methyl {2-(aminocarbonyl)-4-[(2S)-2-[(tert-butoxycarbonyl)amino]-3-oxo-3-(pentylamino)propyl]phenoxy}acetate

Base Information

Chemical Name:methyl {2-(aminocarbonyl)-4-[(2S)-2-[(tert-butoxycarbonyl)amino]-3-oxo-3-(pentylamino)propyl]phenoxy}acetate
CAS No.:402476-76-0
Molecular Formula:C₂₃H₃₅N₃O₇
Molecular Weight:465.547
Hs Code.:

Synonyms:methyl {2-(aminocarbonyl)-4-[(2S)-2-[(tert-butoxycarbonyl)amino]-3-oxo-3-(pentylamino)propyl]phenoxy}acetate

Suppliers and Price of methyl {2-(aminocarbonyl)-4-[(2S)-2-[(tert-butoxycarbonyl)amino]-3-oxo-3-(pentylamino)propyl]phenoxy}acetate

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 {2-(aminocarbonyl)-4-[(2S)-2-[(tert-butoxycarbonyl)amino]-3-oxo-3-(pentylamino)propyl]phenoxy}acetate

Chemical Property:

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Technology Process of methyl {2-(aminocarbonyl)-4-[(2S)-2-[(tert-butoxycarbonyl)amino]-3-oxo-3-(pentylamino)propyl]phenoxy}acetate

There total 1 articles about methyl {2-(aminocarbonyl)-4-[(2S)-2-[(tert-butoxycarbonyl)amino]-3-oxo-3-(pentylamino)propyl]phenoxy}acetate 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:

: 96-32-2
bromoacetic acid methyl ester

: 402476-75-9
tert-butyl (1S)-1-[3-(aminocarbonyl)-4-hydroxybenzyl]-2-oxo-2-(pentylamino)-ethylcarbamate

: 402476-76-0
methyl {2-(aminocarbonyl)-4-[(2S)-2-[(tert-butoxycarbonyl)amino]-3-oxo-3-(pentylamino)propyl]phenoxy}acetate

Guidance literature:: With potassium carbonate; In acetone; at 20 ℃; for 16h;
DOI:10.1021/jm010393s

Reference yield:

: 402476-76-0
methyl {2-(aminocarbonyl)-4-[(2S)-2-[(tert-butoxycarbonyl)amino]-3-oxo-3-(pentylamino)propyl]phenoxy}acetate

: [4-((S)-2-Amino-2-pentylcarbamoyl-ethyl)-2-carbamoyl-phenoxy]-acetic acid methyl ester

Guidance literature:: With trifluoroacetic acid; In dichloromethane; at 0 ℃; for 3h;
DOI:10.1021/jm010393s

Reference yield:

: 402476-76-0
methyl {2-(aminocarbonyl)-4-[(2S)-2-[(tert-butoxycarbonyl)amino]-3-oxo-3-(pentylamino)propyl]phenoxy}acetate

: 402476-77-1
4-{[(1S)-1-[3-(aminocarbonyl)-4-(2-methoxy-2-oxoethoxy)benzyl]-2-oxo-2-(pentylamino)ethyl]amino}-4-oxobutanoic acid

Guidance literature:: Multi-step reaction with 2 steps

1: trifluoroacetic acid / CH₂Cl₂ / 3 h / 0 °C

2: Et₃N / CH₂Cl₂ / 16 h

With triethylamine; trifluoroacetic acid; In dichloromethane;
DOI:10.1021/jm010393s