Reacción #6625

ord-f4b94ff8ba9e4c06ac8d51b313e46253

Condiciones de reacción

Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    Temperaturais heated
  2. 2
    Temperaturaat reflux under nitrogen
  3. 3
    Temperaturathe reaction mixture is heated
  4. 4
    Temperaturaat reflux under nitrogen for an additional 12 hours
  5. 5
    ConcentraciónThe reaction mixture then is concentrated under reduced pressure
  6. 6
    Otrothe residue chromatographed on silica gel
  7. 7
    Lavadoeluting with 20:1 ethyl acetate
  8. 8
    workup.DISSOLUTION) The concentrated material is dissolved in 1:5 ethyl acetate
  9. 9
    workup.WAITether and this solution is refrigerated for 15 hours
  10. 10
    FiltraciónThe solid which forms is collected by filtration
  11. 11
    Lavadowashed with cold ethyl acetate
  12. 12
    Otrodried

Procedimiento

A mixture containing 3.48 g of 3-(3-tetrahydropyr-2-yloxyprop-1-en-1-yl)-4-hydroxy-6-pivaloylaminopyrrolo[2,3-d]pyrimidine, 3.12g (1.2 equiv.) of diethyl N-(4-iodobenzoyl)glutamate, 546 mg (20%) of tris-(2-methylphenyl)phosphine, 201 mg (10%) of palladium acetate and 85.5 mg (5%) of cuprous iodide in 15 ml of triethylamine and 240 ml of acetonitrile is heated at reflux under nitrogen. After 12 hours., 1.17 g of ethyl N-(4-iodobenzoyl)glutamate are added and the reaction mixture is heated at reflux under nitrogen for an additional 12 hours. The reaction mixture then is concentrated under reduced pressure and the residue chromatographed on silica gel, eluting with 20:1 ethyl acetate:hexane. (Any recovered starting material can be recycled through the foregoing procedure.) The concentrated material is dissolved in 1:5 ethyl acetate:ether and this solution is refrigerated for 15 hours. The solid which forms is collected by filtration, washed with cold ethyl acetate and dried to yield diethyl N-[4-{1-(tetrahydropyr-2-yloxy)-3-(4-hydroxy-6-pivaloylaminopyrrolo[2,3-d]pyrimidin-3-yl)prop-2-en-2yl}benzoyl]glutamate.

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US05248775uspto-grants-1993_09