HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1896021Generated: October 27, 2026
1,10-Phenanthroline → 1-{3-[1-(3-Nitropyridin-2-yl)piperidin-4-ylidene]prop-1-ynyl}pyrrolidin-2-one
https://huagongshe.com/reaction/1896021
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 1,10-Phenanthroline | HCID 1318 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 2-Pyrrolidone | HCID 12025 | — |
| Reactant | 2-[4-(3-Bromoprop-2-ynylidene)piperidin-1-yl]-3-nitropyridine | HCID 86762014 | — |
| Solvent | Toluene | HCID 1140 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | 1-{3-[1-(3-Nitropyridin-2-yl)piperidin-4-ylidene]prop-1-ynyl}pyrrolidin-2-one | HCID 86762015 | 1.8% |
Reaction Steps
A mixture of Compound 261a (111 mg, 0.345 mmol), cupric sulphate (11 mg, 0.69 mmol), 1,10-phenantroline (24.9 mg, 0.138 mmol), K2CO3 (95.4 mg, 0.69 mmol), 2-pyrrolidone (39.7 μl, 0.518 mmol) and 5 mL of toluene was stirred at 80° C. for 12 h. The reaction mixture was cooled to r.t., diluted with EtOAc, washed with water, dried over Na2SO4 and evaporated to dryness in vacuo. The crude residue was purified by automated flash liquid chromatography (Horizon™-Biotage) eluting with PE-EtOAc gradient from 98:2 to 0:10, giving the title product (2 mg)
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US08518916B2 |
|---|
| Source dataset | uspto-grants-2013_08 |
|---|
| ORD ID | ord-bde8a51850e041a696718e8f14823a94 |
|---|
| Source note | uspto-grants-2013_08 |
|---|