tert-butyl ((2R,3R)-2-hydroxy-4-(N-((S)-1-((4-methoxybenzyl)oxy)propan-2-yl)-2-((S)-pent-4-en-2-yloxy)-4-(trifluoromethyl)benzamido)-3-methylbutyl)(methyl)carbamate

Base Information

Chemical Name:tert-butyl ((2R,3R)-2-hydroxy-4-(N-((S)-1-((4-methoxybenzyl)oxy)propan-2-yl)-2-((S)-pent-4-en-2-yloxy)-4-(trifluoromethyl)benzamido)-3-methylbutyl)(methyl)carbamate
CAS No.:1403480-56-7
Molecular Formula:C₃₅H₄₉F₃N₂O₇
Molecular Weight:666.778
Hs Code.:

tert-butyl ((2R,3R)-2-hydroxy-4-(N-((S)-1-((4-methoxybenzyl)oxy)propan-2-yl)-2-((S)-pent-4-en-2-yloxy)-4-(trifluoromethyl)benzamido)-3-methylbutyl)(methyl)carbamate

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Chemical Property of tert-butyl ((2R,3R)-2-hydroxy-4-(N-((S)-1-((4-methoxybenzyl)oxy)propan-2-yl)-2-((S)-pent-4-en-2-yloxy)-4-(trifluoromethyl)benzamido)-3-methylbutyl)(methyl)carbamate

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Technology Process of tert-butyl ((2R,3R)-2-hydroxy-4-(N-((S)-1-((4-methoxybenzyl)oxy)propan-2-yl)-2-((S)-pent-4-en-2-yloxy)-4-(trifluoromethyl)benzamido)-3-methylbutyl)(methyl)carbamate

There total 4 articles about tert-butyl ((2R,3R)-2-hydroxy-4-(N-((S)-1-((4-methoxybenzyl)oxy)propan-2-yl)-2-((S)-pent-4-en-2-yloxy)-4-(trifluoromethyl)benzamido)-3-methylbutyl)(methyl)carbamate 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:

: tert-butyl ((2R,3R)-2-((tert-butyldimethylsilyl)oxy)-4-(N-((S)-1-((4-methoxybenzyl)oxy)propan-2-yl)-2-((S)-pent-4-en-2-yloxy)-4-(trifluoromethyl)benzamido)-3-methylbutyl)(methyl)carbamate

: 1403480-56-7
tert-butyl ((2R,3R)-2-hydroxy-4-(N-((S)-1-((4-methoxybenzyl)oxy)propan-2-yl)-2-((S)-pent-4-en-2-yloxy)-4-(trifluoromethyl)benzamido)-3-methylbutyl)(methyl)carbamate

Guidance literature:: With tetrabutyl ammonium fluoride; In tetrahydrofuran; at 0 ℃;
DOI:10.1021/jm500994n

Reference yield:

: 1255212-77-1
tert-butyl ((2R,3S)-2-((tert-butyldimethylsilyl)oxy)-4-(((2S)-1-((4-methoxybenzyl)oxy)propan-2-yl)amino)-3-methyl-4-oxobutyl)(methyl)carbamate

: 1403480-56-7
tert-butyl ((2R,3R)-2-hydroxy-4-(N-((S)-1-((4-methoxybenzyl)oxy)propan-2-yl)-2-((S)-pent-4-en-2-yloxy)-4-(trifluoromethyl)benzamido)-3-methylbutyl)(methyl)carbamate

Guidance literature:: Multi-step reaction with 2 steps

1: N-ethyl-N,N-diisopropylamine; bis-(2-oxo-3-oxazolidinyl)phosphoryl chloride / dichloromethane / 0 - 20 °C

2: tetrabutyl ammonium fluoride / tetrahydrofuran / 0 °C

With tetrabutyl ammonium fluoride; bis-(2-oxo-3-oxazolidinyl)phosphoryl chloride; N-ethyl-N,N-diisopropylamine; In tetrahydrofuran; dichloromethane;
DOI:10.1021/jm500994n

Reference yield:

: 1403480-10-3
(S)-2-(pent-4-en-2-yloxy)-4-(trifluoromethyl)benzoic acid

: 1403480-56-7
tert-butyl ((2R,3R)-2-hydroxy-4-(N-((S)-1-((4-methoxybenzyl)oxy)propan-2-yl)-2-((S)-pent-4-en-2-yloxy)-4-(trifluoromethyl)benzamido)-3-methylbutyl)(methyl)carbamate

Guidance literature:: Multi-step reaction with 2 steps

1: N-ethyl-N,N-diisopropylamine; bis-(2-oxo-3-oxazolidinyl)phosphoryl chloride / dichloromethane / 0 - 20 °C

2: tetrabutyl ammonium fluoride / tetrahydrofuran / 0 °C

With tetrabutyl ammonium fluoride; bis-(2-oxo-3-oxazolidinyl)phosphoryl chloride; N-ethyl-N,N-diisopropylamine; In tetrahydrofuran; dichloromethane;
DOI:10.1021/jm500994n