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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
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Potassium Iodide | HCID 4875 | — |
| 反応物 | Potassium Carbonate | HCID 11430 | — |
| 反応物 | 3-(2-Chloroethyl)-1,3-oxazolidin-2-one | HCID 75633 | — |
| 反応物 | 1-(2-Bromo-10,11-dihydro-dibenzo[b,f]thiepin-10-yl)-piperazine | HCID 21481142 | — |
| 溶媒 | Benzene | HCID 241 | — |
| 溶媒 | Toluene | HCID 1140 | — |
| 生成物 | 3-[2-[4-(2-Bromo-10,11-dihydro-dibenzo[b,f]thiepin-10-yl)-1-piperazinyl]-ethyl]-2-oxazolidinone | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US04006144 |
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| 出典データセット | uspto-grants-1977_02 |
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| ORD ID | ord-45b9e1119c374046b5630580b9367c5c |
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| 出典メモ | uspto-grants-1977_02 |
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