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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1521339Generated: October 29, 2026

Sulfuric Acid → Ethyl 7-bromoimidazo[1,2-a]pyridine-3-carboxylate

https://huagongshe.com/reaction/1521339

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSulfuric AcidHCID 1118—
Reactant2-Amino-4-bromopyridineHCID 693282—
ReactantPotassium (Z)-2-chloro-1-ethoxy-3-oxoprop-1-en-1-olateHCID 86695681—
SolventEthanolHCID 702—
ProductEthyl 7-bromoimidazo[1,2-a]pyridine-3-carboxylateHCID 67260906—

Reaction Conditions

Temperature90 °C

Reaction Steps

A solution of 4-bromopyridin-2-amine (10 g, 57.8 mmol) and potassium (Z)-2-chloro-1-ethoxy-3-oxoprop-1-en-1-olate (step 1) (23.4 g, 124 mmol) in ethanol (200 ml) was cooled to 5° C. Sulfuric acid (7.70 ml, 144 mmol) was added dropwise and the reaction heated to reflux at 90° C. for 3 hrs. The mixture was cooled to RT and TEA (20.03 ml, 144 mmol) was slowly added and heating continued at 90° C. for 18 hrs. After cooling to RT, the mixture was filtered and the solid was partitioned between EtOAc and aqueous 2M HCl. The aqueous layer was basified (NaOH, solid pellets) and extracted using EtOAc. The combined organic extracts were dried (MgSO4) and concentrated in vacuo to afford the title compound;

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09073921B2
Source datasetuspto-grants-2015_07
ORD IDord-0e1f538fa42644ec854d6524197c0261
Source noteuspto-grants-2015_07