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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 609565Generated: October 26, 2026

Pyrrolidine-1-carbonitrile → HCID 178479312, compound

https://huagongshe.com/reaction/609565

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyrrolidine-1-carbonitrileHCID 73737—
Reactant3-(((4-Phenylbutyl)amino)carbonyl)aniline hydrochlorideHCID 19353694—
Catalyst4-(Dimethylamino)pyridineHCID 14284—
SolventChlorobenzeneHCID 7964—
ProductHCID 178479312HCID 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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05998399
Source datasetuspto-grants-1999_12
ORD IDord-6497bc1083d54343bd4263b16d49df8a
Source noteuspto-grants-1999_12