N-substituted carboxylic acid anilides, process for their preparation as well as their use as fungicides 机翻标题: 暂无翻译,请尝试点击翻译按钮。

公开号/公开日
EP0013360 A2 1980-07-23 [EP--13360]EP0013360 A3 1980-08-06 [EP--13360]EP0013360 B1 1982-04-07 [EP--13360] / 1980-07-231980-08-061982-04-07
申请号/申请日
1979EP-0105052 / 1979-12-10
发明人
PLATH, PETER, DR. DIPL.-CHEM.;EICKEN, KARL, DR. DIPL.-CHEM.;ROHR, WOLFGANG, DR. DIPL.-CHEM.;ZEEH, BERND, DR. DIPL.-CHEM.;POMMER, ERNST-HEINRICH, DR.;
申请人
BASF;
主分类号
IPC分类号
A01N-037/22A01N-043/50A01N-043/56A01N-043/653A01N-047/20A01N-047/22A01P-003/00C07C-233/07C07D-213/81C07D-213/82C07D-231/12C07D-233/61C07D-233/68C07D-249/08C07D-261/18C07D-263/34C07D-307/46C07D-307/68C07D-333/38C07D-401/12C07D-405/12C0
摘要
(EP--13360) 1. Claims (for the contracting States : BE, CH, DE, FR, GB, IT, NL, LU, SE) An N-substituted carboxanilide of the formula I see diagramm : EP0013360,P15,F3 where R**1 denotes C1 -C4 -alkyl, R**2 denotes C1 -C4 -alkyl, R**4 denotes methoxy, ethoxy, isopropoxy, phenoxy, benzyl or 1-phenylethyl or unsubstituted phenyl or phenyl monosubstituted by fluors, chloro, bromo, iodo, methyl, methoxy or nitro, or R**4 denotes -CH2 -Y, Y denoting methoxy, ethoxy, phenoxy or benzyloxy, and A denotes pyrazole, imidazole or 1,2,4-triazole attached via a nitrogen atom, and its acid addition salts. 1.  Claims (for contracting state AT) A fungicide containing an N-substituted carboxanilide of the formula I see diagramm : EP0013360,P16,F2 where R**1 denotes C1 -C4 -alkyl, R**2 denotes C1 -C4 -alkyl, R**4 denotes methoxy, ethoxy, isopropoxy, phenoxy, benzyl or 1-phenylethyl or unsubstituted phenyl or phenyl monosubstituted by fluoro, chloro, bromo, iodo, methyl, methoxy or nitro, or R**4 denotes -CH2 -Y, Y denoting methoxy, ethoxy, phenoxy or benzyloxy, and A denotes pyrazole, imidazole or 1,2,4-triazole attached via a nitrogen atom, and its acid addition salts.
机翻摘要
暂无翻译结果,您可以尝试点击头部的翻译按钮。
地址
代理人
代理机构
;
优先权号
1978DE-2854598 1978-12-18
主权利要求
(EP--13360)  1. N-Substituted Carbonsaureanilid of the Formula EMI46.1 where R Hydrogen, C1-C4-Alkyl, C1-C3-Alkoxy or Halogeneous, R Hydrogen, C1-C4-Alkyl or Halogen, R Methyl or Chlorine, R4 @@@@ oder by Halogen substituted C1-C6-Alkyl, C2-C4-Alkenyl, if necessary einfach or by Halo zen several times several times if necessary in the Phenylring substituted Styryl, C3-C6-Cycloalkyl, Benzyle or 1-Phenylathyl except Mono Halogen Acetyl mean or R if necessary by Methyl, Fluorine, Chlorine, Bromine, Iodine, Cyanogen, Nitro, Tri Fluorine Methyl, Methoxy or Methylthio, in or doubly substituted Phenyl, or one if necessary by Methyl or Halogen substituted 5 - oer 6-gliedrigen hetero-cyclic Rest with 1 or 2 Hetero Atoms means or R4 the Rest - CH2-Y or 2. Fungicide, containing a N-Substituted Carbonsaure- anilid the Formula EMI47.3 where G 1 Hydrogen, C1-C4-Alkyl, C1-C3-Alkoxy or Halogeneous, R2 Hydrogen, C1-C4-Alkyl or Halogen, R3 Methyl or Chlorine, R4 in or several times by Halogen substituted C1-C6-Alkyl, C2-C4-Alkenyl, if necessary simply or several times by Halo towards Styryl, C3-Cg-Cycloalkl, substituted in the Phenylring, Benzyle or 1-Phenylathyl except Monohalogenacethyl means or R if necessary if necessary by Methyl, Fluorine, Chlorine, Bromine, Iodine, Nitro, Tri Fluorine Methyl, Methoxy or Methylthio, in or doubly substituted Phenyl, or one if necessary by Methyl or Halogen substituted 5 - or 6-gliedrigen hetero-cyclic Rest with 1 