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| Other names | Proketazine, Carphenazin |
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| Routes of administration | Oral |
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| ECHA InfoCard | 100.018.249 |
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| Formula | C24H31N3O2S |
| Molar mass | 425.59 g·mol−1 |
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Carfenazine (INN) (former developmental code name WY-2445), or carphenazine (BAN), also known as carphenazine maleate (USAN) (brand name Proketazine; former developmental code name NSC-71755), is an antipsychotic and tranquilizer of the phenothiazine group that was withdrawn from the market.[1][2][3]
Synthesis
The alkylation reaction between 2-Propionyl Phenothiazine [92-33-1] (1) and 1-Bromo-3-chloropropane (2) gives 1-[10-(3-chloropropyl)phenothiazin-2-yl]propan-1-one [95157-45-2] (3). A second alkylation step, this time with 2-(1-Piperazinyl)ethanol [103-76-4] (4) completes the synthesis of Carfenazine (5).
NB: Although above procedure is proof-of-concept, bear in mind no protecting group {Other patent uses ketalization technique}
Analogues
- Butaperazine uses butanoyl (Butyryl) and not propanoyl group.
- Fluphenazine selfsame but trifluoromethyl on position 2 of the phenothiazine ring.
References
- ↑ Elks J (14 November 2014). The Dictionary of Drugs: Chemical Data: Chemical Data, Structures and Bibliographies. Springer. pp. 224–. ISBN 978-1-4757-2085-3.
- ↑ William Andrew Publishing (22 October 2013). Pharmaceutical Manufacturing Encyclopedia, 3rd Edition. Elsevier. pp. 862–. ISBN 978-0-8155-1856-3.
- ↑ Briggs GG, Freeman RK, Yaffe SJ (2011). Drugs in Pregnancy and Lactation: A Reference Guide to Fetal and Neonatal Risk. Lippincott Williams & Wilkins. pp. 213–. ISBN 978-1-60831-708-0.
- ↑ Zhuraulev, S.V. et al, Zh. Obshch. Khim., 1962, 32, 2244
- ↑ M. H. Sherlock, N. Sperber, U.S. Patent 2,985,654 (1961 to Schering)
- ↑ R. F. Tislow et al., U.S. Patent 3,023,146 (1962 to American Home Products).
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| Antidepressants (Tricyclic antidepressants (TCAs)) |
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