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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 269782Generated: October 30, 2026

Sodium Iodide → 7-(2-[1,4']Bipiperidinyl-1'-yl-ethoxy)-6-methoxy-4-(4-phenoxy-phenylamino)-quinoline-3-carbonitrile

https://huagongshe.com/reaction/269782

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium IodideHCID 5238—
Reactant1,4'-BipiperidineHCID 78607—
Reactant7-(2-Chloroethoxy)-6-methoxy-4-(4-phenoxyphenylamino)quinoline-3-carbonitrileHCID 68463166—
Solvent1,2-DimethoxyethaneHCID 8071—
Product7-(2-[1,4']Bipiperidinyl-1'-yl-ethoxy)-6-methoxy-4-(4-phenoxy-phenylamino)-quinoline-3-carbonitrileHCID 2525505547.7%

Reaction Conditions

Temperature137.5 °C

Reaction Steps

A mixture of 222.5 mg (0.5 mmol) of 7-(2-chloroethoxy)-6-methoxy-4-(4-phenoxyphenylamino)quinoline-3-carbonitrile, 841.4 mg (5.0 mmol) of 4-piperidinopiperidine and 49.5 mg (0.33 mmol) of sodium iodide in 6.0 mL of ethylene glycol dimethyl ether are heated in a sealed tube at 135-140° C. for 17 hours to yield the crude product. Solvents are removed in vacuo. Purification of the oily residue is carried out by preparative thin layer chromatography (eluting with 85:15 dichloromethane/methanol) to provide 137.7 mg of 7-(2-[1,4′]bipiperidinyl-1′-yl-ethoxy)-6-methoxy-4-(4-phenoxy-phenylamino)-quinoline-3-carbonitrile as a light yellow solid, mp 141° C. (decompose).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07449460B2
Source datasetuspto-grants-2008_11
ORD IDord-9d44d3b9d57840fd968efdaa32841f6c
Source noteuspto-grants-2008_11