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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 601692Generated: October 29, 2026

2-Amino-5-bromopyridine → HCID 23158249, compound

https://huagongshe.com/reaction/601692

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Amino-5-bromopyridineHCID 70622—
ReactantEthyl 5-chloro-3-oxopentanoateHCID 23158165—
SolventEthanolHCID 702—
ProductHCID 23158249HCID 2315824913,903.8%

Reaction Steps

4.28 mg of ethyl 5-chloro-3-oxopentanoate was dissolved in 40 ml of ethanol, 2.94 g of 2-amino-5-bromopyridine was added and the mixture was stirred all night by heating under reflux. The mixture was cooled down to room temperature, and the solvents were distilled outunder reduced pressure. Ethyl acetate followed by saturated sodium bicarbonate aqueous solution were added. Organic layer was dried with anhydrous sodium sulfate, and the solvents were distilled outunder reduced pressure. The obtained residues were purified by preparative thin-layer silicagel chromatography (hexane:ethyl acetate=50:50) to obtain 990 mg of the above compound as crude product.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07902369B2
Source datasetuspto-grants-2011_03
ORD IDord-3a4e54da656f4d77a75691cfecfd2013
Source noteuspto-grants-2011_03