Réaction #7844

ord-8d727bc8a4d84ea78c9269287c4a100c

Équation de réaction

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

Solvants

Conditions de réaction

Conditions détaillées
See reaction.notes.procedure_details.

Traitement

  1. 1
    Autrepurified by automated flash chromatography

Mode opératoire

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)+.

Source

DOI: 10.6084/m9.figshare.5104873.v1Brevet: US07087601B2uspto-grants-2006_08