KR100848407B1 - {2-[1-(3,5-비스-트리플루오로메틸벤질)-5-피리딘-4-일-1h-[1,2,3]트리아졸-4-일]-피리딘-3-일}-(2-클로로페닐)-메탄온의 신규 결정질 형태 - Google Patents

{2-[1-(3,5-비스-트리플루오로메틸벤질)-5-피리딘-4-일-1h-[1,2,3]트리아졸-4-일]-피리딘-3-일}-(2-클로로페닐)-메탄온의 신규 결정질 형태 Download PDF

Info

Publication number
KR100848407B1
KR100848407B1 KR1020067007751A KR20067007751A KR100848407B1 KR 100848407 B1 KR100848407 B1 KR 100848407B1 KR 1020067007751 A KR1020067007751 A KR 1020067007751A KR 20067007751 A KR20067007751 A KR 20067007751A KR 100848407 B1 KR100848407 B1 KR 100848407B1
Authority
KR
South Korea
Prior art keywords
delete delete
pyridin
chlorophenyl
methanone
triazol
Prior art date
Legal status (The legal status 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 status listed.)
Expired - Lifetime
Application number
KR1020067007751A
Other languages
English (en)
Korean (ko)
Other versions
KR20060061388A (ko
Inventor
카르스텐 팀페
알피오 보르게제
데이비드 스코트 코페이
파멜라 카예 풋맨
스티븐 웨인 페더젠
수잔 마리 류트젤-에덴스
쉘라 렌욘가 타메제
카르스텐 웨버
Original Assignee
일라이 릴리 앤드 캄파니
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 일라이 릴리 앤드 캄파니 filed Critical 일라이 릴리 앤드 캄파니
Publication of KR20060061388A publication Critical patent/KR20060061388A/ko
Application granted granted Critical
Publication of KR100848407B1 publication Critical patent/KR100848407B1/ko
Anticipated expiration legal-status Critical
Expired - Lifetime legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D401/00Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom
    • C07D401/14Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing three or more hetero rings
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P1/00Drugs for disorders of the alimentary tract or the digestive system
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P25/00Drugs for disorders of the nervous system
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P25/00Drugs for disorders of the nervous system
    • A61P25/22Anxiolytics
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P25/00Drugs for disorders of the nervous system
    • A61P25/24Antidepressants
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D213/00Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members
    • C07D213/02Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members
    • C07D213/04Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom
    • C07D213/24Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom with substituted hydrocarbon radicals attached to ring carbon atoms
    • C07D213/44Radicals substituted by doubly-bound oxygen, sulfur, or nitrogen atoms, or by two such atoms singly-bound to the same carbon atom
    • C07D213/46Oxygen atoms
    • C07D213/50Ketonic radicals
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D401/00Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom
    • C07D401/02Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings
    • C07D401/04Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings directly linked by a ring-member-to-ring-member bond

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Health & Medical Sciences (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Animal Behavior & Ethology (AREA)
  • Veterinary Medicine (AREA)
  • Public Health (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • General Chemical & Material Sciences (AREA)
  • Medicinal Chemistry (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Engineering & Computer Science (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • General Health & Medical Sciences (AREA)
  • Neurology (AREA)
  • Biomedical Technology (AREA)
  • Neurosurgery (AREA)
  • Pain & Pain Management (AREA)
  • Psychiatry (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Plural Heterocyclic Compounds (AREA)
  • Pyridine Compounds (AREA)
  • Medicinal Preparation (AREA)
KR1020067007751A 2003-10-24 2004-10-12 {2-[1-(3,5-비스-트리플루오로메틸벤질)-5-피리딘-4-일-1h-[1,2,3]트리아졸-4-일]-피리딘-3-일}-(2-클로로페닐)-메탄온의 신규 결정질 형태 Expired - Lifetime KR100848407B1 (ko)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
US51430003P 2003-10-24 2003-10-24
US60/514,300 2003-10-24

Publications (2)

Publication Number Publication Date
KR20060061388A KR20060061388A (ko) 2006-06-07
KR100848407B1 true KR100848407B1 (ko) 2008-07-28

Family

ID=34549327

Family Applications (1)

Application Number Title Priority Date Filing Date
KR1020067007751A Expired - Lifetime KR100848407B1 (ko) 2003-10-24 2004-10-12 {2-[1-(3,5-비스-트리플루오로메틸벤질)-5-피리딘-4-일-1h-[1,2,3]트리아졸-4-일]-피리딘-3-일}-(2-클로로페닐)-메탄온의 신규 결정질 형태

