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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 568303Generated: October 25, 2026

Cyclopentylamine → N-(4-pyridazinyl)-N'-cyclopentylurea

https://huagongshe.com/reaction/568303

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCyclopentylamineHCID 2906—
ReactantPhenyl pyridazin-4-ylcarbamateHCID 14099147—
SolventTetrahydrofuranHCID 8028—
ProductN-(4-pyridazinyl)-N'-cyclopentylureaHCID 1409914910.8%

Reaction Steps

A stirred solution of 2.0 grams (0.009 mole) of phenyl N-(4-pyridazinyl)carbamate and 1.0 ml (0.010 mole) of cyclopentylamine in tetrahydrofuran is heated under reflux for 18 hours. The reaction mixture is filtered and the filtrate concentrated under reduced pressure to a residue. The residue is purified by column chromatography on silica gel. Elution is accomplished with 10% methanol in methylene chloride. The appropriate fractions are combined and concentrated under reduced pressure to yield 0.2 gram of N-(4-pyridazinyl)-N'-cyclopentylurea. This material is combined with the identical product from a previous reaction to yield 0.5 gram; m.p. 192°-195° C., dec. The nmr spectrum is consistent with the proposed structure. The reaction is repeated several times.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04728355
Source datasetuspto-grants-1988_03
ORD IDord-72751b774d7d4e85889ba395ee64ee29
Source noteuspto-grants-1988_03