Phosphorus oxychloride → 4-(Imidazo[1,5-a]pyridin-5-yl)benzonitrile

HRID 477972Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 477972
C([NH:5][C:6]([C:8]1[CH:13]=[CH:12][C:11]([C:14]2[N:19]3[CH:20]=[N:21][CH:22]=[C:18]3[CH:17]=[CH:16][CH:15]=2)=[CH:10][CH:9]=1)=O)(C)(C)C.P(Cl)(Cl)(Cl)=O>C1(C)C=CC=CC=1>[C:6]([C:8]1[CH:9]=[CH:10][C:11]([C:14]2[N:19]3[CH:20]=[N:21][CH:22]=[C:18]3[CH:17]=[CH:16][CH:15]=2)=[CH:12][CH:13]=1)#[N:5]

Komponenten

4

Edukt 2

HCID 24813Phosphorus oxychlorideHCID 136882255-(p-Tert-butylaminocarbonylphenyl)imidazo[1,5-a]pyridine

Produkt 1

HCID 136882234-(Imidazo[1,5-a]pyridin-5-yl)benzonitrile

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 1140TolueneLösungsmittel

Versuchsvorschrift

A solution of 0.1 g of 5-(p-tert-butylaminocarbonylphenyl)imidazo[1,5-a]pyridine in 3 ml of toluene is treated with 40 μl of phosphorus oxychloride at 90° for 5 h. The solvent is evaporated and the residue is redissolved in 30 ml of chloroform at 0°. An ice-cold ammonium hydroxide solution is added and the organic phase is separated, dried over sodium sulfate and evaporated. The residue is chromatographed on silica with ethyl acetate to yield the title compound, m.p. 117°-118°.

Aufarbeitung

  1. customThe solvent is evaporated
  2. dissolutionthe residue is redissolved in 30 ml of chloroform at 0°
  3. additionAn ice-cold ammonium hydroxide solution is added
  4. customthe organic phase is separated
  5. dry with materialdried over sodium sulfate
  6. customevaporated
  7. customThe residue is chromatographed on silica with ethyl acetate

Quellen und Nachweise

ORD-Eintrag
ord-9c024c7e70a947779104c5325a43bd0e
Quelldatensatz
uspto-grants-1989_12
Patentnummer
US04889861

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