It provides the enantiomerically pure 5‑amino‑piperidine scaffold, which is then transformed through protection, functionalization (e.g., conversion to the benzyloxyamino derivative), and cyclization steps to construct the diazabicyclooctane (DABCO) core of Avibactam. This intermediate is essential for ensuring the correct stereochemistry and efficient assembly of the active drug molecule. (tert‑Butyl) 2‑ethyl (2R,5S)‑5‑aminopiperidine‑1,2‑dicarboxylate is a chiral intermediate employed to synthesize the β‑lactamase inhibitor Avibactam.
(tert-Butyl) 2-ethyl (2R,5S)-5-aminopiperidine-1,2-dicarboxylate
| API Name | Avibactam |
|---|---|
| CAS No | 2411590-87-7 |
| Molecular Formula | C13H24N2O4 |
| Molecular Weight | 272.34 g/mol |
| Synonyms | 1-O-tert-butyl 2-O-ethyl (2R,5S)-5-aminopiperidine-1,2-dicarboxylate |
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Frequently Asked Questions
It provides the enantiomerically pure 5‑amino‑piperidine scaffold, which is then transformed through protection, functionalization (e.g., conversion to the benzyloxyamino derivative), and cyclization steps to construct the diazabicyclooctane (DABCO) core of Avibactam. This intermediate is essential for ensuring the correct stereochemistry and efficient assembly of the active drug molecule. (tert‑Butyl) 2‑ethyl (2R,5S)‑5‑aminopiperidine‑1,2‑dicarboxylate is a chiral intermediate employed to synthesize the β‑lactamase inhibitor Avibactam.
The CAS number of (tert-Butyl) 2-ethyl (2R,5S)-5-aminopiperidine-1,2-dicarboxylate is 2411590-87-7.
The molecular formula of (tert-Butyl) 2-ethyl (2R,5S)-5-aminopiperidine-1,2-dicarboxylate is C13H24N2O4.
The listed molecular weight of (tert-Butyl) 2-ethyl (2R,5S)-5-aminopiperidine-1,2-dicarboxylate is 272.34 g/mol.
(tert-Butyl) 2-ethyl (2R,5S)-5-aminopiperidine-1,2-dicarboxylate is listed as being used in connection with the following API: Avibactam.
The listed synonym or IUPAC name for (tert-Butyl) 2-ethyl (2R,5S)-5-aminopiperidine-1,2-dicarboxylate is 1-O-tert-butyl 2-O-ethyl (2R,5S)-5-aminopiperidine-1,2-dicarboxylate.