HRID515995

反应详情

EQUATION

反应方程式

HRID 515995 的结构方程式

AUXILIARIES

试剂、催化剂与溶剂

1

CONDITIONS

反应条件

温度
150 °C

PROCEDURE

实验过程

A mixture of methyl 6-chloro-4-cyano-2-(1-methyl-1H-pyrazol-4-yl)nicotinate (155 mg, 0.560 mmol) and tert-butyl (1S,2R)-2-aminocyclohexylcarbamate (144 mg, 0.672 mmol) in DMA (2 mL) was stirred at 150° C. for 1 h under microwave irradiation. To the resulting mixture were added H2O and EtOAc. The organic phase was washed with H2O (3×) and brine, dried over MgSO4, and evaporated. The residue was purified by chromatography on SiO2 to give the title compound as a yellow oil (100 mg, 39.3%). 1H NMR (500 MHz, CDCl3) δ ppm 1.34-1.95 (m, 17 H), 3.92 (s, 3 H), 3.93 (s, 3 H), 4.87 (br s, 1 H), 5.66 (br s, 1 H), 6.52 (s, 1 H), 7.78-7.83 (m, 2 H). [M+H] calc'd for C23H30N6O4, 455; found, 455.

WORKUP

后处理

  1. washThe organic phase was washed with H2O (3×) and brine
  2. dry with materialdried over MgSO4
  3. customevaporated
  4. customThe residue was purified by chromatography on SiO2