4-(5-(N,N-di-p-tolyl-4-aminophenyl)-thiophen-2-yl)-7-(4-hexyl-5-ethynyl-2-thienyl)-2,1,3-benzothiadiazole

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Chemical Name:4-(5-(N,N-di-p-tolyl-4-aminophenyl)-thiophen-2-yl)-7-(4-hexyl-5-ethynyl-2-thienyl)-2,1,3-benzothiadiazole
CAS No.:1361000-53-4
Molecular Formula:C₄₂H₃₇N₃S₃
Molecular Weight:679.974
Hs Code.:

Synonyms:4-(5-(N,N-di-p-tolyl-4-aminophenyl)-thiophen-2-yl)-7-(4-hexyl-5-ethynyl-2-thienyl)-2,1,3-benzothiadiazole

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Chemical Property of 4-(5-(N,N-di-p-tolyl-4-aminophenyl)-thiophen-2-yl)-7-(4-hexyl-5-ethynyl-2-thienyl)-2,1,3-benzothiadiazole

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Technology Process of 4-(5-(N,N-di-p-tolyl-4-aminophenyl)-thiophen-2-yl)-7-(4-hexyl-5-ethynyl-2-thienyl)-2,1,3-benzothiadiazole

There total 5 articles about 4-(5-(N,N-di-p-tolyl-4-aminophenyl)-thiophen-2-yl)-7-(4-hexyl-5-ethynyl-2-thienyl)-2,1,3-benzothiadiazole 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: 90.0%

: 1361000-50-1
4-(5-(N,N-di-p-tolyl-4-aminophenyl)-thiophen-2-yl)-7-(4-hexyl-5-(trimethylsilylethynyl)-2-thienyl)-2,1,3-benzothiadiazole

: 1361000-53-4
4-(5-(N,N-di-p-tolyl-4-aminophenyl)-thiophen-2-yl)-7-(4-hexyl-5-ethynyl-2-thienyl)-2,1,3-benzothiadiazole

Guidance literature:: With potassium carbonate; In methanol; dichloromethane; at 20 ℃; Inert atmosphere;
DOI:10.1002/chem.201102598

Reference yield:

: 1192689-61-4
4-bromo-7-(4-hexylthiophen-2-yl)benzo[c][1,2,5]thiadiazole

: 1361000-53-4
4-(5-(N,N-di-p-tolyl-4-aminophenyl)-thiophen-2-yl)-7-(4-hexyl-5-ethynyl-2-thienyl)-2,1,3-benzothiadiazole

Guidance literature:: Multi-step reaction with 4 steps

1: tetrakis(triphenylphosphine) palladium⁽⁰⁾ / toluene / 24 h / Inert atmosphere; Reflux

2: N-Bromosuccinimide; acetic acid / chloroform / 20 °C / Inert atmosphere; Darkness; Cooling with ice

3: copper(l) iodide; palladium diacetate; triethylamine; triphenylphosphine / dichloromethane / 50 °C / Inert atmosphere

4: potassium carbonate / methanol; dichloromethane / 20 °C / Inert atmosphere

With N-Bromosuccinimide; copper(l) iodide; tetrakis(triphenylphosphine) palladium⁽⁰⁾; palladium diacetate; potassium carbonate; acetic acid; triethylamine; triphenylphosphine; In methanol; dichloromethane; chloroform; toluene; 1: Stille coupling / 3: Sonogashira coupling;
DOI:10.1002/chem.201102598

Reference yield:

: 1361000-44-3
4-(5-(N,N-di-p-tolyl-4-aminophenyl)-thiophen-2-yl)-7-(4-hexyl-2-thienyl)-2,1,3-benzothiadiazole

: 1361000-53-4
4-(5-(N,N-di-p-tolyl-4-aminophenyl)-thiophen-2-yl)-7-(4-hexyl-5-ethynyl-2-thienyl)-2,1,3-benzothiadiazole

Guidance literature:: Multi-step reaction with 3 steps

1: N-Bromosuccinimide; acetic acid / chloroform / 20 °C / Inert atmosphere; Darkness; Cooling with ice

2: copper(l) iodide; palladium diacetate; triethylamine; triphenylphosphine / dichloromethane / 50 °C / Inert atmosphere

3: potassium carbonate / methanol; dichloromethane / 20 °C / Inert atmosphere

With N-Bromosuccinimide; copper(l) iodide; palladium diacetate; potassium carbonate; acetic acid; triethylamine; triphenylphosphine; In methanol; dichloromethane; chloroform; 2: Sonogashira coupling;
DOI:10.1002/chem.201102598