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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1245570Generated: November 1, 2026

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

https://huagongshe.com/reaction/1245570

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 21912789—

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 lithium chloride (26.7 mg, 0.63). After refluxing for 18 h, the mixture was partitioned between ethyl acetate and aqueous sodium bicarbonate. The aqueous layer was extracted with ethyl acetate (3×). Combined organic phase was washed with brine and dried over anhydrous magnesium sulfate. Concentration followed by flash chromatography eluting with 100% ethyl acetate, then 10% methanol in methylene chloride afforded the title compound 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 numberUS07125887B2
Source datasetuspto-grants-2006_10
ORD IDord-7c6b951a0171476aa68ab7c33eab5782
Source noteuspto-grants-2006_10