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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2183691Generated: November 3, 2026

Pyridine → 7-Iodo-2-methyl-4-pyrrolidin-1-yl-quinoline

https://huagongshe.com/reaction/2183691

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
ReactantPotassium IodideHCID 4875—
ReactantPyrrolidineHCID 31268—
Reactant4-Chloro-7-iodo-2-methylquinolineHCID 22054516—
SolventEthanolHCID 702—
Product7-Iodo-2-methyl-4-pyrrolidin-1-yl-quinolineHCID 1133666387%

Reaction Steps

A suspension of 2 g of 4-chloro-7-iodo-2-methyl-quinoline (European patent application EP 0497371, CA 143946-47-8) in 20 ml absolute ethanol is treated successively with 1.09 ml pyrrolidine, 0.2 ml pyridine and 50 mg potassium iodide under argon. The resulting mixture is refluxed for 24 h. The solvent is then distilled off. The residue is taken up in 50 ml water and basified to pH 12 with a 2N solution of sodium hydroxyde. The solid is filtered upon precipitation and washed with 20 ml of water and 20 ml of diethylether. The final product is dried under vacuum yielding 1.95 g (87%) of 7-iodo-2-methyl-4-pyrrolidin-1-yl-quinoline as an off-white solid. Mp: 99-102° C. MS (EI): peaks at m/e: 338(M+, 100%), 296 (5%), 183(9%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06900226B2
Source datasetuspto-grants-2005_05
ORD IDord-6b9d42dcc07d48849f6e44e377b1177d
Source noteuspto-grants-2005_05