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

Base Information

Chemical Name:3-(benzylamino)-5-n-butyl-4-<(2'-cyanobiphenyl-4-yl)methyl>-4H-1,2,4-triazole
CAS No.:146885-43-0
Molecular Formula:C₂₇H₂₇N₅
Molecular Weight:421.545
Hs Code.:

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

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

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

There total 9 articles about 3-(benzylamino)-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: 68.0%

: 146885-42-9
3-(benzylideneamino)-5-n-butyl-4-<(2'-cyanobiphenyl-4-yl)methyl>-4H-1,2,4-triazole

: 146885-43-0
3-(benzylamino)-5-n-butyl-4-<(2'-cyanobiphenyl-4-yl)methyl>-4H-1,2,4-triazole

Guidance literature:: With sodium tetrahydroborate; In ethanol; for 0.416667h;
DOI:10.1021/jm00057a009

Reference yield:

: 100-52-7
benzaldehyde

: 146885-43-0
3-(benzylamino)-5-n-butyl-4-<(2'-cyanobiphenyl-4-yl)methyl>-4H-1,2,4-triazole

Guidance literature:: Multi-step reaction with 2 steps

1: 90 percent / piperidine / propan-2-ol / 14.5 h / Heating

2: 68 percent / sodium borohydride / ethanol / 0.42 h

With piperidine; sodium tetrahydroborate; In ethanol; isopropyl alcohol;
DOI:10.1021/jm00057a009

Reference yield:

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

: 146885-43-0
3-(benzylamino)-5-n-butyl-4-<(2'-cyanobiphenyl-4-yl)methyl>-4H-1,2,4-triazole

Guidance literature:: Multi-step reaction with 6 steps

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

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

3: 71 percent / ethanol / 144 h / Ambient temperature

4: 64 percent / m-chloroperbenzoic acid / CH₂Cl₂ / 5 h

5: 90 percent / piperidine / propan-2-ol / 14.5 h / Heating

6: 68 percent / sodium borohydride / ethanol / 0.42 h

With piperidine; sodium tetrahydroborate; lithium azide; 3-chloro-benzenecarboperoxoic acid; triphenylphosphine; In ethanol; dichloromethane; dimethyl sulfoxide; isopropyl alcohol;
DOI:10.1021/jm00057a009