(Z)-4-((1-(4-amino-2-isopropoxyphenyl)-5-methyl-1-oxohex-2-en-3-yl)amino)-2-isopropoxybenzamide

Base Information

Chemical Name:(Z)-4-((1-(4-amino-2-isopropoxyphenyl)-5-methyl-1-oxohex-2-en-3-yl)amino)-2-isopropoxybenzamide
CAS No.:1319746-35-4
Molecular Formula:C₂₆H₃₅N₃O₄
Molecular Weight:453.582
Hs Code.:

Synonyms:(Z)-4-((1-(4-amino-2-isopropoxyphenyl)-5-methyl-1-oxohex-2-en-3-yl)amino)-2-isopropoxybenzamide

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Chemical Property of (Z)-4-((1-(4-amino-2-isopropoxyphenyl)-5-methyl-1-oxohex-2-en-3-yl)amino)-2-isopropoxybenzamide

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Technology Process of (Z)-4-((1-(4-amino-2-isopropoxyphenyl)-5-methyl-1-oxohex-2-en-3-yl)amino)-2-isopropoxybenzamide

There total 9 articles about (Z)-4-((1-(4-amino-2-isopropoxyphenyl)-5-methyl-1-oxohex-2-en-3-yl)amino)-2-isopropoxybenzamide 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%

: 1319746-26-3
(Z)-2-isopropoxy-4-((1-(2-isopropoxy-4-nitrophenyl)-5-methyl-1-oxohex-2-en-3-yl)amino)benzamide

: 1319746-35-4
(Z)-4-((1-(4-amino-2-isopropoxyphenyl)-5-methyl-1-oxohex-2-en-3-yl)amino)-2-isopropoxybenzamide

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

: 1319746-35-4
(Z)-4-((1-(4-amino-2-isopropoxyphenyl)-5-methyl-1-oxohex-2-en-3-yl)amino)-2-isopropoxybenzamide

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:

: 1319746-14-9
2-isopropoxy-4-nitrobenzoic acid

: 1319746-35-4
(Z)-4-((1-(4-amino-2-isopropoxyphenyl)-5-methyl-1-oxohex-2-en-3-yl)amino)-2-isopropoxybenzamide

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