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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1615109Generated: November 3, 2026

HCID 178435594, compound → HCID 178525130, compound

https://huagongshe.com/reaction/1615109

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 178435594HCID 178435594—
CatalystCopper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
CatalystDichlorobis(triphenylphosphine)palladiumHCID 6102075—
SolventTetrahydrofuranHCID 8028—
ProductHCID 178525130HCID 17852513039%

Reaction Steps

To a stirring solution of (S)-2-(5-ethynyl-1H-benzoimidazol-2-yl)-piperidine-1-carboxylic acid benzyl ester (26 mg, 0.0723 mmol), CuI (3 mg) and bis(triphenylphosphine)palladium(II)dichloride (8 mg) in THF (1.5 mL) is added TEA (30 μL, 3.4 mmol). The reaction mixture is stirred at room temperature for 12 hours and filtered through celite and the filtrate is concentrated in vacuum to dryness. The residue is purified by flash column chromatography on silica gel (EtOAc/hexanes 0% to 100%) to give the title compound (S)-2-(5-{4-[2-((S)-1-benzyloxycarbonyl-piperidin-2-yl)-1H-benzoimidazol-5-yl]-buta-1,3-diynyl}-1H-benzoimidazol-2-yl)-piperidine-1-carboxylic acid benzyl ester (10 mg, 39%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08765731B2
Source datasetuspto-grants-2014_07
ORD IDord-b59f4dc115164557b2d81c1cfa2e35b4
Source noteuspto-grants-2014_07