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C53H73N11O7

Base Information
  • Chemical Name:C53H73N11O7
  • CAS No.:1427038-84-3
  • Molecular Formula:C53H73N11O7
  • Molecular Weight:976.232
  • Hs Code.:
C<sub>53</sub>H<sub>73</sub>N<sub>11</sub>O<sub>7</sub>

Synonyms:C53H73N11O7

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Chemical Property of C53H73N11O7
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Technology Process of C53H73N11O7

There total 13 articles about C53H73N11O7 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:
Guidance literature:
Multi-step reaction with 10 steps
1.1: sodium carbonate; acetic anhydride / water; acetone / 3 h / 0 - 20 °C
1.2: 3 h / 0 - 20 °C
1.3: 1 h / Reflux; Enzymatic reaction
2.1: sodium hydroxide / water; 1,4-dioxane / 0 °C
3.1: triethylamine / dichloromethane / 0 h / 0 °C / Inert atmosphere
4.1: sodium azide / N,N-dimethyl-formamide / 55 °C / Inert atmosphere
5.1: trifluoroacetic acid / 0.5 h / Inert atmosphere
5.2: 2 h / 4 °C / Inert atmosphere
6.1: N-ethyl-N,N-diisopropylamine / acetonitrile / 2 h
7.1: hydrogen; acetic acid; palladium 10% on activated carbon / methanol / 2 h
8.1: N-ethyl-N,N-diisopropylamine / acetonitrile / 3 h
9.1: 0.5 h / 0 °C
10.1: N-ethyl-N,N-diisopropylamine / acetonitrile / 2 h
With sodium azide; palladium 10% on activated carbon; hydrogen; acetic anhydride; sodium carbonate; acetic acid; triethylamine; N-ethyl-N,N-diisopropylamine; trifluoroacetic acid; sodium hydroxide; In 1,4-dioxane; methanol; dichloromethane; water; N,N-dimethyl-formamide; acetone; acetonitrile;
DOI:10.1021/ja401151v
Guidance literature:
Multi-step reaction with 11 steps
1.1: trifluoroacetic acid; platinum(IV) oxide; hydrogen / methanol / 40.5 h / 20 °C
2.1: sodium carbonate; acetic anhydride / water; acetone / 3 h / 0 - 20 °C
2.2: 3 h / 0 - 20 °C
2.3: 1 h / Reflux; Enzymatic reaction
3.1: sodium hydroxide / water; 1,4-dioxane / 0 °C
4.1: triethylamine / dichloromethane / 0 h / 0 °C / Inert atmosphere
5.1: sodium azide / N,N-dimethyl-formamide / 55 °C / Inert atmosphere
6.1: trifluoroacetic acid / 0.5 h / Inert atmosphere
6.2: 2 h / 4 °C / Inert atmosphere
7.1: N-ethyl-N,N-diisopropylamine / acetonitrile / 2 h
8.1: hydrogen; acetic acid; palladium 10% on activated carbon / methanol / 2 h
9.1: N-ethyl-N,N-diisopropylamine / acetonitrile / 3 h
10.1: 0.5 h / 0 °C
11.1: N-ethyl-N,N-diisopropylamine / acetonitrile / 2 h
With platinum(IV) oxide; sodium azide; palladium 10% on activated carbon; hydrogen; acetic anhydride; sodium carbonate; acetic acid; triethylamine; N-ethyl-N,N-diisopropylamine; trifluoroacetic acid; sodium hydroxide; In 1,4-dioxane; methanol; dichloromethane; water; N,N-dimethyl-formamide; acetone; acetonitrile;
DOI:10.1021/ja401151v
Guidance literature:
Multi-step reaction with 8 steps
1.1: triethylamine / dichloromethane / 0 h / 0 °C / Inert atmosphere
2.1: sodium azide / N,N-dimethyl-formamide / 55 °C / Inert atmosphere
3.1: trifluoroacetic acid / 0.5 h / Inert atmosphere
3.2: 2 h / 4 °C / Inert atmosphere
4.1: N-ethyl-N,N-diisopropylamine / acetonitrile / 2 h
5.1: hydrogen; acetic acid; palladium 10% on activated carbon / methanol / 2 h
6.1: N-ethyl-N,N-diisopropylamine / acetonitrile / 3 h
7.1: 0.5 h / 0 °C
8.1: N-ethyl-N,N-diisopropylamine / acetonitrile / 2 h
With sodium azide; palladium 10% on activated carbon; hydrogen; acetic acid; triethylamine; N-ethyl-N,N-diisopropylamine; trifluoroacetic acid; In methanol; dichloromethane; N,N-dimethyl-formamide; acetonitrile;
DOI:10.1021/ja401151v
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