Reaktion #46951

ord-ce7a1d4f6b89469cbe098ff9fbce3425

Reaktionsgleichung

CCOC(C)=O
ethyl acetate
COc1cc(C(C)C)c(OC(C#N)=CNc2ccccc2)cc1I
2-(5-iodo-2-isopropyl-4-methoxy-phenoxy)-3-phenylamino-acrylonitrile
N=C(N)N.O=C(O)O
guanidine carbonate
CN(C)C=O
DMF
COc1cc(C(C)C)c(Oc2cnc(N)nc2N)cc1I
5-(5-iodo-2-isopropyl-4-methoxy-phenoxy)-pyrimidine-2,4-diamine
Ausbeute 99.1%

Lösungsmittel

Reaktionsbedingungen

Temperatur
60°CELSIUS
Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    Temperaturto maintain an internal temperature of 50° C
  2. 2
    TemperaturThe resulting slurry was cooled to 20° C.
  3. 3
    SonstigePrecipitated solids
  4. 4
    Filtrationwere collected by filtration
  5. 5
    Waschenwashed with water (300 ml)
  6. 6
    Sonstigedried in a vacuum oven (50° C., 24 inches Hg)

Vorschrift

A solution of 2-(5-iodo-2-isopropyl-4-methoxy-phenoxy)-3-phenylamino-acrylonitrile (280 g, 0.64 mol), guanidine carbonate (110 g, 0.61 mol), and 560 ml of DMF was heated to 120° C. for 18 hours. After cooling the mixture to 60° C., 140 ml of ethyl acetate was added. Water (1.12 L) was then added to the mixture at a rate to maintain an internal temperature of 50° C. The resulting slurry was cooled to 20° C. and aged. Precipitated solids were collected by filtration, washed with water (300 ml) followed by isopropanol (500 ml), and dried in a vacuum oven (50° C., 24 inches Hg) to give 242 g of 5-(5-iodo-2-isopropyl-4-methoxy-phenoxy)-pyrimidine-2,4-diamine, 94% yield: m.p. 204.4-205.9 degrees C.; 1HNMR (DMSO) δ=1.2 (d, 6H), 3.3 (m, 1H), 3.8 (s, 3H), 5.85 (s, 2H), 6.4 (s, 2H), 6.9 (d, 2H), 7.35 (s, 1H)

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US07741484B2uspto-grants-2010_06