Methyl iodide → 1-methyl-1H,4H,5H,6H,7H-imidazo[4,5-c]pyridine
Reaction equation
[NH:1]1[C:9]2[CH2:8][CH2:7][NH:6][CH2:5][C:4]=2[N:3]=[CH:2]1.[CH3:10]I>>[CH3:10][N:1]1[C:9]2[CH2:8][CH2:7][NH:6][CH2:5][C:4]=2[N:3]=[CH:2]1Participants
3
Procedure
Operating as in Example 1, but starting from 4,5,6,7-tetrahydroimidazo-[4,5-c]-pyridine and methyl iodide, 1-Methyl-4,5,6,7-tetrahydroimidazo-[4,5-c]-pyridine is obtained as intermediate and successively reacted with methyl isothiocyanate to give 1-Methyl-5-(N-methylthiocarbamoyl)-4,5,6,7-tetrahydroimidazo-[4,5-c]-pyridine in a 78% yield, m.p. 238° C.
Sources & evidence
- ORD record
- ord-f69abc026200451db69fe26f9ec86191
- Source dataset
- uspto-grants-1980_09
- Patent number
- US04223146
Reaction notes
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