4-(4-aminobenzyl)-3-n-butyl-5-(carbomethoxymethylthio)-4H-1,2,4-triazole

Base Information

Chemical Name:4-(4-aminobenzyl)-3-n-butyl-5-(carbomethoxymethylthio)-4H-1,2,4-triazole
CAS No.:134402-56-5
Molecular Formula:C₁₆H₂₂N₄O₂S
Molecular Weight:334.442
Hs Code.:

Synonyms:4-(4-aminobenzyl)-3-n-butyl-5-(carbomethoxymethylthio)-4H-1,2,4-triazole

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Chemical Property of 4-(4-aminobenzyl)-3-n-butyl-5-(carbomethoxymethylthio)-4H-1,2,4-triazole

Chemical Property:

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Technology Process of 4-(4-aminobenzyl)-3-n-butyl-5-(carbomethoxymethylthio)-4H-1,2,4-triazole

There total 7 articles about 4-(4-aminobenzyl)-3-n-butyl-5-(carbomethoxymethylthio)-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:

: tin(II)chloride dihydrate

: 134402-55-4
3-n-butyl-5-<<(methoxycarbonyl)methyl>thio>-4-(4-nitrobenzyl)-4H-1,2,4-triazole

: 134402-56-5
4-(4-aminobenzyl)-3-n-butyl-5-(carbomethoxymethylthio)-4H-1,2,4-triazole

Guidance literature:: With sodium hydroxide; In tetrahydrofuran; hydrogenchloride;

Reference yield:

: 134402-55-4
3-n-butyl-5-<<(methoxycarbonyl)methyl>thio>-4-(4-nitrobenzyl)-4H-1,2,4-triazole

: 134402-56-5
4-(4-aminobenzyl)-3-n-butyl-5-(carbomethoxymethylthio)-4H-1,2,4-triazole

Guidance literature:: With hydrogenchloride; tin(ll) chloride; In tetrahydrofuran; for 2.5h; Ambient temperature;
DOI:10.1021/jm00057a009

Reference yield:

: 34930-06-8
4-(4-nitrobenzyl)-3-thiosemicarbazide

: 134402-56-5
4-(4-aminobenzyl)-3-n-butyl-5-(carbomethoxymethylthio)-4H-1,2,4-triazole

Guidance literature:: Multi-step reaction with 3 steps

1: 62 percent / 2-methoxy-ethanol / 24 h / Heating

2: N,N-diisopropylethylamine / 2-methoxy-ethanol / 3.5 h / Ambient temperature

3: stannous chloride dihydrate, conc. HCl / tetrahydrofuran / 2.5 h / Ambient temperature

With hydrogenchloride; N-ethyl-N,N-diisopropylamine; tin(ll) chloride; In tetrahydrofuran; 2-methoxy-ethanol;
DOI:10.1021/jm00057a009