Sodium Hydroxide → HCID 13747175, compound
Reaction equation
[CH2:1]([NH:4][C:5]1[C:10]([C:11]([O:13]CC)=[O:12])=[CH:9][N:8]=[C:7]2[CH:16]=[N:17][NH:18][C:6]=12)[CH:2]=[CH2:3].[OH-].[Na+]>O>[CH2:1]([NH:4][C:5]1[C:10]([C:11]([OH:13])=[O:12])=[CH:9][N:8]=[C:7]2[CH:16]=[N:17][NH:18][C:6]=12)[CH:2]=[CH2:3]Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
Ethyl 7-allylamino-1H-pyrazolo[4,3-b]pyridine-6-carboxylate (5.0 g, 20 mmol) was added to a solution of sodium hydroxide (2.4 g, 60 mmol) in water (100 ml) and heated under reflux for 60 min. The solution was filtered, diluted with water (200 ml) and made neutral with 5N hydrochloric acid. The solid was filtered off, washed with water and dried to give the title compound (4.25 g, 96%), m.p. 240°-242° C.
Workup
- temperatureheated
- temperatureunder reflux for 60 min
- filtrationThe solution was filtered
- additiondiluted with water (200 ml)
- filtrationThe solid was filtered off
- washwashed with water
- customdried
Sources & evidence
- ORD record
- ord-3713893392a240aab65c48098d0a2b03
- Source dataset
- uspto-grants-1989_06
- Patent number
- US04837238
Reaction notes
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