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HRID 230593作成日:2026年10月25日

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

https://huagongshe.com/reaction/230593

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-(hydroxymethyl)phenyl]methanesulfonamideHCID 68714531—
溶媒MethanolHCID 887—
生成物N-[4-[(1R)-1-aminoethyl]-2-(hydroxymethyl)phenyl]methanesulfonamide hydrochlorideHCID 6880430787%

反応手順

To a solution of N-[4-((1R)-1-{[(R)-tert-butylsulfinyl]amino}ethyl)-2-(hydroxymethyl)phenyl]methanesulfonamide (3.6 g,10 mmol) in methanol (30 ml) was added hydrogenchloride-methanol solution (30 ml). The solution was stirred at room temperature for 30 minutes and then concentrated under reduced pressure. The given residue was recrystallized from methanol-diethyl ether. The precipitate was then filtered, washed with diethyl ether and collected to furnish 2.5 g (87% yield) of the title compound as a yellow oil.

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-89a7101265e44a5d8bed3465caa43f72
出典メモuspto-grants-2009_07