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HRID 2232396作成日:2026年10月26日

Methanesulfonyl chloride → N-{4-[4-(Pyridin-4-yl)piperazin-1-yl]phenyl}methanesulfonamide

https://huagongshe.com/reaction/2232396

反応式

関与物質

役割名称HCID仕込み量
反応物Methanesulfonyl chlorideHCID 31297—
反応物1-(4-Aminophenyl)-4-(4-pyridyl)piperazineHCID 10890461—
溶媒PyridineHCID 1049—
生成物N-{4-[4-(Pyridin-4-yl)piperazin-1-yl]phenyl}methanesulfonamideHCID 1573540742.1%

反応手順

Methanesulphonyl chloride (0.50 g) was added dropwise to a stirred solution of 1-(4-aminophenyl)-4-(4-pyridyl)piperazine (1.00 g) in dry pyridine (10 ml) at room temperature. The mixture was stirred at room temperature for 20 hours and then evaporated. The residue was dissolved in water and the solution was basified with sodium bicarbonate solution and allowed to stand for 2 hours. The solid was filtered off, washed with water, dried and crystallised from methanol/ethyl acetate to give the title compound (0.55 g), m.p. 230°-232° C. Found: C,57.80; H,6.07; N,16.89. C16H20N4O2S requires: C,57.81; H,6.06; N,16.85%.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04788196
出典データセットuspto-grants-1988_11
ORD IDord-4c8f5d71fb2241cbb014594916a86f98
出典メモuspto-grants-1988_11