ES2055652A1 - Procedimiento de obtencion de 2,6-dimetil-4-(2,3-diclorofenil)-1,4-dihidropiridin-3,5-dicarboxilato de 3-etil-5-metil. - Google Patents
Procedimiento de obtencion de 2,6-dimetil-4-(2,3-diclorofenil)-1,4-dihidropiridin-3,5-dicarboxilato de 3-etil-5-metil.Info
- Publication number
- ES2055652A1 ES2055652A1 ES09201890A ES9201890A ES2055652A1 ES 2055652 A1 ES2055652 A1 ES 2055652A1 ES 09201890 A ES09201890 A ES 09201890A ES 9201890 A ES9201890 A ES 9201890A ES 2055652 A1 ES2055652 A1 ES 2055652A1
- Authority
- ES
- Spain
- Prior art keywords
- obtaining
- methyl
- dihydropyridine
- ethyl
- procedure
- 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.)
- Granted
Links
- 238000000034 method Methods 0.000 title abstract 5
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 abstract 2
- KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 abstract 2
- NQRYJNQNLNOLGT-UHFFFAOYSA-N Piperidine Chemical compound C1CCNCC1 NQRYJNQNLNOLGT-UHFFFAOYSA-N 0.000 abstract 2
- YNGDWRXWKFWCJY-UHFFFAOYSA-N 1,4-Dihydropyridine Chemical compound C1C=CNC=C1 YNGDWRXWKFWCJY-UHFFFAOYSA-N 0.000 abstract 1
- LLMLNAVBOAMOEE-UHFFFAOYSA-N 2,3-dichlorobenzaldehyde Chemical compound ClC1=CC=CC(C=O)=C1Cl LLMLNAVBOAMOEE-UHFFFAOYSA-N 0.000 abstract 1
- WRQNANDWMGAFTP-UHFFFAOYSA-N Methylacetoacetic acid Chemical compound COC(=O)CC(C)=O WRQNANDWMGAFTP-UHFFFAOYSA-N 0.000 abstract 1
- 229960000583 acetic acid Drugs 0.000 abstract 1
- 239000003377 acid catalyst Substances 0.000 abstract 1
- PNEYBMLMFCGWSK-UHFFFAOYSA-N aluminium oxide Inorganic materials [O-2].[O-2].[O-2].[Al+3].[Al+3] PNEYBMLMFCGWSK-UHFFFAOYSA-N 0.000 abstract 1
- 239000003153 chemical reaction reagent Substances 0.000 abstract 1
- 125000004925 dihydropyridyl group Chemical group N1(CC=CC=C1)* 0.000 abstract 1
- 230000007613 environmental effect Effects 0.000 abstract 1
- YPMPTULBFPFSEQ-PLNGDYQASA-N ethyl (z)-3-aminobut-2-enoate Chemical compound CCOC(=O)\C=C(\C)N YPMPTULBFPFSEQ-PLNGDYQASA-N 0.000 abstract 1
- 239000012362 glacial acetic acid Substances 0.000 abstract 1
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 abstract 1
- 230000035484 reaction time Effects 0.000 abstract 1
- 239000007790 solid phase Substances 0.000 abstract 1
- 239000002904 solvent Substances 0.000 abstract 1
Landscapes
- Hydrogenated Pyridines (AREA)
Abstract
NUEVO PROCEDIMIENTO DE OBTENCION DE 2,6-DIMETIL-4-(2'', 3''-DICLOROFENIL)-1,4-DIHIDROPIRIDIN-3,5-DICARBOXILATO DE 3-ETIL-5-METIL, VERIFICADO EN DOS ETAPAS. OBTENCION DEL 2-(2'',3''DICLORO) BENCILIDENACETOACETATO DE METILO A PARTIR DEL ACETOACETATO DE METILO Y EL 2,3-DICLOROBENZALDEHIDO EN PRESENCIA DE PIPERIDINA, ACIDO ACETICO GLACIAL E ISOPROPANOL. UN SEGUNDO PASO, DONDE SE TRATA CON 3-AMINOCROTONATO DE ETILO EN PRESENCIA DE ALUMINA ACTIVADA PARA DAR EL PRODUCTO TITULADO. VENTAJAS QUE SE OBTIENEN MEDIANTE ESTE PROCEDIMIENTO EN RELACION AL ESTADO ANTERIOR DE LA TECNICA: A) PROCESOS REALIZADOS EN CONDICIONES RAPIDAS, SUAVES Y SENCILLAS, OBTENIENDOSE PRODUCTOS DE ALTA CALIDAD. B) EL TIEMPO DE REACCION ES MENOR. C) EL ULTIMO PASO SE REALIZA EN FASE SOLIDA, EVITANDO TRAZAS DE DIHIDROPIRIDINAS SIMETRICAS. D) OBTENCION DE LA DIHIDROPIRIDINA SIN DISOLVENTE, MINIMA PRODUCCION DE EFLUENTES CONTAMINANTES. E) UTILIZACION DE CATALIZADORES BASICOS O ACIDOS RECICLABLES. F) BAJO COSTO DE LOS PROCESOS, MINIMIZACION DE REACTIVOS Y RESIDUOS. G) BAJO IMPACTO AMBIENTAL.