Imidazole → 3-(1H-imidazol-1-yl)-5-(trifluoromethyl)-benzonitrile
Reaction equation
F[C:2]1[CH:3]=[C:4]([CH:7]=[C:8]([C:10]([F:13])([F:12])[F:11])[CH:9]=1)[C:5]#[N:6].[NH:14]1[CH:18]=[CH:17][N:16]=[CH:15]1>>[N:14]1([C:2]2[CH:3]=[C:4]([CH:7]=[C:8]([C:10]([F:13])([F:12])[F:11])[CH:9]=2)[C:5]#[N:6])[CH:18]=[CH:17][N:16]=[CH:15]1Participants
3
Procedure
The title compound is prepared using an analogous method as described in Example 1.1, utilising 3-fluoro-5-(trifluoromethyl)-benzonitrile (Lancaster Synthesis GmbH) and imidazole (Fluka, Buchs, Switzerland), with a reaction temperature of 110° C. for 24 hours.
Sources & evidence
- ORD record
- ord-d0dddc637c11435ba0650b48980c4ce9
- Source dataset
- uspto-grants-2010_02
- Patent number
- US07655669B2
Reaction notes
Loading…