NUEVOS DERIVADOS DE BENC(E)INDENO, PROCEDIMIENTO DE PREPARARLOS, COMPOSICION FARMACEUTICA QUE LOS CONTIENE, PROCEDIMIENTO DE PREPARARLA Y UTILIZACION DE AQUELLOS
NUEVOS DERIVADOS DE BENC[E]INDENO, PROCEDIMIENTO DE PREPARARLOS, COMPOSICION FARMACEUTICA QUE LOS CONTIENE, PROCEDIMIENTO DE PREPARARLA Y UTILIZACION DE AQUELLOS. LOS DERIVADOS RESPONDEN A LA FORMULA GENERAL (I) EN LA CUAL A REPRESENTA UN GRUPO DE LA FORMULA ALK-NR1R2 O REPRESENTA PIRIMIDINO, 2,3-EP...
Saved in:
Main Authors | , , , , , |
---|---|
Format | Patent |
Language | Spanish |
Published |
01.02.1998
|
Edition | 6 |
Subjects | |
Online Access | Get full text |
Cover
Loading…
Abstract | NUEVOS DERIVADOS DE BENC[E]INDENO, PROCEDIMIENTO DE PREPARARLOS, COMPOSICION FARMACEUTICA QUE LOS CONTIENE, PROCEDIMIENTO DE PREPARARLA Y UTILIZACION DE AQUELLOS. LOS DERIVADOS RESPONDEN A LA FORMULA GENERAL (I) EN LA CUAL A REPRESENTA UN GRUPO DE LA FORMULA ALK-NR1R2 O REPRESENTA PIRIMIDINO, 2,3-EPOXIPROPILO O UN GRUPO DE LA FORMULA -C(O)NHR3. SE PREPARAN HACIENDO REACCIONAR OTROS DERIVADOS DE BENC[E]INDENO Y, SI SE DESEA, CONVIRTIENDO UN COMPUESTO DE LA FORMULA (I) ASI OBTENIDO EN UNA SAL DE ADICION DE ACIDO O UN DERIVADO DE AMONIO CUATERNARIO FAMACEUTICAMENTE ACEPTABLES, O LIBERANDO UNA BASE LIBRE DE LA FORMULA (I) DE UNA SAL DE LA MISMA Y/O SEPARANDO LOS ESTEREOISOMEROS Y/O LOS ISOMEROS OPTIMAMENTE ACTIVOS. LA INVENCION ES APLICABLE A LA PREPARACION DE COMPOSICIONES QUE POSEEN, ENTRE OTROS, EFECTOS ANTICONVULSIVOS Y ANTIANGINALES Y QUE SE EMPLEAN EN EL TRATAMIENTO DE CIERTAS ENFERMEDADES.
A subject-matter of the invention are benz[e]indene derivatives of the generel formula wherein A represents a group of the formula in which latter alk means a C2-7 alkylene group, optionally substituted by a hydroxy group and R1 and R2 stand independently for hydrogen or a C1-7 alkyl, C2-7 alkenyl, C2-7 alkynyl, C3-7 cycloalkyl, mono-(C1-7)alkylamino-(C1-7)alkyl or di-(C1-7)alkylamino-(C1-7)alkyl group or R1 and R2 together with the nitrogen atom to which they are attached form a 4 to 7 membered heterocyclic ring, optionally comprising an oxygen atom or a further nitrogen atom, which latter may be substituted by a phenyl, benzyl, pyridyl, pyrimidinyl or C1-3 alkyl group which latter ones, in turn, may be substituted by a hydroxy or methoxy group or a halogen atom or a halophenyl group or R1 and R2 together with the nitrogen atom to which they are attached form a phthalimido group or A means a pyrimidino group, a 2,3-(epoxy)-propyl group or a group of the formula in which latter R3 stands for a C1-7 alkyl, C2-7 alkenyl or C3-8 cycloalkyl group and R denotes hydrogen or a C1-7 alkyl group, and their stereoisomers and optically active isomers and mixtures thereof, as well as acid addition salts and quaternary ammonium derivatives of these compounds. Moreover there are provided for a process for preparing these compounds, medicaments containing them and the use of these compounds. |
---|---|
AbstractList | NUEVOS DERIVADOS DE BENC[E]INDENO, PROCEDIMIENTO DE PREPARARLOS, COMPOSICION FARMACEUTICA QUE LOS CONTIENE, PROCEDIMIENTO DE PREPARARLA Y UTILIZACION DE AQUELLOS. LOS DERIVADOS RESPONDEN A LA FORMULA GENERAL (I) EN LA CUAL A REPRESENTA UN GRUPO DE LA FORMULA ALK-NR1R2 O REPRESENTA PIRIMIDINO, 2,3-EPOXIPROPILO O UN GRUPO DE LA FORMULA -C(O)NHR3. SE PREPARAN HACIENDO REACCIONAR OTROS DERIVADOS DE BENC[E]INDENO Y, SI SE DESEA, CONVIRTIENDO UN COMPUESTO DE LA FORMULA (I) ASI OBTENIDO EN UNA SAL DE ADICION DE ACIDO O UN DERIVADO DE AMONIO CUATERNARIO FAMACEUTICAMENTE ACEPTABLES, O LIBERANDO UNA BASE LIBRE DE LA FORMULA (I) DE UNA SAL DE LA MISMA Y/O SEPARANDO LOS ESTEREOISOMEROS Y/O LOS ISOMEROS OPTIMAMENTE ACTIVOS. LA INVENCION ES APLICABLE A LA PREPARACION DE COMPOSICIONES QUE POSEEN, ENTRE OTROS, EFECTOS ANTICONVULSIVOS Y ANTIANGINALES Y QUE SE EMPLEAN EN EL TRATAMIENTO DE CIERTAS ENFERMEDADES.