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| ES9201890A ES2055652B1 (es) | 1992-09-22 | 1992-09-22 | Procedimiento de obtencion de 2,6-dimetil-4-(2,3-diclorofenil)-1,4-dihidropiridin-3,5-dicarboxilato de 3-etil-5-metil. |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| ES9201890A ES2055652B1 (es) | 1992-09-22 | 1992-09-22 | Procedimiento de obtencion de 2,6-dimetil-4-(2,3-diclorofenil)-1,4-dihidropiridin-3,5-dicarboxilato de 3-etil-5-metil. |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| ES2055652A1 true ES2055652A1 (es) | 1994-08-16 |
| ES2055652B1 ES2055652B1 (es) | 1995-03-01 |
Family
ID=8278203
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| ES9201890A Expired - Fee Related ES2055652B1 (es) | 1992-09-22 | 1992-09-22 | Procedimiento de obtencion de 2,6-dimetil-4-(2,3-diclorofenil)-1,4-dihidropiridin-3,5-dicarboxilato de 3-etil-5-metil. |
Country Status (1)
| Country | Link |
|---|---|
| ES (1) | ES2055652B1 (es) |
Cited By (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| EP1089974A4 (en) * | 1995-12-28 | 2001-05-30 | Hoechst Celanese Corp | PROCESS FOR THE PREPARATION OF DIHYDROPYRIDINE AND DERIVATIVES |
| ES2177409A1 (es) * | 2000-08-02 | 2002-12-01 | Liconsa Liberacion Controlada | Procedimiento para la obtencion de 1,4-dihidropiridinas substituida utiles para el tratamiento de la hipertension. |
Families Citing this family (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN101613280B (zh) * | 2009-05-13 | 2012-10-17 | 合肥立方制药股份有限公司 | 非洛地平合成中间体2,3-二氯亚苄基乙酰乙酸甲酯的制备方法 |
Citations (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| EP0234776A2 (en) * | 1986-02-12 | 1987-09-02 | Merck & Co. Inc. | Process for 1,4-dihydropyridine compounds |
| EP0311053A2 (en) * | 1987-10-06 | 1989-04-12 | Banyu Pharmaceutical Co., Ltd. | Ameliorant of cerebral circulation and optical isomer of nb-818, processes for its production and its use |
| EP0383320A1 (en) * | 1989-02-17 | 1990-08-22 | Boehringer Mannheim Italia S.P.A. | A process for preparation of enantiomerically pure polysubstituted 1,4-dihydropyridines |
-
1992
- 1992-09-22 ES ES9201890A patent/ES2055652B1/es not_active Expired - Fee Related
Patent Citations (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| EP0234776A2 (en) * | 1986-02-12 | 1987-09-02 | Merck & Co. Inc. | Process for 1,4-dihydropyridine compounds |
| EP0311053A2 (en) * | 1987-10-06 | 1989-04-12 | Banyu Pharmaceutical Co., Ltd. | Ameliorant of cerebral circulation and optical isomer of nb-818, processes for its production and its use |
| EP0383320A1 (en) * | 1989-02-17 | 1990-08-22 | Boehringer Mannheim Italia S.P.A. | A process for preparation of enantiomerically pure polysubstituted 1,4-dihydropyridines |
Cited By (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| EP1089974A4 (en) * | 1995-12-28 | 2001-05-30 | Hoechst Celanese Corp | PROCESS FOR THE PREPARATION OF DIHYDROPYRIDINE AND DERIVATIVES |
| ES2177409A1 (es) * | 2000-08-02 | 2002-12-01 | Liconsa Liberacion Controlada | Procedimiento para la obtencion de 1,4-dihidropiridinas substituida utiles para el tratamiento de la hipertension. |
Also Published As
| Publication number | Publication date |
|---|---|
| ES2055652B1 (es) | 1995-03-01 |
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Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| PC2A | Transfer of patent |
Owner name: RECORDATI ELMU, S.L. |
|
| FD1A | Patent lapsed |
Effective date: 20001204 |