N-benzyloxycarbonyl-D-phenylalanyl-L-ornithyl(Ac)-D-tryptophyl-L-leucine methyl ester

Base Information

Chemical Name:N-benzyloxycarbonyl-D-phenylalanyl-L-ornithyl(Ac)-D-tryptophyl-L-leucine methyl ester
CAS No.:128718-86-5
Molecular Formula:C₄₂H₅₂N₆O₈
Molecular Weight:768.91
Hs Code.:

Synonyms:N-benzyloxycarbonyl-D-phenylalanyl-L-ornithyl(Ac)-D-tryptophyl-L-leucine methyl ester

Suppliers and Price of N-benzyloxycarbonyl-D-phenylalanyl-L-ornithyl(Ac)-D-tryptophyl-L-leucine methyl 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-benzyloxycarbonyl-D-phenylalanyl-L-ornithyl(Ac)-D-tryptophyl-L-leucine methyl ester

Chemical Property:

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Technology Process of N-benzyloxycarbonyl-D-phenylalanyl-L-ornithyl(Ac)-D-tryptophyl-L-leucine methyl ester

There total 9 articles about N-benzyloxycarbonyl-D-phenylalanyl-L-ornithyl(Ac)-D-tryptophyl-L-leucine methyl 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: 70.0%

: 2466-76-4
N-Acetylimidazole

: 128718-83-2
N-benzyloxycarbonyl-D-phenylalanyl-L-ornithyl-D-tryptophyl-L-leucine methyl ester hydrochloride

: 128718-86-5
N-benzyloxycarbonyl-D-phenylalanyl-L-ornithyl(Ac)-D-tryptophyl-L-leucine methyl ester

Guidance literature:: With triethylamine; In N,N-dimethyl-formamide; at 4 ℃;

Reference yield:

: 2448-45-5
Cbz-D-Phe

: 128718-86-5
N-benzyloxycarbonyl-D-phenylalanyl-L-ornithyl(Ac)-D-tryptophyl-L-leucine methyl ester

Guidance literature:: Multi-step reaction with 3 steps

1: Et₃N, 1-hydroxybenzotriazole (HOBt), dicyclohexylcarbodiimide (DCCI) / dimethylformamide / 4 °C

2: 81.3 percent / 3N HCl / acetic acid / 0.5 h / Ambient temperature

3: 70 percent / Et₃N / dimethylformamide / 4 °C

With hydrogenchloride; benzotriazol-1-ol; triethylamine; dicyclohexyl-carbodiimide; In acetic acid; N,N-dimethyl-formamide;

Reference yield:

: 7517-19-3
methyl (L)-leucinate hydrochloride

: 128718-86-5
N-benzyloxycarbonyl-D-phenylalanyl-L-ornithyl(Ac)-D-tryptophyl-L-leucine methyl ester

Guidance literature:: Multi-step reaction with 7 steps

1: 85.9 percent / dicyclohexylcarbodiimide (DCCI), 1-hydroxybenzotriazole (HOBt), Et₃N / dimethylformamide / 4 °C

2: 83.6 percent / 6N HCl, dithioethane / ethyl acetate / 1 h

3: 75 percent / Et₃N / dimethylformamide / Ambient temperature

4: H₂ / 5percent Pd/C / dimethylformamide; ethanol / 5 h

5: Et₃N, 1-hydroxybenzotriazole (HOBt), dicyclohexylcarbodiimide (DCCI) / dimethylformamide / 4 °C

6: 81.3 percent / 3N HCl / acetic acid / 0.5 h / Ambient temperature

7: 70 percent / Et₃N / dimethylformamide / 4 °C

With hydrogenchloride; hydrogen; benzotriazol-1-ol; ethane-1,2-dithiol; triethylamine; dicyclohexyl-carbodiimide; palladium on activated charcoal; In ethanol; acetic acid; ethyl acetate; N,N-dimethyl-formamide;