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PE20190378A1 - Compuestos de 2,3-dihidro-1h-indol - Google Patents

Compuestos de 2,3-dihidro-1h-indol

Info

Publication number
PE20190378A1
PE20190378A1 PE2018003199A PE2018003199A PE20190378A1 PE 20190378 A1 PE20190378 A1 PE 20190378A1 PE 2018003199 A PE2018003199 A PE 2018003199A PE 2018003199 A PE2018003199 A PE 2018003199A PE 20190378 A1 PE20190378 A1 PE 20190378A1
Authority
PE
Peru
Prior art keywords
hydrogen
fluoro
cancer
dihydro
methyl
Prior art date
Application number
PE2018003199A
Other languages
English (en)
Inventor
Jolie Anne Bastian
Jiehao Chen
Jeffrey Daniel Cohen
James Robert Henry
William Thomas Mcmillen
Bradley Earl Reaman
Almudena Rubio
Daniel Jon Sall
Gaiying Zhao
Original Assignee
Lilly Co Eli
Priority date (The priority date 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 date listed.)
Filing date
Publication date
Application filed by Lilly Co Eli filed Critical Lilly Co Eli
Publication of PE20190378A1 publication Critical patent/PE20190378A1/es

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D405/00Heterocyclic 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
    • C07D405/02Heterocyclic 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
    • C07D405/06Heterocyclic 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 linked by a carbon chain containing only aliphatic carbon atoms
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D405/00Heterocyclic 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
    • C07D405/02Heterocyclic 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
    • C07D405/10Heterocyclic 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 linked by a carbon chain containing aromatic rings
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00Medicinal preparations containing organic active ingredients
    • A61K31/33Heterocyclic compounds
    • A61K31/395Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/40Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with one nitrogen as the only ring hetero atom, e.g. sulpiride, succinimide, tolmetin, buflomedil
    • A61K31/403Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with one nitrogen as the only ring hetero atom, e.g. sulpiride, succinimide, tolmetin, buflomedil condensed with carbocyclic rings, e.g. carbazole
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00Medicinal preparations containing organic active ingredients
    • A61K31/33Heterocyclic compounds
    • A61K31/395Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/40Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with one nitrogen as the only ring hetero atom, e.g. sulpiride, succinimide, tolmetin, buflomedil
    • A61K31/403Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with one nitrogen as the only ring hetero atom, e.g. sulpiride, succinimide, tolmetin, buflomedil condensed with carbocyclic rings, e.g. carbazole
    • A61K31/404Indoles, e.g. pindolol
    • A61K31/4045Indole-alkylamines; Amides thereof, e.g. serotonin, melatonin
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P35/00Antineoplastic agents
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P35/00Antineoplastic agents
    • A61P35/02Antineoplastic agents specific for leukemia
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C233/00Carboxylic acid amides
    • C07C233/57Carboxylic acid amides having carbon atoms of carboxamide groups bound to carbon atoms of rings other than six-membered aromatic rings
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D209/00Heterocyclic compounds containing five-membered rings, condensed with other rings, with one nitrogen atom as the only ring hetero atom
    • C07D209/02Heterocyclic compounds containing five-membered rings, condensed with other rings, with one nitrogen atom as the only ring hetero atom condensed with one carbocyclic ring
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07BGENERAL METHODS OF ORGANIC CHEMISTRY; APPARATUS THEREFOR
    • C07B2200/00Indexing scheme relating to specific properties of organic compounds
    • C07B2200/13Crystalline forms, e.g. polymorphs
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C233/00Carboxylic acid amides
    • C07C233/01Carboxylic acid amides having carbon atoms of carboxamide groups bound to hydrogen atoms or to acyclic carbon atoms
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D309/00Heterocyclic compounds containing six-membered rings having one oxygen atom as the only ring hetero atom, not condensed with other rings

