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HRID 234312作成日:2026年10月27日

5-Amino-3,4-dimethylisoxazole → N-(3,4-dimethyl-5-isoxazolyl)-2-(carbomethoxy)thiophene-3-sulfonamide

https://huagongshe.com/reaction/234312

反応式

関与物質

役割名称HCID仕込み量
反応物5-Amino-3,4-dimethylisoxazoleHCID 88317—
反応物2-Thiophenecarboxylic acid, 3-(chlorosulfonyl)-, methyl esterHCID 2736733—
溶媒PyridineHCID 1049—
生成物N-(3,4-dimethyl-5-isoxazolyl)-2-(carbomethoxy)thiophene-3-sulfonamideHCID 1061532265%

反応手順

2-Methoxycarbonylthiophene-3-sulfonyl chloride (2.50 g, 10.05 mmol) was added to a solution of 5-amino-3,4-dimethylisoxazole(0.98 g, 8.75 mmol) in dry pyridine (5.0 ml). The reaction mixture was stirred at room temperature for 16 h. Pyridine was removed under reduced pressure and the residue was partitioned between water and dichloromethane. The organic layer was washed with 1N HCl (2×50 ml) and dried over anhydrous magnesium sulfate. Evaporation of the solvents left an oily residue, which, after purification by column chromatography over silica gel (1:1 hexanes/ethyl acetate as eluent), yielded 2.20 mg (65%) of a brown solid. Further purification was achieved by recrystallization from ethyl acetate/hexanes, giving the pure product as a white solid, m.p. 113°-116° C.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05594021
出典データセットuspto-grants-1997_01
ORD IDord-a980ca657da34400a5d38a3146522957
出典メモuspto-grants-1997_01