AL-1095

Stimulant drug From Wikipedia, the free encyclopedia

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

ATC code
  • none
Legal status
  • In general: unscheduled
Quick facts Clinical data, ATC code ...
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)
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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

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