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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 928572Generated: November 3, 2026

Triethylamine → HCID 89579370, compound

https://huagongshe.com/reaction/928572

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactant4-Chloro-5-phenylthieno[2,3-d]pyrimidineHCID 708730—
ReactantHCID 87814959HCID 87814959—
CatalystCopper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
SolventEthyl AcetateHCID 8857—
ProductHCID 89579370HCID 89579370—

Reaction Conditions

Temperature100 °C

Reaction Steps

Nitrogen gas was bubbled through a mixture of 4-chloro-5-phenyl-thieno[2,3-d]pyrimidine (1 g, 4.06 mmol), 1-(2-prop-2-ynoxyethyl)pyrrolidine (1.53 g, 10 mmol), bistriphenylphosphine palladium (II) dichloride (180 mg, 0.25 mmol), triethylamine (3.5 mL, 25 mmol), copper (I) iodide (75 mg, 0.4 mmol) in THF (20 mL) for 5 minutes. The reaction was then heated at 100° C. for 60 minutes in a microwave. The reaction was then diluted with ethyl acetate (50 ml) and water (50 ml) and shaken. The ethyl acetate layer was then separated, dried over sodium sulphate and concentrated in vacuum to a gum. The gum was chromatographed on silica in a gradient of 2-15% methanol in dichloromethane. A peak eluted in about 8-12% methanol in dichloromethane to give 5-phenyl-4-[3-(2-pyrrolidine-1-ylethoxy)prop-1-ynyl]thieno[2,3-d]pyrimidine as a gum. (55 mg, 0.15 mmol, 3.7%). LCMS [M+H]+=364; RT=3.04 min.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09290511B2
Source datasetuspto-grants-2016_03
ORD IDord-1158ff429f164d16b3d76a3bbef4ae06
Source noteuspto-grants-2016_03