تفاعل #1616425

ord-465472e6fe1b4ab6b7b6dae9235acdde

المذيبات

ظروف التفاعل

الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    أخرىAfter completion of the reaction
  2. 2
    ترشيحthe reaction mixture is filtered
  3. 3
    أخرىthe product is isolated from the obtained solution by RP-HPLC

الإجراء التجريبي

The title compound is synthesized according to general procedure GP5 starting from 100 mg (0.28 mmol) 4-[3-(6-Amino-pyridin-3-ylethynyl)-2-ethyl-pyridin-4-yl]-2-fluoro-benzoic acid (A-38) using 46 mg (0.36 mmoL) N-acetyl piperazine, 116 mg (0.30 mmol) HATU and 81 μL DIPEA in 1 mL DMF. After completion of the reaction, the reaction mixture is filtered and the product is isolated from the obtained solution by RP-HPLC using a H2O/ACN-gradient. Yield: 69 mg (53%).

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US09090564B2uspto-grants-2015_07