HuagongsheHuagongshe Chemistry Print Report · For research reference only
Pyridine → N-[3-(pyrimidin-5-yl)phenyl]fluorene-1-carboxamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Pyridine | HCID 1049 | — |
| Reactant | Fluorene-1-carbonyl chloride | HCID 255028 | — |
| Reactant | 3-Pyrimidin-5-ylaniline | HCID 7162049 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | N-[3-(pyrimidin-5-yl)phenyl]fluorene-1-carboxamide | HCID 9820411 | 61.2% |
Reaction Steps
To a suspension of 3-(pyrimidin-5-yl)aniline (0. 17g) and pyridine (0.24 ml) in dichloromethane (3 ml) was dropwise added a solution of the fluorene-1-carbonyl chloride (0.23 g) in dichloromethane (5 ml) followed by stirring for 2 hours. The mixture was diluted with dichloromethane and washed with an aqueous solution of sodium hydrogen carbonate and brine. The separated organic layer was dried over sodium sulfate and evaporated. The residue was purified by a silica gel column chromatography eluting with 2% methanol in dichloromethane to give N-[3-(pyrimidin-5-yl)phenyl]fluorene-1-carboxamide (0.222 g, 61.2 %).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06770667B1 |
| Source dataset | uspto-grants-2004_08 |
| ORD ID | ord-a3d307b522294413b85324954a1e0795 |
| Source note | uspto-grants-2004_08 |