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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 19468Generated: October 30, 2026

Triethylamine → HCID 68561395, compound

https://huagongshe.com/reaction/19468

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantEthyl AcetateHCID 8857—
ReactantPhenylacetyleneHCID 10821—
ReactantHCID 67241648HCID 67241648—
CatalystCopper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
CatalystHCID 178418397HCID 178418397—
SolventDimethylformamideHCID 6228—
ProductHCID 68561395HCID 6856139592%

Reaction Steps

3-(β-D-Ribofuranosyl)-5-iodopyridin-2(1H)-one prepared in Example 1(1) (71 mg, 0.20 mmol) was dissolved in DMF (1.0 ml), followed by addition of CuI (6 mg, 0.032 mmol), triethylamine (42 μl, 0.30 mmol), phenylacetylene (33 μl, 0.30 mmol) and Pd(Ph3P)4 (11 mg, 0.010 mol). The reaction mixture was stirred under an argon atmosphere at room temperature for 6 hours. After addition of ethyl acetate (10 ml), the reaction mixture was extracted three times with water (10 ml each). The combined aqueous layers were concentrated under reduced pressure and then purified by reversed-phase HPLC to give 3-(β-D-ribofuranosyl)-5-(2-phenylethynyl)-pyridin-2(1H)-one (60 mg, 92%) as a white product.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07745417B2
Source datasetuspto-grants-2010_06
ORD IDord-2c19a1711fba4c5397acf16d58cb87be
Source noteuspto-grants-2010_06