Methyl iodide → 1-(m-Chlorophenyl)-3-methyl-3-azabicyclo[3.1.0]hexane hydrochloride
Reaction equation
Cl.[Cl:2][C:3]1[CH:4]=[C:5]([C:9]23[CH2:14][CH:13]2[CH2:12][NH:11][CH2:10]3)[CH:6]=[CH:7][CH:8]=1.[CH3:15]I>>[ClH:2].[Cl:2][C:3]1[CH:4]=[C:5]([C:9]23[CH2:14][CH:13]2[CH2:12][N:11]([CH3:15])[CH2:10]3)[CH:6]=[CH:7][CH:8]=1Participants
3
Procedure
By the method of Example 10, 1-(m-chlorophenyl)-N-methyl-1,2-cyclopropanedicarboximide, m.p. 72°-73° C., prepared from 1-(m-chlorophenyl)-1,2-cyclopropanedicarboximide (Example 6) and methyl iodide gives 1-(m-chlorophenyl)-3-methyl-3-azabicyclo[3.1.0]hexane hydrochloride as colorless crystals, m.p. 180°-182° C.
Sources & evidence
- ORD record
- ord-d5f7ffabf2054bcd806513ddadf8c3f0
- Source dataset
- uspto-grants-1980_11
- Patent number
- US04231935
Reaction notes
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