ES2024969A6 - Procedimiento para la obtencion de tetralonas. - Google Patents
Procedimiento para la obtencion de tetralonas.Info
- Publication number
- ES2024969A6 ES2024969A6 ES9003308A ES9003308A ES2024969A6 ES 2024969 A6 ES2024969 A6 ES 2024969A6 ES 9003308 A ES9003308 A ES 9003308A ES 9003308 A ES9003308 A ES 9003308A ES 2024969 A6 ES2024969 A6 ES 2024969A6
- Authority
- ES
- Spain
- Prior art keywords
- group
- alkyl
- atom
- tetralones
- obtaining
- 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 - Lifetime
Links
- 125000004178 (C1-C4) alkyl group Chemical group 0.000 abstract 4
- 125000004435 hydrogen atom Chemical group [H]* 0.000 abstract 3
- 125000000229 (C1-C4)alkoxy group Chemical group 0.000 abstract 2
- 125000005843 halogen group Chemical group 0.000 abstract 2
- 125000002887 hydroxy group Chemical group [H]O* 0.000 abstract 2
- NHQOHKVSCFCWGQ-UHFFFAOYSA-N 2,7b-dihydro-1aH-naphtho[1,2-b]oxiren-3-one Chemical compound O1C2CC(C3=CC=CC=C3C21)=O NHQOHKVSCFCWGQ-UHFFFAOYSA-N 0.000 abstract 1
- IAZDPXIOMUYVGZ-UHFFFAOYSA-N Dimethylsulphoxide Chemical compound CS(C)=O IAZDPXIOMUYVGZ-UHFFFAOYSA-N 0.000 abstract 1
- KEAYESYHFKHZAL-UHFFFAOYSA-N Sodium Chemical compound [Na] KEAYESYHFKHZAL-UHFFFAOYSA-N 0.000 abstract 1
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical group [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 abstract 1
- 150000001408 amides Chemical class 0.000 abstract 1
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical group [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 abstract 1
- 230000008602 contraction Effects 0.000 abstract 1
- 125000004093 cyano group Chemical group *C#N 0.000 abstract 1
- 210000002249 digestive system Anatomy 0.000 abstract 1
- 229960001760 dimethyl sulfoxide Drugs 0.000 abstract 1
- 230000002526 effect on cardiovascular system Effects 0.000 abstract 1
- 239000001257 hydrogen Substances 0.000 abstract 1
- 229910052739 hydrogen Inorganic materials 0.000 abstract 1
- 125000001434 methanylylidene group Chemical group [H]C#[*] 0.000 abstract 1
- 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 abstract 1
- 229910052757 nitrogen Inorganic materials 0.000 abstract 1
- 125000004433 nitrogen atom Chemical group N* 0.000 abstract 1
- 239000001301 oxygen Substances 0.000 abstract 1
- 229910052760 oxygen Inorganic materials 0.000 abstract 1
- -1 polymethylene Polymers 0.000 abstract 1
- 210000002460 smooth muscle Anatomy 0.000 abstract 1
- 229910000104 sodium hydride Inorganic materials 0.000 abstract 1
- 239000012312 sodium hydride Substances 0.000 abstract 1
- 239000002904 solvent Substances 0.000 abstract 1
- 125000000383 tetramethylene group Chemical group [H]C([H])([*:1])C([H])([H])C([H])([H])C([H])([H])[*:2] 0.000 abstract 1
- 125000003258 trimethylene group Chemical group [H]C([H])([*:2])C([H])([H])C([H])([H])[*:1] 0.000 abstract 1
Landscapes
- Nitrogen Condensed Heterocyclic Rings (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
Abstract
PROCEDIMIENTO PARA LA OBTENCION DE TETRALONAS DE FORMULA GENERAL I, UTILES COMO REGULADORES DE LA CONTRACCION DE LA MUSCULATURA LISA EN LOS SISTEMAS CARDIOVASCULAR, BRONCOPULMONAR Y DIGESTIVO: EN DONDE RBS1 REPRESENTA UN ATOMO9 DE HALOGENO O UN GRUPO CIANO, NITRO, CSI1-4 ALCOXI; RBS2 REPRESENTA UN ATOMO DE HIDROGENO O UN GRUPO CSI1-4 ALCOXI; RBS3 REPRESENTA UN ATOMO DE HIDROGENO O UN GRUPO CSI1-4 ALQUILO Y RBS4 ES CSI1-4 ALQUILO O RBS3 Y RBS4 JUNTOS SON POLIMETILENO; RBS5 ES OH O OCOCHSI3 Y RBS6 HIDROGENO, O BIEN RBS5 Y RBS6 JUNTOS FORMAN UN DOBLE ENLACE; RBS7-RBS8 JUNTOS FORMAN UN GRUPO TRIMETILENO O TETRAMETILENO, LOS CUALES ESTAN OPCIONALMENTE SUSTITUIDOS POR UN GRUPO RBS9 O BIEN RBS7-RBS8 REPRESENTAN UN GRUPO -CH=CH-CH=CH- OPCIONALMENTE SUSTITUIDO POR UN GRUPO RBS10 Y UNO DE CUYOS METINOS PUEDE OPCIONALMENTE REEMPLAZARSE POR UN ATOMO DE NITROGENO; RBS9 ES CSI1-4 ALQUILO O HIDROXILO; RBS10 ES UN ATOMO DE HALOGENO O UN GRUPO CSI1-4 ALQUILO O HIDROXILO Y X ES UN ATOMO DE OXIGENO O AZUFRE,CARACTERIZADO PORQUE SE HACE REACCIONAR LA CORRESPONDIENTE 3,4-EPOXITETRALONA CON UNA AMIDA DE FORMULA RBS7NHCORBS8 EN PRESENCIA DE UNA BASE COMO EL HIDRURO SODICO EN UN DISOLVENTE ADECUADO COMO EL DIMETILSULFOXIDO.
Priority Applications (6)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| ES9003308A ES2024969A6 (es) | 1990-12-05 | 1990-12-05 | Procedimiento para la obtencion de tetralonas. |
| EP19910119718 EP0489300A3 (en) | 1990-12-05 | 1991-11-19 | New tetralones with pharmacological activity |
| US07/801,000 US5208246A (en) | 1990-12-05 | 1991-12-02 | Tetralones with pharmacological activity |
| CA002056922A CA2056922A1 (en) | 1990-12-05 | 1991-12-04 | Tetralones with pharmacological activity |
| JP3321840A JPH07113014B2 (ja) | 1990-12-05 | 1991-12-05 | 薬理活性を有する新規なテトラロン |
| US08/006,852 US5272170A (en) | 1990-12-05 | 1993-01-22 | Tetralones with pharmacological activity |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| ES9003308A ES2024969A6 (es) | 1990-12-05 | 1990-12-05 | Procedimiento para la obtencion de tetralonas. |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| ES2024969A6 true ES2024969A6 (es) | 1992-03-01 |
Family
ID=8270210
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| ES9003308A Expired - Lifetime ES2024969A6 (es) | 1990-12-05 | 1990-12-05 | Procedimiento para la obtencion de tetralonas. |
Country Status (1)
| Country | Link |
|---|---|
| ES (1) | ES2024969A6 (es) |
-
1990
- 1990-12-05 ES ES9003308A patent/ES2024969A6/es not_active Expired - Lifetime
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