HuagongsheHuagongshe Chemistry Print Report · For research reference only
Pyrrolidine-1-carbonitrile → HCID 178419712, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Pyrrolidine-1-carbonitrile | HCID 73737 | — |
| Reactant | 4-(3-(4-Aminophenyl)propionyl)morpholine | HCID 19599274 | — |
| Reactant | N,N-diethylaniline hydrobromide | HCID 19599275 | — |
| Catalyst | 4-(Dimethylamino)pyridine | HCID 14284 | — |
| Solvent | Chlorobenzene | HCID 7964 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | HCID 178419712 | HCID 178419712 | — |
Reaction Steps
The product of step (b) (2.22 g, 0.00948 moles) was dissolved in 15 ml chlorobenzene. N,N-diethylaniline hydrobromide (2.18 g, 0.00948 moles) was added followed by 1-pyrrolidinecarbonitrile (1.37 g, 0.01422 moles). A catalytic amount of 4-dimethylaminopyridine was added and the reaction heated to reflux for 6 hours. The reaction was then cooled to room temperature and diluted with 100 ml ethyl acetate. A sticky oil precipitated from solution and was stirred for 24 hours. The resulting solids were filtered and recrystallized from hot isopropanol to give the N-(4(2-((4-morpholinyl)carbonyl)ethyl)phenyl)-1-pyrrolidinecarboximidamide hydrobromide, M.P. 207-209° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05998399 |
| Source dataset | uspto-grants-1999_12 |
| ORD ID | ord-dd7903ff75864863a37c62eaa4813439 |
| Source note | uspto-grants-1999_12 |