C₂₅H₂₉N₃O₃S

Base Information

Chemical Name:C₂₅H₂₉N₃O₃S
CAS No.:1374354-97-8
Molecular Formula:C₂₅H₂₉N₃O₃S
Molecular Weight:451.59
Hs Code.:

C<sub>25</sub>H<sub>29</sub>N<sub>3</sub>O<sub>3</sub>S

Synonyms:

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Chemical Property of C₂₅H₂₉N₃O₃S

Chemical Property:

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Technology Process of C₂₅H₂₉N₃O₃S

There total 17 articles about C₂₅H₂₉N₃O₃S 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:

: 1374354-93-4
C₃₀H₄₄N₂O₂SSi

: 1374354-97-8
C₂₅H₂₉N₃O₃S

Guidance literature:: Multi-step reaction with 4 steps

1: tetrabutyl ammonium fluoride / tetrahydrofuran

2: thionyl chloride / toluene

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

4: water; sodium hydroxide / ethanol

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

Reference yield:

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

: 1374354-97-8
C₂₅H₂₉N₃O₃S

Guidance literature:: Multi-step reaction with 8 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

8: water; sodium hydroxide / ethanol

With Lawessons reagent; pyridine; thionyl chloride; sodium diformamide; 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:

: 175277-27-7
6-formyl-2-(methylthio)nicotinonitrile

: 1374354-97-8
C₂₅H₂₉N₃O₃S

Guidance literature:: Multi-step reaction with 12 steps

1: sodium tetrahydroborate

2: 1H-imidazole

3: 3-chloro-benzenecarboperoxoic acid / ethanol

4: ethylmagnesium bromide / diethyl ether

5: diisobutylaluminium hydride / toluene

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

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

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

9: tetrabutyl ammonium fluoride / tetrahydrofuran

10: thionyl chloride / toluene

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

12: water; sodium hydroxide / ethanol

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