JP2017509676A5 - - Google Patents
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- Publication number
- JP2017509676A5 JP2017509676A5 JP2016560674A JP2016560674A JP2017509676A5 JP 2017509676 A5 JP2017509676 A5 JP 2017509676A5 JP 2016560674 A JP2016560674 A JP 2016560674A JP 2016560674 A JP2016560674 A JP 2016560674A JP 2017509676 A5 JP2017509676 A5 JP 2017509676A5
- Authority
- JP
- Japan
- Prior art keywords
- carboxamide
- pyridine
- cyclopropylmethoxy
- oxadiazol
- cyclopropyl
- 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
Links
- -1 halophenylalkyl Chemical group 0.000 claims description 31
- 150000001875 compounds Chemical class 0.000 claims description 22
- 208000020016 psychiatric disease Diseases 0.000 claims description 18
- 206010003246 arthritis Diseases 0.000 claims description 16
- 208000028017 Psychotic disease Diseases 0.000 claims description 15
- 206010061218 Inflammation Diseases 0.000 claims description 10
- 206010028980 Neoplasm Diseases 0.000 claims description 10
- 206010014599 encephalitis Diseases 0.000 claims description 10
- 230000004054 inflammatory process Effects 0.000 claims description 10
- 201000004792 malaria Diseases 0.000 claims description 10
- 208000001132 Osteoporosis Diseases 0.000 claims description 9
- 208000002193 Pain Diseases 0.000 claims description 9
- 208000006673 asthma Diseases 0.000 claims description 9
- 208000026278 immune system disease Diseases 0.000 claims description 9
- 208000004296 neuralgia Diseases 0.000 claims description 9
- 208000021722 neuropathic pain Diseases 0.000 claims description 9
- 208000018522 Gastrointestinal disease Diseases 0.000 claims description 8
- 206010020751 Hypersensitivity Diseases 0.000 claims description 7
- 230000000172 allergic effect Effects 0.000 claims description 7
- 230000007815 allergy Effects 0.000 claims description 7
- 208000010668 atopic eczema Diseases 0.000 claims description 7
- 230000002265 prevention Effects 0.000 claims description 5
- 208000026935 allergic disease Diseases 0.000 claims description 3
- 238000000034 method Methods 0.000 claims description 3
- 239000008194 pharmaceutical composition Substances 0.000 claims description 3
- 230000000069 prophylactic effect Effects 0.000 claims description 3
- 230000001225 therapeutic effect Effects 0.000 claims description 3
- 239000003814 drug Substances 0.000 claims description 2
- 238000004519 manufacturing process Methods 0.000 claims description 2
- 150000002148 esters Chemical class 0.000 claims 16
- 150000003839 salts Chemical class 0.000 claims 16
- 125000004179 3-chlorophenyl group Chemical group [H]C1=C([H])C(*)=C([H])C(Cl)=C1[H] 0.000 claims 4
- KDLHZDBZIXYQEI-UHFFFAOYSA-N Palladium Chemical compound [Pd] KDLHZDBZIXYQEI-UHFFFAOYSA-N 0.000 claims 4
- 125000003854 p-chlorophenyl group Chemical group [H]C1=C([H])C(*)=C([H])C([H])=C1Cl 0.000 claims 4
- 125000000753 cycloalkyl group Chemical group 0.000 claims 3
- 125000005059 halophenyl group Chemical group 0.000 claims 3
- 229910052739 hydrogen Inorganic materials 0.000 claims 3
- 239000001257 hydrogen Substances 0.000 claims 3
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims 3
- 125000004201 2,4-dichlorophenyl group Chemical group [H]C1=C([H])C(*)=C(Cl)C([H])=C1Cl 0.000 claims 2
- LZPWAYBEOJRFAX-UHFFFAOYSA-N 4,4,5,5-tetramethyl-1,3,2$l^{2}-dioxaborolane Chemical group CC1(C)O[B]OC1(C)C LZPWAYBEOJRFAX-UHFFFAOYSA-N 0.000 claims 2
