WO1996029310A1 - Dimethylamine benzoate or p-anisate catalysed process for the preparation of 4-(nitrophenyl)-dihydropyridines - Google Patents
Dimethylamine benzoate or p-anisate catalysed process for the preparation of 4-(nitrophenyl)-dihydropyridines Download PDFInfo
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- WO1996029310A1 WO1996029310A1 PCT/EP1996/001090 EP9601090W WO9629310A1 WO 1996029310 A1 WO1996029310 A1 WO 1996029310A1 EP 9601090 W EP9601090 W EP 9601090W WO 9629310 A1 WO9629310 A1 WO 9629310A1
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- general formula
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- defined above
- anisate
- meanings defined
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- 238000000034 method Methods 0.000 title claims abstract description 11
- 238000002360 preparation method Methods 0.000 title claims abstract description 11
- CLGPABLPZDWCHL-UHFFFAOYSA-N benzoic acid;n-methylmethanamine Chemical compound CNC.OC(=O)C1=CC=CC=C1 CLGPABLPZDWCHL-UHFFFAOYSA-N 0.000 title claims abstract description 6
- ZEYHEAKUIGZSGI-UHFFFAOYSA-M 4-methoxybenzoate Chemical compound COC1=CC=C(C([O-])=O)C=C1 ZEYHEAKUIGZSGI-UHFFFAOYSA-M 0.000 title claims abstract description 5
- BIWBFFZTZOHCRG-UHFFFAOYSA-N 4-(2-nitrophenyl)-1,2-dihydropyridine Chemical class [O-][N+](=O)C1=CC=CC=C1C1=CCNC=C1 BIWBFFZTZOHCRG-UHFFFAOYSA-N 0.000 title abstract description 3
- 238000006243 chemical reaction Methods 0.000 claims abstract description 11
- HUMNYLRZRPPJDN-UHFFFAOYSA-N benzaldehyde Chemical compound O=CC1=CC=CC=C1 HUMNYLRZRPPJDN-UHFFFAOYSA-N 0.000 claims abstract description 6
- 125000000649 benzylidene group Chemical group [H]C(=[*])C1=C([H])C([H])=C([H])C([H])=C1[H] 0.000 claims abstract description 6
- 150000002081 enamines Chemical class 0.000 claims abstract description 3
- QNGNSVIICDLXHT-UHFFFAOYSA-N para-ethylbenzaldehyde Natural products CCC1=CC=C(C=O)C=C1 QNGNSVIICDLXHT-UHFFFAOYSA-N 0.000 claims abstract description 3
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 claims description 10
- 239000003054 catalyst Substances 0.000 claims description 10
- 150000002148 esters Chemical class 0.000 claims description 6
- 125000004200 2-methoxyethyl group Chemical group [H]C([H])([H])OC([H])([H])C([H])([H])* 0.000 claims description 4
- XYIBRDXRRQCHLP-UHFFFAOYSA-N ethyl acetoacetate Chemical compound CCOC(=O)CC(C)=O XYIBRDXRRQCHLP-UHFFFAOYSA-N 0.000 claims description 4
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 4
- 125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 claims description 3
- CMWKITSNTDAEDT-UHFFFAOYSA-N 2-nitrobenzaldehyde Chemical compound [O-][N+](=O)C1=CC=CC=C1C=O CMWKITSNTDAEDT-UHFFFAOYSA-N 0.000 claims description 2
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 claims description 2
- 125000000959 isobutyl group Chemical group [H]C([H])([H])C([H])(C([H])([H])[H])C([H])([H])* 0.000 claims description 2
- 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 claims description 2
- -1 nitrobenzylidene Chemical class 0.000 claims description 2
- 125000001931 aliphatic group Chemical group 0.000 claims 1
- 239000002904 solvent Substances 0.000 claims 1
