HRID448600

反应详情

EQUATION

反应方程式

HRID 448600 的结构方程式

AUXILIARIES

试剂、催化剂与溶剂

2

PROCEDURE

实验过程

(2S,4S)-5-Biphenyl-4-yl-4-t-butoxycarbonylamino-2-hydroxymethyl-pentanoic acid (50 mg, 120 μmol, 1.0 eq.), DMA (1 mL), DIPEA (0.13 mL, 0.75 mmol) and 1-chloroethyl cyclohexyl carbonate (52 mg, 250 μmol, 2.0 eq.) were combined. The reaction vessel was capped and microwaved at 80° C. for 2 hours. The mixture was dried under vacuum, dissolved in MeCN (2 mL), and combined with 4 M of HCl in dioxane (500 μL). The resulting mixture was stirred at room temperature for 30 minutes. The precipitate was filtered and discarded, and the filtrate containing the intermediate was concentrated down and submitted to next step. 1,2,3-triazole-4-carboxylic acid (14 mg, 120 μmol, 0.5 eq.) and HATU (48 mg, 120 μmol, 1.0 eq) were dissolved in DMF (1 mL) and the resulting solution was stirred for 5 minutes, followed by the addition of DIPEA (44 μL) and the intermediate from last step. The mixture was stirred for 5 minutes. The reaction was quenched with water and the product dried under vacuum. The product was then purified by preparative HPLC to yield the title compound (4.8 mg, 95% purity. MS m/z [M+H]+ calc'd for C30H36N4O7, 565.26. found 565.4.

WORKUP

后处理

  1. customThe reaction vessel was capped
  2. custommicrowaved at 80° C. for 2 hours
  3. customThe mixture was dried under vacuum
  4. dissolutiondissolved in MeCN (2 mL)
  5. filtrationThe precipitate was filtered
  6. additionthe filtrate containing the intermediate
  7. concentrationwas concentrated down
  8. stirringthe resulting solution was stirred for 5 minutes
  9. stirringThe mixture was stirred for 5 minutes
  10. customThe reaction was quenched with water
  11. customthe product dried under vacuum
  12. customThe product was then purified by preparative HPLC