C₄₈H₈₃N₇O₁₇

Base Information

Chemical Name:C₄₈H₈₃N₇O₁₇
CAS No.:1566605-87-5
Molecular Formula:C₄₈H₈₃N₇O₁₇
Molecular Weight:1030.22
Hs Code.:

C<sub>48</sub>H<sub>83</sub>N<sub>7</sub>O<sub>17</sub>

Synonyms:C₄₈H₈₃N₇O₁₇

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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 C₄₈H₈₃N₇O₁₇

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Technology Process of C₄₈H₈₃N₇O₁₇

There total 13 articles about C₄₈H₈₃N₇O₁₇ 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: 86.0%

: 1566605-85-3
C₆₂H₉₅N₇O₁₇

: 1566605-87-5
C₄₈H₈₃N₇O₁₇

Guidance literature:: With palladium 10% on activated carbon; hydrogen; In isopropyl alcohol; at 20 ℃; for 2h;
DOI:10.1021/ol500022n

Reference yield:

: 1566605-79-5
C₄₄H₆₇N₅O₁₄

: 1566605-87-5
C₄₈H₈₃N₇O₁₇

Guidance literature:: Multi-step reaction with 2 steps

1: N-ethyl-N,N-diisopropylamine; benzotriazol-1-yloxyl-tris-(pyrrolidino)-phosphonium hexafluorophosphate / dichloromethane / 1 h / 20 °C / pH 8-9

2: palladium 10% on activated carbon; hydrogen / isopropyl alcohol / 2 h / 20 °C

With palladium 10% on activated carbon; benzotriazol-1-yloxyl-tris-(pyrrolidino)-phosphonium hexafluorophosphate; hydrogen; N-ethyl-N,N-diisopropylamine; In dichloromethane; isopropyl alcohol;
DOI:10.1021/ol500022n

Reference yield:

: 1566605-91-1
1-methoxycarbonylmethyl-1-(4-nitrobenzenesulfonyl)-4,4-bis(tert-butoxycarbonylmethyl)-1,4-diazabutane

: 1566605-87-5
C₄₈H₈₃N₇O₁₇

Guidance literature:: Multi-step reaction with 6 steps

1.1: potassium carbonate; thiophenol / acetonitrile / 4 h / 20 °C

2.1: potassium carbonate / acetonitrile / 72 h / 60 °C

3.1: hydrogenchloride / 1,4-dioxane / 5 h / 20 °C

4.1: acetic anhydride; pyridine / 2 h / 20 °C / Inert atmosphere

4.2: 15 h / 20 °C / Inert atmosphere

5.1: N-ethyl-N,N-diisopropylamine; benzotriazol-1-yloxyl-tris-(pyrrolidino)-phosphonium hexafluorophosphate / dichloromethane / 1 h / 20 °C / pH 8-9

6.1: palladium 10% on activated carbon; hydrogen / isopropyl alcohol / 2 h / 20 °C

With pyridine; hydrogenchloride; palladium 10% on activated carbon; benzotriazol-1-yloxyl-tris-(pyrrolidino)-phosphonium hexafluorophosphate; hydrogen; acetic anhydride; potassium carbonate; thiophenol; N-ethyl-N,N-diisopropylamine; In 1,4-dioxane; dichloromethane; isopropyl alcohol; acetonitrile;
DOI:10.1021/ol500022n