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ES2628005T3 - 2,3-Benzodiazepinas - Google Patents

2,3-Benzodiazepinas Download PDF

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Publication number
ES2628005T3
ES2628005T3 ES13748072T ES13748072T ES2628005T3 ES 2628005 T3 ES2628005 T3 ES 2628005T3 ES 13748072 T ES13748072 T ES 13748072T ES 13748072 T ES13748072 T ES 13748072T ES 2628005 T3 ES2628005 T3 ES 2628005T3
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alkyl
alkoxy
amino
hydroxy
halo
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Stephan Siegel
Stefan BÄURLE
Arwed Cleve
Bernard Haendler
Amaury Ernesto FERNANDEZ-MONTALVAN
Ursula MÖNNING
Sabine Krause
Pascale Lejeune
Norbert Schmees
Matthias BUSEMANN
Simon Holton
Joachim Kuhnke
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Bayer Pharma AG
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Abstract

Compuestos de fórmula general I **Fórmula** A en la que X representa un átomo de oxígeno o de azufre, y A representa un anillo de heteroarilo monocíclico con 5 o 6 átomos de anillo o representa un anillo de fenilo, y R1a representa hidrógeno, halógeno, ciano, carboxi, amino o aminosulfonilo, o representa un resto alcoxi C1-C6, alcoxi C1-C3-alquilo C1-C3, alcoxi C1-C3-alcoxi C2-C3, alquil C1-C6-amino, alquil C1-C6-carbonilamino, alquil C1-C6-amino-alquilo C1-C6, N-(heterociclil)-alquilo C1-C6, N-(heterociclil)-alcoxi C1-C6, hidroxi-alquilo C1-C6, hidroxi-alcoxi C1-C6, halo-alquilo C1-C6, halo-alcoxi C1-C6, alquil C1-C6-carbonilo o alcoxi C1- C6-carbonilo, orepresenta un resto heterociclilo monocíclico con 3 a 8 átomos de anillo que dado el caso puede estar sustituido una o varias veces, de manera igual o diferente, con halógeno, ciano, nitro, hidroxi, amino, oxo, carboxi, alquilo C1-C6, alcoxi C1-C6, alcoxi C1-C6-alquilo C1-C6, hidroxi-alquilo C1-C6, alquil C1-C6-amino, amino-alquilo C1-C6, alquil C1-C6-amino-alquilo C1-C6, halo-alquilo C1-C6, halo-alcoxi C1-C6, cicloalquilo C3-C10, fenilo, halofenilo, fenil-alquilo C1-C6, piridinilo, -NR6C(>=O)-R9, -C(>=O)-NR6R7, -C(>=O)-R8, -S(>=O)2-NR6R7, -S(>=O)-R9, -S(>=O)2-R9, -NH-S(>=O)2-R9 y/o un resto heterociclilo monocíclico con 3 a 8 átomos de anillo, o representa un resto heteroarilo monocíclico con 5 o 6 átomos de anillo que dado el caso puede estar sustituido una o varias veces, de manera igual o diferente, con halógeno, hidroxi, amino, ciano, nitro, carboxi, alquilo C1-C6, alcoxi C1-C6, alcoxi C1-C6-alquilo C1-C6, alquil C1-C6-amino, amino-alquilo C1-C6, alquil C1-C6-amino-alquilo C1-C6, halo-alquilo C1-C6, halo-alcoxi C1-C6, cicloalquilo C3-C10, -C(>=O)-NR6R7, -C(>=O)-R8, -S(>=O)2-NR6R7, -S(>=O)-R9, - S(>=O)2-R9, -NH-S(>=O)2-R9 y/o con un resto heterociclilo monocíclico con 3 a 8 átomos de anillo, y/o con un resto heteroarilo monocíclico con 5 o 