HRP20170572T1 - Derivati pirazina kao agonisti receptora cb2 - Google Patents
Derivati pirazina kao agonisti receptora cb2 Download PDFInfo
- Publication number
- HRP20170572T1 HRP20170572T1 HRP20170572TT HRP20170572T HRP20170572T1 HR P20170572 T1 HRP20170572 T1 HR P20170572T1 HR P20170572T T HRP20170572T T HR P20170572TT HR P20170572 T HRP20170572 T HR P20170572T HR P20170572 T1 HRP20170572 T1 HR P20170572T1
- Authority
- HR
- Croatia
- Prior art keywords
- cyclopropylmethoxy
- difluoro
- azetidin
- pyrazine
- carbonyl
- Prior art date
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- 150000003216 pyrazines Chemical class 0.000 title 1
- 239000000018 receptor agonist Substances 0.000 title 1
- 229940044601 receptor agonist Drugs 0.000 title 1
- -1 oxomorpholinyl Chemical group 0.000 claims 16
- 150000001875 compounds Chemical class 0.000 claims 13
- 125000000623 heterocyclic group Chemical group 0.000 claims 10
- 125000000217 alkyl group Chemical group 0.000 claims 4
- ISHAPNLCSAGSSW-UHFFFAOYSA-N 1-[5-cyclopropyl-6-(cyclopropylmethoxy)pyrazine-2-carbonyl]-4,4-dimethylpyrrolidine-2-carboxamide Chemical compound C1C(C)(C)CC(C(N)=O)N1C(=O)C(N=C1OCC2CC2)=CN=C1C1CC1 ISHAPNLCSAGSSW-UHFFFAOYSA-N 0.000 claims 3
- CUDKBOBOHWXOKN-UHFFFAOYSA-N 1-[6-(cyclopropylmethoxy)-5-(3,3-difluoroazetidin-1-yl)pyrazine-2-carbonyl]-4,4-dimethylpyrrolidine-2-carboxamide Chemical compound C1C(C)(C)CC(C(N)=O)N1C(=O)C(N=C1OCC2CC2)=CN=C1N1CC(F)(F)C1 CUDKBOBOHWXOKN-UHFFFAOYSA-N 0.000 claims 3
- 229910052757 nitrogen Inorganic materials 0.000 claims 3
- 125000004433 nitrogen atom Chemical group N* 0.000 claims 3
- SLGNYEOMLKBLIK-NSHDSACASA-N (2s)-1-[6-(cyclopropylmethoxy)-5-(3,3-difluoroazetidin-1-yl)pyrazine-2-carbonyl]-4,4-difluoropyrrolidine-2-carboxamide Chemical compound NC(=O)[C@@H]1CC(F)(F)CN1C(=O)C(N=C1OCC2CC2)=CN=C1N1CC(F)(F)C1 SLGNYEOMLKBLIK-NSHDSACASA-N 0.000 claims 2
- LNRDCWSMLNFCKY-UHFFFAOYSA-N 1-[6-(cyclopropylmethoxy)-5-(3,3-difluoroazetidin-1-yl)pyrazine-2-carbonyl]piperidine-2-carboxamide Chemical compound NC(=O)C1CCCCN1C(=O)C(N=C1OCC2CC2)=CN=C1N1CC(F)(F)C1 LNRDCWSMLNFCKY-UHFFFAOYSA-N 0.000 claims 2
- GXMVBYITSSGQER-UHFFFAOYSA-N 5-[6-(cyclopropylmethoxy)-5-(3,3-difluoroazetidin-1-yl)pyrazine-2-carbonyl]-5-azaspiro[2.4]heptane-6-carboxamide Chemical compound C1N(C(=O)C=2N=C(OCC3CC3)C(N3CC(F)(F)C3)=NC=2)C(C(=O)N)CC21CC2 GXMVBYITSSGQER-UHFFFAOYSA-N 0.000 claims 2
- CUBFMUJIDHGHON-UHFFFAOYSA-N 6-(cyclopropylmethoxy)-5-(3,3-difluoroazetidin-1-yl)-n-(1-methoxy-2-methylpropan-2-yl)-n-methylpyrazine-2-carboxamide Chemical compound C1CC1COC1=NC(C(=O)N(C)C(C)(C)COC)=CN=C1N1CC(F)(F)C1 CUBFMUJIDHGHON-UHFFFAOYSA-N 0.000 claims 2
- PNKHMUYUQJQQQU-UHFFFAOYSA-N [5-cyclopropyl-6-(cyclopropylmethoxy)pyrazin-2-yl]-(2,2-dimethylpyrrolidin-1-yl)methanone Chemical compound CC1(C)CCCN1C(=O)C(N=C1OCC2CC2)=CN=C1C1CC1 PNKHMUYUQJQQQU-UHFFFAOYSA-N 0.000 claims 2
- MAXRHXDLGBYMAD-UHFFFAOYSA-N [6-(cyclopropylmethoxy)-5-(3,3-difluoroazetidin-1-yl)pyrazin-2-yl]-(2,2-dimethylpyrrolidin-1-yl)methanone Chemical compound CC1(C)CCCN1C(=O)C(N=C1OCC2CC2)=CN=C1N1CC(F)(F)C1 MAXRHXDLGBYMAD-UHFFFAOYSA-N 0.000 claims 2
- RADWJJYFOOUQDK-UHFFFAOYSA-N [6-(cyclopropylmethoxy)-5-(3,3-difluoroazetidin-1-yl)pyrazin-2-yl]-(3,3-dimethylmorpholin-4-yl)methanone Chemical compound CC1(C)COCCN1C(=O)C(N=C1OCC2CC2)=CN=C1N1CC(F)(F)C1 RADWJJYFOOUQDK-UHFFFAOYSA-N 0.000 claims 2
- 206010064930 age-related macular degeneration Diseases 0.000 claims 2
- 125000004183 alkoxy alkyl group Chemical group 0.000 claims 2
- 125000003545 alkoxy group Chemical group 0.000 claims 2
- 230000000735 allogeneic effect Effects 0.000 claims 2
- 125000003917 carbamoyl group Chemical group [H]N([H])C(*)=O 0.000 claims 2
- 208000019425 cirrhosis of liver Diseases 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
- 125000002757 morpholinyl group Chemical group 0.000 claims 2
