HRID71943

反应详情

EQUATION

反应方程式

HRID 71943 的结构方程式

AUXILIARIES

试剂、催化剂与溶剂

2

PROCEDURE

实验过程

5-Aza-spiro[2.4]heptane-5,6-dicarboxylic acid 5-benzyl ester (2.217 g, 7.66 mmol) was dissolved in MeOH (30 mL) and LiOH (1 M in H2O, 15 mL, 15 mmol) was added. After stirring for 15 hours at room temperature, the reaction mixture was poured into 10% HCl and the aqueous phase was extracted 3× with DCM. The combined organics were dried over MgSO4, filtered and concentrated. The residue was treated with MeCN (40 mL), Et3N (1.2 mL, 8.4 mmol) and 2-Bromo-1-(6-bromo-naphthalen-2-yl)-ethanone and the mixture was stirred at room temperature for 20 hours before being filtered over CELITE and concentrated. The resulting oil was dissolved in the minimum amount of DCM and EtOAc (30 mL) was added causing the product to precipitate. The mixture was cooled to 0° C. then the solid was filtered off and rinsed with EtOAc giving clean product (4.00 g, 100%).

WORKUP

后处理

  1. extractionthe aqueous phase was extracted 3× with DCM
  2. dry with materialThe combined organics were dried over MgSO4
  3. filtrationfiltered
  4. concentrationconcentrated
  5. stirringthe mixture was stirred at room temperature for 20 hours
  6. filtrationbefore being filtered over CELITE
  7. concentrationconcentrated
  8. dissolutionThe resulting oil was dissolved in the minimum amount of DCM and EtOAc (30 mL)
  9. additionwas added
  10. customto precipitate
  11. temperatureThe mixture was cooled to 0° C.
  12. filtrationthe solid was filtered off
  13. washrinsed with EtOAc giving clean product (4.00 g, 100%)