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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 39345Generated: October 29, 2026

Sodium Iodide → 8-(benzyloxy)-5-((1R)-1-{[tert-butyl(dimethyl)silyl]oxy}-2-{[6-(2,2-difluoro-2-phenylethoxy)hexyl]amino}ethyl)quinolin-2(1H)-one

https://huagongshe.com/reaction/39345

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium IodideHCID 5238—
ReactantSodium BicarbonateHCID 516892—
Reactant(R)-8-(benzyloxy)-5-(2-bromo-1-((tert-butyldimethylsilyl)oxy)ethyl)quinolin-2(1H)-oneHCID 15606253—
Reactant6-(2,2-Difluoro-2-phenylethoxy)-1-hexanamineHCID 50993080—
SolventDimethyl SulfoxideHCID 679—
SolventWaterHCID 962—
Product8-(benzyloxy)-5-((1R)-1-{[tert-butyl(dimethyl)silyl]oxy}-2-{[6-(2,2-difluoro-2-phenylethoxy)hexyl]amino}ethyl)quinolin-2(1H)-oneHCID 50993081—

Reaction Conditions

Temperature140 °C

Reaction Steps

To a solution of (8-(benzyloxy)-5-((1R)-2-bromo-1-{[tert-butyl(dimethyl)silyl]oxy}ethyl)quinolin-2(1H)-one (V) (4.80 g, 9.83 mmol) and 6-(2,2-Difluoro-2-phenylethoxy)hexyl]amine (IV) (3.04 g, 11.8 mmol) in dimethylsulfoxide (13.5 mL) was added sodium bicarbonate (2.49 g, 29.4 mmol) and sodium iodide (2.22 g, 14.8 mmol). The mixture was heated at 140° C. for 2 hours. After cooling, the reaction was diluted with water (40 mL) and extracted with diethyl ether (2×20 mL). The combined organic extracts were washed with water (2×10 mL) and brine (20 mL), dried (Na2SO4), and the solvent removed under reduced pressure. The title compound was obtained (6.40 g, 98%) as oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08524908B2
Source datasetuspto-grants-2013_09
ORD IDord-75d23ab72cbf46c8ab8ac1060a3e8807
Source noteuspto-grants-2013_09