(S)-2-(Benzyloxycarbonyl-methyl-amino)-3-[4-benzyloxy-3-(1-hydroxy-ethyl)-phenyl]-propionic acid methyl ester

Base Information

Chemical Name:(S)-2-(Benzyloxycarbonyl-methyl-amino)-3-[4-benzyloxy-3-(1-hydroxy-ethyl)-phenyl]-propionic acid methyl ester
CAS No.:110774-05-5
Molecular Formula:C₂₈H₃₁NO₆
Molecular Weight:477.557
Hs Code.:

Synonyms:(S)-2-(Benzyloxycarbonyl-methyl-amino)-3-[4-benzyloxy-3-(1-hydroxy-ethyl)-phenyl]-propionic acid methyl ester

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Chemical Property of (S)-2-(Benzyloxycarbonyl-methyl-amino)-3-[4-benzyloxy-3-(1-hydroxy-ethyl)-phenyl]-propionic acid methyl ester

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Technology Process of (S)-2-(Benzyloxycarbonyl-methyl-amino)-3-[4-benzyloxy-3-(1-hydroxy-ethyl)-phenyl]-propionic acid methyl ester

There total 6 articles about (S)-2-(Benzyloxycarbonyl-methyl-amino)-3-[4-benzyloxy-3-(1-hydroxy-ethyl)-phenyl]-propionic acid methyl 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: 95.0%

: 110774-04-4
L-3-(3-acetyl-4-(benzyloxy)phenyl)-N-(benzyloxycarbonyl)-N-methylalanine methyl ester

: 110774-05-5
(S)-2-(Benzyloxycarbonyl-methyl-amino)-3-[4-benzyloxy-3-(1-hydroxy-ethyl)-phenyl]-propionic acid methyl ester

Guidance literature:: With sodium tetrahydroborate; In methanol; at 25 ℃; for 1h;
DOI:10.1021/jo00232a044

Reference yield:

: 32404-28-7
(S)-3-(3-acetyl-4-hydroxyphenyl)-2-aminopropanoic acid hydrochloride

: 110774-05-5
(S)-2-(Benzyloxycarbonyl-methyl-amino)-3-[4-benzyloxy-3-(1-hydroxy-ethyl)-phenyl]-propionic acid methyl ester

Guidance literature:: Multi-step reaction with 5 steps

1: 74 percent / HCl (g) / 1 h / 25 °C

2: 90 percent / Na₂CO₃ / H₂O; diethyl ether / 3 h / 25 °C

3: 93 percent / K₂CO₃, tetra-n-butylammonium iodide / dimethylformamide / 6 h / 23 °C

4: 97 percent / NaH / tetrahydrofuran; dimethylformamide / 20 h / Heating

5: 95 percent / NaBH₄ / methanol / 1 h / 25 °C

With hydrogenchloride; sodium tetrahydroborate; tetra-(n-butyl)ammonium iodide; sodium hydride; sodium carbonate; potassium carbonate; In tetrahydrofuran; methanol; diethyl ether; water; N,N-dimethyl-formamide;
DOI:10.1021/jo00232a044

Reference yield:

: 60-18-4,18875-48-4,25619-78-7,30704-25-7
L-tyrosine

: 110774-05-5
(S)-2-(Benzyloxycarbonyl-methyl-amino)-3-[4-benzyloxy-3-(1-hydroxy-ethyl)-phenyl]-propionic acid methyl ester

Guidance literature:: Multi-step reaction with 6 steps

1: 77 percent / AlCl₃ / nitrobenzene / 6 h / 100 °C

2: 74 percent / HCl (g) / 1 h / 25 °C

3: 90 percent / Na₂CO₃ / H₂O; diethyl ether / 3 h / 25 °C

4: 93 percent / K₂CO₃, tetra-n-butylammonium iodide / dimethylformamide / 6 h / 23 °C

5: 97 percent / NaH / tetrahydrofuran; dimethylformamide / 20 h / Heating

6: 95 percent / NaBH₄ / methanol / 1 h / 25 °C

With hydrogenchloride; sodium tetrahydroborate; aluminium trichloride; tetra-(n-butyl)ammonium iodide; sodium hydride; sodium carbonate; potassium carbonate; In tetrahydrofuran; methanol; diethyl ether; water; nitrobenzene; N,N-dimethyl-formamide;
DOI:10.1021/jo00232a044