Reaktion #1383377

ord-6abc1cb076a7426eaa6a68c2012b415d

Reaktionsgleichung

COC(=O)c1cc(N)cc(C(=O)OC)c1
5-Amino-1,3-benzenedicarboxylic acid dimethyl ester
NC(CO)CO
2-amino-1,3-dihydroxypropane
Nc1cc(C(=O)NC(CO)CO)cc(C(=O)NC(CO)CO)c1
5-amino-N,N′-bis[2-hydroxy-1-(hydroxymethyl)ethyl]-1,3-benzenedicarboxamide
Ausbeute 90.0%

Lösungsmittel

Reaktionsbedingungen

Temperatur
105°CELSIUS
Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    Sonstigeequipped with a mechanical stirrer
  2. 2
    Temperaturis maintained at this temperature for 150 minutes
  3. 3
    Sonstigeto yield a solution
  4. 4
    TemperaturAfter cooling to 50° C.
  5. 5
    Temperaturthe obtained suspension is maintained for 4 hours at room temperature
  6. 6
    FiltrationThe solid that separates is filtered
  7. 7
    Waschenwashed with methanol (0.3 L)
  8. 8
    Sonstigedried in the oven at 45° C. for 4 hours
  9. 9
    Sonstigeyielding the compound of the title (56.3 g, 0.172 mol, yield: 90%)

Vorschrift

5-Amino-1,3-benzenedicarboxylic acid dimethyl ester (40.0 g, 191 mmol) and 2-amino-1,3-dihydroxypropane (104.5 g, 1.147 mol) are loaded into a 1 L vessel equipped with a mechanical stirrer, a thermometer and a refluxing refrigerator. The suspension is heated up to 105° C., and is maintained at this temperature for 150 minutes to yield a solution. After cooling to 50° C., methanol (0.7 L) is added and the obtained suspension is maintained for 4 hours at room temperature. The solid that separates is filtered, washed with methanol (0.3 L), and dried in the oven at 45° C. for 4 hours yielding the compound of the title (56.3 g, 0.172 mol, yield: 90%).

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US07244864B2uspto-grants-2007_07