1-Acetylnaphthalene → HCID 131716463, Verbindung

HRID 2165463Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 2165463
N1(C[CH:8]2[N:13](N)[C:12]3[CH:15]=[CH:16][CH:17]=[CH:18][C:11]=3[O:10][CH2:9]2)CCOCC1.C1(C(=O)CC(=O)C)C2C(=CC=CC=2)C=CC=1.[N+](C1C=[C:40]([S:44]([OH:47])(=[O:46])=[O:45])C=CC=1)([O-])=O.N1C=CC=CC=1.C1(C(C)=O)C2C(=CC=CC=2)C=CC=1.[H-].[Na+]>CN(C=O)C.C1(C)C=CC=CC=1.C(OCC)C.C(O)C.C(OCC)(=O)C>[CH3:40][S:44]([OH:47])(=[O:46])=[O:45].[O:10]1[C:11]2[CH:18]=[CH:17][CH:16]=[CH:15][C:12]=2[N:13]=[CH:8][CH2:9]1

Komponenten

11

Versuchsvorschrift

Following a procedure similar to that described in Example 2A above, (+)-3-(4-morpholinylmethyl)-5-methyl-6-(1-naphthylcarbonyl)-2,3-dihydropyrrolo1,2,3-de]-1,4-benzoxazine methanesulfonate (11.6 g from methanol/diethyl ether), m.p. 256°-259° C., [α]D25 =+40.2° (1% in DMF) was prepared by reaction of 15.5 g (0.062 mole) of (+)-3-(4-morpholinylmethyl)-4-amino-3,4-dihydro-2H-1,4-benzoxazine with 15.8 g (0.075 mole) of 4-(1-naphthyl)-2,4-butanedione in 500 ml of toluene in the presence of a catalytic amount of pyridine 3-nitrobenzenesulfonate (the 2,4-diketone being prepared by reaction of methyl 1-naphthyl ketone with ethyl acetate in the presence of sodium hydride and ethanol in diethyl ether), followed by cyclization of the resulting hydrazone by refluxing the latter in 300 ml of glacial acetic acid and recrystallization of the product from methanol/diethyl ether.

Aufarbeitung

  1. temperatureby refluxing the
  2. customlatter in 300 ml of glacial acetic acid and recrystallization of the product from methanol/diethyl ether

Quellen und Nachweise

ORD-Eintrag
ord-c1405c4c4c02403bb4c0ca281cf1a4f7
Quelldatensatz
uspto-grants-1990_07
Patentnummer
US04939138

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