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HCID 178487720, Verbindung → Isoxazolo(4,5-c)quinolin-3(2H)-one, 7-methoxy-2-phenyl-

HRID 280110
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Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 280110
O[N:2]([C:18]1[CH:23]=[CH:22][CH:21]=[CH:20][CH:19]=1)[C:3]([C:5]1[CH:6]=[N:7][C:8]2[C:13]([C:14]=1[OH:15])=[CH:12][CH:11]=[C:10]([O:16][CH3:17])[CH:9]=2)=[O:4]>O>[CH3:17][O:16][C:10]1[CH:11]=[CH:12][C:13]2[C:14]3[O:15][N:2]([C:18]4[CH:23]=[CH:22][CH:21]=[CH:20][CH:19]=4)[C:3](=[O:4])[C:5]=3[CH:6]=[N:7][C:8]=2[CH:9]=1
KomponentenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

3

Edukt 1

HCID 178487720HCID 178487720, Verbindung

Produkt 1

HCID 13669238Isoxazolo(4,5-c)quinolin-3(2H)-one, 7-methoxy-2-phenyl-Ausbeute 20,2 %

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 962WaterLösungsmittel

Versuchsvorschrift

Using the procedure of Step B of Example 2, 3.68 g of N,4-dihydroxy-7-methoxy-N-phenyl-3-quinoline carboxamide were reacted and after 18 hours at ambient temperature, the reaction mixture was poured into water and the products which crystallized were extracted with dichloromethane. The organic phase was washed with water and the solvent was eliminated. The residue was chromatographed on silica and eluted with a mixture of methylene chloride-ethyl acetate (9-1) to obtain 0.7 g of 7-methoxy-2-phenylisoxazolo(4,5-c)quinolin-3-(2H)-one melting at 170° C.

Aufarbeitung

  1. customwere reacted and after 18 hours at ambient temperature
  2. customthe products which crystallized
  3. extractionwere extracted with dichloromethane
  4. washThe organic phase was washed with water
  5. customThe residue was chromatographed on silica
  6. washeluted with a mixture of methylene chloride-ethyl acetate (9-1)

Quellen und Nachweise

ORD-Eintrag
ord-60f56b67aef84d349a812300cd540fd3
Quelldatensatz
uspto-grants-1986_05
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US04588731

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