or 2 Hetero Atoms 3. Fungicide, containing a firm or liquid Tra gerstoff and a N-Substituted Carbonsaureanilid of the Formula EMI49.1 where G 1 Hydrogen, C1-C-Alkyl, C1-C3-Alkoxy or Halogeneous, R2 Hydrogen, C1-C4-Alkyl or Halogen, R3 Methyl or Chlorine, gegebenenfalls in or several times by Halogen substituted C1-C6-Alkyl, C2-C4-Alkenyl, if necessary simply or several times by Halo towards Styryl, C3-C6-Cycloalkyl, substituted in the Phenylring, Benzyle or 1-Phenylathyl except Mono Halogen Acetyl means Lt or R if necessary by Methyl, Fluorine, Chlorine, Bromine, Iodine, Cyanogen, Nitro, Tri Fluorine Methyl, Methoxy or Methylthio, in or doubly substituted Phenyl, or one if necessary by Methyl or Halogen substituted 5 - or 6-gliedrigen heterocycllschen Rest with 1 or Hetero Atoms bedeutet or R4 the Rest - CH2-Y or EMI50.1 meant, whereby Y C1-C7-Alkoxy, C1-C4-Alkylthio, or if necessary in or several times means substituted Phenoxy or Phenylthio by Chlorine, Methyl or Tri Fluorine Methyl, or R4 the Rest - X-R5 means, whereby X Oxygen or Sulfur and R' C1-C-Alkyl, Cyclohexyl or if necessary in or several times through Fluor, Chlorine, Bromine, Tri Fluorine Methyl, Methyl, Nitro, Ethyl, Isopropyl, tert. - Buthyl, Methoxy of odeer Methylthio substituted Phenyl means, Z the Remains - CH2 - CH2 (CH2) m, EMI50.2 or EMI50.3 meant, and A means m 1 or 2 if necessary by Methyl, Ethyl, Isopropyl, Nitro, Chlorine or Bromine in or several times substi tuiertes Pyrazol, Imidazole or 1,2,8-Triazol mean and n C, 1 or 2, as well as means their Acid Addition Products and Metallsalzkom piexverbindungen. 4. '4. Verfahren for the Production a Fungicide, by the fact characterized that one a firm or a liquid Carrier Material mixes a N-Substituted with Carbonsaureanilid of the Formula EMI51.1 where G 1 Wasserstoff, C1-C4-Alkyl, C1-C3-Alkoxy or Halogeneous, R2 Hydrogen, C1-C4-Alkyl or Halogen, R Methyl or Chlorine, R4 if necessary in or several times by Halogen substituted C1-C6-Alkyl, C2-C4-Alkenyl, if necessary simply or several times by Halo towards Styryl substituted in the Phenylring, C3-C6-Cycloalkyl, Benzyle or 1-Phenylathyl except Mono Halogen Acetyl mean 4 or R if necessary by Methyl, Fluorine, Chlorine, Bromine, Iodine, Cyanogen, Nitro, Tri Fluorine Methyl, Methoxy or Methylthio, en- or doubly substituted Phenyl, or one if necessary by Methyl or Halogen substituted 5 - or 6-gliedrigen hetero-cyclic Rest with 1 or 2 Hetero Atoms means or R4 the Rest -CH2-Y or EMI51.2 meant, whereby Y means C1-C7-Alkoxy, C1-C4-Alkylthio, if necessary or in or several times by Chlorine, Methyl or Tri Fluorine Methyl substituted Phenoxy or Phenylthio, or R4 the Rest - X-R5 means, whereby X Oxygen or Sulfur and R5 C1-C6-Alkyl, Cyclohexyl or if necessary in or several times by Fluorine, Chlorine, Bromine, Tri Fluorine Methyl, Methyl, Nitro, Methyl, Isopropyl, tert. -, Z the Remains means Buthyl, Methoxy or Methylthio substituted Phenyl - CH2, EMI52.1 or EMI52.2 meant, m 1 or 2 means and A if necessary by Methyl, Athyl, Isopropyl, Nitro, Chlorine or Bromine in or several times substi tuiertes Pyrazol, Imidazole or 1,2,4-Triazol meant and n 0, 1 or 2 mean, as well as their Acid Addition Products and Metallsalzkom plexverbindungen. 