N-(2-bromo-4-methylphenyl)-2-(4-(4-tert-butylphenyl)-5-isopropyl-4H-1,2,4-triazol-3-ylthio)acetamide

Base Information

Chemical Name:N-(2-bromo-4-methylphenyl)-2-(4-(4-tert-butylphenyl)-5-isopropyl-4H-1,2,4-triazol-3-ylthio)acetamide
CAS No.:1492902-42-7
Molecular Formula:C₂₄H₂₉BrN₄OS
Molecular Weight:501.49
Hs Code.:

Synonyms:N-(2-bromo-4-methylphenyl)-2-(4-(4-tert-butylphenyl)-5-isopropyl-4H-1,2,4-triazol-3-ylthio)acetamide

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Chemical Property of N-(2-bromo-4-methylphenyl)-2-(4-(4-tert-butylphenyl)-5-isopropyl-4H-1,2,4-triazol-3-ylthio)acetamide

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Technology Process of N-(2-bromo-4-methylphenyl)-2-(4-(4-tert-butylphenyl)-5-isopropyl-4H-1,2,4-triazol-3-ylthio)acetamide

There total 4 articles about N-(2-bromo-4-methylphenyl)-2-(4-(4-tert-butylphenyl)-5-isopropyl-4H-1,2,4-triazol-3-ylthio)acetamide 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: 41.1%

: 90560-54-6
PCM-0102196

: 1038308-06-3
C₁₅H₂₁N₃S

: 1492902-42-7
N-(2-bromo-4-methylphenyl)-2-(4-(4-tert-butylphenyl)-5-isopropyl-4H-1,2,4-triazol-3-ylthio)acetamide

Guidance literature:: With sodium hydroxide; In ethanol; for 0.5h;
DOI:10.2174/1573406411309070010

Reference yield:

: 1492902-52-9
C₁₅H₂₃N₃OS

: 1492902-42-7
N-(2-bromo-4-methylphenyl)-2-(4-(4-tert-butylphenyl)-5-isopropyl-4H-1,2,4-triazol-3-ylthio)acetamide

Guidance literature:: Multi-step reaction with 2 steps

1: sodium hydroxide / ethanol / 4 h / Reflux

2: sodium hydroxide / ethanol / 0.5 h

With sodium hydroxide; In ethanol;
DOI:10.2174/1573406411309070010

Reference yield:

2-bromo-p-toluidine: 583-68-6
2-bromo-p-toluidine

: 1492902-42-7
N-(2-bromo-4-methylphenyl)-2-(4-(4-tert-butylphenyl)-5-isopropyl-4H-1,2,4-triazol-3-ylthio)acetamide

Guidance literature:: Multi-step reaction with 2 steps

1: triethylamine / dichloromethane / 4 h / 20 °C

2: sodium hydroxide / ethanol / 0.5 h

With triethylamine; sodium hydroxide; In ethanol; dichloromethane;
DOI:10.2174/1573406411309070010