5-(甲基磺酰基)-3-呋喃戊糖基-3H-[1,2,3]三唑并[4,5-d]嘧啶-7-胺合成路线 (共 5 条)
反应条件
1: 1.) p-toluenesulfonic acid, 2.) ethanolic NH3 / 1.) a) RT, 10 min, b) 120 deg C, 15 min, 2.) 90 deg C, 16 h
2: 89 percent / m-chloroperoxybenzoic acid / ethanol / 19 h / Ambient temperature
View Scheme
参考文献
Montgomery, John A.; Shortnacy, Anita T.; Secrist, John A.
Journal of Medicinal Chemistry, 1983 , vol. 26, # 10 p. 1483 - 1489
反应条件
ammonia; toluene-4-sulfonic acid; 3-chloro-benzenecarboperoxoic acid
Multistep reaction;
参考文献
Montgomery, John A.; Shortnacy, Anita T.; Secrist, John A.
Journal of Medicinal Chemistry, 1983 , vol. 26, # 10 p. 1483 - 1489
反应条件
ammonia
48 h; Ambient temperature;
参考文献
Montgomery, John A.; Shortnacy, Anita T.; Secrist, John A.
Journal of Medicinal Chemistry, 1983 , vol. 26, # 10 p. 1483 - 1489
反应条件
ammonia
48 h; Ambient temperature;
参考文献
Montgomery, John A.; Shortnacy, Anita T.; Secrist, John A.
Journal of Medicinal Chemistry, 1983 , vol. 26, # 10 p. 1483 - 1489
反应条件
1: 85 percent / NH3 / 48 h / Ambient temperature
2: 21 percent / 48percent aq. HBF4, KNO2 / 1 h / 5 °C
View Scheme
参考文献
Montgomery, John A.; Shortnacy, Anita T.; Secrist, John A.
Journal of Medicinal Chemistry, 1983 , vol. 26, # 10 p. 1483 - 1489