A subject-matter of the invention are benz[e]indene derivatives of the generel formula wherein A represents a group of the formula in which latter alk means a C2-7 alkylene group, optionally substituted by a hydroxy group and R1 and R2 stand independently for hydrogen or a C1-7 alkyl, C2-7 alkenyl, C2-7 alkynyl, C3-7 cycloalkyl, mono-(C1-7)alkylamino-(C1-7)alkyl or di-(C1-7)alkylamino-(C1-7)alkyl group or R1 and R2 together with the nitrogen atom to which they are attached form a 4 to 7 membered heterocyclic ring, optionally comprising an oxygen atom or a further nitrogen atom, which latter may be substituted by a phenyl, benzyl, pyridyl, pyrimidinyl or C1-3 alkyl group which latter ones, in turn, may be substituted by a hydroxy or methoxy group or a halogen atom or a halophenyl group or R1 and R2 together with the nitrogen atom to which they are attached form a phthalimido group or A means a pyrimidino group, a 2,3-(epoxy)-propyl group or a group of the formula in which latter R3 stands for a C1-7 alkyl, C2-7 alkenyl or C3-8 cycloalkyl group and R denotes hydrogen or a C1-7 alkyl group, and their stereoisomers and optically active isomers and mixtures thereof, as well as acid addition salts and quaternary ammonium derivatives of these compounds. Moreover there are provided for a process for preparing these compounds, medicaments containing them and the use of these compounds. |
Author | BLASKO GABOR GYERTYAN ISTVAN SIMIG GYULA REITER KLARA BUDAI ZOLTAN MEZEI TIBOR |
Author_xml | – fullname: GYERTYAN ISTVAN – fullname: BUDAI ZOLTAN – fullname: BLASKO GABOR – fullname: MEZEI TIBOR – fullname: SIMIG GYULA – fullname: REITER KLARA |
BookMark | eNqNjMsKwjAURLPQha9_uEuFCj5Q7PI2vcVAm8Q0LeimFIkraQv1h_xTo7gWVzMw58yYDZq2cSP2lAWVKoeYjCgx_jSISPI5LYSMSaoAtFGcYpEJkla9d21Io0GTqjwArjKtcsGFkpCgyZBTYQVHOBUEnvCAtF6lX0cIZ_BWKi74OfIbej_1_pQNb_W9d7NvThgkZPlx6bq2cn1XX13jHhXlm1UY7neHaL39A3kB08pGkQ |
ContentType | Patent |
DBID | EVB |
DatabaseName | esp@cenet |
DatabaseTitleList | |
Database_xml | – sequence: 1 dbid: EVB name: esp@cenet url: http://worldwide.espacenet.com/singleLineSearch?locale=en_EP sourceTypes: Open Access Repository |
DeliveryMethod | fulltext_linktorsrc |
Discipline | Medicine Chemistry Sciences |
Edition | 6 |
ExternalDocumentID | ES2099658B1 |
GroupedDBID | EVB |
ID | FETCH-epo_espacenet_ES2099658B13 |
IEDL.DBID | EVB |
IngestDate | Fri Jul 19 13:03:20 EDT 2024 |
IsOpenAccess | true |
IsPeerReviewed | false |
IsScholarly | false |
Language | Spanish |
LinkModel | DirectLink |
MergedId | FETCHMERGED-epo_espacenet_ES2099658B13 |
Notes | Application Number: ES19930002234 |
OpenAccessLink | https://worldwide.espacenet.com/publicationDetails/biblio?FT=D&date=19980201&DB=EPODOC&CC=ES&NR=2099658B1 |
ParticipantIDs | epo_espacenet_ES2099658B1 |
PublicationCentury | 1900 |
PublicationDate | 19980201 |
PublicationDateYYYYMMDD | 1998-02-01 |
PublicationDate_xml | – month: 02 year: 1998 text: 19980201 day: 01 |
