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HRID 2285462作成日:2026年10月25日

Ammonia → 1-(2,3-Ethylenedioxy-5-sulfamoylbenzoyl)-4-(2-pyrimidinyl)-piperazine

https://huagongshe.com/reaction/2285462

反応式

関与物質

役割名称HCID仕込み量
反応物AmmoniaHCID 222—
反応物1,4-DioxaneHCID 31275—
反応物1-(2-Pyrimidinyl)piperazineHCID 88747—
反応物7-Sulfamoyl-2,3-dihydro-1,4-benzodioxine-5-carboxylic acidHCID 20544760—
溶媒WaterHCID 962—
溶媒TriethylamineHCID 8471—
生成物1-(2,3-Ethylenedioxy-5-sulfamoylbenzoyl)-4-(2-pyrimidinyl)-piperazineHCID 2054473940.3%

反応条件

温度10 °C

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° 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

DOI10.6084/m9.figshare.5104873.v1
特許番号US04323503
出典データセットuspto-grants-1982_04
ORD IDord-33ac1fcd06d54492969783daebf86c37
出典メモuspto-grants-1982_04