HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 568303Generated: October 25, 2026
Cyclopentylamine → N-(4-pyridazinyl)-N'-cyclopentylurea
https://huagongshe.com/reaction/568303
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Cyclopentylamine | HCID 2906 | — |
| Reactant | Phenyl pyridazin-4-ylcarbamate | HCID 14099147 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | N-(4-pyridazinyl)-N'-cyclopentylurea | HCID 14099149 | 10.8% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US04728355 |
|---|
| Source dataset | uspto-grants-1988_03 |
|---|
| ORD ID | ord-72751b774d7d4e85889ba395ee64ee29 |
|---|
| Source note | uspto-grants-1988_03 |
|---|