(S)-6-Benzyloxycarbonylamino-2-(4-hydroxy-benzoylamino)-hexanoic acid

Base Information

• Chemical Name: (S)-6-Benzyloxycarbonylamino-2-(4-hydroxy-benzoylamino)-hexanoic acid
• CAS No.: 216880-30-7
• Molecular Formula: C₂₁H₂₄N₂O₆
• Molecular Weight: 400.431
• Mol file: 216880-30-7.mol

Synonyms:(S)-6-Benzyloxycarbonylamino-2-(4-hydroxy-benzoylamino)-hexanoic acid

Chemical Property of (S)-6-Benzyloxycarbonylamino-2-(4-hydroxy-benzoylamino)-hexanoic acid

Chemical Property:

Purity/Quality:

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

Useful:

Technology Process of (S)-6-Benzyloxycarbonylamino-2-(4-hydroxy-benzoylamino)-hexanoic acid

There total 3 articles about (S)-6-Benzyloxycarbonylamino-2-(4-hydroxy-benzoylamino)-hexanoic 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%

(S)-6-Benzyloxycarbonylamino-2-(4-hydroxy-benzoylamino)-hexanoic acid methyl ester (216880-29-4) → (S)-6-Benzyloxycarbonylamino-2-(4-hydroxy-benzoylamino)-hexanoic acid (216880-30-7)

Guidance literature:

With sodium hydroxide; In methanol; at 5 ℃; for 2.5h;

DOI:10.1021/ja980810z

Reference yield:

(S)-methyl 2-amino-6-(benzyloxycarbonylamino)hexanoate (24498-31-5) → (S)-6-Benzyloxycarbonylamino-2-(4-hydroxy-benzoylamino)-hexanoic acid (216880-30-7)

Guidance literature:

Multi-step reaction with 2 steps

1: 69 percent / DCC / tetrahydrofuran / 4 h / Ambient temperature

2: 86 percent / aq. NaOH / methanol / 2.5 h / 5 °C

With sodium hydroxide; dicyclohexyl-carbodiimide; In tetrahydrofuran; methanol;

DOI:10.1021/ja980810z

Reference yield:

4-hydroxy-benzoic acid (99-96-7) → (S)-6-Benzyloxycarbonylamino-2-(4-hydroxy-benzoylamino)-hexanoic acid (216880-30-7)

Guidance literature:

Multi-step reaction with 2 steps

1: 69 percent / DCC / tetrahydrofuran / 4 h / Ambient temperature

2: 86 percent / aq. NaOH / methanol / 2.5 h / 5 °C

With sodium hydroxide; dicyclohexyl-carbodiimide; In tetrahydrofuran; methanol;

DOI:10.1021/ja980810z

upstream raw materials:

(S)-6-Benzyloxycarbonylamino-2-(4-hydroxy-benzoylamino)-hexanoic acid methyl ester

(S)-methyl 2-amino-6-(benzyloxycarbonylamino)hexanoate

4-hydroxy-benzoic acid

Downstream raw materials:

[(S)-5-(4-Hydroxy-benzoylamino)-5-(4-hydroxy-phenylcarbamoyl)-pentyl]-carbamic acid benzyl ester

{(S)-5-[4-(Bis-benzyloxy-phosphoryloxy)-benzoylamino]-5-[4-(bis-benzyloxy-phosphoryloxy)-phenylcarbamoyl]-pentyl}-carbamic acid benzyl ester