C₂₆H₂₄N₂O₄S

Base Information

Chemical Name:C₂₆H₂₄N₂O₄S
CAS No.:1374354-64-9
Molecular Formula:C₂₆H₂₄N₂O₄S
Molecular Weight:460.554
Hs Code.:

C<sub>26</sub>H<sub>24</sub>N<sub>2</sub>O<sub>4</sub>S

Synonyms:

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Chemical Property of C₂₆H₂₄N₂O₄S

Chemical Property:

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Technology Process of C₂₆H₂₄N₂O₄S

There total 12 articles about C₂₆H₂₄N₂O₄S 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:

: 18791-75-8
4-Bromothiophen-2-aldehyde

: 1374354-64-9
C₂₆H₂₄N₂O₄S

Guidance literature:: Multi-step reaction with 10 steps

1: sodium tetrahydroborate / methanol

2: 1H-imidazole

3: 1,3-bis[(diphenylphosphino)propane]dichloronickel(II)

4: n-butyllithium / tetrahydrofuran

5: benzotriazol-1-ol; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; triethylamine / chloroform

6: Burgess Reagent; triethylamine / acetonitrile / 80 °C

7: tetrabutyl ammonium fluoride / tetrahydrofuran

8: thionyl chloride / toluene

9: N-ethyl-N,N-diisopropylamine / acetonitrile

10: water; sodium hydroxide / ethanol

With 1H-imidazole; sodium tetrahydroborate; n-butyllithium; thionyl chloride; Burgess Reagent; 1,3-bis[(diphenylphosphino)propane]dichloronickel(II); tetrabutyl ammonium fluoride; water; benzotriazol-1-ol; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; triethylamine; N-ethyl-N,N-diisopropylamine; sodium hydroxide; In tetrahydrofuran; methanol; ethanol; chloroform; toluene; acetonitrile;
DOI:10.1016/j.bmcl.2012.03.067

Reference yield:

: 913828-80-5
tert-butyl[(4-ethyl-2-thienyl)methoxy]dimethylsilane

: 1374354-64-9
C₂₆H₂₄N₂O₄S

Guidance literature:: Multi-step reaction with 7 steps

1: n-butyllithium / tetrahydrofuran

2: benzotriazol-1-ol; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; triethylamine / chloroform

3: Burgess Reagent; triethylamine / acetonitrile / 80 °C

4: tetrabutyl ammonium fluoride / tetrahydrofuran

5: thionyl chloride / toluene

6: N-ethyl-N,N-diisopropylamine / acetonitrile

7: water; sodium hydroxide / ethanol

With n-butyllithium; thionyl chloride; Burgess Reagent; tetrabutyl ammonium fluoride; water; benzotriazol-1-ol; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; triethylamine; N-ethyl-N,N-diisopropylamine; sodium hydroxide; In tetrahydrofuran; ethanol; chloroform; toluene; acetonitrile;
DOI:10.1016/j.bmcl.2012.03.067

Reference yield:

: C₂₂H₁₉NO₃S

: 1374354-64-9
C₂₆H₂₄N₂O₄S

Guidance literature:: Multi-step reaction with 3 steps

1: thionyl chloride / toluene

2: N-ethyl-N,N-diisopropylamine / acetonitrile

3: water; sodium hydroxide / ethanol

With thionyl chloride; water; N-ethyl-N,N-diisopropylamine; sodium hydroxide; In ethanol; toluene; acetonitrile;
DOI:10.1016/j.bmcl.2012.03.067