http://rdf.ncbi.nlm.nih.gov/pubchem/patent/CN-102796111-B
Outgoing Links
Predicate | Object |
---|---|
assignee | http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_af121e2320f1b2cc3010325ae9e3ada6 |
classificationIPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D491-113 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A01P3-00 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A01N43-90 |
filingDate | 2012-09-10-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
grantDate | 2014-09-24-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
inventor | http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_c3d0c900264e652d02c8980013b119a9 http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_7b913e10ab7e65a629859fa012b590b8 http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_7ee71c3c244a655cd5b5ccbbcaec38aa http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_b13744dc43d89bf8ae85c31020ddb1c5 http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_140bf2c0f5ec123ad7b4e53a29df3c79 http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_548043487b438344a3101e741fe6311e http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_9e78c355fcf0259e66cf98e2ff7b3f16 http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_3ce06db8dc06e84622e8b8a58e31b295 http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_77f03526ec4141aa53343c4f77d3dba3 |
publicationDate | 2014-09-24-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
publicationNumber | CN-102796111-B |
titleOfInvention | Carboxylate (sulfonate) compounds with oxoaza-spiro-amido group, and preparation method and application thereof |
abstract | The invention discloses carboxylate (sulfonate) compounds with oxoaza-spiro-amido group, and a synthesis method and application thereof. The structure of the compounds is disclosed as the following general formula (I). The method comprises the following steps: by using piperidone hydrochloride, glycerol, aromatic acid, substituted aromatic acid, nitrogenous heterocyclic acid, substituted pyrazole acid, acyl chloride and sulfonyl chloride as raw materials, carrying out hydroxy-ketone condensation reaction to obtain an intermediate 1,4-dioxy-8-azaspiro-[4,5]decane-2-alkylmethanol, condensing with different acids to obtain spiro-alcohols containing amide structure, and reacting with acyl chloride and sulfonyl chloride to obtain the target product. The compounds have favorable anti-phytopathogen activity. The general formula (I) is shown in the specification. |
priorityDate | 2012-09-10-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
type | http://data.epo.org/linked-data/def/patent/Publication |
Incoming Links
Total number of triples: 94.