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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 128719Generated: October 25, 2026

(1,1'-Biphenyl)-4-sulphonyl chloride → N-(4-bromo-5-methyl-3-isoxazolyl)-4-biphenylsulfonamide

https://huagongshe.com/reaction/128719

Reaction equation

Participants

RoleNameHCIDCharge
Reactant(1,1'-Biphenyl)-4-sulphonyl chlorideHCID 74192—
Reactant4-Bromo-5-methyl-1,2-oxazol-3-amineHCID 2774464—
ProductN-(4-bromo-5-methyl-3-isoxazolyl)-4-biphenylsulfonamideHCID 154531755%

Reaction Steps

N-(4-bromo-5-methyl-3-isoxazolyl)-4-biphenylsulfonamide was prepared, using the method in Example 1 b, from 3-amino-4-bromo-5-methylisoxazole and 4-biphenylsulfonyl chloride in 5% yield. The product (m.p. 154°-156° C.) was isolated in 51% yield by column chromatography, after recrystallization from ethyl acetate/hexanes. N-(4-Biphenylsulfonyl)-No(4-bromo-5-methyl-3-isoxazolyl)-4-biphenylsulfonamide was obtained in 51% yield.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05464853
Source datasetuspto-grants-1995_11
ORD IDord-07f9636ed4bc404cb5fdb496e88c19bf
Source noteuspto-grants-1995_11