JP2008540547A5 - - Google Patents

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Publication number
JP2008540547A5
JP2008540547A5 JP2008511281A JP2008511281A JP2008540547A5 JP 2008540547 A5 JP2008540547 A5 JP 2008540547A5 JP 2008511281 A JP2008511281 A JP 2008511281A JP 2008511281 A JP2008511281 A JP 2008511281A JP 2008540547 A5 JP2008540547 A5 JP 2008540547A5
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JP
Japan
Prior art keywords
alkyl
heteroaryl
aryl
cycloalkyl
heterocyclo
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JP2008511281A
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English (en)
Japanese (ja)
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JP5047164B2 (ja
JP2008540547A (ja
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Priority claimed from US11/430,215 external-priority patent/US7737279B2/en
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Publication of JP2008540547A publication Critical patent/JP2008540547A/ja
Publication of JP2008540547A5 publication Critical patent/JP2008540547A5/ja
Application granted granted Critical
Publication of JP5047164B2 publication Critical patent/JP5047164B2/ja
Anticipated expiration legal-status Critical
Expired - Fee Related legal-status Critical Current

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JP2008511281A 2005-05-10 2006-05-09 IKK酵素活性の阻害剤としての1,6−ジヒドロ−1,3,5,6−テトラアザ−as−インダセンをベースとした三環式化合物およびそれを含む医薬組成物 Expired - Fee Related JP5047164B2 (ja)

Applications Claiming Priority (5)

Application Number Priority Date Filing Date Title
US67969205P 2005-05-10 2005-05-10
US60/679,692 2005-05-10
US11/430,215 US7737279B2 (en) 2005-05-10 2006-05-08 1,6-dihydro-1,3,5,6-tetraaza-as-indacene based tricyclic compounds and pharmaceutical compositions comprising same
US11/430,215 2006-05-08
PCT/US2006/017950 WO2006122137A1 (en) 2005-05-10 2006-05-09 1, 6 -dihydro- 1,3, 5, 6-tetraaza-as-indacene based tricyclic compounds and pharmaceutical compositions comprising same as inhibitors of ikk enzyme activity

Publications (3)

Publication Number Publication Date
JP2008540547A JP2008540547A (ja) 2008-11-20
JP2008540547A5 true JP2008540547A5 (https=) 2009-06-04
JP5047164B2 JP5047164B2 (ja) 2012-10-10

Family

ID=36808856

Family Applications (1)

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JP2008511281A Expired - Fee Related JP5047164B2 (ja) 2005-05-10 2006-05-09 IKK酵素活性の阻害剤としての1,6−ジヒドロ−1,3,5,6−テトラアザ−as−インダセンをベースとした三環式化合物およびそれを含む医薬組成物

Country Status (15)

Country Link
US (2) US7737279B2 (https=)
EP (1) EP1888584B1 (https=)
JP (1) JP5047164B2 (https=)
AR (1) AR053725A1 (https=)
AT (1) ATE465162T1 (https=)
CY (1) CY1110419T1 (https=)
DE (1) DE602006013816D1 (https=)
DK (1) DK1888584T3 (https=)
ES (1) ES2342976T3 (https=)
PE (1) PE20061424A1 (https=)
PL (1) PL1888584T3 (https=)
PT (1) PT1888584E (https=)
SI (1) SI1888584T1 (https=)
TW (1) TW200718422A (https=)
WO (1) WO2006122137A1 (https=)

