Trifluoroacetic acid → HCID 21498242, compound
Reaction equation
[NH:1]([C:3]1[C:12]2[C:7](=[CH:8][CH:9]=[C:10]([O:13][CH3:14])[CH:11]=2)[CH:6]=[CH:5][N:4]=1)[NH2:2].[F:15][C:16]([F:21])([F:20])[C:17](O)=O>>[F:15][C:16]([F:21])([F:20])[C:17]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]([O:13][CH3:14])=[CH:9][CH:8]=3Participants
3
Procedure
A solution of 1-hydrazino-7-methoxyisoquinoline in excess trifluoroacetic acid was allowed to reflux for 2 hours. Excess acid was removed in vacuo and the residue was slurried in water and treated with sodium bicarbonate solution. The solid was removed by filtration and recrystallized from cyclohexane to give the product in a yield of 70%; m.p. 152°-154°C.
Workup
- temperatureto reflux for 2 hours
- customExcess acid was removed in vacuo
- additiontreated with sodium bicarbonate solution
- customThe solid was removed by filtration
- customrecrystallized from cyclohexane
- customto give the product in a yield of 70%
Sources & evidence
- ORD record
- ord-cb8697c9166b4b75ada6cfd0dbd95a89
- Source dataset
- uspto-grants-1976_11
- Patent number
- US03992539
Reaction notes
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