ChemicalBook CAS DataBase List 4,7-Bis(thiophen-2-yl)benzo[c][1,2,5]thiadiazole

4,7-Bis(thiophen-2-yl)benzo[c][1,2,5]thiadiazole synthesis

10synthesis methods

Product Name:4,7-Bis(thiophen-2-yl)benzo[c][1,2,5]thiadiazole
CAS Number:165190-76-1
Molecular formula:C14H8N2S3
Molecular Weight:300.42

6165-68-0 Synthesis

6165-68-0
400 suppliers
$14.00/5g

15155-41-6
321 suppliers
$20.00/1g

4,7-Bis(thiophen-2-yl)benzo[c][1,2,5]thiadiazole

165190-76-1
95 suppliers
$40.00/250mg

Yield:165190-76-1 95%

Reaction Conditions:

with O₄P^(3-)*3K⁽¹⁺⁾*5H₂O;tris(1-adamantyl)phosphine;{2-[((acetyl-κO)amino)phenyl-κC](tri-1-adamantylphosphine)palladium}(p-toluenesulfonate) in tetrahydrofuran at 20; for 1 h;Suzuki-Miyaura Coupling;

Steps:

To a mixture of 4,7-dibromobenzo[cJ{1,2,5]thiadiazole (147 mg, 0.50 mmol, 1 equiv),thiophen-2-ylboronic acid (192 mg, 1.50 mmol, 3 equiv), and K3P045H20 (0.90 g, 3.0 mmol, 6 equiv) was added THF (900 jiL) then a THF stock solution of 3 and PAd3 (100 iL, 0.25 jtmol ofPd/PAds). The mixture was stirred at room temperature for 1 h. The reaction mixture was diluted with ethyl acetate then extracted with water. The combine organic layers were evaporated andthe crude product was purified by flash chromatography. After drying, 143 mg (95%) of 40 was obtained as an orange solid. NMR spectroscopic data agreed with literature values.

References:

THE TRUSTEES OF PRINCETON UNIVERSITY;CARROW, Brad P.;CHEN, Liye WO2017/75581, 2017, A1 Location in patent:Page/Page column 31

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188290-36-0 Synthesis