- CNGJPRQBRBBAAX-UHFFFAOYSA-N n-tert-butyl-6-(cyclopropylmethoxy)-5-(3,3-difluoroazetidin-1-yl)-n-(2-methoxyethyl)pyrazine-2-carboxamide Chemical compound C1CC1COC1=NC(C(=O)N(CCOC)C(C)(C)C)=CN=C1N1CC(F)(F)C1 CNGJPRQBRBBAAX-UHFFFAOYSA-N 0.000 claims 2
- ICKCVIQXRDRPTI-UHFFFAOYSA-N n-tert-butyl-6-(cyclopropylmethoxy)-5-(3,3-difluoroazetidin-1-yl)-n-methylpyrazine-2-carboxamide Chemical compound C1CC1COC1=NC(C(=O)N(C)C(C)(C)C)=CN=C1N1CC(F)(F)C1 ICKCVIQXRDRPTI-UHFFFAOYSA-N 0.000 claims 2
- 125000000719 pyrrolidinyl group Chemical group 0.000 claims 2
- 125000001424 substituent group Chemical group 0.000 claims 2
- VPJDFQXEQISZLA-CQSZACIVSA-N (2r)-1-[6-(cyclopropylmethoxy)-5-(3,3-difluoroazetidin-1-yl)pyrazine-2-carbonyl]-n,n-dimethylpyrrolidine-2-carbothioamide Chemical compound CN(C)C(=S)[C@H]1CCCN1C(=O)C(N=C1OCC2CC2)=CN=C1N1CC(F)(F)C1 VPJDFQXEQISZLA-CQSZACIVSA-N 0.000 claims 1
- SRCMSCCVZFTWDG-QMMMGPOBSA-N (2s)-1-[5-(3,3-difluoroazetidin-1-yl)-6-(2,2-difluoroethoxy)pyrazine-2-carbonyl]-4,4-difluoropyrrolidine-2-carboxamide Chemical compound NC(=O)[C@@H]1CC(F)(F)CN1C(=O)C(N=C1OCC(F)F)=CN=C1N1CC(F)(F)C1 SRCMSCCVZFTWDG-QMMMGPOBSA-N 0.000 claims 1
- XMKGBINAXSPRKN-LBPRGKRZSA-N (2s)-1-[5-cyclopropyl-6-(cyclopropylmethoxy)pyrazine-2-carbonyl]-4,4-difluoropyrrolidine-2-carboxamide Chemical compound NC(=O)[C@@H]1CC(F)(F)CN1C(=O)C(N=C1OCC2CC2)=CN=C1C1CC1 XMKGBINAXSPRKN-LBPRGKRZSA-N 0.000 claims 1
- AZAQQPJXYPDQCS-WHUIICBVSA-N (2s)-1-[6-(cyclopropylmethoxy)-5-(3,3-difluoroazetidin-1-yl)pyrazine-2-carbonyl]-4-hydroxy-4-methylpyrrolidine-2-carboxamide Chemical compound C1C(C)(O)C[C@@H](C(N)=O)N1C(=O)C(N=C1OCC2CC2)=CN=C1N1CC(F)(F)C1 AZAQQPJXYPDQCS-WHUIICBVSA-N 0.000 claims 1
- DNODHRHZHANYEO-UHFFFAOYSA-N 4-[6-(cyclopropylmethoxy)-5-(3,3-difluoroazetidin-1-yl)pyrazine-2-carbonyl]morpholin-2-one Chemical compound C1C(F)(F)CN1C1=NC=C(C(=O)N2CC(=O)OCC2)N=C1OCC1CC1 DNODHRHZHANYEO-UHFFFAOYSA-N 0.000 claims 1
- PPFSTWQTUYTVGT-UHFFFAOYSA-N 4-[6-(cyclopropylmethoxy)-5-(3,3-difluoroazetidin-1-yl)pyrazine-2-carbonyl]thiomorpholine-3-carboxamide Chemical compound NC(=O)C1CSCCN1C(=O)C(N=C1OCC2CC2)=CN=C1N1CC(F)(F)C1 PPFSTWQTUYTVGT-UHFFFAOYSA-N 0.000 claims 1
- KZMJZRATNJTRNA-UHFFFAOYSA-N 5-cyclopropyl-6-(cyclopropylmethoxy)-n-(1-methoxy-2-methylpropan-2-yl)-n-methylpyrazine-2-carboxamide Chemical compound C1CC1COC1=NC(C(=O)N(C)C(C)(C)COC)=CN=C1C1CC1 KZMJZRATNJTRNA-UHFFFAOYSA-N 0.000 claims 1
- DQGNFQJJQBUCMP-UHFFFAOYSA-N 6-(cyclopropylmethoxy)-5-(3,3-difluoroazetidin-1-yl)-n-ethyl-n-propan-2-ylpyrazine-2-carboxamide Chemical compound C1CC1COC1=NC(C(=O)N(C(C)C)CC)=CN=C1N1CC(F)(F)C1 DQGNFQJJQBUCMP-UHFFFAOYSA-N 0.000 claims 1
- 208000007788 Acute Liver Failure Diseases 0.000 claims 1
- 206010000804 Acute hepatic failure Diseases 0.000 claims 1
- 201000001320 Atherosclerosis Diseases 0.000 claims 1
- 208000031229 Cardiomyopathies Diseases 0.000 claims 1
- 208000032544 Cicatrix Diseases 0.000 claims 1
- 208000007342 Diabetic Nephropathies Diseases 0.000 claims 1
- 206010012689 Diabetic retinopathy Diseases 0.000 claims 1
- JROQHKRCBXRBCD-VXGBXAGGSA-N FC1(F)CN(C1)c1ncc(nc1OCC1CC1)C(=O)N1C[C@H]2C[C@@H]1CO2 Chemical compound FC1(F)CN(C1)c1ncc(nc1OCC1CC1)C(=O)N1C[C@H]2C[C@@H]1CO2 JROQHKRCBXRBCD-VXGBXAGGSA-N 0.000 claims 1
- 206010016654 Fibrosis Diseases 0.000 claims 1
- 208000008069 Geographic Atrophy Diseases 0.000 claims 1
- 208000010412 Glaucoma Diseases 0.000 claims 1
- 206010018364 Glomerulonephritis Diseases 0.000 claims 1
- 206010019280 Heart failures Diseases 0.000 claims 1
- 206010019695 Hepatic neoplasm Diseases 0.000 claims 1
- 206010061218 Inflammation Diseases 0.000 claims 1
- 208000022559 Inflammatory bowel disease Diseases 0.000 claims 1
- 208000002260 Keloid Diseases 0.000 claims 1
- 206010023421 Kidney fibrosis Diseases 0.000 claims 1
- 206010069385 Ocular ischaemic syndrome Diseases 0.000 claims 1
