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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1814102생성일: 2026년 10월 25일

Ethanol → 1-(4-Fluorobenzyl)-5-methanesulfonyl-2-(5-methyl-[1,2,4]oxadiazol-3-yl)indole

https://huagongshe.com/reaction/1814102

반응식

참여 물질

역할이름HCID투입량
반응물EthanolHCID 702—
반응물Potassium HydroxideHCID 14797—
반응물Hydroxyamine hydrochlorideHCID 443297—
반응물2-Cyano-1-(4-fluorobenzyl)-5-methanesulfonylindoleHCID 22504448—
생성물1-(4-Fluorobenzyl)-5-methanesulfonyl-2-(5-methyl-[1,2,4]oxadiazol-3-yl)indoleHCID 22504406—

반응 조건

온도100 °C

반응 단계

A mixture of the compound obtained in Example 24 (1) (68 mg), hydroxylamine hydrochloride (22 mg), potassium hydroxide (18 mg) and ethanol (1 ml) was heated under reflux for 2 hours. After the insolubles were filtered off, the reaction mixture was concentrated under reduced pressure. A mixture of the resulting residue and dimethylacetamide dimethylacetal (1 ml) was stirred at 100° C. for 1 hour. Water was added thereto, and the mixture was extracted with ethyl acetate. The organic layer was washed with water, dried over sodium sulfate and concentrated under reduced pressure. The resulting residue was subjected to silica gel column chromatography (hexane:ethyl acetate=1:1) to obtain 50 mg of the desired product as a white crystal.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06875770B2
출처 데이터셋uspto-grants-2005_04
ORD IDord-df16cd957b9742c8a68b579f24a7ff3b
출처 메모uspto-grants-2005_04