Technology Process of Ergoline-8-methanol, 8,9-didehydro-6-methyl-
There total 6 articles about Ergoline-8-methanol, 8,9-didehydro-6-methyl- 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:
-
With
indole; benzeneseleninic anhydride;
In
tetrahydrofuran;
at 40 ℃;
for 1.5h;
-
-
84936-67-4,84986-20-9,98633-52-4
(3aβ,5aβ,6aβ,11bα,11cβ)-8-benzoyl-5,5a,6,6a,7,8,11b,11c-octahydro-5-methylfuro<3,2-c>indolo<4,3-fg>quinolin-4(3aH)-one
- Guidance literature:
-
Multi-step reaction with 5 steps
1: 1) ozone, 2) LiAlH4 / 1) CHCl3, 2) diethylether, THF, 2 h, reflux
2: 89 percent / pyridine / 0 °C
3: 18 percent / SOCl2 / benzene / 1 h / Heating
4: 66 percent / conc. HCl / methanol / Heating
5: 94 percent / benzeneseleninic anhydride, indole / tetrahydrofuran / 1.5 h / 40 °C
With
pyridine; indole; hydrogenchloride; lithium aluminium tetrahydride; thionyl chloride; benzeneseleninic anhydride; ozone;
In
tetrahydrofuran; methanol; benzene;
- Guidance literature:
-
Multi-step reaction with 5 steps
1: 90 percent / H2, 10percent aq. HCl, 70percent HClO4 / 40percent Pd/C / 4 h / 3420 Torr
2: 89 percent / pyridine / 0 °C
3: 18 percent / SOCl2 / benzene / 1 h / Heating
4: 66 percent / conc. HCl / methanol / Heating
5: 94 percent / benzeneseleninic anhydride, indole / tetrahydrofuran / 1.5 h / 40 °C
With
pyridine; indole; hydrogenchloride; thionyl chloride; perchloric acid; benzeneseleninic anhydride; hydrogen;
palladium on activated charcoal;
In
tetrahydrofuran; methanol; benzene;