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Health & Medical Sciences (AREA)
  • Veterinary Medicine (AREA)
  • Medicinal Chemistry (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Animal Behavior & Ethology (AREA)
  • General Health & Medical Sciences (AREA)
  • Public Health (AREA)
  • Epidemiology (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • General Chemical & Material Sciences (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Hematology (AREA)
  • Oncology (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Plural Heterocyclic Compounds (AREA)
  • Peptides Or Proteins (AREA)
  • Nitrogen Condensed Heterocyclic Rings (AREA)

Abstract

Se refiere a derivados de 2,3-dihidro-1H-indol, en donde: R1a es hidrogeno, metilo, etenilo, ciano, fluoro, cloro, fluorometilo, o difluorometilo; R1b es hidrogeno, fluoro, o cloro; R1c es hidrogeno, hidroxi, fluoro, benciloxi, entre otros; R2 es hidrogeno o metilo; R2a es hidrogeno o metilo; y R3a es tetrahidropiranilo. Entre los compuestos preferidos se tiene el siguiente: 4-fluoro-N-{(1R)}-1-[1-(tetrahidro-2H-piran-4-ilcarbonil)-2,3-dihidro-1H-indol-5-il]etil}benzamida cristalino, el cual se encuentra caracterizado por un patron de difraccion en polvo de rayos X que comprende al menos un pico a 17.38°. Estos compuestos inhiben la conversion de triptofano a cinureina y se emplean en el tratamiento de un cancer seleccionado de melanoma, leucemia mieloide aguda, leucemia linfocitica cronica, cancer colorrectal , cancer de mama , cancer de pulmon, cancer de ovario, carcinoma de trompas de Falopio, carcinoma peritoneal primario, entre otros.
PE2018003199A 2016-06-10 2017-05-31 Compuestos de 2,3-dihidro-1h-indol PE20190378A1 (es)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US201662348457P 2016-06-10 2016-06-10

Publications (1)

Publication Number Publication Date
PE20190378A1 true PE20190378A1 (es) 2019-03-08

Family

ID=59031409

Family Applications (1)

Application Number Title Priority Date Filing Date
PE2018003199A PE20190378A1 (es) 2016-06-10 2017-05-31 Compuestos de 2,3-dihidro-1h-indol

Country Status (40)

Country Link
US (2) US9872853B2 (es)
EP (1) EP3468965B1 (es)
JP (1) JP6632746B2 (es)
KR (1) KR102241258B1 (es)
CN (1) CN109641881B (es)
AR (1) AR108586A1 (es)
AU (1) AU2017277833B2 (es)
BR (1) BR112018072872A2 (es)
CA (1) CA3027035C (es)
CL (1) CL2018003543A1 (es)
CO (1) CO2018013251A2 (es)
CR (1) CR20180579A (es)
CY (1) CY1123660T1 (es)
DK (1) DK3468965T3 (es)
DO (1) DOP2018000278A (es)
EA (1) EA037419B1 (es)
EC (1) ECSP19001734A (es)
ES (1) ES2797981T3 (es)
HR (1) HRP20200769T1 (es)
HU (1) HUE050155T2 (es)
IL (1) IL263497B (es)
JO (1) JOP20170131B1 (es)
LT (1) LT3468965T (es)
MA (1) MA45224B1 (es)
MD (1) MD3468965T2 (es)
ME (1) ME03744B (es)
MX (1) MX382877B (es)
MY (1) MY197462A (es)
NZ (1) NZ748500A (es)
PE (1) PE20190378A1 (es)
PH (1) PH12018502572A1 (es)
PL (1) PL3468965T3 (es)
PT (1) PT3468965T (es)
RS (1) RS60322B1 (es)
SG (1) SG11201809625RA (es)
SI (1) SI3468965T1 (es)
TW (1) TWI671294B (es)
UA (1) UA122526C2 (es)
WO (1) WO2017213919A1 (es)
ZA (1) ZA201807688B (es)

