EA201490744A1 - N-((1r,2s,5r)-5-(трет-бутиламино)-2-((s)-3-(7-трет-бутилпиразоло[1,5-a][1,3,5]триазин-4-иламино)-2-оксопирролидин-1-ил)циклогексил)ацетамид в качестве двойного модулятора активности хемокиновых рецепторов, его кристаллическая форма и способ получения - Google Patents
N-((1r,2s,5r)-5-(трет-бутиламино)-2-((s)-3-(7-трет-бутилпиразоло[1,5-a][1,3,5]триазин-4-иламино)-2-оксопирролидин-1-ил)циклогексил)ацетамид в качестве двойного модулятора активности хемокиновых рецепторов, его кристаллическая форма и способ полученияInfo
- Publication number
- EA201490744A1 EA201490744A1 EA201490744A EA201490744A EA201490744A1 EA 201490744 A1 EA201490744 A1 EA 201490744A1 EA 201490744 A EA201490744 A EA 201490744A EA 201490744 A EA201490744 A EA 201490744A EA 201490744 A1 EA201490744 A1 EA 201490744A1
- Authority
- EA
- Eurasian Patent Office
- Prior art keywords
- tret
- compounds
- oxopyrrolidin
- triazin
- butylamino
- Prior art date
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Abstract
В настоящем изобретении предложен новый антагонист, N-((1R,2S,5R)-5-(трет-бутиламино)-2-((S)-3-(7-трет-бутилпиразоло[1,5-а][1,3,5]триазин-4-иламино)-2-оксопирролидин-1-ил)циклогексил)ацетамидили его фармацевтически приемлемая соль, сольват или пролекарство, обладающий неожиданной двойной активностью в отношении рецепторов CCR-2 и CCR-5. В настоящем изобретении также предложены кристаллические формы, метаболиты, фармацевтические композиции, содержащие указанные соединения, и способы применения этих соединений в качестве агентов для лечения воспалительных заболеваний, аллергических, аутоиммунных, метаболических, раковых и/или сердечно-сосудистых заболеваний. В настоящем изобретении также предложены способы получения соединений формулы (I), таких как предложено в изобретении, включая N-((1R,2S,5R)-5-(трет-бутиламино)-2-((S)-3-(7-трет-бутилпиразоло[1,5-а][1,3,5]триазин-4-иламино)-2-оксопирролидин-1-ил)циклогексил)ацетамид. В данном изобретении также предложены соединения, которые могут быть использованы в качестве промежуточных соединений в способе получения соединений согласно настоящему изобретению.
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
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US25097809P | 2009-10-13 | 2009-10-13 |
Publications (1)
Publication Number | Publication Date |
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EA201490744A1 true EA201490744A1 (ru) | 2014-11-28 |
Family
ID=43063940
Family Applications (2)
Application Number | Title | Priority Date | Filing Date |
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EA201270602A EA020486B1 (ru) | 2009-10-13 | 2010-10-12 | N-((1R,2S,5R)-5-(ТРЕТ-БУТИЛАМИНО)-2-((S)-3-(7-ТРЕТ-БУТИЛПИРАЗОЛО[1,5-a][1,3,5]ТРИАЗИН-4-ИЛАМИНО)-2-ОКСОПИРРОЛИДИН-1-ИЛ)ЦИКЛОГЕКСИЛ)АЦЕТАМИД В КАЧЕСТВЕ ДВОЙНОГО МОДУЛЯТОРА АКТИВНОСТИ ХЕМОКИНОВЫХ РЕЦЕПТОРОВ, ЕГО КРИСТАЛЛИЧЕСКИЕ ФОРМЫ И СПОСОБ ПОЛУЧЕНИЯ |
