methyl {(2S)-2-[(tert-butoxycarbonyl)amino]-3-(2-nitro-5-phenoxypyridin-3-yl)}propanoate

Base Information

Chemical Name:methyl {(2S)-2-[(tert-butoxycarbonyl)amino]-3-(2-nitro-5-phenoxypyridin-3-yl)}propanoate
CAS No.:1258544-93-2
Molecular Formula:C₂₀H₂₃N₃O₇
Molecular Weight:417.419
Hs Code.:

Synonyms:methyl {(2S)-2-[(tert-butoxycarbonyl)amino]-3-(2-nitro-5-phenoxypyridin-3-yl)}propanoate

Suppliers and Price of methyl {(2S)-2-[(tert-butoxycarbonyl)amino]-3-(2-nitro-5-phenoxypyridin-3-yl)}propanoate

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 {(2S)-2-[(tert-butoxycarbonyl)amino]-3-(2-nitro-5-phenoxypyridin-3-yl)}propanoate

Chemical Property:

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Technology Process of methyl {(2S)-2-[(tert-butoxycarbonyl)amino]-3-(2-nitro-5-phenoxypyridin-3-yl)}propanoate

There total 4 articles about methyl {(2S)-2-[(tert-butoxycarbonyl)amino]-3-(2-nitro-5-phenoxypyridin-3-yl)}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: 28.0%

: 1258544-92-1
3-bromo-2-nitro-5-phenoxypyridine

: 170848-34-7,889670-02-4
N-t-butoxycarbonyl-3-iodo-D-alanine methyl ester

: 1258544-93-2
methyl {(2S)-2-[(tert-butoxycarbonyl)amino]-3-(2-nitro-5-phenoxypyridin-3-yl)}propanoate

Guidance literature:: 3-bromo-2-nitro-5-phenoxypyridine; With iodine; zinc; In N,N-dimethyl-formamide;

N-t-butoxycarbonyl-3-iodo-D-alanine methyl ester; With palladium diacetate; XPhos; In N,N-dimethyl-formamide; at 60 ℃; for 12h;
DOI:10.1039/c2md20166f

Reference yield: 16.0%

: 1258544-92-1
3-bromo-2-nitro-5-phenoxypyridine

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

: 1258544-93-2
methyl {(2S)-2-[(tert-butoxycarbonyl)amino]-3-(2-nitro-5-phenoxypyridin-3-yl)}propanoate

Guidance literature:: N-(tert-butoxycarbonyl)-L-3-iodoalanine methyl ester; With chloro-trimethyl-silane; zinc; In N,N-dimethyl-formamide; at 20 ℃; for 0.5h;

3-bromo-2-nitro-5-phenoxypyridine; palladium diacetate; XPhos; In N,N-dimethyl-formamide; at 20 ℃; for 18h; Inert atmosphere;

Reference yield:

: 1258544-91-0
3-bromo-5-fluoro-2-nitropyridine

: 1258544-93-2
methyl {(2S)-2-[(tert-butoxycarbonyl)amino]-3-(2-nitro-5-phenoxypyridin-3-yl)}propanoate

Guidance literature:: Multi-step reaction with 2 steps

1.1: caesium carbonate / acetonitrile / 2 h / 60 °C

2.1: zinc; iodine / N,N-dimethyl-formamide

2.2: 12 h / 60 °C

With iodine; caesium carbonate; zinc; In N,N-dimethyl-formamide; acetonitrile; 2.1: |Negishi Coupling / 2.2: |Negishi Coupling;
DOI:10.1039/c2md20166f