- WDJHALXBUFZDSR-UHFFFAOYSA-M acetoacetate Chemical compound CC(=O)CC([O-])=O WDJHALXBUFZDSR-UHFFFAOYSA-M 0.000 abstract description 3
- KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 description 16
- ROSDSFDQCJNGOL-UHFFFAOYSA-N Dimethylamine Chemical compound CNC ROSDSFDQCJNGOL-UHFFFAOYSA-N 0.000 description 10
- ZEYHEAKUIGZSGI-UHFFFAOYSA-N 4-methoxybenzoic acid Chemical compound COC1=CC=C(C(O)=O)C=C1 ZEYHEAKUIGZSGI-UHFFFAOYSA-N 0.000 description 8
- 238000010438 heat treatment Methods 0.000 description 5
- NQRYJNQNLNOLGT-UHFFFAOYSA-N Piperidine Chemical compound C1CCNCC1 NQRYJNQNLNOLGT-UHFFFAOYSA-N 0.000 description 4
- 239000012267 brine Substances 0.000 description 4
- 125000004925 dihydropyridyl group Chemical group N1(CC=CC=C1)* 0.000 description 4
- HPALAKNZSZLMCH-UHFFFAOYSA-M sodium;chloride;hydrate Chemical compound O.[Na+].[Cl-] HPALAKNZSZLMCH-UHFFFAOYSA-M 0.000 description 4
- 239000000243 solution Substances 0.000 description 4
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 4
- 229940071248 anisate Drugs 0.000 description 3
- 230000015572 biosynthetic process Effects 0.000 description 3
- 239000012535 impurity Substances 0.000 description 3
- 239000000047 product Substances 0.000 description 3
- ZETIVVHRRQLWFW-UHFFFAOYSA-N 3-nitrobenzaldehyde Chemical compound [O-][N+](=O)C1=CC=CC(C=O)=C1 ZETIVVHRRQLWFW-UHFFFAOYSA-N 0.000 description 2
- QGZKDVFQNNGYKY-UHFFFAOYSA-N Ammonia Chemical compound N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 description 2
- 150000001299 aldehydes Chemical class 0.000 description 2
- WPYMKLBDIGXBTP-UHFFFAOYSA-N benzoic acid Chemical compound OC(=O)C1=CC=CC=C1 WPYMKLBDIGXBTP-UHFFFAOYSA-N 0.000 description 2
- 238000001035 drying Methods 0.000 description 2
- YOPMSDPIOQUWFE-XYOKQWHBSA-N ethyl (2e)-2-[(3-nitrophenyl)methylidene]-3-oxobutanoate Chemical compound CCOC(=O)C(\C(C)=O)=C\C1=CC=CC([N+]([O-])=O)=C1 YOPMSDPIOQUWFE-XYOKQWHBSA-N 0.000 description 2
- 238000004128 high performance liquid chromatography Methods 0.000 description 2
- DDIZAANNODHTRB-UHFFFAOYSA-N methyl p-anisate Chemical compound COC(=O)C1=CC=C(OC)C=C1 DDIZAANNODHTRB-UHFFFAOYSA-N 0.000 description 2
- 239000002244 precipitate Substances 0.000 description 2
- 239000011541 reaction mixture Substances 0.000 description 2
- 238000001953 recrystallisation Methods 0.000 description 2
- 231100000331 toxic Toxicity 0.000 description 2
- 230000002588 toxic effect Effects 0.000 description 2
- 238000005406 washing Methods 0.000 description 2
- PVHUJELLJLJGLN-INIZCTEOSA-N (S)-nitrendipine Chemical compound CCOC(=O)C1=C(C)NC(C)=C(C(=O)OC)[C@@H]1C1=CC=CC([N+]([O-])=O)=C1 PVHUJELLJLJGLN-INIZCTEOSA-N 0.000 description 1
- UKVYVZLTGQVOPX-IHWYPQMZSA-N (z)-3-aminobut-2-enoic acid Chemical compound C\C(N)=C\C(O)=O UKVYVZLTGQVOPX-IHWYPQMZSA-N 0.000 description 1
- YNGDWRXWKFWCJY-UHFFFAOYSA-N 1,4-Dihydropyridine Chemical compound C1C=CNC=C1 YNGDWRXWKFWCJY-UHFFFAOYSA-N 0.000 description 1
- ZFFMLCVRJBZUDZ-UHFFFAOYSA-N 2,3-dimethylbutane Chemical group CC(C)C(C)C ZFFMLCVRJBZUDZ-UHFFFAOYSA-N 0.000 description 1
- UVZJPCAZMGLNTB-UKTHLTGXSA-N 2-methoxyethyl (2e)-2-[(3-nitrophenyl)methylidene]-3-oxobutanoate Chemical compound COCCOC(=O)C(\C(C)=O)=C\C1=CC=CC([N+]([O-])=O)=C1 UVZJPCAZMGLNTB-UKTHLTGXSA-N 0.000 description 1
