http://rdf.ncbi.nlm.nih.gov/pubchem/patent/ES-2608628-T3

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classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07F7-10
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classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07F7-08
filingDate 2013-08-05-04:00^^<http://www.w3.org/2001/XMLSchema#date>
grantDate 2017-04-12-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_f5c0dc537d5acb763da08f795d4ee0fa
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_ecf5b777ebfd8e646082c3fb2ffb316e
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publicationDate 2017-04-12-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber ES-2608628-T3
titleOfInvention Procedure for the preparation of heterocyclic ester derivatives
abstract A process for the preparation of a compound of formula (I) ** Formula ** in which A1 is selected from the group consisting of C1-3alkyl; where ** Formula ** is selected from the group consisting of ** Formula ** and ** Formula ** in which each R 4 is independently selected from the group consisting of H, F, Cl, Br, I, -OH , -OCH3, - OCH2CH3, -SC (1-4) alkyl, -SOC (1-4) alkyl, -SO2C (1-4) alkyl, -C (1-3) alkyl, -CO2Rd, -CONReRf, - CCRg, and -CN; and wherein Rd is selected from the group consisting of hydrogen and -C (1-3) alkyl; Re is selected from the group consisting of H and -C (1-3) alkyl; Rf is selected from the group consisting of H and -C (1-3) alkyl; and Rg is selected from the group consisting of H, -CH2OH and -CH2CH2OH; or a pharmaceutically acceptable salt thereof; that includes
priorityDate 2012-08-07-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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