Reaction #86410

ord-c197e5073e5441919dd53cab972b80f6

Solvents

Conditions

Temperature
50°CELSIUS
Detailed conditions
See reaction.notes.procedure_details.

Workup

  1. 1
    FiltrationThe reaction mixture was filtered
  2. 2
    Concentrationthe filtrate was concentrated in vacuo
  3. 3
    Otherto give crude product, which
  4. 4
    Otherwas purified by silica gel column chromatography

Procedure

A mixture of 3-(2,6-dichloro-3,5-dimethoxy-phenyl)-1-[6-(2-nitro-phenylamino)-pyrimidin-4-yl]-1-pyridin-3-ylmethyl-urea (85 g, 0.149 mmol) and Fe (84 g, 1.5 mmol) in AcOH (5 mL) was heated at 50° C. for 2 hours. The reaction mixture was filtered and the filtrate was concentrated in vacuo to give crude product, which was purified by silica gel column chromatography to afford the title compound (53 mg, yield: 66%). MS (ESI): 540 [M+H]+.

Source

DOI: 10.6084/m9.figshare.5104873.v1Patent: US09434697B2uspto-grants-2016_09