Phosphorus oxychloride → 4-Chloropyrrolo(2,1-f)(1,2,4)triazine

HRID 1851095Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 1851095
C(N(C(C)C)CC)(C)C.[CH:10]1[CH:19]=[C:18]2[N:12]([CH:13]=[N:14][NH:15][C:16]2=O)[CH:11]=1.P(Cl)(Cl)([Cl:22])=O.C(=O)(O)[O-].[Na+]>C1(C)C=CC=CC=1>[CH:18]1[CH:19]=[C:10]2[C:11]([Cl:22])=[N:12][CH:13]=[N:14][N:15]2[CH:16]=1

Komponenten

6

Reaktionsbedingungen

Temperatur
100 °C

Versuchsvorschrift

Diisopropylethylamine (3.5 mL, 20.3 mmol) was added to a solution of pyrrolo[1,2-f][1,2,4]triazin-4(3H)-one (2.5 g, 18.5 mmol) dissolved in toluene (37.5 mL) under nitrogen atmosphere. Subsequently, after adding phosphorus oxychloride (5.1 mL, 55.7 mmol), the mixture was heated for 20 hours at 100° C. The resulting reaction mixture was cooled to 0° C. and, after slowly adding sodium bicarbonate aqueous solution, stirred at room temperature for 30 minutes. The resulting aqueous layer was extracted with ethyl acetate, dried with magnesium sulfate, and then filtered. The filtrate was concentrated in vacuum. The resulting yellow solid product was subjected to the next step without purification (2.31 g, 15.0 mmol, 81% yield).

Aufarbeitung

  1. customThe resulting reaction mixture
  2. temperaturewas cooled to 0° C.
  3. extractionThe resulting aqueous layer was extracted with ethyl acetate
  4. dry with materialdried with magnesium sulfate
  5. filtrationfiltered
  6. concentrationThe filtrate was concentrated in vacuum
  7. customThe resulting yellow solid product was subjected to the next step without purification (2.31 g, 15.0 mmol, 81% yield)

Quellen und Nachweise

ORD-Eintrag
ord-aac4df1b1f564c2a90bb7ff55186c652
Quelldatensatz
uspto-grants-2015_02
Patentnummer
US08957102B2

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