1-[2-(4-phenylbutyryl)cyclopent-2-enecarbonyl]pyrrolidine-2(S)-carboxylic acid methyl ester

Base Information

Chemical Name:1-[2-(4-phenylbutyryl)cyclopent-2-enecarbonyl]pyrrolidine-2(S)-carboxylic acid methyl ester
CAS No.:725265-83-8
Molecular Formula:C₂₂H₂₇NO₄
Molecular Weight:369.461
Hs Code.:

Synonyms:1-[2-(4-phenylbutyryl)cyclopent-2-enecarbonyl]pyrrolidine-2(S)-carboxylic acid methyl ester

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Chemical Property of 1-[2-(4-phenylbutyryl)cyclopent-2-enecarbonyl]pyrrolidine-2(S)-carboxylic acid methyl ester

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Technology Process of 1-[2-(4-phenylbutyryl)cyclopent-2-enecarbonyl]pyrrolidine-2(S)-carboxylic acid methyl ester

There total 6 articles about 1-[2-(4-phenylbutyryl)cyclopent-2-enecarbonyl]pyrrolidine-2(S)-carboxylic acid methyl 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: 77.0%

: 2133-40-6
L-proline methyl ester monohydrochloride

: 725265-82-7
(+/-)-2-(4-phenylbutyryl)cyclopent-2-enecarboxylic acid

: 725265-83-8
1-[2-(4-phenylbutyryl)cyclopent-2-enecarbonyl]pyrrolidine-2(S)-carboxylic acid methyl ester

Guidance literature:: (+/-)-2-(4-phenylbutyryl)cyclopent-2-enecarboxylic acid; With pivaloyl chloride; triethylamine; In dichloromethane; at 0 ℃; for 2.5h;

L-proline methyl ester monohydrochloride; With triethylamine; In dichloromethane; at 20 ℃; for 3h;
DOI:10.1021/jm049503w

Reference yield:

: 637-59-2
1-Bromo-3-phenylpropane

: 725265-83-8
1-[2-(4-phenylbutyryl)cyclopent-2-enecarbonyl]pyrrolidine-2(S)-carboxylic acid methyl ester

Guidance literature:: Multi-step reaction with 3 steps

1.1: Mg; I₂ / diethyl ether / Heating

1.2: 69 percent / diethyl ether / 2 h

2.1: 51 percent / (COCl)2; DMSO; Et₃N / CH₂Cl₂ / -78 - 20 °C

3.1: trimethylacetyl chloride; Et₃N / CH₂Cl₂ / 2.5 h / 0 °C

3.2: 77 percent / Et₃N / CH₂Cl₂ / 3 h / 20 °C

With oxalyl dichloride; iodine; pivaloyl chloride; magnesium; dimethyl sulfoxide; triethylamine; In diethyl ether; dichloromethane;
DOI:10.1021/jm049503w

Reference yield:

: 30758-76-0
(+/-)-2-formylcyclopent-2-enecarboxylic acid

: 725265-83-8
1-[2-(4-phenylbutyryl)cyclopent-2-enecarbonyl]pyrrolidine-2(S)-carboxylic acid methyl ester

Guidance literature:: Multi-step reaction with 3 steps

1.1: Mg; I₂ / diethyl ether / Heating

1.2: 69 percent / diethyl ether / 2 h

2.1: 51 percent / (COCl)2; DMSO; Et₃N / CH₂Cl₂ / -78 - 20 °C

3.1: trimethylacetyl chloride; Et₃N / CH₂Cl₂ / 2.5 h / 0 °C

3.2: 77 percent / Et₃N / CH₂Cl₂ / 3 h / 20 °C

With oxalyl dichloride; iodine; pivaloyl chloride; magnesium; dimethyl sulfoxide; triethylamine; In diethyl ether; dichloromethane;
DOI:10.1021/jm049503w