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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 486650Generated: October 30, 2026

4-tert-Butylbenzenesulfonamide → HCID 19095805, compound

https://huagongshe.com/reaction/486650

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-tert-ButylbenzenesulfonamideHCID 222872—
ReactantHCID 19095786HCID 19095786—
SolventDimethyl SulfoxideHCID 679—
ProductHCID 19095805HCID 19095805—

Reaction Steps

A solution of 0.353 g of 4,6-dichloro-5-(2-methoxyphenoxy)-2-(thiophen-2-yl)-pyrimidine in 5 ml of DMSO was heated to 150° C. with 0.376 g of p-tert-butylbenzenesulphonamide for 30 minutes. The solution was concentrated in a high vacuum and the oily residue was poured on to ice, made acid (pH=3) and the suspension was extracted with ethyl acetate. The organic extracts were combined, washed with water, dried over sodium sulfate and concentrated under reduced pressure. The residue was chromatographed on silica gel with toluene-ethyl acetate 9:1 and yielded 4-tert-butyl-N-[6-chloro-5-(2-methoxyphenoxy)-2-(thiophen-2-yl)-pyrimidin-4-yl]-benzenesulphonamide as a white foam.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05292740
Source datasetuspto-grants-1994_03
ORD IDord-90eb69fc4acb4edca6c9145ec56f7e3e
Source noteuspto-grants-1994_03