JP2012506440A5 - - Google Patents
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- JP2012506440A5 JP2012506440A5 JP2011533270A JP2011533270A JP2012506440A5 JP 2012506440 A5 JP2012506440 A5 JP 2012506440A5 JP 2011533270 A JP2011533270 A JP 2011533270A JP 2011533270 A JP2011533270 A JP 2011533270A JP 2012506440 A5 JP2012506440 A5 JP 2012506440A5
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- Prior art keywords
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- aryl
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- 238000000034 method Methods 0.000 claims description 124
- 150000001875 compounds Chemical class 0.000 claims description 100
- 125000003118 aryl group Chemical group 0.000 claims description 54
- QJGQUHMNIGDVPM-UHFFFAOYSA-N nitrogen group Chemical group [N] QJGQUHMNIGDVPM-UHFFFAOYSA-N 0.000 claims description 48
- 238000010438 heat treatment Methods 0.000 claims description 47
- 239000012454 non-polar solvent Substances 0.000 claims description 39
- 239000000203 mixture Substances 0.000 claims description 31
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 claims description 30
- 125000006241 alcohol protecting group Chemical group 0.000 claims description 30
- 239000002798 polar solvent Substances 0.000 claims description 26
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical group [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 claims description 24
- 125000006244 carboxylic acid protecting group Chemical group 0.000 claims description 24
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 claims description 18
- 150000002500 ions Chemical class 0.000 claims description 18
- 239000000706 filtrate Substances 0.000 claims description 15
- 239000011541 reaction mixture Substances 0.000 claims description 15
- 125000000008 (C1-C10) alkyl group Chemical group 0.000 claims description 14
- 238000001914 filtration Methods 0.000 claims description 14
- -1 tetraphenylborate Chemical compound 0.000 claims description 12
- 239000000463 material Substances 0.000 claims description 10
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 claims description 9
- WEVYAHXRMPXWCK-UHFFFAOYSA-N Acetonitrile Chemical compound CC#N WEVYAHXRMPXWCK-UHFFFAOYSA-N 0.000 claims description 9
- YMWUJEATGCHHMB-UHFFFAOYSA-N Dichloromethane Chemical compound ClCCl YMWUJEATGCHHMB-UHFFFAOYSA-N 0.000 claims description 9
- XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 claims description 9
- ZMXDDKWLCZADIW-UHFFFAOYSA-N N,N-Dimethylformamide Chemical compound CN(C)C=O ZMXDDKWLCZADIW-UHFFFAOYSA-N 0.000 claims description 9
- VLKZOEOYAKHREP-UHFFFAOYSA-N n-Hexane Chemical compound CCCCCC VLKZOEOYAKHREP-UHFFFAOYSA-N 0.000 claims description 9
- GOYDNIKZWGIXJT-UHFFFAOYSA-N 1,2-difluorobenzene Chemical compound FC1=CC=CC=C1F GOYDNIKZWGIXJT-UHFFFAOYSA-N 0.000 claims description 6
- 125000006374 C2-C10 alkenyl group Chemical group 0.000 claims description 6
- YNQLUTRBYVCPMQ-UHFFFAOYSA-N Ethylbenzene Chemical compound CCC1=CC=CC=C1 YNQLUTRBYVCPMQ-UHFFFAOYSA-N 0.000 claims description 6
- DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical group C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 claims description 6
- CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical group CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 claims description 6
- URLKBWYHVLBVBO-UHFFFAOYSA-N Para-Xylene Chemical group CC1=CC=C(C)C=C1 URLKBWYHVLBVBO-UHFFFAOYSA-N 0.000 claims description 6
