HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 656478Generated: October 26, 2026
Dimethyl Sulfoxide → 6,7-dihydro-5H-spiro[imidazo[1,5-a]pyridine-8,2'-oxirane]
https://huagongshe.com/reaction/656478
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Dimethyl Sulfoxide | HCID 679 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | Trimethylsulfonium iodide | HCID 75127 | — |
| Reactant | 5H,6H,7H,8H-imidazo(1,5-a)pyridin-8-one | HCID 16752069 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Solvent | Pentane | HCID 8003 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Solvent | Sodium chloride; water | HCID 57417360 | — |
| Product | 6,7-dihydro-5H-spiro[imidazo[1,5-a]pyridine-8,2'-oxirane] | HCID 86629999 | — |
Reaction Steps
Sodium hydride (22 mmol) washed with pentane is admixed under argon with 20 ml of dimethyl sulphoxide. The mixture is heated at 60° C. for an hour and then diluted with 5 ml of tetrahydrofuran. The mixture is cooled to 0° C. and a solution of 21 mmol of trimethyl-sulphonium iodide in 5 ml of N,N-dimethylformamide is added at 0° C., after which the mixture is stirred for 10 minutes. A solution of 20 mmol of 6,7-dihydro-5H-imidazo[1,5-a]pyridin-8-one [426219-51-4] in 5 ml of N,N-dimethylformamide is added and the reaction mixture is stirred at 60° C. for 18 hours. The reaction mixture is poured into cold brine and extracted with tert-butyl methyl ether. The combined organic phases are washed with brine, dried with sodium sulphate and evaporated. From the residue the title compound is identified by means of flash chromatography (SiO2 60 F) on the basis of the Rf value.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08071773B2 |
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| Source dataset | uspto-grants-2011_12 |
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| ORD ID | ord-c8da428b86274a3eba72701e2eee38aa |
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| Source note | uspto-grants-2011_12 |
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