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| Routes of administration | Oral |
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| Formula | C17H13ClN3O |
| Molar mass | 310.76 g·mol−1 |
Trazium (EGYT-3,615) is anantidepressantdrug which was never marketed.[1] It haspsychostimulant-like effects and its actions appear to be mediated by thedopaminergic andadrenergic systems.[2] It was formulated as asalt withethanesulfonic acid and given the generic nametrazium esilate (INN).
Precursors:[3][4][5] Background literature:[6][7][8][9]
Ex 5: The Grignard reaction between para-chlorophenylmagnesium bromide and 1-cyanoisoquinoline [1198-30-7] (1) gave 1-(4-chlorobenzoyl)isoquinoline, PC12243105 (2). The reaction of this with O-tosylhydroxylamine [52913-14-1] gives (2-aminoisoquinolin-2-ium-1-yl)-(4-chlorophenyl)methanone;4-methylbenzenesulfonate, PC23311140 (3). The reaction of this a mixture of formamide and phosphoryl chloride gave the ring. The addition of perchloric acid led to 1-(4-Chlorophenyl)[1,2,4]triazino[6,1-a]isoquinolin-5-ium perchlorate [82319-70-8] (4). The reaction of this with triethylammonium bromide is said to give (4).
Patent:[10]
Ex 1: 1-(4-chlorophenyl)-as-triazino[6,1-a]isoquinolinium-bromide [82319-85-5] (1) is reacted with an aqueous solution of acetonitrile to give the title compound.Ex 2: Treatment with ethanesulfonic acid in acetonitrile then prepares the esilate salt.
