1-(2,4-dichlorophenyl)-5-(5-(2-(4-(trifluoromethyl)phenyl)-ethynyl)thiophene-2-yl)-4-(hydroxymethyl)-N-(piperidin-1-yl)-1H-pyrazole-3-carboxamide

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Chemical Name:1-(2,4-dichlorophenyl)-5-(5-(2-(4-(trifluoromethyl)phenyl)-ethynyl)thiophene-2-yl)-4-(hydroxymethyl)-N-(piperidin-1-yl)-1H-pyrazole-3-carboxamide
CAS No.:1429242-14-7
Molecular Formula:C₂₉H₂₃Cl₂F₃N₄O₂S
Molecular Weight:619.494
Hs Code.:

Synonyms:1-(2,4-dichlorophenyl)-5-(5-(2-(4-(trifluoromethyl)phenyl)-ethynyl)thiophene-2-yl)-4-(hydroxymethyl)-N-(piperidin-1-yl)-1H-pyrazole-3-carboxamide

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Chemical Property of 1-(2,4-dichlorophenyl)-5-(5-(2-(4-(trifluoromethyl)phenyl)-ethynyl)thiophene-2-yl)-4-(hydroxymethyl)-N-(piperidin-1-yl)-1H-pyrazole-3-carboxamide

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Technology Process of 1-(2,4-dichlorophenyl)-5-(5-(2-(4-(trifluoromethyl)phenyl)-ethynyl)thiophene-2-yl)-4-(hydroxymethyl)-N-(piperidin-1-yl)-1H-pyrazole-3-carboxamide

There total 8 articles about 1-(2,4-dichlorophenyl)-5-(5-(2-(4-(trifluoromethyl)phenyl)-ethynyl)thiophene-2-yl)-4-(hydroxymethyl)-N-(piperidin-1-yl)-1H-pyrazole-3-carboxamide 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: 87.0%

: 705-31-7
4-trifluoromethylphenylacetylene

: 1429242-12-5
5-(5-bromothiophene-2-yl)-1-(2,4-dichlorophenyl)-4-(hydroxymethyl)-N-(piperidin-1-yl)-1H-pyrazole-3-carboxamide

: 1429242-14-7
1-(2,4-dichlorophenyl)-5-(5-(2-(4-(trifluoromethyl)phenyl)-ethynyl)thiophene-2-yl)-4-(hydroxymethyl)-N-(piperidin-1-yl)-1H-pyrazole-3-carboxamide

Guidance literature:: With bis-triphenylphosphine-palladium(II) chloride; copper(l) iodide; In tetrahydrofuran; at 80 ℃; for 12h; Inert atmosphere; Sealed tube;
DOI:10.1021/jm401158e

Reference yield: 70.0%

: 705-31-7
4-trifluoromethylphenylacetylene

: 1429242-12-5
5-(5-bromothiophene-2-yl)-1-(2,4-dichlorophenyl)-4-(hydroxymethyl)-N-(piperidin-1-yl)-1H-pyrazole-3-carboxamide

: 141-43-5
ethanolamine

: 1429242-14-7
1-(2,4-dichlorophenyl)-5-(5-(2-(4-(trifluoromethyl)phenyl)-ethynyl)thiophene-2-yl)-4-(hydroxymethyl)-N-(piperidin-1-yl)-1H-pyrazole-3-carboxamide

Guidance literature:: 5-(5-bromothiophene-2-yl)-1-(2,4-dichlorophenyl)-4-(hydroxymethyl)-N-(piperidin-1-yl)-1H-pyrazole-3-carboxamide; ethanolamine; With bis-triphenylphosphine-palladium(II) chloride; copper(l) iodide; In tetrahydrofuran; water; for 0.166667h; Inert atmosphere;

4-trifluoromethylphenylacetylene; In tetrahydrofuran; at 80 ℃; for 12h; Inert atmosphere;

Reference yield:

: 1013649-25-6
5-(5-bromothiophen-2-yl)-1-(2,4-dichloro-phenyl)-4-methyl-5-thiophen-2-yl-1H-pyrazole-3-carboxylic acid ethyl ester

: 1429242-14-7
1-(2,4-dichlorophenyl)-5-(5-(2-(4-(trifluoromethyl)phenyl)-ethynyl)thiophene-2-yl)-4-(hydroxymethyl)-N-(piperidin-1-yl)-1H-pyrazole-3-carboxamide

Guidance literature:: Multi-step reaction with 4 steps

1.1: N-Bromosuccinimide; 2,2'-azobis(isobutyronitrile) / tetrachloromethane / 16 h / Reflux

2.1: silver nitrate; water / acetone / 60 °C

3.1: aluminum (III) chloride / 1,2-dichloro-ethane / 16 h / 0 - 20 °C / Inert atmosphere

4.1: bis-triphenylphosphine-palladium(II) chloride; copper(l) iodide / tetrahydrofuran; water / 0.17 h / Inert atmosphere

4.2: 12 h / 80 °C / Inert atmosphere

With aluminum (III) chloride; bis-triphenylphosphine-palladium(II) chloride; N-Bromosuccinimide; copper(l) iodide; 2,2'-azobis(isobutyronitrile); water; silver nitrate; In tetrahydrofuran; tetrachloromethane; water; 1,2-dichloro-ethane; acetone;