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Hydrochloride methanol → 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 | Hydrochloride methanol | HCID 21893726 | — |
| 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 HCl-methanol (2.0 M, 5.0 mL) and 1,4-dioxane (5.0 mL). The solution was stirred at room temperature for 30 minutes and then concentrated in vacuo. Diethyl ether was added to precipitate amine hydrochloride. The precipitate was then filtered and washed with diethyl ether (450 mg, quant) to furnish the title compound as a white solid.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US07566739B2 |
| 出典データセット | uspto-grants-2009_07 |
| ORD ID | ord-a0458d0345a94e5f8c4dcca15465382a |
| 出典メモ | uspto-grants-2009_07 |