6 átomos de anillo, y/o con un resto fenilo, que a su vez puede estar sustituido dado el caso una o varias veces, de manera igual o diferente, con halógeno, alquilo C1-C3 y/o alcoxi C1-C3, o representa un resto fenilo que dado el caso puede estar sustituido una o varias veces, de manera igual o diferente, con halógeno, amino, hidroxi, ciano, nitro, carboxi, alquilo C1-C6, alcoxi C1-C6, alcoxi C1-C6-alquilo C1- C6, alquil C1-C6-amino, amino-alquilo C1-C6, alquil C1-C6-amino-alquilo C1-C6, -C(>=O)NR6R7, -C(>=O)R8, alquil C1- C3-sulfinilo, alquil C1-C3-sulfonilo, -S(>=O)2NH2, alquil C1-C3-sulfonilamino, alquil C1-C3-aminosulfonilo, cicloalquil C3-C6-aminosulfonilo, halo-alquilo C1-C6, halo-alcoxi C1-C6, hidroxi-alquilo C1-C6, cicloalquilo C3-C10 y/o un resto heterociclilo monocíclico con 3 a 8 átomos de anillo y/o un resto heteroarilo monocíclico con 5 o 6 átomos de anillo, que a su vez dado el caso puede estar sustituido una o varias veces, de manera igual o diferente, con halógeno, alquilo C1-C3 y/o alcoxi C1-C3, y R1b y R1c representan, independientemente entre sí, hidrógeno, halógeno, hidroxi, ciano, nitro y/o representan un resto alquilo C1-C6, alcoxi C1-C6, alcoxi C1-C6-alquilo C1-C6, halo-alquilo C1-C6, halo-alcoxi C1-C6, cicloalquilo C3- C10 y/o un resto heterociclilo monocíclico con 3 a 8 átomos de anillo, y R2 representa un resto alquilo C1-C3 o trifluorometilo o cicloalquilo C3 o C4, y R3 representa ciclopropilo, alquilo C1-C3, alcoxi C1-C3, amino, ciclopropilamino o alquil C1-C3-amino, y R4 y R5 representan, independientemente entre sí, hidrógeno, hidroxi, ciano, nitro, amino, aminocarbonilo, flúor, cloro, bromo, alquilo C1-C6, alcoxi C1-C6, alquil C1-C6-amino, alquil C1-C6-carbonilamino, alquil C1-C6- aminocarbonilo o alquil C1-C6-aminosulfonilo, o representan alquilo C1-C6, alcoxi C1-C6, alquil C1-C6-amino, alquil C1-C6-carbonilamino, alquil C1-C6- aminocarbonilo o alquil C1-C6-aminosulfonilo que dado el caso pueden estar sustituidos una o varias veces, de manera igual o diferente, con halógeno, amino, hidroxi, carboxi, hidroxi-alquilo C1-C6, alcoxi C1-C6, alcoxi C1-C6- alquilo C1-C6, alquil C1-C6-amino, amino-alquilo C1-C6, heterociclilo monocíclico con 3 a 8 átomos de anillo y/o heteroarilo monocíclico con 5 o 6 átomos de anillo, pudiendo estar los restos heterociclilo y heteroarilo monocíclicos mencionados a su vez dado el caso sustituidos una vez con alquilo C1-C3, o representan cicloalquilo C3-C10 que dado el caso puede estar sustituido una o varias veces, de manera igual o diferente, con halógeno, amino, hidroxi, carboxi, alquilo C1-C6, alcoxi C1-C6, alcoxi C1-C6-alquilo C1-C6, alquil C1- C6-amino, amino-alquilo C1-C6, alquil C1-C6-amino-alquilo C1-C6, halo-alquilo C1-C6, halo-alcoxi C1-C6 y/o un resto heterociclilo monocíclico con 3 a 8 átomos de anillo, o