- PLHCSZRZWOWUBW-UHFFFAOYSA-N 2-methoxyethyl 3-oxobutanoate Chemical compound COCCOC(=O)CC(C)=O PLHCSZRZWOWUBW-UHFFFAOYSA-N 0.000 description 1
- JJYPMNFTHPTTDI-UHFFFAOYSA-N 3-methylaniline Chemical compound CC1=CC=CC(N)=C1 JJYPMNFTHPTTDI-UHFFFAOYSA-N 0.000 description 1
- UIAGMCDKSXEBJQ-IBGZPJMESA-N 3-o-(2-methoxyethyl) 5-o-propan-2-yl (4s)-2,6-dimethyl-4-(3-nitrophenyl)-1,4-dihydropyridine-3,5-dicarboxylate Chemical compound COCCOC(=O)C1=C(C)NC(C)=C(C(=O)OC(C)C)[C@H]1C1=CC=CC([N+]([O-])=O)=C1 UIAGMCDKSXEBJQ-IBGZPJMESA-N 0.000 description 1
- QTBSBXVTEAMEQO-UHFFFAOYSA-M Acetate Chemical compound CC([O-])=O QTBSBXVTEAMEQO-UHFFFAOYSA-M 0.000 description 1
- 238000006000 Knoevenagel condensation reaction Methods 0.000 description 1
- VNNMQWJKFKKJLV-UHFFFAOYSA-N acetic acid;n-propan-2-ylpropan-2-amine Chemical compound CC(O)=O.CC(C)NC(C)C VNNMQWJKFKKJLV-UHFFFAOYSA-N 0.000 description 1
- RLKBOGLIOLFMEK-NSCUHMNNSA-N amino (e)-but-2-enoate Chemical compound C\C=C\C(=O)ON RLKBOGLIOLFMEK-NSCUHMNNSA-N 0.000 description 1
- 229910021529 ammonia Inorganic materials 0.000 description 1
- 239000006227 byproduct Substances 0.000 description 1
- 239000007809 chemical reaction catalyst Substances 0.000 description 1
- 150000001875 compounds Chemical class 0.000 description 1
- 238000009833 condensation Methods 0.000 description 1
- 230000005494 condensation Effects 0.000 description 1
- 125000004177 diethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 1
- 125000000118 dimethyl group Chemical group [H]C([H])([H])* 0.000 description 1
- 239000012467 final product Substances 0.000 description 1
- 231100001231 less toxic Toxicity 0.000 description 1
- XKORCTIIRYKLLG-ARJAWSKDSA-N methyl (z)-3-aminobut-2-enoate Chemical compound COC(=O)\C=C(\C)N XKORCTIIRYKLLG-ARJAWSKDSA-N 0.000 description 1
- 239000000203 mixture Substances 0.000 description 1
- 229960000715 nimodipine Drugs 0.000 description 1
- 229960005425 nitrendipine Drugs 0.000 description 1
- VMPITZXILSNTON-UHFFFAOYSA-N o-anisidine Chemical compound COC1=CC=CC=C1N VMPITZXILSNTON-UHFFFAOYSA-N 0.000 description 1
- 238000006053 organic reaction Methods 0.000 description 1
- RAIYODFGMLZUDF-UHFFFAOYSA-N piperidin-1-ium;acetate Chemical compound CC([O-])=O.C1CC[NH2+]CC1 RAIYODFGMLZUDF-UHFFFAOYSA-N 0.000 description 1
- 238000010992 reflux Methods 0.000 description 1
- 150000003839 salts Chemical class 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 238000003786 synthesis reaction Methods 0.000 description 1
- 238000010189 synthetic method Methods 0.000 description 1
- 231100000419 toxicity Toxicity 0.000 description 1
- 230000001988 toxicity Effects 0.000 description 1
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
- C07D211/80—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 two double bonds between ring members or between ring members and non-ring members
- C07D211/84—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 two 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 directly attached to ring carbon atoms
- C07D211/90—Carbon atoms having three bonds to hetero atoms with at the most one bond to halogen
Definitions
- the present invention relates to a process for the preparation of 4-(nitrophenyl)dihydropyridines .
