4-(tert-butoxycarbonyl-(3-(4-(3-(tert-butoxycarbonyl(4-(cyclohexylamino)-4-oxobutyl)amino)prop-1-ynyl)phenyl)prop-2-ynyl)amino)butanoic acid

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Chemical Name:4-(tert-butoxycarbonyl-(3-(4-(3-(tert-butoxycarbonyl(4-(cyclohexylamino)-4-oxobutyl)amino)prop-1-ynyl)phenyl)prop-2-ynyl)amino)butanoic acid
CAS No.:946055-32-9
Molecular Formula:C₃₆H₅₁N₃O₇
Molecular Weight:637.817
Hs Code.:

Synonyms:4-(tert-butoxycarbonyl-(3-(4-(3-(tert-butoxycarbonyl(4-(cyclohexylamino)-4-oxobutyl)amino)prop-1-ynyl)phenyl)prop-2-ynyl)amino)butanoic acid

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Chemical Property of 4-(tert-butoxycarbonyl-(3-(4-(3-(tert-butoxycarbonyl(4-(cyclohexylamino)-4-oxobutyl)amino)prop-1-ynyl)phenyl)prop-2-ynyl)amino)butanoic acid

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Technology Process of 4-(tert-butoxycarbonyl-(3-(4-(3-(tert-butoxycarbonyl(4-(cyclohexylamino)-4-oxobutyl)amino)prop-1-ynyl)phenyl)prop-2-ynyl)amino)butanoic acid

There total 3 articles about 4-(tert-butoxycarbonyl-(3-(4-(3-(tert-butoxycarbonyl(4-(cyclohexylamino)-4-oxobutyl)amino)prop-1-ynyl)phenyl)prop-2-ynyl)amino)butanoic acid 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: 53.0%

: 946055-30-7
4-(tert-butoxycarbonyl-(3-(4-iodophenyl)prop-2-ynyl)amino)butanoic acid

: 946055-31-8
tert-butyl 4-(cyclohexylamino)-4-oxobutyl(prop-2-ynyl)carbamate

: 946055-32-9
4-(tert-butoxycarbonyl-(3-(4-(3-(tert-butoxycarbonyl(4-(cyclohexylamino)-4-oxobutyl)amino)prop-1-ynyl)phenyl)prop-2-ynyl)amino)butanoic acid

Guidance literature:: With copper(l) iodide; triethylamine; bis-triphenylphosphine-palladium(II) chloride; In N,N-dimethyl-formamide; at 80 ℃; for 3.5h;
DOI:10.1021/jm070552t

Reference yield:

: 946055-36-3
4-(tert-butoxycarbonyl(prop-2-ynyl)amino)butanoic acid

: 946055-32-9
4-(tert-butoxycarbonyl-(3-(4-(3-(tert-butoxycarbonyl(4-(cyclohexylamino)-4-oxobutyl)amino)prop-1-ynyl)phenyl)prop-2-ynyl)amino)butanoic acid

Guidance literature:: Multi-step reaction with 2 steps

1: 49 percent / Et₃N; CuI / PdCl₂(PPh₃)2 / dimethylformamide / 0 - 20 °C

2: 53 percent / Et₃N; CuI / PdCl₂(PPh₃)2 / dimethylformamide / 3.5 h / 80 °C

With copper(l) iodide; triethylamine; bis-triphenylphosphine-palladium(II) chloride; In N,N-dimethyl-formamide; 1: Sonogashira-Linstrumelle coupling / 2: Sonogashira-Linstrumelle coupling;
DOI:10.1021/jm070552t

Reference yield:

: 57294-38-9
N-(tert-butoxycarbonyl)-4-aminobutanoic acid

: 946055-32-9
4-(tert-butoxycarbonyl-(3-(4-(3-(tert-butoxycarbonyl(4-(cyclohexylamino)-4-oxobutyl)amino)prop-1-ynyl)phenyl)prop-2-ynyl)amino)butanoic acid

Guidance literature:: Multi-step reaction with 3 steps

1: 77 percent / NaH / dimethylformamide; toluene / 0 - 20 °C

2: 49 percent / Et₃N; CuI / PdCl₂(PPh₃)2 / dimethylformamide / 0 - 20 °C

3: 53 percent / Et₃N; CuI / PdCl₂(PPh₃)2 / dimethylformamide / 3.5 h / 80 °C

With copper(l) iodide; sodium hydride; triethylamine; bis-triphenylphosphine-palladium(II) chloride; In N,N-dimethyl-formamide; toluene; 2: Sonogashira-Linstrumelle coupling / 3: Sonogashira-Linstrumelle coupling;
DOI:10.1021/jm070552t