Ethanol → 1-Methyl-1,4,5,6-Tetrahydro-5-(3-methyl-1,2,4-oxadiazol-5-yl)pyrimidine

HRID 1653709Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 1653709
[H-].[Na+].[C:3](=[N:6][OH:7])([NH2:5])[CH3:4].[CH3:8][N:9]1[CH2:14][CH:13]([C:15](OC)=O)[CH2:12][N:11]=[CH:10]1.C(O)C>C1COCC1>[CH3:8][N:9]1[CH2:14][CH:13]([C:15]2[O:7][N:6]=[C:3]([CH3:4])[N:5]=2)[CH2:12][N:11]=[CH:10]1

Komponenten

6

Edukt 4

HCID 702EthanolHCID 24758Sodium hydrideHCID 30926N-HydroxyacetamidineHCID 152943851-Methyl-5-methoxycarbonyl-1,4,5,6-tetrahydropyrimidine

Produkt 1

HCID 152943861-Methyl-1,4,5,6-Tetrahydro-5-(3-methyl-1,2,4-oxadiazol-5-yl)pyrimidine

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 8028TetrahydrofuranLösungsmittel2×

Reaktionsbedingungen

Temperatur
0 °C

Versuchsvorschrift

Sodium hydride (60% dispersion in mineral oil 112 mg, 2.8 mmol) and acetamidoxime (207 mg, 2.8 mmol) are suspended in dry THF (16 ml) in an oven dried round bottom flask under nitrogen with stirring at 0° C. After 10 minutes the grey suspension is refluxed for 30 minutes giving a white suspension. 1-Methyl-1,4,5,6-tetrahydro-5-methoxycarbonylpyrimidine (593 mg, 2.8 mmol) dissolved in dry THF (4 ml) and anhydrous ethanol (1 ml) is added via syringe and reflux continued 15 hours. The suspension is evaporated in vacuo to a yellow gum and chromatographed (silica, chloroform/methanol, 9:1) to yield 24 mg (rf=0.07, 4%) solids identified by 300 MHz nmr and ms m/z=180.

Aufarbeitung

  1. customdried round bottom flask under nitrogen
  2. temperatureAfter 10 minutes the grey suspension is refluxed for 30 minutes
  3. customgiving a white suspension
  4. temperaturereflux
  5. customThe suspension is evaporated in vacuo to a yellow gum
  6. customchromatographed (silica, chloroform/methanol, 9:1)
  7. customto yield 24 mg (rf=0.07, 4%) solids

Quellen und Nachweise

ORD-Eintrag
ord-779d7402c00047fbbd1bfdc060a9d642
Quelldatensatz
uspto-grants-1995_04
Patentnummer
US05403845

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