EP1776341A1 - Method for preparing n-aminopiperedine and its salts - Google Patents

Method for preparing n-aminopiperedine and its salts

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Publication number
EP1776341A1
EP1776341A1 EP05796225A EP05796225A EP1776341A1 EP 1776341 A1 EP1776341 A1 EP 1776341A1 EP 05796225 A EP05796225 A EP 05796225A EP 05796225 A EP05796225 A EP 05796225A EP 1776341 A1 EP1776341 A1 EP 1776341A1
Authority
EP
European Patent Office
Prior art keywords
formula
compound
solvent
temperature
hai
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.)
Withdrawn
Application number
EP05796225A
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German (de)
French (fr)
Inventor
Pierre Jean Grossi
Raphaël SOLE
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Sanofi SA
Original Assignee
Sanofi Aventis France
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Publication date
Application filed by Sanofi Aventis France filed Critical Sanofi Aventis France
Publication of EP1776341A1 publication Critical patent/EP1776341A1/en
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Classifications

    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D295/00—Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms
    • C07D295/22—Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms with hetero atoms directly attached to ring nitrogen atoms
    • C07D295/28—Nitrogen atoms
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D295/00—Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms
    • C07D295/22—Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms with hetero atoms directly attached to ring nitrogen atoms
    • C07D295/28—Nitrogen atoms
    • C07D295/30—Nitrogen atoms non-acylated
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D211/00—Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings
    • C07D211/92—Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with a hetero atom directly attached to the ring nitrogen atom
    • C07D211/98—Nitrogen atom

Abstract

The invention concerns a novel method for preparing N-aminopiperedine of formula (I).

