HRID1471454

反应详情

EQUATION

反应方程式

HRID 1471454 的结构方程式

AUXILIARIES

试剂、催化剂与溶剂

4

CONDITIONS

反应条件

温度
2.5 °C

PROCEDURE

实验过程

Synthesis of (Z)-azanediylbis(ethane-2,1-diyl) dioleate TFA salt previously described. (Z)-azanediylbis(ethane-2,1-diyl) dioleate TFA salt (4.06 g, 6.41 mmol) was stirred in DCM (60 mL) with 10% K2CO3 (30 mL) at 0-5° C. After 30 min, the organic phase was separated and the aqueous phase was further extracted with DCM (30 mL). The combined organic phases were stirred with anhydrous MgSO4 for a period of 30 minutes at 0-5° C., filtered, and washed with DCM (30 mL). To the combined filtrates were added to 2-((2-(dimethylamino)ethyl)thio)acetic acid (1.26 g, 7.70 mmol), EDC HCl salt (1.84 g, 9.62 mmol), DMAP (78.3 mg, 0.64 mmol). The thin suspension was stirred overnight at room temperature; after which a period of time, the solution became clear. Next day, deionized water (60 mL) and methanol (30 mL) were added. After stirring for 10 minutes, the clear organic layer was isolated. The turbid aqueous phase is extracted with DCM. The combined organic extracts were concentrated. Crude material was filtered through a plug of silica and taken up in DCM (40 mL) and PBS (pH=11, 50 mL) was added. The mixture was stirred at room temperature for 10 min. Then, the organic phase was separated and the aqueous phase is extracted again with DCM (15 mL). The combined organic phases were stirred with anhydrous MgSO4 for a period of 30 min. The mixture was then filtered, and washed with DCM. The combined filtrates were concentrated in vacuo to yield (Z)-((2-((2-(dimethylamino)ethyl)thio)acetyl)azanediyl)bis(ethane-2,1-diyl) dioleate (3.44 g).

WORKUP

后处理

  1. customthe organic phase was separated
  2. extractionthe aqueous phase was further extracted with DCM (30 mL)
  3. filtrationfiltered
  4. washwashed with DCM (30 mL)
  5. stirringThe thin suspension was stirred overnight at room temperature
  6. stirringAfter stirring for 10 minutes
  7. customthe clear organic layer was isolated
  8. extractionThe turbid aqueous phase is extracted with DCM
  9. concentrationThe combined organic extracts were concentrated
  10. filtrationCrude material was filtered through a plug of silica
  11. additionPBS (pH=11, 50 mL) was added
  12. stirringThe mixture was stirred at room temperature for 10 min
  13. customThen, the organic phase was separated
  14. extractionthe aqueous phase is extracted again with DCM (15 mL)
  15. stirringThe combined organic phases were stirred with anhydrous MgSO4 for a period of 30 min
  16. filtrationThe mixture was then filtered
  17. washwashed with DCM
  18. concentrationThe combined filtrates were concentrated in vacuo