Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2042136Generated: October 30, 2026

Triethylamine → 6-Phenylethynyl-pyrazolo[1,5-a]pyrimidine

https://huagongshe.com/reaction/2042136

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantPhenylacetyleneHCID 10821—
ReactantTriphenylphosphineHCID 11776—
Reactant6-Bromopyrazolo[1,5-a]pyrimidineHCID 22236701—
CatalystCopper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
CatalystHCID 178418476HCID 178418476—
SolventTetrahydrofuranHCID 8028—
Product6-Phenylethynyl-pyrazolo[1,5-a]pyrimidineHCID 50914914—

Reaction Conditions

Temperature65 °C

Reaction Steps

Bis-(triphenylphosphine)-palladium (II) dichloride (27 mg, 0.04 mmol) was dissolved in 1 ml of THF. 6-Bromo-pyrazolo[1,5-a]pyrimidine (150 mg, 0.76 mmol) and phenylacetylene (130 μl, 1.21 mmol) were added at room temperature. Triethylamine (310 μl, 2.3 mmol), triphenylphosphine (6 mg, 0.023 mmol) and copper (I) iodide (4 mg, 0.023 mmol) were added and the mixture was stirred for 2 hours at 65° C. The reaction mixture was cooled and extracted with saturated NaHCO3 solution and two times with a small volume of dichloromethane. The crude product was purified by flash chromatography by directly loading the dichloromethane layers onto a silica gel column and eluting with heptane:ethyl acetate 100:0->50:50. The desired compound was obtained as a yellow solid (150 mg, 90% yield), MS: m/e=220.3 (M+H+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08586581B2
Source datasetuspto-grants-2013_11
ORD IDord-b3466dee2c2245f7bf133fe4831f714d
Source noteuspto-grants-2013_11