PublicationDecade | 1990 |
PublicationYear | 1998 |
RelatedCompanies | EGIS GYOGYSZERGYAR RT |
RelatedCompanies_xml | – name: EGIS GYOGYSZERGYAR RT |
Score | 2.4804327 |
Snippet | NUEVOS DERIVADOS DE BENC[E]INDENO, PROCEDIMIENTO DE PREPARARLOS, COMPOSICION FARMACEUTICA QUE LOS CONTIENE, PROCEDIMIENTO DE PREPARARLA Y UTILIZACION DE... |
SourceID | epo |
SourceType | Open Access Repository |
SubjectTerms | ACYCLIC OR CARBOCYCLIC COMPOUNDS CHEMISTRY HETEROCYCLIC COMPOUNDS HUMAN NECESSITIES HYGIENE MEDICAL OR VETERINARY SCIENCE METALLURGY ORGANIC CHEMISTRY PREPARATIONS FOR MEDICAL, DENTAL, OR TOILET PURPOSES SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS ORMEDICINAL PREPARATIONS |
Title | NUEVOS DERIVADOS DE BENC(E)INDENO, PROCEDIMIENTO DE PREPARARLOS, COMPOSICION FARMACEUTICA QUE LOS CONTIENE, PROCEDIMIENTO DE PREPARARLA Y UTILIZACION DE AQUELLOS |
URI | https://worldwide.espacenet.com/publicationDetails/biblio?FT=D&date=19980201&DB=EPODOC&locale=&CC=ES&NR=2099658B1 |
hasFullText | 1 |
inHoldings | 1 |
isFullTextHit | |
isPrint | |
link | http://utb.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwfV3dT8IwEG8IGvVNUSN-pQ-GaMKibmzCw2K6rgszrJ37IOgLoWwmvACRGf8e_1NvFdAXeWt2vUt2y93veuuvRejq7i2XAIxSU_23sluldayxrrVkZhjmCFAiL_nOAbe6aetpYA4qaLLiwqhzQj_V4YgQUWOI90Ll6_lvE8tVeysXt3ICj2aPXmK7jWxFF4Pq577hOjYLhStog1Ibiioe2SVDFMDWgYXSFlTRD2UwsL5TklLmfxHF20fbIRibFgeoki9qaJeuLl6roZ1g-b8bhsvQWxyiL56yvoixCyuvPnHVCDuM02t243OXcdHEYSQocyEdMZ6IUg7-DUlEop6Im5iKIBSxTyF7Yo9EAaEsTXxK8HPKMMyACTwBVbbJEMEvGLR6_itRhkBGQL8H-kcIeyyhXQ3edbj265DFa68Yx6g6nU3zE4RHVkfmmS7LS8hbZnssDalLqVttU7eMTB_VUf1fM6cbZGdo74fPV24FOUfV4v0jvwBAL-Sl-hTfgrWY-Q |
link.rule.ids | 230,309,783,888,25576,76876 |
linkProvider | European Patent Office |
linkToHtml | http://utb.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwfV3dT8IwEG8IGvVNUSN-9sEQTVjUjU14WEzXdWG6tXMfBH0hlM2EFyAy49_jf-ptAvoib82ud8luuftdb_21CF3evmUSgFEqZf-t6FYpHWOkKi2Zapo-BJTICr6zz41u0nrs6_0KGi-5MOU5oZ_l4YgQUSOI97zM17PfJpZd7q2c38gxPJo-OLFpN9IlXQyqn7uGbZksELagDUpNKKp4aBYMUQBbCxZKG1Bh3xfBwHpWQUqZ_UUUZxdtBmBsku-hSjavoW26vHithrb8xf9uGC5Cb76PvnjCeiLCNqy8esQuR9hinF6xa5fbjIsmDkJBmQ3piPFYFHLwb0BCEnoiamIq_EBELoXsiR0S-oSyJHYpwc8JwzADJvAYVNk6QwS_YNDy3FdSGgIZAX0P9A8QdlhMuwq862Dl1wGLVl7RDlF1Mp1kRwgPjY7MUlUWl5C39PZIalKVUjXaumpoqTqso_q_Zo7XyC7Qdjf2vYHn8qcTtPPD7Su2hZyiav7-kZ0BuOfyvPws392Tm-w |
openUrl | ctx_ver=Z39.88-2004&ctx_enc=info%3Aofi%2Fenc%3AUTF-8&rfr_id=info%3Asid%2Fsummon.serialssolutions.com&rft_val_fmt=info%3Aofi%2Ffmt%3Akev%3Amtx%3Apatent&rft.title=NUEVOS+DERIVADOS+DE+BENC%28E%29INDENO%2C+PROCEDIMIENTO+DE+PREPARARLOS%2C+COMPOSICION+FARMACEUTICA+QUE+LOS+CONTIENE%2C+PROCEDIMIENTO+DE+PREPARARLA+Y+UTILIZACION+DE+AQUELLOS&rft.inventor=GYERTYAN+ISTVAN&rft.inventor=BUDAI+ZOLTAN&rft.inventor=BLASKO+GABOR&rft.inventor=MEZEI+TIBOR&rft.inventor=SIMIG+GYULA&rft.inventor=REITER+KLARA&rft.date=1998-02-01&rft.externalDBID=B1&rft.externalDocID=ES2099658B1 |