1-(2,4-Dichlorobenzyl)-4-ethoxycarbonyl-5-<(3-oxo-1-cyclohexen-1-yl)amino>pyrazole

Base Information

Chemical Name:1-(2,4-Dichlorobenzyl)-4-ethoxycarbonyl-5-<(3-oxo-1-cyclohexen-1-yl)amino>pyrazole
CAS No.:137278-80-9
Molecular Formula:C₁₉H₁₉Cl₂N₃O₃
Molecular Weight:408.284
Hs Code.:

Synonyms:1-(2,4-Dichlorobenzyl)-4-ethoxycarbonyl-5-<(3-oxo-1-cyclohexen-1-yl)amino>pyrazole

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Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

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Chemical Property of 1-(2,4-Dichlorobenzyl)-4-ethoxycarbonyl-5-<(3-oxo-1-cyclohexen-1-yl)amino>pyrazole

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Technology Process of 1-(2,4-Dichlorobenzyl)-4-ethoxycarbonyl-5-<(3-oxo-1-cyclohexen-1-yl)amino>pyrazole

There total 1 articles about 1-(2,4-Dichlorobenzyl)-4-ethoxycarbonyl-5-<(3-oxo-1-cyclohexen-1-yl)amino>pyrazole 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: 77.0%

: 504-02-9
1,3-cylohexanedione

: 125240-84-8
ethyl 5-amino-1-(2,4-dichlorobenzyl)-1H-pyrazole-4-carboxylate

: 137278-80-9
1-(2,4-Dichlorobenzyl)-4-ethoxycarbonyl-5-<(3-oxo-1-cyclohexen-1-yl)amino>pyrazole

Guidance literature:: With toluene-4-sulfonic acid; In toluene; for 24h; Heating;

Reference yield: 68.0%

: 137278-80-9
1-(2,4-Dichlorobenzyl)-4-ethoxycarbonyl-5-<(3-oxo-1-cyclohexen-1-yl)amino>pyrazole

: 137278-85-4
4-Carboxy-1-(2,4-dichlorobenzyl)-5-<(3-oxo-1-cyclohexen-1-yl)amino>pyrazole

Guidance literature:: With sodium hydroxide; for 4h; Heating;

Reference yield:

: 137278-80-9
1-(2,4-Dichlorobenzyl)-4-ethoxycarbonyl-5-<(3-oxo-1-cyclohexen-1-yl)amino>pyrazole

: 137279-18-6
1-(2,4-Dichlorobenzyl)-7,8-dihydro-6H,9H-pyrazolo<3,4-b>quinoline-4,5-dione

Guidance literature:: Multi-step reaction with 2 steps

1: 68 percent / 15percent aq. NaOH / 4 h / Heating

2: 85 percent / polyphosphoric ester (PPE) / acetonitrile / 2 h / Heating

With sodium hydroxide; polyphosphoric ester; In acetonitrile;