HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1637111Generated: October 25, 2026
5-(3-Iodophenyl)-3-methyl-1,2,4-oxadiazole → (S)-methyl-3-(3-cyclopentyloxy-4-methoxyphenyl)-5-[3-(3-methyl[1,2,4]oxadiazol-5-yl)phenyl]pent-4ynoate
https://huagongshe.com/reaction/1637111
Participants
| Role | Name | HCID | Charge |
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| Reactant | 5-(3-Iodophenyl)-3-methyl-1,2,4-oxadiazole | HCID 19349979 | — |
| Reactant | (R)-methyl-3-(3-cyclopentyloxy-4-methoxyphenyl)-3-ethynylpropionate | HCID 21967451 | — |
| Catalyst | Copper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI) | HCID 24350 | — |
| Catalyst | HCID 178418397 | HCID 178418397 | — |
| Solvent | Triethylamine | HCID 8471 | — |
| Product | (S)-methyl-3-(3-cyclopentyloxy-4-methoxyphenyl)-5-[3-(3-methyl[1,2,4]oxadiazol-5-yl)phenyl]pent-4ynoate | HCID 21967463 | 31.7% |
Reaction Steps
A solution of (R)-methyl-3-(3-cyclopentyloxy-4-methoxyphenyl)-3-ethynylpropionate (150 mg, 0.5 mmol) and 3-(3-methyl[1,2,4]oxadiazol-5-yl) iodobenzene (144 mg, 0.5 mmol) in Et3N (4 ml) was treated with tetrakis(triphenylphosphine)palladium(0) (10 mg) and copper(I)iodide (10 mg). The reaction was heated to 55° for 30 min, and then the solvent was thoroughly evaporated. The residue was purified by flash chromatography (silica gel CH2Cl2 :hexane:Et2O/10:10:1) and gave the titled compound as an oil (73 mg, 17%) 1H NMR (400 MHz, CDCl3) δ 8.18 (s, 1 H), 8.02 (m, 1 H), 7.60 (m, 1 H), 7.60 (t, 1 H), 6.95 (m, 2 H), 6.86 (d, 1 H), 4.80 (m, 1 H), 4.33 (t, 1 H), 3.84 (s, 3 H), 3.72 (s, 3 H), 2.92 (d of d, 1 H), 2.82 (d of d, 1 H), 2.48 (s, 3 H), 1.78-2.02 (m, 6 H), 1.62 (m, 2 H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06037367 |
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| Source dataset | uspto-grants-2000_03 |
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| ORD ID | ord-536d3aa761ef4e3294ad68bbbb063360 |
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| Source note | uspto-grants-2000_03 |
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