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Napactadine

From Wikipedia, the free encyclopedia
A naphthyl amidine antidepressant.

Pharmaceutical compound
Napactadine
Clinical data
Other namesDL-588
Identifiers
  • N,N'-dimethyl-2-naphthalen-2-ylethanimidamide
CAS Number
PubChemCID
ChemSpider
UNII
ChEMBL
Chemical and physical data
FormulaC14H16N2
Molar mass212.296 g·mol−1
3D model (JSmol)
  • CNC(=NC)CC1=CC2=CC=CC=C2C=C1
  • InChI=1S/C14H16N2/c1-15-14(16-2)10-11-7-8-12-5-3-4-6-13(12)9-11/h3-9H,10H2,1-2H3,(H,15,16)
  • Key:NAHCWQNNENHGNH-UHFFFAOYSA-N

Napactadine (DL-588) is anantidepressant which has structural properties that look similar toPAL-287 ormethamnetamine, but is based on anamidine functional group.[1]

Synthesis

[edit]

The synthesis of napactadine has been described:[2][3]

Napactadine synthesis
Napactadine synthesis

Reaction of N-methyl-2-(naphthalen-2-yl)acetamide [2086-65-9] (1) withtriethyloxonium fluoroborate (Meerwein reagent) [368-39-8] (2) affords the correspondingimino ether (3). Exposure of this intermediate tomethylamine (4) leads to napactidine (5).

References

[edit]
  1. ^Castañer J, Hillier K (1981). "DL-588".Drugs of the Future.6 (6): 348.doi:10.1358/dof.1981.006.06.1003976.
  2. ^McCarthy JR, Wright DL, Schuster AJ, Abdallah AH, Shea PJ, Eyster R (November 1985). "New bicyclic antidepressant agent. Synthesis and activity of napactadine and related compounds".Journal of Medicinal Chemistry.28 (11):1721–7.doi:10.1021/jm00149a031.PMID 4067998.
  3. ^ Jr James R Mccarthy, US3903163 (1975 to Dow Chemical Co).


SSRIsTooltip Selective serotonin reuptake inhibitors
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NaSSAsTooltip Noradrenergic and specific serotonergic antidepressants
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MAOATooltip Monoamine oxidase A-selective
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