3-(N-benzyl-N-methylcarbamoyl)-5-n-butyl-4-<(2'-cyanobiphenyl-4-yl)methyl>-4H-1,2,4-triazole

Base Information

Chemical Name:3-(N-benzyl-N-methylcarbamoyl)-5-n-butyl-4-<(2'-cyanobiphenyl-4-yl)methyl>-4H-1,2,4-triazole
CAS No.:134425-29-9
Molecular Formula:C₂₉H₂₉N₅O
Molecular Weight:463.582
Hs Code.:

Synonyms:3-(N-benzyl-N-methylcarbamoyl)-5-n-butyl-4-<(2'-cyanobiphenyl-4-yl)methyl>-4H-1,2,4-triazole

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Chemical Property of 3-(N-benzyl-N-methylcarbamoyl)-5-n-butyl-4-<(2'-cyanobiphenyl-4-yl)methyl>-4H-1,2,4-triazole

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Technology Process of 3-(N-benzyl-N-methylcarbamoyl)-5-n-butyl-4-<(2'-cyanobiphenyl-4-yl)methyl>-4H-1,2,4-triazole

There total 7 articles about 3-(N-benzyl-N-methylcarbamoyl)-5-n-butyl-4-<(2'-cyanobiphenyl-4-yl)methyl>-4H-1,2,4-triazole 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: 74.0%

: 133690-92-3
[(2'-cyanobiphenyl-4-yl)methyl]amine

: 134425-28-8
ethyl valerate 5-benzyl-5-methylsemioxamazone

: 134425-29-9
3-(N-benzyl-N-methylcarbamoyl)-5-n-butyl-4-<(2'-cyanobiphenyl-4-yl)methyl>-4H-1,2,4-triazole

Guidance literature:: In ethanol; at 45 - 70 ℃;
DOI:10.1021/jm00057a009

Reference yield:

: 128429-34-5
ethyl 2-(benzyl(methyl)amino)-2-oxoacetate

: 134425-29-9
3-(N-benzyl-N-methylcarbamoyl)-5-n-butyl-4-<(2'-cyanobiphenyl-4-yl)methyl>-4H-1,2,4-triazole

Guidance literature:: Multi-step reaction with 3 steps

1: 61 percent / hydrazine hydrate / ethanol / Ambient temperature

2: 100 percent / ethanol / 42.5 h / -10 - 5 °C

3: 74 percent / ethanol / 45 - 70 °C

With hydrazine hydrate; In ethanol;
DOI:10.1021/jm00057a009

Reference yield:

: 114772-54-2
4'-(bromomethyl)-1,1'-biphenyl-2-carbonitrile

: 134425-29-9
3-(N-benzyl-N-methylcarbamoyl)-5-n-butyl-4-<(2'-cyanobiphenyl-4-yl)methyl>-4H-1,2,4-triazole

Guidance literature:: Multi-step reaction with 3 steps

1: 68 percent / lithium azide / dimethylsulfoxide / 1 h / Ambient temperature

2: 89 percent / triphenylphosphine / 2 h / Ambient temperature

3: 74 percent / ethanol / 45 - 70 °C

With lithium azide; triphenylphosphine; In ethanol; dimethyl sulfoxide;
DOI:10.1021/jm00057a009