(Z)-4-((1-(4-amino-2-(benzyloxy)phenyl)-5-methyl-1-oxohex-2-en-3-yl)amino)-2-(benzyloxy)benzamide

Base Information

Chemical Name:(Z)-4-((1-(4-amino-2-(benzyloxy)phenyl)-5-methyl-1-oxohex-2-en-3-yl)amino)-2-(benzyloxy)benzamide
CAS No.:1319746-39-8
Molecular Formula:C₃₄H₃₅N₃O₄
Molecular Weight:549.67
Hs Code.:

Synonyms:(Z)-4-((1-(4-amino-2-(benzyloxy)phenyl)-5-methyl-1-oxohex-2-en-3-yl)amino)-2-(benzyloxy)benzamide

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Chemical Property of (Z)-4-((1-(4-amino-2-(benzyloxy)phenyl)-5-methyl-1-oxohex-2-en-3-yl)amino)-2-(benzyloxy)benzamide

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Technology Process of (Z)-4-((1-(4-amino-2-(benzyloxy)phenyl)-5-methyl-1-oxohex-2-en-3-yl)amino)-2-(benzyloxy)benzamide

There total 9 articles about (Z)-4-((1-(4-amino-2-(benzyloxy)phenyl)-5-methyl-1-oxohex-2-en-3-yl)amino)-2-(benzyloxy)benzamide 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: 100.0%

: 1319746-30-9
(Z)-2-(benzyloxy)-4-((1-(2-(benzyloxy)-4-nitrophenyl)-5-methyl-1-oxohex-2-en-3-yl)amino)benzamide

: 1319746-39-8
(Z)-4-((1-(4-amino-2-(benzyloxy)phenyl)-5-methyl-1-oxohex-2-en-3-yl)amino)-2-(benzyloxy)benzamide

Guidance literature:: With platinum(IV) oxide; hydrogen; potassium carbonate; In methanol; for 0.75h;
DOI:10.1021/jo200917d

Reference yield:

: 619-19-2
2-hydroxy-4-nitrobenzoic acid

: 1319746-39-8
(Z)-4-((1-(4-amino-2-(benzyloxy)phenyl)-5-methyl-1-oxohex-2-en-3-yl)amino)-2-(benzyloxy)benzamide

Guidance literature:: Multi-step reaction with 6 steps

1.1: potassium carbonate / N,N-dimethyl-formamide / 16 h / 80 °C / Inert atmosphere

2.1: oxalyl dichloride; N,N-dimethyl-formamide / dichloromethane / 1 h / 20 °C / Inert atmosphere

3.1: triethylamine / dichloromethane / 2.5 h / 20 °C / Inert atmosphere

4.1: n-butyllithium / tetrahydrofuran / -78 °C / Inert atmosphere

4.2: 1.25 h / -78 - 20 °C / Inert atmosphere

5.1: methanol / 3 h / 120 °C

6.1: platinum(IV) oxide; hydrogen; potassium carbonate / methanol / 0.75 h

With platinum(IV) oxide; n-butyllithium; oxalyl dichloride; hydrogen; potassium carbonate; triethylamine; N,N-dimethyl-formamide; In tetrahydrofuran; methanol; dichloromethane; N,N-dimethyl-formamide;
DOI:10.1021/jo200917d

Reference yield:

: 5340-21-6
2-(benzyloxy)-4-nitrobenzoic acid

: 1319746-39-8
(Z)-4-((1-(4-amino-2-(benzyloxy)phenyl)-5-methyl-1-oxohex-2-en-3-yl)amino)-2-(benzyloxy)benzamide

Guidance literature:: Multi-step reaction with 5 steps

1.1: oxalyl dichloride; N,N-dimethyl-formamide / dichloromethane / 1 h / 20 °C / Inert atmosphere

2.1: triethylamine / dichloromethane / 2.5 h / 20 °C / Inert atmosphere

3.1: n-butyllithium / tetrahydrofuran / -78 °C / Inert atmosphere

3.2: 1.25 h / -78 - 20 °C / Inert atmosphere

4.1: methanol / 3 h / 120 °C

5.1: platinum(IV) oxide; hydrogen; potassium carbonate / methanol / 0.75 h

With platinum(IV) oxide; n-butyllithium; oxalyl dichloride; hydrogen; potassium carbonate; triethylamine; N,N-dimethyl-formamide; In tetrahydrofuran; methanol; dichloromethane;
DOI:10.1021/jo200917d