(R)-2-allyl-2-(((tert-butoxy)carbonyl)amino)-4-{2-chloro-4-((2-((tert-butoxy)carbonyl)hydroxy)-5-ethoxyphenylthio)phenyl}butan-1-ol

Base Information

Chemical Name:(R)-2-allyl-2-(((tert-butoxy)carbonyl)amino)-4-{2-chloro-4-((2-((tert-butoxy)carbonyl)hydroxy)-5-ethoxyphenylthio)phenyl}butan-1-ol
CAS No.:1383617-33-1
Molecular Formula:C₃₁H₄₂ClNO₇S
Molecular Weight:608.196
Hs Code.:

Synonyms:(R)-2-allyl-2-(((tert-butoxy)carbonyl)amino)-4-{2-chloro-4-((2-((tert-butoxy)carbonyl)hydroxy)-5-ethoxyphenylthio)phenyl}butan-1-ol

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Chemical Property of (R)-2-allyl-2-(((tert-butoxy)carbonyl)amino)-4-{2-chloro-4-((2-((tert-butoxy)carbonyl)hydroxy)-5-ethoxyphenylthio)phenyl}butan-1-ol

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Technology Process of (R)-2-allyl-2-(((tert-butoxy)carbonyl)amino)-4-{2-chloro-4-((2-((tert-butoxy)carbonyl)hydroxy)-5-ethoxyphenylthio)phenyl}butan-1-ol

There total 10 articles about (R)-2-allyl-2-(((tert-butoxy)carbonyl)amino)-4-{2-chloro-4-((2-((tert-butoxy)carbonyl)hydroxy)-5-ethoxyphenylthio)phenyl}butan-1-ol 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:

: 24424-99-5
di-tert-butyl dicarbonate

: 1383617-32-0
(R)-2-allyl-2-(((tert-butoxy)carbonyl)amino)-4-{2-chloro-4-((5-ethoxy-2-hydroxyphenyl)thio)phenyl}butan-1-ol

: 1383617-33-1
(R)-2-allyl-2-(((tert-butoxy)carbonyl)amino)-4-{2-chloro-4-((2-((tert-butoxy)carbonyl)hydroxy)-5-ethoxyphenylthio)phenyl}butan-1-ol

Guidance literature:: With triethylamine; In water; acetonitrile; at 15 - 25 ℃; for 60h; Inert atmosphere;

Reference yield:

: 1260511-61-2
methyl (R)-2-allyl-4-(4-bromo-2-chlorophenyl)-2-(((tert-butoxy)carbonyl)amino)butyrate

: 1383617-33-1
(R)-2-allyl-2-(((tert-butoxy)carbonyl)amino)-4-{2-chloro-4-((2-((tert-butoxy)carbonyl)hydroxy)-5-ethoxyphenylthio)phenyl}butan-1-ol

Guidance literature:: Multi-step reaction with 3 steps

1: lithium borohydride; ethanol / tetrahydrofuran / 2 h / Cooling with ice

2: N-ethyl-N,N-diisopropylamine; tris-(dibenzylideneacetone)dipalladium⁽⁰⁾; 4,5-bis(diphenylphosphino)-9,9-dimethylxanthene / 1,4-dioxane / 17 h / Inert atmosphere; Reflux

3: triethylamine / water; acetonitrile / 60 h / 15 - 25 °C / Inert atmosphere

With tris-(dibenzylideneacetone)dipalladium⁽⁰⁾; lithium borohydride; ethanol; triethylamine; N-ethyl-N,N-diisopropylamine; 4,5-bis(diphenylphosphino)-9,9-dimethylxanthene; In tetrahydrofuran; 1,4-dioxane; water; acetonitrile;

Reference yield:

: 7735-56-0
5-hydroxybenzo[d][1,3]oxathiol-2-one

: 1383617-33-1
(R)-2-allyl-2-(((tert-butoxy)carbonyl)amino)-4-{2-chloro-4-((2-((tert-butoxy)carbonyl)hydroxy)-5-ethoxyphenylthio)phenyl}butan-1-ol

Guidance literature:: Multi-step reaction with 4 steps

1: potassium carbonate / N,N-dimethyl-formamide / 4 h / 15 - 25 °C

2: lithium aluminium tetrahydride / tetrahydrofuran / 0.5 h / Inert atmosphere; Cooling with ice

3: N-ethyl-N,N-diisopropylamine; tris-(dibenzylideneacetone)dipalladium⁽⁰⁾; 4,5-bis(diphenylphosphino)-9,9-dimethylxanthene / 1,4-dioxane / 17 h / Inert atmosphere; Reflux

4: triethylamine / water; acetonitrile / 60 h / 15 - 25 °C / Inert atmosphere

With tris-(dibenzylideneacetone)dipalladium⁽⁰⁾; lithium aluminium tetrahydride; potassium carbonate; triethylamine; N-ethyl-N,N-diisopropylamine; 4,5-bis(diphenylphosphino)-9,9-dimethylxanthene; In tetrahydrofuran; 1,4-dioxane; water; N,N-dimethyl-formamide; acetonitrile;