تفاعل #65765

ord-13b8ea75399b459d9ff47abf66674903

ظروف التفاعل

الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    workup.ADDITIONwas added dropwise under ice-
  2. 2
    درجة الحرارةcooling
  3. 3
    workup.WAITleft
  4. 4
    أخرىstanding in a refrigerator overnight
  5. 5
    workup.DISTILLATIONwas distilled off
  6. 6
    استخلاصfollowed by extraction with ethyl acetate
  7. 7
    غسيلThe organic layer was washed with a saturated aqueous solution of sodium chloride
  8. 8
    أخرىdried
  9. 9
    workup.DISTILLATIONThen, the solvent was distilled off
  10. 10
    أخرىThe residue was purified by silica gel column chromatography (eluent:dichloromethane→ethyl acetate)

الإجراء التجريبي

In 250 ml of 1N hydrochloric acid and 100 ml of dioxane was dissolved 32.2 g of 2-amino-3,4-diethoxycarbonyl-6-(4-methoxyethoxymethoxyphenyl)pyridine, whereto a solution of 6.9 g (1.3 eq.) of sodium nitrite dissolved in 30 ml of water was added dropwise under ice-cooling. The mixture was stirred for 1 hour and left standing in a refrigerator overnight. The mixture was neutralized with sodium hydrogencarbonate, and dioxane was distilled off, followed by extraction with ethyl acetate. The organic layer was washed with a saturated aqueous solution of sodium chloride and dried. Then, the solvent was distilled off. The residue was purified by silica gel column chromatography (eluent:dichloromethane→ethyl acetate).

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US05420275uspto-grants-1995_05