- 208000002193 Pain Diseases 0.000 claims 1
- 206010037660 Pyrexia Diseases 0.000 claims 1
- 206010063837 Reperfusion injury Diseases 0.000 claims 1
- 208000017442 Retinal disease Diseases 0.000 claims 1
- 206010038923 Retinopathy Diseases 0.000 claims 1
- 208000006011 Stroke Diseases 0.000 claims 1
- 201000009594 Systemic Scleroderma Diseases 0.000 claims 1
- 206010042953 Systemic sclerosis Diseases 0.000 claims 1
- 208000032109 Transient ischaemic attack Diseases 0.000 claims 1
- 206010046851 Uveitis Diseases 0.000 claims 1
- 208000027418 Wounds and injury Diseases 0.000 claims 1
- UODCOTAUGKQESU-ZDUSSCGKSA-N [(3s)-1-[6-(cyclopropylmethoxy)-5-(3,3-difluoroazetidin-1-yl)pyrazine-2-carbonyl]pyrrolidin-3-yl] acetate Chemical compound C1[C@@H](OC(=O)C)CCN1C(=O)C(N=C1OCC2CC2)=CN=C1N1CC(F)(F)C1 UODCOTAUGKQESU-ZDUSSCGKSA-N 0.000 claims 1
- URASPVATSWONFK-UHFFFAOYSA-N [1-[5-cyclopropyl-6-(cyclopropylmethoxy)pyrazine-2-carbonyl]-3-methylpyrrolidin-3-yl] acetate Chemical compound C1C(OC(=O)C)(C)CCN1C(=O)C(N=C1OCC2CC2)=CN=C1C1CC1 URASPVATSWONFK-UHFFFAOYSA-N 0.000 claims 1
- FFOXXHDQUUDKOV-UHFFFAOYSA-N [1-[6-(cyclopropylmethoxy)-5-(3,3-difluoroazetidin-1-yl)pyrazine-2-carbonyl]-3-methylpyrrolidin-3-yl] acetate Chemical compound C1C(OC(=O)C)(C)CCN1C(=O)C(N=C1OCC2CC2)=CN=C1N1CC(F)(F)C1 FFOXXHDQUUDKOV-UHFFFAOYSA-N 0.000 claims 1
- ZGEGFXUPPMEWHZ-UHFFFAOYSA-N [5-(3,3-difluoroazetidin-1-yl)-6-(2,2,2-trifluoroethoxy)pyrazin-2-yl]-(2,2-dimethylpyrrolidin-1-yl)methanone Chemical compound CC1(C)CCCN1C(=O)C(N=C1OCC(F)(F)F)=CN=C1N1CC(F)(F)C1 ZGEGFXUPPMEWHZ-UHFFFAOYSA-N 0.000 claims 1
- PHCZFHXFRVWXOW-UHFFFAOYSA-N [5-cyclopropyl-6-(cyclopropylmethoxy)pyrazin-2-yl]-(3,3,4,4-tetrafluoropyrrolidin-1-yl)methanone Chemical compound C1C(F)(F)C(F)(F)CN1C(=O)C(N=C1OCC2CC2)=CN=C1C1CC1 PHCZFHXFRVWXOW-UHFFFAOYSA-N 0.000 claims 1
- NZLXQSVAQWMGCX-UHFFFAOYSA-N [5-cyclopropyl-6-(cyclopropylmethoxy)pyrazin-2-yl]-(7-oxa-4-azaspiro[2.5]octan-4-yl)methanone Chemical compound C=1N=C(C2CC2)C(OCC2CC2)=NC=1C(=O)N1CCOCC11CC1 NZLXQSVAQWMGCX-UHFFFAOYSA-N 0.000 claims 1
- MJOBLMCVCVMOJT-LLVKDONJSA-N [5-cyclopropyl-6-(cyclopropylmethoxy)pyrazin-2-yl]-[(2r)-2-methylpyrrolidin-1-yl]methanone Chemical compound C[C@@H]1CCCN1C(=O)C(N=C1OCC2CC2)=CN=C1C1CC1 MJOBLMCVCVMOJT-LLVKDONJSA-N 0.000 claims 1
- ULZLYINESXARHU-UHFFFAOYSA-N [6-(cyclopropylmethoxy)-5-(3,3-difluoroazetidin-1-yl)pyrazin-2-yl]-(2,2-dimethylmorpholin-4-yl)methanone Chemical compound C1COC(C)(C)CN1C(=O)C(N=C1OCC2CC2)=CN=C1N1CC(F)(F)C1 ULZLYINESXARHU-UHFFFAOYSA-N 0.000 claims 1
- WHEVZVDNKRTZHA-UHFFFAOYSA-N [6-(cyclopropylmethoxy)-5-(3,3-difluoroazetidin-1-yl)pyrazin-2-yl]-(2-oxa-7-azaspiro[3.4]octan-7-yl)methanone Chemical compound C1C(F)(F)CN1C1=NC=C(C(=O)N2CC3(COC3)CC2)N=C1OCC1CC1 WHEVZVDNKRTZHA-UHFFFAOYSA-N 0.000 claims 1
- NPOSXWDUCSOJAX-UHFFFAOYSA-N [6-(cyclopropylmethoxy)-5-(3,3-difluoroazetidin-1-yl)pyrazin-2-yl]-(3,3,4,4-tetrafluoropyrrolidin-1-yl)methanone Chemical compound C1C(F)(F)CN1C1=NC=C(C(=O)N2CC(F)(F)C(F)(F)C2)N=C1OCC1CC1 NPOSXWDUCSOJAX-UHFFFAOYSA-N 0.000 claims 1
- JTBMTLQPRDBTQC-UHFFFAOYSA-N [6-(cyclopropylmethoxy)-5-(3,3-difluoroazetidin-1-yl)pyrazin-2-yl]-(3,3-difluoropyrrolidin-1-yl)methanone Chemical compound C1C(F)(F)CN1C1=NC=C(C(=O)N2CC(F)(F)CC2)N=C1OCC1CC1 JTBMTLQPRDBTQC-UHFFFAOYSA-N 0.000 claims 1
- RNHDQIQNRFAOIU-UHFFFAOYSA-N [6-(cyclopropylmethoxy)-5-(3,3-difluoroazetidin-1-yl)pyrazin-2-yl]-(7-oxa-4-azaspiro[2.5]octan-4-yl)methanone Chemical compound C1C(F)(F)CN1C1=NC=C(C(=O)N2C3(CC3)COCC2)N=C1OCC1CC1 RNHDQIQNRFAOIU-UHFFFAOYSA-N 0.000 claims 1
- ZXJWVSDWNJTBJK-LLVKDONJSA-N [6-(cyclopropylmethoxy)-5-(3,3-difluoroazetidin-1-yl)pyrazin-2-yl]-[(2r)-2-methylpyrrolidin-1-yl]methanone Chemical compound C[C@@H]1CCCN1C(=O)C(N=C1OCC2CC2)=CN=C1N1CC(F)(F)C1 ZXJWVSDWNJTBJK-LLVKDONJSA-N 0.000 claims 1
