4-[(S)-2-Benzyloxycarbonylamino-2-({[(S)-1-((S)-1-carbamoyl-3-methylsulfanyl-propylcarbamoyl)-3-methyl-butylcarbamoyl]-methyl}-carbamoyl)-ethyl]-imidazole-1-carboxylic acid benzyl ester

Base Information

Chemical Name:4-[(S)-2-Benzyloxycarbonylamino-2-({[(S)-1-((S)-1-carbamoyl-3-methylsulfanyl-propylcarbamoyl)-3-methyl-butylcarbamoyl]-methyl}-carbamoyl)-ethyl]-imidazole-1-carboxylic acid benzyl ester
CAS No.:103929-14-2
Molecular Formula:C₃₅H₄₅N₇O₈S
Molecular Weight:723.85
Hs Code.:

4-[(S)-2-Benzyloxycarbonylamino-2-({[(S)-1-((S)-1-carbamoyl-3-methylsulfanyl-propylcarbamoyl)-3-methyl-butylcarbamoyl]-methyl}-carbamoyl)-ethyl]-imidazole-1-carboxylic acid benzyl ester

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Chemical Property of 4-[(S)-2-Benzyloxycarbonylamino-2-({[(S)-1-((S)-1-carbamoyl-3-methylsulfanyl-propylcarbamoyl)-3-methyl-butylcarbamoyl]-methyl}-carbamoyl)-ethyl]-imidazole-1-carboxylic acid benzyl ester

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Technology Process of 4-[(S)-2-Benzyloxycarbonylamino-2-({[(S)-1-((S)-1-carbamoyl-3-methylsulfanyl-propylcarbamoyl)-3-methyl-butylcarbamoyl]-methyl}-carbamoyl)-ethyl]-imidazole-1-carboxylic acid benzyl ester

There total 1 articles about 4-[(S)-2-Benzyloxycarbonylamino-2-({[(S)-1-((S)-1-carbamoyl-3-methylsulfanyl-propylcarbamoyl)-3-methyl-butylcarbamoyl]-methyl}-carbamoyl)-ethyl]-imidazole-1-carboxylic acid benzyl 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:

: 40297-96-9
H-Gly-Leu-Met-NH₂ hydrochloride

: 35016-67-2
Z-His(imZ)-OH

: 103929-14-2
4-[(S)-2-Benzyloxycarbonylamino-2-({[(S)-1-((S)-1-carbamoyl-3-methylsulfanyl-propylcarbamoyl)-3-methyl-butylcarbamoyl]-methyl}-carbamoyl)-ethyl]-imidazole-1-carboxylic acid benzyl ester

Guidance literature:: With benzotriazol-1-ol; triethylamine; dicyclohexyl-carbodiimide; In N,N-dimethyl-formamide; at 0 ℃; for 12h;

Reference yield:

: 103929-14-2
4-[(S)-2-Benzyloxycarbonylamino-2-({[(S)-1-((S)-1-carbamoyl-3-methylsulfanyl-propylcarbamoyl)-3-methyl-butylcarbamoyl]-methyl}-carbamoyl)-ethyl]-imidazole-1-carboxylic acid benzyl ester

: 103969-90-0
Boc-Phe-His-Gly-Leu-Met-NH₂

Guidance literature:: Multi-step reaction with 3 steps

1: conc. aq. NH₃ / 0.17 h / Heating

2: 93 percent / HBr / acetic acid / 1 h / Ambient temperature

3: 60 percent / triethylamine / dimethylformamide / 120 h / Ambient temperature

With ammonium hydroxide; hydrogen bromide; triethylamine; In acetic acid; N,N-dimethyl-formamide;

Reference yield:

: 103929-14-2
4-[(S)-2-Benzyloxycarbonylamino-2-({[(S)-1-((S)-1-carbamoyl-3-methylsulfanyl-propylcarbamoyl)-3-methyl-butylcarbamoyl]-methyl}-carbamoyl)-ethyl]-imidazole-1-carboxylic acid benzyl ester

: 90456-49-8
p-Glu-Phe-His-Gly-Leu-Met-NH₂

Guidance literature:: Multi-step reaction with 5 steps

1: conc. aq. NH₃ / 0.17 h / Heating

2: 93 percent / HBr / acetic acid / 1 h / Ambient temperature

3: 60 percent / triethylamine / dimethylformamide / 120 h / Ambient temperature

4: 91 percent / 4.2M HCl / dioxane / 0.5 h

5: 45 percent / triethylamine, dicyclohexylcarbodiimide / dimethylformamide / 24 h

With hydrogenchloride; ammonium hydroxide; hydrogen bromide; triethylamine; dicyclohexyl-carbodiimide; In 1,4-dioxane; acetic acid; N,N-dimethyl-formamide;