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 claims 2
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims 2
- 125000000217 alkyl group Chemical group 0.000 claims 2
- WTEOIRVLGSZEPR-UHFFFAOYSA-N boron trifluoride Chemical group FB(F)F WTEOIRVLGSZEPR-UHFFFAOYSA-N 0.000 claims 2
- 239000003054 catalyst Substances 0.000 claims 2
- 125000005112 cycloalkylalkoxy group Chemical group 0.000 claims 2
- 229910052736 halogen Inorganic materials 0.000 claims 2
- 150000002367 halogens Chemical class 0.000 claims 2
- 229910052757 nitrogen Inorganic materials 0.000 claims 2
- 125000005476 oxopyrrolidinyl group Chemical group 0.000 claims 2
- 229910052763 palladium Inorganic materials 0.000 claims 2
- FPZWZCWUIYYYBU-UHFFFAOYSA-N 2-(2-ethoxyethoxy)ethyl acetate Chemical group CCOCCOCCOC(C)=O FPZWZCWUIYYYBU-UHFFFAOYSA-N 0.000 claims 1
- FACJIODPNQMPJQ-UHFFFAOYSA-N 4-[5-cyclopropyl-6-(cyclopropylmethoxy)pyridine-2-carbonyl]thiomorpholine-3-carboxamide Chemical compound NC(=O)C1CSCCN1C(=O)C(N=C1OCC2CC2)=CC=C1C1CC1 FACJIODPNQMPJQ-UHFFFAOYSA-N 0.000 claims 1
- 125000001255 4-fluorophenyl group Chemical group [H]C1=C([H])C(*)=C([H])C([H])=C1F 0.000 claims 1
- ZOXJGFHDIHLPTG-UHFFFAOYSA-N Boron Chemical compound [B] ZOXJGFHDIHLPTG-UHFFFAOYSA-N 0.000 claims 1
- GHBIFWJMGJLPJL-UHFFFAOYSA-N C1(CC1)COC1=C(C=CC(=N1)C(=O)NC12CC3(CC(CC(C1)C3)C2)O)N2CC(C2)(F)F Chemical compound C1(CC1)COC1=C(C=CC(=N1)C(=O)NC12CC3(CC(CC(C1)C3)C2)O)N2CC(C2)(F)F GHBIFWJMGJLPJL-UHFFFAOYSA-N 0.000 claims 1
- GANJOZPBMGPBDY-UHFFFAOYSA-N CC(C)(CC1=NC(=NO1)C1=CC=CC=C1)NC(=O)C1=NC(OCC(F)(F)F)=CC=C1 Chemical compound CC(C)(CC1=NC(=NO1)C1=CC=CC=C1)NC(=O)C1=NC(OCC(F)(F)F)=CC=C1 GANJOZPBMGPBDY-UHFFFAOYSA-N 0.000 claims 1
- QETRMUBQKBPDKU-UHFFFAOYSA-N CC(C)(CC1=NN=C(O1)C1=CC=CC=C1)NC(=O)C1=NC(OCC(F)(F)F)=CC=C1 Chemical compound CC(C)(CC1=NN=C(O1)C1=CC=CC=C1)NC(=O)C1=NC(OCC(F)(F)F)=CC=C1 QETRMUBQKBPDKU-UHFFFAOYSA-N 0.000 claims 1
- NXTDMSXSJGPTNM-UHFFFAOYSA-N COCCOCC(C)(C)C1=NOC(NC(=O)C2=NC(OCC3CC3)=C(C=C2)N2CC(F)(F)C2)=C1 Chemical compound COCCOCC(C)(C)C1=NOC(NC(=O)C2=NC(OCC3CC3)=C(C=C2)N2CC(F)(F)C2)=C1 NXTDMSXSJGPTNM-UHFFFAOYSA-N 0.000 claims 1
- BWMGKSFFMRANBX-UHFFFAOYSA-N N-[3-(1-azido-2-methylpropan-2-yl)-1,2-oxazol-5-yl]-5-cyclopropyl-6-(cyclopropylmethoxy)pyrazine-2-carboxamide Chemical compound CC(C)(CN=[N+]=[N-])C1=NOC(NC(=O)C2=CN=C(C3CC3)C(OCC3CC3)=N2)=C1 BWMGKSFFMRANBX-UHFFFAOYSA-N 0.000 claims 1
- 239000002253 acid Substances 0.000 claims 1
- NIXOWILDQLNWCW-UHFFFAOYSA-M acrylate group Chemical group C(C=C)(=O)[O-] NIXOWILDQLNWCW-UHFFFAOYSA-M 0.000 claims 1
- 125000005083 alkoxyalkoxy group Chemical group 0.000 claims 1
- 150000001408 amides Chemical class 0.000 claims 1
- 229910052796 boron Inorganic materials 0.000 claims 1
- 125000005620 boronic acid group Chemical group 0.000 claims 1
- 229910052794 bromium Inorganic materials 0.000 claims 1
- 229910052801 chlorine Inorganic materials 0.000 claims 1
- 125000001309 chloro group Chemical group Cl* 0.000 claims 1
- 239000007822 coupling agent Substances 0.000 claims 1
- 125000001559 cyclopropyl group Chemical group [H]C1([H])C([H])([H])C1([H])* 0.000 claims 1
- WJJMNDUMQPNECX-UHFFFAOYSA-N dipicolinic acid Chemical compound OC(=O)C1=CC=CC(C(O)=O)=N1 WJJMNDUMQPNECX-UHFFFAOYSA-N 0.000 claims 1
- 125000004438 haloalkoxy group Chemical group 0.000 claims 1