5. Procedure for the Fight against Mushrooms, thus gekenn draws that one the Mushrooms or the Articles which can be protected against Fungal Attack treated with one N-Sub stituierten Carbonsaureanilid of the Formula EMI52.3 where G 1 Hydrogen, C1-C4-Alkyl, C1-C-Alkoxy or Halogen, R2 Hydrogen, C1-C4-Alkyl or Halogen, R3 Methyl or Chlorine, 14 R if necessary in or several times by Halogen substituted C1-C6-Alkyl, C2-C4-Alkenyl, if necessary simply or several times by Halo towards Styryl substituted in the Phenylring, C3-C6-Cycloalkyl, Benzyle or 1-Phenylathyl except Mono Halogen Acetyl mean or R4 if necessary by Methyl, Fluorine, Chlorine, Bromine, Iodine, Cyanogen, Nitro, Tri Fluorine Methyl, 6. Procedure for the Production one N-substituierten N-Carbonsaureanilids of the Formula EMI54.1 where G 1 Hydrogen, C1-C4-Alkyl, C1-C3-Alkoxy or Halogeneous, R3 Hydrogen, C1-C4-Alkyl or Halogen, R3 Methyl or Chlor5 gegebenenfalls in or several times by Halogen substituted C1-C6-Alkyl, C2-C4-Alkenyl, if necessary simply or several times by Halo towards Styryl substituted in the Phenylring, C3-C6-Cycloalkyl, Benzyle or 1-Phenyl2thyl except Mono Halogen Acetyl means or R if necessary by Methyl, Fluorine, Chlorine, Bromine, Iodine, Cyanogen, Nitro, Trifluormethyt, Methoxy or Methylthio, in or doubly substituted Phenyl the one if necessary by Methyl or halogeneous substituted 5 7. N-Substituted Carbonsaureanilid, manufactured GE mass the preceding Patent Claim. 8. Procedure for the Production N-Substituted Oarbonsaureanilids of the Formula EMI56.1 where R Hydrogen, C1-C4-Alkyl, C1-C3-Alkoxy or Halogen R Hydrogen, C1-C4-Alkyl or Halogen R Methyl or Chlorine.  R if necessary in or several times by Halogen substituted C1-C6-Alkyl, C2-C4-Alkenyl, if necessary simply or several times by Halo towards Styryl substituted in the Phenylring, C3-C6-Cycloalkyl, Benzyle or 1-Phenylathyl except Mono Halogen Acetyl mean 4 or R if necessary by Methyl, Fluorine, Chlorine, Bromine, Iodine, Cyanogen, Nitro, Tri Fluorine Methyl, Methoxy or Methylthio, in or doubly substituted Phenyl, or one if necessary by Methyl or Halogen substituted 5 - or 6-gliedrigen hetero-cyclic Rest with 1 or 2 Hetero Atoms means or R the Rest - CH2-Y or EMI57.1 meant, whereby Y C1-C7-Alkoxy, C1-C4-Alkylthio, means or if necessary in or several times by Chlorine, Methyl or Tri Fluorine Methyl substituted Phenoxy or Phenylthio, or R4 the Rest - X-R5 means, whereby X Oxygen or Sulfur and R5 C1-C6-Alkyl, Cyclohexyl or if necessary in or several times by Fluorine, Chlorine, Bromine, Tri Fluorine Methyl, Methyl, Nitro, Methyl, Isopropyl, tert. - Butyl, Methoxy or Nethylthio substituted Phenyl means, Z den Rest (CH2) 2- > (OH2) 3 - > EMI57.2 or EMI57.3 meant, A if necessary by Methyl, Ethyl, Isopropyl, Nitro, Chlorine or Bromine in or several times substi tuiertes Pyrazol, Imidazole or 1,2,4-Triazol meant and J n 0, 1 or 2 it means, as well as their Acid Addition Products and Metal Salt Complex Connections, by the fact characterized that one a Mol of a secondary Aniline of the Formula EMI58.1 in which R, R, R, A, Z and n indicated the above Meaning, with 1 to 1.2 Mol one Oarbonsaur= of halide of the Formula (V) at a Temperature between -10 and +1500C have converts, in which Hal Halogen, in particular Fluorine, Chlorine or Bromine means, and 4 R the Meaning indicated above hat. 9. N-Substituted Carbonsaureanilid, manufactured GE mass the preceding Patent Claim. 10. N-1,2,4-Triazolyl (1) - methyl-methoxyacetyl-2,6-di- methylanilid. 11. Funizid, containing N-1,2,4-Triazolyl (1) - methyl - methoxyacetyl-2,6-dimethylanilid.
