Dimethylformamide → 6-Chloro-1,3-dimethyl-1H-pyrazolo[3,4-b]pyridine-5-carbaldehyde

HRID 577760Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 577760
C(O[C:5](=[O:7])[CH3:6])(=O)C.[CH3:8][N:9]1[C:13](N)=[CH:12][C:11]([CH3:15])=[N:10]1.P(Cl)(Cl)([Cl:18])=O.C[N:22]([CH:24]=O)[CH3:23]>>[Cl:18][C:24]1[N:22]=[C:23]2[N:9]([CH3:8])[N:10]=[C:11]([CH3:15])[C:12]2=[CH:13][C:6]=1[CH:5]=[O:7]

Komponenten

5

Reaktionsbedingungen

Temperatur
95 °C

Versuchsvorschrift

A mixture of acetic anhydride (6.62 mL, 70 mmol) and 2,5-dimethyl-2H-pyrazol-3-ylamine (5.0 g, 45 mmol) was heated while stirring at 90-100° C. for 4 h. After evaporation of volatiles in vacuo, phosphorus oxychloride (18.5 mL, 200 mmol) was added and the mixture was heated while stirring at 90-95° C. for 3 h. Thereafter, anhydrous DMF (9.2 mL, 120 mmol) was added slowly over the period of 30 min while maintaining the internal temperature of the mixture at 90-95° C. After stirring for an additional 2 h, the reaction mixture was cooled to RT and poured over crushed ice (100-120 g). The precipitated solid was filtered off, washed with water and dried in vacuo. The yellowish solid product was subsequently dissolved in methylene chloride (100 mL), washed with water, dried over sodium sulfate, and the solvent was evaporated in vacuo to give the desired product as light yellow solid (4.1 g), yield: 44%, mp: 152-153° C.

Aufarbeitung

  1. temperaturewas heated
  2. additionwas added
  3. temperaturethe mixture was heated
  4. stirringwhile stirring at 90-95° C. for 3 h
  5. temperaturewhile maintaining the internal temperature of the mixture at 90-95° C
  6. stirringAfter stirring for an additional 2 h
  7. temperaturethe reaction mixture was cooled to RT
  8. additionpoured
  9. filtrationThe precipitated solid was filtered off
  10. washwashed with water
  11. customdried in vacuo
  12. dissolutionThe yellowish solid product was subsequently dissolved in methylene chloride (100 mL)
  13. washwashed with water
  14. dry with materialdried over sodium sulfate
  15. customthe solvent was evaporated in vacuo

Quellen und Nachweise

ORD-Eintrag
ord-b11b9abfeba042fd81ce1ced7bd707fc
Quelldatensatz
uspto-grants-2015_05
Patentnummer
US09040558B2

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