Reaction #336834

ord-ca2f51cef2204ff4b0fd222f9034322c

Reaction equation

Cl
hydrochloric acid
CCOC(=O)CC(=O)C(=O)OCC.[Na]
diethyl oxalacetate sodium salt
[Na+].[OH-]
sodium hydroxide
Cl.N=C(N)C1CC1
cyclopropanecarboximidamide monohydrochloride
O=C(O)c1cc(=O)[nH]c(C2CC2)n1
title compound
Yield 58.4%
O=C(O)c1cc(=O)[nH]c(C2CC2)n1
2-cyclopropyl-1,6-dihydro-6-oxo-4-pyrimidine-carboxylic acid
Yield 58.4%

Conditions

Temperature
30°CELSIUS
Detailed conditions
See reaction.notes.procedure_details.

Workup

  1. 1
    Otherremained at 25-30° C.
  2. 2
    TemperatureThe orange solution was heated to 50° C. over 30 minutes
  3. 3
    TemperatureThe reaction mixture was cooled to 30° C.
  4. 4
    Concentrationconcentrated to half volume at reduced pressure at 35-40° C.
  5. 5
    Other(resulting in foaming) over 30 minutes at 25-30° C. until the pH was about 1-2
  6. 6
    Othercrystallization of the product
  7. 7
    TemperatureAfter the mixture was cooled to 0° C. the solid
  8. 8
    Filtrationwas collected by filtration
  9. 9
    WashThe solid washed with water (3×60 mL)
  10. 10
    Othersuction-dried
  11. 11
    Otherdried in a vacuum-oven at 70° C.

Procedure

To a mixture of diethyl oxalacetate sodium salt (210 g, 950 mmol) in methanol (500 mL) and water (400 mL) was added 50% aqueous sodium hydroxide (80 g, 1.0 mol) in water (60 mL) over 30 minutes, over which time the temperature remained at 25-30° C. and the pH at 11-12. Then the stirred mixture was heated for an additional 30 min at 30° C. To this mixture was added cyclopropanecarboximidamide monohydrochloride (110 g, 910 mol). The orange solution was heated to 50° C. over 30 minutes and held at that temperature for 5 h. The reaction mixture was cooled to 30° C. and concentrated to half volume at reduced pressure at 35-40° C. and concentrated hydrochloric acid (140 g, 1.4 mol) was added gradually (resulting in foaming) over 30 minutes at 25-30° C. until the pH was about 1-2. The mixture was stirred at 5° C. for 1 h to complete crystallization of the product. After the mixture was cooled to 0° C. the solid was collected by filtration. The solid washed with water (3×60 mL), suction-dried, and then dried in a vacuum-oven at 70° C. to afford the title compound as a beige solid (100 g); m.p. 235-236° C. (dec.).

Source

DOI: 10.6084/m9.figshare.5104873.v1Patent: US07863220B2uspto-grants-2011_01