JP2012522763A5 - - Google Patents
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- Publication number
- JP2012522763A5 JP2012522763A5 JP2012503350A JP2012503350A JP2012522763A5 JP 2012522763 A5 JP2012522763 A5 JP 2012522763A5 JP 2012503350 A JP2012503350 A JP 2012503350A JP 2012503350 A JP2012503350 A JP 2012503350A JP 2012522763 A5 JP2012522763 A5 JP 2012522763A5
- Authority
- JP
- Japan
- Prior art keywords
- diyl
- alkyl
- group
- alkoxy
- methyl
- 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.)
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- -1 1,3,4-oxadiazole-2,5-diyl Chemical group 0.000 claims 15
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 claims 3
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 claims 2
- 239000008186 active pharmaceutical agent Substances 0.000 claims 2
- 125000003545 alkoxy group Chemical group 0.000 claims 2
- 125000000217 alkyl group Chemical group 0.000 claims 2
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 claims 2
- 125000001072 heteroaryl group Chemical group 0.000 claims 2
- 229910052739 hydrogen Inorganic materials 0.000 claims 2
- 239000001257 hydrogen Substances 0.000 claims 2
- 125000003253 isopropoxy group Chemical group [H]C([H])([H])C([H])(O*)C([H])([H])[H] 0.000 claims 2
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims 2
- 125000004108 n-butyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 claims 2
- 125000004123 n-propyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])* 0.000 claims 2
- 125000004890 (C1-C6) alkylamino group Chemical group 0.000 claims 1
- 125000004739 (C1-C6) alkylsulfonyl group Chemical group 0.000 claims 1
- 125000006619 (C1-C6) dialkylamino group Chemical group 0.000 claims 1
- 125000000171 (C1-C6) haloalkyl group Chemical group 0.000 claims 1
- YHKWFDPEASWKFQ-UHFFFAOYSA-N 3-nitrobenzene-1,2-diol Chemical class OC1=CC=CC([N+]([O-])=O)=C1O YHKWFDPEASWKFQ-UHFFFAOYSA-N 0.000 claims 1
- MYMOFIZGZYHOMD-UHFFFAOYSA-N Dioxygen Chemical compound O=O MYMOFIZGZYHOMD-UHFFFAOYSA-N 0.000 claims 1
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims 1
- JUJWROOIHBZHMG-UHFFFAOYSA-N Pyridine Chemical group C1=CC=NC=C1 JUJWROOIHBZHMG-UHFFFAOYSA-N 0.000 claims 1
- 125000001931 aliphatic group Chemical group 0.000 claims 1
- 125000004453 alkoxycarbonyl group Chemical group 0.000 claims 1
- 125000003435 aroyl group Chemical group 0.000 claims 1
- 125000003118 aryl group Chemical group 0.000 claims 1
- 125000001589 carboacyl group Chemical group 0.000 claims 1
- 125000002915 carbonyl group Chemical group [*:2]C([*:1])=O 0.000 claims 1
- 150000001875 compounds Chemical class 0.000 claims 1
- 125000004093 cyano group Chemical group *C#N 0.000 claims 1
- 150000002148 esters Chemical class 0.000 claims 1
- 239000008187 granular material Substances 0.000 claims 1
- 229910052736 halogen Inorganic materials 0.000 claims 1
- 150000002367 halogens Chemical class 0.000 claims 1
- 150000004677 hydrates Chemical class 0.000 claims 1
- 150000002431 hydrogen Chemical class 0.000 claims 1
- 125000001570 methylene group Chemical group [H]C([H])([*:1])[*:2] 0.000 claims 1
- 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 claims 1
- 229910052757 nitrogen Inorganic materials 0.000 claims 1
- 229910052760 oxygen Inorganic materials 0.000 claims 1
- 239000001301 oxygen Substances 0.000 claims 1
- 125000002467 phosphate group Chemical class [H]OP(=O)(O[H])O[*] 0.000 claims 1
- 230000004962 physiological condition Effects 0.000 claims 1
- 235000013855 polyvinylpyrrolidone Nutrition 0.000 claims 1
- 229920000036 polyvinylpyrrolidone Polymers 0.000 claims 1
- 239000001267 polyvinylpyrrolidone Substances 0.000 claims 1
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 claims 1
- 150000003839 salts Chemical class 0.000 claims 1
- SNOOUWRIMMFWNE-UHFFFAOYSA-M sodium;6-[(3,4,5-trimethoxybenzoyl)amino]hexanoate Chemical compound [Na+].COC1=CC(C(=O)NCCCCCC([O-])=O)=CC(OC)=C1OC SNOOUWRIMMFWNE-UHFFFAOYSA-M 0.000 claims 1
