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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1427056Generated: November 4, 2026

Dimethyl Sulfoxide → HCID 86730357, compound

https://huagongshe.com/reaction/1427056

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethyl SulfoxideHCID 679—
ReactantN-(4-Chloropyridin-2-yl)acetamideHCID 22832129—
ReactantPotassium tert-butoxideHCID 23665647—
ReactantHCID 86730356HCID 86730356—
SolventWaterHCID 962—
SolventEthyl AcetateHCID 8857—
ProductHCID 86730357HCID 8673035746%

Reaction Conditions

Temperature150 °C

Reaction Steps

Dimethylsulfoxide (25 mL) was added to a mixture of 6-(3-methoxypropoxy)-1H-indol-5-ol described in Production Example 32-5 (3.81 g, 17.2 mmol), N-(4-chloropyridin-2-yl)acetamide described in Production Example 1-5 (3.23 g, 18.9 mmol), and potassium tert-butoxide (2.12 g, 18.9 mmol) under nitrogen atmosphere at room temperature. The liquid mixture was stirred at 150° C. for 14 hours. The reaction liquid was cooled to room temperature, and then ethyl acetate and water were added. The organic layer was washed with a saturated saline solution and then dried over anhydrous sodium sulfate. The drying agent was separated by filtration and then 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=49:1) to obtain the title compound (2.83 g, 46%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08933099B2
Source datasetuspto-grants-2015_01
ORD IDord-726b7afb01e84b58afbf32b5493739fe
Source noteuspto-grants-2015_01