5-{4'-[5-(2-bromo-phenyl)-[1,3,4]oxadiazol-2-ylsulfanylmethyl]-biphenyl-2-yl}-2-trityl-2H-tetrazole

Base Information

Chemical Name:5-{4'-[5-(2-bromo-phenyl)-[1,3,4]oxadiazol-2-ylsulfanylmethyl]-biphenyl-2-yl}-2-trityl-2H-tetrazole
CAS No.:882213-53-8
Molecular Formula:C₄₁H₂₉BrN₆OS
Molecular Weight:733.691
Hs Code.:

5-{4'-[5-(2-bromo-phenyl)-[1,3,4]oxadiazol-2-ylsulfanylmethyl]-biphenyl-2-yl}-2-trityl-2<i>H</i>-tetrazole

Synonyms:5-{4'-[5-(2-bromo-phenyl)-[1,3,4]oxadiazol-2-ylsulfanylmethyl]-biphenyl-2-yl}-2-trityl-2H-tetrazole

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Chemical Property of 5-{4'-[5-(2-bromo-phenyl)-[1,3,4]oxadiazol-2-ylsulfanylmethyl]-biphenyl-2-yl}-2-trityl-2H-tetrazole

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Technology Process of 5-{4'-[5-(2-bromo-phenyl)-[1,3,4]oxadiazol-2-ylsulfanylmethyl]-biphenyl-2-yl}-2-trityl-2H-tetrazole

There total 5 articles about 5-{4'-[5-(2-bromo-phenyl)-[1,3,4]oxadiazol-2-ylsulfanylmethyl]-biphenyl-2-yl}-2-trityl-2H-tetrazole 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: 92.0%

: 203268-68-2,161013-20-3
2-mercapto-5-(2-bromophenyl)-1,3,4-oxadiazole

: 133051-88-4
N-(triphenylmethyl)-5-<4'-(bromomethyl)biphenyl-2-yl>tetrazole

: 882213-53-8
5-{4'-[5-(2-bromo-phenyl)-[1,3,4]oxadiazol-2-ylsulfanylmethyl]-biphenyl-2-yl}-2-trityl-2H-tetrazole

Guidance literature:: 2-mercapto-5-(2-bromophenyl)-1,3,4-oxadiazole; With potassium carbonate; In acetone; for 0.5h; Heating;

N-(triphenylmethyl)-5-<4'-(bromomethyl)biphenyl-2-yl>tetrazole; In acetone; Heating;
DOI:10.1002/jccs.200500079

Reference yield:

: 29418-67-5
2-bromobenzohydrazide

: 882213-53-8
5-{4'-[5-(2-bromo-phenyl)-[1,3,4]oxadiazol-2-ylsulfanylmethyl]-biphenyl-2-yl}-2-trityl-2H-tetrazole

Guidance literature:: Multi-step reaction with 2 steps

1.1: KOH / ethanol / Heating

2.1: K₂CO₃ / acetone / 0.5 h / Heating

2.2: 92 percent / acetone / Heating

With potassium hydroxide; potassium carbonate; In ethanol; acetone;
DOI:10.1002/jccs.200500079

Reference yield:

: 114772-53-1
2-Cyano-4'-methylbiphenyl

: 882213-53-8
5-{4'-[5-(2-bromo-phenyl)-[1,3,4]oxadiazol-2-ylsulfanylmethyl]-biphenyl-2-yl}-2-trityl-2H-tetrazole

Guidance literature:: Multi-step reaction with 4 steps

1.1: 96 percent / ZnCl₂; NaN₃ / dimethylformamide / 36 h / Heating

2.1: 91 percent / aq. NaOH / toluene / 3 h / 20 °C

3.1: 92 percent / N-bromosuccinimide; dibenzoyl peroxide / CCl₄ / 8 h / Heating

4.1: K₂CO₃ / acetone / 0.5 h / Heating

4.2: 92 percent / acetone / Heating

With sodium hydroxide; N-Bromosuccinimide; sodium azide; potassium carbonate; zinc(II) chloride; dibenzoyl peroxide; In tetrachloromethane; N,N-dimethyl-formamide; acetone; toluene;
DOI:10.1002/jccs.200500079