(2S,5S)-5-(2-Benzyloxycarbonylamino-ethyl)-piperidine-1,2-dicarboxylic acid 1-tert-butyl ester 2-ethyl ester

Base Information

Chemical Name:(2S,5S)-5-(2-Benzyloxycarbonylamino-ethyl)-piperidine-1,2-dicarboxylic acid 1-tert-butyl ester 2-ethyl ester
CAS No.:176588-19-5
Molecular Formula:C₂₃H₃₄N₂O₆
Molecular Weight:434.533
Hs Code.:

Synonyms:(2S,5S)-5-(2-Benzyloxycarbonylamino-ethyl)-piperidine-1,2-dicarboxylic acid 1-tert-butyl ester 2-ethyl ester

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Chemical Property of (2S,5S)-5-(2-Benzyloxycarbonylamino-ethyl)-piperidine-1,2-dicarboxylic acid 1-tert-butyl ester 2-ethyl ester

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Technology Process of (2S,5S)-5-(2-Benzyloxycarbonylamino-ethyl)-piperidine-1,2-dicarboxylic acid 1-tert-butyl ester 2-ethyl ester

There total 7 articles about (2S,5S)-5-(2-Benzyloxycarbonylamino-ethyl)-piperidine-1,2-dicarboxylic acid 1-tert-butyl ester 2-ethyl 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: 85.0%

: 501-53-1,94274-21-2
benzyl chloroformate

: 176588-18-4
(2S,5S)-5-(2-Amino-ethyl)-piperidine-1,2-dicarboxylic acid 1-tert-butyl ester 2-ethyl ester

: 176588-19-5
(2S,5S)-5-(2-Benzyloxycarbonylamino-ethyl)-piperidine-1,2-dicarboxylic acid 1-tert-butyl ester 2-ethyl ester

Guidance literature:: With triethylamine; In dichloromethane;
DOI:10.1016/0040-4039(96)00140-2

Reference yield:

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

: 176588-19-5
(2S,5S)-5-(2-Benzyloxycarbonylamino-ethyl)-piperidine-1,2-dicarboxylic acid 1-tert-butyl ester 2-ethyl ester

Guidance literature:: Multi-step reaction with 6 steps

1: 82 percent / DMAP / CH₂Cl₂

2: 1.) LiHMDS / 1.) THF, -78 deg C

3: LiEt₃BH / tetrahydrofuran

4: Et₃SiH, BF₃*OEt₂ / CH₂Cl₂

5: 89 percent / H₂ / PtO₂ / ethanol; CHCl₃

6: 85 percent / Et₃N / CH₂Cl₂

With triethylsilane; dmap; boron trifluoride diethyl etherate; hydrogen; lithium triethylborohydride; triethylamine; lithium hexamethyldisilazane; platinum(IV) oxide; In tetrahydrofuran; ethanol; dichloromethane; chloroform;
DOI:10.1016/0040-4039(96)00140-2

Reference yield:

: 149733-38-0
(S)-6-oxo-piperidine-1,2-dicarboxylic acid 1-tert-butyl ester 2-ethyl ester

: 176588-19-5
(2S,5S)-5-(2-Benzyloxycarbonylamino-ethyl)-piperidine-1,2-dicarboxylic acid 1-tert-butyl ester 2-ethyl ester

Guidance literature:: Multi-step reaction with 5 steps

1: 1.) LiHMDS / 1.) THF, -78 deg C

2: LiEt₃BH / tetrahydrofuran

3: Et₃SiH, BF₃*OEt₂ / CH₂Cl₂

4: 89 percent / H₂ / PtO₂ / ethanol; CHCl₃

5: 85 percent / Et₃N / CH₂Cl₂

With triethylsilane; boron trifluoride diethyl etherate; hydrogen; lithium triethylborohydride; triethylamine; lithium hexamethyldisilazane; platinum(IV) oxide; In tetrahydrofuran; ethanol; dichloromethane; chloroform;
DOI:10.1016/0040-4039(96)00140-2