Technology Process of 2-[2-(p-t-butoxycarbonylphenyl)ethyl amino]-adenosine
There total 6 articles about 2-[2-(p-t-butoxycarbonylphenyl)ethyl amino]-adenosine 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
N-ethyl-N,N-diisopropylamine;
In
i-Amyl alcohol;
at 140 ℃;
for 48h;
DOI:10.1021/jm00112a035
- Guidance literature:
-
Multi-step reaction with 4 steps
1: 5 g / palladium acetate, tri-o-tolylphosphine, N,N-diisopropylethylamine / acetonitrile / 90 °C
2: 5 g / H2 / 10percent Pd/C / ethanol; tetrahydrofuran / 2585.7 Torr
3: hydrazine hydrate / ethanol / 1.5 h / 80 °C
4: 68 percent / N,N-diisopropylethylamine / 3-methyl-butan-1-ol / 48 h / 140 °C
With
hydrogen; palladium diacetate; hydrazine hydrate; N-ethyl-N,N-diisopropylamine; tris-(o-tolyl)phosphine;
palladium on activated charcoal;
In
tetrahydrofuran; ethanol; i-Amyl alcohol; acetonitrile;
DOI:10.1021/jm00112a035
- Guidance literature:
-
Multi-step reaction with 3 steps
1: 5 g / H2 / 10percent Pd/C / ethanol; tetrahydrofuran / 2585.7 Torr
2: hydrazine hydrate / ethanol / 1.5 h / 80 °C
3: 68 percent / N,N-diisopropylethylamine / 3-methyl-butan-1-ol / 48 h / 140 °C
With
hydrogen; hydrazine hydrate; N-ethyl-N,N-diisopropylamine;
palladium on activated charcoal;
In
tetrahydrofuran; ethanol; i-Amyl alcohol;
DOI:10.1021/jm00112a035
