反应条件
1: 72 percent / p-toluenesulfonic acid / CH2Cl2 / 2 h / Ambient temperature
2: 17 percent / aq. NH4OH / methanol; tetrahydrofuran / 168 h / Ambient temperature
3: 1.) pyridine, 2.) 2 N aq. HCl / 1.) CH2Cl2, RT, 16 h, 2.) aq. EtOH, RT, 22 h
View Scheme
参考文献
Kaneko; Schmitz; Essery; Rose; Howell; O'Herron; Nachfolger; Huftalen; Bradner; Partyka; Doyle; Davies; Cundliffe
Journal of Medicinal Chemistry, 1982 , vol. 25, # 5 p. 579 - 589