Allyl bromide → HCID 21193027, compound
Reaction equation
[NH:1]1[C:5]2[CH:6]=[CH:7][CH:8]=[CH:9][C:4]=2[N:3]=[C:2]1[CH:10]1[CH2:15][CH2:14][N:13]([C:16](=[O:18])[CH3:17])[CH2:12][CH2:11]1.[H-].[Na+].[CH2:21](Br)[CH:22]=[CH2:23]>CN(C=O)C>[CH2:23]([N:1]1[C:5]2[CH:6]=[CH:7][CH:8]=[CH:9][C:4]=2[N:3]=[C:2]1[CH:10]1[CH2:11][CH2:12][N:13]([C:16](=[O:18])[CH3:17])[CH2:14][CH2:15]1)[CH:22]=[CH2:21]Participants
5
Reactant 3
Product 1
Reagents, catalysts & solvents 1
Procedure
The title compound was prepared from 1-(4-(1-H-benzoimidazol-2-yl)-piperidin-1-yl)ethanone (from Step A), sodium hydride, allyl bromide and DMF.
Sources & evidence
- ORD record
- ord-fb53e85d37f94bc9bd01c9dd380fcdc3
- Source dataset
- uspto-grants-2001_06
- Patent number
- US06248755B1
Reaction notes
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