Reaction #87888

ord-4263173b978647c9b6d01246878d03fb

Conditions

Detailed conditions
See reaction.notes.procedure_details.

Workup

  1. 1
    Otherthe resulting solution was evaporated to dryness under reduced pressure
  2. 2
    workup.DISSOLUTIONThe residue was dissolved in dry tetrahydrofuran (5 mL)
  3. 3
    workup.STIRRINGThe reaction was stirred at room temperature for 1 hour
  4. 4
    FiltrationThe resulting precipitate of crude product (100 mg) was collected by filtration
  5. 5
    ExtractionThe filtrate was extracted with chloroform (3×30 mL) and ethyl acetate (20 mL)
  6. 6
    WashThe combined organic extracts were washed with 2M aqueous sodium hydroxide (20 mL), water (20 mL)
  7. 7
    Dryingdried (Na2SO4)
  8. 8
    Concentrationconcentrated under reduced pressure

Procedure

Oxalyl chloride (0.68 mL, 7.8 mmol) was added to a suspension of 2,3-methylenedioxycinnamic acid (500 mg, 2.6 mmol) in dichloromethane (5 mL) containing a drop of dimethylformamide. The mixture was stirred for 2.5 hours and the resulting solution was evaporated to dryness under reduced pressure. The residue was dissolved in dry tetrahydrofuran (5 mL) and added to a solution of guanidine hydrochloride (1.24 g, 13 mmol) in 2M aqueous sodium hydroxide (8 mL). The reaction was stirred at room temperature for 1 hour and chloroform was then added. The resulting precipitate of crude product (100 mg) was collected by filtration. The filtrate was extracted with chloroform (3×30 mL) and ethyl acetate (20 mL). The combined organic extracts were washed with 2M aqueous sodium hydroxide (20 mL), water (20 mL), dried (Na2SO4) and concentrated under reduced pressure to give a further quantity of crude product (400 mg). The two crops of crude product were combined, suspended in chloroform (10 mL) and stirred vigorously for 20 minutes. The resulting 2,3-methylenedioxycinnamoylguanidine (420 mg) was collected by filtration and dried under vacuum.

Source

DOI: 10.6084/m9.figshare.5104873.v1Patent: US09440926B2uspto-grants-2016_09