HRID445267

反应详情

EQUATION

反应方程式

HRID 445267 的结构方程式

AUXILIARIES

试剂、催化剂与溶剂

1

PROCEDURE

实验过程

A mixture of 4-nitrophenyl 1-(4-(trifluoromethyl)phenyl)-3,4-dihydroisoquinoline-2(1H)-carboxylate (350 mg, 0.79 mmol, example 15) and (R)-1-Boc-3-amino-piperidine (1.6 mL, 7.91 mmol) was subjected to a microwave irradiation at 120° C. for 45 min. Then, MeOH (2 mL) was added to the mixture and the mixture was filtered. The solution mixture was purified by preparative HPLC (10%-100% of MeCN (0.1% TFA)/H2O (0.1% TFA). All fractions of the product were combined, saturated NaHCO3 (1 mL) was added and the solvents were removed. Then, an additional amount of saturated NaHCO3 (10 mL) was added and the aqueous mixture was extracted with EtOAc (2×10 mL). The combined organic extracts were dried over MgSO4 and concentrated to give the title compound as a white solid. MS (ESI, positive ion) m/z: 504 (M+H).

WORKUP

后处理

  1. customwas subjected to a microwave irradiation at 120° C. for 45 min
  2. filtrationthe mixture was filtered
  3. customThe solution mixture was purified by preparative HPLC (10%-100% of MeCN (0.1% TFA)/H2O (0.1% TFA)
  4. additionsaturated NaHCO3 (1 mL) was added
  5. customthe solvents were removed
  6. additionThen, an additional amount of saturated NaHCO3 (10 mL) was added
  7. extractionthe aqueous mixture was extracted with EtOAc (2×10 mL)
  8. dry with materialThe combined organic extracts were dried over MgSO4
  9. concentrationconcentrated