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PE20240220A1 - SAL TARTRATO DE 1-{(2S)-2-AMINO-4-[2,4-BIS(TRIFLUOROMETIL)-5,8-DI-HIDROPIRIDO[3,4-d]PIRIMIDIN-7(6H)-IL]-4-OXOBUTIL}-5,5-DIFLUORO-PIPERIDIN-2-ONA 1,5 HIDRATO - Google Patents

SAL TARTRATO DE 1-{(2S)-2-AMINO-4-[2,4-BIS(TRIFLUOROMETIL)-5,8-DI-HIDROPIRIDO[3,4-d]PIRIMIDIN-7(6H)-IL]-4-OXOBUTIL}-5,5-DIFLUORO-PIPERIDIN-2-ONA 1,5 HIDRATO

Info

Publication number
PE20240220A1
PE20240220A1 PE2023001454A PE2023001454A PE20240220A1 PE 20240220 A1 PE20240220 A1 PE 20240220A1 PE 2023001454 A PE2023001454 A PE 2023001454A PE 2023001454 A PE2023001454 A PE 2023001454A PE 20240220 A1 PE20240220 A1 PE 20240220A1
Authority
PE
Peru
Prior art keywords
piperidin
difluoro
hydrate
trifluoromethyl
bis
Prior art date
Application number
PE2023001454A
Other languages
English (en)
Inventor
Ki Sook Park
Jung Min Yun
Bong Chan Kim
Kyu Young Kim
Ji Hye Lee
Original Assignee
Lg Chemical Ltd
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=45995015&utm_source=google_patent&utm_medium=platform_link&utm_campaign=public_patent_search&patent=PE20240220(A1) "Global patent litigation dataset” by Darts-ip is licensed under a Creative Commons Attribution 4.0 International License.
Application filed by Lg Chemical Ltd filed Critical Lg Chemical Ltd
Publication of PE20240220A1 publication Critical patent/PE20240220A1/es

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D471/00Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00
    • C07D471/02Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00 in which the condensed system contains two hetero rings
    • C07D471/04Ortho-condensed systems
    • 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
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P3/00Drugs for disorders of the metabolism
    • A61P3/04Anorexiants; Antiobesity agents
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P3/00Drugs for disorders of the metabolism
    • A61P3/08Drugs for disorders of the metabolism for glucose homeostasis
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P3/00Drugs for disorders of the metabolism
    • A61P3/08Drugs for disorders of the metabolism for glucose homeostasis
    • A61P3/10Drugs for disorders of the metabolism for glucose homeostasis for hyperglycaemia, e.g. antidiabetics
    • 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

Landscapes

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

Abstract

La presente invencion se refiere al 1,5 hidrato de tartrato de 1-{(2S)-2-amino-4-[2,4-bis(trifluorometil)-5,8-dihidropirido[3,4-d]pirimidin-7(6H)-il]-4-oxobutil}-5,5-difluoro-piperidin-2-ona; caracterizados porque los valores del pico 2 theta en el difractograma de XRD son de 14.7766°, 15.4912°, 17.835°, 20.036°, 21.322° y 22.694°; las absorbancias caracteristicas en el espectro infrarrojo (EI) son 3591, 3401, 3128, 1712, 1655, 1636, 1229, 1205, 1129 y 1058 cm-1; y el espectro de calorimetria de barrido diferencial tiene el pico endotermico de 118.17°C en rangos de temperatura de 90-130 °C y el pico endotermico de 153.44°C en el rango de temperatura de 130-160 °C; un contenido de agua en el rango de 3,5-5,5% y un cambio de peso de 0,8% o menos dependiendo del cambio de humedad externa en el rango de 5 a 95% HR. Este compuesto tiene actividad inhibitoria superior contra la dipeptidil peptidasa-IV (DPP-IV). Tambien se refiere a un proceso para preparar dicho compuesto y una composicion farmaceutica que lo comprende.
PE2023001454A 2010-11-01 2011-10-31 SAL TARTRATO DE 1-{(2S)-2-AMINO-4-[2,4-BIS(TRIFLUOROMETIL)-5,8-DI-HIDROPIRIDO[3,4-d]PIRIMIDIN-7(6H)-IL]-4-OXOBUTIL}-5,5-DIFLUORO-PIPERIDIN-2-ONA 1,5 HIDRATO PE20240220A1 (es)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
KR20100107868 2010-11-01
PCT/KR2011/008186 WO2012060590A2 (en) 2010-11-01 2011-10-31 Hydrate of 1-{(2s)-2-amino-4-[2,4-bis(trifluoromethyl)-5,8-di- hydropyrido[3,4-d]pyrimidin-7(6h)-yl]-4-oxobutyl}-5,5-difluoro-piperidin-2-one tartrate