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WO2016183266A1 (en) 2015-05-13 2016-11-17 Enanta Pharmaceuticals, Inc. Ehpatitis b antiviral agents
PL3426245T3 (pl) 2016-03-07 2023-05-22 Enanta Pharmaceuticals, Inc. Środki przeciwwirusowe zapalenia wątroby typu b
EP3675637A4 (en) 2017-08-28 2021-05-19 Enanta Pharmaceuticals, Inc. Hepatitis b antiviral agents
US12275729B2 (en) * 2017-11-01 2025-04-15 Merck Sharp & Dohme Llc Substituted tetrahydroquinolin compounds as indoleamine 2,3-dioxygenase (IDO) inhibitors
EP3727374A4 (en) * 2017-12-21 2021-11-10 Merck Patent GmbH COMBINATION OF AN ANTI-PD-L1 ANTIBODY AND AN IDO1 INHIBITOR FOR THE TREATMENT OF CANCER
WO2019143902A2 (en) 2018-01-22 2019-07-25 Enanta Pharmaceuticals, Inc. Substituted heterocycles as antiviral agents
WO2020036837A1 (en) * 2018-08-17 2020-02-20 Merck Sharp & Dohme Corp. Novel substituted tetrahydroquinoline compounds as indoleamine 2,3-dioxygenase inhibitors
AR116474A1 (es) 2018-09-21 2021-05-12 Enanta Pharm Inc DERIVADOS DEL ÁCIDO 6,7-DIHIDRO-2H-BENZOFURO[2,3-a]QUINOLIZIN-3-CARBOXÍLICO COMO AGENTES ANTIVIRALES PARA EL TRATAMIENTO O PREVENCIÓN DE UNA INFECCIÓN POR HBV
US12065438B2 (en) 2018-11-06 2024-08-20 Merck Sharp & Dohme Llc Substituted tricyclic compounds as indoleamine 2,3-dioxygenase inhibitors
EP3883570A4 (en) 2018-11-21 2022-07-13 Enanta Pharmaceuticals, Inc. FUNCTIONALIZED HETEROCYCLES AS ANTIVIRAL AGENTS
US11236111B2 (en) 2019-06-03 2022-02-01 Enanta Pharmaceuticals, Inc. Hepatitis B antiviral agents
US11760755B2 (en) 2019-06-04 2023-09-19 Enanta Pharmaceuticals, Inc. Hepatitis B antiviral agents
WO2020247575A1 (en) 2019-06-04 2020-12-10 Enanta Pharmaceuticals, Inc. Hepatitis b antiviral agents
US11738019B2 (en) 2019-07-11 2023-08-29 Enanta Pharmaceuticals, Inc. Substituted heterocycles as antiviral agents
WO2021055425A2 (en) 2019-09-17 2021-03-25 Enanta Pharmaceuticals, Inc. Functionalized heterocycles as antiviral agents
WO2021188414A1 (en) 2020-03-16 2021-09-23 Enanta Pharmaceuticals, Inc. Functionalized heterocyclic compounds as antiviral agents
CN114105961B (zh) * 2021-12-10 2023-09-12 海南梵圣生物科技有限公司 一种ido1抑制剂(ly-3381916)制备方法
CN114213310B (zh) * 2021-12-31 2024-02-23 中国药科大学 吲哚啉化合物及其衍生物、制备方法、药物组合物和应用
WO2025072355A1 (en) * 2023-09-25 2025-04-03 Biohybrid Solutions Holdings, Inc. Methods for and compositions of non-peg bioconjugates with ultra-high drug-to-agent ratio
WO2025140363A1 (zh) * 2023-12-27 2025-07-03 海思科医药集团股份有限公司 一种苯基哌啶衍生物的制备方法

Family Cites Families (10)

