methyl (S)-3-(2-bromo-5-methoxyphenyl)2-((tert-butyloxycarbonyl)amino)propanoate

Base Information

Chemical Name:methyl (S)-3-(2-bromo-5-methoxyphenyl)2-((tert-butyloxycarbonyl)amino)propanoate
CAS No.:1300035-21-5
Molecular Formula:C₁₆H₂₂BrNO₅
Molecular Weight:388.258
Hs Code.:

Synonyms:methyl (S)-3-(2-bromo-5-methoxyphenyl)2-((tert-butyloxycarbonyl)amino)propanoate

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Chemical Property of methyl (S)-3-(2-bromo-5-methoxyphenyl)2-((tert-butyloxycarbonyl)amino)propanoate

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Technology Process of methyl (S)-3-(2-bromo-5-methoxyphenyl)2-((tert-butyloxycarbonyl)amino)propanoate

There total 8 articles about methyl (S)-3-(2-bromo-5-methoxyphenyl)2-((tert-butyloxycarbonyl)amino)propanoate 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: 94.0%

: 184176-05-4
methyl (S)-2-((tert-butyloxycarbonyl)amino)-3-(3-methoxyphenyl)propanoate

: 1300035-21-5
methyl (S)-3-(2-bromo-5-methoxyphenyl)2-((tert-butyloxycarbonyl)amino)propanoate

Guidance literature:: With N-Bromosuccinimide; In acetonitrile; at 20 ℃; for 2h; Inert atmosphere;
DOI:10.1021/ol200725m

Reference yield: 61.0%

: 4897-68-1
2-iodo-4-methoxybromobenzene

: 93267-04-0,170848-34-7,889670-02-4
N-(tert-butoxycarbonyl)-L-3-iodoalanine methyl ester

: 1300035-21-5
methyl (S)-3-(2-bromo-5-methoxyphenyl)2-((tert-butyloxycarbonyl)amino)propanoate

Guidance literature:: With tris-(dibenzylideneacetone)dipalladium⁽⁰⁾; tris-(o-tolyl)phosphine; zinc; In N,N-dimethyl-formamide; at 20 ℃; for 12h; Inert atmosphere;
DOI:10.1021/ol200725m

Reference yield:

: 766-85-8
3-methoxy-1-iodobenzene

: 1300035-21-5
methyl (S)-3-(2-bromo-5-methoxyphenyl)2-((tert-butyloxycarbonyl)amino)propanoate

Guidance literature:: Multi-step reaction with 2 steps

1: bromine; acetic acid / 24 h / 20 °C / Inert atmosphere

2: tris-(dibenzylideneacetone)dipalladium⁽⁰⁾; tris-(o-tolyl)phosphine; zinc / N,N-dimethyl-formamide / 12 h / 20 °C / Inert atmosphere

With tris-(dibenzylideneacetone)dipalladium⁽⁰⁾; bromine; acetic acid; tris-(o-tolyl)phosphine; zinc; In N,N-dimethyl-formamide;
DOI:10.1021/ol200725m