HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 251623Generated: October 31, 2026
3-Methoxypropyne → 6-(2,6-Diethyl-phenyl)-4-(3-methoxy-prop-1-ynyl)-2-methyl-nicotinic acid ethyl ester
https://huagongshe.com/reaction/251623
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 3-Methoxypropyne | HCID 69393 | — |
| Reactant | 4-Bromo-6-(2,6-diethyl-phenyl)-2-methyl-nicotinic ethyl ester | HCID 66993565 | — |
| Catalyst | Copper iodide | HCID 83717 | — |
| Catalyst | HCID 178418397 | HCID 178418397 | — |
| Solvent | Diisopropylamine | HCID 7912 | — |
| Product | 6-(2,6-Diethyl-phenyl)-4-(3-methoxy-prop-1-ynyl)-2-methyl-nicotinic acid ethyl ester | HCID 66993646 | — |
Reaction Steps
A mixture of 4-bromo-6-(2,6-diethyl-phenyl)-2-methyl-nicotinic ethyl ester (308 mg, 0.82 mmol), methyl propargyl ether (0.69 mL, 8.2 mmol), Pd(PPh3)4 (95 mg, 0.082 mmol), and copper iodide (8 mg, 0.041 mmol) in diisopropylamine (8 mL) is heated at 105° C. in a sealed tube. After filtration through celite, the filtrate is concentrated in vacuo and the residue purified by flash chromatography to give 6-(2,6-diethyl-phenyl)-4-(3-methoxy-propyn-1-yl)-2-methyl-nicotinic acid ethyl ester as a yellow oil. 1H NMR (CDCl3) 7.36-7.29 (m, 2H), 7.20-7.15 (m, 2H), 4.47 (q, 2H), 4.32 (s, 2H), 3.41 (s, 3H), 2.62 (s, 3H), 2.38-2.27 (m, 4H), 1.41 (t, 3H), 1.06 (t, 6H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07863454B2 |
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| Source dataset | uspto-grants-2011_01 |
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| ORD ID | ord-e8b6344efb5347e184583b4edba59183 |
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| Source note | uspto-grants-2011_01 |
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