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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 54529Generated: October 25, 2026

Potassium Carbonate → 7-(2-Cyanoethyl)-1-[3-[2-E-(7-chloroquinolin-2-yl)ethenyl]benzyl]-2,3-dihydroindole

https://huagongshe.com/reaction/54529

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
Reactanttrans-3-[2-(7-Chloroquinolin-2-yl)ethenyl]benzyl chlorideHCID 19369489—
Reactant7-(2-Cyanoethyl)-2,3-dihydroindoleHCID 19959109—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
SolventEthyl AcetateHCID 8857—
Product7-(2-Cyanoethyl)-1-[3-[2-E-(7-chloroquinolin-2-yl)ethenyl]benzyl]-2,3-dihydroindoleHCID 1533792947%

Reaction Conditions

Temperature85 °C

Reaction Steps

A mixture of 7-(2-cyanoethyl)-2,3-dihydroindole (690 mg, 4.01 mmol), 3-[2-E-(7-chloroquinolin-2-yl)ethenyl]benzyl chloride (product of Example 3), 1.29 g, 4.10 mmol), and potassium carbonate (1.10 g, 7.97 mmol) in DMF (100 mL), was heated in an oil bath at 85° C. for 16 hours. The mixture was cooled and diluted with water and ethyl acetate. The organic solution was separated, washed once with water, once with saturated sodium chloride solution, then dried (over sodium sulfate), filtered, and concentrated in vacuo. Chromatography (silica gel, 70% hexane/30% ether) of the resulting residue provided 850 mg (47%) of the intermediate.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05622969
Source datasetuspto-grants-1997_04
ORD IDord-91fd433367b04121bc9403d0a1de8b60
Source noteuspto-grants-1997_04