Reaktion #1262

ord-db70288e9ca54cb89358931186bc5974

Reaktionsgleichung

Nc1cc(Cl)nc(N)n1
4-chloro-2,6-diaminopyrimidine
CC(=O)[O-].[Na+]
sodium acetate
N#[N+]c1ccc(Cl)cc1.[Cl-]
4-chlorobenzenediazonium chloride
Nc1nc(N)c(N=Nc2ccc(Cl)cc2)c(Cl)n1
6-chloro-5-[(4-chlorophenyl)azo]-2,4-pyrimidinediamine
Ausbeute 41.4%

Lösungsmittel

Reaktionsbedingungen

Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    Temperaturwith cooling over 30 minutes at a rate that
  2. 2
    Sonstigethe reaction at 18°
  3. 3
    workup.STIRRINGThe reaction was stirred overnight at room temperature
  4. 4
    Filtrationthe orange crystals were filtered
  5. 5
    Waschenwashed with water (4×400 ml)
  6. 6
    Sonstigedried in vacuo

Vorschrift

To a suspension of 4-chloro-2,6-diaminopyrimidine (21.68 g, 0.150 mol) in water (750 ml) and acetic acid (750 ml) was added sodium acetate (300 g). Solution occurred after stirring for 20 minutes, and then the solution of 4-chlorobenzenediazonium chloride (0.166 mol) was added with cooling over 30 minutes at a rate that kept the reaction at 18°. The reaction was stirred overnight at room temperature, and the orange crystals were filtered, washed with water (4×400 ml), and dried in vacuo to give 17.6 g of 6-chloro-5-[(4-chlorophenyl)azo]-2,4-pyrimidinediamine. The mother liquors were cooled to 5° for 20 hours, and the crystals were collected and dried in vacuo to give 6.94 g of additional 6-chloro-5-[(4-chlorophenyl)azo]-2,4-pyrimidineadiamine.

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US05723609uspto-grants-1998_03