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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2363752Generated: October 29, 2026

Trimethylsilylacetylene → Ethyl 6-[(trimethylsilyl)ethynyl]imidazo[1,2-a]pyridine-2-carboxylate

https://huagongshe.com/reaction/2363752

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrimethylsilylacetyleneHCID 66111—
ReactantEthyl 6-iodoimidazo[1,2-a]pyridine-2-carboxylateHCID 3681971—
CatalystHCID 178418476HCID 178418476—
ProductEthyl 6-[(trimethylsilyl)ethynyl]imidazo[1,2-a]pyridine-2-carboxylateHCID 44136341—

Reaction Conditions

Temperature50 °C

Reaction Steps

A mixture of 4 g of ethyl 6-iodoimidazo[1,2-a]pyridine-2-carboxylate, 2.63 mL of ethynyltrimethylsilane and 888 mg of dichlorobis(triphenylphosphine)palladium is degassed under vacuum. 240 mg of degassed N,N-dimethylformamide and 3.52 mL of triethylamine are added. The reaction mixture is degassed under argon, stirred at 50° C. for 50 hours and then cooled and diluted with 20 mL of water. The precipitate is filtered off by suction and washed with 5 mL of water and then chromatographed on silica, eluting with mixtures of ethyl acetate and hexane (from 50/50 to 90/10). The fractions containing the expected product are combined and concentrated to dryness under reduced pressure to give 3.6 g of ethyl 6-[(trimethylsilyl)ethynyl]imidazo[1,2-a]pyridine-2-carboxylate in the form of an off-white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08691990B2
Source datasetuspto-grants-2014_04
ORD IDord-ca67b75e54e749fc82854ca95a158990
Source noteuspto-grants-2014_04