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

Base Information

Chemical Name:methyl (R)-2-allyl-4-(4-bromo-2-chlorophenyl)-2-(((tert-butoxy)carbonyl)amino)butyrate
CAS No.:1260511-61-2
Molecular Formula:C₁₉H₂₅BrClNO₄
Molecular Weight:446.769
Hs Code.:

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

Suppliers and Price of methyl (R)-2-allyl-4-(4-bromo-2-chlorophenyl)-2-(((tert-butoxy)carbonyl)amino)butyrate

Supply Marketing:

Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

Manufacturers and distributors:

Manufacture/Brand
Chemicals and raw materials
Packaging
price

Total 0 raw suppliers

Chemical Property of methyl (R)-2-allyl-4-(4-bromo-2-chlorophenyl)-2-(((tert-butoxy)carbonyl)amino)butyrate

Chemical Property:

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Technology Process of methyl (R)-2-allyl-4-(4-bromo-2-chlorophenyl)-2-(((tert-butoxy)carbonyl)amino)butyrate

There total 5 articles about methyl (R)-2-allyl-4-(4-bromo-2-chlorophenyl)-2-(((tert-butoxy)carbonyl)amino)butyrate 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

: 1260511-59-8
(2R,5R)-2-allyl-2-(4-bromo-2-chlorophenyl)ethyl-3,6-dimethoxy-5-(isopropyl)-2,5-dihydropyrazine

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

Guidance literature:: (2R,5R)-2-allyl-2-(4-bromo-2-chlorophenyl)ethyl-3,6-dimethoxy-5-(isopropyl)-2,5-dihydropyrazine; With trifluoroacetic acid; In water; at 20 ℃; for 1h;

di-tert-butyl dicarbonate; In acetonitrile; at 20 ℃; for 1h;

Reference yield:

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

: C₁₄H₁₇BrClNO₂

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

Guidance literature:: In acetonitrile; at 15 - 25 ℃; for 1h;

Reference yield:

: 190079-30-2
(5R)-2-allyl-2,5-dihydro-3,6-dimethoxy-5-isopropylpyrazine

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

Guidance literature:: Multi-step reaction with 3 steps

1.1: n-butyllithium / tetrahydrofuran; hexane / 0.5 h / -78 °C / Inert atmosphere

1.2: 1.5 h / -78 - 0 °C / Inert atmosphere

2.1: trifluoroacetic acid / water / 1 h / 15 - 25 °C

3.1: acetonitrile / 1 h / 15 - 25 °C

With n-butyllithium; trifluoroacetic acid; In tetrahydrofuran; hexane; water; acetonitrile;