Reaktion #70581

ord-19e4ce7f9b13484ca7fa92967721689b

Reaktionsbedingungen

Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    SonstigeThe title compound was prepared by the method

Vorschrift

The title compound was prepared by the method described in Example 1, Step D, except that 5-(1-benzyl-5-phenyl-1H-imidazol-2-yl)-2-phenylpyrimidine (this Example, Step B) was used instead of 5-(1-benzyl-2-phenyl-1H-imidazol-5-yl)-2-phenylpyrimidine. The title compound was isolated as a white solid (0.044 g, 62% yield); Rf 0.26 with 95:5 v/v dichloromethane-methanol; melting point 238° C.; 1H-NMR (400 MHz; DMSO-d6) δ 9.40 (s, 2H), 8.43 (m, 2H), 7.99-7.84 (m, 2H), 7.58-7.20 (m, 8H); MS (ESI+) m/z 299.1 (M+1); H-PGDS FPBA IC50: 2.8 μM.

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US08536185B2uspto-grants-2013_09