- EP 0,124,743 and EP 0,173,126 disclose the preparation of the benzylidene derivatives with suitable catalysts, such as piperidine acetate in the first Patent and, inte -alia, o-anisidine and m- toluidine in the second Patent.
- EP 319,814 discloses the final closure reaction of one of these important dihydropyridines, catalyzed by diisopropylamine acetate or dimethylbenzyla ine acetate.
- dihydropyridine asymmetric esters can be prepared in high yield and purity, with remarkable savings in time and energy, and therefore with a low cost, using as reaction catalysts organic salts that up to now have never been considered.
- the dihydropyridines of the invention have the general formula ( I )
- R 1 is a nitro group at the 2 or 3 position
- R 2 and R3, which are different from each other, are a methyl, ethyl, isopropyl, 2-methoxyethyl or isobutyl group, whereas R ⁇ and R ⁇ are methyl groups.
- R3 and R5 have the meanings defined above.
- the benzylidene derivative (II) is in turn prepared by reacting a benzaldehyde of general formula (IV)
- R 2 and R 4 have the meanings defined above.
- Both the above reactions can be carried out in a lower C 1-4 alcohol and are catalyzed by dimethyla ine benzoate or p-anisate.
- reaction temperature ranging from 20 * to 40*C.
- dimethylamine anisate or benzoate minimizes the formation of the main undesired impurities of these dihydropyridines, i.e. the corresponding dicarboxylic symmetric esters of general formula (II) wherein 2 and R3 are the same.
- the catalyst moles range from 0.01 to 0.06 per mole of nitrobenzaldehyde and from 0.005 to 0.015 per mole of nitrobenzylidene derivative. From the comparison between the data deducible from the Registry of Toxic Effects of Chemical Substance, moreover, the catalysts of the invention turn out to be less toxic than those used up to now in the above cited patents. For example, in EP 0,124,743 piperidine is used as the catalyst. Said product involves evident handling problems due to its characteristics of toxicity.
- EXAMPLE 1 a) 300 kg of ethyl acetoacetate and 348 kg of 3-nitrobenzaldehyde are suspended in 1550 1 of isopropanol. After that 5.235 kg of p-anisic acid and 4.4 kg of 33% dimethylamine in ethanol are added. The mixture is warmed for about 30' at about 35 * C to obtain a solution. The reaction mixture is left to cool at 20/25'C and then it is cooled for about 12 hours with running water and for a further 24 hours at about 0 ⁇ C with brine, then is centrifuged, washing with isopropanol.
- reaction mixture is left to cool at 20/25 * C and then it is cooled for about 12 hours with running water and for a further 24 hours at about 0 * C with brine, then is centrifuged, washing with isopropanol.
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Hydrogenated Pyridines (AREA)
- Low-Molecular Organic Synthesis Reactions Using Catalysts (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Pyridine Compounds (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
Abstract
A method for the preparation of 4-(nitrophenyl)-dihydropyridines, by reacting a benzaldehyde with an acetoacetate and subsequently reacting the resulting benzylidene derivative with an enamine derivative. Both reactions are catalyzed by dimethylamine benzoate or p-anisate.
