HuagongsheHuagongshe Chemistry Print Report · For research reference only
Pyrrolidine-1-carbonitrile → HCID 178479312, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Pyrrolidine-1-carbonitrile | HCID 73737 | — |
| Reactant | 3-(((4-Phenylbutyl)amino)carbonyl)aniline hydrochloride | HCID 19353694 | — |
| Catalyst | 4-(Dimethylamino)pyridine | HCID 14284 | — |
| Solvent | Chlorobenzene | HCID 7964 | — |
| Product | HCID 178479312 | HCID 178479312 | — |
Reaction Steps
To a stirred suspension of the product of step (a), 2.0 g, 0.006 moles, in 35 ml of chlorobenzene was added 4-dimethylaminopyridine. To this was added 1-pyrrolidinecarbonitrile, 1.5 ml; 0.008 moles, and the reaction was heated to reflux for 4 hours. The reaction cooled to room temperature and the solvent was decanted. To the residue was added 25 ml of isopropanol and 150 ml of ethyl acetate. A solid crystallized and was collected by filtration. The above solid was then dried at 80° C. for 24 hours to give N-[3-(((4-phenylbutyl)amino)carbonyl)phenyl]-1-pyrrolidinecarboximidamide hydrochloride, 2.3 g, m.p. 197-198° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05998399 |
| Source dataset | uspto-grants-1999_12 |
| ORD ID | ord-6497bc1083d54343bd4263b16d49df8a |
| Source note | uspto-grants-1999_12 |