Pyridinium chloride → HCID 178450137, compound
Reaction equation
[CH3:1][CH:2]([CH3:40])[C:3]([C:29]1[CH:34]=[CH:33][CH:32]=[C:31]([C:35]2[CH:39]=[CH:38][S:37][CH:36]=2)[CH:30]=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:34]=[CH:33][CH:32]=[C:31]([C:35]3[CH:39]=[CH:38][S:37][CH:36]=3)[CH:30]=2)([OH:4])[CH:2]([CH3:40])[CH3:1])[N:6]=[CH:7]1Participants
3
Procedure
By the reaction in the same manner as in Example 4-(iii) using 2-methyl-1-[3-(3-thienyl)phenyl]-1-(1-trityl-1H-imidazol-4-yl)-1-propanol (1.43 g) and pyridine hydrochloride (550 mg), the title compound (585 mg) was obtained as colorless plate crystals.
Workup
- customBy the reaction in the same manner as in Example
Sources & evidence
- ORD record
- ord-5fab4b288e0c406db078820e82b87e8a
- Source dataset
- uspto-grants-2003_02
- Patent number
- US06518257B1
Reaction notes
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