- ZXJWVSDWNJTBJK-NSHDSACASA-N [6-(cyclopropylmethoxy)-5-(3,3-difluoroazetidin-1-yl)pyrazin-2-yl]-[(2s)-2-methylpyrrolidin-1-yl]methanone Chemical compound C[C@H]1CCCN1C(=O)C(N=C1OCC2CC2)=CN=C1N1CC(F)(F)C1 ZXJWVSDWNJTBJK-NSHDSACASA-N 0.000 claims 1
- FZQXJJYOPAWXBR-UHFFFAOYSA-N [6-(cyclopropylmethoxy)-5-(3,3-difluoroazetidin-1-yl)pyrazin-2-yl]-[4-(2-hydroxyethyl)piperazin-1-yl]methanone Chemical compound C1CN(CCO)CCN1C(=O)C(N=C1OCC2CC2)=CN=C1N1CC(F)(F)C1 FZQXJJYOPAWXBR-UHFFFAOYSA-N 0.000 claims 1
- 230000001154 acute effect Effects 0.000 claims 1
- 231100000836 acute liver failure Toxicity 0.000 claims 1
- 125000004453 alkoxycarbonyl group Chemical group 0.000 claims 1
- 125000005078 alkoxycarbonylalkyl group Chemical group 0.000 claims 1
- 125000005196 alkyl carbonyloxy group Chemical group 0.000 claims 1
- 206010002026 amyotrophic lateral sclerosis Diseases 0.000 claims 1
- 230000033228 biological regulation Effects 0.000 claims 1
- 210000000988 bone and bone Anatomy 0.000 claims 1
- 230000001684 chronic effect Effects 0.000 claims 1
- 125000000753 cycloalkyl group Chemical group 0.000 claims 1
- 125000001559 cyclopropyl group Chemical group [H]C1([H])C([H])([H])C1([H])* 0.000 claims 1
- 230000006378 damage Effects 0.000 claims 1
- 206010012601 diabetes mellitus Diseases 0.000 claims 1
- 208000033679 diabetic kidney disease Diseases 0.000 claims 1
- FRWMYAZAWIIHDG-UHFFFAOYSA-N ethyl 2-[tert-butyl-[6-(cyclopropylmethoxy)-5-(3,3-difluoroazetidin-1-yl)pyrazine-2-carbonyl]amino]acetate Chemical compound C1CC1COC1=NC(C(=O)N(CC(=O)OCC)C(C)(C)C)=CN=C1N1CC(F)(F)C1 FRWMYAZAWIIHDG-UHFFFAOYSA-N 0.000 claims 1
- 230000027950 fever generation Effects 0.000 claims 1
- 230000004761 fibrosis Effects 0.000 claims 1
- 208000007565 gingivitis Diseases 0.000 claims 1
- 125000004438 haloalkoxy group Chemical group 0.000 claims 1
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims 1
- 125000002768 hydroxyalkyl group Chemical group 0.000 claims 1
- 230000001969 hypertrophic effect Effects 0.000 claims 1
- 230000004054 inflammatory process Effects 0.000 claims 1
- 208000014674 injury Diseases 0.000 claims 1
- 208000012947 ischemia reperfusion injury Diseases 0.000 claims 1
- 210000001117 keloid Anatomy 0.000 claims 1
- 208000017169 kidney disease Diseases 0.000 claims 1
- 208000014018 liver neoplasm Diseases 0.000 claims 1
- 208000002780 macular degeneration Diseases 0.000 claims 1
- 238000000034 method Methods 0.000 claims 1
- GRZKZDYFLDPNBM-CYBMUJFWSA-N methyl (2r)-1-[6-(cyclopropylmethoxy)-5-(3,3-difluoroazetidin-1-yl)pyrazine-2-carbonyl]pyrrolidine-2-carboxylate Chemical compound COC(=O)[C@H]1CCCN1C(=O)C(N=C1OCC2CC2)=CN=C1N1CC(F)(F)C1 GRZKZDYFLDPNBM-CYBMUJFWSA-N 0.000 claims 1
- PIZOYHRQRIQRPT-AWEZNQCLSA-N methyl (2s)-1-[5-cyclopropyl-6-(cyclopropylmethoxy)pyrazine-2-carbonyl]pyrrolidine-2-carboxylate Chemical compound COC(=O)[C@@H]1CCCN1C(=O)C(N=C1OCC2CC2)=CN=C1C1CC1 PIZOYHRQRIQRPT-AWEZNQCLSA-N 0.000 claims 1
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims 1
- 208000010125 myocardial infarction Diseases 0.000 claims 1
- 208000031225 myocardial ischemia Diseases 0.000 claims 1
- FIAAIGAANUVTAQ-UHFFFAOYSA-N n-tert-butyl-5-(3,3-difluoroazetidin-1-yl)-n-methyl-6-(2,2,2-trifluoroethoxy)pyrazine-2-carboxamide Chemical compound FC(F)(F)COC1=NC(C(=O)N(C)C(C)(C)C)=CN=C1N1CC(F)(F)C1 FIAAIGAANUVTAQ-UHFFFAOYSA-N 0.000 claims 1
- 230000004770 neurodegeneration Effects 0.000 claims 1
- 239000008194 pharmaceutical composition Substances 0.000 claims 1
- 125000004193 piperazinyl group Chemical group 0.000 claims 1
- 125000003386 piperidinyl group Chemical group 0.000 claims 1
- 230000002028 premature Effects 0.000 claims 1
- 238000011321 prophylaxis Methods 0.000 claims 1
- 208000005069 pulmonary fibrosis Diseases 0.000 claims 1
- 208000004644 retinal vein occlusion Diseases 0.000 claims 1
- 150000003839 salts Chemical class 0.000 claims 1
- 231100000241 scar Toxicity 0.000 claims 1
