2-chloro-1H-imidazole → HCID 58405414, compound
Reaction equation
Cl[C:2]1[N:11]=[CH:10][C:9]2[N:8]([CH3:12])[C:7](=[O:13])[C@@H:6]([CH2:14][CH3:15])[N:5]([CH:16]3[CH2:20][CH2:19][CH2:18][CH2:17]3)[C:4]=2[N:3]=1.[Cl:21][C:22]1[NH:23][CH:24]=[CH:25][N:26]=1>>[Cl:21][C:22]1[N:23]([C:2]2[N:11]=[CH:10][C:9]3[N:8]([CH3:12])[C:7](=[O:13])[C@@H:6]([CH2:14][CH3:15])[N:5]([CH:16]4[CH2:20][CH2:19][CH2:18][CH2:17]4)[C:4]=3[N:3]=2)[CH:24]=[CH:25][N:26]=1Participants
3
Procedure
The title compound was prepared similarly to the methods described in Example 185, with Intermediate B instead of Intermediate C and 2-chloro-1H-imidazole instead of 2-(3,5-dichlorophenyl)-1H-imidazole. LCMS: 361.2 m/z (M+H)+; ret. Time 10.06 min (Analytical Method C).
Sources & evidence
- ORD record
- ord-e71c86cd3cf9420387d3275af668b893
- Source dataset
- uspto-grants-2013_09
- Patent number
- US08541418B2
Reaction notes
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