Réaction #322997

ord-48b605eb739444d7ad11458a312f483c

Solvants

Conditions de réaction

Température
4°CELSIUS
Conditions détaillées
See reaction.notes.procedure_details.

Traitement

  1. 1
    workup.DISSOLUTIONis dissolved
  2. 2
    Autrethe crystallised solid is separated by filtration
  3. 3
    Lavagewashed with ethanol (10 cc)
  4. 4
    Autredried at 45° C. under reduced pressure (0.067 kPa)

Mode opératoire

The procedure is similar to that described in Example 1, but starting with 2,6-difluorobenzoic acid (5.1 g), N,N'-carbonyldiimidazole (5.2 g) and 2-amino-7-methoxy-1,8-naphthyridine (4.4 g). The product produced by precipitation in water (4.5 g; m.p. 215°-217° C.) is dissolved in boiling ethanol (70 cc). After 1 hour's cooling at 4° C., the crystallised solid is separated by filtration, washed with ethanol (10 cc) and dried at 45° C. under reduced pressure (0.067 kPa). N-(7-methoxy-1,8-naphthyridin-2-yl)-2,6-difluorobenzamide (3.2 g) is produced, m.p. 219°-220° C.

Source

DOI: 10.6084/m9.figshare.5104873.v1Brevet: US04642308uspto-grants-1987_02