ES2587284T3 - 5-Fluoro-pirimidinas 2,4-disustituidas como inhibidores selectivos de CDK9 - Google Patents
5-Fluoro-pirimidinas 2,4-disustituidas como inhibidores selectivos de CDK9 Download PDFInfo
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- ES2587284T3 ES2587284T3 ES12761590.4T ES12761590T ES2587284T3 ES 2587284 T3 ES2587284 T3 ES 2587284T3 ES 12761590 T ES12761590 T ES 12761590T ES 2587284 T3 ES2587284 T3 ES 2587284T3
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- acetylamino
- alkyl
- fluoroalkoxy
- alkoxy
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D239/00—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings
- C07D239/02—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings
- C07D239/24—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings having three or more double bonds between ring members or between ring members and non-ring members
- C07D239/28—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings having three or more double bonds between ring members or between ring members and non-ring members with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, directly attached to ring carbon atoms
- C07D239/32—One oxygen, sulfur or nitrogen atom
- C07D239/42—One nitrogen atom
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/495—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with two or more nitrogen atoms as the only ring heteroatoms, e.g. piperazine or tetrazines
- A61K31/505—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/495—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with two or more nitrogen atoms as the only ring heteroatoms, e.g. piperazine or tetrazines
- A61K31/505—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim
- A61K31/506—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim not condensed and containing further heterocyclic rings
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P1/00—Drugs for disorders of the alimentary tract or the digestive system
- A61P1/04—Drugs for disorders of the alimentary tract or the digestive system for ulcers, gastritis or reflux esophagitis, e.g. antacids, inhibitors of acid secretion, mucosal protectants
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P11/00—Drugs for disorders of the respiratory system
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P13/00—Drugs for disorders of the urinary system
- A61P13/08—Drugs for disorders of the urinary system of the prostate
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P15/00—Drugs for genital or sexual disorders; Contraceptives
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P17/00—Drugs for dermatological disorders
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P31/00—Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
- A61P31/12—Antivirals
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P35/00—Antineoplastic agents
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P9/00—Drugs for disorders of the cardiovascular system
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D401/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom
- C07D401/02—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings
- C07D401/12—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings linked by a chain containing hetero atoms as chain links
-
- 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
- C07D407/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having oxygen atoms as the only ring hetero atoms, not provided for by group C07D405/00
- C07D407/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having oxygen atoms as the only ring hetero atoms, not provided for by group C07D405/00 containing two hetero rings
- C07D407/04—Heterocyclic compounds containing two or more hetero rings, at least one ring having oxygen atoms as the only ring hetero atoms, not provided for by group C07D405/00 containing two hetero rings directly linked by a ring-member-to-ring-member bond
Abstract
Un compuesto de fórmula general (I) en la que R1 representa un grupo seleccionado de alquilo C1-C6, cicloalquilo C3-C7, heterociclil-, fenilo, heteroarilo, fenilalquilo C1-C3 o heteroarilalquilo C1-C3, en el que dicho grupo está opcionalmente sustituido con uno o dos o tres sustituyentes, de forma idéntica o de forma diferente, seleccionados del grupo de hidroxi, ciano, halógeno, haloalquil C1-C3-, alcoxi C1-C6-, fluoroalcoxi C1-C3-, -NH2, alquilamino-, dialquilamino-, acetilamino-, N-metil-N-acetilamino-, aminas cíclicas; R2 representa un grupo seleccionado de R3, R4 representan, independientemente el uno del otro, un grupo seleccionado de un átomo de hidrógeno, un átomo fluoro, un átomo cloro, alquil C1-C3-, alcoxi