Styrene Oxide → Dimethyl 4-[2-[2-(beta-hydroxyphenethylamino)ethoxy]-5-nitrophenyl]-2,6-dimethyl-1,4-dihydropyridine-3,5-dicarboxylate

HRID 4662

Reaktionsgleichung

Reaktionsgleichung von HRID 4662
[NH2:1][CH2:2][CH2:3][O:4][C:5]1[CH:10]=[CH:9][C:8]([N+:11]([O-:13])=[O:12])=[CH:7][C:6]=1[CH:14]1[C:19]([C:20]([O:22][CH3:23])=[O:21])=[C:18]([CH3:24])[NH:17][C:16]([CH3:25])=[C:15]1[C:26]([O:28][CH3:29])=[O:27].[CH2:30]1[O:38][CH:31]1[C:32]1[CH:37]=[CH:36][CH:35]=[CH:34][CH:33]=1>CN(C)C=O>[OH:38][CH:31]([C:32]1[CH:37]=[CH:36][CH:35]=[CH:34][CH:33]=1)[CH2:30][NH:1][CH2:2][CH2:3][O:4][C:5]1[CH:10]=[CH:9][C:8]([N+:11]([O-:13])=[O:12])=[CH:7][C:6]=1[CH:14]1[C:19]([C:20]([O:22][CH3:23])=[O:21])=[C:18]([CH3:24])[NH:17][C:16]([CH3:25])=[C:15]1[C:26]([O:28][CH3:29])=[O:27]

Komponenten

4

Versuchsvorschrift

In 30 ml of N,N-dimethylformamide were dissolved 2 g of dimethyl 4-[2-(2-aminoethoxy)-5-nitrophenyl]-2,6-dimethyl-1,4-dihydropyridine-3,5-dicarboxylate and 0.6 g of styrene oxide, and the solution thus formed was allowed to stand for 2 days at room temperature. The reaction solution was concentrated under reduced pressure, and the residue was subjected to silica gel column chromatography. The product was eluted with chloroform-methanol (95:5 v/v). Crude crystals were recrystallized from ethyl acetate to give 500 mg of dimethyl 4-[2-[2-(β-hydroxyphenethylamino)ethoxy]-5-nitrophenyl]-2,6-dimethyl-1,4-dihydropyridine-3,5-dicarboxylate.

Aufarbeitung

  1. customthe solution thus formed
  2. concentrationThe reaction solution was concentrated under reduced pressure
  3. washThe product was eluted with chloroform-methanol (95:5 v/v)
  4. customCrude crystals were recrystallized from ethyl acetate

Quellen und Nachweise

ORD-Eintrag
ord-d45e5598631844f08585adfaf6246f37
Quelldatensatz
uspto-grants-1988_02
Patentnummer
US04727082

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