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Morpholine → HCID 86659725, Verbindung

HRID 1878567
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 1878567
[Cl:1][C:2]1[CH:7]=[C:6](Cl)[N:5]2[N:9]=[C:10]([CH3:12])[CH:11]=[C:4]2[N:3]=1.[NH:13]1[CH2:18][CH2:17][O:16][CH2:15][CH2:14]1>O1CCOCC1>[Cl:1][C:2]1[CH:7]=[C:6]([N:13]2[CH2:18][CH2:17][O:16][CH2:15][CH2:14]2)[N:5]2[N:9]=[C:10]([CH3:12])[CH:11]=[C:4]2[N:3]=1
KomponentenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

4

Edukt 2

HCID 8083MorpholineHCID 497615345,7-Dichloro-2-methylpyrazolo[1,5-A]pyrimidine

Produkt 1

HCID 86659725HCID 86659725, VerbindungAusbeute 74 %

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 312751,4-DioxaneLösungsmittel

Versuchsvorschrift

There was dissolved, in 1,4-dioxane (20 mL), 5,7-dichloro-2-methyl-pyrazolo-[1,5-a]pyrimidine (1.00 g, 4.95 mM), then morpholine (863 μL, 9.90 mM) was added to the solution and the mixture was stirred at room temperature for one hour. The solvent was then distilled off from this reaction mixture, the resulting residue was diluted with water and the mixture was extracted with methylene chloride. The resulting extracts were combined, dried over anhydrous sodium sulfate, the solvent was distilled off and the resulting solid was washed with methanol to thus give the title compound (927 mg, yield: 74%).

Aufarbeitung

  1. distillationThe solvent was then distilled off from this reaction mixture
  2. additionthe resulting residue was diluted with water
  3. extractionthe mixture was extracted with methylene chloride
  4. dry with materialdried over anhydrous sodium sulfate
  5. distillationthe solvent was distilled off
  6. washthe resulting solid was washed with methanol

Quellen und Nachweise

ORD-Eintrag
ord-a39b1f5f4140499a950ca3e8833e43be
Quelldatensatz
uspto-grants-2012_11
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US08314098B2

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