1098-60-8

White powder

Triflupromazine is a phenothiazine with diverse biological activities. It binds to muscarinic receptors in isolated rat corpus striatum (IC₅₀ = 100 μM in a radioligand binding assay). Triflupromazine inhibits serotonin (5-HT) uptake by isolated rat brainstem synaptosomes (IC₅₀ = 0.8 μM). It inhibits T. cruzi infection in mouse peritoneal macrophages when used at a concentration of 12.5 μM. Triflupromazine is active against S. aureus, shigellae, and vibrios (MICs = 2-100 μg/ml) in vitro and is protective against S. typhimurium infection in mice when administered at a dose of 30 μg per animal. Formulations containing triflupromazine were previously used as antipsychotics.

Vesprin,Squibb,US,1957

analgesic, antiinflammatory, antipyretic, COX-II inhibitor

Approximately 3.8 grams of sodamide is freshly prepared from 2.25 grams of sodium, 90 grams of liquid ammonia and a catalytic trace of ferric nitrate. The ammonia is allowed to evaporate. A solution of 19.1 grams of 2-trifluoromethylphenothiazine (prepared by the Bernthsen thionation of 3- trifluoromethyldiphenylamine) in 160 ml of dry benzene is added to the reaction flask followed by 18 grams of 3-chloro-1-dimethylaminopropane. The reaction mixture is heated at reflux for 20 hours. After washing the cooled mixture with 130 ml of water, the organic layer is extracted with several portions of dilute hydrochloric acid. The acid extracts are combined and neutralized with ammonium hydroxide solution. The oily free base is extracted into benzene and purified by distillation to give 19.6 grams of 10-(3'- dimethylaminopropyl)-2-trifluoromethylphenothiazine, boiling point 177° to 181°C at 1 mm. The free base (7 grams) is converted to the hydrochloride salt by reacting an alcoholic solution of the base with hydrogen chloride gas.
Evaporation of the volatiles in vacuo leaves an amorphous solid which is recrystallized from ethanol/ether to pink crystals, MP 173° to 174°C, the hydrochloride salt of the free base prepared above.

Vesprin (Bristol-Myers Squibb).

Tranquilizer

Triflupromazinehydrochloride, 10-[3-(dimethylamino)propyl]-2-(trifluoromethyl)phenothiazine monohydrochloride (Vesprin), has agreater milligram potency as an antipsychotic, higher EPS,but lower sedative and hypotensive effects than chlorpromazine.The 2-CF₃ versus the 2-Cl is associated with thesechanges. Overall, the drug has uses analogous to those ofchlorpromazine.

Store at -20°C

[1] SOLOMON H. SNYDER  Henry I Y  David Greenberg. Antischizophrenic drugs: Affinity for muscarinic cholinergic receptor sites in the brain predicts extrapyramidal effects[J]. Journal of psychiatric research, 1974, 11: Pages 91-95. DOI: 10.1016/0022-3956(74)90078-8
[2] TUOMISTO J. A new modification for studying 5-HT uptake by blood platelets: a re-evaluation of tricyclic antidepressants as uptake inhibitors*[J]. Journal of Pharmacy and Pharmacology, 1974, 26 2: 92-100. DOI: 10.1111/j.2042-7158.1974.tb09231.x
[3] S L DE CASTRO  M de N D M  M N Soeiro. Trypanosoma cruzi: effect of phenothiazines on the parasite and its interaction with host cells.[J]. Memorias do Instituto Oswaldo Cruz, 1992, 87 2: 209-215. DOI: 10.1590/s0074-02761992000200007
[4] S. DASTIDAR. Triflupromazine: a microbicide non-antibiotic compound.[J]. Acta microbiologica et immunologica Hungarica, 2004, 51 1-2 1: 75-83. DOI: 10.1556/amicr.51.2004.1-2.5