HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → 4-Ethoxy-2-pyrrolidin-1-ylpyrimidine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Pyrrolidine | HCID 31268 | — |
| Reactant | 2-Chloro-4-ethoxypyrimidine | HCID 4737280 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 4-Ethoxy-2-pyrrolidin-1-ylpyrimidine | HCID 59525896 | — |
Reaction Steps
To a solution of 2-chloro-4-ethoxypyrimidine (3 g, 19 mol) in THF (410 mL) was added pyrrolidine (2.7 g, 38 mmol) and Et3N (5.8 g, 57 mmol) and the reaction mixture was heated to reflux overnight. The solvent was evaporated and the residue was partioned between water and EtOAc. The aqueous phase was extracted with EtOAc. The combined organic phases were dried over sodium sulfate, filtered, and concentrated to give the title compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08367706B2 |
| Source dataset | uspto-grants-2013_02 |
| ORD ID | ord-7a911ec2b8604f458f43e5d3f63a6713 |
| Source note | uspto-grants-2013_02 |