Ethanol → HCID 21258509, Verbindung

HRID 635350Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 635350
[Br:1][CH2:2][C:3]([C:5]1([C:9]2[CH:18]=[CH:17][C:16]3[C:11](=[CH:12][CH:13]=[CH:14][CH:15]=3)[CH:10]=2)[CH2:8][CH2:7][CH2:6]1)=O.[NH:19]1[CH2:23][CH2:22][NH:21][C:20]1=[S:24].C(O)C>C(O)(=O)C>[BrH:1].[CH:10]1[C:11]2[C:16](=[CH:15][CH:14]=[CH:13][CH:12]=2)[CH:17]=[CH:18][C:9]=1[C:5]1([C:3]2[N:21]3[CH2:22][CH2:23][N:19]=[C:20]3[S:24][CH:2]=2)[CH2:8][CH2:7][CH2:6]1

Komponenten

5

Versuchsvorschrift

A mixture of the crude 2-bromo-1-[1-(2-naphthyl)cyclobutyl]ethanone described above, imidazolidine-2-thione (5.1 g), ethanol (60 ml) and acetic acid (40 ml) was heated under reflux for 18 hours then allowed to cool to ambient temperature. The solvents were removed in vacuo and the residue was triturated with a hot mixture of ethyl acetate (100 ml) and acetone (20 ml). The resulting solid was collected by filtration, washed with ethyl acetate (50 ml), dried in vacuo at 60° C., then crystallised from ethanol. The resulting solid was collected by filtration, washed with ethanol (30 ml), and dried in vacuo at 60° C. to give 3-[1-(2-naphthyl)cyclobutyl]-5,6-dihydroimidazo[2,1-b]thiazole hydrobromide as pale yellow prisms (10 g), m.p. 239-241° C.

Aufarbeitung

  1. temperaturewas heated
  2. temperatureunder reflux for 18 hours
  3. customThe solvents were removed in vacuo
  4. customthe residue was triturated with a hot mixture of ethyl acetate (100 ml) and acetone (20 ml)
  5. filtrationThe resulting solid was collected by filtration
  6. washwashed with ethyl acetate (50 ml)
  7. customdried in vacuo at 60° C.
  8. customcrystallised from ethanol
  9. filtrationThe resulting solid was collected by filtration
  10. washwashed with ethanol (30 ml)
  11. customdried in vacuo at 60° C.

Quellen und Nachweise

ORD-Eintrag
ord-156e456459d84c7eb20ad2eda81b4488
Quelldatensatz
uspto-grants-2001_02
Patentnummer
US06187802B1

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