تفاعل #543780

ord-f263539c0f034394aa574992f4747d22

ظروف التفاعل

درجة الحرارة
60°CELSIUS
الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    تركيزThe solvent was concentrated
  2. 2
    workup.ADDITIONthe residue was diluted with water
  3. 3
    استخلاصextracted with diethyl ether
  4. 4
    أخرىto remove the unreacted quinoxaline
  5. 5
    استخلاصextracted with ethyl acetate
  6. 6
    تجفيفThe organic phase was dried over magnesium sulfate
  7. 7
    تركيزconcentrated
  8. 8
    أخرىThe residue was chromatographed on silica gel eluting with dichloromethane-methanol (first 95-5

الإجراء التجريبي

A solution of diethylamine hydrochloride (3.82 g, 35 mmol) and triethylamine (0.23 ml) in ethanol (1.75 ml) and water (1.75 ml) was added dropwise, at 60° C., to a mixture of 2-methyl-quinoxaline (5.0 g, 35 mmol), formaldehyde (2.81 g of 37% solution, 35 mmol), triethylamine (0.17 ml) and ethanol (4.6 ml). The pH was adjusted to 7–7.5 by mean of dilute aqueous hydrochloric acid. Stirring was maintained 16 hours at 60° C. The solvent was concentrated, the residue was diluted with water and extracted with diethyl ether to remove the unreacted quinoxaline. The aqueous phase was basified with 20% aqueous sodium hydroxide (10 ml) and extracted with ethyl acetate. The organic phase was dried over magnesium sulfate and concentrated. The residue was chromatographed on silica gel eluting with dichloromethane-methanol (first 95-5 then 90-10 and finally 90-10 plus 0.1% of ammonia) to give diethyl-(2-quinoxalin-2-yl-ethyl)-amine (2.67 g, 37%).

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US07186730B2uspto-grants-2007_03