HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1377477Generated: October 30, 2026
Sodium Iodide → 8-(6-Methyl-2-nitrobenzylamino)-2,3-dimethylimidazo[1,2-a]pyridine
https://huagongshe.com/reaction/1377477
Participants
| Role | Name | HCID | Charge |
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| Reactant | Sodium Iodide | HCID 5238 | — |
| Reactant | Sodium Carbonate | HCID 10340 | — |
| Reactant | 2-(chloromethyl)-1-methyl-3-nitroBenzene | HCID 12204070 | — |
| Reactant | 2,3-Dimethylimidazo[1,2-a]pyridin-8-amine | HCID 21873980 | — |
| Solvent | Acetone | HCID 180 | — |
| Product | 8-(6-Methyl-2-nitrobenzylamino)-2,3-dimethylimidazo[1,2-a]pyridine | HCID 15382424 | 49.5% |
Reaction Steps
Sodium iodide (15.0 g) and sodium carbonate (31.0 g) are added to a solution of 8-amino-2,3-dimethylimidazo[1,2-a]pyridine (14.7 g) and 6-methyl-2-nitrobenzylchloride (18.6 g) in acetone (100 ml) at RT and are heated to reflux for 6 h. After cooling to RT and evaporation of the solvent, the residue is dissolved in a mixture of ethyl acetate (200 ml) and water (200 ml), and the organic phase is separated off. After three further extractions with ethyl acetate (100 ml) the combined organic layers are dried over magnesium sulfate and concentrated to a volume of 80 ml. 12.1 g of the title compound crystallize as a faintly yellow solid. The mother liquor is evaporated and the residue is purified by chromatography on silica gel (toluene/dioxane=6:1 as eluent) to yield additional 14 g of crystalline material. After recrystallization of both fractions from ethyl acetate, 21.5 g (76%) of the title compound of m.p. 160°-162° C. are isolated.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05665730 |
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| Source dataset | uspto-grants-1997_09 |
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| ORD ID | ord-8cbea724bf9f43308866fc1c1827829d |
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| Source note | uspto-grants-1997_09 |
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