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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1644652Generated: October 30, 2026

Pyridine → HCID 57551218, compound

https://huagongshe.com/reaction/1644652

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
Reactant2-AminothiazoleHCID 2155—
Reactant4-Bromo-2-cyanobenzenesulfonyl chlorideHCID 17978377—
ProductHCID 57551218HCID 575512187.3%

Reaction Steps

To 2-AMINOTHIAZOLE (0.21 g, 0.0021 mol) in Pyridine (1 mL, 0.01 mol) was added portion-wise the crude 4-Bromo-2-cyano-benzenesulfonyl chloride (0.40 g, 0.0014 mol). The reaction mixture was stirred at room temperature overnight. The reaction mixture was concentrated under reduced pressure, diluted with Ethyl acetate, washed with 1.0 N HCl, H2O and brine, dried with anhydrous sodium sulfate, filtered and concentrated to give the crude product, which was purified on ISCO (25% to 100% Ethyl acetate in hexanes). 35 mg of the product was obtained as a light yellow solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08124610B2
Source datasetuspto-grants-2012_02
ORD IDord-f91bcbd577f6492595c2a6b53e56d25f
Source noteuspto-grants-2012_02