Acetic Acid → 4-[(2-Butyl pyrazolo(1,5-a) pyridin-3-yl) carbonyl]benzoic acid
Reaction equation
[CH2:1]([C:5]1[C:13]([C:14]([C:16]2[CH:23]=[CH:22]C=C[C:17]=2[C:18]#N)=[O:15])=[C:8]2[CH:9]=[CH:10][CH:11]=[CH:12][N:7]2[N:6]=1)[CH2:2][CH2:3][CH3:4].S(=O)(=O)(O)O.[C:29]([OH:32])(=[O:31])[CH3:30]>O>[CH2:1]([C:5]1[C:13]([C:14]([C:16]2[CH:23]=[CH:22][C:30]([C:29]([OH:32])=[O:31])=[CH:18][CH:17]=2)=[O:15])=[C:8]2[CH:9]=[CH:10][CH:11]=[CH:12][N:7]2[N:6]=1)[CH2:2][CH2:3][CH3:4]Participants
5
Procedure
A mixture of 845 mg of the product of Example 2 and 15 ml of a mixture in equal proportions of sulfuric acid, acetic acid and water was refluxed for 2 hours and the mixture was cooled down, taken up in water, filtered, washed with water and dried at 80° C. under reduced pressure.
Workup
- temperaturewas refluxed for 2 hours
- temperaturethe mixture was cooled down
- filtrationfiltered
- washwashed with water
- customdried at 80° C. under reduced pressure
Sources & evidence
- ORD record
- ord-61b16523a7764a7a8d917dd5cae5cf31
- Source dataset
- uspto-grants-1995_05
- Patent number
- US05420138
Reaction notes
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