반응 #7844

ord-8d727bc8a4d84ea78c9269287c4a100c

반응 방정식

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

용매

반응 조건

상세 조건
See reaction.notes.procedure_details.

후처리

  1. 1
    기타purified by automated flash chromatography

실험 절차

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)+.

출처

DOI: 10.6084/m9.figshare.5104873.v1특허: US07087601B2uspto-grants-2006_08