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HRID 435689作成日:2026年10月24日

Potassium Iodide → 3-[2-[4-(2-Bromo-10,11-dihydro-dibenzo[b,f]thiepin-10-yl)-1-piperazinyl]-ethyl]-2-oxazolidinone

https://huagongshe.com/ja/reaction/435689

反応式

関与物質

役割名称HCID仕込み量
反応物Potassium IodideHCID 4875—
反応物Potassium CarbonateHCID 11430—
反応物3-(2-Chloroethyl)-1,3-oxazolidin-2-oneHCID 75633—
反応物1-(2-Bromo-10,11-dihydro-dibenzo[b,f]thiepin-10-yl)-piperazineHCID 21481142—
溶媒BenzeneHCID 241—
溶媒TolueneHCID 1140—
生成物3-[2-[4-(2-Bromo-10,11-dihydro-dibenzo[b,f]thiepin-10-yl)-1-piperazinyl]-ethyl]-2-oxazolidinoneHCID 21481155—

反応手順

12.5 g of 1-(2-bromo-10,11-dihydro-dibenzo[b,f]thiepin-10-yl)-piperazine are treated, together with 13 g of powdered potassium carbonate, 0.2 g of potassium iodide and 1 litre of toluene, with 13.2 g of N-(β-chloroethyl)-oxazolidinone and the mixture is heated under reflux for 25 hours. Then the mixture is poured on to ice-water and diluted with benzene. The benzene solution is washed neutral with water and extracted with 2-N hydrochloric acid. The aqueous phase is made alkaline with sodium hydroxide and extracted with benzene. The organic phase is washed with water, dried over magnesium sulphate and concentrated under reduced pressure. There is obtained crude 3-[ 2-[4-(2-bromo-10,11-dihydro-dibenzo[b,f]thiepin-10-yl)-1-piperazinyl]-ethyl ]-2-oxazolidinone which is converted into the maleate of melting point 170°-172° C by treatment with maleic acid.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04006144
出典データセットuspto-grants-1977_02
ORD IDord-45b9e1119c374046b5630580b9367c5c
出典メモuspto-grants-1977_02