N-{2-(1-benzyl-1H-1,2,3-triazol-4-yl)propan-2-yl}-[1,1’-biphenyl]-4-carboxamide

Base Information

Chemical Name:N-{2-(1-benzyl-1H-1,2,3-triazol-4-yl)propan-2-yl}-[1,1’-biphenyl]-4-carboxamide
CAS No.:1623775-10-9
Molecular Formula:C₂₅H₂₄N₄O
Molecular Weight:396.492
Hs Code.:

Synonyms:N-{2-(1-benzyl-1H-1,2,3-triazol-4-yl)propan-2-yl}-[1,1’-biphenyl]-4-carboxamide

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Chemical Property of N-{2-(1-benzyl-1H-1,2,3-triazol-4-yl)propan-2-yl}-[1,1’-biphenyl]-4-carboxamide

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Technology Process of N-{2-(1-benzyl-1H-1,2,3-triazol-4-yl)propan-2-yl}-[1,1’-biphenyl]-4-carboxamide

There total 3 articles about N-{2-(1-benzyl-1H-1,2,3-triazol-4-yl)propan-2-yl}-[1,1’-biphenyl]-4-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: 86.0%

: 1310826-33-5
2-(1-benzyl-1H-1,2,3-triazol-4-yl)propan-2-amine

: 14002-51-8
4-biphenyl-carboxylic acid chloride

: 1623775-10-9
N-{2-(1-benzyl-1H-1,2,3-triazol-4-yl)propan-2-yl}-[1,1’-biphenyl]-4-carboxamide

Guidance literature:: With triethylamine; In dichloromethane; at 0 - 20 ℃; for 12h; Inert atmosphere; Schlenk technique;
DOI:10.1002/anie.201311024

Reference yield:

: 2978-58-7
1,1-dimethylprop-3-ynylamine

: 1623775-10-9
N-{2-(1-benzyl-1H-1,2,3-triazol-4-yl)propan-2-yl}-[1,1’-biphenyl]-4-carboxamide

Guidance literature:: Multi-step reaction with 2 steps

1: copper(ll) sulfate pentahydrate; sodium L-ascorbate / tert-butyl alcohol; water / 24 h / 20 °C / Inert atmosphere; Schlenk technique

2: triethylamine / dichloromethane / 12 h / 0 - 20 °C / Inert atmosphere; Schlenk technique

With copper(ll) sulfate pentahydrate; sodium L-ascorbate; triethylamine; In dichloromethane; water; tert-butyl alcohol;
DOI:10.1002/anie.201311024

Reference yield:

: 622-79-7
benzyl azide

: 1623775-10-9
N-{2-(1-benzyl-1H-1,2,3-triazol-4-yl)propan-2-yl}-[1,1’-biphenyl]-4-carboxamide

Guidance literature:: Multi-step reaction with 2 steps

1: copper(ll) sulfate pentahydrate; sodium L-ascorbate / tert-butyl alcohol; water / 24 h / 20 °C / Inert atmosphere; Schlenk technique

2: triethylamine / dichloromethane / 12 h / 0 - 20 °C / Inert atmosphere; Schlenk technique

With copper(ll) sulfate pentahydrate; sodium L-ascorbate; triethylamine; In dichloromethane; water; tert-butyl alcohol;
DOI:10.1002/anie.201311024