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1-(5-(4-(bis(4-methoxybenzyl)amino)-6-methyl-1,3,5-triazin-2-yl)-6-((5-fluoro-6-methoxypyridin-3-yl)amino)pyridin-3-yl)ethyl methanesulfonate

Base Information
  • Chemical Name:1-(5-(4-(bis(4-methoxybenzyl)amino)-6-methyl-1,3,5-triazin-2-yl)-6-((5-fluoro-6-methoxypyridin-3-yl)amino)pyridin-3-yl)ethyl methanesulfonate
  • CAS No.:1253575-95-9
  • Molecular Formula:C34H36FN7O6S
  • Molecular Weight:689.768
  • Hs Code.:
1-(5-(4-(bis(4-methoxybenzyl)amino)-6-methyl-1,3,5-triazin-2-yl)-6-((5-fluoro-6-methoxypyridin-3-yl)amino)pyridin-3-yl)ethyl methanesulfonate

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Chemical Property of 1-(5-(4-(bis(4-methoxybenzyl)amino)-6-methyl-1,3,5-triazin-2-yl)-6-((5-fluoro-6-methoxypyridin-3-yl)amino)pyridin-3-yl)ethyl methanesulfonate
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Technology Process of 1-(5-(4-(bis(4-methoxybenzyl)amino)-6-methyl-1,3,5-triazin-2-yl)-6-((5-fluoro-6-methoxypyridin-3-yl)amino)pyridin-3-yl)ethyl methanesulfonate

There total 7 articles about 1-(5-(4-(bis(4-methoxybenzyl)amino)-6-methyl-1,3,5-triazin-2-yl)-6-((5-fluoro-6-methoxypyridin-3-yl)amino)pyridin-3-yl)ethyl 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:
Guidance literature:
Multi-step reaction with 4 steps
1: lithium hexamethyldisilazane / tetrahydrofuran / 0.58 h / Cooling with ice; Inert atmosphere
2: hydrogenchloride; water / tetrahydrofuran; methanol / 0.17 h / 20 °C / Inert atmosphere
3: tetrahydrofuran; diethyl ether / 0.42 h / 0 °C
4: triethylamine / dichloromethane / 2 h
With hydrogenchloride; water; triethylamine; lithium hexamethyldisilazane; In tetrahydrofuran; methanol; diethyl ether; dichloromethane;
DOI:10.1021/jm300846z
Guidance literature:
Multi-step reaction with 2 steps
1: tetrahydrofuran; diethyl ether / 0.42 h / 0 °C
2: triethylamine / dichloromethane / 2 h
With triethylamine; In tetrahydrofuran; diethyl ether; dichloromethane;
DOI:10.1021/jm300846z
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