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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 648428Generated: October 25, 2026

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

https://huagongshe.com/reaction/648428

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCyclopentylamineHCID 2906—
ReactantPhenyl pyridazin-4-ylcarbamateHCID 14099147—
SolventTetrahydrofuranHCID 8028—
ProductN-(4-pyridazinyl)-N'-cyclopentylureaHCID 14099149—

Reaction Steps

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

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04735650
Source datasetuspto-grants-1988_04
ORD IDord-44ba51dd1dd34f9db57b60a204cfea36
Source noteuspto-grants-1988_04