HuagongsheHuagongshe Chemistry Print Report · For research reference only
Dichloromethane → 3-Chloro-6-(4-[1,2,3]triazol-1-yl-but-1-ynyl)-pyridazine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Dichloromethane | HCID 6344 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 3-Chloro-6-iodopyridazine | HCID 15418839 | — |
| Reactant | 1-But-3-ynyl-1H-[1,2,3]triazole | HCID 18453522 | — |
| Catalyst | Copper iodide | HCID 83717 | — |
| Catalyst | HCID 178418397 | HCID 178418397 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 3-Chloro-6-(4-[1,2,3]triazol-1-yl-but-1-ynyl)-pyridazine | HCID 86074067 | — |
Reaction Steps
3-Chloro-6-iodo-pyridazine (11.56 g, 48.1 mmol), 1-but-3-ynyl-1H-[1,2,3]triazole (6.99 g, 57.7 mmol) and triethyl amine (NEt3) (94 ml) are dissolved in DMF (188 ml) and copper iodide (CuI) (0.981 g, 5.15 mmol) is added under stirring. After passing a stream of argon through the mixture for 10 min tetrakis(triphenylphosphine)palladium(0) (2.836 g, 2.43 mmol) is added and stirring is continued for 6 h at r.t. Dichloromethane (300 ml) is added, the mixture is washed with 0.5N hydrochloric acid (HCl) and brine, dried over Na2SO4 and concentrated in vacuo. The crude product is purified by flash column chromatography (ethyl acetate) yielding 3-chloro-6-(4-[1,2,3]triazol-1-yl-but-1-ynyl)-pyridazine as a colorless solid. Yield 9.52 g (85%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07179812B2 |
| Source dataset | uspto-grants-2007_02 |
| ORD ID | ord-6c77992320494766b8912a493564a18b |
| Source note | uspto-grants-2007_02 |