Benzoyl chloride → HCID 67147870, compound
Reaction equation
[Br:1][C:2]1[CH:3]=[C:4]([CH2:8][NH:9][CH3:10])[CH:5]=[N:6][CH:7]=1.[C:11](Cl)(=[O:18])[C:12]1[CH:17]=[CH:16][CH:15]=[CH:14][CH:13]=1>>[Br:1][C:2]1[CH:3]=[C:4]([CH2:8][N:9]([CH3:10])[C:11](=[O:18])[C:12]2[CH:17]=[CH:16][CH:15]=[CH:14][CH:13]=2)[CH:5]=[N:6][CH:7]=1Participants
3
Procedure
In a manner similar to that of Example 2(f), starting with 0.5 g (3 mmol) of (5-bromopyrid-3-ylmethyl)methylamine and 0.4 ml (3.6 mmol) of benzoyl chloride, 0.8 g (90%) of N-(5-bromopyrid-3-ylmethyl) -N-methylbenzamide is obtained.
Sources & evidence
- ORD record
- ord-5cec06fb61594d9287754a4e6c8c15e3
- Source dataset
- uspto-grants-2011_09
- Patent number
- US08022079B2
Reaction notes
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