Ethyl (3R,8Ar)-5-(4-Nitrophenyl)-3-Phenyl-3,7,8,8A-Tetrahydro-2H-Oxazolo[3,2-A]Pyridine-6-Carboxylate置于硫酸,Palladium 10% On Activated Carbon,氢气,Potassium Carbonate,溶剂黄146,甲基磺酰氯,N,N-二异丙基乙胺体系中,用 乙醇,二氯甲烷,甲基叔丁基醚,水 用作溶剂,95.0 °C,379.22 Kpa 条件下,反应 115.5H,反应生成(2R,3S)-2-[4-(环戊基氨基)苯基]-1-(2-氟-6-甲基苯甲酰基)-N-[4-甲基3-(三氟甲基)苯基]哌啶-3-甲酰胺
参考文献:Processes And Intermediates In The Preparation Of C5Ar Antagonists
标题:Processes And Intermediates In The Preparation Of C5Ar Antagonists
摘要:提供了中间体和方法,用于制备选择的c5Ar拮抗剂化合物.