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filingDate 1982-11-26-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_7bd71d109aa57eca1f529d9f3fd685f6
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publicationDate 1984-06-06-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber JP-S5998023-A
titleOfInvention Novel preparation of 5-aryl-1h-tetrazole derivative and its intermediate
abstract PURPOSE: To obtain the titled substance useful as an intermediate for drugs inexpensively, by reacting a reaction product of a toluene derivative and N- bromosuccinimide, etc. with an alkali metal azide, etc. to give diamidomethylbenzene, decomposing it thermally. n CONSTITUTION: A compound shown by the formula I (R 1 and R 2 are H, halogen, nitro, or alkoxy) is reacted with N-bromo or chlorosuccinimide in an inert solvent (e.g., benzene, CCl 4 ) to give a compound shown by the formula II (X 1 and X 2 are Br, or Cl), which is reacted with an alkaline (earth) metal azide or ammonium azide in an inert solvent (e.g., DMF, DMSO, acetone) to give a compound shown by the formula III, which is thermally decomposed in a solvent such as DMF, acetic acid, toluene, etc. at 50W200°C in an inert gas atmosphere, to give a compound shown by the formula IV. n EFFECT: This process is economic because an inexpensive compound shown by the formula I is used as a starting raw material. n COPYRIGHT: (C)1984,JPO&Japio
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