representan heteroarilo monocíclico con 5 o 6 átomos de anillo que dado el caso puede estar sustituido una o varias veces, de manera igual o diferente, con halógeno, amino, hidroxi, ciano, nitro, carboxi, alquilo C1-C6, alcoxi C1-C6, alcoxi C1-C6-alquilo C1-C6, hidroxi-alquilo C1-C6, alquil C1-C6-amino, amino-alquilo C1-C6, alquil C1-C6- amino-alquilo C1-C6, halo-alquilo C1-C6, halo-alcoxi C1-C6, cicloalquilo C3-C10, -C(>=O)R8, -S(>=O)2R9, -NR6R7 y/o un resto heterociclilo monocíclico con 3 a 8 átomos de anillo, o representan heterociclilo monocíclico con 3 a 8 átomos de anillo que dado el caso puede estar sustituido una o varias veces, de manera igual o diferente, con halógeno, amino, hidroxi, ciano, oxo, carboxi, alquilo C1-C6, alcoxi C1-C6, alcoxi C1-C6-alquilo C1-C6, alquil C1-C6-amino, amino-alquilo C1-C6, alquil C1-C6-amino-alquilo C1-C6, hidroxi-alquilo C1-C6, halo-alquilo C1-C6, halo-alcoxi C1-C6, cicloalquilo C3-C10, -C(>=O)R8, -S(>=O)2R9, -NR6R7 y/o un resto heterociclilo monocíclico con 3 a 8 átomos de anillo, o representan fenilo que dado el caso puede estar sustituido una o varias veces, de manera igual o diferente, con halógeno, amino, hidroxi, ciano, nitro, carboxi, alquilo C1-C6, alcoxi C1-C6, alcoxi C1-C6-alquilo C1-C6, alquil C1-C6- amino, amino-alquilo C1-C6, alquil C1-C6-aminocarbonilo, alquil C1-C6-aminosulfonilo, alquil C1-C6-amino-alquilo C1-C6, hidroxi-alquilo C1-C6, halo-alquilo C1-C6, halo-alcoxi C1-C6, cicloalquilo C3-C10 y/o un resto heterociclilo monocíclico con 3 a 8 átomos de anillo, y R6 y R7 representan, independientemente entre sí, hidrógeno, alquilo C1-C3, ciclopropilo, di-alquil C1-C3-amino-alquilo C1-C3 o fluoropiridilo, y R8 representa hidroxi, alquilo C1-C6, halo-alquilo C1-C3, hidroxi-alquilo C1-C3, alcoxi C1-C3-alquilo C1-C3, 30 cicloalquilo C3-C8, fenilo, heterociclilo monocíclico con 3 a 8 átomos de anillo o heteroarilo monocíclico con 5 o 6 átomos de anillo, pudiendo estar fenilo, heteroarilo y heterociclilo dado el caso sustituidos una o dos veces con halógeno, alcoxi C1-C3 o alquilo C1-C3, y R9 representa hidrógeno, alquilo C1-C6 o alcoxi C1-C4, así como sus polimorfos, enantiómeros, diaestereómeros, racematos, tautómeros, solvatos, sales fisiológicamente aceptables y solvatos de estas sales, con la condición de que si A representa un anillo de fenilo y R4 y R5 representan, independientemente entre sí, hidrógeno, hidroxi, ciano, nitro, amino, aminocarbonilo, flúor, cloro, bromo, alquilo C1-C6, alcoxi C1-C6, alquil C1-C6-amino, alquil C1-C6- carbonilamino, alquil C1-C6-aminocarbonilo o alquil C1-C6-aminosulfonilo, o representan alquilo C1-C6, alcoxi C1-C6, alquil C1-C6-amino, alquil C1-C6-carbonilamino, alquil C1-C6-aminocarbonilo o alquil C1-C6-aminosulfonilo que dado el caso pueden estar sustituidos una o varias veces, de manera igual