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Sodium methanolate methanol → 2-Methoxypyrido[2,3-d]pyrimidin-7(8H)-one

HRID 385555
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 385555
[NH2:1][C:2]1[C:7](/[CH:8]=[CH:9]/[C:10](OCC)=[O:11])=[CH:6][N:5]=[C:4]([O:15][CH3:16])[N:3]=1.C[O-].[Na+].CO>CO>[CH3:16][O:15][C:4]1[N:5]=[CH:6][C:7]2[CH:8]=[CH:9][C:10](=[O:11])[NH:1][C:2]=2[N:3]=1
KomponentenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

4

Edukt 2

HCID 23694274Sodium methanolate methanolHCID 68105238HCID 68105238, Verbindung

Produkt 1

HCID 578153292-Methoxypyrido[2,3-d]pyrimidin-7(8H)-oneAusbeute 79,7 %

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 887MethanolLösungsmittel

Versuchsvorschrift

To a solution of 0.87 g of ethyl (2E)-3-(4-amino-2-methoxypyrimidin-5-yl)acrylate in 50 mL of methanol, 2.31 g of a 28% sodium methoxide/methanol solution was added at room temperature, and the mixture was heated under reflux while stirring for 4 hours. The reaction mixture was cooled to room temperature, and the solvent was then distilled off under reduced pressure. To the resultant residue, a saturated aqueous ammonium chloride solution and chloroform were added, the organic layer was separated, and the aqueous layer was extracted with chloroform. The organic layer and the extract were combined, the resultant solution was dried over anhydrous magnesium sulfate, and the solvent was distilled off under reduced pressure. The solid thus obtained was washed with diethyl ether to obtain 0.55 g of 2-methoxypyrido(2,3-d)pyrimidin-7(8H)-one as a yellow solid.

Aufarbeitung

  1. temperaturethe mixture was heated
  2. temperatureunder reflux
  3. distillationthe solvent was then distilled off under reduced pressure
  4. additionTo the resultant residue, a saturated aqueous ammonium chloride solution and chloroform were added
  5. customthe organic layer was separated
  6. extractionthe aqueous layer was extracted with chloroform
  7. dry with materialthe resultant solution was dried over anhydrous magnesium sulfate
  8. distillationthe solvent was distilled off under reduced pressure
  9. customThe solid thus obtained
  10. washwas washed with diethyl ether

Quellen und Nachweise

ORD-Eintrag
ord-bf848f12d5564931a95692bc58a65987
Quelldatensatz
uspto-grants-2013_02
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US08367831B2

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