(2S,5R)-1-Benzyl-5-((S)-1-benzyloxycarbonyl-propyl)-pyrrolidine-2-carboxylic acid methyl ester

Base Information

Chemical Name:(2S,5R)-1-Benzyl-5-((S)-1-benzyloxycarbonyl-propyl)-pyrrolidine-2-carboxylic acid methyl ester
CAS No.:130516-29-9
Molecular Formula:C₂₄H₂₉NO₄
Molecular Weight:395.499
Hs Code.:

Synonyms:(2S,5R)-1-Benzyl-5-((S)-1-benzyloxycarbonyl-propyl)-pyrrolidine-2-carboxylic acid methyl ester

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Chemical Property of (2S,5R)-1-Benzyl-5-((S)-1-benzyloxycarbonyl-propyl)-pyrrolidine-2-carboxylic acid methyl ester

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Technology Process of (2S,5R)-1-Benzyl-5-((S)-1-benzyloxycarbonyl-propyl)-pyrrolidine-2-carboxylic acid methyl ester

There total 8 articles about (2S,5R)-1-Benzyl-5-((S)-1-benzyloxycarbonyl-propyl)-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: 70.0%

: 130516-27-7,130516-28-8
(S)-1-Benzyl-5-[1-benzyloxycarbonyl-prop-(Z)-ylidene]-pyrrolidine-2-carboxylic acid methyl ester

: 130516-29-9
(2S,5R)-1-Benzyl-5-((S)-1-benzyloxycarbonyl-propyl)-pyrrolidine-2-carboxylic acid methyl ester

: 130607-80-6
(2S,5R)-1-Benzyl-5-((R)-1-benzyloxycarbonyl-propyl)-pyrrolidine-2-carboxylic acid methyl ester

Guidance literature:: With hydrogen; platinum on activated charcoal; In ethyl acetate; under 2280 Torr; Ambient temperature;
DOI:10.1016/S0040-4039(00)94734-8

Reference yield:

: 56-86-0,21675-62-7,23009-64-5,25104-13-6,84960-48-5,25513-46-6
L-glutamic acid

: 130516-29-9
(2S,5R)-1-Benzyl-5-((S)-1-benzyloxycarbonyl-propyl)-pyrrolidine-2-carboxylic acid methyl ester

Guidance literature:: Multi-step reaction with 6 steps

1: NaBH₄

2: H₂O / Heating

3: HCl

4: P₄S₁₀ / tetrahydrofuran / Ambient temperature

5: 2.) Ph₃P, N-methylpiperidine / 1.) CH₃CN, rt, overnight, 2.) rt, 6 h

6: 70 percent / H₂ / Pt/C / ethyl acetate / 2280 Torr / Ambient temperature

With N-methylcyclohexylamine; hydrogenchloride; sodium tetrahydroborate; tetraphosphorus decasulfide; hydrogen; triphenylphosphine; platinum on activated charcoal; In tetrahydrofuran; water; ethyl acetate;
DOI:10.1016/S0040-4039(00)94734-8

Reference yield:

: 77539-18-5,73914-82-6
(S)-(+)-2-benzylamino glutaric acid

: 130516-29-9
(2S,5R)-1-Benzyl-5-((S)-1-benzyloxycarbonyl-propyl)-pyrrolidine-2-carboxylic acid methyl ester

Guidance literature:: Multi-step reaction with 5 steps

1: H₂O / Heating

2: HCl

3: P₄S₁₀ / tetrahydrofuran / Ambient temperature

4: 2.) Ph₃P, N-methylpiperidine / 1.) CH₃CN, rt, overnight, 2.) rt, 6 h

5: 70 percent / H₂ / Pt/C / ethyl acetate / 2280 Torr / Ambient temperature

With N-methylcyclohexylamine; hydrogenchloride; tetraphosphorus decasulfide; hydrogen; triphenylphosphine; platinum on activated charcoal; In tetrahydrofuran; water; ethyl acetate;
DOI:10.1016/S0040-4039(00)94734-8