Methyl iodide → 7-Bromo-2-methyl-1,2,3,4-tetrahydroisoquinoline
Reaction equation
Cl.[Br:2][C:3]1[CH:12]=[C:11]2[C:6]([CH2:7][CH2:8][NH:9][CH2:10]2)=[CH:5][CH:4]=1.I[CH3:14]>>[Br:2][C:3]1[CH:12]=[C:11]2[C:6]([CH2:7][CH2:8][N:9]([CH3:14])[CH2:10]2)=[CH:5][CH:4]=1Participants
3
Procedure
Following the procedure described for Intermediate 3 using 7-bromo-1,2,3,4-tetrahydroisoquinoline hydrochloride and iodomethane provided the title compound. ESMS [M+H]+: 226.0.
Sources & evidence
- ORD record
- ord-867928a9d6124e3582c9442395bb78cd
- Source dataset
- uspto-grants-2007_10
- Patent number
- US07282588B2
Reaction notes
Loading…