Description
DIMETHYLAMINE BENZOATE OR P-ANISATE CATALYSED PROCESS FOR THE PREPARATION
OF 4-(NITR0PHENYL)-DIHYDR0PYRIDINES
The present invention relates to a process for the preparation of 4-(nitrophenyl)dihydropyridines .
These products are widely used due to their remarkable pharmaceutical properties, and up to now they were prepared according to different synthetic methods.
For example, Hantzsch's synthesis (Ann. 215, 1, 72;
1882) is made use of to prepare in a single step the
3 , 5-dicarboxylic acid symmetric esters, using a mole of aldehyde, 2 moles of acetoacetic ester and ammonia. On the other hand, for the preparation of the asymmetric esters, Knoevenagel synthesis is employed,
(Ber. 31, 370; 1898) first reacting an aldehyde with an acetoacetate in the presence of piperidine, subsequently treating the resulting benzylidene derivative with the suitable aminocrotonate.
Knoevanagel condensation is exhaustively described by G. Jones in Organic Reactions, 15, 1967, p. 204-599.
A number of methods and patents concerning the preparation of dihydropyridines exist in literature. Among these, EP 0,124,743 and EP 0,173,126 disclose the preparation of the benzylidene derivatives with suitable catalysts, such as piperidine acetate in the first Patent and, inte -alia, o-anisidine and m- toluidine in the second Patent. On the other hand, EP 319,814 discloses the final closure reaction of one of these important dihydropyridines, catalyzed by diisopropylamine acetate or dimethylbenzyla ine acetate.
Now it has surprisingly been found that
dihydropyridine asymmetric esters can be prepared in high yield and purity, with remarkable savings in time and energy, and therefore with a low cost, using as reaction catalysts organic salts that up to now have never been considered.
The dihydropyridines of the invention have the general formula ( I )
Compounds (I) are prepared, according to the invention, from a benzylidene derivative of general formula (II)
wherein \R^ f R2 an R4 have the meanings defined above, by reaction with an enamine derivative of general formula (III)
wherein R3 and R5 have the meanings defined above.
The benzylidene derivative (II) is in turn prepared by reacting a benzaldehyde of general formula (IV)
wherein R^ has the meanings defined above, with an acetoacetic ester of general formula (V)
wherein R2 and R4 have the meanings defined above.
Both the above reactions can be carried out in a lower C1-4 alcohol and are catalyzed by dimethyla ine benzoate or p-anisate.
The use of the catalyst according to the invention makes it surprisingly possible to carry out the reaction
necessary for the preparation of (II) in mild conditions
(reaction temperature ranging from 20* to 40*C). In this way, the formation of undesired side-products is restricted and a highly pure intermediate (II) is obtained in a high yield, with remarkable energetic savings and therefore at lower costs.
The use of dimethylamine benzoate or anisate in the subsequent reaction, moreover, makes it possible for (I) to form already after a few hours heating, also affording in this case the advantage of energetic savings and consequent low costs.
On the contrary, when the reaction for the preparation of the main product (I) is carried out with no use of catalysts, heating under reflux up to 24 hours is necessary (as disclosed, for example, in EP 124,743).
Moreover, the use of dimethylamine anisate or benzoate minimizes the formation of the main undesired impurities of these dihydropyridines, i.e. the corresponding dicarboxylic symmetric esters of general formula (II) wherein 2 and R3 are the same.
In the process of the invention, the catalyst moles range from 0.01 to 0.06 per mole of nitrobenzaldehyde and from 0.005 to 0.015 per mole of nitrobenzylidene derivative. From the comparison between the data deducible from the Registry of Toxic Effects of Chemical Substance, moreover, the catalysts of the invention turn out to be less toxic than those used up to now in the above cited patents. For example, in EP 0,124,743 piperidine is used as the catalyst. Said product involves evident handling
problems due to its characteristics of toxicity.