C1-C3-, haloalquil C1-C3-, fluoroalcoxi C1-C3-; R5 representa un grupo seleccionado de**Fórmula** a) un grupo alquilo C1-C6, que está opcionalmente sustituido con uno o dos o tres sustituyentes, de forma idéntica o de forma diferente, seleccionados de halógeno, hidroxi, -NH2, alquilamino-, dialquilamino-, acetilamino-, N-metil-N-acetilamino-, aminas cíclicas, ciano, alquil C1-C3-, haloalquil C1-C3-, fluoroalcoxi C1-C3-, alcoxi C1-C3-, alquenil C2-C3-, alquinil C2-C3-, cicloalquil C3-C7-, heterociclil-, fenilo, heteroarilo, en el que dicho grupo cicloalquil C3-C7-, heterociclil-, fenilo o heteroarilo está opcionalmente sustituido con uno, dos o tres sustituyentes, de forma idéntica o de forma diferente, seleccionados de halógeno, hidroxi, alquil C1-C3-, alcoxi C1-C3-, -NH2, alquilamino-, dialquilamino-, acetilamino-, N-metil-N-acetilamino-, aminas cíclicas, haloalquil C1- C3-, fluoroalcoxi C1-C3-; b) un grupo cicloalquil C3-C7-, que está opcionalmente sustituido con uno o dos o tres sustituyentes, de forma idéntica o de forma diferente, seleccionados del grupo de halógeno, hidroxi, -NH2, alquilamino-, dialquilamino- , acetilamino-, N-metil-N-acetilamino-, aminas cíclicas, ciano, alquil C1-C3-, haloalquil C1-C3-, fluoroalcoxi C1- C3-, alcoxi C1-C3-, alquenil C2-C3-, alquinil C2-C3-; c) un grupo heterociclil-, que está opcionalmente sustituido con uno o dos o tres sustituyentes, de forma idéntica o de forma diferente, seleccionados del grupo de halógeno, hidroxi, -NH2, alquilamino-, dialquilamino- , acetilamino-, N-metil-N-acetilamino-, aminas cíclicas, ciano, alquil C1-C3-, haloalquil C1-C3-, fluoroalcoxi C1-C3-, alcoxi C1-C3-, alquenil C2-C3-, alquinil C2-C3-; d) un grupo fenilo, que está opcionalmente sustituido con uno o dos o tres sustituyentes, de forma idéntica o de forma diferente, seleccionados del grupo de halógeno, hidroxi, -NH2, alquilamino-, dialquilamino-, acetilamino-, N-metil-N-acetilamino-, aminas cíclicas, ciano, alquil C1-C3-, haloalquil C1-C3-, fluoroalcoxi C1-C3-, alcoxi C1-C3-; e) un grupo heteroarilo, que está opcionalmente sustituido con uno o dos o tres sustituyentes, de forma idéntica o de forma diferente, seleccionados del grupo de halógeno, hidroxi, -NH2, alquilamino-, dialquilamino- , acetilamino-, N-metil-N-acetilamino-, aminas cíclicas, ciano, alquil C1-C3-, haloalquil C1-C3-, fluoroalcoxi C1- C3-, alcoxi C1-C3-; f) un grupo fenilalquil C1-C3-, cuyo grupo fenilo está opcionalmente sustituido con uno o dos o tres sustituyentes, de forma idéntica o de forma diferente, seleccionados del grupo de halógeno, hidroxi, -NH2, alquilamino-, dialquilamino-, acetilamino-, N-metil-N-acetilamino-, aminas cíclicas, ciano, alquil C1-C3-, 5 haloalquil C1-C3-, fluoroalcoxi C1-C3-, alcoxi C1-C3-; g) un grupo heteroarilalquil C1-C3-, cuyo grupo heteroarilo está opcionalmente sustituido con uno o dos o tres sustituyentes, de forma idéntica o de forma diferente, seleccionados del grupo de halógeno, hidroxi, -NH2, alquilamino-, dialquilamino-, acetilamino-, N-metil-N-acetilamino-, aminas cíclicas, ciano, alquil C1-C3-, haloalquil C1-C3-, fluoroalcoxi C1-C3-, alcoxi C1-C3-; h) un grupo cicloalquil C3-C6-alquil C1-C3-, cuyo grupo cicloalquilo C3-C6 está opcionalmente sustituido con uno o dos o tres sustituyentes, de forma idéntica o de forma diferente, seleccionados de halógeno, alquil C1- C3-, alcoxi C1-C3-, haloalquil C1-C3-, fluoroalcoxi C1-C3-; i) un grupo heterociclilalquil C1-C3-, cuyo grupo heterociclilo está opcionalmente sustituido con uno o dos o tres sustituyentes, de forma idéntica o de forma diferente, seleccionados de halógeno, alquil C1-C3-, alcoxi C1-C3-, haloalquil C1-C3-, fluoroalcoxi C1-C3-; j) grupo fenil-cicropropil-, cuyo grupo fenilo está opcionalmente sustituido con uno o dos o tres sustituyentes, de forma idéntica o de forma diferente, seleccionados del grupo de halógeno, hidroxi, NH2, alquilamino-, dialquilamino-, acetilamino-, N-metil-N-acetilamino-, aminas cíclicas, ciano, alquil C1-C3-, haloalquil C1-C3-, fluoroalcoxi C1-C3-, alcoxi C1-C3-; k) un grupo heteroaril-ciclopropil-, cuyo grupo heteroarilo está opcionalmente sustituido con uno o dos o tres sustituyentes, de forma idéntica o de forma diferente, seleccionados del grupo de halógeno, hidroxi, NH2, alquilamino-, dialquilamino-, acetilamino-, N-metil-N-acetilamino-, aminas cíclicas, ciano, alquil C1-C3-, haloalquil C1-C3-, fluoroalcoxi C1-C3-, alcoxi C1-C3-; R6, R7 representan, independientemente el uno del otro, un grupo seleccionado de un átomo de hidrógeno, un átomo fluoro, un átomo cloro, alquil C1-C3-, alcoxi C1-C3-, haloalquil C1-C3-, fluoroalcoxi C1-C3-; o sus sales, solvatos o sales de solvatos.
