C₂₃H₃₃N₃O₂S

Base Information

Chemical Name:C₂₃H₃₃N₃O₂S
CAS No.:1391848-00-2
Molecular Formula:C₂₃H₃₃N₃O₂S
Molecular Weight:415.6
Hs Code.:

C<sub>23</sub>H<sub>33</sub>N<sub>3</sub>O<sub>2</sub>S

Synonyms:C₂₃H₃₃N₃O₂S

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Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

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Chemical Property of C₂₃H₃₃N₃O₂S

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Technology Process of C₂₃H₃₃N₃O₂S

There total 6 articles about C₂₃H₃₃N₃O₂S 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: 99.0%

: 1391848-03-5
C₂₈H₄₁N₃O₄S

: 1391848-00-2
C₂₃H₃₃N₃O₂S

Guidance literature:: With triphenylphosphine; In tetrahydrofuran; water;
DOI:10.1016/j.bmcl.2012.06.059

Reference yield:

: 1391847-99-6
C₁₆H₂₆N₂O₄

: 1391848-00-2
C₂₃H₃₃N₃O₂S

Guidance literature:: Multi-step reaction with 2 steps

1: triethylamine / dichloromethane / 15 h / 20 °C

2: triphenylphosphine / tetrahydrofuran; water

With triethylamine; triphenylphosphine; In tetrahydrofuran; dichloromethane; water; 2: Staudinger reduction;
DOI:10.1016/j.bmcl.2012.06.059

Reference yield:

: C₁₁H₁₆ClNO₂

: 1391848-00-2
C₂₃H₃₃N₃O₂S

Guidance literature:: Multi-step reaction with 4 steps

1.1: sodium azide; tetrabutylammomium bromide; potassium iodide / toluene / Reflux

2.1: palladium on activated charcoal; hydrogen / ethanol / 20 °C

2.2: 2 h / 80 °C

2.3: 15 h / 20 °C

3.1: triethylamine / dichloromethane / 15 h / 20 °C

4.1: triphenylphosphine / tetrahydrofuran; water

With sodium azide; palladium on activated charcoal; tetrabutylammomium bromide; hydrogen; triethylamine; triphenylphosphine; potassium iodide; In tetrahydrofuran; ethanol; dichloromethane; water; toluene; 4.1: Staudinger reduction;
DOI:10.1016/j.bmcl.2012.06.059