http://rdf.ncbi.nlm.nih.gov/pubchem/patent/AR-106299-A1
Outgoing Links
| Predicate | Object |
|---|---|
| assignee | http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_d43a9787b2c506fa5fd3940c28329e87 |
| classificationCPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D401-04 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A01P3-00 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D213-70 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A01N47-40 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A01N55-00 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A01N47-02 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A01N25-00 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07F7-12 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D213-64 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A01N43-40 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D213-643 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D211-84 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D211-86 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D405-12 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07F7-0812 |
| classificationIPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A01N43-40 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A01N55-00 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A01N47-40 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D401-04 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D213-70 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D213-64 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A01N47-02 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07F7-12 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D211-86 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D211-84 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D405-12 |
| filingDate | 2016-10-07-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| inventor | http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_48da03611691d98d8b101e11eb7451ea http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_049ba274c2f45efffe233c7eafaee3ec http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_8e4940a903c676c2c27482a0919ee153 http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_56621c7920695b4c9e7627893cde30bb http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_f3cda54cb66726ba4b226e25be56a1a3 http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_2ef55378d44ed9ab4dc1c2f1300464bc http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_1a60469355d22e63f986e7dcd06131f5 http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_0a400f99dea353b67e906e26d9b8a784 |
| publicationDate | 2018-01-03-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| publicationNumber | AR-106299-A1 |
| titleOfInvention | PIRIDONA COMPOUNDS AND AGRICULTURAL AND HERTICAL FUNGICIDES CONTAINING THESE COMPOUNDS AS ACTIVE INGREDIENT |
| abstract | Claim 1: A compound represented by the formula (1) or a salt thereof, [characterized in that R¹ represents a hydroxy group, a cyano group, a C₁₋₆ alkyl group optionally substituted with substituent A, a C₁₋₆ haloalkyl group , a C₃₋₈ cycloalkyl group optionally substituted with substituent A, a C₂₋₆ alkenyl group optionally substituted with substituent A, a C₂₋₆ haloalkenyl group, a C₂₋₆ alkynyl group optionally substituted with substituent A, a haloalkynyl group C₂₋₆, a C₁₋₆ alkoxy group optionally substituted with substituent A, a C₁₋₆ haloalkoxy group, a C₃₋₈ cycloalkoxy group optionally substituted with substituent A, C₂₋₆-oxy alkenyl group optionally substituted with substituent A , a C₂₋₆-oxy haloalkenyl group, a C₃₋₆-oxy alkynyl group optionally substituted with substituent A, a C₃₋₆-oxy haloalkynyl group, or an R ⁰R¹¹N- (where R¹⁰ and R¹¹ in each represent, independently, a hydrogen atom or an alkyl C₁₋₆); R² represents a halogen atom, a hydroxy group, a cyano group, a nitro group, a C₁₋₆ alkyl group optionally substituted with the substituent B, a C₁₋₆ haloalkyl group, a C₃₋₈ cycloalkyl group optionally substituted with the substituent B, a C₂₋₆ alkenyl group optionally substituted with substituent B, a C₂₋₆ haloalkenyl group, a C₂₋₆ alkynyl group optionally substituted with substituent B, a C₂₋₆ haloalkynyl group, an optionally substituted C₁₋₆ alkoxy group with substituent B, a C₁₋₆ haloalkoxy group, a C₃₋₈ cycloalkoxy group optionally substituted with substituent B, a C₂₋₆-oxy alkenyl group optionally substituted with substituent B, a C₂₋₆-oxy haloalkenyl group, a C₃₋₆-oxy alkynyl group optionally substituted with substituent B, a C₃₋₆-oxy haloalkynyl group, a R²⁰C (= O) - (where R²⁰ represents a C₁₋ alkyl group , a C₁₋₆ haloalkyl group, a C₃₋₈ cycloalkyl group, a C₁₋₆ alkoxy group, a C₁₋₆ haloalkoxy group, a C₃₋₈ cycloalkoxy group or an R²¹R²²N- (where R²¹ and R²² each represent, of independently, a hydrogen atom, a C₁₋₆ alkyl group optionally substituted with the substituent B¹, a C₁₋₆ haloalkyl group or a C₃₋₈ or R²¹ and R²² cycloalkyl group in combination with the nitrogen atom to which they are attached form an aziridinyl group, an azetidinyl group, a pyrrolidinyl group, a piperidinyl group, a homopiperidinyl group or