Hydrochloric Acid → HCID 86755876, Verbindung

HRID 365403Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 365403
[CH3:1][O:2][C:3]1[CH:4]=[C:5]2[C:14](=[CH:15][C:16]=1[O:17][CH3:18])[C@H:13]1[C@H:8]([CH2:9][CH2:10][CH2:11][CH2:12]1)[N:7]=[C:6]2[C:19]1[CH:24]=[CH:23][C:22]([N+:25]([O-])=O)=[CH:21][CH:20]=1.Cl.O>CO.[Fe]>[CH3:1][O:2][C:3]1[CH:4]=[C:5]2[C:14](=[CH:15][C:16]=1[O:17][CH3:18])[C@H:13]1[C@H:8]([CH2:9][CH2:10][CH2:11][CH2:12]1)[N:7]=[C:6]2[C:19]1[CH:20]=[CH:21][C:22]([NH2:25])=[CH:23][CH:24]=1

Komponenten

6

Versuchsvorschrift

8.5 g of (+/-)-cis-8,9-dimethoxy-6-(4-nitrophenyl)-1,2,3,4,4a,10b-hexahydrophenanthridine are dissolved in 200 ml of methanol, and the solution is treated with 5 ml of concentrated hydrochloric acid, 20 ml of water and 800 mg of iron powder and stirred overnight at RT. The reaction mixture is filtered, the filtrate is concentrated, the residue is extracted with sodium hydrogencarbonate solution/ethyl acetate, and the organic phase is dried using sodium sulfate and concentrated. The residue is chromatographed on silica gel using a mixture of toluene/dioxane/triethylamine in the ratio 40:20:2. After concentration of the corresponding eluate fractions, 5.5 g (70.5% of theory) of the title compound of m.p. 159.5-161° C. are obtained.

Aufarbeitung

  1. filtrationThe reaction mixture is filtered
  2. concentrationthe filtrate is concentrated
  3. extractionthe residue is extracted with sodium hydrogencarbonate solution/ethyl acetate
  4. customthe organic phase is dried
  5. concentrationconcentrated
  6. customThe residue is chromatographed on silica gel using
  7. additiona mixture of toluene/dioxane/triethylamine in the ratio 40:20:2

Quellen und Nachweise

ORD-Eintrag
ord-6895fa458b574598b57bfeb2c250ff46
Quelldatensatz
uspto-grants-2000_10
Patentnummer
US06127378

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