Reaction equation
[NH2:1][C:2]1[CH:7]=[C:6]([CH3:8])[CH:5]=[CH:4][N:3]=1.[CH3:9][O:10][C:11]1[CH:12]=[C:13]([CH:18]=[CH:19][C:20]=1[O:21][CH3:22])[C:14](=O)[CH2:15]Br>>[CH3:9][O:10][C:11]1[CH:12]=[C:13]([C:14]2[N:1]=[C:2]3[CH:7]=[C:6]([CH3:8])[CH:5]=[CH:4][N:3]3[CH:15]=2)[CH:18]=[CH:19][C:20]=1[O:21][CH3:22]Participants
3
Procedure
The title compound, pale yellow solid, m.p. 163° C. and MS: m/e=268.1 (M+), was prepared in accordance with the general method of example 1 from 2-amino-4-methyl-pyridine and 3,4-dimethoxy-phenacylbromide.
Sources & evidence
- ORD record
- ord-92ebbf9ab99f42cf967f66593f2093da
- Source dataset
- uspto-grants-2005_07
- Patent number
- US06916826B2
Linked notes
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