Reaktion #7844

ord-8d727bc8a4d84ea78c9269287c4a100c

Reaktionsgleichung

C1CCNC1
Pyrrolidine
COc1cc(-c2nc3ccccc3o2)ccc1CBr
2-[4-(bromomethyl)-3-methoxyphenyl]-1,3-benzoxazole
CCN(CC)CC
triethylamine
COc1cc(-c2nc3ccccc3o2)ccc1CN1CCCC1
2-[3-methoxy-4-(pyrrolidin-1-ylmethyl)phenyl]-1,3-benzoxazole

Lösungsmittel

Reaktionsbedingungen

Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    Sonstigepurified by automated flash chromatography

Vorschrift

Pyrrolidine (226 μL, 2.83 mmol) was added to a stirring solution of 2-[4-(bromomethyl)-3-methoxyphenyl]-1,3-benzoxazole (300 mg, 0.94 mmol) and triethylamine (390 μL, 2.8 mmol) in CH2Cl2 (5 mL). The mixture was stirred at rt overnight. Crude mixture was adsorbed onto silica gel and purified by automated flash chromatography using an EtOAc/hexanes gradient to afford the desired 2-[3-methoxy-4-(pyrrolidin-1-ylmethyl)phenyl]-1,3-benzoxazole as a colorless solid: 1H NMR (CDCl3, 300 MHz) δ 7.82–7.80 (m, 1H), 7.77–7.74 (m, 1H), 7.71 (s, 1H), 7.56–7.50 (m, 2H), 7.35–7.30 (m, 2H), 3.94 (s, 3H), 3.71 (s, 2H), 2.59 (s, 4H), 1.81–1.78 (m, 4H). MS (ESI) 309 (M+H)+.

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US07087601B2uspto-grants-2006_08