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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1427039Generated: October 26, 2026

Dimethyl Sulfoxide → N-(4-((6-(2-Ethoxyethoxy)-1H-indol-5-yl)oxy)pyridin-2-yl)acetamide

https://huagongshe.com/reaction/1427039

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethyl SulfoxideHCID 679—
ReactantN-(4-Chloropyridin-2-yl)acetamideHCID 22832129—
ReactantPotassium tert-butoxideHCID 23665647—
Reactant6-(2-Ethoxyethoxy)-1H-indol-5-olHCID 86730341—
SolventWaterHCID 962—
SolventEthyl AcetateHCID 8857—
ProductN-(4-((6-(2-Ethoxyethoxy)-1H-indol-5-yl)oxy)pyridin-2-yl)acetamideHCID 8673034248%

Reaction Conditions

Temperature150 °C

Reaction Steps

Dimethylsulfoxide (20 mL) was added to a mixture of 6-(2-ethoxyethoxy)-1H-indol-5-ol described in Production Example 24-5 (3.28 g, 14.8 mmol), N-(4-chloropyridin-2-yl)acetamide described in Production Example 1-5 (2.78 g, 16.3 mmol), and potassium tert-butoxide (1.83 g, 16.3 mmol) under nitrogen atmosphere at room temperature. The liquid mixture was stirred at 150° C. overnight. The reaction liquid was allowed to stand to cool to room temperature and then diluted with water and ethyl acetate. The organic layer was washed with a saturated saline solution and dried over anhydrous sodium sulfate, and then the drying agent was separated by filtration. The filtrate was concentrated under vacuum. The residue was purified with silica gel column chromatography (n-heptane:ethyl acetate=1:1-0:1-ethyl acetate:methanol=99:1-19:1) to obtain the title compound (2.5 g, 48%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08933099B2
Source datasetuspto-grants-2015_01
ORD IDord-9cd462329aa84014b77b2e0e837efd04
Source noteuspto-grants-2015_01