3-氨基-5-甲硫基-1H-1,2,4-三唑合成路线 （共 33 条）
反应条件
benzyl halide; sodium hydride in N,N-dimethyl-formamide
T=50°C; Heatingother temp.; Product distribution;
参考文献
Reiter, J.; Somorai, T.; Dvortsak, P.; Bujtas, Gy.
Journal of Heterocyclic Chemistry, 1985 , vol. 22, p. 385 - 394
反应条件
sodium hydride
1) toluene, DMF, 0 deg C, 0.5 h, 2) 0 deg C, 3 h, r.t.; Yield given. Multistep reaction. Yields of byproduct given;
参考文献
Reiter, J.; Somorai, T.; Dvortsak, P.; Bujtas, Gy.
Journal of Heterocyclic Chemistry, 1985 , vol. 22, p. 385 - 394
反应条件
sodium hydride
1) toluene, DMF, 0 deg C, 0.5 h, 2) 0 deg C, 3 h, r.t.; Yield given. Multistep reaction. Yields of byproduct given;
参考文献
Reiter, J.; Somorai, T.; Dvortsak, P.; Bujtas, Gy.
Journal of Heterocyclic Chemistry, 1985 , vol. 22, p. 385 - 394
反应条件
benzyl halide; sodium hydride in N,N-dimethyl-formamide
T=50°C; Heatingother temp.; Product distribution;
参考文献
Reiter, J.; Somorai, T.; Dvortsak, P.; Bujtas, Gy.
Journal of Heterocyclic Chemistry, 1985 , vol. 22, p. 385 - 394
反应条件
sodium hydride
1) toluene, DMF, 0 deg C, 0.5 h, 2) 0 deg C, 3 h, r.t.; Yield given. Multistep reaction. Yields of byproduct given;
参考文献
Reiter, J.; Somorai, T.; Dvortsak, P.; Bujtas, Gy.
Journal of Heterocyclic Chemistry, 1985 , vol. 22, p. 385 - 394
反应条件
sodium hydride
1) toluene, DMF, 0 deg C, 0.5 h, 2) 0 deg C, 3 h, r.t.; Yield given. Multistep reaction. Yields of byproduct given;
参考文献
Reiter, J.; Somorai, T.; Dvortsak, P.; Bujtas, Gy.
Journal of Heterocyclic Chemistry, 1985 , vol. 22, p. 385 - 394
反应条件
sodium hydride
1) toluene, DMF, 0 deg C, 0.5 h, 2) 0 deg C, 3 h, r.t.; Yield given. Multistep reaction. Yields of byproduct given;
参考文献
Reiter, J.; Somorai, T.; Dvortsak, P.; Bujtas, Gy.
Journal of Heterocyclic Chemistry, 1985 , vol. 22, p. 385 - 394
反应条件
in acetic acid
5 h; Heating;
参考文献
Reiter; Pongo; Dvortsak
Journal of Heterocyclic Chemistry, 1987 , vol. 24, # 4 p. 1149 - 1154
参考文献
Reiter, Jozsef; Pongo, Laszlo; Dvortsak, Peter
Journal of Heterocyclic Chemistry, 1987 , vol. 24, p. 127 - 142
参考文献
Allen et al.
Journal of Organic Chemistry, 1959 , vol. 24, p. 787,792
