(R)-ethyl 2-(4-(((S)-3-((R)-3-(tert-butoxycarbonylamino)-4-(2,4,5-trifluorophenyl)-butanoyl)thiazolidine-2-carboxamido)methyl)phenylamino)-3-methylbutanoate

Base Information

Chemical Name:(R)-ethyl 2-(4-(((S)-3-((R)-3-(tert-butoxycarbonylamino)-4-(2,4,5-trifluorophenyl)-butanoyl)thiazolidine-2-carboxamido)methyl)phenylamino)-3-methylbutanoate
CAS No.:1041612-31-0
Molecular Formula:C₃₃H₄₃F₃N₄O₆S
Molecular Weight:680.789
Hs Code.:

(R)-ethyl 2-(4-(((S)-3-((R)-3-(tert-butoxycarbonylamino)-4-(2,4,5-trifluorophenyl)-butanoyl)thiazolidine-2-carboxamido)methyl)phenylamino)-3-methylbutanoate

Synonyms:(R)-ethyl 2-(4-(((S)-3-((R)-3-(tert-butoxycarbonylamino)-4-(2,4,5-trifluorophenyl)-butanoyl)thiazolidine-2-carboxamido)methyl)phenylamino)-3-methylbutanoate

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Chemical Property of (R)-ethyl 2-(4-(((S)-3-((R)-3-(tert-butoxycarbonylamino)-4-(2,4,5-trifluorophenyl)-butanoyl)thiazolidine-2-carboxamido)methyl)phenylamino)-3-methylbutanoate

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Technology Process of (R)-ethyl 2-(4-(((S)-3-((R)-3-(tert-butoxycarbonylamino)-4-(2,4,5-trifluorophenyl)-butanoyl)thiazolidine-2-carboxamido)methyl)phenylamino)-3-methylbutanoate

There total 10 articles about (R)-ethyl 2-(4-(((S)-3-((R)-3-(tert-butoxycarbonylamino)-4-(2,4,5-trifluorophenyl)-butanoyl)thiazolidine-2-carboxamido)methyl)phenylamino)-3-methylbutanoate 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: 70.0%

: 1041612-05-8
(S)-3-((R)-3-(tert-butoxycarbonylamino)-4-(2,4,5-trifluorophenyl)butanoyl)thiazolidine-2-carboxylic acid

: 1041612-30-9
(R)-ethyl 2-(4-(aminomethyl)phenylamino)-3-methylbutanoate hydrochloride

: 1041612-31-0
(R)-ethyl 2-(4-(((S)-3-((R)-3-(tert-butoxycarbonylamino)-4-(2,4,5-trifluorophenyl)-butanoyl)thiazolidine-2-carboxamido)methyl)phenylamino)-3-methylbutanoate

Guidance literature:: With 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; triethylamine; In dichloromethane; at 20 ℃; for 10h;
DOI:10.1016/j.bmcl.2011.01.041

Reference yield: 67.0%

: 1041612-31-0
(R)-ethyl 2-(4-(((S)-3-((R)-3-(tert-butoxycarbonylamino)-4-(2,4,5-trifluorophenyl)-butanoyl)thiazolidine-2-carboxamido)methyl)phenylamino)-3-methylbutanoate

Guidance literature:

Reference yield:

: 1041612-08-1
(S)-ethyl 3-((R)-3-(tert-butoxycarbonylamino)-4-(2,4,5-trifluorophenyl)butanoyl)-thiazolidine-2-carboxylate

: 1041612-31-0
(R)-ethyl 2-(4-(((S)-3-((R)-3-(tert-butoxycarbonylamino)-4-(2,4,5-trifluorophenyl)-butanoyl)thiazolidine-2-carboxamido)methyl)phenylamino)-3-methylbutanoate

Guidance literature:: Multi-step reaction with 2 steps

1: water; lithium hydroxide / tetrahydrofuran; methanol / 3 h / 20 °C

2: 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; triethylamine / dichloromethane / 10 h / 20 °C

With water; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; triethylamine; lithium hydroxide; In tetrahydrofuran; methanol; dichloromethane;
DOI:10.1016/j.bmcl.2011.01.041