2-((1-(4-nitrophenyl)-1H-1,2,3-triazol-4-yl)methylthio)benzo[d]thiazole

Base Information

Chemical Name:2-((1-(4-nitrophenyl)-1H-1,2,3-triazol-4-yl)methylthio)benzo[d]thiazole
CAS No.:1362125-14-1
Molecular Formula:C₁₆H₁₁N₅O₂S₂
Molecular Weight:369.428
Hs Code.:

Synonyms:2-((1-(4-nitrophenyl)-1H-1,2,3-triazol-4-yl)methylthio)benzo[d]thiazole

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Chemical Property of 2-((1-(4-nitrophenyl)-1H-1,2,3-triazol-4-yl)methylthio)benzo[d]thiazole

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Technology Process of 2-((1-(4-nitrophenyl)-1H-1,2,3-triazol-4-yl)methylthio)benzo[d]thiazole

There total 2 articles about 2-((1-(4-nitrophenyl)-1H-1,2,3-triazol-4-yl)methylthio)benzo[d]thiazole 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: 93.0%

: 42477-59-8
2-(prop-2-yn-1-ylsulfanyl)-1,3-benzothiazole

: 1516-60-5
4-nitrophenyl azide

: 1362125-14-1
2-((1-(4-nitrophenyl)-1H-1,2,3-triazol-4-yl)methylthio)benzo[d]thiazole

Guidance literature:: 2-(prop-2-yn-1-ylsulfanyl)-1,3-benzothiazole; With copper(ll) sulfate pentahydrate; sodium L-ascorbate; In water; tert-butyl alcohol; at 20 ℃; for 0.25h;

4-nitrophenyl azide; In water; tert-butyl alcohol; at 20 ℃; for 8h;
DOI:10.1016/j.ejmech.2012.01.032

Reference yield:

: 149-30-4,118090-09-8
2-Mercaptobenzothiazole

: 1362125-14-1
2-((1-(4-nitrophenyl)-1H-1,2,3-triazol-4-yl)methylthio)benzo[d]thiazole

Guidance literature:: Multi-step reaction with 2 steps

1.1: triethylamine / 1,4-dioxane / Reflux

2.1: copper(ll) sulfate pentahydrate; sodium L-ascorbate / water; tert-butyl alcohol / 0.25 h / 20 °C

2.2: 8 h / 20 °C

With copper(ll) sulfate pentahydrate; sodium L-ascorbate; triethylamine; In 1,4-dioxane; water; tert-butyl alcohol;
DOI:10.1016/j.ejmech.2012.01.032