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HRID 1983134作成日:2026年10月26日

Sodium Carbonate → 4-{3-Methoxy-4-[5-(5-methyl-3-phenyl-isoxazol-4-yl)-[1,3,4]oxadiazol-2-yl]-phenyl}-thiomorpholine 1-oxide

https://huagongshe.com/reaction/1983134

反応式

関与物質

役割名称HCID仕込み量
反応物Sodium CarbonateHCID 10340—
反応物4-{3-Methoxy-4-[5-(5-methyl-3-phenyl-isoxazol-4-yl)-[1,3,4]oxadiazol-2-yl]-phenyl}-thiomorpholineHCID 16722646—
反応物Sodium BisulfiteHCID 23665763—
反応物Potassium hydroxy sulfiteHCID 23707502—
溶媒MethanolHCID 887—
溶媒WaterHCID 962—
溶媒DichloromethaneHCID 6344—
生成物4-{3-Methoxy-4-[5-(5-methyl-3-phenyl-isoxazol-4-yl)-[1,3,4]oxadiazol-2-yl]-phenyl}-thiomorpholine 1-oxideHCID 1672285215%

反応条件

温度60 °C

反応手順

To a solution of 4-{3-methoxy-4-[5-(5-methyl-3-phenyl-isoxazol-4-yl)-[1,3,4]oxadiazol-2-yl]-phenyl}-thiomorpholine (660 mg, 1.52 mmol) in dichloromethane (7 mL), methanol (7 mL) and water (0.1 mL) was added oxone (1.87 g, 3.04 mmol) and stirred for 8 h at 60° C. The reaction mixture was cooled to ambient temperature and aqueous sodium bisulfite (38%, 5 mL) was added and stirred for 1 h. After the addition of aqueous sodium carbonate (saturated, 30 mL) the mixture was extracted with dichloromethane (30 mL) and washed with aqueous sodium carbonate (half-saturated, 30 mL). Drying over sodium sulfate and purification by chromatography (SiO2, heptane:ethyl acetate:dichloromethane:methanol=40:40:20:0 to 0:75:20:5) afforded the title compound (102 mg, 15%) as an off-white solid. MS: m/e=451.1 [M+H]+.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07541372B2
出典データセットuspto-grants-2009_06
ORD IDord-519a25e8541e4fb4b9436dce27030fa6
出典メモuspto-grants-2009_06