Finally, the use of a single, scarcely toxic catalyst makes the search for any traces thereof in the final product (I) easier. The following examples further illustrate the process of the invention without limiting it.
EXAMPLE 1 a) 300 kg of ethyl acetoacetate and 348 kg of 3-nitrobenzaldehyde are suspended in 1550 1 of isopropanol. After that 5.235 kg of p-anisic acid and 4.4 kg of 33% dimethylamine in ethanol are added. The mixture is warmed for about 30' at about 35*C to obtain a solution. The reaction mixture is left to cool at 20/25'C and then it is cooled for about 12 hours with running water and for a further 24 hours at about 0βC with brine, then is centrifuged, washing with isopropanol. After drying, 578 kg of ethyl 2- (3-nitrobenzylidene)acetoacetate are obtained, in an about 95% yield. b) 362 kg of ethyl 2-(3-nitrobenzylidene)acetoacetate and 158.3 kg of methyl 3-aminocrotonate are suspended in 840 1 of isopropanol and treated with 2.2 kg of p-anisic acid and 1.85 kg of 33% dimethylamine in ethanol. Upon heating, a solution is obtained which is refluxed for about 12 hours, after that it is cooled with water and then with brine at about -5*C and the resulting precipitate is centryfuged. By recrystallization from isopropanol, 476 kg of Nitrendipine are obtained in an about 96% yield.
6 The content in dimethyl and diethyl esters, by HPLC analysis, turns out to be lower than 0.1% for each of said impurities.
EXAMPLE 2
5 a) 200 kg of 2-methoxyethyl acetoacetate and 185.1 kg of 3-nitrobenzaldehyde are suspended in 800 1 of isopropanol. Then 5.65 kg of p-anisic acid and 5.05 kg of 33% dimethylamine in ethanol are added, heating for about 30' at about 35*C to obtain a
10 solution. The reaction mixture is left to cool at 20/25*C and then it is cooled for about 12 hours with running water and for a further 24 hours at about 0*C with brine, then is centrifuged, washing with isopropanol.
15 After drying, 327 kg of 2-methoxyethyl
2-(3-nitrobenzylidene) acetoacetate are obtained, in an about 91% yield. b) 490 kg of 2-methoxyethyl 2-(3-nitrobenzylidene) acetoacetate and 244.4 kg of isopropyl
20 3-aminocrotonate are suspended in 1500 1 of isopropanol and treated with 3 kg of p-anisic acid and 2.5 kg of 33% dimethylamine in ethanol. Upon heating, a solution is obtained which is refluxed for about 10 hours, after that it is cooled with
25 water and then with brine at about 0*C and the resulting precipitate is centrifuged. By recrystallization from isopropanol, 657 kg of Nimodipine are obtained in an about 94% yield. The content in 2-methoxyethyl and diisopropyl
30 esters, by HPLC analysis, turns out to be lower than 0.1% for each of said impurities.
Claims
1. A process for the preparation of asymmetric esters of 4-(nitrophenyl)dihydroρyridines of general formula
(I)
(II)
wherein R , R2 and R4 have the meanings defined above, with an enamine derivative of general formula (III) 
wherein R3 and Re have the meanings defined above, chacterized in that said reaction is carried out ir. the presence of dimethylamine benzoate or p-anisate as the catalyst.
2. A process for the preparation of a benzyliiene derivative of general formula (II)
wherein R1, R2 and R4 have the meanings defined above, in which a benzaldehyde of general formula (IV)
wherein R, has the meanings defined above, is reacted with an acetoacetic ester of general formula ( V )
wherein R and R4 have the meanings defined above, characterized in that the reaction is carried out in the presence of dimethylamine benzoate or p-anisate as the catalyst, at a temperature ranging from 20"C to 40'C.
3. A process according to claims 1 and 2, characterized in that the catalyst is present in molar amounts from 0.01 to 0.06 moles per mole of nitrobenzaldehyde and from 0.005 to 0.015 moles per mole of nitrobenzylidene derivative.
