C₂₆H₂₆N₄O₆S₂

Base Information

Chemical Name:C₂₆H₂₆N₄O₆S₂
CAS No.:1445860-12-7
Molecular Formula:C₂₆H₂₆N₄O₆S₂
Molecular Weight:554.648
Hs Code.:

C<sub>26</sub>H<sub>26</sub>N<sub>4</sub>O<sub>6</sub>S<sub>2</sub>

Synonyms:C₂₆H₂₆N₄O₆S₂

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Chemical Property of C₂₆H₂₆N₄O₆S₂

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Technology Process of C₂₆H₂₆N₄O₆S₂

There total 9 articles about C₂₆H₂₆N₄O₆S₂ 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: 100.0%

: 1445860-21-8
C₂₇H₂₈N₄O₆S₂

: 1445860-12-7
C₂₆H₂₆N₄O₆S₂

Guidance literature:: With lithium hydroxide monohydrate; In methanol; at 20 ℃; for 8h; Inert atmosphere;
DOI:10.1021/ol401412v

Reference yield:

: 478937-39-2
(S)-2-(3-t-butoxycarbonyl-2,2-dimethyl-1,3-oxazolidin-4-yl)-1,3-thiazole-4-thiocarboxamide

: 1445860-12-7
C₂₆H₂₆N₄O₆S₂

Guidance literature:: Multi-step reaction with 2 steps

1.1: potassium hydrogencarbonate / 1,2-dimethoxyethane / 20 °C / Inert atmosphere

1.2: 3 h / 0 - 20 °C / Inert atmosphere

1.3: 0.33 h / 20 °C / Inert atmosphere

2.1: lithium hydroxide monohydrate / methanol / 8 h / 20 °C / Inert atmosphere

With lithium hydroxide monohydrate; potassium hydrogencarbonate; In methanol; 1,2-dimethoxyethane; 1.1: |Hantzsch Thiazole Synthesis / 1.2: |Hantzsch Thiazole Synthesis / 1.3: |Hantzsch Thiazole Synthesis;
DOI:10.1021/ol401412v

Reference yield:

: 478937-33-6
ethyl (S)-2-(3-t-butoxycarbonyl-2,2-dimethyl-1,3-oxazolidin-4-yl)-1,3-thiazole-4-carboxylate

: 1445860-12-7
C₂₆H₂₆N₄O₆S₂

Guidance literature:: Multi-step reaction with 4 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

4.1: lithium hydroxide monohydrate / methanol / 8 h / 20 °C / Inert atmosphere

With Lawessons reagent; ammonium hydroxide; lithium hydroxide monohydrate; 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