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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1068231Generated: October 31, 2026

Lithium Chloride → 2-Ethyl-3-(4-pyridyl)-imidazo[1,2-a]pyridine

https://huagongshe.com/reaction/1068231

Reaction equation

Participants

RoleNameHCIDCharge
ReactantLithium ChlorideHCID 433294—
Reactant4-(Tri-n-butylstannyl)pyridineHCID 2737318—
Reactant3-Bromo-2-ethyl-imidazo[1,2-a]pyridineHCID 21912741—
CatalystPalladiumHCID 23938—
SolventTolueneHCID 1140—
Product2-Ethyl-3-(4-pyridyl)-imidazo[1,2-a]pyridineHCID 2191278938.7%

Reaction Steps

To a solution of 3-bromo-2-ethyl-imidazo[1,2-a]pyridine (1.4 g, 6.28 mmol), 4-tributylstannylpyridine (2.31 g, 6.28 mmol) and Pd (II) (Ph3P)2Cl2 (442 mg, 0.63 mmol) in toluene (5 mL) was added LiCl (26.7 mg, 0.63). After refluxing for 18 h, the mixture was partitioned between EtOAc and aqueous NaHCO3. The aqueous layer was extracted with EtOAc (3×). Combined organic phase was washed with brine and dried over anhydrous MgSO4. Concentration followed by flash chromatography eluting with 100% EtOAc, then 10% MeOH in CH2Cl2 afforded the title compound (543 mg) as a viscous oil. 1H NMR (500 MHz, CDCl3): δ 1.36 (t, J=7.5 Hz, 3H), 2.84 (q, J=7.5 Hz, 2H), 6.68 (dt, J=6.8, 1.1 Hz, 1H), 7.21 (m, 1H), 7.39 (dd, J=5.9, 1.6 Hz, 2H), 7.61 (dd, J=8.9, 1.0 Hz, 1H), 8.75 (d, J=5.9 Hz, 2H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06248755B1
Source datasetuspto-grants-2001_06
ORD IDord-b5a748f8ba6a4881905b534cf7e1f8f7
Source noteuspto-grants-2001_06