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carbonic acid 5-{(R)-(4-{amino[2-propoxycarbonylimino]methyl}phenylamino)-[2-fluoro-3-(2-hydroxyethoxy)-5-methoxyphenyl]methyl}-2-pyrimidin-2-yl-2H-[1,2,4]triazol-3-yloxymethyl ester2-fluoro-1,l-dimethylethyl ester

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  • Chemical Name:carbonic acid 5-{(R)-(4-{amino[2-propoxycarbonylimino]methyl}phenylamino)-[2-fluoro-3-(2-hydroxyethoxy)-5-methoxyphenyl]methyl}-2-pyrimidin-2-yl-2H-[1,2,4]triazol-3-yloxymethyl ester2-fluoro-1,l-dimethylethyl ester
  • CAS No.:1350551-81-3
  • Molecular Formula:C33H38F2N8O9
  • Molecular Weight:728.71
  • Hs Code.:
carbonic acid 5-{(R)-(4-{amino[2-propoxycarbonylimino]methyl}phenylamino)-[2-fluoro-3-(2-hydroxyethoxy)-5-methoxyphenyl]methyl}-2-pyrimidin-2-yl-2H-[1,2,4]triazol-3-yloxymethyl ester2-fluoro-1,l-dimethylethyl ester

Synonyms:carbonic acid 5-{(R)-(4-{amino[2-propoxycarbonylimino]methyl}phenylamino)-[2-fluoro-3-(2-hydroxyethoxy)-5-methoxyphenyl]methyl}-2-pyrimidin-2-yl-2H-[1,2,4]triazol-3-yloxymethyl ester2-fluoro-1,l-dimethylethyl ester

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Chemical Property of carbonic acid 5-{(R)-(4-{amino[2-propoxycarbonylimino]methyl}phenylamino)-[2-fluoro-3-(2-hydroxyethoxy)-5-methoxyphenyl]methyl}-2-pyrimidin-2-yl-2H-[1,2,4]triazol-3-yloxymethyl ester2-fluoro-1,l-dimethylethyl ester
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Technology Process of carbonic acid 5-{(R)-(4-{amino[2-propoxycarbonylimino]methyl}phenylamino)-[2-fluoro-3-(2-hydroxyethoxy)-5-methoxyphenyl]methyl}-2-pyrimidin-2-yl-2H-[1,2,4]triazol-3-yloxymethyl ester2-fluoro-1,l-dimethylethyl ester

