1-{4-[5-(4-Nitro-phenyl)-[1,3,4]thiadiazol-2-ylsulfanyl]-but-2-ynyl}-azepane

Base Information

Chemical Name:1-{4-[5-(4-Nitro-phenyl)-[1,3,4]thiadiazol-2-ylsulfanyl]-but-2-ynyl}-azepane
CAS No.:84459-71-2
Molecular Formula:C₁₈H₂₀N₄O₂S₂
Molecular Weight:388.514
Hs Code.:

Synonyms:1-{4-[5-(4-Nitro-phenyl)-[1,3,4]thiadiazol-2-ylsulfanyl]-but-2-ynyl}-azepane

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Chemical Property of 1-{4-[5-(4-Nitro-phenyl)-[1,3,4]thiadiazol-2-ylsulfanyl]-but-2-ynyl}-azepane

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Technology Process of 1-{4-[5-(4-Nitro-phenyl)-[1,3,4]thiadiazol-2-ylsulfanyl]-but-2-ynyl}-azepane

There total 4 articles about 1-{4-[5-(4-Nitro-phenyl)-[1,3,4]thiadiazol-2-ylsulfanyl]-but-2-ynyl}-azepane 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: 58.0%

: 111-49-9
hexamethylene imine

: 50-00-0,30525-89-4,61233-19-0
formaldehyd

: 84459-85-8
2-(4-Nitro-phenyl)-5-prop-2-ynylsulfanyl-[1,3,4]thiadiazole

: 84459-71-2
1-{4-[5-(4-Nitro-phenyl)-[1,3,4]thiadiazol-2-ylsulfanyl]-but-2-ynyl}-azepane

Guidance literature:: copper(l) chloride; In 1,4-dioxane; at 70 ℃; for 3h;

Reference yield:

: 636-97-5
N-amino-(4-nitrophenyl)carboxamide

: 84459-71-2
1-{4-[5-(4-Nitro-phenyl)-[1,3,4]thiadiazol-2-ylsulfanyl]-but-2-ynyl}-azepane

Guidance literature:: Multi-step reaction with 4 steps

1: 52.5 percent / potassium hydroxide / methanol / 5 h / Ambient temperature

2: 40 percent / polyphosphoric acid / Ambient temperature

3: 63 percent / potassium hydroxide / ethanol / 1 h / Heating

4: 58 percent / cuprous chloride / dioxane / 3 h / 70 °C

With potassium hydroxide; PPA; copper(l) chloride; In 1,4-dioxane; methanol; ethanol;

Reference yield:

: 5-p-nitrophenyl-1,3,4-thiadiazole-2-thione

: 84459-71-2
1-{4-[5-(4-Nitro-phenyl)-[1,3,4]thiadiazol-2-ylsulfanyl]-but-2-ynyl}-azepane

Guidance literature:: Multi-step reaction with 2 steps

1: 63 percent / potassium hydroxide / ethanol / 1 h / Heating

2: 58 percent / cuprous chloride / dioxane / 3 h / 70 °C

With potassium hydroxide; copper(l) chloride; In 1,4-dioxane; ethanol;