法律状态
(EP--13360) LEGAL DETAILS FOR EP0013360  Actual or expected expiration date=1999-12-10    Legal state=DEAD    Status=EXPIRED     Event publication date=1979-12-10  Event code=EP/APP  Event indicator=Pos  Event type=Examination events  Application details  Application country=EP EP79105052  Application date=1979-12-10  Standardized application number=1979EP-0105052     Event publication date=1980-07-23  Event code=EP/A2  Event type=Examination events  Application published without search report  Publication country=EP  Publication number=EP0013360  Publication stage Code=A2  Publication date=1980-07-23  Standardized publication number=EP--13360     Event publication date=1980-07-23  Event code=EP/AK  Event indicator=Pos  Event type=Designated states  Designated contracting states: Benannte vertragsstaaten AT BE CH DE FR GB IT LU NL SE    Event publication date=1980-08-06  Event code=EP/A3  Event indicator=Pos  Event type=Examination events  Published search report  Publication country=EP  Publication number=EP0013360  Publication stage Code=A3  Publication date=1980-08-06  Standardized publication number=EP--13360     Event publication date=1980-08-06  Event code=EP/AK  Event indicator=Pos  Event type=Designated states  Designated contracting states: Benannte vertragsstaaten AT BE CH DE FR GB IT LU NL SE    Event publication date=1980-09-03  Event code=EP/17P  Event indicator=Pos  Event type=Examination events  Request for examination filed Pruefungsantrag gestellt    Event publication date=1982-04-07  Event code=EP/B1  Event indicator=Pos  Event type=Event indicating In Force  Patent specification  Publication country=EP  Publication number=EP0013360  Publication stage Code=B1  Publication date=1982-04-07  Standardized publication number=EP--13360     Event publication date=1982-04-07  Event code=EP/AK  Event indicator=Pos  Event type=Designated states  Designated contracting states: Benannte vertragsstaaten AT BE CH DE FR GB IT LU NL SE    Event publication date=1999-12-10  Event code=EP/EEDX  Event indicator=Neg  Event type=Event indicating Not In Force  Patent has expired MEMBER STATE LEGAL DETAILS FOR AT821  Actual or expected expiration date=1984-12-10    Legal state=DEAD    Status=LAPSED   Corresponding cc:  Designated or member state=AT Corresponding appl: AT79105052  Application date in the designated or member state=1979-12-10   Application number in the designated or member state=1979AT-0105052T Corresponding cc:  Designated or member state=AT Corresponding pat: AT821  Publication stage code in the designated or member state=T  Publication date in the designated or member state=1982-04-15   Publication number in the designated or member state=ATE000821    Event publication date=1982-04-07  Event code=EP/REF  Event type=Entry into national phase  Corresponds to: Corresponding cc:  Designated or member state=AT     Event publication date=1983-11-30  Event code=EP/PGFP  Event indicator=Pos  Event type=Event indicating In Force  Event type=Payment or non-payment notifications  Postgrant: annual fees paid to national office   Annual fees payment date=1983-11-30     Year of payment of annual fees=5  Corresponding cc:  Designated or member state=AT     Event publication date=1984-12-10  Event code=EP/PG25  Event indicator=Neg  Event type=Event indicating Not In Force  Event type=Payment or non-payment notifications  Lapsed in a contracting state announced via postgrant inform. from nat. office to EPO Corresponding cc:  Designated or member state=AT   Effective date of the event=1984-12-10  MEMBER STATE LEGAL DETAILS FOR BE  Actual or expected expiration date=1984-12-10    Legal state=DEAD    Status=LAPSED   Corresponding cc:  Designated or member state=BE     Event publication date=1983-12-31  Event code=EP/PGFP  Event indicator=Pos  Event type=Event indicating In Force  Event type=Payment or non-payment notifications  Postgrant: annual fees paid to national office   Annual fees payment date=1983-12-31     Year of payment of annual fees=5  Corresponding cc:  Designated or member state=BE     Event publication date=1984-12-31  Event code=EP/PG25  Event indicator=Neg  Event type=Event indicating Not In Force  Event type=Payment or non-payment notifications  Lapsed in a contracting state announced via postgrant inform. from nat. office to EPO Corresponding