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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 964946생성일: 2026년 10월 26일

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

https://huagongshe.com/reaction/964946

반응식

참여 물질

역할이름HCID투입량
반응물EthanolHCID 702—
반응물1H-2,3-Benzothiazin-4(3H)-one 2,2-dioxideHCID 89042—
반응물SodiumHCID 5360545—
반응물1-Chloro-3-morpholin-4-yl-propan-2-olHCID 10080987—
생성물3-(2-ethoxy3-morpholinopropyl)-1H-2,3-benzothiazin-4(3H)-one 2,2-dioxideHCID 1907438220%
생성물3-(2-hydroxy-3-morpholinopropyl)-1H-2,3-benzothiazin-4(3H)-one 2,2-dioxideHCID 1907441563%

반응 조건

온도50 °C

반응 단계

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.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05773437
출처 데이터셋uspto-grants-1998_06
ORD IDord-453b986b65ad4d428d6cef8b43f374de
출처 메모uspto-grants-1998_06