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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 2196107생성일: 2026년 10월 25일

Hydrogen Peroxide → 2-(3,5-Dichloro-1-oxido-pyridin-4-yl)-1-{9-methoxy-spiro[2H-1,5-benzodioxepin-3(4H),3'-oxetane]-6-yl}ethanone

https://huagongshe.com/reaction/2196107

반응식

참여 물질

역할이름HCID투입량
반응물Hydrogen PeroxideHCID 784—
반응물2-(3,5-Dichloropyridin-4-yl)-1-{9-methoxy-spiro[2H-1,5-benzodioxepin-3(4H),3'-oxetane]-6-yl}ethanoneHCID 25005168—
촉매Manganese dioxideHCID 14801—
촉매HCID 178477782HCID 178477782—
용매DichloromethaneHCID 6344—
생성물2-(3,5-Dichloro-1-oxido-pyridin-4-yl)-1-{9-methoxy-spiro[2H-1,5-benzodioxepin-3(4H),3'-oxetane]-6-yl}ethanoneHCID 25005169—

반응 단계

To a solution of 2-(3,5-Dichloropyridin-4-yl)-1-{9-methoxy-spiro[2H-1,5-benzodioxepin-3(4H),3′-oxetane]-6-yl}ethanone [121] (20.5 mg, 50 μmol) in CH2Cl2 (1 mL) was added 30% H2O2 (15 μL) and methyltrioxorhenium(VII) (5 mg). The mixture was stirred for 18 h, added MnO2 (5 mg) and was stirred for another hour. CH2Cl2 (10 mL) was added and the organic phase was washed with water. The combined organic phase was dried over MgSO4 and evaporated to dryness under reduced pressure. Standard HPLC purification afforded 14 mg of the product.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08338431B2
출처 데이터셋uspto-grants-2012_12
ORD IDord-0eb6c5e22bcb453e93177ccfb4df0523
출처 메모uspto-grants-2012_12