C₂₄H₂₃F₂N₅O₄S

Base Information

Chemical Name:C₂₄H₂₃F₂N₅O₄S
CAS No.:1616277-62-3
Molecular Formula:C₂₄H₂₃F₂N₅O₄S
Molecular Weight:515.541
Hs Code.:

C<sub>24</sub>H<sub>23</sub>F<sub>2</sub>N<sub>5</sub>O<sub>4</sub>S

Synonyms:C₂₄H₂₃F₂N₅O₄S

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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 C₂₄H₂₃F₂N₅O₄S

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Technology Process of C₂₄H₂₃F₂N₅O₄S

There total 17 articles about C₂₄H₂₃F₂N₅O₄S 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:

: 1616278-44-4
C₂₅H₂₅F₂N₅O₄S

: 1616277-62-3
C₂₄H₂₃F₂N₅O₄S

Guidance literature:: With lithium chloride; In N,N-dimethyl-formamide; at 100 ℃; for 1h;

Reference yield:

: 1616277-94-1
C₁₄H₁₈O₇

: 1616277-62-3
C₂₄H₂₃F₂N₅O₄S

Guidance literature:: Multi-step reaction with 11 steps

1.1: hydrogenchloride / ethyl acetate / 1 h / 0 - 20 °C

2.1: oxalyl dichloride; N,N-dimethyl-formamide / N,N-dimethyl-formamide; toluene / 2 h / 0 - 20 °C / Inert atmosphere

3.1: chloroform / 16 h / 20 °C

4.1: 1-methyl-1H-imidazole / 5 h / 60 °C

5.1: lithium hydroxide; water / ethanol / 20 h / 45 °C

6.1: ammonium chloride; chloro-N,N,N',N'-bis(tetramethylene)formamidinium hexafluorophosphate; N-ethyl-N,N-diisopropylamine / 20 °C

7.1: toluene-4-sulfonic acid / 1,2-dichloro-ethane / 2 h / 90 °C

8.1: caesium carbonate / N,N-dimethyl-formamide / 1.5 h / 20 °C

9.1: sodium hydroxide; water / methanol / 60 °C

10.1: triethylamine; isobutyl chloroformate / tetrahydrofuran / 0.25 h / 0 °C

10.2: -78 °C

11.1: lithium chloride / N,N-dimethyl-formamide / 1 h / 100 °C

With 1-methyl-1H-imidazole; hydrogenchloride; oxalyl dichloride; water; chloro-N,N,N',N'-bis(tetramethylene)formamidinium hexafluorophosphate; ammonium chloride; caesium carbonate; toluene-4-sulfonic acid; triethylamine; N-ethyl-N,N-diisopropylamine; N,N-dimethyl-formamide; lithium chloride; sodium hydroxide; lithium hydroxide; isobutyl chloroformate; In tetrahydrofuran; methanol; ethanol; chloroform; ethyl acetate; 1,2-dichloro-ethane; N,N-dimethyl-formamide; toluene;

Reference yield:

: 1616277-93-0
C₁₂H₂₁NO₄

: 1616277-62-3
C₂₄H₂₃F₂N₅O₄S

Guidance literature:: Multi-step reaction with 12 steps

1.1: lithium hexamethyldisilazane / tetrahydrofuran / 0.5 h / -70 °C / Inert atmosphere

1.2: 1 h / -70 °C

2.1: hydrogenchloride / ethyl acetate / 1 h / 0 - 20 °C

3.1: oxalyl dichloride; N,N-dimethyl-formamide / N,N-dimethyl-formamide; toluene / 2 h / 0 - 20 °C / Inert atmosphere

4.1: chloroform / 16 h / 20 °C

5.1: 1-methyl-1H-imidazole / 5 h / 60 °C

6.1: lithium hydroxide; water / ethanol / 20 h / 45 °C

7.1: ammonium chloride; chloro-N,N,N',N'-bis(tetramethylene)formamidinium hexafluorophosphate; N-ethyl-N,N-diisopropylamine / 20 °C

8.1: toluene-4-sulfonic acid / 1,2-dichloro-ethane / 2 h / 90 °C

9.1: caesium carbonate / N,N-dimethyl-formamide / 1.5 h / 20 °C

10.1: sodium hydroxide; water / methanol / 60 °C

11.1: triethylamine; isobutyl chloroformate / tetrahydrofuran / 0.25 h / 0 °C

11.2: -78 °C

12.1: lithium chloride / N,N-dimethyl-formamide / 1 h / 100 °C

With 1-methyl-1H-imidazole; hydrogenchloride; oxalyl dichloride; water; chloro-N,N,N',N'-bis(tetramethylene)formamidinium hexafluorophosphate; ammonium chloride; caesium carbonate; toluene-4-sulfonic acid; triethylamine; N-ethyl-N,N-diisopropylamine; N,N-dimethyl-formamide; lithium chloride; sodium hydroxide; lithium hydroxide; lithium hexamethyldisilazane; isobutyl chloroformate; In tetrahydrofuran; methanol; ethanol; chloroform; ethyl acetate; 1,2-dichloro-ethane; N,N-dimethyl-formamide; toluene;