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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Imidazole | HCID 795 | — |
| Reactant | Sodium Iodide | HCID 5238 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | 5-(2-Chloroethoxy)-alpha-(3,4-dimethoxyphenyl)-1,3-dihydro-6-methoxy-alpha-[[4-methylphenyl)thio]-2H-isoindole-2-heptanenitrile | HCID 10746053 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Toluene | HCID 1140 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | alpha-(3,4-Dimethoxyphenyl)-1,3-dihydro-5-[2-(1H-imidazol-1-yl)ethoxy]-6-methoxy-alpha-[(4-methylphenyl)-thio]-2H-isoindole-2-heptanenitrile | HCID 10699180 | — |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05561141 |
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| Source dataset | uspto-grants-1996_10 |
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| ORD ID | ord-4bcb7cafa20346af9b3f0fbcfa3c51ac |
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| Source note | uspto-grants-1996_10 |
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