4,14-dibenzyl-2,5,13,16-tetraoxo-3,6,12,15,21-pentaazabicyclo[15,3,1]heneicosa-1⁽²¹⁾,17⁽¹⁸⁾,19-triene-11-carboxylic acid methyl ester

Base Information

• Chemical Name: 4,14-dibenzyl-2,5,13,16-tetraoxo-3,6,12,15,21-pentaazabicyclo[15,3,1]heneicosa-1⁽²¹⁾,17⁽¹⁸⁾,19-triene-11-carboxylic acid methyl ester
• CAS No.: 335265-92-4
• Molecular Formula: C₃₂H₃₅N₅O₆
• Molecular Weight: 585.66

Synonyms:4,14-dibenzyl-2,5,13,16-tetraoxo-3,6,12,15,21-pentaazabicyclo[15,3,1]heneicosa-1⁽²¹⁾,17⁽¹⁸⁾,19-triene-11-carboxylic acid methyl ester

Chemical Property of 4,14-dibenzyl-2,5,13,16-tetraoxo-3,6,12,15,21-pentaazabicyclo[15,3,1]heneicosa-1⁽²¹⁾,17⁽¹⁸⁾,19-triene-11-carboxylic acid methyl ester

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Technology Process of 4,14-dibenzyl-2,5,13,16-tetraoxo-3,6,12,15,21-pentaazabicyclo[15,3,1]heneicosa-1⁽²¹⁾,17⁽¹⁸⁾,19-triene-11-carboxylic acid methyl ester

There total 4 articles about 4,14-dibenzyl-2,5,13,16-tetraoxo-3,6,12,15,21-pentaazabicyclo[15,3,1]heneicosa-1⁽²¹⁾,17⁽¹⁸⁾,19-triene-11-carboxylic acid 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:

Reference yield:

L-lysine methyl ester (687-64-9) + C31H31N3O10 → 4,14-dibenzyl-2,5,13,16-tetraoxo-3,6,12,15,21-pentaazabicyclo[15,3,1]heneicosa-1(21),17(18),19-triene-11-carboxylic acid methyl ester (335265-92-4)

Guidance literature:

With TEA; In tetrahydrofuran; at 20 ℃; for 12h;

Reference yield:

N,N'-bis[(S)-1-methoxycarbonyl-2-phenylethyl]-2,6-pyridinecarboxamide (158946-83-9) → 4,14-dibenzyl-2,5,13,16-tetraoxo-3,6,12,15,21-pentaazabicyclo[15,3,1]heneicosa-1(21),17(18),19-triene-11-carboxylic acid methyl ester (335265-92-4)

Guidance literature:

Multi-step reaction with 3 steps

1: 79 percent / 1 N aq. NaOH / methanol / 12 h / 20 °C

2: Et₃N / tetrahydrofuran / 0.25 h / -30 °C

3: TEA / tetrahydrofuran / 12 h / 20 °C

With sodium hydroxide; TEA; triethylamine; In tetrahydrofuran; methanol;

Reference yield:

N2,N6-bis(3-phenylpropanoic acid-2-yl)pyridine-2,6-dicarboxamide (158946-78-2) → 4,14-dibenzyl-2,5,13,16-tetraoxo-3,6,12,15,21-pentaazabicyclo[15,3,1]heneicosa-1(21),17(18),19-triene-11-carboxylic acid methyl ester (335265-92-4)

Guidance literature:

Multi-step reaction with 2 steps

1: Et₃N / tetrahydrofuran / 0.25 h / -30 °C

2: TEA / tetrahydrofuran / 12 h / 20 °C

With TEA; triethylamine; In tetrahydrofuran;

upstream raw materials:

L-lysine methyl ester

N,N'-bis[(S)-1-methoxycarbonyl-2-phenylethyl]-2,6-pyridinecarboxamide

N²,N⁶-bis(3-phenylpropanoic acid-2-yl)pyridine-2,6-dicarboxamide

N²,N^2'-(Pyridine-2,6-dicarbonyl)di(S)phenylalaninehydrazide

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