Methyl iodide → HCID 11426171, compound
Reaction equation
[NH2:1][C:2]1[CH:11]=[CH:10][CH:9]=[C:8]2[C:3]=1[CH:4]=[CH:5][N:6]=[CH:7]2.[I:12][CH3:13]>CC(C)=O>[I-:12].[NH2:1][C:2]1[CH:11]=[CH:10][CH:9]=[C:8]2[C:3]=1[CH:4]=[CH:5][N+:6]([CH3:13])=[CH:7]2Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
To a solution of 5-aminoisoquinoline (14.4 g, 100 mmol) in acetone (300 ml) was added iodomethane (14.4 ml). The solution was briefly stirred and then allowed to stand for 2 h. The yellow precipitate was then filtered, washed with acetone and dried to afford the title compound as a yellow solid (18.8 g).
Workup
- filtrationThe yellow precipitate was then filtered
- washwashed with acetone
- customdried
Sources & evidence
- ORD record
- ord-03f83c946ffc443e83813e76deb81850
- Source dataset
- uspto-grants-2001_08
- Patent number
- US06274594B1
Reaction notes
Loading…