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HRID 1925707作成日:2026年10月24日

Methyl 3-amino-2-thiophenecarboxylate → Methyl 3-(4-tert-butylphenylsulfonamido)thiophene-2-carboxylate

https://huagongshe.com/ja/reaction/1925707

反応式

関与物質

役割名称HCID仕込み量
反応物Methyl 3-amino-2-thiophenecarboxylateHCID 89652—
反応物4-t-Butylbenzenesulfonyl chlorideHCID 139882—
溶媒PyridineHCID 1049—
溶媒DichloromethaneHCID 6344—
生成物Methyl 3-(4-tert-butylphenylsulfonamido)thiophene-2-carboxylateHCID 801564366%

反応条件

温度40 °C

反応手順

To a solution of methyl 3-aminothiophene-2-carboxylate (0.55 g; 3.5 mmol) in pyridine (2 mL) and dichloromethane (2 mL) was added 4-tert-butylbenzenesulfonyl chloride (0.98 g; 4.2 mmol). The resulting mixture was warmed to 40° C. to aid in solubility, then stirred at room temperature for 48 hours. The reaction mixture was diluted with dichloromethane and washed with aqueous hydrochloric acid (2N). The aqueous layer was separated and extracted with dichloromethane. The organic layers were combined, dried over anhydrous sodium sulfate, decanted, and filtered through a and of silica. The silica was washed with dichloromethane. The eluant was combined with hexanes and allowed to stand. After 24 hours the resulting solid product was collected by filtration to give the desired product as a white solid (817 mg).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08178699B2
出典データセットuspto-grants-2012_05
ORD IDord-4fc1342cfdfe4611b700d4c23e1bcb89
出典メモuspto-grants-2012_05