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assignee http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_b502fde933db1d6126d10bbcbddb83ea
classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D277-74
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D249-12
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D277-74
filingDate 1992-10-05-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_755aa963fff277d4b6f48cbb7fa94c84
publicationDate 1994-04-07-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber DE-4233397-A1
titleOfInvention Process for the preparation of omega-acylaminoalkylthio compounds
abstract Prodn. of acylamino-alkylthio cpds. of formula (I) comprises reacting a 2-oxazoline or 5,6-dihydro-4H-1,3-oxazine of formula (II) with an equimolar amt. of a mercapto cpd. of formula XSH (III) at elevated temp.: R is 1-21C alkyl, 2-21C alkenyl or Ph; R1-R4 are H, 1-8C alkyl, 2-21C alkenyl or Ph; Z is a direct bond or CR5R6; R5 and R6 are H, Me or Et; X is (CR7R'7)nCOOR8, C(R9)=NY or a C-bonded heterocyclic gp., opt. fused with other aromatic rings; R7 and R'7 are H or 1-4C alkyl; n is 1-4; R8 is H or 1-22C alkyl; R9 is 1-6C alkyl, Ph or NH2; Y is H, 1-12C alkyl or Ph. USE/ADVANTAGE - (I) are useful as antimicrobial agents (claimed), antiparasitic agents and radiodiagnostic agents for kidney imaging. The process gives high yields (mostly above 80%), even when R is higher alkyl.
priorityDate 1992-10-05-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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