Pyridinium chloride → HCID 178450098, compound
Reaction equation
[CH:1]1([NH:4][C:5]([C:7]2[CH:8]=[C:9]([C:13]3[CH:18]=[CH:17][C:16]([C:19]([OH:47])([C:23]4[N:24]=[CH:25][N:26](C(C5C=CC=CC=5)(C5C=CC=CC=5)C5C=CC=CC=5)[CH:27]=4)[CH:20]([CH3:22])[CH3:21])=[CH:15][CH:14]=3)[CH:10]=[CH:11][CH:12]=2)=[O:6])[CH2:3][CH2:2]1.Cl.N1C=CC=CC=1>>[CH:1]1([NH:4][C:5]([C:7]2[CH:8]=[C:9]([C:13]3[CH:18]=[CH:17][C:16]([C:19]([OH:47])([C:23]4[N:24]=[CH:25][NH:26][CH:27]=4)[CH:20]([CH3:22])[CH3:21])=[CH:15][CH:14]=3)[CH:10]=[CH:11][CH:12]=2)=[O:6])[CH2:3][CH2:2]1Participants
3
Procedure
By the reaction in the same manner as in Example 4-(iii) using N-cyclopropyl-4′-[1-hydroxy-2-methyl-1-(1-trityl-1H-imidazol-4-yl)propyl][1,1′-biphenyl]-3-carboxamide (2.13 g) and pyridine hydrochloride (650 mg), the title compound (375 mg) was obtained as colorless powder crystals.
Workup
- customBy the reaction in the same manner as in Example
Sources & evidence
- ORD record
- ord-63961c582c084933b7e9ba461d5c02c3
- Source dataset
- uspto-grants-2003_02
- Patent number
- US06518257B1
Reaction notes
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