반응 #323041

ord-5e9f7f2c77d5410e97f5ab8929bd8415

반응 방정식

CCO
ethanol
O=C(O)c1ccco1
2-furancarboxylic acid
Nc1ccc2ccc(Oc3ccccc3)nc2n1
2-amino-7-phenoxy-1,8-naphthyridine
O=C(Nc1ccc2ccc(Oc3ccccc3)nc2n1)c1ccco1
N-(7-Phenoxy-1,8-naphthyridin-2-yl)-2-furancarboxamide
수율 86.7%

용매

반응 조건

온도
4°CELSIUS
상세 조건
See reaction.notes.procedure_details.

후처리

  1. 1
    workup.DISSOLUTIONis dissolved
  2. 2
    기타the crystallised solid is separated by filtration
  3. 3
    세척washed with ethanol (15 cc)
  4. 4
    기타dried at 40° C. under reduced pressure (0.067 kPa)

실험 절차

The procedure is similar to that described in Example 1, but starting with 2-furancarboxylic acid (7.5 g), N,N'-carbonyldiimidazole (10.9 g) and 2-amino-7-phenoxy-1,8-naphthyridine (11.9 g). The product produced by precipitation in water (15.7 g; m.p. 164° C.) is dissolved in boiling ethanol (200 cc). After 2 hours' cooling at 4° C., the crystallised solid is separated by filtration, washed with ethanol (15 cc) and dried at 40° C. under reduced pressure (0.067 kPa). N-(7-Phenoxy-1,8-naphthyridin-2-yl)-2-furancarboxamide (14.4 g) is produced, m.p. 167° C.

출처

DOI: 10.6084/m9.figshare.5104873.v1특허: US04642308uspto-grants-1987_02