(S)-1-((S)-5-Hexanoylamino-4-oxo-6-phenyl-hexanoyl)-pyrrolidine-2-carboxylic acid

Base Information

Chemical Name:(S)-1-((S)-5-Hexanoylamino-4-oxo-6-phenyl-hexanoyl)-pyrrolidine-2-carboxylic acid
CAS No.:83084-94-0
Molecular Formula:C₂₃H₃₂N₂O₅
Molecular Weight:416.517
Hs Code.:

Synonyms:(S)-1-((S)-5-Hexanoylamino-4-oxo-6-phenyl-hexanoyl)-pyrrolidine-2-carboxylic acid

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Chemical Property of (S)-1-((S)-5-Hexanoylamino-4-oxo-6-phenyl-hexanoyl)-pyrrolidine-2-carboxylic acid

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Technology Process of (S)-1-((S)-5-Hexanoylamino-4-oxo-6-phenyl-hexanoyl)-pyrrolidine-2-carboxylic acid

There total 10 articles about (S)-1-((S)-5-Hexanoylamino-4-oxo-6-phenyl-hexanoyl)-pyrrolidine-2-carboxylic 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:

: 5874-61-3,21453-79-2,51127-19-6,75658-67-2
4-benzyl-2-phenyl-2-oxazolin-5-one

: 83084-94-0
(S)-1-((S)-5-Hexanoylamino-4-oxo-6-phenyl-hexanoyl)-pyrrolidine-2-carboxylic acid

Guidance literature:: Multi-step reaction with 9 steps

1: Et₃N / tetrahydrofuran / 16 h / Ambient temperature

2: pyridine, HOAc / 1 h / 100 °C

3: 0.5 N aq. NaOH / tetrahydrofuran / 4 h / Ambient temperature

4: 78 percent / conc. aq. HCl, acetic acid / 24 h / Heating

5: HCl / 18 h

6: 55 percent / Na₂CO₃ / H₂O / 1 h

7: 1N aq. NaOH / methanol / 0.17 h

8: Et₃N, DCC / CH₂Cl₂ / 1.) 0 deg C, 30 min, 2.) RT, 18 h

9: H₂, acetic acid / 10percent Pd/C / 16 h / 760 Torr / Ambient temperature

With pyridine; hydrogenchloride; sodium hydroxide; hydrogen; sodium carbonate; acetic acid; triethylamine; dicyclohexyl-carbodiimide; palladium on activated charcoal; In tetrahydrofuran; methanol; dichloromethane; water;
DOI:10.1021/jm00353a005

Reference yield:

: 77982-73-1
(R,S)-5-benzoylamino-4-oxo-6-phenylhexanoic acid methyl ester

: 83084-94-0
(S)-1-((S)-5-Hexanoylamino-4-oxo-6-phenyl-hexanoyl)-pyrrolidine-2-carboxylic acid

Guidance literature:: Multi-step reaction with 7 steps

1: 0.5 N aq. NaOH / tetrahydrofuran / 4 h / Ambient temperature

2: 78 percent / conc. aq. HCl, acetic acid / 24 h / Heating

3: HCl / 18 h

4: 55 percent / Na₂CO₃ / H₂O / 1 h

5: 1N aq. NaOH / methanol / 0.17 h

6: Et₃N, DCC / CH₂Cl₂ / 1.) 0 deg C, 30 min, 2.) RT, 18 h

7: H₂, acetic acid / 10percent Pd/C / 16 h / 760 Torr / Ambient temperature

With hydrogenchloride; sodium hydroxide; hydrogen; sodium carbonate; acetic acid; triethylamine; dicyclohexyl-carbodiimide; palladium on activated charcoal; In tetrahydrofuran; methanol; dichloromethane; water;
DOI:10.1021/jm00353a005

Reference yield:

: 83084-67-7
2-Phenyl-4-benzyl-4-β-carbomethoxypropionyloxazolone

: 83084-94-0
(S)-1-((S)-5-Hexanoylamino-4-oxo-6-phenyl-hexanoyl)-pyrrolidine-2-carboxylic acid

Guidance literature:: Multi-step reaction with 8 steps

1: pyridine, HOAc / 1 h / 100 °C

2: 0.5 N aq. NaOH / tetrahydrofuran / 4 h / Ambient temperature

3: 78 percent / conc. aq. HCl, acetic acid / 24 h / Heating

4: HCl / 18 h

5: 55 percent / Na₂CO₃ / H₂O / 1 h

6: 1N aq. NaOH / methanol / 0.17 h

7: Et₃N, DCC / CH₂Cl₂ / 1.) 0 deg C, 30 min, 2.) RT, 18 h

8: H₂, acetic acid / 10percent Pd/C / 16 h / 760 Torr / Ambient temperature

With pyridine; hydrogenchloride; sodium hydroxide; hydrogen; sodium carbonate; acetic acid; triethylamine; dicyclohexyl-carbodiimide; palladium on activated charcoal; In tetrahydrofuran; methanol; dichloromethane; water;
DOI:10.1021/jm00353a005