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HRID 1638908作成日:2026年10月25日

Butyl isocyanate → N-(n-butylcarbamoyl)-4-ethoxycarbonyl-1-(2-pyridyl)pyrazole-5-sulfonamide

https://huagongshe.com/reaction/1638908

反応式

関与物質

役割名称HCID仕込み量
反応物Butyl isocyanateHCID 8110—
反応物Potassium CarbonateHCID 11430—
反応物4-Ethoxycarbonyl-1-(2-pyridyl)pyrazole-5-sulfonamideHCID 14049155—
溶媒AcetoneHCID 180—
生成物N-(n-butylcarbamoyl)-4-ethoxycarbonyl-1-(2-pyridyl)pyrazole-5-sulfonamideHCID 1983937495.2%

反応手順

To a 70 ml acetone mixture of 8.5 g of 4-ethoxycarbonyl-1-(2-pyridyl)pyrazole-5-sulfonamide and 6.0 g of anhydrous potassium carbonate, added was 3.3 g of n-butylisocyanate at room temperature, followed by heating under reflux for 3 hours. After the reaction was completed, acetone was evaporated under reduced pressure, and then the residue was emptied into ice water to filter insolbles off, and then the filtrate was precipitated with hydrochloric acid. Crystals precipitated was filtered, washed with water and dried to obtain 10.8 g of N-(n-butylcarbamoyl)-4-ethoxycarbonyl-1-(2-pyridyl)pyrazole-5-sulfonamide. m.p.: 180° to 181° C.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04881965
出典データセットuspto-grants-1989_11
ORD IDord-f49a1aa730cb47e18a9058c083cdc71e
出典メモuspto-grants-1989_11