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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1899694Generated: October 30, 2026

1-Naphthalenesulfonyl chloride → N-(4-Methyl-3-trifluoromethyl-5-isoxazolyl)-1-naphthalenesulfonamide

https://huagongshe.com/reaction/1899694

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-Naphthalenesulfonyl chlorideHCID 66560—
Reactant4-Methyl-3-(trifluoromethyl)isoxazol-5-amineHCID 15613878—
ProductN-(4-Methyl-3-trifluoromethyl-5-isoxazolyl)-1-naphthalenesulfonamideHCID 2337291985%

Reaction Steps

N-(4-Methyl-3-trifluoromethyl-5-isoxazolyl)-1-naphthalenesulfonamide was prepared, as described in Example 90, from 5-amino-4-methyl-3-trifluoromethylisoxazole and 1-naphthalenesulfonyl chloride in 85% yield. Purification was achieved by recrystallization from methanol/water to give white needed, m.p. 154°-155° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05571821
Source datasetuspto-grants-1996_11
ORD IDord-5730c4a9f959427db5f063a3d44243eb
Source noteuspto-grants-1996_11