Cyanoacetic acid → 6-Amino-1-cyclopropyl-1,2,3,4-tetrahydropyrimidine-2,4-dione

HRID 464595Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 464595
[C:1]([CH2:3][C:4](O)=[O:5])#[N:2].[CH:7]1([NH:10][C:11]([NH2:13])=[O:12])[CH2:9][CH2:8]1>C(OC(=O)C)(=O)C>[NH2:2][C:1]1[N:10]([CH:7]2[CH2:9][CH2:8]2)[C:11](=[O:12])[NH:13][C:4](=[O:5])[CH:3]=1

Komponenten

4

Edukt 2

HCID 9740Cyanoacetic acidHCID 2726261-Cyclopropylurea

Produkt 1

HCID 71315486-Amino-1-cyclopropyl-1,2,3,4-tetrahydropyrimidine-2,4-dione

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 7918Acetic AnhydrideLösungsmittel

Versuchsvorschrift

To a solution of 64 g (0.75 mol) cyanoacetic acid and 250 ml of acetic anhydride was added 70 g (0.7 mol) of cyclopropylurea. The solution was stirred at 60°-70° C. for 2 hours. After cooling white crystals were filtered off and washed with ethanol. Yield 76.7 g (66%) (I). This was suspended in 200 ml of hot water and 55 ml of 5N NaOH was added in portions so the solution the whole time was basic. The reaction mixture was refluxed for 20 minutes and then neutralized with 5N HCl. After cooling, white crystals were filtered off. Yield 31.7 g (42%) (II) NMR.

Aufarbeitung

  1. temperatureAfter cooling white crystals
  2. filtrationwere filtered off
  3. washwashed with ethanol
  4. addition55 ml of 5N NaOH was added in portions so the solution the whole time
  5. temperatureThe reaction mixture was refluxed for 20 minutes
  6. temperatureAfter cooling
  7. filtrationwhite crystals were filtered off

Quellen und Nachweise

ORD-Eintrag
ord-cdfdd993758f4a81aa647f6de18584f0
Quelldatensatz
uspto-grants-1985_10
Patentnummer
US04548818

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