C₅₈H₉₂IN₁₅O₁₄

Base Information

Chemical Name:C₅₈H₉₂IN₁₅O₁₄
CAS No.:1316857-51-8
Molecular Formula:C₅₈H₉₂IN₁₅O₁₄
Molecular Weight:1350.37
Hs Code.:

C<sub>58</sub>H<sub>92</sub>IN<sub>15</sub>O<sub>14</sub>

Synonyms:

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Chemical Property of C₅₈H₉₂IN₁₅O₁₄

Chemical Property:

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Technology Process of C₅₈H₉₂IN₁₅O₁₄

There total 10 articles about C₅₈H₉₂IN₁₅O₁₄ 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:

: 168827-67-6
C₁₄H₂₆N₆O₄

: C₃₀H₄₀IN₃O₆

: 1316857-51-8
C₅₈H₉₂IN₁₅O₁₄

Guidance literature:: With copper(l) iodide; N-ethyl-N,N-diisopropylamine; In tetrahydrofuran; at 25 ℃; for 15h;
DOI:10.1039/c1ob05606a

Reference yield:

: 1316857-59-6
C₁₄H₁₇IO₄

: 1316857-51-8
C₅₈H₉₂IN₁₅O₁₄

Guidance literature:: Multi-step reaction with 6 steps

1: hydrogenchloride; methanol / 4 h / 50 °C

2: sodium hydroxide / water; dimethyl sulfoxide / 18 h / 25 °C

3: zinc trifluoromethanesulfonate; triethylamine / dichloromethane / 20 h / 25 °C

4: copper(l) iodide; N-ethyl-N,N-diisopropylamine / tetrahydrofuran / 15 h / 25 °C

5: methanol; potassium carbonate / 1.5 h / 25 °C

6: copper(l) iodide; N-ethyl-N,N-diisopropylamine / tetrahydrofuran / 15 h / 25 °C

With hydrogenchloride; methanol; copper(l) iodide; zinc trifluoromethanesulfonate; potassium carbonate; triethylamine; N-ethyl-N,N-diisopropylamine; sodium hydroxide; In tetrahydrofuran; dichloromethane; water; dimethyl sulfoxide; 4: Huisgen-Sharpless 1,3-dipolar cycloaddition / 6: Huisgen-Sharpless 1,3-dipolar cycloaddition;
DOI:10.1039/c1ob05606a

Reference yield:

: 1316857-42-7
C₁₂H₁₇IO₄

: 1316857-51-8
C₅₈H₉₂IN₁₅O₁₄

Guidance literature:: Multi-step reaction with 5 steps

1: sodium hydroxide / water; dimethyl sulfoxide / 18 h / 25 °C

2: zinc trifluoromethanesulfonate; triethylamine / dichloromethane / 20 h / 25 °C

3: copper(l) iodide; N-ethyl-N,N-diisopropylamine / tetrahydrofuran / 15 h / 25 °C

4: methanol; potassium carbonate / 1.5 h / 25 °C

5: copper(l) iodide; N-ethyl-N,N-diisopropylamine / tetrahydrofuran / 15 h / 25 °C

With methanol; copper(l) iodide; zinc trifluoromethanesulfonate; potassium carbonate; triethylamine; N-ethyl-N,N-diisopropylamine; sodium hydroxide; In tetrahydrofuran; dichloromethane; water; dimethyl sulfoxide; 3: Huisgen-Sharpless 1,3-dipolar cycloaddition / 5: Huisgen-Sharpless 1,3-dipolar cycloaddition;
DOI:10.1039/c1ob05606a