N,N′-((3R,7R,11R)-11-(2,3-bis(benzyloxy)-5-((E)-prop-1-en-1-yl)benzamido)-2,6,10-trioxo-1,5,9-trioxacyclododecane-3,7-diyl)bis(2,3-bis(benzyloxy)benzamide)

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Chemical Name:N,N′-((3R,7R,11R)-11-(2,3-bis(benzyloxy)-5-((E)-prop-1-en-1-yl)benzamido)-2,6,10-trioxo-1,5,9-trioxacyclododecane-3,7-diyl)bis(2,3-bis(benzyloxy)benzamide)
CAS No.:1407510-71-7
Molecular Formula:C₇₅H₆₇N₃O₁₅
Molecular Weight:1250.37
Hs Code.:

Synonyms:N,N′-((3R,7R,11R)-11-(2,3-bis(benzyloxy)-5-((E)-prop-1-en-1-yl)benzamido)-2,6,10-trioxo-1,5,9-trioxacyclododecane-3,7-diyl)bis(2,3-bis(benzyloxy)benzamide)

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Chemical Property of N,N′-((3R,7R,11R)-11-(2,3-bis(benzyloxy)-5-((E)-prop-1-en-1-yl)benzamido)-2,6,10-trioxo-1,5,9-trioxacyclododecane-3,7-diyl)bis(2,3-bis(benzyloxy)benzamide)

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Technology Process of N,N′-((3R,7R,11R)-11-(2,3-bis(benzyloxy)-5-((E)-prop-1-en-1-yl)benzamido)-2,6,10-trioxo-1,5,9-trioxacyclododecane-3,7-diyl)bis(2,3-bis(benzyloxy)benzamide)

There total 1 articles about N,N′-((3R,7R,11R)-11-(2,3-bis(benzyloxy)-5-((E)-prop-1-en-1-yl)benzamido)-2,6,10-trioxo-1,5,9-trioxacyclododecane-3,7-diyl)bis(2,3-bis(benzyloxy)benzamide) 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: 15.0%

: (E)-2,3-bis(benzyloxy)-5-(prop-1-en-1-yl)benzoic acid

: 74272-78-9
2,3-dibenzyloxybenzoic acid

: C₉H₁₅N₃O₆

: 1407510-71-7
N,N′-((3R,7R,11R)-11-(2,3-bis(benzyloxy)-5-((E)-prop-1-en-1-yl)benzamido)-2,6,10-trioxo-1,5,9-trioxacyclododecane-3,7-diyl)bis(2,3-bis(benzyloxy)benzamide)

Guidance literature:: With benzotriazol-1-yloxyl-tris-(pyrrolidino)-phosphonium hexafluorophosphate; N-ethyl-N,N-diisopropylamine; In dimethyl sulfoxide; at 20 ℃; for 2h;
DOI:10.1021/ja3077268