Technology Process of 3-Benzyloxycarbonyl-5-(3-benzyloxypropyl)-1,2,4,5,6,7,8,9-octahydro-3H-azecino<5,4-b>indol-8-carbonsaeure
There total 12 articles about 3-Benzyloxycarbonyl-5-(3-benzyloxypropyl)-1,2,4,5,6,7,8,9-octahydro-3H-azecino<5,4-b>indol-8-carbonsaeure which
guide to synthetic route it.
The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:
synthetic route:
- Guidance literature:
-
Multi-step reaction with 9 steps
1: 97 percent / glacial acetic acid / 7 h / Heating
2: 1) aq. NaOH / 1) ethanol, 30 min, reflux, 2) 180 deg C, vacuum
3: 95 percent / LiAlH4 / tetrahydrofuran / 1.5 h / Heating
4: 70 percent / 15 percent K2CO3 / tetrahydrofuran / 3 h / Heating
5: 96 percent / 4-dimethylaminopyridine, pyridine / CH2Cl2 / 2 h / Ambient temperature
6: 91 percent / TBAB, NaI / toluene / 8 h / Heating
7: 5.41 g / NaOH, 31percent H2O2 / ethanol / 5 h / 45 °C
8: 67 percent / AmberlystR 15 / 90 h / 60 °C
9: 0.52 g / KOH / methanol / 8 h / Heating
With
pyridine; dmap; potassium hydroxide; sodium hydroxide; lithium aluminium tetrahydride; AmberlystR 15; tetrabutylammomium bromide; dihydrogen peroxide; potassium carbonate; acetic acid; sodium iodide;
In
tetrahydrofuran; methanol; ethanol; dichloromethane; toluene;
DOI:10.1016/S0040-4020(01)86686-2
- Guidance literature:
-
Multi-step reaction with 10 steps
1: 1) Na / 1) ethanol, 5 deg C, 2) 1.5 h, r.t.
2: 97 percent / glacial acetic acid / 7 h / Heating
3: 1) aq. NaOH / 1) ethanol, 30 min, reflux, 2) 180 deg C, vacuum
4: 95 percent / LiAlH4 / tetrahydrofuran / 1.5 h / Heating
5: 70 percent / 15 percent K2CO3 / tetrahydrofuran / 3 h / Heating
6: 96 percent / 4-dimethylaminopyridine, pyridine / CH2Cl2 / 2 h / Ambient temperature
7: 91 percent / TBAB, NaI / toluene / 8 h / Heating
8: 5.41 g / NaOH, 31percent H2O2 / ethanol / 5 h / 45 °C
9: 67 percent / AmberlystR 15 / 90 h / 60 °C
10: 0.52 g / KOH / methanol / 8 h / Heating
With
pyridine; dmap; potassium hydroxide; sodium hydroxide; lithium aluminium tetrahydride; AmberlystR 15; tetrabutylammomium bromide; dihydrogen peroxide; sodium; potassium carbonate; acetic acid; sodium iodide;
In
tetrahydrofuran; methanol; ethanol; dichloromethane; toluene;
DOI:10.1016/S0040-4020(01)86686-2
- Guidance literature:
-
Multi-step reaction with 9 steps
1: 97 percent / glacial acetic acid / 7 h / Heating
2: 1) aq. NaOH / 1) ethanol, 30 min, reflux, 2) 180 deg C, vacuum
3: 95 percent / LiAlH4 / tetrahydrofuran / 1.5 h / Heating
4: 70 percent / 15 percent K2CO3 / tetrahydrofuran / 3 h / Heating
5: 96 percent / 4-dimethylaminopyridine, pyridine / CH2Cl2 / 2 h / Ambient temperature
6: 91 percent / TBAB, NaI / toluene / 8 h / Heating
7: 5.41 g / NaOH, 31percent H2O2 / ethanol / 5 h / 45 °C
8: 67 percent / AmberlystR 15 / 90 h / 60 °C
9: 0.52 g / KOH / methanol / 8 h / Heating
With
pyridine; dmap; potassium hydroxide; sodium hydroxide; lithium aluminium tetrahydride; AmberlystR 15; tetrabutylammomium bromide; dihydrogen peroxide; potassium carbonate; acetic acid; sodium iodide;
In
tetrahydrofuran; methanol; ethanol; dichloromethane; toluene;
DOI:10.1016/S0040-4020(01)86686-2