- ZLMJMSJWJFRBEC-UHFFFAOYSA-N Potassium Chemical group [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 claims description 6
- WYURNTSHIVDZCO-UHFFFAOYSA-N Tetrahydrofuran Chemical compound C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 claims description 6
- 125000000304 alkynyl group Chemical group 0.000 claims description 6
- 229910052792 caesium Inorganic materials 0.000 claims description 6
- TVFDJXOCXUVLDH-UHFFFAOYSA-N caesium atom Chemical group [Cs] TVFDJXOCXUVLDH-UHFFFAOYSA-N 0.000 claims description 6
- MVPPADPHJFYWMZ-UHFFFAOYSA-N chlorobenzene Chemical compound ClC1=CC=CC=C1 MVPPADPHJFYWMZ-UHFFFAOYSA-N 0.000 claims description 6
- 125000001188 haloalkyl group Chemical group 0.000 claims description 6
- 125000001072 heteroaryl group Chemical group 0.000 claims description 6
- IVSZLXZYQVIEFR-UHFFFAOYSA-N m-xylene Chemical group CC1=CC=CC(C)=C1 IVSZLXZYQVIEFR-UHFFFAOYSA-N 0.000 claims description 6
- LQNUZADURLCDLV-UHFFFAOYSA-N nitrobenzene Chemical compound [O-][N+](=O)C1=CC=CC=C1 LQNUZADURLCDLV-UHFFFAOYSA-N 0.000 claims description 6
- 229910052700 potassium Inorganic materials 0.000 claims description 6
- 239000011591 potassium Substances 0.000 claims description 6
- 229910052708 sodium Inorganic materials 0.000 claims description 6
- 239000011734 sodium Chemical group 0.000 claims description 6
- 125000001424 substituent group Chemical group 0.000 claims description 6
- VZGDMQKNWNREIO-UHFFFAOYSA-N tetrachloromethane Chemical compound ClC(Cl)(Cl)Cl VZGDMQKNWNREIO-UHFFFAOYSA-N 0.000 claims description 6
- 239000000047 product Substances 0.000 claims description 5
- 230000002285 radioactive effect Effects 0.000 claims description 5
- CPELXLSAUQHCOX-UHFFFAOYSA-M Bromide Chemical compound [Br-] CPELXLSAUQHCOX-UHFFFAOYSA-M 0.000 claims description 4
- VEXZGXHMUGYJMC-UHFFFAOYSA-M Chloride anion Chemical compound [Cl-] VEXZGXHMUGYJMC-UHFFFAOYSA-M 0.000 claims description 4
- DTQVDTLACAAQTR-UHFFFAOYSA-M Trifluoroacetate Chemical compound [O-]C(=O)C(F)(F)F DTQVDTLACAAQTR-UHFFFAOYSA-M 0.000 claims description 4
- XMBWDFGMSWQBCA-UHFFFAOYSA-N hydrogen iodide Chemical compound I XMBWDFGMSWQBCA-UHFFFAOYSA-N 0.000 claims description 4
- GETTZEONDQJALK-UHFFFAOYSA-N (trifluoromethyl)benzene Chemical compound FC(F)(F)C1=CC=CC=C1 GETTZEONDQJALK-UHFFFAOYSA-N 0.000 claims description 3
- NLMDJJTUQPXZFG-UHFFFAOYSA-N 1,4,10,13-tetraoxa-7,16-diazacyclooctadecane Chemical compound C1COCCOCCNCCOCCOCCN1 NLMDJJTUQPXZFG-UHFFFAOYSA-N 0.000 claims description 3
- PXACTUVBBMDKRW-UHFFFAOYSA-M 4-bromobenzenesulfonate Chemical compound [O-]S(=O)(=O)C1=CC=C(Br)C=C1 PXACTUVBBMDKRW-UHFFFAOYSA-M 0.000 claims description 3
- SPXOTSHWBDUUMT-UHFFFAOYSA-M 4-nitrobenzenesulfonate Chemical compound [O-][N+](=O)C1=CC=C(S([O-])(=O)=O)C=C1 SPXOTSHWBDUUMT-UHFFFAOYSA-M 0.000 claims description 3
- XDTMQSROBMDMFD-UHFFFAOYSA-N Cyclohexane Chemical compound C1CCCCC1 XDTMQSROBMDMFD-UHFFFAOYSA-N 0.000 claims description 3
- WHXSMMKQMYFTQS-UHFFFAOYSA-N Lithium Chemical compound [Li] WHXSMMKQMYFTQS-UHFFFAOYSA-N 0.000 claims description 3
- AFVFQIVMOAPDHO-UHFFFAOYSA-N Methanesulfonic acid Chemical group CS(O)(=O)=O AFVFQIVMOAPDHO-UHFFFAOYSA-N 0.000 claims description 3
- 150000003983 crown ethers Chemical class 0.000 claims description 3
- 239000002739 cryptand Substances 0.000 claims description 3
- 150000002159 estradiols Chemical class 0.000 claims description 3
- 238000001722 flash pyrolysis Methods 0.000 claims description 3
- 150000002410 histidine derivatives Chemical group 0.000 claims description 3
