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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1418848Generated: November 1, 2026

Pyrrolidine-1-carbonitrile → HCID 178479312, compound

https://huagongshe.com/reaction/1418848

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 4hours. 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 numberUS05885985
Source datasetuspto-grants-1999_03
ORD IDord-5fb39d25ad864577ab14403b0fbed7cc
Source noteuspto-grants-1999_03