Publications (1)

Publication Number Publication Date
PE20240220A1 true PE20240220A1 (es) 2024-02-16

Family

ID=45995015

Family Applications (3)

Application Number Title Priority Date Filing Date
PE2013000904A PE20140392A1 (es) 2010-11-01 2011-10-31 HIDRATO DE TARTRATO DE 1-{(2S)-2-AMINO-4-[2,4-BIS(TRIFLUOROMETIL)-5,8-DI-HIDROPIRIDO[3,4-d]PIRIMIDIN-7(6H)-IL]-4-OXOBUTIL}-5,5-DIFLUORO-PIPERIDIN-2-ONA
PE2018000088A PE20180464A1 (es) 2010-11-01 2011-10-31 HIDRATO DE TARTRATO DE 1-{(2S)-2-AMINO-4-[2,4-BIS(TRIFLUOROMETIL)-5,8-DI-HIDROPIRIDO[3,4-d]PIRIMIDIN-7(6H)-IL]-4-OXOBUTIL}-5,5-DIFLUORO-PIPERIDIN-2-ONA
PE2023001454A PE20240220A1 (es) 2010-11-01 2011-10-31 SAL TARTRATO DE 1-{(2S)-2-AMINO-4-[2,4-BIS(TRIFLUOROMETIL)-5,8-DI-HIDROPIRIDO[3,4-d]PIRIMIDIN-7(6H)-IL]-4-OXOBUTIL}-5,5-DIFLUORO-PIPERIDIN-2-ONA 1,5 HIDRATO

Family Applications Before (2)

Application Number Title Priority Date Filing Date
PE2013000904A PE20140392A1 (es) 2010-11-01 2011-10-31 HIDRATO DE TARTRATO DE 1-{(2S)-2-AMINO-4-[2,4-BIS(TRIFLUOROMETIL)-5,8-DI-HIDROPIRIDO[3,4-d]PIRIMIDIN-7(6H)-IL]-4-OXOBUTIL}-5,5-DIFLUORO-PIPERIDIN-2-ONA
PE2018000088A PE20180464A1 (es) 2010-11-01 2011-10-31 HIDRATO DE TARTRATO DE 1-{(2S)-2-AMINO-4-[2,4-BIS(TRIFLUOROMETIL)-5,8-DI-HIDROPIRIDO[3,4-d]PIRIMIDIN-7(6H)-IL]-4-OXOBUTIL}-5,5-DIFLUORO-PIPERIDIN-2-ONA

Country Status (29)

Country Link
US (1) US8859567B2 (es)
EP (1) EP2635580B1 (es)
JP (1) JP6193762B2 (es)
KR (1) KR101446789B1 (es)
CN (1) CN103189375B (es)
AP (1) AP3287A (es)
AR (1) AR083591A1 (es)
AU (1) AU2011324253B2 (es)
BR (1) BR112013010586A2 (es)
CA (1) CA2814357C (es)
CL (1) CL2013001137A1 (es)
CO (1) CO6710945A2 (es)
DO (1) DOP2013000090A (es)
EA (1) EA024679B1 (es)
EC (1) ECSP13012599A (es)
GE (1) GEP20156218B (es)
IL (1) IL225808A (es)
MA (1) MA34625B1 (es)
MX (1) MX341584B (es)
MY (1) MY156428A (es)
NZ (1) NZ609644A (es)
PE (3) PE20140392A1 (es)
PH (1) PH12013500685A1 (es)
SG (1) SG189931A1 (es)
TW (1) TWI519533B (es)
UA (1) UA106445C2 (es)
UY (1) UY33696A (es)
WO (1) WO2012060590A2 (es)
ZA (1) ZA201302646B (es)