- 230000037387 scars Effects 0.000 claims 1
- 239000000126 substance Substances 0.000 claims 1
- 230000009885 systemic effect Effects 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
- 125000004568 thiomorpholinyl group Chemical group 0.000 claims 1
- 201000010875 transient cerebral ischemia Diseases 0.000 claims 1
- 238000011282 treatment Methods 0.000 claims 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D401/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom
- C07D401/14—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing three or more hetero rings
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D498/00—Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen and oxygen atoms as the only ring hetero atoms
- C07D498/02—Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen and oxygen atoms as the only ring hetero atoms in which the condensed system contains two hetero rings
- C07D498/08—Bridged systems
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P1/00—Drugs for disorders of the alimentary tract or the digestive system
- A61P1/02—Stomatological preparations, e.g. drugs for caries, aphtae, periodontitis
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P1/00—Drugs for disorders of the alimentary tract or the digestive system
- A61P1/16—Drugs for disorders of the alimentary tract or the digestive system for liver or gallbladder disorders, e.g. hepatoprotective agents, cholagogues, litholytics
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P11/00—Drugs for disorders of the respiratory system
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P13/00—Drugs for disorders of the urinary system
- A61P13/12—Drugs for disorders of the urinary system of the kidneys
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P17/00—Drugs for dermatological disorders
- A61P17/02—Drugs for dermatological disorders for treating wounds, ulcers, burns, scars, keloids, or the like
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P19/00—Drugs for skeletal disorders
-
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- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
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Claims (12)
1. Spoj, naznačen time, da ima sljedeću formulu (I):
[image]
u kojoj
R1 je cikloalkilalkoksi ili haloalkoksi;
R2 je cikloalkil ili haloazetidinil;
R3 i R4 su neovisno odabrani od sljedećih: alkil, alkoksi, alkoksialkil i alkoksikarbonilalkil; ili R3 i R4 zajedno s atomom dušika na kojega su priključeni, tvore heterociklil ili supstituirani heterociklil, pri čemu je heterociklil
sljedeći: pirolidinil, morfolinil, oksomorfolinil, 2-okso-5-aza-biciklo[2.2.1]heptil, 7-oksa-4-aza-spiro[2.5]oktil, piperazinil, 2-oksa-6-aza-spiro[3.4]oktil, piperidinil, tiomorfolinil ili 5-aza-spiro[2.4]heptil, te je pritom supstituirani heterociklil takav heterociklil koji je supstituiran s jednim do četiri supstituenta neovisno odabrana od sljedećih: alkil, halogen, aminokarbonil, hidroksialkil,
alkoksikarbonil, alkiltiokarbamoil, alkilkarboniloksi i hidroksil;
ili njegova farmaceutski prihvatljiva sol.
2. Spoj prema zahtjevu 1, naznačen time, da R1 je cikloalkilalkoksi.
3. Spoj prema zahtjevu 1 ili 2, naznačen time, da R1 je ciklopropilmetoksi.
4. Spoj prema bilo kojem od zahtjeva 1 do 3, naznačen time, da R2 je ciklopropil ili difluoroazetidinil.
5. Spoj prema bilo kojem od zahtjeva 1 do 4, naznačen time, da su R3 i R4 neovisno odabrani od sljedećih: alkil, alkoksi i alkoksialkil, ili R3 i R4 zajedno s atomom dušika na kojega su priključeni, tvore heterociklil ili supstituirani heterociklil, pri čemu je heterociklil sljedeći: pirolidinil, morfolinil ili 5-azaspiro[2.4]heptil, te je pritom supstituirani heterociklil takav heterociklil koji je supstituiran s jednim do tri supstituenta neovisno odabrana od sljedećih: alkil, halogen i aminokarbonil.
