(R)-Amino-(4-{3-[4-((R)-amino-ethoxycarbonyl-methyl)-phenoxymethyl]-benzyloxy}-phenyl)-acetic acid ethyl ester

Base Information

Chemical Name:(R)-Amino-(4-{3-[4-((R)-amino-ethoxycarbonyl-methyl)-phenoxymethyl]-benzyloxy}-phenyl)-acetic acid ethyl ester
CAS No.:458550-66-8
Molecular Formula:C₂₈H₃₂N₂O₆
Molecular Weight:492.572
Hs Code.:

Synonyms:(R)-Amino-(4-{3-[4-((R)-amino-ethoxycarbonyl-methyl)-phenoxymethyl]-benzyloxy}-phenyl)-acetic acid ethyl ester

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Chemical Property of (R)-Amino-(4-{3-[4-((R)-amino-ethoxycarbonyl-methyl)-phenoxymethyl]-benzyloxy}-phenyl)-acetic acid ethyl ester

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Technology Process of (R)-Amino-(4-{3-[4-((R)-amino-ethoxycarbonyl-methyl)-phenoxymethyl]-benzyloxy}-phenyl)-acetic acid ethyl ester

There total 4 articles about (R)-Amino-(4-{3-[4-((R)-amino-ethoxycarbonyl-methyl)-phenoxymethyl]-benzyloxy}-phenyl)-acetic acid ethyl 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: 91.0%

: 458550-62-4
tert-butoxycarbonylamino-(4-{3-[4-(tert-butoxycarbonylamino-ethoxycarbonyl-methyl)-phenoxymethyl]-benzyloxy}-phenyl)-acetic acid ethyl ester

: 458550-66-8
(R)-Amino-(4-{3-[4-((R)-amino-ethoxycarbonyl-methyl)-phenoxymethyl]-benzyloxy}-phenyl)-acetic acid ethyl ester

Guidance literature:: With 20percent TFA; In dichloromethane; for 2h;
DOI:10.1021/jm020093q

Reference yield:

: 22818-40-2
D-4-hydroxyphenylglycine

: 458550-66-8
(R)-Amino-(4-{3-[4-((R)-amino-ethoxycarbonyl-methyl)-phenoxymethyl]-benzyloxy}-phenyl)-acetic acid ethyl ester

Guidance literature:: Multi-step reaction with 4 steps

1: 100 percent / SOCl₂ / 10 h / 20 °C

2: 95 percent / aq. NaHCO₃ / dioxane / 7 h / 0 - 20 °C

3: 49 percent / EtOH / 23 h / 20 °C

4: 91 percent / 20percent TFA / CH₂Cl₂ / 2 h

With thionyl chloride; ethanol; sodium hydrogencarbonate; In 1,4-dioxane; dichloromethane; 3: Williamson synthesis;
DOI:10.1021/jm020093q

Reference yield:

: 37763-23-8
D-2-p-hydroxyphenylglycine methyl ester

: 458550-66-8
(R)-Amino-(4-{3-[4-((R)-amino-ethoxycarbonyl-methyl)-phenoxymethyl]-benzyloxy}-phenyl)-acetic acid ethyl ester

Guidance literature:: Multi-step reaction with 3 steps

1: 95 percent / aq. NaHCO₃ / dioxane / 7 h / 0 - 20 °C

2: 49 percent / EtOH / 23 h / 20 °C

3: 91 percent / 20percent TFA / CH₂Cl₂ / 2 h

With ethanol; sodium hydrogencarbonate; In 1,4-dioxane; dichloromethane; 2: Williamson synthesis;
DOI:10.1021/jm020093q