HCID 178478845, Verbindung → 1-[4-(Amidino)-2,3-dihydro-1H-inden-1-ylideneamino]-2-amino-4,5-di-hydro-imidazole dihydrochloride

HRID 357611

Reaktionsgleichung

Reaktionsgleichung von HRID 357611
[ClH:1].Cl.O[NH:4][C:5]([C:7]1[CH:15]=[CH:14][CH:13]=[C:12]2[C:8]=1[CH2:9][CH2:10][C:11]2=[N:16][N:17]1[CH2:21][CH2:20][N:19]=[C:18]1[NH2:22])=[NH:6]>[Ni].O>[ClH:1].[ClH:1].[C:5]([C:7]1[CH:15]=[CH:14][CH:13]=[C:12]2[C:8]=1[CH2:9][CH2:10][C:11]2=[N:16][N:17]1[CH2:21][CH2:20][N:19]=[C:18]1[NH2:22])(=[NH:4])[NH2:6]

Komponenten

4

Versuchsvorschrift

Analogously to Example 2, approximately 2.0 g of Raney nickel are added to a solution of 4.75 g (0.0138 mol) of 1-[4-(N-hydroxyamidino)-2,3-dihydro-1H-inden-1-ylideneamino]-2-amino-4,5-dihydro-imidazole dihydrochloride in 240 ml of water, and hydrogenation is carried out at room temperature and under normal pressure until the absorption of hydrogen has ceased. The reaction mixture is then filtered, adjusted to pH 4 with a small amount of 2N alcoholic hydrochloric acid and concentrated to dryness by evaporation. The residue is recrystallized from water, yielding the title compound in the form of the monohydrate, m.p. 280° C. (decomp.), 1H-NMR (DMSO/D2O): δ=8.17 (d, 1H); 7.66 (d, 1H); 7.54 (t, 1H); 4.18 (t, 2H); 3.70 (t, 2H); 3.25 (m, 2H); 3.13 (m, 2H).

Aufarbeitung

  1. customis carried out at room temperature and under normal pressure until the absorption of hydrogen
  2. filtrationThe reaction mixture is then filtered
  3. concentrationconcentrated to dryness by evaporation
  4. customThe residue is recrystallized from water

Quellen und Nachweise

ORD-Eintrag
ord-3d0783ad72a14ddf96c3ca397da557a8
Quelldatensatz
uspto-grants-1998_11
Patentnummer
US05840911

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