6. Spoj prema bilo kojem od zahtjeva 1 do 5, naznačen time, da su R3 i R4 neovisno odabrani od sljedećih: metil, tert-butil, metoksietil ili metoksibutil, ili R3 i R4 zajedno s atomom dušika na kojega su priključeni, tvore sljedeće: dimetilmorfolinil, dimetilpirolidinil, (aminokarbonil)(difluoro) pirolidinil, (aminokarbonil)(dimetil)pirolidinil, ili (aminokarbonil)-5-azaspiro[2.4]heptil.
7. Spoj prema bilo kojem od zahtjeva 1 do 6, naznačen time, da je odabran od sljedećih:
(5-ciklopropil-6-ciklopropilmetoksi-pirazin-2-il)-((R)-2-metil-pirolidin-1-il)-metanon;
[6-ciklopropilmetoksi-5-(3,3-difluoro-azetidin-1-il)-pirazin-2-il]-((R)-2-metil-pirolidin-1-il)-metanon;
6-ciklopropilmetoksi-5-(3,3-difluoro-azetidin-1-il)-pirazin-2-karboksilna kiselina-tert-butil-(2-metoksi-etil)-amid;
[6-ciklopropilmetoksi-5-(3,3-difluoro-azetidin-1-il)-pirazin-2-il]-(3,3-dimetil-morfolin-4-il)-metanon;
[6-ciklopropilmetoksi-5-(3,3-difluoro-azetidin-1-il)-pirazin-2-il]-((S)-2-metil-pirolidin-1-il)-metanon;
[6-ciklopropilmetoksi-5-(3,3-difluoro-azetidin-1-il)-pirazin-2-il]-((1R,4R)-2-oksa-5-aza-biciklo[2.2.1]hept-5-il)-metanon;
6-ciklopropilmetoksi-5-(3,3-difluoro-azetidin-1-il)-pirazin-2-karboksilna kiselina-tert-butil-metil-amid;
[6-ciklopropilmetoksi-5-(3,3-difluoro-azetidin-1-il)-pirazin-2-il]-(3,3-difluoro-pirolidin-1-il)-metanon;
6-ciklopropilmetoksi-5-(3,3-difluoro-azetidin-1-il)-pirazin-2-karboksilna kiselina-etil-izopropil-amid;
[6-ciklopropilmetoksi-5-(3,3-difluoro-azetidin-1-il)-pirazin-2-il]-(7-oksa-4-aza-spiro[2.5]okt-4-il)-metanon;
{tert-butil-[6-ciklopropilmetoksi-5-(3,3-difluoro-azetidin-1-il)-pirazin-2-karbonil]-amino}-octena kiselina-etilester;
6-ciklopropilmetoksi-5-(3,3-difluoro-azetidin-1-il)-pirazin-2-karboksilna kiselina-(2-metoksi-1,1-dimetil-etil)-metil-amid;
[6-ciklopropilmetoksi-5-(3,3-difluoro-azetidin-1-il)-pirazin-2-il]-(2,2-dimetil-morfolin-4-il)-metanon;
5-ciklopropil-6-ciklopropilmetoksi-pirazin-2-karboksilna kiselina-(2-metoksi-1,1-dimetil-etil)-metil-amid;
(5-ciklopropil-6-ciklopropilmetoksi-pirazin-2-il)-(2,2-dimetil-pirolidin-1-il)-metanon;
(S)-1-(5-ciklopropil-6-ciklopropilmetoksi-pirazin-2-karbonil)-pirolidin-2-karboksilna kiselina-metil-ester;
(5-ciklopropil-6-ciklopropilmetoksi-pirazin-2-il)-(7-oksa-4-aza-spiro[2.5]okt-4-il)-metanon;
(S)-1-(5-ciklopropil-6-ciklopropilmetoksi-pirazin-2-karbonil)-4,4-difluoro-pirolidin-2-karboksilna kiselina-amid;
(S)-1-[6-ciklopropilmetoksi-5-(3,3-difluoro-azetidin-1-il)-pirazin-2-karbonil]-4,4-difluoro-pirolidin-2-karboksilna kiselina-amid;
[6-ciklopropilmetoksi-5-(3,3-difluoro-azetidin-1-il)-pirazin-2-il]-[4-(2-hidroksietil)-piperazin-1-il]-metanon;
[6-ciklopropilmetoksi-5-(3,3-difluoro-azetidin-1-il)-pirazin-2-il]-(2,2-dimetil-pirolidin-1-il)-metanon;
(R)-1-[6-ciklopropilmetoksi-5-(3,3-difluoro-azetidin-1-il)-pirazin-2-karbonil]-pirolidin-2-karboksilna kiselina-metil-ester;
4-[6-ciklopropilmetoksi-5-(3,3-difluoro-azetidin-1-il)-pirazin-2-karbonil]-morfolin-2-on;
(R)-1-[6-ciklopropilmetoksi-5-(3,3-difluoro-azetidin-1-il)-pirazin-2-karbonil]-pirolidin-2-karbotioična kiselina-dimetil-amid;
octena kiselina-1-(5-ciklopropil-6-ciklopropilmetoksi-pirazin-2-karbonil)-3-metilpirolidin-3-il-ester;
(5-ciklopropil-6-ciklopropilmetoksi-pirazin-2-il)-(3,3,4,4-tetrafluoro-pirolidin-1-il)-metanon;
octena kiselina-(S)-1-[6-ciklopropilmetoksi-5-(3,3-difluoro-azetidin-1-il)-pirazin-2-karbonil]-pirolidin-3-il-ester;
[6-ciklopropilmetoksi-5-(3,3-difluoro-azetidin-1-il)-pirazin-2-il]-(2-oksa-6-aza-spiro[3.4]okt-6-il)-metanon;
octena kiselina-1-[6-ciklopropilmetoksi-5-(3,3-difluoro-azetidin-1-il)-pirazin-2-karbonil]-3-metil-pirolidin-3-il-ester;
[6-ciklopropilmetoksi-5-(3,3-difluoro-azetidin-1-il)-pirazin-2-il]-(3,3,4,4-tetrafluoro-pirolidin-1-il)-metanon;
5-(3,3-difluoro-azetidin-1-il)-6-(2,2,2-trifluoro-etoksi)-pirazin-2-karboksilna kiselina-tert-butil-metil-amid;
[5-(3,3-difluoro-azetidin-1-il)-6-(2,2,2-trifluoro-etoksi)-pirazin-2-il]-(2,2-dimetil-pirolidin-1-il)-metanon;
