1,3-Propanediamine → HCID 57718193, Verbindung

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 (1H, s, py); 6.77 (1H, s, py); 4.50 (2H, br s, NH2); 4.24 (2H, t, OCH2); 1.72 (2H, m, OCH2CH2); 1.32 (4H, m, OCH2CH2CH2CH2CH3); 0.81 (3H, t, CH2CH3).

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

ORD-Eintrag

ord-841c0deeed134f70a93dd59be0f96402

Quelldatensatz

uspto-grants-2009_06

DOI

10.6084/m9.figshare.5104873.v1

Patentnummer

US07544702B2