4. A process according to claims 1 and 2, characterized in that both reactions are carried out in a lower aliphatic C1-4 alcohol as the solvent.
Priority Applications (8)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE69602596T DE69602596T2 (en) | 1995-03-20 | 1996-03-14 | DIMETHYLAMINE BENZOATE IDER P-ANISATE CATALYZED PROCESS FOR PRODUCING 4-8NITROPHENYL) -DIHYDROPYRIDINES |
| JP52805396A JP3916252B2 (en) | 1995-03-20 | 1996-03-14 | Process for producing 4- (nitrophenyl) -dihydropyridines with dimethylamine benzoate or anisate catalyst |
| EP96907468A EP0819117B1 (en) | 1995-03-20 | 1996-03-14 | Dimethylamine benzoate or p-anisate catalysed process for the preparation of 4-(nitrophenyl)-dihydropyridines |
| AU51086/96A AU703214B2 (en) | 1995-03-20 | 1996-03-14 | Dimethylamine benzoate or p-anisate catalysed process for the preparation of (nitrophenyl)-dihydropyridines |
| CA002215837A CA2215837C (en) | 1995-03-20 | 1996-03-14 | Dimethylamine benzoate or p-anisate catalysed process for the preparation of 4-(nitrophenyl)-dihydropyridines |
| DK96907468T DK0819117T3 (en) | 1995-03-20 | 1996-03-14 | Dimethylamine benzoate or β-anisate catalyzed process for the preparation of 4- (nitrophenyl) dihydropyridines |
| US08/894,389 US6015906A (en) | 1995-03-20 | 1996-03-14 | Dimethylamine benzoate or p-anisate catalysed process for the preparation of 4-(nitrophenyl)-dihydropyridines |
| GR990402119T GR3031041T3 (en) | 1995-03-20 | 1999-08-19 | Dimethylamine benzoate or p-anisate catalysed process for the preparation of 4-(nitrophenyl)-dihydropyridines |
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| ITMI95A000540 | 1995-03-20 | ||
| IT95MI000540A IT1275939B1 (en) | 1995-03-20 | 1995-03-20 | PROCEDURE FOR THE PREPARATION OF 4 (NITROFENIL) DIIDROPIRIDINE |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| WO1996029310A1 true WO1996029310A1 (en) | 1996-09-26 |
Family
ID=11370961
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| PCT/EP1996/001090 WO1996029310A1 (en) | 1995-03-20 | 1996-03-14 | Dimethylamine benzoate or p-anisate catalysed process for the preparation of 4-(nitrophenyl)-dihydropyridines |
Country Status (12)
| Country | Link |
|---|---|
| US (1) | US6015906A (en) |
| EP (1) | EP0819117B1 (en) |
| JP (1) | JP3916252B2 (en) |
| AT (1) | ATE180471T1 (en) |
| AU (1) | AU703214B2 (en) |
| CA (1) | CA2215837C (en) |
| DE (1) | DE69602596T2 (en) |
| DK (1) | DK0819117T3 (en) |
| ES (1) | ES2131394T3 (en) |
| GR (1) | GR3031041T3 (en) |
| IT (1) | IT1275939B1 (en) |
| WO (1) | WO1996029310A1 (en) |
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN104860873A (en) * | 2015-05-28 | 2015-08-26 | 石家庄学院 | Preparation method for (S)-1,4-dihydropyridine calcium ion antagonist |
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| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| EP2115008B1 (en) | 2007-03-01 | 2019-09-18 | De Staat der Nederlanden, vert. door de Minister van Volksgezondheid, Welzijn en Sport, namens de Minister, Projectdirectie ALT, het INTRAVACC | Biodegradable material based on opened starch |
