تفاعل #1616424
ord-6e7ad02202e8407c94ba815f34ed26e1
معادلة التفاعل
المتفاعلات
الكواشف
لا شيء
ظروف التفاعل
الظروف التفصيلية
See reaction.notes.procedure_details.
المعالجة
- 1أخرىAfter completion of the reaction
- 2ترشيحthe reaction mixture is filtered
- 3أخرىthe 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 (0.27 mmol) 4-[2-Ethyl-3-(6-methylamino-pyridin-3-ylethynyl)-pyridin-4-yl]-2-fluoro-benzoic acid (A-46) using 68 mg (0.40 mmoL) tetrahydro-pyran-4-yl piperazine, 101 mg (0.27 mmol) HATU and 50 μL DIPEA in 1.5 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: 59 mg (42%).