Propanal → HCID 86750388, Verbindung

HRID 1451772Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 1451772
[CH:1](=O)[CH2:2][CH3:3].[NH2:5][CH2:6][CH:7]1[CH2:15][C:14]2[C:9](=[CH:10][CH:11]=[C:12]([C:16]3[CH2:17][CH2:18][C:19](=[O:22])[NH:20][N:21]=3)[CH:13]=2)[CH2:8]1.[BH4-].[Na+]>CO>[CH2:1]([CH:8]1[CH2:9][C:10]2[C:15](=[CH:14][CH:13]=[C:12]([C:16]3[CH2:17][CH2:18][C:19](=[O:22])[NH:20][N:21]=3)[CH:11]=2)[CH:7]1[CH2:6][NH2:5])[CH2:2][CH3:3]

Komponenten

5

Versuchsvorschrift

Propanal (1.51 g) dissolved in 5 ml of methanol was added dropwise to 6.15 g of 2-aminomethyl-5-[4,5-dihydro-pyridazin-3(2H)-on-6-yl]indane dissolved in 60 ml of methanol. The mixture was stirred at room temperature for 30 minutes. Then, under ice cooling, 1.03 g of sodium borohydride was added to the mixture. The resulting mixture was stirred at the same temperature for 20 minutes and then stirred at room temperature for 1 hour. After methanol was removed, water was added to the residue, and the residue was extracted with ethyl acetate. The organic layer was collected by filtration, washed with water and dried, and the solvent was removed. The residue was purified by silica gel column chromatography (solvent; chloroform: methanol (15:1)) to obtain 5.22 g of 2-propyl-aminomethyl-5-[4,5-dihydropyridazin-3(2H)-on-6-yl]indane.

Aufarbeitung

  1. stirringThe resulting mixture was stirred at the same temperature for 20 minutes
  2. stirringstirred at room temperature for 1 hour
  3. customAfter methanol was removed
  4. additionwater was added to the residue
  5. extractionthe residue was extracted with ethyl acetate
  6. filtrationThe organic layer was collected by filtration
  7. washwashed with water
  8. customdried
  9. customthe solvent was removed
  10. customThe residue was purified by silica gel column chromatography (solvent; chloroform: methanol (15:1))

Quellen und Nachweise

ORD-Eintrag
ord-6fcda02b438c4904aace4c2ad43b59e1
Quelldatensatz
uspto-grants-1997_02
Patentnummer
US05605901

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