HRID1591722

反应详情

EQUATION

反应方程式

HRID 1591722 的结构方程式

AUXILIARIES

试剂、催化剂与溶剂

4

CONDITIONS

反应条件

温度
105 °C

PROCEDURE

实验过程

(1S,2R,4R)—N-[2-(4-Bromo-benzenesulfonylmethyl)-4-(isopropyl-methyl-amino)-cyclohexyl]-2-(4-trifluoromethyl-1H-benzoimidazol-2-yl)-acetamide, Example 3, (30 mg) was dissolved in DMA (1 ml) prior to the addition of Zn(CN)2 (34 mg), Pd2(dba)3 (10 mg), dppf (11 mg) and Zn powder (4 mg). The resulting solution was heated at 105° C. oil bath for over night. After cooling, the solution was concentrated. EtOAc and 10% amminum hydroxide (aq) were added. The organic layer was dried, filtered, and concentrated. Reverse phase HPLC purification (gradient elution, water/acetonitrile/TFA) of the resulting residue provided the title compound (8 mg). MS found: (M+H)+=576.5.

WORKUP

后处理

  1. temperatureAfter cooling
  2. concentrationthe solution was concentrated
  3. additionEtOAc and 10% amminum hydroxide (aq) were added
  4. customThe organic layer was dried
  5. filtrationfiltered
  6. concentrationconcentrated
  7. customReverse phase HPLC purification (gradient elution, water/acetonitrile/TFA) of the resulting residue