(3R,5S)-N-benzyloxycarbonyl-L-phenylalanine-3-phenyl-5-(trans-1-propenyl)-L-proline methyl ester

Base Information

Chemical Name:(3R,5S)-N-benzyloxycarbonyl-L-phenylalanine-3-phenyl-5-(trans-1-propenyl)-L-proline methyl ester
CAS No.:212612-52-7
Molecular Formula:C₃₂H₃₄N₂O₅
Molecular Weight:526.632
Hs Code.:

Synonyms:(3R,5S)-N-benzyloxycarbonyl-L-phenylalanine-3-phenyl-5-(trans-1-propenyl)-L-proline methyl ester

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Chemical Property of (3R,5S)-N-benzyloxycarbonyl-L-phenylalanine-3-phenyl-5-(trans-1-propenyl)-L-proline methyl ester

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Technology Process of (3R,5S)-N-benzyloxycarbonyl-L-phenylalanine-3-phenyl-5-(trans-1-propenyl)-L-proline methyl ester

There total 7 articles about (3R,5S)-N-benzyloxycarbonyl-L-phenylalanine-3-phenyl-5-(trans-1-propenyl)-L-proline 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: 75.0%

: 1161-13-3
N-Cbz-L-Phe

: 212612-60-7
(2S,3R,5S)-3-Phenyl-5-((E)-propenyl)-pyrrolidine-2-carboxylic acid methyl ester

: 212612-52-7
(3R,5S)-N-benzyloxycarbonyl-L-phenylalanine-3-phenyl-5-(trans-1-propenyl)-L-proline methyl ester

Guidance literature:: With N-Ethylmaleimide; In dichloromethane;
DOI:10.1016/S0960-894X(98)00289-3

Reference yield:

: 212612-51-6
(3R)-N-tert-butyloxycarbonyl-5-methoxy-3-phenyl-L-proline methyl ester

: 212612-52-7
(3R,5S)-N-benzyloxycarbonyl-L-phenylalanine-3-phenyl-5-(trans-1-propenyl)-L-proline methyl ester

Guidance literature:: Multi-step reaction with 3 steps

1.1: Li / diethyl ether / 2 h / -20 °C

1.2: coppr(I) bromide*Me₂S / diethyl ether / 1 h / -40 °C

1.3: 75 percent / BF₃*Et₂O / diethyl ether / 0.25 h / -78 °C

2.1: BF₃*Et₂O / diethyl ether / 18 h / 20 °C

3.1: cyanuric fluoride; pyridine / CH₂Cl₂ / 1.5 h / -20 °C

3.2: 60 percent / N-ethylmorpholine / CH₂Cl₂ / 18 h / 20 °C

With pyridine; trifluoro-[1,3,5]triazine; boron trifluoride diethyl etherate; lithium; In diethyl ether; dichloromethane; 1.1: Metallation / 1.2: Substitution / 1.3: Substitution / 2.1: Substitution / 3.1: Fluorination / 3.2: Acylation;
DOI:10.1021/jo991649t

Reference yield:

: 212612-58-3
(3R,5S)-N-tert-butyloxycarbonyl-3-phenyl-5-(trans-1-propenyl)-L-proline methyl ester

: 212612-52-7
(3R,5S)-N-benzyloxycarbonyl-L-phenylalanine-3-phenyl-5-(trans-1-propenyl)-L-proline methyl ester

Guidance literature:: Multi-step reaction with 2 steps

1.1: BF₃*Et₂O / diethyl ether / 18 h / 20 °C

2.1: cyanuric fluoride; pyridine / CH₂Cl₂ / 1.5 h / -20 °C

2.2: 60 percent / N-ethylmorpholine / CH₂Cl₂ / 18 h / 20 °C

With pyridine; trifluoro-[1,3,5]triazine; boron trifluoride diethyl etherate; In diethyl ether; dichloromethane; 1.1: Substitution / 2.1: Fluorination / 2.2: Acylation;
DOI:10.1021/jo991649t