PE20120907A1 - Sal de clorhidrato de ((1s,2s,4r)-4-{4-[(1s)-2,3-dihidro-1h-inden-1-ilamino]-7h-pirrolo[2,3-d]pirimidin-7-il}-2-hidroxiciclopentil)metilsulfamato - Google Patents

Sal de clorhidrato de ((1s,2s,4r)-4-{4-[(1s)-2,3-dihidro-1h-inden-1-ilamino]-7h-pirrolo[2,3-d]pirimidin-7-il}-2-hidroxiciclopentil)metilsulfamato

Info

Publication number
PE20120907A1
PE20120907A1 PE2011001962A PE2011001962A PE20120907A1 PE 20120907 A1 PE20120907 A1 PE 20120907A1 PE 2011001962 A PE2011001962 A PE 2011001962A PE 2011001962 A PE2011001962 A PE 2011001962A PE 20120907 A1 PE20120907 A1 PE 20120907A1
Authority
PE
Peru
Prior art keywords
xrpd
peaks
presenting
methylsulfamate
pirrolo
Prior art date
Application number
PE2011001962A
Other languages
English (en)
Inventor
Ian G Armitage
Reenu Chopra
Martin Ian Cooper
Marianne Langton
Original Assignee
Millennium Pharm Inc
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 Millennium Pharm Inc filed Critical Millennium Pharm Inc
Publication of PE20120907A1 publication Critical patent/PE20120907A1/es

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Classifications

    • 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
    • A61K31/495Heterocyclic 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
    • A61K31/505Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim
    • A61K31/519Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim ortho- or peri-condensed with heterocyclic 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
    • A61K31/495Heterocyclic 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
    • A61K31/505Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim
    • A61K31/519Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim ortho- or peri-condensed with heterocyclic rings
    • A61K31/52Purines, e.g. adenine
    • A61K31/522Purines, e.g. adenine having oxo groups directly attached to the heterocyclic ring, e.g. hypoxanthine, guanine, acyclovir
    • 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
    • A61P35/00Antineoplastic agents
    • A61P35/04Antineoplastic agents specific for metastasis
    • 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
    • C07D487/00Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00
    • C07D487/02Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00 in which the condensed system contains two hetero rings
    • C07D487/04Ortho-condensed systems

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

Abstract

SE REFIERE A UNA SAL DE CLORHIDRATO DE ((1S,2S,4R)-4-{4-[(1S)-2,3-DIHIDRO-1H-INDEN-1-ILAMINO]-7H-PIRROLO[2,3-D]PIRIMIDIN-7-IL}-2-HIDROXICICLOPENTIL)METILSULFAMATO QUE COMPRENDE: (A) UNA FORMA 1 QUE SE CARACTERIZA POR PRESENTAR UN PATRON DE DIFRACCION DE POLVO DE RAYOS X (XRPD) CON PICOS EN ANGULOS 2THETA DE: 9.6º, 13.6º Y 19.1º O 9.6º, 13.6º, 14.5º, 19.1º Y 23.7º; (B) UNA FORMA 2 QUE SE CARACTERIZA POR PRESENTAR UN XRPD CON PICOS EN ANGULOS 2THETA DE: 8.7º, 18.2º Y 23.8º O 8.7º, 18.2º, 19.4º, 23.8º, 24.3º Y 27.5º; (C) UNA FORMA 3A QUE SE CARACTERIZA POR PRESENTAR UN XRPD CON PICOS EN ANGULOS 2THETA DE: 10.9º, 14.6º, 19.5º Y 24.0º O 10.9º, 14.6º, 16.9º, 19.5º, 24.0º Y 25.9º; (D) UNA FORMA 3B QUE SE CARACTERIZA POR PRESENTAR UN XRPD CON PICOS EN ANGULOS 2THETA DE: 10.8º, 16.9º, 23.7º Y 24.0º O 10.8º, 14.5º, 16.9º, 19.3º, 21.2º, 23.7º, 24.0º Y 28.8º; (E) UNA FORMA 3C QUE SE CARACTERIZA POR PRESENTAR UN XRPD CON PICOS EN ANGULOS 2THETA DE: 11.0º, 12.2º Y 24.4º; 11.0º, 12.2º, 14.9º, 19.8º, 24.0º Y 24.4º; (F) UNA FORMA 5 QUE SE CARACTERIZA POR PRESENTAR UN XRPD CON PICOS EN ANGULOS 2THETA DE: 16.7º Y 22.9º O 16.7º, 17.2º, 18.1º Y 22.9º; (G) UNA FORMA 7 QUE SE CARACTERIZA POR PRESENTAR UN XRPD CON PICOS EN ANGULOS 2THETA DE: 15.4º, 17.3º, 19.6º Y 22.5º O 10.0º, 15.4º, 16.6º, 17.3º, 18.0º, 18.3º, 19.6º, 22.0º Y 22.5º. DICHO COMPUESTO ES UN INHIBIDOR DE ENZIMA ACTIVANTE DE E1 UTIL EN EL TRATAMIENTO DEL CANCER
PE2011001962A 2009-05-14 2010-05-13 Sal de clorhidrato de ((1s,2s,4r)-4-{4-[(1s)-2,3-dihidro-1h-inden-1-ilamino]-7h-pirrolo[2,3-d]pirimidin-7-il}-2-hidroxiciclopentil)metilsulfamato PE20120907A1 (es)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US21622109P 2009-05-14 2009-05-14