- 239000002198 insoluble material Substances 0.000 claims description 3
- 229910052744 lithium Inorganic materials 0.000 claims description 3
- PYLWMHQQBFSUBP-UHFFFAOYSA-N monofluorobenzene Chemical compound FC1=CC=CC=C1 PYLWMHQQBFSUBP-UHFFFAOYSA-N 0.000 claims description 3
- 229940078552 o-xylene Drugs 0.000 claims description 3
- VLTRZXGMWDSKGL-UHFFFAOYSA-M perchlorate Inorganic materials [O-]Cl(=O)(=O)=O VLTRZXGMWDSKGL-UHFFFAOYSA-M 0.000 claims description 3
- VLTRZXGMWDSKGL-UHFFFAOYSA-N perchloric acid Chemical compound OCl(=O)(=O)=O VLTRZXGMWDSKGL-UHFFFAOYSA-N 0.000 claims description 3
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims description 3
- 150000002993 phenylalanine derivatives Chemical class 0.000 claims description 3
- 150000003839 salts Chemical class 0.000 claims description 3
- 239000002904 solvent Substances 0.000 claims description 3
- YLQBMQCUIZJEEH-UHFFFAOYSA-N tetrahydrofuran Natural products C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 claims description 3
- JOXIMZWYDAKGHI-UHFFFAOYSA-N toluene-4-sulfonic acid Chemical compound CC1=CC=C(S(O)(=O)=O)C=C1 JOXIMZWYDAKGHI-UHFFFAOYSA-N 0.000 claims description 3
- 125000002827 triflate group Chemical group FC(S(=O)(=O)O*)(F)F 0.000 claims description 3
- 150000003667 tyrosine derivatives Chemical class 0.000 claims description 3
- PXGOKWXKJXAPGV-UHFFFAOYSA-N Fluorine Chemical compound FF PXGOKWXKJXAPGV-UHFFFAOYSA-N 0.000 claims description 2
- 229910052731 fluorine Inorganic materials 0.000 claims description 2
- 239000011737 fluorine Substances 0.000 claims description 2
- 0 CC(CCC1*=CC=C1)C1CC1 Chemical compound CC(CCC1*=CC=C1)C1CC1 0.000 description 8
- 239000002253 acid Substances 0.000 description 7
- 125000000217 alkyl group Chemical group 0.000 description 4
- 150000002222 fluorine compounds Chemical group 0.000 description 3
- QGZKDVFQNNGYKY-UHFFFAOYSA-O Ammonium Chemical class [NH4+] QGZKDVFQNNGYKY-UHFFFAOYSA-O 0.000 description 2
- 229910019142 PO4 Inorganic materials 0.000 description 2
- ZMZDMBWJUHKJPS-UHFFFAOYSA-M Thiocyanate anion Chemical group [S-]C#N ZMZDMBWJUHKJPS-UHFFFAOYSA-M 0.000 description 2
- RHQDFWAXVIIEBN-UHFFFAOYSA-N Trifluoroethanol Chemical group OCC(F)(F)F RHQDFWAXVIIEBN-UHFFFAOYSA-N 0.000 description 2
- 150000001540 azides Chemical group 0.000 description 2
- 150000007942 carboxylates Chemical class 0.000 description 2
- XLJMAIOERFSOGZ-UHFFFAOYSA-M cyanate Chemical group [O-]C#N XLJMAIOERFSOGZ-UHFFFAOYSA-M 0.000 description 2
- ZMZDMBWJUHKJPS-UHFFFAOYSA-N hydrogen thiocyanate Chemical group SC#N ZMZDMBWJUHKJPS-UHFFFAOYSA-N 0.000 description 2
- 125000005010 perfluoroalkyl group Chemical group 0.000 description 2
- ISWSIDIOOBJBQZ-UHFFFAOYSA-M phenolate Chemical group [O-]C1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-M 0.000 description 2
- NBIIXXVUZAFLBC-UHFFFAOYSA-K phosphate Chemical group [O-]P([O-])([O-])=O NBIIXXVUZAFLBC-UHFFFAOYSA-K 0.000 description 2
- 239000010452 phosphate Chemical group 0.000 description 2
- XYFCBTPGUUZFHI-UHFFFAOYSA-O phosphonium Chemical compound [PH4+] XYFCBTPGUUZFHI-UHFFFAOYSA-O 0.000 description 2
- 150000007944 thiolates Chemical group 0.000 description 2
- ITMCEJHCFYSIIV-UHFFFAOYSA-M triflate Chemical group [O-]S(=O)(=O)C(F)(F)F ITMCEJHCFYSIIV-UHFFFAOYSA-M 0.000 description 2
- QTBSBXVTEAMEQO-UHFFFAOYSA-M Acetate Chemical group CC([O-])=O QTBSBXVTEAMEQO-UHFFFAOYSA-M 0.000 description 1
