N^α-tert-butyloxycarbonyl-L-p-aminophenylalanyl-L-leucine tert-butyl ester

Base Information

Chemical Name:N^α-tert-butyloxycarbonyl-L-p-aminophenylalanyl-L-leucine tert-butyl ester
CAS No.:309729-32-6
Molecular Formula:C₂₄H₃₉N₃O₅
Molecular Weight:449.591
Hs Code.:

N<sup>α</sup>-tert-butyloxycarbonyl-L-p-aminophenylalanyl-L-leucine tert-butyl ester

Synonyms:N^α-tert-butyloxycarbonyl-L-p-aminophenylalanyl-L-leucine tert-butyl ester

Suppliers and Price of N^α-tert-butyloxycarbonyl-L-p-aminophenylalanyl-L-leucine tert-butyl ester

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 N^α-tert-butyloxycarbonyl-L-p-aminophenylalanyl-L-leucine tert-butyl ester

Chemical Property:

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Technology Process of N^α-tert-butyloxycarbonyl-L-p-aminophenylalanyl-L-leucine tert-butyl ester

There total 3 articles about N^α-tert-butyloxycarbonyl-L-p-aminophenylalanyl-L-leucine tert-butyl ester 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%

: 309729-31-5
N^α-tert-butyloxycarbonyl-L-p-nitrophenylalanyl-L-leucine tert-butyl ester

: 309729-32-6
N^α-tert-butyloxycarbonyl-L-p-aminophenylalanyl-L-leucine tert-butyl ester

Guidance literature:: With ammonium formate; 10percent Pd/C; In methanol; for 0.5h;
DOI:10.1021/jm000123u

Reference yield:

: 33305-77-0
Boc-Phe(p-NO₂)-OH

: 309729-32-6
N^α-tert-butyloxycarbonyl-L-p-aminophenylalanyl-L-leucine tert-butyl ester

Guidance literature:: Multi-step reaction with 3 steps

1: N-methylmorpholine / tetrahydrofuran / 0.03 h / -15 °C

2: N-methylmorpholine / dimethylformamide; tetrahydrofuran / -15 - 20 °C

3: 94 percent / aq. NH₄HCO₂ / 10percent Pd/C / methanol / 0.5 h

With 4-methyl-morpholine; ammonium formate; 10percent Pd/C; In tetrahydrofuran; methanol; N,N-dimethyl-formamide; 1: Acylation / 2: Condensation / 3: Reduction;
DOI:10.1021/jm000123u

Reference yield:

: C₁₉H₂₆N₂O₈

: 309729-32-6
N^α-tert-butyloxycarbonyl-L-p-aminophenylalanyl-L-leucine tert-butyl ester

Guidance literature:: Multi-step reaction with 2 steps

1: N-methylmorpholine / dimethylformamide; tetrahydrofuran / -15 - 20 °C

2: 94 percent / aq. NH₄HCO₂ / 10percent Pd/C / methanol / 0.5 h

With 4-methyl-morpholine; ammonium formate; 10percent Pd/C; In tetrahydrofuran; methanol; N,N-dimethyl-formamide; 1: Condensation / 2: Reduction;
DOI:10.1021/jm000123u