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HRID 232748作成日:2026年10月27日

Thiophene-3-sulfonyl Chloride → N-(4-bromo-3-methyl-5-isoxazolyl)thiophene-3-sulfonamide

https://huagongshe.com/reaction/232748

反応式

関与物質

役割名称HCID仕込み量
反応物Thiophene-3-sulfonyl ChlorideHCID 2776378—
反応物4-Bromo-3-methylisoxazol-5-amineHCID 10487519—
生成物N-(4-bromo-3-methyl-5-isoxazolyl)thiophene-3-sulfonamideHCID 1214637522%

反応手順

N-(4-Bromo-3-methyl-5-isoxazolyl)thiophene-3-sulfonamide was prepared in the same manner as described in Example 2 from thiophene-3-sulfonyl chloride with 5-amino-4-bromo-3-methylisoxazole in 22% yield. Purification by column chromatography using 10% MeOH/CHCl3 as eluent gave a pale brown oil.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05591761
出典データセットuspto-grants-1997_01
ORD IDord-5648f23a8a5649a0a6503bd53864150c
出典メモuspto-grants-1997_01