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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 256992Generated: October 27, 2026

4-Methylpiperidine → 3-(3-(4-Methylpiperidino)-1,2,5-thiadiazol-4-yl)pyridine

https://huagongshe.com/reaction/256992

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-MethylpiperidineHCID 69381—
Reactant3-Chloro-4-(pyridin-3-yl)-1,2,5-thiadiazoleHCID 10488164—
SolventDimethylformamideHCID 6228—
Product3-(3-(4-Methylpiperidino)-1,2,5-thiadiazol-4-yl)pyridineHCID 19075317—

Reaction Steps

A solution of 3-(4-chloro-1,2,5-thiadiazol-3-yl)pyridine (10.80 g, 4 mmol) and 4-methylpiperidine (1.96 g, 20 mmol) in DMF (10 ml) was heated at 100° C. for 3 h. After evaporation water was added to the residue and extracted with ether. The combined and dried organic phases were evaporated and the residue purified by column chromatography (SiO2, eluent: ethyl acetate/methylene chloride (1:2)). Yield: 0.8 g (77%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05260311
Source datasetuspto-grants-1993_11
ORD IDord-9424db1be5c1493dab03199190450abe
Source noteuspto-grants-1993_11