[1-(3-tert-Butoxycarbonylamino-2,2-dimethyl-3-phenyl-propionyl)-piperidin-4-yl]-acetic acid benzyl ester

Base Information

Chemical Name:[1-(3-tert-Butoxycarbonylamino-2,2-dimethyl-3-phenyl-propionyl)-piperidin-4-yl]-acetic acid benzyl ester
CAS No.:200490-83-1
Molecular Formula:C₃₀H₄₀N₂O₅
Molecular Weight:508.658
Hs Code.:

Synonyms:[1-(3-tert-Butoxycarbonylamino-2,2-dimethyl-3-phenyl-propionyl)-piperidin-4-yl]-acetic acid benzyl ester

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Chemical Property of [1-(3-tert-Butoxycarbonylamino-2,2-dimethyl-3-phenyl-propionyl)-piperidin-4-yl]-acetic acid benzyl ester

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Technology Process of [1-(3-tert-Butoxycarbonylamino-2,2-dimethyl-3-phenyl-propionyl)-piperidin-4-yl]-acetic acid benzyl ester

There total 3 articles about [1-(3-tert-Butoxycarbonylamino-2,2-dimethyl-3-phenyl-propionyl)-piperidin-4-yl]-acetic acid benzyl 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: 98.0%

: benzyl (piperidin-4-yl)acetate

: 208397-32-4
3-((tert-butoxycarbonyl)amino)-2,2-dimethyl-3-phenylpropanoic acid

: 200490-83-1
[1-(3-tert-Butoxycarbonylamino-2,2-dimethyl-3-phenyl-propionyl)-piperidin-4-yl]-acetic acid benzyl ester

Guidance literature:: With N-ethyl-N,N-diisopropylamine; N-[(dimethylamino)-3-oxo-1H-1,2,3-triazolo[4,5-b]pyridin-1-yl-methylene]-N-methylmethanaminium hexafluorophosphate; In dichloromethane; for 18h; Ambient temperature;
DOI:10.1021/jm980126v

Reference yield:

: 24424-99-5
di-tert-butyl dicarbonate

: 200490-83-1
[1-(3-tert-Butoxycarbonylamino-2,2-dimethyl-3-phenyl-propionyl)-piperidin-4-yl]-acetic acid benzyl ester

Guidance literature:: Multi-step reaction with 2 steps

1: 95 percent / 10percent aq. Na₂CO₃ / dioxane / Ambient temperature

2: 98 percent / HATU, DIEA / CH₂Cl₂ / 18 h / Ambient temperature

With sodium carbonate; N-ethyl-N,N-diisopropylamine; N-[(dimethylamino)-3-oxo-1H-1,2,3-triazolo[4,5-b]pyridin-1-yl-methylene]-N-methylmethanaminium hexafluorophosphate; In 1,4-dioxane; dichloromethane;
DOI:10.1021/jm980126v

Reference yield:

: β-phenyl-α,α-dimethyl-β-alanine hydrochloride

: 200490-83-1
[1-(3-tert-Butoxycarbonylamino-2,2-dimethyl-3-phenyl-propionyl)-piperidin-4-yl]-acetic acid benzyl ester

Guidance literature:: Multi-step reaction with 2 steps

1: 95 percent / 10percent aq. Na₂CO₃ / dioxane / Ambient temperature

2: 98 percent / HATU, DIEA / CH₂Cl₂ / 18 h / Ambient temperature

With sodium carbonate; N-ethyl-N,N-diisopropylamine; N-[(dimethylamino)-3-oxo-1H-1,2,3-triazolo[4,5-b]pyridin-1-yl-methylene]-N-methylmethanaminium hexafluorophosphate; In 1,4-dioxane; dichloromethane;
DOI:10.1021/jm980126v