Reacción #657272

ord-445e9cfb716949de991987b91306f145

Ecuación de reacción

O=C1CCC(=O)N1O
N-hydroxysuccinimide
C(=NC1CCCCC1)=NC1CCCCC1
dicyclohexylcarbodiimide
O=C(O)CSc1ncccn1
(Pyrimidin-2-ylsulfanyl)-acetic acid
O=C(CSc1ncccn1)ON1C(=O)CCC1=O
(Pyrimidin-2-ylsulfanyl)-acetic acid-(2,5-dioxo-pyrrolidine-1-yl)-ester

Disolventes

Condiciones de reacción

Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    FiltraciónThe residue was filtered
  2. 2
    Otrothe filtrate was evaporated in vacuo to dryness
  3. 3
    workup.DISSOLUTIONThe remaining product was dissolved
  4. 4
    Temperaturaunder reflux in 400 ml ethyl acetate
  5. 5
    Filtraciónthe hot solution was filtered
  6. 6
    Otrothe mixture was subjected to a chromatographic purification (Florisil)
  7. 7
    OtroThe compound was then recrystallised from ethyl acetate

Procedimiento

12.31 g (107 mMol) N-hydroxysuccinimide and 22.70 g (110 mMol) dicyclohexylcarbodiimide were added at −35° C. to a solution of 18.27 g (107 mMol) (Pyrimidin-2-ylsulfanyl)-acetic acid (a) dissolved in 200 ml DMF. The reaction mixture was stirred for 16 h under argon. The residue was filtered and the filtrate was evaporated in vacuo to dryness. The remaining product was dissolved under reflux in 400 ml ethyl acetate, the hot solution was filtered and the mixture was subjected to a chromatographic purification (Florisil) using ethyl acetate. The compound was then recrystallised from ethyl acetate.

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US09023656B2uspto-grants-2015_05