- WNXSQUQBVYNQGJ-BUSXIPJBSA-N CCCC(OC(N([C@@H](Cc(cc(c(OC)c1)OC)c1F)C(OC)=O)C(OC(C)(C)C)=O)=O)I Chemical compound CCCC(OC(N([C@@H](Cc(cc(c(OC)c1)OC)c1F)C(OC)=O)C(OC(C)(C)C)=O)=O)I WNXSQUQBVYNQGJ-BUSXIPJBSA-N 0.000 description 1
- KRHYYFGTRYWZRS-UHFFFAOYSA-M Fluoride anion Chemical compound [F-] KRHYYFGTRYWZRS-UHFFFAOYSA-M 0.000 description 1
- 125000005599 alkyl carboxylate group Chemical group 0.000 description 1
- WPYMKLBDIGXBTP-UHFFFAOYSA-N benzoic acid Chemical group OC(=O)C1=CC=CC=C1 WPYMKLBDIGXBTP-UHFFFAOYSA-N 0.000 description 1
- 150000004820 halides Chemical group 0.000 description 1
- 238000012986 modification Methods 0.000 description 1
- 230000004048 modification Effects 0.000 description 1
- UEZVMMHDMIWARA-UHFFFAOYSA-M phosphonate Chemical group [O-]P(=O)=O UEZVMMHDMIWARA-UHFFFAOYSA-M 0.000 description 1
- XRBCRPZXSCBRTK-UHFFFAOYSA-N phosphonous acid Chemical group OPO XRBCRPZXSCBRTK-UHFFFAOYSA-N 0.000 description 1
Applications Claiming Priority (5)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US10715608P | 2008-10-21 | 2008-10-21 | |
| US61/107,156 | 2008-10-21 | ||
| US23603709P | 2009-08-21 | 2009-08-21 | |
| US61/236,037 | 2009-08-21 | ||
| PCT/US2009/061308 WO2010048170A2 (en) | 2008-10-21 | 2009-10-20 | Fluorination of aromatic ring systems |
Related Child Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2015107073A Division JP6049804B2 (ja) | 2008-10-21 | 2015-05-27 | 環系芳香族のフッ素化 |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JP2012506440A JP2012506440A (ja) | 2012-03-15 |
| JP2012506440A5 true JP2012506440A5 (enExample) | 2012-11-29 |
Family
ID=42119938
Family Applications (2)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2011533270A Withdrawn JP2012506440A (ja) | 2008-10-21 | 2009-10-20 | 環系芳香族のフッ素化 |
| JP2015107073A Active JP6049804B2 (ja) | 2008-10-21 | 2015-05-27 | 環系芳香族のフッ素化 |
Family Applications After (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2015107073A Active JP6049804B2 (ja) | 2008-10-21 | 2015-05-27 | 環系芳香族のフッ素化 |
Country Status (7)
| Country | Link |
|---|---|
| US (1) | US8604213B2 (enExample) |
| EP (3) | EP3284736B1 (enExample) |
| JP (2) | JP2012506440A (enExample) |
| AU (1) | AU2009307715B2 (enExample) |
| CA (1) | CA2741967A1 (enExample) |
| ES (2) | ES2627825T3 (enExample) |
| WO (1) | WO2010048170A2 (enExample) |
Families Citing this family (16)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| ES2627825T3 (es) | 2008-10-21 | 2017-07-31 | Nutech Ventures | Fluoración de sistemas de anillos aromáticos |
| US9302990B2 (en) * | 2008-10-21 | 2016-04-05 | Nutech Ventures | Fluorination of aromatic ring systems |
| US8377704B2 (en) * | 2009-10-20 | 2013-02-19 | Nutech Ventures | Detection and quantification of anions |
| US8546578B2 (en) | 2010-02-04 | 2013-10-01 | Nutech Ventures | Iodonium Cyclophanes for SECURE arene functionalization |
| US20120309796A1 (en) | 2011-06-06 | 2012-12-06 | Fariborz Firooznia | Benzocycloheptene acetic acids |
| CA2875622A1 (en) | 2012-06-05 | 2013-12-12 | Nutech Ventures | Processes and reagents for making diaryliodonium salts |
| WO2014022224A1 (en) * | 2012-08-02 | 2014-02-06 | The Penn State Research Foundation | Polymer conductor for lithium-ion batteries |
| US9018172B2 (en) | 2012-09-26 | 2015-04-28 | Massachusetts Institute Of Technology | Modification of peptides via SNAr reactions of thiols with fluorinated aromatics |
| WO2014066772A1 (en) * | 2012-10-27 | 2014-05-01 | Ground Fluor Pharmaceuticals, Inc. | Processes and reagents for making diaryliodonium salts |
| CA2935856A1 (en) * | 2014-01-03 | 2015-10-01 | Nutech Ventures | Radioiodinated compounds |