1-[6-ciklopropilmetoksi-5-(3,3-difluoro-azetidin-1-il)-pirazin-2-karbonil]-piperidin-2-karboksilna kiselina-amid;
1-(5-ciklopropil-6-ciklopropilmetoksi-pirazin-2-karbonil)-4,4-dimetil-pirolidin-2-karboksilna kiselina-amid;
1-[6-ciklopropilmetoksi-5-(3,3-difluoro-azetidin-1-il)-pirazin-2-karbonil]-4,4-dimetil-pirolidin-2-karboksilna kiselina-amid;
(-)-1-[6-ciklopropilmetoksi-5-(3,3-difluoro-azetidin-1-il)-pirazin-2-karbonil]-piperidin-2-karboksilna kiselina-amid;
(-)-4-[6-ciklopropilmetoksi-5-(3,3-difluoro-azetidin-1-il)-pirazin-2-karbonil]-tiomorfolin-3-karboksilna kiselina-amid;
(-)-1-[6-ciklopropilmetoksi-5-(3,3-difluoro-azetidin-1-il)-pirazin-2-karbonil]-4,4-dimetil-pirolidin-2-karboksilna kiselina-amid;
(-)-1-(5-ciklopropil-6-ciklopropilmetoksi-pirazin-2-karbonil)-4,4-dimetil-pirolidin-2-karboksilna kiselina-amid;
(±)-5-[6-(ciklopropilmetoksi)-5-(3,3-difluoro-azetidin-1-il)-pirazin-2-karbonil]-5-azaspiro[2.4]heptan-6-karboksamid;
(2S)-1-[6-(ciklopropilmetoksi)-5-(3,3-difluoro-azetidin-1-il)-pirazin-2-karbonil]-4-hidroksi-4-metil-pirolidin-2-karboksamid; i
(2S)-1-[5-(3,3-difluoro-azetidin-1-il)-6-(2,2-difluoro-etoksi)-pirazin-2-karbonil]-4,4-difluoro-pirolidin-2-karboksamid.
8. Spoj prema bilo kojem od zahtjeva 1 do 7, naznačen time, da je odabran od sljedećih:
6-ciklopropilmetoksi-5-(3,3-difluoro-azetidin-1-il)-pirazin-2-karboksilna kiselina-tert-butil-(2-metoksi-etil)-amid;
[6-ciklopropilmetoksi-5-(3,3-difluoro-azetidin-1-il)-pirazin-2-il]-(3,3-dimetil-morfolin-4-il)-metanon;
6-ciklopropilmetoksi-5-(3,3-difluoro-azetidin-1-il)-pirazin-2-karboksilna kiselina-tert-butil-metil-amid;
6-ciklopropilmetoksi-5-(3,3-difluoro-azetidin-1-il)-pirazin-2-karboksilna kiselina-(2-metoksi-1,1-dimetil-etil)-metil-amid;
(5-ciklopropil-6-ciklopropilmetoksi-pirazin-2-il)-(2,2-dimetil-pirolidin-1-il)-metanon;
(S)-1-[6-ciklopropilmetoksi-5-(3,3-difluoro-azetidin-1-il)-pirazin-2-karbonil]-4,4-difluoro-pirolidin-2-karboksilna kiselina-amid;
[6-ciklopropilmetoksi-5-(3,3-difluoro-azetidin-1-il)-pirazin-2-il]-(2,2-dimetil-pirolidin-1-il)-metanon;
1-(5-ciklopropil-6-ciklopropilmetoksi-pirazin-2-karbonil)-4,4-dimetil-pirolidin-2-karboksilna kiselina-amid;
(-)-1-[6-ciklopropilmetoksi-5-(3,3-difluoro-azetidin-1-il)-pirazin-2-karbonil]-4,4-dimetil-pirolidin-2-karboksilna kiselina-amid; i
(±)-5-[6-(ciklopropilmetoksi)-5-(3,3-difluoro-azetidin-1-il)-pirazin-2-karbonil]-5-azaspiro[2.4]heptan-6-karboksamid.
9. Postupak za proizvodnju spoja prema bilo kojem od zahtjeva 1 do 8, naznačen time, da obuhvaća reakciju spoja sljedeće formule (II):
[image]
u prisutnosti NHR3R4, amidnog sredstva za vezanje te baze, pri čemu su R1 do R4 isti kao što su definirani u bilo kojem od zahtjeva 1 do 6.
10. Spoj prema bilo kojem od zahtjeva 1 do 8, naznačen time, da se upotrebljava kao terapeutski djelotvorna tvar.
11. Farmaceutski sastav, naznačen time, da obuhvaća spoj prema bilo kojem od zahtjeva 1 do 8, te terapeutski inertan nosač.
12. Spoj prema bilo kojem od zahtjeva 1 do 8, naznačen time, da se upotrebljava u liječenju ili profilaksi sljedećih stanja: bol, ateroskleroza, makularna degeneracija povezana sa starošću, dijabetska retinopatija, glaukom, okluzija retinalne vene, retinopatija kod prerano rođene djece, okularni ishemijski sindrom, geografska atrofija, dijabetes melitus, upala, upalna bolest crijeva, ishemijsko-reperfuzijska ozljeda, akutno zatajenje jetre, fibroza jetre, fibroza pluća, fibroza bubrega, sustavna fibroza, akutno odbacivanje alogenskih presadaka, kronična alogenska nefropatija, dijabetska nefropatija, glomerulonefropatija, kardiomiopatija, zatajenje srca, ishemija miokarda, infarkt miokarda, sustavna skleroza, termalna ozljeda, opekotina, hipertrofični ožiljci, keloidi, gingivitis pireksija, ciroza jetre ili tumori jetre, regulacija koštane mase, neurodegeneracija, amiotrofna lateralna skleroza, moždani udar, prolazni ishemijski napad ili uveitis.