- 150000002431 hydrogen Chemical class 0.000 claims 1
- 229910052740 iodine Inorganic materials 0.000 claims 1
- 125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 claims 1
- 239000000463 material Substances 0.000 claims 1
- STUHQDIOZQUPGP-UHFFFAOYSA-N morpholin-4-ium-4-carboxylate Chemical compound OC(=O)N1CCOCC1 STUHQDIOZQUPGP-UHFFFAOYSA-N 0.000 claims 1
- 125000004433 nitrogen atom Chemical group N* 0.000 claims 1
- IBBMAWULFFBRKK-UHFFFAOYSA-N picolinamide Chemical compound NC(=O)C1=CC=CC=N1 IBBMAWULFFBRKK-UHFFFAOYSA-N 0.000 claims 1
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 claims 1
- 125000000999 tert-butyl group Chemical group [H]C([H])([H])C(*)(C([H])([H])[H])C([H])([H])[H] 0.000 claims 1
- ITMCEJHCFYSIIV-UHFFFAOYSA-M triflate Chemical compound [O-]S(=O)(=O)C(F)(F)F ITMCEJHCFYSIIV-UHFFFAOYSA-M 0.000 claims 1
- 102000009135 CB2 Cannabinoid Receptor Human genes 0.000 description 3
- 108010073376 CB2 Cannabinoid Receptor Proteins 0.000 description 3
- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 description 3
- 239000005557 antagonist Substances 0.000 description 2
- 201000010099 disease Diseases 0.000 description 2
- 241000124008 Mammalia Species 0.000 description 1
- 239000013543 active substance Substances 0.000 description 1
- 239000000556 agonist Substances 0.000 description 1
- 201000011510 cancer Diseases 0.000 description 1
- 230000001079 digestive effect Effects 0.000 description 1
- 208000035475 disorder Diseases 0.000 description 1
- 239000002621 endocannabinoid Substances 0.000 description 1
- 239000003446 ligand Substances 0.000 description 1
- 150000002632 lipids Chemical class 0.000 description 1
- 230000007170 pathology Effects 0.000 description 1
- 230000001681 protective effect Effects 0.000 description 1
- 239000000018 receptor agonist Substances 0.000 description 1
- 229940044601 receptor agonist Drugs 0.000 description 1
- 239000002469 receptor inverse agonist Substances 0.000 description 1
- 230000000630 rising effect Effects 0.000 description 1
- 230000011664 signaling Effects 0.000 description 1
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| EP14163555 | 2014-04-04 | ||
| EP14163555.7 | 2014-04-04 | ||
| PCT/EP2015/057151 WO2015150440A1 (en) | 2014-04-04 | 2015-04-01 | Pyridine-2-amides useful as cb2 agonists |
Publications (3)
| Publication Number | Publication Date |
|---|---|
| JP2017509676A JP2017509676A (ja) | 2017-04-06 |
| JP2017509676A5 true JP2017509676A5 (cg-RX-API-DMAC7.html) | 2019-05-16 |
| JP6654574B2 JP6654574B2 (ja) | 2020-02-26 |
Family
ID=50424143
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2016560674A Expired - Fee Related JP6654574B2 (ja) | 2014-04-04 | 2015-04-01 | Ｃｂ２アゴニストとして有用なピリジン−２−アミド |
Country Status (19)
Families Citing this family (9)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CA2899168A1 (en) | 2013-03-26 | 2014-10-02 | F. Hoffmann-La Roche Ag | Novel pyridine derivatives |
| DK3126354T3 (da) | 2014-04-04 | 2020-03-09 | H Lundbeck As | Halogenerede quinazolin-thf-aminer som pde1-inhibitorer |
| DK3386951T3 (en) * | 2015-12-09 | 2020-04-27 | Hoffmann La Roche | Phenylderivater som cannabinoidreceptor-2-agonister |
| EP3429997A1 (de) | 2016-03-16 | 2019-01-23 | Bayer CropScience Aktiengesellschaft | N-(cyanbenzyl)-6-(cyclopropylcarbonylamino)-4-(phenyl)-pyridin-2-carboxamid-derivate und verwandte verbindungen als pestizide pflanzenschutzmittel |
