反应 #657272

ord-445e9cfb716949de991987b91306f145

反应方程式

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

溶剂

反应条件

详细条件
See reaction.notes.procedure_details.

后处理

  1. 1
    过滤The residue was filtered
  2. 2
    其他the filtrate was evaporated in vacuo to dryness
  3. 3
    workup.DISSOLUTIONThe remaining product was dissolved
  4. 4
    温度under reflux in 400 ml ethyl acetate
  5. 5
    过滤the hot solution was filtered
  6. 6
    其他the mixture was subjected to a chromatographic purification (Florisil)
  7. 7
    其他The compound was then recrystallised from ethyl acetate

实验过程

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.

来源

DOI: 10.6084/m9.figshare.5104873.v1专利: US09023656B2uspto-grants-2015_05