tert-butyl (2S)-[N-[(2S)-[(tert-butoxy)carbonylamino]-5-[[imino[[(2,4,6-trimethylphenyl)sulfonyl]amino]methyl]amino]pentyl](phenylmethoxy)carbonylamino]-3-(2-naphthyl)propanoate

Base Information

Chemical Name:tert-butyl (2S)-[N-[(2S)-[(tert-butoxy)carbonylamino]-5-[[imino[[(2,4,6-trimethylphenyl)sulfonyl]amino]methyl]amino]pentyl](phenylmethoxy)carbonylamino]-3-(2-naphthyl)propanoate
CAS No.:842166-63-6
Molecular Formula:C₄₅H₅₉N₅O₈S
Molecular Weight:830.058
Hs Code.:

tert-butyl (2S)-[N-[(2S)-[(tert-butoxy)carbonylamino]-5-[[imino[[(2,4,6-trimethylphenyl)sulfonyl]amino]methyl]amino]pentyl](phenylmethoxy)carbonylamino]-3-(2-naphthyl)propanoate

Synonyms:tert-butyl (2S)-[N-[(2S)-[(tert-butoxy)carbonylamino]-5-[[imino[[(2,4,6-trimethylphenyl)sulfonyl]amino]methyl]amino]pentyl](phenylmethoxy)carbonylamino]-3-(2-naphthyl)propanoate

Suppliers and Price of tert-butyl (2S)-[N-[(2S)-[(tert-butoxy)carbonylamino]-5-[[imino[[(2,4,6-trimethylphenyl)sulfonyl]amino]methyl]amino]pentyl](phenylmethoxy)carbonylamino]-3-(2-naphthyl)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 tert-butyl (2S)-[N-[(2S)-[(tert-butoxy)carbonylamino]-5-[[imino[[(2,4,6-trimethylphenyl)sulfonyl]amino]methyl]amino]pentyl](phenylmethoxy)carbonylamino]-3-(2-naphthyl)propanoate

Chemical Property:

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Technology Process of tert-butyl (2S)-[N-[(2S)-[(tert-butoxy)carbonylamino]-5-[[imino[[(2,4,6-trimethylphenyl)sulfonyl]amino]methyl]amino]pentyl](phenylmethoxy)carbonylamino]-3-(2-naphthyl)propanoate

There total 6 articles about tert-butyl (2S)-[N-[(2S)-[(tert-butoxy)carbonylamino]-5-[[imino[[(2,4,6-trimethylphenyl)sulfonyl]amino]methyl]amino]pentyl](phenylmethoxy)carbonylamino]-3-(2-naphthyl)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: 77.0%

: 501-53-1,94274-21-2
benzyl chloroformate

: 842166-62-5
tert-butyl (2S)-[[(2S)-[(tert-butoxy)carbonylamino]-5-[[imino[[(2,4,6-trimethylphenyl)sulfonyl]amino]methyl]amino]pentyl]amino]-3-(2-naphthyl) propanoate

: 842166-63-6
tert-butyl (2S)-[N-[(2S)-[(tert-butoxy)carbonylamino]-5-[[imino[[(2,4,6-trimethylphenyl)sulfonyl]amino]methyl]amino]pentyl](phenylmethoxy)carbonylamino]-3-(2-naphthyl)propanoate

Guidance literature:: With triethylamine; In N,N-dimethyl-formamide; at 20 ℃; for 8h;
DOI:10.1021/jm049429h

Reference yield:

: 68262-71-5,200122-85-6
Boc-Arg(MTS)-OH

: 842166-63-6
tert-butyl (2S)-[N-[(2S)-[(tert-butoxy)carbonylamino]-5-[[imino[[(2,4,6-trimethylphenyl)sulfonyl]amino]methyl]amino]pentyl](phenylmethoxy)carbonylamino]-3-(2-naphthyl)propanoate

Guidance literature:: Multi-step reaction with 4 steps

1.1: 100 percent / potassium bicarbonate / dimethylformamide / 10 h / 20 °C

2.1: DIBAL-H / toluene; CH₂Cl₂ / 2 h / -78 °C

3.1: AcOH / 1,2-dichloro-ethane; dimethylformamide / 0.17 h / 4 °C

3.2: 3.4 g / NaBH(OAc)3 / 1,2-dichloro-ethane; dimethylformamide / 8 h / 20 °C

4.1: 77 percent / Et₃N / dimethylformamide / 8 h / 20 °C

With diisobutylaluminium hydride; potassium hydrogencarbonate; acetic acid; triethylamine; In dichloromethane; 1,2-dichloro-ethane; N,N-dimethyl-formamide; toluene;
DOI:10.1021/jm049429h

Reference yield:

: 199588-96-0
tert-butyl (S)-2-amino-3-(2-naphthyl)propanoate

: 842166-63-6
tert-butyl (2S)-[N-[(2S)-[(tert-butoxy)carbonylamino]-5-[[imino[[(2,4,6-trimethylphenyl)sulfonyl]amino]methyl]amino]pentyl](phenylmethoxy)carbonylamino]-3-(2-naphthyl)propanoate

Guidance literature:: Multi-step reaction with 2 steps

1.1: AcOH / 1,2-dichloro-ethane; dimethylformamide / 0.17 h / 4 °C

1.2: 3.4 g / NaBH(OAc)3 / 1,2-dichloro-ethane; dimethylformamide / 8 h / 20 °C

2.1: 77 percent / Et₃N / dimethylformamide / 8 h / 20 °C

With acetic acid; triethylamine; In 1,2-dichloro-ethane; N,N-dimethyl-formamide;
DOI:10.1021/jm049429h