cc:  Designated or member state=BE   Effective date of the event=1984-12-31     Event publication date=1985-06-30  Event code=EP/BERE  Event indicator=Neg  Event type=Event indicating Not In Force  BE: Lapsed BE: Dechu Corresponding cc:  Designated or member state=BE   Effective date of the event=1984-12-10  MEMBER STATE LEGAL DETAILS FOR CH  Actual or expected expiration date=1984-12-31    Legal state=DEAD    Status=EXPIRED   Corresponding cc:  Designated or member state=CH     Event publication date=1983-11-22  Event code=EP/PGFP  Event indicator=Pos  Event type=Event indicating In Force  Event type=Payment or non-payment notifications  Postgrant: annual fees paid to national office   Annual fees payment date=1983-11-22     Year of payment of annual fees=5  Corresponding cc:  Designated or member state=CH     Event publication date=1984-12-31  Event code=EP/PG25  Event indicator=Neg  Event type=Event indicating Not In Force  Event type=Payment or non-payment notifications  Lapsed in a contracting state announced via postgrant inform. from nat. office to EPO Corresponding cc:  Designated or member state=CH   Effective date of the event=1984-12-31     Event publication date=1985-08-30  Event code=EP/REG  Event code=CH/PL  Event indicator=Neg  Event type=Event indicating Not In Force  Reference to a national code Patent ceased Loeschung/radiation/radiazion Corresponding cc:  Designated or member state=CH  MEMBER STATE LEGAL DETAILS FOR DE  Actual or expected expiration date=1984-02-15    Legal state=DEAD    Status=LAPSED   Corresponding cc:  Designated or member state=DE Corresponding appl: DE2962483    Event publication date=1982-05-19  Event code=EP/REF  Event type=Entry into national phase  Corresponds to: Corresponding cc:  Designated or member state=DE     Event publication date=1983-11-25  Event code=EP/PGFP  Event indicator=Pos  Event type=Event indicating In Force  Event type=Payment or non-payment notifications  Postgrant: annual fees paid to national office   Annual fees payment date=1983-11-25     Year of payment of annual fees=5  Corresponding cc:  Designated or member state=DE     Event publication date=1984-02-15  Event code=EP/PG25  Event indicator=Neg  Event type=Event indicating Not In Force  Event type=Payment or non-payment notifications  Lapsed in a contracting state announced via postgrant inform. from nat. office to EPO Corresponding cc:  Designated or member state=DE   Effective date of the event=1984-02-15     Event publication date=1984-04-26  Event code=DE/STCHG  Patent status changed by the national office Corresponding cc:  Designated or member state=DE  MEMBER STATE LEGAL DETAILS FOR FR  Actual or expected expiration date=1985-08-30    Legal state=DEAD    Status=LAPSED   Corresponding cc:  Designated or member state=FR     Event publication date=1983-11-24  Event code=EP/PGFP  Event indicator=Pos  Event type=Event indicating In Force  Event type=Payment or non-payment notifications  Postgrant: annual fees paid to national office   Annual fees payment date=1983-11-24     Year of payment of annual fees=5  Corresponding cc:  Designated or member state=FR     Event publication date=1985-08-30  Event code=EP/PG25  Event indicator=Neg  Event type=Event indicating Not In Force  Event type=Payment or non-payment notifications  Lapsed in a contracting state announced via postgrant inform. from nat. office to EPO Corresponding cc:  Designated or member state=FR   Effective date of the event=1985-08-30  LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES     Event publication date=1985-10-25  Event code=EP/REG  Event code=FR/ST  Event indicator=Neg  Event type=Event indicating Not In Force  Event type=Payment or non-payment notifications  Reference to a national code Notification of lapse Constatation de decheances Corresponding cc:  Designated or member state=FR  MEMBER STATE LEGAL DETAILS FOR GB  Actual or expected expiration date=1988-11-18    Legal state=DEAD    Status=LAPSED   Corresponding cc:  Designated or member state=GB     Event publication date=1985-07-31  Event code=EP/GBPC  Event indicator=Neg  Event type=Event indicating Not In Force  Event type=Payment or non-payment notifications  GB: European patent ceased through non-payment of renewal fee Corresponding cc:  Designated or member state=GB     Event publication