Hydrochloric Acid → 4-(3-chlorophenyl)-1-ethyl-7-(1-hydroxyethyl)pyrido[2,3-d]pyrimidin-2(1H)-one

HRID 368990Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 368990
[OH-].[Na+].C([O:6][CH:7]([C:9]1[CH:10]=[CH:11][C:12]2[C:17]([C:18]3[CH:23]=[CH:22][CH:21]=[C:20]([Cl:24])[CH:19]=3)=[N:16][C:15](=[O:25])[N:14]([CH2:26][CH3:27])[C:13]=2[N:28]=1)[CH3:8])(=O)C.Cl>CO>[Cl:24][C:20]1[CH:19]=[C:18]([C:17]2[C:12]3[CH:11]=[CH:10][C:9]([CH:7]([OH:6])[CH3:8])=[N:28][C:13]=3[N:14]([CH2:26][CH3:27])[C:15](=[O:25])[N:16]=2)[CH:23]=[CH:22][CH:21]=1

Komponenten

5

Versuchsvorschrift

Methanol (30 ml) and 30 ml of 1 N sodium hydroxide aqueous solution were added to 6.78 g (18.2 mmol) of 7-(1-acetoxyethyl)-4-(3-chlorophenyl)-1-ethylpyrido[2,3-d]pyrimidin-2(1H)-one, followed by stirring for 20 minutes at room temperature. The reaction solution was neutralized by adding 1 N hydrochloric acid and extracted with chloroform. The organic layer was washed with brine and dried over anhydrous magnesium sulfate, magnesium sulfate was removed by filtration and the resulting filtrate was concentrated under a reduced pressure. Thereafter, the resulting residue was purified by silica gel column chromatography (chloroform) to give 4.50 g of 4-(3-chlorophenyl)-1-ethyl-7-(1-hydroxyethyl)pyrido[2,3-d]pyrimidin-2(1H)-one in the form of crystals. The yield was 75%.

Aufarbeitung

  1. extractionextracted with chloroform
  2. washThe organic layer was washed with brine
  3. dry with materialdried over anhydrous magnesium sulfate, magnesium sulfate
  4. customwas removed by filtration
  5. concentrationthe resulting filtrate was concentrated under a reduced pressure
  6. customThereafter, the resulting residue was purified by silica gel column chromatography (chloroform)

Quellen und Nachweise

ORD-Eintrag
ord-4d99e4ddd71d4555b5391b4d277b92fe
Quelldatensatz
uspto-grants-2000_10
Patentnummer
US06136810

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