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 sthand for 2h. The yellow precipithate was then filtered, washed with acetone and dried to afford the title compound as a yellow solid (18.8 g).
Workup
- filtrationThe yellow precipithate was then filtered
- washwashed with acetone
- customdried
Sources & evidence
- ORD record
- ord-1393fedd38a24ce8839b7aed18fa7a4a
- Source dataset
- uspto-grants-2000_08
- Patent number
- US06110934
Reaction notes
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