http://rdf.ncbi.nlm.nih.gov/pubchem/patent/JP-S54106466-A

Outgoing Links

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classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D231-22
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D231-20
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D285-16
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filingDate 1978-02-06-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_e4a7685fa08d060d9f937acad819c99a
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_af875d0930b208ac2025f14d72722048
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publicationDate 1979-08-21-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber JP-S54106466-A
titleOfInvention Preparation of heterocyclic compound
abstract PURPOSE: To prepare a heterocyclic compound useful as an intermediate for medicines and pesticides, in high yield in a simple operation advantageously, by reacting safe and easily handleable acyl Medlrm's acid or its homolog with an amino compound. n CONSTITUTION: An acyl derivative of Meldrums acid of formula I: (R 1 , R 2 , and R 3 are lower alkyl groups) or its homolog is reacted with a compound of formula II: (R 4 is H, alkyl, or (un)substituted phenyl group; X is -CO-,-CS-, or -SO 2 -), hydroxylamine (hydrochloride, sulfate, etc.) or a hydrazine of the formula R 5 NH NH 2 (R 5 is the same as R 4 ) under heating or melting, and, if necessary, in an inert solvent, at room temperature to refluxing one to give a hetercyclic compound consisting of a compound of formula III, an isoxazole derivative of formula IV, or a pyrazole derivative of formula V. The raw material can be readily obtained by acylating Meldrum's acid according to the conventional method. n COPYRIGHT: (C)1979,JPO&Japio
priorityDate 1978-02-06-04:00^^<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: 30.