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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 2-Iodoadenosine | HCID 169662 | — |
| Reactant | 7-Cyano-1-heptyne | HCID 13133500 | — |
| Catalyst | HCID 178418476 | HCID 178418476 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 2-(7-Cyano-1-heptynyl)-Adenosine | HCID 69595306 | 199.3% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06936596B2 |
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| Source dataset | uspto-grants-2005_08 |
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| ORD ID | ord-3b80021d64b74106a8a6c624e16175f5 |
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| Source note | uspto-grants-2005_08 |
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