o diferente, con halógeno, amino, hidroxi, carboxi, hidroxi-alquilo C1-C6, alcoxi C1-C6, alcoxi C1-C6-alquilo C1-C6, alquil C1-C6-amino, amino-alquilo C1-C6, heterociclilo monocíclico con 3 a 8 átomos de anillo y/o heteroarilo monocíclico con 5 o 6 átomos de anillo, pudiendo estar los restos heterociclilo y heteroarilo monocíclicos mencionados a su vez dado el caso sustituidos una vez con alquilo C1-C3, R1a no representa hidrógeno, halógeno, ciano, carboxi, amino o aminosulfonilo, o representa un resto alcoxi C1-C6, alcoxi C1-C3-alquilo C1-C3, alcoxi C1-C3-alcoxi C2-C3, alquil C1-C6-amino, alquil C1-C6-carbonilamino, alquil C1-C6- amino-alquilo C1-C6, N-(heterociclil)-alquilo C1-C6, N-(heterociclil)-alcoxi C1-C6, hidroxi-alquilo C1-C6, hidroxi-alcoxi C1-C6, halo-alquilo C1-C6, halo-alcoxi C1-C6, alquil C1-C6-carbonilo o alcoxi C1-C6-carbonilo, y no comprendiendo la condición aquellos compuestos de fórmula general (I) en la que A representa fenilo y R4 representa hidrógeno, flúor, cloro o bromo y R5 representa alcoxi C1-C6 que está sustituido una o varias veces, de manera igual o diferente, con halógeno y R1a representa halógeno, y tampoco aquellos compuestos de fórmula general (I) en la que A representa fenilo y R4 representa hidrógeno y R5 representa alcoxi C1-C6 que está sustituido una o varias veces, de manera igual o diferente, con un resto heterociclilo monocíclico con 3 a 8 átomos de anillo y/o un resto heteroarilo monocíclico con 5 o 6 átomos de anillo, pudiendo estar los restos heterociclilo y heteroarilo monocíclicos mencionados a su vez dado el caso sustituidos una vez con alquilo C1-C3, y R1a representa halógeno.
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Families Citing this family (28)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
TWI568722B (zh) 2012-06-15 2017-02-01 葛蘭馬克製藥公司 作爲ｍＰＧＥＳ－１抑制劑之三唑酮化合物
CA2901352A1 (en) * 2013-02-19 2014-08-28 Bayer Pharma Aktiengesellschaft Bicyclo 2,3-benzodiazepines and spirocyclically substituted 2,3-benzodiazepines
TWI719464B (zh) 2013-03-15 2021-02-21 美商英塞特控股公司 作為bet蛋白抑制劑之三環雜環
JP2016523964A (ja) 2013-07-08 2016-08-12 インサイト・ホールディングス・コーポレイションＩｎｃｙｔｅ Ｈｏｌｄｉｎｇｓ Ｃｏｒｐｏｒａｔｉｏｎ Ｂｅｔタンパク質阻害剤としての三環式複素環
WO2015081203A1 (en) 2013-11-26 2015-06-04 Incyte Corporation Bicyclic heterocycles as bet protein inhibitors
WO2015081189A1 (en) 2013-11-26 2015-06-04 Incyte Corporation Bicyclic heterocycles as bet protein inhibitors
US9309246B2 (en) 2013-12-19 2016-04-12 Incyte Corporation Tricyclic heterocycles as BET protein inhibitors
WO2015121226A1 (de) * 2014-02-13 2015-08-20 Bayer Pharma Aktiengesellschaft 6-substituierte 2,3-benzodiazepine
KR20240134245A (ko) 2014-04-23 2024-09-06 인사이트 홀딩스 코포레이션 BET 단백질의 저해제로서의 1H-피롤로[2,3-c]피리딘-7(6H)-온 및 피라졸로[3,4-c]피리딘-7(6H)-온
US9527864B2 (en) 2014-09-15 2016-12-27 Incyte Corporation Tricyclic heterocycles as BET protein inhibitors
