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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 378444Generated: October 30, 2026

N-bromobutanimide → N-(4-bromo-3-methyl-5-isoxazolyl)-4-(3-methoxyphenyl)benzenesulfonamide

https://huagongshe.com/reaction/378444

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-bromobutanimideHCID 67184—
ReactantN-(3-methyl-5-isoxazolyl)-4-(3-methoxyphenyl)benzenesulfonamideHCID 15453194—
ProductN-(4-bromo-3-methyl-5-isoxazolyl)-4-(3-methoxyphenyl)benzenesulfonamideHCID 15453188—

Reaction Steps

N-(4-bromo-3-methyl-5-isoxazolyl)-4-(3-methoxyphenyl)benzenesulfonamide was prepared in the same manner as described in Example 15 using N-(3-methyl-5-isoxazolyl)-4-(3-methoxyphenyl)benzenesulfonamide and NBS (reaction time 30 min at room temperature). The crude product was purified by column chromatography on silica gel using ethyl acetate as eluent giving the final product, after recrystallization using hexane/ethyl acetate, in 75% yield, m.p. 140-144° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06030991
Source datasetuspto-grants-2000_02
ORD IDord-663c9898fcbd476781ff0bc4ca3fa3f5
Source noteuspto-grants-2000_02