4-Aminopyridine → HCID 22934764, compound
Reaction equation
[NH2:1][C:2]1[CH:7]=[CH:6][N:5]=[CH:4][CH:3]=1.Cl[C:9](=[O:14])[C:10]([O:12][CH3:13])=[O:11]>>[CH3:13][O:12][C:10](=[O:11])[C:9](=[O:14])[NH:1][C:2]1[CH:7]=[CH:6][N:5]=[CH:4][CH:3]=1Participants
3
Procedure
In a manner similar to that employed in Referential Example 242, the title compound was prepared from 4-aminopyridine and methyl chlorooxoacetate.
Sources & evidence
- ORD record
- ord-f21e108a1b9348d092e3c33e1ba222a2
- Source dataset
- uspto-grants-2009_08
- Patent number
- US07576135B2
Reaction notes
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