AL-1095

In this article, we will thoroughly explore the topic of AL-1095 and how it has impacted different aspects of society. From its emergence to its evolution over time, AL-1095 has been the subject of debate and controversy, but it has also been a source of inspiration and change. We will analyze its influence on culture, politics, economics and other areas, as well as its role in the formation of identity and community. Through a multidisciplinary approach, we will examine the various perspectives that exist on AL-1095, seeking to understand its scope and meaning in the current context. Likewise, we will examine whether AL-1095 has a positive or negative impact on society and how it can be understood through different theoretical and methodological approaches. Ultimately, this article aims to provide a complete and balanced view of AL-1095, so that the reader can form an informed opinion on this topic.

AL-1095
Clinical data
ATC code
  • none
Legal status
Legal status
  • In general: unscheduled
Identifiers
  • 2-(1-phenyl-1-(p-chlorophenyl)methyl)-3-hydroxyquinuclidine
CAS Number
PubChem CID
ChemSpider
UNII
CompTox Dashboard (EPA)
Chemical and physical data
FormulaC20H22ClNO
Molar mass327.85 g·mol−1
3D model (JSmol)
  • OC(C1CCN2CC1)C2C(C3=CC=C(Cl)C=C3)C4=CC=CC=C4
  • InChI=1S/C20H22ClNO/c21-17-8-6-15(7-9-17)18(14-4-2-1-3-5-14)19-20(23)16-10-12-22(19)13-11-16/h1-9,16,18-20,23H,10-13H2/t18?,19-,20+/m0/s1 checkY
  • Key:JXCMZYHEZWCLOD-NRRUETGQSA-N checkY
 ☒NcheckY (what is this?)  (verify)

AL-1095,[1] is a centrally acting stimulant drug with comparable effects to amphetamine,[2] developed by Bristol in the 1970s.[3]

Synthesis

Correction:[4]

The first-step is a mixed-aldol condensation between 3-quinuclidinone (1) and benzaldehyde (2) gives 2-benzylidene-3-oxoquinuclidine (3). The conjugate addition of the Grignard reagent formed from 4-bromochlorobenzene (4) to the enone gives the benzhydryl (5). MPV reduction of the carbonyl gives the syn stereoisomers, whereas borohydride gave trans. Both diastereoisomers are active but in only one of the enantiomers.

See also

References

  1. ^ US 3506673, Warawa ED, Mueller NJ, "2-(4'Halo)-Benzhydryl-3-Quinuclidinols", issued 14 April 1970, assigned to Aldrich Chemical Company 
  2. ^ Hedblom P, Grinspoon L (1975). The Speed Culture: Amphetamine Use and Abuse in America. Cambridge: Harvard University Press. p. 50. ISBN 0-674-83192-6.
  3. ^ Warawa EJ, Mueller NJ (January 1975). "Quinuclidine Chemistry. 3. β-cis-2-(4'-Chlorobenzhydryl)-3-quinuclidinol, a New Central Nervous System Stimulant. Importance of the Benzhydryl Configuration". Journal of Medicinal Chemistry. 18 (1): 71–4. doi:10.1021/jm00235a016. PMID 803245.
  4. ^ Warawa, E., Mueller, N., & Gylys, J. (1975). Additions and Corrections - Quinuclidine Chemistry. 3. β-cis-2-(4’-Chlorobenzhydryl)-3-quinuclidinol, a New Central Nervous System Stimulant. Importance of the Benzhydryl Configuration. Journal of Medicinal Chemistry, 18(12), 1275–1275. https://doi.org/10.1021/jm00246a600.
Stub icon

This drug article relating to the nervous system is a stub. You can help Wikipedia by expanding it.