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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1251856Generated: November 3, 2026

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

https://huagongshe.com/reaction/1251856

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 206b, using N-(3-methyl-5-isoxazolyl)-4-bromobenzenesulfonamide (Example 206a) and 4-methoxybenzeneboronic acid resulting in an 82% yield of the final product, m.p. 1 94-1 96° C. The product was recrystallized using hexane/ethyl acetate.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06342610B2
Source datasetuspto-grants-2002_01
ORD IDord-f05e6e6ef1e14ecfaf824f50ecbd6e70
Source noteuspto-grants-2002_01