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Sulfuric Acid → [7-[3-(Ethylamino)phenyl]pyrazolo[1,5-a]pyrimidin-3-yl]-2-furanylmethanone

HRID 1247968
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 1247968
[CH2:1]([N:3]([C:14]1[CH:19]=[CH:18][CH:17]=[C:16]([C:20]2[N:25]3[N:26]=[CH:27][C:28]([C:29]([C:31]4[O:32][CH:33]=[CH:34][CH:35]=4)=[O:30])=[C:24]3[N:23]=[CH:22][CH:21]=2)[CH:15]=1)S(C1C=CC(C)=CC=1)(=O)=O)[CH3:2].S(=O)(=O)(O)O.[OH-].[NH4+]>O>[CH2:1]([NH:3][C:14]1[CH:15]=[C:16]([C:20]2[N:25]3[N:26]=[CH:27][C:28]([C:29]([C:31]4[O:32][CH:33]=[CH:34][CH:35]=4)=[O:30])=[C:24]3[N:23]=[CH:22][CH:21]=2)[CH:17]=[CH:18][CH:19]=1)[CH3:2]
KomponentenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

5

Edukt 3

HCID 1118Sulfuric AcidHCID 14923Ammonium HydroxideHCID 20280467N-ethyl-N-[3-[3-(2-furanylcarbonyl)pyrazolo[1,5-a]pyrimidin-7-yl]phenyl]-4-methylbenzenesulfonamide

Produkt 1

HCID 13475999[7-[3-(Ethylamino)phenyl]pyrazolo[1,5-a]pyrimidin-3-yl]-2-furanylmethanone

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 962Water
Lösungsmittel

Versuchsvorschrift

A 10.7 g portion of N-ethyl-N-[3-[3-(2-furanylcarbonyl)pyrazolo[1,5-a]pyrimidin-7-yl]phenyl]-4-methylbenzenesulfonamide was added to a mixture of 90 ml of water and 210 ml of concentrated sulfuric acid. This mixture was heated to 140°-145° C., allowed to cool slowly to room temperature, then cooled to -10° C., poured onto ice, made basic with 550 ml of concentrated ammonium hydroxide and cooled to 0° C. This mixture was extracted with dichloromethane. The extract was passed through hydrous magnesium silicate and washed with 200 ml of dichloromethane. The dichloromethane filtrate and wash was combined with 300 ml of hexane, concentrated to 300 ml, diluted to 800 ml with hexane, treated with charcoal, clarified and cooled to -10° C. This material was filtered, the filtrate concentrated to turbidity and cooled at -10° C. The precipitate was collected, washed with hexane and dried at 60° C. in vacuo, giving 2.3 g of the desired product, mp 142°-143° C.

Aufarbeitung

  1. temperatureThis mixture was heated to 140°-145° C.
  2. temperaturecooled to -10° C.
  3. additionpoured onto ice
  4. temperaturecooled to 0° C
  5. extractionThis mixture was extracted with dichloromethane
  6. washwashed with 200 ml of dichloromethane
  7. washThe dichloromethane filtrate and wash
  8. concentrationconcentrated to 300 ml
  9. additiondiluted to 800 ml with hexane
  10. additiontreated with charcoal
  11. temperaturecooled to -10° C
  12. filtrationThis material was filtered
  13. concentrationthe filtrate concentrated to turbidity
  14. temperaturecooled at -10° C
  15. customThe precipitate was collected
  16. washwashed with hexane
  17. customdried at 60° C. in vacuo

Quellen und Nachweise

ORD-Eintrag
ord-6e58576fa90d407d940edf49071d3708
Quelldatensatz
uspto-grants-1985_06
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US04521422

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