1,3-Propanediamine → HCID 57718193, Verbindung

HRID 1366821Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 1366821
[CH3:1][O:2][C:3](=[O:12])[C:4]1[C:9](Br)=[CH:8][N:7]=[C:6]([NH2:11])[CH:5]=1.[I-:13].[Na+].NC[CH2:17][CH2:18]N.C(O[CH2:24][CH3:25])(=O)C>C(O)CCCC.[Cu](I)I>[CH2:1]([O:2][C:3](=[O:12])[C:4]1[C:9]([I:13])=[CH:8][N:7]=[C:6]([NH2:11])[CH:5]=1)[CH2:17][CH2:18][CH2:24][CH3:25]

Komponenten

7

Versuchsvorschrift

2-amino-5-bromo-isonicotinic acid methyl ester (1.79 g, 7.75 mmol) was added to a stirred mixture of copper iodide (145 mg, 0.76 mmol), sodium iodide (2.36 g, 15.73 mmol) and 1,3-diaminopropane (0.13 ml, 1.55 mmol) in n-pentanol (20 ml) and heated to reflux overnight. The reaction was cooled to room temperature, ethyl acetate (100 ml) added and washed with NaHCO3 solution (50 ml) and brine (50 ml) before being dried (MgSO4) and concentrated under reduced pressure. The residue was purified by flash column chromatography using ethyl acetate 1/4 hexane as eluent to afford 2-amino-5-iodo-isonicotinic acid pentyl ester as a yellow solid (1.51 g, 58%). 1H NMR (CDCl3): 8.36 (1 H, s, py); 6.77 (1 H, s, py); 4.50 (2 H, br s, NH2); 4.24 (2 H, t, OCH2); 1.72 (2 H, m, OCH2CH2); 1.32 (4 H, m, OCH2CH2CH2CH2CH3); 0.81 (3 H, t, CH2CH3).

Aufarbeitung

  1. temperatureheated
  2. temperatureto reflux overnight
  3. washwashed with NaHCO3 solution (50 ml) and brine (50 ml)
  4. dry with materialbefore being dried (MgSO4)
  5. concentrationconcentrated under reduced pressure
  6. customThe residue was purified by flash column chromatography

Quellen und Nachweise

ORD-Eintrag
ord-0b145ad523ed42d09a276ce2f8de7648
Quelldatensatz
uspto-grants-2011_02
Patentnummer
US07893077B2

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