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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1943679생성일: 2026년 10월 25일

Hydrochloric Acid → 4-(2,3-Dihydro-pyrido[4,3-b][1,4]oxazin-4-sulfonyl)-phenol

https://huagongshe.com/reaction/1943679

반응식

참여 물질

역할이름HCID투입량
반응물Hydrochloric AcidHCID 313—
반응물Boron tribromideHCID 25134—
반응물Sodium BicarbonateHCID 516892—
반응물4-(4-methoxy-benzenesulfonyl)-3,4-dihydro-2H-pyrido[4,3-b][1,4]oxazineHCID 66936616—
용매DichloromethaneHCID 6344—
생성물4-(2,3-Dihydro-pyrido[4,3-b][1,4]oxazin-4-sulfonyl)-phenolHCID 4460837656.2%

반응 단계

In a 100 ml flask, 4-(4-methoxy-benzenesulfonyl)-3,4-dihydro-2H-pyrido[4,3-b][1,4]oxazine (699 mg, 2.282 mmol) was dissolved in dichloromethane (30 ml) and the mixture was cooled to 0□. 1.0M Boron tribromide dissolved in dichloromethane (11.4 ml, 11.4 mmol) was added thereto and stirred at room temperature for 16 hours. After neutralizing with saturated solution of sodium hydrogen carbonate to pH 8 to 9, the mixture was adjusted to pH 6 again by using 1N hydrochloric acid and extracted with dichloromethane. The combined organic layer was washed with saturated saline solution and dried over anhydrous sodium sulfate (Na2SO4), filtered and evaporated under reduced pressure. The residue was purified by column chromatography on silica eluting with a solvent of methanol:dichloromethane=1:20. The fractions containing the product were collected and evaporated to obtain white solid (375 mg, 56.2%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08394792B2
출처 데이터셋uspto-grants-2013_03
ORD IDord-8b44fec77661458f8dae130767dce7fa
출처 메모uspto-grants-2013_03