Trifluoroacetic acid → HCID 21498217, compound
Reaction equation
[NH:1]([C:3]1[C:12]2[C:7](=[CH:8][CH:9]=[C:10]([CH3:13])[CH:11]=2)[CH:6]=[CH:5][N:4]=1)[NH2:2].[F:14][C:15]([F:20])([F:19])[C:16](O)=O>>[F:14][C:15]([F:20])([F:19])[C:16]1[N:4]2[CH:5]=[CH:6][C:7]3[C:12]([C:3]2=[N:1][N:2]=1)=[CH:11][C:10]([CH3:13])=[CH:9][CH:8]=3Participants
3
Procedure
A solution of 1-hydrazino-7-methylisoquinoline in excess trifluoroacetic acid was allowed to reflux for two hours. Removal of the excess acid in vacuo, treatment of the residue with sodium bicarbonate solution and filtration provided the crude product which was recrystallized from cyclohexane to give the product in a yield of 20%; m.p. 205°-206°C.
Workup
- temperatureto reflux for two hours
- customRemoval of the excess acid in vacuo, treatment of the residue
- filtrationwith sodium bicarbonate solution and filtration
Sources & evidence
- ORD record
- ord-55867833854d4bd5a2b458ea5632e3c4
- Source dataset
- uspto-grants-1976_11
- Patent number
- US03992539
Reaction notes
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