HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → 4-(Isoquinolin-4-yl)but-3-yn-1-ol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 3-Butyn-1-OL | HCID 13566 | — |
| Reactant | 4-Bromoisoquinoline | HCID 73743 | — |
| Catalyst | Dichlorobis(triphenylphosphine)palladium | HCID 6102075 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 4-(Isoquinolin-4-yl)but-3-yn-1-ol | HCID 10631793 | 71.7% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04927838 |
| Source dataset | uspto-grants-1990_05 |
| ORD ID | ord-17290ca0c62749fd817a7b69f4c256a9 |
| Source note | uspto-grants-1990_05 |