[3-tert-butoxycarbonylamino-4-(2-carbamoyl-piperidin-1-yl)-4-oxo-butyl]-(4-chloro-benzyl)-carbamic acid tert-butyl ester

Base Information

Chemical Name:[3-tert-butoxycarbonylamino-4-(2-carbamoyl-piperidin-1-yl)-4-oxo-butyl]-(4-chloro-benzyl)-carbamic acid tert-butyl ester
CAS No.:697797-46-9
Molecular Formula:C₂₇H₄₁ClN₄O₆
Molecular Weight:553.099
Hs Code.:

[3-<i>tert</i>-butoxycarbonylamino-4-(2-carbamoyl-piperidin-1-yl)-4-oxo-butyl]-(4-chloro-benzyl)-carbamic acid <i>tert</i>-butyl ester

Synonyms:[3-tert-butoxycarbonylamino-4-(2-carbamoyl-piperidin-1-yl)-4-oxo-butyl]-(4-chloro-benzyl)-carbamic acid tert-butyl ester

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Chemical Property of [3-tert-butoxycarbonylamino-4-(2-carbamoyl-piperidin-1-yl)-4-oxo-butyl]-(4-chloro-benzyl)-carbamic acid tert-butyl ester

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Technology Process of [3-tert-butoxycarbonylamino-4-(2-carbamoyl-piperidin-1-yl)-4-oxo-butyl]-(4-chloro-benzyl)-carbamic acid tert-butyl ester

There total 5 articles about [3-tert-butoxycarbonylamino-4-(2-carbamoyl-piperidin-1-yl)-4-oxo-butyl]-(4-chloro-benzyl)-carbamic acid 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:

: 25691-37-6,80445-78-9
(2S)-4-amino-2-[(tert-butoxycarbonyl)amino]butanoic acid

: 697797-46-9
[3-tert-butoxycarbonylamino-4-(2-carbamoyl-piperidin-1-yl)-4-oxo-butyl]-(4-chloro-benzyl)-carbamic acid tert-butyl ester

Guidance literature:: Multi-step reaction with 3 steps

1: NaCNBH₃; CH₃COOH / methanol / 20 °C

2: triethylamine / dioxane; H₂O

3: triethylamine; TBTU / dimethylformamide / 20 °C

With sodium cyanoborohydride; O-(benzotriazol-1-yl)-N,N,N',N'-tetramethyluronium tetrafluoroborate; acetic acid; triethylamine; In 1,4-dioxane; methanol; water; N,N-dimethyl-formamide;
DOI:10.1021/jm031122f

Reference yield:

: 19889-77-1,24735-67-9,65057-28-5,78088-51-4
(2S)-2-piperidinecarboxamide

: 697797-44-7
2-tert-butoxycarbonylamino-4-[tert-butoxycarbonyl-(4-chloro-benzyl)-amino]-butyric acid

: 697797-46-9
[3-tert-butoxycarbonylamino-4-(2-carbamoyl-piperidin-1-yl)-4-oxo-butyl]-(4-chloro-benzyl)-carbamic acid tert-butyl ester

Guidance literature:: With O-(benzotriazol-1-yl)-N,N,N',N'-tetramethyluronium tetrafluoroborate; triethylamine; In N,N-dimethyl-formamide; at 20 ℃;
DOI:10.1021/jm031122f

Reference yield:

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

: 697797-46-9
[3-tert-butoxycarbonylamino-4-(2-carbamoyl-piperidin-1-yl)-4-oxo-butyl]-(4-chloro-benzyl)-carbamic acid tert-butyl ester

Guidance literature:: Multi-step reaction with 2 steps

1: triethylamine / dioxane; H₂O

2: triethylamine; TBTU / dimethylformamide / 20 °C

With O-(benzotriazol-1-yl)-N,N,N',N'-tetramethyluronium tetrafluoroborate; triethylamine; In 1,4-dioxane; water; N,N-dimethyl-formamide;
DOI:10.1021/jm031122f