Miconazole → HCID 178425461, compound
Reaction equation
[Cl:1][C:2]1[CH:24]=[C:23]([Cl:25])[CH:22]=[CH:21][C:3]=1[CH:4]([O:11][CH2:12][C:13]1[CH:18]=[CH:17][C:16]([Cl:19])=[CH:15][C:14]=1[Cl:20])[CH2:5][N:6]1[CH:10]=[CH:9][N:8]=[CH:7]1.[CH3:26][C:27]1[CH:34]=[CH:33][C:30]([CH2:31][Br:32])=[CH:29][CH:28]=1>>[Br-:32].[Cl:1][C:2]1[CH:24]=[C:23]([Cl:25])[CH:22]=[CH:21][C:3]=1[CH:4]([O:11][CH2:12][C:13]1[CH:18]=[CH:17][C:16]([Cl:19])=[CH:15][C:14]=1[Cl:20])[CH2:5][N+:6]1[CH:10]=[CH:9][N:8]([CH2:26][C:27]2[CH:34]=[CH:33][C:30]([CH3:31])=[CH:29][CH:28]=2)[CH:7]=1Participants
3
Procedure
mp. 152.2° C., by the reaction of 1-[2,4-dichloro-β-(2,4-dichlorobenzyloxy)phenethyl]-imidazole and p-methylbenzyl bromide.
Sources & evidence
- ORD record
- ord-fa392695d4be4ebd9d1c7ab4b47d6098
- Source dataset
- uspto-grants-1976_11
- Patent number
- US03991202
Reaction notes
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