Acetic Anhydride → 1-[2-(Propan-2-yl)pyrazolo[1,5-a]pyridin-3-yl]ethan-1-one

HRID 839792Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 839792
[CH:1]([C:4]1[CH:12]=[C:7]2[CH:8]=[CH:9][CH:10]=[CH:11][N:6]2[N:5]=1)([CH3:3])[CH3:2].[C:13](OC(=O)C)(=[O:15])[CH3:14]>S(=O)(=O)(O)O.[OH-].[K+]>[C:13]([C:12]1[C:4]([CH:1]([CH3:3])[CH3:2])=[N:5][N:6]2[CH:11]=[CH:10][CH:9]=[CH:8][C:7]=12)(=[O:15])[CH3:14]

Komponenten

5

Edukt 2

HCID 7918Acetic AnhydrideHCID 113786582-Isopropylpyrazolo[1,5-a]pyridine

Produkt 1

HCID 159338551-[2-(Propan-2-yl)pyrazolo[1,5-a]pyridin-3-yl]ethan-1-oneAusbeute 81,1 %

Reagenzien, Katalysatoren, Lösungsmittel 2

HCID 1118Sulfuric AcidKatalysatorHCID 14797Potassium HydroxideLösungsmittel

Versuchsvorschrift

A mixture of 4.2g of 2-isopropylpyrazolo[1,5-a]-pyridine, 10.2g of acetic anhydride and 2-3 drops of concentrated sulfuric acid was refluxed for 7 hr. After cooling, the mixture was added to 200 ml of 4M potassium hydroxide solution and stirred for 1 hr. The solution was extracted with chloroform and the chloroform solution was dried over sodium sulfate. The dried chloroform solution was concentrated and the residue was columnchromatographed over alumina to isolate objective product. Recrystallization from n-hexane gave 4.3g of colorless needles, mp 74° C. Yield 67%.

Aufarbeitung

  1. temperaturewas refluxed for 7 hr
  2. temperatureAfter cooling
  3. extractionThe solution was extracted with chloroform
  4. dry with materialthe chloroform solution was dried over sodium sulfate
  5. concentrationThe dried chloroform solution was concentrated
  6. customto isolate objective product
  7. customRecrystallization from n-hexane

Quellen und Nachweise

ORD-Eintrag
ord-7501d1dc34534a46a42280ac97b4d82c
Quelldatensatz
uspto-grants-1978_06
Patentnummer
US04097483

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