Chemistry:AL-1095

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Short description: Stimulant drug
AL-1095
AL-1095 Structure.svg
Clinical data
ATC code
  • none
Legal status
Legal status
  • In general: unscheduled
Identifiers
CAS Number
PubChem CID
ChemSpider
UNII
Chemical and physical data
FormulaC20H22ClNO
Molar mass327.85 g·mol−1
3D model (JSmol)
 ☒N☑Y (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 [3731-38-2] (1) and benzaldehyde (2) gives 2-benzylidene-3-oxoquinuclidine [24123-89-5] (3). The conjugate addition of the Grignard reagent formed from 4-bromochlorobenzene [106-39-8] (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. Warawa ED, Mueller NJ, "2-(4'Halo)-Benzhydryl-3-Quinuclidinols", US patent 3506673, issued 14 April 1970, assigned to Aldrich Chemical Company
  2. The Speed Culture: Amphetamine Use and Abuse in America. Cambridge: Harvard University Press. 1975. p. 50. ISBN 0-674-83192-6. https://archive.org/details/speedcultureamph0000grin_n3i0. 
  3. "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. January 1975. 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.