N-(4-(3,4-dichlorophenyl)butan-2-yl)-4-hydroxy-5-oxo-1-(3-(4-(trifluoromethoxy)phenyl)prop-2-ynyl)-2,5-dihydro-1H-pyrrole-3-carboxamide

Base Information

Chemical Name:N-(4-(3,4-dichlorophenyl)butan-2-yl)-4-hydroxy-5-oxo-1-(3-(4-(trifluoromethoxy)phenyl)prop-2-ynyl)-2,5-dihydro-1H-pyrrole-3-carboxamide
CAS No.:1429293-60-6
Molecular Formula:C₂₅H₂₁Cl₂F₃N₂O₄
Molecular Weight:541.354
Hs Code.:

Synonyms:N-(4-(3,4-dichlorophenyl)butan-2-yl)-4-hydroxy-5-oxo-1-(3-(4-(trifluoromethoxy)phenyl)prop-2-ynyl)-2,5-dihydro-1H-pyrrole-3-carboxamide

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Chemical Property of N-(4-(3,4-dichlorophenyl)butan-2-yl)-4-hydroxy-5-oxo-1-(3-(4-(trifluoromethoxy)phenyl)prop-2-ynyl)-2,5-dihydro-1H-pyrrole-3-carboxamide

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Technology Process of N-(4-(3,4-dichlorophenyl)butan-2-yl)-4-hydroxy-5-oxo-1-(3-(4-(trifluoromethoxy)phenyl)prop-2-ynyl)-2,5-dihydro-1H-pyrrole-3-carboxamide

There total 6 articles about N-(4-(3,4-dichlorophenyl)butan-2-yl)-4-hydroxy-5-oxo-1-(3-(4-(trifluoromethoxy)phenyl)prop-2-ynyl)-2,5-dihydro-1H-pyrrole-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: 18.0%

: 407-14-7
1-bromo-4-(trifluoromethoxy)benzene

: 1429293-59-3
N-(4-(3,4-dichlorophenyl)butan-2-yl)-4-methoxy-5-oxo-1-(prop-2-ynyl)-2,5-dihydro-1H-pyrrole-3-carboxamide

: 1429293-60-6
N-(4-(3,4-dichlorophenyl)butan-2-yl)-4-hydroxy-5-oxo-1-(3-(4-(trifluoromethoxy)phenyl)prop-2-ynyl)-2,5-dihydro-1H-pyrrole-3-carboxamide

Guidance literature:: With bis-triphenylphosphine-palladium(II) chloride; copper(l) iodide; diethylamine; triphenylphosphine; In N,N-dimethyl-formamide; at 120 ℃; for 0.333333h; Inert atmosphere; Microwave irradiation;

Reference yield:

: 42160-40-7
4-(3,4-dichlorophenyl)butan-2-one

: 1429293-60-6
N-(4-(3,4-dichlorophenyl)butan-2-yl)-4-hydroxy-5-oxo-1-(3-(4-(trifluoromethoxy)phenyl)prop-2-ynyl)-2,5-dihydro-1H-pyrrole-3-carboxamide

Guidance literature:: Multi-step reaction with 4 steps

1.1: ammonium acetate / methanol / 0.17 h / 20 °C

1.2: 18 h / 20 °C

2.1: benzotriazol-1-yloxyl-tris-(pyrrolidino)-phosphonium hexafluorophosphate; N-ethyl-N,N-diisopropylamine / N,N-dimethyl-formamide / 2 h / 20 °C

3.1: N-ethyl-N,N-diisopropylamine / methanol / 0.17 h / 60 °C / Microwave irradiation

3.2: 0.25 h / 100 °C / Microwave irradiation

3.3: 18 h / 20 °C

4.1: copper(l) iodide; bis-triphenylphosphine-palladium(II) chloride; diethylamine; triphenylphosphine / N,N-dimethyl-formamide / 0.33 h / 120 °C / Inert atmosphere; Microwave irradiation

With bis-triphenylphosphine-palladium(II) chloride; copper(l) iodide; ammonium acetate; benzotriazol-1-yloxyl-tris-(pyrrolidino)-phosphonium hexafluorophosphate; diethylamine; N-ethyl-N,N-diisopropylamine; triphenylphosphine; In methanol; N,N-dimethyl-formamide;

Reference yield:

: 1429293-58-2
N-(4-(3,4-dichlorophenyl)butan-2-yl)-2-(2,2-dimethyl-5-oxo-1,3-dioxolan-4-ylidene)acetamide

: 1429293-60-6
N-(4-(3,4-dichlorophenyl)butan-2-yl)-4-hydroxy-5-oxo-1-(3-(4-(trifluoromethoxy)phenyl)prop-2-ynyl)-2,5-dihydro-1H-pyrrole-3-carboxamide

Guidance literature:: Multi-step reaction with 2 steps

1.1: N-ethyl-N,N-diisopropylamine / methanol / 0.17 h / 60 °C / Microwave irradiation

1.2: 0.25 h / 100 °C / Microwave irradiation

1.3: 18 h / 20 °C

2.1: copper(l) iodide; bis-triphenylphosphine-palladium(II) chloride; diethylamine; triphenylphosphine / N,N-dimethyl-formamide / 0.33 h / 120 °C / Inert atmosphere; Microwave irradiation

With bis-triphenylphosphine-palladium(II) chloride; copper(l) iodide; diethylamine; N-ethyl-N,N-diisopropylamine; triphenylphosphine; In methanol; N,N-dimethyl-formamide;