(N-tert-butoxycarbonyl-1-carbobenzyloxy-2-iodo-L-tryptophanyl)-L-phenylalanine methyl ester

Base Information

Chemical Name:(N-tert-butoxycarbonyl-1-carbobenzyloxy-2-iodo-L-tryptophanyl)-L-phenylalanine methyl ester
CAS No.:1053208-73-3
Molecular Formula:C₃₄H₃₆IN₃O₇
Molecular Weight:725.58
Hs Code.:

Synonyms:(N-tert-butoxycarbonyl-1-carbobenzyloxy-2-iodo-L-tryptophanyl)-L-phenylalanine methyl ester

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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-tert-butoxycarbonyl-1-carbobenzyloxy-2-iodo-L-tryptophanyl)-L-phenylalanine methyl ester

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Technology Process of (N-tert-butoxycarbonyl-1-carbobenzyloxy-2-iodo-L-tryptophanyl)-L-phenylalanine methyl ester

There total 1 articles about (N-tert-butoxycarbonyl-1-carbobenzyloxy-2-iodo-L-tryptophanyl)-L-phenylalanine methyl 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: 96.0%

: 1053209-09-8
(N-tert-butoxycarbonyl-1-carbobenzyloxy-L-tryptophanyl)-L-phenylalanine methyl ester

: 1053208-73-3
(N-tert-butoxycarbonyl-1-carbobenzyloxy-2-iodo-L-tryptophanyl)-L-phenylalanine methyl ester

Guidance literature:: (N-tert-butoxycarbonyl-1-carbobenzyloxy-L-tryptophanyl)-L-phenylalanine methyl ester; With mercury(II) trifluoroacetate; In dichloromethane; Inert atmosphere;

With iodine; regioselective reaction; Inert atmosphere;
DOI:10.1021/ol8015513

Reference yield: 45.0%

: 1053208-73-3
(N-tert-butoxycarbonyl-1-carbobenzyloxy-2-iodo-L-tryptophanyl)-L-phenylalanine methyl ester

: 1053208-74-4
C₃₄H₃₅N₃O₇

Guidance literature:: With potassium phosphate; copper(l) iodide; trans-1,2-Diaminocyclohexane; In toluene; at 110 ℃; diastereoselective reaction; Inert atmosphere;
DOI:10.1021/ol8015513