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C27H28N4O6S2

Base Information
  • Chemical Name:C27H28N4O6S2
  • CAS No.:1445860-21-8
  • Molecular Formula:C27H28N4O6S2
  • Molecular Weight:568.675
  • Hs Code.:
C<sub>27</sub>H<sub>28</sub>N<sub>4</sub>O<sub>6</sub>S<sub>2</sub>

Synonyms:C27H28N4O6S2

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Chemical Property of C27H28N4O6S2
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Technology Process of C27H28N4O6S2

There total 8 articles about C27H28N4O6S2 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:
Guidance literature:
C13H10BrNO4; (S)-2-(3-t-butoxycarbonyl-2,2-dimethyl-1,3-oxazolidin-4-yl)-1,3-thiazole-4-thiocarboxamide; With potassium hydrogencarbonate; In 1,2-dimethoxyethane; at 20 ℃; Inert atmosphere;
With pyridine; trifluoroacetic anhydride; In 1,2-dimethoxyethane; at 0 - 20 ℃; for 3h; Inert atmosphere;
With triethylamine; In 1,2-dimethoxyethane; at 20 ℃; for 0.333333h; Inert atmosphere;
DOI:10.1021/ol401412v
Guidance literature:
Multi-step reaction with 3 steps
1.1: ammonium hydroxide / methanol / Inert atmosphere
2.1: Lawessons reagent / benzene / 16 h / Inert atmosphere; Reflux
3.1: potassium hydrogencarbonate / 1,2-dimethoxyethane / 20 °C / Inert atmosphere
3.2: 3 h / 0 - 20 °C / Inert atmosphere
3.3: 0.33 h / 20 °C / Inert atmosphere
With Lawessons reagent; ammonium hydroxide; potassium hydrogencarbonate; In methanol; 1,2-dimethoxyethane; benzene; 3.1: |Hantzsch Thiazole Synthesis / 3.2: |Hantzsch Thiazole Synthesis / 3.3: |Hantzsch Thiazole Synthesis;
DOI:10.1021/ol401412v
Guidance literature:
Multi-step reaction with 6 steps
1.1: ammonium hydroxide / methanol / 12 h / Inert atmosphere
2.1: Lawessons reagent / tetrahydrofuran / 16 h / Inert atmosphere; Reflux
3.1: potassium hydrogencarbonate / 1,2-dimethoxyethane / 20 °C / Inert atmosphere
3.2: 3 h / 0 - 20 °C / Inert atmosphere
3.3: 1 h / 20 °C / Inert atmosphere
4.1: ammonium hydroxide / methanol / Inert atmosphere
5.1: Lawessons reagent / benzene / 16 h / Inert atmosphere; Reflux
6.1: potassium hydrogencarbonate / 1,2-dimethoxyethane / 20 °C / Inert atmosphere
6.2: 3 h / 0 - 20 °C / Inert atmosphere
6.3: 0.33 h / 20 °C / Inert atmosphere
With Lawessons reagent; ammonium hydroxide; potassium hydrogencarbonate; In tetrahydrofuran; methanol; 1,2-dimethoxyethane; benzene; 3.1: |Hantzsch Thiazole Synthesis / 3.2: |Hantzsch Thiazole Synthesis / 3.3: |Hantzsch Thiazole Synthesis / 6.1: |Hantzsch Thiazole Synthesis / 6.2: |Hantzsch Thiazole Synthesis / 6.3: |Hantzsch Thiazole Synthesis;
DOI:10.1021/ol401412v
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