- Chemical Name:(1R,2R)-2-azaniumylcyclohexane-1-carboxylate
- CAS No.:5691-19-0
- Molecular Formula:C7H13 N O2
- Molecular Weight:143.186
- Hs Code.:2922499990
- Mol file:5691-19-0.mol
Synonyms:
Synonyms:
98%,99%, *data from raw suppliers
trans-2-Aminocyclohexanecarboxylic acid *data from reagent suppliers
There total 59 articles about (1R,2R)-2-azaniumylcyclohexane-1-carboxylate 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:
Reference yield: 100.0%
Reference yield: 92.0%
Reference yield: 89.0%
The research describes a method for the synthesis of enantiomerically pure cis- and trans-2-aminocyclohexane-1-carboxylic acids, which are significant due to their potential therapeutic applications and role in forming stable secondary structures in β-peptides. The study utilizes 2-aminobenzamide as a chiral block to assemble quinazolinone, aiming to provide a new synthesis route for all four isomers of 2-aminocyclohexanecarboxylic acid. The process involves chemoselective and diastereoselective hydrogenation of 2,3-dihydro-3-[(S)-α-methylbenzyl]-4-quinazolinone to produce octahydroquinazolinones, which can be epimerized to form their respective stereoisomers. Hydrolysis of these octahydroquinazolinones with HCl yields the desired enantiomerically pure amino acids.