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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2232145Generated: October 31, 2026

Triethylamine → 4-(Isoquinolin-4-yl)but-3-yn-1-ol

https://huagongshe.com/reaction/2232145

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactant3-Butyn-1-OLHCID 13566—
Reactant4-BromoisoquinolineHCID 73743—
CatalystHCID 178418476HCID 178418476—
SolventDichloromethaneHCID 6344—
Product4-(Isoquinolin-4-yl)but-3-yn-1-olHCID 1063179371.7%

Reaction Steps

In an inert atmosphere, 0.268 g of bis(triphenylphosphine)palladium dichloride and 0.072 g of cuprous iodide was added with stirring to a deoxygenated solution of 5 g of 4-bromoisoquinoline, 3.02 g of 3-butyn-1-ol and 10 mL of triethylamine in 20 mL of dichloromethane. The reaction was stirred at room temperature for 1 hour and then at reflux for 18 hours. The cooled mixture was filtered and the filtrate was washed with water. The dried (Na2SO4) organic phase was concentrated in vacuo and the residual oil was purified by HPLC (ethyl acetate-toluene; 2:3) to yield 3.4 g of 4-(4-isoquinolinyl)-3-butyn-1-ol as an oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04786646
Source datasetuspto-grants-1988_11
ORD IDord-fcc3a29609bc4c44b7a3dfc12d1b6ada
Source noteuspto-grants-1988_11