C₂₆H₂₃N₃O₅S

Base Information

Chemical Name:C₂₆H₂₃N₃O₅S
CAS No.:329042-64-0
Molecular Formula:C₂₆H₂₃N₃O₅S
Molecular Weight:489.552
Hs Code.:

C<sub>26</sub>H<sub>23</sub>N<sub>3</sub>O<sub>5</sub>S

Synonyms:

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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 C₂₆H₂₃N₃O₅S

Chemical Property:

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Technology Process of C₂₆H₂₃N₃O₅S

There total 3 articles about C₂₆H₂₃N₃O₅S 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: 10.0%

: C₁₈H₁₄ClNO₂

: 144-80-9
sulphaacetamide

: 329042-64-0
C₂₆H₂₃N₃O₅S

Guidance literature:: With 4-methyl-morpholine; In dichloromethane; at 0 ℃; for 12h;
DOI:10.1002/anie.201505054

Reference yield:

: 91-56-5,1186480-61-4,84788-92-1
indole-2,3-dione

: 329042-64-0
C₂₆H₂₃N₃O₅S

Guidance literature:: Multi-step reaction with 3 steps

1: potassium hydroxide / ethanol / 12 h / Reflux; Molecular sieve

2: thionyl chloride / dichloromethane / 3 h / Reflux

3: 4-methyl-morpholine / dichloromethane / 12 h / 0 °C

With 4-methyl-morpholine; thionyl chloride; potassium hydroxide; In ethanol; dichloromethane; 1: |Pfitzinger Quinoline Synthesis;
DOI:10.1002/anie.201505054

Reference yield:

: 1676-63-7
4'-ethoxyacetophenone

: 329042-64-0
C₂₆H₂₃N₃O₅S

Guidance literature:: Multi-step reaction with 3 steps

1: potassium hydroxide / ethanol / 12 h / Reflux; Molecular sieve

2: thionyl chloride / dichloromethane / 3 h / Reflux

3: 4-methyl-morpholine / dichloromethane / 12 h / 0 °C

With 4-methyl-morpholine; thionyl chloride; potassium hydroxide; In ethanol; dichloromethane; 1: |Pfitzinger Quinoline Synthesis;
DOI:10.1002/anie.201505054