反应 #1880993

ord-2be807cb949b4a0b8de75f9622fc0f63

反应方程式

Cl
HCl
[Na+].[OH-]
NaOH
CCCn1c(=O)[nH]c(=S)c2[nH]c(C34CCC(O)(CC3)CC4)nc21
8-(4-Hydroxy-bicyclo[2.2.2]oct-1-yl)-3-propyl-6-thioxo-1,3,6,7-tetrahydro-purin-2-one
CI
MeI
CCCn1c(=O)nc(SC)c2[nH]c(C34CCC(O)(CC3)CC4)nc21
titled compound
CCCn1c(=O)nc(SC)c2[nH]c(C34CCC(O)(CC3)CC4)nc21
8-(4-Hydroxy-bicyclo[2.2.2]oct-1-yl)-6-methylsulfanyl-3-propyl-3,7-dihydro-purin-2-one

反应条件

详细条件
See reaction.notes.procedure_details.

后处理

  1. 1
    萃取extracted with CHCl3
  2. 2
    干燥The combined organic layers were dried (Na2SO4)
  3. 3
    浓缩concentrated under reduced pressure

实验过程

8-(4-Hydroxy-bicyclo[2.2.2]oct-1-yl)-3-propyl-6-thioxo-1,3,6,7-tetrahydro-purin-2-one (120 mg, 0.36 mmol) was suspended in 3 mL of H2O and 1.5 mL of EtOH. NaOH was added as a solution in 0.4 mL of H2O, followed by MeI. The reaction mixture was stirred at rt for 1 h. It was then neutralized with 0.1 N HCl and extracted with CHCl3. The combined organic layers were dried (Na2SO4) and concentrated under reduced pressure to afford essentially quantitative amount of the titled compound.

来源

DOI: 10.6084/m9.figshare.5104873.v1专利: US07022686B2uspto-grants-2006_04