HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2389289Generated: October 31, 2026
Chloroacetaldehyde → HCID 67458178, compound
https://huagongshe.com/reaction/2389289
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Chloroacetaldehyde | HCID 33 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | HCID 67453699 | HCID 67453699 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 67458178 | HCID 67458178 | 24% |
Reaction Steps
6-Amino-5-bromo-N-ethyl-N-methylnicotinamide (250 mg, 0.97 mmol) obtained in Step 1 of Example 170 was dissolved in ethanol (2.5 mL), and a 50% aqueous chloroacetaldehyde solution was added thereto, and the mixture was stirred overnight under reflux. After the mixture was left to cool to room temperature, an aqueous sodium hydrogen carbonate solution was added thereto, and the mixture was extracted with a chloroform/isopropanol (6/1) mixed solution. The organic layer was washed with saturated brine and dried over anhydrous magnesium sulfate, and the solvent was evaporated under reduced pressure. The residue was purified by silica gel column chromatography (chloroform/methanol=98/2) to give 8-bromo-N-ethyl-N-methylimidazo[1,2-a]pyridine-6-carboxamide (65 mg, 0.23 mmol, yield: 24%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08273738B2 |
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| Source dataset | uspto-grants-2012_09 |
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| ORD ID | ord-9a6ccf1b15d349b8840a1ac8123495d3 |
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| Source note | uspto-grants-2012_09 |
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