Description

PROCEDE DE PREPARATION DE LA N-AMINOPIPERIDINE ET DE SES SELS. PROCESS FOR THE PREPARATION OF N-AMINOPIPERIDINE AND ITS SALTS
La présente invention a pour objet un nouveau procédé de préparation de la N- 5 . aminopipéridine de formule :The subject of the present invention is a new process for preparing N-5. aminopiperidine of formula:
1010
Plusieurs procédés de préparation de la N-aminopipéridine sont connus dans la littérature :Several processes for the preparation of N-aminopiperidine are known in the literature:
- procédé Raschig utilisant de la pipéridine et de la chloramine ;Raschig process using piperidine and chloramine;
- procédé via Phydrazine et la N-acétylaminopipéridine ;- process via hydrazine and N-acetylaminopiperidine;
- procédé via la N-nitrosopipéridine (Lunn, Keefer, J. Org. Chem. 1984, 49 (19), 3470) ;- process via N-nitrosopiperidine (Lunn, Keefer, J. Org Chem 1984, 49 (19), 3470);
- procédé via le glutaraldéhyde et le benzotriazole (Katritzky A.R., Wei-Quiang Fan, J. Org. Chem. 1990, 55, 3205-3209).- process via glutaraldehyde and benzotriazole (Katritzky A.R., Wei-Quiang Fan, J. Org Chem 1990, 55, 3205-3209).
Le procédé de préparation de la N-aminopipéridine (I) et de ses sels selon la présente invention est caractérisé en ce que : a) on traite un carbazate de formule :The process for the preparation of N-aminopiperidine (I) and its salts according to the present invention is characterized in that: a) a carbazate of formula:
NH2-NH-COOR (II) dans laquelle R représente un groupe (Ci-Cg)alkyle, un phényle ou un benzyle, par un 1,5-dihalogénure de pentyle de formule :NH 2 -NH-COOR (II) in which R represents a (C 1 -C 8) alkyl group, a phenyl or a benzyl, with a pentyl 1,5-dihalide of the formula:
25 Hal-(CH2)5-Hal (III) dans laquelle HaI représente un atome d'halogène ; b) on traite le pipéridin-l-ylcarbamate ainsi obtenu de formule : 25 Hal- (CH 2) 5 -Hal (III) in which Hal represents a halogen atom; b) treating the piperidin-1-ylcarbamate thus obtained of formula:
dans laquelle R représente un groupe (Ci-C6)alkyle, un phényle ou un benzyle en milieu acide ou en milieu basique pour obtenir la N-aminopipéridine attendue. or Le cas échéant, on peut préparer un sel de la N-aminopipéridine (I) par action d'un acide minéral ou organique. Par atome d'halogène on entend un atome de brome, de chlore ou d'iode. L'étape a) est réalisée dans un solvant tel que l'acétonitrile ou le toluène, à une température comprise entre la température ambiante et la température de reflux du solvant. L'étape b) est réalisée soit en milieu acide, par exemple en présence d'acide chlorhydrique ou bromhydrique, soit en milieu basique, par exemple en présence de potasse ou de soude dans un solvant tel que l'eau ou l'éthanol et à une température comprise entre la température ambiante et la température de reflux du solvant. wherein R represents a (C 1 -C 6) alkyl group, a phenyl or a benzyl in an acid medium or in a basic medium to obtain the expected N-aminopiperidine. If necessary, a salt of N-aminopiperidine (I) can be prepared by the action of a mineral or organic acid. By halogen atom is meant a bromine, chlorine or iodine atom. Step a) is carried out in a solvent such as acetonitrile or toluene, at a temperature between room temperature and the reflux temperature of the solvent. Step b) is carried out either in an acid medium, for example in the presence of hydrochloric or hydrobromic acid, or in a basic medium, for example in the presence of potassium hydroxide or sodium hydroxide in a solvent such as water or ethanol and at a temperature between room temperature and the reflux temperature of the solvent.
Selon un mode de réalisation préféré de la présente invention, à l'étape a) on traite un composé de formule (II) dans laquelle R représente un radical éthyle par un composé de formule (III) dans laquelle HaI représente un atome de brome, dans de l'acétonitrile, en chauffant à reflux du solvant.According to a preferred embodiment of the present invention, in step a) a compound of formula (II) in which R represents an ethyl radical is treated with a compound of formula (III) in which HaI represents a bromine atom, in acetonitrile, while refluxing the solvent.
Selon un mode de réalisation préféré de la présente invention, à l'étape b), on traite le composé de formule (IV) dans laquelle R représente un radical éthyle par de la soude dans de l'eau en chauffant à reflux du solvant.According to a preferred embodiment of the present invention, in step b), the compound of formula (IV) in which R represents an ethyl radical is treated with sodium hydroxide in water while heating at reflux of the solvent.
