Réaction #657272

ord-445e9cfb716949de991987b91306f145

Équation de réaction

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

Solvants

Conditions de réaction

Conditions détaillées
See reaction.notes.procedure_details.

Traitement

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

Mode opératoire

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.

Source

DOI: 10.6084/m9.figshare.5104873.v1Brevet: US09023656B2uspto-grants-2015_05