Реакция #1653

ord-560dc193ecc34b789acc357ab3f450a5

Уравнение реакции

CCN(C(C)C)C(C)C
diisopropylethylamine
CC(=O)Nc1nc(C(=O)N(c2ccccc2)c2ccccc2)c2ncn(COCC[Se]c3ccccc3)c2n1
2-acetamido-6-diphenylcarbamoyl-9-[2-(phenylselenyl)ethoxymethyl]purine
OO
H2O2
O=C([O-])O.[Na+]
sodium bicarbonate
C=COCn1cnc2c(C(=O)N(c3ccccc3)c3ccccc3)nc(NC(C)=O)nc21
title compound
C=COCn1cnc2c(C(=O)N(c3ccccc3)c3ccccc3)nc(NC(C)=O)nc21
2-Acetamido-6-diphenylcarbamoyl-9-(vinyloxymethyl)purine

Растворители

Условия реакции

Температура
60°CELSIUS
Подробные условия
See reaction.notes.procedure_details.

Обработка

  1. 1
    КонцентрированиеThe reaction was then concentrated to about 10 mL
  2. 2
    workup.ADDITIONdiluted with ethyl acetate (100 mL)
  3. 3
    Сушкаdried (MgSO4)
  4. 4
    Другоеthe solvents were removed in vacuo
  5. 5
    workup.DISSOLUTIONThe residue was dissolved in dioxane (40 mL)
  6. 6
    Температураthe solution was heated at 80° C. for 30 min under nitrogen
  7. 7
    ДругоеThe solvent was evaporated in vacuo
  8. 8
    Другоеthe residual oil was chromatographed on silica gel

Методика

To a solution of 2-acetamido-6-diphenylcarbamoyl-9-[2-(phenylselenyl)ethoxymethyl]purine (4.92 g, 8.16 mmol) in dioxane (80 mL) was added 30% H2O2 (4 mL, 35 mmol) and sodium bicarbonate (2.1 g, 24.5 mmol). The mixture was heated at 60° C. for 20 min. The reaction was then concentrated to about 10 mL, diluted with ethyl acetate (100 mL), dried (MgSO4) and the solvents were removed in vacuo. The residue was dissolved in dioxane (40 mL), diisopropylethylamine (1.27 g, 10 mmol) was added and the solution was heated at 80° C. for 30 min under nitrogen. The solvent was evaporated in vacuo and the residual oil was chromatographed on silica gel using CH2Cl2 -ethyl acetate (1:1) as eluent to give the title compound as a yellowish powder: yield 2.3 g (65%).

Источник

DOI: 10.6084/m9.figshare.5104873.v1Патент: US05726174uspto-grants-1998_03