HRID81702

反应详情

EQUATION

反应方程式

HRID 81702 的结构方程式

AUXILIARIES

试剂、催化剂与溶剂

1

CONDITIONS

反应条件

温度
100 °C

PROCEDURE

实验过程

A mixture of Pd[PPh3]4 (75 mg, 0.065 mmol) and Cs2CO3 (550 mg, 1.69 mmol) was evacuated and purged with nitrogen. Toluene (12 mL) was then added followed by 4-bromo-2-(trifluoromethyl)aniline (187 μL, 1.33 mmol) and Triisopropylsilanethiol (TIPS-SH) (363 μL, 1.69 mmol). The mixture was heated at 100° C. for 24 h then cooled to room temperature. Saturated aqueous NH4Cl (5 mL) was added then diluted with water and extracted twice with EtOAc. The combined extracts were washed with water, brine then dried (Na2SO4). The solvent was removed under reduced pressure to give the crude TIPS thiophenol as a dark red oil (675 mg). This oil was dissolved in THE (13 mL), 2,4-dichloro-5-methylpyrimidine (190 μL, 1.62 mmol) was added and the solution was cooled to 0° C. Tetrabutyl ammonium fluoride (TBAF) (1.0 M in THF, 2.6 mL, 2.6 mmol) was added dropwise and the mixture was allowed to warm to room temperature and stirred for 3 h. Water was added and the mixture was extracted three times with EtOAc. The combined extracts were washed with water, brine then dried (Na2SO4). Solvent removal under reduced pressure and the resulting residue was purified by silica gel chromatography with 30% EtOAc/Petrol as eluent to give 4-[(2-chloro-5-methylpyrimidin-4-yl)thio]-2-(trifluoromethyl)aniline (410 mg, 95%). 1H NMR (CDCl3, 300 MHz) δ 8.07 (d, J=0.9 Hz, 1H), 7.58 (d, J=2.4 Hz, 1H), 7.43 (dd, J=8.7, 2.4 Hz, 1H), 6.81 (d, J=8.4 Hz, 1H), 4.43 (br s, 2H), 2.25 (d, J=0.6 Hz, 3H); LRMS (ESI): m/z calcd for [M+H]+320.0, found 320.2.

WORKUP

后处理

  1. customwas evacuated
  2. custompurged with nitrogen
  3. additionToluene (12 mL) was then added
  4. temperaturethen cooled to room temperature
  5. extractionextracted twice with EtOAc
  6. washThe combined extracts were washed with water, brine
  7. dry with materialthen dried (Na2SO4)
  8. customThe solvent was removed under reduced pressure
  9. customto give the crude TIPS thiophenol as a dark red oil (675 mg)
  10. additionwas added
  11. temperaturethe solution was cooled to 0° C
  12. temperatureto warm to room temperature
  13. extractionthe mixture was extracted three times with EtOAc
  14. washThe combined extracts were washed with water, brine
  15. dry with materialthen dried (Na2SO4)
  16. customSolvent removal under reduced pressure
  17. customthe resulting residue was purified by silica gel chromatography with 30% EtOAc/Petrol as eluent