N-(benzyloxycarbonyl)-D-alanyl-L-2-amino-7-(tert-butyloxycarbonyl)heptanoyl-D-proline methyl ester

Base Information

Chemical Name:N-(benzyloxycarbonyl)-D-alanyl-L-2-amino-7-(tert-butyloxycarbonyl)heptanoyl-D-proline methyl ester
CAS No.:104848-88-6
Molecular Formula:C₂₉H₄₃N₃O₈
Molecular Weight:561.676
Hs Code.:

Synonyms:N-(benzyloxycarbonyl)-D-alanyl-L-2-amino-7-(tert-butyloxycarbonyl)heptanoyl-D-proline methyl ester

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Chemical Property of N-(benzyloxycarbonyl)-D-alanyl-L-2-amino-7-(tert-butyloxycarbonyl)heptanoyl-D-proline methyl ester

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Technology Process of N-(benzyloxycarbonyl)-D-alanyl-L-2-amino-7-(tert-butyloxycarbonyl)heptanoyl-D-proline methyl ester

There total 3 articles about N-(benzyloxycarbonyl)-D-alanyl-L-2-amino-7-(tert-butyloxycarbonyl)heptanoyl-D-proline 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:

: 49645-27-4
(S)-2-(((benzyloxy)carbonyl)amino)-8-(tert-butoxy)-8-oxooctanoic acid

: 104848-88-6
N-(benzyloxycarbonyl)-D-alanyl-L-2-amino-7-(tert-butyloxycarbonyl)heptanoyl-D-proline methyl ester

Guidance literature:: Multi-step reaction with 3 steps

1: 100 percent / N-methylmorpholine (NMM), dicyclohexylcarbodiimide (DCC), 1-hydroxybenzotriazole (HOBt) / CH₂Cl₂ / -5 - 20 °C

2: conc. HCl, H₂ / 10percent Pd/C / methanol / 1.5 h

3: diisopropylethylamine (DIEA), 1-hydroxybenzotriazole (HOBt) / dimethylformamide / 2 h / Ambient temperature

With 4-methyl-morpholine; hydrogenchloride; hydrogen; benzotriazol-1-ol; N-ethyl-N,N-diisopropylamine; dicyclohexyl-carbodiimide; palladium on activated charcoal; In methanol; dichloromethane; N,N-dimethyl-formamide;
DOI:10.1021/jm00384a013

Reference yield:

: 104848-86-4
N-(benzyloxycarbonyl)-L-2-amino-7-(tert-butyloxycarbonyl)heptanoyl-D-proline methyl ester

: 104848-88-6
N-(benzyloxycarbonyl)-D-alanyl-L-2-amino-7-(tert-butyloxycarbonyl)heptanoyl-D-proline methyl ester

Guidance literature:: Multi-step reaction with 2 steps

1: conc. HCl, H₂ / 10percent Pd/C / methanol / 1.5 h

2: diisopropylethylamine (DIEA), 1-hydroxybenzotriazole (HOBt) / dimethylformamide / 2 h / Ambient temperature

With hydrogenchloride; hydrogen; benzotriazol-1-ol; N-ethyl-N,N-diisopropylamine; palladium on activated charcoal; In methanol; N,N-dimethyl-formamide;
DOI:10.1021/jm00384a013

Reference yield:

: 26607-51-2
N-benzyloxycarbonyl-D-alanine

: 104848-88-6
N-(benzyloxycarbonyl)-D-alanyl-L-2-amino-7-(tert-butyloxycarbonyl)heptanoyl-D-proline methyl ester

Guidance literature:: Multi-step reaction with 2 steps

1: 73 percent / dicyclohexylcarbodiimide (DCC) / ethyl acetate / 2.5 h / -5 - 20 °C

2: diisopropylethylamine (DIEA), 1-hydroxybenzotriazole (HOBt) / dimethylformamide / 2 h / Ambient temperature

With benzotriazol-1-ol; N-ethyl-N,N-diisopropylamine; dicyclohexyl-carbodiimide; In ethyl acetate; N,N-dimethyl-formamide;
DOI:10.1021/jm00384a013