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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1006144Generated: November 1, 2026

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

https://huagongshe.com/reaction/1006144

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
ReactantPyrrolidineHCID 31268—
Reactant4-Chloro-7-iodo-2-methylquinolineHCID 22054516—
CatalystPotassium IodideHCID 4875—
SolventEthanolHCID 702—
Product7-Iodo-2-methyl-4-pyrrolidin-1-yl-quinolineHCID 1133666387.5%

Reaction Steps

A suspension of 4-chloro-7-iodo-2-methylquinoline (EP497371, 2.00 g, 6.59 mmol) in ethanol (20 mL) was treated sucessively with pyrrolidine (1.28 g, 18.0 mmol), pyridine (0.2 mL) and potassium iodide (50 mg, 0.30 mmol), and the resulting mixture was refluxed for 24 h. After concentration in vacuo, the residue was taken up in water (50 mL) and basified to pH 12 by addition of 2 M aq. sodium hydroxide solution. The precipitate was collected by filtration, washed with water (20 mL) and ether (20 mL) and dried to afford the title compound (1.95 g, 87%). Off-white solid, m.p. 99-102° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06787558B2
Source datasetuspto-grants-2004_09
ORD IDord-e2ec37c419c749a1900f33b7547f5062
Source noteuspto-grants-2004_09