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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 228926Generated: October 26, 2026

2-Iodo-6-methylpyridin-3-ol → 7-Benzyloxy-4-(2-iodo-6-methyl-pyridin-3-yloxy)-6-methoxyquinoline

https://huagongshe.com/reaction/228926

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Iodo-6-methylpyridin-3-olHCID 89957—
Reactant7-(Benzyloxy)-4-chloro-6-methoxyquinolineHCID 22646562—
Catalyst4-(Dimethylamino)pyridineHCID 14284—
Solvent1,2-DichlorobenzeneHCID 7239—
Product7-Benzyloxy-4-(2-iodo-6-methyl-pyridin-3-yloxy)-6-methoxyquinolineHCID 2307832346%

Reaction Conditions

Temperature125 °C

Reaction Steps

2-Iodo-6-picolin-3-ol (10 g), 4-chloro-7-benzyloxy-6-methoxyquinoline (6.8 g), and 4-(N,N-dimethylamino)-pyridine (12.2 g) were dissolved in 1,2-dichlorobenzene (400 ml) to prepare a solution, and the mixture was stirred at 125° C. overnight. The reaction solution was cooled to room temperature, and the solvent was then removed by distillation under the reduced pressure. Water was added to the residue, the mixture was extracted with chloroform, and the chloroform layer was then washed with water and was dried over anhydrous sodium sulfate. The solvent was removed by distillation under the reduced pressure. The residue was purified by column chromatography using chloroform-acetone to give 7-benzyloxy-4-(2-iodo-6-methyl-pyridin-3-yloxy)-6-methoxy-quinoline (5.2 g, yield 31%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07560558B2
Source datasetuspto-grants-2009_07
ORD IDord-7827b17d3f3644edb1816e665f69888b
Source noteuspto-grants-2009_07