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HRID 730220作成日:2026年10月25日

6-Methoxy-m-toluenesulfonyl chloride → Benzo[b]thiophene-2sulfonic acid [2-(2-methoxy-5-methylbenzenesulfonylamino)phenyl]-amide

https://huagongshe.com/reaction/730220

反応式

関与物質

役割名称HCID仕込み量
反応物6-Methoxy-m-toluenesulfonyl chlorideHCID 145149—
反応物Benzo[b]thiophene-2-sulfonic acid (2-aminophenyl)amideHCID 86240018—
溶媒PyridineHCID 1049—
溶媒DichloromethaneHCID 6344—
生成物Benzo[b]thiophene-2sulfonic acid [2-(2-methoxy-5-methylbenzenesulfonylamino)phenyl]-amideHCID 1151877679.8%

反応手順

To a solution of benzo[b]thiophene-2-sulfonic acid (2-aminophenyl)-amide (1 mmol, prepared as in Example 1) in DCM (2 mL) and pyridine (2 mL), 2-methoxy-5-methylbenzenesulfonyl chloride (1.1 mmol) was added at RT and the reaction mixture was then allowed to stir at RT overnight. The reaction mixture was then diluted with DCM (10 mL). The organic phase was washed with 10% aqueous HCl (10 mL), water (10 mL) and brine (10 mL). The organic phase was dried over anhydrous sodium sulfate and concentrated under vacuum. The residue obtained was purified by flash column chromatography eluting with DCM/EtOAc to obtain 390 mg of benzo[b]thiophene-2-sulfonic acid [2-(2-methoxy-5-methylbenzenesulfonylamino)phenyl]-amide. LC: Tr 1.25 min; MS: 489.1 (M+1)+.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07582673B2
出典データセットuspto-grants-2009_09
ORD IDord-a1631ad6ce614e76885649047060fa4d
出典メモuspto-grants-2009_09