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CN106103446B (zh) 2014-03-26 2019-07-30 豪夫迈·罗氏有限公司 作为自分泌运动因子(atx)和溶血磷脂酸(lpa)生产抑制剂的二环化合物
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CA2992889A1 (en) 2015-09-04 2017-03-09 F. Hoffmann-La Roche Ag Phenoxymethyl derivatives
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AU2016328365B2 (en) 2015-09-24 2020-04-23 F. Hoffmann-La Roche Ag New bicyclic compounds as dual ATX/CA inhibitors
CR20180057A (es) 2015-09-24 2018-04-02 Hoffmann La Roche Nuevos compuestos biciclicos como inhibidores duales de atx/ca.
US11512092B2 (en) 2015-10-16 2022-11-29 Abbvie Inc. Processes for the preparation of (3S,4R)-3-ethyl-4-(3H-imidazo[1,2-a]pyrrolo[2,3-e]-pyrazin-8-yl)-n-(2,2,2-trifluoroethyl)pyrrolidine-1-carboxamide and solid state forms thereof
US11365198B2 (en) 2015-10-16 2022-06-21 Abbvie Inc. Processes for the preparation of (3S,4R)-3-ethyl-4-(3H-imidazo[1,2-a]pyrrolo[2,3-e]-pyrazin-8-yl)-N-(2,2,2-trifluoroethyl)pyrrolidine-1-carboxamide and solid state forms thereof
US11524964B2 (en) 2015-10-16 2022-12-13 Abbvie Inc. Processes for the preparation of (3S,4R)-3-ethyl-4-(3H-imidazo[1,2-a]pyrrolo[2,3-e]-pyrazin-8-yl)-n-(2,2,2-trifluoroethyl)pyrrolidine-1-carboxamide and solid state forms thereof
US10550126B2 (en) 2015-10-16 2020-02-04 Abbvie Inc. Processes for the preparation of (3S,4R)-3-ethyl-4-(3H-imidazo[1,2-A]pyrrolo[2,3-e]-pyrazin-8-yl)-N-(2,2,2-trifluoroethyl)pyrrolidine-1-carboxamide and solid state forms thereof
US11780848B2 (en) 2015-10-16 2023-10-10 Abbvie Inc. Processes for the preparation of (3S,4R)-3-ethyl-4-(3H-imidazo[1,2-a]pyrrolo[2,3-e]-pyrazin-8-yl)-n-(2,2,2-trifluoroethyl)pyrrolidine-1- carboxamide and solid state forms thereof
US12365689B2 (en) 2015-10-16 2025-07-22 Abbvie Inc. Processes for the preparation of (3S,4R)-3-ethyl-4-(3H-imidazo[1,2-a]pyrrolo[2,3-e]-pyrazin-8-yl)-n-(2,2,2-trifluoroethyl)pyrrolidine-1-carboxamide and solid state forms thereof
EP3362455A1 (en) 2015-10-16 2018-08-22 AbbVie Inc. PROCESSES FOR THE PREPARATION OF (3S,4R)-3-ETHYL-4-(3H-IMIDAZO[1,2-a]PYRROLO[2,3-e]-PYRAZIN-8-YL)-N-(2,2,2-TRIFLUOROETHYL)PYRROLIDINE-1-CARBOXAMIDE AND SOLID STATE FORMS THEREOF
CA3158951A1 (en) * 2016-08-15 2018-02-22 Purdue Research Foundation 4-substituted aminoisoquinoline derivatives
JOP20190144A1 (ar) 2016-12-16 2019-06-16 Janssen Pharmaceutica Nv إيميدازو بيرولو بيريدين كمثبطات لعائلة jak الخاصة بإنزيمات الكيناز
LT3555097T (lt) 2016-12-16 2022-08-25 Janssen Pharmaceutica Nv Imidazo[4,5-d]pirolo[2,3-b]piridino junginiai kaip janus kinazės inhibitoriai
SG11201908560SA (en) 2017-03-16 2019-10-30 Hoffmann La Roche Heterocyclic compounds useful as dual atx/ca inhibitors
WO2018167113A1 (en) 2017-03-16 2018-09-20 F. Hoffmann-La Roche Ag New bicyclic compounds as atx inhibitors
TW202016110A (zh) 2018-06-15 2020-05-01 比利時商健生藥品公司 Jak激酶家族之小分子抑制劑
US20230374011A1 (en) * 2020-10-08 2023-11-23 Unichem Laboratories Ltd. Substituted tricyclic compounds
JP7805363B2 (ja) 2020-11-02 2026-01-23 ベーリンガー インゲルハイム インターナショナル ゲゼルシャフト ミット ベシュレンクテル ハフツング EGFR阻害薬としての置換1H-ピラゾロ[4,3-c]及び誘導体
BR112023018286A2 (pt) 2021-03-11 2023-10-31 Janssen Pharmaceutica Nv Lorpucitinib para uso no tratamento de distúrbios mediados por jak

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