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HRID 230586作成日:2026年10月26日

Hydrochloride methanol → N-{4-[(1R)-1-aminoethyl]-2-methylphenyl)methanesulfonamide hydrochloride

https://huagongshe.com/reaction/230586

反応式

関与物質

役割名称HCID仕込み量
反応物Hydrochloride methanolHCID 21893726—
反応物N-[4-((1R)-1-{[(R)-tert-butylsulfinyl]amino}ethyl)-2-methylphenyl]methanesulfonamideHCID 58640404—
溶媒1,4-DioxaneHCID 31275—
生成物N-{4-[(1R)-1-aminoethyl]-2-methylphenyl)methanesulfonamide hydrochlorideHCID 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

DOI10.6084/m9.figshare.5104873.v1
特許番号US07566739B2
出典データセットuspto-grants-2009_07
ORD IDord-a0458d0345a94e5f8c4dcca15465382a
出典メモuspto-grants-2009_07