HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1789197Generated: November 1, 2026
Imidazo[1,2-a]pyridin-8-ylmethanol → HCID 178488119, compound
https://huagongshe.com/reaction/1789197
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Imidazo[1,2-a]pyridin-8-ylmethanol | HCID 11029987 | — |
| Reactant | HCID 178488032 | HCID 178488032 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Solvent | Hydrogen Bromide | HCID 260 | — |
| Product | HCID 178488119 | HCID 178488119 | — |
Reaction Steps
A mixture of 2.92 g (23 mmole) of 3-hydroxymethyl-2-pyridinamine, 6.15 g (35 mmole) of chloroacetaldehyde, and 2.0 g (35 mmole) of sodium bicarbonate in 100 ml of ethanol was heated at reflux for 1.5 hours. The mixture was filtered and the filtrate was concentrated in vacuo to a solid. Recrystallization from diethyl ether yielded 4.4 g of 8-hydroxymethylimidazo[1,2-a]pyridine, as confirmed by the nmr and infrared spectra. A mixture of 683 mg (3.8 mmole) of 2-mercapto-5-methoxybenzimidazole and 700 mg (3.8 mmole) of 8-hydroxymethylimidazo[1,2-a]pyridine was dissolved in 3 ml of 30% hydrogen bromide in acetic acid and heated on a steam bath. After being cooled to room temperature, the mixture was partitioned between 5% aqueous sodium hydroxide and dichloromethane. The organic layer was dried over sodium sulfate, filtered, and concentrated to yield the title compound as an oil. Structure assignment was supported by the nmr and infrared spectra.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04687775 |
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| Source dataset | uspto-grants-1987_08 |
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| ORD ID | ord-fa237b32af6b4b098a33a40beb816430 |
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| Source note | uspto-grants-1987_08 |
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