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Phosphorus oxychloride → 7-Chloro-2-(4-fluorophenyl)-oxazolo[5,4-d]pyrimidine

HRID 1396735
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 1396735
O[C:2]1[C:7]([NH:8][C:9](=[O:17])[C:10]2[CH:15]=[CH:14][C:13]([F:16])=[CH:12][CH:11]=2)=[C:6](O)[N:5]=[CH:4][N:3]=1.C(N(C(C)C)CC)(C)C.O=P(Cl)(Cl)[Cl:30]>>[Cl:30][C:6]1[C:7]2[N:8]=[C:9]([C:10]3[CH:11]=[CH:12][C:13]([F:16])=[CH:14][CH:15]=3)[O:17][C:2]=2[N:3]=[CH:4][N:5]=1
KomponentenReaktionsbedingungenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

4

Edukt 3

HCID 24813Phosphorus oxychlorideHCID 81531DiisopropylethylamineHCID 178522470HCID 178522470, Verbindung

Produkt 1

HCID 866624407-Chloro-2-(4-fluorophenyl)-oxazolo[5,4-d]pyrimidineAusbeute 30 %

Reaktionsbedingungen

Temperatur
90 °C

Versuchsvorschrift

To a solution of N-(4,6-dihydroxypyrimidin-5-yl)-4-fluorobenzamide (0.30 g, 1.20 mmol) in POCl3 (6 ml) was added diisopropylethylamine (0.42 ml, 2.41 mmol). The reaction mixture was stirred under N2 at 90° C. for 3.5 hours. The reaction mixture was allowed to cool down to room temperature and the volatiles were evaporated to dryness. The residue was diluted with water and the aqueous phase was extracted with diethyl ether. The combined organic layers were washed with a saturated NaHCO3 solution and brine, dried over Na2SO4, and concentrated under reduced pressure. The residue was purified by chromatography on silica gel (CH2Cl2/MeOH 100:1) to yield the title compound as a white solid (0.13 g, 30%).

Aufarbeitung

  1. temperatureto cool down to room temperature
  2. customthe volatiles were evaporated to dryness
  3. additionThe residue was diluted with water
  4. extractionthe aqueous phase was extracted with diethyl ether
  5. washThe combined organic layers were washed with a saturated NaHCO3 solution and brine
  6. dry with materialdried over Na2SO4
  7. concentrationconcentrated under reduced pressure
  8. customThe residue was purified by chromatography on silica gel (CH2Cl2/MeOH 100:1)

Quellen und Nachweise

ORD-Eintrag
ord-201d20b98e814882829147fbbd3214da
Quelldatensatz
uspto-grants-2014_12
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US08901132B2

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