ES2038660T3 - Un procedimiento para la preparacion de nuevos benzopiranos con actividad farmacologica. - Google Patents
Un procedimiento para la preparacion de nuevos benzopiranos con actividad farmacologica.Info
- Publication number
- ES2038660T3 ES2038660T3 ES198787303967T ES87303967T ES2038660T3 ES 2038660 T3 ES2038660 T3 ES 2038660T3 ES 198787303967 T ES198787303967 T ES 198787303967T ES 87303967 T ES87303967 T ES 87303967T ES 2038660 T3 ES2038660 T3 ES 2038660T3
- Authority
- ES
- Spain
- Prior art keywords
- alkyl
- hydrogen
- optionally replaced
- group
- alcoxi
- 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
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D405/00—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom
- C07D405/02—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing two hetero rings
- C07D405/04—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing two hetero rings directly linked by a ring-member-to-ring-member bond
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D311/00—Heterocyclic compounds containing six-membered rings having one oxygen atom as the only hetero atom, condensed with other rings
- C07D311/02—Heterocyclic compounds containing six-membered rings having one oxygen atom as the only hetero atom, condensed with other rings ortho- or peri-condensed with carbocyclic rings or ring systems
- C07D311/04—Benzo[b]pyrans, not hydrogenated in the carbocyclic ring
- C07D311/58—Benzo[b]pyrans, not hydrogenated in the carbocyclic ring other than with oxygen or sulphur atoms in position 2 or 4
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D311/00—Heterocyclic compounds containing six-membered rings having one oxygen atom as the only hetero atom, condensed with other rings
- C07D311/02—Heterocyclic compounds containing six-membered rings having one oxygen atom as the only hetero atom, condensed with other rings ortho- or peri-condensed with carbocyclic rings or ring systems
- C07D311/04—Benzo[b]pyrans, not hydrogenated in the carbocyclic ring
- C07D311/58—Benzo[b]pyrans, not hydrogenated in the carbocyclic ring other than with oxygen or sulphur atoms in position 2 or 4
- C07D311/68—Benzo[b]pyrans, not hydrogenated in the carbocyclic ring other than with oxygen or sulphur atoms in position 2 or 4 with nitrogen atoms directly attached in position 4
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D405/00—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom
- C07D405/14—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing three or more hetero rings
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
Abstract
COMPUESTOS DE LA FORMULA (I) Y LAS SALES FARMACEUTICAMENTE ACEPTABLES DE LOS MISMOS: EN DONDE: Y ES N O (CUANDO R3 ES HIDROXI, ALCOXI C1-6 O ACILOXI C1-7) CH; UNO DE R1 Y R2 ES HIDROGENO O ALQUILO C1-4 Y EL OTRO ES ALQUILO C1-4 O R1 Y R2 JUNTOS SON POLIMETILENO C2-5; R3 ES HIDROGENO, HIDROXI, ALCOXI C1-6 O ACILOXI C1-7; R4 ES UN GRUPO CICLOALQUILO C3-8 O UN GRUPO ALQUILO C1-6 OPCIONALMENTE SUSTITUIDO POR UN GRUPO R7 QUE ES HIDROXI, ALCOXI C1-6, AMINO OPCIONALMENTE SUSTITUIDO POR UNO O MAS GRUPOS ALQUILO C1-6; ALCANOILAMINO C1-7, CICLOALQUILOXI C3-8, CICLOALQUILAMINO C3-8 O 1,3-DIOXO-2-ISOINDOLINA; CUANDO Y ES N, R5 ES HIDROGENO, ALQUILO C1-6 OPCIONALMENTE SUSTITUIDO POR HALOGENO, HIDROXI, ALCOXI C1-6, ALCOXICARBONILO C1-6, CARBOXI O AMINO OPCIONALMENTE SUSTITUIDO POR UNO O DOS GRUPOS ALQUILO C1-6 