Technology Process of Inosine, 1-[(2-methoxyethoxy)methyl]-8-(4-methoxyphenyl)-,
2',3',5'-triacetate
There total 5 articles about Inosine, 1-[(2-methoxyethoxy)methyl]-8-(4-methoxyphenyl)-,
2',3',5'-triacetate 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
dichloromethane;
at 20 ℃;
for 3.5h;
DOI:10.1055/s-2004-831249
- Guidance literature:
-
Multi-step reaction with 4 steps
1: 73 percent / aq. K2CO3 / Pd(PPh3)4 / 1,2-dimethoxy-ethane / 16 h / 90 °C
2: 91 percent / pyridine / 16 h / 20 °C
3: 79 percent / aq. NaNO2; AcOH / 19 h / 20 °C
4: 75 percent / N,N-diisopropylethylamine / CH2Cl2 / 3.5 h / 20 °C
With
pyridine; potassium carbonate; acetic acid; N-ethyl-N,N-diisopropylamine; sodium nitrite;
tetrakis(triphenylphosphine) palladium(0);
In
1,2-dimethoxyethane; dichloromethane;
1: Suzuki-Miyaura cross-coupling;
DOI:10.1055/s-2004-831249
- Guidance literature:
-
Multi-step reaction with 5 steps
1: 81 percent / Br2 / acetate buffer / 47 h / 20 °C / pH 4
2: 73 percent / aq. K2CO3 / Pd(PPh3)4 / 1,2-dimethoxy-ethane / 16 h / 90 °C
3: 91 percent / pyridine / 16 h / 20 °C
4: 79 percent / aq. NaNO2; AcOH / 19 h / 20 °C
5: 75 percent / N,N-diisopropylethylamine / CH2Cl2 / 3.5 h / 20 °C
With
pyridine; bromine; potassium carbonate; acetic acid; N-ethyl-N,N-diisopropylamine; sodium nitrite;
tetrakis(triphenylphosphine) palladium(0);
In
1,2-dimethoxyethane; dichloromethane; acetate buffer;
2: Suzuki-Miyaura cross-coupling;
DOI:10.1055/s-2004-831249
