http://rdf.ncbi.nlm.nih.gov/pubchem/patent/PT-86821-B

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classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D405-06
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classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C02F11-00
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D257-04
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filingDate 1988-02-24-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_af649bcf471ff2fac7c1e871a139791c
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_1bf6a40fbfb4ce0d72d7cf9cb02723a4
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_af92c0fcd3eace69f0cd8edbbf87b47f
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_c9837000f182e31c17d194eb4ba2438c
publicationDate 1992-05-29-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber PT-86821-B
titleOfInvention METHOD FOR THE PREPARATION OF NEW TETRAZOLE COMPOUNDS USED AS INTERMEDIATE COMPOUNDS IN THE PREPARATION OF ANTI-HYBRESTEROLETEROLIC COMPOUNDS
abstract This invention provides novel tetrazole intermediates of the formula <IMAGE> wherein R1 and R4 each are independently hydrogen, halogen, C1-4 alkyl, C1-4 alkoxy or trifluoromethyl; R2,R3,R5 and R6 each are independently hydrogen, halogen, C1-4 alkyl or C1-4 alkoxy; B is hydrogen, C1-4 alkoxycarbonyl, CH2Y or CH2Z; Y is hydrogen, hydroxyl or X; Z is <IMAGE> X is bromo, chloro or iodo; R10 is C1-4 alkyl; and R11 is phenyl which is unsubstituted or substituted by one or two C1-4 alkyl or chloro substituents. and processes thereof which are useful for the preparation of antihypercholesterolemic agents.
priorityDate 1987-02-25-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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