(R)-4-[5-(5-fluoro-4'-{2-[(S)-1-((S)-2-methoxycarbonylamino-3-methyl-butyryl)pyrrolidin-2-yl]-1H-imidazol-4-yl}-2-trifluoromethoxy-biphenyl-4-ylcarbamoyl)pyridin-2-yl]-3-methyl-piperazine-1-carboxylic acid tert butyl ester

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Chemical Name:(R)-4-[5-(5-fluoro-4'-{2-[(S)-1-((S)-2-methoxycarbonylamino-3-methyl-butyryl)pyrrolidin-2-yl]-1H-imidazol-4-yl}-2-trifluoromethoxy-biphenyl-4-ylcarbamoyl)pyridin-2-yl]-3-methyl-piperazine-1-carboxylic acid tert butyl ester
CAS No.:1374892-14-4
Molecular Formula:C₄₃H₅₀F₄N₈O₇
Molecular Weight:866.913
Hs Code.:

(R)-4-[5-(5-fluoro-4'-{2-[(S)-1-((S)-2-methoxycarbonylamino-3-methyl-butyryl)pyrrolidin-2-yl]-1H-imidazol-4-yl}-2-trifluoromethoxy-biphenyl-4-ylcarbamoyl)pyridin-2-yl]-3-methyl-piperazine-1-carboxylic acid tert butyl ester

Synonyms:(R)-4-[5-(5-fluoro-4'-{2-[(S)-1-((S)-2-methoxycarbonylamino-3-methyl-butyryl)pyrrolidin-2-yl]-1H-imidazol-4-yl}-2-trifluoromethoxy-biphenyl-4-ylcarbamoyl)pyridin-2-yl]-3-methyl-piperazine-1-carboxylic acid tert butyl ester

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Chemical Property of (R)-4-[5-(5-fluoro-4'-{2-[(S)-1-((S)-2-methoxycarbonylamino-3-methyl-butyryl)pyrrolidin-2-yl]-1H-imidazol-4-yl}-2-trifluoromethoxy-biphenyl-4-ylcarbamoyl)pyridin-2-yl]-3-methyl-piperazine-1-carboxylic acid tert butyl ester

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Technology Process of (R)-4-[5-(5-fluoro-4'-{2-[(S)-1-((S)-2-methoxycarbonylamino-3-methyl-butyryl)pyrrolidin-2-yl]-1H-imidazol-4-yl}-2-trifluoromethoxy-biphenyl-4-ylcarbamoyl)pyridin-2-yl]-3-methyl-piperazine-1-carboxylic acid tert butyl ester

There total 10 articles about (R)-4-[5-(5-fluoro-4'-{2-[(S)-1-((S)-2-methoxycarbonylamino-3-methyl-butyryl)pyrrolidin-2-yl]-1H-imidazol-4-yl}-2-trifluoromethoxy-biphenyl-4-ylcarbamoyl)pyridin-2-yl]-3-methyl-piperazine-1-carboxylic 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:

: 1374892-13-3
{(S)-1-[(S)-2-(4-{5'-fluoro-4'-[(6-fluoro-pyridine-3-carbonyl)amino]-2'-trifluoromethoxy-biphenyl-4-yl}-1H-imidazol-2-yl)pyrrolidine-1-carbonyl]-2-methyl-propyl}carbamic acid methyl ester

: 163765-44-4
(R)-tert-butyl 3-methylpiperazine-1-carboxylate

: 1374892-14-4
(R)-4-[5-(5-fluoro-4'-{2-[(S)-1-((S)-2-methoxycarbonylamino-3-methyl-butyryl)pyrrolidin-2-yl]-1H-imidazol-4-yl}-2-trifluoromethoxy-biphenyl-4-ylcarbamoyl)pyridin-2-yl]-3-methyl-piperazine-1-carboxylic acid tert butyl ester

Guidance literature:: With N-ethyl-N,N-diisopropylamine; In dimethyl sulfoxide; at 120 ℃; Inert atmosphere;

Reference yield:

: 116369-23-4
2-fluoro-5-(trifluoromethoxy)aniline

: 1374892-14-4
(R)-4-[5-(5-fluoro-4'-{2-[(S)-1-((S)-2-methoxycarbonylamino-3-methyl-butyryl)pyrrolidin-2-yl]-1H-imidazol-4-yl}-2-trifluoromethoxy-biphenyl-4-ylcarbamoyl)pyridin-2-yl]-3-methyl-piperazine-1-carboxylic acid tert butyl ester

Guidance literature:: Multi-step reaction with 4 steps

1: N-Bromosuccinimide / N,N-dimethyl-formamide / 1 h / 20 °C / Inert atmosphere

2: potassium carbonate; tetrakis(triphenylphosphine) palladium⁽⁰⁾ / toluene; water / 100 °C / Inert atmosphere

3: dichloromethane / 0.08 h / 20 °C / Inert atmosphere

4: N-ethyl-N,N-diisopropylamine / dimethyl sulfoxide / 120 °C / Inert atmosphere

With N-Bromosuccinimide; tetrakis(triphenylphosphine) palladium⁽⁰⁾; potassium carbonate; N-ethyl-N,N-diisopropylamine; In dichloromethane; water; dimethyl sulfoxide; N,N-dimethyl-formamide; toluene;

Reference yield:

: 116367-67-0
4-bromo-2-fluoro-5-trifluoromethoxy-phenylamine

: 1374892-14-4
(R)-4-[5-(5-fluoro-4'-{2-[(S)-1-((S)-2-methoxycarbonylamino-3-methyl-butyryl)pyrrolidin-2-yl]-1H-imidazol-4-yl}-2-trifluoromethoxy-biphenyl-4-ylcarbamoyl)pyridin-2-yl]-3-methyl-piperazine-1-carboxylic acid tert butyl ester

Guidance literature:: Multi-step reaction with 3 steps

1: potassium carbonate; tetrakis(triphenylphosphine) palladium⁽⁰⁾ / toluene; water / 100 °C / Inert atmosphere

2: dichloromethane / 0.08 h / 20 °C / Inert atmosphere

3: N-ethyl-N,N-diisopropylamine / dimethyl sulfoxide / 120 °C / Inert atmosphere

With tetrakis(triphenylphosphine) palladium⁽⁰⁾; potassium carbonate; N-ethyl-N,N-diisopropylamine; In dichloromethane; water; dimethyl sulfoxide; toluene;