Boc-Dopa(diCH2Ph)-Lys2(Cl)> p-nitrophenyl ester

Base Information

Chemical Name:Boc-Dopa(diCH2Ph)-Lys2(Cl)> p-nitrophenyl ester
CAS No.:111104-08-6
Molecular Formula:C₄₈H₅₁ClN₄O₁₁
Molecular Weight:895.406
Hs Code.:

Boc-Dopa(diCH2Ph)-Lys<Z<sup>2</sup>(Cl)> p-nitrophenyl ester

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Chemical Property of Boc-Dopa(diCH2Ph)-Lys2(Cl)> p-nitrophenyl ester

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Technology Process of Boc-Dopa(diCH2Ph)-Lys2(Cl)> p-nitrophenyl ester

There total 3 articles about Boc-Dopa(diCH2Ph)-Lys2(Cl)> p-nitrophenyl ester 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:

: 30033-24-0
(2S)-3-(3,4-dihydroxyphenyl)-2-[(tert-butoxy)carbonylamino]propanoic acid

: 111104-08-6
Boc-Dopa(diCH2Ph)-Lys2(Cl)> p-nitrophenyl ester

Guidance literature:: Multi-step reaction with 2 steps

1: 51 percent / potassium carbonate, sodium iodide

2: 1.) N-methylmorpholine; 2.) DCCI / 2.) chloroform; 3.) chloroform, 0 deg C, 2 h, 5 deg C, overnight

With 4-methyl-morpholine; potassium carbonate; dicyclohexyl-carbodiimide; sodium iodide;

Reference yield:

: 100-44-7
benzyl chloride

: 111104-08-6
Boc-Dopa(diCH2Ph)-Lys2(Cl)> p-nitrophenyl ester

Guidance literature:: Multi-step reaction with 2 steps

1: 51 percent / potassium carbonate, sodium iodide

2: 1.) N-methylmorpholine; 2.) DCCI / 2.) chloroform; 3.) chloroform, 0 deg C, 2 h, 5 deg C, overnight

With 4-methyl-morpholine; potassium carbonate; dicyclohexyl-carbodiimide; sodium iodide;

Reference yield:

: 59727-98-9
3-[3,4-di(benzyloxy)phenyl]-2-{[(tert-butoxy)carbonyl]amino}propanoic acid

: 82650-26-8
Lys2(Cl)> p-nitrophenyl ester hydrochloride

: 111104-08-6
Boc-Dopa(diCH2Ph)-Lys2(Cl)> p-nitrophenyl ester

Guidance literature:: With 4-methyl-morpholine; dicyclohexyl-carbodiimide; Yield given. Multistep reaction; 2.) chloroform; 3.) chloroform, 0 deg C, 2 h, 5 deg C, overnight;