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Publication number Priority date Publication date Assignee Title
EP2239012A3 (en) * 2003-04-11 2011-06-15 High Point Pharmaceuticals, LLC Substituted amide derivatives and pharmaceutical uses thereof
ES2401482T3 (es) * 2005-05-10 2013-04-22 Incyte Corporation Moduladores de la indolamina 2,3-dioxigenasa y métodos de uso de los mismos
US7622495B2 (en) * 2006-10-03 2009-11-24 Neurim Pharmaceuticals (1991) Ltd. Substituted aryl-indole compounds and their kynurenine/kynuramine-like metabolites as therapeutic agents
JP2011511800A (ja) 2008-02-07 2011-04-14 アボット・ラボラトリーズ 正のアロステリックな修飾物質としてのアミド誘導体およびこれらの使用方法
HRP20141094T1 (hr) * 2008-07-08 2015-01-16 Incyte Corporation 1,2,5-oksadiazoli kao inhibitori indolamin 2,3-dioksigenaze
NO2694640T3 (es) * 2011-04-15 2018-03-17
JP6313415B2 (ja) * 2013-03-15 2018-04-18 ブリストル−マイヤーズ スクイブ カンパニーBristol−Myers Squibb Company Ido阻害剤
AU2015239886B2 (en) * 2014-04-04 2018-02-01 Iomet Pharma Ltd Indole derivatives for use in medicine
UY36391A (es) * 2014-11-05 2016-06-01 Flexus Biosciences Inc Compuestos moduladores de la enzima indolamina 2,3-dioxigenasa (ido1), sus métodos de síntesis y composiciones farmacèuticas que las contienen
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Also Published As

Publication number Publication date
LT3468965T (lt) 2020-06-10
KR102241258B1 (ko) 2021-04-16
EA037419B1 (ru) 2021-03-25
ES2797981T3 (es) 2020-12-04
PT3468965T (pt) 2020-07-16
JP2019518027A (ja) 2019-06-27
PH12018502572A1 (en) 2019-10-28
CR20180579A (es) 2019-02-08
DK3468965T3 (da) 2020-06-15
CA3027035A1 (en) 2017-12-14
IL263497A (en) 2019-01-31
US9872853B2 (en) 2018-01-23
EP3468965A1 (en) 2019-04-17
CY1123660T1 (el) 2022-03-24
PL3468965T3 (pl) 2020-09-21
ME03744B (me) 2021-04-20
ECSP19001734A (es) 2019-01-31
CN109641881B (zh) 2022-01-07
CO2018013251A2 (es) 2019-01-18
WO2017213919A1 (en) 2017-12-14
TWI671294B (zh) 2019-09-11
US20170354641A1 (en) 2017-12-14
SI3468965T1 (sl) 2020-07-31
US10759786B2 (en) 2020-09-01
KR20190003750A (ko) 2019-01-09
BR112018072872A2 (pt) 2019-03-06
EA201892479A1 (ru) 2019-07-31
IL263497B (en) 2020-11-30
CA3027035C (en) 2021-05-04
HUE050155T2 (hu) 2020-12-28
US20190161477A1 (en) 2019-05-30
JOP20170131B1 (ar) 2021-08-17
MD3468965T2 (ro) 2020-08-31
SG11201809625RA (en) 2018-11-29
AR108586A1 (es) 2018-09-05
CN109641881A (zh) 2019-04-16
MX2018015275A (es) 2019-04-11
HRP20200769T1 (hr) 2020-07-24
MY197462A (en) 2023-06-19
MX382877B (es) 2025-03-13
UA122526C2 (uk) 2020-11-25
JP6632746B2 (ja) 2020-01-22
DOP2018000278A (es) 2018-12-31
AU2017277833A1 (en) 2018-11-15
TW201806948A (zh) 2018-03-01
EP3468965B1 (en) 2020-04-29
NZ748500A (en) 2020-04-24
ZA201807688B (en) 2020-08-26
RS60322B1 (sr) 2020-07-31
CL2018003543A1 (es) 2019-03-22
AU2017277833B2 (en) 2020-07-02
MA45224B1 (fr) 2020-06-30

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