(2E)-N-(4-methoxybenzyloxy)-3-(1-((E)-1-(naphthalen-1-yl)-4-phenylbut-3-en-2-yl)-1H-1,2,3-triazol-4-yl)acrylamide

Base Information

Chemical Name:(2E)-N-(4-methoxybenzyloxy)-3-(1-((E)-1-(naphthalen-1-yl)-4-phenylbut-3-en-2-yl)-1H-1,2,3-triazol-4-yl)acrylamide
CAS No.:1314802-34-0
Molecular Formula:C₃₃H₃₀N₄O₃
Molecular Weight:530.626
Hs Code.:

Synonyms:(2E)-N-(4-methoxybenzyloxy)-3-(1-((E)-1-(naphthalen-1-yl)-4-phenylbut-3-en-2-yl)-1H-1,2,3-triazol-4-yl)acrylamide

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Chemical Property of (2E)-N-(4-methoxybenzyloxy)-3-(1-((E)-1-(naphthalen-1-yl)-4-phenylbut-3-en-2-yl)-1H-1,2,3-triazol-4-yl)acrylamide

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Technology Process of (2E)-N-(4-methoxybenzyloxy)-3-(1-((E)-1-(naphthalen-1-yl)-4-phenylbut-3-en-2-yl)-1H-1,2,3-triazol-4-yl)acrylamide

There total 7 articles about (2E)-N-(4-methoxybenzyloxy)-3-(1-((E)-1-(naphthalen-1-yl)-4-phenylbut-3-en-2-yl)-1H-1,2,3-triazol-4-yl)acrylamide 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: 60.0%

: 1312592-14-5
C₁₃H₁₃NO₃

: 1314802-18-0
1-((E)-2-azido-4-phenylbut-3-enyl)naphthalene

: 1314802-34-0
(2E)-N-(4-methoxybenzyloxy)-3-(1-((E)-1-(naphthalen-1-yl)-4-phenylbut-3-en-2-yl)-1H-1,2,3-triazol-4-yl)acrylamide

Guidance literature:: With triethylphosphite copper(I) iodide complex; N-ethyl-N,N-diisopropylamine; In tetrahydrofuran; at 20 ℃;
DOI:10.1016/j.ejmech.2011.04.027

Reference yield:

: 1092115-32-6
(E)-N-(4-methoxybenzyloxy)-5-(trimethylsilyl)pent-2-en-4-ynamide

: 1314802-34-0
(2E)-N-(4-methoxybenzyloxy)-3-(1-((E)-1-(naphthalen-1-yl)-4-phenylbut-3-en-2-yl)-1H-1,2,3-triazol-4-yl)acrylamide

Guidance literature:: Multi-step reaction with 2 steps

1: cesium fluoride

2: triethylphosphite copper(I) iodide complex; N-ethyl-N,N-diisopropylamine / tetrahydrofuran / 20 °C

With triethylphosphite copper(I) iodide complex; N-ethyl-N,N-diisopropylamine; cesium fluoride; In tetrahydrofuran;
DOI:10.1016/j.ejmech.2011.04.027

Reference yield:

: 1092115-41-7
(2-methoxyethoxy)methyl (2E)-5-(trimethylsilyl)pent-2-en-4-ynoate

: 1314802-34-0
(2E)-N-(4-methoxybenzyloxy)-3-(1-((E)-1-(naphthalen-1-yl)-4-phenylbut-3-en-2-yl)-1H-1,2,3-triazol-4-yl)acrylamide

Guidance literature:: Multi-step reaction with 4 steps

1.1: hydrogenchloride / water

2.1: oxalyl dichloride; N,N-dimethyl-formamide / dichloromethane

2.2: 0 - 20 °C

3.1: cesium fluoride

4.1: triethylphosphite copper(I) iodide complex; N-ethyl-N,N-diisopropylamine / tetrahydrofuran / 20 °C

With hydrogenchloride; oxalyl dichloride; triethylphosphite copper(I) iodide complex; N-ethyl-N,N-diisopropylamine; N,N-dimethyl-formamide; cesium fluoride; In tetrahydrofuran; dichloromethane; water;
DOI:10.1016/j.ejmech.2011.04.027