Phosphorus oxychloride → Benzonitrile, 4-(5,6,7,8-tetrahydroimidazo(1,5-a)pyridin-5-yl)-, hydrochloride (1:1)

HRID 477978

Reaktionsgleichung

Reaktionsgleichung von HRID 477978
[C:1]([C:4]1[CH:9]=[CH:8][C:7]([CH:10]2[N:15]3[CH:16]=[N:17][CH:18]=[C:14]3[CH2:13][CH2:12][CH2:11]2)=[CH:6][CH:5]=1)(=O)[NH2:2].P(Cl)(Cl)([Cl:21])=O>C(Cl)(Cl)Cl>[ClH:21].[C:1]([C:4]1[CH:5]=[CH:6][C:7]([CH:10]2[N:15]3[CH:16]=[N:17][CH:18]=[C:14]3[CH2:13][CH2:12][CH2:11]2)=[CH:8][CH:9]=1)#[N:2]

Komponenten

4

Edukt 2

HCID 24813Phosphorus oxychlorideHCID 136882214-(5,6,7,8-Tetrahydroimidazo[1,5-a]pyridin-5-yl)benzamide

Produkt 1

HCID 59694Benzonitrile, 4-(5,6,7,8-tetrahydroimidazo(1,5-a)pyridin-5-yl)-, hydrochloride (1:1)

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 6212ChloroformLösungsmittel

Versuchsvorschrift

A solution of 1.13 g of 5-(p-carbamoylphenyl)-5,6,7,8-tetrahydroimidazo[1,5-a]pyridine and 1.0 ml of phosphorus oxychloride in 30 ml of chloroform is refluxed for 15 h, cooled and evaporated with toluene. The resulting oil is redissolved in 30 ml of methylene chloride, cooled to 0° and 30 ml of an ice-cold solution of 50% ammonium hydroxide solution is added. The organic phase is separated, dried and evaporated to an oil. Filtration through 20 g of silica with ethyl acetate yields the free title compound which is dissolved in 20 ml of acetone and treated with 1.2 ml of 3N ethereal hydrogen chloride to yield its hydrochloride, m.p. 209°-210°.

Aufarbeitung

  1. temperaturecooled
  2. customevaporated with toluene
  3. dissolutionThe resulting oil is redissolved in 30 ml of methylene chloride
  4. temperaturecooled to 0°
  5. addition30 ml of an ice-cold solution of 50% ammonium hydroxide solution is added
  6. customThe organic phase is separated
  7. customdried
  8. customevaporated to an oil
  9. filtrationFiltration through 20 g of silica with ethyl acetate

Quellen und Nachweise

ORD-Eintrag
ord-98b9cb803bd44262a6d94bcbb4dfae67
Quelldatensatz
uspto-grants-1989_12
Patentnummer
US04889861

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