L-2-(benzhydrylidene-amino)-N-{2-[2-(benzhydrylidene-amino)-3-phenyl-propionylamino]-phenyl}-3-phenyl-propionamide

Base Information

Chemical Name:L-2-(benzhydrylidene-amino)-N-{2-[2-(benzhydrylidene-amino)-3-phenyl-propionylamino]-phenyl}-3-phenyl-propionamide
CAS No.:197431-88-2
Molecular Formula:C₅₀H₄₂N₄O₂
Molecular Weight:730.909
Hs Code.:

Synonyms:L-2-(benzhydrylidene-amino)-N-{2-[2-(benzhydrylidene-amino)-3-phenyl-propionylamino]-phenyl}-3-phenyl-propionamide

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Chemical Property of L-2-(benzhydrylidene-amino)-N-{2-[2-(benzhydrylidene-amino)-3-phenyl-propionylamino]-phenyl}-3-phenyl-propionamide

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Technology Process of L-2-(benzhydrylidene-amino)-N-{2-[2-(benzhydrylidene-amino)-3-phenyl-propionylamino]-phenyl}-3-phenyl-propionamide

There total 6 articles about L-2-(benzhydrylidene-amino)-N-{2-[2-(benzhydrylidene-amino)-3-phenyl-propionylamino]-phenyl}-3-phenyl-propionamide 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: 74.0%

: 1013-88-3
Benzophenone imine

: L-2-amino-N-[2-(2-amino-3-phenyl-propionylamino)-phenyl]-3-phenyl-propionamide-bis-hydrochloride

: 197431-88-2
L-2-(benzhydrylidene-amino)-N-{2-[2-(benzhydrylidene-amino)-3-phenyl-propionylamino]-phenyl}-3-phenyl-propionamide

Guidance literature:: DOI:10.1021/ja972135j

Reference yield:

: 197431-84-8
L-{1-[2-(2-tert-butoxycarbonylamino-3-phenyl-propionylamino)-phenylcarbamoyl]-2-phenyl-ethyl}-carbamic acid tert-butyl ester

: 197431-88-2
L-2-(benzhydrylidene-amino)-N-{2-[2-(benzhydrylidene-amino)-3-phenyl-propionylamino]-phenyl}-3-phenyl-propionamide

Guidance literature:: Multi-step reaction with 2 steps

1: 11 g / methanol; AcCl / 24 h / 20 °C

2: 72 percent / CH₂Cl₂ / 12 h / 20 °C

With methanol; acetyl chloride; In dichloromethane; 1: Elimination / 2: Substitution;
DOI:10.1021/ol0063151

Reference yield:

: 13734-34-4
N-tert-butoxycarbonyl-L-phenylalanine

: 197431-88-2
L-2-(benzhydrylidene-amino)-N-{2-[2-(benzhydrylidene-amino)-3-phenyl-propionylamino]-phenyl}-3-phenyl-propionamide

Guidance literature:: Multi-step reaction with 3 steps

1: 90 percent / DCC / other reagent

2: 100 percent / HCl / methanol

3: 74 percent

With hydrogenchloride; dicyclohexyl-carbodiimide; In methanol;
DOI:10.1021/ja972135j