C₅₄H₇₁N₅O₁₀

Base Information

Chemical Name:C₅₄H₇₁N₅O₁₀
CAS No.:1017967-93-9
Molecular Formula:C₅₄H₇₁N₅O₁₀
Molecular Weight:950.185
Hs Code.:

C<sub>54</sub>H<sub>71</sub>N<sub>5</sub>O<sub>10</sub>

Synonyms:C₅₄H₇₁N₅O₁₀

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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 C₅₄H₇₁N₅O₁₀

Chemical Property:

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Technology Process of C₅₄H₇₁N₅O₁₀

There total 7 articles about C₅₄H₇₁N₅O₁₀ 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: 90.0%

: 1220709-66-9
C₅₉H₇₉N₅O₁₂

: 1017967-93-9
C₅₄H₇₁N₅O₁₀

Guidance literature:: With trifluoroacetic acid; In dichloromethane; for 6h; Inert atmosphere; Reflux;
DOI:10.1039/b9nj00305c

Reference yield:

: 303-38-8
2,3-Dihydroxybenzoic acid

: 1017967-93-9
C₅₄H₇₁N₅O₁₀

Guidance literature:: Multi-step reaction with 8 steps

1.1: potassium carbonate / acetonitrile / 1 h / 80 °C / Inert atmosphere

1.2: 17 h / 70 °C / Inert atmosphere

2.1: trifluoro-[1,3,5]triazine; pyridine / dichloromethane / 17 h / 0 - 20 °C / Inert atmosphere

3.1: N-ethyl-N,N-diisopropylamine / dichloromethane / 61.5 h / 20 °C / Inert atmosphere

4.1: tetrabutyl ammonium fluoride / tetrahydrofuran / 3 h / 0 °C / Inert atmosphere; Reflux

5.1: dimethyl sulfoxide; oxalyl dichloride / dichloromethane / -60 - -30 °C / Inert atmosphere

6.1: aminosulfonic acid; sodium chlorite / tetrahydrofuran; water / 13 h / 20 °C / Inert atmosphere

7.1: dicyclohexyl-carbodiimide; dmap; benzotriazol-1-ol / dichloromethane / 60 h / 20 °C / Inert atmosphere

8.1: trifluoroacetic acid / dichloromethane / 6 h / Inert atmosphere; Reflux

With pyridine; dmap; sodium chlorite; trifluoro-[1,3,5]triazine; oxalyl dichloride; aminosulfonic acid; tetrabutyl ammonium fluoride; potassium carbonate; benzotriazol-1-ol; dimethyl sulfoxide; N-ethyl-N,N-diisopropylamine; dicyclohexyl-carbodiimide; trifluoroacetic acid; In tetrahydrofuran; dichloromethane; water; acetonitrile;

Reference yield:

: 130432-57-4
2,3-diallyloxybenzoic acid

: 1017967-93-9
C₅₄H₇₁N₅O₁₀

Guidance literature:: Multi-step reaction with 7 steps

1: trifluoro-[1,3,5]triazine; pyridine / dichloromethane / 17 h / 0 - 20 °C / Inert atmosphere

2: N-ethyl-N,N-diisopropylamine / dichloromethane / 61.5 h / 20 °C / Inert atmosphere

3: tetrabutyl ammonium fluoride / tetrahydrofuran / 3 h / 0 °C / Inert atmosphere; Reflux

4: dimethyl sulfoxide; oxalyl dichloride / dichloromethane / -60 - -30 °C / Inert atmosphere

5: aminosulfonic acid; sodium chlorite / tetrahydrofuran; water / 13 h / 20 °C / Inert atmosphere

6: dicyclohexyl-carbodiimide; dmap; benzotriazol-1-ol / dichloromethane / 60 h / 20 °C / Inert atmosphere

7: trifluoroacetic acid / dichloromethane / 6 h / Inert atmosphere; Reflux

With pyridine; dmap; sodium chlorite; trifluoro-[1,3,5]triazine; oxalyl dichloride; aminosulfonic acid; tetrabutyl ammonium fluoride; benzotriazol-1-ol; dimethyl sulfoxide; N-ethyl-N,N-diisopropylamine; dicyclohexyl-carbodiimide; trifluoroacetic acid; In tetrahydrofuran; dichloromethane; water;