date=1988-11-18  Event code=EP/PG25  Event indicator=Neg  Event type=Event indicating Not In Force  Event type=Payment or non-payment notifications  Lapsed in a contracting state announced via postgrant inform. from nat. office to EPO Corresponding cc:  Designated or member state=GB   Effective date of the event=1988-11-18  MEMBER STATE LEGAL DETAILS FOR IT  Actual or expected expiration date=1999-12-10    Legal state=DEAD    Status=EXPIRED   Corresponding cc:  Designated or member state=IT     Event publication date=1980-11-11  Event code=EP/ITCL  Event indicator=Pos  Event type=Entry into national phase  IT: Translation for ep claims filed IT: Deposito traduzione di rivendicazioni europee Corresponding cc:  Designated or member state=IT     Event publication date=1981-11-27  Event code=EP/ITF  Event indicator=Pos  Event type=Examination events  IT: Translation for a EP patent filed IT: Deposito traduzione di brevetto europeo Corresponding cc:  Designated or member state=IT  MEMBER STATE LEGAL DETAILS FOR LU  Actual or expected expiration date=1999-12-10    Legal state=DEAD    Status=EXPIRED   Corresponding cc:  Designated or member state=LU     Event publication date=1982-12-31  Event code=EP/PG25  Event indicator=Neg  Event type=Event indicating Not In Force  Event type=Payment or non-payment notifications  Lapsed in a contracting state announced via postgrant inform. from nat. office to EPO Corresponding cc:  Designated or member state=LU   Effective date of the event=1982-12-31  LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES     Event publication date=1983-11-30  Event code=EP/PGFP  Event indicator=Pos  Event type=Event indicating In Force  Event type=Payment or non-payment notifications  Postgrant: annual fees paid to national office   Annual fees payment date=1983-11-30     Year of payment of annual fees=5  Corresponding cc:  Designated or member state=LU  MEMBER STATE LEGAL DETAILS FOR NL  Actual or expected expiration date=1985-07-01    Legal state=DEAD    Status=LAPSED   Corresponding cc:  Designated or member state=NL     Event publication date=1983-12-01  Event code=EP/PGFP  Event indicator=Pos  Event type=Event indicating In Force  Event type=Payment or non-payment notifications  Postgrant: annual fees paid to national office   Annual fees payment date=1983-12-01     Year of payment of annual fees=5  Corresponding cc:  Designated or member state=NL     Event publication date=1985-07-01  Event code=EP/PG25  Event indicator=Neg  Event type=Event indicating Not In Force  Event type=Payment or non-payment notifications  Lapsed in a contracting state announced via postgrant inform. from nat. office to EPO Corresponding cc:  Designated or member state=NL   Effective date of the event=1985-07-01     Event publication date=1985-08-16  Event code=EP/NLV4  Event indicator=Neg  Event type=Event indicating Not In Force  Event type=Payment or non-payment notifications  NL: Lapsed or anulled due to non-payment of the annual fee NL: Vervallen wegens niet betalen van een jaarcijns Corresponding cc:  Designated or member state=NL  MEMBER STATE LEGAL DETAILS FOR SE  Actual or expected expiration date=1985-10-08    Legal state=DEAD    Status=LAPSED   Corresponding cc:  Designated or member state=SE Corresponding appl: SE79105052.9    Event publication date=1983-11-30  Event code=EP/PGFP  Event indicator=Pos  Event type=Event indicating In Force  Event type=Payment or non-payment notifications  Postgrant: annual fees paid to national office   Annual fees payment date=1983-11-30     Year of payment of annual fees=5  Corresponding cc:  Designated or member state=SE     Event publication date=1984-12-11  Event code=EP/PG25  Event indicator=Neg  Event type=Event indicating Not In Force  Event type=Payment or non-payment notifications  Lapsed in a contracting state announced via postgrant inform. from nat. office to EPO Corresponding cc:  Designated or member state=SE   Effective date of the event=1984-12-11     Event publication date=1995-01-31  Event code=EP/EUG  Event indicator=Neg  Event type=Event indicating Not In Force  SE: European patent has lapsed SE: Europeiskt patent har upphoert att gaella Corresponding cc:  Designated or member state=SE   Effective date of the event=1985-10-08
专利类型码
A2A3B1
国别省市代码
若您需要申请原文,请登录。

最新评论

暂无评论。

登录后可以发表评论

意见反馈
返回顶部