INDEPENDIENTES O ALQUENILO C2-6, AMINO OPCIONALMENTE SUSTITUIDO POR UN GRUPO ALQUILO C1-6, CICLOALQUILO C3-8 O ALQUENILO C1-6 O POR UN GRUPO ALCANOILO C1-6 OPCIONALMENTE SUSTITUIDO POR HASTA TRES ATOMOS DE HALO, POR UN GRUPO FENILO OPCIONALMENTE SUSTITUIDO POR ALQUILO C1-6, ALCOXI C1-6 O HALOGENO O ARILO O HETEROARILO, SIENDO BIEN OPCIONALMENTE SUSTITUIDO POR UNO O MAS GRUPOS O ATOMOS SELECCIONADOS DE LA CLASE DE ALQUILO C1-6, ALCOXI C1-6, HIDROXI, HALOGENO, TRIFLUOROMETILO, NITRO, CIANO, ACILO CARBOXILICO C1-12 O AMINO O AMINOCARBONILO OPCIONALMENTE SUSTITUIDO POR UNO O DOS GRUPOS ALQUILO C1-6 Y R6 ES HIDROGENO O ALQUILO C1-6 O R5 Y R6 JUNTOS SON -CH2-(CH2)N-Z(CH2)MNDE M Y N SON DE 0 A 2 DE TAL MODO QUE M + N ES 1 O 2 Y Z ES CH2, O, S O NR EN DONDE R ES HIDROGENO, ALQUILO C1-9, ALCANOILO C2-7, FENILALQUILO C1-4, NAFTILCARBONILO, FENILCARBONILO O BENCILCARBONILO OPCIONALMENTE SUSTITUIDO EN EL ANILLO FENILO O NAFTILO POR UNO O DOS DE ALQUILO C1-6, ALCOXI C16 O HALOGENO; HETEROARILCARBONILO MONO 8R9 EN DONDE R8 Y R9 SON, INDEPENDIENTEMENTE, ALQUILO C1-6, R8 ES HIDROGENO Y R9 ES ALQUILO C1-6 O R8 Y R9 JUNTOS SON POLIMETILENO C4-5; O R6 Y R8 JUNTO SON -(CH2)P R9 ES HIDROGENO O ALQUILO C1-6; O R5 ES CH2R10 EN DONDE R10 ES HIDROGENO O ALQUILO C1-5; O R6 Y R10 SON -(CH2)Q 2 O 3; X ES OXIGENO O AZUFRE; O R5, R6, X E Y (CUANDO ES N) SON JUNTOS TETRAHIDROISOQUINOLINONA O TETRAHIDROISOQUINOLINTIONA, OPCIONALMENTE SUSTITUIDAS EN EL ANILLO DE FENILO TAL Y COMO SE HA DEFINIDO ANTES PARA R; EL GRUPO QUE CONTIENE NITROGENO SE ENCUENTRA EN LA POSICION 4 SIENDO TRANS AL GRUPO R3 CUANDO R3 ES HIDROXI, ALCOXI C1-6 O ACILOXI C1-7; TIENE UNA ACTIVIDAD ACTIVADORA DEL CANAL K +, PROCESOS PARA SU PREPARACION Y SU USO COMO PRODUCTOS FARMACEUTICOS.
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GB868610911A GB8610911D0 (en) | 1986-05-03 | 1986-05-03 | Active compounds |
GB868623768A GB8623768D0 (en) | 1986-10-03 | 1986-10-03 | Active compounds |
Publications (1)
Publication Number | Publication Date |
---|---|
ES2038660T3 true ES2038660T3 (es) | 1993-08-01 |
Family
ID=26290724
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
ES198787303967T Expired - Lifetime ES2038660T3 (es) | 1986-05-03 | 1987-05-01 | Un procedimiento para la preparacion de nuevos benzopiranos con actividad farmacologica. |
Country Status (10)
Country | Link |
---|---|
US (2) | US4943582A (es) |
EP (1) | EP0250077B1 (es) |
AU (1) | AU599975B2 (es) |
CA (1) | CA1308105C (es) |
DE (1) | DE3775628D1 (es) |
DK (1) | DK224687A (es) |
ES (1) | ES2038660T3 (es) |
GR (1) | GR3003504T3 (es) |
NZ (1) | NZ220171A (es) |
PT (1) | PT84806B (es) |
Families Citing this family (30)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4971982A (en) * | 1987-07-06 | 1990-11-20 | Hoffmann-La Roche Inc. | Benzopyran derivatives |
GB8800199D0 (en) * | 1988-01-06 | 1988-02-10 | Beecham Group Plc | Pharmaceutical preparation |
US5021432A (en) * | 1988-04-26 | 1991-06-04 | Yoshitomi Pharmaceutical Industries, Ltd. | Benzopyran compound and its pharmaceutical use |
EP0346724A1 (de) * | 1988-06-16 | 1989-12-20 | MERCK PATENT GmbH | Chromanderivate |
US5364878A (en) * | 1988-07-19 | 1994-11-15 | Hoechst Aktiengesellschaft | Use of substituted 3,4-dihydro-2H-benzopyrans as remedies for obstructive functional disorders of the lungs |
ES2071668T3 (es) * | 1988-12-13 | 1995-07-01 | Beecham Group Plc | Benzopirano y compuestos relacionados. |
