تفاعل #515715
ord-1234166dc00344a789f5f352bdf2b2ae
معادلة التفاعل
الكواشف
المذيبات
ظروف التفاعل
المعالجة
- 1درجة الحرارةwere heated
- 2درجة الحرارةat reflux under N2 for 3 hours
- 3ترشيحthe reaction was filtered through celite
- 4غسيلwashing with excess methanol
- 5تركيزThe filtrate was concentrated
- 6workup.ADDITIONdiluted with CH2Cl2 (50 mL)
- 7غسيلwashed with saturated aqueous NaHCO3
- 8استخلاصThe aqueous layer was extracted with CH2Cl2 (2×50 mL)
- 9تجفيفThe combined organic layers were dried over anhydrous sodium sulfate
- 10ترشيحfiltered
- 11تركيزconcentrated in vacuo
الإجراء التجريبي
A mixture of 1-benzyl-4-(6-methoxy-2-methylquinolin-8-yl)piperazine (0.527 g, 1.52 mmol), 10% Pd/C (0.20 g), and ammonium formate (0.96 g, 15.2 mmol) in methanol (10 mL) were heated at reflux under N2 for 3 hours. TLC analysis (35% EtOAc/hexane) indicated only a trace of starting material remained. After cooling to room temperature, the reaction was filtered through celite, washing with excess methanol. The filtrate was concentrated, diluted with CH2Cl2 (50 mL), and washed with saturated aqueous NaHCO3. The aqueous layer was extracted with CH2Cl2 (2×50 mL). The combined organic layers were dried over anhydrous sodium sulfate, filtered, and concentrated in vacuo to afford 0.37 g (95%) of the title compound as a yellow oil, which was used in the subsequent reaction without purification.