HRID876010

反应详情

EQUATION

反应方程式

HRID 876010 的结构方程式

AUXILIARIES

试剂、催化剂与溶剂

6

CONDITIONS

反应条件

温度
120 °C

PROCEDURE

实验过程

A 10 mL reaction vessel was charged with compound 245 (100 mg, 369 μmol), compound 300 (109 mg, 387 μmol), tris(dibenzylideneacetone)dipalladium (0) (25.3 mg, 27.6 μmol), 4,5-bis(diphenylphosphino)-9,9-dimethyl-9H-xanthene (32.0 mg, 55.3 μmol), sodium t-butoxide (70.8 mg, 737 μmol), and dioxane (2.5 mL). The reaction was purged with argon and heated with microwave energy (300 W) for 2.5 hours at 120° C. The reaction was added to aqueous K2CO3 (10%, 30 mL) and extracted with dichloromethane+10% methanol (3×30 mL). The combined organics were dried (MgSO4) and evaporated to give an orange oil. Preparative reverse phase HPLC (gradient elution 0.1% TFA in water/10-70% acetonitrile) afforded. a yellow oil. This residue was taken up in aqueous K2CO3 (30 mL) and extracted with dichloromethane+10% methanol (3×30 mL). The combined organics were dried (MgSO4) and evaporated to give a yellow solid. This was taken up in methanol (2 mL) and 1M HCl in ethanol (0.5 mL) was added. Diethyl ether (10 mL) was added to precipitate the product, which was filtered and dried in vacuo to give compound 299 as a yellow solid (32 mg, 17%). 1H NMR (500 MHz, DMSO-d6) δ 9.43-9.61 (m, 1 H) 9.27-9.40 (m, 1 H) 8.01-8.12 (m, 1 H) 7.91-8.01 (m, 1 H) 7.75-7.91 (m, 3 H) 7.62-7.75 (m, 1 H) 5.27-5.42 (m, 1 H) 4.14-4.28 (m, 3 H) 3.10-3.18 (m, 3 H) 3.06 (none, 3 H) 2.68 (d, J=4.65 Hz, 8 H) 2.06-2.18 (m, 2 H) 1.93-2.06 (m, 2 H) 1.80-1.93 (m, 3 H) 1.48-1.69 (m, 3 H) ppm.

WORKUP

后处理

  1. customA 10 mL reaction vessel
  2. customThe reaction was purged with argon
  3. additionThe reaction was added to aqueous K2CO3 (10%, 30 mL)
  4. extractionextracted with dichloromethane+10% methanol (3×30 mL)
  5. dry with materialThe combined organics were dried (MgSO4)
  6. customevaporated
  7. customto give an orange oil
  8. washPreparative reverse phase HPLC (gradient elution 0.1% TFA in water/10-70% acetonitrile)
  9. customafforded
  10. extractionextracted with dichloromethane+10% methanol (3×30 mL)
  11. dry with materialThe combined organics were dried (MgSO4)
  12. customevaporated
  13. customto give a yellow solid
  14. customto precipitate the product, which
  15. filtrationwas filtered
  16. customdried in vacuo