Applications Claiming Priority (3)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
EP11181545 | 2011-09-16 | ||
EP11181545 | 2011-09-16 | ||
PCT/EP2012/067966 WO2013037896A1 (en) | 2011-09-16 | 2012-09-13 | Disubstituted 5-fluoro-pyrimidines |
Publications (1)
Publication Number | Publication Date |
---|---|
ES2587284T3 true ES2587284T3 (es) | 2016-10-21 |
Family
ID=46880699
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
ES12761590.4T Active ES2587284T3 (es) | 2011-09-16 | 2012-09-13 | 5-Fluoro-pirimidinas 2,4-disustituidas como inhibidores selectivos de CDK9 |
Country Status (8)
Country | Link |
---|---|
US (1) | US9108926B2 (es) |
EP (1) | EP2755956B1 (es) |
JP (1) | JP5982490B2 (es) |
CN (1) | CN103917527B (es) |
CA (1) | CA2848616A1 (es) |
ES (1) | ES2587284T3 (es) |
HK (1) | HK1199448A1 (es) |
WO (1) | WO2013037896A1 (es) |
Families Citing this family (19)
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TWI555737B (zh) | 2011-05-24 | 2016-11-01 | 拜耳知識產權公司 | 含有硫醯亞胺基團之4-芳基-n-苯基-1,3,5-三氮雜苯-2-胺 |
ES2597232T3 (es) * | 2012-10-18 | 2017-01-17 | Bayer Pharma Aktiengesellschaft | 4-(orto)-fluorofenil-5-fluoropirimidin-2-il aminas que contienen un grupo sulfona |
US9708293B2 (en) | 2012-10-18 | 2017-07-18 | Bayer Pharma Aktiengesellschaft | N-(pyridin-2-yl)pyrimidin-4-amine derivatives containing a sulfone group |
EP2909176B1 (en) | 2012-10-18 | 2016-07-20 | Bayer Pharma Aktiengesellschaft | 5-fluoro-n-(pyridin-2-yl)pyridin-2-amine derivatives containing a sulfone group |
TW201418243A (zh) | 2012-11-15 | 2014-05-16 | Bayer Pharma AG | 含有磺醯亞胺基團之n-(吡啶-2-基)嘧啶-4-胺衍生物 |
RS55580B1 (sr) | 2012-11-15 | 2017-06-30 | Bayer Pharma AG | Derivati 5-fluoro-n-(piridin-2-il)piridin-2-amina koji sadrže sulfoksiminsku grupu |
CA2917096C (en) | 2013-07-04 | 2021-05-18 | Bayer Pharma Aktiengesellschaft | Sulfoximine substituted 5-fluoro-n-(pyridin-2-yl)pyridin-2-amine derivatives and their use as cdk9 kinase inhibitors |
CN106232596A (zh) * | 2014-03-13 | 2016-12-14 | 拜耳医药股份有限公司 | 含有砜基团的5‑氟‑n‑(吡啶‑2‑基)吡啶‑2‑胺衍生物 |
EP3126338B1 (en) * | 2014-04-01 | 2019-09-04 | Bayer Pharma Aktiengesellschaft | Disubstituted 5-fluoro pyrimidine derivatives containing a sulfondiimine group |
ES2743799T3 (es) * | 2014-04-11 | 2020-02-20 | Bayer Pharma AG | Nuevos compuestos macrocíclicos |
CA2964683A1 (en) * | 2014-10-16 | 2016-04-21 | Bayer Pharma Aktiengesellschaft | Fluorinated benzofuranyl-pyrimidine derivatives containing a sulfone group |
WO2016059086A1 (en) | 2014-10-16 | 2016-04-21 | Bayer Pharma Aktiengesellschaft | Fluorinated benzofuranyl-pyrimidine derivatives containing a sulfoximine group |
CA2999931A1 (en) | 2015-09-29 | 2017-04-06 | Bayer Pharma Aktiengesellschaft | Novel macrocyclic sulfondiimine compounds |
