Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 378441Generated: October 27, 2026

(4-Methoxyphenyl)boronic acid → N-(3-methyl-5-isoxazolyl)-4-(4-methoxyphenyl)benzenesulfonamide

https://huagongshe.com/reaction/378441

Reaction equation

Participants

RoleNameHCIDCharge
Reactant(4-Methoxyphenyl)boronic acidHCID 201262—
ReactantN-(3-methyl-5-isoxazolyl)-4-bromobenzenesulfonamideHCID 15453181—
ProductN-(3-methyl-5-isoxazolyl)-4-(4-methoxyphenyl)benzenesulfonamideHCID 1545318682%

Reaction Steps

N-(3-methyl-5-isoxazolyl)-4-(4-methoxyphenyl)benzenesulfonamide was prepared in the same manner as described in Example 14b, using N-(3-methyl-5-isoxazolyl)-4-bromobenzenesulfonamide (Example 14a) and 4-methoxybenzeneboronic acid resulting in an 82% yield of the final product, m.p. 194-196° C. The product was recrystallized using hexane/ethyl acetate.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06030991
Source datasetuspto-grants-2000_02
ORD IDord-7f76b8e106524257a8958e80f1ff79fb
Source noteuspto-grants-2000_02