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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 586124Generated: October 26, 2026

Triethylamine → 2-(7-Cyano-1-heptynyl)-Adenosine

https://huagongshe.com/reaction/586124

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactant2-IodoadenosineHCID 169662—
Reactant7-Cyano-1-heptyneHCID 13133500—
CatalystHCID 178418476HCID 178418476—
SolventDimethylformamideHCID 6228—
Product2-(7-Cyano-1-heptynyl)-AdenosineHCID 69595306199.3%

Reaction Conditions

Temperature60 °C

Reaction Steps

Under argon, to a solution of 2-iodoadenosine (200 mg, 0.51 mmol) and bis(triphenylphosphine)palladium dichloride (36 mg, 10 mol %) dissolved in N,N-dimethylformamide (5 mL), triethylamine (0.09 mL, 0.61 mmol, 1.2 eq.) and 7-cyano-1-heptyne (74 mg, 0.1 mmol, 1.2 eq.) were added, and, under ice-cooling conditions, cuprous iodide (10 mg, 5 mol %) was added thereto, followed by stirring at 60° C. for 24 hours. The reaction mixture was cooled to room temperature, and the solvent was removed under reduced pressure. The residue was purified by dry packed silica gel column chromatography (chloroform:methanol=10:1), to thereby yield the above-titled compound as a pale yellow powder (yield: 77 mg, percent yield: 39%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06936596B2
Source datasetuspto-grants-2005_08
ORD IDord-3b80021d64b74106a8a6c624e16175f5
Source noteuspto-grants-2005_08