(S)-1-(5-Butoxycarbonylamino-2-methyl-4-oxo-6-phenyl-hexanoyl)-pyrrolidine-2-carboxylic acid benzyl ester

Base Information

Chemical Name:(S)-1-(5-Butoxycarbonylamino-2-methyl-4-oxo-6-phenyl-hexanoyl)-pyrrolidine-2-carboxylic acid benzyl ester
CAS No.:83450-64-0
Molecular Formula:C₃₀H₃₈N₂O₆
Molecular Weight:522.642
Hs Code.:

Synonyms:(S)-1-(5-Butoxycarbonylamino-2-methyl-4-oxo-6-phenyl-hexanoyl)-pyrrolidine-2-carboxylic acid benzyl ester

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Chemical Property of (S)-1-(5-Butoxycarbonylamino-2-methyl-4-oxo-6-phenyl-hexanoyl)-pyrrolidine-2-carboxylic acid benzyl ester

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Technology Process of (S)-1-(5-Butoxycarbonylamino-2-methyl-4-oxo-6-phenyl-hexanoyl)-pyrrolidine-2-carboxylic acid benzyl ester

There total 8 articles about (S)-1-(5-Butoxycarbonylamino-2-methyl-4-oxo-6-phenyl-hexanoyl)-pyrrolidine-2-carboxylic acid benzyl 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: 59.7%

: 16652-71-4
benzyl (2S)-2-pyrrolidinecarboxylate hydrochloride

: 83084-91-7
5-n-Butyloxycarbonylamino-4-oxo-2-methyl-6-phenylhexanoic acid

: 83450-64-0
(S)-1-(5-Butoxycarbonylamino-2-methyl-4-oxo-6-phenyl-hexanoyl)-pyrrolidine-2-carboxylic acid benzyl ester

Guidance literature:: With triethylamine; dicyclohexyl-carbodiimide; In dichloromethane; 1.) 0 deg C, 30 min, 2.) RT, 18 h;
DOI:10.1021/jm00353a005

Reference yield:

: 21307-96-0,22644-27-5,63163-08-6,1604-11-1
methyl 2-methylsuccinate

: 83450-64-0
(S)-1-(5-Butoxycarbonylamino-2-methyl-4-oxo-6-phenyl-hexanoyl)-pyrrolidine-2-carboxylic acid benzyl ester

Guidance literature:: Multi-step reaction with 9 steps

1: 1.) KOH, 2.) oxalyl chloride / 1.) methanol, 5 deg C, 50 h, 2.) benzene, 35 deg C, 3 h

2: 42.5 g / Et₃N / tetrahydrofuran / 16 h / Ambient temperature

3: pyridine, HOAc / 1 h / 100 °C

4: 58 percent / 0.5 N aq. NaOH / tetrahydrofuran / 4 h / Ambient temperature

5: conc. aq. HCl, acetic acid / 24 h / Heating

6: HCl / 18 h

7: 82 percent / Na₂CO₃ / H₂O / 1 h

8: 94.9 percent / 1N aq. NaOH / methanol / 0.17 h

9: 59.7 percent / Et₃N, DCC / CH₂Cl₂ / 1.) 0 deg C, 30 min, 2.) RT, 18 h

With pyridine; hydrogenchloride; potassium hydroxide; sodium hydroxide; oxalyl dichloride; sodium carbonate; acetic acid; triethylamine; dicyclohexyl-carbodiimide; In tetrahydrofuran; methanol; dichloromethane; water;
DOI:10.1021/jm00353a005

Reference yield:

: 83084-90-6
methyl 5-n-butyloxycarbonylamino-4-oxo-2-methyl-6-phenylhexanoate

: 83450-64-0
(S)-1-(5-Butoxycarbonylamino-2-methyl-4-oxo-6-phenyl-hexanoyl)-pyrrolidine-2-carboxylic acid benzyl ester

Guidance literature:: Multi-step reaction with 2 steps

1: 94.9 percent / 1N aq. NaOH / methanol / 0.17 h

2: 59.7 percent / Et₃N, DCC / CH₂Cl₂ / 1.) 0 deg C, 30 min, 2.) RT, 18 h

With sodium hydroxide; triethylamine; dicyclohexyl-carbodiimide; In methanol; dichloromethane;
DOI:10.1021/jm00353a005