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Methanol → HCID 14989569, Verbindung

HRID 1590865
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 1590865
[CH3:1][O-:2].[Na+].Cl.[NH2:5][C:6]1([C:12]2[CH:13]=[CH:14][C:15](=[O:18])[NH:16][CH:17]=2)[CH2:11][CH2:10][CH2:9][CH2:8][CH2:7]1.[CH3:19]O>>[O:18]=[C:15]1[NH:16][CH:17]=[C:12]([C:6]2([NH:5][C:1](=[O:2])[CH3:19])[CH2:7][CH2:8][CH2:9][CH2:10][CH2:11]2)[CH:13]=[CH:14]1
KomponentenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

4

Edukt 3

HCID 887MethanolHCID 10942334Sodium MethoxideHCID 19768457HCID 19768457, Verbindung

Produkt 1

HCID 14989569HCID 14989569, Verbindung

Versuchsvorschrift

Sodium methoxide solution (25% in methanol, 6 ml) was added to a suspension of 5-(1-aminocyclohexyl)-2(1H)-pyridinone hydrochloride (6.0 g) in 100 ml of methanol, and the mixture was stirred at room temperature for 10 minutes. The solvent was removed in vacuo, and the residual solids were suspended in 260 ml of dichloromethane. Poly-4-vinylpyridine (5.42 g), acetic anhydride (2.67 g) and a catalytic amount of 4-(N,N-dimethylamino)pyridine were added, and the mixture was stirred at room temperature for 2 hours. The suspension was filtered and the solid residue was washed with methanol. The filtrate was concentrated, leaving 4.9 g of solid. Recrystallization from methanol gave 1.69 g of product (m.p. 238°-242° C. dec) in two crops, each of which was analytically pure.

Aufarbeitung

  1. customThe solvent was removed in vacuo
  2. additionPoly-4-vinylpyridine (5.42 g), acetic anhydride (2.67 g) and a catalytic amount of 4-(N,N-dimethylamino)pyridine were added
  3. stirringthe mixture was stirred at room temperature for 2 hours
  4. filtrationThe suspension was filtered
  5. washthe solid residue was washed with methanol
  6. concentrationThe filtrate was concentrated

Quellen und Nachweise

ORD-Eintrag
ord-4a1882f0a55c46caa3baac4938eac980
Quelldatensatz
uspto-grants-1993_04
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US05204480

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