N,N-Diethylethylenediamine → HCID 68129580, compound
Reaction equation
[CH3:1][O:2][C:3]([C:5]1[CH:10]([C:11]2[CH:16]=[CH:15][C:14](Cl)=[C:13]([N+:18]([O-:20])=[O:19])[CH:12]=2)[C:9]([C:21]([O:23][CH3:24])=[O:22])=[C:8]([CH3:25])[NH:7][C:6]=1[CH3:26])=[O:4].[CH2:27]([N:29]([CH2:33][CH3:34])[CH2:30][CH2:31][NH2:32])[CH3:28]>CCOCC>[CH3:1][O:2][C:3]([C:5]1[CH:10]([C:11]2[CH:16]=[CH:15][C:14]([NH:32][CH2:31][CH2:30][N:29]([CH2:33][CH3:34])[CH2:27][CH3:28])=[C:13]([N+:18]([O-:20])=[O:19])[CH:12]=2)[C:9]([C:21]([O:23][CH3:24])=[O:22])=[C:8]([CH3:25])[NH:7][C:6]=1[CH3:26])=[O:4]Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
Ten grams of 2,6-dimethyl-4-(3-nitro-4-chlorophenyl)-1,4-dihydropyridine-3,5-dicarboxylic acid dimethyl ester and 8 g of 2-(diethylamino)ethylamine are heated to 100° (external temperature) overnight. After cooling, ether is added and the product collected by filtration to yield orange crystals of melting poing 161°C after recrystallization from 80 ml of methanol.
Workup
- temperatureAfter cooling
- filtrationthe product collected by filtration
- customto yield orange crystals
- customof melting poing 161°C
- customafter recrystallization from 80 ml of methanol
Sources & evidence
- ORD record
- ord-8c7933bb7c094a4eab3b1e265b0ebe09
- Source dataset
- uspto-grants-1976_07
- Patent number
- US03968117
Reaction notes
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