Реакция #1605868
ord-41d3f93e2b374f28a706def75df6e5b5
Уравнение реакции
Реактанты
Реагенты
Условия реакции
Обработка
- 1ТемператураAfter cooling the reaction mixture to 0° C.
- 2Другоеreaction mixture
- 3Другоеwas quenched
- 4workup.ADDITIONby adding a saturated ammonium chloride solution (10 ml)
- 5Экстракцияthe resulting mixture was extracted with ethyl acetate (2×20 ml)
- 6СушкаThe combined organic layer was dried over anhydrous Na2SO4
- 7ДругоеThe solvent in the dried organic layer was evaporated under a reduced pressure
- 8Другоеto obtain a crude product, which
- 9Другоеwas purified by column chromatography over silica gel (100-200 mesh)
Методика
To a stirred solution of 3-(4-(N-((dimethylamino)methylene) sulfamoyl)phenyl)-N-methoxy-N,4-dimethyl-5-morpholinothiophene-2-carboxamide (compound 24f, 0.120 g, 0.25 mmol) in anhydrous THF (10 ml) at 25° C., Grignard reagent (ethyl magnesium bromide, 0.17 g, 1.25 ml, 1.25 mmol) was added dropwise and the reaction mixture was heated to 70-75° C. for 1 hr. The progress of the reaction was monitored by TLC. After cooling the reaction mixture to 0° C., reaction mixture was quenched by adding a saturated ammonium chloride solution (10 ml) and the resulting mixture was extracted with ethyl acetate (2×20 ml). The combined organic layer was dried over anhydrous Na2SO4. The solvent in the dried organic layer was evaporated under a reduced pressure to obtain a crude product, which was purified by column chromatography over silica gel (100-200 mesh) using 40-45% ethyl acetate in hexane as an eluent to obtain the title compound which was further purified by precipitation by dissolving 0.056 g of this compound in ethyl acetate (1.0 ml) and precipitating it by the slow addition of diisopropyl ether. The precipitate was filtered to obtain the title compound. (0.047 g, 48%).