تفاعل #42275

ord-4776f860dc374479bbd3bed71c13955f

المذيبات

ظروف التفاعل

درجة الحرارة
22.5°CELSIUS
الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    workup.STIRRINGthe mixture is stirred for 15 hours at 20-25 degrees C
  2. 2
    workup.STIRRINGafter stirring for another 3 hours
  3. 3
    أخرىAfter a total of 39 hours
  4. 4
    أخرىthe acetone is removed under reduced pressure
  5. 5
    استخلاصThe mixture is extracted with dichloromethane
  6. 6
    أخرىthe organic layer is separated
  7. 7
    غسيلwashed with hydrochloric acid (0.5 N)
  8. 8
    تجفيفthe organic phase is dried with anhydrous magnesium sulfate to a solid
  9. 9
    أخرىThe solid is crystallized from dichloromethane/hexane/methanol

الإجراء التجريبي

A mixture of 3-cyano-5-[(dipropylamino)carbonyl]benzoic acid (IX/XXXII, PREPARATION 7, 0.602 g, 2.19 mmol), potassium carbonate (0.212 g, 1.53 mmol), and acetone (2.5 mL) is stirred at 20-25 degrees C. Water (2.5 mL) and urea-hydrogen peroxide adduct (0.825 g, 8.78 mmol) are added and the mixture is stirred for 15 hours at 20-25 degrees C., at which time additional urea-hydrogen peroxide adduct (0.204 g) is added; after stirring for another 3 hours, an additional 0.205 g of urea-hydrogen peroxide is added. After a total of 39 hours has elapsed, the acetone is removed under reduced pressure and the residue is acidified with hydrochloric acid (3N) to pH=2-4. The mixture is extracted with dichloromethane, the organic layer is separated and washed with hydrochloric acid (0.5 N), and the organic phase is dried with anhydrous magnesium sulfate to a solid. The solid is crystallized from dichloromethane/hexane/methanol to give the title compound, MS (ESI+) for C15H20N2O4 m/z (M+H)+=293.2.

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US07727997B2uspto-grants-2010_06