HRID465717

反应详情

EQUATION

反应方程式

HRID 465717 的结构方程式

CONDITIONS

反应条件

温度
50 °C

PROCEDURE

实验过程

To 800 mL of an aqueous pH 6.0, 50 mM citrate buffer, prepared as described in Example 2c, was added 2-amino-6-(cyclopropylmethylamino)-9H-purine (0.204 g, 0.8 mmol) and 3'-azido-3'-deoxythymidine (1.069 g, 4.0 mmol). Solution was achieved by heating the mixture at 50° C. with sonication. A sample was removed as a control. A 40 mL solution of trans-N-deoxyribosylase (Example 2b) with an activity of 1500 units/mL was added. The reaction was heated at 50° C. Six days later, 0.204 g, 0.8 mmol, of 2-amino-6-cyclopropylmethylpurine was added to the reaction. Twenty-one days after the reaction was started, another 0.204 g, 0.8 mmol, of 2-amino-6-cyclopropylpurine and 0.428 g, 1.6 mmol, of 3'-azido-3'-deoxythymidine were added to the reaction. The reaction was stopped after thirty-three days by heating to 80° C. to precipitate the enzyme. The aqueous solution was extracted with ethyl acetate to remove the product. The combined ethyl acetate fractions were dried with magnesium sulfate, filtered and the solvent was removed in vacuo to give a foam. The foam was chromatographed on basic alumina grade 1 eluted with chloroform/methanol (97:3, v/v). The product containing fractions were combined and the solvent was removed in vacuo to give the product as a foam 0.237 g, 29% yield. mp=104°-106° C.

WORKUP

后处理

  1. customwith sonication
  2. customA sample was removed as a control
  3. additionA 40 mL solution of trans-N-deoxyribosylase (Example 2b) with an activity of 1500 units/mL was added
  4. temperatureThe reaction was heated at 50° C
  5. additionSix days later, 0.204 g, 0.8 mmol, of 2-amino-6-cyclopropylmethylpurine was added to the reaction
  6. customTwenty-one days
  7. additionanother 0.204 g, 0.8 mmol, of 2-amino-6-cyclopropylpurine and 0.428 g, 1.6 mmol, of 3'-azido-3'-deoxythymidine were added to the reaction
  8. waitThe reaction was stopped after thirty-three days
  9. temperatureby heating to 80° C.
  10. customto precipitate the enzyme
  11. extractionThe aqueous solution was extracted with ethyl acetate
  12. customto remove the product
  13. dry with materialThe combined ethyl acetate fractions were dried with magnesium sulfate
  14. filtrationfiltered
  15. customthe solvent was removed in vacuo
  16. customto give a foam
  17. customThe foam was chromatographed on basic alumina grade 1
  18. washeluted with chloroform/methanol (97:3
  19. additionThe product containing fractions
  20. customthe solvent was removed in vacuo