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HRID 1291939作成日:2026年10月23日

Water → 2,5-Bis[4-(3,4-dimethyl-5-isoxazolyl)sulfamoylanilino]terephthalic acid

https://huagongshe.com/ja/reaction/1291939

反応式

関与物質

役割名称HCID仕込み量
反応物WaterHCID 962—
反応物Sulfuric AcidHCID 1118—
反応物SulfisoxazoleHCID 5344—
反応物Potassium HydroxideHCID 14797—
反応物Sodium 3-nitrobenzenesulfonateHCID 31389—
反応物Dimethylsuccinyl succinateHCID 131720661—
溶媒MethanolHCID 887—
生成物2,5-Bis[4-(3,4-dimethyl-5-isoxazolyl)sulfamoylanilino]terephthalic acidHCID 1891370870.4%

反応条件

温度50 °C

反応手順

To 150 g of methanol was added with stirring 20 g (87.6 mmol) of dimethylsuccinyl succinate, 53.9 g (201.6 mmol) of 4-amino-N-(3,4-dimethyl-5-isoxazolyl)benzenesulfonamide (Aldrich Chemical Co.), and 0.7 g of concentrated sulfuric acid. The reaction mixture was heated slowly to 95° to 97° C. and maintained at that temperature for five hours. After the reaction mixture was cooled to 50° C., 26 g of sodium 3-nitrobenzenesulfonate, 2 g of water, and 75 g of 45% aqueous potassium hydroxide were slowly added with stirring. The resultant mixture was then slowly heated to 90° C and maintained at that temperature for four hours. The reaction mixture was cooled to room temperature and added to 500 ml of water. Concentrated sulfuric acid was slowly added to produce a solid that was collected by filtration and washed with water. The wet presscake was dried in an oven to give 43 g (70.4% of theory) of 2,5-bis[4-(3,4-dimethyl-5-isoxazolyl)sulfamoylanilino]terephthalic acid.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05755873
出典データセットuspto-grants-1998_05
ORD IDord-5bf4fed710744353ab0975c0e0ea28b7
出典メモuspto-grants-1998_05