N-[6-(苯氧基)-2,3-二氢-1H-茚-5-基]甲烷磺酰胺合成路线 (共 10 条)
反应条件
1: 50 percent / cc H2SO4, HNO3 / 1./ 0.5 h. 2./ 1 h. room temp.
2: 1./ cc H2SO4, NaNO2, acetic acid, 2./ CuBr, NaBr, 16percent HBr / 1./ water, 1 h. 3-5 deg C.
3: 82 percent / CuCl, K2CO3 / pyridine / 3 h / Heating
4: 92 percent / H2 / Raney-nickel / methanol / 4 h / 52504.2 Torr
5: 94 percent / pyridine / 1./ 3 h. 0 deg C. 2./ room temp. overnight.
View Scheme
参考文献
Schroder; Lehmann; Rufer; Bottcher
European Journal of Medicinal Chemistry, 1982 , vol. 17, # 1 p. 35 - 42
反应条件
in pyridine; chloroform
参考文献
Schering, Aktiengesellschaft
Patent: US4244960 A1, 1981 ;
反应条件
1: 92 percent / H2 / Raney-nickel / methanol / 4 h / 52504.2 Torr
2: 94 percent / pyridine / 1./ 3 h. 0 deg C. 2./ room temp. overnight.
View Scheme
参考文献
Schroder; Lehmann; Rufer; Bottcher
European Journal of Medicinal Chemistry, 1982 , vol. 17, # 1 p. 35 - 42
反应条件
1: 37 percent / HNO3 / 0.25 h / 0 - 5 °C
2: 82 percent / CuCl, K2CO3 / pyridine / 3 h / Heating
3: 92 percent / H2 / Raney-nickel / methanol / 4 h / 52504.2 Torr
4: 94 percent / pyridine / 1./ 3 h. 0 deg C. 2./ room temp. overnight.
View Scheme
参考文献
Schroder; Lehmann; Rufer; Bottcher
European Journal of Medicinal Chemistry, 1982 , vol. 17, # 1 p. 35 - 42
反应条件
1: 1./ cc H2SO4, NaNO2, acetic acid, 2./ CuBr, NaBr, 16percent HBr / 1./ water, 1 h. 3-5 deg C.
2: 82 percent / CuCl, K2CO3 / pyridine / 3 h / Heating
3: 92 percent / H2 / Raney-nickel / methanol / 4 h / 52504.2 Torr
4: 94 percent / pyridine / 1./ 3 h. 0 deg C. 2./ room temp. overnight.
View Scheme
参考文献
Schroder; Lehmann; Rufer; Bottcher
European Journal of Medicinal Chemistry, 1982 , vol. 17, # 1 p. 35 - 42
反应条件
1: 100 percent / 5n HCl / 1.5 h / Heating
2: 1./ cc H2SO4, NaNO2, acetic acid, 2./ CuBr, NaBr, 16percent HBr / 1./ water, 1 h. 3-5 deg C.
3: 82 percent / CuCl, K2CO3 / pyridine / 3 h / Heating
4: 92 percent / H2 / Raney-nickel / methanol / 4 h / 52504.2 Torr
5: 94 percent / pyridine / 1./ 3 h. 0 deg C. 2./ room temp. overnight.
View Scheme
参考文献
Schroder; Lehmann; Rufer; Bottcher
European Journal of Medicinal Chemistry, 1982 , vol. 17, # 1 p. 35 - 42
反应条件
1: 82 percent / CuCl, K2CO3 / pyridine / 3 h / Heating
2: 92 percent / H2 / Raney-nickel / methanol / 4 h / 52504.2 Torr
3: 94 percent / pyridine / 1./ 3 h. 0 deg C. 2./ room temp. overnight.
View Scheme
参考文献
Schroder; Lehmann; Rufer; Bottcher
European Journal of Medicinal Chemistry, 1982 , vol. 17, # 1 p. 35 - 42
反应条件
1: 75 percent / HNO3 / acetic acid / 2 h / Ambient temperature
2: 100 percent / 5n HCl / 1.5 h / Heating
3: 1./ cc H2SO4, NaNO2, acetic acid, 2./ CuBr, NaBr, 16percent HBr / 1./ water, 1 h. 3-5 deg C.
4: 82 percent / CuCl, K2CO3 / pyridine / 3 h / Heating
5: 92 percent / H2 / Raney-nickel / methanol / 4 h / 52504.2 Torr
6: 94 percent / pyridine / 1./ 3 h. 0 deg C. 2./ room temp. overnight.
View Scheme
参考文献
Schroder; Lehmann; Rufer; Bottcher
European Journal of Medicinal Chemistry, 1982 , vol. 17, # 1 p. 35 - 42
反应条件
pyridine
1./ 3 h. 0 deg C. 2./ room temp. overnight.;
参考文献
Schroder; Lehmann; Rufer; Bottcher
European Journal of Medicinal Chemistry, 1982 , vol. 17, # 1 p. 35 - 42
反应条件
acetic anhydride in water; acetic acid
参考文献
Schering, Aktiengesellschaft
Patent: US4244960 A1, 1981 ;