an azocanyl group)), an R²⁰C (= O) O- (where R²⁰ is as defined hereinbefore), a 3 to 6 member ring group containing 1 to 2 oxygen atoms, a R²³-L²- (where R²³ represents a C₁₋₆ alkyl group or a C₁₋₆ haloalkyl group and L² is S, SO or SO₂) , an R²¹R²²N- (where R²¹ and R²² are as defined were previously initiated herein), or an R²⁴C (= O) N (R²⁵) - (where R²⁴ represents a hydrogen atom, a C₁₋₆ alkyl group, a C₁₋₆ haloalkyl group, a C₃₋₈ cycloalkyl group , a C₁₋₆ alkoxy group, a C₁₋₆ haloalkoxy group, a C₃₋₈ cycloalkoxy group or an R²¹R²²N- (where R²¹ and R²² are as defined hereinbefore) and R²⁵ represents a hydrogen atom, a C₁₋₆ alkyl group optionally substituted with the substituent B¹, a C₁₋₆ haloalkyl group or a C₃₋₈ cycloalkyl group); R³ represents a hydrogen atom, a halogen atom, a nitro group, a C₁₋₆ alkyl group optionally substituted with the C substituent, a C₁₋₆ haloalkyl group, a C₃₋₈ cycloalkyl group optionally substituted with the C substituent, a C₁₋₆ alkoxy group optionally substituted with substituent C, a C₁₋₆ haloalkoxy group, a C₂₋₆ alkenyl group optionally substituted with substituent C, a C₂₋₆ haloalkenyl group, a C₂₋₆ alkynyl group optionally substituted with substituent C , a haloalkynyl group C₂₋₆, a R³⁰-L³- (where R³⁰ has the same definition as R²³ and L³ has the same definition as L²), a R³¹R³²N- (where R³¹ and R³² have the same definition as R²¹ and R²² ), or an R³³C (= O) - (where R³³ represents a C₁₋₆ alkyl group, a C₁₋₆ haloalkyl group or a C₃₋₈ cycloalkyl group); n represents an integer from 0 to 5 (provided that when n is 2 or more, the two or more R² represent independent substituents); X represents an oxygen atom or a sulfur atom; And it represents a phenyl group, a pyridyl group, a pyridazinyl group, a pyrimidinyl group, a pyrazinyl group, a triazinyl group, a tetrazinyl group, a thienyl group, a thiazolyl group, an isothiazolyl group or a thiadiazolyl group, the phenyl group is substituted with the substituent D in an ortho position and in addition it is substituted with 0 to 4 independent substituents D¹ appropriately, the pyridyl group, the pyrazinyl group, the pyrimidinyl group, the pyridazinyl group, the triazinyl group or the tetrazinyl group is substituted with substituent D in an ortho position and in addition is substituted with 0 to 3 independent substituents D¹ appropriately, the thienyl group, the thiazolyl group, the isothiazolyl group or the thiadiazolyl group is substituted with the substituent D in an ortho position and is substituted with 0 to 2 independent substituents D¹ appropriately; the link with a dotted line indicates a double bond or a single bond, the substituent A is at least one selected from the group consisting of: a hydroxy group, a cyano group, a C₃₋₈ cycloalkyl group, a C₁₋ alkoxy group ₆, a C₁₋₆ haloalkoxy group, a C₃₋₈ cycloalkoxy group, a R¹²R¹³N- (where R¹² and R¹³ each independently represent a hydrogen atom, a C₁₋₆ alkyl group, a C₁₋ haloalkyl group ₆ or a C₃₋₈ or R¹² and R¹³ cycloalkyl group in combination with the nitrogen atom to which they are attached form an aziridinyl group, an azetidinyl group, a pyrrolidinyl group, a piperidinyl group, a homopiperidinyl group or an azocanyl group) and a R¹⁴-L¹- (where R¹⁴ represents a C₁₋₆ alkyl group or a C₁₋₆ haloalkyl group and L¹ represents S, SO or SO₂); the substituent B is at least one selected from the group consisting of: a hydroxy group, a cyano group, a C₃₋₈ cycloalkyl group, a C₁₋₆ alkoxy group, a C₁₋₆ haloalkoxy group, a C₃₋₈ cycloalkoxy group, an alkoxyalkoxy group C₂₋₆, an R²¹R²²N- (where R²¹ and R²² are as defined hereinbefore), an R²³-L²- (where R²³ and L² are as defined hereinbefore), a R²⁶R²⁷R²⁸Si- (where R²⁶, R²⁷ and R²⁸ each independently represent a C alquilo alkyl group), a R²⁶R²⁷R²⁸Si- (CH₂) ₛ-O- (where s represents an integer from 1 to 3 and R²⁶ , R²⁷ and R²⁸ are as defined hereinbefore), an R²⁰C (= O) - (where R²⁰ is as defined hereinbefore) and a 3 to 6 member ring group containing 1 at 2 oxygen atoms; the substituent B¹ is at least one selected from the group consisting of: a cyano group, a C alco alkoxy group, a C₁₋₆ haloalkoxy group and a C₃₋₈ cycloalkoxy group; the substituent C is at least one selected from the group consisting of: a hydroxy group, a cyano group, a C₃₋₈ cycloalkyl group, a C₁₋₆ alkoxy group, a C₁₋₆ haloalkoxy group, a C₃₋₈ cycloalkoxy group, a R³¹R³²N- (where R³¹ and R³² have the same definition as R²¹ and R²²) and a R³⁰-L³- (where R³⁰ has the same definition as R¹⁴ and L³ has the same definition as L¹); the substituent D is at least one selected from the group consisting of: a halogen atom, a C₁₋₆ alkyl group, a C₁₋₆ haloalkyl group, a C₁₋₆ alkoxy group and a C₁₋₆ haloalkoxy group; and the substituent D¹ is at least one selected from the group consisting of: a hydroxy group, a halogen atom, a C₁₋₆ alkyl group, a C₁₋₆ haloalkyl group, a C₃₋₈ cycloalkyl group, a C₁₋ alkoxy group ₆, a C₁₋₆ haloalkoxy group and a C₃₋₈ cycloalkoxy group.] |
| priorityDate | 2015-10-09-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| type | http://data.epo.org/linked-data/def/patent/Publication |
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Total number of triples: 52.