反应详情

温度

-30 °C

In this preparation 0.1 mole of 2-ethylthio-5-carboxythiazole is dissolved in 300 ml. of anhydrous tetrahydrofuran, under nitrogen, and 0.1 mole of triethylamine is added and the resulting mixture cooled to -30° C. 0.1 Mole of ethylchloroformate is then added dropwise with stirring and the resulting mixture allowed to warm to 0° C. The mixture is then stirred for ten minutes, then cooled to -30° C and 0.11 mole of 2-(bicyclo[2.2.1]hept-7-yl)ethylamine in 50 ml. of tetrahydrofuran added dropwise. The mixture is allowed to warm to room temperature (about 20° C), poured into 500 ml. of ethyl acetate, washed with water, then washed with saturated aqueous sodium chloride solution, and dried over anhydrous magnesium sulfate. The mixture is then filtered and the resulting filtrate evaporated under vacuum yielding 2-ethylthio-5-[2-(bicyclo[2.2.1]hept-7-yl)ethylaminocarbonyl]-thiazole as a solid, which is then further purified by recrystallization from ethyl acetate.

1. dissolutionis dissolved in 300 ml
2. temperatureto warm to 0° C
3. stirringThe mixture is then stirred for ten minutes
4. temperaturecooled to -30° C
5. temperatureto warm to room temperature (about 20° C)
6. additionpoured into 500 ml
7. washof ethyl acetate, washed with water
8. washwashed with saturated aqueous sodium chloride solution
9. dry with materialdried over anhydrous magnesium sulfate
10. filtrationThe mixture is then filtered
11. customthe resulting filtrate evaporated under vacuum