Réaction #84097

ord-0c6c5bb0a5c943cab6c7cb134fb85ce2

Équation de réaction

COc1ccc2nc(Cl)ccc2c1
2-chloro-6-methoxyquinoline
COC(=O)c1ccc(B(O)O)cc1
4-(methoxycarbonyl) phenylboronic acid
O=C([O-])[O-].[Na+].[Na+]
sodium carbonate
COC(=O)c1ccc(-c2ccc3cc(OC)ccc3n2)cc1
product
COC(=O)c1ccc(-c2ccc3cc(OC)ccc3n2)cc1
methyl 4-(6-methoxyquinolin-2-yl)benzoate

Conditions de réaction

Température
120°CELSIUS
Conditions détaillées
See reaction.notes.procedure_details.

Traitement

  1. 1
    FiltrationThe precipitates were filtered
  2. 2
    Lavagewashed with EtOAc (10 mL), acetone (10 mL) and water (10 mL) separately
  3. 3
    Autredried

Mode opératoire

A mixture of 2-chloro-6-methoxyquinoline (see U.S. 61/391,225 for synthesis) (200 mg, 1.0 mmol), 4-(methoxycarbonyl) phenylboronic acid (205 mg, 1.1 mmol), Pd(dppf)Cl2 (366 mg, 0.5 mmol) and sodium carbonate (212 mg, 2.0 mmol) in 1,4-dioxane/water (3 mL/0.6 mL) was heated to 120° C. by microwave for 1 h. The precipitates were filtered; washed with EtOAc (10 mL), acetone (10 mL) and water (10 mL) separately; dried to give the product as a black solid. (120 mg, 40.9%).

Source

DOI: 10.6084/m9.figshare.5104873.v1Brevet: US09433618B2uspto-grants-2016_09