Préférentiellement, on prépare un sel de N-aminopipéridine tel que le bromhydrate, le chlorhydrate ou l'oxalate. Par exemple, on peut préparer le bromhydrate de N-aminopipéridine dans un solvant tel que le méthyl-fert-butyléther (MTBE). EXEMPLEPreferentially, an N-aminopiperidine salt such as hydrobromide, hydrochloride or oxalate is prepared. For example, N-aminopiperidine hydrobromide can be prepared in a solvent such as methyl-fert-butyl ether (MTBE). EXAMPLE
A - Pipéridin-1-yl-carbamate d'éthyleA - Piperidin-1-yl-ethyl carbamate
On prépare un mélange de 565,3 g de carbazate d'éthyle dans 373 ml d'acétonitrile. On coule 415,4 g de 1,5-dibromopentane sur le mélange précédent porté au reflux. Le reflux est maintenu 3 heures. L'acétonitrile est éliminé par concentration sous vide. Le résidu ainsi obtenu est dissous dans un mélange toluène/eau. Le mélange biphasique est amené à pH = 5 par addition de NaOH à 30 %.A mixture of 565.3 g of ethyl carbazate in 373 ml of acetonitrile is prepared. 415.4 g of 1,5-dibromopentane are poured onto the preceding mixture brought to reflux. Reflux is maintained for 3 hours. Acetonitrile is removed by concentration in vacuo. The residue thus obtained is dissolved in a toluene / water mixture. The biphasic mixture is brought to pH = 5 by addition of 30% NaOH.
La phase aqueuse est décantée et réextraite par du toluène. De l'eau et de l'HCl à 36% sont additionnées aux phase toluéniques jointes. La phase aqueuse "riche" est lavée 3 à 4 fois par du méthyl fert-butyléther (MTBE) pour éliminer les neutres (impuretés, carbazate de diéthyle, dibromopentane résiduel). La phase aqueuse acide est basifiée par NaOH puis NaHCÛ3 en présence de toluène. La phase aqueuse est réextraite par du toluène. Les phases toluéniques sont lavées séparément par de l'eau afin d'appauvrir en éthylcarbazate résiduel. Les phases toluéniques sont concentrées à sec.The aqueous phase is decanted and reextracted with toluene. Water and 36% HCl are added to the attached toluene phases. The "rich" aqueous phase is washed 3 to 4 times with methyl-but-butyl ether (MTBE) to remove the neutral (impurities, diethyl carbazate, residual dibromopentane). The acidic aqueous phase is basified with NaOH and then NaHCO3 in the presence of toluene. The aqueous phase is reextracted with toluene. The toluene phases are washed separately with water in order to deplete residual ethylcarbazate. The toluene phases are concentrated to dryness.
On obtient 252 g du produit attendu sous forme d'une poudre blanche que l'on purifie par recristallisation dans le méthylcyclohexane. Spectre de RMN1H à 300 MHz : δ (ppm) : 1,23 : t : 3H ; 4,14 : qd : 2H ; 2,70 : t : 4H ; 1,66 : qt : 4H ; 1,36 : qt : 2H ; 5,54 : se : IH. B - N-aminopipéridine252 g of the expected product are obtained in the form of a white powder which is purified by recrystallization from methylcyclohexane. 1 H NMR spectrum at 300 MHz: δ (ppm): 1.23: t: 3H; 4.14: qd: 2H; 2.70: t: 4H; 1.66: qt: 4H; 1.36: qt: 2H; 5.54: se: 1H. B - N-aminopiperidine
On porte au reflux sous balayage d'Argon pendant 3 heures un mélange de 160 g de composé obtenu à l'étape précédente, 214 ml d'eau et 120 g de soude perles. Après refroidissement, on introduit 640 ml de MTBE avant de filtrer les minéraux présents. On obtient ainsi une solution de N-aminopipéridine brute dans MTBE. C - Préparation du bromhydrate de N-aminopipéridine brute.A mixture of 160 g of compound obtained in the preceding step, 214 ml of water and 120 g of sodium bead is refluxed under Argon for 3 hours. After cooling, 640 ml of MTBE are introduced before filtering the minerals present. A solution of crude N-aminopiperidine in MTBE is thus obtained. C - Preparation of crude N-aminopiperidine hydrobromide
On coule environ 1 volume d'éthanol bromhydrique à 36% pds/pds, à 25 °C et en 0,5 heure sur la solution de N-aminopipéridine dans MTBE obtenue à l'étape précédente. On observe la formation d'un précipité et l'on maintient sous agitation 1 heure. Le bromhydrate est filtré à 20°C, lavé par de l'éthanol, puis par du MTBE, il est ensuite séché sous vide à 45-50°C et l'on obtient 156 g du composé attendu. F = 177-177,5°C (littérature 174-1750C). About 1 volume of 36% w / w hydrobromic ethanol is poured at 25 ° C. and 0.5 hour onto the N-aminopiperidine solution in MTBE obtained in the previous step. The formation of a precipitate is observed and the mixture is stirred for 1 hour. The hydrobromide is filtered at 20 ° C, washed with ethanol, then with MTBE, it is then dried under vacuum at 45-50 ° C and 156 g of the expected compound is obtained. Mp 177-177.5 ° C (literature 174-175 ° C.).

