C₅₇H₃₂F₁₀N₆O₅S

Base Information

Chemical Name:C₅₇H₃₂F₁₀N₆O₅S
CAS No.:1420764-87-9
Molecular Formula:C₅₇H₃₂F₁₀N₆O₅S
Molecular Weight:1102.97
Hs Code.:

C<sub>57</sub>H<sub>32</sub>F<sub>10</sub>N<sub>6</sub>O<sub>5</sub>S

Synonyms:C₅₇H₃₂F₁₀N₆O₅S

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Chemical Property of C₅₇H₃₂F₁₀N₆O₅S

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Technology Process of C₅₇H₃₂F₁₀N₆O₅S

There total 6 articles about C₅₇H₃₂F₁₀N₆O₅S 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: 6.6%

: 1420764-54-0
2-{2-[(acetylsulfanyl)methyl]-3-{[(2-formylphenyl)carbamoyl]methoxy}phenoxy}-N-(2-formylphenyl)acetamide

: 167482-91-9
5-(pentafluorophenyl)dipyrromethane

: 1420764-87-9
C₅₇H₃₂F₁₀N₆O₅S

Guidance literature:: 2-{2-[(acetylsulfanyl)methyl]-3-{[(2-formylphenyl)carbamoyl]methoxy}phenoxy}-N-(2-formylphenyl)acetamide; 5-(pentafluorophenyl)dipyrromethane; With trifluoroacetic acid; In dichloromethane; at 20 ℃; Inert atmosphere;

With 2,3-dicyano-5,6-dichloro-p-benzoquinone; In dichloromethane; at 20 ℃; for 7h; Inert atmosphere;

With triethylamine; In dichloromethane; at 20 ℃; for 0.5h; Inert atmosphere;
DOI:10.1002/cssc.201200572

Reference yield:

: 608-25-3
2-methylbenzene-1,3-diol

: 1420764-87-9
C₅₇H₃₂F₁₀N₆O₅S

Guidance literature:: Multi-step reaction with 6 steps

1.1: potassium carbonate / acetone / 2 h / 60 °C / Inert atmosphere

1.2: 48 h / Reflux; Inert atmosphere

2.1: N-Bromosuccinimide; dibenzoyl peroxide / tetrachloromethane / Reflux; Inert atmosphere

3.1: acetone / 20 °C / Inert atmosphere

4.1: trifluoroacetic acid / dichloromethane / 20 °C / Inert atmosphere

5.1: 2-chloro-1-methyl-pyridinium iodide; triethylamine / dichloromethane / 20 °C / Inert atmosphere

6.1: trifluoroacetic acid / dichloromethane / 20 °C / Inert atmosphere

6.2: 7 h / 20 °C / Inert atmosphere

6.3: 0.5 h / 20 °C / Inert atmosphere

With N-Bromosuccinimide; 2-chloro-1-methyl-pyridinium iodide; potassium carbonate; triethylamine; trifluoroacetic acid; dibenzoyl peroxide; In tetrachloromethane; dichloromethane; acetone;
DOI:10.1002/cssc.201200572

Reference yield:

: 1420764-40-4
1-bromomentyl-2,6-bis(tert-butoxycarbonylmethoxy)benzene

: 1420764-87-9
C₅₇H₃₂F₁₀N₆O₅S

Guidance literature:: Multi-step reaction with 4 steps

1.1: acetone / 20 °C / Inert atmosphere

2.1: trifluoroacetic acid / dichloromethane / 20 °C / Inert atmosphere

3.1: 2-chloro-1-methyl-pyridinium iodide; triethylamine / dichloromethane / 20 °C / Inert atmosphere

4.1: trifluoroacetic acid / dichloromethane / 20 °C / Inert atmosphere

4.2: 7 h / 20 °C / Inert atmosphere

4.3: 0.5 h / 20 °C / Inert atmosphere

With 2-chloro-1-methyl-pyridinium iodide; triethylamine; trifluoroacetic acid; In dichloromethane; acetone;
DOI:10.1002/cssc.201200572