Pyridinium chloride → HCID 178450134, compound
Reaction equation
[CH3:1][CH:2]([CH3:46])[C:3]([C:29]1[CH:30]=[C:31]([C:35]2[CH:40]=[CH:39][C:38]([O:41][C:42]([F:45])([F:44])[F:43])=[CH:37][CH:36]=2)[CH:32]=[CH:33][CH:34]=1)([C:5]1[N:6]=[CH:7][N:8](C(C2C=CC=CC=2)(C2C=CC=CC=2)C2C=CC=CC=2)[CH:9]=1)[OH:4].Cl.N1C=CC=CC=1>>[NH:8]1[CH:9]=[C:5]([C:3]([C:29]2[CH:30]=[C:31]([C:35]3[CH:36]=[CH:37][C:38]([O:41][C:42]([F:43])([F:44])[F:45])=[CH:39][CH:40]=3)[CH:32]=[CH:33][CH:34]=2)([OH:4])[CH:2]([CH3:1])[CH3:46])[N:6]=[CH:7]1Participants
3
Procedure
By the reaction in the same manner as in Example 4-(iii) using 2-methyl-1-[4′-(trifluoromethoxy)[1,1′-biphenyl]-3-yl]-1-(1-trityl-1H-imidazol-4-yl)-1-propanol (3.63 g) and pyridine hydrochloride (1.22 g), the title compound (3.76 g) was obtained as colorless needle crystals.
Workup
- customBy the reaction in the same manner as in Example
Sources & evidence
- ORD record
- ord-514caae71e7241f8a3a9cc4ea2d171a3
- Source dataset
- uspto-grants-2003_02
- Patent number
- US06518257B1
Reaction notes
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