HRID1631792

反应详情

EQUATION

反应方程式

HRID 1631792 的结构方程式

AUXILIARIES

试剂、催化剂与溶剂

4

CONDITIONS

反应条件

温度
120 °C

PROCEDURE

实验过程

A mixture of (R)-tert-butyl 2-(2-chloro-6a,7,9,10-tetrahydro-[1,4]oxazino[3,4-h]pteridin-5(6H)-yl)acetate (PREPARATION x24, 100 mg, 0.293 mmol), indole-4-boronic acid (70.8 mg, 0.440 mmol), tetrakis(triphenylphosphine)palladium(0) (33.9 mg, 0.029 mmol) and sodium carbonate (62.2 mg, 0.587 mmol) in 1,4-dioxane (1 mL) and water (0.5 mL) was heated to 120° C. for 30 minutes in a microwave. After cooling to room temperature, the reaction mixture was diluted with EtOAc, filtered through Celite, washed with water and brine, dried over Na2SO4, filtered, and concentrated in vacuo. The residue was purified by column chromatography (SiO2, 20-80% EtOAc/hexane gradient) to afford the title compound as an off-white solid (110 mg, 89%). 1H NMR (400 MHz, CDCl3) δ 1.48 (s, 9H), 3.07-3.36 (m, 3H), 3.42-3.51 (m, 1H), 3.62-3.79 (m, 3H), 3.93 (dd, J=10.86, 3.28 Hz, 1H), 4.01-4.16 (m, 2H), 4.77 (dd, J=13.39, 2.02 Hz, 1H), 7.22-7.31 (m, 2H), 7.39-7.46 (m, 2H), 7.66 (s, 1H), 8.01 (dd, J=7.45, 0.88 Hz, 1H), 8.26 (br s, 1H). ESI-MS m/z [M+H]+ calc'd for C23H27N5O3, 422.21. found 422.3.

WORKUP

后处理

  1. temperatureAfter cooling to room temperature
  2. filtrationfiltered through Celite
  3. washwashed with water and brine
  4. dry with materialdried over Na2SO4
  5. filtrationfiltered
  6. concentrationconcentrated in vacuo
  7. customThe residue was purified by column chromatography (SiO2, 20-80% EtOAc/hexane gradient)