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assignee http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_c1c80109783a6f3a25a27e07efcecd14
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D209-52
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D333-80
filingDate 1997-05-28-04:00^^<http://www.w3.org/2001/XMLSchema#date>
grantDate 1999-06-20-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_4a1d2922cc31aadda8f51262406e6a63
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_bf8be59e12a1bca4ecf9d7aff04b71b0
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_5f80edcc1292c569da0b2a8667c4a42b
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_6a8c5f6ccca324095b56eeaf402f1129
publicationDate 1999-06-20-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber RU-2131871-C1
titleOfInvention Method of preparing 1,3-dimethyl-4,8-dialcoxy-6-r-pyrrolo(thieno)-[c]- tropilium salts
abstract FIELD: organic synthesis. SUBSTANCE: compounds of general formula I: (I) wherein Z is S, N-H, N-R (R is C 1 -C 10 -alkyl, C 1 -C 10 -alkoxy, and carbethoxy radicals); R 1 is hydrogen atom, styryl, phenyl, mono- or dihydroxyphenyl, mono- or dihydroxy-C 1 -C 10 -alkoxy, methylenedioxy, and di-C 1 -C 6 -alkylamino groups; R 2 is C 1 -C 10 =alkyl; and X is ClO 4 , HSO 4 , or Br; are prepared by heating 3,4-diacetylhexanedione (formula II: (II)) with hydrogen sulfide in acetic acid or by melting it with alkylamines, arylamines, their acetate salts, or ammonium acetate to form 2,5-dimethyl-3,4-diacetylpyrrols(thiophenes), which, in the same reactor or after intermediate isolation from reaction mixture, are brought into interaction with trialkyl-ortho-formiates and inorganic acid (to form compounds I with R 1 = H) or with aromatic aldehydes R 1 - CHO in presence of perchloric acid followed by treatment with trialkyl- ortho-formiate (to form compounds I with R 1 = styryl, or optionally substituted phenyl). Compounds I are potential biologically active compounds, which manifest high reactivity in reactions with nucleophils and can be used for production of various known and new biologically active compounds of pyrrolo(thyeno)-[C]-tropilium and azaazulene types. EFFECT: extended choice of biologically active compounds. 7 cl, 2 tbl, 21 ex
priorityDate 1997-05-28-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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