반응 #41512

ord-1391e643d8c940e99a991612b0e29915

반응 방정식

O=Cc1ccccn1
pyridine-2-carboxaldehyde
O=[N+]([O-])c1ccccc1
nitrobenzene
Nc1cc(Oc2cccnc2)c(Oc2cccnc2)cc1N
4,5-bis(pyridin-3-yloxy)-benzene-1,2-diamine
c1ccc(-c2nc3cc(Oc4cccnc4)c(Oc4cccnc4)cc3[nH]2)nc1
2-pyridin-2-yl-5,6-bis(pyridin-3-yloxy)-1H-benzimidazole

반응 조건

상세 조건
See reaction.notes.procedure_details.

후처리

  1. 1
    기타the reaction liquid
  2. 2
    기타The reaction mixture was purified through reversed-phase middle-pressure liquid chromatography [ODS-AS-360-CC (by YMC), mobile phase: water-acetonitrile-0.1% trifluoroacetic acid]
  3. 3
    기타The solvent of the resulting fraction was evaporated away under reduced pressure
  4. 4
    기타this was purified
  5. 5
    기타through partitioning thin-layer chromatography (Kieselgel™ 60F254, Art 5744 (by Merck), chloroform/methanol=20/1)
  6. 6
    기타to obtain the entitled compound as a yellow oily substance

실험 절차

0.01 ml of pyridine-2-carboxaldehyde was added to a nitrobenzene (0.3 ml) solution of 30 mg of 4,5-bis(pyridin-3-yloxy)-benzene-1,2-diamine at 120° C., and the reaction liquid was stirred at the same temperature for 2 hours. The reaction mixture was purified through reversed-phase middle-pressure liquid chromatography [ODS-AS-360-CC (by YMC), mobile phase: water-acetonitrile-0.1% trifluoroacetic acid]. The solvent of the resulting fraction was evaporated away under reduced pressure, and this was purified through partitioning thin-layer chromatography (Kieselgel™ 60F254, Art 5744 (by Merck), chloroform/methanol=20/1) to obtain the entitled compound as a yellow oily substance.

출처

DOI: 10.6084/m9.figshare.5104873.v1특허: US07728025B2uspto-grants-2010_06