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filingDate 2000-07-08-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_e09586e32bc8970923e7457aa9abe8d8
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_0acb8e30f974a31a8a3b85825645d408
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_b103d8824651bf6eba16817e84856ae7
publicationDate 2002-12-28-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber HU-0201939-A2
titleOfInvention 1,4,5,6-Tetrahydro-pyrimidine derivative with a vitronectin inhibitory activity, a method for its preparation, a pharmaceutical composition comprising it and the intermediates of the compound
abstract The present invention relates to ethyl (2S) -2- (naphthalene-1-sulfonylamino) -3- (4- (2- (1,4,5,6-tetrahydropyrimidin-2-ylcarbamoyl) ethyl) formula (I). ) ethyl ethyl benzoylamino) propionate hemifumarate. The present invention relates to the preparation of an abase comprising 4- (2- (1,4,5,6-tetrahydropyrimidin-2-ylcarbamoyl) ethyl) benzoic acid or a derivative thereof and ethyl (2S) -3-amino- 2- (Naphthalene-1-sulfonylamino) -propionate is reacted. The compound of formula (I) is a valuable drug that can be used, for example, to treat or prevent diseases that can be affected by inhibition of the vitronectin receptor, in particular acne diseases, e.g. osteoporosis. The invention also relates to chemical intermediates of formula (XIII) and (XV) useful in the preparation of a compound of formula (I), wherein Y is a chlorine or bromine atom or a hydroxyl group. SHE
priorityDate 1999-07-21-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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