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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 387836Generated: October 26, 2026

Diisopropylethylamine → 4-(2-Chloro-6-iodopyridin-3-yloxy)-6,7-dimethoxyquinoline

https://huagongshe.com/reaction/387836

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiisopropylethylamineHCID 81531—
Reactant4-Chloro-6,7-dimethoxyquinolineHCID 459610—
Reactant2-Chloro-3-hydroxy-6-iodopyridineHCID 10777417—
ReactantTetrahydrofuran ethyl acetateHCID 21939870—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
SolventHexaneHCID 8058—
SolventEthyl AcetateHCID 8857—
Product4-(2-Chloro-6-iodopyridin-3-yloxy)-6,7-dimethoxyquinolineHCID 2293658549%

Reaction Steps

4-Chloro-6,7-dimethoxyquinoline (2.23 g, 10.0 mmol), 2-chloro-6-iodopyridin-3-ol (2.55 g, 22.0 mmol) and diisopropylethylamine (1.29 g, 10.0 mmol) were heated and stirred in dimethylformamide (5 ml) at 130° C. for 3 hours. The reaction solution was distributed between an ethyl acetate-tetrahydrofuran mixed solvent and water, the organic layer was washed with water and saturated saline and dried over anhydrous magnesium sulfate, the drying agent was filtered off and the filtrate was distilled off under reduced pressure. The obtained crude product was subjected to silica gel column chromatography (eluent-ethyl acetate:hexane=3:1), and the fraction containing the target substance was concentrated, suspended in ethyl acetate and diluted with hexane, after which the crystals were filtered out, washed with hexane and then blow-dried to obtain the title compound (2.16 g, 4.88 mmol, 49%) as colorless crystals.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08372981B2
Source datasetuspto-grants-2013_02
ORD IDord-6475a32341fd4fa49824925d780aa525
Source noteuspto-grants-2013_02