Publications (1)

Publication Number Publication Date
PE20120907A1 true PE20120907A1 (es) 2012-08-18

Family

ID=42396430

Family Applications (2)

Application Number Title Priority Date Filing Date
PE2016001604A PE20161222A1 (es) 2009-05-14 2010-05-13 Sal de clorhidrato de ((1s,2s,4r)-4-{4-[(1s)-2,3-dihidro-1h-inden-1-ilamino]-7h-pirrolo[2,3-d]pirimidin-7-il}-2-hidroxiciclopentil)metilsulfamato
PE2011001962A PE20120907A1 (es) 2009-05-14 2010-05-13 Sal de clorhidrato de ((1s,2s,4r)-4-{4-[(1s)-2,3-dihidro-1h-inden-1-ilamino]-7h-pirrolo[2,3-d]pirimidin-7-il}-2-hidroxiciclopentil)metilsulfamato

Family Applications Before (1)

Application Number Title Priority Date Filing Date
PE2016001604A PE20161222A1 (es) 2009-05-14 2010-05-13 Sal de clorhidrato de ((1s,2s,4r)-4-{4-[(1s)-2,3-dihidro-1h-inden-1-ilamino]-7h-pirrolo[2,3-d]pirimidin-7-il}-2-hidroxiciclopentil)metilsulfamato

Country Status (18)

Country Link
US (2) US9187482B2 (es)
EP (2) EP2430026A1 (es)
JP (3) JP2012526808A (es)
KR (2) KR20120024715A (es)
CN (2) CN104016987A (es)
AU (1) AU2010248151B2 (es)
BR (1) BRPI1012142A2 (es)
CA (1) CA2761256C (es)
IL (1) IL216201A (es)
MX (1) MX2011012108A (es)
NZ (2) NZ621128A (es)
PE (2) PE20161222A1 (es)
PH (1) PH12015501925A1 (es)
RU (1) RU2562245C2 (es)
SG (2) SG10201402148SA (es)
UA (1) UA108986C2 (es)
WO (1) WO2010132110A1 (es)
ZA (1) ZA201108347B (es)

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JP2020534331A (ja) 2017-09-21 2020-11-26 ミレニアム ファーマシューティカルズ, インコーポレイテッドMillennium Pharmaceuticals, Inc. ((1s,2s,4r)−4−{4−[(1s)−2,3−ジヒドロ−1h−インデン−1−イルアミノ]−7h−ピロロ[2,3−d]ピリミジン−7−イル}−2−ヒドロキシシクロペンチル)メチルスルファメートの共結晶形態、その製剤及び使用
JP2022521972A (ja) * 2019-02-26 2022-04-13 ミレニアム ファーマシューティカルズ, インコーポレイテッド アジュバントとして有用な化合物
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Also Published As

Publication number Publication date
CA2761256C (en) 2021-01-05
EP3091020B1 (en) 2020-12-30
US20170000792A9 (en) 2017-01-05
BRPI1012142A2 (pt) 2016-03-29
KR20170102381A (ko) 2017-09-08
WO2010132110A1 (en) 2010-11-18
AU2010248151A1 (en) 2011-12-01
US20160030432A1 (en) 2016-02-04
US9187482B2 (en) 2015-11-17
EP3091020A3 (en) 2017-01-11
PE20161222A1 (es) 2016-12-01
SG175929A1 (en) 2011-12-29
PH12015501925A1 (en) 2018-01-22
CN102421780A (zh) 2012-04-18
IL216201A0 (en) 2012-01-31
MX2011012108A (es) 2011-12-08
EP3091020A2 (en) 2016-11-09
JP2017105816A (ja) 2017-06-15
UA108986C2 (uk) 2015-07-10
CA2761256A1 (en) 2010-11-18
JP2012526808A (ja) 2012-11-01
US20110021544A1 (en) 2011-01-27
RU2562245C2 (ru) 2015-09-10
EP2430026A1 (en) 2012-03-21
CN104016987A (zh) 2014-09-03
AU2010248151B2 (en) 2016-07-14
JP2015096547A (ja) 2015-05-21
NZ621128A (en) 2015-08-28
RU2011150826A (ru) 2013-06-20
ZA201108347B (en) 2014-05-26
IL216201A (en) 2015-11-30
SG10201402148SA (en) 2014-07-30
US10016427B2 (en) 2018-07-10
NZ596470A (en) 2014-04-30
KR20120024715A (ko) 2012-03-14

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