関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Ammonia | HCID 222 | — |
| 反応物 | 1,4-Dioxane | HCID 31275 | — |
| 反応物 | 1-(2-Pyrimidinyl)piperazine | HCID 88747 | — |
| 反応物 | 7-Sulfamoyl-2,3-dihydro-1,4-benzodioxine-5-carboxylic acid | HCID 20544760 | — |
| 溶媒 | Water | HCID 962 | — |
| 溶媒 | Triethylamine | HCID 8471 | — |
| 生成物 | 1-(2,3-Ethylenedioxy-5-sulfamoylbenzoyl)-4-(2-pyrimidinyl)-piperazine | HCID 20544739 | 40.3% |
反応手順
146 g of 7-sulfamoyl-1,4-benzodioxane-5-carboxylic acid, 300 ml of dioxane and 57 g of triethylamine were introduced into a 1-liter 3-neck flask provided with an agitator, a thermometer and an introduction funnel. The mixture was heated to 40°-50° C. and 80 ml of water was added. The solution was cooled to a temperature of from 5°-10° l C. and 61.5 g of ethyl chloroformiate was added. Agitation of the mixture was maintained for one hour at 10° C. and 93 g of 1-(2-pyrimidinyl)-piperazine was added without the temperature rising above 15° C. Agitation of the mixture was continued for one hour at ambient temperature and then, after the addition of 1,500 ml of water, the mixture was rendered alkaline to a pH of 10 with ammonia. The crystals produced after distillation under vacuum of the solvents and cooling were dried off, washed with water, dried in a drying oven at 50° C. and then purified by treatment with 120 ml of chloroform. After filtration and drying, 92 g of 1-(2,3-ethylenedioxy-5-sulfamoylbenzoyl)-4-(2-pyrimidinyl)-piperazine was produced (M.P.: 239° C.; yield: 40.2%). The structure was confirmed by nuclear magnetic resonance.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US04306072 |
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| 出典データセット | uspto-grants-1981_12 |
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| ORD ID | ord-46da4b7979574d43a73484f46d52a21b |
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| 出典メモ | uspto-grants-1981_12 |
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