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HRID 1432253作成日:2026年10月27日

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

https://huagongshe.com/reaction/1432253

反応式

関与物質

役割名称HCID仕込み量
反応物1,1-Dimethoxyethyl(dimethyl)amineHCID 87835—
反応物1-(4-Fluorobenzyl)-5-methanesulfonylindole-2-carboxamideHCID 22504369—
生成物1-(4-Fluorobenzyl)-5-methanesulfonyl-2-(3-methyl-[1,2,4]oxadiazol-5-yl)indoleHCID 12094553—

反応条件

温度110 °C

反応手順

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.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07612070B2
出典データセットuspto-grants-2009_11
ORD IDord-0dfbf076857c498d9d030cb27cec8a4d
出典メモuspto-grants-2009_11