Hydrochloric Acid → HCID 21163085, compound
Reaction equation
[N:1]1[CH:6]=[CH:5][CH:4]=[C:3]([C:7]2[N:12]3[N:13]=[CH:14][C:15]([CH2:16][OH:17])=[C:11]3[N:10]=[CH:9][CH:8]=2)[CH:2]=1.Cl.[CH3:19]O>>[CH3:19][O:17][CH2:16][C:15]1[CH:14]=[N:13][N:12]2[C:7]([C:3]3[CH:2]=[N:1][CH:6]=[CH:5][CH:4]=3)=[CH:8][CH:9]=[N:10][C:11]=12Participants
4
Procedure
To a mixture of 0.01 mole of 7-(3-pyridyl)pyrazolo-[1,5-a]pyrimidine-3-methanol in 50 ml. of methanol is added anhydrous hydrochloric acid in 10 ml. of methanol. The mixture is heated on a steam bath for 3 hours and the solvent removed. The residue is partitioned between dichloromethane and aqueous sodium bicarbonate. The dichloromethane solution is dried over magnesium sulfate, concentrated and diluted with hexane to give the product of the example.
Workup
- temperatureThe mixture is heated on a steam bath for 3 hours
- customthe solvent removed
- customThe residue is partitioned between dichloromethane and aqueous sodium bicarbonate
- dry with materialThe dichloromethane solution is dried over magnesium sulfate
- concentrationconcentrated
- additiondiluted with hexane
- customto give the product of the example
Sources & evidence
- ORD record
- ord-f5620bc89ecd4c4ab9827a403433e477
- Source dataset
- uspto-grants-1981_07
- Patent number
- US04281000
Reaction notes
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