(S)-4-{(S)-2-Acetylamino-3-[4-(2-methoxycarbonyl-2-oxo-acetyl)-phenyl]-propionylamino}-4-[(S)-3-tert-butoxycarbonyl-1-((1S,2S)-1-carbamoyl-2-methyl-butylcarbamoyl)-propylcarbamoyl]-butyric acid tert-butyl ester

Base Information

Chemical Name:(S)-4-{(S)-2-Acetylamino-3-[4-(2-methoxycarbonyl-2-oxo-acetyl)-phenyl]-propionylamino}-4-[(S)-3-tert-butoxycarbonyl-1-((1S,2S)-1-carbamoyl-2-methyl-butylcarbamoyl)-propylcarbamoyl]-butyric acid tert-butyl ester
CAS No.:367266-81-7
Molecular Formula:C₃₉H₅₇N₅O₁₃
Molecular Weight:803.907
Hs Code.:

(S)-4-{(S)-2-Acetylamino-3-[4-(2-methoxycarbonyl-2-oxo-acetyl)-phenyl]-propionylamino}-4-[(S)-3-tert-butoxycarbonyl-1-((1S,2S)-1-carbamoyl-2-methyl-butylcarbamoyl)-propylcarbamoyl]-butyric acid tert-butyl ester

Synonyms:(S)-4-{(S)-2-Acetylamino-3-[4-(2-methoxycarbonyl-2-oxo-acetyl)-phenyl]-propionylamino}-4-[(S)-3-tert-butoxycarbonyl-1-((1S,2S)-1-carbamoyl-2-methyl-butylcarbamoyl)-propylcarbamoyl]-butyric acid tert-butyl ester

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Chemical Property of (S)-4-{(S)-2-Acetylamino-3-[4-(2-methoxycarbonyl-2-oxo-acetyl)-phenyl]-propionylamino}-4-[(S)-3-tert-butoxycarbonyl-1-((1S,2S)-1-carbamoyl-2-methyl-butylcarbamoyl)-propylcarbamoyl]-butyric acid tert-butyl ester

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Technology Process of (S)-4-{(S)-2-Acetylamino-3-[4-(2-methoxycarbonyl-2-oxo-acetyl)-phenyl]-propionylamino}-4-[(S)-3-tert-butoxycarbonyl-1-((1S,2S)-1-carbamoyl-2-methyl-butylcarbamoyl)-propylcarbamoyl]-butyric acid tert-butyl ester

There total 8 articles about (S)-4-{(S)-2-Acetylamino-3-[4-(2-methoxycarbonyl-2-oxo-acetyl)-phenyl]-propionylamino}-4-[(S)-3-tert-butoxycarbonyl-1-((1S,2S)-1-carbamoyl-2-methyl-butylcarbamoyl)-propylcarbamoyl]-butyric acid 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: 62.0%

: 367266-82-8
(S)-4-((S)-2-Acetylamino-3-{4-[2-methoxycarbonyl-2-(triphenyl-λ⁵-phosphanylidene)-acetyl]-phenyl}-propionylamino)-4-[(S)-3-tert-butoxycarbonyl-1-((1S,2S)-1-carbamoyl-2-methyl-butylcarbamoyl)-propylcarbamoyl]-butyric acid tert-butyl ester

: 367266-81-7
(S)-4-{(S)-2-Acetylamino-3-[4-(2-methoxycarbonyl-2-oxo-acetyl)-phenyl]-propionylamino}-4-[(S)-3-tert-butoxycarbonyl-1-((1S,2S)-1-carbamoyl-2-methyl-butylcarbamoyl)-propylcarbamoyl]-butyric acid tert-butyl ester

Guidance literature:: With ozone; In methanol; at -78 - 20 ℃; for 0.5h;
DOI:10.1016/S0960-894X(01)00269-4

Reference yield:

: 150618-07-8
4-((S)-2-Benzyloxycarbonyl-2-tert-butoxycarbonylamino-ethyl)-benzoic acid

: 367266-81-7
(S)-4-{(S)-2-Acetylamino-3-[4-(2-methoxycarbonyl-2-oxo-acetyl)-phenyl]-propionylamino}-4-[(S)-3-tert-butoxycarbonyl-1-((1S,2S)-1-carbamoyl-2-methyl-butylcarbamoyl)-propylcarbamoyl]-butyric acid tert-butyl ester

Guidance literature:: Multi-step reaction with 6 steps

1: 42 percent / EDC; DMAP / tetrahydrofuran / 28 h / 20 °C

2: H₂ / Pd/C / methanol / 0.5 h / 20 °C

3: TFA / CH₂Cl₂ / 0.5 h / 20 °C

4: 81 percent / Et₃N / 1,2-dimethoxy-ethane / 18 h / 20 °C

5: 57 percent / EDC; HOBt / CH₂Cl₂; dimethylformamide / 4.5 h / 20 °C

6: 62 percent / O₃ / methanol / 0.5 h / -78 - 20 °C

With dmap; hydrogen; benzotriazol-1-ol; ozone; N-(3-dimethylaminopropyl)-N-ethylcarbodiimide; triethylamine; trifluoroacetic acid; palladium on activated charcoal; In tetrahydrofuran; methanol; 1,2-dimethoxyethane; dichloromethane; N,N-dimethyl-formamide;
DOI:10.1016/S0960-894X(01)00269-4

Reference yield:

: 123993-20-4
N-tert.-butoxycarbonyl-(4-trifluoromethanesulfonyloxy)-L-phenylalanine benzyl ester

: 367266-81-7
(S)-4-{(S)-2-Acetylamino-3-[4-(2-methoxycarbonyl-2-oxo-acetyl)-phenyl]-propionylamino}-4-[(S)-3-tert-butoxycarbonyl-1-((1S,2S)-1-carbamoyl-2-methyl-butylcarbamoyl)-propylcarbamoyl]-butyric acid tert-butyl ester

Guidance literature:: Multi-step reaction with 8 steps

1: 90 percent / Pd(OAc)2; dppp; Et₃N / dimethylsulfoxide / 2 h / 80 °C

2: 80 percent / Bu₄NF / tetrahydrofuran / 5 h / 20 °C

3: 42 percent / EDC; DMAP / tetrahydrofuran / 28 h / 20 °C

4: H₂ / Pd/C / methanol / 0.5 h / 20 °C

5: TFA / CH₂Cl₂ / 0.5 h / 20 °C

6: 81 percent / Et₃N / 1,2-dimethoxy-ethane / 18 h / 20 °C

7: 57 percent / EDC; HOBt / CH₂Cl₂; dimethylformamide / 4.5 h / 20 °C

8: 62 percent / O₃ / methanol / 0.5 h / -78 - 20 °C

With dmap; palladium diacetate; 1,3-bis-(diphenylphosphino)propane; tetrabutyl ammonium fluoride; hydrogen; benzotriazol-1-ol; ozone; N-(3-dimethylaminopropyl)-N-ethylcarbodiimide; triethylamine; trifluoroacetic acid; palladium on activated charcoal; In tetrahydrofuran; methanol; 1,2-dimethoxyethane; dichloromethane; dimethyl sulfoxide; N,N-dimethyl-formamide;
DOI:10.1016/S0960-894X(01)00269-4