(S)-2-[2-((S)-2-{(S)-2-[2-(4-Fluoro-phenyl)-acetylamino]-3-phenyl-propionylamino}-3-phenyl-propionylamino)-acetylamino]-4-methyl-pentanoic acid ((S)-1-carbamoyl-3-methylsulfanyl-propyl)-amide

Base Information

• Chemical Name: (S)-2-[2-((S)-2-{(S)-2-[2-(4-Fluoro-phenyl)-acetylamino]-3-phenyl-propionylamino}-3-phenyl-propionylamino)-acetylamino]-4-methyl-pentanoic acid ((S)-1-carbamoyl-3-methylsulfanyl-propyl)-amide
• CAS No.: 119372-40-6
• Molecular Formula: C₃₉H₄₉FN₆O₆S
• Molecular Weight: 748.919

Synonyms:

Chemical Property of (S)-2-[2-((S)-2-{(S)-2-[2-(4-Fluoro-phenyl)-acetylamino]-3-phenyl-propionylamino}-3-phenyl-propionylamino)-acetylamino]-4-methyl-pentanoic acid ((S)-1-carbamoyl-3-methylsulfanyl-propyl)-amide

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Technology Process of (S)-2-[2-((S)-2-{(S)-2-[2-(4-Fluoro-phenyl)-acetylamino]-3-phenyl-propionylamino}-3-phenyl-propionylamino)-acetylamino]-4-methyl-pentanoic acid ((S)-1-carbamoyl-3-methylsulfanyl-propyl)-amide

There total 9 articles about (S)-2-[2-((S)-2-{(S)-2-[2-(4-Fluoro-phenyl)-acetylamino]-3-phenyl-propionylamino}-3-phenyl-propionylamino)-acetylamino]-4-methyl-pentanoic acid ((S)-1-carbamoyl-3-methylsulfanyl-propyl)-amide 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: 66.0%

H-Phe-Phe-Gly-Leu-Met-NH2 (51165-05-0,78081-73-9) + (4-Fluoro-phenyl)-acetic acid 2,4,5-trichloro-phenyl ester → (S)-2-[2-((S)-2-{(S)-2-[2-(4-Fluoro-phenyl)-acetylamino]-3-phenyl-propionylamino}-3-phenyl-propionylamino)-acetylamino]-4-methyl-pentanoic acid ((S)-1-carbamoyl-3-methylsulfanyl-propyl)-amide (119372-40-6)

Guidance literature:

DOI:10.1016/0223-5234(88)90006-2

Reference yield:

N-tert-butoxycarbonyl-L-phenylalanine (13734-34-4) → (S)-2-[2-((S)-2-{(S)-2-[2-(4-Fluoro-phenyl)-acetylamino]-3-phenyl-propionylamino}-3-phenyl-propionylamino)-acetylamino]-4-methyl-pentanoic acid ((S)-1-carbamoyl-3-methylsulfanyl-propyl)-amide (119372-40-6)

Guidance literature:

Multi-step reaction with 5 steps

1: 70 percent / NMM, IBCF / dimethylformamide / -15 °C

2: 85 percent / 1N NaOH / dioxane; methanol / 0 deg C, 5 h, RT

3: 54.6 percent / IBCF, NMMole / dimethylformamide / -20 °C

4: TFA, anisole / CH₂Cl₂ / 1 h / 0 °C

5: 66 percent

With 4-methyl-morpholine; sodium hydroxide; methoxybenzene; trifluoroacetic acid; isobutyl chloroformate; In 1,4-dioxane; methanol; dichloromethane; N,N-dimethyl-formamide;

DOI:10.1016/0223-5234(88)90006-2

Reference yield:

N-tert-butoxycarbonyl-L-leucine (13139-15-6,53296-34-7) → (S)-2-[2-((S)-2-{(S)-2-[2-(4-Fluoro-phenyl)-acetylamino]-3-phenyl-propionylamino}-3-phenyl-propionylamino)-acetylamino]-4-methyl-pentanoic acid ((S)-1-carbamoyl-3-methylsulfanyl-propyl)-amide (119372-40-6)

Guidance literature:

Multi-step reaction with 5 steps

1: 93.6 percent / NMM, IBCF / dimethylformamide / -20 °C

2: TFA, anisole / CH₂Cl₂ / 1 h / 0 °C

3: 54.6 percent / IBCF, NMMole / dimethylformamide / -20 °C

4: TFA, anisole / CH₂Cl₂ / 1 h / 0 °C

5: 66 percent

With 4-methyl-morpholine; methoxybenzene; trifluoroacetic acid; isobutyl chloroformate; In dichloromethane; N,N-dimethyl-formamide;

DOI:10.1016/0223-5234(88)90006-2

upstream raw materials:

H-Phe-Phe-Gly-Leu-Met-NH₂

N-tert-butoxycarbonyl-L-leucine

N-tert-butoxycarbonyl-L-leucyl-L-methioninamide

N-tert-butoxycarbonyl-L-phenylalanine

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