((R)-2-{(S)-2-[(S)-1-(Benzyloxycarbonylamino-imino-methyl)-2-oxo-piperidin-3-ylcarbamoyl]-pyrrolidin-1-yl}-2-oxo-1-phenyl-ethyl)-carbamic acid tert-butyl ester

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Chemical Name:((R)-2-{(S)-2-[(S)-1-(Benzyloxycarbonylamino-imino-methyl)-2-oxo-piperidin-3-ylcarbamoyl]-pyrrolidin-1-yl}-2-oxo-1-phenyl-ethyl)-carbamic acid tert-butyl ester
CAS No.:141973-00-4
Molecular Formula:C₃₂H₄₀N₆O₇
Molecular Weight:620.706
Hs Code.:

((R)-2-{(S)-2-[(S)-1-(Benzyloxycarbonylamino-imino-methyl)-2-oxo-piperidin-3-ylcarbamoyl]-pyrrolidin-1-yl}-2-oxo-1-phenyl-ethyl)-carbamic acid tert-butyl ester

Synonyms:((R)-2-{(S)-2-[(S)-1-(Benzyloxycarbonylamino-imino-methyl)-2-oxo-piperidin-3-ylcarbamoyl]-pyrrolidin-1-yl}-2-oxo-1-phenyl-ethyl)-carbamic acid tert-butyl ester

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Chemical Property of ((R)-2-{(S)-2-[(S)-1-(Benzyloxycarbonylamino-imino-methyl)-2-oxo-piperidin-3-ylcarbamoyl]-pyrrolidin-1-yl}-2-oxo-1-phenyl-ethyl)-carbamic acid tert-butyl ester

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Technology Process of ((R)-2-{(S)-2-[(S)-1-(Benzyloxycarbonylamino-imino-methyl)-2-oxo-piperidin-3-ylcarbamoyl]-pyrrolidin-1-yl}-2-oxo-1-phenyl-ethyl)-carbamic acid tert-butyl ester

There total 3 articles about ((R)-2-{(S)-2-[(S)-1-(Benzyloxycarbonylamino-imino-methyl)-2-oxo-piperidin-3-ylcarbamoyl]-pyrrolidin-1-yl}-2-oxo-1-phenyl-ethyl)-carbamic acid tert-butyl 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:

: 2900-27-8
(2S)-2-[(tert-butoxycarbonyl)amino]-2-phenylethanoic acid

: 141973-00-4
((R)-2-{(S)-2-[(S)-1-(Benzyloxycarbonylamino-imino-methyl)-2-oxo-piperidin-3-ylcarbamoyl]-pyrrolidin-1-yl}-2-oxo-1-phenyl-ethyl)-carbamic acid tert-butyl ester

Guidance literature:: Multi-step reaction with 3 steps

1: DCC / ethyl acetate / 2.5 h / 0 - 20 °C

2: pyridine, triethylemine / 24 h / Ambient temperature

3: 1.) N-methylmorpholine, isobutyl chloroformate / 1.) DMF, -15 deg C, 2 min, 2.) DMF, a.) -15 deg C, 4 h, b.) RT, 24 h

With 4-methyl-morpholine; pyridine; triethylamine; dicyclohexyl-carbodiimide; isobutyl chloroformate; In ethyl acetate;
DOI:10.1021/jm00055a002

Reference yield:

: C₂₀H₁₈Cl₃NO₆

: 141973-00-4
((R)-2-{(S)-2-[(S)-1-(Benzyloxycarbonylamino-imino-methyl)-2-oxo-piperidin-3-ylcarbamoyl]-pyrrolidin-1-yl}-2-oxo-1-phenyl-ethyl)-carbamic acid tert-butyl ester

Guidance literature:: Multi-step reaction with 2 steps

1: pyridine, triethylemine / 24 h / Ambient temperature

2: 1.) N-methylmorpholine, isobutyl chloroformate / 1.) DMF, -15 deg C, 2 min, 2.) DMF, a.) -15 deg C, 4 h, b.) RT, 24 h

With 4-methyl-morpholine; pyridine; triethylamine; isobutyl chloroformate;
DOI:10.1021/jm00055a002

Reference yield:

: (R)-1-((R)-2-tert-Butoxycarbonylamino-2-phenyl-acetyl)-pyrrolidine-2-carboxylic acid

: TFA-Arg(Z) lactam

: 141973-00-4
((R)-2-{(S)-2-[(S)-1-(Benzyloxycarbonylamino-imino-methyl)-2-oxo-piperidin-3-ylcarbamoyl]-pyrrolidin-1-yl}-2-oxo-1-phenyl-ethyl)-carbamic acid tert-butyl ester

Guidance literature:: With 4-methyl-morpholine; isobutyl chloroformate; Multistep reaction; 1.) DMF, -15 deg C, 2 min, 2.) DMF, a.) -15 deg C, 4 h, b.) RT, 24 h;
DOI:10.1021/jm00055a002