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Phosphorus oxychloride → 6-Bromo-4-chloropyrrolo[1,2-b]pyridazine-3-carbonitrile

HRID 1408908
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 1408908
[Br:1][C:2]1[CH:3]=[C:4]2[C:9](O)=[C:8]([C:11]#[N:12])[CH:7]=[N:6][N:5]2[CH:13]=1.O=P(Cl)(Cl)[Cl:16]>>[Br:1][C:2]1[CH:3]=[C:4]2[C:9]([Cl:16])=[C:8]([C:11]#[N:12])[CH:7]=[N:6][N:5]2[CH:13]=1
KomponentenReaktionsbedingungenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

3

Edukt 2

HCID 24813Phosphorus oxychlorideHCID 178510449HCID 178510449, Verbindung

Produkt 1

HCID 682911366-Bromo-4-chloropyrrolo[1,2-b]pyridazine-3-carbonitrileAusbeute 47,7 %

Reaktionsbedingungen

Temperatur
75 °C

Versuchsvorschrift

To a 25 mL round bottom flask was added 6-bromo-4-hydroxypyrrolo[1,2-b]pyridazine-3-carbonitrile (16.5 g, 69.47 mmol) and POCl3 (85 mL, 0.88 mol) and the reaction mixture was stirred and heated at 75° C. for 3 hours. The POCl3 was removed under vacuum and the resulting residue was dissolved in CH2Cl2. The solution was cooled to 0° C. and saturated aq. NaHCO3 solution was added and the biphasic mixture was stirred vigorously while allowing to warm to rt. The organic layer was separated and concentrated and the obtained residue was purified by flash silica gel column chromatography to yield 8.5 g (29%) of the title compound as a yellow solid. HPLC (condition P): retention time=16.74 min. 1H NMR (400 MHz, CDCl3) δ ppm: 8.09 (1H, s), 7.94 (1H, d, 2.0 Hz), 7.06 (1H, d, 2.0 Hz).

Aufarbeitung

  1. customThe POCl3 was removed under vacuum
  2. dissolutionthe resulting residue was dissolved in CH2Cl2
  3. temperatureThe solution was cooled to 0° C.
  4. additionsaturated aq. NaHCO3 solution was added
  5. stirringthe biphasic mixture was stirred vigorously
  6. temperatureto warm to rt
  7. customThe organic layer was separated
  8. concentrationconcentrated
  9. customthe obtained residue was purified by flash silica gel column chromatography

Quellen und Nachweise

ORD-Eintrag
ord-25fefe339fe7491090dbf13679b24407
Quelldatensatz
uspto-grants-2014_12
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US08921368B2

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