HRID454895

反应详情

EQUATION

反应方程式

HRID 454895 的结构方程式

AUXILIARIES

试剂、催化剂与溶剂

3

PROCEDURE

实验过程

To a suspension of activated zinc dust (84.4 g, 1.29 mol, 1.94 eq.) in anhydrous DMA (270 mL) was added 1,2-dibromoethane (9.1 mL, 0.106 mol, 0.16 eq.), followed by the slow addition of chlorotrimethylsilane (13.5 mL, 0.106 mol, 0.16 eq.) over a period of 5 min. The resulting mixture was stirred for 15 min under nitrogen. Then a solution of tert-butyl 4-iodopiperidine-1-carboxylate (329 g, 1.06 mol, 1.59 eq.) in anhydrous DMA (670 mL) was added to the above suspension over a period of 45 min keeping the internal temperature below 65° C. The resulting mixture was stirred for 1 hour while cooling back to room temperature. The prepared zinc reagent was allowed to stand and the upper clear solution was transferred to a degassed and well stirred solution of 2,3-dichloropyrazine (99 g, 0.664 mol, 1 eq.), PdCl2(dppf) CH2Cl2 (16.3 g, 19.9 mmol, 0.03 eq.) and Cul (7.8 g, 41.2 mmol, 0.062 eq.) in anhydrous DMA (670 mL) using a cannula. DMA (400 mL) was used to rinse the remaining zinc dust and added to the above mixture. The resulting mixture was heated to 80° C. under nitrogen and stirred overnight (19 hours). The mixture was cooled to room temperature and diluted with brine (1 L) and ethyl acetate (6 L). The aqueous phase was extracted with ethyl acetate (4 L) and organic extracts were combined, washed with brine (1 L), dried and concentrated. The resulting residue was purified by column chromatography (eluting with hexanes/ethyl acetate=9:1 to 6:1) to give 92 g of tert-butyl 4-(3-chloropyrazin-2-yl)piperidine-1-carboxylate.

WORKUP

后处理

  1. customthe internal temperature below 65° C
  2. stirringThe resulting mixture was stirred for 1 hour
  3. customa degassed
  4. washto rinse the remaining zinc dust
  5. additionadded to the above mixture
  6. temperatureThe resulting mixture was heated to 80° C. under nitrogen
  7. stirringstirred overnight (19 hours)
  8. temperatureThe mixture was cooled to room temperature
  9. additiondiluted with brine (1 L) and ethyl acetate (6 L)
  10. extractionThe aqueous phase was extracted with ethyl acetate (4 L) and organic extracts
  11. washwashed with brine (1 L)
  12. customdried
  13. concentrationconcentrated
  14. customThe resulting residue was purified by column chromatography (eluting with hexanes/ethyl acetate=9:1 to 6:1)