HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethynylpyridine → HCID 86599493, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethynylpyridine | HCID 137268 | — |
| Reactant | ethyl 8-iodo-6-(trifluoromethoxy)-2-(trifluoromethyl)-2H-chromene-3-carboxylate | HCID 86599457 | — |
| Catalyst | Copper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI) | HCID 24350 | — |
| Catalyst | HCID 178418807 | HCID 178418807 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | HCID 86599493 | HCID 86599493 | 77% |
Reaction Steps
A mixture of ethyl 8-iodo-6-(trifluoromethoxy)-2-(trifluoromethyl)-2H-chromene-3-carboxylate prepared as in Example 21a, Step 2 (1.00 g, 2.07 mmole), 2-pyridylacetylene (419 uL, 4.15 mmole), CuI (39 mg, 0.207 mmole), PdCl2(dppf)2-CH2Cl2 (169 mg, 0.207 mmole) and TEA (0.866 mL, 6.21 mmole) in anhydrous toluene (10 mL) was stirred at room temperature for 5 days under a N2 atmosphere. The mixture was then diluted with hexanes and purified by silica chromatography (0% to 75% EtOAc:hexanes gradient) to give 0.73 g (77% yield) the title product as a pale yellow crystalline solid: ESHRMS m/z 458.0849 (M+H, C21H14F6NO4, Calc'd 458.0822).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07259266B2 |
| Source dataset | uspto-grants-2007_08 |
| ORD ID | ord-a845c58339c643d3b9f56784ba1f5ba5 |
| Source note | uspto-grants-2007_08 |