(2R,3R,4R,5S)-3-((4R,5R)-1,3-Dimethyl-4,5-diphenyl-imidazolidin-2-yl)-5-phenyl-pyrrolidine-2,4-dicarboxylic acid dimethyl ester

Base Information

Chemical Name:(2R,3R,4R,5S)-3-((4R,5R)-1,3-Dimethyl-4,5-diphenyl-imidazolidin-2-yl)-5-phenyl-pyrrolidine-2,4-dicarboxylic acid dimethyl ester
CAS No.:135212-34-9
Molecular Formula:C₃₁H₃₅N₃O₄
Molecular Weight:513.637
Hs Code.:

Synonyms:(2R,3R,4R,5S)-3-((4R,5R)-1,3-Dimethyl-4,5-diphenyl-imidazolidin-2-yl)-5-phenyl-pyrrolidine-2,4-dicarboxylic acid dimethyl ester

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Chemical Property of (2R,3R,4R,5S)-3-((4R,5R)-1,3-Dimethyl-4,5-diphenyl-imidazolidin-2-yl)-5-phenyl-pyrrolidine-2,4-dicarboxylic acid dimethyl ester

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Technology Process of (2R,3R,4R,5S)-3-((4R,5R)-1,3-Dimethyl-4,5-diphenyl-imidazolidin-2-yl)-5-phenyl-pyrrolidine-2,4-dicarboxylic acid dimethyl ester

There total 10 articles about (2R,3R,4R,5S)-3-((4R,5R)-1,3-Dimethyl-4,5-diphenyl-imidazolidin-2-yl)-5-phenyl-pyrrolidine-2,4-dicarboxylic acid dimethyl 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:

: 951-87-1,5700-60-7,16635-95-3,29841-69-8,35132-20-8,107133-00-6
rac-1,2-diphenylethylene-1,2-diamine

: 135075-67-1,135212-34-9
(2S,3S,4S,5R)-3-((4S,5S)-1,3-Dimethyl-4,5-diphenyl-imidazolidin-2-yl)-5-phenyl-pyrrolidine-2,4-dicarboxylic acid dimethyl ester

Guidance literature:: Multi-step reaction with 4 steps

1: 97 percent / ethanol / 0.17 h / Ambient temperature

2: 98 percent / LiAlH₄ / tetrahydrofuran / 9.5 h / Heating

3: 59 percent / pyridinium p-toluenesulfonate / CHCl₃ / Ambient temperature; a few minutes

4: 1a.) lithium diisopropylamide, 1b.) methanol / 1.) THF, hexane, -78 deg C, 2.) -78 deg C, 1 h

With methanol; lithium aluminium tetrahydride; pyridinium p-toluenesulfonate; lithium diisopropyl amide; In tetrahydrofuran; ethanol; chloroform;
DOI:10.1021/jo00014a028

Reference yield:

: 5837-72-9
methyl (E)-4-oxo-2-butenoate

: 135212-34-9
(2R,3R,4R,5S)-3-((4R,5R)-1,3-Dimethyl-4,5-diphenyl-imidazolidin-2-yl)-5-phenyl-pyrrolidine-2,4-dicarboxylic acid dimethyl ester

Guidance literature:: Multi-step reaction with 2 steps

1: pyridinium p-toluenesulfonate / CHCl₃ / 0.17 h / Ambient temperature

2: 1a.) lithium diisopropylamide, 1b.) methanol / 1.) THF, hexane, -78 deg C, 2.) -78 deg C

With methanol; pyridinium p-toluenesulfonate; lithium diisopropyl amide; In chloroform;
DOI:10.1021/jo00014a028

Reference yield:

: 5837-72-9
methyl (E)-4-oxo-2-butenoate

: 135075-67-1,135212-34-9
(2S,3S,4S,5R)-3-((4S,5S)-1,3-Dimethyl-4,5-diphenyl-imidazolidin-2-yl)-5-phenyl-pyrrolidine-2,4-dicarboxylic acid dimethyl ester

Guidance literature:: Multi-step reaction with 2 steps

1: 59 percent / pyridinium p-toluenesulfonate / CHCl₃ / Ambient temperature; a few minutes

2: 1a.) lithium diisopropylamide, 1b.) methanol / 1.) THF, hexane, -78 deg C, 2.) -78 deg C, 1 h

With methanol; pyridinium p-toluenesulfonate; lithium diisopropyl amide; In chloroform;
DOI:10.1021/jo00014a028