{(S)-1-[2-(2-{(3,4-di(oleyloxy)benzoyl)amino}-ethyldisulfanyl)-ethylcarbamoyl]-4-tert-butoxycarbonylaminobutyl}-carbamic acid tert-butyl ester

Base Information

Chemical Name:{(S)-1-[2-(2-{(3,4-di(oleyloxy)benzoyl)amino}-ethyldisulfanyl)-ethylcarbamoyl]-4-tert-butoxycarbonylaminobutyl}-carbamic acid tert-butyl ester
CAS No.:1323443-54-4
Molecular Formula:C₆₂H₁₁₀N₄O₈S₂
Molecular Weight:1103.71
Hs Code.:

Synonyms:{(S)-1-[2-(2-{(3,4-di(oleyloxy)benzoyl)amino}-ethyldisulfanyl)-ethylcarbamoyl]-4-tert-butoxycarbonylaminobutyl}-carbamic acid tert-butyl ester

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Chemical Property of {(S)-1-[2-(2-{(3,4-di(oleyloxy)benzoyl)amino}-ethyldisulfanyl)-ethylcarbamoyl]-4-tert-butoxycarbonylaminobutyl}-carbamic acid tert-butyl ester

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Technology Process of {(S)-1-[2-(2-{(3,4-di(oleyloxy)benzoyl)amino}-ethyldisulfanyl)-ethylcarbamoyl]-4-tert-butoxycarbonylaminobutyl}-carbamic acid tert-butyl ester

There total 6 articles about {(S)-1-[2-(2-{(3,4-di(oleyloxy)benzoyl)amino}-ethyldisulfanyl)-ethylcarbamoyl]-4-tert-butoxycarbonylaminobutyl}-carbamic acid tert-butyl 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: 84.0%

: 57133-29-6
(S)-2,5-bis((tert-butoxycarbonyl)amino)pentanoic acid

: 1323443-53-3
N-[2-(2-aminoethyldisulfanyl)-ethyl]-3,4-di(oleyloxy)benzamide trifluoroacetate

: 1323443-54-4
{(S)-1-[2-(2-{(3,4-di(oleyloxy)benzoyl)amino}-ethyldisulfanyl)-ethylcarbamoyl]-4-tert-butoxycarbonylaminobutyl}-carbamic acid tert-butyl ester

Guidance literature:: With O-(benzotriazol-1-yl)-N,N,N',N'-tetramethyluronium tetrafluoroborate; N-ethyl-N,N-diisopropylamine; In dichloromethane; for 18h;
DOI:10.1016/j.bbamem.2011.04.020

Reference yield:

: 143-28-2,593-47-5,84286-21-5
oleoyl alcohol

: 1323443-54-4
{(S)-1-[2-(2-{(3,4-di(oleyloxy)benzoyl)amino}-ethyldisulfanyl)-ethylcarbamoyl]-4-tert-butoxycarbonylaminobutyl}-carbamic acid tert-butyl ester

Guidance literature:: Multi-step reaction with 5 steps

1: triphenylphosphine; diethylazodicarboxylate / tetrahydrofuran; toluene / 5 - 50 °C

2: ethanol; potassium hydroxide / 4 h / Inert atmosphere; Reflux

3: O-(benzotriazol-1-yl)-N,N,N',N'-tetramethyluronium tetrafluoroborate; N-ethyl-N,N-diisopropylamine / dichloromethane / 18 h / Inert atmosphere

4: Inert atmosphere; Cooling with ice

5: O-(benzotriazol-1-yl)-N,N,N',N'-tetramethyluronium tetrafluoroborate; N-ethyl-N,N-diisopropylamine / dichloromethane / 18 h

With ethanol; O-(benzotriazol-1-yl)-N,N,N',N'-tetramethyluronium tetrafluoroborate; N-ethyl-N,N-diisopropylamine; triphenylphosphine; potassium hydroxide; diethylazodicarboxylate; In tetrahydrofuran; dichloromethane; toluene; 1: Mitsunobu reaction;
DOI:10.1016/j.bbamem.2011.04.020

Reference yield:

: 1323443-51-1
[2-(2-{[3,4-di(oleyloxy)benzoyl]amino}-ethyldisulfanyl)ethyl]-carbamic acid tert-butyl ester

: 1323443-54-4
{(S)-1-[2-(2-{(3,4-di(oleyloxy)benzoyl)amino}-ethyldisulfanyl)-ethylcarbamoyl]-4-tert-butoxycarbonylaminobutyl}-carbamic acid tert-butyl ester

Guidance literature:: Multi-step reaction with 2 steps

1: Inert atmosphere; Cooling with ice

2: O-(benzotriazol-1-yl)-N,N,N',N'-tetramethyluronium tetrafluoroborate; N-ethyl-N,N-diisopropylamine / dichloromethane / 18 h

With O-(benzotriazol-1-yl)-N,N,N',N'-tetramethyluronium tetrafluoroborate; N-ethyl-N,N-diisopropylamine; In dichloromethane;
DOI:10.1016/j.bbamem.2011.04.020