Реакция #1605863
ord-286d6959668f4cffaf6c853064fcb7cd
Уравнение реакции
Реактанты
Реагенты
Условия реакции
Обработка
- 1ТемператураAfter cooling the reaction mixture to 0° C.
- 2Другоеthe reaction mixture was quenched
- 3workup.ADDITIONby adding a solution of saturated ammonium chloride (40 ml)
- 4Экстракцияthe resulting mixture was extracted with ethyl acetate (3×50 ml)
- 5СушкаThe combined organic layer was dried over anhydrous Na2SO4
- 6ДругоеThe solvent was evaporated from the dried organic layer under reduced pressure
- 7Другоеto obtain a crude product
- 8Другоеwhich was purified by column chromatography over silica gel (100-200 mesh)
Методика
To a stirred solution of 5-(4-chlorophenyl)-3-(4-(N-((dimethylamino)methylene) sulfamoyl)phenyl)-N-methoxy-N,4-dimethylthiophene-2-carboxamide (compound 1d, 2.3 g, 4.55 mmol) in anhydrous THF (40 ml) at 25° C., Grignard reagent (ethyl magnesium bromide, 3.04 g, 22.8 ml, 22.77 mmol) was added dropwise and the reaction mixture was heated at 70-75° C. for 1 hr. The progress of the reaction was monitored by TLC. After cooling the reaction mixture to 0° C., the reaction mixture was quenched by adding a solution of saturated ammonium chloride (40 ml) and the resulting mixture was extracted with ethyl acetate (3×50 ml). The combined organic layer was dried over anhydrous Na2SO4. The solvent was evaporated from the dried organic layer under reduced pressure to obtain a crude product; which was purified by column chromatography over silica gel (100-200 mesh) using 30-35% ethyl acetate in hexane as an eluent to obtain the title compound which was further purified by precipitation by dissolving 1.1 g of the compound in dichloromethane (10 ml) and precipitating it by slow addition of diisopropyl ether. (0.89 g, 47%)