反应详情

Mix (2-benzothiazolyl)(4-piperidinyl)methanone.CF3CO2H (2.56 g, 7.13 mmol), 2-phenylethyl bromide (1.45 g, 7.84 mmol), 18-Crown-6 (188 mg, 0.71 mmol), potassium carbonate (9.85 g, 71.3 mmol) and methylene chloride (100 mL). Stir at room temperature under an argon atmosphere for 2 hours, then add potassium iodide (200 mg). Stir at room temperature for an additional 2 hours then heat at reflux overnight. Add additional 2-phenylethyl bromide (1.45 g, 7.84 mmol) and heat at reflux overnight. Add additional 2-phenylethyl bromide (1.45 g, 7.84 mmol) and heat at reflux overnight. Cool the reaction to room temperature and pour into water (150 mL). Separate the organic phase, wash with water (100 mL) and dry (Na2SO4). Evaporate the solvent in vacuo and purify by chromatography (20% ethyl acetate/hexane with 2% triethylamine) to give the title compound as a yellow solid; mp 108.5°-109.5° C.

1. stirringStir at room temperature for an additional 2 hours
2. temperaturethen heat
3. temperatureat reflux overnight
4. temperatureheat
5. temperatureat reflux overnight
6. temperatureheat
7. temperatureat reflux overnight
8. temperatureCool
9. customthe reaction to room temperature
10. customSeparate the organic phase
11. washwash with water (100 mL)
12. dry with materialdry (Na2SO4)
13. customEvaporate the solvent in vacuo
14. custompurify by chromatography (20% ethyl acetate/hexane with 2% triethylamine)