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HRID 128715作成日:2026年10月26日

(1,1'-Biphenyl)-4-sulphonyl chloride → N-(4-biphenylsulfonyl)-N-(4-bromo-3-methyl-5-isoxazolyl)-4-biphenylsulfonamide

https://huagongshe.com/reaction/128715

反応式

関与物質

役割名称HCID仕込み量
反応物(1,1'-Biphenyl)-4-sulphonyl chlorideHCID 74192—
反応物4-Bromo-3-methylisoxazol-5-amineHCID 10487519—
溶媒PyridineHCID 1049—
溶媒DichloromethaneHCID 6344—
生成物N-(4-biphenylsulfonyl)-N-(4-bromo-3-methyl-5-isoxazolyl)-4-biphenylsulfonamideHCID 1545317164%

反応手順

5-Amino-4-bromo-3-methylisoxazole (0.179 g, 1.0 mmol) was dissolved in dry pyridine (2 ml). 4-Biphenylsulfonyl chloride (0.509 g, 2.2 mmol) was added with stirring at ambient temperature. N,N-Dimethylaminopyridine (5 mg) was added, and stirring was continued at 50° C. for 16 h. The reaction mixture was diluted with dichloromethane (75 ml), washed with 1N HCl (2×50 ml) and the organic phase was dried over magnesium sulfate. The solvent was removed under reduced pressure to yield a crude product, which was purified by column chromatography using 8:2, hexanes/ethyl acetate, to give 0.390 g (60% yield) of N-(4-biphenylsulfonyl)-N-(4-bromo-3-methyl-5-isoxazolyl)-4-biphenylsulfonamide.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05464853
出典データセットuspto-grants-1995_11
ORD IDord-29d7b972a1b24a0f8965d753a85afb9c
出典メモuspto-grants-1995_11