تفاعل #1616417
ord-45c2a7f397d545a6b7606fd69a53b666
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 (0.28 mmol) 4-[3-(6-Amino-pyridin-3-ylethynyl)-2-ethyl-pyridin-4-yl]-2-fluoro-benzoic acid (A-38) using 38 mg (0.33 mmoL) N-ethyl 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/MeOH-gradient. Yield: 36 mg (28%).