Benzyl Bromide → HCID 68437018, compound
Reaction equation
[N:1]1[C:10]2[CH:9]=[CH:8][CH:7]=[C:6]([OH:11])[C:5]=2[CH:4]=[CH:3][CH:2]=1.[CH2:12](Br)[C:13]1[CH:18]=[CH:17][CH:16]=[CH:15][CH:14]=1.[CH3:20][O:21][C:22]1[CH:29]=[CH:28][CH:27]=[CH:26][C:23]=1[CH2:24][NH2:25]>>[CH2:12]([O:11][C:6]1[CH:7]=[CH:8][CH:9]=[C:10]2[C:5]=1[CH:4]=[CH:3][C:2]([NH:25][CH2:24][C:23]1[CH:26]=[CH:27][CH:28]=[CH:29][C:22]=1[O:21][CH3:20])=[N:1]2)[C:13]1[CH:18]=[CH:17][CH:16]=[CH:15][CH:14]=1Participants
4
Procedure
The title compound, MS: m/e=371.4 (M+H+), was prepared in accordance with the general method of example 47 from 5-quinolinol (CAS 578-67-6), benzyl bromide and 2-methoxybenzylamine.
Sources & evidence
- ORD record
- ord-5b287e5c154b449c80dfe46488fe8c05
- Source dataset
- uspto-grants-2010_11
- Patent number
- US07825253B2
Reaction notes
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