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EP12196024 | 2012-12-07 | ||
EP13799545.2A EP2928882B1 (en) | 2012-12-07 | 2013-12-04 | Pyrazine derivatives as cb2 receptor agonists |
PCT/EP2013/075444 WO2014086807A1 (en) | 2012-12-07 | 2013-12-04 | Novel pyrazine derivatives as cb2 receptor agonists |
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HRP20170572T1 true HRP20170572T1 (hr) | 2017-06-16 |
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HRP20170572TT HRP20170572T1 (hr) | 2012-12-07 | 2017-04-10 | Derivati pirazina kao agonisti receptora cb2 |
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US (1) | US9512141B2 (hr) |
EP (1) | EP2928882B1 (hr) |
JP (1) | JP6322646B2 (hr) |
KR (1) | KR20150092156A (hr) |
CN (1) | CN104837830B (hr) |
AR (1) | AR093804A1 (hr) |
AU (1) | AU2013354115B2 (hr) |
BR (1) | BR112015009603A2 (hr) |
CA (1) | CA2885418A1 (hr) |
CL (1) | CL2015001318A1 (hr) |
CR (1) | CR20150210A (hr) |
CY (1) | CY1118808T1 (hr) |
DK (1) | DK2928882T3 (hr) |
EA (1) | EA025840B1 (hr) |
ES (1) | ES2621958T3 (hr) |
HK (1) | HK1208030A1 (hr) |
HR (1) | HRP20170572T1 (hr) |
HU (1) | HUE030836T2 (hr) |
IL (1) | IL237982A (hr) |
IN (1) | IN2015DN03145A (hr) |
LT (1) | LT2928882T (hr) |
MA (1) | MA38217B1 (hr) |
MX (1) | MX2015006036A (hr) |
PE (1) | PE20151060A1 (hr) |
PH (1) | PH12015501072B1 (hr) |
PL (1) | PL2928882T3 (hr) |
PT (1) | PT2928882T (hr) |
RS (1) | RS55951B1 (hr) |
SG (1) | SG11201504011UA (hr) |
SI (1) | SI2928882T1 (hr) |
TW (1) | TW201427960A (hr) |
UA (1) | UA116894C2 (hr) |
WO (1) | WO2014086807A1 (hr) |
Families Citing this family (12)
Publication number | Priority date | Publication date | Assignee | Title |
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MY176797A (en) | 2013-03-07 | 2020-08-21 | Hoffmann La Roche | Novel pyrazol derivatives |
ES2661737T3 (es) | 2013-03-26 | 2018-04-03 | F. Hoffmann-La Roche Ag | Derivados de piridina novedosos |
UA116801C2 (uk) | 2013-05-02 | 2018-05-10 | Ф. Хоффманн-Ля Рош Аг | ПОХІДНІ ПІРОЛО[2,3-d]ПІРИМІДИНУ ЯК АГОНІСТИ РЕЦЕПТОРА CB2 |
MX2015014757A (es) | 2013-05-02 | 2016-03-11 | Hoffmann La Roche | Derivados de purina como agonistas del receptor de cannabinoides 2 (cb2). |
CN105555788B (zh) | 2013-09-06 | 2018-11-23 | 豪夫迈·罗氏有限公司 | 三唑并[4,5-d]嘧啶衍生物 |
JP6654574B2 (ja) * | 2014-04-04 | 2020-02-26 | エフ.ホフマン−ラ ロシュ アーゲーF. Hoffmann−La Roche Aktiengesellschaft | Cb2アゴニストとして有用なピリジン−2−アミド |
MX2018006802A (es) | 2015-12-09 | 2018-09-05 | Hoffmann La Roche | Derivados de fenilo como agonistas del receptor de canabinoides 2. |
CN110753690B (zh) | 2017-06-20 | 2023-12-05 | 豪夫迈·罗氏有限公司 | 吡啶衍生物 |
PE20210368A1 (es) | 2018-06-27 | 2021-02-26 | Eth Zuerich | Nuevos compuestos de piridina y pirazina como inhibidores del receptor cannabinoide 2 |
JP7454512B2 (ja) | 2018-06-27 | 2024-03-22 | エフ. ホフマン-ラ ロシュ アーゲー | 優先的カンナビノイド2アゴニストとしてのピリジン及びピラジン誘導体 |
JP7456948B2 (ja) | 2018-06-27 | 2024-03-27 | エフ. ホフマン-ラ ロシュ アーゲー | 放射性標識カンナビノイド受容体2リガンド |
WO2022128050A1 (en) | 2020-12-14 | 2022-06-23 | Symrise Ag | Medicament for fighting inflammation and pain |
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US7629346B2 (en) * | 2006-06-19 | 2009-12-08 | Hoffmann-La Roche Inc. | Pyrazinecarboxamide derivatives as CB1 antagonists |
KR101114704B1 (ko) * | 2006-10-04 | 2012-03-14 | 에프. 호프만-라 로슈 아게 | Cb2 수용체 조절제로서 피라진-2-카복스아마이드 유도체 |
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 |
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2013
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- 2013-12-04 CN CN201380063228.9A patent/CN104837830B/zh not_active Expired - Fee Related
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- 2013-12-04 PT PT137995452T patent/PT2928882T/pt unknown
- 2013-12-04 ES ES13799545.2T patent/ES2621958T3/es active Active
- 2013-12-04 EP EP13799545.2A patent/EP2928882B1/en not_active Not-in-force
- 2013-12-04 WO PCT/EP2013/075444 patent/WO2014086807A1/en active Application Filing
- 2013-12-04 MX MX2015006036A patent/MX2015006036A/es unknown
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- 2013-12-04 US US14/648,399 patent/US9512141B2/en not_active Expired - Fee Related
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