Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 79491Generated: October 25, 2026

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

https://huagongshe.com/reaction/79491

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
Reactant1,4-DioxaneHCID 31275—
Reactant2-Amino-4-bromopyridineHCID 693282—
ReactantPotassium (E)-2-chloro-3-ethoxy-3-oxoprop-1-en-1-olateHCID 23711836—
SolventTolueneHCID 1140—
ProductEthyl 7-bromoimidazo[1,2-a]pyridine-3-carboxylateHCID 6726090674.3%

Reaction Steps

Potassium (E)-2-chloro-3-ethoxy-3-oxoprop-1-en-1-olate (4.4 g, 23 mmol; prepared as in Example 65, step B1) was suspended in toluene (40 mL) and a 4M solution of HCl in dioxane (2.0 mL, 8.1 mmol). The mixture was stirred at ambient temperature for 5 minutes. 4-Bromopyridin-2-amine (2.0 g, 12 mmol) was added to the mixture and heated to 40° C. for 22 hours. The mixture was cooled to ambient temperature and extracted with 2M HCl (3×75 mL). Solid K2CO3 was added to the combined aqueous extracts until CO2 evolution ceased. The aqueous phase was extracted with MTBE (2×50 mL), dried over MgSO4, filtered and concentrated to give the product (2.4 g). MS (ES+APCI) m/z=268.7 (M+H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08841455B2
Source datasetuspto-grants-2014_09
ORD IDord-78e23bd9e68a406c9c5de6f9f892a1c3
Source noteuspto-grants-2014_09