Dimethylamine → HCID 21182833, compound
Reaction equation
[Br:1][C:2]1[CH:3]=[C:4]([CH:9]=[CH:10][C:11]=1[CH2:12]Br)[C:5]([O:7][CH3:8])=[O:6].[CH3:14][NH:15][CH3:16]>>[Br:1][C:2]1[CH:3]=[C:4]([CH:9]=[CH:10][C:11]=1[CH2:12][N:15]([CH3:16])[CH3:14])[C:5]([O:7][CH3:8])=[O:6]Participants
3
Procedure
By following essentially the procedure of Example 137, Part B, the title compound was prepared from methyl 3-bromo-4-bromomethylbenzoate (Example 137, Part A) and dimethylamine (40%), in 70% yield. The flash chromatography was carried out by eluting with a gradient of hexanes(100-80%)/EtOAc(0-20%).
Workup
- washby eluting with a gradient of hexanes(100-80%)/EtOAc(0-20%)
Sources & evidence
- ORD record
- ord-945f748f00d44130b1c7f98aec74c142
- Source dataset
- uspto-grants-2001_07
- Patent number
- US06265575B1
Reaction notes
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