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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2400993Generated: October 31, 2026

4-(Trifluoromethyl)benzenesulfonyl chloride → HCID 58530732, compound

https://huagongshe.com/reaction/2400993

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-(Trifluoromethyl)benzenesulfonyl chlorideHCID 2777399—
ReactantHCID 58530605HCID 58530605—
ProductHCID 58530732HCID 58530732—

Reaction Steps

N-{2-[(5Z)-5-({1-[4-Chloro-2-(trifluoromethyl)benzyl]-1H-indazol-5-yl}methylidene)-2,4-dioxo-1,3-thiazolidin-3-yl]ethyl}-4-(trifluoromethyl)benzenesulfonamide was prepared from 3-(2-aminoethyl)-(5Z)-5-({1-[4-chloro-2-(trifluoromethyl)benzyl]-1H-indazol-5-yl}methylidene)-1,3-thiazolidine-2,4-dione (from Example 49) and p-trifluoromethyl-benzenesulfonyl chloride following General Procedure U.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08796256B2
Source datasetuspto-grants-2014_08
ORD IDord-ad451429bfea406382df4ba741ea3280
Source noteuspto-grants-2014_08