N,N',N''-tris[2-hydroxy, 3-methoxy(benzoyl)carbonyl]cyclotriseryl trilactone

Base Information

Chemical Name:N,N',N''-tris[2-hydroxy, 3-methoxy(benzoyl)carbonyl]cyclotriseryl trilactone
CAS No.:905719-10-0
Molecular Formula:C₃₃H₃₃N₃O₁₅
Molecular Weight:711.636
Hs Code.:

Synonyms:N,N',N''-tris[2-hydroxy, 3-methoxy(benzoyl)carbonyl]cyclotriseryl trilactone

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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 N,N',N''-tris[2-hydroxy, 3-methoxy(benzoyl)carbonyl]cyclotriseryl trilactone

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Technology Process of N,N',N''-tris[2-hydroxy, 3-methoxy(benzoyl)carbonyl]cyclotriseryl trilactone

There total 2 articles about N,N',N''-tris[2-hydroxy, 3-methoxy(benzoyl)carbonyl]cyclotriseryl trilactone 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: 70.0%

: C₅₄H₅₁N₃O₁₅

: 905719-10-0
N,N',N''-tris[2-hydroxy, 3-methoxy(benzoyl)carbonyl]cyclotriseryl trilactone

Guidance literature:: With hydrogen; palladium on activated charcoal; In ethanol; ethyl acetate; at 20 ℃; for 24h; atmospheric pressure;
DOI:10.1021/ja062046j

Reference yield:

: 104530-71-4
(3S,7S,11S)-3,7,11-triamino-1,5,9-trioxacyclodecane-2,6,10-trione trihydrochloride

: 905719-10-0
N,N',N''-tris[2-hydroxy, 3-methoxy(benzoyl)carbonyl]cyclotriseryl trilactone

Guidance literature:: Multi-step reaction with 2 steps

1: 63 percent / triethylamine / tetrahydrofuran / 20 °C

2: 70 percent / hydrogen / Pd-C / ethyl acetate; ethanol / 24 h / 20 °C / atmospheric pressure

With hydrogen; triethylamine; palladium on activated charcoal; In tetrahydrofuran; ethanol; ethyl acetate;
DOI:10.1021/ja062046j