Claims

REVENDICATIONS
1. Procédé de préparation de la N-aminopipéridine de formule :1. Process for the preparation of N-aminopiperidine of formula:
et de ses sels avec un acide minéral ou organique, caractérisé en ce que : a) on traite un carbazate de formule : and its salts with a mineral or organic acid, characterized in that: a) a carbazate of formula
NH2-NH-COOR (II) dans laquelle R représente un groupe (Ci-C6)alkyle, un phényle ou un benzyle, par un 1,5-dihalogénure de pentyle de formule :NH 2 -NH-COOR (II) in which R represents a (C 1 -C 6) alkyl group, a phenyl or a benzyl, with a pentyl 1,5-dihalide of formula:
HaI-(CH2)S-HaI (III) dans laquelle HaI représente un atome d'halogène ; b) on traite le pipéridin-1-ylcarbamate ainsi obtenu de formule :HaI- (CH 2 ) S-HaI (III) wherein Hal represents a halogen atom; b) treating the piperidin-1-ylcarbamate thus obtained of formula:
dans laquelle R est tel que défini ci-dessus, en milieu acide ou en milieu basique pour obtenir le composé de formule (I). in which R is as defined above, in acidic medium or in basic medium to obtain the compound of formula (I).
2. Procédé selon la revendication 1 caractérisé en ce que, à l'étape a), la réaction 2^ s'effectue dans un solvant choisi parmi l'acétonitrile ou le toluène, à une température comprise entre la température ambiante et la température de reflux du solvant.2. Method according to claim 1 characterized in that, in step a), the reaction 2 ^ is carried out in a solvent selected from acetonitrile or toluene, at a temperature between room temperature and the temperature of reflux of the solvent.
3. Procédé selon la revendication 1 ou 2 caractérisé en ce que, à l'étape b), la réaction s'effectue en utilisant soit un acide choisi parmi l'acide chlorhydrique ou on l'acide bromhydrique, soit une base choisi parmi la potasse ou la soude, dans un solvant choisi parmi l'eau ou l'éthanol, à une température comprise entre la température ambiante et la température de reflux du solvant.3. Method according to claim 1 or 2 characterized in that, in step b), the reaction is carried out using either an acid selected from hydrochloric acid or hydrobromic acid, or a base selected from potash or soda, in a solvent selected from water or ethanol, at a temperature between room temperature and the reflux temperature of the solvent.
4. Procédé selon l'une quelconque des revendications 1 à 3 caractérisé en ce que, à l'étape a), on traite un composé de formule (II) dans laquelle R représente un4. Method according to any one of claims 1 to 3 characterized in that, in step a), a compound of formula (II) is treated in which R represents a
« radical éthyle par un composé de formule (III) dans laquelle HaI représente un atome de brome, dans de l'acétonitrile, en chauffant à reflux du solvant. "Ethyl radical with a compound of formula (III) wherein HaI represents a bromine atom, in acetonitrile, by refluxing the solvent.
5. Procédé selon l'une quelconque des revendications 1 à 4 caractérisé en ce que, à l'étape b), on traite un composé de formule (TV) dans laquelle R représente un radical éthyle par de la soude, dans de l'eau, en chauffant à reflux du solvant.5. Method according to any one of claims 1 to 4 characterized in that, in step b), a compound of formula (TV) is treated in which R represents an ethyl radical by sodium hydroxide, in water, by refluxing the solvent.
6. Procédé selon l'une quelconque des revendications 1 à 5 caractérisé en ce que l'on prépare un sel du composé de formule (I) choisi parmi le bromhydrate, le chlorhydrate ou l'oxalate.6. Process according to any one of Claims 1 to 5, characterized in that a salt of the compound of formula (I) chosen from hydrobromide, hydrochloride or oxalate is prepared.
7. Procédé selon l'une quelconque des revendications 1 à 6 caractérisé en ce que l'on prépare le bromhydrate du composé de formule (I) dans le méthyl-tert-butyléther. 7. Process according to any one of Claims 1 to 6, characterized in that the hydrobromide of the compound of formula (I) is prepared in methyl-tert-butyl ether.
EP05796225A 2004-08-05 2005-08-02 Method for preparing n-aminopiperedine and its salts Withdrawn EP1776341A1 (en)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
FR0408700A FR2874013B1 (en) 2004-08-05 2004-08-05 PROCESS FOR THE PREPARATION OF N-AMINOPIPERIDINE AND ITS SALTS
PCT/FR2005/002016 WO2006024778A1 (en) 2004-08-05 2005-08-02 Method for preparing n-aminopiperedine and its salts

