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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 269273Generated: October 29, 2026

5-Bromo-2-thiophenesulfonamide → 5-[8-Methyl-6-(4-trifluoromethyl-phenyl)-imidazo[1,2-a]pyridin-3-ylethynyl]-thiophene-2-sulfonic acid amide

https://huagongshe.com/reaction/269273

Reaction equation

Participants

RoleNameHCIDCharge
Reactant5-Bromo-2-thiophenesulfonamideHCID 1241304—
Reactant3-Ethynyl-8-methyl-6-(4-trifluoromethyl-phenyl)-imidazo[1,2-a]pyridineHCID 86608095—
Product5-[8-Methyl-6-(4-trifluoromethyl-phenyl)-imidazo[1,2-a]pyridin-3-ylethynyl]-thiophene-2-sulfonic acid amideHCID 16738465—

Reaction Steps

The title compound was prepared from 3-ethynyl-8-methyl-6-(4-trifluoromethyl-phenyl)-imidazo[1,2-a]pyridine (example C.20) (300 mg, 1 mmol) and commercially available 5-bromothiophene-2-sulfonamide (230 mg, 1 mmol) according to general procedure II. Obtained as a light brown solid (200 mg, 50%). MS (ISP) 462 [(M+H)+]; mp 270° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07446113B2
Source datasetuspto-grants-2008_11
ORD IDord-1be160d3f0444458b5b99ed8bbef4f29
Source noteuspto-grants-2008_11