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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1838362생성일: 2026년 10월 27일

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

https://huagongshe.com/reaction/1838362

반응식

참여 물질

역할이름HCID투입량
반응물1,1-Dimethoxyethyl(dimethyl)amineHCID 87835—
반응물1-(4-Fluorobenzyl)-5-methanesulfonylindole-2-carboxamideHCID 22504369—
생성물1-(4-Fluorobenzyl)-5-methanesulfonyl-2-(3-methyl-[1,2,4]oxadiazol-5-yl)indoleHCID 12094553—

반응 조건

온도110 °C

반응 단계

A mixture of 1-(4-fluorobenzyl)-5-methanesulfonylindole-2-carboxamide (63 mg) and dimethylacetamide dimethylacetal (1 ml) was stirred at 110° C. for 1 hour. The reaction mixture was concentrated under reduced pressure. A mixture of the resulting residue, hydroxylamine hydrochloride (25 mg), a 2N aqueous sodium hydroxide solution (0.18 ml), 1,4-dioxane (0.4 ml) and acetic acid (0.4 ml) was stirred at 90° C. for 2 hours. 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 번호US06673797B1
출처 데이터셋uspto-grants-2004_01
ORD IDord-d46a96f9a4d54aa2a09adb46796b391f
출처 메모uspto-grants-2004_01