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Piperidine → 8-Fluoro-3-hydroxy-1-methyl-4-quinolone

HRID 358674
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 358674
C([O:9][C:10]1[C:19](=[O:20])[C:18]2[C:13](=[C:14]([F:21])[CH:15]=[CH:16][CH:17]=2)[N:12]([CH3:22])[CH:11]=1)(=O)C1C=CC=CC=1.N1CCCCC1>ClCCl>[F:21][C:14]1[CH:15]=[CH:16][CH:17]=[C:18]2[C:13]=1[N:12]([CH3:22])[CH:11]=[C:10]([OH:9])[C:19]2=[O:20]
KomponentenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

4

Edukt 2

HCID 8082Piperidine2×HCID 544988888-Fluoro-1-methyl-4-oxo-1,4-dihydroquinol-3-yl benzoate

Produkt 1

HCID 231281098-Fluoro-3-hydroxy-1-methyl-4-quinolone

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 6344DichloromethaneLösungsmittel

Versuchsvorschrift

A mixture of 8-fluoro-1-methyl-4-oxo-1 ,4-dihydro-quinol-3-yl benzoate (10 g), piperidine (3.18 g) and dichloromethane (200 ml) was stirred for 24 hours, a further portion of piperidine (1.7 ml) was added and the stirring continued for a further 24 hours. The solvent was removed by distillation and the residue was triturated with diethyl ether (300 ml). The resultant solid was extracted with aqueous sodium hydroxide (0.1 M, 100 ml) and the extract was neutralised with hydrochloric acid (5M, 2 ml). The resultant precipitate was collected by filtration to give the novel compound 8-fluoro-3-hydroxy-1 -methyl-4-quinolone, m.p. 248°.

Aufarbeitung

  1. waitthe stirring continued for a further 24 hours
  2. customThe solvent was removed by distillation
  3. customthe residue was triturated with diethyl ether (300 ml)
  4. extractionThe resultant solid was extracted with aqueous sodium hydroxide (0.1 M, 100 ml)
  5. filtrationThe resultant precipitate was collected by filtration

Quellen und Nachweise

ORD-Eintrag
ord-f9b726113c9b44cd958e86b9b0386765
Quelldatensatz
uspto-grants-1991_03
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US04997840

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