(2R,3S)-1-[(R)-1-phenylethyl]-3-[1-(phenylsulfonyl)ethyl]pyrrolidine-2-carboxylic acid methyl ester

Base Information

Chemical Name:(2R,3S)-1-[(R)-1-phenylethyl]-3-[1-(phenylsulfonyl)ethyl]pyrrolidine-2-carboxylic acid methyl ester
CAS No.:506420-69-5
Molecular Formula:C₂₂H₂₇NO₄S
Molecular Weight:401.527
Hs Code.:

Synonyms:(2R,3S)-1-[(R)-1-phenylethyl]-3-[1-(phenylsulfonyl)ethyl]pyrrolidine-2-carboxylic acid methyl ester

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Chemical Property of (2R,3S)-1-[(R)-1-phenylethyl]-3-[1-(phenylsulfonyl)ethyl]pyrrolidine-2-carboxylic acid methyl ester

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Technology Process of (2R,3S)-1-[(R)-1-phenylethyl]-3-[1-(phenylsulfonyl)ethyl]pyrrolidine-2-carboxylic acid methyl ester

There total 4 articles about (2R,3S)-1-[(R)-1-phenylethyl]-3-[1-(phenylsulfonyl)ethyl]pyrrolidine-2-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: 93.0%

: 506420-67-3
(2R,3S)-1-[(R)-1-phenylethyl]-3-[(phenylsulfonyl)methyl]pyrrolidine-2-carboxylic acid methyl ester

: 74-88-4
methyl iodide

: 506420-69-5
(2R,3S)-1-[(R)-1-phenylethyl]-3-[1-(phenylsulfonyl)ethyl]pyrrolidine-2-carboxylic acid methyl ester

Guidance literature:: With lithium diisopropyl amide; In tetrahydrofuran; at -78 - 20 ℃;
DOI:10.1021/jo026535n

Reference yield:

: 177944-16-0
(R)-N-(but-3-en-1-yl)-N-(α-methylbenzyl)amine

: 506420-69-5
(2R,3S)-1-[(R)-1-phenylethyl]-3-[1-(phenylsulfonyl)ethyl]pyrrolidine-2-carboxylic acid methyl ester

Guidance literature:: Multi-step reaction with 4 steps

1.1: 91.5 percent / K₂CO₃ / tetrahydrofuran; various solvent(s) / 0 - 20 °C

2.1: LDA; ZnBr₂ / tetrahydrofuran; diethyl ether / 4 h / -78 - 20 °C

2.2: 74 percent / CuCN; lithium chloride / tetrahydrofuran; diethyl ether / 0 - 20 °C

3.1: 80 percent / mCPBA; TFA / CH₂Cl₂ / 1 h / 0 °C

4.1: 93 percent / LDA / tetrahydrofuran; various solvent(s) / -78 - 20 °C

With potassium carbonate; 3-chloro-benzenecarboperoxoic acid; trifluoroacetic acid; zinc dibromide; lithium diisopropyl amide; In tetrahydrofuran; diethyl ether; dichloromethane;
DOI:10.1021/jo026535n

Reference yield:

: 186653-18-9
(R)-[(but-3-enyl)(1-phenylethyl)amino]acetic acid methyl ester

: 506420-69-5
(2R,3S)-1-[(R)-1-phenylethyl]-3-[1-(phenylsulfonyl)ethyl]pyrrolidine-2-carboxylic acid methyl ester

Guidance literature:: Multi-step reaction with 3 steps

1.1: LDA; ZnBr₂ / tetrahydrofuran; diethyl ether / 4 h / -78 - 20 °C

1.2: 74 percent / CuCN; lithium chloride / tetrahydrofuran; diethyl ether / 0 - 20 °C

2.1: 80 percent / mCPBA; TFA / CH₂Cl₂ / 1 h / 0 °C

3.1: 93 percent / LDA / tetrahydrofuran; various solvent(s) / -78 - 20 °C

With 3-chloro-benzenecarboperoxoic acid; trifluoroacetic acid; zinc dibromide; lithium diisopropyl amide; In tetrahydrofuran; diethyl ether; dichloromethane;
DOI:10.1021/jo026535n