Dimethylformamide → Fadrozole

HRID 22548

Reaktionsgleichung

Reaktionsgleichung von HRID 22548
Br[C:2]1[CH:7]=[CH:6][C:5]([CH:8]2[N:13]3[CH:14]=[N:15][CH:16]=[C:12]3[CH2:11][CH2:10][CH2:9]2)=[CH:4][CH:3]=1.[CH3:17][N:18](C)C=O>O>[C:17]([C:2]1[CH:7]=[CH:6][C:5]([CH:8]2[N:13]3[CH:14]=[N:15][CH:16]=[C:12]3[CH2:11][CH2:10][CH2:9]2)=[CH:4][CH:3]=1)#[N:18]

Komponenten

4

Versuchsvorschrift

A mixture of 85 mg of 5-(p-bromophenyl)-5,6,7,8-tetrahydroimidazo[1,5-a]pyridine and 74 mg of cuprous cyanide in 1 ml of N,N-dimethylformamide is heated under nitrogen at 120° for 11 h. The reaction mixture is cooled, diluted with 10 ml of water and extracted with ethyl acetate. The organic extracts are dried over sodium sulfate and evaporated. The resulting oil is chromatographed on silica gel with ethyl acetate to yield the title compound, m.p. 117°-118°.

Aufarbeitung

  1. temperatureis heated under nitrogen at 120° for 11 h
  2. temperatureThe reaction mixture is cooled
  3. extractionextracted with ethyl acetate
  4. dry with materialThe organic extracts are dried over sodium sulfate
  5. customevaporated
  6. customThe resulting oil is chromatographed on silica gel with ethyl acetate

Quellen und Nachweise

ORD-Eintrag
ord-00f7638125924cf68d1eb79ce35a532a
Quelldatensatz
uspto-grants-1995_06
Patentnummer
US05428160

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