- 239000012453 solvate Substances 0.000 claims 1
- 229910052717 sulfur Inorganic materials 0.000 claims 1
- 125000004434 sulfur atom Chemical group 0.000 claims 1
- 125000002023 trifluoromethyl group Chemical group FC(F)(F)* 0.000 claims 1
- GBXQPDCOMJJCMJ-UHFFFAOYSA-M trimethyl-[6-(trimethylazaniumyl)hexyl]azanium;bromide Chemical compound [Br-].C[N+](C)(C)CCCCCC[N+](C)(C)C GBXQPDCOMJJCMJ-UHFFFAOYSA-M 0.000 claims 1
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US16577809P | 2009-04-01 | 2009-04-01 | |
| US61/165,778 | 2009-04-01 | ||
| PCT/PT2010/000014 WO2010114404A1 (en) | 2009-04-01 | 2010-03-31 | Pharmaceutical formulations comprising nitrocatechol derivatives and methods of making thereof |
Related Child Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2015168152A Division JP6239561B2 (ja) | 2009-04-01 | 2015-08-27 | ニトロカテコール誘導体を含む医薬製剤及びその製造方法 |
Publications (3)
| Publication Number | Publication Date |
|---|---|
| JP2012522763A JP2012522763A (ja) | 2012-09-27 |
| JP2012522763A5 true JP2012522763A5 (https=) | 2013-05-16 |
| JP5864409B2 JP5864409B2 (ja) | 2016-02-17 |
Family
ID=42225014
Family Applications (2)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2012503350A Active JP5864409B2 (ja) | 2009-04-01 | 2010-03-31 | ニトロカテコール誘導体を含む医薬製剤及びその製造方法 |
| JP2015168152A Active JP6239561B2 (ja) | 2009-04-01 | 2015-08-27 | ニトロカテコール誘導体を含む医薬製剤及びその製造方法 |
Family Applications After (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2015168152A Active JP6239561B2 (ja) | 2009-04-01 | 2015-08-27 | ニトロカテコール誘導体を含む医薬製剤及びその製造方法 |
Country Status (16)
| Country | Link |
|---|---|
| US (5) | US9132094B2 (https=) |
| EP (1) | EP2413912B1 (https=) |
| JP (2) | JP5864409B2 (https=) |
| KR (4) | KR20210009441A (https=) |
| CN (2) | CN102448444B (https=) |
| AU (1) | AU2010231961B2 (https=) |
| BR (1) | BRPI1014865B1 (https=) |
| CA (1) | CA2757411C (https=) |
| DK (1) | DK2413912T3 (https=) |
| ES (1) | ES2730678T3 (https=) |
| MX (1) | MX340360B (https=) |
| PL (1) | PL2413912T3 (https=) |
| PT (1) | PT2413912T (https=) |
| RU (2) | RU2011144145A (https=) |
| TR (1) | TR201908590T4 (https=) |
| WO (1) | WO2010114404A1 (https=) |
Families Citing this family (20)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| ITMI20110713A1 (it) | 2011-04-29 | 2012-10-30 | Bracco Imaging Spa | Processo per la preparazione di un derivato solfatato di3,5-diiodo-o-[3-iodofenil]-l-tirosina |
| ITMI20022394A1 (it) | 2002-11-13 | 2004-05-14 | Bracco Spa | Uso di triiodotironina 3-solfato come farmaco ad attivita' tireomimetica e relative formulazioni farmaceutiche. |
| PL1907382T3 (pl) | 2005-07-26 | 2016-01-29 | Bial Portela & Ca Sa | Pochodne nitrokatecholowe jako inhibitory COMT |
| EP1845097A1 (en) | 2006-04-10 | 2007-10-17 | Portela & Ca., S.A. | Oxadiazole derivatives as COMT inhibitors |
| BRPI0721213B1 (pt) | 2007-01-31 | 2021-11-09 | Bial - Portela & Ca, S.A. | Uso de nitrocatecóis substituídos, e embalagem |
| WO2009116882A1 (en) | 2008-03-17 | 2009-09-24 | Portela & Ca., S.A. | Crystal forms of 5- [3- (2, 5-dichloro-4, 6-dimethyl-1-oxy-pyridine-3-yl) [1,2,3] oxadiazol-5-yl] -3-nit robenzene-1, 2-diol |
| PT2413912T (pt) | 2009-04-01 | 2019-06-11 | Bial Portela & Ca Sa | Formulações farmacêuticas compreendendo derivados de nitrocatecol e métodos para as produzir |
| US20140045900A1 (en) * | 2011-02-11 | 2014-02-13 | Bial-Portela & Ca, S.A. | Administration regime for nitrocatechols |
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| JP6456143B2 (ja) | 2011-12-13 | 2019-01-23 | ノヴィファーマ，エス．アー． | カテコール−ｏ−メチル転移酵素阻害剤を調製するための中間体として有用な化学的化合物 |
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| WO2021182981A1 (en) | 2020-03-13 | 2021-09-16 | BIAL - PORTELA & Cª, S.A. | Micronised opicapone |
| TW202200138A (zh) * | 2020-05-26 | 2022-01-01 | 日商小野藥品工業股份有限公司 | 包含奧匹卡朋（ｏｐｉｃａｐｏｎｅ）之錠劑 |
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| EP4262798A1 (en) | 2020-12-17 | 2023-10-25 | Bial-Portela & CA, S.A. | Treatment regimens for early idiopathic parkinson's disease |
