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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1263659Generated: November 2, 2026

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

https://huagongshe.com/reaction/1263659

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-bromobutanimideHCID 67184—
ReactantN-(3-methyl-5-isoxazolyl)-4-(4-methoxyphenyl)benzenesulfonamideHCID 15453186—
ProductN-(4-bromo-3-methyl-5-isoxazolyl)-4-(4-methoxyphenyl)benzenesulfonamideHCID 15453187—

Reaction Steps

N-(4-bromo-3-methyl-5-isoxazolyl)-4-(4-methoxyphenyl) benzenesulfonamide was prepared in the same manner as described in Example 15 using N-(3-methyl-5-isoxazolyl)-4-(4-methoxyphenyl)benzenesulfonamide (Example 19) 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 in 78% yield, m.p. 208° C. (dec). The product was recrystallized using hexane/ethyl acetate.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06541498B2
Source datasetuspto-grants-2003_04
ORD IDord-0e683fae737b443d82680810be0c3cb0
Source noteuspto-grants-2003_04