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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1746141생성일: 2026년 10월 26일

Hydrazine → Oxadiazole

https://huagongshe.com/reaction/1746141

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참여 물질

역할이름HCID투입량
반응물HydrazineHCID 9321—
반응물Methyl 3-HydroxybenzoateHCID 88068—
반응물3-Bromo-1,2-oxazoleHCID 13933891—
반응물TriethylorthoaceateHCID 21875354—
용매MethanolHCID 887—
용매WaterHCID 962—
용매Ethyl AcetateHCID 8857—
생성물OxadiazoleHCID 10197612—
생성물3-Phenoxy-4,5-dihydroisoxazoleHCID 14960467—

반응 단계

3-(phenoxy)-4,5-dihydroisoxazole I-222a and I-222b were prepared in 3 steps according to the following procedures: 3-hydroxy benzoic acid methyl ester is reacted with racemic bromoisoxazole I-75 using Method 5. The resulting methyl ester (1.0 equiv) is dissolved in methanol (0.08 M) after which hydrazine (50 equiv, 50% by weight in water) is added and the reaction is allowed to stir for 14 h. The reaction mixture is then concentrated under vacuum and used directly in the next step. Triethylorthoacetate (8.0 equiv) is added and the reaction is sealed and heated to reflux for 14 h. The reaction is then transferred to a separatory funnel with excess ethyl acetate and water. The organic layer was washed water and brine, drive over sodium sulfate and concentrated under vacuum to provide crude material which was purified using flash silica gel chromatography (gradient ethyl acetate/hexanes) to provide the desired racemic oxadiazole I-222. These compounds can be separated using chiral HPLC methods known in the art. For example, see chiral HPLC Method disclosed herein. [M+H]+=420.5 m/z. Activity: A

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09149465B2
출처 데이터셋uspto-grants-2015_10
ORD IDord-f536457a541c48679e23dba2d2c8050f
출처 메모uspto-grants-2015_10