1-(3,3-dimethyl-2-oxo-pentanoyl)-piperidine-2-carboxylic acid 1-(2-tert-butoxycarbonylamino-ethyl)-4-phenyl-butyl ester

Base Information

Chemical Name:1-(3,3-dimethyl-2-oxo-pentanoyl)-piperidine-2-carboxylic acid 1-(2-tert-butoxycarbonylamino-ethyl)-4-phenyl-butyl ester
CAS No.:344462-70-0
Molecular Formula:C₃₀H₄₆N₂O₆
Molecular Weight:530.705
Hs Code.:

1-(3,3-dimethyl-2-oxo-pentanoyl)-piperidine-2-carboxylic acid 1-(2-<i>tert</i>-butoxycarbonylamino-ethyl)-4-phenyl-butyl ester

Synonyms:1-(3,3-dimethyl-2-oxo-pentanoyl)-piperidine-2-carboxylic acid 1-(2-tert-butoxycarbonylamino-ethyl)-4-phenyl-butyl ester

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Chemical Property of 1-(3,3-dimethyl-2-oxo-pentanoyl)-piperidine-2-carboxylic acid 1-(2-tert-butoxycarbonylamino-ethyl)-4-phenyl-butyl ester

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Technology Process of 1-(3,3-dimethyl-2-oxo-pentanoyl)-piperidine-2-carboxylic acid 1-(2-tert-butoxycarbonylamino-ethyl)-4-phenyl-butyl ester

There total 7 articles about 1-(3,3-dimethyl-2-oxo-pentanoyl)-piperidine-2-carboxylic acid 1-(2-tert-butoxycarbonylamino-ethyl)-4-phenyl-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:

: 58885-58-8
N-tert-butoxycarbonyl-3-aminopropanol

: 344462-70-0
1-(3,3-dimethyl-2-oxo-pentanoyl)-piperidine-2-carboxylic acid 1-(2-tert-butoxycarbonylamino-ethyl)-4-phenyl-butyl ester

Guidance literature:: Multi-step reaction with 3 steps

1: 28 percent / Dess-Martin periodinane / CH₂Cl₂

2: 22 percent / tetrahydrofuran / -78 - 20 °C

3: 3-ethyl-1-dimethylaminopropylcarbodiimide; 4-dimethylaminopyridine / CH₂Cl₂

With dmap; Dess-Martin periodane; N-(3-dimethylaminopropyl)-N-ethylcarbodiimide; In tetrahydrofuran; dichloromethane; 1: Oxidation / 2: Addition / 3: Esterification;
DOI:10.1016/S0960-894X(00)00045-7

Reference yield:

: 18328-11-5
3-benzyl propionaldehyde

: 344462-70-0
1-(3,3-dimethyl-2-oxo-pentanoyl)-piperidine-2-carboxylic acid 1-(2-tert-butoxycarbonylamino-ethyl)-4-phenyl-butyl ester

Guidance literature:: Multi-step reaction with 4 steps

1: 27 percent / LDA / tetrahydrofuran / -78 °C

2: H₂; AcOH / Pd/C / ethyl acetate

4: 3-ethyl-1-dimethylaminopropylcarbodiimide; 4-dimethylaminopyridine / CH₂Cl₂

With dmap; hydrogen; acetic acid; N-(3-dimethylaminopropyl)-N-ethylcarbodiimide; lithium diisopropyl amide; palladium on activated charcoal; In tetrahydrofuran; dichloromethane; ethyl acetate; 1: Condensation / 2: Hydrogenation / 3: N-protection / 4: Esterification;
DOI:10.1016/S0960-894X(00)00045-7

Reference yield:

: 862490-90-2
3-hydroxy-6-phenylhexanitrile

: 344462-70-0
1-(3,3-dimethyl-2-oxo-pentanoyl)-piperidine-2-carboxylic acid 1-(2-tert-butoxycarbonylamino-ethyl)-4-phenyl-butyl ester

Guidance literature:: Multi-step reaction with 3 steps

1: H₂; AcOH / Pd/C / ethyl acetate

3: 3-ethyl-1-dimethylaminopropylcarbodiimide; 4-dimethylaminopyridine / CH₂Cl₂

With dmap; hydrogen; acetic acid; N-(3-dimethylaminopropyl)-N-ethylcarbodiimide; palladium on activated charcoal; In dichloromethane; ethyl acetate; 1: Hydrogenation / 2: N-protection / 3: Esterification;
DOI:10.1016/S0960-894X(00)00045-7