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HRID 2411226作成日:2026年10月27日

Diisopropylethylamine → 1-(4,6-Dimethylpyridin-3-yl)-4-(toluene-4-sulfonyl)piperazine

https://huagongshe.com/reaction/2411226

反応式

関与物質

役割名称HCID仕込み量
反応物DiisopropylethylamineHCID 81531—
反応物N,N-bis(2-chloroethyl)-p-toluenesulphonamideHCID 96039—
反応物4,6-Dimethylpyridin-3-amineHCID 7060669—
溶媒WaterHCID 962—
生成物1-(4,6-Dimethylpyridin-3-yl)-4-(toluene-4-sulfonyl)piperazineHCID 7125218115.7%

反応手順

To 5-amino-2,4-dimethylpyridine (883 mg) were added N,N-diisopropylethylamine (2.1 mL) and N,N-bis(2-chloroethyl)-p-toluenesulfonamide (2.08 g), and the mixture was stirred with heating under reflux. After completion of the reaction, water was added to the reaction mixture, the mixture was extracted with chloroform, and the solvent was evaporated. The obtained residue was purified by column chromatography (chloroform:methanol) to give 1-(4,6-dimethylpyridin-3-yl)-4-(toluene-4-sulfonyl)piperazine (380 mg). The obtained 1-(4,6-dimethylpyridin-3-yl)-4-(toluene-4-sulfonyl)piperazine (380 mg) was dissolved in acetic acid (2 mL), 40% hydrobromic acid (2 mL) was added, and the mixture was stirred at 100° C. After completion of the reaction, the reaction mixture was neutralized with aqueous sodium hydroxide solution, and the mixture was extracted with ethyl acetate. The solvent was evaporated from the organic layer to give the title compound (131 mg).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08816079B2
出典データセットuspto-grants-2014_08
ORD IDord-eb0674f3edd244f3995b85e2b604a5a1
出典メモuspto-grants-2014_08