Reaction equation
[NH2:1][C:2]1[CH:7]=[C:6]([O:8][CH3:9])[CH:5]=[CH:4][N:3]=1.[CH3:10][O:11][C:12]1[CH:13]=[C:14]([CH:19]=[CH:20][C:21]=1[O:22][CH3:23])[C:15](=O)[CH2:16]Br>>[CH3:10][O:11][C:12]1[CH:13]=[C:14]([C:15]2[N:1]=[C:2]3[CH:7]=[C:6]([O:8][CH3:9])[CH:5]=[CH:4][N:3]3[CH:16]=2)[CH:19]=[CH:20][C:21]=1[O:22][CH3:23]Participants
3
Procedure
The title compound, pale yellow solid, m.p. 142° C. and MS: m/e=284.1 (M+), was prepared in accordance with the general method of example 1 from 2-amino-4-methoxy-pyridine and 3,4-dimethoxy-phenacylbromide.
Sources & evidence
- ORD record
- ord-8f3e79917a7e42a8a3fc4eb62e4e26ab
- Source dataset
- uspto-grants-2005_07
- Patent number
- US06916826B2
Linked notes
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