Ammonium Chloride → HCID 178515422, Verbindung

HRID 1112520Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 1112520
[O:1]=[C:2]1[N:7]2[CH:8]=[CH:9][CH:10]=[CH:11][C:6]2=[N:5][CH:4]=[C:3]1[C:12]#[N:13].[N-:14]=[N+:15]=[N-:16].[Na+].[Cl-].[NH4+]>CN(C)C=O>[NH:14]1[C:12]([C:3]2[C:2](=[O:1])[N:7]3[CH:8]=[CH:9][CH:10]=[CH:11][C:6]3=[N:5][CH:4]=2)=[N:13][N:16]=[N:15]1

Komponenten

5

Edukt 3

HCID 25517Ammonium ChlorideHCID 33557Sodium AzideHCID 13480904HCID 13480904, Verbindung

Produkt 1

HCID 178515422HCID 178515422, VerbindungAusbeute 19,1 %

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 6228DimethylformamideLösungsmittel

Versuchsvorschrift

A stirred mixture of 4-oxo-4H-pyrido[1,2-a]-pyrimidine-3-carbonitrile (2.17 g., 0.0127 mole), sodium azide (0.911 g., 0.014 mole), and ammonium chloride (0.75 g., 0.014 mole) in N,N-dimethylformamide (20 ml.) was heated by means of an oil bath maintained at 120° for 19 hours. The solvent was removed and the residue treated with hot aqueous sodium bicarbonate. The mixture was filtered. The filtrate was acidified with acetic acid. The precipitate was collected and recrystallized from acetic acid to give the title compound (0.52 g., 19%) m.p. 308°-309° (decomp). Recrystallization from acetic acid with charcoal treatment gave analytical material, m.p. 311°-312° (decomp).

Aufarbeitung

  1. temperaturewas heated by means of an oil bath
  2. temperaturemaintained at 120° for 19 hours
  3. customThe solvent was removed
  4. additionthe residue treated with hot aqueous sodium bicarbonate
  5. filtrationThe mixture was filtered
  6. customThe precipitate was collected
  7. customrecrystallized from acetic acid

Quellen und Nachweise

ORD-Eintrag
ord-2c24545ebfa34e55a7aa5fddfada5bbb
Quelldatensatz
uspto-grants-1978_10
Patentnummer
US04122274

Notizen zur Reaktion

Wird geladen…