HuagongsheHuagongshe Chemistry Print Report · For research reference only
1,10-Phenanthroline → HCID 118023303, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1,10-Phenanthroline | HCID 1318 | — |
| Reactant | Cerous carbonate | HCID 160516 | — |
| Reactant | 2-Fluorothiophenol | HCID 520216 | — |
| Reactant | tert-Butyl 4-(5-bromopyrimidin-2-yl)piperazine-1-carboxylate | HCID 21914476 | — |
| Catalyst | Copper iodide | HCID 83717 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | HCID 118023303 | HCID 118023303 | — |
Reaction Steps
A mixture of tert-butyl 4-(5-bromopyrimidin-2-yl)piperazine-1-carboxylate (5.0 g, 14.6 mmol), 2-fluorobenzenethiol (9.3 g, 73 mmol), 1,10-Phenanthroline (7.9 g, 43.8 mmol), copper iodide (13.9 g, 73 mmol) and cerium carbonate (28.6 g, 87.6 mmol) in dioxane (100 mL) was refluxed for 3 days. The reaction mixture was cooled to RT and concentrated. The residue was directly purified by silica gel chromatography to give the title compound. MS (ES+) C19H23FN4O2S requires: 390. found: 391 [M+H]+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09200002B2 |
| Source dataset | uspto-grants-2015_12 |
| ORD ID | ord-395908b6efea4186aad34a8c4daa773e |
| Source note | uspto-grants-2015_12 |