| EP3642200B1 (en) | 2017-06-20 | 2023-05-03 | F. Hoffmann-La Roche AG | Pyridine derivatives |
| EP3813888B1 (en) | 2018-06-27 | 2025-11-26 | F. Hoffmann-La Roche AG | Radiolabeled cannabinoid receptor 2 ligand |
| MA53002A (fr) * | 2018-06-27 | 2021-05-05 | Eth Zuerich | Nouveaux composés de pyridine et de pyrazine en tant qu'inhibiteurs du récepteur cannabinoïde 2 |
| JP7478672B2 (ja) | 2018-06-27 | 2024-05-07 | エフ． ホフマン－ラ ロシュ アーゲー | カンナビノイド受容体２の阻害剤としての新規なアゼチジン置換ピリジン及びピラジン化合物 |
| CN112074513B (zh) | 2018-06-27 | 2024-06-14 | 豪夫迈·罗氏有限公司 | 作为优先大麻素2激动剂的吡啶和吡嗪衍生物 |
Family Cites Families (9)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| AU2006230292A1 (en) | 2005-03-31 | 2006-10-05 | Schering Corporation | Spirocyclic thrombin receptor antagonists |
| FR2887550A1 (fr) | 2005-06-24 | 2006-12-29 | Sanofi Aventis Sa | Derives de 1-benzylpyrazole-3-acetamide, leur preparation et leur application en therapeutique |
| US20110206607A1 (en) * | 2007-05-10 | 2011-08-25 | Roger Olsson | Imidazol (1,2-a)pyridines and related compounds with activity at cannabinoid cb2 receptors |
| EP2311443A1 (en) | 2009-10-15 | 2011-04-20 | Rheinische Friedrich-Wilhelms-Universität | Pharmaceutical composition containing cannabinoid-receptor 2 antagonists |
| WO2012031817A1 (en) * | 2010-09-09 | 2012-03-15 | F. Hoffmann-La Roche Ag | Determination of abca1 protein levels in cells |
| US9321727B2 (en) * | 2011-06-10 | 2016-04-26 | Hoffmann-La Roche Inc. | Pyridine derivatives as agonists of the CB2 receptor |
| US9403808B2 (en) * | 2011-10-28 | 2016-08-02 | Hoffmann-La Roche Inc. | Pyrazine derivatives |
| KR20150092156A (ko) * | 2012-12-07 | 2015-08-12 | 에프. 호프만-라 로슈 아게 | Cb2 수용체 작용제로서 신규한 피라진 유도체 |
| PT2928868T (pt) * | 2012-12-07 | 2017-10-04 | Hoffmann La Roche | Piridina-2-amidas úteis como agonistas do cb2 |
-
2015
- 2015-04-01 EA EA201691983A patent/EA030116B1/ru not_active IP Right Cessation
- 2015-04-01 SG SG10201809066TA patent/SG10201809066TA/en unknown
- 2015-04-01 CA CA2943013A patent/CA2943013A1/en not_active Abandoned
- 2015-04-01 CN CN201580017199.1A patent/CN106132958A/zh active Pending
- 2015-04-01 PE PE2016001656A patent/PE20161370A1/es unknown
- 2015-04-01 KR KR1020167030780A patent/KR20160142365A/ko not_active Withdrawn
- 2015-04-01 JP JP2016560674A patent/JP6654574B2/ja not_active Expired - Fee Related
- 2015-04-01 SG SG11201608108SA patent/SG11201608108SA/en unknown
- 2015-04-01 CR CR20160448A patent/CR20160448A/es unknown
- 2015-04-01 EP EP15713492.5A patent/EP3126359A1/en not_active Withdrawn
- 2015-04-01 MX MX2016012689A patent/MX2016012689A/es unknown
- 2015-04-01 MA MA039843A patent/MA39843A/fr unknown
- 2015-04-01 AR ARP150100985A patent/AR099933A1/es unknown
- 2015-04-01 AU AU2015239539A patent/AU2015239539A1/en not_active Abandoned
- 2015-04-01 WO PCT/EP2015/057151 patent/WO2015150440A1/en not_active Ceased
- 2015-04-02 TW TW104111026A patent/TW201623276A/zh unknown
-
2016
- 2016-09-09 US US15/260,826 patent/US20160376262A1/en not_active Abandoned
- 2016-09-14 IL IL247817A patent/IL247817A0/en unknown
- 2016-09-22 PH PH12016501865A patent/PH12016501865A1/en unknown
- 2016-09-30 CL CL2016002483A patent/CL2016002483A1/es unknown
-
2018
- 2018-07-24 US US16/044,320 patent/US20180327396A1/en not_active Abandoned