Methanesulfonic acid (3R,5R)-1-benzyl-5-(pyrrolidine-1-carbonyl)-pyrrolidin-3-yl ester

Base Information

Chemical Name:Methanesulfonic acid (3R,5R)-1-benzyl-5-(pyrrolidine-1-carbonyl)-pyrrolidin-3-yl ester
CAS No.:114676-95-8
Molecular Formula:C₁₇H₂₄N₂O₄S
Molecular Weight:352.455
Hs Code.:

Synonyms:Methanesulfonic acid (3R,5R)-1-benzyl-5-(pyrrolidine-1-carbonyl)-pyrrolidin-3-yl ester

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Chemical Property of Methanesulfonic acid (3R,5R)-1-benzyl-5-(pyrrolidine-1-carbonyl)-pyrrolidin-3-yl ester

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Technology Process of Methanesulfonic acid (3R,5R)-1-benzyl-5-(pyrrolidine-1-carbonyl)-pyrrolidin-3-yl ester

There total 5 articles about Methanesulfonic acid (3R,5R)-1-benzyl-5-(pyrrolidine-1-carbonyl)-pyrrolidin-3-yl 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:

: 100-44-7
benzyl chloride

: 114676-95-8
Methanesulfonic acid (3R,5R)-1-benzyl-5-(pyrrolidine-1-carbonyl)-pyrrolidin-3-yl ester

Guidance literature:: Multi-step reaction with 3 steps

1: 84 percent / triethylamine / CH₂Cl₂ / 7 h / Heating

2: 650 mg / CH₂Cl₂ / 1.) room temperature, 85 min, 2.) 105 deg C, 5 h

3: 390 mg / triethylamine / CH₂Cl₂ / 8 h / Ambient temperature

With triethylamine; In dichloromethane;
DOI:10.1021/jm00403a020

Reference yield:

: 114676-53-8
(2R,4R)-methyl 1-benzyl-4-hydroxypyrrolidine-2-carboxylate

: 114676-95-8
Methanesulfonic acid (3R,5R)-1-benzyl-5-(pyrrolidine-1-carbonyl)-pyrrolidin-3-yl ester

Guidance literature:: Multi-step reaction with 2 steps

1: 650 mg / CH₂Cl₂ / 1.) room temperature, 85 min, 2.) 105 deg C, 5 h

2: 390 mg / triethylamine / CH₂Cl₂ / 8 h / Ambient temperature

With triethylamine; In dichloromethane;
DOI:10.1021/jm00403a020

Reference yield:

: 114676-59-4
(2R,4R)-4-hydroxy-2-methoxycarbonylpyrrolidine hydrochloride

: 114676-95-8
Methanesulfonic acid (3R,5R)-1-benzyl-5-(pyrrolidine-1-carbonyl)-pyrrolidin-3-yl ester

Guidance literature:: Multi-step reaction with 3 steps

1: 84 percent / triethylamine / CH₂Cl₂ / 7 h / Heating

2: 650 mg / CH₂Cl₂ / 1.) room temperature, 85 min, 2.) 105 deg C, 5 h

3: 390 mg / triethylamine / CH₂Cl₂ / 8 h / Ambient temperature

With triethylamine; In dichloromethane;
DOI:10.1021/jm00403a020