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

HRID 877664
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 877664
[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. H1 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-fc1127327c534886a8293e75b0e966ec
Quelldatensatz
uspto-grants-2015_03
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US08987268B2

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