N-[3-[1,1'-biphenyl]-4-yl-2-[[hydroxy[2-phenyl-1-[[(phenylmethoxy)carbonyl]amino]ethyl]phosphinyl]methyl]-1-oxopropyl]-L-alanine

Base Information

Chemical Name:N-[3-[1,1'-biphenyl]-4-yl-2-[[hydroxy[2-phenyl-1-[[(phenylmethoxy)carbonyl]amino]ethyl]phosphinyl]methyl]-1-oxopropyl]-L-alanine
CAS No.:207286-85-9
Molecular Formula:C₃₅H₃₇N₂O₇P
Molecular Weight:628.662
Hs Code.:

Synonyms:N-[3-[1,1'-biphenyl]-4-yl-2-[[hydroxy[2-phenyl-1-[[(phenylmethoxy)carbonyl]amino]ethyl]phosphinyl]methyl]-1-oxopropyl]-L-alanine

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Chemical Property of N-[3-[1,1'-biphenyl]-4-yl-2-[[hydroxy[2-phenyl-1-[[(phenylmethoxy)carbonyl]amino]ethyl]phosphinyl]methyl]-1-oxopropyl]-L-alanine

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Technology Process of N-[3-[1,1'-biphenyl]-4-yl-2-[[hydroxy[2-phenyl-1-[[(phenylmethoxy)carbonyl]amino]ethyl]phosphinyl]methyl]-1-oxopropyl]-L-alanine

There total 6 articles about N-[3-[1,1'-biphenyl]-4-yl-2-[[hydroxy[2-phenyl-1-[[(phenylmethoxy)carbonyl]amino]ethyl]phosphinyl]methyl]-1-oxopropyl]-L-alanine 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: 100.0%

: 207286-84-8
methyl N-[3-[1,1'-biphenyl]-4-yl-2-[[hydroxy[2-phenyl-1-[[(phenylmethoxy)carbonyl]amino]ethyl]phosphinyl]methyl]-1-oxopropyl]-L-alaninate

: 207286-85-9
N-[3-[1,1'-biphenyl]-4-yl-2-[[hydroxy[2-phenyl-1-[[(phenylmethoxy)carbonyl]amino]ethyl]phosphinyl]methyl]-1-oxopropyl]-L-alanine

Guidance literature:

Reference yield:

: 115961-49-4
[2-phenyl-1-[[(phenylmethoxy)carbonyl]amino]ethyl]phosphinic acid

: 207286-85-9
N-[3-[1,1'-biphenyl]-4-yl-2-[[hydroxy[2-phenyl-1-[[(phenylmethoxy)carbonyl]amino]ethyl]phosphinyl]methyl]-1-oxopropyl]-L-alanine

Guidance literature:: Multi-step reaction with 5 steps

1: 84.1 percent / N,O-bistrimethylsilylacetamide

2: 80 percent / Pd(PPh₃)4; 2 M aq. Na₂CO₃ / toluene / 10 h / 80 °C

3: 97.4 percent / 1 M aq. NaOH / ethanol / 20 °C

4: Et₃N; BOP / dimethylformamide / 0.5 h / 20 °C

5: 1 M aq. LiOH / ethanol / 8 h / 20 °C

With lithium hydroxide; sodium hydroxide; tetrakis(triphenylphosphine) palladium⁽⁰⁾; N,O-bis-(trimethylsilyl)-acetamide; sodium carbonate; (benzotriazo-1-yloxy)tris(dimethylamino)phosphonium hexafluorophosphate; triethylamine; In ethanol; N,N-dimethyl-formamide; toluene; 1: Addition / 2: Phenylation / 3: Hydrolysis / 4: Acylation / 5: Hydrolysis;
DOI:10.1021/jm990483l

Reference yield:

: 207286-80-4
ethyl 4-bromo-α-methylenebenzenepropanoate

: 207286-85-9
N-[3-[1,1'-biphenyl]-4-yl-2-[[hydroxy[2-phenyl-1-[[(phenylmethoxy)carbonyl]amino]ethyl]phosphinyl]methyl]-1-oxopropyl]-L-alanine

Guidance literature:: Multi-step reaction with 5 steps

1: 84.1 percent / N,O-bistrimethylsilylacetamide

2: 80 percent / Pd(PPh₃)4; 2 M aq. Na₂CO₃ / toluene / 10 h / 80 °C

3: 97.4 percent / 1 M aq. NaOH / ethanol / 20 °C

4: Et₃N; BOP / dimethylformamide / 0.5 h / 20 °C

5: 1 M aq. LiOH / ethanol / 8 h / 20 °C

With lithium hydroxide; sodium hydroxide; tetrakis(triphenylphosphine) palladium⁽⁰⁾; N,O-bis-(trimethylsilyl)-acetamide; sodium carbonate; (benzotriazo-1-yloxy)tris(dimethylamino)phosphonium hexafluorophosphate; triethylamine; In ethanol; N,N-dimethyl-formamide; toluene; 1: Addition / 2: Phenylation / 3: Hydrolysis / 4: Acylation / 5: Hydrolysis;
DOI:10.1021/jm990483l