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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2389289Generated: October 31, 2026

Chloroacetaldehyde → HCID 67458178, compound

https://huagongshe.com/reaction/2389289

Reaction equation

Participants

RoleNameHCIDCharge
ReactantChloroacetaldehydeHCID 33—
ReactantSodium BicarbonateHCID 516892—
ReactantHCID 67453699HCID 67453699—
SolventEthanolHCID 702—
ProductHCID 67458178HCID 6745817824%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08273738B2
Source datasetuspto-grants-2012_09
ORD IDord-9a6ccf1b15d349b8840a1ac8123495d3
Source noteuspto-grants-2012_09