ethyl 2-benzoyl-1-(4-(hept-1-yn-1-yl)phenyl)-5-phenyl-1H-pyrrole-3-carboxylate

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Chemical Name:ethyl 2-benzoyl-1-(4-(hept-1-yn-1-yl)phenyl)-5-phenyl-1H-pyrrole-3-carboxylate
CAS No.:1396396-27-2
Molecular Formula:C₃₃H₃₁NO₃
Molecular Weight:489.614
Hs Code.:

Synonyms:ethyl 2-benzoyl-1-(4-(hept-1-yn-1-yl)phenyl)-5-phenyl-1H-pyrrole-3-carboxylate

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Chemical Property of ethyl 2-benzoyl-1-(4-(hept-1-yn-1-yl)phenyl)-5-phenyl-1H-pyrrole-3-carboxylate

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Technology Process of ethyl 2-benzoyl-1-(4-(hept-1-yn-1-yl)phenyl)-5-phenyl-1H-pyrrole-3-carboxylate

There total 3 articles about ethyl 2-benzoyl-1-(4-(hept-1-yn-1-yl)phenyl)-5-phenyl-1H-pyrrole-3-carboxylate 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: 88.0%

: 628-71-7
1-Heptyne

: 1396396-19-2
ethyl 2-benzoyl-1-(4-iodophenyl)-5-phenyl-1H-pyrrole-3-carboxylate

: 1396396-27-2
ethyl 2-benzoyl-1-(4-(hept-1-yn-1-yl)phenyl)-5-phenyl-1H-pyrrole-3-carboxylate

Guidance literature:: ethyl 2-benzoyl-1-(4-iodophenyl)-5-phenyl-1H-pyrrole-3-carboxylate; With bis-triphenylphosphine-palladium(II) chloride; copper(l) iodide; triethylamine; In N,N-dimethyl-formamide; at 20 ℃; for 0.5h; Inert atmosphere;

1-Heptyne; In N,N-dimethyl-formamide; at 50 - 60 ℃; Inert atmosphere;
DOI:10.1016/j.bmcl.2012.06.100

Reference yield:

: 70-11-1
α-bromoacetophenone

: 1396396-27-2
ethyl 2-benzoyl-1-(4-(hept-1-yn-1-yl)phenyl)-5-phenyl-1H-pyrrole-3-carboxylate

Guidance literature:: Multi-step reaction with 2 steps

1.1: N,N-dimethyl-formamide / 1 h / 20 °C

1.2: 10 h / 50 °C

2.1: copper(l) iodide; bis-triphenylphosphine-palladium(II) chloride; triethylamine / N,N-dimethyl-formamide / 0.5 h / 20 °C / Inert atmosphere

2.2: 50 - 60 °C / Inert atmosphere

With bis-triphenylphosphine-palladium(II) chloride; copper(l) iodide; triethylamine; In N,N-dimethyl-formamide; 2.1: Sonogashira coupling / 2.2: Sonogashira coupling;
DOI:10.1016/j.bmcl.2012.06.100

Reference yield:

: 540-37-4
p-aminoiodobenzene

: 1396396-27-2
ethyl 2-benzoyl-1-(4-(hept-1-yn-1-yl)phenyl)-5-phenyl-1H-pyrrole-3-carboxylate

Guidance literature:: Multi-step reaction with 2 steps

1.1: N,N-dimethyl-formamide / 1 h / 20 °C

1.2: 10 h / 50 °C

2.1: copper(l) iodide; bis-triphenylphosphine-palladium(II) chloride; triethylamine / N,N-dimethyl-formamide / 0.5 h / 20 °C / Inert atmosphere

2.2: 50 - 60 °C / Inert atmosphere

With bis-triphenylphosphine-palladium(II) chloride; copper(l) iodide; triethylamine; In N,N-dimethyl-formamide; 2.1: Sonogashira coupling / 2.2: Sonogashira coupling;
DOI:10.1016/j.bmcl.2012.06.100