Novel tricyclic compounds and their use in medicine; process for their preparation and pharmaceutical compositions containing them
a tricyclic compound and compound technology, applied in the field of new tricyclic compounds, can solve the problems of severe affecting the quality of life of a large population
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example 2
[0204] Ethyl (E / Z)-3-[4-[2-[phenothiazin-10-yl)methylbenzofuran-5-yl)-2-et-hoxypropenoate: 25
[0205] The title compound was obtained as E:Z isomers (38:62) (as measured by .sup.1H NMR) (1.5g, 100%) as a colorless liquid from 5-formyl-2-(phenothiazin-10-yl) methylbenzofuran (1.14 g, 3.2 mmol) by a procedure similar to that described for preparation 1.
[0206] .sup.1HNMR (CDCl.sub.3, 200 MHz): .delta. 1.23-1.45 (complex, 6H), 3.55-3.78 (complex, 1H), 3.88-4.19 (complex, 1H), 4.22-4.35 (complex, 2H), 5.14 (s, 2H), 6.18 (s, 0.38H, olefinic proton of E isomer) 6.47 and 6.54 (combined, 1H), 6.78-7.12 (complex, 8.62H), 7.37-7.48 (complex, 1H), 7.71 (d, J=7.57 Hz, 1H), 7.95 (s, 1H).
example 3
[0207] Ethyl (E / Z)-3-[4-[2-(phenoxazin-10-yl)ethoxy]phenyl]-2-ethoxypropen-oate: 26
[0208] The title compound (14.4 g, 76%) was obtained as E:Z isomers (36:64) (as measured by .sup.1H NMR) as a white solid from 4-[2-(phenoxazin-10-yl)ethoxy]benzaldehyde (14.0 g, 42.3 mmol) by an analogous procedure to that described for preparation 1. mp: 110-112.degree. C.
[0209] .sup.1H NMR (CDCl.sub.3, 200 MHz): .delta. 1.16 and 1.38 (combined, 6H, isomeric --OCH.sub.2CH.sub.3 triplet signals), 3.89-4.05 (complex, 4H), 4.14-4.31 (complex, 4H), 6.06 (s, 0.36H, olefinic proton of E isomer), 6.66-6.95 (complex, 10.64H), 7.75 (d, J=8.76 Hz, 2H).
example 4
[0210] Methyl 3-[4-[2-(phenotliiazin-10-yl)ethoxy]phenyl]-2-ethoxypropanoa-te: 27
[0211] The title compound (1.3 g, 94%) was prepared as a gummy liquid from ethyl (E / Z)-3-[4-[2-(phenothiazin-10-yl)ethoxy]phenyl]-2-ethoxypropenoate (1.43 g, 3.10 mmol) obtained in example 1 by an analogous procedure to that described in preparation 2.
[0212] .sup.1H NMR (CDCl.sub.3, 200 MHz):.delta. 1.15 (t, J=7.0 Hz, 3H), 2.93(d, J=6.64 Hz, 2H), 3.33-3.42 (complex, 1H), 3.52-3.63 (complex, 1H), 3.69 (s, 3H), 3.97 (t, J=6.2 Hz,1H), 4.29 (s,4H), 6.81 (d, J=8.62 Hz, 2H), 6.92-6.96 (complex, 4H), 7.12-7.22 (complex, 6H).
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