| EP4719374A1 (en) | 2023-05-25 | 2026-04-08 | Bial-Portela & CA, S.A. | Treatment regimens for early idiopathic parkinson's disease |
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| KR101669432B1 (ko) | 2007-08-27 | 2016-10-26 | 다트 뉴로사이언스 (케이만) 엘티디. | 치료적 이속사졸 화합물 |
| JP4976500B2 (ja) * | 2007-09-19 | 2012-07-18 | アサヒグループホールディングス株式会社 | 漢方エキス、生薬エキスあるいは天然物抽出エキスまたはそれらの混合物等の天然物由来物質を含有する顆粒物の製造方法およびその顆粒物から製造する錠剤の製造方法 |
| MX2010009043A (es) * | 2008-02-28 | 2010-10-25 | Bial Portela & Ca Sa | Composicion farmaceutica para farmacos poco solubles. |
| WO2009116882A1 (en) * | 2008-03-17 | 2009-09-24 | Portela & Ca., S.A. | Crystal forms of 5- [3- (2, 5-dichloro-4, 6-dimethyl-1-oxy-pyridine-3-yl) [1,2,3] oxadiazol-5-yl] -3-nit robenzene-1, 2-diol |
| ES2723729T3 (es) * | 2008-07-29 | 2019-08-30 | Bial Portela & Ca Sa | Régimen de administración de nitrocatecoles |
| US8827197B2 (en) * | 2008-11-04 | 2014-09-09 | Microgreen Polymers Inc | Apparatus and method for interleaving polymeric roll for gas impregnation and solid-state foam processing |
| PT2413912T (pt) | 2009-04-01 | 2019-06-11 | Bial Portela & Ca Sa | Formulações farmacêuticas compreendendo derivados de nitrocatecol e métodos para as produzir |
| BRPI1016132B8 (pt) | 2009-04-01 | 2021-05-25 | Bial Portela & Ca Sa | composição, formulação farmacêutica, processo de obtenção de uma formulação farmacêutica estável |
| EA026419B1 (ru) | 2010-03-04 | 2017-04-28 | Орион Корпорейшн | Применение леводопы, карбидопы и энтакапона для лечения болезни паркинсона |
| US20140045900A1 (en) | 2011-02-11 | 2014-02-13 | Bial-Portela & Ca, S.A. | Administration regime for nitrocatechols |
| JP6456143B2 (ja) | 2011-12-13 | 2019-01-23 | ノヴィファーマ，エス．アー． | カテコール−ｏ−メチル転移酵素阻害剤を調製するための中間体として有用な化学的化合物 |
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2010
- 2010-03-31 PT PT10713380T patent/PT2413912T/pt unknown
- 2010-03-31 PL PL10713380T patent/PL2413912T3/pl unknown
- 2010-03-31 CN CN201080022653.XA patent/CN102448444B/zh active Active
- 2010-03-31 RU RU2011144145/15A patent/RU2011144145A/ru not_active Application Discontinuation
- 2010-03-31 WO PCT/PT2010/000014 patent/WO2010114404A1/en not_active Ceased
- 2010-03-31 CN CN201610250582.8A patent/CN105878242A/zh active Pending
- 2010-03-31 AU AU2010231961A patent/AU2010231961B2/en active Active
- 2010-03-31 TR TR2019/08590T patent/TR201908590T4/tr unknown
- 2010-03-31 KR KR1020217001609A patent/KR20210009441A/ko not_active Ceased
- 2010-03-31 KR KR1020177009828A patent/KR102023255B1/ko active Active
- 2010-03-31 MX MX2011010415A patent/MX340360B/es active IP Right Grant
- 2010-03-31 KR KR1020187024054A patent/KR102329271B1/ko active Active
- 2010-03-31 ES ES10713380T patent/ES2730678T3/es active Active
- 2010-03-31 KR KR20117026011A patent/KR20120027197A/ko not_active Ceased
- 2010-03-31 JP JP2012503350A patent/JP5864409B2/ja active Active
- 2010-03-31 RU RU2016152167A patent/RU2701731C2/ru active
- 2010-03-31 CA CA2757411A patent/CA2757411C/en active Active
- 2010-03-31 DK DK10713380.3T patent/DK2413912T3/da active
- 2010-03-31 EP EP10713380.3A patent/EP2413912B1/en active Active
- 2010-03-31 US US12/750,956 patent/US9132094B2/en active Active
- 2010-03-31 BR BRPI1014865-5A patent/BRPI1014865B1/pt active IP Right Grant
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2015
- 2015-08-13 US US14/825,600 patent/US10071085B2/en active Active
- 2015-08-27 JP JP2015168152A patent/JP6239561B2/ja active Active
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2018
- 2018-07-31 US US16/050,602 patent/US10583130B2/en active Active
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2020
- 2020-03-05 US US16/809,662 patent/US20210023067A1/en not_active Abandoned
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2024
- 2024-09-27 US US18/899,225 patent/US20250262196A1/en active Pending
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