Réaction #2328985

ord-98a6bc0f06ab4ea683206b64f38480ad

Équation de réaction

COc1ccc(NC(=O)c2ccc(Cl)nc2)c(O)c1
6-Chloro-N-(2-hydroxy-4-methoxyphenyl)nicotinamide
CN(C)C=O
DMF
O
water
COc1ccc2nc(-c3ccc(N(C)C)nc3)oc2c1
title compound
COc1ccc2nc(-c3ccc(N(C)C)nc3)oc2c1
5-(6-Methoxy-1,3-benzoxazol-2-yl)-N,N-dimethylpyridin-2-amine

Conditions de réaction

Conditions détaillées
See reaction.notes.procedure_details.

Traitement

  1. 1
    Autrethe solid was collected
  2. 2
    Lavagerinsed with water
  3. 3
    Autredried
  4. 4
    AutreThe crude product was purified by flash column chromatography

Mode opératoire

6-Chloro-N-(2-hydroxy-4-methoxyphenyl)nicotinamide (40 mg, 0.14 mmol) was dissolved in DMF (1.5 mL) and one drop of sulfuric acid was added. The reaction was run at 230° C. for 20 minutes in a microwave reactor. The mixture was added to water, the solid was collected, rinsed with water and dried. The crude product was purified by flash column chromatography using 40% ethyl acetate in hexane, giving the title compound (14 mg) as an orange solid. 1H NMR (400 MHz, CHLOROFORM-d) δ ppm 8.96 (d, 1H) 8.19 (dd, 1 H) 7.57 (d, 1H) 7.10 (d, 1H) 6.92 (dd, 1H) 6.60 (d, 1H) 3.88 (s, 3H) 3.20 (s, 6H); MS m/z (M+H) 270.

Source

DOI: 10.6084/m9.figshare.5104873.v1Brevet: US07670591B2uspto-grants-2010_03