methyl (S)-3-((((9H-fluoren-9-yl)methoxy)carbonyl)amino)-4-(benzyl(N-benzyl-4-(benzylcarbamoyl)piperidin-4-yl)amino)-4-oxobutanoate

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Chemical Name:methyl (S)-3-((((9H-fluoren-9-yl)methoxy)carbonyl)amino)-4-(benzyl(N-benzyl-4-(benzylcarbamoyl)piperidin-4-yl)amino)-4-oxobutanoate
CAS No.:1621105-37-0
Molecular Formula:C₄₇H₄₈N₄O₆
Molecular Weight:764.921
Hs Code.:

Synonyms:methyl (S)-3-((((9H-fluoren-9-yl)methoxy)carbonyl)amino)-4-(benzyl(N-benzyl-4-(benzylcarbamoyl)piperidin-4-yl)amino)-4-oxobutanoate

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Chemical Property of methyl (S)-3-((((9H-fluoren-9-yl)methoxy)carbonyl)amino)-4-(benzyl(N-benzyl-4-(benzylcarbamoyl)piperidin-4-yl)amino)-4-oxobutanoate

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Technology Process of methyl (S)-3-((((9H-fluoren-9-yl)methoxy)carbonyl)amino)-4-(benzyl(N-benzyl-4-(benzylcarbamoyl)piperidin-4-yl)amino)-4-oxobutanoate

There total 1 articles about methyl (S)-3-((((9H-fluoren-9-yl)methoxy)carbonyl)amino)-4-(benzyl(N-benzyl-4-(benzylcarbamoyl)piperidin-4-yl)amino)-4-oxobutanoate 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: 88.0%

: 3612-20-2
1-phenylmethyl-4-piperidone

: 88333-03-3,10340-91-7
Benzyl isocyanide

: 100-46-9
benzylamine

: 145038-53-5
(S)-2-((((9H-fluoren-9-yl)methoxy)carbonyl)amino)-4-methoxy-4-oxobutanoic acid

: 1621105-37-0
methyl (S)-3-((((9H-fluoren-9-yl)methoxy)carbonyl)amino)-4-(benzyl(N-benzyl-4-(benzylcarbamoyl)piperidin-4-yl)amino)-4-oxobutanoate

Guidance literature:: 1-phenylmethyl-4-piperidone; Benzyl isocyanide; benzylamine; (S)-2-((((9H-fluoren-9-yl)methoxy)carbonyl)amino)-4-methoxy-4-oxobutanoic acid; In methanol; at 20 ℃; for 96h;

With hydrogenchloride; In methanol; at 20 ℃; for 0.5h;
DOI:10.1016/j.ejmech.2014.06.026