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Hydrochloric Acid → N-{4-[(1R)-1-aminoethyl]-2-methylphenyl)methanesulfonamide hydrochloride
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Hydrochloric Acid | HCID 313 | — |
| 反応物 | N-[4-((1R)-1-{[(R)-tert-butylsulfinyl]amino}ethyl)-2-methylphenyl]methanesulfonamide | HCID 58640404 | — |
| 溶媒 | 1,4-Dioxane | HCID 31275 | — |
| 生成物 | N-{4-[(1R)-1-aminoethyl]-2-methylphenyl)methanesulfonamide hydrochloride | HCID 21097519 | — |
反応手順
To N-[4-((1R)-1-{[(R)-tert-butylsulfinyl]amino}ethyl)-2-methylphenyl]methanesulfonamide (530 mg,1.60 mmol) was added 10% methanolic hydrogen chloride (5.0 ml) and dioxane (5.0 ml). The solution was stirred at ambient temperature for 30 minutes and then concentrated under reduced pressure. Diethyl ether was added to precipitate amine hydrochloride. The precipitate was then filtered, washed with diethyl ether and collected to furnish 450 mg (quant.) of the title compound as a white solid.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US07214824B2 |
| 出典データセット | uspto-grants-2007_05 |
| ORD ID | ord-8b544fffb3e84e5e96885c6b82505aac |
| 出典メモ | uspto-grants-2007_05 |