C₂₆H₃₁N₃O₃S

Base Information

Chemical Name:C₂₆H₃₁N₃O₃S
CAS No.:1374354-95-6
Molecular Formula:C₂₆H₃₁N₃O₃S
Molecular Weight:465.616
Hs Code.:

C<sub>26</sub>H<sub>31</sub>N<sub>3</sub>O<sub>3</sub>S

Synonyms:

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Chemical Property of C₂₆H₃₁N₃O₃S

Chemical Property:

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Technology Process of C₂₆H₃₁N₃O₃S

There total 15 articles about C₂₆H₃₁N₃O₃S 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:

: 913829-25-1
2-(methylthio)-6-{[(triisopropylsilyl)oxy]methyl}nicotinonitrile

: 1374354-95-6
C₂₆H₃₁N₃O₃S

Guidance literature:: Multi-step reaction with 9 steps

1: 3-chloro-benzenecarboperoxoic acid / ethanol

2: ethylmagnesium bromide / diethyl ether

3: diisobutylaluminium hydride / toluene

4: sodium chlorite; potassium dihydrogenphosphate; 2-methyl-but-2-ene

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

6: Lawessons reagent; pyridine / toluene / 100 °C

7: tetrabutyl ammonium fluoride / tetrahydrofuran

8: thionyl chloride / toluene

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

With Lawessons reagent; pyridine; sodium chlorite; potassium dihydrogenphosphate; thionyl chloride; 2-methyl-but-2-ene; ethylmagnesium bromide; tetrabutyl ammonium fluoride; diisobutylaluminium hydride; benzotriazol-1-ol; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; triethylamine; N-ethyl-N,N-diisopropylamine; 3-chloro-benzenecarboperoxoic acid; In tetrahydrofuran; diethyl ether; ethanol; chloroform; toluene; acetonitrile;
DOI:10.1016/j.bmcl.2012.03.067

Reference yield:

: 1374354-93-4
C₃₀H₄₄N₂O₂SSi

: 1374354-95-6
C₂₆H₃₁N₃O₃S

Guidance literature:: Multi-step reaction with 3 steps

1: tetrabutyl ammonium fluoride / tetrahydrofuran

2: thionyl chloride / toluene

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

With thionyl chloride; tetrabutyl ammonium fluoride; N-ethyl-N,N-diisopropylamine; In tetrahydrofuran; toluene; acetonitrile;
DOI:10.1016/j.bmcl.2012.03.067

Reference yield:

: 1-(4-isopropoxy-3-methylphenyl)ethanone

: 1374354-95-6
C₂₆H₃₁N₃O₃S

Guidance literature:: Multi-step reaction with 7 steps

1: PhMe₂NBr₃

2: sodium diformamide

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

4: Lawessons reagent; pyridine / toluene / 100 °C

5: tetrabutyl ammonium fluoride / tetrahydrofuran

6: thionyl chloride / toluene

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

With Lawessons reagent; pyridine; thionyl chloride; sodium diformamide; tetrabutyl ammonium fluoride; benzotriazol-1-ol; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; triethylamine; N-ethyl-N,N-diisopropylamine; In tetrahydrofuran; chloroform; toluene; acetonitrile;
DOI:10.1016/j.bmcl.2012.03.067