4]=[C:3]([CH2:2][OH:1])[CH:7]=2)=[CH:13][CH:12]=[CH:11][N:10]=1Participants
5
Reactant 3
Product 1
Reagents, catalysts & solvents 1
Conditions
- Temperature
- 58.5 °C
Procedure
To a mixture of N-{3-[3-(hydroxymethyl)isoxazol-5-yl]pyridin-2-yl}-2,2 dimethylpropanamide (82.8 g) obtained in Example 4 and methanol (350 mL) was added 5N aqueous sodium hydroxide (350 mL) at room temperature, which was stirred at 57 to 60° C. for 14 hours. To the reaction mixture was added acetic acid (100 mL) and the precipitated solid was filtered, so as to obtain the title compound (42.2 g) as a grayish white solid.
Workup
- filtrationthe precipitated solid was filtered
Sources & evidence
- ORD record
- ord-f646affc504e4a35a38c516f83bd9b7c
- Source dataset
- uspto-grants-2013_04
- Patent number
- US08410277B2
Reaction notes
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