Pyridine →
Reaction equation
[Cl:1][CH2:2][C:3](=[O:9])[CH2:4][C:5]([O:7]C)=[O:6].[N:10]1[CH:15]=[CH:14][CH:13]=[CH:12][CH:11]=1>>[Cl-:1].[C:5]([O-:7])(=[O:6])[CH2:4][C:3]([CH3:2])=[O:9].[CH3:2][C:11]1[CH:12]=[CH2+:13][CH:14]=[CH:15][N:10]=1.[CH3:2][C:3]1[CH:4]=[CH2+:5][CH:12]=[CH:11][N:10]=1Participants
2
Reactant 2
Product 0
No Product data yet.
Procedure
The title compound was prepared as described in Example 1 from pyridine and methyl 4-chloroacetoacetate in a yield of 74%.
Sources & evidence
- ORD record
- ord-2c36a8b728ed4392a13229a68088c081
- Source dataset
- uspto-grants-1995_08
- Patent number
- US05438140
Reaction notes
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