HCID 4362726, Verbindung → 7-[1-(2,4-Dichlorophenoxy)ethyl]-[1,2,4]triazolo[1,5-a]pyrimidine

HRID 1290812Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 1290812
[Cl:1][C:2]1[CH:17]=[C:16]([Cl:18])[CH:15]=[CH:14][C:3]=1[O:4][CH:5]([CH3:13])[C:6](=O)[CH:7]=[CH:8][N:9](C)[CH3:10].[NH2:19][C:20]1N=C[NH:22][N:21]=1>C(O)(=O)C>[Cl:1][C:2]1[CH:17]=[C:16]([Cl:18])[CH:15]=[CH:14][C:3]=1[O:4][CH:5]([C:6]1[N:22]2[N:21]=[CH:20][N:19]=[C:10]2[N:9]=[CH:8][CH:7]=1)[CH3:13]

Komponenten

4

Edukt 2

HCID 4362726HCID 4362726, VerbindungHCID 178418311HCID 178418311, Verbindung

Produkt 1

HCID 38014747-[1-(2,4-Dichlorophenoxy)ethyl]-[1,2,4]triazolo[1,5-a]pyrimidine

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 176Acetic AcidLösungsmittel2×

Versuchsvorschrift

A solution of 4-(2,4-dichlorophenoxy)-1-(dimethylamino)-1-penten-3-one (2.9 g) in glacial acetic acid (25 ml) was added to a stirred solution of 3-amino-1,2,4-triazole (0.93 g) also in glacial acetic acid (25 ml). The mixture was heated under reflux for 5 hours and then cooled to room temperature. The mixture was then poured into 200 ml of ice-water and extracted with toluene. The toluene extracts were washed with a 10% aqueous solution of sodium hydrogen carbonate followed by water, then dried over anhydrous magnesium sulphate and the solvent was evaporated under reduced pressure. The residue was triturated with cold diethyl ether and the solid was collected by filtration, followed by recrystallisation from a mixture of ethyl acetate and petroleum ether (b.p. 40°-60° C.) to give 7-[1-(2,4-dichlorophenoxy)ethyl]-1,2,4-triazolo[1,5-a]pyrimidine. Yield 2.02 g, (mp 137°-138° C.).

Aufarbeitung

  1. temperatureThe mixture was heated
  2. temperatureunder reflux for 5 hours
  3. extractionextracted with toluene
  4. washThe toluene extracts were washed with a 10% aqueous solution of sodium hydrogen carbonate
  5. dry with materialdried over anhydrous magnesium sulphate
  6. customthe solvent was evaporated under reduced pressure
  7. customThe residue was triturated with cold diethyl ether
  8. filtrationthe solid was collected by filtration
  9. customfollowed by recrystallisation from a mixture of ethyl acetate and petroleum ether (b.p. 40°-60° C.)

Quellen und Nachweise

ORD-Eintrag
ord-4f36e255efb64a5483ec38ca23ccfbd9
Quelldatensatz
uspto-grants-1998_05
Patentnummer
US05753665

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