Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1814100생성일: 2026년 10월 25일
1,1-Dimethoxyethyl(dimethyl)amine → 1-(4-Fluorobenzyl)-5-methanesulfonyl-2-(3-methyl-[1,2,4]oxadiazol-5-yl)indole
https://huagongshe.com/reaction/1814100
참여 물질
| 역할 | 이름 | HCID | 투입량 |
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| 반응물 | 1,1-Dimethoxyethyl(dimethyl)amine | HCID 87835 | — |
| 반응물 | 1-(4-Fluorobenzyl)-5-methanesulfonylindole-2-carboxamide | HCID 22504369 | — |
| 생성물 | 1-(4-Fluorobenzyl)-5-methanesulfonyl-2-(3-methyl-[1,2,4]oxadiazol-5-yl)indole | HCID 12094553 | — |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US06875770B2 |
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| 출처 데이터셋 | uspto-grants-2005_04 |
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| ORD ID | ord-89192e409dbb4128a0dfdd7d17f223aa |
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| 출처 메모 | uspto-grants-2005_04 |
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