Technology Process of Glycine,
N-[2-[2-[5-(2,7-difluoro-3,6-dihydroxy-9H-xanthen-9-yl)-2-[(2-methoxy-2-
oxoethyl)amino]phenoxy]ethoxy]-4-methoxyphenyl]-N-(2-methoxy-2-oxo
ethyl)-, methyl ester
There total 7 articles about Glycine,
N-[2-[2-[5-(2,7-difluoro-3,6-dihydroxy-9H-xanthen-9-yl)-2-[(2-methoxy-2-
oxoethyl)amino]phenoxy]ethoxy]-4-methoxyphenyl]-N-(2-methoxy-2-oxo
ethyl)-, methyl ester 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 4 steps
1: 88 percent / potassium carbonate / dimethylformamide / 3 h / 100 °C
2: 49 percent / H2 / platinum oxide / ethyl acetate; methanol; 1,2-dichloro-ethane / 8 h / 1034.32 Torr
3: 40 percent / diisopropylethylamine / dimethylformamide / 90 °C
4: 98 percent / methanesulfonic acid
With
methanesulfonic acid; hydrogen; potassium carbonate; N-ethyl-N,N-diisopropylamine;
platinum(IV) oxide;
In
methanol; ethyl acetate; 1,2-dichloro-ethane; N,N-dimethyl-formamide;
DOI:10.1021/ja011774y
- Guidance literature:
-
Multi-step reaction with 6 steps
1: 77 percent / potassium carbonate / dimethylformamide / 2 h / 100 °C
2: 97 percent / p-toluenesulfonic acid / 24 h / Heating
3: 88 percent / potassium carbonate / dimethylformamide / 3 h / 100 °C
4: 49 percent / H2 / platinum oxide / ethyl acetate; methanol; 1,2-dichloro-ethane / 8 h / 1034.32 Torr
5: 40 percent / diisopropylethylamine / dimethylformamide / 90 °C
6: 98 percent / methanesulfonic acid
With
methanesulfonic acid; hydrogen; potassium carbonate; toluene-4-sulfonic acid; N-ethyl-N,N-diisopropylamine;
platinum(IV) oxide;
In
methanol; ethyl acetate; 1,2-dichloro-ethane; N,N-dimethyl-formamide;
DOI:10.1021/ja011774y