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Methane → HCID 19867724, Verbindung

HRID 1198944
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 1198944
[CH3:1][C:2]1[C:11]2[C:6](=[C:7]([CH3:13])[CH:8]=[C:9]([NH2:12])[CH:10]=2)[NH:5][C:4](=[O:14])[CH:3]=1.C>C(O)C>[CH3:1][CH:2]1[C:11]2[C:6](=[C:7]([CH3:13])[CH:8]=[C:9]([NH2:12])[CH:10]=2)[NH:5][C:4](=[O:14])[CH2:3]1
KomponentenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

4

Edukt 2

HCID 297MethaneHCID 198677256-Amino-4,8-dimethyl-2(1H)-quinolinone

Produkt 1

HCID 19867724HCID 19867724, Verbindung

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 702EthanolLösungsmittel

Versuchsvorschrift

A suspension of 4-methyl-6-amino-8-methyl-2-(1H)-quinolone (0.38 g) in absolute ethanol (50 cm3) was hydrogenated at 100° and 2000 p.s.i. (13.7×106Pa) pressure over 10% palladised charcoal (0.05 g) for 72 hours. The cooled solution was then filtered through "Solkafloc" (Trade mark for a cellulose-base filtering aid) and evaporated in vacuo to give a solid which was chromtographed on silica (Merck "MK 60.9385" [Trade Mark]) eluting with methanol:chloroform, 1:50 by volume. Combination and evaporation of appropriate fractions gave a residue which on trituration with ethyl acetate afforded the title compound, m.p. 207°-10°, (0.22 g).

Aufarbeitung

  1. customwas hydrogenated at 100°
  2. filtrationThe cooled solution was then filtered through "Solkafloc" (Trade mark for a cellulose-base
  3. filtrationfiltering aid) and
  4. customevaporated in vacuo
  5. customto give a solid which
  6. washeluting with methanol
  7. customCombination and evaporation of appropriate fractions
  8. customgave a residue which on trituration with ethyl acetate

Quellen und Nachweise

ORD-Eintrag
ord-b515485c515f42048d12646d4f660d01
Quelldatensatz
uspto-grants-1990_02
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US04898872

Notizen zur Reaktion

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