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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2232726Generated: November 2, 2026

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

https://huagongshe.com/reaction/2232726

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactant3-Butyn-1-OLHCID 13566—
Reactant4-BromoisoquinolineHCID 73743—
CatalystDichlorobis(triphenylphosphine)palladiumHCID 6102075—
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 numberUS04788206
Source datasetuspto-grants-1988_11
ORD IDord-88ef171e4aa84e92adff2b94f2431650
Source noteuspto-grants-1988_11