AR100095A1 - Formas sólidas del ácido {[(2r,3s,4r,5s)-4-(4-cloro-2-fluoro-fenil)-3-(3-cloro-2-fluoro-fenil)-4-ciano-5-(2,2-dimetil-propil)-pirrolidin-2-carbonil]-amino}-3-metoxi-benzoico - Google Patents

Formas sólidas del ácido {[(2r,3s,4r,5s)-4-(4-cloro-2-fluoro-fenil)-3-(3-cloro-2-fluoro-fenil)-4-ciano-5-(2,2-dimetil-propil)-pirrolidin-2-carbonil]-amino}-3-metoxi-benzoico

Info

Publication number
AR100095A1
AR100095A1 ARP150101148A ARP150101148A AR100095A1 AR 100095 A1 AR100095 A1 AR 100095A1 AR P150101148 A ARP150101148 A AR P150101148A AR P150101148 A ARP150101148 A AR P150101148A AR 100095 A1 AR100095 A1 AR 100095A1
Authority
AR
Argentina
Prior art keywords
fluoro
chloro
phenyl
solid forms
compound
Prior art date
Application number
ARP150101148A
Other languages
English (en)
Original Assignee
Hoffmann La Roche
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 Hoffmann La Roche filed Critical Hoffmann La Roche
Publication of AR100095A1 publication Critical patent/AR100095A1/es

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Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D207/00Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom
    • C07D207/02Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom with only hydrogen or carbon atoms directly attached to the ring nitrogen atom
    • C07D207/04Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having no double bonds between ring members or between ring members and non-ring members
    • C07D207/10Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having no 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, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
    • C07D207/16Carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals
    • 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
    • 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
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P43/00Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D207/00Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom
    • C07D207/02Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom with only hydrogen or carbon atoms directly attached to the ring nitrogen atom
    • C07D207/04Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having no double bonds between ring members or between ring members and non-ring members
    • C07D207/10Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having no 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, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
    • 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

Abstract

La presente solicitud describe formas sólidas del compuesto de fórmula (1), los métodos para producirlos, así como composiciones que comprenden dichas formas sólidas. Reivindicación 1: Una forma sólida del compuesto de fórmula (1), seleccionado de e) una forma sustancialmente amorfa del compuesto de fórmula (1); f) un hemihidrato, hidrato, hemisolvato o solvato del compuesto de fórmula (1); o g) un polimorfo del compuesto de fórmula (1); o h) una sal farmacéuticamente aceptable del compuesto de fórmula (1).
ARP150101148A 2014-04-15 2015-04-15 Formas sólidas del ácido {[(2r,3s,4r,5s)-4-(4-cloro-2-fluoro-fenil)-3-(3-cloro-2-fluoro-fenil)-4-ciano-5-(2,2-dimetil-propil)-pirrolidin-2-carbonil]-amino}-3-metoxi-benzoico AR100095A1 (es)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US201461979649P 2014-04-15 2014-04-15

Publications (1)

Publication Number Publication Date
AR100095A1 true AR100095A1 (es) 2016-09-07

Family

ID=52815005

Family Applications (1)

Application Number Title Priority Date Filing Date
ARP150101148A AR100095A1 (es) 2014-04-15 2015-04-15 Formas sólidas del ácido {[(2r,3s,4r,5s)-4-(4-cloro-2-fluoro-fenil)-3-(3-cloro-2-fluoro-fenil)-4-ciano-5-(2,2-dimetil-propil)-pirrolidin-2-carbonil]-amino}-3-metoxi-benzoico

Country Status (18)

Country Link
US (1) US10227298B2 (es)
EP (2) EP3459933B1 (es)
JP (2) JP6621761B2 (es)
KR (1) KR20160138307A (es)
CN (1) CN106458886A (es)
AR (1) AR100095A1 (es)
AU (1) AU2015249018A1 (es)
BR (1) BR112016023767A2 (es)
CA (1) CA2943571A1 (es)
ES (1) ES2928706T3 (es)
IL (1) IL247974A0 (es)
MA (1) MA39877A (es)
MX (1) MX2016013439A (es)
PL (1) PL3459933T3 (es)
RU (1) RU2016144187A (es)
SG (1) SG11201608559QA (es)
WO (1) WO2015158648A1 (es)
ZA (1) ZA201606653B (es)

Families Citing this family (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
PL3458101T3 (pl) 2016-05-20 2021-05-31 F. Hoffmann-La Roche Ag Koniugaty PROTAC-przeciwciało i sposoby ich stosowania
WO2019213106A1 (en) 2018-04-30 2019-11-07 Teva Pharmaceuticals International Gmbh Solid state forms of idasanutlin
WO2023056069A1 (en) 2021-09-30 2023-04-06 Angiex, Inc. Degrader-antibody conjugates and methods of using same

Family Cites Families (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US8354444B2 (en) * 2008-09-18 2013-01-15 Hoffmann-La Roche Inc. Substituted pyrrolidine-2-carboxamides
US8993614B2 (en) * 2012-03-15 2015-03-31 F. Hoffmann-La Roche Ag Substituted pyrrolidine-2-carboxamides
US9216170B2 (en) * 2012-03-19 2015-12-22 Hoffmann-La Roche Inc. Combination therapy for proliferative disorders
US20130245089A1 (en) * 2012-03-19 2013-09-19 Hoffmann-La Roche Inc. Method for administration
BR112014029530A2 (pt) * 2012-05-30 2017-06-27 Hoffmann La Roche compostos, composição farmacêutica e uso de um composto
MY192032A (en) * 2013-01-22 2022-07-24 Hoffmann La Roche Pharmaceutical composition with improved bioavailability
EP2958893B1 (en) 2013-02-21 2017-05-03 F. Hoffmann-La Roche AG Asymmetric synthesis of a substituted pyrrolidine-2-carboxamide

Also Published As

Publication number Publication date
EP3459933B1 (en) 2022-08-24
JP6887980B2 (ja) 2021-06-16
EP3459933A2 (en) 2019-03-27
SG11201608559QA (en) 2016-11-29
RU2016144187A3 (es) 2018-11-13
AU2015249018A1 (en) 2016-10-06
EP3459933A3 (en) 2019-05-29
BR112016023767A2 (pt) 2017-08-15
MA39877A (fr) 2017-02-22
CN106458886A (zh) 2017-02-22
JP6621761B2 (ja) 2019-12-18
IL247974A0 (en) 2016-11-30
JP2017511362A (ja) 2017-04-20
US20170037005A1 (en) 2017-02-09
JP2019055960A (ja) 2019-04-11
ZA201606653B (en) 2018-05-30
KR20160138307A (ko) 2016-12-02
RU2016144187A (ru) 2018-05-16
WO2015158648A1 (en) 2015-10-22
US10227298B2 (en) 2019-03-12
MX2016013439A (es) 2016-11-17
EP3131878A1 (en) 2017-02-22
ES2928706T3 (es) 2022-11-22
CA2943571A1 (en) 2015-10-22
PL3459933T3 (pl) 2023-01-23

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