Propiophenone derivatives in the treatment of pathological muscular conditions
Märksõnad
Patendiinfo
| Patendi number | 3995047 |
| Esitatud | 03/10/1976 |
| Patendi kuupäev | 11/29/1976 |
Abstraktne
Nõuded
1. A method for the treatment of pathological muscular contracture, spastic paralysis due to cerebral apoplexy, and spinal and cerebral palysies, which comprises administering a therapeutically effective amount of a 4'-substituted 2-methyl-3-piperidino-propiophenone derivative represented by the formula: ##SPC4##
wherein R stands for a lower alkyl group having 2 to 3 carbon atoms or a pharmacologically acceptable acid-addition salt thereof to a human patient
2. A method according to claim 1 wherein the derivative is 4'-ethyl-2-methyl-3-piperidino-propiophenone or a pharmacologically
3. A method according to claim 1 wherein the derivative is 4'-n-propyl-2-methyl-3-piperidino-Propiophenone or a pharmacologically
4. A method according to claim 1 wherein the derivative is 4'-isopropyl-2-methyl-3-piperidino-propiophenone or a pharmacologically acceptable acid-addition salt thereof.
Kirjeldus
Following Examples will serve to illustrate the embodiments of the production of the compounds contemplated in the invention, but the invention, of course, is not intended to be limited thereby.
EXAMPLE 1
Preparation of 4'-ethyl-2-methyl-3-piperidino-propiophenone
To 60 mls. of isopropanol, there are introduced 120 grs. of 4-ethyl-propiophenone, 28.8 grs. of paraformaldehyde and 107 grs. of piperidine hydrochloride, and the resulting mixture is heated to reflux on an oil bath with stirring. The heating is continued, and when the reaction mixture solidifies, the state being a sign of completion of the reaction, there are added 500 mls. of acetone thereinto. The solidified mass is pulverized by crush, recovered by filtration and washed with acetone. 144 Grs. of the crude crystalline substance are thus obtained which are the hydrochloride of the purposed product. The hydrochloride is recrystallized from isopropanol, and there are obtained the crystalline needles having the melting point of 170.degree.-172.degree. C.
Elementary analysis of the product presumed as C.sub.17 H.sub.25 NO.HCl gives:
______________________________________ C H N ______________________________________ Calculated (%): 69.00 8.87 4.73 Found (%): 68.99 8.92 4.59 ______________________________________
EXAMPLE 2
Preparation of 4'-isopropyl-2-methyl-3-piperidino-propiophenone
To 350 mls. of isopropanol, there are introduced 350 grs. of 4-isopropyl-propiophenone, 270 grs. of a 30% aqeous formaldehyde and 266 grs. of piperidine hydrochloride together with 5 mls. of concentrated hydrochloric acid. The resulting mixture is heated to reflux on an oil bath with stirring for three hours. 500 mls. of acetone are then added to the reaction mixture with stirring. Crystals separate out from the reaction mixture are recovered by filtration and washed with acetone. There is thus obtained the crude hydrochloride of the purposed product in a crystalline form. The yield of the product amounts to 440 grs. The product is recrystallized from isopropanol and shows the melting point of 172.degree.-174.degree. C.
Elementary analysis of the product presumed as C.sub.18 H.sub.27 NO.HCl gives:
______________________________________ C H H ______________________________________ Calculated (%): 69.75 9.12 4.52 Found (%): 69.86 9.21 4.29 ______________________________________
EXAMPLE 3
A compound depicted in the following Table is prepared in accordance with the procedure disclosed in Example 1.
Table ______________________________________ Elementary Analysis Molecular Formula Calculated (%) R (Melting Point) (Found) (%) ______________________________________ C H N C.sub.18 H.sub.27 NO . HCl 69.75 9.12 4.52 --CH.sub.2 CH.sub.2 CH.sub.3 (168.degree. - 169.degree. C.) (69.40) (9.21) (4.43) ______________________________________
