Methyl iodide → HCID 178488729, Verbindung

HRID 66016

Reaktionsgleichung

Reaktionsgleichung von HRID 66016
[CH3:1][O:2][C:3]1[CH:8]=[CH:7][C:6]([C:9]2[N:10]=[C:11]3[CH:16]=[CH:15][CH:14]=[CH:13][N:12]3[CH:17]=2)=[CH:5][CH:4]=1.[CH3:18][I:19]>C(#N)C>[I-:19].[CH3:18][N+:10]1[C:9]([C:6]2[CH:5]=[CH:4][C:3]([O:2][CH3:1])=[CH:8][CH:7]=2)=[CH:17][N:12]2[CH:13]=[CH:14][CH:15]=[CH:16][C:11]=12

Komponenten

4

Edukt 2

HCID 6328Methyl iodide2×HCID 6949632-(4-Methoxyphenyl)imidazo[1,2-a]pyridine

Produkt 1

HCID 178488729HCID 178488729, Verbindung

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 6342AcetonitrileLösungsmittel

Versuchsvorschrift

To 2.23 g. of 2-(4-methoxyphenyl)imidazo[1,2-a]pyridine in 50 ml. of acetonitrile is added 2.84 g. of methyl iodide, and the resulting reaction mixture refluxed for 3 hrs. Additional methyl iodide (2 ml.) is added and reflux continued for one hour. The solids which precipitate on cooling are filtered and partially dissolved in boiling isopropanol and filtered. The isopropanol filtrate is cooled and treated with diethyl ether. The crystallized product is filtered and dried to give 1.03 g., m.p. 194-196° C.

Aufarbeitung

  1. temperaturerefluxed for 3 hrs
  2. temperaturereflux
  3. customThe solids which precipitate
  4. temperatureon cooling
  5. filtrationare filtered
  6. dissolutionpartially dissolved
  7. filtrationfiltered
  8. temperatureThe isopropanol filtrate is cooled
  9. additiontreated with diethyl ether
  10. filtrationThe crystallized product is filtered
  11. customdried
  12. customto give 1.03 g

Quellen und Nachweise

ORD-Eintrag
ord-8a708d5803164077b7f4629a7c0c7d9b
Quelldatensatz
uspto-grants-1978_12
Patentnummer
US04129567

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