ES412584A1 - Procedure for preparation of (alcohil-4-piperidil-4) - oxialcanols. (Machine-translation by Google Translate, not legally binding) - Google Patents
Procedure for preparation of (alcohil-4-piperidil-4) - oxialcanols. (Machine-translation by Google Translate, not legally binding)Info
- Publication number
- ES412584A1 ES412584A1 ES412584A ES412584A ES412584A1 ES 412584 A1 ES412584 A1 ES 412584A1 ES 412584 A ES412584 A ES 412584A ES 412584 A ES412584 A ES 412584A ES 412584 A1 ES412584 A1 ES 412584A1
- Authority
- ES
- Spain
- Prior art keywords
- formula
- product
- radical
- translation
- carbon atoms
- 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
- C07D491/00—Heterocyclic compounds containing in the condensed ring system both one or more rings having oxygen atoms as the only ring hetero atoms and one or more rings having nitrogen atoms as the only ring hetero atoms, not provided for by groups C07D451/00 - C07D459/00, C07D463/00, C07D477/00 or C07D489/00
- C07D491/02—Heterocyclic compounds containing in the condensed ring system both one or more rings having oxygen atoms as the only ring hetero atoms and one or more rings having nitrogen atoms as the only ring hetero atoms, not provided for by groups C07D451/00 - C07D459/00, C07D463/00, C07D477/00 or C07D489/00 in which the condensed system contains two hetero rings
- C07D491/10—Spiro-condensed systems
-
- 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)
- Hydrogenated Pyridines (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
Abstract
Preparation procedure for (alcohol-4-piperidyl-4) -oxy-alkanols of formula 1: **(See formula)** where R represents a hydrogen atom or an alcohol radical containing a maximum of 4 carbon atoms, Z represents a linear or branched alcohol radical containing a maximum of 10 carbon atoms, n may take the values 0, 1 or 2, and A represents a hydrogen atom or a radical -CO-R1 in which R1 represents a polymethoxyphenyl radical or an alcohol radical containing a maximum of 18 carbon atoms and which can carry a double bond or an oxy radical (-0-), characterized in that a cyclic acetyl of benzylpiperidone of formula 2 is reacted in anhydrous medium: **(See formula)** in which R and n have the aforementioned meaning, with an organ-magnesium of formula 3: Z-Mg-Hal (3) in which Hal represents a chlorine, bromine or iodine atom and Z has the previously indicated meaning, the product of formula 4 is made to act: **(See formula)** resulting either hydrogen in the presence of a palladium-based catalyst to obtain a product of formula 1 in which A represents a hydrogen atom, or an acid chloride of formula Cl-CO-R1 in which R1 has the meaning indicated above, to obtain a product of formula 5: **(See formula)** wherein R, R1, Z and n have the aforementioned meaning and said product of formula 5 is actuated, hydrogen in the presence of a palladium-based catalyst to obtain a product of formula 1, in which A represents a radical -CO-R1. (Machine-translation by Google Translate, not legally binding)
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
FR7208801A FR2175564A1 (en) | 1972-03-14 | 1972-03-14 | 2(4-alkyl-4-piperidyloxy)alkanols - inters for human and veterinary drugs |
Publications (1)
Publication Number | Publication Date |
---|---|
ES412584A1 true ES412584A1 (en) | 1976-01-16 |
Family
ID=9095159
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
ES412584A Expired ES412584A1 (en) | 1972-03-14 | 1973-03-13 | Procedure for preparation of (alcohil-4-piperidil-4) - oxialcanols. (Machine-translation by Google Translate, not legally binding) |
Country Status (2)
Country | Link |
---|---|
ES (1) | ES412584A1 (en) |
FR (1) | FR2175564A1 (en) |
-
1972
- 1972-03-14 FR FR7208801A patent/FR2175564A1/en active Granted
-
1973
- 1973-03-13 ES ES412584A patent/ES412584A1/en not_active Expired
Also Published As
Publication number | Publication date |
---|---|
FR2175564B1 (en) | 1975-04-25 |
FR2175564A1 (en) | 1973-10-26 |
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