반응 #7288

ord-42e2736d1d544ffaa239652e6a28183b

용매

반응 조건

상세 조건
See reaction.notes.procedure_details.

후처리

  1. 1
    기타The catalyst was removed by filtration
  2. 2
    농축the filtrate was concentrated

실험 절차

A solution of (4-hydroxymethyl-benzyl)-(3-hydroxy-pyridin-2-ylmethyl)-carbamic acid tert-butyl ester (0.99 g, 2.9 mmol) in CH2Cl2 (14 mL) was stirred at room temperature with a suspension of 85% MnO2 (3.0 g, 29 mmol) for 15 hours. The catalyst was removed by filtration, and the filtrate was concentrated to give orange crystals (818 mg, 83%). 1H NMR (CDCl3) □ 1.44 (s, 9H), 4.54 (s, 2H), 4.61 (s, 2H), 7.17 (dd, 1H, J=8.1, 4.5 Hz), 7.26 (dd, 1H, J=8.1, 1.5 Hz), 7.37 (d, 2H, J=8.1 Hz), 7.84 (d, 2H, J=8.1 Hz), 8.03 (dd, 1H, J=4.5, 1.2 Hz), 9.55 (s, 1H), 10.00 (s, 1H).

출처

DOI: 10.6084/m9.figshare.5104873.v1특허: US07084155B2uspto-grants-2006_08