HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1284102Generated: November 1, 2026
Sulfuric Acid → 1-[4-(Imidazo[1,2-a]pyridin-2-yl)phenyl]ethan-1-one
https://huagongshe.com/reaction/1284102
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sulfuric Acid | HCID 1118 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | 4-imidazo[1,2-a]pyridin-2-ylbenzonitrile | HCID 821107 | — |
| Reactant | HCID 178418373 | HCID 178418373 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 1-[4-(Imidazo[1,2-a]pyridin-2-yl)phenyl]ethan-1-one | HCID 21515561 | — |
Reaction Steps
A solution of methylmagnesium iodide (prepared from 3.6 g of magnesium and 22 g of methyl iodide) in 40 ml of ether is added dropwise to a mixture of 6.5 g of 4-(imidazo[1,2-a]pyridin-2-yl)benzonitrile and 50 ml of tetrahydrofuran with stirring on an ice bath. The mixture is heated under reflux for 3 hours, and the reaction mixture is cooled with salt and ice. 100 ml of 50% sulfuric acid is added dropwise to the reaction mixture, water is added, and the whole mixture is adjusted to pH 8 by addition of 20% sodium hydroxide. The crystalline precipitate is filtered off, washed with water and recrystallized from dimethylformamide to give 4.2 g of 2-(4-acetylphenyl)-imidazo[1,2-a]pyridine as colorless crystals melting at 209°-210°C. 2.2 g of the thus-obtained 2-(4-acetylphenyl)-imidazo[1,2-a]pyridine is heated with 0.45 g of sulfur and 10 ml of morpholine under reflux for 6 hours. The reaction mixture is cooled, and ethanol is added. The crystalline precipitate is filtered off and washed with ethanol to give 1.4 g of 4-(imidazo[1,2-a]pyridin-2-yl)phenylacetothiomorpholide as yellowish brown crystals melting at 204°-206°C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US03978071 |
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| Source dataset | uspto-grants-1976_08 |
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| ORD ID | ord-15ce9d84be9546278c8b765da23a2fe7 |
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| Source note | uspto-grants-1976_08 |
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