HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 606889Generated: October 27, 2026
Triethylamine → 2-Fluoro-5-(5-methoxypyridin-3-ylethynyl)-benzonitrile
https://huagongshe.com/reaction/606889
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 2-Fluoro-5-iodobenzonitrile | HCID 2778928 | — |
| Reactant | 3-Ethynyl-5-methoxypyridine | HCID 21097349 | — |
| Catalyst | Copper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI) | HCID 24350 | — |
| Catalyst | HCID 178419050 | HCID 178419050 | — |
| Product | 2-Fluoro-5-(5-methoxypyridin-3-ylethynyl)-benzonitrile | HCID 67047609 | 90% |
Reaction Steps
Add bis(triphenylphosphine)palladium (II) dichloride (77 mg, 0.1 mmol), copper (I) iodide (44 mg, 0.23 mmol), and 3-ethynyl-5-methoxypyridine (300 mg, 2.3 mmol), (prepared as described in PREPARATION 10), to a solution of 2-fluoro-5-iodobenzonitrile (670 mg, 2.7 mmol) in triethylamine (3.4 mL, 34 mmol) and heat at 60° C. for 2.75 h. Cool to room temperature and concentrate. Purify the residue by silica gel chromatography, eluting with 100:0 to 80:20 dichloromethane/ethyl acetate followed by a second silica gel chromatography, eluting with 75:25 to 60:40 hexanes:ethyl acetate to give the title compound as a white solid (510 mg, 90%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07915424B2 |
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| Source dataset | uspto-grants-2011_03 |
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| ORD ID | ord-7e0beb338e42442d8e7bf97e48221d7a |
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| Source note | uspto-grants-2011_03 |
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