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EP1776341A1 true EP1776341A1 (en) 2007-04-25

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Country Status (16)

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US (2) US20070173648A1 (en)
EP (1) EP1776341A1 (en)
JP (1) JP2008509114A (en)
KR (1) KR20070048765A (en)
CN (1) CN101001839A (en)
AR (1) AR050089A1 (en)
AU (1) AU2005279087A1 (en)
BR (1) BRPI0514076A (en)
CA (1) CA2576718A1 (en)
FR (1) FR2874013B1 (en)
IL (1) IL180870A0 (en)
MX (1) MX2007001140A (en)
RU (1) RU2373196C2 (en)
TW (1) TW200621713A (en)
UY (1) UY29045A1 (en)
WO (1) WO2006024778A1 (en)

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Publication number Priority date Publication date Assignee Title
FR2864081B1 (en) * 2003-12-17 2006-04-28 Isochem Sa PROCESS FOR THE SYNTHESIS OF EXOCYCLIC CYCLOALKYL HYDRAZINE DERIVATIVES AND EXOCYCLIC HETEROCYCLOALKYL HYDRAZINE DERIVATIVES

Family Cites Families (7)

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Publication number Priority date Publication date Assignee Title
DE338609C (en) 1919-10-15 1921-06-22 Fritz Sommer Dr Process for the preparation of hydrazine and its alkyl or aryl substitution products
US3317607A (en) * 1959-07-30 1967-05-02 Fmc Corp Chemical reduction of nitrosamines
DE4138142C2 (en) * 1991-11-20 1996-04-25 Cassella Ag Process for the preparation of 1-amino-2,6-dimethylpiperidine
US5977360A (en) * 1996-12-27 1999-11-02 Japan Hydrazine Co., Ltd. Process for producing cyclic hydrazine derivatives, tetra-hydropyridazine and hexahydropyridazine
JP4118559B2 (en) * 2001-12-19 2008-07-16 日本曹達株式会社 Method for producing alicyclic hydrazine
JP2004137181A (en) * 2002-10-17 2004-05-13 Nippon Soda Co Ltd Method for producing n-aminopiperidine
JP2004137182A (en) * 2002-10-17 2004-05-13 Nippon Soda Co Ltd Method for producing n-aminopiperidine

Non-Patent Citations (1)

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Title
See references of WO2006024778A1 *

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US7951952B2 (en) 2011-05-31
FR2874013B1 (en) 2006-09-29
RU2373196C2 (en) 2009-11-20
JP2008509114A (en) 2008-03-27
US20080306274A1 (en) 2008-12-11
IL180870A0 (en) 2009-02-11
AR050089A1 (en) 2006-09-27
UY29045A1 (en) 2006-03-31
CN101001839A (en) 2007-07-18
CA2576718A1 (en) 2006-03-09
US20070173648A1 (en) 2007-07-26
TW200621713A (en) 2006-07-01
MX2007001140A (en) 2007-04-19
AU2005279087A1 (en) 2006-03-09
KR20070048765A (en) 2007-05-09
RU2007107806A (en) 2008-09-10
BRPI0514076A (en) 2008-05-27
FR2874013A1 (en) 2006-02-10
WO2006024778A1 (en) 2006-03-09

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