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Clocinizine

From Wikipedia, the free encyclopedia
Chemical compound
Pharmaceutical compound
Clocinizine
Clinical data
Trade namesSenioral (withPPATooltip phenylpropanolamine)
AHFS/Drugs.comInternational Drug Names
Routes of
administration
By mouth
ATC code
  • none
Identifiers
  • 1-[(4-chlorophenyl)-phenylmethyl]-4-[(E)-3-phenylprop-2-enyl]piperazine
CAS Number
PubChemCID
ChemSpider
UNII
ChEMBL
Chemical and physical data
FormulaC26H27ClN2
Molar mass402.97 g·mol−1
3D model (JSmol)
  • Clc1ccc(cc1)C(c2ccccc2)N3CCN(CC3)C\C=C\c4ccccc4

Clocinizine is afirst-generation antihistamine of thediphenylmethylpiperazine class. It is marketed inSpain incombination withphenylpropanolamine under the brand nameSenioral.[1]

Synthesis

[edit]
Synthesis:[2] Patent:[3]

The reduction of 4-Chlorobenzophenone [134-85-0] (1) with NBH gives 4-Chlorobenzhydrol [119-56-2] (2). Halogenation of the alcohol in muriatic acid afforded 4-Chlorobenzhydryl chloride [134-83-8] (3). Alkylation with one equivalent of piperazine gives 1-(4-Chlorobenzhydryl)piperazine [303-26-4] (4). Alkylation of the remaining nitrogen with Cinnamyl Bromide [4392-24-9] (5) completed the synthesis of Clocinizine (6).

References

[edit]
  1. ^Fookes C (September 2022)."List of Common Antihistamines + Uses & Side Effects".Drugs.com.
  2. ^Venkat Narsaiah A, Narsimha P (April 2012). "Efficient synthesis of antihistamines clocinizine and chlorcyclizine".Medicinal Chemistry Research.21 (4):538–541.doi:10.1007/s00044-011-9556-x.S2CID 253636495.
  3. ^DE 2220242, Kato H, Kurata S, "Antiarrhythmic piperazine derivs prepn - from benzhydrylpiperazine cinnamaldehyde by leuckart reaction", issued 1972, assigned to Hokuriku Pharmaceutical 
Benzimidazoles(*)
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Ethylenediamines
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Fortopical use
H1
Agonists
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H2
Agonists
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H3
Agonists
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H4
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