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Dimethylamine methanol → 1-(4,4-Dimethylpentanoyl)-4-{4-[5-(dimethylamino)-1,2,4-oxadiazol-3-yl]pyridin-2-yl}piperazine
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Dimethylamine methanol | HCID 22497844 | — |
| 反応物 | 1-(4,4-Dimethylpentanoyl)-4-{4-[5-(trichloromethyl)-1,2,4-oxadiazol-3-yl]pyridin-2-yl}piperazine | HCID 66673767 | — |
| 溶媒 | Methanol | HCID 887 | — |
| 生成物 | 1-(4,4-Dimethylpentanoyl)-4-{4-[5-(dimethylamino)-1,2,4-oxadiazol-3-yl]pyridin-2-yl}piperazine | HCID 11993187 | — |
反応手順
1-(4,4-Dimethylpentanoyl)-4-{4-[5-(trichloromethyl)-1,2,4-oxadiazol-3-yl]pyridin-2-yl}piperazine (48.1 mg) was dissolved in methanol (2 mL), and 2.0 M dimethylamine/methanol solution (1 mL) was added thereto and stirred at room temperature for 2 hours. Then, the solvent was evaporated away and the resulting residue was isolated and purified through thin-layer silica gel chromatography (hexane/ethyl acetate=1/1) to obtain 17.5 mg of the entitled compound as a yellow oil.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US08101618B2 |
| 出典データセット | uspto-grants-2012_01 |
| ORD ID | ord-929b559e0a4a45d289c8eaf60911fd45 |
| 出典メモ | uspto-grants-2012_01 |