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HRID 271138作成日:2026年10月27日

Nitrogen mustard hydrochloride → 8-(4-Methyl-piperazin-1-yl)-3phenylsulfonylquinoline

https://huagongshe.com/reaction/271138

反応式

関与物質

役割名称HCID仕込み量
反応物Nitrogen mustard hydrochlorideHCID 5935—
反応物Sodium CarbonateHCID 10340—
反応物Sodium ThiosulfateHCID 24477—
反応物Sodium BicarbonateHCID 516892—
反応物3-(Phenylsulfonyl)-8-quinolinamineHCID 53425502—
溶媒1-ButanolHCID 263—
生成物8-(4-Methyl-piperazin-1-yl)-3phenylsulfonylquinolineHCID 9929162—

反応条件

温度100 °C

反応手順

A solution of 8-amino-3-phenylsulfonylquinoline (D5) (38.8 g, 137 mmol) in n-butanol (360 ml) was treated with bis-(2-chloroethyl)-methyl-amine hydrochloride (40 g, 138 mmol) and sodium carbonate (72 g, 0.68 mol). The mixture was heated to a vigorous reflux (˜100° C.) for 16 h then a further portion of bis-(2-chloroethyl)-methyl-amine hydrochloride (25 g, 86 mmol) introduced and heating continued for a further 4 h. The solution was cooled and a 1:1 mixture of saturated aqueous sodium bicarbonate and aqueous 10% sodium thiosulphate solution (2 L) added. Stirring was continued at ambient temperature for 16 h then the aqueous phase was extracted with dichloromethane (3×500 ml), the combined organic phase dried over magnesium sulphate, evaporated in vacuo and subjected to chromatography on a Biotage Flash 75 apparatus (1 kg Silica gel) to afford the title compound (E1) as the free base form (11.6 g), identical spectroscopically to that prepared by the first method.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07452888B2
出典データセットuspto-grants-2008_11
ORD IDord-01b565316634446383e9b2ede5e8e759
出典メモuspto-grants-2008_11