Citations (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| EP0124743A2 (en) | 1983-04-05 | 1984-11-14 | Bayer Ag | Process for the preparation of asymmetric 1,4-dihydropyridine-carboxylic acid esters |
| EP0173126A1 (en) | 1984-08-07 | 1986-03-05 | Otsuka Pharmaceutical Co., Ltd. | Process for preparing novel dihydropyridine derivatives |
| EP0319814A2 (en) | 1987-12-08 | 1989-06-14 | Bayer Ag | Method of preparing asymmetrical dihydropyridines |
| JPH04173761A (en) * | 1990-11-06 | 1992-06-22 | Daicel Chem Ind Ltd | Production of alpha-alkylacrolein |
-
1995
- 1995-03-20 IT IT95MI000540A patent/IT1275939B1/en active IP Right Grant
-
1996
- 1996-03-14 WO PCT/EP1996/001090 patent/WO1996029310A1/en active IP Right Grant
- 1996-03-14 DK DK96907468T patent/DK0819117T3/en active
- 1996-03-14 US US08/894,389 patent/US6015906A/en not_active Expired - Lifetime
- 1996-03-14 DE DE69602596T patent/DE69602596T2/en not_active Expired - Lifetime
- 1996-03-14 CA CA002215837A patent/CA2215837C/en not_active Expired - Lifetime
- 1996-03-14 AT AT96907468T patent/ATE180471T1/en active
- 1996-03-14 EP EP96907468A patent/EP0819117B1/en not_active Expired - Lifetime
- 1996-03-14 AU AU51086/96A patent/AU703214B2/en not_active Expired
- 1996-03-14 ES ES96907468T patent/ES2131394T3/en not_active Expired - Lifetime
- 1996-03-14 JP JP52805396A patent/JP3916252B2/en not_active Expired - Lifetime
-
1999
- 1999-08-19 GR GR990402119T patent/GR3031041T3/en unknown
Patent Citations (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| EP0124743A2 (en) | 1983-04-05 | 1984-11-14 | Bayer Ag | Process for the preparation of asymmetric 1,4-dihydropyridine-carboxylic acid esters |
| EP0173126A1 (en) | 1984-08-07 | 1986-03-05 | Otsuka Pharmaceutical Co., Ltd. | Process for preparing novel dihydropyridine derivatives |
| EP0319814A2 (en) | 1987-12-08 | 1989-06-14 | Bayer Ag | Method of preparing asymmetrical dihydropyridines |
| JPH04173761A (en) * | 1990-11-06 | 1992-06-22 | Daicel Chem Ind Ltd | Production of alpha-alkylacrolein |
Non-Patent Citations (3)
| Title |
|---|
| BER., vol. 31, pages 370 |
| G. JONES, ORGANIC REACTIONS, vol. 15, 1967, pages 204 - 599 |
| PATENT ABSTRACTS OF JAPAN vol. 016, no. 473 (C - 0991) 2 October 1992 (1992-10-02) * |
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN104860873A (en) * | 2015-05-28 | 2015-08-26 | 石家庄学院 | Preparation method for (S)-1,4-dihydropyridine calcium ion antagonist |
Also Published As
| Publication number | Publication date |
|---|---|
| CA2215837C (en) | 2007-10-30 |
| AU703214B2 (en) | 1999-03-18 |
| AU5108696A (en) | 1996-10-08 |
| ES2131394T3 (en) | 1999-07-16 |
| DE69602596D1 (en) | 1999-07-01 |
| IT1275939B1 (en) | 1997-10-24 |
| JP3916252B2 (en) | 2007-05-16 |
| DK0819117T3 (en) | 1999-11-08 |
| DE69602596T2 (en) | 1999-09-23 |
| JPH11505518A (en) | 1999-05-21 |
| EP0819117B1 (en) | 1999-05-26 |
| GR3031041T3 (en) | 1999-12-31 |
| ATE180471T1 (en) | 1999-06-15 |
| US6015906A (en) | 2000-01-18 |
| CA2215837A1 (en) | 1996-09-26 |
| ITMI950540A0 (en) | 1995-03-20 |
| ITMI950540A1 (en) | 1996-09-20 |
| EP0819117A1 (en) | 1998-01-21 |
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