There total 21 articles about carbonic acid 5-{(R)-(4-{amino[2-propoxycarbonylimino]methyl}phenylamino)-[2-fluoro-3-(2-hydroxyethoxy)-5-methoxyphenyl]methyl}-2-pyrimidin-2-yl-2H-[1,2,4]triazol-3-yloxymethyl ester2-fluoro-1,l-dimethylethyl 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 15 steps
1.1: guanidine hydrochloride / methanol / 1.5 h / 40 °C / Inert atmosphere
1.2: 22 h / 40 °C
2.1: potassium carbonate; sodium iodide / N,N-dimethyl-formamide / 13.5 h / 70 °C / Inert atmosphere
3.1: water; diammonium sulfide / tetrahydrofuran; methanol / 20 °C
4.1: acetonitrile / 0.83 h / 20 °C / Cooling
5.1: 2,4,6-trimethyl-pyridine / ethyl acetate; toluene / 85 °C
6.1: triethylamine / toluene / 4.17 h / 50 - 110 °C
7.1: acetic acid; 2-picoline borane complex / water; methanol / 24 h / 20 °C
8.1: sodium hydroxide; water / tetrahydrofuran; methanol / 23.5 h / 20 °C
8.2: 0.33 h
9.1: acetyl chloride; methanol / 18.5 h / 5 - 10 °C
9.2: 18 h / 10 - 20 °C
9.3: 18 h / 20 °C
10.1: triethylamine / methanol / 0.25 h / 60 °C
10.2: 23 h / 0 - 20 °C
11.1: hydrogenchloride / ethanol; water; methanol / 20 °C
12.1: potassium carbonate / dimethyl sulfoxide / 96 h / 20 °C
13.1: rubidium carbonate / N,N-dimethyl acetamide / 1 h / 85 °C / Inert atmosphere
14.1: tetrakis(triphenylphosphine) palladium(0) / N,N-dimethyl-formamide / 15 h / 45 °C / Inert atmosphere
15.1: pyridine / 20 °C
With rubidium carbonate; pyridine; 2,4,6-trimethyl-pyridine; hydrogenchloride; methanol; diammonium sulfide; 2-picoline borane complex; water; guanidine hydrochloride; potassium carbonate; acetic acid; triethylamine; acetyl chloride; sodium iodide; sodium hydroxide; tetrakis(triphenylphosphine) palladium(0); In tetrahydrofuran; methanol; ethanol; N,N-dimethyl acetamide; water; dimethyl sulfoxide; ethyl acetate; N,N-dimethyl-formamide; toluene; acetonitrile;
Guidance literature:
Multi-step reaction with 18 steps
1.1: n-butyllithium; N,N,N',N'',N'''-pentamethyldiethylenetriamine / hexane; tetrahydrofuran / -70 °C / Inert atmosphere
1.2: 1 h
1.3: -10 - 20 °C
2.1: triethylamine / tetrahydrofuran / 20 °C / Cooling with ice; Inert atmosphere
3.1: n-butyllithium; N,N,N',N'',N'''-pentamethyldiethylenetriamine / hexane; tetrahydrofuran / 3 h / -72 - -56 °C / Inert atmosphere
3.3: 10 - 20 °C
4.1: guanidine hydrochloride / methanol / 1.5 h / 40 °C / Inert atmosphere
4.2: 22 h / 40 °C
5.1: potassium carbonate; sodium iodide / N,N-dimethyl-formamide / 13.5 h / 70 °C / Inert atmosphere
6.1: water; diammonium sulfide / tetrahydrofuran; methanol / 20 °C
7.1: acetonitrile / 0.83 h / 20 °C / Cooling
8.1: 2,4,6-trimethyl-pyridine / ethyl acetate; toluene / 85 °C
9.1: triethylamine / toluene / 4.17 h / 50 - 110 °C
10.1: acetic acid; 2-picoline borane complex / water; methanol / 24 h / 20 °C
11.1: sodium hydroxide; water / tetrahydrofuran; methanol / 23.5 h / 20 °C
11.2: 0.33 h
12.1: acetyl chloride; methanol / 18.5 h / 5 - 10 °C
12.2: 18 h / 10 - 20 °C
12.3: 18 h / 20 °C
13.1: triethylamine / methanol / 0.25 h / 60 °C
13.2: 23 h / 0 - 20 °C
14.1: hydrogenchloride / ethanol; water; methanol / 20 °C
15.1: potassium carbonate / dimethyl sulfoxide / 96 h / 20 °C
16.1: rubidium carbonate / N,N-dimethyl acetamide / 1 h / 85 °C / Inert atmosphere
17.1: tetrakis(triphenylphosphine) palladium(0) / N,N-dimethyl-formamide / 15 h / 45 °C / Inert atmosphere
18.1: pyridine / 20 °C
With rubidium carbonate; pyridine; 2,4,6-trimethyl-pyridine; hydrogenchloride; methanol; diammonium sulfide; n-butyllithium; 2-picoline borane complex; N,N,N',N'',N'''-pentamethyldiethylenetriamine; water; guanidine hydrochloride; potassium carbonate; acetic acid; triethylamine; acetyl chloride; sodium iodide; sodium hydroxide; tetrakis(triphenylphosphine) palladium(0); In tetrahydrofuran; methanol; ethanol; hexane; N,N-dimethyl acetamide; water; dimethyl sulfoxide; ethyl acetate; N,N-dimethyl-formamide; toluene; acetonitrile;
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