JP2007509143A5 - - Google Patents

Download PDF

Info

Publication number
JP2007509143A5
JP2007509143A5 JP2006536635A JP2006536635A JP2007509143A5 JP 2007509143 A5 JP2007509143 A5 JP 2007509143A5 JP 2006536635 A JP2006536635 A JP 2006536635A JP 2006536635 A JP2006536635 A JP 2006536635A JP 2007509143 A5 JP2007509143 A5 JP 2007509143A5
Authority
JP
Japan
Prior art keywords
pyridin
methanone
chlorophenyl
bistrifluoromethylbenzyl
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.)
Granted
Application number
JP2006536635A
Other languages
English (en)
Japanese (ja)
Other versions
JP2007509143A (ja
JP4959336B2 (ja
Filing date
Publication date
Application filed filed Critical
Priority claimed from PCT/US2004/030914 external-priority patent/WO2005042515A1/en
Publication of JP2007509143A publication Critical patent/JP2007509143A/ja
Publication of JP2007509143A5 publication Critical patent/JP2007509143A5/ja
Application granted granted Critical
Publication of JP4959336B2 publication Critical patent/JP4959336B2/ja
Anticipated expiration legal-status Critical
Expired - Lifetime legal-status Critical Current

Links

JP2006536635A 2003-10-24 2004-10-12 {2−[1−(3,5−ビストリフルオロメチルベンジル)−5−ピリジン−4−イル−1h−[1,2,3]トリアゾル−4−イル]−ピリジン−3−イル}−(2−クロロフェニル)−メタノンの新規の結晶形態 Expired - Lifetime JP4959336B2 (ja)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
US51430003P 2003-10-24 2003-10-24
US60/514,300 2003-10-24
PCT/US2004/030914 WO2005042515A1 (en) 2003-10-24 2004-10-12 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

Publications (3)

Publication Number Publication Date
JP2007509143A JP2007509143A (ja) 2007-04-12
JP2007509143A5 true JP2007509143A5 (https=) 2007-10-18
JP4959336B2 JP4959336B2 (ja) 2012-06-20

Family

ID=34549327

Family Applications (1)

Application Number Title Priority Date Filing Date
JP2006536635A Expired - Lifetime JP4959336B2 (ja) 2003-10-24 2004-10-12 {2−[1−(3,5−ビストリフルオロメチルベンジル)−5−ピリジン−4−イル−1h−[1,2,3]トリアゾル−4−イル]−ピリジン−3−イル}−(2−クロロフェニル)−メタノンの新規の結晶形態

Country Status (28)

Country Link
US (1) US7381826B2 (https=)
JP (1) JP4959336B2 (https=)
KR (1) KR100848407B1 (https=)
CN (1) CN1863791B (https=)
AR (1) AR046131A1 (https=)
AT (1) ATE462700T1 (https=)
AU (1) AU2004285855B8 (https=)
BR (1) BRPI0415010B8 (https=)
CA (1) CA2542140C (https=)
CL (2) CL2009001311A1 (https=)
CR (1) CR8353A (https=)
DE (1) DE602004026333D1 (https=)
DK (1) DK1675846T3 (https=)
EA (1) EA008881B1 (https=)
EC (1) ECSP066517A (https=)
ES (1) ES2340772T3 (https=)
HR (1) HRP20100207T1 (https=)
IL (1) IL174926A0 (https=)
MA (1) MA28329A1 (https=)
MY (1) MY157375A (https=)
NO (1) NO335090B1 (https=)
NZ (2) NZ545917A (https=)
PE (1) PE20050481A1 (https=)
PT (1) PT1675846E (https=)
TW (1) TW200524906A (https=)
UA (1) UA82901C2 (https=)
WO (1) WO2005042515A1 (https=)
ZA (1) ZA200603234B (https=)

Families Citing this family (17)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
BRPI0721069A2 (pt) 2006-12-20 2014-02-04 Lilly Co Eli Intermediários e processo útil na preparação de {2-[1-(3,5-bis-trifluorometil-benzil)-5-piridin-4-il-1h[1,2, 3]triazol-4-il]-piridin-3-il}-2-clorofenil)-metanona
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
ES2824552T3 (es) 2015-03-04 2021-05-12 Vanda Pharmaceuticals Inc Método de tratamiento con tradipitant
WO2017031215A1 (en) * 2015-08-17 2017-02-23 Eli Lilly And Company Process development of a pyridine-containing nk-1 receptor antagonist
AU2018331267B2 (en) 2017-09-13 2024-03-07 Vanda Pharmaceuticals Inc. Improved treatment of atopic dermatitis with tradipitant
CN119074729A (zh) * 2017-11-17 2024-12-06 万达制药公司 使用川地匹坦治疗胃肠疾病的方法
CA3101210A1 (en) * 2018-06-08 2019-12-12 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
HUE070000T2 (hu) 2018-09-28 2025-04-28 Vanda Pharmaceuticals Inc Tradipitant alkalmazása utazási betegségben
WO2020117811A1 (en) * 2018-12-03 2020-06-11 Vanda Pharmaceuticals Inc. Method of treatment with tradipitant
KR20220145844A (ko) 2020-02-25 2022-10-31 반다 파마슈티칼즈, 인코퍼레이티드. 트라디피탄트를 이용한 아토피 피부염의 개선된 치료
JP7791832B2 (ja) 2020-03-26 2025-12-24 バンダ・ファーマシューティカルズ・インコーポレイテッド トラジピタントによる下気道感染症の治療
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
AU2023413130A1 (en) 2022-12-21 2025-06-05 Vanda Pharmaceuticals Inc. Methods of treatment with tradipitant
EP4599831A1 (en) 2024-02-09 2025-08-13 Vanda Pharmaceuticals Inc. Treatment of gastroparesis with tradipitant

