AR104176A1 - Inhibidores de ido (indolamina-2,3-dioxigenasa) - Google Patents

Inhibidores de ido (indolamina-2,3-dioxigenasa)

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Publication number
AR104176A1
AR104176A1 ARP160100897A ARP160100897A AR104176A1 AR 104176 A1 AR104176 A1 AR 104176A1 AR P160100897 A ARP160100897 A AR P160100897A AR P160100897 A ARP160100897 A AR P160100897A AR 104176 A1 AR104176 A1 AR 104176A1
Authority
AR
Argentina
Prior art keywords
optionally substituted
cycloalkyl
alkyl
heteroaryl
heterocyclyl
Prior art date
Application number
ARP160100897A
Other languages
English (en)
Inventor
Pulicharla Nagalakshmi
Kanyaboina Yadagiri
Thangathirupathy Srinivasan
Cheruku Srinivas
Kumar Sistla Ramesh
Thangavel Soodamani
Roy Saumya
Jethanand Nara Susheel
Murugesan Natesan
K Williams David
Shan Weifang
P Seitz Steven
A Markwalder Jay
Huang Audris
Guo Weiwei
Charlotte Cherney Emily
Aaron Balog James
Original Assignee
Bristol Myers Squibb Co
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
Family has litigation
First worldwide family litigation filed litigation Critical https://patents.darts-ip.com/?family=55702190&utm_source=***_patent&utm_medium=platform_link&utm_campaign=public_patent_search&patent=AR104176(A1) "Global patent litigation dataset” by Darts-ip is licensed under a Creative Commons Attribution 4.0 International License.
Application filed by Bristol Myers Squibb Co filed Critical Bristol Myers Squibb Co
Publication of AR104176A1 publication Critical patent/AR104176A1/es

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    • C07C229/00Compounds containing amino and carboxyl groups bound to the same carbon skeleton
    • C07C229/40Compounds containing amino and carboxyl groups bound to the same carbon skeleton having amino groups bound to carbon atoms of at least one six-membered aromatic ring and carboxyl groups bound to acyclic carbon atoms of the same carbon skeleton
    • C07C229/42Compounds containing amino and carboxyl groups bound to the same carbon skeleton having amino groups bound to carbon atoms of at least one six-membered aromatic ring and carboxyl groups bound to acyclic carbon atoms of the same carbon skeleton with carboxyl groups linked to the six-membered aromatic ring, or to the condensed ring system containing that ring, by saturated carbon chains
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    • A61K31/17Amides, e.g. hydroxamic acids having the group >N—C(O)—N< or >N—C(S)—N<, e.g. urea, thiourea, carmustine
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    • A61K31/19Carboxylic acids, e.g. valproic acid
    • A61K31/195Carboxylic acids, e.g. valproic acid having an amino group
    • A61K31/196Carboxylic acids, e.g. valproic acid having an amino group the amino group being directly attached to a ring, e.g. anthranilic acid, mefenamic acid, diclofenac, chlorambucil
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Abstract

Reivindicación 1: Un compuesto caracterizado por la fórmula (1) en donde: Y es N, CH o CF; V es N, CH o CF; R¹ es -COOH, -COOC₁₋₆ alquilo, -CONH₂, -CN, heterociclilo opcionalmente sustituido, heteroarilo opcionalmente sustituido, -NHCONHR¹³, -CONHSO₂R¹⁴, -CONHCOR¹³, -SO₂NHCOR¹³, -CONR¹³, -CONHSO₂NR¹³R¹⁴, -SO₂NHR¹³, -NHCONHSO₂R¹³, -CHCF₃OH, -COCF₃, -CR²R³OH o -NHSO₂R¹³; R¹³ es H, C₁₋₁₀ alquilo opcionalmente sustituido, C₃₋₈ cicloalquilo opcionalmente sustituido, C₂₋₁₀ alquenilo opcionalmente sustituido, C₂₋₁₀ alquinilo opcionalmente sustituido, heterociclilo opcionalmente sustituido, fenilo opcionalmente sustituido o heteroarilo opcionalmente sustituido; R¹⁴ es H, C₁₋₁₀ alquilo opcionalmente sustituido; fenilo o C₃₋₈ cicloalquilo; R² y R³ son independientemente -hidrógeno, C₁₋₁₀ alquilo opcionalmente sustituido, C₃₋₈ cicloalquilo opcionalmente sustituido o fenilo opcionalmente sustituido; o R² y R³ se toman junto con el carbono al cual están unidos para formar un anillo carbocíclico o heterocíclico de 3 a 6 miembros opcionalmente sustituido; R⁴ y R⁵ son independientemente H, C₁₋₁₀ alquilo opcionalmente sustituido, C₁₋₁₀ alcoxi-C₁₋₁₀ alquilo opcionalmente sustituido, C₁₋₁₀ alcoxi opcionalmente sustituido, arilo opcionalmente sustituido, aril-C₁₋₁₀ alquilo opcionalmente sustituido, heteroarilo de 5 a 8 miembros opcionalmente sustituido, C₃₋₈ cicloalquilo opcionalmente sustituido o heterociclilo opcionalmente sustituido; o R⁴ y R⁵ se toman junto con el nitrógeno al cual están unidos para formar un anillo heterocíclico de 4 a 8 miembros opcionalmente sustituido que contiene 0 - 3 heteroátomos adicionales seleccionados de -N-, -S- y -O-; o R⁴ y R⁵ se toman junto con el nitrógeno al cual están unidos para formar un anillo heterobicíclico de 6 a 10 miembros opcionalmente sustituido que contiene 0 - 3 heteroátomos adicionales seleccionados de -N-, -S- y -O-; R⁶ es arilo opcionalmente sustituido, heteroarilo opcionalmente sustituido, C₃₋₈ cicloalquilo opcionalmente sustituido, heterociclilo opcionalmente sustituido o -COR⁷; R⁷ es -CR²R³-arilo opcionalmente sustituido, -CR²R³-heteroarilo opcionalmente sustituido, -CR²R³-heterociclilo, arilo opcionalmente sustituido, heteroarilo opcionalmente sustituido, C₃₋₈ cicloalquilo opcionalmente sustituido o heterociclilo opcionalmente sustituido; y Rˣ y Rʸ son, cada uno independientemente, H, C₁₋₁₀ alquilo opcionalmente sustituido, C₁₋₁₀ alcoxi opcionalmente sustituido o C₃₋₈ cicloalquilo opcionalmente sustituido; o Rˣ y Rʸ se toman junto con el carbono al cual están unidos para formar un anillo heterocíclico de 3 a 7 miembros que contiene 0 - 3 heteroátomos adicionales seleccionados de -N-, -S- y -O-; y/o un estereoisómero, un tautómero o una sal de aquel aceptable desde el punto de vista farmacéutico. Reivindicación 21: Uso de un compuesto de acuerdo con cualquiera de las reivindicaciones anteriores en un medicamento para tratar el cáncer. Reivindicación 23: El uso de acuerdo con la reivindicación 22, que también comprende un agente antineoplásico adicional.
ARP160100897A 2015-04-03 2016-04-01 Inhibidores de ido (indolamina-2,3-dioxigenasa) AR104176A1 (es)

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