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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 863911Generated: October 27, 2026

Imidazole → alpha-(3,4-Dimethoxyphenyl)-1,3-dihydro-5-[2-(1H-imidazol-1-yl)ethoxy]-6-methoxy-alpha-[(4-methylphenyl)-thio]-2H-isoindole-2-heptanenitrile

https://huagongshe.com/reaction/863911

Reaction equation

Participants

RoleNameHCIDCharge
ReactantImidazoleHCID 795—
ReactantSodium IodideHCID 5238—
ReactantSodium hydrideHCID 24758—
Reactant5-(2-Chloroethoxy)-alpha-(3,4-dimethoxyphenyl)-1,3-dihydro-6-methoxy-alpha-[[4-methylphenyl)thio]-2H-isoindole-2-heptanenitrileHCID 10746053—
SolventWaterHCID 962—
SolventTolueneHCID 1140—
SolventDimethylformamideHCID 6228—
Productalpha-(3,4-Dimethoxyphenyl)-1,3-dihydro-5-[2-(1H-imidazol-1-yl)ethoxy]-6-methoxy-alpha-[(4-methylphenyl)-thio]-2H-isoindole-2-heptanenitrileHCID 10699180—

Reaction Conditions

Temperature75 °C

Reaction Steps

To a solution of 0.11 g of imidazole in 6 mL of N,N-dimethylformamide, under argon, is added 0.036 g of 60% of sodium hydride in oil. After stirring for 40 minutes, a solution of 0.3 g of 5-(2-chloroethoxy)-α-(3,4-dimethoxyphenyl)-1,3-dihydro-6-methoxy-α-[(4-methylphenyl)thio]-2H-isoindole-2-heptanenitrile in 8 mL of toluene is added followed by 0.3 g of sodium iodide. The resulting solution is heated at 75° C. for 21 hours. The solution is cooled and and poured into water. The solution is extracted with ethyl acetate and the organic layer washed with brine and dried over sodium sulfate. The solvent is removed at reduce pressure and the residual oil purified via column chromatography using a gradient elution from 4% methyl alcohol in methylene chloride to 9% methyl alcohol in methylene chloride. This affords 0.196 g of the desired product as a beige oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05561141
Source datasetuspto-grants-1996_10
ORD IDord-4bcb7cafa20346af9b3f0fbcfa3c51ac
Source noteuspto-grants-1996_10