Ammonia → HCID 20429203, compound
Reaction equation
[C:1]([O:7]CC)(=O)[CH2:2][C:3]([CH3:5])=O.N.C(OC(C1C(C2[N+:27]([O-:28])=[C:26]([CH3:29])[CH:25]=CC=2)C(C(OCC)=O)=C(C)NC=1C)=O)C>C(O)C>[CH3:29][C:26]1[CH:25]=[CH:5][CH:3]=[C:2]([CH:1]=[O:7])[N+:27]=1[O-:28]Participants
5
Reactant 3
Product 1
Reagents, catalysts & solvents 1
Procedure
Analogously to the process described in Example 1 there is obtained from 24.1 g of 2-methylpyridine-6-carboxaldehyde-1-oxide, 40 ml of ethanol, 50.4 ml of ethyl acetoacetate and 20 ml of 25% aqueous ammonia, 2,6-dimethyl-4-(2-methyl-1-oxido-6-pyridyl)-1,4-dihydropyridine-3,5-dicarboxylic acid diethyl ester which, after recrystallisation from ethanol, melts at 224°-225° (with decomposition).
Sources & evidence
- ORD record
- ord-e120f27f439549e5950a85ffe9ba1615
- Source dataset
- uspto-grants-1985_02
- Patent number
- US04497808
Reaction notes
Loading…