ES412585A1 - Procedure for the preparation of derivatives of (alcoxy-4-alcohil-4-piperidinoalcohil) -10-phenotyazines. (Machine-translation by Google Translate, not legally binding) - Google Patents
Procedure for the preparation of derivatives of (alcoxy-4-alcohil-4-piperidinoalcohil) -10-phenotyazines. (Machine-translation by Google Translate, not legally binding)Info
- Publication number
- ES412585A1 ES412585A1 ES412585A ES412585A ES412585A1 ES 412585 A1 ES412585 A1 ES 412585A1 ES 412585 A ES412585 A ES 412585A ES 412585 A ES412585 A ES 412585A ES 412585 A1 ES412585 A1 ES 412585A1
- Authority
- ES
- Spain
- Prior art keywords
- formula
- radical
- reacted
- alcohol
- mineral
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Expired
Links
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D211/00—Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings
- C07D211/04—Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with only hydrogen or carbon atoms directly attached to the ring nitrogen atom
- C07D211/06—Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having no double bonds between ring members or between ring members and non-ring members
- C07D211/36—Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having no double bonds between ring members or between ring members and non-ring members with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
- C07D211/40—Oxygen atoms
- C07D211/44—Oxygen atoms attached in position 4
- C07D211/48—Oxygen atoms attached in position 4 having an acyclic carbon atom attached in position 4
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
Abstract
Preparation process of derivatives of (alkoxy-4-alcohol-4-piperidino-alcoholic) -10-phenothiazines and their addition salts with mineral or organic acids, said derivatives responding to formula 1: **(See formula)** in which X represents a hydrogen or chlorine atom or a trifluoromethyl, methoxy or methylthio radical, B and R, identical or different, represent a hydrogen atom or an alcohol radical comprising at most 4 carbon atoms, Z represents a linear or branched alcohol radical containing a maximum of 10 carbon atoms, p represents values 0 or 1, n represents values 0, 1 or 2, and A represents a hydrogen atom or a -COR1 radical, in which R1 represents a polymethoxy-phenyl radical or an alcohol radical containing a maximum of 18 carbon atoms and which may contain a double bond or an oxy (-O-) radical, or A represents a -COOR2 radical in which R2 represents a linear alcohol radical containing a maximum of 15 carbon atoms, a procedure characterized in that a halogen-alcohol-10-phenothiazine of formula 2 is reacted: **(See formula)** in which X, B and p have the aforementioned meanings and Y represents a chlorine or bromine atom, with a piperidine derivative of formula 3: **(See formula)** in which A, Z, R and n have the meanings indicated above, and either the product of formula 1 obtained is isolated and reacted, if desired, with a mineral or organic acid to form the salt thereof, or when A represents a hydrogen atom, said product is reacted, either with an acid chloride of formula Cl-CO-R1, in which R1 has the aforementioned meaning and the resulting product of formula 1 is isolated in which A represents a radical -COR1 that is reacted, if desired, with a mineral or organic acid to form the salt thereof, either with an alcoholic chloroformate of the formula Cl-COOR2 in which R2 has the previously indicated meaning and is isolated the resulting product of formula 1 in which A represents a radical -COOR2, which is reacted, if desired, with a mineral or organic acid to form the salt thereof. (Machine-translation by Google Translate, not legally binding)
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
FR7208802A FR2175565A1 (en) | 1972-03-14 | 1972-03-14 | 10-(4-alkoxy-4-alkylpiperidinoalkyl)phenothiazines - - with neuroleptic,antihistaminic,analgesic and spasmolytic activity |
Publications (1)
Publication Number | Publication Date |
---|---|
ES412585A1 true ES412585A1 (en) | 1976-01-16 |
Family
ID=9095160
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
ES412585A Expired ES412585A1 (en) | 1972-03-14 | 1973-03-13 | Procedure for the preparation of derivatives of (alcoxy-4-alcohil-4-piperidinoalcohil) -10-phenotyazines. (Machine-translation by Google Translate, not legally binding) |
Country Status (2)
Country | Link |
---|---|
ES (1) | ES412585A1 (en) |
FR (1) | FR2175565A1 (en) |
Family Cites Families (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
FR1344593A (en) * | 1961-11-25 | 1963-11-29 | Boehringer & Soehne Gmbh | Process for the preparation of novel alkoxy-piperidine derivatives and their salts |
FR1578731A (en) * | 1967-11-24 | 1969-08-22 |
-
1972
- 1972-03-14 FR FR7208802A patent/FR2175565A1/en active Granted
-
1973
- 1973-03-13 ES ES412585A patent/ES412585A1/en not_active Expired
Also Published As
Publication number | Publication date |
---|---|
FR2175565A1 (en) | 1973-10-26 |
FR2175565B1 (en) | 1975-03-14 |
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