Reaktion #58061

ord-d9c1a501838d44b187f008901b681277

Reaktionsgleichung

O=C(O)c1cc2cc(F)ccc2[nH]1
5-fluoro-1H-indole-2-carboxylic acid
CCN=C=NCCCN(C)C
EDCI
NCCCO
3-amino-propan-1-ol
O=C(NCCCO)c1cc2cc(F)ccc2[nH]1
5-fluoro-1H-indole-2-carboxylic acid (3-hydroxy-propyl)-amide

Lösungsmittel

Reaktionsbedingungen

Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    SonstigeAfter the solvent is removed under vacuum, 5% HCl (100 mL)
  2. 2
    workup.ADDITIONis added to the mixture
  3. 3
    ExtraktionIt is extracted with EtOAc (100 mL×3)
  4. 4
    WaschenThe combined organic layers are washed with saturated aqueous NaHCO3 (100 mL), brine (100 mL)
  5. 5
    Trocknendried with Na2SO4
  6. 6
    SonstigeSolvent is removed

Vorschrift

To a solution of 5-fluoro-1H-indole-2-carboxylic acid (2.27 g, 12.7 mmol) in CH2Cl2 (100 mL) is added DMAP (4.64 g, 38 mmol), EDCI (3.64 g, 19 mmol), 3-amino-propan-1-ol (1.90 g, 25 mmol). The mixture is stirred at room temperature for 24 hours. After the solvent is removed under vacuum, 5% HCl (100 mL) is added to the mixture. It is extracted with EtOAc (100 mL×3). The combined organic layers are washed with saturated aqueous NaHCO3 (100 mL), brine (100 mL) and dried with Na2SO4. Solvent is removed to give 5-fluoro-1H-indole-2-carboxylic acid (3-hydroxy-propyl)-amide; 1H NMR (DMSO-d6) δ 1.69 (quint, 2H, J=6.4 Hz), 3.34 (q, 2H, J=6.0 Hz), 3.48 (t, 2H, J=6.4 Hz), 4.48 (bs, 1H), 6.99-7.10 (m, 2H), 7.36-7.44 (m, 2H), 8.47 (t, 1H, J=5.6 Hz), 11.63 (s, 1H); m/z [M++1] 237.1.

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US07423031B2uspto-grants-2008_09