| WO2015157597A1 (en) * | 2014-04-11 | 2015-10-15 | The Regents Of The University Of Michigan | Copper catalyzed [18f]fluorination of iodonium salts |
| US9181297B1 (en) | 2014-05-15 | 2015-11-10 | Massachusetts Institute Of Technology | Cysteine arylation directed by a genetically encodable π-clamp |
| US20170001957A1 (en) * | 2015-06-12 | 2017-01-05 | Nutech Ventures | Radioiodinated bioconjugation reagents |
| CN109384806B (zh) * | 2017-08-03 | 2021-04-27 | 王璐 | 一种[18f]fbpa新型制备方法 |
| JP7545813B2 (ja) * | 2019-04-24 | 2024-09-05 | 住友化学株式会社 | レジスト組成物及びレジストパターンの製造方法 |
| CN110862367A (zh) * | 2019-11-18 | 2020-03-06 | 上海兆维科技发展有限公司 | 一种香豆素芳基醚类化合物及其制备方法与应用 |
Family Cites Families (17)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPH0611718B2 (ja) * | 1986-06-26 | 1994-02-16 | 財団法人相模中央化学研究所 | 芳香族フツ素化合物の製造方法 |
| GB0115927D0 (en) * | 2001-06-29 | 2001-08-22 | Nycomed Amersham Plc | Solid-phase nucleophilic fluorination |
| GB0206117D0 (en) | 2002-03-15 | 2002-04-24 | Imaging Res Solutions Ltd | Use of microfabricated devices |
| GB0229683D0 (en) | 2002-12-20 | 2003-01-29 | Imaging Res Solutions Ltd | Preparation of radiopharmaceuticals |
| GB0320313D0 (en) | 2003-08-29 | 2003-10-01 | Ic Innovations Ltd | Process |
| GB0329716D0 (en) | 2003-12-23 | 2004-01-28 | Amersham Plc | Radical trap |
| GB0407952D0 (en) * | 2004-04-08 | 2004-05-12 | Amersham Plc | Fluoridation method |
| US20060128031A1 (en) | 2004-12-15 | 2006-06-15 | Robotti Karla M | Addressable recovery of bound analytes from an evanescent wave sensor |
| JP4931181B2 (ja) * | 2006-01-31 | 2012-05-16 | 独立行政法人放射線医学総合研究所 | １８ｆ標識フルオロベンゼン環を有する放射性リガンドの合成法 |
| PT2046396E (pt) | 2006-07-18 | 2013-12-09 | Univ Nebraska | Agentes de fluoração anidro 18f radioactivamente marcados e métodos para a sua produção e utilização |
| GB0808986D0 (en) | 2008-05-16 | 2008-06-25 | Univ Newcastle | Formation of 18F and 19F fluoroarenes bearing reactive functionalities |
| WO2010008522A2 (en) | 2008-07-14 | 2010-01-21 | The Regents Of The University Of California | Nucleophilic fluorination of aromatic compounds |
| GB0814893D0 (en) | 2008-08-14 | 2008-09-17 | Ge Healthcare Ltd | Improved fluoridation of iodonium salts |
| ES2627825T3 (es) | 2008-10-21 | 2017-07-31 | Nutech Ventures | Fluoración de sistemas de anillos aromáticos |
| US9302990B2 (en) | 2008-10-21 | 2016-04-05 | Nutech Ventures | Fluorination of aromatic ring systems |
| US8377704B2 (en) | 2009-10-20 | 2013-02-19 | Nutech Ventures | Detection and quantification of anions |
| US8546578B2 (en) | 2010-02-04 | 2013-10-01 | Nutech Ventures | Iodonium Cyclophanes for SECURE arene functionalization |
-
2009
- 2009-10-20 ES ES12185395.6T patent/ES2627825T3/es active Active
- 2009-10-20 WO PCT/US2009/061308 patent/WO2010048170A2/en not_active Ceased
- 2009-10-20 US US13/125,209 patent/US8604213B2/en active Active
- 2009-10-20 EP EP17173035.1A patent/EP3284736B1/en active Active
- 2009-10-20 EP EP12185395.6A patent/EP2537826B1/en active Active
- 2009-10-20 EP EP09822555A patent/EP2349977A4/en not_active Withdrawn
- 2009-10-20 ES ES17173035T patent/ES2861578T3/es active Active
- 2009-10-20 CA CA2741967A patent/CA2741967A1/en not_active Abandoned
- 2009-10-20 AU AU2009307715A patent/AU2009307715B2/en active Active
- 2009-10-20 JP JP2011533270A patent/JP2012506440A/ja not_active Withdrawn
-
2015
- 2015-05-27 JP JP2015107073A patent/JP6049804B2/ja active Active
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