CA3000633C (en) 2014-10-14 2023-10-03 The Regents Of The University Of California Use of cdk9 and brd4 inhibitors to inhibit inflammation
WO2016062688A1 (de) * 2014-10-23 2016-04-28 Bayer Pharma Aktiengesellschaft 1-phenyl-4,5-dihydro-3h-2,3-benzodiazepine derivatives
GB201504694D0 (en) 2015-03-19 2015-05-06 Glaxosmithkline Ip Dev Ltd Covalent conjugates
WO2017005711A1 (de) * 2015-07-09 2017-01-12 Bayer Pharma Aktiengesellschaft Phosphor- und schwefel-substituierte benzodiazepin-derivate
WO2017063959A1 (de) * 2015-10-15 2017-04-20 Bayer Pharma Aktiengesellschaft N-sulfoximinophenyl-substituierte benzodiazepin-derivate als bet-proteininhibitoren
US20170121347A1 (en) 2015-10-29 2017-05-04 Incyte Corporation Amorphous solid form of a bet protein inhibitor
US10167293B2 (en) * 2016-05-26 2019-01-01 Bayer Pharma Aktiengesellschaft [8-(phenylsulfonyl)-3,8-diazabicyclo[3.2.1]oct-3-yl](1H-1,2,3-triazol-4-yl)methanones
DE102017005089A1 (de) 2016-05-30 2017-11-30 Bayer Pharma Aktiengesellschaft Substitulerte 3,4-Dihydrochinoxalin-2(1H)-one
DE102017005091A1 (de) 2016-05-30 2017-11-30 Bayer Pharma Aktiengesellschaft Substituierte 3,4-Dihydropyrido[2,3-b]pyrazin-2(1H)-one
EP4234554A3 (en) 2016-06-20 2023-12-27 Incyte Corporation Crystalline solid forms of a bet inhibitor
MX384407B (es) 2016-08-15 2025-03-14 Givaudan Sa Derivados de indanona que poseen propiedades olfativas frutales y florales.
CN109406685B (zh) * 2018-12-27 2021-05-25 湖南泰新医药科技有限公司 一种分离卡非佐米和其异构体的高效液相色谱方法
WO2020242923A1 (en) * 2019-05-24 2020-12-03 Emory University Uses of radiation and benzodiazepine derivatives in cancer therapies
WO2021138391A1 (en) 2019-12-30 2021-07-08 Tyra Biosciences, Inc. Indazole compounds
WO2021152113A1 (en) 2020-01-31 2021-08-05 Bayer Aktiengesellschaft Substituted 2,3-benzodiazepines derivatives
US11833155B2 (en) 2020-06-03 2023-12-05 Incyte Corporation Combination therapy for treatment of myeloproliferative neoplasms
CN114920727B (zh) * 2022-05-26 2023-07-25 重庆华邦制药有限公司 一种卢帕他定的制备方法
WO2023229535A1 (en) 2022-05-27 2023-11-30 Engine Biosciences Pte. Ltd. Bet polypeptide therapeutic agents for generating synthetic lethality in tumors

Family Cites Families (30)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3483186A (en) * 1966-11-22 1969-12-09 Mcneilab Inc 2-benzazepine derivatives
HU208429B (en) 1991-05-03 1993-10-28 Gyogyszerkutato Intezet Process for producing 1-/3-chloro-phenyl/-4-methyl-7,8-dimethoxy-5h-2,3-benzodiazepine of high purity
CA2120939A1 (en) 1991-10-11 1993-04-15 Tetsuya Tahara Therapeutic agent for osteoporosis and diazepine compound
WO1994006802A1 (fr) 1992-09-18 1994-03-31 Yoshitomi Pharmaceutical Industries, Ltd. Compose de thienodiazepine et son utilisation medicinale
KR960702444A (ko) 1993-05-13 1996-04-27 고야 마사시 3-아미노아제핀 화합물 및 그 의약 용도(3-aminoazepine compound and pharmaceutical use thereof)
