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HRID 964946作成日:2026年10月27日

Ethanol → 3-(2-hydroxy-3-morpholinopropyl)-1H-2,3-benzothiazin-4(3H)-one 2,2-dioxide

https://huagongshe.com/reaction/964946

反応式

関与物質

役割名称HCID仕込み量
反応物EthanolHCID 702—
反応物1H-2,3-Benzothiazin-4(3H)-one 2,2-dioxideHCID 89042—
反応物SodiumHCID 5360545—
反応物1-Chloro-3-morpholin-4-yl-propan-2-olHCID 10080987—
生成物3-(2-ethoxy3-morpholinopropyl)-1H-2,3-benzothiazin-4(3H)-one 2,2-dioxideHCID 1907438220%
生成物3-(2-hydroxy-3-morpholinopropyl)-1H-2,3-benzothiazin-4(3H)-one 2,2-dioxideHCID 1907441563%

反応条件

温度50 °C

反応手順

In dry ethanol (10 mL) was dissolved metallic sodium (23 mg, 1 mmol.), and to the solution was added 1H-2,3-benzothiazin-4(3H)-one 2,2-dioxide (197 mg, 1 mmol.). The mixture was stirred at 50° C. for 30 min. To the reaction solution was added 1-chloro-3-morpholino-2-propanol (198 mg, 1.1 mmol.). The mixture was then heated for 6 hours under refluxing. The reaction liquid was placed under reduced pressure to distill the solvent off. The resulting residue was treated with 1N hydrochloric acid and ethyl acetate. The aqueous layer was taken out, and made basic by addition of potassium carbonate. The oil precipitated and was extracted with ethyl acetate. The ethyl acetate portion was washed with an aqueous saturated sodium chloride solution, and then dried over anhydrous sodium sulfate. The dried ethyl acetate portion was placed under reduced pressure to distill the solvent off. The resulting residue was treated by silica gel column chromatography (chloroform/methanol=40/1) to give 3-(2-hydroxy-3-morpholinopropyl)-1H-2,3-benzothiazin-4(3H)-one 2,2-dioxide (215 mg, yield 63%) as a colorless oil, and 3-(2 -ethoxy3-morpholinopropyl)-1H-2,3-benzothiazin-4(3H)-one 2,2-dioxide (70 mg, yield 20%) as an colorless oil.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05773437
出典データセットuspto-grants-1998_06
ORD IDord-453b986b65ad4d428d6cef8b43f374de
出典メモuspto-grants-1998_06