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HRID 130424作成日:2026年10月25日

5-Bromothiophene-2-sulfonyl chloride → 5-Bromo-N-[2-chloro-5-(cis-3,5-dimethyl-1-piperazinyl)phenyl]-2-thiophenesulfonamide

https://huagongshe.com/reaction/130424

反応式

関与物質

役割名称HCID仕込み量
反応物5-Bromothiophene-2-sulfonyl chlorideHCID 2733924—
反応物5-(cis-3,5-Dimethyl-1-piperazinyl)-2-chloroanilineHCID 59007078—
溶媒Pyridine methylene chlorideHCID 21875418—
生成物5-Bromo-N-[2-chloro-5-(cis-3,5-dimethyl-1-piperazinyl)phenyl]-2-thiophenesulfonamideHCID 59007109—

反応手順

A solution of 5-(cis-3,5-Dimethyl-1-piperazinyl)-2-chloroaniline (D34) (100 mg, 0.42 mmol) in pyridine:dichloromethane (1:1, 4 ml) was treated with 5-bromo-2-thiophenesulfonyl chloride (132 mg, 0.51 mmol). The solution was stirred at room temperature for 2 hours, quenched with methanol and concentrated in vacuo. The residue was applied to a SCX cartridge (Varian bond-elute, 5 g) and washed with methanol and 2M ammonia in methanol. The combined basic fractions were concentrated in vacuo and the resulting residue was purified by column chromatography (FlashMaster) (gradient of dichloromethane to 4% metlianol:dichloromethane) to afford the title product (D36). MS (ES+) m/e 464/466/468 [M+H]+.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07381728B2
出典データセットuspto-grants-2008_06
ORD IDord-b25f89cab3aa45d48fefb505f715d870
出典メモuspto-grants-2008_06