US5104890A (en) * | 1989-03-28 | 1992-04-14 | Fujisawa Pharmaceutical Company, Ltd. | Benzopyran derivatives and processes for preparation thereof |
DE3918041A1 (de) * | 1989-06-02 | 1990-12-06 | Merck Patent Gmbh | Chromanderivate |
DE3926001A1 (de) * | 1989-08-05 | 1991-02-07 | Merck Patent Gmbh | Chromanderivate |
GB8918298D0 (en) * | 1989-08-10 | 1989-09-20 | Beecham Group Plc | Novel compounds |
GB8924373D0 (en) * | 1989-10-30 | 1989-12-20 | Beecham Group Plc | Novel compounds |
GB9002458D0 (en) * | 1990-02-03 | 1990-04-04 | Beecham Group Plc | Pharmaceuticals |
FR2661676A1 (fr) * | 1990-05-02 | 1991-11-08 | Lipha | Derives d'amino benzocycloalcanes, procedes de preparation et medicaments les contenant. |
US5276168A (en) * | 1990-06-18 | 1994-01-04 | E. R. Squibb & Sons, Inc. | Benzopyran derivatives and heterocyclic analogs thereof as antiischemic agents |
FR2670780B1 (fr) * | 1990-12-20 | 1993-07-09 | Synthelabo | Derives de 4-(acylamino)benzopyranes, leur preparation et leur application en therapeutique. |
EP0508425A1 (en) | 1991-04-12 | 1992-10-14 | Schering Corporation | Bicyclic amides as inhibitors of acyl-coenzyme a: cholesterol acyl transferase |
GB9112721D0 (en) * | 1991-06-13 | 1991-07-31 | Smithkline Beecham Plc | Novel treatment |
US5624954A (en) * | 1991-06-13 | 1997-04-29 | Smithkline Beecham P.L.C. | Benzo- and pyridopyran derivatives having anxiolytic and anti-convulsant activity |
US5240943A (en) * | 1991-12-19 | 1993-08-31 | G. D. Searle & Co. | Benzopyran class iii antiarrhythmic agents |
US5416118A (en) * | 1992-04-09 | 1995-05-16 | Schering Corporation | Bicyclic amides as inhibitors of acyl-coenzyme A: cholesterol acyl transferase |
GR1002276B (el) * | 1992-10-08 | 1996-05-02 | Smithkline Beecham P.L.C. | Παραγωγα βενζοπυρανιου τα οποια κεκτηνται δραση κνς. |
AP360A (en) * | 1992-12-04 | 1994-09-07 | Smithkline Beecham Plc | Benzo-and pyridopyran derivatives having anxiolytic and anticonvulsant activity. |
US5837702A (en) * | 1993-10-07 | 1998-11-17 | Bristol-Myers Squibb Co. | 4-arylamino-benzopyran and related compounds |
GB9411635D0 (en) * | 1994-06-10 | 1994-08-03 | Smithkline Beecham Plc | Novel treatment |
US5574049A (en) * | 1994-07-22 | 1996-11-12 | Sandoz Ltd. | 2,2-dialkyl- and 2,2-dialkyl-3,4-dihydro-3-hydroxy-2H-1-benzopyrans |
US5629429A (en) * | 1995-06-07 | 1997-05-13 | Bristol-Myers Squibb Company | Process for preparing 4-arylamino-benzopyran and related compounds |
US5612370A (en) * | 1995-06-07 | 1997-03-18 | Bristol-Myers Squibb Company | Phenylglycine and phenylalaninen amido benzopyran derivatives |
US5612323A (en) * | 1995-06-07 | 1997-03-18 | Bristol-Myers Squibb Company | Phosphinic ester substituted benzopyran derivatives |
US5869478A (en) * | 1995-06-07 | 1999-02-09 | Bristol-Myers Squibb Company | Sulfonamido substituted benzopyran derivatives |
FR2763335B1 (fr) * | 1997-05-16 | 2000-11-24 | Adir | Nouveaux composes heterocycliques substitues, leur procede de preparation et les compositions pharmaceutiques qui les contiennent |
Family Cites Families (20)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4062870A (en) * | 1974-05-31 | 1977-12-13 | Beecham Group Limited | Chroman derivatives |
US4016226A (en) * | 1975-02-10 | 1977-04-05 | The Babcock & Wilcox Company | Method of making porous nuclear fuel |
NZ183551A (en) * | 1976-04-02 | 1978-09-20 | Beecham Group Ltd | Aminochromanols and pharmaceutical compositions containingthem |
