(R)-2-(3-((R)-2-(3-((R)-2-(3-aminophenoxy)propanamido)phenoxy)propanamido)phenoxy)propanoic acid

Base Information

Chemical Name:(R)-2-(3-((R)-2-(3-((R)-2-(3-aminophenoxy)propanamido)phenoxy)propanamido)phenoxy)propanoic acid
CAS No.:1595156-81-2
Molecular Formula:C₂₇H₂₉N₃O₇
Molecular Weight:507.543
Hs Code.:

Synonyms:(R)-2-(3-((R)-2-(3-((R)-2-(3-aminophenoxy)propanamido)phenoxy)propanamido)phenoxy)propanoic acid

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Chemical Property of (R)-2-(3-((R)-2-(3-((R)-2-(3-aminophenoxy)propanamido)phenoxy)propanamido)phenoxy)propanoic acid

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Technology Process of (R)-2-(3-((R)-2-(3-((R)-2-(3-aminophenoxy)propanamido)phenoxy)propanamido)phenoxy)propanoic acid

There total 8 articles about (R)-2-(3-((R)-2-(3-((R)-2-(3-aminophenoxy)propanamido)phenoxy)propanamido)phenoxy)propanoic acid 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: 86.0%

: 1595156-77-6
(R)-methyl 2-(3-((R)-2-(3-((R)-2-(3-aminophenoxy)propanamido)phenoxy)propanamido)phenoxy)propanoate

: 1595156-81-2
(R)-2-(3-((R)-2-(3-((R)-2-(3-aminophenoxy)propanamido)phenoxy)propanamido)phenoxy)propanoic acid

Guidance literature:: With lithium hydroxide; In tetrahydrofuran; at 20 ℃; for 1h;
DOI:10.1016/j.tetlet.2014.02.066

Reference yield:

: 554-84-7
meta-nitrophenol

: 1595156-81-2
(R)-2-(3-((R)-2-(3-((R)-2-(3-aminophenoxy)propanamido)phenoxy)propanamido)phenoxy)propanoic acid

Guidance literature:: Multi-step reaction with 5 steps

1: triphenylphosphine; diethylazodicarboxylate / tetrahydrofuran / 28.5 h / 0 - 20 °C

2: lithium hydroxide / tetrahydrofuran; water / 7.5 h / 20 °C

3: 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; benzotriazol-1-ol / tetrahydrofuran / 26.5 h / 0 - 20 °C

4: palladium 10% on activated carbon / tetrahydrofuran / 46 h / 20 °C

5: lithium hydroxide / tetrahydrofuran / 1 h / 20 °C

With palladium 10% on activated carbon; benzotriazol-1-ol; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; triphenylphosphine; lithium hydroxide; diethylazodicarboxylate; In tetrahydrofuran; water; 1: |Mitsunobu Displacement;
DOI:10.1016/j.tetlet.2014.02.066

Reference yield:

: 153546-07-7
methyl (R)-2-(3-nitrophenoxy)propionate

: 1595156-81-2
(R)-2-(3-((R)-2-(3-((R)-2-(3-aminophenoxy)propanamido)phenoxy)propanamido)phenoxy)propanoic acid

Guidance literature:: Multi-step reaction with 4 steps

1: lithium hydroxide / tetrahydrofuran; water / 7.5 h / 20 °C

2: 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; benzotriazol-1-ol / tetrahydrofuran / 26.5 h / 0 - 20 °C

3: palladium 10% on activated carbon / tetrahydrofuran / 46 h / 20 °C

4: lithium hydroxide / tetrahydrofuran / 1 h / 20 °C

With palladium 10% on activated carbon; benzotriazol-1-ol; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; lithium hydroxide; In tetrahydrofuran; water;
DOI:10.1016/j.tetlet.2014.02.066