EA201490744A EA201490744A1 (ru) | 2009-10-13 | 2010-10-12 | N-((1r,2s,5r)-5-(трет-бутиламино)-2-((s)-3-(7-трет-бутилпиразоло[1,5-a][1,3,5]триазин-4-иламино)-2-оксопирролидин-1-ил)циклогексил)ацетамид в качестве двойного модулятора активности хемокиновых рецепторов, его кристаллическая форма и способ получения |
Family Applications Before (1)
Application Number | Title | Priority Date | Filing Date |
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EA201270602A EA020486B1 (ru) | 2009-10-13 | 2010-10-12 | N-((1R,2S,5R)-5-(ТРЕТ-БУТИЛАМИНО)-2-((S)-3-(7-ТРЕТ-БУТИЛПИРАЗОЛО[1,5-a][1,3,5]ТРИАЗИН-4-ИЛАМИНО)-2-ОКСОПИРРОЛИДИН-1-ИЛ)ЦИКЛОГЕКСИЛ)АЦЕТАМИД В КАЧЕСТВЕ ДВОЙНОГО МОДУЛЯТОРА АКТИВНОСТИ ХЕМОКИНОВЫХ РЕЦЕПТОРОВ, ЕГО КРИСТАЛЛИЧЕСКИЕ ФОРМЫ И СПОСОБ ПОЛУЧЕНИЯ |
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US (3) | US8383812B2 (ru) |
EP (2) | EP2664620A3 (ru) |
JP (1) | JP5759999B2 (ru) |
KR (1) | KR20120102052A (ru) |
CN (1) | CN102648201B (ru) |
AR (1) | AR078627A1 (ru) |
AU (1) | AU2010306968B2 (ru) |
BR (1) | BR112012008650B1 (ru) |
CA (1) | CA2777563A1 (ru) |
CL (1) | CL2014000753A1 (ru) |
CO (1) | CO6460737A2 (ru) |
DK (1) | DK2488523T3 (ru) |
EA (2) | EA020486B1 (ru) |
ES (1) | ES2442897T3 (ru) |
HK (1) | HK1174614A1 (ru) |
HR (1) | HRP20140072T1 (ru) |
IL (2) | IL219121A0 (ru) |
MX (1) | MX2012003720A (ru) |
NZ (2) | NZ613580A (ru) |
PE (1) | PE20121349A1 (ru) |
PL (1) | PL2488523T3 (ru) |
PT (1) | PT2488523E (ru) |
RS (1) | RS53131B (ru) |
SI (1) | SI2488523T1 (ru) |
SM (1) | SMT201400020B (ru) |
TN (1) | TN2012000132A1 (ru) |
TW (1) | TW201120042A (ru) |
WO (1) | WO2011046916A1 (ru) |
ZA (1) | ZA201305994B (ru) |
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US8383812B2 (en) * | 2009-10-13 | 2013-02-26 | Bristol-Myers Squibb Company | N-((1R,2S,5R)-5-(tert-butylamino)-2-((S)-3-(7-tert-butylpyrazolo[1,5-A][1,3,5]triazin-4-ylamino)-2-oxopyrrolidin-1-yl)cyclohexyl)acetamide, a dual modulator of chemokine receptor activity, crystalline forms and processes |
JP2016029037A (ja) | 2014-07-17 | 2016-03-03 | 参天製薬株式会社 | 後眼部疾患の予防または治療剤 |
WO2018051229A1 (en) | 2016-09-14 | 2018-03-22 | Novartis Ag | Novel regimes of fxr agonists |
JOP20190040A1 (ar) | 2016-09-14 | 2019-03-10 | Novartis Ag | توليفة من ناهضات fxr |
PT3655395T (pt) | 2017-07-20 | 2022-02-22 | Bristol Myers Squibb Co | Processo para a preparação de n-((1r,2s,5r)-5-(tercbutilamino)- 2-((s)-3-(7-terc-butilpirazolo[1,5- a][1,3,5]triazin-4-ilamino)-2-oxopirrolidin-1- il)ciclohexil)acetamida |
BR112020014574A2 (pt) * | 2018-01-22 | 2020-12-08 | Bristol-Myers Squibb Company | Composições e métodos para o tratamento do câncer |
US12006318B2 (en) * | 2019-11-13 | 2024-06-11 | Rapt Therapeutics, Inc. | Crystalline forms of C-C chemokine receptor type 4 antagonist and uses thereof |
WO2022032187A1 (en) | 2020-08-07 | 2022-02-10 | Bristol-Myers Squibb Company | Fgf21 combined with ccr2/5 antagonists for the treatment of fibrosis |
WO2023092049A1 (en) * | 2021-11-19 | 2023-05-25 | Bristol-Myers Squibb Company | Azirine pharmaceutical compositions |
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