تفاعل #56847

ord-582a73f2ba0f47c68b8c414e243374b1

معادلة التفاعل

O=C([O-])[O-].[Na+].[Na+]
sodium carbonate
Nc1nc(Cl)cc(Cl)n1
4,6-dichloro-pyrimidin-2-ylamine
CCOc1ccc(Cl)cc1B(O)O
5-chloro-2-ethoxy-phenyl boronic acid
c1ccc(P(c2ccccc2)c2ccccc2)cc1
triphenylphosphine
CCOc1ccc(Cl)cc1-c1cc(Cl)nc(N)n1
4-chloro-6-(5-chloro-2-ethoxy-phenyl)-pyrimidin-2-ylamine
المردود 73.3%

المذيبات

ظروف التفاعل

الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    ترشيحthe mixture was filtered through a pad of celite under suction
  2. 2
    تركيزThe filtrated was concentrated under reduced pressure
  3. 3
    أخرىthe residue was purified by flash chromatography on silica gel eluting with 15% ethyl acetate-hexane

الإجراء التجريبي

To a mixture of 4,6-dichloro-pyrimidin-2-ylamine (0.50 g, 3.0 mmol), 5-chloro-2-ethoxy-phenyl boronic acid (0.61 g, 3.0 mmol), palladium (II) acetate (0.10 g, 0.46 mmol), and triphenylphosphine (0.24 g, 0.91 mmol) was added a solution of sodium carbonate (1.6 g, 15.2 mmol) in water (5 ml) followed by glyme (20 ml). The mixture was stirred under an argon atmosphere at room temperature for 3.5 hours. Acetone (20 ml) was added and the mixture was filtered through a pad of celite under suction. The filtrated was concentrated under reduced pressure and the residue was purified by flash chromatography on silica gel eluting with 15% ethyl acetate-hexane followed by 20% ethyl acetate-hexane to provide 4-chloro-6-(5-chloro-2-ethoxy-phenyl)-pyrimidin-2-ylamine (0.625 g, 73% yield) as a white powder.

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US07419984B2uspto-grants-2008_09