HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1253564Generated: November 2, 2026
Hydrochloric Acid → 7-Iodo-5-methoxyimidazo[1,2-a]pyridine
https://huagongshe.com/reaction/1253564
Participants
| Role | Name | HCID | Charge |
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| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | 2-Bromo-1,1-dimethoxyethane | HCID 81672 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | 4-Iodo-6-methoxypyridin-2-amine | HCID 67204680 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | 7-Iodo-5-methoxyimidazo[1,2-a]pyridine | HCID 67207747 | — |
Reaction Steps
To a mixture of bromoacetaldehyde dimethylacetal (4.50 ml, 37.1 mmol) in water (126 ml) was added a 1M solution of hydrochloric acid (8.40 ml, 8.40 mmol). After 2.5 h the reaction mixture was heated to 80° C. resulting in a clear solution. After 40 minutes the reaction mixture was cooled to ambient temperature and sodium bicarbonate (3.83 g, 45.6 mmol) and 4-iodo-6-methoxypyridin-2-amine (5.25 g, 21.0 mmol) were added. After 16 hours the reaction mixture was diluted with ethyl acetate, washed with water, then dried over magnesium sulfate, filtered, and concentrated. The residue was purified by column chromatography on silica gel (methanol/dichloromethane gradient) to give 7-iodo-5-methoxyimidazo[1,2-a]pyridine. LRMS (ESI) calculated for C8H8IN2O [M+H]+, 275.0 found 274.9.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08455477B2 |
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| Source dataset | uspto-grants-2013_06 |
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| ORD ID | ord-369cb5a8b09e495ea775380a7c6dfb85 |
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| Source note | uspto-grants-2013_06 |
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