(4S)-1-benzoyl-4-<(carboxymethyl)methylamino>-L-proline 4-tert-butyl ester

Base Information

Chemical Name:(4S)-1-benzoyl-4-<(carboxymethyl)methylamino>-L-proline 4-tert-butyl ester
CAS No.:84520-87-6
Molecular Formula:C₁₉H₂₆N₂O₅
Molecular Weight:362.426
Hs Code.:

Synonyms:(4S)-1-benzoyl-4-<(carboxymethyl)methylamino>-L-proline 4-tert-butyl ester

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Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

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Chemical Property of (4S)-1-benzoyl-4-<(carboxymethyl)methylamino>-L-proline 4-tert-butyl ester

Chemical Property:

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Technology Process of (4S)-1-benzoyl-4-<(carboxymethyl)methylamino>-L-proline 4-tert-butyl ester

There total 6 articles about (4S)-1-benzoyl-4-<(carboxymethyl)methylamino>-L-proline 4-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: 62.0%

: 84520-85-4
(4S)-1-benzoyl-4-<(carboxymethyl)methylamino>-L-proline 4-tert-butyl methyl ester

: 84520-87-6
(4S)-1-benzoyl-4-<(carboxymethyl)methylamino>-L-proline 4-tert-butyl ester

Guidance literature:: With sodium hydroxide; In methanol; for 3h; Ambient temperature;
DOI:10.1021/jm00358a017

Reference yield:

: 84520-72-9
(4S)-1-benzoyl-1-azido-L-proline methyl ester

: 84520-87-6
(4S)-1-benzoyl-4-<(carboxymethyl)methylamino>-L-proline 4-tert-butyl ester

Guidance literature:: Multi-step reaction with 4 steps

1: concd. HCl, H₂ / 10percent Pd/C / methanol / 2 h / 760 Torr

2: dioxane; dimethylformamide / 48 h / 50 °C

3: 75 percent / NaBH₃CN / acetonitrile / 0.25 h / Ambient temperature

4: 62 percent / NaOH / methanol / 3 h / Ambient temperature

With hydrogenchloride; sodium hydroxide; hydrogen; sodium cyanoborohydride; palladium on activated charcoal; In 1,4-dioxane; methanol; N,N-dimethyl-formamide; acetonitrile;
DOI:10.1021/jm00358a017

Reference yield:

: 65-85-0,8013-63-6
benzoic acid

: 84520-87-6
(4S)-1-benzoyl-4-<(carboxymethyl)methylamino>-L-proline 4-tert-butyl ester

Guidance literature:: Multi-step reaction with 5 steps

1: DCC / 48 h

2: concd. HCl, H₂ / 10percent Pd/C / methanol / 2 h / 760 Torr

3: dioxane; dimethylformamide / 48 h / 50 °C

4: 75 percent / NaBH₃CN / acetonitrile / 0.25 h / Ambient temperature

5: 62 percent / NaOH / methanol / 3 h / Ambient temperature

With hydrogenchloride; sodium hydroxide; hydrogen; sodium cyanoborohydride; dicyclohexyl-carbodiimide; palladium on activated charcoal; In 1,4-dioxane; methanol; N,N-dimethyl-formamide; acetonitrile;
DOI:10.1021/jm00358a017