3,4,5-Trimethoxybenzaldehyde → HCID 21853792, Verbindung

HRID 1580938

Reaktionsgleichung

Reaktionsgleichung von HRID 1580938
C[O-].[Na+].[CH3:4][C:5]1[N:6]=[C:7]2[C:16]([CH3:17])=[CH:15][CH:14]=[CH:13][N:8]2[C:9](=[O:12])[C:10]=1[CH3:11].[CH3:18][O:19][C:20]1[CH:21]=[C:22]([CH:25]=[C:26]([O:30][CH3:31])[C:27]=1[O:28][CH3:29])[CH:23]=O>C(O)C>[CH3:11][C:10]1[C:9](=[O:12])[N:8]2[CH:13]=[CH:14][CH:15]=[C:16]([CH3:17])[C:7]2=[N:6][C:5]=1/[CH:4]=[CH:23]/[C:22]1[CH:25]=[C:26]([O:30][CH3:31])[C:27]([O:28][CH3:29])=[C:20]([O:19][CH3:18])[CH:21]=1

Komponenten

5

Edukt 3

HCID 68583,4,5-TrimethoxybenzaldehydeHCID 10942334Sodium MethoxideHCID 123397192,3,9-Trimethyl-4H-pyrido[1,2-a]pyrimidin-4-one

Produkt 1

HCID 21853792HCID 21853792, Verbindung

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 702EthanolLösungsmittel

Versuchsvorschrift

To a solution of 1.3g of sodium methoxide in 75ml of absolute ethanol is added 2.0g of 2,3,9-trimethyl-4H-pyrido-[1,2-a]pyrimidin-4-one, followed by 4.0g of 3,4,5-trimethoxybenzaldehyde. The mixture is stirred and heated under reflux for 89 hours. The reaction mixture is cooled, the solid is filtered, washed with 20ml of ether and 25ml of water, dried, and recrystallized from 75ml of acetonitrile to yield the title compound, melting point 218°-219°C dec.

Aufarbeitung

  1. temperatureheated
  2. temperatureunder reflux for 89 hours
  3. temperatureThe reaction mixture is cooled
  4. filtrationthe solid is filtered
  5. washwashed with 20ml of ether and 25ml of water
  6. customdried
  7. customrecrystallized from 75ml of acetonitrile

Quellen und Nachweise

ORD-Eintrag
ord-d89cf70173b24f458c8421a5b15a938f
Quelldatensatz
uspto-grants-1976_01
Patentnummer
US03935197

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