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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1622639생성일: 2026년 10월 25일

9-[(7-Methoxynaphthalen-2-yl)oxy]-3,4-dihydropyrido[2,1-c][1,2,4]thiadiazine 2,2-dioxide → 9-[(7-Methoxynaphthalen-2-yl)oxy]-3,4,6,7,8,9-hexahydropyrido[2,1-c][1,2,4]thiadiazine 2,2-dioxide

https://huagongshe.com/reaction/1622639

반응식

참여 물질

역할이름HCID투입량
반응물9-[(7-Methoxynaphthalen-2-yl)oxy]-3,4-dihydropyrido[2,1-c][1,2,4]thiadiazine 2,2-dioxideHCID 66748979—
촉매Adams' catalystHCID 345198—
용매Acetic AcidHCID 176—
생성물9-[(7-Methoxynaphthalen-2-yl)oxy]-3,4,6,7,8,9-hexahydropyrido[2,1-c][1,2,4]thiadiazine 2,2-dioxideHCID 6674861122.6%

반응 단계

A mixture of 9-[(7-methoxynaphthalen-2-yl)oxy]-3,4-dihydropyrido[2,1-c][1,2,4]thiadiazine 2,2-dioxide (120 mg), platinum(IV) oxide (76 mg) and acetic acid (10 mL) was stirred under a hydrogen atmosphere at room temperature overnight. The reaction mixture was filtered, and concentrated under reduced pressure. To the residue was added a saturated aqueous sodium hydrogen carbonate solution and the mixture was extracted with ethyl acetate. The organic layer was washed with saturated aqueous sodium hydrogen carbonate solution and saturated brine, dried over anhydrous magnesium sulfate, and concentrated under reduced pressure. The residue was crystallized from ethyl acetate and hexane to give the title compound (27.4 mg) as a gray white solid.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08778934B2
출처 데이터셋uspto-grants-2014_07
ORD IDord-3128a84d1a2a402abf1389c7b5fb0738
출처 메모uspto-grants-2014_07