1-((4-methoxyphenyl)ethynyl)-3-(4-trifluoromethylphenylethynyl)imidazo[1,5-a]pyridine

Base Information

Chemical Name:1-((4-methoxyphenyl)ethynyl)-3-(4-trifluoromethylphenylethynyl)imidazo[1,5-a]pyridine
CAS No.:1379574-54-5
Molecular Formula:C₂₅H₁₅F₃N₂O
Molecular Weight:416.402
Hs Code.:

Synonyms:1-((4-methoxyphenyl)ethynyl)-3-(4-trifluoromethylphenylethynyl)imidazo[1,5-a]pyridine

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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-((4-methoxyphenyl)ethynyl)-3-(4-trifluoromethylphenylethynyl)imidazo[1,5-a]pyridine

Chemical Property:

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Technology Process of 1-((4-methoxyphenyl)ethynyl)-3-(4-trifluoromethylphenylethynyl)imidazo[1,5-a]pyridine

There total 6 articles about 1-((4-methoxyphenyl)ethynyl)-3-(4-trifluoromethylphenylethynyl)imidazo[1,5-a]pyridine 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: 80.0%

: 705-31-7
4-trifluoromethylphenylacetylene

: 1379574-50-1
1-(4-methoxyphenyl)(ethynyl)imidazo[1,5-a]pyridine

: 1379574-54-5
1-((4-methoxyphenyl)ethynyl)-3-(4-trifluoromethylphenylethynyl)imidazo[1,5-a]pyridine

: 1379574-63-6
1,1'-bis(4-methoxyphenylethynyl)-3,3'-biimidazo[1,5-a]-pyridinyl

: 151362-06-0
1,4-bis[4-(trifluoromethyl)phenyl]buta-1,3-diyne

Guidance literature:: With palladium diacetate; acetic acid; silver carbonate; In dimethyl sulfoxide; N,N-dimethyl-formamide; at 120 ℃; for 1h; Inert atmosphere;
DOI:10.1021/jo3008385

Reference yield:

: 274-47-5
imidazo[1,5-a]pyridine

: 1379574-54-5
1-((4-methoxyphenyl)ethynyl)-3-(4-trifluoromethylphenylethynyl)imidazo[1,5-a]pyridine

Guidance literature:: Multi-step reaction with 3 steps

1: N-Bromosuccinimide / dichloromethane / 1.5 h / -78 - 20 °C / Inert atmosphere

2: copper(l) iodide; bis(benzonitrile)palladium(II) dichloride; N-ethyl-N,N-diisopropylamine; tri-t-butylphosphonium tetraphenylborate complex / acetonitrile / 24 h / 60 °C / Inert atmosphere

3: palladium diacetate; acetic acid; silver carbonate / dimethyl sulfoxide / 1 h / 120 °C / Inert atmosphere

With N-Bromosuccinimide; copper(l) iodide; bis(benzonitrile)palladium(II) dichloride; palladium diacetate; acetic acid; N-ethyl-N,N-diisopropylamine; silver carbonate; tri-t-butylphosphonium tetraphenylborate complex; In dichloromethane; dimethyl sulfoxide; acetonitrile; 2: Sonogashira coupling;
DOI:10.1021/jo3008385

Reference yield:

: 274-47-5
imidazo[1,5-a]pyridine

: 1379574-54-5
1-((4-methoxyphenyl)ethynyl)-3-(4-trifluoromethylphenylethynyl)imidazo[1,5-a]pyridine

: 1379574-63-6
1,1'-bis(4-methoxyphenylethynyl)-3,3'-biimidazo[1,5-a]-pyridinyl

Guidance literature:: Multi-step reaction with 3 steps

1: N-Bromosuccinimide / dichloromethane / 1.5 h / -78 - 20 °C / Inert atmosphere

2: copper(l) iodide; bis(benzonitrile)palladium(II) dichloride; N-ethyl-N,N-diisopropylamine; tri-t-butylphosphonium tetraphenylborate complex / acetonitrile / 24 h / 60 °C / Inert atmosphere

3: palladium diacetate; acetic acid; silver carbonate / dimethyl sulfoxide; N,N-dimethyl-formamide / 3 h / 120 °C / Inert atmosphere

With N-Bromosuccinimide; copper(l) iodide; bis(benzonitrile)palladium(II) dichloride; palladium diacetate; acetic acid; N-ethyl-N,N-diisopropylamine; silver carbonate; tri-t-butylphosphonium tetraphenylborate complex; In dichloromethane; dimethyl sulfoxide; N,N-dimethyl-formamide; acetonitrile; 2: Sonogashira coupling;
DOI:10.1021/jo3008385