Reacción #336836

ord-4eadabf1fb634b8b852c75df87c7aa67

Ecuación de reacción

O=C(O)c1cc(=O)[nH]c(C2CC2)n1
2-cyclopropyl-1,6-dihydro-6-oxo-4-pyrimidinecarboxylic acid
O=C(O)c1cc(=O)[nH]c(C2CC2)n1
product
O=C(O)c1cc(=O)[nH]c(C2CC2)n1
2-cyclopropyl-1,6-dihydro-6-oxo-4-pyrimidinecarboxylic acid
O=S([O-])O.[Na+]
sodium bisulfite
[Na+].[O-]Cl
sodium hypochlorite
O=C(O)c1nc(C2CC2)[nH]c(=O)c1Cl
title compound
O=C(O)c1nc(C2CC2)[nH]c(=O)c1Cl
5-chloro-2-cyclopropyl-1,6-dihydro-6-oxo-4-pyrimidinecarboxylic acid

Disolventes

Condiciones de reacción

Temperatura
9°CELSIUS
Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    Concentraciónconcentrated hydrochloric
  2. 2
    Temperaturawith cooling the reaction mixture
  3. 3
    Otrowas obtained
  4. 4
    TemperaturaThe mixture was cooled to 5° C.
  5. 5
    Otrothe suspended product was isolated by filtration
  6. 6
    Lavadowashed with a minimum amount of cold water
  7. 7
    OtroThe product was then dried to constant weight in vacuum-oven at 50° C.

Procedimiento

To a mixture of 2-cyclopropyl-1,6-dihydro-6-oxo-4-pyrimidinecarboxylic acid (i.e. the product of Step A1 or A2) (184 g, 1.02 mol) in water (45 mL) and concentrated hydrochloric, acid (292 g, 3 mol) at 8-12° C. was added dropwise aqueous sodium hypochlorite solution, (8.4%, 1.02 kg, 1.15 mol) over 2 h so that with cooling the reaction mixture was maintained at 8-10° C. The mixture was then held at 10-12° C. for 1 h and the conversion was monitored by HPLC. When less than 5% of the starting material remained solid sodium bisulfite was added until a negative KI starch paper test was obtained. The mixture was cooled to 5° C., and the suspended product was isolated by filtration and washed with a minimum amount of cold water. The product was then dried to constant weight in vacuum-oven at 50° C. to afford the title compound (194 g); m.p. 189-190° C.

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US07863220B2uspto-grants-2011_01