US10214542B2 (en) | 2015-10-08 | 2019-02-26 | Bayer Pharma Aktiengesellschaft | Modified macrocyclic compounds |
WO2017060322A2 (en) | 2015-10-10 | 2017-04-13 | Bayer Pharma Aktiengesellschaft | Ptefb-inhibitor-adc |
CN109476677A (zh) * | 2016-08-08 | 2019-03-15 | 南京明德新药研发股份有限公司 | 抗hcmv病毒化合物 |
US11254690B2 (en) | 2017-03-28 | 2022-02-22 | Bayer Pharma Aktiengesellschaft | PTEFb inhibiting macrocyclic compounds |
WO2018177889A1 (en) | 2017-03-28 | 2018-10-04 | Bayer Aktiengesellschaft | Novel ptefb inhibiting macrocyclic compounds |
AU2019221019A1 (en) | 2018-02-13 | 2020-07-23 | Bayer Aktiengesellschaft | Use of 5-Fluoro-4-(4-fluoro-2-methoxyphenyl)-N-{4-[(S-methylsulfonimidoyl)methyl]pyridin-2-yl}pyridin-2-amine for treating diffuse large B-cell lymphoma |
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EP1218360B1 (en) | 1999-10-07 | 2008-05-28 | Amgen Inc., | Triazine kinase inhibitors |
GB0103926D0 (en) | 2001-02-17 | 2001-04-04 | Astrazeneca Ab | Chemical compounds |
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EP1611125A1 (en) | 2003-02-07 | 2006-01-04 | Vertex Pharmaceuticals Incorporated | Heteroaryl substituted pyrolls useful as inhibitors of protein kinases |
WO2005026129A1 (en) | 2003-09-15 | 2005-03-24 | Gpc Biotech Ag | Pharmaceutically active 4,6-disubstituted aminopyrimidine derivatives as modulators of protein kinases |
GB0427699D0 (en) * | 2004-12-17 | 2005-01-19 | Astrazeneca Ab | Chemical compounds |
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DE102006041382A1 (de) | 2006-08-29 | 2008-03-20 | Bayer Schering Pharma Ag | Carbamoyl-Sulfoximide als Proteinkinaseinhibitoren |
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-
2012
- 2012-09-13 JP JP2014530222A patent/JP5982490B2/ja not_active Expired - Fee Related
- 2012-09-13 CA CA2848616A patent/CA2848616A1/en not_active Abandoned
- 2012-09-13 ES ES12761590.4T patent/ES2587284T3/es active Active
- 2012-09-13 CN CN201280054032.9A patent/CN103917527B/zh not_active Expired - Fee Related
- 2012-09-13 US US14/343,983 patent/US9108926B2/en not_active Expired - Fee Related
- 2012-09-13 WO PCT/EP2012/067966 patent/WO2013037896A1/en active Application Filing
- 2012-09-13 EP EP12761590.4A patent/EP2755956B1/en not_active Not-in-force
-
2014
- 2014-12-29 HK HK14113032.7A patent/HK1199448A1/xx not_active IP Right Cessation
Also Published As
Publication number | Publication date |
---|---|
WO2013037896A1 (en) | 2013-03-21 |
US20140228387A1 (en) | 2014-08-14 |
HK1199448A1 (en) | 2015-07-03 |
CA2848616A1 (en) | 2013-03-21 |
CN103917527B (zh) | 2017-05-31 |
EP2755956B1 (en) | 2016-05-18 |
JP2014526489A (ja) | 2014-10-06 |
CN103917527A (zh) | 2014-07-09 |
US9108926B2 (en) | 2015-08-18 |
EP2755956A1 (en) | 2014-07-23 |
JP5982490B2 (ja) | 2016-08-31 |
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