HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1895951Generated: November 2, 2026
2-Bromo-6-methylpyridine → 2-{4-[3-(6-Methylpyridin-2-yl)prop-2-ynylidene]piperidin-1-yl}-3-nitropyridine
https://huagongshe.com/reaction/1895951
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 2-Bromo-6-methylpyridine | HCID 79205 | — |
| Reactant | 3-Nitro-2-(4-prop-2-ynylidenepiperidin-1-yl)pyridine | HCID 86627335 | — |
| Catalyst | Copper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI) | HCID 24350 | — |
| Catalyst | HCID 178418397 | HCID 178418397 | — |
| Product | 2-{4-[3-(6-Methylpyridin-2-yl)prop-2-ynylidene]piperidin-1-yl}-3-nitropyridine | HCID 25183668 | 69.6% |
Reaction Steps
A mixture of Compound 1c (0.21 g, 0.86 mmol), 2-bromo-6-methylpyridine (0.11 mL, 0.95 mmol), tetrakis(triphenylphosphine)palladium(0) (70 mg, 0.06 mmol), CuI (16 mg, 0.09 mmol) in anhydrous and degassed triethylamine (10 mL) was heated at 80° C. under a nitrogen atmosphere for 2 h in sealed vessel. The reaction mixture was cooled, poured into water and extracted with EtOAc. The combined organic layers were washed with brine, dried on Na2SO4 and evaporated to dryness in vacuo to afford a residue, which was purified by flash chromatography (EtOAc—Petroleum Ether 3.5:6.5) affording the title product (0.20 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08518916B2 |
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| Source dataset | uspto-grants-2013_08 |
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| ORD ID | ord-364c87f6c7544ea3b84d53f2d13c04b3 |
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| Source note | uspto-grants-2013_08 |
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