Acetonitrile → HCID 178419382, Verbindung
Reaktionsgleichung
[CH:1]1[N:2]=[CH:3][N:4]2[CH:9]=[CH:8][CH:7]=[CH:6][C:5]=12.C(#N)C.[Br:13][CH2:14][C:15]1[CH:20]=[CH:19][CH:18]=[CH:17][CH:16]=1>C(OCC)C>[Br-:13].[CH2:14]([C:1]1[NH+:2]=[CH:3][N:4]2[CH:9]=[CH:8][CH:7]=[CH:6][C:5]=12)[C:15]1[CH:20]=[CH:19][CH:18]=[CH:17][CH:16]=1Komponenten
5
Edukt 3
Produkt 1
Reagenzien, Katalysatoren, Lösungsmittel 1
Versuchsvorschrift
Imidazo[1,5-a]pyridine (3.9 g.) in 100 ml. of dry acetonitrile is treated with 6.8 g. of α-bromotoluene, and the resulting reaction mixture heated under reflux for 3 hrs. The solution is cooled and diluted with 250 ml. of diethyl ether. The resulting precipitate is filtered and recrystallized from isopropanol-diethyl ether, 7.92 g., m.p. 172-176° C.
Aufarbeitung
- temperatureheated
- temperatureunder reflux for 3 hrs
- temperatureThe solution is cooled
- additiondiluted with 250 ml
- filtrationThe resulting precipitate is filtered
- customrecrystallized from isopropanol-diethyl ether, 7.92 g
Quellen und Nachweise
- ORD-Eintrag
- ord-52b39dafd60e443fa79424fe2b0238b5
- Quelldatensatz
- uspto-grants-1978_12
- Patentnummer
- US04129567
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