Family Cites Families (8)

* 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
DE69736390T2 (de) * 1996-10-07 2007-07-26 Merck Sharp & Dohme Ltd., Hoddesdon Zns-penetrierende nk-1 rezeptorantagonisten als antidepressivum und / oder anxiolytikum
BR0013551A (pt) * 1999-08-13 2003-06-17 Vertex Pharma Inibidores de cinases n-terminal cjun (jnk) e outras cinases de proteìnas
AU1343901A (en) * 1999-10-29 2001-05-14 Merck & Co., Inc. Polymorphic form of a tachykinin receptor antagonist
US20020044971A1 (en) * 2000-07-07 2002-04-18 Amidon Gordon L. Dissolution rate of poorly soluble drugs
AU2003230829B8 (en) 2002-04-26 2008-12-11 Eli Lilly And Company Triazole derivatives as tachykinin receptor antagonists

Similar Documents

Publication Publication Date Title
JP2007509143A5 (https=)
JP4624667B2 (ja) 1−4−(5−シアノインドール−3−イル)ブチル−4−(2−カルバモイルベンゾフラン−5−イル)ピペラジン塩酸塩の多形相
JP4336106B2 (ja) 非晶質アトルバスタチンカルシウムの調製
BG64508B1 (bg) Кристален полиморфен (+)-(s)- клопидогрел хидрогенсулфат, метод за получаването му и фармацевтичен състав, който го съдържа
JP2004501191A (ja) カルベジロール
JP2007504160A5 (https=)
CA3097312A1 (en) Crystalline forms of a tlr7/tlr8 inhibitor
JP2002509136A (ja) Hivプロテアーゼ抑制剤重硫酸塩
JP2006514626A5 (https=)
RU2000128658A (ru) Тиенилазолилалкоксиэтанамны, их производные и их применение в качестве лекарственных средств
SG184721A1 (en) Method of treating polycystic kidney diseases with ceramide derivatives
JP2023548160A (ja) 1-(3-シアノ-1-イソプロピル-インドール-5-イル)ピラゾール-4-カルボン酸の結晶性粒子の製造方法およびそれを含む薬学的組成物
CA2542140A1 (en) 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
CN104098570A (zh) 替卡格雷晶型及其制备方法和用途
JP2024517431A5 (https=)
TWI445697B (zh) 塔適那偉(atazanavir)硫酸氫鹽之製法及其新穎的形式
RU2193560C2 (ru) Новая соль
CA2518999A1 (en) Crystalline and amorphous solids of pantoprazole and processes for their preparation
HUP0300596A2 (hu) Amorf toraszemid módosulat, eljárás az előállítására, alkalmazása és ezt tartalmazó gyógyszerkészítmények
JP2018521055A (ja) サクビトリルカルシウム塩
JP2016539994A (ja) α,ω‐二置換ジヒドロキシシクロペンチル化合物の固体形態、並びにその製造及び使用方法
HUP0302135A2 (hu) A toraszemid új V. polimorf módosulata, eljárás előállítására, alkalmazása nyersanyagként, valamint ilyen módosulatot tartalmazó gyógyászati készítmények
TWI819279B (zh) 2-[(4s)-8-氟-2-[4-(3-甲氧基苯基)哌嗪-1-基]-3-[2-甲氧基-5-(三氟甲基)苯基]-4h-喹唑啉-4-基]乙酸之鉀鹽
JP2007528349A (ja) 高い安定性を有する無定形アムロジピンカムシレート、その製造方法及びこれを含む経口投与用組成物
CN115581118A (zh) 制造结晶形式的2-[(4s)-8-氟-2-[4-(3-甲氧基苯基)哌嗪-1-基]-3-[2-甲氧基-5-(三氟甲基)苯基]-4h-喹唑啉-4-基]乙酸钠三水合物的方法