Reaction #446031

ord-74e1eea7522a424985bec55ffcbbcc6e

Solvents

Conditions

Detailed conditions
See reaction.notes.procedure_details.

Workup

  1. 1
    workup.STIRRINGthe resulting red solution is stirred for 2 hours at 80° C.
  2. 2
    Filtrationfiltered with suction
  3. 3
    Otherthe crystals are dried
  4. 4
    workup.DISSOLUTIONdissolved in 50 ml of saturated sodium chloride solution
  5. 5
    Extractionextracted three times with 100 ml of ethyl acetate each time
  6. 6
    DryingThe organic phase is dried over magnesium sulphate
  7. 7
    Filtrationfiltered off with suction
  8. 8
    Concentrationconcentrated by evaporation
  9. 9
    OtherThe residue crystallises from ether/hexane 1:2 yielding 2.8 g of the above acid, which

Procedure

5 g of potassium tert.-butoxide are added in portions at a temperature of 80° C. to a solution of 5.7 g of 6-methoxymethyl-5-methylpyridine-2,3-dicarboxylic acid diethyl ester and 2.6 g of 2-amino-2,3-dimethylbutyramide in 200 ml of dry toluene while stirring. Once the addition of the potassium tert.-butoxide is complete, the resulting red solution is stirred for 2 hours at 80° C., the potassium salt of 2-(5-isopropyl-5-methyl-4-oxoimidazolin-2-yl)-5-ethylpyridine-3-carboxylic acid being deposited in the form of a thick crystalline slurry. The mixture is cooled to room temperature and filtered with suction, and the crystals are dried and then dissolved in 50 ml of saturated sodium chloride solution. The solution is adjusted to pH 4 with concentrated hydrochloric acid and then extracted three times with 100 ml of ethyl acetate each time. The organic phase is dried over magnesium sulphate, filtered off with suction and concentrated by evaporation. The residue crystallises from ether/hexane 1:2 yielding 2.8 g of the above acid, which has a melting point of 151°-153° C.

Source

DOI: 10.6084/m9.figshare.5104873.v1Patent: US04997947uspto-grants-1991_03