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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2384550Generated: October 31, 2026

1-Bromo-3-chloropropane → 5-(5-[(3-chloropropyl)thio]-4-methyl-4H-1,2,4-triazol-3-yl)-2-methylquinoline

https://huagongshe.com/reaction/2384550

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-Bromo-3-chloropropaneHCID 8006—
ReactantSodium hydrideHCID 24758—
Reactant4-methyl-5-(2-methyl-5-quinolinyl)-4H-1,2,4-triazole-3-thiolHCID 44627570—
SolventEthanolHCID 702—
Product5-(5-[(3-chloropropyl)thio]-4-methyl-4H-1,2,4-triazol-3-yl)-2-methylquinolineHCID 25105050—

Reaction Steps

To 4-methyl-5-(2-methyl-5-quinolinyl)-2,4-dihydro-3H-1,2,4-triazole-3-thione (3.6 g, prepared in analogy to the method described in WO200240471) in ethanol (60 mL) containing 1-bromo-3-chloropropane (2.0 mL) was carefully added with stirring sodium hydride (0.60 g, 60% in petrolium). The mixture was heated at reflux for 45 min. Volatiles were evaporated in vacuo and the residue submitted to column chromatography (EtOAc—acetone gradient). The material thus obtained was precipitated from hot EtOAc (20 mL) by adding petroleum ether (40-60, 50 mL), cooled and collected by filtration to provide the title compound as colourless crystals (2.1 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08263782B2
Source datasetuspto-grants-2012_09
ORD IDord-7d39dd457cd94e7c87baeaca39a9619f
Source noteuspto-grants-2012_09