Country Status (28)

Country Link
US (1) US7381826B2 (enExample)
JP (1) JP4959336B2 (enExample)
KR (1) KR100848407B1 (enExample)
CN (1) CN1863791B (enExample)
AR (1) AR046131A1 (enExample)
AT (1) ATE462700T1 (enExample)
AU (1) AU2004285855B8 (enExample)
BR (1) BRPI0415010B8 (enExample)
CA (1) CA2542140C (enExample)
CL (2) CL2009001310A1 (enExample)
CR (1) CR8353A (enExample)
DE (1) DE602004026333D1 (enExample)
DK (1) DK1675846T3 (enExample)
EA (1) EA008881B1 (enExample)
EC (1) ECSP066517A (enExample)
ES (1) ES2340772T3 (enExample)
HR (1) HRP20100207T1 (enExample)
IL (1) IL174926A0 (enExample)
MA (1) MA28329A1 (enExample)
MY (1) MY157375A (enExample)
NO (1) NO335090B1 (enExample)
NZ (2) NZ580480A (enExample)
PE (1) PE20050481A1 (enExample)
PT (1) PT1675846E (enExample)
TW (1) TW200524906A (enExample)
UA (1) UA82901C2 (enExample)
WO (1) WO2005042515A1 (enExample)
ZA (1) ZA200603234B (enExample)

Families Citing this family (17)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP2121610B1 (en) * 2006-12-20 2014-04-02 Eli Lilly & Company Novel intermediate and process useful in the preparation of {2-[1-(3,5-bis-trifluoromethyl-benzyl)-5-pyridin-4-yl-1h-[1,2,3]triazol-4-yl]-pyridin-3-yl}-(2-chlorophenyl)-methanone
WO2009075778A2 (en) * 2007-12-06 2009-06-18 The Regents Of The University Of California Nonpeptidic inhibitors of cruzain
US8080568B1 (en) * 2010-06-29 2011-12-20 Ewha University - Industry Collaboration Foundation 2-pyridyl substituted imidazoles as therapeutic ALK5 and/or ALK4 inhibitors
KR20170122777A (ko) 2015-03-04 2017-11-06 반다 파마슈티칼즈, 인코퍼레이티드. 트라디피턴트에 의한 치료 방법
US10287287B2 (en) 2015-08-17 2019-05-14 Eli Lilly And Company Process development of a pyridine-containing NK-1 receptor antagonist
KR20200054232A (ko) 2017-09-13 2020-05-19 반다 파마슈티칼즈, 인코퍼레이티드. 트라디피탄트를 이용한 아토피 피부염의 개선된 치료
KR20250140655A (ko) * 2017-11-17 2025-09-25 반다 파마슈티칼즈, 인코퍼레이티드. 트라디피탄트를 이용한 위장 질환의 치료 방법
US20210228555A1 (en) 2018-06-08 2021-07-29 Vanda Pharmaceuticals Inc. Method of treatment with tradipitant
US10821099B2 (en) 2018-09-28 2020-11-03 Vanda Pharmaceuticals Inc. Use of tradipitant in motion sickness
CN111918701B (zh) 2018-09-28 2024-08-02 万达制药公司 曲地匹坦在晕动病中的用途
WO2020117811A1 (en) * 2018-12-03 2020-06-11 Vanda Pharmaceuticals Inc. Method of treatment with tradipitant
WO2021173641A1 (en) 2020-02-25 2021-09-02 Vanda Pharmaceuticals Inc. Improved treatment of atopic dermatitis with tradipitant
WO2021195205A1 (en) 2020-03-26 2021-09-30 Vanda Pharmaceuticals Inc. Treatment of lower respiratory tract infection with tradipitant
WO2023019084A1 (en) 2021-08-12 2023-02-16 Vanda Pharmaceuticals Inc. Treatment of gastric accommodation with tradipitant
US20240350469A1 (en) 2021-08-31 2024-10-24 Vanda Pharmaceuticals Inc. Treatment of lower respiratory tract infection with tradipitant
WO2024138040A1 (en) 2022-12-21 2024-06-27 Vanda Pharmaceuticals Inc. Methods of treatment with tradipitant
US20250255855A1 (en) 2024-02-09 2025-08-14 Vanda Pharmaceuticals Inc. Method of treatment with tradipitant

Citations (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US6432952B1 (en) 1999-10-29 2002-08-13 Merck & Co., Inc. Polymorphic form of a tachykinin receptor antagonist
WO2003091226A1 (en) * 2002-04-26 2003-11-06 Eli Lilly And Company Triazole derivatives as tachykinin receptor antagonists

