HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 568303Erstellt: 25. Oktober 2026
Cyclopentylamine → N-(4-pyridazinyl)-N'-cyclopentylurea
https://huagongshe.com/reaction/568303
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Cyclopentylamine | HCID 2906 | — |
| Edukt | Phenyl pyridazin-4-ylcarbamate | HCID 14099147 | — |
| Lösungsmittel | Tetrahydrofuran | HCID 8028 | — |
| Produkt | N-(4-pyridazinyl)-N'-cyclopentylurea | HCID 14099149 | 10,8% |
Reaktionsschritte
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.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US04728355 |
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| Quelldatensatz | uspto-grants-1988_03 |
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| ORD ID | ord-72751b774d7d4e85889ba395ee64ee29 |
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| Quellennotiz | uspto-grants-1988_03 |
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