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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 128717Generated: October 26, 2026

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

https://huagongshe.com/reaction/128717

Reaction equation

Participants

RoleNameHCIDCharge
Reactant(1,1'-Biphenyl)-4-sulphonyl chlorideHCID 74192—
Reactant4-Methyl-3-(trifluoromethyl)isoxazol-5-amineHCID 15613878—
ProductN-(4-Methyl-3-trifluoromethyl-5-isoxazolyl)-4-biphenylsulfonamideHCID 1545317478%

Reaction Steps

N-(4-Methyl- 3-trifluoromethyl-5-isoxazolyl)-4-biphenylsulfonamide was prepared in the same manner as described in Example 2b from 5-amino-4-methyl-3-trifluoromethyl-isoxazole and 4-biphenylsulfonyl chloride in 78% yield. Purification was achieved by recrystallization from methanol/water to give a white solid, m.p. 139°-140° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05464853
Source datasetuspto-grants-1995_11
ORD IDord-4c73efb1315242f48afe96f8d56d0ff9
Source noteuspto-grants-1995_11