Family Cites Families (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US20020099067A1 (en) 1993-07-08 2002-07-25 Ulrich Posanski Pharmaceutical compositions for sparingly soluble therapeutic agents
GB9505492D0 (en) * 1995-03-18 1995-05-03 Merck Sharp & Dohme Therapeutic agents
GB9525296D0 (en) * 1995-12-11 1996-02-07 Merck Sharp & Dohme Therapeutic agents
JP2001502311A (ja) * 1996-10-07 2001-02-20 メルク シヤープ エンド ドーム リミテツド 抗鬱及び/又は抗不安薬としてのcns浸透性nk―1受容体拮抗薬
AR032130A1 (es) * 1999-08-13 2003-10-29 Vertex Pharma Un compuesto inhibidor de quinasas proteicas, una composicion farmaceutica que lo incluye, y un metodo para tratar afecciones con dicho compuesto
US20020044971A1 (en) 2000-07-07 2002-04-18 Amidon Gordon L. Dissolution rate of poorly soluble drugs

Patent Citations (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US6432952B1 (en) 1999-10-29 2002-08-13 Merck & Co., Inc. Polymorphic form of a tachykinin receptor antagonist
WO2003091226A1 (en) * 2002-04-26 2003-11-06 Eli Lilly And Company Triazole derivatives as tachykinin receptor antagonists

Also Published As

Publication number Publication date
AR046131A1 (es) 2005-11-23
JP4959336B2 (ja) 2012-06-20
CL2009001311A1 (es) 2009-10-02
NZ545917A (en) 2009-11-27
MY157375A (en) 2016-06-15
NZ580480A (en) 2010-02-26
ES2340772T3 (es) 2010-06-09
MA28329A1 (fr) 2006-12-01
CN1863791B (zh) 2011-12-07
HRP20100207T1 (hr) 2010-05-31
CR8353A (es) 2006-06-06
ATE462700T1 (de) 2010-04-15
CL2009001310A1 (es) 2009-12-04
US7381826B2 (en) 2008-06-03
DK1675846T3 (da) 2010-05-31
AU2004285855A1 (en) 2005-05-12
AU2004285855B8 (en) 2011-04-28
TW200524906A (en) 2005-08-01
PT1675846E (pt) 2010-04-20
PE20050481A1 (es) 2005-09-20
CA2542140C (en) 2012-05-29
NO20062371L (no) 2006-05-24
AU2004285855B2 (en) 2010-12-23
CN1863791A (zh) 2006-11-15
EA008881B1 (ru) 2007-08-31
KR20060061388A (ko) 2006-06-07
ZA200603234B (en) 2007-07-25
BRPI0415010A8 (pt) 2018-05-08
IL174926A0 (en) 2006-08-20
NO335090B1 (no) 2014-09-08
DE602004026333D1 (de) 2010-05-12
EA200600829A1 (ru) 2006-08-25
WO2005042515A1 (en) 2005-05-12
CA2542140A1 (en) 2005-05-12
UA82901C2 (en) 2008-05-26
BRPI0415010B1 (pt) 2019-07-09
US20070078166A1 (en) 2007-04-05
ECSP066517A (es) 2006-10-10
BRPI0415010B8 (pt) 2021-05-25
BRPI0415010A (pt) 2006-11-07
JP2007509143A (ja) 2007-04-12

