http://rdf.ncbi.nlm.nih.gov/pubchem/patent/US-3657229-A

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classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D233-22
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http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/B01J27-00
filingDate 1968-05-02-04:00^^<http://www.w3.org/2001/XMLSchema#date>
grantDate 1972-04-18-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_853506b45de3d56e44eb379b5d222913
publicationDate 1972-04-18-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber US-3657229-A
titleOfInvention 1 3-diaza-2 3-cycloalkene derivatives
abstract 2-(A-(LOWER-ALKOXY) BENZYL) -2-IMIDZOLINES,-1,4,5,6TETRAHYDROPYRIMIDINES AND -4,5,6,7-TETRAHYDRO-1H-1,3-DIAZEPINES, HAVING PHARMACOLOGICAL PROPERTIES, E.G., HYPOGLYCEMIC, DIURETIC, ANTI-INFLAMMATORY, ARE PREPARED BY HEATING A 2-(LOWER-ALKOXY)-2-PHENYLALKANENITRILE WITH AN ALKANEDIAMINE, WHEREIN 2,3 OR 4 CARBON ATOMS, RESPECTIVELY INTERVENE BETWEEN THE TWO AMINO GROUPS, IN THE PRESENCE OF A CATALYTIC AMOUNT OF CARBON DISULFIDE OR HYDROGEN SULFIDE. THE INTERMEDIATE 2-(LOWER-ALKOXY)-2PHENYLALKANENITRILES ARE PREPARED PREFERABLY BY FIRST REACTING A BENZALDEHYDE WITH A TRI-(LOWER-ALKYL) ORTHOFORMATE TO FORM THE ALDEHYDE DI-(LOWER-ALKYL) ACETAL, REACTING THE LATTER WITH AN ACYL HALIDE TO FORM THE CORRESPONDING AHALOBENZYL LOWER-ALKYL ETHER AND REACTING SAID ETHER WITH AN ALKALI CYANIDE TO YIELD SAID INTERMEDIATE NITRILE.
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http://rdf.ncbi.nlm.nih.gov/pubchem/patent/US-3996207-A
http://rdf.ncbi.nlm.nih.gov/pubchem/patent/US-4260626-A
priorityDate 1968-05-02-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID419548762
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID71444885
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID431932144
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http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID419588938
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID419519637
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID451245303
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID431923961
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http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID424468465
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID415887006
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http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID426194970
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID81770
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http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID33643
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID415834942
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID454263208
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID432589
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID8929
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID75469
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID6348
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID6451252
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID158922606
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http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID521998
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID3744783
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID432453620
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http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID420292159
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http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID422925159
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID6340
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID420910461
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID78109
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID56229
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID7841
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http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID419566143
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Total number of triples: 356.