5-(2,4-dihydroxy-5-isopropylphenyl)-4-[4-(4-methylpiperazin-1-yl)benzoylamino]isoxazole-3-carboxylic acid ethylamide trifluoroacetate

Base Information

Chemical Name:5-(2,4-dihydroxy-5-isopropylphenyl)-4-[4-(4-methylpiperazin-1-yl)benzoylamino]isoxazole-3-carboxylic acid ethylamide trifluoroacetate
CAS No.:1350722-62-1
Molecular Formula:C₂HF₃O₂*C₂₇H₃₃N₅O₅
Molecular Weight:621.613
Hs Code.:

5-(2,4-dihydroxy-5-isopropylphenyl)-4-[4-(4-methylpiperazin-1-yl)benzoylamino]isoxazole-3-carboxylic acid ethylamide trifluoroacetate

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Chemical Property of 5-(2,4-dihydroxy-5-isopropylphenyl)-4-[4-(4-methylpiperazin-1-yl)benzoylamino]isoxazole-3-carboxylic acid ethylamide trifluoroacetate

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Technology Process of 5-(2,4-dihydroxy-5-isopropylphenyl)-4-[4-(4-methylpiperazin-1-yl)benzoylamino]isoxazole-3-carboxylic acid ethylamide trifluoroacetate

There total 3 articles about 5-(2,4-dihydroxy-5-isopropylphenyl)-4-[4-(4-methylpiperazin-1-yl)benzoylamino]isoxazole-3-carboxylic acid ethylamide trifluoroacetate 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:

: 747414-21-7
5-(2,4-bis(benzyloxy)-5-isopropylphenyl)isoxazole-3-carboxylic acid ethylamide

: 1350722-62-1
5-(2,4-dihydroxy-5-isopropylphenyl)-4-[4-(4-methylpiperazin-1-yl)benzoylamino]isoxazole-3-carboxylic acid ethylamide trifluoroacetate

Guidance literature:: Multi-step reaction with 4 steps

1: nitric acid; acetic anhydride / 70 h / 0 - 10 °C / Inert atmosphere

2: water; ammonium chloride; zinc / tetrahydrofuran / 0.75 h / 0 °C

3: triethylamine / dichloromethane / 5 h / Inert atmosphere

4: boron trichloride / dichloromethane / 1.17 h / 0 - 20 °C / Inert atmosphere

With water; nitric acid; acetic anhydride; boron trichloride; ammonium chloride; triethylamine; zinc; In tetrahydrofuran; dichloromethane;
DOI:10.1021/jm201155e

Reference yield:

: 1202920-71-5
5-[2,4-bis(benzyloxy)-5-isopropylphenyl]-4-nitroisoxazole-3-carboxylic acid ethylamide

: 1350722-62-1
5-(2,4-dihydroxy-5-isopropylphenyl)-4-[4-(4-methylpiperazin-1-yl)benzoylamino]isoxazole-3-carboxylic acid ethylamide trifluoroacetate

Guidance literature:: Multi-step reaction with 3 steps

1: water; ammonium chloride; zinc / tetrahydrofuran / 0.75 h / 0 °C

2: triethylamine / dichloromethane / 5 h / Inert atmosphere

3: boron trichloride / dichloromethane / 1.17 h / 0 - 20 °C / Inert atmosphere

With water; boron trichloride; ammonium chloride; triethylamine; zinc; In tetrahydrofuran; dichloromethane;
DOI:10.1021/jm201155e

Reference yield:

: 401495-67-8
4-(4-methylpiperazin-4-ium-1-yl)benzoyl chloride

: 1202920-72-6
4-amino-5-[2,4-bis(benzyloxy)-5-isopropylphenyl]isoxazole-3-carboxylic acid ethylamide

: 1350722-62-1
5-(2,4-dihydroxy-5-isopropylphenyl)-4-[4-(4-methylpiperazin-1-yl)benzoylamino]isoxazole-3-carboxylic acid ethylamide trifluoroacetate

Guidance literature:: Multi-step reaction with 2 steps

1: triethylamine / dichloromethane / 5 h / Inert atmosphere

2: boron trichloride / dichloromethane / 1.17 h / 0 - 20 °C / Inert atmosphere

With boron trichloride; triethylamine; In dichloromethane;
DOI:10.1021/jm201155e