Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 439393Generated: October 30, 2026

Benzenesulfonyl chloride → HCID 10784030, compound

https://huagongshe.com/reaction/439393

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzenesulfonyl chlorideHCID 7369—
ReactantHCID 10584549HCID 10584549—
ProductHCID 10784030HCID 1078403085%

Reaction Steps

N-(4-Methoxycarbonyl-3-trifluoromethyl-5-isoxazolyl)benzenesulfonamide was prepared as described in Example 25 from 5-amino-4-methoxycarbonyl-3-trifluoromethylisoxazole and benzenesulfonyl chloride in 85% yield. The crude product was purified by recrystallization from methanol/water to give a solid, m.p. 100°-101° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05514691
Source datasetuspto-grants-1996_05
ORD IDord-31154794d8d3437389e6f76553e40f99
Source noteuspto-grants-1996_05