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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1263661Generated: November 4, 2026

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

https://huagongshe.com/reaction/1263661

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 numberUS06541498B2
Source datasetuspto-grants-2003_04
ORD IDord-2d33c0fd44224aa9ab7c1897b59ce0f8
Source noteuspto-grants-2003_04