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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1637120Generated: November 3, 2026

HCID 19349925, compound → HCID 54557479, compound

https://huagongshe.com/reaction/1637120

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 19349925HCID 19349925—
ReactantHCID 54129593HCID 54129593—
CatalystCopper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
SolventTriethylamineHCID 8471—
ProductHCID 54557479HCID 5455747971%

Reaction Conditions

Temperature80 °C

Reaction Steps

A mixture (+/-)-3-(3-cyclopentyloxy-4-methoxyphenyl)pent-4-ynal (0.20 g, 0.73 mmol) and 1-iodo-3-(5-methyl-[1,2,4]oxadiazol-3-yl)benzene (0.21 g, 0.73 mmol) and trace tetrakistriphenylphosphine palladium (0) and trace copper(I)iodide in triethylamine (5 mL)under an argon atmosphere was heated at 80° C. for 0.25 h. The mixture was cooled to room temperature and was evaporated. The residue was purified by flash chromatography (silica gel, 35% EtOAc/Hex) to provide the title compound as a yellow oil (0.22 g, 71%).1H NMR (250 Mhz, CDCl3) δ 9.86 (t, J=1.7 Hz, 1 H), 8.15, (d, J=1.4 Hz, 1 H), 8.01 (dt, J=7.8 and 1.4 Hz, 1 H), 7.54 (dt, J=7.8 and 1.4 Hz, 1 H), 7.42 (t, J=7.8 Hz),lH), 6.95 (m. 2 H), 6.84 (d, J=8.5 Hz, 1 H), 4.8 (m, 1 H), 4.40 (t, J=7 Hz, 1 H), 3.85 (s, 3 H), 2.86-3.10 (m, 2 H), 2.66 (s, 3 H), 1.80-2.05 (m, 6 H), 1.60-1.69 (m, 2 H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06037367
Source datasetuspto-grants-2000_03
ORD IDord-396b962fab7d476b8db2c7bcaedb7458
Source noteuspto-grants-2000_03