Piperazine → 1-(3-Piperazinylpropyl)-3-n-hexylurea

HRID 1380199Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 1380199
Cl[CH2:2][CH2:3][CH2:4][NH:5][C:6]([NH:8][CH2:9][CH2:10][CH2:11][CH2:12][CH2:13][CH3:14])=[O:7].[NH:15]1[CH2:20][CH2:19][NH:18][CH2:17][CH2:16]1>C(O)C>[N:15]1([CH2:2][CH2:3][CH2:4][NH:5][C:6]([NH:8][CH2:9][CH2:10][CH2:11][CH2:12][CH2:13][CH3:14])=[O:7])[CH2:20][CH2:19][NH:18][CH2:17][CH2:16]1

Komponenten

4

Edukt 2

HCID 4837PiperazineHCID 136067321-(3-Chloropropyl)-3-n-hexylurea

Produkt 1

HCID 571432471-(3-Piperazinylpropyl)-3-n-hexylureaAusbeute 39 %

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 702EthanolLösungsmittel

Versuchsvorschrift

A mixture of 1-(3-chloropropyl)-3-n-hexylurea (11.0 g; 50 mmole), piperazine (43.0 g; 500 mmole) and reagent ethanol (250 ml) was refluxed for 2 hours. The solvent was removed in vacuo, and the solid residue was dissolved in water. The resulting solution was extracted with methylene chloride, concentrated in vacuo, and the residue was chromatographed on silica gel to give 1-(3-piperazinylpropyl)-3-n-hexylurea as a light yellow oil (6.7 g; 39% yield).

Aufarbeitung

  1. temperaturewas refluxed for 2 hours
  2. customThe solvent was removed in vacuo
  3. dissolutionthe solid residue was dissolved in water
  4. extractionThe resulting solution was extracted with methylene chloride
  5. concentrationconcentrated in vacuo
  6. customthe residue was chromatographed on silica gel

Quellen und Nachweise

ORD-Eintrag
ord-d0f86b9766324726a753e3dba896e77d
Quelldatensatz
uspto-grants-1986_04
Patentnummer
US04579947

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