反应条件
1: 86 percent / ammonia, methanol / 10 h / Ambient temperature 2: 78 percent / 2 M oxalyl chloride, dimethyl sulfoxide, triethylamine / CH2Cl2 / -60 °C 3: 97 percent / p-toluenesulfonic acid / benzene / 4 h / Heating 4: 91 percent / sodium hydroxide, water / tetrahydrofuran / 4 h / 24 °C 5: 70 percent / pyridine, chromium trioxide / CH2Cl2 / 0.5 h / 23 °C 6: 1) sodium methylsulfinylmethide / 1) dimethyl sulfoxide, tetrahydrofuran, 0 deg C, 2 min, 2) tetrahydrofuran, 0 deg C, 30 min, then 25 deg C, 1 h 7: 51 percent / benzene; methanol / 16 h / Heating 8: 84 percent / hydrogen, triethylamine / 5 percent palladium on carbon / ethanol / 775.7 Torr 9: hydrochloric acid / methanol View Scheme
参考文献
Weerawarna; Guha-Biswas; Nelson
Journal of Heterocyclic Chemistry, 1991 , vol. 28, # 5 p. 1395 - 1403