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Phosphorus oxychloride → 4-chloro-N-(3,5-dimethylphenyl)pyrimidin-2-amine

HRID 968254
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Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 968254
[CH3:1][C:2]1[CH:3]=[C:4]([NH:9][C:10]2[NH:15][C:14](=O)[CH:13]=[CH:12][N:11]=2)[CH:5]=[C:6]([CH3:8])[CH:7]=1.O=P(Cl)(Cl)[Cl:19]>>[Cl:19][C:14]1[CH:13]=[CH:12][N:11]=[C:10]([NH:9][C:4]2[CH:3]=[C:2]([CH3:1])[CH:7]=[C:6]([CH3:8])[CH:5]=2)[N:15]=1
KomponentenReaktionsbedingungenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

3

Edukt 2

HCID 24813Phosphorus oxychlorideHCID 14038592-(3,5-dimethylphenylamino)-3H-pyrimidin-4-one

Produkt 1

HCID 222884124-chloro-N-(3,5-dimethylphenyl)pyrimidin-2-amine

Reaktionsbedingungen

Temperatur
100 °C

Versuchsvorschrift

2-(3,5-Dimethyl-phenylamino)-3H-pyrimidin-4-one (2.01 g, 9.34 mmol) was dissolved in POCl3 (8.70 ml, 93.4 mmol) and the mixture was heated to 100° C. in a round bottom flask equipped with a reflux condenser and a drying tube. After 5 hours the reaction was cooled to room temperature and concentrated in vacuo. The residue was quenched by the addition of sat NaHCO3 (aq) and was extracted 3× with DCM. The combined organic extracts were dried over Na2SO4, filtered and concentrated. The residue was purified by flash column chromatography (dissolved sample in DCM, eluted with 85:15 hexane/EtOAc) to afford 4-chloro-N-(3,5-dimethylphenyl)pyrimidin-2-amine (4-3).

Aufarbeitung

  1. customequipped with a reflux condenser and a drying tube
  2. temperatureAfter 5 hours the reaction was cooled to room temperature
  3. concentrationconcentrated in vacuo
  4. customThe residue was quenched by the addition of sat NaHCO3 (aq)
  5. extractionwas extracted 3× with DCM
  6. dry with materialThe combined organic extracts were dried over Na2SO4
  7. filtrationfiltered
  8. concentrationconcentrated
  9. customThe residue was purified by flash column chromatography (dissolved sample in DCM, eluted with 85:15 hexane/EtOAc)

Quellen und Nachweise

ORD-Eintrag
ord-afc888e2ccc9446f894e8863ebd9fc93
Quelldatensatz
uspto-grants-2005_10
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US06958340B2

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