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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1068807Generated: November 1, 2026

Acetonitrile → HCID 53654791, compound

https://huagongshe.com/reaction/1068807

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetonitrileHCID 6342—
Reactantethyl imidazo[1,2-a]pyridine-5-carboxylateHCID 11127069—
ReactantN,N-dimethylmethyleneammoniumiodideHCID 21892197—
ProductHCID 53654791HCID 53654791—

Reaction Steps

To a solution of 1.90 g (10.0 mmol) of 5-ethoxycarbonylimidazo[1,2-a]pyridine in 40 ml of acetonitrile was added 2.41 g (13.0 mmol) of N,N-dimethylmethyleneammonium iodide. The mixture was heated for two hours under reflux. The solvent was distilled off. To the residue was added methylene chloride. The mixture was washed with an aqueous solution of sodium thiosulfate and an aqueous solution of sodium hydrogencarbonate, successively, dried over anhydrous magnesium sulfate. The solvent was distilled off, and the residue was purified by column chromatography (eluent: ethyl acetate) to afford 1.496 g of the desired compound (60.6%, a pale yellow solid). This product was recrystallized from ethyl acetate to afford the desired compound (colorless crystals), m.p.117.0-118.0° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06251905B1
Source datasetuspto-grants-2001_06
ORD IDord-7d5e627c3c984e7cb08c3a5582e108a0
Source noteuspto-grants-2001_06