Synthesis and asymmetric resolution of substituted 2-aminoindane and 2-aminotetralin derivatives
Akincioglu, Akin, Akbaba, Yusuf, Kose, Leyla Polat, Akyuz, Leyla Demirkol, Goksu, Sueleyman
We performed the racemic synthesis and asymmetric resolution of one 2-aminoindane and three 2-aminotertalins due to their crucial biological roles in the central nervous system (CNS). For this reason, desired (+/-)-2-aminoindane and (+/-)-2-aminotetralin derivatives were synthesized starting from appropriate reagents. While highly enantio pure (+)-39, (+)-40, and ( inverted exclamation )-40 were obtained from the reaction of racemic amines with (R)-O-acetylmandeloyl chloride followed by crystallization, hydrolysis with KOH and acidification with HCl, (S)-42 and (-)-43 were synthesized via the reaction of racemic amines with (S)-mandelic acid and hydrolysis.(c) 2023 Elsevier Ltd. All rights reserved.
- Dergi
- TETRAHEDRON
- Yıl
- 2023
- Cilt
- 133
- ISSN
- 0040-4020
- eISSN
- 1464-5416
- DOI
- 10.1016/j.tet.2023.133277
- WoS UID
- WOS:000944002300001