DE3064285D1 (en) * | 1979-09-28 | 1983-08-25 | Beecham Group Plc | Chromanol derivatives, a process for their preparation and a pharmaceutical composition comprising them |
EP0028064B1 (en) * | 1979-09-28 | 1983-07-20 | Beecham Group Plc | Chromanol derivatives, a process for their preparation and a pharmaceutical composition comprising them |
ATE23718T1 (de) * | 1981-09-25 | 1986-12-15 | Beecham Group Plc | Benzopyran-verbindungen mit pharmazeutischer wirkung. |
NZ213469A (en) * | 1981-09-25 | 1986-04-11 | Beecham Group Plc | Benzopyran compounds as intermediates |
DE3368629D1 (en) * | 1982-04-28 | 1987-02-05 | Beecham Group Plc | Novel chromenes and chromans |
DE3368057D1 (en) * | 1982-05-21 | 1987-01-15 | Beecham Group Plc | Pharmaceutically active aminobenzopyrans |
GB8308064D0 (en) * | 1983-03-24 | 1983-05-05 | Beecham Group Plc | Active compounds |
GB8308062D0 (en) * | 1983-03-24 | 1983-05-05 | Beecham Group Plc | Active compounds |
EP0126367B1 (en) * | 1983-05-18 | 1994-10-12 | Beecham Group Plc | Chroman and chromene derivatives |
GB8313679D0 (en) * | 1983-05-18 | 1983-06-22 | Beecham Group Plc | Active compounds |
DE3479726D1 (de) * | 1983-05-18 | 1989-10-19 | Beecham Group Plc | Benzopyran derivatives. |
EP0139992B1 (en) * | 1983-09-01 | 1988-12-28 | Beecham Group Plc | Chromanol derivatives |
GB8419515D0 (en) * | 1984-07-31 | 1984-09-05 | Beecham Group Plc | Treatment |
GB8419516D0 (en) * | 1984-07-31 | 1984-09-05 | Beecham Group Plc | Treatment |
GB8513369D0 (en) * | 1985-05-28 | 1985-07-03 | Beecham Group Plc | Treatment |
EP0218373B1 (en) * | 1985-09-11 | 1990-03-07 | Beecham Group Plc | Chroman derivatives and analogues having antihypertensive activity |
US4853410A (en) * | 1986-01-17 | 1989-08-01 | Pfizer Inc. | Hydroxyacetic acid derivatives for the treatment of diabetic complications |
-
1987
- 1987-04-30 PT PT84806A patent/PT84806B/pt not_active IP Right Cessation
- 1987-05-01 US US07/045,626 patent/US4943582A/en not_active Expired - Fee Related
- 1987-05-01 EP EP87303967A patent/EP0250077B1/en not_active Expired - Lifetime
- 1987-05-01 NZ NZ220171A patent/NZ220171A/xx unknown
- 1987-05-01 ES ES198787303967T patent/ES2038660T3/es not_active Expired - Lifetime
- 1987-05-01 DE DE8787303967T patent/DE3775628D1/de not_active Expired - Fee Related
- 1987-05-01 DK DK224687A patent/DK224687A/da not_active Application Discontinuation
- 1987-05-01 CA CA000536173A patent/CA1308105C/en not_active Expired - Fee Related
- 1987-05-01 AU AU72429/87A patent/AU599975B2/en not_active Ceased
-
1989
- 1989-12-06 US US07/447,002 patent/US5075460A/en not_active Expired - Fee Related
-
1992
- 1992-01-03 GR GR910402053T patent/GR3003504T3/el unknown
Also Published As
Publication number | Publication date |
---|---|
US5075460A (en) | 1991-12-24 |
DK224687D0 (da) | 1987-05-01 |
CA1308105C (en) | 1992-09-29 |
AU7242987A (en) | 1987-11-05 |
EP0250077B1 (en) | 1992-01-02 |
AU599975B2 (en) | 1990-08-02 |
PT84806B (pt) | 1989-12-29 |
DE3775628D1 (de) | 1992-02-13 |
NZ220171A (en) | 1990-05-28 |
US4943582A (en) | 1990-07-24 |
GR3003504T3 (es) | 1993-03-16 |
EP0250077A3 (en) | 1988-01-07 |
PT84806A (en) | 1987-05-01 |
EP0250077A2 (en) | 1987-12-23 |
DK224687A (da) | 1987-11-04 |
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Legal Events
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FG2A | Definitive protection |
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