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Phosphorus oxychloride → Methyl 2-(7-chloro-5-methyl-3-phenylpyrazolo[1,5-a]pyrimidin-6-yl)acetate

HRID 472825
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Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 472825
O[CH:2]1[N:7]2[N:8]=[CH:9][C:10]([C:11]3[CH:16]=[CH:15][CH:14]=[CH:13][CH:12]=3)=[C:6]2[NH:5][C:4]([CH3:17])=[C:3]1[CH2:18][C:19]([O:21][CH3:22])=[O:20].O=P(Cl)(Cl)[Cl:25]>>[Cl:25][C:2]1[N:7]2[N:8]=[CH:9][C:10]([C:11]3[CH:16]=[CH:15][CH:14]=[CH:13][CH:12]=3)=[C:6]2[N:5]=[C:4]([CH3:17])[C:3]=1[CH2:18][C:19]([O:21][CH3:22])=[O:20]
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Komponenten

3

Edukt 2

HCID 24813Phosphorus oxychlorideHCID 136350318Methyl2-(7-hydroxy-5-methyl-3-phenyl-4,7-dihydropyrazolo[1,5-a]pyrimidin-6-yl)acetate

Produkt 1

HCID 86670268Methyl 2-(7-chloro-5-methyl-3-phenylpyrazolo[1,5-a]pyrimidin-6-yl)acetateAusbeute 90 %

Versuchsvorschrift

To methyl 2-(7-hydroxy-5-methyl-3-phenyl-4,7-dihydropyrazolo[1,5-a]pyrimidin-6-yl)acetate (0.5 g, 1.68 mmol) was added POCl3 (1 mL). The reaction mixture was heated at reflux for 1 h. After cooling, the reaction mixture was added drop-wise to ice-water. A brown solid precipitated. The solid were filtered and washed with water, then dissolved in ethyl acetate. The organic solution was washed with saturated NaHCO3 and dried over sodium sulfate. The solvent was evaporated to give the title compound (0.48 g, 90%). 1H-NMR (500 MHz, MeOD) δ ppm 2.66 (3H, s), 3.77 (3H, s), 4.04 (2H, s), 7.26 (1H, s), 7.42 (2H, s), 8.09 (2H, s), 8.57 (1H, s).

Aufarbeitung

  1. temperatureThe reaction mixture was heated
  2. temperatureat reflux for 1 h
  3. temperatureAfter cooling
  4. customA brown solid precipitated
  5. filtrationThe solid were filtered
  6. washwashed with water
  7. dissolutiondissolved in ethyl acetate
  8. washThe organic solution was washed with saturated NaHCO3
  9. dry with materialdried over sodium sulfate
  10. customThe solvent was evaporated

Quellen und Nachweise

ORD-Eintrag
ord-511faa31591e4bb7b8a30e30928ab0f8
Quelldatensatz
uspto-grants-2014_01
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US08633200B2

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