http://rdf.ncbi.nlm.nih.gov/pubchem/patent/SU-1421740-A1

Outgoing Links

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assignee http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_80a983bee27c9d7f4381e026b87db519
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D233-20
filingDate 1987-03-30-04:00^^<http://www.w3.org/2001/XMLSchema#date>
grantDate 1988-09-07-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_8ade6a37a50eafc36b8687845415f273
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_5fd79afedcdedbf696cf114547fa22ce
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_dd8a556f171dda252571b11cf2cb2bcb
publicationDate 1988-09-07-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber SU-1421740-A1
titleOfInvention Method of 2-alkylthiomethyl-2-imidazolines
abstract This invention relates to heterocyclic compounds, in particular. to obtain 2-alkylthiomep-2-imide zolines of the formula (R) -NH-C (K) N, where K is R, SCHj, and 1) K, -Rj-Hj 2) R-Rj-H; 3) .R, j - C4H9, R - H; 4), R -, R., - CH 5) R - ,, R - CH3; 6) R, -, Rj - CHj, which can be used as intermediates in organic synthesis. The goal is to get new connections in a new way. Synthesis is carried out from alkylthiochloroacetylene of the formula, where Ri is, CzH7, C4Hz, and 1,2-diamine of the formula H, jNCHR. Hg, where R-2 is H, CHe, at a ratio of 1: 2 in benzene. The method is simple to perform, the starting compounds are readily available. with s
priorityDate 1987-03-30-04:00^^<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: 25.