4-pyridinecarboxylic acid 2-(3-{(R)-(4-{amino[benzoylimino]methyl}phenylamino)-[5-(3-methoxy-2,2-dimethylpropionyloxymethoxy)-1-pyrimidin-2-yl-1H-[1,2,4]triazol-3-yl]methyl}-2-fluoro-5-methoxyphenoxy)ethyl ester methanesulfonate

Base Information

Chemical Name:4-pyridinecarboxylic acid 2-(3-{(R)-(4-{amino[benzoylimino]methyl}phenylamino)-[5-(3-methoxy-2,2-dimethylpropionyloxymethoxy)-1-pyrimidin-2-yl-1H-[1,2,4]triazol-3-yl]methyl}-2-fluoro-5-methoxyphenoxy)ethyl ester methanesulfonate
CAS No.:1350551-54-0
Molecular Formula:CH₄O₃S*C₄₃H₄₂FN₉O₉
Molecular Weight:943.967
Hs Code.:

4-pyridinecarboxylic acid 2-(3-{(R)-(4-{amino[benzoylimino]methyl}phenylamino)-[5-(3-methoxy-2,2-dimethylpropionyloxymethoxy)-1-pyrimidin-2-yl-1H-[1,2,4]triazol-3-yl]methyl}-2-fluoro-5-methoxyphenoxy)ethyl ester methanesulfonate

Synonyms:4-pyridinecarboxylic acid 2-(3-{(R)-(4-{amino[benzoylimino]methyl}phenylamino)-[5-(3-methoxy-2,2-dimethylpropionyloxymethoxy)-1-pyrimidin-2-yl-1H-[1,2,4]triazol-3-yl]methyl}-2-fluoro-5-methoxyphenoxy)ethyl ester methanesulfonate

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Chemical Property of 4-pyridinecarboxylic acid 2-(3-{(R)-(4-{amino[benzoylimino]methyl}phenylamino)-[5-(3-methoxy-2,2-dimethylpropionyloxymethoxy)-1-pyrimidin-2-yl-1H-[1,2,4]triazol-3-yl]methyl}-2-fluoro-5-methoxyphenoxy)ethyl ester methanesulfonate

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Technology Process of 4-pyridinecarboxylic acid 2-(3-{(R)-(4-{amino[benzoylimino]methyl}phenylamino)-[5-(3-methoxy-2,2-dimethylpropionyloxymethoxy)-1-pyrimidin-2-yl-1H-[1,2,4]triazol-3-yl]methyl}-2-fluoro-5-methoxyphenoxy)ethyl ester methanesulfonate

There total 8 articles about 4-pyridinecarboxylic acid 2-(3-{(R)-(4-{amino[benzoylimino]methyl}phenylamino)-[5-(3-methoxy-2,2-dimethylpropionyloxymethoxy)-1-pyrimidin-2-yl-1H-[1,2,4]triazol-3-yl]methyl}-2-fluoro-5-methoxyphenoxy)ethyl ester methanesulfonate 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:

Reference yield:

: 75-75-2,98527-29-8
methanesulfonic acid

: 1350551-35-7
4-pyridinecarboxylic acid 2-(3-{(R)-(4-{amino[benzoylimino]methyl}phenylamino)-[5-(3-methoxy-2,2-dimethylpropionyloxymethoxy)-1-pyrimidin-2-yl-1H-[1,2,4]triazol-3-yl]methyl}-2-fluoro-5-methoxyphenoxy)ethyl ester

: 1350551-54-0
4-pyridinecarboxylic acid 2-(3-{(R)-(4-{amino[benzoylimino]methyl}phenylamino)-[5-(3-methoxy-2,2-dimethylpropionyloxymethoxy)-1-pyrimidin-2-yl-1H-[1,2,4]triazol-3-yl]methyl}-2-fluoro-5-methoxyphenoxy)ethyl ester methanesulfonate

Guidance literature:: In dichloromethane; tert-butyl methyl ether; at 20 ℃; Sonographic reaction;

Reference yield:

: 959-22-8
p-nitrophenylbenzoate

: 1350551-54-0
4-pyridinecarboxylic acid 2-(3-{(R)-(4-{amino[benzoylimino]methyl}phenylamino)-[5-(3-methoxy-2,2-dimethylpropionyloxymethoxy)-1-pyrimidin-2-yl-1H-[1,2,4]triazol-3-yl]methyl}-2-fluoro-5-methoxyphenoxy)ethyl ester methanesulfonate

Guidance literature:: Multi-step reaction with 5 steps

1.1: triethylamine / 50 °C

2.1: caesium carbonate / N,N-dimethyl-formamide / 4 h / 60 °C

3.1: triethylamine; fluoro-N,N,N',N'-tetramethylformamidinium hexafluorophosphate / dichloromethane / 1 h / Inert atmosphere

3.2: 20 °C

4.1: SUMICHIRAL OA-2500S / methanol / Resolution of racemate

5.1: dichloromethane; tert-butyl methyl ether / 20 °C / Sonographic reaction

With caesium carbonate; triethylamine; fluoro-N,N,N',N'-tetramethylformamidinium hexafluorophosphate; In methanol; dichloromethane; tert-butyl methyl ether; N,N-dimethyl-formamide;

Reference yield:

: 951803-95-5
4-({[2-fluoro-3-(2-hydroxyethoxy)-5-methoxyphenyl]-(5-oxo-1-pyrimidin-2-yl-4,5-dihydro-1H-[1,2,4]triazol-3-yl)methyl}amino)benzamidine acetate

: 1350551-54-0
4-pyridinecarboxylic acid 2-(3-{(R)-(4-{amino[benzoylimino]methyl}phenylamino)-[5-(3-methoxy-2,2-dimethylpropionyloxymethoxy)-1-pyrimidin-2-yl-1H-[1,2,4]triazol-3-yl]methyl}-2-fluoro-5-methoxyphenoxy)ethyl ester methanesulfonate

Guidance literature:: Multi-step reaction with 5 steps

1.1: triethylamine / 50 °C

2.1: caesium carbonate / N,N-dimethyl-formamide / 4 h / 60 °C

3.1: triethylamine; fluoro-N,N,N',N'-tetramethylformamidinium hexafluorophosphate / dichloromethane / 1 h / Inert atmosphere

3.2: 20 °C

4.1: SUMICHIRAL OA-2500S / methanol / Resolution of racemate

5.1: dichloromethane; tert-butyl methyl ether / 20 °C / Sonographic reaction

With caesium carbonate; triethylamine; fluoro-N,N,N',N'-tetramethylformamidinium hexafluorophosphate; In methanol; dichloromethane; tert-butyl methyl ether; N,N-dimethyl-formamide;