反応 #1519108

ord-0ca89ac5282d4a8a8d087fc9c8772636

反応方程式

Oc1cc(-c2cc(Cl)ccn2)nc(-c2ccccn2)n1
6-(4-chloropyrid-2-yl)-2-pyrid-2-yl-pyrimidin-4-ol
Cl.N=C(N)c1ccccn1
2-amidinopyridine hydrochloride
Cl.N=C(N)c1cc(Cl)ccn1
2-amidino-4-chloropyridine hydrochloride
Oc1cc(-c2cc(Cl)ccn2)nc(-c2cc(Cl)ccn2)n1
2,6-Bis(4-chloropyrid-2-yl)-pyrimidin-4-ol

反応条件

詳細条件
See reaction.notes.procedure_details.

後処理

  1. 1
    その他After recrystallisation from DMSO, 2,6-bis(4-chloropyrid-2-yl)-pyrimidin-4-ol (ligand PM5)is
  2. 2
    その他obtained in the form of a colourless solid

実験手順

The procedure is as described in the case of 6-(4-chloropyrid-2-yl)-2-pyrid-2-yl-pyrimidin-4-ol (ligand PM1) in Example 3 except that, instead of 2-amidinopyridine hydrochloride, the 2-amidino-4-chloropyridine hydrochloride from Example 8 is used. After recrystallisation from DMSO, 2,6-bis(4-chloropyrid-2-yl)-pyrimidin-4-ol (ligand PM5)is obtained in the form of a colourless solid. 1H-NMR (360 MHz, DMSO-d6): 12.53 (br s, 1H): 8.74 (d, J=5.0 Hz, 1H): 8.74 (s, 1H): 8.71 (d, J=5.0 Hz, 1H): 8.64 (d, J=2.3 Hz, 1H): 7.83 (dd, J=5.0, 2.3 Hz, 1H); 7.71 (dd, J=5.0, 2.3 Hz, 1H): 7.30 (s, 1H).

出典

DOI: 10.6084/m9.figshare.5104873.v1特許: US07612010B2uspto-grants-2009_11