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N2,3-dihydroxy-4-(hydroxymethyl)-N5-(4-methoxybenzyl)pyridine-2,5-dicarboxamide

Base Information
  • Chemical Name:N2,3-dihydroxy-4-(hydroxymethyl)-N5-(4-methoxybenzyl)pyridine-2,5-dicarboxamide
  • CAS No.:1198620-34-6
  • Molecular Formula:C16H17N3O6
  • Molecular Weight:347.327
  • Hs Code.:
N<sub>2</sub>,3-dihydroxy-4-(hydroxymethyl)-N<sub>5</sub>-(4-methoxybenzyl)pyridine-2,5-dicarboxamide

Synonyms:N2,3-dihydroxy-4-(hydroxymethyl)-N5-(4-methoxybenzyl)pyridine-2,5-dicarboxamide

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Chemical Property of N2,3-dihydroxy-4-(hydroxymethyl)-N5-(4-methoxybenzyl)pyridine-2,5-dicarboxamide
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Technology Process of N2,3-dihydroxy-4-(hydroxymethyl)-N5-(4-methoxybenzyl)pyridine-2,5-dicarboxamide

There total 10 articles about N2,3-dihydroxy-4-(hydroxymethyl)-N5-(4-methoxybenzyl)pyridine-2,5-dicarboxamide 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 3 steps
1: manganese(IV) oxide / dichloromethane / 20 °C
2: 0.5 h / 70 °C
3: hydrogen / palladium 10% on activated carbon / methanol / 1 h
With manganese(IV) oxide; hydrogen; palladium 10% on activated carbon; In methanol; dichloromethane;
Guidance literature:
Multi-step reaction with 5 steps
1.1: lithium hexamethyldisilazane / tetrahydrofuran / -78 °C
1.2: 0.5 h / -78 °C
2.1: formic acid / tetrahydrofuran; water / 2 h / 70 °C
3.1: manganese(IV) oxide / dichloromethane / 20 °C
4.1: 0.5 h / 70 °C
5.1: hydrogen / palladium 10% on activated carbon / methanol / 1 h
With manganese(IV) oxide; formic acid; hydrogen; lithium hexamethyldisilazane; palladium 10% on activated carbon; In tetrahydrofuran; methanol; dichloromethane; water;
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