The preparation method of tropisetron hydrochloride
The technology for tropisetron hydrochloride and compound is applied in the field of preparation of tropisetron hydrochloride bulk drug, and can solve the problems of difficult completion of reaction, poor system solubility, inconvenient production and the like
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Embodiment 1
[0029] The synthesis of embodiment 1 indole-3-formyl chloride
[0030] At 15-30°C, add 125.9g of compound (II) (0.78mol) and N,N-dimethylformamide (400mL) into the reaction flask, stir to dissolve, slowly add thionyl chloride, and complete; room temperature React for 5 hours. The reaction solution was directly carried out to the next reaction without treatment.
Embodiment 2
[0031] Example 2 Synthesis of Tropisetron Hydrochloride (I)
[0032] Control the temperature at 10-30°C, add 100.0 g of compound (III) (0.71 mol) to the prepared indole-3-carbonyl chloride (Example 1), and stir for 8 hours.
[0033] Add ethyl acetate (600mL) to the reaction system and stir for 1 hour, filter with suction and wash the filter cake with a mixed solvent of N,N-dimethylformamide / ethyl acetate (2:3), and reduce the filter cake at 50 °C. After pressing and drying for 6 hours, 215.8 g of an off-white solid was obtained, with a yield of 95.0% and a purity of 99.47%.
Embodiment 3
[0034] The preparation of embodiment 3 tropisetron hydrochloride crude drug
[0035] Add 100 g of crude tropisetron hydrochloride, ethanol (505 mL), and water (35 mL) into the reaction flask, heat up and stir to dissolve, add activated carbon, heat to reflux and stir to react for 0.5 h, then heat filter. Collect the filtrate and add concentrated hydrochloric acid to adjust the pH to 2~3.
[0036] The reaction system was stirred and cooled to 0-20°C, filtered with suction, and the filter cake was dried under reduced pressure at 50°C for 10 hours to obtain 90.5 g of a white crystalline solid with a yield of 90.5% and a purity of 99.98%.
[0037] 1 H NMR (600 MHz, DMSO- d 6 ): δ 12.197 (s, 1H), 11.082 (s, 1H), 8.090 (d, J = 3.0Hz, 1H), 8.048 (d, J = 7.2 Hz, 1H), 7.547 (d, J = 7.2 Hz, 1H), 7.192~7.241 (m, 2H), 5.145~5.130 (t, J = 4.8 Hz s, 1H), 3.890 (s, 1H), 2.690~2.750 (m, 2H), 2.688 (d, J = 4.8 Hz s, 3H), 2.230~2.360 (m, 4H), 2.118 (d, J = 4.2 Hz s, 2H) ppm. 13 C NMR (15...
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