Similar Documents

Publication Publication Date Title
KR100848407B1 (ko) {2-[1-(3,5-비스-트리플루오로메틸벤질)-5-피리딘-4-일-1h-[1,2,3]트리아졸-4-일]-피리딘-3-일}-(2-클로로페닐)-메탄온의 신규 결정질 형태
EP4025572B1 (en) Heterocyclic rip1 kinase inhibitors
EP3580220B1 (en) Aminotriazolopyridines as kinase inhibitors
DE60112791T2 (de) Piperidin mch antagonisten und ihre verwendung in der behandlung von obesität
JP6476205B2 (ja) RORγ修飾因子としてのヘテロ環式スルホン
EP2121610B1 (en) Novel intermediate and process useful in the preparation of {2-[1-(3,5-bis-trifluoromethyl-benzyl)-5-pyridin-4-yl-1h-[1,2,3]triazol-4-yl]-pyridin-3-yl}-(2-chlorophenyl)-methanone
CN107849011A (zh) 作为bace1抑制剂的2‑氨基‑3‑氟‑3‑(氟甲基)‑6‑甲基‑6‑苯基‑3,4,5,6‑四氢吡啶
JP2021501184A (ja) P2x3及び/又はp2x2/3受容体アンタゴニスト、それを含む医薬組成物及びその使用
CA3095415A1 (en) Compound with anticancer activity
JP6619503B2 (ja) Cgrp受容体アンタゴニスト
EP2504330A1 (en) Amino heteroaryl compounds as beta-secretase modulators and methods of use
JP2003514905A (ja) ピラジノン系トロンビン阻害薬
AU2017277002B2 (en) Pharmaceutically acceptable salt as renal outer medullary potassium channel inhibitor
EP1675846B1 (en) Novel crystalline forms of {2-[1-(3,5-bis-trifluoromethylbenzyl)-5-pyridin-4-yl-1h- [1,2,3]triazol-4-yl]-pyridin-3-yl}-(2-chlorophenyl)-methanone
MXPA06004444A (en) Novel crystalline forms of {2-[1-(3, 5-bis-trifluoromethylbenzyl) -5-pyridin-4-yl -1h-[1, 2, 3]triazol -4-yl]- pyridin-3-yl}- (2-chlorophenyl) -methanone
EP4620950A1 (en) Piperidine derivative, salt of same, and pharmaceutical composition containing same as active ingredient
TW202521108A (zh) 作為激酶抑制劑之三唑并吡啶醚連接化合物
TW201514162A (zh) 作爲鉀離子通道抑制劑之呔
HK1215574B (en) Diazacarbazole derivatives as tau-pet-ligands

Legal Events

Date Code Title Description
A201 Request for examination
PA0105 International application

Patent event date: 20060421

Patent event code: PA01051R01D

Comment text: International Patent Application

PA0201 Request for examination

Patent event code: PA02012R01D

Patent event date: 20060421

Comment text: Request for Examination of Application

PG1501 Laying open of application
E902 Notification of reason for refusal
PE0902 Notice of grounds for rejection

Comment text: Notification of reason for refusal

Patent event date: 20070427

Patent event code: PE09021S01D

E902 Notification of reason for refusal
PE0902 Notice of grounds for rejection

Comment text: Notification of reason for refusal

Patent event date: 20071024

Patent event code: PE09021S01D

E701 Decision to grant or registration of patent right
PE0701 Decision of registration

Patent event code: PE07011S01D

Comment text: Decision to Grant Registration

Patent event date: 20080424

GRNT Written decision to grant
PR0701 Registration of establishment

Comment text: Registration of Establishment

Patent event date: 20080718

Patent event code: PR07011E01D

PR1002 Payment of registration fee

Payment date: 20080718

End annual number: 3

Start annual number: 1

PG1601 Publication of registration
PR1001 Payment of annual fee

Payment date: 20110629

Start annual number: 4

End annual number: 4

PR1001 Payment of annual fee

Payment date: 20120628

Start annual number: 5

End annual number: 5

FPAY Annual fee payment

Payment date: 20130705

Year of fee payment: 6

PR1001 Payment of annual fee

Payment date: 20130705

Start annual number: 6

End annual number: 6

FPAY Annual fee payment

Payment date: 20140708

Year of fee payment: 7

PR1001 Payment of annual fee

Payment date: 20140708

Start annual number: 7

End annual number: 7

FPAY Annual fee payment

Payment date: 20150706

Year of fee payment: 8

PR1001 Payment of annual fee

Payment date: 20150706

Start annual number: 8

End annual number: 8

FPAY Annual fee payment

Payment date: 20160706

Year of fee payment: 9

PR1001 Payment of annual fee

Payment date: 20160706

Start annual number: 9

End annual number: 9

FPAY Annual fee payment

Payment date: 20170710

Year of fee payment: 10

PR1001 Payment of annual fee

Payment date: 20170710

Start annual number: 10

End annual number: 10

FPAY Annual fee payment

Payment date: 20180710

Year of fee payment: 11

PR1001 Payment of annual fee

Payment date: 20180710

Start annual number: 11

End annual number: 11

FPAY Annual fee payment

Payment date: 20190709

Year of fee payment: 12

PR1001 Payment of annual fee

Payment date: 20190709

Start annual number: 12

End annual number: 12

PR1001 Payment of annual fee

Payment date: 20200708

Start annual number: 13

End annual number: 13

PR1001 Payment of annual fee

Payment date: 20220705

Start annual number: 15

End annual number: 15

PR1001 Payment of annual fee

Payment date: 20230705

Start annual number: 16

End annual number: 16

PC1801 Expiration of term

Termination date: 20250412

Termination category: Expiration of duration