Families Citing this family (9)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP5066175B2 (ja) 2006-03-31 2012-11-07 ジヤンセン・フアーマシユーチカ・ナームローゼ・フエンノートシヤツプ ヒスタミンh4受容体のモジュレーターとしてのベンゾイミダゾール−2−イルピリミジンおよびピラジン
US9371311B2 (en) 2008-06-30 2016-06-21 Janssen Pharmaceutica Nv Benzoimidazol-2-yl pyrimidine derivatives
WO2012170702A1 (en) 2011-06-08 2012-12-13 Arena Pharmaceuticals, Inc. Modulators of the gpr119 receptor and the treatment of disorders related thereto
MY180726A (en) 2013-03-06 2020-12-08 Janssen Pharmaceutica Nv Benzoimidazol-2-yl pyrimidine modulators of the histamine h4 receptor
PH12023550900A1 (en) * 2020-10-13 2024-03-04 Lg Chemical Ltd Oral combined formulation including gemigliptin and dapagliflozin and preparation method therefor
KR20250137744A (ko) 2024-03-11 2025-09-19 엠에프씨 주식회사 제미글립틴의 신규 결정형 및 이의 제조방법
KR20250147756A (ko) 2024-03-27 2025-10-14 엠에프씨 주식회사 신규한 형태의 제미글립틴 말산염 결정형 및 이의 제조방법
KR20250155700A (ko) 2024-04-24 2025-10-31 주식회사 다산제약 제미글립틴 산부가염 제조방법 및 이를 유효성분으로 포함하는 dpp-4 저해용 조성물
CN119285630B (zh) * 2024-09-05 2025-05-27 安徽峆一药业股份有限公司 一种吉格列汀草酸盐及其晶型、制备方法与应用

Family Cites Families (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
ATE451369T1 (de) 2002-07-15 2009-12-15 Merck & Co Inc Piperidinopyrimidindipeptidylpeptidaseinhibitor n zur behandlung von diabetes
EP1592689A4 (en) * 2003-01-31 2008-12-24 Merck & Co Inc 3-AMINO-4-PHENYLBUTANEAN DERIVATIVES AS DIPEPTIDYLPEPTIDASE INHIBITORS FOR THE TREATMENT OR PREVENTION OF DIABETES
TWI357902B (en) * 2005-04-01 2012-02-11 Lg Life Science Ltd Dipeptidyl peptidase-iv inhibiting compounds, meth

Also Published As

Publication number Publication date
ECSP13012599A (es) 2013-07-31
UY33696A (es) 2012-04-30
CN103189375B (zh) 2016-08-10
MX2013004776A (es) 2013-11-04
CA2814357A1 (en) 2012-05-10
TW201245189A (en) 2012-11-16
AP3287A (en) 2015-05-31
KR101446789B1 (ko) 2014-10-01
NZ609644A (en) 2016-02-26
AR083591A1 (es) 2013-03-06
PH12013500685A1 (en) 2015-10-02
PE20140392A1 (es) 2014-03-22
CL2013001137A1 (es) 2013-09-06
MY156428A (en) 2016-02-26
CN103189375A (zh) 2013-07-03
BR112013010586A2 (pt) 2016-08-09
UA106445C2 (ru) 2014-08-26
EA024679B1 (ru) 2016-10-31
MX341584B (es) 2016-08-25
CO6710945A2 (es) 2013-07-15
GEP20156218B (en) 2015-01-12
MA34625B1 (fr) 2013-10-02
KR20120046069A (ko) 2012-05-09
SG189931A1 (en) 2013-06-28
US8859567B2 (en) 2014-10-14
IL225808A (en) 2016-08-31
AU2011324253A1 (en) 2013-05-02
WO2012060590A3 (en) 2012-06-28
EA201390644A1 (ru) 2014-11-28
US20130203787A1 (en) 2013-08-08
EP2635580A2 (en) 2013-09-11
TWI519533B (zh) 2016-02-01
EP2635580A4 (en) 2014-04-02
CA2814357C (en) 2015-07-07
AU2011324253B2 (en) 2015-10-29
AP2013006866A0 (en) 2013-05-31
ZA201302646B (en) 2014-01-29
JP6193762B2 (ja) 2017-09-06
WO2012060590A2 (en) 2012-05-10
JP2013540810A (ja) 2013-11-07
DOP2013000090A (es) 2018-06-30
PE20180464A1 (es) 2018-03-06
EP2635580B1 (en) 2015-08-12
IL225808A0 (en) 2013-06-27

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