N,N-Diethylethylenediamine → HCID 68129580, compound

HRID 917869Notes

Reaction equation

HRID 917869 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

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

  1. temperatureAfter cooling
  2. filtrationthe product collected by filtration
  3. customto yield orange crystals
  4. customof melting poing 161°C
  5. 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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