N-(tert-butoxycarbonyl)-N'-(3,5-dimethylphenyl)-(4R)-hydroxy-L-prolinamide

Base Information

Chemical Name:N-(tert-butoxycarbonyl)-N'-(3,5-dimethylphenyl)-(4R)-hydroxy-L-prolinamide
CAS No.:744253-70-1
Molecular Formula:C₁₈H₂₆N₂O₄
Molecular Weight:334.415
Hs Code.:

Synonyms:N-(tert-butoxycarbonyl)-N'-(3,5-dimethylphenyl)-(4R)-hydroxy-L-prolinamide

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Chemical Property of N-(tert-butoxycarbonyl)-N'-(3,5-dimethylphenyl)-(4R)-hydroxy-L-prolinamide

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Technology Process of N-(tert-butoxycarbonyl)-N'-(3,5-dimethylphenyl)-(4R)-hydroxy-L-prolinamide

There total 1 articles about N-(tert-butoxycarbonyl)-N'-(3,5-dimethylphenyl)-(4R)-hydroxy-L-prolinamide 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: 86.0%

: 13726-69-7,946610-68-0
(2S,4R)-4-hydroxy-1-[(2-methylpropan-2-yl)oxycarbonyl]pyrrolidine-2-carboxylic acid

: 108-69-0
3,5-dimethylaminoaniline

: 744253-70-1
N-(tert-butoxycarbonyl)-N'-(3,5-dimethylphenyl)-(4R)-hydroxy-L-prolinamide

Guidance literature:: With N-ethoxycarbonyl-2-ethoxy-1,2-dihydroquinoline; In dichloromethane; at 20 ℃; for 24h;
DOI:10.1055/s-2004-822384

Reference yield: 60.0%

: 6613-44-1
3,5-dimethylbenzoyl chloride

: 744253-70-1
N-(tert-butoxycarbonyl)-N'-(3,5-dimethylphenyl)-(4R)-hydroxy-L-prolinamide

: 744253-71-2
N-(tert-butoxycarbonyl)-N'-(3,5-dimethylphenyl)-(4R)-(3,5-dimethylbenzoyloxy)-L-prolinamide

Guidance literature:: With sodium hydroxide; In chloroform; at 20 ℃; for 24h;
DOI:10.1055/s-2004-822384

Reference yield:

: 744253-70-1
N-(tert-butoxycarbonyl)-N'-(3,5-dimethylphenyl)-(4R)-hydroxy-L-prolinamide

: N'-(3,5-dimethylphenyl)-(4R)-(3,5-dimethylbenzoyloxy)-L-prolinamide

Guidance literature:: Multi-step reaction with 2 steps

1: 60 percent / aq. NaOH / CHCl₃ / 24 h / 20 °C

2: 92 percent / TFA / CH₂Cl₂ / 0.5 h / 20 °C

With sodium hydroxide; trifluoroacetic acid; In dichloromethane; chloroform;
DOI:10.1055/s-2004-822384