(S)-2-Benzyloxycarbonylamino-3-{4-[ethoxy-(phenyl-trimethylsilanyloxy-methyl)-phosphinoylmethyl]-phenyl}-propionic acid benzyl ester

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Chemical Name:(S)-2-Benzyloxycarbonylamino-3-{4-[ethoxy-(phenyl-trimethylsilanyloxy-methyl)-phosphinoylmethyl]-phenyl}-propionic acid benzyl ester
CAS No.:313342-58-4
Molecular Formula:C₃₇H₄₄NO₇PSi
Molecular Weight:673.818
Hs Code.:

Synonyms:(S)-2-Benzyloxycarbonylamino-3-{4-[ethoxy-(phenyl-trimethylsilanyloxy-methyl)-phosphinoylmethyl]-phenyl}-propionic acid benzyl ester

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Chemical Property of (S)-2-Benzyloxycarbonylamino-3-{4-[ethoxy-(phenyl-trimethylsilanyloxy-methyl)-phosphinoylmethyl]-phenyl}-propionic acid benzyl ester

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Technology Process of (S)-2-Benzyloxycarbonylamino-3-{4-[ethoxy-(phenyl-trimethylsilanyloxy-methyl)-phosphinoylmethyl]-phenyl}-propionic acid benzyl ester

There total 6 articles about (S)-2-Benzyloxycarbonylamino-3-{4-[ethoxy-(phenyl-trimethylsilanyloxy-methyl)-phosphinoylmethyl]-phenyl}-propionic 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: 78.0%

: 75-77-4
chloro-trimethyl-silane

: 100-52-7
benzaldehyde

: 313342-47-1
(S)-2-Benzyloxycarbonylamino-3-(4-ethoxyphosphinoylmethyl-phenyl)-propionic acid benzyl ester

: 313342-58-4
(S)-2-Benzyloxycarbonylamino-3-{4-[ethoxy-(phenyl-trimethylsilanyloxy-methyl)-phosphinoylmethyl]-phenyl}-propionic acid benzyl ester

Guidance literature:: With N-ethyl-N,N-diisopropylamine; In dichloromethane; at 20 ℃; for 4.5h;
DOI:10.1016/S0960-894X(00)00476-5

Reference yield:

: 21209-51-8
N-benzyloxycarbonyl-L-serine benzyl ester

: 313342-58-4
(S)-2-Benzyloxycarbonylamino-3-{4-[ethoxy-(phenyl-trimethylsilanyloxy-methyl)-phosphinoylmethyl]-phenyl}-propionic acid benzyl ester

Guidance literature:: Multi-step reaction with 4 steps

1.1: 64 percent / PPh₃; imidazole; iodine / acetonitrile; diethyl ether / 0.75 h / 0 °C

2.1: Zn; TMSCl / various solvent(s)

2.2: 77 percent / (2-furyl)3P; Pd₂dba3 / N,N-dimethyl-acetamide; tetrahydrofuran / 60 °C

3.1: 73 percent / TMSCl / CH₂Cl₂; ethanol / 20 °C

4.1: 78 percent / iPr₂EtN / CH₂Cl₂ / 4.5 h / 20 °C

With 1H-imidazole; chloro-trimethyl-silane; iodine; N-ethyl-N,N-diisopropylamine; triphenylphosphine; zinc; In diethyl ether; ethanol; dichloromethane; acetonitrile; 1.1: Iodination / 2.1: Metallation / 2.2: Arylation / 3.1: dealkylation / 4.1: Addition;
DOI:10.1016/S0960-894X(00)00476-5

Reference yield:

: 16004-15-2
1-bromomethyl-4-iodobenzene

: 313342-58-4
(S)-2-Benzyloxycarbonylamino-3-{4-[ethoxy-(phenyl-trimethylsilanyloxy-methyl)-phosphinoylmethyl]-phenyl}-propionic acid benzyl ester

Guidance literature:: Multi-step reaction with 4 steps

1.1: 94 percent / NaH / tetrahydrofuran / -10 - 20 °C

2.1: Zn; TMSCl / various solvent(s)

2.2: 77 percent / (2-furyl)3P; Pd₂dba3 / N,N-dimethyl-acetamide; tetrahydrofuran / 60 °C

3.1: 73 percent / TMSCl / CH₂Cl₂; ethanol / 20 °C

4.1: 78 percent / iPr₂EtN / CH₂Cl₂ / 4.5 h / 20 °C

With chloro-trimethyl-silane; sodium hydride; N-ethyl-N,N-diisopropylamine; zinc; In tetrahydrofuran; ethanol; dichloromethane; 1.1: Alkylation / 2.1: Metallation / 2.2: Arylation / 3.1: dealkylation / 4.1: Addition;
DOI:10.1016/S0960-894X(00)00476-5