Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 842872Generated: October 29, 2026

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

https://huagongshe.com/reaction/842872

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 numberUS06376523B1
Source datasetuspto-grants-2002_04
ORD IDord-dc5a8dd43acf419ab8a7e09c58210b66
Source noteuspto-grants-2002_04