Sulfuric Acid → HCID 13195827, compound
Reaction equation
[C:1]([C:9]1[C:10]([NH:24][CH:25]([CH2:27][CH3:28])[CH3:26])=[C:11]2[C:17](C)=[N:16][N:15](C3OC=CC=3)[C:12]2=[N:13][CH:14]=1)(=[O:8])[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.S(=O)(=O)(O)O>>[C:1]([C:9]1[C:10]([NH:24][CH:25]([CH2:27][CH3:28])[CH3:26])=[C:11]2[CH:17]=[N:16][NH:15][C:12]2=[N:13][CH:14]=1)(=[O:8])[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1Participants
3
Procedure
3.7 g. of 5-benzoyl-4-sec.butylamino-1-(2-furanyl)-methyl-1H-pyrazolo[3,4-b]pyridine are stirred in 20 ml. of conc. sulfuric acid for 3 hours at 50°. The mixture is decomposed with 30 ml. of water and filtered. The filtrate is made alkaline with 30% aqueous ammonia and the white precipitate of 5-benzoyl-4-sec.butylamino-1H-pyrazolo[3,4-b]-pyridine is filtered off, yield 1.7 g. (58%), m.p. 186°-187°.
Workup
- filtrationof water and filtered
- filtrationthe white precipitate of 5-benzoyl-4-sec.butylamino-1H-pyrazolo[3,4-b]-pyridine is filtered off
Sources & evidence
- ORD record
- ord-d47dfd0795ac4954a06c438a11a8adb8
- Source dataset
- uspto-grants-1976_10
- Patent number
- US03987051
Reaction notes
Loading…