DE19604920A1 (de) 1996-02-01 1997-08-07 Schering Ag Neue 2,3-Benzodiazepinderivate, deren Herstellung und Verwendung als Arzneimittel
US5891871A (en) 1996-03-21 1999-04-06 Cocensys, Inc. Substituted 2,3-benzodiazepin-4-ones and the use thereof
HU9600871D0 (en) * 1996-04-04 1996-05-28 Gyogyszerkutato Intezet New 2,3-benzodiazepine derivatives
CN1227555A (zh) 1996-06-12 1999-09-01 日本烟草产业株式会社 细胞因子生成抑制剂、三氮䓬化合物及其中间体
DE69717160T2 (de) 1996-09-13 2003-05-08 Mitsubishi Pharma Corp., Osaka Thienotriazolodiazepinverbindungen und ihre medizinischen anwendungen
US6887867B2 (en) 2000-06-16 2005-05-03 Transgenomic, Inc. 5H-2,3-benzodiazepine antagonists of excitatory amino acid receptors
HU225100B1 (hu) * 2000-12-21 2006-06-28 Egyt Gyogyszervegyeszeti Gyar 2,3-Benzodiazepinszármazékok, ilyen hatóanyagot tartalmazó gyógyászati készítmények és alkalmazásuk
CA2482382A1 (en) 2002-04-12 2003-10-23 Pfizer Inc. Pyrazole compounds as anti-inflammatory and analgesic agents
US6858605B2 (en) * 2003-02-04 2005-02-22 Ivax Drug Research Institute, Ltd. Substituted 2,3-benzodiazepine derivatives
GB0425196D0 (en) 2004-11-15 2004-12-15 Black James Foundation Gastrin and cholecystokinin receptor ligands
GB0503962D0 (en) 2005-02-25 2005-04-06 Kudos Pharm Ltd Compounds
WO2006129623A1 (ja) 2005-05-30 2006-12-07 Mitsubishi Tanabe Pharma Corporation チエノトリアゾロジアゼピン化合物及びその医薬としての用途
AU2006334172A1 (en) * 2005-12-30 2007-07-12 Egis Gyogyszergyar Nyilvanosan Mukodo Reszvenytarsasag Optical isomers of dihydro-2,3-benzodiazepines and their stereoselective synthesis
DE102006042439A1 (de) 2006-09-09 2008-03-27 Saltigo Gmbh Verfahren zur katalytischen Herstellung von aromatischen oder heteroaromatischen Nitrilen
TW200902024A (en) * 2007-04-02 2009-01-16 Teva Pharma Novel 2,3-benzodiazepine derivatives and their use as antipsychotic agents
JP2008308491A (ja) * 2007-05-11 2008-12-25 Gunma Univ がん治療用の遊走阻害剤
CN101910182B (zh) 2007-12-28 2013-07-17 田边三菱制药株式会社 抗癌剂
KR101435729B1 (ko) * 2009-09-28 2014-09-01 닛뽕소다 가부시키가이샤 함질소 헤테로 고리 화합물 및 그의 염, 그리고 농원예용 살균제
EP3050885B1 (en) 2009-11-05 2017-10-18 GlaxoSmithKline LLC Benzodiazepine bromodomain inhibitor
GB0919432D0 (en) 2009-11-05 2009-12-23 Glaxosmithkline Llc Use
ES2652304T3 (es) 2009-11-05 2018-02-01 Glaxosmithkline Llc Compuesto de benzodiacepina novedoso
GB0919426D0 (en) 2009-11-05 2009-12-23 Glaxosmithkline Llc Novel compounds
HUE031073T2 (en) 2010-05-14 2017-06-28 Dana Farber Cancer Inst Inc Thieno triazolo-diazepine compounds for the treatment of neoplasia
AR084070A1 (es) 2010-12-02 2013-04-17 Constellation Pharmaceuticals Inc Inhibidores del bromodominio y usos de los mismos
WO2012075456A1 (en) 2010-12-02 2012-06-07 Constellation Pharmaceuticals Bromodomain inhibitors and uses thereof

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