(S)-5-Benzyloxycarbonylamino-2-[2-(5-octyloxy-naphthalen-1-yloxy)-acetylamino]-pentanoic acid

Base Information

Chemical Name:(S)-5-Benzyloxycarbonylamino-2-[2-(5-octyloxy-naphthalen-1-yloxy)-acetylamino]-pentanoic acid
CAS No.:656248-73-6
Molecular Formula:C₃₃H₄₂N₂O₇
Molecular Weight:578.706
Hs Code.:

Synonyms:(S)-5-Benzyloxycarbonylamino-2-[2-(5-octyloxy-naphthalen-1-yloxy)-acetylamino]-pentanoic acid

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Chemical Property of (S)-5-Benzyloxycarbonylamino-2-[2-(5-octyloxy-naphthalen-1-yloxy)-acetylamino]-pentanoic acid

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Technology Process of (S)-5-Benzyloxycarbonylamino-2-[2-(5-octyloxy-naphthalen-1-yloxy)-acetylamino]-pentanoic acid

There total 6 articles about (S)-5-Benzyloxycarbonylamino-2-[2-(5-octyloxy-naphthalen-1-yloxy)-acetylamino]-pentanoic 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:

: 656248-71-4
(S)-5-Benzyloxycarbonylamino-2-[2-(5-octyloxy-naphthalen-1-yloxy)-acetylamino]-pentanoic acid methyl ester

: 656248-73-6
(S)-5-Benzyloxycarbonylamino-2-[2-(5-octyloxy-naphthalen-1-yloxy)-acetylamino]-pentanoic acid

Guidance literature:: With lithium hydroxide; In tetrahydrofuran; water; at 20 ℃; for 4h;
DOI:10.1021/jo035149i

Reference yield:

: 111-83-1
1-bromo-octane

: 656248-73-6
(S)-5-Benzyloxycarbonylamino-2-[2-(5-octyloxy-naphthalen-1-yloxy)-acetylamino]-pentanoic acid

Guidance literature:: Multi-step reaction with 5 steps

1: 22 percent / potassium carbonate; potassium iodide / acetone / 10 h / Heating

2: sodium hydroxide / acetone / 10 h / Heating

3: 2.00 g / sodium hydroxide / acetone; H₂O / 2 h

4: 87 percent / dicyclohexylcarbodiimide; 1-hydroxybenzotriazole; N-methylmorpholine / CH₂Cl₂ / 14 h / 0 - 20 °C

5: 2.30 g / LiOH*H₂O / tetrahydrofuran; H₂O / 4 h / 20 °C

With 4-methyl-morpholine; lithium hydroxide; sodium hydroxide; potassium carbonate; benzotriazol-1-ol; dicyclohexyl-carbodiimide; potassium iodide; In tetrahydrofuran; dichloromethane; water; acetone;
DOI:10.1021/jo035149i

Reference yield:

: 83-56-7
1,5-dihydroxynaphthalene

: 656248-73-6
(S)-5-Benzyloxycarbonylamino-2-[2-(5-octyloxy-naphthalen-1-yloxy)-acetylamino]-pentanoic acid

Guidance literature:: Multi-step reaction with 5 steps

1: 22 percent / potassium carbonate; potassium iodide / acetone / 10 h / Heating

2: sodium hydroxide / acetone / 10 h / Heating

3: 2.00 g / sodium hydroxide / acetone; H₂O / 2 h

4: 87 percent / dicyclohexylcarbodiimide; 1-hydroxybenzotriazole; N-methylmorpholine / CH₂Cl₂ / 14 h / 0 - 20 °C

5: 2.30 g / LiOH*H₂O / tetrahydrofuran; H₂O / 4 h / 20 °C

With 4-methyl-morpholine; lithium hydroxide; sodium hydroxide; potassium carbonate; benzotriazol-1-ol; dicyclohexyl-carbodiimide; potassium iodide; In tetrahydrofuran; dichloromethane; water; acetone;
DOI:10.1021/jo035149i