http://rdf.ncbi.nlm.nih.gov/pubchem/patent/EP-0469685-A1

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classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D239-04
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D239-06
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classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A01N43-54
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A01N43-90
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D239-14
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D239-06
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D239-18
filingDate 1991-07-29-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_1eb212bd081b0ea26ac20de94bbfc883
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_41c041c163b37140a78b8c6097f9d4d5
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_f154cbff28174204504314993f5846ea
publicationDate 1992-02-05-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber EP-0469685-A1
titleOfInvention Tetrahydropyrimidine derivatives
abstract The invention provides a fungicidal composition comprising a carrier and, as active ingredient, certain tetrahydropyrimidine derivatives of the general formulan or an acid-addition salt or metal salt complex thereof, in which n is 0, 1, 2 or 3; R represents an optionally substituted alkyl, aryl or aralkyl group; R 1 represents a hydrogen atom or an optionally substituted alkyl or aralkyl group; R 2 represents an optionally substituted aryl group; p is 0 or 1; X represents a group -NR 3- or -NR 3- NR 3- where each R 3 independently represents a hydrogen atom or an optionally substituted alkyl, aryl or aralkyl group or R 1 and (X)p-A-R 2 together represent a group -(CR 4 R 5 ) q -N(A-R 2 )- where q is 2 or 3 and each of R 4 and R 5 is independently selected from a group consisting of hydrogen atoms and optionally substituted alkyl groups; and A represents a group -(CR 6 R 7 ) m - where m is 0, 1, 2, 3 or 4 and each of R 6 and R 7 is independently selected from a group consisting of hydrogen atoms and optionally substituted alkyl groups with the provisos thatn (i) when p is 1, X is NH, m is 0, R 1 is H and n is 0 then R 2 is not a naphthyl group, a phenyl group substituted at the 4-position by a cyclohexyl, C 4 - 12 alkyl, C 6 - 12 alkoxy, C 4 - 8 alkylthio, (C 6 - 8 alkoxy)carbonyl, 4-methylphenylthio, 4-chlorophenylthio, benzyl, phenylethyl or dibutylamino group, a phenyl group substituted at the 3-position by a hexylthio group or a phenyl group substituted at the 3- and 4-position by a -(CH 2 ) 4 - group; (ii) when p is 1, X is NH, m is 0, R 1 is CH 3 and n is 0 then R 2 is not a phenyl group substituted at the 4- position by a cyclohexyl or C 4-6 alkyl group; and (iii) when p is 1, X is NH, m is 0, R 1 is H, n is 2 and R is 5,5-dimethyl then R 2 is not a phenyl group substituted at the 4-position by a cyclohexyl group; and their use as fungicides. Certain of the tetrahydropyrimidine derivatives are novel and a process for the preparation of these compounds is also provided.
isCitedBy http://rdf.ncbi.nlm.nih.gov/pubchem/patent/WO-2011085170-A1
http://rdf.ncbi.nlm.nih.gov/pubchem/patent/JP-2013516483-A
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priorityDate 1990-07-31-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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